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L-Type Ca(2+) Channel Function Is Linked to Dystrophin Expression in Mammalian Muscle
BACKGROUND: In dystrophic mdx skeletal muscle, aberrant Ca(2+) homeostasis and fibre degeneration are found. The absence of dystrophin in models of Duchenne muscular dystrophy (DMD) has been connected to altered ion channel properties e.g. impaired L-type Ca(2+) currents. In regenerating mdx muscle,...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2408559/ https://ncbi.nlm.nih.gov/pubmed/18516256 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0001762 |
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