A carregar...
TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy
Myotonic dystrophy type 1 (DM1), the most prevalent muscular dystrophy in adults, is characterized by progressive muscle wasting and multi-systemic complications. DM1 is the prototype for disorders caused by RNA toxicity. Currently, no therapies exist. Here, we identify that fibroblast growth factor...
Na minha lista:
| Publicado no: | Hum Mol Genet |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4355029/ https://ncbi.nlm.nih.gov/pubmed/25504044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu617 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|