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    <title>Recent uci_som_derm items</title>
    <link>https://escholarship.org/uc/uci_som_derm/rss</link>
    <description>Recent eScholarship items from Department of Dermatology</description>
    <pubDate>Wed, 24 Jun 2026 02:42:08 +0000</pubDate>
    <item>
      <title>Collagen remodeling in murine melanoma therapy response through second-harmonic generation imaging</title>
      <link>https://escholarship.org/uc/item/7rr7g0s2</link>
      <description>The study by Heaton et al. marks a significant advancement in understanding the role of collagen remodeling within the melanoma tumor microenvironment during immunotherapy. Using in vivo second-harmonic generation imaging, the authors quantitatively tracked dynamic changes in collagen morphology in a preclinical melanoma model, revealing a shift toward a healthier phenotype associated with treatment. These findings enhance our understanding of tumor extracellular matrix dynamics and highlight the potential of optical imaging technologies to guide and optimize cancer immunotherapy. This commentary will explore these findings, contextualize them within the broader field of tumor immunology, and discuss their implications for improving immunotherapy strategies in melanoma and other cancers.</description>
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      <pubDate>Mon, 16 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>Label-free human skin imaging with enhanced molecular contrast via time-resolved fluorescence and advanced phasor analysis</title>
      <link>https://escholarship.org/uc/item/15r1d639</link>
      <description>Current state-of-the-art clinical skin imaging using label-free multiphoton microscopy (MPM) faces challenges due to limited molecular specificity, which hampers the accurate characterization of skin tissues because of overlapping fluorescence signals from multiple molecular components. In this study, we present a novel approach to enhance molecular contrast in MPM clinical skin imaging by leveraging advanced strategies to effectively unmix the various endogenous fluorophores present in the skin with the performance capabilities of a recently developed imaging platform for in vivo time-resolved fluorescence imaging of human skin. By identifying phasor positions of key endogenous skin fluorophores – such as keratin, melanin, free NADH, and protein-bound NADH – we effectively perform multicomponent unmixing in different skin types and conditions, including those with varying levels of pigmentation and metabolic states. The phasor analysis allows for the mapping and quantification...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/15r1d639</guid>
      <pubDate>Mon, 26 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ranjit, Suman</name>
      </author>
      <author>
        <name>Torrado, Belen</name>
      </author>
      <author>
        <name>Vallmitjana, Alexander</name>
      </author>
      <author>
        <name>Durkin, Amanda Fedyk</name>
        <uri>https://orcid.org/0000-0001-9880-7651</uri>
      </author>
      <author>
        <name>Dvornikov, Alexander</name>
      </author>
      <author>
        <name>Ganesan, Anand</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>Treatment preferences by disease severity in alopecia areata: A cross-sectional survey study</title>
      <link>https://escholarship.org/uc/item/0p28108q</link>
      <description>Treatment preferences by disease severity in alopecia areata: A cross-sectional survey study</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0p28108q</guid>
      <pubDate>Mon, 26 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Biba, Ursula</name>
      </author>
      <author>
        <name>Sanchez, Katherine</name>
      </author>
      <author>
        <name>Gregoire, Samantha</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Waldman, Monique</name>
      </author>
      <author>
        <name>Anderson, Lisa</name>
      </author>
      <author>
        <name>Mostaghimi, Arash</name>
      </author>
    </item>
    <item>
      <title>Consensus guidelines for cellular label-free optical metabolic imaging: ensuring accuracy and reproducibility in metabolic profiling</title>
      <link>https://escholarship.org/uc/item/6m95q5zb</link>
      <description>Significance: Cellular metabolism plays a central role in health and disease, making its study critical for advancing diagnostics and therapies. Label-free optical metabolic imaging using endogenous fluorescence from reduced nicotinamide adenine dinucleotide (phosphate) [NAD(P)H] and flavin adenine dinucleotide (FAD) provides nondestructive, high-resolution insights into metabolic function and heterogeneity from the sub-cellular to the tissue level. Standardized approaches are essential to ensure reproducibility and comparability across studies.
Aim: We aim to establish a consensus framework for the acquisition, calibration, and reporting of microscopic imaging metabolic function assessments based on fluorescence intensity and lifetime measurements of NAD(P)H and FAD.
Approach: We present best practices for calibrating, analyzing, and reporting fluorescence intensity-based optical redox ratios and fluorescence lifetime data using multiexponential fitting and phasor analysis. Guidelines...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6m95q5zb</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Georgakoudi, Irene</name>
      </author>
      <author>
        <name>Skala, Melissa C</name>
      </author>
      <author>
        <name>Quinn, Kyle P</name>
      </author>
      <author>
        <name>Stringari, Chiara</name>
      </author>
      <author>
        <name>Sorrells, Janet E</name>
      </author>
      <author>
        <name>Heikal, Ahmed A</name>
      </author>
      <author>
        <name>Li, Lin Z</name>
      </author>
      <author>
        <name>Xu, He N</name>
      </author>
      <author>
        <name>You, Sixian</name>
      </author>
      <author>
        <name>Walsh, Alex J</name>
      </author>
      <author>
        <name>Datta, Rupsa</name>
      </author>
      <author>
        <name>Samimi, Kayvan</name>
      </author>
      <author>
        <name>Gillette, Amani A</name>
      </author>
      <author>
        <name>Eliceiri, Kevin W</name>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Boppart, Stephen A</name>
      </author>
      <author>
        <name>Digman, Michelle A</name>
        <uri>https://orcid.org/0000-0003-4611-7100</uri>
      </author>
      <author>
        <name>Dunning, Kylie R</name>
      </author>
      <author>
        <name>Evans, Conor L</name>
      </author>
      <author>
        <name>Garcia, Alba Alfonso</name>
      </author>
      <author>
        <name>Houston, Jessica P</name>
      </author>
      <author>
        <name>Hwang, Wonsang</name>
      </author>
      <author>
        <name>Lindley, Matthew M</name>
      </author>
      <author>
        <name>Li, Xingde</name>
      </author>
      <author>
        <name>Liu, Zhiyi</name>
      </author>
      <author>
        <name>Marcu, Laura</name>
        <uri>https://orcid.org/0000-0003-2369-0748</uri>
      </author>
      <author>
        <name>Murugkar, Sangeeta</name>
      </author>
      <author>
        <name>Nichols, Michael G</name>
      </author>
      <author>
        <name>Niesner, Raluca</name>
      </author>
      <author>
        <name>Parekh, Sapun H</name>
      </author>
      <author>
        <name>Rajaram, Narasimhan</name>
      </author>
      <author>
        <name>Ranjit, Suman</name>
      </author>
      <author>
        <name>Shen, Keyue</name>
      </author>
      <author>
        <name>Shi, Lingyan</name>
        <uri>https://orcid.org/0000-0003-1373-3206</uri>
      </author>
      <author>
        <name>Torrado, Belén</name>
      </author>
      <author>
        <name>Vallmitjana, Alexander</name>
      </author>
      <author>
        <name>Wang-Evers, Michael</name>
      </author>
      <author>
        <name>Zemp, Roger</name>
      </author>
    </item>
    <item>
      <title>Currently managed US prevalence of cutaneous venous malformations (cVMs): a nationally representative, retrospective, real-world, subject-blinded, physician-observational probability study</title>
      <link>https://escholarship.org/uc/item/9g09s6mj</link>
      <description>BackgroundCutaneous venous malformations (cVMs) are rare vascular anomalies characterized by progressive vessel ectasia, leading to disfigurement, pain, ulceration, and bleeding. These lesions often evade early detection and are notoriously difficult to treat due to the limited dermal bioavailability of systemic therapies. Unlike deep venous malformations, cVMs present unique management challenges and currently lack FDA-approved treatments. To address the paucity of epidemiologic data, we conducted a nationally representative, blinded, real-world observational probability&amp;nbsp;study to estimate the annual treatment prevalence of cVM in the United States.A geographically representative sample of dermatologists, hematologist-oncologists, pediatricians, radiologists, and vascular surgeons was recruited via blinded invitations. Participants self-reported the number of cVM patients treated in the prior 12&amp;nbsp;months. Estimates were adjusted for comanagement to calculate the national...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9g09s6mj</guid>
      <pubDate>Fri, 17 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gallagher, Jack Ray</name>
      </author>
      <author>
        <name>Carroll, Susan</name>
      </author>
      <author>
        <name>Martini, Jeffrey</name>
      </author>
      <author>
        <name>Kelly, Michael</name>
      </author>
      <author>
        <name>Buethe, Maria Gnarra</name>
      </author>
    </item>
    <item>
      <title>Label-free multiphoton microscopy of human skin: longitudinal studies capturing cell dynamics</title>
      <link>https://escholarship.org/uc/item/9dg9r03p</link>
      <description>This study presents recent advances in an imaging platform developed by our lab, the fast large area multiphoton exoscope (FLAME), a microscope designed for clinical skin imaging. Its dual-scanning modality enables reliable, cellular-scale imaging of the same skin locations over extended time periods across areas up to 1 cm&lt;sup&gt;2&lt;/sup&gt;. Enabling fluorescence lifetime imaging microscopy, this device, for the first time &lt;i&gt;in vivo&lt;/i&gt;, allows detailed longitudinal tracking of cellular dynamics in human skin, such as responses to injury, significantly advancing the capabilities of dermatological research. By overcoming previous limitations in large-area, high-resolution skin imaging, FLAME opens new opportunities for monitoring therapy responses, tracking cellular dynamics, and understanding skin biology at the cellular level.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9dg9r03p</guid>
      <pubDate>Wed, 1 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Vallmitjana, Alexander</name>
      </author>
      <author>
        <name>Durkin, Amanda</name>
      </author>
      <author>
        <name>Dvornikov, Alexander</name>
      </author>
      <author>
        <name>Torrado, Belén</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Shiu, Jessica</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>Fast large-area multiphoton exoscope for label-free in vivo imaging of immune cells in human skin</title>
      <link>https://escholarship.org/uc/item/8952x5pf</link>
      <description>Fast large-area multiphoton exoscope for label-free in vivo imaging of immune cells in human skin</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8952x5pf</guid>
      <pubDate>Wed, 1 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Torrado, Belen</name>
      </author>
      <author>
        <name>Ranjit, Suman</name>
      </author>
      <author>
        <name>Durkin, Amanda</name>
      </author>
      <author>
        <name>Vallmitjana, Alexander</name>
      </author>
      <author>
        <name>Wakida, Nicole</name>
      </author>
      <author>
        <name>Hinchee-Rodriguez, Kathryn</name>
      </author>
      <author>
        <name>Shiu, Jessica</name>
      </author>
      <author>
        <name>Ganesan, Anand N</name>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>Minoxidil as a treatment for onychodystrophy: a systematic review</title>
      <link>https://escholarship.org/uc/item/9xj6s292</link>
      <description>Minoxidil as a treatment for onychodystrophy: a systematic review</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9xj6s292</guid>
      <pubDate>Tue, 5 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Thiagarajan, Anagha B</name>
      </author>
      <author>
        <name>Woll, Jack P</name>
      </author>
      <author>
        <name>Hirpara, Milan M</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Horton, Luke</name>
      </author>
    </item>
    <item>
      <title>CDC42-effector interaction inhibitors alter patterns of vessel arborization in skin and tumors in vivo</title>
      <link>https://escholarship.org/uc/item/6112t5qh</link>
      <description>Skin tumors require a vascular supply to grow beyond 1 mm in depth, yet existing anti-angiogenesis agents are largely ineffective at treating melanoma tumors arising in skin. Using an approach that integrates antibody infusion, optical tissue clearing, multiphoton imaging, and vessel tracing, we identified the CDC42 GTPase RhoJ as a critical regulator of skin vessel arborization. Small molecules that target both RhoJ and CDC42 (CDC42 interaction inhibitors), but not those that target only CDC42 (CASIN), inhibit vessel branching in mouse skin &lt;i&gt;in vivo&lt;/i&gt; and vascular organoids &lt;i&gt;in vitro&lt;/i&gt;. This anti-vascular effect was not limited to skin, as CDC42 interaction inhibitors blocked melanoma tumor vascularization and inhibited tumor growth to a similar degree as Braf inhibitors. Taken together, this work identifies small molecules that target RhoJ as selective tumor anti-vascular agents. RhoJ-targeting drugs have a particular proclivity for blocking skin vascularization, nominating...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6112t5qh</guid>
      <pubDate>Tue, 5 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Vuong, Linh M</name>
      </author>
      <author>
        <name>Hachey, Stephanie</name>
      </author>
      <author>
        <name>Shiu, Jessica</name>
      </author>
      <author>
        <name>Xie, Danny F</name>
      </author>
      <author>
        <name>Salvador, Noel</name>
      </author>
      <author>
        <name>Brindani, Nicoletta</name>
      </author>
      <author>
        <name>Bertozzi, Sine Mandrup</name>
      </author>
      <author>
        <name>Summa, Maria</name>
      </author>
      <author>
        <name>Bertorelli, Rosalia</name>
      </author>
      <author>
        <name>Armirotti, Andrea</name>
      </author>
      <author>
        <name>Pham, Rachel</name>
      </author>
      <author>
        <name>Ku, Vance SH</name>
      </author>
      <author>
        <name>Limbekar, Swara D</name>
      </author>
      <author>
        <name>Nguyen, Terry</name>
      </author>
      <author>
        <name>Choi, Bernard</name>
        <uri>https://orcid.org/0000-0002-4380-8291</uri>
      </author>
      <author>
        <name>Hughes, Christopher CW</name>
      </author>
      <author>
        <name>De Vivo, Marco</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
    </item>
    <item>
      <title>Statement from the frontal fibrosing alopecia international expert alliance: SOFFIA 2024</title>
      <link>https://escholarship.org/uc/item/49f829tj</link>
      <description>BACKGROUND: As the incidence of frontal fibrosing alopecia (FFA) continues to rise, there is a need for an optimal treatment algorithm for FFA.
OBJECTIVE: To produce an international consensus statement on the treatment modalities and prognostic indicators of FFA.
METHODS: Sixty-nine hair experts from six continents were invited to participate in a three-round Delphi process. The final stage was held as a virtual meeting facilitated via Zoom. The consensus threshold was set at ≥66%.
RESULTS: Of 365 questions, expert consensus was achieved in 204 (56%) questions following completion of the three rounds. Three additional questions were included at the final meeting. The category with the strongest consensus agreement was disease monitoring (9; 100%). Questions pertaining to physical therapies achieved the least category consensus (15; 40%), followed by systemic therapy (45; 43%).
LIMITATIONS: The study lacked sufficient representation from Africa and South America.
CONCLUSION: SOFFIA...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/49f829tj</guid>
      <pubDate>Tue, 5 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Meah, Nekma</name>
      </author>
      <author>
        <name>Li, Jane</name>
      </author>
      <author>
        <name>Wall, Dmitri</name>
      </author>
      <author>
        <name>York, Katherine</name>
      </author>
      <author>
        <name>Bhoyrul, Bevin</name>
      </author>
      <author>
        <name>Bokhari, Laita</name>
      </author>
      <author>
        <name>Coulthard, Lachlan</name>
      </author>
      <author>
        <name>Asfour, Leila</name>
      </author>
      <author>
        <name>Abraham, Leonardo Spagnol</name>
      </author>
      <author>
        <name>Asz‐Sigall, Daniel</name>
      </author>
      <author>
        <name>Bergfeld, Wilma F</name>
      </author>
      <author>
        <name>Betz, Regina C</name>
      </author>
      <author>
        <name>Blume‐Peytavi, Ulrike</name>
      </author>
      <author>
        <name>Callender, Valerie</name>
      </author>
      <author>
        <name>Chitreddy, Vijaya</name>
      </author>
      <author>
        <name>Combalia, Andrea</name>
      </author>
      <author>
        <name>Cotsarelis, George</name>
      </author>
      <author>
        <name>Craiglow, Brittany</name>
      </author>
      <author>
        <name>Dhurat, Rachita</name>
      </author>
      <author>
        <name>Dlova, Ncoza</name>
      </author>
      <author>
        <name>Donovan, Jeff</name>
      </author>
      <author>
        <name>Doroshkevich, Andrei</name>
      </author>
      <author>
        <name>Eisman, Samantha</name>
      </author>
      <author>
        <name>Farrant, Paul</name>
      </author>
      <author>
        <name>Gadzhigoroeva, Aida</name>
      </author>
      <author>
        <name>Green, Jack</name>
      </author>
      <author>
        <name>Grimalt, Ramon</name>
      </author>
      <author>
        <name>Harries, Matthew</name>
      </author>
      <author>
        <name>Hordinsky, Maria</name>
      </author>
      <author>
        <name>Irvine, Alan D</name>
      </author>
      <author>
        <name>Jolliffe, Victoria</name>
      </author>
      <author>
        <name>Kaiumov, Spartak</name>
      </author>
      <author>
        <name>King, Brett</name>
      </author>
      <author>
        <name>Kossard, Steven</name>
      </author>
      <author>
        <name>Lee, Joyce</name>
      </author>
      <author>
        <name>Lee, Won‐Soo</name>
      </author>
      <author>
        <name>Lortkipanidze, Nino</name>
      </author>
      <author>
        <name>McMichael, Amy</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha Atanaskova</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Messenger, Andrew</name>
      </author>
      <author>
        <name>Mirmirani, Paradi</name>
      </author>
      <author>
        <name>Olsen, Elise</name>
      </author>
      <author>
        <name>Orlow, Seth J</name>
      </author>
      <author>
        <name>Ovcharenko, Yuliya</name>
      </author>
      <author>
        <name>Piraccini, Bianca Maria</name>
      </author>
      <author>
        <name>Pirmez, Rodrigo</name>
      </author>
      <author>
        <name>Rakowska, Adriana</name>
      </author>
      <author>
        <name>Reygagne, Pascal</name>
      </author>
      <author>
        <name>Roberts, Janet</name>
      </author>
      <author>
        <name>Rudnicka, Lidia</name>
      </author>
      <author>
        <name>Saceda‐Corralo, David</name>
      </author>
      <author>
        <name>Shapiro, Jerry</name>
      </author>
      <author>
        <name>Sharma, Pooja</name>
      </author>
      <author>
        <name>Silyuk, Tatiana</name>
      </author>
      <author>
        <name>Suchonwanit, Poonkiat</name>
      </author>
      <author>
        <name>Takwale, Anita</name>
      </author>
      <author>
        <name>Tosti, Antonella</name>
      </author>
      <author>
        <name>Visser, WI</name>
      </author>
      <author>
        <name>Vañó‐Galván, Sergio</name>
      </author>
      <author>
        <name>Vogt, Annika</name>
      </author>
      <author>
        <name>Wade, Martin</name>
      </author>
      <author>
        <name>Yip, Leona</name>
      </author>
      <author>
        <name>Zlotogorski, Abraham</name>
      </author>
      <author>
        <name>Zhou, Cheng</name>
      </author>
      <author>
        <name>Sinclair, Rodney</name>
      </author>
    </item>
    <item>
      <title>Uncovering minimal pathways in melanoma initiation</title>
      <link>https://escholarship.org/uc/item/3w50b46j</link>
      <description>Melanomas are genetically heterogeneous, displaying mitogen-activated protein kinase mutations and homozygous loss of tumor suppressor genes. Mouse models combining such mutations produce fast-growing tumors. In contrast, rare, slow-growing tumors arise in mice combining Braf activation with heterozygous loss of Pten. Here we show that similar tumors can arise in albino mice bearing only a Braf mutation. Incidence kinetics suggest a stochastic event underlies tumorigenesis in tumors that arise with only a Braf mutation, yet de novo mutations or structural variants that could explain the incidence of most tumors could not be found. Single-cell transcriptomics of tumors identify a cell type resembling “neural crest-like” cells in human and mouse melanomas. These exist in normal mouse skin, expand upon Braf activation, and persist through serial transplantation; analyses of gene expression suggest they serve as precursors of malignant cells. This state may serve as an intermediate...</description>
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      <pubDate>Tue, 5 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Xiao, Hui</name>
      </author>
      <author>
        <name>Shiu, Jessica</name>
      </author>
      <author>
        <name>Chen, Chi-Fen</name>
      </author>
      <author>
        <name>Wu, Jie</name>
      </author>
      <author>
        <name>Zhou, Peijie</name>
      </author>
      <author>
        <name>Telang, Sahil S</name>
      </author>
      <author>
        <name>Ruiz-Vega, Rolando</name>
      </author>
      <author>
        <name>Edwards, Robert A</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Lander, Arthur D</name>
        <uri>https://orcid.org/0000-0002-4380-5525</uri>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
    </item>
    <item>
      <title>Increasing baricitinib accessibility through prescription discounts</title>
      <link>https://escholarship.org/uc/item/2xs6d2m0</link>
      <description>Increasing baricitinib accessibility through prescription discounts</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2xs6d2m0</guid>
      <pubDate>Tue, 5 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Woll, Jack</name>
      </author>
      <author>
        <name>Hirpara, Milan</name>
      </author>
      <author>
        <name>Kincaid, Colin</name>
      </author>
      <author>
        <name>Di Tomasso, Pamela Maree</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Isotretinoin Effects on Nasal Contouring: The Role of Facial Landmark Detection Technology</title>
      <link>https://escholarship.org/uc/item/9kt6153d</link>
      <description>Isotretinoin Effects on Nasal Contouring: The Role of Facial Landmark Detection Technology</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9kt6153d</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hirpara, Milan M</name>
      </author>
      <author>
        <name>Woll, Jack</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Autologous cell harvesting device provides repigmentation and improves quality-of-life for patients with stable vitiligo lesions in a large and diverse patient population</title>
      <link>https://escholarship.org/uc/item/8qt702bk</link>
      <description>INTRODUCTION: The mental health burden associated with vitiligo can significantly impact patients' quality-of-life. Although successful for repigmentation of stable vitiligo, adoption of surgical melanocyte transplantation remains limited due to time and skilled-expertise requirements. A cell harvesting device prepares autologous skin cell suspension (ASCS) at point of care, simplifying the process.
