<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:atom="http://www.w3.org/2005/Atom" version="2.0">
  <channel>
    <docs>http://www.rssboard.org/rss-specification</docs>
    <atom:link rel="self" type="application/rss+xml" href="https://escholarship.org/uc/bcoe_be_oapolicydeposits/rss"/>
    <ttl>720</ttl>
    <title>Recent bcoe_be_oapolicydeposits items</title>
    <link>https://escholarship.org/uc/bcoe_be_oapolicydeposits/rss</link>
    <description>Recent eScholarship items from Bioengineering Department Open Access Policy Deposits</description>
    <pubDate>Sun, 21 Jun 2026 06:23:18 +0000</pubDate>
    <item>
      <title>Examining iron‐related off‐target binding effects of 18F‐AV1451 PET in the cortex of Aβ+ individuals</title>
      <link>https://escholarship.org/uc/item/6bh2b8ms</link>
      <description>The presence of neurofibrillary tangles containing hyper-phosphorylated tau is a characteristic of Alzheimer's disease (AD) pathology. The positron emission tomography (PET) radioligand sensitive to tau neurofibrillary tangles (&lt;sup&gt;18&lt;/sup&gt;F-AV1451) also binds with iron. This off-target binding effect may be enhanced in older adults on the AD spectrum, particularly those with amyloid-positive biomarkers. Here, we examined group differences in &lt;sup&gt;18&lt;/sup&gt;F-AV1451 PET after controlling for iron-sensitive measures from magnetic resonance imaging (MRI) and its relationships to tissue microstructure and cognition in 40 amyloid beta positive (Aβ+) individuals, 20 amyloid beta negative (Aβ-) with MCI and 31 Aβ- control participants. After controlling for iron, increased &lt;sup&gt;18&lt;/sup&gt;F-AV1451 PET uptake was found in the temporal lobe and hippocampus of Aβ+ participants compared to Aβ- MCI and control participants. Within the Aβ+ group, significant correlations were seen between &lt;sup&gt;18&lt;/sup&gt;F-AV1451...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6bh2b8ms</guid>
      <pubDate>Thu, 11 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Langley, Jason</name>
      </author>
      <author>
        <name>Bennett, Ilana J</name>
        <uri>https://orcid.org/0000-0002-5330-4679</uri>
      </author>
      <author>
        <name>Hu, Xiaoping P</name>
        <uri>https://orcid.org/0000-0002-8155-7040</uri>
      </author>
      <author>
        <name>Initiative, for the Alzheimer's Disease Neuroimaging</name>
      </author>
    </item>
    <item>
      <title>Locus Coeruleus Engagement Drives Network Connectivity Dynamics In Humans And Rats</title>
      <link>https://escholarship.org/uc/item/41t6h49z</link>
      <description>Locus Coeruleus Engagement Drives Network Connectivity Dynamics In Humans And Rats</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/41t6h49z</guid>
      <pubDate>Thu, 11 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hussain, Sana</name>
      </author>
      <author>
        <name>Shalchy, Mahsa Alizadeh</name>
      </author>
      <author>
        <name>Yaghoubi, Kimia C</name>
      </author>
      <author>
        <name>Langley, Jason</name>
      </author>
      <author>
        <name>Chen, Xu</name>
      </author>
      <author>
        <name>Bennett, Ilana J</name>
        <uri>https://orcid.org/0000-0002-5330-4679</uri>
      </author>
      <author>
        <name>Huang, Ringo</name>
      </author>
      <author>
        <name>Clewett, David</name>
      </author>
      <author>
        <name>Nielsen, Shawn E</name>
      </author>
      <author>
        <name>Velasco, Rico</name>
      </author>
      <author>
        <name>Kennedy, Briana</name>
      </author>
      <author>
        <name>Han, Sophia</name>
      </author>
      <author>
        <name>Tu, Kristie</name>
      </author>
      <author>
        <name>Seitz, Aaron R</name>
      </author>
      <author>
        <name>Zhang, Nanyin</name>
      </author>
      <author>
        <name>Mather, Mara</name>
      </author>
      <author>
        <name>Hu, Xiaoping</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>Associations between iron and mean kurtosis in iron-rich grey matter nuclei in aging.</title>
      <link>https://escholarship.org/uc/item/1458d4j5</link>
      <description>OBJECTIVE: Elevated kurtosis values have been observed in subcortical grey matter structures of patients with neurodegenerative diseases. Here, we examined relationships between iron measures and kurtosis in iron-rich subcortical grey matter structures.Please check and confirm the affiliation 4 for the author "Xiaoping P. Hu".Affiliation 4 for Xiaoping P. Hu was incorrect since he is not associated with that department. We have removed this affiliation. Thanks!&amp;nbsp; MATERIALS AND METHODS: Multi-shell diffusion and multi-echo gradient echo acquisitions were used to derive mean kurtosis and iron measures (R&lt;sub&gt;2&lt;/sub&gt;* and magnetic susceptibility), respectively, in subcortical grey matter nuclei and white matter tracts in a discovery cohort (110 healthy older and 63 younger adults) and replication cohort (72 healthy older adults).Please confirm if the author names are presented accurately and in the correct sequence (Ilana J. Bennett and Xiaoping P. Hu). Also, kindly confirm the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1458d4j5</guid>
      <pubDate>Thu, 11 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Langley, Jason</name>
      </author>
      <author>
        <name>Solis, Kitzia</name>
      </author>
      <author>
        <name>Masjedizadeh, Vala</name>
      </author>
      <author>
        <name>Shao, Murphy</name>
      </author>
      <author>
        <name>Bennett, Ilana J</name>
        <uri>https://orcid.org/0000-0002-5330-4679</uri>
      </author>
      <author>
        <name>Hu, Xiaoping P</name>
        <uri>https://orcid.org/0000-0002-8155-7040</uri>
      </author>
    </item>
    <item>
      <title>The regenerative role of neural crest stem cells in physical stimuli-enhanced peripheral nerve repair</title>
      <link>https://escholarship.org/uc/item/6mb2926w</link>
      <description>Neural crest stem cells (NCSCs), capable of differentiating into neurons and Schwann cells, are essential for peripheral nerve regeneration. This study investigates the role of endogenous NCSC-like cells in mechano-electrical stimulation (MES)-enhanced peripheral nerve repair. In a critical-sized nerve injury model, MES leads to complete nerve reconnection, accompanied by a significant increase in NCSC-like cells at the injury sites. In vitro, MES promotes the simultaneous differentiation of NCSC-like cells into neurons and Schwann cells, with elevated neuregulin 1 (NRG1) expression, a key factor in Schwann cell development. Mechanistically, MES activates BMP/Smad signaling, driving neuronal differentiation and subsequent NRG1 secretion, which in turn promotes Schwann cell maturation through the ErBB/NFAT pathway. These findings demonstrate that MES enhances peripheral nerve regeneration by activating and directing stem cell differentiation, supporting a novel therapeutic approach...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6mb2926w</guid>
      <pubDate>Thu, 9 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Tai, Youyi</name>
      </author>
      <author>
        <name>Jin, Lu</name>
      </author>
      <author>
        <name>Tonmoy, Thamidul Islam</name>
      </author>
      <author>
        <name>Park, B Hyle</name>
      </author>
      <author>
        <name>Nam, Jin</name>
        <uri>https://orcid.org/0000-0001-5117-8958</uri>
      </author>
    </item>
    <item>
      <title>Connectome-based predictive modelling predicts frailty levels in older adults</title>
      <link>https://escholarship.org/uc/item/5jc775rx</link>
      <description>Frailty is characterized by a persistent and progressive decline in physiological reserves, leading to increased vulnerability to stressors and a heightened risk of adverse health outcomes, both physically and mentally. Despite frailty's prevalence in older adults, there is limited research on its neural substrates, especially using task-based brain functional connectivity. In this study, we used connectome-based predictive modelling (CPM) to find a linear relationship between task-based connectomes - taken from tasks that involved similar handgrip manipulations - and a separate measure of frailty: the maximum grip strength in older adults. We observed that the task-based connectomes were able to explain individual differences in grip strength, with the Subcortical and Cerebellum network, particularly the caudate nucleus, functional connectivity being the strongest predictor. These findings demonstrate that task-based functional connectomes can serve as personalized markers that...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5jc775rx</guid>
      <pubDate>Thu, 26 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ghaffari, Amin</name>
      </author>
      <author>
        <name>abouzaki, Majd</name>
      </author>
      <author>
        <name>Romero, Yasmine</name>
      </author>
      <author>
        <name>Sun, Andrew</name>
      </author>
      <author>
        <name>Seitz, Aaron</name>
      </author>
      <author>
        <name>Langley, Jason</name>
      </author>
      <author>
        <name>Bennett, Ilana J</name>
      </author>
      <author>
        <name>Hu, Xiaoping</name>
        <uri>https://orcid.org/0000-0002-8155-7040</uri>
      </author>
    </item>
    <item>
      <title>Fuel-driven filamentous phage nanomotors</title>
      <link>https://escholarship.org/uc/item/1jp9t542</link>
      <description>Virus-based nanocarriers have shown great potential for noninvasive delivery of drugs, diagnostics, and imaging agents to hard-to-reach anatomical locations. Yet, they largely depend on diffusion for transport, often lacking the force to actively penetrate biological barriers, and navigation to guide therapeutic agents. In these studies, the M13 bacteriophage, a linearly shaped virus, was converted from passive nanocarrier to actively propelled, fuel-driven nanomotor. Using the distinctive low symmetry of its capsid, a single Pt nanoparticle was added to one end of the M13 virus to form a tadpole-like structure. The Pt/M13 head/tail nanomotors exhibited notably enhanced diffusion in the presence of hydrogen peroxide fuel, and significantly improved uptake by SVOK3 ovarian cancer cells &lt;i&gt;in vitro&lt;/i&gt;. Given the successes of the M13 bacteriophage as a nanocarrier, the demonstration of this simple, but comparatively mobile M13-based nanomotor platform represents an important step...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1jp9t542</guid>
      <pubDate>Thu, 26 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ding, Xi</name>
      </author>
      <author>
        <name>Zaman, Shamima</name>
      </author>
      <author>
        <name>Africa, Emily P</name>
      </author>
      <author>
        <name>Anvari, Bahman</name>
        <uri>https://orcid.org/0000-0002-2511-5854</uri>
      </author>
      <author>
        <name>Haberer, Elaine D</name>
        <uri>https://orcid.org/0000-0002-3676-9079</uri>
      </author>
    </item>
    <item>
      <title>Investigating the correlation between force output, strains, and pressure for active skeletal muscle contractions.</title>
      <link>https://escholarship.org/uc/item/4x70q09f</link>
      <description>Measuring the forces of individual muscles in a muscle group around a joint is non-trivial, and researchers have suggested using surrogates for individual muscle forces instead. Traditionally, experimentalists have shown that the force output of the skeletal muscle tissue can be correlated to the intra-muscular pressure (IMP) generated by the muscle belly. However, IMP proves difficult to measure in vivo, due to variations from sensor placement and invasiveness of the procedure. Numerical biomechanical simulations offer a tool to analyze muscle contractions, enabling new insights into the correlations among non-invasive experimentally measurable quantities, such as strains and the force output. In this work, we investigate the correlations between the muscle force output, the principal, shear and volumetric strains experienced by the muscle, as well as the pressure developed within the muscle belly as the tissue undergoes isometric contractions with varying activation profiles...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4x70q09f</guid>
      <pubDate>Sat, 21 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Taneja, Karan</name>
      </author>
      <author>
        <name>He, Xiaolong</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
      <author>
        <name>Hodgson, John</name>
      </author>
      <author>
        <name>Sinha, Usha</name>
      </author>
      <author>
        <name>Sinha, Shantanu</name>
      </author>
      <author>
        <name>Chen, Jiun-Shyan</name>
      </author>
    </item>
    <item>
      <title>Identifying indicators of consciousness in AI systems</title>
      <link>https://escholarship.org/uc/item/9wp8t1n8</link>
      <description>Rapid progress in artificial intelligence (AI) capabilities has drawn fresh attention to the prospect of consciousness in AI. There is an urgent need for rigorous methods to assess AI systems for consciousness, but significant uncertainty about relevant issues in consciousness science. We present a method for assessing AI systems for consciousness that involves exploring what follows from existing or future neuroscientific theories of consciousness. Indicators derived from such theories can be used to inform credences about whether particular AI systems are conscious. This method allows us to make meaningful progress because some influential theories of consciousness, notably including computational functionalist theories, have implications for AI that can be investigated empirically.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9wp8t1n8</guid>
      <pubDate>Thu, 15 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Butlin, Patrick</name>
      </author>
      <author>
        <name>Long, Robert</name>
      </author>
      <author>
        <name>Bayne, Tim</name>
      </author>
      <author>
        <name>Bengio, Yoshua</name>
      </author>
      <author>
        <name>Birch, Jonathan</name>
      </author>
      <author>
        <name>Chalmers, David</name>
      </author>
      <author>
        <name>Constant, Axel</name>
      </author>
      <author>
        <name>Deane, George</name>
      </author>
      <author>
        <name>Elmoznino, Eric</name>
      </author>
      <author>
        <name>Fleming, Stephen M</name>
      </author>
      <author>
        <name>Ji, Xu</name>
      </author>
      <author>
        <name>Kanai, Ryota</name>
      </author>
      <author>
        <name>Klein, Colin</name>
      </author>
      <author>
        <name>Lindsay, Grace</name>
      </author>
      <author>
        <name>Michel, Matthias</name>
      </author>
      <author>
        <name>Mudrik, Liad</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Schwitzgebel, Eric</name>
      </author>
      <author>
        <name>Simon, Jonathan</name>
      </author>
      <author>
        <name>VanRullen, Rufin</name>
      </author>
    </item>
    <item>
      <title>Air-powered logic circuits for error detection in pneumatic systems</title>
      <link>https://escholarship.org/uc/item/8x34n9dr</link>
      <description>Air-powered logic circuits for error detection in pneumatic systems</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8x34n9dr</guid>
      <pubDate>Thu, 28 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hoang, Shane</name>
      </author>
      <author>
        <name>Shehada, Mabel</name>
      </author>
      <author>
        <name>Patel, Zinal</name>
      </author>
      <author>
        <name>Tran, Minh-Huy</name>
      </author>
      <author>
        <name>Karydis, Konstantinos</name>
      </author>
      <author>
        <name>Brisk, Philip</name>
        <uri>https://orcid.org/0000-0003-0083-9781</uri>
      </author>
      <author>
        <name>Grover, William H</name>
        <uri>https://orcid.org/0000-0001-6854-8951</uri>
      </author>
    </item>
    <item>
      <title>Rapid development and optimization of paper microfluidic designs using software automation</title>
      <link>https://escholarship.org/uc/item/8sq5n0s9</link>
      <description>Paper microfluidic or lateral flow devices have found many applications, especially in medical diagnostics. Their low cost and ease of use makes them particularly valuable in resource-limited and point-of-care applications. However, the process of developing new paper microfluidic devices is slowed by the need to find optimal values for their various design parameters, which determine the overall size and fluid volume requirements of the device. Often, researchers must design and test several different versions of a device to find a combination of parameters that functions as intended. To accelerate the development of new paper microfluidics, we developed a software framework that automatically designs custom paper microfluidic devices for a given application. Once the user specifies the desired device parameters, the software generates printable image files of the resulting devices, ready to output to a conventional wax ink color printer and test. As a proof-of-concept, we used...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8sq5n0s9</guid>
      <pubDate>Thu, 28 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Potter, Joshua</name>
      </author>
      <author>
        <name>Brisk, Philip</name>
        <uri>https://orcid.org/0000-0003-0083-9781</uri>
      </author>
      <author>
        <name>Grover, William H</name>
        <uri>https://orcid.org/0000-0001-6854-8951</uri>
      </author>
    </item>
    <item>
      <title>Multi-Objective Design Automation for Microfluidic Capture Chips</title>
      <link>https://escholarship.org/uc/item/8pf0w33t</link>
      <description>Microfluidic capture chips are useful for preparing or analyzing a wide range of different chemical, biological, and medical samples. A typical microfluidic capture chip contains features that capture certain targets (i.e. molecules, particles, cells) as they flow through the chip. However, creating optimal capture chip designs is difficult because of the inherent relationship between capture efficiency and flow resistance: as more capture features are added to the chip, the capture efficiency increases, but the additional features slow the flow of fluid through the chip. This paper introduces the use of multi-objective optimization to generate capture chip designs that balance the trade-off between maximizing target capture efficiency and minimizing resistance to fluid flow. Design automation for this important class of microfluidic chips has not been attempted previously. Our approach automatically produces a Pareto front of non-dominated chip designs in a reasonable amount...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8pf0w33t</guid>
      <pubDate>Thu, 28 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Lisa</name>
      </author>
      <author>
        <name>Grover, William H</name>
        <uri>https://orcid.org/0000-0001-6854-8951</uri>
      </author>
      <author>
        <name>Sridharan, Manu</name>
      </author>
      <author>
        <name>Brisk, Philip</name>
        <uri>https://orcid.org/0000-0003-0083-9781</uri>
      </author>
    </item>
    <item>
      <title>Controlling Biomedical Devices Using Pneumatic Logic</title>
      <link>https://escholarship.org/uc/item/6gz9231c</link>
      <description>Many biomedical devices are powered and controlled by electrical components. These electronics add to the cost of a device (possibly making the device too expensive for use in resource-limited or point-of-care settings) and can also render the device unsuitable for use in some environments (for example, high-humidity areas such as incubators where condensation could cause electrical short circuits, ovens where electronic components may overheat, or explosive or flammable environments where electric sparks could cause serious accidents). In this work, we show that pneumatic logic can be used to power and control biomedical devices without the need for electricity or electric components. Originally developed for controlling microfluidic “lab-on-a-chip” devices, these circuits use microfluidic valves like transistors in air-powered logic “circuits.” We show that a modification to the basic valve design—adding additional air channels in parallel through the valve—creates a “high-flow”...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6gz9231c</guid>
      <pubDate>Thu, 28 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hoang, Shane</name>
      </author>
      <author>
        <name>Shehada, Mabel</name>
      </author>
      <author>
        <name>Karydis, Konstantinos</name>
      </author>
      <author>
        <name>Brisk, Philip</name>
        <uri>https://orcid.org/0000-0003-0083-9781</uri>
      </author>
      <author>
        <name>Grover, William H</name>
        <uri>https://orcid.org/0000-0001-6854-8951</uri>
      </author>
    </item>
    <item>
      <title>Optimization of deep learning–based denoising for arterial spin labeling: Effects of averaging and training strategies</title>
      <link>https://escholarship.org/uc/item/4t53590x</link>
      <description>PURPOSE: Systematic study of the effects of averaging and other relevant training strategies in deep learning (DL)-based denoising is required to optimize such processing pipelines for improving the quality of arterial spin labeling (ASL) images.
