Department of Cellular & Molecular Medicine - Open Access Policy Deposits
Parent: School of Medicine
eScholarship stats: Breakdown by Item for March through June, 2026
| Item | Title | Total requests | Download | View-only | %Dnld |
|---|---|---|---|---|---|
| 7rs018c6 | Gain-of-function cardiomyopathic mutations in RBM20 rewire splicing regulation and re-distribute ribonucleoprotein granules within processing bodies | 774 | 681 | 93 | 88.0% |
| 9wk3d379 | Guidelines for the use and interpretation of assays for monitoring autophagy | 622 | 307 | 315 | 49.4% |
| 9044v022 | Brain organoids, consciousness, ethics and moral status | 556 | 347 | 209 | 62.4% |
| 172879gx | Age-Dependent Brain Gene Expression and Copy Number Anomalies in Autism Suggest Distinct Pathological Processes at Young Versus Mature Ages | 531 | 62 | 469 | 11.7% |
| 0jb936p7 | Mechanism of STMN2 cryptic splice-polyadenylation and its correction for TDP-43 proteinopathies | 470 | 205 | 265 | 43.6% |
| 551458jj | APOE4/4 is linked to damaging lipid droplets in Alzheimer’s disease microglia | 469 | 259 | 210 | 55.2% |
| 3pv76061 | E-cigarettes compromise the gut barrier and trigger inflammation | 419 | 198 | 221 | 47.3% |
| 5s47j042 | First Organoid Intelligence (OI) workshop to form an OI community | 410 | 206 | 204 | 50.2% |
| 0914g67c | A comparative atlas of single-cell chromatin accessibility in the human brain | 395 | 240 | 155 | 60.8% |
| 00g3j9wp | Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated Alzheimer’s disease | 392 | 239 | 153 | 61.0% |
| 70c3m48j | Spindle assembly checkpoint activation and silencing at kinetochores | 377 | 207 | 170 | 54.9% |
| 28k88901 | Transcription Factor 4 loss-of-function is associated with deficits in progenitor proliferation and cortical neuron content | 366 | 252 | 114 | 68.9% |
| 3cv2t1d1 | Mechanism and reconstitution of circadian transcription in cyanobacteria | 356 | 203 | 153 | 57.0% |
| 4bd0d5ws | An environment-dependent transcriptional network specifies human microglia identity | 346 | 186 | 160 | 53.8% |
| 2nz1949j | A large-scale binding and functional map of human RNA-binding proteins | 343 | 232 | 111 | 67.6% |
| 0r30n2q3 | Adipose tissue macrophages secrete small extracellular vesicles that mediate rosiglitazone-induced insulin sensitization | 339 | 193 | 146 | 56.9% |
| 1jm982xv | Decoding ALS: from genes to mechanism | 339 | 182 | 157 | 53.7% |
| 10h0243m | Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection | 332 | 190 | 142 | 57.2% |
| 8fz9q8fw | Lipid-associated macrophages’ promotion of fibrosis resolution during MASH regression requires TREM2 | 329 | 238 | 91 | 72.3% |
| 2pp4w8dz | The complexity of tobacco smoke-induced mutagenesis in head and neck cancer | 327 | 191 | 136 | 58.4% |
| 3mk2678t | Exploring the consequences of redirecting an exocytic Rab onto endocytic vesicles | 318 | 253 | 65 | 79.6% |
| 2bq0m1f2 | Reduced signal for polygenic adaptation of height in UK Biobank | 298 | 162 | 136 | 54.4% |
| 68k9w7dj | A living organoid biobank of patients with Crohn’s disease reveals molecular subtypes for personalized therapeutics | 291 | 209 | 82 | 71.8% |
| 1m706149 | Reversing a model of Parkinson’s disease with in situ converted nigral neurons | 288 | 189 | 99 | 65.6% |
| 4vt1n111 | A phage nucleus-associated RNA-binding protein is required for jumbo phage infection | 284 | 102 | 182 | 35.9% |