OBJECTIVE: To confirm early and favorable repigmentation response and evaluate health-related quality-of-life changes following ASCS treatment of stable vitiligo.
METHODS: In this large (N = 107), prospective, multicenter study, vitiligo lesions were laser-ablated and received ASCS treatment followed by at-home phototherapy.
RESULTS: All Fitzpatrick skin types and major vitiligo subtypes were represented. Excellent repigmentation response (≥80%) was observed by week 4. By week-24, all lesions demonstrated improvement; 67% achieved &amp;gt;50% repigmentation, 42% achieved ≥80% repigmentation,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8qt702bk</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pandya, Amit G</name>
      </author>
      <author>
        <name>Mahmoud, Bassel H</name>
      </author>
      <author>
        <name>Huggins, Richard H</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Silverberg, Nanette B</name>
      </author>
      <author>
        <name>Munavalli, Girish</name>
      </author>
      <author>
        <name>Weiss, Eduardo</name>
      </author>
      <author>
        <name>Zubair, Raheel</name>
      </author>
      <author>
        <name>Lal, Karan</name>
      </author>
      <author>
        <name>Jensen, J Daniel</name>
      </author>
      <author>
        <name>Skelsey, Maral Kibarian</name>
      </author>
      <author>
        <name>Ezra, Navid</name>
      </author>
      <author>
        <name>Siperstein, Robyn</name>
      </author>
      <author>
        <name>Noell, Claire</name>
      </author>
      <author>
        <name>Grekin, Steven K</name>
      </author>
      <author>
        <name>Hamzavi, Iltefat H</name>
      </author>
    </item>
    <item>
      <title>History of acne is associated with new-onset acne development in patients with alopecia areata treated with Janus kinase inhibitors</title>
      <link>https://escholarship.org/uc/item/8q0801j1</link>
      <description>History of acne is associated with new-onset acne development in patients with alopecia areata treated with Janus kinase inhibitors</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8q0801j1</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gordon, Emily R</name>
      </author>
      <author>
        <name>Salas, Jesse</name>
      </author>
      <author>
        <name>Hashemi, Kimia</name>
      </author>
      <author>
        <name>Sarabi, Ali</name>
      </author>
      <author>
        <name>Amin, Pouya</name>
      </author>
      <author>
        <name>Hirpara, Milan</name>
      </author>
      <author>
        <name>Nguyen, Megan</name>
      </author>
      <author>
        <name>Benromdhane, Rania</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Efficacy and safety of etrasimod in alopecia areata: A multicentre, randomized, double‐blind, placebo‐controlled, Phase 2 study</title>
      <link>https://escholarship.org/uc/item/89f499wj</link>
      <description>BACKGROUND: Etrasimod, an oral, selective sphingosine 1-phosphate 1, 4 and 5 receptor modulator approved for the treatment of ulcerative colitis, has been studied in immune-mediated inflammatory diseases, including alopecia areata (AA).
OBJECTIVES: To evaluate the efficacy and safety of etrasimod in adults with moderate to severe AA.
METHODS: This Phase 2, randomized, double-blind, placebo-controlled trial included patients (aged ≥18 years) with moderate to severe AA, defined as a Severity of Alopecia Tool (SALT) score of ≥25. Patients were sequentially enrolled into two cohorts. Cohort 1 included patients (SALT score of ≥50) randomized 2:1 to etrasimod 2 mg or placebo. Cohort 2 included patients (SALT score ≥25 to &amp;lt;95) randomized 4:1:2 to etrasimod 3 mg, 2 mg or placebo. Patients completed a 24-week double-blind and 28-week open-label extension period. The primary endpoint was percent change from baseline (%CFB) in SALT score at Week 24. Safety was monitored throughout the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/89f499wj</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>King, B</name>
      </author>
      <author>
        <name>Mesinkovska, N</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Senna, M</name>
      </author>
      <author>
        <name>Luo, X</name>
      </author>
      <author>
        <name>Minkiewicz, J</name>
      </author>
      <author>
        <name>Selfridge, A</name>
      </author>
    </item>
    <item>
      <title>The Relationship between Stigma and Healthcare Interaction in Alopecia Areata</title>
      <link>https://escholarship.org/uc/item/7xs5q2s7</link>
      <description>Introduction: People with alopecia areata (AA) experience stigma, but little is known about how this affects healthcare interaction (HCI). We aim to explore the relationship between stigma and HCI in AA.
Methods: A cross-sectional survey of 500 members of the National Alopecia Areata Foundation was performed. Survey items related to stigma and HCI were summed and sorted into low, medium, and high tertiles. Multinomial logistic regressions were performed to control for demographic and clinical factors.
Results: Respondents (&lt;i&gt;n&lt;/i&gt; = 500) were white (80.0%), female (86.2%), and insured (96.0%), with a plurality earning over USD 100,000 annually (34.2%). Participants in the high-stigma subgroup were more likely to be in the low-HCI subgroup (relative risk ratio [RRR]: 2.22; 95% CI: 1.31-3.76; &lt;i&gt;p&lt;/i&gt; = 0.003), in comparison to participants in the low- or moderate-stigma subgroups (RRR for both: 0.45; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05). This relationship was independent of demographics and clinical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7xs5q2s7</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Biba, Ursula</name>
      </author>
      <author>
        <name>Gregoire, Samantha</name>
      </author>
      <author>
        <name>Sanchez, Katherine</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha Atanaskova</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Waldman, Monique Margaret</name>
      </author>
      <author>
        <name>Anderson, Lisa</name>
      </author>
      <author>
        <name>Mostaghimi, Arash</name>
      </author>
    </item>
    <item>
      <title>Evidence-based consensus on the clinical application of photobiomodulation</title>
      <link>https://escholarship.org/uc/item/68j64451</link>
      <description>BACKGROUND: There is a lack of evidence-based consensus to assist clinicians in using photobiomodulation (PBM).
OBJECTIVE: To create a consensus on the safe and effective use of PBM.
METHODS: A systematic literature review of Embase and MEDLINE was conducted in June 2022 to identify publications reporting research on PBM. An international multidisciplinary panel was convened to draft recommendations informed by the systematic search; they were refined through 2 rounds of Delphi survey, 2 consensus meetings, and iterative review by all panelists until unanimous consensus was achieved.
RESULTS: A multidisciplinary panel of experts (n = 21) was assembled based on publication history. The key findings that informed the consensus developed by the expert panel were as follows: PBM is a safe treatment modality for adult patients and red light PBM does not induce DNA damage. PBM is an effective treatment option for peripheral neuropathy, androgenic alopecia, wound ulcers due to multiple...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/68j64451</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Maghfour, Jalal</name>
      </author>
      <author>
        <name>Mineroff, Jessica</name>
      </author>
      <author>
        <name>Ozog, David M</name>
      </author>
      <author>
        <name>Jagdeo, Jared</name>
      </author>
      <author>
        <name>Lim, Henry W</name>
      </author>
      <author>
        <name>Kohli, Indermeet</name>
      </author>
      <author>
        <name>Anderson, Rox</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Mamalis, Andrew</name>
      </author>
      <author>
        <name>Munavalli, Gilly</name>
      </author>
      <author>
        <name>Cleber, Ferraresi</name>
      </author>
      <author>
        <name>Siegel, Daniel</name>
      </author>
      <author>
        <name>Geneva, Ivayla</name>
      </author>
      <author>
        <name>Weiss, Robert</name>
      </author>
      <author>
        <name>Morita, Akimich</name>
      </author>
      <author>
        <name>Juanita, Anders</name>
      </author>
      <author>
        <name>Goldman, Mitchel P</name>
      </author>
      <author>
        <name>Arany, Paraveen R</name>
      </author>
      <author>
        <name>Sliney, David</name>
      </author>
      <author>
        <name>Ibrahimi, Omar A</name>
      </author>
      <author>
        <name>Chopp, Michael</name>
      </author>
      <author>
        <name>Esmat, Samia</name>
      </author>
      <author>
        <name>Tuner, Jan</name>
      </author>
    </item>
    <item>
      <title>Adding to Your Tool Box: Laser Therapy for Vascular Anomalies</title>
      <link>https://escholarship.org/uc/item/5xz8d75m</link>
      <description>Adjuvant laser therapy of vascular anomalies is based on the principle of selective photo-thermolysis, through targeted destruction of selected chromophores with minimal injury to surrounding tissue. Choice of laser wavelength, treatment parameters, and predicted response to therapy are dependent on the dominant chromophore within the vascular anomaly, lesional location, and target depth, with relatively superficial and mucosal lesions producing the best response to therapy. Lasers can be safely combined with multi-modal approaches for vascular anomalies, including sclerotherapy, surgical excision, and systemic therapy. In this manuscript, we review the laser literature on a range of vascular anomalies, and provide indications, appropriate therapeutic and warning endpoints in the skin, pearls/pitfalls, and multi-disciplinary approaches for pediatric dermatologists pursuing laser as adjuvant therapy for vascular anomalies.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xz8d75m</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Thomas, Kevin V</name>
      </author>
      <author>
        <name>Le, Todd</name>
      </author>
      <author>
        <name>Messele, Feben</name>
      </author>
      <author>
        <name>Garland, Catharine B</name>
      </author>
      <author>
        <name>Monroe, Eric J</name>
      </author>
      <author>
        <name>Metry, Denise</name>
      </author>
      <author>
        <name>Levin, Yakir</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Arkin, Lisa M</name>
      </author>
    </item>
    <item>
      <title>Summation and recommendations for the safe and effective use of topical and oral minoxidil</title>
      <link>https://escholarship.org/uc/item/5d42s0q7</link>
      <description>BACKGROUND: Topical minoxidil, approved for the treatment of androgenetic alopecia, also has efficacy in many other hair loss disorders, its use is limited due to the need for at least daily application. Oral minoxidil, in doses below those likely to lower blood pressure (so called "low dose oral minoxidil") has increasingly been used off label to treat a variety of hair loss conditions but without any standard recommended best practices.
OBJECTIVES: To provide a review of how experts in hair loss use the available literature on topical and low dose oral minoxidil to educate and treat safely and effectively patients with hair loss.
METHODS: Dermatologists with expertise in hair disorders met by teleconference and email to review the literature and share their direct experience with topical and oral minoxidil.
RESULTS: Provision of basic knowledge of the key aspects of the use of topical or oral minoxidil to insure safe and effective use of either in treating hair loss.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5d42s0q7</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Olsen, Elise A</name>
      </author>
      <author>
        <name>Sinclair, Rodney</name>
      </author>
      <author>
        <name>Hordinsky, Maria</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Sadick, Neil</name>
      </author>
      <author>
        <name>Shapiro, Jerry</name>
      </author>
      <author>
        <name>Bergfeld, Wilma</name>
      </author>
    </item>
    <item>
      <title>Consensus Statement on the Prevention and Management of Complications of Fully Ablative Laser Resurfacing of the Face</title>
      <link>https://escholarship.org/uc/item/58d2m60g</link>
      <description>OBJECTIVES: To achieve consensus among expert laser surgeons on standards for the prevention and management of adverse events from fully ablative laser resurfacing of the face.
MATERIALS AND METHODS: Delphi study with two rounds of ratings and revisions until consensus was achieved. The draft set of statements was developed by a steering committee based on expert clinical experience. This was followed by two rounds of rating and revisions completed by an expert panel, then a virtual consensus meeting. In both rounds, respondents rated the draft statements on a 9-point Likert scale (1 = strongly disagree; 9 = strongly agree) and optionally provided comments. The consensus meeting was supplemented by the results of a systematic review of the literature (from 2000 to 2023).
RESULTS: Two rounds of Delphi survey were completed by 34 participants across four countries. Represented specialties were dermatology, facial plastic surgery, plastic surgery, and oculoplastic surgery. The initial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/58d2m60g</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kang, Bianca Y</name>
      </author>
      <author>
        <name>Cohen, Joel L</name>
      </author>
      <author>
        <name>Geronemus, Roy</name>
      </author>
      <author>
        <name>Kilmer, Suzanne L</name>
      </author>
      <author>
        <name>Ross, Edward Victor</name>
      </author>
      <author>
        <name>Tanzi, Elizabeth L</name>
      </author>
      <author>
        <name>Waibel, Jill S</name>
      </author>
      <author>
        <name>Wong, Brian JF</name>
        <uri>https://orcid.org/0000-0001-6318-7384</uri>
      </author>
      <author>
        <name>Alam, Murad</name>
      </author>
      <author>
        <name>Alexiades, Macrene</name>
      </author>
      <author>
        <name>Arndt, Kenneth A</name>
      </author>
      <author>
        <name>Avram, Mathew</name>
      </author>
      <author>
        <name>Bhatia, Ashish C</name>
      </author>
      <author>
        <name>Biesman, Brian Stuart</name>
      </author>
      <author>
        <name>Bloom, Jason D</name>
      </author>
      <author>
        <name>Burns, A Jay</name>
      </author>
      <author>
        <name>Chan, Henry HL</name>
      </author>
      <author>
        <name>DiGiorgio, Catherine M</name>
      </author>
      <author>
        <name>Dover, Jeffrey S</name>
      </author>
      <author>
        <name>Fathizadeh, Sam</name>
      </author>
      <author>
        <name>Esteves, Sara C</name>
      </author>
      <author>
        <name>Gold, Michael H</name>
      </author>
      <author>
        <name>Goldberg, Gerald N</name>
      </author>
      <author>
        <name>Haedersdal, Merete</name>
      </author>
      <author>
        <name>Hoss, Elika</name>
      </author>
      <author>
        <name>Ibrahimi, Omar A</name>
      </author>
      <author>
        <name>Jalian, H Ray</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Manuskiatti, Woraphong</name>
      </author>
      <author>
        <name>Marks, Lisa A</name>
      </author>
      <author>
        <name>Munavalli, Girish S</name>
      </author>
      <author>
        <name>Pozner, Jason N</name>
      </author>
      <author>
        <name>Robb, Chris W</name>
      </author>
      <author>
        <name>Rossi, Anthony M</name>
      </author>
      <author>
        <name>Saedi, Nazanin</name>
      </author>
      <author>
        <name>Shumaker, Peter R</name>
      </author>
      <author>
        <name>Stankiewicz, Kelly</name>
      </author>
      <author>
        <name>Wanner, Molly</name>
      </author>
      <author>
        <name>Wu, Douglas C</name>
      </author>
      <author>
        <name>Wulkan, Adam J</name>
      </author>
      <author>
        <name>Ortiz, Arisa</name>
      </author>
    </item>
    <item>
      <title>Acetyl Hexapeptide-8 as a Topical Alternative to Botulinum Toxin: A Review of the Literature.</title>
      <link>https://escholarship.org/uc/item/4rm1w2hc</link>
      <description>Acetyl Hexapeptide-8 as a Topical Alternative to Botulinum Toxin: A Review of the Literature.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4rm1w2hc</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lum, Kalisa</name>
      </author>
      <author>
        <name>M Hirpara, Milan</name>
      </author>
      <author>
        <name>Pham, Christine</name>
      </author>
      <author>
        <name>Nguyen, Megan</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Components of Severity in Alopecia Areata</title>
      <link>https://escholarship.org/uc/item/24b6z0q8</link>
      <description>Introduction: Severity of alopecia areata (AA) has been commonly defined by clinician assessment of scalp hair loss. Our aim was to characterize patient-reported factors beyond scalp hair loss that contribute to AA severity while modifying for socioeconomic factors.
Methods: Patients with AA were recruited to take a survey. Multivariable linear regression was performed to evaluate lifetime AA severity while adjusting for socioeconomic variables, current AA severity at the time of survey, and patient-reported disease burden.
Results: Patient-reported AA severity was associated with scalp hair loss (OR: 4.19, 95% CI: [1.35-13], &lt;i&gt;p&lt;/i&gt; = 0.013), facial hair loss (OR: 3.55, 95% CI: [1.75-7.21], &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), increased financial burden (OR: 2.41, 95% CI: [1.21-4.8], &lt;i&gt;p&lt;/i&gt; = 0.013), and greater emotional burden (OR: 2.96, 95% CI: [1.48-5.93], &lt;i&gt;p&lt;/i&gt; = 0.002), while presence of comorbidities were linked to less severe AA (OR: 0.38, 95% CI: [0.17-0.84], &lt;i&gt;p&lt;/i&gt; = 0.017).
