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Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals conserved gene alterations linked to Parkinson's disease
1,2,5,6 1Department of Cellular and Molecular Medicine, University of California San Diego, School of Medicine, La Jolla, California 92093, USA; 2Center for Epigenomics, University of California San Diego, School of Medicine, La Jolla, California 92093, USA; 3Westlake Laboratory of Life Sciences and Biomedicine, School of Life Sciences, Westlake University, Hangzhou, Zhejiang 310024, China; 4Department of Neuroscience, University of California San Diego, La Jolla, California 92093, USA...
Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals conserved gene alterations linked to Parkinson's disease
1,4 1 University of California San Diego, School of Medicine; 2 Westlake University; 3 University of California San Diego ↵* Corresponding author; email: br2833{at}cumc.columbia.edu Received June 23, 2025. Accepted March 2, 2026. This manuscript is Open Access. This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International license), as described at http://creativecommons.org/licenses/by-nc/4.0/.
CryoET reveals organelle phenotypes in huntington disease patient iPSC-derived and mouse primary neurons - Nature Communications
Abstract Huntington’s disease (HD) is caused by an expanded CAG repeat in the huntingtin gene, yielding a Huntingtin protein with an expanded polyglutamine tract. While experiments with patient-derived induced pluripotent stem cells (iPSCs) can help understand disease, defining pathological biomarkers remains challenging.
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