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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:BMC Cell Biol
Päätekijät: Cea, Luis A., Bevilacqua, Jorge A., Arriagada, Christian, Cárdenas, Ana María, Bigot, Anne, Mouly, Vincent, Sáez, Juan C., Caviedes, Pablo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2016
Aiheet:
Research
Linkit: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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