Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis.

The transepithelial chloride permeability of airway and sweat ductal epithelium has been reported to be decreased in patients with cystic fibrosis (CF). In the present study, we investigated whether the airway epithelial defect was in the cell path by characterizing the relative ion permeabilities o...

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Pubblicato in:	J Clin Invest
Autori principali:	Cotton, C U, Stutts, M J, Knowles, M R, Gatzy, J T, Boucher, R C
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Clinical Investigation 1987
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423991/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3793933/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112812
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