載入...
Linker molecules between laminins and dystroglycan ameliorate laminin-α2–deficient muscular dystrophy at all disease stages
Mutations in laminin-α2 cause a severe congenital muscular dystrophy, called MDC1A. The two main receptors that interact with laminin-α2 are dystroglycan and α7β1 integrin. We have previously shown in mouse models for MDC1A that muscle-specific overexpression of a miniaturized form of agrin (mini-ag...
Na minha lista:
| Main Authors: | , , , , |
|---|---|
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
The Rockefeller University Press
2007
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2064083/ https://ncbi.nlm.nih.gov/pubmed/17389231 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200611152 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|