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Editorial Focus: CFTR‐dependent bicarbonate secretion by Calu‐3 cells

Cystic Fibrosis is an autosomal recessive multisystem disease caused by the severely impaired or absent function of the Cystic Fibrosis Transmembrane Conductance Regulator, CFTR. While CFTR is best recognized as a Cl‐ channel, impairment of CFTR‐dependent bicarbonate transport is increasingly recogn...

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Detalles Bibliográficos
Autor principal:	Rubenstein, Ronald C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2018
Materias:	Editorial
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974715/ https://www.ncbi.nlm.nih.gov/pubmed/29845767 http://dx.doi.org/10.14814/phy2.13691

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