Characterisation of Progressive Skeletal Muscle Fibrosis in the Mdx Mouse Model of Duchenne Muscular Dystrophy: An In Vivo and In Vitro Study

Duchenne muscular dystrophy (DMD) is a rare genetic disease leading to progressive muscle wasting, respiratory failure, and cardiomyopathy. Although muscle fibrosis represents a DMD hallmark, the organisation of the extracellular matrix and the molecular changes in its turnover are still not fully u...

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Detalles Bibliográficos
Autores principales: Giovarelli, Matteo, Arnaboldi, Francesca, Zecchini, Silvia, Cornaghi, Laura Brigida, Nava, Ambra, Sommariva, Michele, Clementi, Emilio Giuseppe Ignazio, Gagliano, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369129/
https://www.ncbi.nlm.nih.gov/pubmed/35955872
http://dx.doi.org/10.3390/ijms23158735

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369129/
https://www.ncbi.nlm.nih.gov/pubmed/35955872
http://dx.doi.org/10.3390/ijms23158735

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