interaction of haloacetonitriles with glutathione and glutathione-s-transferase

interaction of haloacetonitriles with glutathione and glutathione-s-transferase S-transferase: A versatile dynamic enzyme Glutathione Transferase Health risk assessment of haloacetonitriles

Name: interaction of haloacetonitriles with glutathione and glutathione-s-transferase S-transferase: A versatile dynamic enzyme Glutathione Transferase Health risk assessment of haloacetonitriles
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Health risk assessment of haloacetonitriles in drinking water based on internal dose ScienceDirect Haloacetonitrile stability in cell culture media used in vitro toxicological studies ScienceDirect Overexpression of Glutathione S Transferases in Human Diseases: Drug Targets and Therapeutic Implications Glutathione S Transferases as Potential Targets for Modulation of Nitric Oxide Mediated Vasodilation

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This notion receives some support from microarray analysis of GRX gene expression in mutants with pertur- bations in leaf glutathione redox state, in which specic members of class III were the only GRX that were found to respond (Mhamdi et al

For example, wild-type TP53 is able to inhibit glycolysis by suppressing the expression of GLUT1, GLUT3, and GLUT4 (160, 161), and regulating the expression of enzymes involved in the glycolytic pathway, such as HK2 (162), phosphofructokinase 1 (PFK1) (163), phosphoglycerate mutase (PGM) (163), pyruvate dehydrogenase (PDH), parkin 2 (PARK2) (164), and pyruvate dehydrogenase kinase (PDK2) (165)