glutathione deficiency cystic fibrosis Rethinking pathology: the critical role of abnormal reduced (GSH) transport caused by CFTR mutation Oxidative Stress Biomarkers in Cystic
Description
10.1016/s0165-5728(00)00231-9 J
Therefore, GH maintains triglyceride storage in the liver through three mechanisms, inhibiting intrahepatic triglyceride lipolysis, inhibiting lipid oxidation, and enhancing lipogenesis ( More recently, the surface proteins of lipid droplets (LD) have been studied for their multiple functions, including the regulation of lipolysis
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Yon L., Feuilloley M., Charnay Y., Vaudry H