Conclusion:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/24b6z0q8</guid>
      <pubDate>Mon, 30 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sanchez, Katherine</name>
      </author>
      <author>
        <name>Biba, Ursula</name>
      </author>
      <author>
        <name>Gregoire, Samantha</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha Atanaskova</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Waldman, Monique Margaret</name>
      </author>
      <author>
        <name>Anderson, Lisa</name>
      </author>
      <author>
        <name>Mostaghimi, Arash</name>
      </author>
    </item>
    <item>
      <title>Standardizing multiphoton microscopy for clinical melanoma diagnosis</title>
      <link>https://escholarship.org/uc/item/95q5h21j</link>
      <description>Standardizing multiphoton microscopy for clinical melanoma diagnosis</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/95q5h21j</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ranjit, Suman</name>
      </author>
      <author>
        <name>Vallmitjana Lees, Alexander</name>
      </author>
      <author>
        <name>Durkin, Amanda</name>
      </author>
      <author>
        <name>Torrado, Belen</name>
      </author>
      <author>
        <name>Messele, Faben F</name>
      </author>
      <author>
        <name>Kelly, Kristen</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>Non-invasive, label-free, two-photon detection of epithelial metabolic precursors to repigmentation in vitiligo micrografts</title>
      <link>https://escholarship.org/uc/item/80q540q3</link>
      <description>Non-invasive, label-free, two-photon detection of epithelial metabolic precursors to repigmentation in vitiligo micrografts</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/80q540q3</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Polleys, Christopher</name>
      </author>
      <author>
        <name>Lentsch, Griffin</name>
      </author>
      <author>
        <name>Tromberg, Bruce</name>
        <uri>https://orcid.org/0000-0002-7481-7975</uri>
      </author>
      <author>
        <name>Ganesan, Anand</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Rius-Diaz, Francisca</name>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Georgakoudi, Irene</name>
      </author>
    </item>
    <item>
      <title>In-vivo optical microscopy and single cell transcriptomics approaches provide insights into therapeutic response of vitiligo</title>
      <link>https://escholarship.org/uc/item/4cn251sf</link>
      <description>In-vivo optical microscopy and single cell transcriptomics approaches provide insights into therapeutic response of vitiligo</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4cn251sf</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lentsch, Griffin R</name>
      </author>
      <author>
        <name>Shiu, Jessica</name>
      </author>
      <author>
        <name>Flesher, Jessica</name>
      </author>
      <author>
        <name>Mobasher, Pezhman</name>
      </author>
      <author>
        <name>Polleys, Christopher</name>
      </author>
      <author>
        <name>Mizzoni, Craig</name>
      </author>
      <author>
        <name>König, Karsten</name>
      </author>
      <author>
        <name>Jin, Suoqin</name>
      </author>
      <author>
        <name>Zhang, Lihua</name>
      </author>
      <author>
        <name>Tromberg, Bruce J</name>
        <uri>https://orcid.org/0000-0002-7481-7975</uri>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Georgakoudi, Irene</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>In vivo optical imaging of vitiligo skin grafting treatment using multiphoton microscopy and reflectance confocal microscopy (Conference Presentation)</title>
      <link>https://escholarship.org/uc/item/31p7g3c3</link>
      <description>In vivo optical imaging of vitiligo skin grafting treatment using multiphoton microscopy and reflectance confocal microscopy (Conference Presentation)</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/31p7g3c3</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lentsch, Griffin R</name>
      </author>
      <author>
        <name>Mobasher, Pezhman</name>
      </author>
      <author>
        <name>Mizzoni, Craig</name>
      </author>
      <author>
        <name>Koenig, Karsten</name>
      </author>
      <author>
        <name>Tromberg, Bruce</name>
        <uri>https://orcid.org/0000-0002-7481-7975</uri>
      </author>
      <author>
        <name>Georgakoudi, Irene</name>
      </author>
      <author>
        <name>Ganesan, Anand</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>Meeting Highlights The 4th Marie Skłodowska-Curie Symposium on cancer research and care: Mechanisms of support for regional &amp;amp; international collaborations</title>
      <link>https://escholarship.org/uc/item/2vm8g9d4</link>
      <description>The Marie Skłodowska-Curie Symposia on Cancer Research and Care (MSCS-CRC) promote collaborations between cancer researchers and care providers in the United States, Canada and Central and Eastern European Countries (CEEC) to accelerate the development of new cancer therapies, new strategies for early detection and prevention, and improve cancer care and the quality of life for patients and their families. The 4th MSCS-CRC (September 25-27, 2024, Buffalo, New York) brought together 147 participants from the US, Canada, Croatia, Czechia, Lithuania, Poland, Romania and Ukraine, and involved representatives of the US Centers for Disease Control and Prevention (CDC), National Cancer Institute (NCI) and their counterparts from Poland, Ukraine Lithuania and other CEECs. They were accompanied by New York State (NYS) and local representatives of the NYS Empire State Development, and of the Translational Research Consortium of Cancer Centers (TRCCC), involving 13 cancer centers from the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2vm8g9d4</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kalinski, Pawel</name>
      </author>
      <author>
        <name>Kokolus, Kathleen M</name>
      </author>
      <author>
        <name>Ahluwalia, Indu</name>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Balwicki, Łukasz</name>
      </author>
      <author>
        <name>Baran, Brygida</name>
      </author>
      <author>
        <name>Beine, Loretta</name>
      </author>
      <author>
        <name>Berezin, Mikhail</name>
      </author>
      <author>
        <name>Berindan-Neagoe, Ioana</name>
      </author>
      <author>
        <name>Beznosenko, Andriy</name>
      </author>
      <author>
        <name>Borowiec, Blanka</name>
      </author>
      <author>
        <name>Bozsányi, Szabolcs</name>
      </author>
      <author>
        <name>Bramson, Jonathan</name>
      </author>
      <author>
        <name>Czerniecki, Brian</name>
      </author>
      <author>
        <name>Everatt, Rūta</name>
      </author>
      <author>
        <name>Fendler, Wojciech</name>
      </author>
      <author>
        <name>Forsyth, Peter</name>
      </author>
      <author>
        <name>Gershenwald, Jeffrey E</name>
      </author>
      <author>
        <name>Goniewicz, Maciej</name>
      </author>
      <author>
        <name>Guru, Khurshid</name>
      </author>
      <author>
        <name>Hyland, Andrew</name>
      </author>
      <author>
        <name>James, Smitha</name>
      </author>
      <author>
        <name>Kirac, Iva</name>
      </author>
      <author>
        <name>Koczkodaj, Pawel</name>
      </author>
      <author>
        <name>Kotula, Leszek</name>
      </author>
      <author>
        <name>Łuba, Maciej</name>
      </author>
      <author>
        <name>Ługowska, Iwona</name>
      </author>
      <author>
        <name>Luke, Elizabeth</name>
      </author>
      <author>
        <name>Lungulescu, Cristian</name>
      </author>
      <author>
        <name>Matosevic, Sandro</name>
      </author>
      <author>
        <name>Nanavati, Kaushal</name>
      </author>
      <author>
        <name>Nemeth, Michael</name>
      </author>
      <author>
        <name>Nowak, Karolina</name>
      </author>
      <author>
        <name>Noyes, Katia</name>
      </author>
      <author>
        <name>Parascandola, Mark</name>
      </author>
      <author>
        <name>Priebe, Waldemar</name>
      </author>
      <author>
        <name>Rutkowski, Piotr</name>
      </author>
      <author>
        <name>Seshadri, Mukund</name>
      </author>
      <author>
        <name>Sheffer, Christine E</name>
      </author>
      <author>
        <name>Stanciu, Ioana-Miruna</name>
      </author>
      <author>
        <name>Stanson, Joanna</name>
      </author>
      <author>
        <name>Stewart, Telisa</name>
      </author>
      <author>
        <name>Sužiedėlienė, Edita</name>
      </author>
      <author>
        <name>Sužiedėlis, Kęstutis</name>
      </author>
      <author>
        <name>Tanasiichuk, Iryna</name>
      </author>
      <author>
        <name>Vlad, Anda M</name>
      </author>
      <author>
        <name>Wei, Wei-Zen</name>
      </author>
      <author>
        <name>Williams, Dylan</name>
      </author>
      <author>
        <name>Wojtowicz, Malgorzata</name>
      </author>
      <author>
        <name>Zdrojewski, Tomasz</name>
      </author>
    </item>
    <item>
      <title>Advancements in time-resolved detection for in vivo multiphoton microscopy of human skin</title>
      <link>https://escholarship.org/uc/item/0v5186nv</link>
      <description>Advancements in time-resolved detection for in vivo multiphoton microscopy of human skin</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0v5186nv</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Vallmitjana, Alexander</name>
      </author>
      <author>
        <name>Durkin, Amanda</name>
      </author>
      <author>
        <name>Dvornikov, Alexander</name>
      </author>
      <author>
        <name>Torrado, Belen</name>
      </author>
      <author>
        <name>Ranjit, Suman</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
    </item>
    <item>
      <title>Nicolau Syndrome After Glatiramer Acetate Injection in Close Proximity to Administration of SARS-CoV-2 mRNA Vaccine</title>
      <link>https://escholarship.org/uc/item/8239h9gd</link>
      <description>Nicolau Syndrome After Glatiramer Acetate Injection in Close Proximity to Administration of SARS-CoV-2 mRNA Vaccine</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8239h9gd</guid>
      <pubDate>Wed, 14 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sy, Michael Yu</name>
      </author>
      <author>
        <name>Fromm, Erin</name>
      </author>
      <author>
        <name>Doan, Linda</name>
        <uri>https://orcid.org/0000-0003-0274-2529</uri>
      </author>
      <author>
        <name>Rojek, Nathan</name>
      </author>
      <author>
        <name>Brandt, Alexander Ulrich</name>
      </author>
    </item>
    <item>
      <title>GSLab: open-source platform for advanced phasor analysis in fluorescence microscopy</title>
      <link>https://escholarship.org/uc/item/3q894731</link>
      <description>SUMMARY: GSLab addresses the need for effective image analysis tools in fluorescence microscopy by providing an open-source platform that enhances traditional phasor analysis with advanced features. Key capabilities include machine learning-based clustering, real-time monitoring, and quantitative unmixing of fluorescent species. Designed for both commercial and custom systems, GSLab provides researchers with comprehensive lifetime and spectral phasor image analysis tools to tackle complex biological problems.
AVAILABILITY AND IMPLEMENTATION: The software is written as a MATLAB app. It is available for download at: https://doi.org/10.6084/m9.figshare.27921966. Example files and tutorials are also available: https://doi.org/10.6084/m9.figshare.28067108. For developers who wish to contribute please use: https://github.com/AlexVallmitjana/GSLab. A compiled Windows installer (does not require MATLAB) is available at: https://doi.org/10.6084/m9.figshare.28655276.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3q894731</guid>
      <pubDate>Wed, 14 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Vallmitjana, Alexander</name>
      </author>
      <author>
        <name>Torrado, Belén</name>
      </author>
      <author>
        <name>Durkin, Amanda F</name>
        <uri>https://orcid.org/0000-0001-9880-7651</uri>
      </author>
      <author>
        <name>Dvornikov, Alexander</name>
      </author>
      <author>
        <name>Rajil, Navid</name>
      </author>
      <author>
        <name>Ranjit, Suman</name>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>A rare case of pediatric cutaneous bullous mastocytosis</title>
      <link>https://escholarship.org/uc/item/122470wk</link>
      <description>A rare case of pediatric cutaneous bullous mastocytosis</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/122470wk</guid>
      <pubDate>Wed, 14 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Roux, Jennifer</name>
      </author>
      <author>
        <name>Pham, Christine T</name>
      </author>
      <author>
        <name>Yale, Katerina</name>
      </author>
      <author>
        <name>Rojek, Nathan W</name>
      </author>
      <author>
        <name>Linden, Kenneth</name>
      </author>
      <author>
        <name>Doan, Linda</name>
        <uri>https://orcid.org/0000-0003-0274-2529</uri>
      </author>
    </item>
    <item>
      <title>Effective and durable repigmentation for stable vitiligo: A randomized within-subject controlled trial assessing treatment with autologous skin cell suspension transplantation</title>
      <link>https://escholarship.org/uc/item/5fp4x7zc</link>
      <description>BACKGROUND: Vitiligo lesions are often challenging to repigment with conventional medical therapies. Surgical autologous melanocyte transfer methods can be utilized for stable vitiligo but demand specialized skills and equipment. A point-of-care autologous cell harvesting device was designed enabling simple preparation of autologous skin cell suspension (ASCS) containing melanocytes, keratinocytes, and fibroblasts providing a straightforward approach for cellular transplantation.
OBJECTIVE: To evaluate the safety and effectiveness of ASCS for repigmentation of stable vitiligo lesions among adults.
METHODS: A US multicenter, randomized, within-subject controlled trial compared ASCS to narrow band ultraviolet B only (Control) in similar vitiligo lesions. ASCS was applied after laser skin resurfacing and followed by narrow band ultraviolet B treatment. The primary effectiveness endpoint was the proportion of lesions achieving ≥80% repigmentation at week-24. Repigmentation durability...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5fp4x7zc</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hamzavi, Iltefat H</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Mahmoud, Bassel H</name>
      </author>
      <author>
        <name>Weiss, Eduardo</name>
      </author>
      <author>
        <name>Ahmed, Ammar M</name>
      </author>
      <author>
        <name>Robinson, Deanne</name>
      </author>
      <author>
        <name>Goldman, Mitchel P</name>
      </author>
      <author>
        <name>Munavalli, Girish</name>
      </author>
      <author>
        <name>Kahn, Steven A</name>
      </author>
      <author>
        <name>Huang, Victor</name>
      </author>
      <author>
        <name>Waibel, Jill</name>
      </author>
      <author>
        <name>Desai, Alpesh</name>
      </author>
      <author>
        <name>Elbuluk, Nada</name>
      </author>
      <author>
        <name>Desai, Seemal</name>
      </author>
      <author>
        <name>Pandya, Amit G</name>
      </author>
    </item>
    <item>
      <title>Parsing patterns: Emerging roles of tissue self-organization in health and disease</title>
      <link>https://escholarship.org/uc/item/51x3v3b6</link>
      <description>Patterned morphologies, such as segments, spirals, stripes, and spots, frequently emerge during embryogenesis through self-organized coordination between cells. Yet, complex patterns also emerge in adults, suggesting that the capacity for spontaneous self-organization is a ubiquitous property of biological tissues. We review current knowledge on the principles and mechanisms of self-organized patterning in embryonic tissues and explore how these principles and mechanisms apply to adult tissues that exhibit features of patterning. We discuss how and why spontaneous pattern generation is integral to homeostasis and healing of tissues, illustrating it with examples from regenerative biology. We examine how aberrant self-organization underlies diverse pathological states, including inflammatory skin disorders and tumors. Lastly, we posit that based on such blueprints, targeted engineering of pattern-driving molecular circuits can be leveraged for synthetic biology and the generation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/51x3v3b6</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ramos, Raul</name>
      </author>
      <author>
        <name>Swedlund, Benjamin</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Morsut, Leonardo</name>
      </author>
      <author>
        <name>Maini, Philip K</name>
      </author>
      <author>
        <name>Monuki, Edwin S</name>
      </author>
      <author>
        <name>Lander, Arthur D</name>
        <uri>https://orcid.org/0000-0002-4380-5525</uri>
      </author>
      <author>
        <name>Chuong, Cheng-Ming</name>
      </author>
      <author>
        <name>Plikus, Maksim V</name>
      </author>
    </item>
    <item>
      <title>Exosomes What Is Going on?</title>
      <link>https://escholarship.org/uc/item/4bm530rn</link>
      <description>Exosomes What Is Going on?</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4bm530rn</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hirpara, Milan Minesh</name>
      </author>
      <author>
        <name>Nguyen, Megan</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Alopecia as an Adverse Event of Immune Checkpoint Inhibitor Therapies: Clinical Evidence and Outcomes.</title>
      <link>https://escholarship.org/uc/item/3mw8s3fj</link>
      <description>Immunotherapy utilizing immune checkpoint inhibitors (ICIs) such as PD-1, PD-L1, and CTLA-4 inhibitors has revolutionized cancer therapy by enhancing T cell recognition and attack against cancer cells.1 Immune-related adverse events (irAEs) are a limitation of ICI therapy, encompassing various manifestations such as colitis and cutaneous adverse events such as dermatitis, alopecia, and vitiligo.2 Hair loss is a common concern of cancer patients as they embark on their therapeutic paths. The evidence on alopecia from isolated clinical trials with ICI therapies is limited and largely lacks diagnostic and prognostic details to help guide patients.3,4 In this systematic review, we examined the types of alopecia as part of the irAEs of ICI therapy, timing of onset, prognosis, and treatment approaches. Our analysis includes 19 studies describing new-onset non-scarring or scarring alopecia following ICI treatment. Alopecia was a rare adverse event in the setting of ICIs (n=26) with the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3mw8s3fj</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Park, Minjun</name>
      </author>
      <author>
        <name>Suh, Susie</name>
      </author>
      <author>
        <name>Kincaid, Colin</name>
      </author>
      <author>
        <name>Yale, Katerina</name>
      </author>
      <author>
        <name>Atanaskova Mesinkovska, Natasha</name>
      </author>
    </item>
    <item>
      <title>Interruption of the intratumor CD8+ T&amp;nbsp;cell:Treg crosstalk improves the efficacy of PD-1 immunotherapy</title>
      <link>https://escholarship.org/uc/item/1v85h4rw</link>
      <description>PD-1 blockade unleashes potent antitumor activity in CD8&lt;sup&gt;+&lt;/sup&gt; T&amp;nbsp;cells but can also promote immunosuppressive T regulatory (Treg) cells, which may worsen the response to immunotherapy. Tumor-Treg inhibition is a promising strategy to improve the efficacy of checkpoint blockade immunotherapy; however, our understanding of the mechanisms supporting tumor-Tregs during PD-1 immunotherapy is incomplete. Here, we show that PD-1 blockade increases tumor-Tregs in mouse models of melanoma and metastatic melanoma patients. Mechanistically, Treg accumulation is not caused by Treg-intrinsic inhibition of PD-1 signaling but depends on an indirect effect of activated CD8&lt;sup&gt;+&lt;/sup&gt; T&amp;nbsp;cells. CD8&lt;sup&gt;+&lt;/sup&gt; T&amp;nbsp;cells produce IL-2 and colocalize with Tregs in mouse and human melanomas. IL-2 upregulates the anti-apoptotic protein ICOS on tumor-Tregs, promoting their accumulation. Inhibition of ICOS signaling before PD-1 immunotherapy improves control over immunogenic melanoma....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1v85h4rw</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Geels, Shannon N</name>
      </author>
      <author>
        <name>Moshensky, Alexander</name>
      </author>
      <author>
        <name>Sousa, Rachel S</name>
      </author>
      <author>
        <name>Murat, Claire</name>
      </author>
      <author>
        <name>Bustos, Matias A</name>
      </author>
      <author>
        <name>Walker, Benjamin L</name>
      </author>
      <author>
        <name>Singh, Rima</name>
      </author>
      <author>
        <name>Harbour, Stacey N</name>
      </author>
      <author>
        <name>Gutierrez, Giselle</name>
      </author>
      <author>
        <name>Hwang, Michael</name>
      </author>
      <author>
        <name>Mempel, Thorsten R</name>
      </author>
      <author>
        <name>Weaver, Casey T</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Hoon, Dave SB</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Othy, Shivashankar</name>
      </author>
      <author>
        <name>Marangoni, Francesco</name>
      </author>
    </item>
    <item>
      <title>TONE: A Large, Prospective Post-Approval Study Investigating the Repigmentation of Stable Vitiligo Lesions Using a Point-of-Care Autologous Cell Harvesting Device</title>
      <link>https://escholarship.org/uc/item/1bx5t793</link>
      <description>Introduction: Vitiligo is a depigmenting autoimmune skin disorder caused by loss of melanocytes, impacting 0.5% to 2% of the global population.1-3 &amp;nbsp;For patients with stable vitiligo, surgery allows for physical transplantation of healthy melanocytes to a lesion lacking functional melanocytes.1,4 A combination approach incorporating vitiligo surgery with pharmacotherapy may be recommended in some patients, as employing multiple modalities can improve repigmentation response.4 A point-of-care Autologous Cell Harvesting Device, FDA-approved for the repigmentation of stable vitiligo lesions, prepares autologous skin cell suspension (ASCS) to be applied onto laser-ablated lesions.5 Previously reported, the randomized, within-subject controlled pivotal trial found that 36% of ASCS-treated lesions achieved ≥80% repigmentation at 24 weeks post-treatment, versus 0% of control lesions.6 Here, we report on TONE, a post-approval trial using this device.
