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Scientific Reports|June 29, 2016
Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophyMarc-Olivier Deguise, Justin G Boyer, Emily R McFall, et al.
Skeletal Muscle|October 15, 2013
Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophyJustin G Boyer, Lyndsay M Murray, Kyle Scott, et al.
Neuromuscular Disorders : NMD|May 24, 2005
A 1.3 kb promoter fragment confers spatial and temporal expression of utrophin A mRNA in mouse skeletal muscle fibersMark A Stocksley, Joe V Chakkalakal, Amanda Bradford, et al.
Development (Cambridge, England)|November 13, 2009
Cdx2 regulation of posterior development through non-Hox targetsJoanne G A Savory, Nathalie Bouchard, Vicki Pierre, et al.
Autophagy|June 6, 2015
Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum miceAndrew Ferrier, Yves De Repentigny, Anisha Lynch-Godrei, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 30, 2006
The mouse dystrophin muscle promoter/enhancer drives expression of mini-dystrophin in transgenic mdx mice and rescues the dystrophy in these miceCarrie L Anderson, Yves De Repentigny, Carlo Cifelli, et al.
Frontiers in Cellular Neuroscience|August 22, 2022
Suppression of the necroptotic cell death pathways improves survival in <i>Smn</i> <sup>2</sup> miceLucia Chehade, Marc-Olivier Deguise, Yves De Repentigny, et al.
Neurogastroenterology and Motility|December 10, 2019
Characterization of gastrointestinal pathologies in the dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VIAnisha Lynch-Godrei, Yves De Repentigny, Rebecca A Yaworski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 20, 2005
Physiological maturation of photoreceptors depends on the voltage-gated sodium channel NaV1.6 (Scn8a)Patrice D Côté, Yves De Repentigny, Stuart G Coupland, et al.
Transgenic Research|July 9, 2009
Mice with podocyte-specific overexpression of wild type alpha-actinin-4 are healthy controls for K256E-alpha-actinin-4 mutant transgenic miceJean-Louis Michaud, Erin Stitt-Cavanaugh, Nicole Endlich, et al.
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