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CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes

The cystic fibrosis transmembrane conductance regulator (CFTR) plays a crucial role in regulating fluid secretion by the airways, intestines, sweat glands and other epithelial tissues. It is well established that the CFTR is a cAMP-activated, nucleotide-dependent anion channel, but additional functi...

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Autores principales: Nagel, G, Barbry, P, Chabot, H, Brochiero, E, Hartung, K, Grygorczyk, R
Formato: Artigo
Lenguaje:Inglês
Publicado: Blackwell Science Inc 2005
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1464468/
https://ncbi.nlm.nih.gov/pubmed/15746174
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2004.079046
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