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The absence of dysferlin induces the expression of functional connexin-based hemichannels in human myotubes

BACKGROUND: Mutations in the gene encoding for dysferlin cause recessive autosomal muscular dystrophies called dysferlinopathies. These mutations induce several alterations in skeletal muscles, including, inflammation, increased membrane permeability and cell death. Despite the fact that the etiolog...

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Detalhes bibliográficos
Publicado no:BMC Cell Biol
Main Authors: Cea, Luis A., Bevilacqua, Jorge A., Arriagada, Christian, Cárdenas, Ana María, Bigot, Anne, Mouly, Vincent, Sáez, Juan C., Caviedes, Pablo
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4896263/
https://ncbi.nlm.nih.gov/pubmed/27229680
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12860-016-0096-6
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