Proteome Profiling of the Dystrophic mdx Mice Diaphragm

Mdx mice with a spontaneous mutation in exon 23 of the Dmd gene represent the most common model to investigate the pathophysiology of Duchenne muscular dystrophy (DMD). The disease, caused by the lack of functional dystrophin, is characterized by irreversible impairment of muscle functions, with the...

Descripción completa

Detalles Bibliográficos
Autores principales: Mucha, Olga, Myszka, Małgorzata, Podkalicka, Paulina, Świderska, Bianka, Malinowska, Agata, Dulak, Józef, Łoboda, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669179/
https://www.ncbi.nlm.nih.gov/pubmed/38002330
http://dx.doi.org/10.3390/biom13111648

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669179/
https://www.ncbi.nlm.nih.gov/pubmed/38002330
http://dx.doi.org/10.3390/biom13111648

Ejemplares similares