Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is the most frequent genetic myopathy in childhood and leads to progressive muscle atrophy, weakness, and premature death. So far, there is no curative treatment available. Therapeutic development from bench to bedside takes time, and promising therapies need to be...

Descripción completa

Detalles Bibliográficos
Autores principales: Donandt, Tina, Hintze, Stefan, Krause, Sabine, Wolf, Eckhard, Schoser, Benedikt, Walter, Maggie C., Meinke, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604785/
https://www.ncbi.nlm.nih.gov/pubmed/36295103
http://dx.doi.org/10.3390/life12101668

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604785/
https://www.ncbi.nlm.nih.gov/pubmed/36295103
http://dx.doi.org/10.3390/life12101668

Ejemplares similares