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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2020
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Materias: | |
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 |
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