BK(Ca) Activator NS1619 Improves the Structure and Function of Skeletal Muscle Mitochondria in Duchenne Dystrophy

Duchenne muscular dystrophy (DMD) is a progressive hereditary disease caused by the absence of the dystrophin protein. This is secondarily accompanied by a dysregulation of ion homeostasis, in which mitochondria play an important role. In the present work, we show that mitochondrial dysfunction in t...

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Detalles Bibliográficos
Autores principales: Dubinin, Mikhail V., Starinets, Vlada S., Belosludtseva, Natalia V., Mikheeva, Irina B., Chelyadnikova, Yuliya A., Igoshkina, Anastasia D., Vafina, Aliya B., Vedernikov, Alexander A., Belosludtsev, Konstantin N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696041/
https://www.ncbi.nlm.nih.gov/pubmed/36365155
http://dx.doi.org/10.3390/pharmaceutics14112336

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