METHODS: Different averaging strategies, including windowed and interleaved averaging methods, and different levels of averaging before and after convolutional neural network-based and transformer-based denoising were studied. The experiments were performed on 152 single-delay ASL scans from 152 subjects, including pulsed and pseudo-continuous ASL acquisitions. Four-fold cross-validation was implemented in all experiments. The effect of including calibration scans (M&lt;sub&gt;0&lt;/sub&gt;) was studied and compared across images of different levels of signal-to-noise ratio (SNR). The generalizability of DL denoising was examined in experiments using low-SNR ground truth in training. The results were assessed using image-quality metrics including...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4t53590x</guid>
      <pubDate>Thu, 28 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Guo, Jia</name>
        <uri>https://orcid.org/0000-0003-3371-5857</uri>
      </author>
      <author>
        <name>Sharma, Arun</name>
      </author>
      <author>
        <name>Zaharchuk, Greg</name>
      </author>
      <author>
        <name>Rahimzadeh, Hossein</name>
      </author>
      <author>
        <name>Ilyas, Naveed</name>
      </author>
    </item>
    <item>
      <title>Characterization of the critical lift-off of a single flat-plate microchip particle in straight rectangular microchannel flows</title>
      <link>https://escholarship.org/uc/item/8pp875qr</link>
      <description>Characterization of the critical lift-off of a single flat-plate microchip particle in straight rectangular microchannel flows</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8pp875qr</guid>
      <pubDate>Thu, 14 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Yeung, Raymond</name>
      </author>
      <author>
        <name>Sainz, Cynthia</name>
      </author>
      <author>
        <name>Mandala, Jason</name>
      </author>
      <author>
        <name>Brisk, Philip</name>
        <uri>https://orcid.org/0000-0003-0083-9781</uri>
      </author>
      <author>
        <name>Grover, William H</name>
        <uri>https://orcid.org/0000-0001-6854-8951</uri>
      </author>
      <author>
        <name>Rodgers, Victor GJ</name>
        <uri>https://orcid.org/0000-0002-1857-8025</uri>
      </author>
    </item>
    <item>
      <title>Acoustic Side Channel Attack Against DNA Synthesis Machines: Poster Abstract</title>
      <link>https://escholarship.org/uc/item/5xf6h587</link>
      <description>Synthetic DNA molecules play an essential role in genomics research and are a promising, high-capacity data storage medium. Currently, researchers use automated DNA synthesizers to custom-build sequences of oligonucleotides (short DNA strands) using the nucleobases: Adenine (A), Guanine (G), Cytosine (C), and Thymine (T). Research laboratories invest large amounts of capital to engineer unique oligonucleotide sequences. In our work, we demonstrate the vulnerability of commonly used DNA synthesizers to acoustic side-channel attacks, where confidentiality can be breached to steal precious DNA sequences. We introduce a novel methodology to reverse engineer the acoustic noise generated by the DNA synthesizer and extract the type and order of the nucleobases delivered to the output. To the best of our knowledge, this is the first work which highlights the possibility of physical-to-cyber attacks in DNA synthesis technologies.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xf6h587</guid>
      <pubDate>Thu, 14 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Faezi, Sina</name>
      </author>
      <author>
        <name>Chhetri, Sujit Rokka</name>
      </author>
      <author>
        <name>Malawade, Arnav Vaibhav</name>
      </author>
      <author>
        <name>Chaput, John Charles</name>
      </author>
      <author>
        <name>Grover, William</name>
        <uri>https://orcid.org/0000-0001-6854-8951</uri>
      </author>
      <author>
        <name>Brisk, Philip</name>
        <uri>https://orcid.org/0000-0003-0083-9781</uri>
      </author>
      <author>
        <name>Al Faruque, Mohammad Abdullah</name>
      </author>
    </item>
    <item>
      <title>Enhanced neuromorphogenesis of neural stem cells via the optimization of physical stimulus-responsive signaling pathways</title>
      <link>https://escholarship.org/uc/item/8725j3pw</link>
      <description>BackgroundNeural stem cells hold significant promise for developing in vitro nerve models due to their capacity to differentiate into diverse neural cell types. While traditional biochemical approaches often restrict differentiation to a single phenotype, limiting the ability to study critical neuron-glia interactions, physical stimuli have been explored due to their capacity to drive multi-phenotypic differentiation of neural stem cells. However, underlying molecular mechanisms mediating the physical stimulation-induced neural stem cell differentiation, with an emphasis on electrical stimulation and mechanical stimulation, remain inadequately explored, hindering the comprehensive optimization and application of physical stimulation for enhanced neuromorphogenesis.MethodsIn this study, we explored the signaling pathways driving mechano-electrical stimulation-induced multi-phenotypic differentiation of NSCs using a piezoelectric platform with signaling inhibitors. The signaling...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8725j3pw</guid>
      <pubDate>Tue, 5 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Tai, Youyi</name>
      </author>
      <author>
        <name>Brinkley, Natasha</name>
      </author>
      <author>
        <name>Jin, Lu</name>
      </author>
      <author>
        <name>Chang, Yu Wei</name>
      </author>
      <author>
        <name>Liakhovetski, Allen</name>
      </author>
      <author>
        <name>Nam, Jin</name>
        <uri>https://orcid.org/0000-0001-5117-8958</uri>
      </author>
    </item>
    <item>
      <title>Controllable Doping for Tunable and Multimodal Emission in ZnS-Based Mechanoluminescent Nanocrystals</title>
      <link>https://escholarship.org/uc/item/2ds6x41n</link>
      <description>Scaling mechanoluminescent materials to the nanoscale enhances their potential for biomedical applications due to improved sensitivity, resolution, and biocompatibility. Here, we report a versatile strategy for synthesizing wavelength-tunable mechanoluminescent ZnS nanocrystals doped with Ag&lt;sup&gt;+&lt;/sup&gt;, Cu&lt;sup&gt;2+&lt;/sup&gt;, or Mn&lt;sup&gt;2+&lt;/sup&gt;. The method involves coassembly of ZnS and metal sulfide nanocrystals within silica nanoreactors, followed by high-temperature calcination to induce solid-state doping and phase transformation. The resulting ZnS:Ag&lt;sup&gt;+&lt;/sup&gt;, ZnS:Cu&lt;sup&gt;2+&lt;/sup&gt;, and ZnS:Mn&lt;sup&gt;2+&lt;/sup&gt; nanocrystals exhibit focused ultrasound-induced mechanoluminescence at 480, 500, and 585 nm, respectively. Notably, ZnS:Ag&lt;sup&gt;+&lt;/sup&gt; also shows photoluminescence and afterglow upon UV excitation. The luminescence intensity is highly dependent on Ag&lt;sup&gt;+&lt;/sup&gt; concentration, with 0.15% yielding the optimal emission. These nanocrystals were further applied to stimulate neuronal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2ds6x41n</guid>
      <pubDate>Tue, 5 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Zhongxiang</name>
      </author>
      <author>
        <name>Jin, Lu</name>
      </author>
      <author>
        <name>Ni, Haoyang</name>
      </author>
      <author>
        <name>Kim, Hwangsun</name>
      </author>
      <author>
        <name>Zeng, Yushun</name>
      </author>
      <author>
        <name>Zhou, Qifa</name>
      </author>
      <author>
        <name>Chi, Miaofang</name>
      </author>
      <author>
        <name>Nam, Jin</name>
        <uri>https://orcid.org/0000-0001-5117-8958</uri>
      </author>
      <author>
        <name>Yin, Yadong</name>
        <uri>https://orcid.org/0000-0003-0218-3042</uri>
      </author>
    </item>
    <item>
      <title>Beyond Stress Granules: G3BP1 and G3BP2 Redundantly Suppress SARS-CoV-2 Infection</title>
      <link>https://escholarship.org/uc/item/0mj492rw</link>
      <description>The global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has posed unprecedented challenges to public health and economic stability. Central to SARS-CoV-2 pathogenesis is its ability to evade the host immune response by hijacking host pathways via the interaction between viral and host proteins. We identified Ras-GTPase-activating protein SH3 domain-binding protein 1/2 (G3BP1/G3BP2) as a critical host factor that interacts with the viral nucleocapsid (N) protein, emerging from a comparative analysis of proteomic data from multiple studies. We revisited the underlying molecular mechanisms by confirming the residues required for the interaction between G3BP1/G3BP2 and SARS-CoV-2 N protein and showed that this interaction disrupts stress granule formation. Intriguingly, we observed that the ablation of both G3BP1 and G3BP2 enhanced SARS-CoV-2 replication. Our data collectively supports the notion that G3BP1 and G3BP2 play a critical role in modulating...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0mj492rw</guid>
      <pubDate>Fri, 25 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Xu, Duo</name>
        <uri>https://orcid.org/0000-0003-2554-3602</uri>
      </author>
      <author>
        <name>Biswal, Mahamaya</name>
      </author>
      <author>
        <name>Zhang, Quanqing</name>
      </author>
      <author>
        <name>Light, Christine</name>
      </author>
      <author>
        <name>Wu, Yijie</name>
      </author>
      <author>
        <name>Ye, Chenjin</name>
      </author>
      <author>
        <name>Martínez-Sobrido, Luis</name>
      </author>
      <author>
        <name>Song, Jikui</name>
      </author>
      <author>
        <name>Hai, Rong</name>
      </author>
    </item>
    <item>
      <title>Reasoning Goals and Representational Decisions in Computational Cognitive Neuroscience: Lessons From the Drift Diffusion Model</title>
      <link>https://escholarship.org/uc/item/78p7p6rv</link>
      <description>Computational cognitive models are powerful tools for enhancing the quantitative and theoretical rigor of cognitive neuroscience. It is thus imperative that model users-researchers who develop models, use existing models, or integrate model-based findings into their own research-understand how these tools work and what factors need to be considered when engaging with them. To this end, we developed a philosophical toolkit that addresses core questions about computational cognitive models in the brain and behavioral sciences. Drawing on recent advances in the philosophy of modeling, we highlight the central role of model users' reasoning goals in the application and interpretation of formal models. We demonstrate the utility of this perspective by first offering a philosophical introduction to the highly popular drift diffusion model (DDM) and then providing a novel conceptual analysis of a long-standing debate about decision thresholds in the DDM. Contrary to most existing work,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/78p7p6rv</guid>
      <pubDate>Thu, 3 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Khoudary, Ari</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Bornstein, Aaron M</name>
        <uri>https://orcid.org/0000-0001-6251-6000</uri>
      </author>
    </item>
    <item>
      <title>Portable dual-mode microfluidic sensor for rapid and sensitive detection of DPA on chip</title>
      <link>https://escholarship.org/uc/item/6wb4q760</link>
      <description>In this work, we developed a dual-mode portable device that integrated a 3D-printed microfluidic chip for detection of dipicolinic acid (DPA) on chip. The system uses a ratiometric fluorescence nanoprobe formed by embedding carbon dots (CDs) into an Eu3⁺ metal–organic framework (Eu-MOF). Upon reaction with DPA in the microchannel, red fluorescence was enhanced and blue fluorescence suppressed, enabling sensitive ratiometric detection of DPA on chip with a detection limit (LOD) of 0.04 µM. Interestingly, the composite EuMOF/CDs/DPA also exhibits peroxidase-like activity, catalyzing the oxidation of TMB into a blue-colored product (oxTMB), which allows for colorimetric detection with an LOD of 10.14 µM. To improve usability and reduce environmental or instrumental variability, incorporating a microfluidic chip into a semi-portable device and utilizing a smartphone, making the system portable and miniaturized for easy operation. In the smartphone-assisted mode, the LODs were 0.33...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6wb4q760</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Cao, Zhengyang</name>
      </author>
      <author>
        <name>Zeng, Shiyu</name>
      </author>
      <author>
        <name>Zhu, Haoyu</name>
      </author>
      <author>
        <name>Zhai, Kairui</name>
      </author>
      <author>
        <name>Yin, Binfeng</name>
      </author>
      <author>
        <name>Zhang, Cheng</name>
      </author>
      <author>
        <name>Peng, Tao</name>
      </author>
      <author>
        <name>Cheng, Teng</name>
      </author>
      <author>
        <name>Zhang, Biao</name>
      </author>
    </item>
    <item>
      <title>Turning brain MRI into diagnostic PET: 15O-water PET CBF synthesis from multi-contrast MRI via attention-based encoder–decoder networks</title>
      <link>https://escholarship.org/uc/item/7cx705xv</link>
      <description>Accurate quantification of cerebral blood flow (CBF) is essential for the diagnosis and assessment of a wide range of neurological diseases. Positron emission tomography (PET) with radiolabeled water (&lt;sup&gt;15&lt;/sup&gt;O-water) is the gold-standard for the measurement of CBF in humans, however, it is not widely available due to its prohibitive costs and the use of short-lived radiopharmaceutical tracers that require onsite cyclotron production. Magnetic resonance imaging (MRI), in contrast, is more accessible and does not involve ionizing radiation. This study presents a convolutional encoder-decoder network with attention mechanisms to predict the gold-standard &lt;sup&gt;15&lt;/sup&gt;O-water PET CBF from multi-contrast MRI scans, thus eliminating the need for radioactive tracers. The model was trained and validated using 5-fold cross-validation in a group of 126 subjects consisting of healthy controls and cerebrovascular disease patients, all of whom underwent simultaneous &lt;sup&gt;15&lt;/sup&gt;O-water...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7cx705xv</guid>
      <pubDate>Tue, 15 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hussein, Ramy</name>
      </author>
      <author>
        <name>Shin, David</name>
      </author>
      <author>
        <name>Zhao, Moss Y</name>
      </author>
      <author>
        <name>Guo, Jia</name>
        <uri>https://orcid.org/0000-0003-3371-5857</uri>
      </author>
      <author>
        <name>Davidzon, Guido</name>
      </author>
      <author>
        <name>Steinberg, Gary</name>
      </author>
      <author>
        <name>Moseley, Michael</name>
      </author>
      <author>
        <name>Zaharchuk, Greg</name>
      </author>
    </item>
    <item>
      <title>Whole-brain causal discovery using fMRI</title>
      <link>https://escholarship.org/uc/item/9gx4g09v</link>
      <description>Despite significant research, discovering causal relationships from fMRI remains a challenge. Popular methods such as Granger causality and dynamic causal modeling fall short in handling contemporaneous effects and latent common causes. Methods from causal structure learning literature can address these limitations but often scale poorly with network size and need acyclicity. In this study, we first provide a taxonomy of existing methods and compare their accuracy and efficiency on simulated fMRI from simple topologies. This analysis demonstrates a pressing need for more accurate and scalable methods, motivating the design of Causal discovery for Large-scale Low-resolution Time-series with Feedback (CaLLTiF). CaLLTiF is a constraint-based method that uses conditional independence between contemporaneous and lagged variables to extract causal relationships. On simulated fMRI from the macaque connectome, CaLLTiF achieves significantly higher accuracy and scalability than all tested...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9gx4g09v</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Arab, Fahimeh</name>
      </author>
      <author>
        <name>Ghassami, AmirEmad</name>
      </author>
      <author>
        <name>Jamalabadi, Hamidreza</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Nozari, Erfan</name>
        <uri>https://orcid.org/0000-0002-1981-8959</uri>
      </author>
    </item>
    <item>
      <title>Evaluation of affine fiber kinematics in porcine tricuspid valve leaflets using polarized spatial frequency domain imaging and planar biaxial testing</title>
      <link>https://escholarship.org/uc/item/64j6s86c</link>
      <description>Collagen fibers are the primary load-bearing microstructural constituent of bodily soft tissues, and, when subjected to external loading, the collagen fibers reorient, uncrimp, and elongate. Specific to the atrioventricular heart valve leaflets, the collagen fiber kinematics form the basis of many constitutive models; however, some researchers claim that modeling the affine fiber kinematics (AFK) are sufficient for accurately predicting the macroscopic tissue deformations, while others state that modeling the non-affine kinematics (i.e., fiber uncrimping together with elastic elongation) is required. Experimental verification of the AFK theory has been previously performed for the mitral valve leaflets in the left-side heart; however, this same evaluation has yet to be performed for the morphologically distinct tricuspid valve (TV) leaflets in the right-side heart. In this work, we, for the first time, evaluated the AFK theory for the TV leaflets using an integrated biaxial testing-polarized...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/64j6s86c</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ross, Colton J</name>
      </author>
      <author>
        <name>Mullins, Brennan T</name>
      </author>
      <author>
        <name>Hillshafer, Clare E</name>
      </author>
      <author>
        <name>Mir, Arshid</name>
      </author>
      <author>
        <name>Burkhart, Harold M</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
    <item>
      <title>A Physics-Guided Neural Operator Learning Approach to Model Biological Tissues From Digital Image Correlation Measurements.</title>
      <link>https://escholarship.org/uc/item/5kc8g2mk</link>
      <description>We present a data-driven workflow to biological tissue modeling, which aims to predict the displacement field based on digital image correlation (DIC) measurements under unseen loading scenarios, without postulating a specific constitutive model form nor possessing knowledge of the material microstructure. To this end, a material database is constructed from the DIC displacement tracking measurements of multiple biaxial stretching protocols on a porcine tricuspid valve anterior leaflet, with which we build a neural operator learning model. The material response is modeled as a solution operator from the loading to the resultant displacement field, with the material microstructure properties learned implicitly from the data and naturally embedded in the network parameters. Using various combinations of loading protocols, we compare the predictivity of this framework with finite element analysis based on three conventional constitutive models. From in-distribution tests, the predictivity...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5kc8g2mk</guid>
      <pubDate>Fri, 4 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>You, Huaiqian</name>
      </author>
      <author>
        <name>Zhang, Quinn</name>
      </author>
      <author>
        <name>Ross, Colton J</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
      <author>
        <name>Hsu, Ming-Chen</name>
      </author>
      <author>
        <name>Yu, Yue</name>
      </author>
    </item>
    <item>
      <title>Investigation on submicron particle separation and deflection using tilted-angle standing surface acoustic wave microfluidics</title>
      <link>https://escholarship.org/uc/item/9gh484hj</link>
      <description>With the development of in vitro diagnostics, extracting submicron scale particles from mixed body fluids samples is crucial. In recent years, microfluidic separation has attracted much attention due to its high efficiency, label-free, and inexpensive nature. Among the microfluidic-based separation, the separation based on ultrasonic standing waves has gradually become a powerful tool. A microfluid environment containing a tilted-angle ultrasonic standing surface acoustic wave (taSSAW) field has been widely adapted and designed to separate submicron particles for biochemical applications. This paper investigated submicron particle defection in microfluidics using taSSAWs analytically. Particles with 0.1-1&amp;nbsp;μm diameters were analyzed under acoustic pressure, flow rate, tilted angle, and SSAW frequency. According to different acoustic radiation forces acting on the particles, the motion of large-diameter particles was more likely to deflect to the direction of the nodal lines....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9gh484hj</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Peng, Tao</name>
      </author>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Li, Luming</name>
      </author>
      <author>
        <name>Huang, Lei</name>
      </author>
      <author>
        <name>Jiang, Bingyan</name>
      </author>
      <author>
        <name>Jia, Yanwei</name>
      </author>
    </item>
    <item>
      <title>The Generation and Control of Harmful Products in Food Processing</title>
