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Reversible Silencing of CFTR Chloride Channels by Glutathionylation
The cystic fibrosis transmembrane conductance regulator (CFTR) is a phosphorylation- and ATP-dependent chloride channel that modulates salt and water transport across lung and gut epithelia. The relationship between CFTR and oxidized forms of glutathione is of potential interest because reactive glu...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Rockefeller University Press
2005
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2217496/ https://ncbi.nlm.nih.gov/pubmed/15657297 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.200409115 |
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