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Duchenne muscular dystrophy models show their age
The lack of appropriate animal models has hampered efforts to develop therapies for Duchenne muscular dystrophy (DMD). A new mouse model lacking both dystrophin and telomerase (Sacco et al., 2010) closely mimics the pathological progression of human DMD and shows that muscle stem cell activity is a...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3038548/ https://ncbi.nlm.nih.gov/pubmed/21183068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2010.12.005 |
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