      <link>https://escholarship.org/uc/item/6xr4k3z8</link>
      <description>Food processing is an integral part of the modern food industry aimed at improving the quality, taste, and preservation of food products [...].</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6xr4k3z8</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Zhang, Biao</name>
      </author>
      <author>
        <name>Zeng, Maomao</name>
      </author>
    </item>
    <item>
      <title>An Ultrasensitive Fluorescence Sensor with Simple Operation for Cu2+ Specific Detection in Drinking Water</title>
      <link>https://escholarship.org/uc/item/6nr0d9f5</link>
      <description>Whether short-term or long-term, overexposure to an abnormal amount of copper ion does significant harm to human health. Considering its nonbiodegradability, it is critical to sensitively detect copper ion. Herein, a novel fluorescent strategy with a "turn-on" signal was developed for highly sensitive and specific detection of copper ion (Cu&lt;sup&gt;2+&lt;/sup&gt;). In the present investigation, we found that Cu&lt;sup&gt;2+&lt;/sup&gt; exhibits excellent peroxidase-like catalytic activity toward oxidizing the nonfluorescent substrate of Amplex Red into the product of resofurin with outstanding fluorescence emission under the aid of H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;. Thus, an enzyme-free and label-free sensing system was constructed for copper ion detection with quite simple operation. To ensure the detection sensitivity and reproducibility, the amount of H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; and incubation time were optimized. The limit of detection can reach as low as 1.0 nM. In addition, the developed assay demonstrated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6nr0d9f5</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gao, Jinting</name>
      </author>
      <author>
        <name>Yin, Jinjin</name>
      </author>
      <author>
        <name>Tao, Zhanhui</name>
      </author>
      <author>
        <name>Liu, Yaqing</name>
      </author>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Deng, Jiankang</name>
      </author>
      <author>
        <name>Wang, Shuo</name>
      </author>
    </item>
    <item>
      <title>A Smartphone Colorimetric Sensor Based on Pt@Au Nanozyme for Visual and Quantitative Detection of Omethoate</title>
      <link>https://escholarship.org/uc/item/5v51m8b9</link>
      <description>A smartphone colorimetric sensor based on the Pt@Au nanozyme was successfully developed for the visual and quantitative detection of omethoate in fruit and vegetables. The anti-omethoate antibody was conjugated on the surface of the Pt@Au nanozyme as a catalytic functional signal probe, and coating antigen conjugated on the surface of magnetic polystyrene microspheres (MPMs) was used as a separation capture probe. In the sensing system, when the catalytic functional signal probe was combined with a separation capture probe containing no omethoate, the visible blue color appeared with the addition of tetramethylbenzidine (TMB) chromogenic solution, and the maximum B value of the sensing system was obtained via the smartphone. With increasing concentrations of omethoate, the visualization of the sensing system decreased, and the B-value obtained via the smartphone dropped. Under optimal detection conditions, the omethoate could be detected in a linear range of 0.5-50 μg/L (R&lt;sup&gt;2&lt;/sup&gt;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5v51m8b9</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Biao</name>
      </author>
      <author>
        <name>Zhou, Ruofan</name>
      </author>
      <author>
        <name>Zhang, Huiqi</name>
      </author>
      <author>
        <name>Cai, Danfeng</name>
      </author>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Lang, Yihan</name>
      </author>
      <author>
        <name>Qiu, Yulou</name>
      </author>
      <author>
        <name>Shentu, Xuping</name>
      </author>
      <author>
        <name>Ye, Zihong</name>
      </author>
      <author>
        <name>Yu, Xiaoping</name>
      </author>
    </item>
    <item>
      <title>Implementation of cascade logic gates and majority logic gate on a simple and universal molecular platform</title>
      <link>https://escholarship.org/uc/item/59v9h39t</link>
      <description>Wiring a series of simple logic gates to process complex data is significantly important and a large challenge for untraditional molecular computing systems. The programmable property of DNA endows its powerful application in molecular computing. In our investigation, it was found that DNA exhibits excellent peroxidase-like activity in a colorimetric system of TMB/H2O2/Hemin (TMB, 3,3′, 5,5′-Tetramethylbenzidine) in the presence of K+ and Cu2+, which is significantly inhibited by the addition of an antioxidant. According to the modulated catalytic activity of this DNA-based catalyst, three cascade logic gates including AND-OR-INH (INHIBIT), AND-INH and OR-INH were successfully constructed. Interestingly, by only modulating the concentration of Cu2+, a majority logic gate with a single-vote veto function was realized following the same threshold value as that of the cascade logic gates. The strategy is quite straightforward and versatile and provides an instructive method for constructing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/59v9h39t</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gao, Jinting</name>
      </author>
      <author>
        <name>Liu, Yaqing</name>
      </author>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Deng, Jiankang</name>
      </author>
      <author>
        <name>Yin, Jinjin</name>
      </author>
      <author>
        <name>Wang, Shuo</name>
      </author>
    </item>
    <item>
      <title>Multiple advanced logic gates made of DNA-Ag nanocluster and the application for intelligent detection of pathogenic bacterial genes</title>
      <link>https://escholarship.org/uc/item/51c4z7d1</link>
      <description>The integration of multiple DNA logic gates on a universal platform to implement advance logic functions is a critical challenge for DNA computing. Herein, a straightforward and powerful strategy in which a guanine-rich DNA sequence lighting up a silver nanocluster and fluorophore was developed to construct a library of logic gates on a simple DNA-templated silver nanoclusters (DNA-AgNCs) platform. This library included basic logic gates, YES, AND, OR, INHIBIT, and XOR, which were further integrated into complex logic circuits to implement diverse advanced arithmetic/non-arithmetic functions including half-adder, half-subtractor, multiplexer, and demultiplexer. Under UV irradiation, all the logic functions could be instantly visualized, confirming an excellent repeatability. The logic operations were entirely based on DNA hybridization in an enzyme-free and label-free condition, avoiding waste accumulation and reducing cost consumption. Interestingly, a DNA-AgNCs-based multiplexer...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/51c4z7d1</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Liu, Yaqing</name>
      </author>
      <author>
        <name>Deng, Jiankang</name>
      </author>
      <author>
        <name>Lyu, Yanlong</name>
      </author>
      <author>
        <name>Qian, Pengcheng</name>
      </author>
      <author>
        <name>Li, Yunfei</name>
      </author>
      <author>
        <name>Wang, Shuo</name>
      </author>
    </item>
    <item>
      <title>Review on bile dynamics and microfluidic-based component detection: Advancing the understanding of bilestone pathogenesis in the biliary tract</title>
      <link>https://escholarship.org/uc/item/411524xp</link>
      <description>Bilestones are solid masses found in the gallbladder or biliary tract, which block the normal bile flow and eventually result in severe life-threatening complications. Studies have shown that bilestone formation may be related to bile flow dynamics and the concentration level of bile components. The bile flow dynamics in the biliary tract play a critical role in disclosing the mechanism of bile stasis and transportation. The concentration of bile composition is closely associated with processes such as nucleation and crystallization. Recently, microfluidic-based biosensors have been favored for multiple advantages over traditional benchtop detection assays for their less sample consumption, portability, low cost, and high sensitivity for real-time detection. Here, we reviewed the developments in bile dynamics study and microfluidics-based bile component detection methods. These studies may provide valuable insights into the bilestone formation mechanisms and better treatment,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/411524xp</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Peng, Tao</name>
      </author>
      <author>
        <name>Zhou, Chenxiao</name>
      </author>
      <author>
        <name>Zhang, Zhexin</name>
      </author>
      <author>
        <name>Liu, Yingying</name>
      </author>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
      <author>
        <name>Ye, Yongqing</name>
      </author>
      <author>
        <name>Zhong, Yunlong</name>
      </author>
      <author>
        <name>Wang, Ping</name>
      </author>
      <author>
        <name>Jia, Yanwei</name>
      </author>
    </item>
    <item>
      <title>Dual-Channel Fluorescent/Colorimetric-Based OPD-Pd/Pt NFs Sensor for High-Sensitivity Detection of Silver Ions</title>
      <link>https://escholarship.org/uc/item/39f603gj</link>
      <description>Silver ions (Ag&lt;sup&gt;+&lt;/sup&gt;) exist widely in various areas of human life, and the food contamination caused by them poses a serious threat to human health. Among the numerous methods used for the detection of Ag&lt;sup&gt;+&lt;/sup&gt;, fluorescence and colorimetric analysis have attracted much attention due to their inherent advantages, such as high sensitivity, simple operation, short time, low cost and visualized detection. In this work, Pd/Pt nanoflowers (NFs) specifically responsive to Ag&lt;sup&gt;+&lt;/sup&gt; were synthesized in a simple way to oxidize o-phenylenediamine (OPD) into 2,3-diaminophenazine (DAP). The interaction of Ag&lt;sup&gt;+&lt;/sup&gt; with the surface of Pd/Pt NFs inhibits the catalytic activity of Pd/Pt NFs towards the substrate OPD. A novel dual-channel nanosensor was constructed for the detection of Ag&lt;sup&gt;+&lt;/sup&gt;, using the fluorescence intensity and UV-vis absorption intensity of DAP as output signals. This dual-mode analysis combines their respective advantages to significantly...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/39f603gj</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Fang, Yuan</name>
      </author>
      <author>
        <name>Ding, Shusen</name>
      </author>
      <author>
        <name>Li, Weiran</name>
      </author>
      <author>
        <name>Zhang, Jingjing</name>
      </author>
      <author>
        <name>Sun, Hui</name>
      </author>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
    </item>
    <item>
      <title>Microfluidics-Based POCT for SARS-CoV-2 Diagnostics</title>
      <link>https://escholarship.org/uc/item/2bb5s7m2</link>
      <description>A microfluidic chip is a tiny reactor that can confine and flow a specific amount of fluid into channels of tens to thousands of microns as needed and can precisely control fluid flow, pressure, temperature, etc. Point-of-care testing (POCT) requires small equipment, has short testing cycles, and controls the process, allowing single or multiple laboratory facilities to simultaneously analyze biological samples and diagnose infectious diseases. In general, rapid detection and stage assessment of viral epidemics are essential to overcome pandemic situations and diagnose promptly. Therefore, combining microfluidic devices with POCT improves detection efficiency and convenience for viral disease SARS-CoV-2. At the same time, the POCT of microfluidic chips increases user accessibility, improves accuracy and sensitivity, shortens detection time, etc., which are beneficial in detecting SARS-CoV-2. This review shares recent advances in POCT-based testing for COVID-19 and how it is better...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2bb5s7m2</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Yin, Binfeng</name>
      </author>
      <author>
        <name>Wan, Xinhua</name>
      </author>
      <author>
        <name>Sohan, ASM Muhtasim Fuad</name>
      </author>
      <author>
        <name>Lin, Xiaodong</name>
        <uri>https://orcid.org/0000-0002-0639-0017</uri>
      </author>
    </item>
    <item>
      <title>Meibomian gland lipid alterations and ocular surface sequela in Awat2 knockout murine model of meibomian gland dysfunction and evaporative dry eye disease</title>
      <link>https://escholarship.org/uc/item/72z6q207</link>
      <description>PURPOSE: There is an urgent need for animal models of meibomian gland dysfunction (MGD) and evaporative dry eye disease (EDED) to understand their pathophysiology and investigate novel therapeutics. This study sought to further define the acyl-CoA: wax alcohol acyltransferase 2 knockout (Awat2 KO) mouse as a model of EDED using a combination of novel clinical, biochemical, and biophysical endpoints.
METHODS: Wildtype and Awat2 KO mice between 1 and 18 months of age were used. Ocular examinations and advanced imaging were performed. The lipidomic composition and in situ melting temperature of meibum were determined. qPCR was performed to define ocular surface gene and pro-inflammatory transcript expression. Dynamic contact angle goniometry was performed to assess the adherence capability of the ocular surface.
RESULTS: Awat2 KO mice have mild, white, hyperreflective corneal opacities of the anterior stroma and significantly enlarged apical epithelial cells (P&amp;nbsp;=&amp;nbsp;0.0004)....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/72z6q207</guid>
      <pubDate>Tue, 1 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hisey, Erin A</name>
      </author>
      <author>
        <name>Wong, Sydni</name>
      </author>
      <author>
        <name>Park, Sangwan</name>
      </author>
      <author>
        <name>Gamarra, Kevin Aguirre</name>
      </author>
      <author>
        <name>Adelman, Sara A</name>
      </author>
      <author>
        <name>Knickelbein, Kelly E</name>
      </author>
      <author>
        <name>Quan, Melinda</name>
      </author>
      <author>
        <name>Ferneding, Michelle H</name>
      </author>
      <author>
        <name>McCorkell, Michelle</name>
      </author>
      <author>
        <name>Daley, Nicole</name>
      </author>
      <author>
        <name>Ureno, Vanessa</name>
      </author>
      <author>
        <name>Le, Sophie</name>
      </author>
      <author>
        <name>Ardon, Monica</name>
        <uri>https://orcid.org/0009-0006-2314-9010</uri>
      </author>
      <author>
        <name>Williams, Liana</name>
      </author>
      <author>
        <name>Puentes, Bryan</name>
      </author>
      <author>
        <name>Bowman, Morgan</name>
      </author>
      <author>
        <name>Motta, Monica J</name>
      </author>
      <author>
        <name>Pham, Hoang Quoc Hai</name>
      </author>
      <author>
        <name>Wilkerson, Amber</name>
      </author>
      <author>
        <name>Yuksel, Seher</name>
      </author>
      <author>
        <name>Jester, James V</name>
        <uri>https://orcid.org/0000-0002-9246-0981</uri>
      </author>
      <author>
        <name>Thomasy, Sara M</name>
        <uri>https://orcid.org/0000-0001-5617-9677</uri>
      </author>
      <author>
        <name>Morgan, Joshua T</name>
        <uri>https://orcid.org/0000-0001-8033-0285</uri>
      </author>
      <author>
        <name>Butovich, Igor A</name>
      </author>
      <author>
        <name>Leonard, Brian C</name>
        <uri>https://orcid.org/0000-0003-2080-8480</uri>
      </author>
    </item>
    <item>
      <title>How Rigid Are Anthranilamide Molecular Electrets?</title>
      <link>https://escholarship.org/uc/item/35r8j3gr</link>
      <description>As important as molecular electrets are for electronic materials and devices, conformational fluctuations strongly impact their macrodipoles and intrinsic properties. Herein, we employ molecular dynamics (MD) simulations with the polarizable charge equilibrium (PQEq) method to investigate the persistence length (&lt;i&gt;L&lt;/i&gt;&lt;sub&gt;&lt;i&gt;P&lt;/i&gt;&lt;/sub&gt;) of molecular electrets composed of anthranilamide (Aa) residues. The PQEq-MD dissipates the accepted static notions about Aa macromolecules, and &lt;i&gt;L&lt;/i&gt;&lt;sub&gt;&lt;i&gt;P&lt;/i&gt;&lt;/sub&gt; represents the shortest Aa rigid segments. The classical model with a single &lt;i&gt;L&lt;/i&gt;&lt;sub&gt;&lt;i&gt;P&lt;/i&gt;&lt;/sub&gt; value does not describe these oligomers. Introducing multiple &lt;i&gt;L&lt;/i&gt;&lt;sub&gt;&lt;i&gt;P&lt;/i&gt;&lt;/sub&gt; values for the same macromolecule follows the observed trends and discerns the enhanced rigidity in their middle sections from the reduced stiffness at their terminal regions. Furthermore, &lt;i&gt;L&lt;/i&gt;&lt;sub&gt;&lt;i&gt;P&lt;/i&gt;&lt;/sub&gt; distinctly depends on solvent polarity. The Aa oligomers maintain...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/35r8j3gr</guid>
      <pubDate>Tue, 1 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>O’Mari, Omar</name>
      </author>
      <author>
        <name>Yang, Moon Young</name>
      </author>
      <author>
        <name>Goddard, William</name>
      </author>
      <author>
        <name>Vullev, Valentine I</name>
      </author>
    </item>
    <item>
      <title>Graph theory approaches for molecular dynamics simulations</title>
      <link>https://escholarship.org/uc/item/1rr587dw</link>
      <description>Graph theory, a branch of mathematics that focuses on the study of graphs (networks of nodes and edges), provides a robust framework for analysing the structural and functional properties of biomolecules. By leveraging molecular dynamics (MD) simulations, atoms or groups of atoms can be represented as nodes, while their dynamic interactions are depicted as edges. This network-based approach facilitates the characterization of properties such as connectivity, centrality, and modularity, which are essential for understanding the behaviour of molecular systems. This review details the application and development of graph theory-based models in studying biomolecular systems. We introduce key concepts in graph theory and demonstrate their practical applications, illustrating how innovative graph theory approaches can be employed to design biomolecular systems with enhanced functionality. Specifically, we explore the integration of graph theoretical methods with MD simulations to gain...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1rr587dw</guid>
      <pubDate>Tue, 1 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Patel, Amun C</name>
      </author>
      <author>
        <name>Sinha, Souvik</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
    </item>
    <item>
      <title>On the Feasibility of SERS-Based Monitoring of Drug Loading Efficiency in Exosomes for Targeted Delivery</title>
      <link>https://escholarship.org/uc/item/3j42d4t8</link>
      <description>Cancer, a significant cause of mortality, necessitates improved drug delivery strategies. Exosomes, as natural drug carriers, offer a more efficient, targeted, and less toxic drug delivery system compared to direct dispersal methods via ingestion or injection. To be successfully implemented as drug carriers, efficient loading of drugs into exosomes is crucial, and a deeper understanding of the loading mechanism remains to be solved. This study introduces surface-enhanced Raman scattering (SERS) to monitor drug loading efficacy at the single vesicle level. By enhancing the Raman signal, SERS overcomes limitations in Raman spectroscopy. A gold nanopyramids array-based SERS substrate assesses exosome heterogeneity in drug-loading capabilities with the help of single-layer graphene for precise quantification. This research advances targeted drug delivery by presenting a more efficient method of evaluating drug-loading efficiency into individual exosomes through SERS-based monitoring....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3j42d4t8</guid>
      <pubDate>Wed, 26 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Jun</name>
        <uri>https://orcid.org/0000-0002-9670-1033</uri>
      </author>
      <author>
        <name>Srivastava, Siddharth</name>
      </author>
      <author>
        <name>Li, Tieyi</name>
      </author>
      <author>
        <name>Moujane, Faycal</name>
      </author>
      <author>
        <name>Lee, John Y</name>
      </author>
      <author>
        <name>Chen, Yiqing</name>
      </author>
      <author>
        <name>Liu, Huinan</name>
        <uri>https://orcid.org/0000-0001-9366-6204</uri>
      </author>
      <author>
        <name>Deng, Sophie X</name>
      </author>
      <author>
        <name>Xie, Ya-Hong</name>
      </author>
    </item>
    <item>
      <title>Systematic Review and Meta-Analysis of Endovascular Therapy Effectiveness for Unruptured Saccular Intracranial Aneurysms.</title>
      <link>https://escholarship.org/uc/item/4zv42366</link>
      <description>Background: Currently, endovascular treatment of intracranial aneurysms (ICAs) is limited by low complete occlusion rates. The advent of novel endovascular technology has expanded the applicability of endovascular therapy; however, the superiority of novel embolic devices over the traditional Guglielmi detachable coils (GDCs) is still debated. We performed a systematic review of literature that reported Raymond-Roy occlusion classification (RROC) rates of modern endovascular devices to determine their immediate and follow-up occlusion effectiveness for the treatment of unruptured saccular ICAs.
