Rashmi Kothary, Ph.D
Affiliations: | Ottawa Hospital Research Institute |
Area:
Muscle and nervous system integrity, pathology of neuromuscular diseasesWebsite:
http://www.ohri.ca/profiles/kothary.aspGoogle:
"Rashmi Kothary"Bio:
Mean distance: 15.95 (cluster 57)
Children
Sign in to add trainee| Scott D. Ryan | post-doc | Sanford Burnham Research Institute | |
| Patrice D. Cote | post-doc | 2001-2005 | OHRI |
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Publications
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| Reilly A, Yaworski R, Beauvais A, et al. (2023) Long term peripheral AAV9-SMN gene therapy promotes survival in a mouse model of spinal muscular atrophy. Human Molecular Genetics |
| Chehade L, Deguise MO, De Repentigny Y, et al. (2022) Suppression of the necroptotic cell death pathways improves survival in mice. Frontiers in Cellular Neuroscience. 16: 972029 |
| Khayrullina G, Alipio-Gloria ZA, Deguise MO, et al. (2022) Survival motor neuron protein deficiency alters microglia reactivity. Glia |
| Lynch-Godrei A, De Repentigny Y, Ferrier A, et al. (2020) Dystonin loss-of-function leads to impaired autophagy-endolysosomal pathway dynamics. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire |
| 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 |
| Deguise MO, Beauvais A, Schneider BL, et al. (2020) Blood Flow to the Spleen is Altered in a Mouse Model of Spinal Muscular Atrophy. Journal of Neuromuscular Diseases |
| Lynch-Godrei A, Kothary R. (2020) HSAN-VI: A spectrum disorder based on dystonin isoform expression. Neurology. Genetics. 6: e389 |
| 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 |