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Human Molecular Genetics|April 3, 2014
Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophyJustin G Boyer, Marc-Olivier Deguise, Lyndsay M Murray, et al.
Journal of Cell Science|September 28, 2006
Disruption of MEF2 activity in cardiomyoblasts inhibits cardiomyogenesisChristina Karamboulas, Gabriel D Dakubo, Jun Liu, et al.
The Journal of Biological Chemistry|July 28, 2009
Bin1 SRC homology 3 domain acts as a scaffold for myofiber sarcomere assemblyPasan Fernando, Jacqueline S Sandoz, Wen Ding, et al.
Human Molecular Genetics|January 11, 2017
Oligodendrocyte development and CNS myelination are unaffected in a mouse model of severe spinal muscular atrophyRyan W O'Meara, Sarah E Cummings, Yves De Repentigny, et al.
Molecular Biology of the Cell|December 23, 2011
Neuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and functionScott D Ryan, Andrew Ferrier, Tadasu Sato, et al.
Communications Biology|July 4, 2024
Loss of miR-145 promotes remyelination and functional recovery in a model of chronic central demyelinationSamantha F Kornfeld, Sarah E Cummings, Rebecca Yaworski, et al.
The Journal of Experimental Medicine|February 20, 2003
Transgenic expression of the activating natural killer receptor Ly49H confers resistance to cytomegalovirus in genetically susceptible miceSeung-Hwan Lee, Ahmed Zafer, Yves de Repentigny, et al.
Plos One|July 11, 2013
Six1 regulates MyoD expression in adult muscle progenitor cellsYubing Liu, Imane Chakroun, Dabo Yang, et al.
Human Molecular Genetics|January 2, 2014
Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VIAndrew Ferrier, Tadasu Sato, Yves De Repentigny, et al.
Investigative Ophthalmology & Visual Science|August 1, 2020
XIAP Protects Retinal Ganglion Cells in the Mutant ND4 Mouse Model of Leber Hereditary Optic NeuropathySarah J Wassmer, Yves De Repentigny, Derek Sheppard, et al.
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