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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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| Udgivet i: | Int J Mol Sci |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5618545/ https://ncbi.nlm.nih.gov/pubmed/28869532 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18091896 |
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