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Transplantation of PSC-derived myogenic progenitors counteracts disease phenotypes in FSHD mice
Facioscapulohumeral muscular dystrophy (FSHD) is a genetically dominant progressive myopathy caused by improper silencing of the DUX4 gene, leading to fibrosis, muscle atrophy, and fatty replacement. Approaches focused on muscle regeneration through the delivery of stem cells represent an attractive...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440030/ https://www.ncbi.nlm.nih.gov/pubmed/36056021 http://dx.doi.org/10.1038/s41536-022-00249-0 |