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Utrophin regulates modal gating of mechanosensitive ion channels in dystrophic skeletal muscle
Dystrophin is a large, submembrane cytoskeletal protein, absence of which causes Duchenne muscular dystrophy. Utrophin is a dystrophin homologue found in both muscle and brain whose physiological function is unknown. Recordings of single-channel activity were made from membrane patches on skeletal m...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BlackWell Publishing Ltd
2014
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4146377/ https://ncbi.nlm.nih.gov/pubmed/24879867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2014.274332 |
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