Bernard J. Jasmin

Affiliations: 
University of Ottawa, Ottawa, ON, Canada 
Area:
Neuroscience Biology
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"Bernard Jasmin"
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Publications

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Roussel MP, Ravel-Chapuis A, Gobin J, et al. (2024) Changes in Physiopathological Markers in Myotonic Dystrophy Type 1 Skeletal Muscle: A 3-Year Follow-up Study. Journal of Neuromuscular Diseases
Freeman E, Langlois S, Leyba MF, et al. (2024) Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice. Skeletal Muscle. 14: 8
Neault N, Ravel-Chapuis A, Baird SD, et al. (2023) Vorinostat Improves Myotonic Dystrophy Type 1 Splicing Abnormalities in DM1 Muscle Cell Lines and Skeletal Muscle from a DM1 Mouse Model. International Journal of Molecular Sciences. 24
Osseni A, Ravel-Chapuis A, Belotti E, et al. (2022) Pharmacological inhibition of HDAC6 improves muscle phenotypes in dystrophin-deficient mice by downregulating TGF-β via Smad3 acetylation. Nature Communications. 13: 7108
Péladeau C, Jasmin BJ. (2022) Identifying FDA-Approved Drugs that Upregulate Utrophin A as a Therapeutic Strategy for Duchenne Muscular Dystrophy. Methods in Molecular Biology (Clifton, N.J.). 2587: 495-510
Misquitta NS, Ravel-Chapuis A, Jasmin BJ. (2022) Combinatorial treatment with exercise and AICAR potentiates the rescue of myotonic dystrophy type 1 mouse muscles in a sex-specific manner. Human Molecular Genetics
Freeman E, Langlois S, Scott K, et al. (2022) Sex-dependent role of Pannexin 1 in regulating skeletal muscle and satellite cell function. Journal of Cellular Physiology
Ravel-Chapuis A, Duchesne E, Jasmin BJ. (2022) Pharmacological and exercise-induced activation of AMPK as emerging therapies for myotonic dystrophy type 1 patients. The Journal of Physiology
Guilhot C, Fovet T, Delobel P, et al. (2022) Severe Muscle Deconditioning Triggers Early Extracellular Matrix Remodeling and Resident Stem Cell Differentiation into Adipocytes in Healthy Men. International Journal of Molecular Sciences. 23
Ravel-Chapuis A, Jasmin BJ. (2022) Combinatorial therapies for rescuing myotonic dystrophy type 1 skeletal muscle defects. Trends in Molecular Medicine. 28: 439-442
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