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Plos One|June 24, 2011
Motor unit abnormalities in Dystonia musculorum miceYves De Repentigny, Andrew Ferrier, Scott D Ryan, et al.
Human Molecular Genetics|January 22, 2017
Immune dysregulation may contribute to disease pathogenesis in spinal muscular atrophy miceMarc-Olivier Deguise, Yves De Repentigny, Emily McFall, et al.
Elife|February 20, 2025
Impact of liver-specific survival motor neuron (SMN) depletion on central nervous system and peripheral tissue pathologyMonique Marylin Alves de Almeida, Yves De Repentigny, Sabrina Gagnon, et al.
Human Molecular Genetics|February 2, 2002
Neurodevelopmental defects resulting from ATRX overexpression in transgenic miceNathalie G Bérubé, Magdalena Jagla, Cecelia Smeenk, et al.
Molecular and Cellular Biology|November 3, 2010
Wnt11 promotes cardiomyocyte development by caspase-mediated suppression of canonical Wnt signalsMohammad Abdul-Ghani, Daniel Dufort, Rebecca Stiles, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 2, 2002
Mouse dystrophin enhancer preferentially targets lacZ expression in skeletal and cardiac musclePhilip Marshall, Nathalie Chartrand, Yves De Repentigny, et al.
The Journal of Cell Biology|March 14, 2012
Microtubule stability, Golgi organization, and transport flux require dystonin-a2-MAP1B interactionScott D Ryan, Kunal Bhanot, Andrew Ferrier, et al.
Plos One|February 18, 2016
Cytoskeletal Linker Protein Dystonin Is Not Critical to Terminal Oligodendrocyte Differentiation or CNS MyelinationSamantha F Kornfeld, Anisha Lynch-Godrei, Sawyer R Bonin, et al.
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