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The emerging potential of autophagy-based therapies in the treatment of cystic fibrosis lung infections

Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR), a channel that normally transports anions across epithelial cell membranes. The most common manifestation of CF is buildup of mucus in the airways and bacterial colonization of the lower respiratory tra...

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Detalhes bibliográficos
Main Authors: Junkins, Robert D, McCormick, Craig, Lin, Tong-Jun
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4077897/
https://ncbi.nlm.nih.gov/pubmed/24434788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/auto.27750
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