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Cell|June 17, 2006
Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtinRona K Graham, Yu Deng, Elizabeth J Slow, et al.The EMBO Journal|July 4, 2003
Disruption of the endocytic protein HIP1 results in neurological deficits and decreased AMPA receptor traffickingMartina Metzler, Bo Li, Lu Gan, et al.Human Molecular Genetics|July 22, 2011
Altered palmitoylation and neuropathological deficits in mice lacking HIP14Roshni R Singaraja, Kun Huang, Shaun S Sanders, et al.CMAJ Open|April 27, 2017
Characteristics and outcomes of Canadian MD/PhD program graduates: a cross-sectional surveyMichael A Skinnider, Jordan W Squair, David D W Twa, et al.EMBO Molecular Medicine|July 29, 2010
Inhibition of transglutaminase 2 mitigates transcriptional dysregulation in models of Huntington diseaseStephen J McConoughey, Manuela Basso, Zoya V Niatsetskaya, et al.Journal of Lipid Research|November 22, 2024
The bile acid chenodeoxycholic acid associates with reduced stroke in humans and miceVera F Monteiro-Cardoso, Xin Yi Yeo, Han-Gyu Bae, et al.Neurology|December 4, 2016
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington diseaseAndrew McGarry, Michael McDermott, Karl Kieburtz, et al.Pageof 12