Methods: A search was conducted using electronic databases (PUBMED, Cochrane, ClinicalTrials.gov, Web of Science). We retrieved studies published between 2000-2022 reporting immediate and follow-up RROC rates of subjects treated with different endovascular ICA therapies. We extracted demographic information of the treated patients and their reported angiographic RROC rates.
Results: A total...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4zv42366</guid>
      <pubDate>Wed, 19 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pineda‐Castillo, Sergio A</name>
      </author>
      <author>
        <name>Jones, Evan R</name>
      </author>
      <author>
        <name>Laurence, Keely A</name>
      </author>
      <author>
        <name>Thoendel, Lauren R</name>
      </author>
      <author>
        <name>Cabaniss, Tanner L</name>
      </author>
      <author>
        <name>Zhao, Yan D</name>
      </author>
      <author>
        <name>Bohnstedt, Bradley N</name>
      </author>
      <author>
        <name>Lee, Chung‐Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
    <item>
      <title>Bayesian Optimization-Based Inverse Finite Element Analysis for Atrioventricular Heart Valves</title>
      <link>https://escholarship.org/uc/item/2zw7h8h3</link>
      <description>Inverse finite element analysis (iFEA) of the atrioventricular heart valves (AHVs) can provide insights into the in-vivo valvular function, such as in-vivo tissue strains; however, there are several limitations in the current state-of-the-art that iFEA has not been widely employed to predict the in-vivo, patient-specific AHV leaflet mechanical responses. In this exploratory study, we propose the use of Bayesian optimization (BO) to study the AHV functional behaviors in-vivo. We analyzed the efficacy of Bayesian optimization to estimate the&amp;nbsp;isotropic Lee–Sacks material coefficients in three benchmark problems: (i)&amp;nbsp;an inflation test, (ii)&amp;nbsp;a simplified leaflet contact model, and (iii)&amp;nbsp;an idealized AHV model. Then, we applied the developed BO-iFEA framework to predict the leaflet properties for a patient-specific tricuspid valve under a congenital heart defect condition. We found that the BO could accurately construct the objective function surface compared to...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2zw7h8h3</guid>
      <pubDate>Tue, 18 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ross, Colton J</name>
      </author>
      <author>
        <name>Laurence, Devin W</name>
      </author>
      <author>
        <name>Aggarwal, Ankush</name>
      </author>
      <author>
        <name>Hsu, Ming-Chen</name>
      </author>
      <author>
        <name>Mir, Arshid</name>
      </author>
      <author>
        <name>Burkhart, Harold M</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
    <item>
      <title>Effects of blood type and number concentration on the circulation time of micro-sized erythrocyte-derived optical particles in mice</title>
      <link>https://escholarship.org/uc/item/8k13m6k5</link>
      <description>Erythrocyte-derived optical microparticles containing near infrared (NIR) dyes such as indocyanine green (ICG) present a promising platform for fluorescence imaging and laser treatment of abnormal vasculature, including port wine birthmarks. Herein, we have investigated the effects of blood type utilized in fabricating these microparticles, and the number density of the particles on their circulation time in mice by real-time NIR fluorescence imaging of the dermal vasculature. We find that the emission half-life of microparticles engineered from human O+ blood type increases by approximately two-fold as compared to those engineered from B+ blood type. Increasing the number density of the microparticles fabricated from O+ blood type from ~0.5 millions/µl to 1.6 millions/µl is associated with nearly a fourfold increase in the emission half-life of the particles. These findings emphasize the importance of blood type and number density in engineering erythrocyte-derived particles...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8k13m6k5</guid>
      <pubDate>Fri, 7 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Swajian, G</name>
      </author>
      <author>
        <name>Zaman, S</name>
      </author>
      <author>
        <name>Lee, C-H</name>
      </author>
      <author>
        <name>Nguyen, E</name>
      </author>
      <author>
        <name>Huynh, C</name>
      </author>
      <author>
        <name>Lai, O</name>
      </author>
      <author>
        <name>Nelson, JS</name>
        <uri>https://orcid.org/0000-0002-2697-9152</uri>
      </author>
      <author>
        <name>Choi, B</name>
        <uri>https://orcid.org/0000-0002-4380-8291</uri>
      </author>
      <author>
        <name>Jia, W</name>
        <uri>https://orcid.org/0000-0002-5021-3827</uri>
      </author>
      <author>
        <name>Anvari, B</name>
        <uri>https://orcid.org/0000-0002-2511-5854</uri>
      </author>
    </item>
    <item>
      <title>Flexibility in PAM recognition expands DNA targeting in xCas9</title>
      <link>https://escholarship.org/uc/item/2wr0z6pv</link>
      <description>xCas9 is an evolved variant of the CRISPR-Cas9 genome editing system, engineered to improve specificity and reduce undesired off-target effects. How xCas9 expands the DNA targeting capability of Cas9 by recognising a series of alternative protospacer adjacent motif (PAM) sequences while ignoring others is unknown. Here, we elucidate the molecular mechanism underlying xCas9's expanded PAM recognition and provide critical insights for expanding DNA targeting. We demonstrate that while wild-type Cas9 enforces stringent guanine selection through the rigidity of its interacting arginine dyad, xCas9 introduces flexibility in R1335, enabling selective recognition of specific PAM sequences. This increased flexibility confers a pronounced entropic preference, which also improves recognition of the canonical TGG PAM. Furthermore, xCas9 enhances DNA binding to alternative PAM sequences during the early evolution cycles, while favouring binding to the canonical PAM in the final evolution...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2wr0z6pv</guid>
      <pubDate>Mon, 3 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hossain, Kazi A</name>
      </author>
      <author>
        <name>Nierzwicki, Lukasz</name>
      </author>
      <author>
        <name>Orozco, Modesto</name>
      </author>
      <author>
        <name>Czub, Jacek</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
    </item>
    <item>
      <title>Mechanical Regulation of Retinal Vascular Inflammation and Degeneration in Diabetes.</title>
      <link>https://escholarship.org/uc/item/2w369394</link>
      <description>Vascular inflammation is known to cause degeneration of retinal capillaries in early diabetic retinopathy (DR), a major microvascular complication of diabetes. Past studies investigating these diabetes-induced retinal vascular abnormalities have focused primarily on the role of molecular or biochemical cues. Here we show that retinal vascular inflammation and degeneration in diabetes are also mechanically regulated by the increase in retinal vascular stiffness caused by overexpression of the collagen-cross-linking enzyme lysyl oxidase (LOX). Treatment of diabetic mice with LOX inhibitor β-aminopropionitrile (BAPN) prevented the increase in retinal capillary stiffness, vascular intracellular adhesion molecule-1 overexpression, and leukostasis. Consistent with these anti-inflammatory effects, BAPN treatment of diabetic mice blocked the upregulation of proapoptotic caspase-3 in retinal vessels, which concomitantly reduced retinal capillary degeneration, pericyte ghost formation,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2w369394</guid>
      <pubDate>Fri, 14 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chandrakumar, Sathishkumar</name>
      </author>
      <author>
        <name>Santiago Tierno, Irene</name>
      </author>
      <author>
        <name>Agarwal, Mahesh</name>
      </author>
      <author>
        <name>Lessieur, Emma M</name>
        <uri>https://orcid.org/0000-0001-9120-0291</uri>
      </author>
      <author>
        <name>Du, Yunpeng</name>
      </author>
      <author>
        <name>Tang, Jie</name>
      </author>
      <author>
        <name>Kiser, Jianying</name>
      </author>
      <author>
        <name>Yang, Xiao</name>
      </author>
      <author>
        <name>Rodriguez, Anthony</name>
      </author>
      <author>
        <name>Kern, Timothy S</name>
        <uri>https://orcid.org/0000-0003-1188-0739</uri>
      </author>
      <author>
        <name>Ghosh, Kaustabh</name>
      </author>
    </item>
    <item>
      <title>Facile and Green Synthesis of Multicolor Fluorescence Carbon Dots from Curcumin: In Vitro and in Vivo Bioimaging and Other Applications</title>
      <link>https://escholarship.org/uc/item/4cj9z56k</link>
      <description>Early detection is the critical phase in the prognostic strategy of various life-threatening maladies like infectious diseases and cancer. The mortality rate caused by these diseases could be considerably reduced if they were diagnosed in the early stages of disease development. Carbon dots (C-dots), a relatively new and promising candidate in the fluorescent nanomaterial category, possess a perceptible impact on various bioapplications. Herein, we report a one-step facile hydrothermal synthesis that yields a novel surface-passivated carbon dot (CDP) from curcumin (as a green substrate) displaying high aqueous solubility. The physico-chemical characterization of thus synthesized C-dots was accomplished by an UV-visible spectrophotometer, fluorescence spectrophotometer, zetasizer, TEM, and FE-SEM to understand the formation of carbon dots with a 4-5 nm size near spherical nanoparticle with high colloidal stability. &lt;i&gt;E. coli&lt;/i&gt; DH5α was engaged as the Gram-negative test organism...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4cj9z56k</guid>
      <pubDate>Fri, 31 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pal, Tathagata</name>
        <uri>https://orcid.org/0000-0002-2473-6974</uri>
      </author>
      <author>
        <name>Mohiyuddin, Shanid</name>
      </author>
      <author>
        <name>Packirisamy, Gopinath</name>
      </author>
    </item>
    <item>
      <title>Engineering the Ratios of Nanoparticles Dispersed in Triphasic Nanocomposites for Biomedical Applications</title>
      <link>https://escholarship.org/uc/item/81r6b94m</link>
      <description>Polymer/ceramic nanocomposites integrated the advantages of both polymers and ceramics for a wide range of biomedical applications, such as bone tissue repair. Here, we reported triphasic poly(lactic-&lt;i&gt;co&lt;/i&gt;-glycolic acid) (PLGA, LA/GA = 90:10) nanocomposites with improved dispersion of hydroxyapatite (HA) and magnesium oxide (MgO) nanoparticles using a process that integrated the benefits of ultrasonic energy and dual asymmetric centrifugal mixing. We characterized the microstructure and composition of the nanocomposites and evaluated the effects of the HA/MgO ratios on degradation behavior and cell-material interactions. The PLGA/HA/MgO nanocomposites were composed of 70 wt % PLGA and 30 wt % nanoparticles made of 20:10, 25:5, and 29:1% by weight of HA and MgO, respectively. The results showed that the nanocomposites had a homogeneous nanoparticle distribution and as-designed elemental composition. The cell study indicated that reducing the MgO content in the triphasic nanocomposite...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/81r6b94m</guid>
      <pubDate>Thu, 30 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wetteland, Cheyann</name>
      </author>
      <author>
        <name>Xu, Changlu</name>
      </author>
      <author>
        <name>Wang, Sebo Michelle</name>
      </author>
      <author>
        <name>Zhang, Chaoxing</name>
      </author>
      <author>
        <name>Ang, Elizabeth Juntilla</name>
      </author>
      <author>
        <name>Azevedo, Cole Gabriel</name>
      </author>
      <author>
        <name>Liu, Huinan Hannah</name>
        <uri>https://orcid.org/0000-0001-9366-6204</uri>
      </author>
    </item>
    <item>
      <title>Task relevant autoencoding enhances machine learning for human neuroscience</title>
      <link>https://escholarship.org/uc/item/2xh0x1ff</link>
      <description>In human neuroscience, machine learning can help reveal lower-dimensional neural representations relevant to subjects’ behavior. However, state-of-the-art models typically require large datasets to train, and so are prone to overfitting on human neuroimaging data that often possess few samples but many input dimensions. Here, we capitalized on the fact that the features we seek in human neuroscience are precisely those relevant to subjects’ behavior rather than noise or other irrelevant factors. We thus developed a Task-Relevant Autoencoder via Classifier Enhancement (TRACE) designed to identify behaviorally-relevant target neural patterns. We benchmarked TRACE against a standard autoencoder and other models for two severely truncated machine learning datasets (to match the data typically available in functional magnetic resonance imaging [fMRI] data for an individual subject), then evaluated all models on fMRI data from 59 subjects who observed animals and objects. TRACE outperformed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2xh0x1ff</guid>
      <pubDate>Thu, 30 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Orouji, Seyedmehdi</name>
      </author>
      <author>
        <name>Taschereau-Dumouchel, Vincent</name>
      </author>
      <author>
        <name>Cortese, Aurelio</name>
      </author>
      <author>
        <name>Odegaard, Brian</name>
      </author>
      <author>
        <name>Cushing, Cody</name>
      </author>
      <author>
        <name>Cherkaoui, Mouslim</name>
      </author>
      <author>
        <name>Kawato, Mitsuo</name>
      </author>
      <author>
        <name>Lau, Hakwan</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>CIMNE-CRISPR: A novel amplification-free diagnostic for rapid early detection of African Swine Fever Virus</title>
      <link>https://escholarship.org/uc/item/03n8t47m</link>
      <description>African Swine Fever Virus (ASFV) is a highly contagious pathogen with nearly 100% mortality in swine, causing severe global economic loss. Current detection methods rely on nucleic acid amplification, which requires specialized equipment and skilled operators, limiting accessibility in resource-constrained settings. To address these challenges, we developed the Covalently Immobilized Magnetic Nanoparticles Enhanced CRISPR (CIMNE-CRISPR) system. This amplification-free diagnostic system seamlessly combines target recognition, sequence-specific enrichment, and signal generation. This approach uses covalent immobilization of CRISPR-LbCas12a-crRNA complexes on Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;@SiO&lt;sub&gt;2&lt;/sub&gt; core-shell magnetic nanoparticles, which improves enzyme specificity and robustness over traditional adsorption. The CIMNE-CRISPR assay reached a limit of detection (LOD) of 8.1&amp;nbsp;×&amp;nbsp;10&lt;sup&gt;4&lt;/sup&gt; copies/μL and a limit of quantification (LOQ) of 4.2&amp;nbsp;×&amp;nbsp;10&lt;sup&gt;5&lt;/sup&gt;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/03n8t47m</guid>
      <pubDate>Thu, 30 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pal, Tathagata</name>
        <uri>https://orcid.org/0000-0002-2473-6974</uri>
      </author>
      <author>
        <name>Liu, Zilong</name>
      </author>
      <author>
        <name>Chen, Juhong</name>
        <uri>https://orcid.org/0000-0002-6484-2739</uri>
      </author>
    </item>
    <item>
      <title>Development of a self-powered digital LAMP microfluidic chip (SP-dChip) for the detection of emerging viruses</title>
      <link>https://escholarship.org/uc/item/9196g03f</link>
      <description>Point-of-care (POC) diagnostics have emerged as a crucial technology for emerging pathogen detections to enable rapid and on-site detection of infectious diseases. However, current POC devices often suffer from limited sensitivity with poor reliability to provide quantitative readouts. In this paper, we present a self-powered digital loop-mediated isothermal amplification (dLAMP) microfluidic chip (SP-dChip) for the rapid and quantitative detection of nucleic acids. The SP-dChip utilizes a vacuum lung design to passively digitize samples into individual nanoliter wells for high-throughput analysis. The superior digitization scheme is further combined with reverse transcription loop-mediated isothermal amplification (RT-LAMP) to demonstrate dLAMP detection of Zika virus (ZIKV). Firstly, the LAMP assay is loaded into the chip and passively digitized into individual wells. Mineral oil is then pipetted through the chip to differentiate each well as an individual reactor. The chip...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9196g03f</guid>
      <pubDate>Fri, 24 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kasputis, Tom</name>
      </author>
      <author>
        <name>Yeh, Po-Chen</name>
      </author>
      <author>
        <name>Liu, Li</name>
      </author>
      <author>
        <name>Marano, Jeffrey</name>
      </author>
      <author>
        <name>Weger-Lucarelli, James</name>
      </author>
      <author>
        <name>Du, Ke</name>
        <uri>https://orcid.org/0000-0003-2560-3281</uri>
      </author>
      <author>
        <name>Lin, Liwei</name>
      </author>
      <author>
        <name>Chen, Juhong</name>
        <uri>https://orcid.org/0000-0002-6484-2739</uri>
      </author>
    </item>
    <item>
      <title>Dimerization of the deaminase domain and locking interactions with Cas9 boost base editing efficiency in ABE8e</title>
      <link>https://escholarship.org/uc/item/8mx3c60v</link>
      <description>CRISPR-based DNA adenine base editors (ABEs) hold remarkable promises to address human genetic diseases caused by point mutations. ABEs were developed by combining CRISPR-Cas9 with a transfer RNA (tRNA) adenosine deaminase enzyme and through directed evolution, conferring the ability to deaminate DNA. However, the molecular mechanisms driving the efficient DNA deamination in the evolved ABEs remain unresolved. Here, extensive molecular simulations and biochemical experiments reveal the biophysical basis behind the astonishing base editing efficiency of ABE8e, the most efficient ABE to date. We demonstrate that the ABE8e's DNA deaminase domain, TadA8e, forms remarkably stable dimers compared to its tRNA-deaminating progenitor and that the strength of TadA dimerization is crucial for DNA deamination. The TadA8e dimer forms robust interactions involving its R98 and R129 residues, the RuvC domain of Cas9 and the DNA. These locking interactions are exclusive to ABE8e, distinguishing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8mx3c60v</guid>
      <pubDate>Mon, 6 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Arantes, Pablo R</name>
        <uri>https://orcid.org/0000-0003-1946-2750</uri>
      </author>
      <author>
        <name>Chen, Xiaoyu</name>
      </author>
      <author>
        <name>Sinha, Souvik</name>
      </author>
      <author>
        <name>Saha, Aakash</name>
      </author>
      <author>
        <name>Patel, Amun C</name>
      </author>
      <author>
        <name>Sample, Matthew</name>
      </author>
      <author>
        <name>Nierzwicki, Łukasz</name>
      </author>
      <author>
        <name>Lapinaite, Audrone</name>
        <uri>https://orcid.org/0000-0002-9427-9342</uri>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
    </item>
    <item>
      <title>Substrate-independent activation pathways of the CRISPR-Cas9 HNH nuclease</title>
      <link>https://escholarship.org/uc/item/785050nr</link>
      <description>A hallmark of tightly regulated high-fidelity enzymes is that they become activated only after encountering cognate substrates, often by an induced-fit mechanism rather than conformational selection. Upon analysis of molecular dynamics trajectories, we recently discovered that the Cas9 HNH domain exists in three conformations: 1) Y836 (which is two residues away from the catalytic D839 and H840 residues) is hydrogen bonded to the D829 backbone amide, 2) Y836 is hydrogen bonded to the backbone amide of D861 (which is one residue away from the third catalytic residue N863), and 3) Y836 is not hydrogen bonded to either residue. Each of the three conformers differs from the active state of HNH. The conversion between the inactive and active states involves a local unfolding-refolding process that displaces the Cα and side chain of the catalytic N863 residue by ∼5&amp;nbsp;Å and ∼10&amp;nbsp;Å, respectively. In this study, we report the two largest principal components of coordinate variance...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/785050nr</guid>
      <pubDate>Thu, 2 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Jimin</name>
      </author>
      <author>
        <name>Maschietto, Federica</name>
      </author>
      <author>
        <name>Qiu, Tianyin</name>
      </author>
      <author>
        <name>Arantes, Pablo R</name>
      </author>
      <author>
        <name>Skeens, Erin</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
      <author>
        <name>Lisi, George P</name>
      </author>
      <author>
        <name>Batista, Victor S</name>
      </author>
    </item>
    <item>
      <title>MetaNO: How to transfer your knowledge on learning hidden physics</title>
      <link>https://escholarship.org/uc/item/25q1h70n</link>
      <description>Gradient-based meta-learning methods have primarily been applied to classical machine learning tasks such as image classification. Recently, PDE-solving deep learning methods, such as neural operators, are starting to make an important impact on learning and predicting the response of a complex physical system directly from observational data. Taking the material modeling problems for example, the neural operator approach learns a surrogate mapping from the loading field to the corresponding material response field, which can be seen as learning the solution operator of a hidden PDE. The microstructure and mechanical parameters of each material specimen correspond to the (possibly heterogeneous) parameter field in this hidden PDE. Due to the limitation on experimental measurement techniques, the data acquisition for each material specimen is commonly challenging and costly. This fact calls for the utilization and transfer of existing knowledge to new and unseen material specimens,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/25q1h70n</guid>
      <pubDate>Tue, 24 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Lu</name>
      </author>
      <author>
        <name>You, Huaiqian</name>
      </author>
      <author>
        <name>Gao, Tian</name>
      </author>
      <author>
        <name>Yu, Mo</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
      <author>
        <name>Yu, Yue</name>
      </author>
    </item>
    <item>
      <title>Potent strategy towards strongly emissive nitroaromatics through a weakly electron-deficient core</title>
      <link>https://escholarship.org/uc/item/9gd7p4sx</link>
