Defective fluid transport by cystic fibrosis airway epithelia.

Cystic fibrosis (CF) airway epithelia exhibit defective transepithelial electrolyte transport: cAMP-stimulated Cl- secretion is abolished because of the loss of apical membrane cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channels, and amiloride-sensitive Na+ absorption is increase...

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Pubblicato in:	J Clin Invest
Autori principali:	Smith, J J, Karp, P H, Welsh, M J
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Clinical Investigation 1994
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC294089/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8132771/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI117087
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