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| Q72596028 | Extracellular metabolism of glutathione accounts for its disappearance from the basolateral circulation of the kidney |
| Q35359325 | Formation of gamma-glutamycyst(e)ine in vivo is catalyzed by gamma-glutamyl transpeptidase |
| Q46576674 | Gamma-glutamyl transpeptidase in glutathione biosynthesis |
| Q34307571 | Glutathione is required for intestinal function |
| Q83216917 | Glutathione-indole-3-acetonitrile is required for camalexin biosynthesis in Arabidopsis thaliana |
| Q37270914 | Glutathione: overview of its protective roles, measurement, and biosynthesis |
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| Q37706607 | Identification of a highly reactive threonine residue at the active site of gamma-glutamyl transpeptidase |
| Q44016819 | Increased macrophage glutathione content reduces cell-mediated oxidation of LDL and atherosclerosis in apolipoprotein E-deficient mice |
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| Q46057381 | Nonenzymatic, self-elimination degradation mechanism of glutathione. |
| Q40085021 | On the Cycles of Glutathione Metabolism and Transport |
| Q43976703 | Oxidative stress increases the expression of the angiotensin-II receptor type 1 in mouse peritoneal macrophages |
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| Q54440299 | The effect of H2O2 on lens epithelial cell glutathione. |
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