      <description>Nitroaromatics seldom fluoresce. The importance of electron-deficient (n-type) conjugates, however, has inspired a number of strategies for suppressing the emission-quenching effects of the strongly electron-withdrawing nitro group. Here, we demonstrate how such strategies yield fluorescent nitroaryl derivatives of dipyrrolonaphthyridinedione (DPND). Nitro groups near the DPND core quench its fluorescence. Conversely, nitro groups placed farther from the core allow some of the highest fluorescence quantum yields ever recorded for nitroaromatics. This strategy of preventing the known processes that compete with photoemission, however, leads to the emergence of unprecedented alternative mechanisms for fluorescence quenching, involving transitions to dark nπ* singlet states and aborted photochemistry. Forming nπ* triplet states from ππ* singlets is a classical pathway for fluorescence quenching. In nitro-DPNDs, however, these ππ* and nπ* excited states are both singlets, and they...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9gd7p4sx</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sadowski, Bartłomiej</name>
      </author>
      <author>
        <name>Kaliszewska, Marzena</name>
      </author>
      <author>
        <name>Poronik, Yevgen M</name>
      </author>
      <author>
        <name>Czichy, Małgorzata</name>
      </author>
      <author>
        <name>Janasik, Patryk</name>
      </author>
      <author>
        <name>Banasiewicz, Marzena</name>
      </author>
      <author>
        <name>Mierzwa, Dominik</name>
      </author>
      <author>
        <name>Gadomski, Wojciech</name>
      </author>
      <author>
        <name>Lohrey, Trevor D</name>
      </author>
      <author>
        <name>Clark, John A</name>
      </author>
      <author>
        <name>Łapkowski, Mieczysław</name>
      </author>
      <author>
        <name>Kozankiewicz, Bolesław</name>
      </author>
      <author>
        <name>Vullev, Valentine I</name>
      </author>
      <author>
        <name>Sobolewski, Andrzej L</name>
      </author>
      <author>
        <name>Piatkowski, Piotr</name>
      </author>
      <author>
        <name>Gryko, Daniel T</name>
      </author>
    </item>
    <item>
      <title>How does tautomerization affect the excited-state dynamics of an amino acid-derivatized corrole?</title>
      <link>https://escholarship.org/uc/item/97m2g9d8</link>
      <description>In the first two decades of the XXI century, corroles have emerged as an important class of porphyrinoids for photonics and biomedical photonics. In comparison with porphyrins, corroles have lower molecular symmetry and higher electron density, which leads to uniquely complementary properties. In macrocycles of free-base corroles, for example, three protons are distributed among four pyrrole nitrogens. It results in distinct tautomers that have different thermodynamic energies. Herein, we focus on the excited-state dynamics of a corrole modified with l-phenylalanine. The tautomerization in the singlet-excited state occurs in the timescales of about 10–100 picoseconds and exhibits substantial kinetic isotope effects. It, however, does not discernably affect nanosecond deactivation of the photoexcited corrole and its basic photophysics. Nevertheless, this excited-state tautomerization dynamics can strongly affect photoinduced processes with comparable or shorter timescales, considering...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/97m2g9d8</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Clark, John A</name>
      </author>
      <author>
        <name>Orłowski, Rafał</name>
      </author>
      <author>
        <name>Derr, James B</name>
      </author>
      <author>
        <name>Espinoza, Eli M</name>
      </author>
      <author>
        <name>Gryko, Daniel T</name>
      </author>
      <author>
        <name>Vullev, Valentine I</name>
      </author>
    </item>
    <item>
      <title>The magic of biaryl linkers: the electronic coupling through them defines the propensity for excited-state symmetry breaking in quadrupolar acceptor–donor–acceptor fluorophores</title>
      <link>https://escholarship.org/uc/item/8379x9n8</link>
      <description>Charge transfer (CT) is key for molecular photonics, governing the optical properties of chromophores comprising electron-rich and electron-deficient components. In photoexcited dyes with an acceptor-donor-acceptor or donor-acceptor-donor architecture, CT breaks their quadrupolar symmetry and yields dipolar structures manifesting pronounced solvatochromism. Herein, we explore the effects of electronic coupling through biaryl linkers on the excited-state symmetry breaking of such hybrid dyes composed of an electron-rich core, &lt;i&gt;i.e.&lt;/i&gt;, 1,4-dihydropyrrolo[3,2-&lt;i&gt;b&lt;/i&gt;]pyrrole (DHPP), and pyrene substituents that can act as electron acceptors. Experimental and theoretical studies reveal that strengthening the donor-acceptor electronic coupling decreases the CT rates and the propensity for symmetry breaking. We ascribe this unexpected result to effects of electronic coupling on the CT thermodynamics, which in its turn affects the CT kinetics. In cases of intermediate electronic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8379x9n8</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Clark, John A</name>
      </author>
      <author>
        <name>Kusy, Damian</name>
      </author>
      <author>
        <name>Vakuliuk, Olena</name>
      </author>
      <author>
        <name>Krzeszewski, Maciej</name>
      </author>
      <author>
        <name>Kochanowski, Krzysztof J</name>
      </author>
      <author>
        <name>Koszarna, Beata</name>
      </author>
      <author>
        <name>O'Mari, Omar</name>
      </author>
      <author>
        <name>Jacquemin, Denis</name>
      </author>
      <author>
        <name>Gryko, Daniel T</name>
      </author>
      <author>
        <name>Vullev, Valentine I</name>
        <uri>https://orcid.org/0000-0002-3416-9686</uri>
      </author>
    </item>
    <item>
      <title>Deciphering the unusual fluorescence in weakly coupled bis-nitro-pyrrolo[3,2-b]pyrroles</title>
      <link>https://escholarship.org/uc/item/6pb240f8</link>
      <description>Electron-deficient π-conjugated functional dyes lie at the heart of organic optoelectronics. Adding nitro groups to aromatic compounds usually quenches their fluorescence via inter-system crossing (ISC) or internal conversion (IC). While strong electronic coupling of the nitro groups with the dyes ensures the benefits from these electron-withdrawing substituents, it also leads to fluorescence quenching. Here, we demonstrate how such electronic coupling affects the photophysics of acceptor–donor–acceptor fluorescent dyes, with nitrophenyl acceptors and a pyrrolo[3,2-b]pyrrole donor. The position of the nitro groups and the donor-acceptor distance strongly affect the fluorescence properties of the bis-nitrotetraphenylpyrrolopyrroles. Concurrently, increasing solvent polarity quenches the emission that recovers upon solidifying the media. Intramolecular charge transfer (CT) and molecular dynamics, therefore, govern the fluorescence of these nitro-aromatics. While balanced donor-acceptor...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6pb240f8</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Poronik, Yevgen M</name>
      </author>
      <author>
        <name>Baryshnikov, Glib V</name>
      </author>
      <author>
        <name>Deperasińska, Irena</name>
      </author>
      <author>
        <name>Espinoza, Eli M</name>
      </author>
      <author>
        <name>Clark, John A</name>
      </author>
      <author>
        <name>Ågren, Hans</name>
      </author>
      <author>
        <name>Gryko, Daniel T</name>
      </author>
      <author>
        <name>Vullev, Valentine I</name>
      </author>
    </item>
    <item>
      <title>Role of intramolecular hydrogen bonds in promoting electron flow through amino acid and oligopeptide conjugates</title>
      <link>https://escholarship.org/uc/item/5mw9f9d6</link>
      <description>Elucidating the factors that control charge transfer rates in relatively flexible conjugates is of importance for understanding energy flows in biology as well as assisting the design and construction of electronic devices. Here, we report ultrafast electron transfer (ET) and hole transfer (HT) between a corrole (Cor) donor linked to a perylene-diimide (PDI) acceptor by a tetrameric alanine (Ala)&lt;sub&gt;4&lt;/sub&gt; Selective photoexcitation of the donor and acceptor triggers subpicosecond and picosecond ET and HT. Replacement of the (Ala)&lt;sub&gt;4&lt;/sub&gt; linker with either a single alanine or phenylalanine does not substantially affect the ET and HT kinetics. We infer that electronic coupling in these reactions is not mediated by tetrapeptide backbone nor by direct donor-acceptor interactions. Employing a combination of NMR, circular dichroism, and computational studies, we show that intramolecular hydrogen bonding brings the donor and the acceptor into proximity in a "scorpion-shaped" molecular...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5mw9f9d6</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Orłowski, Rafał</name>
      </author>
      <author>
        <name>Clark, John A</name>
      </author>
      <author>
        <name>Derr, James B</name>
      </author>
      <author>
        <name>Espinoza, Eli M</name>
      </author>
      <author>
        <name>Mayther, Maximilian F</name>
      </author>
      <author>
        <name>Staszewska-Krajewska, Olga</name>
      </author>
      <author>
        <name>Winkler, Jay R</name>
      </author>
      <author>
        <name>Jędrzejewska, Hanna</name>
      </author>
      <author>
        <name>Szumna, Agnieszka</name>
      </author>
      <author>
        <name>Gray, Harry B</name>
      </author>
      <author>
        <name>Vullev, Valentine I</name>
        <uri>https://orcid.org/0000-0002-3416-9686</uri>
      </author>
      <author>
        <name>Gryko, Daniel T</name>
      </author>
    </item>
    <item>
      <title>Solvent-induced selectivity of Williamson etherification in the pursuit of amides resistant against oxidative degradation</title>
      <link>https://escholarship.org/uc/item/0zx123k0</link>
      <description>This article reports two discoveries. (1) 2-Methoxyethanol induces unprecedented selectivity for etherification of 5-hydroxy-2-nitrobenzic acids without forming undesired esters. (2) Such compounds are precursors for amides showing unusual robustness against oxidative degradation, essential for molecular electrets that transfer strongly oxidizing holes at about -6.4 eV &lt;i&gt;vs.&lt;/i&gt; vacuum.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0zx123k0</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Derr, James B</name>
      </author>
      <author>
        <name>Clark, John A</name>
      </author>
      <author>
        <name>Morales, Maryann</name>
      </author>
      <author>
        <name>Espinoza, Eli M</name>
      </author>
      <author>
        <name>Vadhin, Sandra</name>
      </author>
      <author>
        <name>Vullev, Valentine I</name>
        <uri>https://orcid.org/0000-0002-3416-9686</uri>
      </author>
    </item>
    <item>
      <title>Piezoelectric silk fibroin nanofibers: Structural optimization to enhance piezoelectricity and biostability for neural tissue engineering</title>
      <link>https://escholarship.org/uc/item/73h3z4b7</link>
      <description>Silk fibroin (SF) has garnered significant interest in tissue engineering due to its excellent biocompatibility and bioactivity. Notably, SF exhibits piezoelectric properties that can be harnessed to electrically stimulate cells, enhancing tissue morphogenesis. However, a systematic approach to control SF's piezoelectricity and biodegradation, and its application in neural morphogenesis, has not been fully explored. In this study, SF was electrospun into nanofibers of various sizes and subjected to a post-electrospinning chemical treatment to examine the effects of phase composition, especially the β-sheet formation, on the piezoelectricity and biostability of SF. The optimized SF scaffolds having a nanofiber diameter of 750 nm and a scaffold thickness of 250 µm allowed for the maintenance of nanofibrous structure for at least 6 weeks in aqueous environments while maintaining piezoelectric potential outputs of at least 200 mVp-p. This enabled cell membrane depolarization over...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/73h3z4b7</guid>
      <pubDate>Thu, 21 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Jin, Lu</name>
      </author>
      <author>
        <name>Tai, Youyi</name>
      </author>
      <author>
        <name>Nam, Jin</name>
        <uri>https://orcid.org/0000-0001-5117-8958</uri>
      </author>
    </item>
    <item>
      <title>CytoNet: an efficient dual attention based automatic prediction of cancer sub-types in cytology studies</title>
      <link>https://escholarship.org/uc/item/3zz6s92t</link>
      <description>Computer-assisted diagnosis (CAD) plays a key role in cancer diagnosis or screening. Whereas, current CAD performs poorly on whole slide image (WSI) analysis, and thus fails to generalize well. This research aims to develop an automatic classification system to distinguish between different types of carcinomas. Obtaining rich deep features in multi-class classification while achieving high accuracy is still a challenging problem. The detection and classification of cancerous cells in WSI are quite challenging due to the misclassification of normal lumps and cancerous cells. This is due to cluttering, occlusion, and irregular cell distribution. Researchers in the past mostly obtained the hand-crafted features while neglecting the above-mentioned challenges which led to a reduction of the classification accuracy. To mitigate this problem we proposed an efficient dual attention-based network (CytoNet). The proposed network is composed of two main modules (i) Efficient-Net and (ii)...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3zz6s92t</guid>
      <pubDate>Wed, 13 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ilyas, Naveed</name>
      </author>
      <author>
        <name>Naseer, Farhat</name>
      </author>
      <author>
        <name>Khan, Anwar</name>
      </author>
      <author>
        <name>Raja, Aamir</name>
      </author>
      <author>
        <name>Lee, Yong-Moon</name>
      </author>
      <author>
        <name>Park, Jae Hyun</name>
      </author>
      <author>
        <name>Lee, Boreom</name>
      </author>
    </item>
    <item>
      <title>An investigation of how specimen dimensions affect biaxial mechanical characterizations with CellScale BioTester and constitutive modeling of porcine tricuspid valve leaflets</title>
      <link>https://escholarship.org/uc/item/72h795r9</link>
      <description>Biaxial mechanical characterizations are the accepted approach to determine the mechanical response of many biological soft tissues. Although several computational and experimental studies have examined how experimental factors (e.g., clamped vs. suture mounting) affect the acquired tissue mechanical behavior, little is known about the role of specimen dimensions in data acquisition and the subsequent modeling. In this study, we combined our established mechanical characterization framework with an iterative size-reduction protocol to test the hypothesis that specimen dimensions affect the observed mechanical behavior of biaxial characterizations. Our findings indicated that there were non-significant differences in the peak equibiaxial stretches of tricuspid valve leaflets across four specimen dimensions ranging from 4.5×4.5mm to 9 × 9mm. Further analyses revealed that there were significant differences in the low-tensile modulus of the circumferential tissue direction. These...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/72h795r9</guid>
      <pubDate>Fri, 8 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Laurence, Devin W</name>
      </author>
      <author>
        <name>Wang, Shuodao</name>
      </author>
      <author>
        <name>Xiao, Rui</name>
      </author>
      <author>
        <name>Qian, Jin</name>
      </author>
      <author>
        <name>Mir, Arshid</name>
      </author>
      <author>
        <name>Burkhart, Harold M</name>
      </author>
      <author>
        <name>Holzapfel, Gerhard A</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
    <item>
      <title>Modulation of Smooth Muscle Cell Phenotype for Translation of Tissue-Engineered Vascular Grafts</title>
      <link>https://escholarship.org/uc/item/69j9n7zw</link>
      <description>Translation of small-diameter tissue-engineered vascular grafts (TEVGs) for the treatment of coronary artery disease (CAD) remains an unfulfilled promise. This is largely due to the limited integration of TEVGs into the native vascular wall-a process hampered by the insufficient smooth muscle cell (SMC) infiltration and extracellular matrix deposition, and low vasoactivity. These processes can be promoted through the judicious modulation of the SMC toward a synthetic phenotype to promote remodeling and vascular integration; however, the expression of synthetic markers is often accompanied by a decrease in the expression of contractile proteins. Therefore, techniques that can precisely modulate the SMC phenotypical behavior could have the potential to advance the translation of TEVGs. In this review, we describe the phenotypic diversity of SMCs and the different environmental cues that allow the modulation of SMC gene expression. Furthermore, we describe the emerging biomaterial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/69j9n7zw</guid>
      <pubDate>Fri, 8 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Pineda-Castillo, Sergio A</name>
      </author>
      <author>
        <name>Acar, Handan</name>
      </author>
      <author>
        <name>Detamore, Michael S</name>
      </author>
      <author>
        <name>Holzapfel, Gerhard A</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
    <item>
      <title>Aligning consciousness science and U.S. funding agency priorities</title>
      <link>https://escholarship.org/uc/item/3cr3s175</link>
      <description>We recently completed the Fund Consciousness Science! Project: a workshop and subawards program aimed to align United States federal funding mechanisms and consciousness research. Here we describe the project’s motivation, execution, and outcomes to motivate similar efforts both locally and globally.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3cr3s175</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bradford, Nora A</name>
      </author>
      <author>
        <name>Shen, Angela</name>
      </author>
      <author>
        <name>Odegaard, Brian</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>Engineering Triphasic Nanocomposite Coatings on Pretreated Mg Substrates for Biomedical Applications</title>
      <link>https://escholarship.org/uc/item/5dd3500m</link>
      <description>Biodegradable polymer-based nanocomposite coatings provide multiple advantages to modulate the corrosion resistance and cytocompatibility of magnesium (Mg) alloys for biomedical applications. Biodegradable poly(glycerol sebacate) (PGS) is a promising candidate used for medical implant applications. In this study, we synthesized a new PGS nanocomposite system consisting of hydroxyapatite (HA) and magnesium oxide (MgO) nanoparticles and developed a spray coating process to produce the PGS nanocomposite layer on pretreated Mg substrates, which improved the coating adhesion at the interface and their cytocompatibility with bone marrow derived mesenchymal stem cells (BMSCs). Prior to the spray coating process of polymer-based nanocomposites, the Mg substrates were pretreated in alkaline solutions to enhance the interfacial adhesion strength of the polymer-based nanocomposite coatings. The addition of HA and MgO nanoparticles (nHA and nMgO) to the PGS matrix, as well as the alkaline...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5dd3500m</guid>
      <pubDate>Tue, 5 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Chai, Xijuan</name>
      </author>
      <author>
        <name>Lin, Jiajia</name>
      </author>
      <author>
        <name>Xu, Changlu</name>
      </author>
      <author>
        <name>Sun, Dongwei</name>
      </author>
      <author>
        <name>Liu, Huinan Hannah</name>
        <uri>https://orcid.org/0000-0001-9366-6204</uri>
      </author>
    </item>
    <item>
      <title>Chitosan–Polyethylene Glycol Inspired Polyelectrolyte Complex Hydrogel Templates Favoring NEO-Tissue Formation for Cardiac Tissue Engineering</title>
      <link>https://escholarship.org/uc/item/6951v314</link>
      <description>Neo-tissue formation and host tissue regeneration determine the success of cardiac tissue engineering where functional hydrogel scaffolds act as cardiac (extracellular matrix) ECM mimic. Translationally, the hydrogel templates promoting neo-cardiac tissue formation are currently limited; however, they are highly demanding in cardiac tissue engineering. The current study focused on the development of a panel of four chitosan-based polyelectrolyte hydrogels as cardiac scaffolds facilitating neo-cardiac tissue formation to promote cardiac regeneration. Chitosan-PEG (CP), gelatin-chitosan-PEG (GCP), hyaluronic acid-chitosan-PEG (HACP), and combined CP (CoCP) polyelectrolyte hydrogels were engineered by solvent casting and assessed for physiochemical, thermal, electrical, biodegradable, mechanical, and biological properties. The CP, GCP, HACP, and CoCP hydrogels exhibited excellent porosity (4.24 ± 0.18, 13.089 ± 1.13, 12.53 ± 1.30 and 15.88 ± 1.10 for CP, GCP, HACP and CoCP, respectively),...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6951v314</guid>
      <pubDate>Fri, 11 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Keklikian, Angelo</name>
      </author>
      <author>
        <name>de Barros, Natan Roberto</name>
      </author>
      <author>
        <name>Rashad, Ahmad</name>
      </author>
      <author>
        <name>Chen, Yiqing</name>
      </author>
      <author>
        <name>Tan, Jinrui</name>
      </author>
      <author>
        <name>Sheng, Ruoyu</name>
      </author>
      <author>
        <name>Sun, Dongwei</name>
      </author>
      <author>
        <name>Liu, Huinan</name>
        <uri>https://orcid.org/0000-0001-9366-6204</uri>
      </author>
      <author>
        <name>Thankam, Finosh G</name>
      </author>
    </item>
    <item>
      <title>Preliminary evaluation of safety and migration of immune activated mesenchymal stromal cells administered by subconjunctival injection for equine recurrent uveitis</title>
      <link>https://escholarship.org/uc/item/04x6c2n4</link>
      <description>Introduction: Equine recurrent uveitis (ERU), an immune mediated disease characterized by repeated episodes of intra-ocular inflammation, affects 25% of horses in the USA and is the most common cause of glaucoma, cataracts, and blindness. Mesenchymal stromal cells (MSCs) have immunomodulatory properties, which are upregulated by preconditioning with toll-like receptor agonists. The objective was to evaluate safety and migration of TLR-3 agonist polyinosinic, polycytidylic acid (pIC)-activated MSCs injected subconjunctivally in healthy horses prior to clinical application in horses with ERU. We hypothesized that activated allogeneic MSCs injected subconjunctivally would not induce ocular or systemic inflammation and would remain in the conjunctiva for &amp;gt;14 days.
