Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.

Cystic fibrosis is caused by mutations in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR). To further our understanding of CFTR's function and regulation, we used confocal immunofluorescence microscopy to localize CFTR in cells stained with monoclonal antibodies ag...

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Veröffentlicht in:	J Clin Invest
Hauptverfasser:	Denning, G M, Ostedgaard, L S, Cheng, S H, Smith, A E, Welsh, M J
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Clinical Investigation 1992
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC442854/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1370301/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115582
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