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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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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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John Wiley and Sons Inc.
2018
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| 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 |