Methods: Bulbar subconjunctiva of two horses was injected with 10 × 10&lt;sup&gt;6&lt;/sup&gt; pIC-activated (10 μg/mL, 2 h) GFP-labeled MSCs from one donor three times at two-week intervals. Vehicle (saline) control was injected...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/04x6c2n4</guid>
      <pubDate>Fri, 11 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Cassano, Jennifer M</name>
      </author>
      <author>
        <name>Leonard, Brian C</name>
      </author>
      <author>
        <name>Martins, Bianca C</name>
      </author>
      <author>
        <name>Vapniarsky, Natalia</name>
      </author>
      <author>
        <name>Morgan, Joshua T</name>
        <uri>https://orcid.org/0000-0001-8033-0285</uri>
      </author>
      <author>
        <name>Dow, Steven W</name>
      </author>
      <author>
        <name>Wotman, Kathryn L</name>
      </author>
      <author>
        <name>Pezzanite, Lynn M</name>
      </author>
    </item>
    <item>
      <title>Erythrocyte nano-ghosts with dual optical and magnetic resonance characteristics</title>
      <link>https://escholarship.org/uc/item/9p7564r8</link>
      <description>Significance: Fluorescent organic dyes provide imaging capabilities at cellular and sub-cellular levels. However, a common problem associated with some of the existing dyes such as the US FDA-approved indocyanine green (ICG) is their weak fluorescence emission. Alternative dyes with greater emission characteristics would be useful in various imaging applications. Complementing optical imaging, magnetic resonance (MR) imaging enables deep tissue imaging. Nano-sized delivery systems containing dyes with greater fluorescence emission as well as MR contrast agents present a promising dual-mode platform with high optical sensitivity and deep tissue imaging for image-guided surgical applications.
Aim: We have engineered a nano-sized platform, derived from erythrocyte ghosts (EGs), with dual near-infrared fluorescence and MR characteristics by co-encapsulation of a brominated carbocyanine dye and gadobenate dimeglumine (Gd-BOPTA).
Approach: We have investigated the use of three brominated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9p7564r8</guid>
      <pubDate>Mon, 9 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Chi-Hua</name>
      </author>
      <author>
        <name>Zaman, Shamima</name>
      </author>
      <author>
        <name>Kundra, Vikas</name>
      </author>
      <author>
        <name>Anvari, Bahman</name>
        <uri>https://orcid.org/0000-0002-2511-5854</uri>
      </author>
    </item>
    <item>
      <title>Heuristic use of perceptual evidence leads to dissociation between performance and metacognitive sensitivity</title>
      <link>https://escholarship.org/uc/item/9kn5d5pv</link>
      <description>Zylberberg et al. [Zylberberg, Barttfeld, &amp;amp; Sigman (Frontiers in Integrative Neuroscience, 6; 79, 2012), Frontiers in Integrative Neuroscience 6:79] found that confidence decisions, but not perceptual decisions, are insensitive to evidence against a selected perceptual choice. We present a signal detection theoretic model to formalize this insight, which gave rise to a counter-intuitive empirical prediction: that depending on the observer’s perceptual choice, increasing task performance can be associated with decreasing metacognitive sensitivity (i.e., the trial-by-trial correspondence between confidence and accuracy). The model also provides an explanation as to why metacognitive sensitivity tends to be less than optimal in actual subjects. These predictions were confirmed robustly in a psychophysics experiment. In a second experiment we found that, in at least some subjects, the effects were replicated even under performance feedback designed to encourage optimal behavior....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9kn5d5pv</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maniscalco, Brian</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Lau, Hakwan</name>
      </author>
    </item>
    <item>
      <title>Normal observers show no evidence for blindsight in facial emotion perception</title>
      <link>https://escholarship.org/uc/item/88d4h17n</link>
      <description>Some researchers have argued that normal human observers can exhibit "blindsight-like" behavior: the ability to discriminate or identify a stimulus without being aware of it. However, we recently used a bias-free task to show that what looks like blindsight may in fact be an artifact of typical experimental paradigms' susceptibility to response bias. While those findings challenge previous reports of blindsight in normal observers, they do not rule out the possibility that different stimuli or techniques could still reveal perception without awareness. One intriguing candidate is emotion processing, since processing of emotional stimuli (e.g. fearful/happy faces) has been reported to potentially bypass conscious visual circuits. Here we used the bias-free blindsight paradigm to investigate whether emotion processing might reveal "featural blindsight," i.e. ability to identify a face's emotion without introspective access to the task-relevant features that led to the discrimination...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/88d4h17n</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Rajananda, Sivananda</name>
      </author>
      <author>
        <name>Zhu, Jeanette</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>Behavioral and neural measures of confidence using a novel auditory pitch identification task</title>
      <link>https://escholarship.org/uc/item/626239p3</link>
      <description>Observers can discriminate between correct versus incorrect perceptual decisions with feelings of confidence. The centro-parietal positivity build-up rate (CPP slope) has been suggested as a likely neural signature of accumulated evidence, which may guide both perceptual performance and confidence. However, CPP slope also covaries with reaction time, which also covaries with confidence in previous studies, and performance and confidence typically covary; thus, CPP slope may index signatures of perceptual performance rather than confidence per se. Moreover, perceptual metacognition-including neural correlates-has largely been studied in vision, with few exceptions. Thus, we lack understanding of domain-general neural signatures of perceptual metacognition outside vision. Here we designed a novel auditory pitch identification task and collected behavior with simultaneous 32-channel EEG in healthy adults. Participants saw two tone labels which varied in tonal distance on each trial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/626239p3</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Tang, Tamara</name>
      </author>
      <author>
        <name>Samaha, Jason</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>Transcranial magnetic stimulation to visual cortex induces suboptimal introspection</title>
      <link>https://escholarship.org/uc/item/60p8f87d</link>
      <description>Blindsight patients with damage to the visual cortex can discriminate objects but report no conscious visual experience. This provides an intriguing opportunity to allow the study of subjective awareness in isolation from objective performance capacity. However, blindsight is rare, so one promising way to induce the effect in neurologically intact observers is to apply transcranial magnetic stimulation (TMS) to the visual cortex. Here, we used a recently-developed criterion-free method to conclusively rule out an important alternative interpretation of TMS-induced performance without awareness: that TMS-induced blindsight may be just due to conservative reporting biases for conscious perception. Critically, using this criterion-free paradigm we have previously shown that introspective judgments were optimal even under visual masking. However, here under TMS, observers were suboptimal, as if they were metacognitively blind to the visual disturbances caused by TMS. We argue that...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/60p8f87d</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Fesi, Jeremy</name>
      </author>
      <author>
        <name>Amendi, Namema</name>
      </author>
      <author>
        <name>Knotts, Jeffrey D</name>
      </author>
      <author>
        <name>Lau, Hakwan</name>
      </author>
      <author>
        <name>Ro, Tony</name>
      </author>
    </item>
    <item>
      <title>Unconscious Perception of Vernier Offsets</title>
      <link>https://escholarship.org/uc/item/4200z206</link>
      <description>The comparison between conscious and unconscious perception is a cornerstone of consciousness science. However, most studies reporting above-chance discrimination of unseen stimuli do not control for criterion biases when assessing awareness. We tested whether observers can discriminate subjectively invisible offsets of Vernier stimuli when visibility is probed using a bias-free task. To reduce visibility, stimuli were either backward masked or presented for very brief durations (1-3 milliseconds) using a modern-day Tachistoscope. We found some behavioral indicators of perception without awareness, and yet, no conclusive evidence thereof. To seek more decisive proof, we simulated a series of Bayesian observer models, including some that produce visibility judgements alongside type-1 judgements. Our data are best accounted for by observers with slightly suboptimal conscious access to sensory evidence. Overall, the stimuli and visibility manipulations employed here induced mild...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4200z206</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Amerio, Pietro</name>
      </author>
      <author>
        <name>Michel, Matthias</name>
      </author>
      <author>
        <name>Goerttler, Stephan</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Cleeremans, Axel</name>
      </author>
    </item>
    <item>
      <title>An investigation of how relative precision of target encoding influences metacognitive performance</title>
      <link>https://escholarship.org/uc/item/2252n7kz</link>
      <description>Detection failures in perceptual tasks can result from different causes: sometimes we may fail to see something because perceptual information is noisy or degraded, and sometimes we may fail to see something due to the limited capacity of attention. Previous work indicates that metacognitive capacities for detection failures may differ depending on the specific stimulus visibility manipulation employed. In this investigation, we measured metacognition while matching performance in two visibility manipulations: phase-scrambling and the attentional blink. As in previous work, metacognitive asymmetries emerged: despite matched type 1 performance, metacognitive ability (measured by area under the ROC curve) for reporting stimulus absence was higher in the attentional blink condition, which was mainly driven by metacognitive ability in correct rejection trials. We performed Signal Detection Theoretic (SDT) modeling of the results, showing that differences in metacognition under equal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2252n7kz</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kellij, Sanne</name>
      </author>
      <author>
        <name>Fahrenfort, Johannes</name>
      </author>
      <author>
        <name>Lau, Hakwan</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Odegaard, Brian</name>
      </author>
    </item>
    <item>
      <title>Toward ‘Computational-Rationality’ Approaches to Arbitrating Models of Cognition: A Case Study Using Perceptual Metacognition</title>
      <link>https://escholarship.org/uc/item/21w887nh</link>
      <description>Perceptual confidence results from a metacognitive process which evaluates how likely our percepts are to be correct. Many competing models of perceptual metacognition enjoy strong empirical support. Arbitrating these models traditionally proceeds via researchers conducting experiments and then fitting several models to the data collected. However, such a process often includes conditions or paradigms that may not best arbitrate competing models: Many models make similar predictions under typical experimental conditions. Consequently, many experiments are needed, collectively (sub-optimally) sampling the space of conditions to compare models. Here, instead, we introduce a variant of optimal experimental design which we call a &lt;i&gt;computational-rationality&lt;/i&gt; approach to generative models of cognition, using perceptual metacognition as a case study. Instead of designing experiments and post-hoc specifying models, we &lt;i&gt;began&lt;/i&gt; with comprehensive model comparison among four competing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/21w887nh</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Rong, Yingqi</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>Tuned inhibition in perceptual decision-making circuits can explain seemingly suboptimal confidence behavior</title>
      <link>https://escholarship.org/uc/item/1jg0498c</link>
      <description>Current dominant views hold that perceptual confidence reflects the probability that a decision is correct. Although these views have enjoyed some empirical support, recent behavioral results indicate that confidence and the probability of being correct can be dissociated. An alternative hypothesis suggests that confidence instead reflects the magnitude of evidence in favor of a decision while being relatively insensitive to the evidence opposing the decision. We considered how this alternative hypothesis might be biologically instantiated by developing a simple neural network model incorporating a known property of sensory neurons: tuned inhibition. The key idea of the model is that the level of inhibition that each accumulator unit receives from units with the opposite tuning preference, i.e. its inhibition 'tuning', dictates its contribution to perceptual decisions versus confidence judgments, such that units with higher tuned inhibition (computing relative evidence for different...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1jg0498c</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maniscalco, Brian</name>
      </author>
      <author>
        <name>Odegaard, Brian</name>
      </author>
      <author>
        <name>Grimaldi, Piercesare</name>
      </author>
      <author>
        <name>Cho, Seong Hah</name>
      </author>
      <author>
        <name>Basso, Michele A</name>
      </author>
      <author>
        <name>Lau, Hakwan</name>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>Multi-omics analysis of green lineage osmotic stress pathways unveils crucial roles of different cellular compartments</title>
      <link>https://escholarship.org/uc/item/5w63g55x</link>
      <description>Maintenance of water homeostasis is a fundamental cellular process required by all living organisms. Here, we use the single-celled green alga Chlamydomonas reinhardtii to establish a foundational understanding of osmotic-stress signaling pathways through transcriptomics, phosphoproteomics, and functional genomics approaches. Comparison of pathways identified through these analyses with yeast and Arabidopsis allows us to infer their evolutionary conservation and divergence across these lineages. 76 genes, acting across diverse cellular compartments, were found to be important for osmotic-stress tolerance in Chlamydomonas through their functions in cytoskeletal organization, potassium transport, vesicle trafficking, mitogen-activated protein kinase and chloroplast signaling. We show that homologs for five of these genes have conserved functions in stress tolerance in Arabidopsis and reveal a novel PROFILIN-dependent stage of acclimation affecting the actin cytoskeleton that ensures...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5w63g55x</guid>
      <pubDate>Fri, 2 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Vilarrasa-Blasi, Josep</name>
      </author>
      <author>
        <name>Vellosillo, Tamara</name>
      </author>
      <author>
        <name>Jinkerson, Robert E</name>
        <uri>https://orcid.org/0000-0001-9399-1613</uri>
      </author>
      <author>
        <name>Fauser, Friedrich</name>
      </author>
      <author>
        <name>Xiang, Tingting</name>
        <uri>https://orcid.org/0000-0001-9062-2273</uri>
      </author>
      <author>
        <name>Minkoff, Benjamin B</name>
      </author>
      <author>
        <name>Wang, Lianyong</name>
      </author>
      <author>
        <name>Kniazev, Kiril</name>
      </author>
      <author>
        <name>Guzman, Michael</name>
      </author>
      <author>
        <name>Osaki, Jacqueline</name>
      </author>
      <author>
        <name>Barrett-Wilt, Gregory A</name>
      </author>
      <author>
        <name>Sussman, Michael R</name>
      </author>
      <author>
        <name>Jonikas, Martin C</name>
      </author>
      <author>
        <name>Dinneny, José R</name>
      </author>
    </item>
    <item>
      <title>High-Fidelity Identification of Single Nucleotide Polymorphism by Type V CRISPR Systems</title>
      <link>https://escholarship.org/uc/item/79p217r2</link>
      <description>Accurate and sensitive detection of single nucleotide polymorphism (SNP) holds significant clinical implications, especially in the field of cancer diagnosis. Leveraging its high accuracy and programmability, the CRISPR system emerges as a promising platform for advancing the identification of SNPs. In this study, we compared two type V CRISPR/Cas systems (Cas12a and Cas14a) for the identification of cancer-related SNP. Their identification performances were evaluated by characterizing their mismatch tolerance to the BRAF gene. We found that the CRISPR/Cas14a system exhibited superior accuracy and robustness over the CRISPR/Cas12a system for SNP detection. Furthermore, blocker displacement amplification (BDA) was combined with the CRISPR/Cas14a system to eliminate the interference of the wild type (WT) and increase the detection accuracy. In this strategy, we were able to detect BRAF V600E as low as 10&lt;sup&gt;3&lt;/sup&gt; copies with a sensitivity of 0.1% variant allele frequency. Moreover,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/79p217r2</guid>
      <pubDate>Mon, 22 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>He, Yawen</name>
      </author>
      <author>
        <name>Shao, Shengjie</name>
      </author>
      <author>
        <name>Chen, Juhong</name>
        <uri>https://orcid.org/0000-0002-6484-2739</uri>
      </author>
    </item>
    <item>
      <title>Development of Nanobody-Displayed Whole-Cell Biosensors for the Colorimetric Detection of SARS-CoV‑2</title>
      <link>https://escholarship.org/uc/item/7x616151</link>
      <description>The accurate and effective detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is essential to preventing the spread of infectious diseases and ensuring human health. Herein, a nanobody-displayed whole-cell biosensor was developed for colorimetric detection of SARS-CoV-2 spike proteins. Serving as bioreceptors, yeast surfaces were genetically engineered to display SARS-CoV-2 binding of llama-derived single-domain antibodies (nanobodies) with high capture efficiency, facilitating the concentration and purification of SARS-CoV-2. Gold nanoparticles (AuNPs) employed as signal transductions were functionalized with horseradish peroxidase (HRP) and anti-SARS monoclonal antibodies to enhance the detection sensitivity. In the presence of SARS-CoV-2 spike proteins, the sandwiched binding will be formed by linking engineered yeast, SARS-CoV-2 spike proteins, and reporter AuNPs. The colorimetric signal was generated by the enzymatic reaction of HRP and its corresponding...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7x616151</guid>
      <pubDate>Fri, 19 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>He, Yawen</name>
        <uri>https://orcid.org/0009-0001-4898-5465</uri>
      </author>
      <author>
        <name>Xu, Zhiyuan</name>
      </author>
      <author>
        <name>Kasputis, Tom</name>
      </author>
      <author>
        <name>Zhao, Xue</name>
      </author>
      <author>
        <name>Ibañez, Itati</name>
      </author>
      <author>
        <name>Pavan, Florencia</name>
      </author>
      <author>
        <name>Bok, Marina</name>
      </author>
      <author>
        <name>Malito, Juan Pablo</name>
      </author>
      <author>
        <name>Parreno, Viviana</name>
      </author>
      <author>
        <name>Yuan, Lijuan</name>
      </author>
      <author>
        <name>Wright, R Clay</name>
      </author>
      <author>
        <name>Chen, Juhong</name>
        <uri>https://orcid.org/0000-0002-6484-2739</uri>
      </author>
    </item>
    <item>
      <title>Locus coeruleus contrast and diffusivity metrics differentially relate to age and memory performance</title>
      <link>https://escholarship.org/uc/item/64c787fh</link>
