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Journal Abstract Search

180 related items for PubMed ID: 4018089

  • 1.
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  • 2. Malarial parasite hexokinase and hexokinase-dependent glutathione reduction in the Plasmodium falciparum-infected human erythrocyte.
    Roth EF.
    J Biol Chem; 1987 Nov 15; 262(32):15678-82. PubMed ID: 3316204
    [Abstract] [Full Text] [Related]

  • 3. Multiple NADPH-producing pathways control glutathione (GSH) content in retina.
    Winkler BS, DeSantis N, Solomon F.
    Exp Eye Res; 1986 Nov 15; 43(5):829-47. PubMed ID: 3803464
    [Abstract] [Full Text] [Related]

  • 4. Hexose monophosphate shunt activity in erythrocytes related to cell age.
    Ouwerkerk R, Damen P, de Haan K, Staal GE, Rijksen G.
    Eur J Haematol; 1989 Nov 15; 43(5):441-7. PubMed ID: 2612618
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  • 7. Glutathione Depletion, Pentose Phosphate Pathway Activation, and Hemolysis in Erythrocytes Protecting Cancer Cells from Vitamin C-induced Oxidative Stress.
    Zhang ZZ, Lee EE, Sudderth J, Yue Y, Zia A, Glass D, Deberardinis RJ, Wang RC.
    J Biol Chem; 2016 Oct 28; 291(44):22861-22867. PubMed ID: 27660392
    [Abstract] [Full Text] [Related]

  • 8. Role of hexokinase in the regulation of erythrocyte hexose monophosphate pathway under oxidative stress.
    Magnani M, Rossi L, Bianchi M, Serafini G, Stocchi V.
    Biochem Biophys Res Commun; 1988 Aug 30; 155(1):423-8. PubMed ID: 3415698
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  • 9. Interrelations between glycolysis and the hexose monophosphate shunt in erythrocytes as studied on the basis of a mathematical model.
    Schuster R, Holzhütter HG, Jacobasch G.
    Biosystems; 1988 Aug 30; 22(1):19-36. PubMed ID: 3191218
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  • 10. Intracellular restraint: a new basis for the limitation in response to oxidative stress in human erythrocytes containing low-activity variants of glucose-6-phosphate dehydrogenase.
    Gaetani GD, Parker JC, Kirkman HN.
    Proc Natl Acad Sci U S A; 1974 Sep 30; 71(9):3584-7. PubMed ID: 4154443
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  • 11. Ribose metabolism and nucleic acid synthesis in normal and glucose-6-phosphate dehydrogenase-deficient human erythrocytes infected with Plasmodium falciparum.
    Roth EF, Ruprecht RM, Schulman S, Vanderberg J, Olson JA.
    J Clin Invest; 1986 Apr 30; 77(4):1129-35. PubMed ID: 2420826
    [Abstract] [Full Text] [Related]

  • 12. Defenses against oxidation in human erythrocytes: role of glutathione reductase in the activation of glucose decarboxylation by hemolytic drugs.
    Hohl RJ, Kennedy EJ, Frischer H.
    J Lab Clin Med; 1991 Apr 30; 117(4):325-31. PubMed ID: 1901343
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  • 13. Toxicity of aromatic thiols in the human red blood cell.
    Amrolia P, Sullivan SG, Stern A, Munday R.
    J Appl Toxicol; 1989 Apr 30; 9(2):113-8. PubMed ID: 2715566
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  • 14. Stimulation of the hexose monophosphate shunt in bovine ciliary body under oxidative stress.
    Shichi H, Hodder WA, Giblin FJ.
    J Ocul Pharmacol; 1986 Apr 30; 2(1):59-66. PubMed ID: 3503098
    [Abstract] [Full Text] [Related]

  • 15. Comparison of computer simulations of the F-type and L-type non-oxidative hexose monophosphate shunts with 31P-NMR experimental data from human erythrocytes.
    McIntyre LM, Thorburn DR, Bubb WA, Kuchel PW.
    Eur J Biochem; 1989 Mar 15; 180(2):399-420. PubMed ID: 2924774
    [Abstract] [Full Text] [Related]

  • 16. Useful agents for the study of glutathione metabolism in erythroyctes. Organic hydroperoxides.
    Srivastava SK, Awasthi YC, Beutler E.
    Biochem J; 1974 May 15; 139(2):289-95. PubMed ID: 4447610
    [Abstract] [Full Text] [Related]

  • 17. The malaria parasite supplies glutathione to its host cell--investigation of glutathione transport and metabolism in human erythrocytes infected with Plasmodium falciparum.
    Atamna H, Ginsburg H.
    Eur J Biochem; 1997 Dec 15; 250(3):670-9. PubMed ID: 9461289
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  • 18.
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  • 19. Role of protein -SH groups in redox homeostasis--the erythrocyte as a model system.
    Di Simplicio P, Cacace MG, Lusini L, Giannerini F, Giustarini D, Rossi R.
    Arch Biochem Biophys; 1998 Jul 15; 355(2):145-52. PubMed ID: 9675020
    [Abstract] [Full Text] [Related]

  • 20. Substrates of hexokinase, glucose-6-phosphate dehydrogenase, and glyceraldehyde-3-phosphate dehydrogenase prevent the inhibitory response induced by ascorbic acid/iron and dehydroascorbic acid in rabbit erythrocytes.
    Fiorani M, De Sanctis R, Scarlatti F, Stocchi V.
    Arch Biochem Biophys; 1998 Aug 15; 356(2):159-66. PubMed ID: 9705206
    [Abstract] [Full Text] [Related]

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