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Lifetime analysis of mdx skeletal muscle reveals a progressive pathology that leads to myofiber loss
The muscular dystrophy X-linked mouse (mdx) is the most commonly used preclinical model for Duchenne muscular dystrophy. Although disease progression in the mouse does not perfectly model the human disease, it shares many pathological features. Early characterizations of the model reported severe pa...
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| 出版年: | Sci Rep |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group UK
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7560899/ https://ncbi.nlm.nih.gov/pubmed/33057110 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-74192-9 |
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