Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator
CFTR is a cyclic AMP (cAMP)-activated chloride (Cl(−)) channel and a regulator of outwardly rectifying Cl(−) channels (ORCCs) in airway epithelia. CFTR regulates ORCCs by facilitating the release of ATP out of cells. Once released from cells, ATP stimulates ORCCs by means of a purinergic receptor. T...
Uloženo v:
| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1998
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC19458/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9482946/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.95.5.2674 |
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