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Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD
Lack of dystrophin expression is the underlying genetic basis for Duchenne muscular dystrophy (DMD). However, disease severity varies between patients, based on specific genetic modifiers. D2-mdx is a model for severe DMD that exhibits exacerbated muscle degeneration and failure to regenerate even i...
Autores principales: | Mázala, Davi A. G., Hindupur, Ravi, Moon, Young Jae, Shaikh, Fatima, Gamu, Iteoluwakishi H., Alladi, Dhruv, Panci, Georgiana, Weiss-Gayet, Michèle, Chazaud, Bénédicte, Partridge, Terence A., Novak, James S., Jaiswal, Jyoti K. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319851/ https://www.ncbi.nlm.nih.gov/pubmed/37402716 http://dx.doi.org/10.1038/s41420-023-01503-0 |
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