&amp;nbsp;
Objective: This multi-center,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1bx5t793</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pandya, Amit G</name>
      </author>
    </item>
    <item>
      <title>624 - Vitiligo biomarker CXCL10 correlates with clinical response in the phase 2 randomized, double-blind, vehicle-controlled TRuE-V mechanism of action study</title>
      <link>https://escholarship.org/uc/item/0sp3z97g</link>
      <description>Abstract: 

               
                  Introduction/Background: 

                  Ruxolitinib cream is a topical formulation of the selective Janus kinase (JAK) 1/JAK2 inhibitor ruxolitinib and is the first and only repigmentation treatment approved by the US Food and Drug Administration and European Commission for nonsegmental vitiligo in patients ≥12 years old. 

               
               
                  Objectives: 

                  To evaluate treatment-associated changes in biomarkers among patients with vitiligo, correlate changes in key biomarkers with efficacy, and assess the safety and tolerability of ruxolitinib cream. 

               
               
                  Methods: 

                  The phase 2, randomized, double-blind, vehicle-controlled TRuE-V mechanism of action study (NCT04896385) was conducted in adult patients (≥18 years) with vitiligo ≤50% of total body surface area. Patients were randomized 2:1 to twice-daily 1.5% ruxolitinib...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0sp3z97g</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Passeron, Thierry</name>
      </author>
      <author>
        <name>Lebwohl, Mark</name>
      </author>
      <author>
        <name>Lynde, Charles</name>
      </author>
      <author>
        <name>Alam, Maryam Shayesteh</name>
      </author>
      <author>
        <name>Laquer, Vivian T</name>
      </author>
      <author>
        <name>Beecker, Jennifer</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Volkova, Angelina</name>
      </author>
      <author>
        <name>Soltanalizadeh, Babak</name>
      </author>
      <author>
        <name>Kornacki, Deanna</name>
      </author>
      <author>
        <name>Smith, Susan H</name>
      </author>
    </item>
    <item>
      <title>The emerging role of photodynamic therapy in the treatment of cutaneous infections.</title>
      <link>https://escholarship.org/uc/item/0c02r328</link>
      <description>INTRODUCTION: Cutaneous infections pose ongoing challenges to standard treatments due to resistance and limited efficacy. Photodynamic therapy (PDT) emerges as a promising supplement or an alternative to address complicated cases. In this review, we comprehensively review PDT's safety and efficacy in treating cutaneous infections.
EVIDENCE ACQUISITION: A PubMed systematic review with search terms for PDT treatment, hair, skin, and nail infections.
EVIDENCE SYNTHESIS: There were a total of 43 studies on the use of PDT in cutaneous infections which discussed the treatment of viral (N.=20), bacterial (N.=11), fungal (N.=9), and protozoal (N.=3) infections. There is evidence for using PDT, mostly 5-aminolevulinic acid (5-ALA) and methyl aminolevulinate (MAL), in the treatment of cutaneous infections. Most evidence for viral infections involved treatment with 5-ALA PDT in condyloma acuminatum (CoAc), verruca vulgaris, and molluscum contagiosum. In bacterial infections, 5-ALA and MB...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0c02r328</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Anagu, Olive</name>
      </author>
      <author>
        <name>Salas, Jesse</name>
      </author>
      <author>
        <name>Choe, Sarah</name>
      </author>
      <author>
        <name>Birda, Abhinav</name>
      </author>
      <author>
        <name>Sharma, Ajay</name>
      </author>
      <author>
        <name>Baker, Gabrielle</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Immune checkpoint inhibitor-associated linear IgA bullous dermatosis with recalcitrant ocular involvement: a rare presentation</title>
      <link>https://escholarship.org/uc/item/0hn3v6sz</link>
      <description>Programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1) receptor inhibitors have become imperative in the treatment of advanced solid organ malignancies such as metastatic melanoma. With this disinhibition of certain immune responses to induce an antitumour response, numerous adverse events have been reported, many of which affect the skin. While rare, PD-1/PD-L1 inhibitor-associated severe cutaneous adverse reactions (SCARs) can cause significant morbidity and/or mortality. New SCARs are reported with increasing frequency as immune checkpoint inhibitors become more widely used. Here, we present a rare case of recalcitrant ocular linear IgA bullous dermatosis associated with a PD-1 inhibitor. Awareness of this entity will allow more rapid recognition and initiation of appropriate management and treatment, which would reduce the morbidity and/or mortality associated with these serious adverse reactions.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0hn3v6sz</guid>
      <pubDate>Fri, 4 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Saeed, Lina</name>
      </author>
      <author>
        <name>Hosking, Anna-Marie</name>
      </author>
      <author>
        <name>Grando, Sergei A</name>
        <uri>https://orcid.org/0000-0001-5769-8938</uri>
      </author>
    </item>
    <item>
      <title>The AhR-Ovol1-Id1 regulatory axis in keratinocytes promotes epidermal and immune homeostasis in atopic dermatitis-like skin inflammation</title>
      <link>https://escholarship.org/uc/item/6j3475zh</link>
      <description>The skin is our outer permeability and immune defense barrier against myriad external assaults. Aryl hydrocarbon receptor (AhR) senses environmental factors and regulates barrier robustness and immune homeostasis. AhR agonists have been approved by the FDA for psoriasis treatment and are in clinical trials for the treatment of atopic dermatitis (AD), but the underlying mechanism of action remains poorly defined. Here, we report that OVOL1/Ovol1 is a conserved and direct transcriptional target of AhR in epidermal keratinocytes. We show that OVOL1/Ovol1 influences AhR-mediated regulation of keratinocyte gene expression and that OVOL1/Ovol1 ablation in keratinocytes impairs the barrier-promoting function of AhR, exacerbating AD-like inflammation. Mechanistically, we&amp;nbsp;have identified Ovol1’s direct downstream targets genome-wide and provided in vivo evidence supporting the role of Id1 as a functional target in barrier maintenance, disease suppression, and neutrophil accumulation....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6j3475zh</guid>
      <pubDate>Tue, 1 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Zeyu</name>
      </author>
      <author>
        <name>Dragan, Morgan</name>
      </author>
      <author>
        <name>Sun, Peng</name>
      </author>
      <author>
        <name>Haensel, Daniel</name>
      </author>
      <author>
        <name>Vu, Remy</name>
      </author>
      <author>
        <name>Cui, Lian</name>
      </author>
      <author>
        <name>Zhu, Peiyao</name>
      </author>
      <author>
        <name>Yang, Nan</name>
      </author>
      <author>
        <name>Shi, Yuling</name>
      </author>
      <author>
        <name>Dai, Xing</name>
        <uri>https://orcid.org/0000-0001-8134-1365</uri>
      </author>
    </item>
    <item>
      <title>The effects of age and dysfunction on meibomian gland population dynamics</title>
      <link>https://escholarship.org/uc/item/1z18n6sm</link>
      <description>PURPOSE: While meibomian gland dysfunction (MGD) is widely recognized as a major cause of evaporative dry eye disease, little is known about normal gland differentiation and lipid synthesis or the mechanism underlying gland atrophy and abnormal lipid secretion. The purpose of this study was to use single-cell and spatial transcriptomics to probe changes in cell composition, differentiation, and gene expression associated with two murine models of MGD: age-related gland atrophy in wild-type mice and altered meibum quality in acyl-CoA wax alcohol acyltransferase 2 (Awat2) knockout (KO) mice.
METHODS: Young (6 month) and old (22 month) wild type, C57Bl/6 mice and young (3 month) and old (13 month) Awat2 KO mice were used in these studies. For single-cell analysis, the tarsal plate was dissected from the upper and lower eyelids, and single cells isolated and submitted to the UCI Genomic Core, while for the spatial analysis frozen tissue sections were shipped to Resolve Biosciences...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1z18n6sm</guid>
      <pubDate>Mon, 24 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wiedemann, Julie</name>
      </author>
      <author>
        <name>Kashgari, Ghaidaa</name>
      </author>
      <author>
        <name>Lane, Shelley</name>
      </author>
      <author>
        <name>Leonard, Brian C</name>
      </author>
      <author>
        <name>Knickelbein, Kelly E</name>
      </author>
      <author>
        <name>Andersen, Bogi</name>
        <uri>https://orcid.org/0000-0001-7181-2768</uri>
      </author>
      <author>
        <name>Jester, James V</name>
        <uri>https://orcid.org/0000-0002-9246-0981</uri>
      </author>
    </item>
    <item>
      <title>Insights Into Demographics, Comorbidities, and Risk Factors in Keloids and Hypertrophic Scars: A Retrospective Study.</title>
      <link>https://escholarship.org/uc/item/9x64w0jw</link>
      <description>Hypertrophic scars and keloids represent abnormal wound healing, manifesting as raised scars confined to or extending beyond the wound margin, respectively. Understanding the risk factors associated with these scarring types is crucial for prevention and management. Utilizing the TriNetX global health research network database, we analyzed the data of 6,249 patients with hypertrophic scars or keloids. We employed the ICD-10 code L91.0 for identification, generating a control cohort matched by age, sex, and race. Associations between scarring and race, ethnicity, and various comorbidities were quantified. The analysis revealed that hypertrophic scars and keloids were more commonly associated with Black/African American individuals (OR=1.74, P&amp;lt;0.01) and less so with White races and Hispanic ethnicity. Significant comorbidities associated with increased risk included scarring alopecia, rosacea, atopic dermatitis, and acne. Inadequate sample size limited analysis for conditions...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9x64w0jw</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sharma, Ajay N</name>
      </author>
      <author>
        <name>Birda, Abhinav</name>
      </author>
      <author>
        <name>Park, Minjun</name>
      </author>
      <author>
        <name>Choe, Sarah</name>
      </author>
      <author>
        <name>Salas, Jesse</name>
      </author>
      <author>
        <name>Kincaid, Colin</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Legislative efforts to expand insurance coverage of wigs for individuals with medical causes of alopecia</title>
      <link>https://escholarship.org/uc/item/7c07001r</link>
      <description>Legislative efforts to expand insurance coverage of wigs for individuals with medical causes of alopecia</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7c07001r</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kim, Richard W</name>
      </author>
      <author>
        <name>McClain, Weston</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Min, Michelle S</name>
      </author>
    </item>
    <item>
      <title>INDIVIDUAL ARTICLE: Insights on the Impact of Scalp Barrier Condition on Hair Health.</title>
      <link>https://escholarship.org/uc/item/6mq4h8dv</link>
      <description>Scalp health is essential for healthy hair growth and may be affected by intrinsic or extrinsic factors. Reactive oxygens species are key contributors to aging and can have a detrimental impact on scalp health. Oxidative stress on the scalp is thought to be a factor in developing dandruff. We present consensus statements on scalp barrier health and its effects on hair through a systematic literature search and expert panel discussion. Three dermatologists with extensive experience in hair were selected to form a panel that formulated consensus statements that would best capture the current understanding of scalp health. The consensus statements developed and presented in this manuscript highlight the current literature and broader discussion surrounding scalp health and its impact on hair and dandruff. It also highlights the often-overlooked effects of scalp conditions on hair health and growth. Through our research, we found that there has been minimal emphasis on scalp health...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6mq4h8dv</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hordinsky, Maria</name>
      </author>
      <author>
        <name>Andriessen, Anneke</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Woolery-Lloyd, Heather</name>
      </author>
    </item>
    <item>
      <title>Current evidence on safety of Janus kinase inhibitors in pregnancy and lactation</title>
      <link>https://escholarship.org/uc/item/2z43m4c5</link>
      <description>Current evidence on safety of Janus kinase inhibitors in pregnancy and lactation</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2z43m4c5</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gordon, Emily R</name>
      </author>
      <author>
        <name>Hanson, Mitchell</name>
      </author>
      <author>
        <name>Bhutani, Tina</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Low-Dose Oral Minoxidil Initiation for Patients With Hair Loss</title>
      <link>https://escholarship.org/uc/item/2pp1b5gc</link>
      <description>Importance: The results of small studies suggest that off-label use of low-dose oral minoxidil (LDOM) may be safe and effective for patients with hair loss, but larger trials and standardized guidelines are lacking.
Objective: To create an expert consensus statement for LDOM prescribing for patients with hair loss.
Evidence Review: The current literature on the pharmacological properties, adverse effect profile, and use of LDOM for patients with hair loss was reviewed. Topics of interest were identified, and a modified Delphi consensus process was created. A total of 43 hair loss specialist dermatologists from 12 countries participated in a modified Delphi process. Consensus was reached if at least 70% agreed or strongly agreed on a 5-point Likert scale.
Findings: Over 4 survey rounds, 180 items in the first round, 121 items in the second round, 16 items in the third round, and 11 items in the fourth round were considered and revised. A total of 76 items achieved consensus including...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2pp1b5gc</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Akiska, Yagiz Matthew</name>
      </author>
      <author>
        <name>Mirmirani, Paradi</name>
      </author>
      <author>
        <name>Roseborough, Ingrid</name>
      </author>
      <author>
        <name>Mathes, Erin</name>
      </author>
      <author>
        <name>Bhutani, Tina</name>
      </author>
      <author>
        <name>Ambrosy, Andrew</name>
      </author>
      <author>
        <name>Aguh, Crystal</name>
      </author>
      <author>
        <name>Bergfeld, Wilma</name>
      </author>
      <author>
        <name>Callender, Valerie D</name>
      </author>
      <author>
        <name>Castelo-Soccio, Leslie</name>
      </author>
      <author>
        <name>Cotsarelis, George</name>
      </author>
      <author>
        <name>Craiglow, Brittany Gareth</name>
      </author>
      <author>
        <name>Desai, Nisha S</name>
      </author>
      <author>
        <name>Doche, Isabella</name>
      </author>
      <author>
        <name>Duque-Estrada, Bruna</name>
      </author>
      <author>
        <name>Elston, Dirk M</name>
      </author>
      <author>
        <name>Goh, Carolyn</name>
      </author>
      <author>
        <name>Goldberg, Lynne J</name>
      </author>
      <author>
        <name>Grimalt, Ramon</name>
      </author>
      <author>
        <name>Jabbari, Ali</name>
      </author>
      <author>
        <name>Jolliffe, Victoria</name>
      </author>
      <author>
        <name>King, Brett A</name>
      </author>
      <author>
        <name>LaSenna, Charlotte</name>
      </author>
      <author>
        <name>Lenzy, Yolanda</name>
      </author>
      <author>
        <name>Lester, Jenna C</name>
      </author>
      <author>
        <name>Lortkipanidze, Nino</name>
      </author>
      <author>
        <name>Sicco, Kristen I Lo</name>
      </author>
      <author>
        <name>McMichael, Amy</name>
      </author>
      <author>
        <name>Meah, Nekma</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Miteva, Mariya</name>
      </author>
      <author>
        <name>Mostaghimi, Arash</name>
      </author>
      <author>
        <name>Ovcharenko, Yuliya</name>
      </author>
      <author>
        <name>Piliang, Melissa</name>
      </author>
      <author>
        <name>Piraccini, Bianca Maria</name>
      </author>
      <author>
        <name>Rakowska, Adriana</name>
      </author>
      <author>
        <name>Salkey, Kimberly S</name>
      </author>
      <author>
        <name>Schmidt, Adriana</name>
      </author>
      <author>
        <name>Shapiro, Jerry</name>
      </author>
      <author>
        <name>Sibbald, Cathryn</name>
      </author>
      <author>
        <name>Sinclair, Rodney</name>
      </author>
      <author>
        <name>Suchonwanit, Poonkiat</name>
      </author>
      <author>
        <name>Taylor, Susan</name>
      </author>
      <author>
        <name>Tosti, Antonella</name>
      </author>
      <author>
        <name>Vañó-Galván, Sergio</name>
      </author>
      <author>
        <name>Wall, Dmitri Robert</name>
      </author>
      <author>
        <name>Fu, Jennifer M</name>
      </author>
    </item>
    <item>
      <title>INDIVIDUAL ARTICLE: Etiology, Treatment Challenges, and the Role of Scalp and Haircare in Managing Dandruff.</title>
      <link>https://escholarship.org/uc/item/1r8348dt</link>
      <description>Dandruff and seborrheic dermatitis are associated with a disrupted scalp barrier that contributes to irritation, pruritus, and flaking of the scalp. The flaking and itch associated with dandruff can significantly impact an individual's self-esteem and quality of life. While the exact pathogenesis of dandruff is still not completely understood, scalp barrier health and its microbiome are thought to play significant roles in disease propagation. Five expert dermatologists with extensive experience in hair, dandruff, and seborrheic dermatitis were selected to participate in discussions that would result in five consensus statements focused on scalp barrier health and dandruff. Results of a systematic literature search and expert panel discussion are presented. These consensus statements aim to reflect expert opinions on the current understanding of scalp health in the context of dandruff and seborrheic dermatitis. The panel addressed challenges to promote scalp health, improve patient...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1r8348dt</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hordinsky, Maria</name>
      </author>
      <author>
        <name>Andriessen, Anneke</name>
      </author>
      <author>
        <name>Day, Doris</name>
      </author>
      <author>
        <name>McMichael, Amy</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Woolery-Lloyd, Heather</name>
      </author>
    </item>
    <item>
      <title>Leveraging gene correlations in single cell transcriptomic data</title>
      <link>https://escholarship.org/uc/item/9v96001h</link>
      <description>BACKGROUND: Many approaches have been developed to overcome technical noise in single cell RNA-sequencing (scRNAseq). As researchers dig deeper into data-looking for rare cell types, subtleties of cell states, and details of gene regulatory networks-there is a growing need for algorithms with controllable accuracy and fewer &lt;i&gt;ad hoc&lt;/i&gt; parameters and thresholds. Impeding this goal is the fact that an appropriate null distribution for scRNAseq cannot simply be extracted from data when ground truth about biological variation is unknown (i.e., usually).
