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Interaction between mesenchymal stem cells and myoblasts in the context of facioscapulohumeral muscular dystrophy contributes to the disease phenotype
Facioscapulohumeral muscular dystrophy (FSHD) is a genetic disease associated with ectopic expression of the DUX4 gene in skeletal muscle. Muscle degeneration in FSHD is accompanied by muscle tissue replacement with fat and connective tissue. Expression of DUX4 in myoblasts stimulates mesenchymal st...
Autores principales: | Kiseleva, Ekaterina, Serbina, Olesya, Karpukhina, Anna, Mouly, Vincent, Vassetzky, Yegor S. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545833/ https://www.ncbi.nlm.nih.gov/pubmed/35621301 http://dx.doi.org/10.1002/jcp.30789 |
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