CFTR-NHERF2-LPA(2) Complex in the Airway and Gut Epithelia

The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP- and cGMP-regulated chloride (Cl(−)) and bicarbonate (HCO(3)(−)) channel localized primarily at the apical plasma membrane of epithelial cells lining the airway, gut and exocrine glands, where it is responsible for transepithel...

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Detalles Bibliográficos
Autores principales: Zhang, Weiqiang, Zhang, Zhihong, Zhang, Yanhui, Naren, Anjaparavanda P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618545/
https://www.ncbi.nlm.nih.gov/pubmed/28869532
http://dx.doi.org/10.3390/ijms18091896

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618545/
https://www.ncbi.nlm.nih.gov/pubmed/28869532
http://dx.doi.org/10.3390/ijms18091896

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