RESULTS: We approach this problem analytically, assuming that scRNAseq data reflect only cell heterogeneity (what we seek to characterize), transcriptional noise (temporal fluctuations randomly distributed across cells), and sampling error (i.e., Poisson noise). We analyze scRNAseq data without normalization-a step that skews distributions, particularly for sparse data-and calculate &lt;i&gt;p&lt;/i&gt;-values associated with key statistics....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9v96001h</guid>
      <pubDate>Mon, 3 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Silkwood, Kai</name>
      </author>
      <author>
        <name>Dollinger, Emmanuel</name>
      </author>
      <author>
        <name>Gervin, Josh</name>
      </author>
      <author>
        <name>Atwood, Scott</name>
        <uri>https://orcid.org/0000-0001-7407-9792</uri>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Lander, Arthur D</name>
        <uri>https://orcid.org/0000-0002-4380-5525</uri>
      </author>
    </item>
    <item>
      <title>PILOT STUDY ON IN VIVO MULTIPHOTON-MICROSCOPY OF LASER-INDUCED OPTICAL BREAKDOWN IN HUMAN SKIN</title>
      <link>https://escholarship.org/uc/item/80n73113</link>
      <description>PILOT STUDY ON IN VIVO MULTIPHOTON-MICROSCOPY OF LASER-INDUCED OPTICAL BREAKDOWN IN HUMAN SKIN</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/80n73113</guid>
      <pubDate>Thu, 20 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Lentsch, Griffin</name>
      </author>
      <author>
        <name>Korta, Dorota</name>
      </author>
      <author>
        <name>Koenig, Karsten</name>
      </author>
      <author>
        <name>Kelly, Kristen</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Tromberg, Bruce</name>
      </author>
      <author>
        <name>Zachary, Christopher</name>
        <uri>https://orcid.org/0000-0002-5883-5188</uri>
      </author>
    </item>
    <item>
      <title>ASSESSMENT OF SKIN STRUCTURE BY COMBINED PHOTOTHERMAL RADIOMETRY AND OPTICAL SPECTROSCOPY: COREGISTRATION WITH MULTI-PHOTON MICROSCOPY</title>
      <link>https://escholarship.org/uc/item/6t0569c4</link>
      <description>ASSESSMENT OF SKIN STRUCTURE BY COMBINED PHOTOTHERMAL RADIOMETRY AND OPTICAL SPECTROSCOPY: COREGISTRATION WITH MULTI-PHOTON MICROSCOPY</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6t0569c4</guid>
      <pubDate>Thu, 20 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Verdel, Nina</name>
      </author>
      <author>
        <name>Lentsch, Griffin</name>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Tromberg, Bruce</name>
      </author>
      <author>
        <name>Majaron, Boris</name>
      </author>
    </item>
    <item>
      <title>Picking a Side: Preferential Laterality in Scalp Hair Density</title>
      <link>https://escholarship.org/uc/item/9vs8q1p7</link>
      <description>Introduction: Clinical examinations of the scalp have shown that patients may grow hair preferentially at higher density on one side of their scalp, yet review of the literature to date has not yield studies that directly assess differences in scalp hair density laterality. The objective of this study was to examine whether scalp hair growth occurs preferentially and on which side of the scalp, the right or left, in healthy patients.
Method: Scalps of healthy subjects with no history of hair loss or scalp disease were imaged with digital trichoscopy at a university dermatology clinic. Bilateral temporal photos were uploaded to trichoscopy software for quantitative analysis.
Results: Scalp hair laterality was observed in both male and female, with no trend in left or right preference. While subjects who identified as Asian or Hispanic exhibited a strong laterality preference, statistical significance was not reached among African American or Caucasian subjects.
Conclusion: No overall...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9vs8q1p7</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Duong, Amanda N</name>
      </author>
      <author>
        <name>Kincaid, Colin</name>
      </author>
      <author>
        <name>Phong, Celine</name>
      </author>
      <author>
        <name>Babadjouni, Arash</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha Atanaskova</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Premature hair graying: a multifaceted phenomenon</title>
      <link>https://escholarship.org/uc/item/9k7664mr</link>
      <description>Premature hair graying (PHG) is the early loss of natural hair color, influenced by genetic, biological, and environmental factors. This review discusses the significant psychological impacts of PHG and explores its underlying mechanisms, related health conditions, and available treatments. The review examines the roles of genetics, oxidative stress, and lifestyle factors such as smoking and diet in premature graying. It also considers associated medical conditions and current and emerging treatment options. This overview aims to improve understanding of PHG and its broader implications.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9k7664mr</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Desai, Deesha D</name>
      </author>
      <author>
        <name>Karim, Maria</name>
      </author>
      <author>
        <name>Nohria, Ambika</name>
      </author>
      <author>
        <name>Needle, Carli</name>
      </author>
      <author>
        <name>Brinks, Anna</name>
      </author>
      <author>
        <name>Kearney, Caitlin A</name>
      </author>
      <author>
        <name>Ridge, Amy</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Shapiro, Jerry</name>
      </author>
      <author>
        <name>Sicco, Kristen I Lo</name>
      </author>
    </item>
    <item>
      <title>Efficacy and safety of deuruxolitinib, an oral selective Janus kinase inhibitor, in adults with alopecia areata: Results from the Phase 3 randomized, controlled trial (THRIVE-AA1)</title>
      <link>https://escholarship.org/uc/item/875833fw</link>
      <description>BACKGROUND: Alopecia areata (AA) is a hair loss disorder that can seriously impact quality of life. Janus kinase (JAK) inhibitors, including deuruxolitinib, have previously demonstrated significant hair regrowth in AA.
OBJECTIVE: The Phase 3 THRIVE-AA1 randomized, double-blinded, placebo-controlled trial (NCT04518995) evaluated the safety and efficacy of the oral JAK1/JAK2 inhibitor deuruxolitinib in adult patients with AA.
METHODS: Patients aged 18-65&amp;nbsp;years with ≥50% hair loss were randomized to deuruxolitinib 8&amp;nbsp;mg twice daily, deuruxolitinib 12&amp;nbsp;mg twice daily, or placebo for 24&amp;nbsp;weeks. The primary end point was the percentage of patients achieving a Severity of Alopecia Tool score ≤20. A key secondary end point was the percentage of satisfaction of hair patient-reported outcome responders.
RESULTS: Significantly higher proportions of patients taking deuruxolitinib met the primary end point (8&amp;nbsp;mg 29.6%; 12&amp;nbsp;mg 41.5% versus placebo 0.8%). Both deuruxolitinib...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/875833fw</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>King, Brett</name>
      </author>
      <author>
        <name>Senna, Maryanne M</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Lynde, Charles</name>
      </author>
      <author>
        <name>Zirwas, Matthew</name>
      </author>
      <author>
        <name>Maari, Catherine</name>
      </author>
      <author>
        <name>Prajapati, Vimal H</name>
      </author>
      <author>
        <name>Sapra, Sheetal</name>
      </author>
      <author>
        <name>Brzewski, Pawel</name>
      </author>
      <author>
        <name>Osman, Lawrence</name>
      </author>
      <author>
        <name>Hanna, Sameh</name>
      </author>
      <author>
        <name>Wiseman, Marni C</name>
      </author>
      <author>
        <name>Hamilton, Colleen</name>
      </author>
      <author>
        <name>Cassella, James</name>
      </author>
    </item>
    <item>
      <title>Evaluating Anti-Inflammatory Potential of Platelet-Rich Plasma in Scarring Alopecia: A Systematic Review.</title>
      <link>https://escholarship.org/uc/item/83d8z1f0</link>
      <description>Scarring alopecia, also known as cicatricial alopecia, is a group of hair loss disorders characterized by inflammatory destruction of hair follicles, leading to hair loss and scar tissue formation. Treating scarring alopecia is challenging due to the irreversible damage caused by the inflammatory process. Consequently, early intervention targeting inflammation is crucial for improving prognosis.1 Recently, several reports have emerged supporting the use of platelet-rich plasma (PRP) as a non-conventional therapy for scarring alopecia, suggesting its potential benefits in mitigating inflammation and halting disease progression. While there is a growing body of evidence demonstrating the efficacy and safety of PRP in nonscarring alopecia, such as androgenetic alopecia (AGA) and alopecia areata (AA), there remains a scarcity of evidence regarding the clinical benefits of PRP in scarring alopecias.2-7 In this study, we conducted a literature review exploring the effectiveness and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/83d8z1f0</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Suh, Susie</name>
      </author>
      <author>
        <name>Park, Minjun</name>
      </author>
      <author>
        <name>Babadjouni, Arash</name>
      </author>
      <author>
        <name>Atanaskova Mesinkovska, Natasha</name>
      </author>
    </item>
    <item>
      <title>Efficacy and safety of ritlecitinib, an oral JAK3/TEC family kinase inhibitor, in adolescent and adult patients with alopecia totalis and alopecia universalis</title>
      <link>https://escholarship.org/uc/item/7ns7f6p9</link>
      <description>This post-hoc analysis of the ALLEGRO phase 2b/3 study (NCT03732807) evaluated the efficacy and safety of ritlecitinib, an oral Janus kinase 3/TEC family kinase inhibitor, in patients with alopecia totalis (AT) and alopecia universalis (AU). Patients aged ≥ 12 years with alopecia areata (AA) and ≥50% scalp hair loss received once-daily ritlecitinib 50 or 30 mg (± 4-week 200-mg loading dose) or placebo for 24 weeks. In a subsequent 24-week extension period, the ritlecitinib groups continued their doses and patients initially assigned to placebo switched to ritlecitinib (200/50 or 50 mg daily). In this analysis, clinician- and patient-reported hair regrowth outcomes were assessed at weeks 24 and 48 in four AA subgroups: AT/AU, AT, AU, and non-AT/AU. Safety was monitored throughout. Of the 718 randomized patients, 151 (21%) and 147 (20%) were defined as having AT or AU, respectively. At week 24, Severity of Alopecia Tool (SALT) score ≤20 (≤20% scalp hair loss) response rates were...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7ns7f6p9</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>King, Brett</name>
      </author>
      <author>
        <name>Zhang, Xingqi</name>
      </author>
      <author>
        <name>Guttman‐Yassky, Emma</name>
      </author>
      <author>
        <name>Magnolo, Nina</name>
      </author>
      <author>
        <name>Sinclair, Rodney</name>
      </author>
      <author>
        <name>Mizuashi, Masato</name>
      </author>
      <author>
        <name>Shapiro, Jerry</name>
      </author>
      <author>
        <name>Peeva, Elena</name>
      </author>
      <author>
        <name>Banerjee, Anindita</name>
      </author>
      <author>
        <name>Takiya, Liza</name>
      </author>
      <author>
        <name>Cox, Lori Ann</name>
      </author>
      <author>
        <name>Wajsbrot, Dalia</name>
      </author>
      <author>
        <name>Kerkmann, Urs</name>
      </author>
      <author>
        <name>Law, Ernest</name>
      </author>
      <author>
        <name>Wolk, Robert</name>
      </author>
      <author>
        <name>Schaefer, Gregor</name>
      </author>
    </item>
    <item>
      <title>Characterizing low-dose oral minoxidil-induced peripheral edema in alopecia patients</title>
      <link>https://escholarship.org/uc/item/7n0448pq</link>
      <description>Characterizing low-dose oral minoxidil-induced peripheral edema in alopecia patients</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7n0448pq</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Salas, Jesse</name>
      </author>
      <author>
        <name>Esse, Ilhan</name>
      </author>
      <author>
        <name>Kincaid, Colin M</name>
      </author>
      <author>
        <name>Birda, Abhinav</name>
      </author>
      <author>
        <name>Choe, Sarah</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Clinical Significance of Mottling Rashes in Diving Decompression Sickness.</title>
      <link>https://escholarship.org/uc/item/6522z7kx</link>
      <description>&lt;b&gt;INTRODUCTION:&lt;/b&gt; Decompression sickness (DCS) is a medical condition caused by outgassing of dissolved nitrogen following rapid ascent by divers and aviators. Cutaneous DCS, historically termed cutis marmorata (CM), presents as a predominantly truncal reticular violaceous-to-dusky eruption. The prevailing theories for its pathogenesis include: localized cutaneous outgassing, paradoxical embolism across a right-to-left shunt (RLS), and brainstem emboli disrupting autonomic control of cutaneous microcirculation.&lt;b&gt;METHODS:&lt;/b&gt; We conducted a systematic review of reports of cutaneous DCS to investigate relationships among CM, RLS, and neurological sequelae to better elucidate the mechanism of CM. A literature search examining reports of cutaneous DCS yielded 31 eligible studies, comprising a pooled total of 128 patients.&lt;b&gt;RESULTS:&lt;/b&gt; Of the patients with documented workup, 84% showed evidence of RLS with CM. Subsequently 18 patients underwent percutaneous closure of intracardiac...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6522z7kx</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Breen, Ilana D</name>
      </author>
      <author>
        <name>Stepanek, Jan</name>
      </author>
      <author>
        <name>Marks, Lisa</name>
      </author>
      <author>
        <name>Yale, Katerina</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Swanson, David</name>
      </author>
    </item>
    <item>
      <title>Correction to: Integrated Safety Analysis of Ritlecitinib, an Oral JAK3/TEC Family Kinase Inhibitor, for the Treatment of Alopecia Areata from the ALLEGRO Clinical Trial Program</title>
      <link>https://escholarship.org/uc/item/4b21w76h</link>
      <description>A video abstract is now available for this publication, which can be viewed online. The video abstract can also be accessed on the article’s Figshare page here: https://doi.org/10.6084/m9.figshare.24749436 and in the parent article as Supplementary file 3. 2xeqpp-jg_FT7HrQkW1y9mVideo abstract: Integrated safety analysis of ritlecitinib in patients aged ≥ 12 years with alopecia areata (MP4 1.03 gb)Video abstract: Integrated safety analysis of ritlecitinib in patients aged ≥ 12 years with alopecia areata (MP4 1.03 gb) Video abstract: Integrated safety analysis of ritlecitinib in patients aged ≥ 12 years with alopecia areata (MP4 1.03 gb). In Supplementary file2, Table S11, “Lymphocytes, n/N1 (%)&lt;sup&gt;c&lt;/sup&gt;, Grade 3 (200 to &amp;lt; 500/mm&lt;sup&gt;3&lt;/sup&gt;)” row, “Any ritlecitinib (n=1294)” column, the data that previously read: “27/128 (2.1)” should have read: “27/1286 (2.1)” The original Supplementary file 2 has been corrected.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4b21w76h</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>King, Brett</name>
      </author>
      <author>
        <name>Soung, Jennifer</name>
      </author>
      <author>
        <name>Tziotzios, Christos</name>
      </author>
      <author>
        <name>Rudnicka, Lidia</name>
      </author>
      <author>
        <name>Joly, Pascal</name>
      </author>
      <author>
        <name>Gooderham, Melinda</name>
      </author>
      <author>
        <name>Sinclair, Rodney</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Paul, Carle</name>
      </author>
      <author>
        <name>Gong, Yankun</name>
      </author>
      <author>
        <name>Anway, Susan D</name>
      </author>
      <author>
        <name>Tran, Helen</name>
      </author>
      <author>
        <name>Wolk, Robert</name>
      </author>
      <author>
        <name>Zwillich, Samuel H</name>
      </author>
      <author>
        <name>Lejeune, Alexandre</name>
      </author>
    </item>
    <item>
      <title>Patient-Reported Satisfaction with Hair Regrowth in a Study of Ritlecitinib in Alopecia Areata: Results from ALLEGRO-2b/3</title>
      <link>https://escholarship.org/uc/item/4728n4c7</link>
      <description>&lt;h4&gt;Introduction&lt;/h4&gt;Patients with alopecia areata (AA) report high levels of dissatisfaction with commonly used treatments. Patient-reported outcomes are essential to understanding patients' experiences with AA treatments. The objective of this study was to evaluate patient-reported satisfaction with hair growth among patients with AA receiving ritlecitinib or placebo and the correlation between clinician-assessed efficacy and patient-reported satisfaction.&lt;h4&gt;Methods&lt;/h4&gt;In the ALLEGRO-2b/3 (NCT03732807) trial, patients with AA and ≥50% scalp hair loss were randomized to daily ritlecitinib or placebo for 24 weeks, with a 24-week extension of continued ritlecitinib or switch from placebo to ritlecitinib. The Patient Satisfaction with Hair Growth (P-Sat) measure evaluated patients' satisfaction with hair growth in 3 domains: amount, quality, and overall satisfaction with hair growth. The prespecified analysis evaluated the proportion of patients who were slightly, moderately,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4728n4c7</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sinclair, Rodney</name>
      </author>
      <author>
        <name>Law, Ernest H</name>
      </author>
      <author>
        <name>Zhang, Xingqi</name>
      </author>
      <author>
        <name>Zhang, Fan</name>
      </author>
      <author>
        <name>Napatalung, Lynne</name>
      </author>
      <author>
        <name>Zwillich, Samuel H</name>
      </author>
      <author>
        <name>King, Brett</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Baricitinib Withdrawal and Retreatment in Patients With Severe Alopecia Areata</title>
      <link>https://escholarship.org/uc/item/3gn7984f</link>
      <description>Importance: Baricitinib has demonstrated efficacy for treating severe alopecia areata in adults. There is currently limited information about the need for continuous therapy after achieving scalp hair regrowth.
Objective: To report results from the randomized withdrawal period of the BRAVE-AA1 trial.
Design, Setting, and Participants: BRAVE-AA1 was a randomized, placebo-controlled, phase 3 randomized clinical trial with a treatment withdrawal substudy that was conducted at 70 centers in 3 countries beginning in March 2019. It included 654 adults with severe alopecia areata (AA) (Severity of Alopecia Tool [SALT] score ≥50) who were randomized 3:2:2 to receive treatment with baricitinib, 4 mg; baricitinib, 2 mg; or placebo. Data were analyzed in August 2023.
Intervention: At week 52, 154 patients who were responders (SALT score ≤20) were rerandomized 3:1 to continue to take their current dose of baricitinib or transition to placebo (randomized withdrawal). Responders randomized...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3gn7984f</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>King, Brett</name>
      </author>
      <author>
        <name>Ko, Justin</name>
      </author>
      <author>
        <name>Kwon, Ohsang</name>
      </author>
      <author>
        <name>Vañó-Galván, Sergio</name>
      </author>
      <author>
        <name>Piraccini, Bianca Maria</name>
      </author>
      <author>
        <name>Dutronc, Yves</name>
      </author>
      <author>
        <name>Yu, Guanglei</name>
      </author>
      <author>
        <name>Liu, Chunyuan</name>
      </author>
      <author>
        <name>Somani, Najwa</name>
      </author>
      <author>
        <name>Ball, Susan</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Evaluation of Pericardial Effusions in Alopecia Patients on Low-Dose Oral Minoxidil Therapy.</title>
      <link>https://escholarship.org/uc/item/32t130hn</link>
      <description>BACKGROUND: Minoxidil is an anti-hypertensive vasodilator increasingly used off-label for the treatment of alopecia. It is associated with an increased risk of pericardial effusions, with recent reports even in patients on low-dose oral minoxidil (LDOM) therapy.