      <description>Neurocognitive aging researchers are increasingly focused on the locus coeruleus, a neuromodulatory brainstem structure that degrades with age. With this rapid growth, the field will benefit from consensus regarding which magnetic resonance imaging (MRI) metrics of locus coeruleus structure are most sensitive to age and cognition. To address this need, the current study acquired magnetization transfer- and diffusion-weighted MRI images in younger and older adults who also completed a free recall memory task. Results revealed significantly larger differences between younger and older adults for maximum than average magnetization transfer-weighted contrast (MTC), axial than mean or radial single-tensor diffusivity (DTI), and free than restricted multi-compartment diffusion (NODDI) metrics in the locus coeruleus; with maximum MTC being the best predictor of age group. Age effects for all imaging modalities interacted with sex, with larger age group differences in males than females...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/64c787fh</guid>
      <pubDate>Tue, 16 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bennett, Ilana J</name>
        <uri>https://orcid.org/0000-0002-5330-4679</uri>
      </author>
      <author>
        <name>Langley, Jason</name>
      </author>
      <author>
        <name>Sun, Andrew</name>
      </author>
      <author>
        <name>Solis, Kitzia</name>
      </author>
      <author>
        <name>Seitz, Aaron R</name>
      </author>
      <author>
        <name>Hu, Xiaoping P</name>
        <uri>https://orcid.org/0000-0002-8155-7040</uri>
      </author>
    </item>
    <item>
      <title>CRISPR/Cas14 and G‑Quadruplex DNAzyme-Driven Biosensor for Paper-Based Colorimetric Detection of African Swine Fever Virus</title>
      <link>https://escholarship.org/uc/item/1vh6846g</link>
      <description>The highly contagious nature and 100% fatality rate contribute to the ongoing and expanding impact of the African swine fever virus (ASFV), causing significant economic losses worldwide. Herein, we developed a cascaded colorimetric detection using the combination of a CRISPR/Cas14a system, G-quadruplex DNAzyme, and microfluidic paper-based analytical device. This CRISPR/Cas14a-G4 biosensor could detect ASFV as low as 5 copies/μL and differentiate the wild-type and mutated ASFV DNA with 2-nt difference. Moreover, this approach was employed to detect ASFV in porcine plasma. A broad linear detection range was observed, and the limit of detection in spiked porcine plasma was calculated to be as low as 42-85 copies/μL. Our results indicate that the developed paper platform exhibits the advantages of high sensitivity, excellent specificity, and low cost, making it promising for clinical applications in the field of DNA disease detection and suitable for popularization in low-resourced areas.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1vh6846g</guid>
      <pubDate>Tue, 16 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhao, Xue</name>
      </author>
      <author>
        <name>He, Yawen</name>
        <uri>https://orcid.org/0009-0001-4898-5465</uri>
      </author>
      <author>
        <name>Shao, Shengjie</name>
      </author>
      <author>
        <name>Ci, Qiaoqiao</name>
      </author>
      <author>
        <name>Chen, Lin</name>
      </author>
      <author>
        <name>Lu, Xiaonan</name>
      </author>
      <author>
        <name>Liu, Qian</name>
      </author>
      <author>
        <name>Chen, Juhong</name>
        <uri>https://orcid.org/0000-0002-6484-2739</uri>
      </author>
    </item>
    <item>
      <title>Nanofiber-microwell cell culture system for spatially patterned differentiation of pluripotent stem cells in 3D</title>
      <link>https://escholarship.org/uc/item/6bw661h1</link>
      <description>The intricate interplay between biochemical and physical cues dictates pluripotent stem cell (PSC) differentiation to form various tissues. While biochemical modulation has been extensively studied, the role of biophysical microenvironments in early lineage commitment remains elusive. Here, we introduce a novel 3D cell culture system combining electrospun nanofibers with microfabricated polydimethylsiloxane (PDMS) patterns. This system enables the controlled formation of semispherical human induced pluripotent stem cell (hiPSC) colonies, facilitating the investigation of local mechanical stem cell niches on mechano-responsive signaling and lineage specification. Our system unveiled spatially organized RhoA activity coupled with actin-myosin cable formation, suggesting mechano-dependent hiPSC behaviors. Nodal network analysis of RNA-seq data revealed RhoA downstream regulation of YAP signaling, DNA histone modifications, and patterned germ layer specification. Notably, altering...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6bw661h1</guid>
      <pubDate>Thu, 20 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Tai, Youyi</name>
      </author>
      <author>
        <name>Goodrich, Robyn</name>
      </author>
      <author>
        <name>Maldonado, Maricela</name>
      </author>
      <author>
        <name>Ortiz, Jessica</name>
      </author>
      <author>
        <name>Martinez, Jeniree</name>
      </author>
      <author>
        <name>Ico, Gerardo</name>
      </author>
      <author>
        <name>Ko, Angel</name>
      </author>
      <author>
        <name>Shih, Hung Ping</name>
      </author>
      <author>
        <name>Nam, Jin</name>
        <uri>https://orcid.org/0000-0001-5117-8958</uri>
      </author>
    </item>
    <item>
      <title>A predictor-informed multi-subject bayesian approach for dynamic functional connectivity</title>
      <link>https://escholarship.org/uc/item/7235p795</link>
      <description>Dynamic functional connectivity investigates how the interactions among brain regions vary over the course of an fMRI experiment. Such transitions between different individual connectivity states can be modulated by changes in underlying physiological mechanisms that drive functional network dynamics, e.g., changes in attention or cognitive effort. In this paper, we develop a multi-subject Bayesian framework where the estimation of dynamic functional networks is informed by time-varying exogenous physiological covariates that are simultaneously recorded in each subject during the fMRI experiment. More specifically, we consider a dynamic Gaussian graphical model approach where a non-homogeneous hidden Markov model is employed to classify the fMRI time series into latent neurological states. We assume the state-transition probabilities to vary over time and across subjects as a function of the underlying covariates, allowing for the estimation of recurrent connectivity patterns...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7235p795</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Jaylen</name>
      </author>
      <author>
        <name>Hussain, Sana</name>
      </author>
      <author>
        <name>Warnick, Ryan</name>
      </author>
      <author>
        <name>Vannucci, Marina</name>
      </author>
      <author>
        <name>Menchaca, Isaac</name>
      </author>
      <author>
        <name>Seitz, Aaron R</name>
      </author>
      <author>
        <name>Hu, Xiaoping</name>
        <uri>https://orcid.org/0000-0002-8155-7040</uri>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
      <author>
        <name>Guindani, Michele</name>
        <uri>https://orcid.org/0000-0002-6363-9907</uri>
      </author>
    </item>
    <item>
      <title>Synthesis and bioluminescence of thioluciferin</title>
      <link>https://escholarship.org/uc/item/7rj8q2pw</link>
      <description>The firefly luciferin analog thioluciferin (S-luc) was synthesised as a key element of bioluminescent reporters for oxidation state and thiol/disulfide equilibria. It shows blue-shifts in absorption and fluorescence compared to luciferin, and is a modest luciferase substrate. These features are attributed to a π-system that is less conjugated than luciferin.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7rj8q2pw</guid>
      <pubDate>Thu, 23 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Pirrung, Michael C</name>
        <uri>https://orcid.org/0000-0003-4585-8353</uri>
      </author>
      <author>
        <name>Carlson, Andrew D</name>
      </author>
      <author>
        <name>De Howitt, Natalie</name>
      </author>
      <author>
        <name>Liao, Jiayu</name>
        <uri>https://orcid.org/0000-0002-2624-5781</uri>
      </author>
    </item>
    <item>
      <title>RNA targeting and cleavage by the type III-Dv CRISPR effector complex</title>
      <link>https://escholarship.org/uc/item/8286g1zz</link>
      <description>CRISPR-Cas are adaptive immune systems in bacteria and archaea that utilize CRISPR RNA-guided surveillance complexes to target complementary RNA or DNA for destruction1–5. Target RNA cleavage at regular intervals is characteristic of type III effector complexes6–8. Here, we determine the structures of the Synechocystis type III-Dv complex, an apparent evolutionary intermediate from multi-protein to single-protein type III effectors9,10, in pre- and post-cleavage states. The structures show how multi-subunit fusion proteins in the effector are tethered together in an unusual arrangement to assemble into an active and programmable RNA endonuclease and how the effector utilizes a distinct mechanism for target RNA seeding from other type III effectors. Using structural, biochemical, and quantum/classical molecular dynamics simulation, we study the structure and dynamics of the three catalytic sites, where a 2′-OH of the ribose on the target RNA acts as a nucleophile for in line self-cleavage...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8286g1zz</guid>
      <pubDate>Sat, 27 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Schwartz, Evan A</name>
      </author>
      <author>
        <name>Bravo, Jack PK</name>
      </author>
      <author>
        <name>Ahsan, Mohd</name>
      </author>
      <author>
        <name>Macias, Luis A</name>
      </author>
      <author>
        <name>McCafferty, Caitlyn L</name>
      </author>
      <author>
        <name>Dangerfield, Tyler L</name>
      </author>
      <author>
        <name>Walker, Jada N</name>
      </author>
      <author>
        <name>Brodbelt, Jennifer S</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
      <author>
        <name>Fineran, Peter C</name>
      </author>
      <author>
        <name>Fagerlund, Robert D</name>
      </author>
      <author>
        <name>Taylor, David W</name>
      </author>
    </item>
    <item>
      <title>Theta-frequency medial septal nucleus deep brain stimulation increases neurovascular activity in MK-801-treated mice</title>
      <link>https://escholarship.org/uc/item/5f1916nj</link>
      <description>Introduction: Deep brain stimulation (DBS) has shown remarkable success treating neurological and psychiatric disorders including Parkinson's disease, essential tremor, dystonia, epilepsy, and obsessive-compulsive disorder. DBS is now being explored to improve cognitive and functional outcomes in other psychiatric conditions, such as those characterized by reduced N-methyl-D-aspartate (NMDA) function (i.e., schizophrenia). While DBS for movement disorders generally involves high-frequency (&amp;gt;100 Hz) stimulation, there is evidence that low-frequency stimulation may have beneficial and persisting effects when applied to cognitive brain networks.
Methods: In this study, we utilize a novel technology, functional ultrasound imaging (fUSI), to characterize the cerebrovascular impact of medial septal nucleus (MSN) DBS under conditions of NMDA antagonism (pharmacologically using Dizocilpine [MK-801]) in anesthetized male mice.
Results: Imaging from a sagittal plane across a variety...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5f1916nj</guid>
      <pubDate>Thu, 18 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Crown, Lindsey M</name>
      </author>
      <author>
        <name>Agyeman, Kofi A</name>
      </author>
      <author>
        <name>Choi, Wooseong</name>
      </author>
      <author>
        <name>Zepeda, Nancy</name>
      </author>
      <author>
        <name>Iseri, Ege</name>
      </author>
      <author>
        <name>Pahlavan, Pooyan</name>
      </author>
      <author>
        <name>Siegel, Steven J</name>
      </author>
      <author>
        <name>Liu, Charles</name>
      </author>
      <author>
        <name>Christopoulos, Vasileios</name>
      </author>
      <author>
        <name>Lee, Darrin J</name>
      </author>
    </item>
    <item>
      <title>Single-cell dissociation of the model cnidarian sea anemone Exaiptasia diaphana</title>
      <link>https://escholarship.org/uc/item/6j97367s</link>
      <description>The sea anemone Exaiptasia diaphana (Aiptasia) is a versatile model in studying cellular mechanisms that govern cnidarian-Symbiodiniaceae symbiosis, the foundation of coral reef ecosystems. Here, we provide a protocol to efficiently dissociate adult Aiptasia tissue into a single-cell suspension using enzymatic digestion. We detail steps including washing animals, dissociating tissue with pronase digestion, and evaluating dissociated single cells using fluorescence imaging. This procedure can be applied to other cnidarians, including coral polyps. For complete details on the use and execution of this protocol, please refer to Jinkerson et&amp;nbsp;al. (2022).&lt;sup&gt;1&lt;/sup&gt;.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6j97367s</guid>
      <pubDate>Fri, 12 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kirk, Andrea L</name>
      </author>
      <author>
        <name>Xiang, Tingting</name>
      </author>
    </item>
    <item>
      <title>Biosynthesis of chlorophyll c in a dinoflagellate and heterologous production in planta</title>
      <link>https://escholarship.org/uc/item/1n63w1qs</link>
      <description>Chlorophyll c is a key photosynthetic pigment that has been used historically to classify eukaryotic algae. Despite its importance in global photosynthetic productivity, the pathway for its biosynthesis has remained elusive. Here we define the CHLOROPHYLL C SYNTHASE (CHLCS) discovered through investigation of a dinoflagellate mutant deficient in chlorophyll c. CHLCSs are proteins with chlorophyll a/b binding and 2-oxoglutarate-Fe(II) dioxygenase (2OGD) domains found in peridinin-containing dinoflagellates; other chlorophyll c-containing algae utilize enzymes with only the 2OGD domain or an unknown synthase to produce chlorophyll c. 2OGD-containing synthases across dinoflagellate, diatom, cryptophyte, and haptophyte lineages form a monophyletic group, 8 members of which were also shown to produce chlorophyll c. Chlorophyll c&lt;sub&gt;1&lt;/sub&gt; to c&lt;sub&gt;2&lt;/sub&gt; ratios in marine algae are dictated in part by chlorophyll c synthases. CHLCS heterologously expressed in planta results in the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1n63w1qs</guid>
      <pubDate>Thu, 11 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Jinkerson, Robert E</name>
        <uri>https://orcid.org/0000-0001-9399-1613</uri>
      </author>
      <author>
        <name>Poveda-Huertes, Daniel</name>
      </author>
      <author>
        <name>Cooney, Elizabeth C</name>
      </author>
      <author>
        <name>Cho, Anna</name>
      </author>
      <author>
        <name>Ochoa-Fernandez, Rocio</name>
      </author>
      <author>
        <name>Keeling, Patrick J</name>
      </author>
      <author>
        <name>Xiang, Tingting</name>
        <uri>https://orcid.org/0000-0001-9062-2273</uri>
      </author>
      <author>
        <name>Andersen-Ranberg, Johan</name>
      </author>
    </item>
    <item>
      <title>A Novel Hidden Markov Approach to Studying Dynamic Functional Connectivity States in Human Neuroimaging</title>
      <link>https://escholarship.org/uc/item/4hf2q6mg</link>
      <description>&lt;b&gt;&lt;i&gt;Introduction:&lt;/i&gt;&lt;/b&gt; Hidden Markov models (HMMs) are a popular choice to extract and examine recurring patterns of activity or functional connectivity in neuroimaging data, both in terms of spatial patterns and their temporal progression. Although many diverse HMMs have been applied to neuroimaging data, most have defined states based on activity levels (intensity-based [IB] states) rather than patterns of functional connectivity between brain areas (connectivity-based states), which is problematic if we want to understand connectivity dynamics: IB states are unlikely to provide comprehensive information about dynamic connectivity patterns. &lt;b&gt;&lt;i&gt;Methods:&lt;/i&gt;&lt;/b&gt; We addressed this problem by introducing a new HMM that defines states based on full functional connectivity (FFC) profiles among brain regions. We empirically explored the behavior of this new model in comparison to existing approaches based on IB or summed functional connectivity states using the Human Connectome...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4hf2q6mg</guid>
      <pubDate>Tue, 9 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Hussain, Sana</name>
      </author>
      <author>
        <name>Langley, Jason</name>
      </author>
      <author>
        <name>Seitz, Aaron R</name>
      </author>
      <author>
        <name>Hu, Xiaoping P</name>
        <uri>https://orcid.org/0000-0002-8155-7040</uri>
      </author>
      <author>
        <name>Peters, Megan AK</name>
        <uri>https://orcid.org/0000-0002-0248-0816</uri>
      </author>
    </item>
    <item>
      <title>Enhanced peripheral nerve regeneration by mechano-electrical stimulation</title>
      <link>https://escholarship.org/uc/item/8p42j106</link>
      <description>To address limitations in current approaches for treating large peripheral nerve defects, the presented study evaluated the feasibility of functional material-mediated physical stimuli on peripheral nerve regeneration. Electrospun piezoelectric poly(vinylidene fluoride-trifluoroethylene) nanofibers were utilized to deliver mechanical actuation-activated electrical stimulation to nerve cells/tissues in a non-invasive manner. Using morphologically and piezoelectrically optimized nanofibers for neurite extension and Schwann cell maturation based on in vitro experiments, piezoelectric nerve conduits were synthesized and implanted in a rat sciatic nerve transection model to bridge a critical-sized sciatic nerve defect (15 mm). A therapeutic shockwave system was utilized to periodically activate the piezoelectric effect of the implanted nerve conduit on demand. The piezoelectric nerve conduit-mediated mechano-electrical stimulation (MES) induced enhanced peripheral nerve regeneration,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8p42j106</guid>
      <pubDate>Thu, 28 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Tai, Youyi</name>
      </author>
      <author>
        <name>Tonmoy, Thamidul Islam</name>
      </author>
      <author>
        <name>Win, Shwe</name>
      </author>
      <author>
        <name>Brinkley, Natasha T</name>
      </author>
      <author>
        <name>Park, B Hyle</name>
      </author>
      <author>
        <name>Nam, Jin</name>
        <uri>https://orcid.org/0000-0001-5117-8958</uri>
      </author>
    </item>
    <item>
      <title>High-fidelity, hyper-accurate, and evolved mutants rewire atomic-level communication in CRISPR-Cas9</title>
      <link>https://escholarship.org/uc/item/6k391466</link>
      <description>The high-fidelity (HF1), hyper-accurate (Hypa), and evolved (Evo) variants of the CRISPR-associated protein 9 (Cas9) endonuclease are critical tools to mitigate off-target effects in the application of CRISPR-Cas9 technology. The mechanisms by which mutations in recognition subdomain 3 (Rec3) mediate specificity in these variants are poorly understood. Here, solution nuclear magnetic resonance and molecular dynamics simulations establish the structural and dynamic effects of high-specificity mutations in Rec3, and how they propagate the allosteric signal of Cas9. We reveal conserved structural changes and dynamic differences at regions of Rec3 that interface with the RNA:DNA hybrid, transducing chemical signals from Rec3 to the catalytic His-Asn-His (HNH) domain. The variants remodel the communication sourcing from the Rec3 α helix 37, previously shown to sense target DNA complementarity, either directly or allosterically. This mechanism increases communication between the DNA...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6k391466</guid>
      <pubDate>Sat, 16 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Skeens, Erin</name>
      </author>
      <author>
        <name>Sinha, Souvik</name>
      </author>
      <author>
        <name>Ahsan, Mohd</name>
      </author>
      <author>
        <name>D'Ordine, Alexandra M</name>
      </author>
      <author>
        <name>Jogl, Gerwald</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
      <author>
        <name>Lisi, George P</name>
      </author>
    </item>
    <item>
      <title>Proteomes of Micro- and Nanosized Carriers Engineered from Red Blood Cells</title>
      <link>https://escholarship.org/uc/item/3jn831t6</link>
