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The tissue activity of the H 2 O 2 metabolizing enzyme glutathione peroxidase was determined using glutathione reductase and then measuring the rate of NADPH oxidation at an absorbance of 340 nm using H 2 O 2 as the substrate [28]

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We next comparatively assessed the rate of reaction of WT or GLRX mutants with diE-GSSG or E-GS-BSA

Cisplatin-induced renal cell apoptosis: Caspase 3-dependent and -independent pathways