載入...
Sarcolipin deletion in mdx mice impairs calcineurin signalling and worsens dystrophic pathology
Duchenne muscular dystrophy (DMD) is the most severe form of muscular dystrophy affecting 1 in 3500 live male births. Although there is no cure for DMD, therapeutic strategies aimed at enhancing calcineurin signalling and promoting the slow fibre phenotype have shown promise in mdx mice, which is th...
Na minha lista:
| 發表在: | Hum Mol Genet |
|---|---|
| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2018
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6240731/ https://ncbi.nlm.nih.gov/pubmed/30137316 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy302 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|