Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.

Cystic fibrosis (CF) is characterized by an abnormality in cAMP-regulated chloride transport that results from a primary defect in the protein product of the CF gene, the CF transmembrane conductance regulator (CFTR). In this report, antibodies against CFTR peptides were used to localize the CFTR pr...

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Detalles Bibliográficos

Publicado en:	J Clin Invest
Autores principales:	Marino, C R, Matovcik, L M, Gorelick, F S, Cohn, J A
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	American Society for Clinical Investigation 1991
Materias:	Research Article
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC295422/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1713921/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115358
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