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Human Molecular Genetics|April 15, 2014
The novel Parkinson's disease linked mutation G51D attenuates in vitro aggregation and membrane binding of α-synuclein, and enhances its secretion and nuclear localization in cellsMohamed-Bilal Fares, Nadine Ait-Bouziad, Igor Dikiy, et al.Nature Genetics|February 3, 2009
Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicityAaron D Gitler, Alessandra Chesi, Melissa L Geddie, et al.Biorxiv : the Preprint Server for Biology|December 15, 2025
TDP-43 suppression of ATP8A2 cryptic splicing implicates phosphatidylserine-driven neuroinflammation in ALS/FTDJames T O'Connor, Hui Qi Loo, Caiwei Guo, et al.Nature Neuroscience|October 21, 2025
TDP-43 nuclear loss in FTD/ALS causes widespread alternative polyadenylation changesYi Zeng, Anastasiia Lovchykova, Tetsuya Akiyama, et al.Nature Genetics|October 30, 2012
Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease modelsMaria Armakola, Matthew J Higgins, Matthew D Figley, et al.Aging and Disease|December 3, 2019
Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral SclerosisZhi-Jun Liu, Hui-Xia Lin, Qiao Wei, et al.Elife|October 7, 2020
A versatile system to record cell-cell interactionsRui Tang, Christopher W Murray, Ian L Linde, et al.Plos One|June 16, 2017
ERAD defects and the HFE-H63D variant are associated with increased risk of liver damages in Alpha 1-Antitrypsin DeficiencyPhilippe Joly, Hélène Vignaud, Julie Di Martino, et al.Proceedings of the National Academy of Sciences of the United States of America|December 29, 2007
The Parkinson's disease protein alpha-synuclein disrupts cellular Rab homeostasisAaron D Gitler, Brooke J Bevis, James Shorter, et al.Nature Genetics|February 24, 2009
Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicityEsti Yeger-Lotem, Laura Riva, Linhui Julie Su, et al.Pageof 18