| 4ch9n51h | Mitotic tethering enables inheritance of shattered micronuclear chromosomes | 280 | 146 | 134 | 52.1% |
| 0503r9x1 | Adult stem cell-derived complete lung organoid models emulate lung disease in COVID-19 | 275 | 182 | 93 | 66.2% |
| 7m89k316 | Nuclear miR-320 Mediates Diabetes-Induced Cardiac Dysfunction by Activating Transcription of Fatty Acid Metabolic Genes to Cause Lipotoxicity in the Heart | 274 | 187 | 87 | 68.2% |
| 0063305k | Sequential regulatory loops as key gatekeepers for neuronal reprogramming in human cells | 270 | 67 | 203 | 24.8% |
| 16h8932r | Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants | 268 | 116 | 152 | 43.3% |
| 6nt244k4 | Generation of ‘semi-guided’ cortical organoids with complex neural oscillations | 267 | 156 | 111 | 58.4% |
| 9jp3g347 | The SARS-CoV-2 nucleocapsid phosphoprotein forms mutually exclusive condensates with RNA and the membrane-associated M protein | 262 | 118 | 144 | 45.0% |
| 01j548f4 | Perspectives on ENCODE | 260 | 165 | 95 | 63.5% |
| 0bw638xs | Architecture and self-assembly of the jumbo bacteriophage nuclear shell | 260 | 120 | 140 | 46.2% |
| 8vw4s1s8 | Robust transcriptome-wide discovery of RNA-binding protein binding sites with enhanced CLIP (eCLIP) | 257 | 96 | 161 | 37.4% |
| 60k166zd | The sustained expression of Cas9 targeting toxic RNAs reverses disease phenotypes in mouse models of myotonic dystrophy type 1 | 251 | 54 | 197 | 21.5% |
| 0tt0x846 | Mechanisms underlying HIV-associated cognitive impairment and emerging therapies for its management | 248 | 121 | 127 | 48.8% |
| 1k65z54f | Microbiome–microglia connections via the gut–brain axis | 248 | 138 | 110 | 55.6% |
| 2gr9g49c | Liver-Derived Signals Sequentially Reprogram Myeloid Enhancers to Initiate and Maintain Kupffer Cell Identity | 243 | 72 | 171 | 29.6% |
| 6z9096mf | An in vivo neuroimmune organoid model to study human microglia phenotypes | 242 | 105 | 137 | 43.4% |
| 8670n4cq | Three-dimensional bioprinted glioblastoma microenvironments model cellular dependencies and immune interactions | 240 | 102 | 138 | 42.5% |
| 0xm8q84f | Circular ecDNA promotes accessible chromatin and high oncogene expression | 237 | 62 | 175 | 26.2% |
| 3pd6q5r4 | Promoter-proximal CTCF binding promotes distal enhancer-dependent gene activation | 237 | 82 | 155 | 34.6% |
| 8bg9p9r4 | Messenger RNA Oxidation Occurs Early in Disease Pathogenesis and Promotes Motor Neuron Degeneration in ALS | 237 | 136 | 101 | 57.4% |
| 9093x51q | Complex Oscillatory Waves Emerging from Cortical Organoids Model Early Human Brain Network Development | 237 | 77 | 160 | 32.5% |
| 27v4m3md | Role of H3K4 monomethylation in gene regulation | 236 | 81 | 155 | 34.3% |
| 4vs4p782 | Endosomal escape of RNA therapeutics: How do we solve this rate-limiting problem? | 236 | 109 | 127 | 46.2% |
| 8f133727 | SREBP1 Contributes to Resolution of Pro-inflammatory TLR4 Signaling by Reprogramming Fatty Acid Metabolism | 235 | 61 | 174 | 26.0% |
| 20t6f25j | Rebuilding Chromosomes After Catastrophe: Emerging Mechanisms of Chromothripsis | 232 | 67 | 165 | 28.9% |
| 13v7056h | Identification of the bacteriophage nucleus protein interaction network | 231 | 81 | 150 | 35.1% |
Note: Due to the evolving nature of web traffic, the data presented here should be considered approximate and subject to revision. Learn more.