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

Mostrar otras versiones (1)

Lack of dystrophin is the genetic basis for the 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 in the juvenile sta...

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: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081277/
https://www.ncbi.nlm.nih.gov/pubmed/37034785
http://dx.doi.org/10.1101/2023.03.27.534413

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081277/
https://www.ncbi.nlm.nih.gov/pubmed/37034785
http://dx.doi.org/10.1101/2023.03.27.534413

Ejemplares similares