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Akademický článek

Pendrin stimulates a chloride absorption pathway to increase CFTR‐mediated chloride secretion from Cystic Fibrosis airway epithelia

Autor: Jeffrey Bajko, Mei Duguid, Steve Altmann, Gregory D. Hurlbut, J. Stefan Kaczmarek

Publikováno v: FASEB BioAdvances, Vol 2, Iss 9, Pp 526-537 (2020)

Abstract Cystic Fibrosis (CF), an inherited multi‐system disease, is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) that disrupt its ability to secrete anions from epithelia. Recovery of functional anion secre

Externí odkaz: https://doaj.org/article/226b8725f8634eb099cd8b16bb7bd856

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Pendrin stimulates a chloride absorption pathway to increase CFTR‐mediated chloride secretion from Cystic Fibrosis airway epithelia

Autor: Gregory D. Hurlbut, J. Stefan Kaczmarek, Jeffrey Bajko, Steve Altmann, Mei Duguid

Publikováno v: FASEB BioAdvances, Vol 2, Iss 9, Pp 526-537 (2020)
FASEB BioAdvances

Cystic Fibrosis (CF), an inherited multi‐system disease, is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) that disrupt its ability to secrete anions from epithelia. Recovery of functional anion secretion may

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::598e756a0326d917917215a033b44040
https://doaj.org/article/226b8725f8634eb099cd8b16bb7bd856

Zobrazit plný text záznamu

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