      <description>Red blood cell (RBC)-derived systems offer a potential platform for delivery of biomedical cargos. Although the importance of specific proteins associated with the biodistribution and pharmacokinetics of these particles has been recognized, it remains to be explored whether some of the key transmembrane and cytoskeletal proteins responsible for immune-modulatory effects and mechanical integrity of the particles are retained. Herein, using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and quantitative tandem mass tag mass spectrometry in conjunction with bioinformatics analysis, we have examined the proteomes of micro- and nanosized erythrocyte ghosts doped with indocyanine green and compared them with those of RBCs. We identified a total of 884 proteins in each set of RBCs, micro-, and nanosized particles, of which 8 and 45 proteins were expressed at significantly different relative abundances when comparing micro-sized particles vs RBCs and nanosized particles...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3jn831t6</guid>
      <pubDate>Tue, 12 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Chi-Hua</name>
      </author>
      <author>
        <name>Tang, Jack C</name>
      </author>
      <author>
        <name>Hendricks, Nathan G</name>
      </author>
      <author>
        <name>Anvari, Bahman</name>
        <uri>https://orcid.org/0000-0002-2511-5854</uri>
      </author>
    </item>
    <item>
      <title>Carboxymethyl cellulose–alginate interpenetrating hydroxy ethyl methacrylate crosslinked polyvinyl alcohol reinforced hybrid hydrogel templates with improved biological performance for cardiac tissue engineering</title>
      <link>https://escholarship.org/uc/item/2c58x6wk</link>
      <description>Cardiac tissue engineering is an emerging approach for cardiac regeneration utilizing the inherent healing responses elicited by the surviving heart using biomaterial templates. In this study, we aimed to develop hydrogel scaffolds for cardiac tissue regeneration following myocardial infarction (MI). Two superabsorbent hydrogels, CAHA2A and CAHA2AP, were developed employing interpenetration chemistry. CAHA2A was constituted with alginate, carboxymethyl cellulose, (hydroxyethyl) methacrylate, and acrylic acid, where CAHA2AP was prepared by interpenetrated CAHA2A with polyvinyl alcohol. Both hydrogels displayed superior physiochemical characteristics, as determined by attenuated total reflection infrared spectroscopy spectral analysis, differential scanning calorimetry&amp;nbsp;measurements, tensile testing, contact angle, water profiling, dye release, and conductivity. In vitro degradation of the hydrogels displayed acceptable weight composure and pH changes. Both hydrogels were hemocompatible,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2c58x6wk</guid>
      <pubDate>Tue, 12 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sedighim, Sharona</name>
      </author>
      <author>
        <name>Chen, Yiqing</name>
      </author>
      <author>
        <name>Xu, Changlu</name>
      </author>
      <author>
        <name>Mohindra, Rohit</name>
      </author>
      <author>
        <name>Liu, Huinan</name>
        <uri>https://orcid.org/0000-0001-9366-6204</uri>
      </author>
      <author>
        <name>Agrawal, Devendra K</name>
      </author>
      <author>
        <name>Thankam, Finosh G</name>
      </author>
    </item>
    <item>
      <title>An alpha-helical lid guides the target DNA toward catalysis in CRISPR-Cas12a</title>
      <link>https://escholarship.org/uc/item/0h2107mr</link>
      <description>CRISPR-Cas12a is a powerful RNA-guided genome-editing system that generates double-strand DNA breaks using its single RuvC nuclease domain by a sequential mechanism in which initial cleavage of the non-target strand is followed by target strand cleavage. How the spatially distant DNA target strand traverses toward the RuvC catalytic core is presently not understood. Here, continuous tens of microsecond-long molecular dynamics and free-energy simulations reveal that an α-helical lid, located within the RuvC domain, plays a pivotal role in the traversal of the DNA target strand by anchoring the crRNA:target strand duplex and guiding the target strand toward the RuvC core, as also corroborated by DNA cleavage experiments. In this mechanism, the REC2 domain pushes the crRNA:target strand duplex toward the core of the enzyme, while the Nuc domain aids the bending and accommodation of the target strand within the RuvC core by bending inward. Understanding of this critical process underlying...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0h2107mr</guid>
      <pubDate>Mon, 4 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Saha, Aakash</name>
      </author>
      <author>
        <name>Ahsan, Mohd</name>
      </author>
      <author>
        <name>Arantes, Pablo R</name>
      </author>
      <author>
        <name>Schmitz, Michael</name>
      </author>
      <author>
        <name>Chanez, Christelle</name>
      </author>
      <author>
        <name>Jinek, Martin</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
    </item>
    <item>
      <title>Strain energy density as a Gaussian process and its utilization in stochastic finite element analysis: Application to planar soft tissues</title>
      <link>https://escholarship.org/uc/item/8bt9c13m</link>
      <description>Data-based approaches are promising alternatives to the traditional analytical constitutive models for solid mechanics. Herein, we propose a Gaussian process (GP) based constitutive modeling framework, specifically focusing on planar, hyperelastic and incompressible soft tissues. The strain energy density of soft tissues is modeled as a GP, which can be regressed to experimental stress-strain data obtained from biaxial experiments. Moreover, the GP model can be weakly constrained to be convex. A key advantage of a GP-based model is that, in addition to the mean value, it provides a probability density (i.e. associated uncertainty) for the strain energy density. To simulate the effect of this uncertainty, a non-intrusive stochastic finite element analysis (SFEA) framework is proposed. The proposed framework is verified against an artificial dataset based on the Gasser-Ogden-Holzapfel model and applied to a real experimental dataset of a porcine aortic valve leaflet tissue. Results...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8bt9c13m</guid>
      <pubDate>Fri, 16 Feb 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Aggarwal, Ankush</name>
      </author>
      <author>
        <name>Jensen, Bjørn Sand</name>
      </author>
      <author>
        <name>Pant, Sanjay</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
    <item>
      <title>Unveiling the RNA-mediated allosteric activation discloses functional hotspots in CRISPR-Cas13a</title>
      <link>https://escholarship.org/uc/item/07c9089p</link>
      <description>Cas13a is a recent addition to the CRISPR-Cas toolkit that exclusively targets RNA, which makes it a promising tool for RNA detection. It utilizes a CRISPR RNA (crRNA) to target RNA sequences and trigger a composite active site formed by two 'Higher Eukaryotes and Prokaryotes Nucleotide' (HEPN) domains, cleaving any solvent-exposed RNA. In this system, an intriguing form of allosteric communication controls the RNA cleavage activity, yet its molecular details are unknown. Here, multiple-microsecond molecular dynamics simulations are combined with graph theory to decipher this intricate activation mechanism. We show that the binding of a target RNA acts as an allosteric effector, by amplifying the communication signals over the dynamical noise through interactions of the crRNA at the buried HEPN1-2 interface. By introducing a novel Signal-to-Noise Ratio (SNR) of communication efficiency, we reveal critical allosteric residues-R377,&amp;nbsp;N378, and&amp;nbsp;R973-that rearrange their...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/07c9089p</guid>
      <pubDate>Sat, 3 Feb 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sinha, Souvik</name>
      </author>
      <author>
        <name>Vargas, Adrian M Molina</name>
      </author>
      <author>
        <name>Arantes, Pablo R</name>
      </author>
      <author>
        <name>Patel, Amun</name>
      </author>
      <author>
        <name>O’Connell, Mitchell R</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
    </item>
    <item>
      <title>A Bayesian constitutive model selection framework for biaxial mechanical testing of planar soft tissues: Application to porcine aortic valves</title>
      <link>https://escholarship.org/uc/item/8mj7p92t</link>
      <description>A variety of constitutive models have been developed for soft tissue mechanics. However, there is no established criterion to select a suitable model for a specific application. Although the model that best fits the experimental data can be deemed the most suitable model, this practice often can be insufficient given the inter-sample variability of experimental observations. Herein, we present a Bayesian approach to calculate the relative probabilities of constitutive models based on biaxial mechanical testing of tissue samples. Forty-six samples of porcine aortic valve tissue were tested using a biaxial stretching setup. For each sample, seven ratios of stresses along and perpendicular to the fiber direction were applied. The probabilities of eight invariant-based constitutive models were calculated based on the experimental data using the proposed model selection framework. The calculated probabilities showed that, out of the considered models and based on the information available...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8mj7p92t</guid>
      <pubDate>Fri, 2 Feb 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Aggarwal, Ankush</name>
      </author>
      <author>
        <name>Hudson, Luke T</name>
      </author>
      <author>
        <name>Laurence, Devin W</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
      <author>
        <name>Pant, Sanjay</name>
      </author>
    </item>
    <item>
      <title>Disruption of electrostatic contacts in the HNH nuclease from a thermophilic Cas9 rewires allosteric motions and enhances high-temperature DNA cleavage</title>
      <link>https://escholarship.org/uc/item/1ck54309</link>
      <description>Allosteric signaling within multidomain proteins is a driver of communication between spatially distant functional sites. Understanding the mechanism of allosteric coupling in large multidomain proteins is the most promising route to achieving spatial and temporal control of the system. The recent explosion of CRISPR-Cas9 applications in molecular biology and medicine has created a need to understand how the atomic level protein dynamics of Cas9, which are the driving force of its allosteric crosstalk, influence its biophysical characteristics. In this study, we used a synergistic approach of nuclear magnetic resonance (NMR) and computation to pinpoint an allosteric hotspot in the HNH domain of the thermostable GeoCas9. We show that mutation of K597 to alanine disrupts a salt-bridge network, which in turn alters the structure, the timescale of allosteric motions, and the thermostability of the GeoHNH domain. This homologous lysine-to-alanine mutation in the extensively studied...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1ck54309</guid>
      <pubDate>Wed, 27 Dec 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Belato, Helen B</name>
      </author>
      <author>
        <name>Norbrun, Carmelissa</name>
      </author>
      <author>
        <name>Luo, Jinping</name>
      </author>
      <author>
        <name>Pindi, Chinmai</name>
      </author>
      <author>
        <name>Sinha, Souvik</name>
      </author>
      <author>
        <name>D’Ordine, Alexandra M</name>
      </author>
      <author>
        <name>Jogl, Gerwald</name>
      </author>
      <author>
        <name>Palermo, Giulia</name>
        <uri>https://orcid.org/0000-0003-1404-8737</uri>
      </author>
      <author>
        <name>Lisi, George P</name>
      </author>
    </item>
    <item>
      <title>Protocol for the generation of Symbiodiniaceae mutants using UV mutagenesis</title>
      <link>https://escholarship.org/uc/item/69b6566w</link>
      <description>Genetic approaches are limited in the dinoflagellate family, Symbiodiniaceae, causing a bottleneck in the discovery of useful mutants toward the goal of preventing future coral bleaching events. In this protocol, we demonstrate the application of UV exposure, coupled with downstream phenotypic screening and mutant isolation, to form a UV mutagenesis pipeline. This pipeline provides an avenue to generate Symbiodiniaceae mutants to help link genotype to phenotype, as well as address previously unanswered questions surrounding relationships with host organisms, like coral. For complete details on the use and execution of this protocol, please refer to Jinkerson et&amp;nbsp;al. (2022).&lt;sup&gt;1&lt;/sup&gt;.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/69b6566w</guid>
      <pubDate>Tue, 19 Dec 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Russo, Joseph A</name>
      </author>
      <author>
        <name>Xiang, Tingting</name>
        <uri>https://orcid.org/0000-0001-9062-2273</uri>
      </author>
      <author>
        <name>Jinkerson, Robert E</name>
        <uri>https://orcid.org/0000-0001-9399-1613</uri>
      </author>
    </item>
    <item>
      <title>Characterization of age-related microstructural changes in locus coeruleus and substantia nigra pars compacta</title>
      <link>https://escholarship.org/uc/item/32610525</link>
      <description>Locus coeruleus (LC) and substantia nigra pars compacta (SNpc) degrade with normal aging, but not much is known regarding how these changes manifest in MRI images, or whether these markers predict aspects of cognition. Here, we use high-resolution diffusion-weighted MRI to investigate microstructural and compositional changes in LC and SNpc in young and older adult cohorts, as well as their relationship with cognition. In LC, the older cohort exhibited a significant reduction in mean and radial diffusivity, but a significant increase in fractional anisotropy compared with the young cohort. We observed a significant correlation between the decrease in LC mean, axial, and radial diffusivities and measures examining cognition (Rey Auditory Verbal Learning Test delayed recall) in the older adult cohort. This observation suggests that LC is involved in retaining cognitive abilities. In addition, we observed that iron deposition in SNpc occurs early in life and continues during normal aging.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32610525</guid>
      <pubDate>Sun, 22 Oct 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Langley, Jason</name>
      </author>
      <author>
        <name>Hussain, Sana</name>
      </author>
      <author>
        <name>Flores, Justino J</name>
      </author>
      <author>
        <name>Bennett, Ilana J</name>
        <uri>https://orcid.org/0000-0002-5330-4679</uri>
      </author>
      <author>
        <name>Hu, Xiaoping</name>
        <uri>https://orcid.org/0000-0002-8155-7040</uri>
      </author>
    </item>
    <item>
      <title>Mechanics of the Tricuspid Valve—From Clinical Diagnosis/Treatment, In-Vivo and In-Vitro Investigations, to Patient-Specific Biomechanical Modeling</title>
      <link>https://escholarship.org/uc/item/9zk528w2</link>
      <description>Proper tricuspid valve (TV) function is essential to unidirectional blood flow through the right side of the heart. Alterations to the tricuspid valvular components, such as the TV annulus, may lead to functional tricuspid regurgitation (FTR), where the valve is unable to prevent undesired backflow of blood from the right ventricle into the right atrium during systole. Various treatment options are currently available for FTR; however, research for the tricuspid heart valve, functional tricuspid regurgitation, and the relevant treatment methodologies are limited due to the pervasive expectation among cardiac surgeons and cardiologists that FTR will naturally regress after repair of left-sided heart valve lesions. Recent studies have focused on (i) understanding the function of the TV and the initiation or progression of FTR using both in-vivo and in-vitro methods, (ii) quantifying the biomechanical properties of the tricuspid valve apparatus as well as its surrounding heart tissue,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9zk528w2</guid>
      <pubDate>Fri, 29 Sep 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
      <author>
        <name>Laurence, Devin W</name>
      </author>
      <author>
        <name>Ross, Colton J</name>
      </author>
      <author>
        <name>Kramer, Katherine E</name>
      </author>
      <author>
        <name>Babu, Anju R</name>
      </author>
      <author>
        <name>Johnson, Emily L</name>
      </author>
      <author>
        <name>Hsu, Ming-Chen</name>
      </author>
      <author>
        <name>Aggarwal, Ankush</name>
      </author>
      <author>
        <name>Mir, Arshid</name>
      </author>
      <author>
        <name>Burkhart, Harold M</name>
      </author>
      <author>
        <name>Towner, Rheal A</name>
      </author>
      <author>
        <name>Baumwart, Ryan</name>
      </author>
      <author>
        <name>Wu, Yi</name>
      </author>
    </item>
    <item>
      <title>A pilot study on biaxial mechanical, collagen microstructural, and morphological characterizations of a resected human intracranial aneurysm tissue</title>
      <link>https://escholarship.org/uc/item/9xq1k3rh</link>
      <description>Intracranial aneurysms (ICAs) are focal dilatations that imply a weakening of the brain artery. Incidental rupture of an ICA is increasingly responsible for significant mortality and morbidity in the American’s aging population. Previous studies have quantified the pressure-volume characteristics, uniaxial mechanical properties, and morphological features of human aneurysms. In this pilot study, for the first time, we comprehensively quantified the mechanical, collagen fiber microstructural, and morphological properties of one resected human posterior inferior cerebellar artery aneurysm. The tissue from the dome of a right posterior inferior cerebral aneurysm was first mechanically characterized using biaxial tension and stress relaxation tests. Then, the load-dependent collagen fiber architecture of the aneurysm tissue was quantified using an in-house polarized spatial frequency domain imaging system. Finally, optical coherence tomography and histological procedures were used...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9xq1k3rh</guid>
      <pubDate>Fri, 29 Sep 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Laurence, Devin W</name>
      </author>
      <author>
        <name>Homburg, Hannah</name>
      </author>
      <author>
        <name>Yan, Feng</name>
      </author>
      <author>
        <name>Tang, Qinggong</name>
      </author>
      <author>
        <name>Fung, Kar-Ming</name>
      </author>
      <author>
        <name>Bohnstedt, Bradley N</name>
      </author>
      <author>
        <name>Holzapfel, Gerhard A</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
    <item>
      <title>Shape Memory Polyurethane with Porous Architectures for Potential Applications in Intracranial Aneurysm Treatment</title>
      <link>https://escholarship.org/uc/item/9x15s5wr</link>
      <description>Conventional endovascular embolization of intracranial (or brain) aneurysms using helical detachable platinum coils can be time-consuming and occasionally requires retreatment due to incomplete coil packing. These shortcomings create a need for new biomedical devices and methods of achieving brain aneurysm occlusion. This paper presents a biocompatible and highly porous shape memory polymer (SMP) material with potential applications in the development of novel endovascular devices for treating complex intracranial aneurysms. The novel highly porous polyurethane SMP is synthesized as an open cell foam material with a glass transition temperature (&lt;i&gt;T&lt;/i&gt;&lt;sub&gt;g&lt;/sub&gt;) of 39 °C using a sugar particle leaching method. Once heated above the &lt;i&gt;T&lt;/i&gt;&lt;sub&gt;g&lt;/sub&gt;, the compressed SMP foam is able to quickly return to its original shape. An electrical resistance heating method is also employed to demonstrate a potential triggering design for the shape recovery process in future medical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9x15s5wr</guid>
      <pubDate>Fri, 29 Sep 2023 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Jingyu</name>
      </author>
      <author>
        <name>Kunkel, Robert</name>
      </author>
      <author>
        <name>Luo, Jishan</name>
      </author>
      <author>
        <name>Li, Yuhua</name>
      </author>
      <author>
        <name>Liu, Hong</name>
      </author>
      <author>
        <name>Bohnstedt, Bradley N</name>
      </author>
      <author>
        <name>Liu, Yingtao</name>
      </author>
      <author>
        <name>Lee, Chung-Hao</name>
        <uri>https://orcid.org/0000-0002-8019-3329</uri>
      </author>
    </item>
  </channel>
</rss>
