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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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Denning, G M, Ostedgaard, L S, Cheng, S H, Smith, A E, Welsh, M J
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1992
Assuntos:	Research Article
Acesso em linha:	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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