Actin Polymerization Defects Induce Mitochondrial Dysfunction in Cellular Models of Nemaline Myopathies

Actin Polymerization Defects Induce Mitochondrial Dysfunction in Cellular Models of Nemaline Myopathies

Nemaline myopathy (NM) is one of the most common forms of congenital myopathy and it is identified by the presence of “nemaline bodies” (rods) in muscle fibers by histopathological examination. The most common forms of NM are caused by mutations in the <i>Actin Alpha 1</i> (<i>ACTA...

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Détails bibliographiques
Auteurs principaux: Rocío Piñero-Pérez, Alejandra López-Cabrera, Mónica Álvarez-Córdoba, Paula Cilleros-Holgado, Marta Talaverón-Rey, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, David Gómez-Fernández, Diana Reche-López, Ana Romero-González, José Manuel Romero-Domínguez, Rocío M. de Pablos, José A. Sánchez-Alcázar
Format: Article
Langue:English
Publié: MDPI AG 2023-11-01
Collection:Antioxidants
Sujets:
nemaline myopathy
actin polymerization
mitochondria
linoleic acid
L-carnitine
Accès en ligne:https://www.mdpi.com/2076-3921/12/12/2023

Internet

https://www.mdpi.com/2076-3921/12/12/2023

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