Absence of Desmin Results in Impaired Adaptive Response to Mechanical Overloading of Skeletal Muscle

Background: Desmin is a muscle-specific protein belonging to the intermediate filament family. Desmin mutations are linked to skeletal muscle defects, including inherited myopathies with severe clinical manifestations. The aim of this study was to examine the role of desmin in skeletal muscle remode...

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Detalles Bibliográficos
Autores principales: Joanne, Pierre, Hovhannisyan, Yeranuhi, Bencze, Maximilien, Daher, Marie-Thérèse, Parlakian, Ara, Toutirais, Geraldine, Gao-Li, Jacqueline, Lilienbaum, Alain, Li, Zhenlin, Kordeli, Ekaterini, Ferry, Arnaud, Agbulut, Onnik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320001/
https://www.ncbi.nlm.nih.gov/pubmed/34336827
http://dx.doi.org/10.3389/fcell.2021.662133

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320001/
https://www.ncbi.nlm.nih.gov/pubmed/34336827
http://dx.doi.org/10.3389/fcell.2021.662133

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