Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD

Mostrar otras versiones (1)

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...

Descripción completa

Detalles Bibliográficos
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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
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

Internet

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

Ejemplares similares