OBJECTIVE: To evaluate whether LDOM is associated with increased prevalence of pericardial effusions in patients with alopecia.
METHODS: In this cross-sectional study, point-of-care ultrasound was used to screen alopecia patients at dermatology appointments. Scans were evaluated by two independent cardiologists for the presence and size of effusions. The prevalence of effusions was compared between patients on LDOM therapy and patients not on minoxidil therapy.
RESULTS: A total of 100 patients were evaluated for pericardial effusion: 51 LDOM patients and 49 control patients. The two groups were similar in terms of age (53.7 vs 54.1; P=0.91), sex (86% vs 73% female; P=0.14), and race. Small pericardial effusions (&amp;lt;1...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32t130hn</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kincaid, Colin M</name>
      </author>
      <author>
        <name>Sharma, Ajay N</name>
      </author>
      <author>
        <name>Sargent, Brynn</name>
      </author>
      <author>
        <name>Gradus-Pizlo, Irmina</name>
        <uri>https://orcid.org/0000-0002-3558-9439</uri>
      </author>
      <author>
        <name>Dineen, Elizabeth H</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>The overturn of Roe v Wade: Google searches for teratogenic medications following the U.S. Supreme Court ruling</title>
      <link>https://escholarship.org/uc/item/2vw8x31z</link>
      <description>The overturn of Roe v Wade: Google searches for teratogenic medications following the U.S. Supreme Court ruling</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2vw8x31z</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Nohria, Ambika</name>
      </author>
      <author>
        <name>Desai, Deesha</name>
      </author>
      <author>
        <name>Klein, Elizabeth J</name>
      </author>
      <author>
        <name>Senna, Maryanne M</name>
      </author>
      <author>
        <name>Aguh, Crystal</name>
      </author>
      <author>
        <name>Farah, Ronda S</name>
      </author>
      <author>
        <name>Bordone, Lindsey</name>
      </author>
      <author>
        <name>Krueger, Loren D</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Cummins, Donna</name>
      </author>
      <author>
        <name>Sicco, Kristen I Lo</name>
      </author>
    </item>
    <item>
      <title>The Burden of Melasma: Race, Ethnicity, and Comorbidities.</title>
      <link>https://escholarship.org/uc/item/2q02m8rv</link>
      <description>INTRODUCTION: In an effort to define the characteristics of populations affected by melasma, we utilized a large global health research network database from 108 health care organizations (TriNetx) to quantify the associations between race, ethnicity, and comorbidities.
METHODS: We identified the cohort of all patients with melasma from the TriNetx database, and subsequently generated a control cohort. ICD-10 codes were used to identify the prevalence of various comorbidities associated with melasma.
RESULTS: A total of 41,283 patients with melasma (93% female, mean [SD] age 48.8 [12.6] year) were identified. The most frequently associated risk factors included hypertension (25% of the melasma cohort) and hormonal contraception (24%). Rosacea (OR=5.1), atopic dermatitis (OR=3.3), lupus (OR=2.5), history of skin cancer (OR=2.5), history of internal malignancy (OR=2.1), and hormonal contraception use (OR=2.1) possessed the highest odds ratios for development of melasma (all P&amp;lt;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2q02m8rv</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sharma, Ajay N</name>
      </author>
      <author>
        <name>Kincaid, Colin M</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>In Vivo Imaging Techniques for the Human Scalp: A Systematic Review of the Literature</title>
      <link>https://escholarship.org/uc/item/2g83d629</link>
      <description>&lt;h4&gt;Objective&lt;/h4&gt;Scalp inflammation and alopecia are distressing conditions for which patients regularly present to dermatology. Although some diagnoses can be made clinically, others require biopsy, which carries the risk of pain, infection, bleeding, and scarring. This review examines the existing literature regarding noninvasive in vivo imaging techniques and their evidence and utility in evaluating scalp pathology, with a focus on the diagnostics of hair conditions.&lt;h4&gt;Methods&lt;/h4&gt;A systematic literature search was conducted using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines without timeframe restrictions. The PubMed and Clarivate (Web of Science) databases were searched using the terms ("imaging" OR "in-vivo imaging" OR "non-invasive imaging" OR "non-invasive in vivo imaging" "imaging," "in-vivo imaging) AND ("human scalp disorders" OR "scalp" OR "hair loss" OR "alopecia"). Peer-reviewed randomized control trials (RCTs), prospective...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2g83d629</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hedayati, Bobak</name>
      </author>
      <author>
        <name>Horton, Luke</name>
      </author>
      <author>
        <name>Urso, Brittany</name>
      </author>
      <author>
        <name>Ekelem, Chloe</name>
      </author>
      <author>
        <name>Babadjouni, Arash</name>
      </author>
      <author>
        <name>Sharma, Ajay N</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha Atanaskova</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Characterization of scalp involvement in dermatomyositis based on myositis-specific antibody subsets</title>
      <link>https://escholarship.org/uc/item/1vz22830</link>
      <description>Characterization of scalp involvement in dermatomyositis based on myositis-specific antibody subsets</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1vz22830</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Arora, Jagmeet S</name>
      </author>
      <author>
        <name>Kincaid, Colin M</name>
      </author>
      <author>
        <name>Sharma, Ajay N</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Min, Michelle S</name>
      </author>
    </item>
    <item>
      <title>Liposurfomas: Acquired bilateral chest wall fibrolipomas in surfers—7 cases</title>
      <link>https://escholarship.org/uc/item/16f3b7pt</link>
      <description>Liposurfomas: Acquired bilateral chest wall fibrolipomas in surfers—7 cases</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/16f3b7pt</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Klein, Paytra A</name>
      </author>
      <author>
        <name>Barr, Ronald J</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Klein, Jeffrey A</name>
      </author>
    </item>
    <item>
      <title>Isobutylamido Thiazolyl Resorcinol (Thiamidol) for Combatting Hyperpigmentation: A Systematic Review of Clinical Studies.</title>
      <link>https://escholarship.org/uc/item/0w14s3cm</link>
      <description>BACKGROUND: Tyrosinase is the rate-limiting enzyme of melanogenesis and thus an ideal inhibitory target for treating hyperpigmentation. There are many commercially available tyrosinase inhibitors with limited clinical efficacy. A recent screen of 50,000 compounds found isobutylamido thiazolyl resorcinol (ITR) to be the most potent inhibitor of human tyrosinase.
OBJECTIVE: To summarize the current evidence on the efficacy and adverse effects of ITR in treating hyperpigmentation.
METHODS: A literature search was conducted using PubMed and Google Scholar databases in June 2022. Fourteen clinical studies investigating the use of topical ITR in hyperpigmentation treatment or prevention were identified.
RESULTS: Most studies (n=13) investigated topical ITR as a treatment, while only one investigated ITR as a preventative measure against hyperpigmentation. All studies (n=14) found ITR to provide statistically significant improvements to hyperpigmentation conditions, including facial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0w14s3cm</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Klein, Paytra A</name>
      </author>
      <author>
        <name>Kincaid, Colin</name>
      </author>
      <author>
        <name>Babadjouni, Arash</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Alopecia areata: Mortality trends from a population-based cohort study reflect increased survival</title>
      <link>https://escholarship.org/uc/item/0s77v384</link>
      <description>Alopecia areata: Mortality trends from a population-based cohort study reflect increased survival</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0s77v384</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Birda, Abhinav</name>
      </author>
      <author>
        <name>Choe, Sarah</name>
      </author>
      <author>
        <name>Salas, Jesse</name>
      </author>
      <author>
        <name>Horton, Luke</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha A</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
    </item>
    <item>
      <title>Race and Ethnicity Sub-Groups of Alopecia Areata Patients have Differing Clinical Characteristics: TARGET-DERM AA</title>
      <link>https://escholarship.org/uc/item/0fr8x47r</link>
      <description>Introduction Alopecia areata (AA) is a chronic, autoimmune disease that disproportionately impacts particular subgroups.1 Methods United States and Canadian clinics enrolled participants in the TARGET-DERM AA registry (December 2021 - June 2024, data collection ongoing). Those who completed a baseline patient questionnaire [self-reported race / ethnicity, Patient Global Impression of Severity (PGIS-AA)] and clinician-reported outcome measures [Severity of Alopecia Tool (SALT), ClinRO Measure for Eyebrow / Eyelash Hair Loss] were summarized. Results Of the 267 AA patients, 61.4% were female; 53.2% were adults, 28.5% identified as Hispanic, 52.1% Non-Hispanic (NH)-White, 8.6% NH Black and 6.4% as NH Asian. 47.1% of NH Asian patients had severe disease (SALT&amp;gt;50) and represented the group with the highest proportion of SALT&amp;gt;50, followed by 34.8% of NH Black, 31.7% NH White, and 19.7% Hispanic AA patients. 47.1% of NH Asian patients reported PGIS-AA ‘severe/very severe’ disease,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0fr8x47r</guid>
      <pubDate>Wed, 5 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hordinsky, Maria</name>
      </author>
      <author>
        <name>Bristow, Claire</name>
      </author>
      <author>
        <name>Richter, Sven</name>
      </author>
      <author>
        <name>Soliman, Ahmed</name>
      </author>
      <author>
        <name>Knapp, Keith</name>
      </author>
      <author>
        <name>Munoz, Breda</name>
      </author>
      <author>
        <name>Crawford, Julie</name>
      </author>
      <author>
        <name>Paller, Amy</name>
      </author>
      <author>
        <name>Chapman, Shane</name>
      </author>
      <author>
        <name>Wine Lee, Lara</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Ungar, Benjamin</name>
      </author>
    </item>
    <item>
      <title>Single-cell transcriptomics of human-skin-equivalent organoids</title>
      <link>https://escholarship.org/uc/item/7km904sz</link>
      <description>Several methods for generating human-skin-equivalent (HSE) organoid cultures are in use to study skin biology; however, few studies thoroughly characterize these systems. To fill this gap, we use single-cell transcriptomics to compare in&amp;nbsp;vitro HSEs, xenograft HSEs, and in&amp;nbsp;vivo epidermis. By combining differential gene expression, pseudotime analyses, and spatial localization, we reconstruct HSE keratinocyte differentiation trajectories that recapitulate known in&amp;nbsp;vivo epidermal differentiation pathways and show that HSEs contain major in&amp;nbsp;vivo cellular states. However, HSEs also develop unique keratinocyte states, an expanded basal stem cell program, and disrupted terminal differentiation. Cell-cell communication modeling shows aberrant epithelial-to-mesenchymal transition (EMT)-associated signaling pathways that alter upon epidermal growth factor (EGF) supplementation. Last, xenograft HSEs at early time points post transplantation significantly rescue many in&amp;nbsp;vitro...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7km904sz</guid>
      <pubDate>Sat, 1 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Stabell, Adam R</name>
      </author>
      <author>
        <name>Lee, Grace E</name>
      </author>
      <author>
        <name>Jia, Yunlong</name>
      </author>
      <author>
        <name>Wong, Kirsten N</name>
      </author>
      <author>
        <name>Wang, Shuxiong</name>
      </author>
      <author>
        <name>Ling, Ji</name>
      </author>
      <author>
        <name>Nguyen, Sandrine D</name>
      </author>
      <author>
        <name>Sen, George L</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Atwood, Scott X</name>
        <uri>https://orcid.org/0000-0001-7407-9792</uri>
      </author>
    </item>
    <item>
      <title>Label-free multiphoton microscopy of immune cells in human skin</title>
      <link>https://escholarship.org/uc/item/3s606350</link>
      <description>This presentation will highlight the latest advances in utilizing a custom-designed clinical multiphoton imaging platform. The goal is to identify and distinguish immune cell populations in human skin using label-free molecular contrast.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3s606350</guid>
      <pubDate>Wed, 29 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Vallmitjana, A</name>
      </author>
      <author>
        <name>Durkin, A</name>
      </author>
      <author>
        <name>Rajil, N</name>
      </author>
      <author>
        <name>Shiu, J</name>
      </author>
      <author>
        <name>Ganesan, AK</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Balu, M</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
    </item>
    <item>
      <title>Patient-Reported Hair Loss and Its Impacts as Measured by the Alopecia Areata Patient Priority Outcomes Instrument in Patients Treated with Ritlecitinib: The ALLEGRO Phase 2b/3 Randomized Clinical Trial</title>
      <link>https://escholarship.org/uc/item/1fn6451r</link>
      <description>BackgroundThe ALLEGRO phase 2b/3 study investigated the efficacy and safety of ritlecitinib in patients with alopecia areata (AA).ObjectiveTo describe the impact of ritlecitinib on patient-reported hair loss using the Alopecia Areata Patient Priority Outcomes (AAPPO) instrument and evaluate the relationship between clinically meaningful hair regrowth and improvements in patient-reported impacts.MethodsIn ALLEGRO-2b/3, patients aged ≥ 12 years with AA and ≥ 50% scalp hair loss received once-daily ritlecitinib 50 or 30 mg (± 4-week 200-mg daily loading dose), 10 mg, or placebo for 24 weeks and&amp;nbsp;then continued ritlecitinib or switched from placebo to ritlecitinib 200/50 or 50 mg for 24 weeks. The AAPPO instrument evaluated improvement in hair loss, emotional symptoms (ES), and activity limitations (AL) from weeks 4 to 48 (secondary endpoint). Mean changes in ES and AL domain scores and individual items at weeks 24 and 48 were calculated for Severity of Alopecia Tool (SALT) score...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1fn6451r</guid>
      <pubDate>Mon, 27 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sinclair, Rodney</name>
      </author>
      <author>
        <name>Mesinkovska, Natasha</name>
        <uri>https://orcid.org/0000-0002-2705-7002</uri>
      </author>
      <author>
        <name>Mitra, Debanjali</name>
      </author>
      <author>
        <name>Wajsbrot, Dalia</name>
      </author>
      <author>
        <name>Law, Ernest H</name>
      </author>
      <author>
        <name>Wolk, Robert</name>
      </author>
      <author>
        <name>King, Brett</name>
      </author>
    </item>
    <item>
      <title>Round Bodies Detected by Treponema pallidum Immunohistochemical Stain in Two Cases of Cutaneous Syphilitic Gummata</title>
      <link>https://escholarship.org/uc/item/94n4p1s6</link>
      <description>ABSTRACT: Tertiary syphilis may present a diagnostic challenge due to negative nontreponemal serologies in up to 30% of cases and frequent lack of identifiable spirochetes on histopathology or other direct detection tests. We report 2 cases of round bodies staining with Treponema pallidum immunohistochemistry by light microscopy in biopsies from cutaneous syphilitic gummata. In 1 case, the finding was validated 3 times by 2 independent laboratories; in the other case, T. pallidum was detected by polymerase chain reaction in the biopsy sample. Spirochete round bodies have previously been reported in the setting of electron microscopy and fluorography, but to the best of our knowledge, have not been reported by light microscopy in a routine skin biopsy. Although the clinical implications are unclear, this may represent a helpful new paradigm for the diagnosis of tertiary syphilis.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/94n4p1s6</guid>
      <pubDate>Tue, 5 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Birmingham, Suzanne W</name>
      </author>
      <author>
        <name>Saeed, Lina</name>
      </author>
      <author>
        <name>Thurlow, Charles M</name>
      </author>
      <author>
        <name>Vilfort, Kendra</name>
      </author>
      <author>
        <name>Pillay, Allan</name>
      </author>
      <author>
        <name>Rojek, Nathan W</name>
      </author>
      <author>
        <name>Doan, Linda T</name>
        <uri>https://orcid.org/0000-0003-0274-2529</uri>
      </author>
      <author>
        <name>Lee, Bonnie A</name>
      </author>
    </item>
    <item>
      <title>1.7-micron Optical Coherence Tomography Angiography for Diagnosis and Monitoring of Hereditary Hemorrhagic Telangiectasia - A Pilot Study</title>
      <link>https://escholarship.org/uc/item/6h76g4h5</link>
      <description>OBJECTIVE: Develop a multi-functional imaging system that combines 1.7 µm optical coherence tomography/angiography (OCT/OCTA) to accurately interrogate Hereditary Hemorrhagic Telangiectasia (HHT) skin lesions.
METHODS: The study involved imaging HHT skin lesions on five subjects including lips, hands, and chest. We assessed the attributes of both HHT lesions and the healthy vasculature around them in these individuals, employing quantifiable measures such as vascular density and diameter. Additionally, we performed scans on an HHT patient who had undergone anti-angiogenic therapy, allowing us to observe changes in vasculature before and after treatment.
RESULTS: The results from this pilot study demonstrate the feasibility of evaluating the HHT lesion using this novel methodology and suggest the potential of OCTA to non-invasively track HHT lesions over time. The average percentage change in density between HHT patients' lesions and control was 37%. The percentage increase in...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6h76g4h5</guid>
      <pubDate>Tue, 29 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Murthy, Raksha Sreeramachandra</name>
      </author>
      <author>
        <name>Elsanadi, Rachel</name>
      </author>
      <author>
        <name>Soliman, John</name>
      </author>
      <author>
        <name>Li, Yan</name>
      </author>
      <author>
        <name>Chou, Li-Dek</name>
        <uri>https://orcid.org/0009-0001-3113-0401</uri>
      </author>
      <author>
        <name>Sprecher, Dennis</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Chen, Zhongping</name>
        <uri>https://orcid.org/0000-0002-4584-4560</uri>
      </author>
    </item>
    <item>
      <title>Optical coherence tomography-measured blood vessel characteristics of port-wine birthmarks by depth: A cross-sectional study</title>
      <link>https://escholarship.org/uc/item/6dd4h014</link>
      <description>BACKGROUND: Port-Wine Birthmarks (PWB) are congenital capillary malformations requiring multiple treatments. Optical coherence tomography (OCT), a noninvasive imaging technique, characterizes vessels in cutaneous vascular lesions, including PWBs.
OBJECTIVE: To assess variability in blood vessel characteristics within and between individual PWBs.
METHODS: OCT was used to measure blood vessel density (%) and modal vessel diameter (micrometers) at increments of 0.05&amp;nbsp;mm from the skin surface to a depth of 0.50&amp;nbsp;mm at several adjacent spots of single PWBs in this cross-sectional study. Average ratios of vessel density and diameter in affected to control skin were obtained for each PWB by averaging data for all spots within a lesion. Statistical analysis was performed with a linear mixed effects model using SPSS software (IBM Corporation).
