Sertoli Cells Improve Myogenic Differentiation, Reduce Fibrogenic Markers, and Induce Utrophin Expression in Human DMD Myoblasts

Duchenne muscular dystrophy (DMD) is an X-linked disease caused by mutations in DMD gene translating in lack of functional dystrophin and resulting in susceptibility of myofibers to rupture during contraction. Inflammation and fibrosis are critical hallmarks of DMD muscles, which undergo progressive...

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Detalles Bibliográficos
Autores principales: Salvadori, Laura, Chiappalupi, Sara, Arato, Iva, Mancuso, Francesca, Calvitti, Mario, Marchetti, Maria Cristina, Riuzzi, Francesca, Calafiore, Riccardo, Luca, Giovanni, Sorci, Guglielmo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533898/
https://www.ncbi.nlm.nih.gov/pubmed/34680138
http://dx.doi.org/10.3390/biom11101504

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533898/
https://www.ncbi.nlm.nih.gov/pubmed/34680138
http://dx.doi.org/10.3390/biom11101504

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