Showing results (81-90 of 109) with videos related to

Sort By:
Pageof 11
Neuron|January 19, 2022
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosisSai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
Deep learning modeling of rare noncoding genetic variants in human motor neurons defines CCDC146 as a therapeutic target for ALSSai Zhang, Tobias Moll, Jasper Rubin-Sigler, et al.
Genome Biology|November 20, 2024
Considerations in the search for epistasisMarleen Balvert, Johnathan Cooper-Knock, Julian Stamp, et al.
Research Square|June 12, 2026
Single-nucleus multiomic atlas of ALS primary motor cortex nominates neuroprotective WDR49-expressing astrocytesJohnathan Cooper-Knock, Sam Bonsall, Rodrigo Kazu, et al.
BMJ Neurology Open|February 23, 2026
Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALSKoen Cedric Demaegd, Wouter Koole, Joke Jfa van Vugt, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2025
Human Body Single-Cell Atlas of 3D Genome Organization and DNA MethylationJingtian Zhou, Yue Wu, Hanqing Liu, et al.
Molecular Cell|November 20, 2020
Spatiotemporal Proteomic Analysis of Stress Granule Disassembly Using APEX Reveals Regulation by SUMOylation and Links to ALS PathogenesisHagai Marmor-Kollet, Aviad Siany, Nancy Kedersha, et al.
Science (New York, N.Y.)|July 23, 2026
Human body single-cell atlas of three-dimensional genome organization and DNA methylationJingtian Zhou, Yue Wu, Hanqing Liu, et al.
Cell Reports|February 28, 2019
Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral SclerosisJohnathan Cooper-Knock, Tobias Moll, Tennore Ramesh, et al.
Heliyon|February 6, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosisCalum Harvey, Marcel Weinreich, James A K Lee, et al.
Pageof 11