Article
Altered muscle niche contributes to myogenic deficit in the D2- <i>mdx</i> model of severe DMD
2023-03-28
Abstract excerpt
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 stage of the disease. We show that poor regeneration of juvenile D2- mdx muscles is associated with enhanced inflamma...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 37f713d4-eb5d-5aca-9604-df137d02bbb9
- DOI
- 10.1101/2023.03.27.534413
