SMN promotes mitochondrial metabolic maturation during myogenesis by regulating the MYOD-miRNA axis

Spinal muscular atrophy (SMA) is a congenital neuromuscular disease caused by the mutation or deletion of the survival motor neuron 1 (SMN1) gene. Although the primary cause of progressive muscle atrophy in SMA has classically been considered the degeneration of motor neurons, recent studies have in...

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Detalles Bibliográficos
Autores principales: Ikenaka, Akihiro, Kitagawa, Yohko, Yoshida, Michiko, Lin, Chuang-Yu, Niwa, Akira, Nakahata, Tatsutoshi, Saito, Megumu K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834662/
https://www.ncbi.nlm.nih.gov/pubmed/36604149
http://dx.doi.org/10.26508/lsa.202201457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834662/
https://www.ncbi.nlm.nih.gov/pubmed/36604149
http://dx.doi.org/10.26508/lsa.202201457

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