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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Bibliografiske detaljer

Udgivet i:	J Clin Invest
Principais autores:	Denning, G M, Ostedgaard, L S, Cheng, S H, Smith, A E, Welsh, M J
Format:	Artigo
Sprog:	Inglês
Udgivet:	American Society for Clinical Investigation 1992
Fag:	Research Article
Online adgang:	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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