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Human Molecular Genetics|February 25, 2016
Interactome network analysis identifies multiple caspase-6 interactors involved in the pathogenesis of HDSean-Patrick Riechers, Stefanie Butland, Yu Deng, et al.
Acta Neuropathologica Communications|September 13, 2013
Topography of FUS pathology distinguishes late-onset BIBD from aFTLD-UEdward B Lee, Jenny Russ, Hyunjoo Jung, et al.
Plos Genetics|August 24, 2012
Identification of human proteins that modify misfolding and proteotoxicity of pathogenic ataxin-1Spyros Petrakis, Tamás Raskó, Jenny Russ, et al.
Frontiers in Neurology|December 17, 2020
RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's DiseaseMiguel A Andrade-Navarro, Katja Mühlenberg, Eike J Spruth, et al.
Nucleic Acids Research|January 1, 2013
Development and application of a DNA microarray-based yeast two-hybrid systemBernhard Suter, Jean-Fred Fontaine, Reha Yildirimman, et al.
Acta Neuropathologica|November 13, 2014
Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifierJenny Russ, Elaine Y Liu, Kathryn Wu, et al.
The Journal of Clinical Investigation|October 27, 2020
mTOR-dependent translation amplifies microglia priming in aging miceLily Keane, Ignazio Antignano, Sean-Patrick Riechers, et al.
Genome Research|April 25, 2015
Systematic interaction network filtering identifies CRMP1 as a novel suppressor of huntingtin misfolding and neurotoxicityMartin Stroedicke, Yacine Bounab, Nadine Strempel, et al.
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