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A role for CFTR in the elevation of glutathione levels in the lung by oral glutathione administration

The cystic fibrosis transmembrane conductance regulator (CFTR) protein is the only known apical glutathione (GSH) transporter in the lung. The purpose of these studies was to determine whether oral GSH or glutathione disulfide (GSSG) treatment could increase lung epithelial lining fluid (ELF) GSH le...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Kariya, Chirag, Leitner, Heather, Min, Elysia, van Heeckeren, Christiaan, van Heeckeren, Anna, Day, Brian J.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2007
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3983954/
https://ncbi.nlm.nih.gov/pubmed/17369290
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00365.2006
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