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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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Bibliografiske detaljer
Udgivet i:J Clin Invest
Principais autores: Cotton, C U, Stutts, M J, Knowles, M R, Gatzy, J T, Boucher, R C
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Clinical Investigation 1987
Fag:
Online adgang: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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