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Generation of human myogenic progenitors from pluripotent stem cells for in vivo regeneration
Muscular dystrophy encompasses a large number of heterogeneous genetic disorders characterized by progressive and devastating muscle wasting. Cell-based replacement strategies aimed at promoting skeletal muscle regeneration represent a candidate therapeutic approach to treat muscular dystrophies. Du...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer International Publishing
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270264/ https://www.ncbi.nlm.nih.gov/pubmed/35802202 http://dx.doi.org/10.1007/s00018-022-04434-8 |