Metabolic reprogramming of fibro/adipogenic progenitors facilitates muscle regeneration

In Duchenne muscular dystrophy (DMD), the absence of the dystrophin protein causes a variety of poorly understood secondary effects. Notably, muscle fibers of dystrophic individuals are characterized by mitochondrial dysfunctions, as revealed by a reduced ATP production rate and by defective oxidati...

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Detalles Bibliográficos
Autores principales: Reggio, Alessio, Rosina, Marco, Krahmer, Natalie, Palma, Alessandro, Petrilli, Lucia Lisa, Maiolatesi, Giuliano, Massacci, Giorgia, Salvatori, Illari, Valle, Cristiana, Testa, Stefano, Gargioli, Cesare, Fuoco, Claudia, Castagnoli, Luisa, Cesareni, Gianni, Sacco, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003708/
https://www.ncbi.nlm.nih.gov/pubmed/32019766
http://dx.doi.org/10.26508/lsa.202000660

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003708/
https://www.ncbi.nlm.nih.gov/pubmed/32019766
http://dx.doi.org/10.26508/lsa.202000660

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