RESULTS: There was great variability in vessel density and diameter within and between PWBs. Depths where average ratios of vessel density...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6dd4h014</guid>
      <pubDate>Tue, 29 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Elsanadi, Rachel Ann</name>
      </author>
      <author>
        <name>Messele, Feben</name>
      </author>
      <author>
        <name>Lee, Jaylen</name>
      </author>
      <author>
        <name>Choi, Bernard</name>
        <uri>https://orcid.org/0000-0002-4380-8291</uri>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
    </item>
    <item>
      <title>Early detection of cutaneous neurofibromas using spatial frequency domain imaging and optical coherence tomography</title>
      <link>https://escholarship.org/uc/item/5bx111pp</link>
      <description>Early detection of cutaneous neurofibromas using spatial frequency domain imaging and optical coherence tomography</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5bx111pp</guid>
      <pubDate>Tue, 29 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Junsoo</name>
      </author>
      <author>
        <name>Jia, Wangcun</name>
        <uri>https://orcid.org/0000-0002-5021-3827</uri>
      </author>
      <author>
        <name>Kennedy, Gordon</name>
      </author>
      <author>
        <name>Katta, Nitesh</name>
      </author>
      <author>
        <name>Sierra, Rafael</name>
      </author>
      <author>
        <name>Johnson, James E</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Durkin, Anthony J</name>
      </author>
      <author>
        <name>Nelson, J Stuart</name>
        <uri>https://orcid.org/0000-0002-2697-9152</uri>
      </author>
      <author>
        <name>Milner, Thomas</name>
        <uri>https://orcid.org/0000-0002-7532-0004</uri>
      </author>
    </item>
    <item>
      <title>Intradermal Delivery of Calcium Hydroxylapatite With Fractionated Ablation</title>
      <link>https://escholarship.org/uc/item/4776b258</link>
      <description>OBJECTIVES: The absorption of biostimulatory particulate matter following its application to fractional skin defects remains poorly understood, and even less is known about its in vivo impact in terms of tissue integration. The objectives of this study are twofold: (1) to evaluate the potential of calcium hydroxylapatite (CaHA) to penetrate through skin treated with a fractional laser; and (2) to assess the effectiveness of clinical laser scanning microscopy technologies in monitoring the effects of such treatment over time.
METHODS: One area on a volunteer's arm was treated with a fractional erbium laser (Sciton Inc., Palo Alto, CA), while a second area received the same laser treatment followed by CaHA topical application. We used reflectance confocal microscopy (RCM) and multiphoton microscopy (MPM) to noninvasively image beneath the surface of the treated skin to study and monitor the effects of these treatments within 1 h of treatment and at four additional time points over...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4776b258</guid>
      <pubDate>Mon, 28 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Driscoll, William</name>
      </author>
      <author>
        <name>Golbari, Nicole M</name>
      </author>
      <author>
        <name>Vallmitjana, Alexander</name>
      </author>
      <author>
        <name>Durkin, Amanda F</name>
      </author>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Zachary, Christopher B</name>
        <uri>https://orcid.org/0000-0002-5883-5188</uri>
      </author>
    </item>
    <item>
      <title>Strategies for overcoming obstacles to hands-on cosmetic and laser training in dermatology residency</title>
      <link>https://escholarship.org/uc/item/6n6837pc</link>
      <description>Strategies for overcoming obstacles to hands-on cosmetic and laser training in dermatology residency</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6n6837pc</guid>
      <pubDate>Tue, 8 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kang, Bianca Y</name>
      </author>
      <author>
        <name>Aristizabal, Miguel</name>
      </author>
      <author>
        <name>Stratman, Erik J</name>
      </author>
      <author>
        <name>Hu, Jenny C</name>
      </author>
      <author>
        <name>Petronic-Rosic, Vesna</name>
      </author>
      <author>
        <name>Minkis, Kira</name>
      </author>
      <author>
        <name>Elsanadi, Rachel</name>
      </author>
      <author>
        <name>Alvarez, Gabriella</name>
      </author>
      <author>
        <name>Nadir, Umer</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Saikaly, Sami K</name>
      </author>
      <author>
        <name>Bolotin, Diana</name>
      </author>
      <author>
        <name>Levin, Yakir S</name>
      </author>
      <author>
        <name>Orringer, Jeffrey S</name>
      </author>
      <author>
        <name>Alam, Murad</name>
      </author>
    </item>
    <item>
      <title>Leveraging gene correlations in single cell transcriptomic data</title>
      <link>https://escholarship.org/uc/item/15k712w5</link>
      <description>BackgroundMany approaches have been developed to overcome technical noise in single cell RNA-sequencing (scRNAseq). As researchers dig deeper into data—looking for rare cell types, subtleties of cell states, and details of gene regulatory networks—there is a growing need for algorithms with controllable accuracy and fewer ad hoc parameters and thresholds. Impeding this goal is the fact that an appropriate null distribution for scRNAseq cannot simply be extracted from data in which ground truth about biological variation is unknown (i.e., usually).ResultsWe approach this problem analytically, assuming that scRNAseq data reflect only cell heterogeneity (what we seek to characterize), transcriptional noise (temporal fluctuations randomly distributed across cells), and sampling error (i.e., Poisson noise). We analyze scRNAseq data without normalization—a step that skews distributions, particularly for sparse data—and calculate p values associated with key statistics. We develop an...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/15k712w5</guid>
      <pubDate>Thu, 26 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Silkwood, Kai</name>
      </author>
      <author>
        <name>Dollinger, Emmanuel</name>
      </author>
      <author>
        <name>Gervin, Joshua</name>
      </author>
      <author>
        <name>Atwood, Scott</name>
        <uri>https://orcid.org/0000-0001-7407-9792</uri>
      </author>
      <author>
        <name>Nie, Qing</name>
      </author>
      <author>
        <name>Lander, Arthur D</name>
        <uri>https://orcid.org/0000-0002-4380-5525</uri>
      </author>
    </item>
    <item>
      <title>Ergonomics in Dermatologic Laser Procedures.</title>
      <link>https://escholarship.org/uc/item/8nw0k12w</link>
      <description>Due to working in static positions and use of repetitive movements over long periods of time, dermatologists are at increased risk of work-related musculoskeletal injury. Historically, studies on procedural ergonomics have focused on dermatologic surgery, however, laser procedures can also have a significant cumulative effect on physician posture. Here, we aim to highlight ergonomic challenges specific to dermatologic laser procedures and suggest areas of improvement in operating room organization, patient positioning, physician mechanics, and instrumentation. For the operating room, it is beneficial to store several devices in the same room, have central placement of electrical outlets, and to position the devices on the same side of the bed as the laser operator. When considering patient positioning, a Trendelenburg bed position can be helpful for vascular lesions on the head, and frequent repositioning of the patient can prevent uncomfortable bending of the operator and laser...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8nw0k12w</guid>
      <pubDate>Mon, 16 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Yale, Katerina</name>
      </author>
      <author>
        <name>Cox, Surget</name>
      </author>
      <author>
        <name>Grushchak, Solomiya</name>
      </author>
      <author>
        <name>Lee, Patrick K</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
    </item>
    <item>
      <title>A Roadmap for a Consensus Human Skin Cell Atlas and Single-Cell Data Standardization</title>
      <link>https://escholarship.org/uc/item/1qg450st</link>
      <description>Single-cell technologies have become essential to driving discovery in both basic and translational investigative dermatology. Despite the multitude of available datasets, a central reference atlas of normal human skin, which can serve as a reference resource for skin cell types, cell states, and their molecular signatures, is still lacking. For any such atlas to receive broad acceptance, participation by many investigators during atlas construction is an essential prerequisite. As part of the Human Cell Atlas project, we have assembled a Skin Biological Network to build a consensus Human Skin Cell Atlas and outline a roadmap toward that goal. We define the drivers of skin diversity to be considered when selecting sequencing datasets for the atlas and list practical hurdles during skin sampling that can result in data gaps and impede comprehensive representation and technical considerations for tissue processing and computational analysis, the accounting for which should minimize...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1qg450st</guid>
      <pubDate>Tue, 10 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Almet, Axel A</name>
      </author>
      <author>
        <name>Yuan, Hao</name>
      </author>
      <author>
        <name>Annusver, Karl</name>
      </author>
      <author>
        <name>Ramos, Raul</name>
      </author>
      <author>
        <name>Liu, Yingzi</name>
      </author>
      <author>
        <name>Wiedemann, Julie</name>
      </author>
      <author>
        <name>Sorkin, Dara H</name>
        <uri>https://orcid.org/0000-0003-0742-9240</uri>
      </author>
      <author>
        <name>Landén, Ning Xu</name>
      </author>
      <author>
        <name>Sonkoly, Enikö</name>
      </author>
      <author>
        <name>Haniffa, Muzlifah</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Lichtenberger, Beate M</name>
      </author>
      <author>
        <name>Luecken, Malte D</name>
      </author>
      <author>
        <name>Andersen, Bogi</name>
        <uri>https://orcid.org/0000-0001-7181-2768</uri>
      </author>
      <author>
        <name>Tsoi, Lam C</name>
      </author>
      <author>
        <name>Watt, Fiona M</name>
      </author>
      <author>
        <name>Gudjonsson, Johann E</name>
      </author>
      <author>
        <name>Plikus, Maksim V</name>
      </author>
      <author>
        <name>Kasper, Maria</name>
      </author>
    </item>
    <item>
      <title>Increasing Endoglin Deletion in Endothelial Cells Exacerbates the Severity of Brain Arteriovenous Malformation in Mouse</title>
      <link>https://escholarship.org/uc/item/4kt413dq</link>
      <description>Endoglin (&lt;i&gt;ENG&lt;/i&gt;) mutation causes type 1 hereditary hemorrhagic telangiectasia (HHT1). HHT1 patients have arteriovenous malformations (AVMs) in multiple organs, including the brain. In mice, &lt;i&gt;Eng&lt;/i&gt; deletion induced by R26RCreER or SM22αCre leads to AVM development in the brain and other organs. We hypothesized that an increase in Eng- negative ECs will enhance AVM severity. To increase EC &lt;i&gt;Eng&lt;/i&gt; deletion, we used a codon-improved cre (icre), which is more potent in recombination of the floxed alleles than the wild-type (WT) cre. R26RCreER;&lt;i&gt;Eng&lt;/i&gt;&lt;sup&gt;f/f&lt;/sup&gt; mice that have a Rosa promoter driving and tamoxifen (TM)-inducible WT cre expression globally, and PdgfbiCreER;&lt;i&gt;Eng&lt;/i&gt;&lt;sup&gt;f/f&lt;/sup&gt; mice that have a Pdgfb promoter driving and TM-inducible icre expression in ECs were treated with three intra-peritoneal injections of TM (2.5 mg/25 g of body weight) to delete &lt;i&gt;Eng&lt;/i&gt; globally or in the ECs. AAV-VEGF was stereotactically injected into the brain to induce...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4kt413dq</guid>
      <pubDate>Wed, 4 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shabani, Zahra</name>
      </author>
      <author>
        <name>Do Prado, Leandro Barbosa</name>
      </author>
      <author>
        <name>Zhang, Rui</name>
      </author>
      <author>
        <name>Zhu, Wan</name>
      </author>
      <author>
        <name>Shaligram, Sonali S</name>
      </author>
      <author>
        <name>Yadav, Alka</name>
      </author>
      <author>
        <name>Wang, Calvin</name>
      </author>
      <author>
        <name>Su, Hua</name>
        <uri>https://orcid.org/0000-0003-1566-9877</uri>
      </author>
    </item>
    <item>
      <title>Ergonomics in Dermatologic Laser Procedures.</title>
      <link>https://escholarship.org/uc/item/63n667nc</link>
      <description>Due to working in static positions and use of repetitive movements over long periods of time, dermatologists are at increased risk of work-related musculoskeletal injury. Historically, studies on procedural ergonomics have focused on dermatologic surgery, however, laser procedures can also have a significant cumulative effect on physician posture. Here, we aim to highlight ergonomic challenges specific to dermatologic laser procedures and suggest areas of improvement in operating room organization, patient positioning, physician mechanics, and instrumentation. For the operating room, it is beneficial to store several devices in the same room, have central placement of electrical outlets, and to position the devices on the same side of the bed as the laser operator. When considering patient positioning, a Trendelenburg bed position can be helpful for vascular lesions on the head, and frequent repositioning of the patient can prevent uncomfortable bending of the operator and laser...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/63n667nc</guid>
      <pubDate>Mon, 2 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Yale, Katerina</name>
      </author>
      <author>
        <name>Cox, Surget</name>
      </author>
      <author>
        <name>Grushchak, Solomiya</name>
      </author>
      <author>
        <name>Lee, Patrick</name>
      </author>
      <author>
        <name>Kelly, Kristen</name>
      </author>
    </item>
    <item>
      <title>Metastatic pilomatrix carcinoma treated with stereotactic body radiation therapy</title>
      <link>https://escholarship.org/uc/item/3xm5v56x</link>
      <description>Metastatic pilomatrix carcinoma treated with stereotactic body radiation therapy</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3xm5v56x</guid>
      <pubDate>Wed, 28 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Banks, Rufus</name>
      </author>
      <author>
        <name>Park, Jino</name>
        <uri>https://orcid.org/0000-0001-5228-3880</uri>
      </author>
      <author>
        <name>Doan, Linda</name>
        <uri>https://orcid.org/0000-0003-0274-2529</uri>
      </author>
      <author>
        <name>Healy, Erin</name>
      </author>
      <author>
        <name>Harris, Jeremy P</name>
        <uri>https://orcid.org/0000-0003-1231-4798</uri>
      </author>
    </item>
    <item>
      <title>Best Practices for Achieving Compliance with the NIH Public Access Mandate</title>
      <link>https://escholarship.org/uc/item/7bq61487</link>
      <description>NIH Public Access Policy requires that published journal articles resulting from NIH-funded research be made available to the public no later than 12 months after the date of publication. The public access mandate has been extended to NSF-funded research as well, and the government is moving toward making it a requirement for ALL federal funding. Non-compliance with this policy affects researchers because federal funding could be withheld. This presentation will introduce best practices for achieving compliance, and provide access to helpful resources, like the NIH Public Access Compliance video produced by UCI’s Office of Research.

The presentation by Brown was supported by funding from a LAUC (Librarians Association of the University of California) Mini-Grant for Travel and Presentation.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7bq61487</guid>
      <pubDate>Mon, 19 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Frazer, Kim</name>
      </author>
      <author>
        <name>Kim, Hanna</name>
      </author>
      <author>
        <name>Brown, Mitchell C</name>
        <uri>https://orcid.org/0000-0002-3366-1281</uri>
      </author>
    </item>
    <item>
      <title>Defining Epidermal Basal Cell States during Skin Homeostasis and Wound Healing Using Single-Cell Transcriptomics</title>
      <link>https://escholarship.org/uc/item/7v17t2hh</link>
      <description>Our knowledge of transcriptional heterogeneities in epithelial stem and progenitor cell compartments is limited. Epidermal basal cells sustain cutaneous tissue maintenance and drive wound healing. Previous studies have probed basal cell heterogeneity in stem and progenitor potential, but a comprehensive dissection of basal cell dynamics during differentiation is lacking. Using single-cell RNA sequencing coupled with RNAScope and fluorescence lifetime imaging, we identify three non-proliferative and one proliferative basal cell state in homeostatic skin that differ in metabolic preference and become spatially partitioned during wound re-epithelialization. Pseudotemporal trajectory and RNA velocity analyses predict a quasi-linear differentiation hierarchy where basal cells progress from Col17a1&lt;sup&gt;Hi&lt;/sup&gt;/Trp63&lt;sup&gt;Hi&lt;/sup&gt; state to early-response state, proliferate at the juncture of these two states, or become growth arrested before differentiating into spinous cells. Wound...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7v17t2hh</guid>
      <pubDate>Sun, 18 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Haensel, Daniel</name>
      </author>
      <author>
        <name>Jin, Suoqin</name>
      </author>
      <author>
        <name>Sun, Peng</name>
      </author>
      <author>
        <name>Cinco, Rachel</name>
      </author>
      <author>
        <name>Dragan, Morgan</name>
      </author>
      <author>
        <name>Nguyen, Quy</name>
      </author>
      <author>
        <name>Cang, Zixuan</name>
      </author>
      <author>
        <name>Gong, Yanwen</name>
      </author>
      <author>
        <name>Vu, Remy</name>
      </author>
      <author>
        <name>MacLean, Adam L</name>
      </author>
      <author>
        <name>Kessenbrock, Kai</name>
      </author>
      <author>
        <name>Gratton, Enrico</name>
        <uri>https://orcid.org/0000-0002-6450-7391</uri>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Dai, Xing</name>
        <uri>https://orcid.org/0000-0001-8134-1365</uri>
      </author>
    </item>
    <item>
      <title>Circadian control of interferon-sensitive gene expression in murine skin</title>
      <link>https://escholarship.org/uc/item/34h42478</link>
      <description>The circadian clock coordinates a variety of immune responses with signals from the external environment to promote survival. We investigated the potential reciprocal relationship between the circadian clock and skin inflammation. We treated mice topically with the Toll-like receptor 7 (TLR7) agonist imiquimod (IMQ) to activate IFN-sensitive gene (ISG) pathways and induce psoriasiform inflammation. IMQ transiently altered core clock gene expression, an effect mirrored in human patient psoriatic lesions. In mouse skin 1 d after IMQ treatment, ISGs, including the key ISG transcription factor &lt;i&gt;IFN regulatory factor 7&lt;/i&gt; (&lt;i&gt;Irf7),&lt;/i&gt; were more highly induced after treatment during the day than the night. Nuclear localization of phosphorylated-IRF7 was most prominently time-of-day dependent in epidermal leukocytes, suggesting that these cell types play an important role in the diurnal ISG response to IMQ. Mice lacking &lt;i&gt;Bmal1&lt;/i&gt; systemically had exacerbated and arrhythmic ISG&lt;i&gt;/Irf7&lt;/i&gt;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/34h42478</guid>
      <pubDate>Sun, 18 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Greenberg, Elyse Noelani</name>
      </author>
      <author>
        <name>Marshall, Michaela Ellen</name>
      </author>
      <author>
        <name>Jin, Suoqin</name>
      </author>
      <author>
        <name>Venkatesh, Sanan</name>
      </author>
      <author>
        <name>Dragan, Morgan</name>
      </author>
      <author>
        <name>Tsoi, Lam C</name>
      </author>
      <author>
        <name>Gudjonsson, Johann E</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Takahashi, Joseph S</name>
      </author>
      <author>
        <name>Andersen, Bogi</name>
        <uri>https://orcid.org/0000-0001-7181-2768</uri>
      </author>
    </item>
    <item>
      <title>Alternative mRNA splicing events and regulators in epidermal differentiation</title>
      <link>https://escholarship.org/uc/item/6tq7z5sc</link>
