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Rashmi Kothary

Showing results (61-70 of 151) with videos related to

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Journal of Proteome Research|July 3, 2019
Pathologic Alterations in the Proteome of Synaptosomes from a Mouse Model of Spinal Muscular AtrophyMehdi Eshraghi, Robert Gombar, Yves De Repentigny, et al.
The Journal of Biological Chemistry|April 29, 2011
Biochemical, proteomic, structural, and thermodynamic characterizations of integrin-linked kinase (ILK): cross-validation of the pseudokinaseKoichi Fukuda, James D R Knight, Grzegorz Piszczek, et al.
Human Molecular Genetics|November 6, 2024
SMN depletion impairs skeletal muscle formation and maturation in a mouse model of SMAHong Liu, Lucia Chehade, Marc-Olivier Deguise, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|December 21, 2020
Dystonin loss-of-function leads to impaired autophagosome-endolysosome pathway dynamicsAnisha Lynch-Godrei, Yves De Repentigny, Andrew Ferrier, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 13, 2005
Genetic alterations at the Bpag1 locus in dt mice and their impact on transcript expressionMadeline Pool, Céline Boudreau Larivière, Gilbert Bernier, et al.
Brain : a Journal of Neurology|June 25, 2026
Multiple spinal muscular atrophy disease-modifying effects of a Hspa8G470R synaptic chaperone variantYoon-Ra Her, Andrea Fuentes-Moliz, Rashmi Kothary, et al.
Human Molecular Genetics|July 9, 2018
Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VIAnisha Lynch-Godrei, Yves De Repentigny, Sabrina Gagnon, et al.
Journal of Cellular Physiology|July 1, 2020
MiRNA-145-5p prevents differentiation of oligodendrocyte progenitor cells by regulating expression of myelin gene regulatory factorSamantha F Kornfeld, Sarah E Cummings, Samaneh Fathi, et al.
BMC Medicine|March 9, 2012
Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophyMelissa Bowerman, Lyndsay M Murray, Justin G Boyer, et al.
Biorxiv : the Preprint Server for Biology|March 26, 2026
Protein-stabilizing and neurotransmission-potentiating activities of a synaptic chaperone modify spinal muscular atrophy in model miceYoon-Ra Her, Andrea Fuentes-Moliz, Rashmi Kothary, et al.
Pageof 16

Showing results (61-70 of 151) with videos related to

Sort By:
Pageof 16
Journal of Proteome Research|July 3, 2019
Pathologic Alterations in the Proteome of Synaptosomes from a Mouse Model of Spinal Muscular AtrophyMehdi Eshraghi, Robert Gombar, Yves De Repentigny, et al.
The Journal of Biological Chemistry|April 29, 2011
Biochemical, proteomic, structural, and thermodynamic characterizations of integrin-linked kinase (ILK): cross-validation of the pseudokinaseKoichi Fukuda, James D R Knight, Grzegorz Piszczek, et al.
Human Molecular Genetics|November 6, 2024
SMN depletion impairs skeletal muscle formation and maturation in a mouse model of SMAHong Liu, Lucia Chehade, Marc-Olivier Deguise, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|December 21, 2020
Dystonin loss-of-function leads to impaired autophagosome-endolysosome pathway dynamicsAnisha Lynch-Godrei, Yves De Repentigny, Andrew Ferrier, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 13, 2005
Genetic alterations at the Bpag1 locus in dt mice and their impact on transcript expressionMadeline Pool, Céline Boudreau Larivière, Gilbert Bernier, et al.
Brain : a Journal of Neurology|June 25, 2026
Multiple spinal muscular atrophy disease-modifying effects of a Hspa8G470R synaptic chaperone variantYoon-Ra Her, Andrea Fuentes-Moliz, Rashmi Kothary, et al.
Human Molecular Genetics|July 9, 2018
Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VIAnisha Lynch-Godrei, Yves De Repentigny, Sabrina Gagnon, et al.
Journal of Cellular Physiology|July 1, 2020
MiRNA-145-5p prevents differentiation of oligodendrocyte progenitor cells by regulating expression of myelin gene regulatory factorSamantha F Kornfeld, Sarah E Cummings, Samaneh Fathi, et al.
BMC Medicine|March 9, 2012
Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophyMelissa Bowerman, Lyndsay M Murray, Justin G Boyer, et al.
Biorxiv : the Preprint Server for Biology|March 26, 2026
Protein-stabilizing and neurotransmission-potentiating activities of a synaptic chaperone modify spinal muscular atrophy in model miceYoon-Ra Her, Andrea Fuentes-Moliz, Rashmi Kothary, et al.
Pageof 16