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Overexpression of Staufen1 in DM1 mouse skeletal muscle exacerbates dystrophic and atrophic features
In myotonic dystrophy type 1 (DM1), the CUG expansion (CUG(exp)) in the 3′ untranslated region of the dystrophia myotonica protein kinase messenger ribonucleic acid affects the homeostasis of ribonucleic acid-binding proteins, causing the multiple symptoms of DM1. We have previously reported that St...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7399530/ https://ncbi.nlm.nih.gov/pubmed/32504084 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddaa111 |
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