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Heregulin ameliorates the dystrophic phenotype in mdx mice
Duchenne's muscular dystrophy (DMD) is a fatal neuromuscular disease caused by absence of dystrophin. Utrophin is a chromosome 6-encoded dystrophin-related protein (DRP), sharing functional motifs with dystrophin. Utrophin's ability to compensate for dystrophin during development and when...
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| 發表在: | Proc Natl Acad Sci U S A |
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| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
National Academy of Sciences
2004
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC518764/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15365169/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0405972101 |
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