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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Detalles Bibliográficos
Autores principales: Cea, Luis A., Bevilacqua, Jorge A., Arriagada, Christian, Cárdenas, Ana María, Bigot, Anne, Mouly, Vincent, Sáez, Juan C., Caviedes, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896263/
https://www.ncbi.nlm.nih.gov/pubmed/27229680
http://dx.doi.org/10.1186/s12860-016-0096-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896263/
https://www.ncbi.nlm.nih.gov/pubmed/27229680
http://dx.doi.org/10.1186/s12860-016-0096-6

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