Vitamin C controls the cystic fibrosis transmembrane conductance regulator chloride channel
Vitamin C (l-ascorbate) is present in the respiratory lining fluid of human lungs, and local deficits occur during oxidative stress. Here we report a unique function of vitamin C on the cystic fibrosis (CF) transmembrane conductance regulator (CFTR), a cAMP-dependent Cl channel that regulates epithe...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2004
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC373524/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14993613/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0308393100 |
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