CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity

The cystic fibrosis transmembrane conductance regulator (CFTR) mutation ΔF508CFTR still causes regulatory defects when rescued to the apical membrane, suggesting that the intracellular milieu might affect its ability to respond to cAMP regulation. We recently reported that overexpression of the Na(+...

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Detalhes bibliográficos
Main Authors: Monterisi, Stefania, Favia, Maria, Guerra, Lorenzo, Cardone, Rosa A., Marzulli, Domenico, Reshkin, Stephan J., Casavola, Valeria, Zaccolo, Manuela
Formato: Artigo
Idioma:Inglês
Publicado em: Company of Biologists 2012
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3324578/
https://ncbi.nlm.nih.gov/pubmed/22302988
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.089086
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