      <description>Alternative splicing (AS) of messenger RNAs occurs in ∼95% of multi-exon human genes and generates diverse RNA and protein isoforms. We investigated AS events associated with human epidermal differentiation, a process crucial for skin function. We identified 6,413 AS events, primarily involving cassette exons. We also predicted 34 RNA-binding proteins (RBPs) regulating epidermal AS, including 19 previously undescribed candidate regulators. From these results, we identified FUS as an RBP that regulates the balance between keratinocyte proliferation and differentiation. Additionally, we characterized the function of a cassette exon AS event in MAP3K7, which encodes a kinase involved in cell signaling. We found that a switch from the short to long isoform of MAP3K7, triggered during differentiation, enforces the demarcation between proliferating basal progenitors and overlying differentiated strata. Our findings indicate that AS occurs extensively in the human epidermis and has critical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6tq7z5sc</guid>
      <pubDate>Sat, 17 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Takashima, Shota</name>
      </author>
      <author>
        <name>Sun, Wujianan</name>
      </author>
      <author>
        <name>Otten, Auke BC</name>
      </author>
      <author>
        <name>Cai, Pengfei</name>
      </author>
      <author>
        <name>Peng, Shaohong Isaac</name>
      </author>
      <author>
        <name>Tong, Elton</name>
      </author>
      <author>
        <name>Bui, Jolina</name>
      </author>
      <author>
        <name>Mai, McKenzie</name>
      </author>
      <author>
        <name>Amarbayar, Oyumergen</name>
      </author>
      <author>
        <name>Cheng, Binbin</name>
      </author>
      <author>
        <name>Odango, Rowen Jane</name>
      </author>
      <author>
        <name>Li, Zongkai</name>
      </author>
      <author>
        <name>Qu, Kun</name>
      </author>
      <author>
        <name>Sun, Bryan K</name>
      </author>
    </item>
    <item>
      <title>Clinical features in adults with acquired cutis laxa: a retrospective review</title>
      <link>https://escholarship.org/uc/item/7sz5p5hx</link>
      <description>Acquired cutis laxa (ACL) is a very rare dermatological condition with numerous proposed aetiologies. Herein, we report on 10 adult patients&amp;nbsp;with ACL, three of which&amp;nbsp;were found to have genetic mutations suggesting a genetic predisposition for the development of ACL following exposure to an environmental insult. Four patients were presumed to develop ACL in association with medication exposure. Overall,&amp;nbsp;if a case of potential ACL arises, providers should carefully review patient history and comorbidities, perform thorough systemic investigations based on symptomatology, and consider genetic analysis.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7sz5p5hx</guid>
      <pubDate>Wed, 14 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>O’Connell, Katie A</name>
      </author>
      <author>
        <name>Schaefer, Morgan</name>
      </author>
      <author>
        <name>Atzmony, Lihi</name>
      </author>
      <author>
        <name>Vleugels, Ruth Ann</name>
      </author>
      <author>
        <name>Choate, Keith</name>
      </author>
      <author>
        <name>LaChance, Avery H</name>
      </author>
      <author>
        <name>Min, Michelle S</name>
      </author>
    </item>
    <item>
      <title>Treatment With Mycophenolate Mofetil for Salt-and-Pepper Dyspigmentation Caused by Autoimmune Sclerosing Disease</title>
      <link>https://escholarship.org/uc/item/6gm5v086</link>
      <description>This case report describes 3 patients with systemic sclerosis or mixed connective tissue disease with scleroderma features who experienced salt-and-pepper dyspigmentation that responded to treatment with mycophenolate mofetil.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6gm5v086</guid>
      <pubDate>Wed, 14 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Min, Michelle S</name>
      </author>
      <author>
        <name>Mazori, Daniel R</name>
      </author>
      <author>
        <name>Kassamali, Bina</name>
      </author>
      <author>
        <name>Cobos, Gabriela</name>
      </author>
      <author>
        <name>Ho, Allen</name>
      </author>
      <author>
        <name>LaChance, Avery H</name>
      </author>
      <author>
        <name>Vleugels, Ruth Ann</name>
      </author>
    </item>
    <item>
      <title>Ritlecitinib, a JAK3/TEC family kinase inhibitor, stabilizes active lesions and repigments stable lesions in vitiligo</title>
      <link>https://escholarship.org/uc/item/3qz833wt</link>
      <description>The efficacy of ritlecitinib, an oral JAK3/TEC family kinase inhibitor, on active and stable lesions was evaluated in patients with active non-segmental vitiligo in a phase 2b trial (NCT03715829). Patients were randomized to placebo or daily ritlecitinib 50&amp;nbsp;mg (with or without 4-week 100-mg or 200-mg loading dose), 30&amp;nbsp;mg, or 10&amp;nbsp;mg for 24 weeks. Active lesions showed greater baseline expression of inflammatory/immune markers IFNG and CCL5, levels of CD103, and T-cell infiltrates than stable lesions. Patients with more active than stable vitiligo lesions showed higher baseline serum levels of CXCL9 and PD-L1, while patients with more stable than active lesions showed higher baseline serum levels of HO-1. At Week 24, ritlecitinib 50&amp;nbsp;mg significantly stabilized mean percent change from baseline in depigmentation extent in both active lesions and stable lesions vs. placebo-response, with stable lesions showing greater repigmentation. After 24 weeks of treatment,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3qz833wt</guid>
      <pubDate>Fri, 2 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Yamaguchi, Yuji</name>
      </author>
      <author>
        <name>Peeva, Elena</name>
      </author>
      <author>
        <name>Duca, Ester Del</name>
      </author>
      <author>
        <name>Facheris, Paola</name>
      </author>
      <author>
        <name>Bar, Jonathan</name>
      </author>
      <author>
        <name>Shore, Ronald</name>
      </author>
      <author>
        <name>Cox, Lori Ann</name>
      </author>
      <author>
        <name>Sloan, Abigail</name>
      </author>
      <author>
        <name>Thaçi, Diamant</name>
      </author>
      <author>
        <name>Ganesan, Anand</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>Han, George</name>
      </author>
      <author>
        <name>Ezzedine, Khaled</name>
      </author>
      <author>
        <name>Ye, Zhan</name>
      </author>
      <author>
        <name>Guttman-Yassky, Emma</name>
      </author>
    </item>
    <item>
      <title>Epithelial Migration and Non-adhesive Periderm Are Required for Digit Separation during Mammalian Development</title>
      <link>https://escholarship.org/uc/item/3hd8g0gc</link>
      <description>The fusion of digits or toes, syndactyly, can be part of complex syndromes, including van der Woude syndrome. A subset of van der Woude cases is caused by dominant-negative mutations in the epithelial transcription factor Grainyhead like-3 (GRHL3), and Grhl3&lt;sup&gt;-/-&lt;/sup&gt;mice have soft-tissue syndactyly. Although impaired interdigital cell death of mesenchymal cells causes syndactyly in multiple genetic mutants, Grhl3&lt;sup&gt;-/-&lt;/sup&gt; embryos had normal interdigital cell death, suggesting alternative mechanisms for syndactyly. We found that in digit separation, the overlying epidermis forms a migrating interdigital epithelial tongue (IET) when the epithelium invaginates to separate the digits. Normally, the non-adhesive surface periderm allows the IET to bifurcate as the digits separate. In contrast, in Grhl3&lt;sup&gt;-/-&lt;/sup&gt; embryos, the IET moves normally between the digits but fails to bifurcate because of abnormal adhesion of the periderm. Our study identifies epidermal developmental...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3hd8g0gc</guid>
      <pubDate>Sun, 21 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kashgari, Ghaidaa</name>
      </author>
      <author>
        <name>Meinecke, Lina</name>
      </author>
      <author>
        <name>Gordon, William</name>
      </author>
      <author>
        <name>Ruiz, Bryan</name>
      </author>
      <author>
        <name>Yang, Jady</name>
      </author>
      <author>
        <name>Lan, Amy</name>
      </author>
      <author>
        <name>Xie, Yilu</name>
      </author>
      <author>
        <name>Ho, Hsiang</name>
      </author>
      <author>
        <name>Plikus, Maksim V</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Jester, James V</name>
        <uri>https://orcid.org/0000-0002-9246-0981</uri>
      </author>
      <author>
        <name>Andersen, Bogi</name>
        <uri>https://orcid.org/0000-0001-7181-2768</uri>
      </author>
    </item>
    <item>
      <title>Port Wine Birthmark Therapy: A New Direction</title>
      <link>https://escholarship.org/uc/item/4tj4x8rv</link>
      <description>Port Wine Birthmark Therapy: A New Direction</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4tj4x8rv</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Messele, Feben</name>
      </author>
      <author>
        <name>Van Trigt, William</name>
      </author>
      <author>
        <name>Arkin, Lisa</name>
      </author>
      <author>
        <name>Hughes, Christopher CW</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
    </item>
    <item>
      <title>Availability of lasers and hands-on training in cosmetic dermatology in residency</title>
      <link>https://escholarship.org/uc/item/4rv2z0mf</link>
      <description>Availability of lasers and hands-on training in cosmetic dermatology in residency</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4rv2z0mf</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kang, Bianca Y</name>
      </author>
      <author>
        <name>Stratman, Erik J</name>
      </author>
      <author>
        <name>Hu, Jenny C</name>
      </author>
      <author>
        <name>Elsanadi, Rachel</name>
      </author>
      <author>
        <name>Greywal, Tanya</name>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Ortiz, Arisa</name>
      </author>
      <author>
        <name>Saikaly, Sami K</name>
      </author>
      <author>
        <name>Suozzi, Kathleen C</name>
      </author>
      <author>
        <name>Bolotin, Diana</name>
      </author>
      <author>
        <name>Minkis, Kira</name>
      </author>
      <author>
        <name>Alam, Murad</name>
      </author>
      <author>
        <name>Group, Cosmetic and Laser Education Working</name>
      </author>
      <author>
        <name>Antonovich, Diana D</name>
      </author>
      <author>
        <name>Bar, Anna</name>
      </author>
      <author>
        <name>Boucher, Alison</name>
      </author>
      <author>
        <name>Chow, Maggie L</name>
      </author>
      <author>
        <name>Council, M Laurin</name>
      </author>
      <author>
        <name>Dave, Loma</name>
      </author>
      <author>
        <name>Deng, Min</name>
      </author>
      <author>
        <name>Eshaq, Milad</name>
      </author>
      <author>
        <name>Farah, Ronda S</name>
      </author>
      <author>
        <name>Ghareeb, Erica</name>
      </author>
      <author>
        <name>Robinson, Carolyn Hardin</name>
      </author>
      <author>
        <name>Hooper, Deirdre</name>
      </author>
      <author>
        <name>Hoss, Elika</name>
      </author>
      <author>
        <name>Hisham, Farhana Ikmal</name>
      </author>
      <author>
        <name>Joo, Jayne</name>
      </author>
      <author>
        <name>Kelly, Erica B</name>
      </author>
      <author>
        <name>Kibbi, Nour</name>
      </author>
      <author>
        <name>Kole, Lauren CS</name>
      </author>
      <author>
        <name>Kourosh, A Shadi</name>
      </author>
      <author>
        <name>Kuhn, Helena</name>
      </author>
      <author>
        <name>Labadie, Jessica G</name>
      </author>
      <author>
        <name>Lawrence, Naomi</name>
      </author>
      <author>
        <name>Levin, Yakir S</name>
      </author>
      <author>
        <name>Luke, Janiene</name>
      </author>
      <author>
        <name>Nadir, Umer</name>
      </author>
      <author>
        <name>Nawas, Zeena Y</name>
      </author>
      <author>
        <name>Orringer, Jeffrey S</name>
      </author>
      <author>
        <name>Pearlstein, Michelle V</name>
      </author>
      <author>
        <name>Petronic-Rosic, Vesna</name>
      </author>
      <author>
        <name>Roberts, Jared E</name>
      </author>
      <author>
        <name>Schenck, Olivia L</name>
      </author>
      <author>
        <name>Schlick, Cynthia A</name>
      </author>
      <author>
        <name>Shah, Kalee</name>
      </author>
      <author>
        <name>Shahabi, Ladan</name>
      </author>
      <author>
        <name>Suggs, Amanda K</name>
      </author>
      <author>
        <name>Tolaymat, Leila</name>
      </author>
      <author>
        <name>Vashi, Neelam A</name>
      </author>
      <author>
        <name>Ward, Kimberley HM</name>
      </author>
      <author>
        <name>Wyles, Saranya P</name>
      </author>
      <author>
        <name>Yi, Michael</name>
      </author>
      <author>
        <name>Yoo, Simon S</name>
      </author>
    </item>
    <item>
      <title>Discovery of CDC42 Inhibitors with a Favorable Pharmacokinetic Profile and Anticancer In Vivo Efficacy</title>
      <link>https://escholarship.org/uc/item/3db4936c</link>
      <description>We previously reported trisubstituted pyrimidine lead compounds, namely, ARN22089 and ARN25062, which block the interaction between CDC42 with its specific downstream effector, a PAK protein. This interaction is crucial for the progression of multiple tumor types. Such inhibitors showed anticancer efficacy in vivo. Here, we describe a second class of CDC42 inhibitors with favorable drug-like properties. Out of the 25 compounds here reported, compound &lt;b&gt;15&lt;/b&gt; (ARN25499) stands out as the best lead compound with an improved pharmacokinetic profile, increased bioavailability, and efficacy in an in vivo PDX tumor mouse model. Our results indicate that these CDC42 inhibitors represent a promising chemical class toward the discovery of anticancer drugs, with ARN25499 as an additional lead candidate for preclinical development.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3db4936c</guid>
      <pubDate>Sat, 6 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Brindani, Nicoletta</name>
      </author>
      <author>
        <name>Vuong, Linh M</name>
      </author>
      <author>
        <name>La Serra, Maria Antonietta</name>
      </author>
      <author>
        <name>Salvador, Noel</name>
      </author>
      <author>
        <name>Menichetti, Andrea</name>
      </author>
      <author>
        <name>Acquistapace, Isabella Maria</name>
      </author>
      <author>
        <name>Ortega, Jose Antonio</name>
      </author>
      <author>
        <name>Veronesi, Marina</name>
      </author>
      <author>
        <name>Bertozzi, Sine Mandrup</name>
      </author>
      <author>
        <name>Summa, Maria</name>
      </author>
      <author>
        <name>Girotto, Stefania</name>
      </author>
      <author>
        <name>Bertorelli, Rosalia</name>
      </author>
      <author>
        <name>Armirotti, Andrea</name>
      </author>
      <author>
        <name>Ganesan, Anand K</name>
        <uri>https://orcid.org/0000-0003-4944-9274</uri>
      </author>
      <author>
        <name>De Vivo, Marco</name>
      </author>
    </item>
    <item>
      <title>A Randomized, Double-Blind, Placebo-Controlled Phase II Clinical Trial of Lovastatin for Various Endpoints of Melanoma Pathobiology</title>
      <link>https://escholarship.org/uc/item/7v68d1p8</link>
      <description>On the basis of large cardiovascular clinical trials of lipid-lowering agents that showed a considerable decrease in the incidence of primary melanomas in the active agent arm, we have carried out a randomized, double-blind clinical trial examining the impact of lovastatin on various biomarkers of melanoma pathogenesis. Subjects with at least two clinically atypical nevi were randomized to receive oral lovastatin or placebo for a 6-month period. Clinical, histopathologic, and molecular biomarkers were evaluated for change in the two groups. Eighty subjects were randomized, evaluable, and included in the analyses. Lovastatin showed no benefit in comparison with placebo in the primary endpoint of decreasing the level of histopathologic atypia, nor in any of the secondary endpoints of decreasing clinical atypia, impact on nevus number, nor in showing significant changes in any of the molecular biomarkers. There were no significant differences in adverse event profiles for lovastatin...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7v68d1p8</guid>
      <pubDate>Mon, 17 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Linden, Kenneth G</name>
      </author>
      <author>
        <name>Leachman, Sancy A</name>
      </author>
      <author>
        <name>Zager, Jonathan S</name>
      </author>
      <author>
        <name>Jakowatz, James G</name>
      </author>
      <author>
        <name>Viner, Jaye L</name>
      </author>
      <author>
        <name>McLaren, Christine E</name>
        <uri>https://orcid.org/0000-0002-7932-9903</uri>
      </author>
      <author>
        <name>Barr, Ronald J</name>
      </author>
      <author>
        <name>Carpenter, Philip M</name>
      </author>
      <author>
        <name>Chen, Wen-Pin</name>
      </author>
      <author>
        <name>Elmets, Craig A</name>
      </author>
      <author>
        <name>Tangrea, Joseph A</name>
      </author>
      <author>
        <name>Lim, Sung-Jig</name>
      </author>
      <author>
        <name>Cochran, Alistair J</name>
      </author>
      <author>
        <name>Meyskens, Frank L</name>
        <uri>https://orcid.org/0000-0002-8827-4334</uri>
      </author>
    </item>
    <item>
      <title>Distinguishing between Benign and Malignant Melanocytic Nevi by In Vivo Multiphoton Microscopy</title>
      <link>https://escholarship.org/uc/item/6rr7z879</link>
      <description>Monitoring of atypical nevi is an important step in early detection of melanoma, a clinical imperative in preventing the disease progression. Current standard diagnosis is based on biopsy and histopathologic examination, a method that is invasive and highly dependent upon physician experience. In this work, we used a clinical multiphoton microscope to image in vivo and noninvasively melanocytic nevi at three different stages: common nevi without dysplastic changes, dysplastic nevi with structural and architectural atypia, and melanoma. We analyzed multiphoton microscopy (MPM) images corresponding to 15 lesions (five in each group) both qualitatively and quantitatively. For the qualitative analysis, we identified the morphologic features characteristic of each group. MPM images corresponding to dysplastic nevi and melanoma were compared with standard histopathology to determine correlations between tissue constituents and morphology and to evaluate whether standard histopathology...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6rr7z879</guid>
      <pubDate>Mon, 17 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Balu, Mihaela</name>
        <uri>https://orcid.org/0000-0002-8018-5134</uri>
      </author>
      <author>
        <name>Kelly, Kristen M</name>
        <uri>https://orcid.org/0000-0002-5988-2197</uri>
      </author>
      <author>
        <name>Zachary, Christopher B</name>
        <uri>https://orcid.org/0000-0002-5883-5188</uri>
      </author>
      <author>
        <name>Harris, Ronald M</name>
      </author>
      <author>
        <name>Krasieva, Tatiana B</name>
      </author>
      <author>
        <name>König, Karsten</name>
      </author>
      <author>
        <name>Durkin, Anthony J</name>
        <uri>https://orcid.org/0000-0001-9124-6388</uri>
      </author>
      <author>
        <name>Tromberg, Bruce J</name>
        <uri>https://orcid.org/0000-0002-7481-7975</uri>
      </author>
    </item>
    <item>
      <title>The Ets Transcription Factor EHF as a Regulator of Cornea Epithelial Cell Identity*</title>
      <link>https://escholarship.org/uc/item/9fr540qb</link>
      <description>The cornea is the clear, outermost portion of the eye composed of three layers: an epithelium that provides a protective barrier while allowing transmission of light into the eye, a collagen-rich stroma, and an endothelium monolayer. How cornea development and aging is controlled is poorly understood. Here we characterize the mouse cornea transcriptome from early embryogenesis through aging and compare it with transcriptomes of other epithelial tissues, identifying cornea-enriched genes, pathways, and transcriptional regulators. Additionally, we profiled cornea epithelium and stroma, defining genes enriched in these layers. Over 10,000 genes are differentially regulated in the mouse cornea across the time course, showing dynamic expression during development and modest expression changes in fewer genes during aging. A striking transition time point for gene expression between postnatal days 14 and 28 corresponds with completion of cornea development at the transcriptional level....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9fr540qb</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Stephens, Denise N</name>
      </author>
      <author>
        <name>Klein, Rachel Herndon</name>
      </author>
      <author>
        <name>Salmans, Michael L</name>
      </author>
      <author>
        <name>Gordon, William</name>
      </author>
      <author>
        <name>Ho, Hsiang</name>
      </author>
      <author>
        <name>Andersen, Bogi</name>
        <uri>https://orcid.org/0000-0001-7181-2768</uri>
      </author>
    </item>
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