Rashmi Kothary, Ph.D

Affiliations: 
Ottawa Hospital Research Institute 
Area:
Muscle and nervous system integrity, pathology of neuromuscular diseases
Website:
http://www.ohri.ca/profiles/kothary.asp
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"Rashmi Kothary"
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Mean distance: 15.95 (cluster 57)
 
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Publications

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Deguise MO, De Repentigny Y, Tierney A, et al. (2020) Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy. Ebiomedicine. 55: 102750
Lynch-Godrei A, De Repentigny Y, Yaworski RA, et al. (2019) Characterization of gastrointestinal pathologies in the dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI. Neurogastroenterology and Motility : the Official Journal of the European Gastrointestinal Motility Society. e13773
Alvarez-Saavedra M, Yan K, De Repentigny Y, et al. (2019) Snf2h Drives Chromatin Remodeling to Prime Upper Layer Cortical Neuron Development. Frontiers in Molecular Neuroscience. 12: 243
Deguise MO, Baranello G, Mastella C, et al. (2019) Abnormal fatty acid metabolism is a core component of spinal muscular atrophy. Annals of Clinical and Translational Neurology. 6: 1519-1532
Eshraghi M, Gombar R, De Repentigny Y, et al. (2019) Pathologic alterations in the proteome of synaptosomes from a mouse model of spinal muscular atrophy. Journal of Proteome Research
Walter LM, Deguise MO, Meijboom KE, et al. (2018) Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy Mice. Ebiomedicine
Bowerman M, Murrray LM, Scamps F, et al. (2017) Pathogenic commonalities between spinal muscular atrophy and amyotrophic lateral sclerosis: Converging roads to therapeutic development. European Journal of Medical Genetics
Nash LA, McFall ER, Perozzo AM, et al. (2017) Survival Motor Neuron Protein is Released from Cells in Exosomes: A Potential Biomarker for Spinal Muscular Atrophy. Scientific Reports. 7: 13859
Deguise MO, De Repentigny Y, McFall E, et al. (2017) Immune dysregulation may contribute to disease pathogenesis in spinal muscular atrophy mice. Human Molecular Genetics
O'Meara RW, Cummings SE, De Repentigny Y, et al. (2017) Oligodendrocyte development and CNS myelination are unaffected in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics
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