These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 10486308)

  • 1. Glutathione conjugation of 4-hydroxy-trans-2,3-nonenal in the rat in vivo, the isolated perfused liver and erythrocytes.
    Boon PJ; Marinho HS; Oosting R; Mulder GJ
    Toxicol Appl Pharmacol; 1999 Sep; 159(3):214-23. PubMed ID: 10486308
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Glutathione conjugates of 4-hydroxy-2(E)-nonenal as biomarkers of hepatic oxidative stress-induced lipid peroxidation in rats.
    Völkel W; Alvarez-Sánchez R; Weick I; Mally A; Dekant W; Pähler A
    Free Radic Biol Med; 2005 Jun; 38(11):1526-36. PubMed ID: 15890627
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Glutathionylated 4-hydroxy-2-(E)-alkenal enantiomers in rat organs and their contributions toward the disposal of 4-hydroxy-2-(E)-nonenal in rat liver.
    Sadhukhan S; Han Y; Jin Z; Tochtrop GP; Zhang GF
    Free Radic Biol Med; 2014 May; 70():78-85. PubMed ID: 24556413
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of intermediate pathways of 4-hydroxynonenal metabolism in the rat.
    Alary J; Fernandez Y; Debrauwer L; Perdu E; Guéraud F
    Chem Res Toxicol; 2003 Mar; 16(3):320-7. PubMed ID: 12641432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multidrug resistance-associated protein2 (MRP2) plays an important role in the biliary excretion of glutathione conjugates of 4-hydroxynonenal.
    Ji B; Ito K; Suzuki H; Sugiyama Y; Horie T
    Free Radic Biol Med; 2002 Aug; 33(3):370-8. PubMed ID: 12126759
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Is the glutathione conjugate of trans-4-hydroxy-2-nonenal transported by the multispecific organic anion transporting-ATPase of human erythrocytes?
    Dygas A; Makowski P; Pikuła S
    Acta Biochim Pol; 1998; 45(1):59-65. PubMed ID: 9701496
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis in the rat of 4-hydroxynonenal metabolites excreted in bile: evidence of enterohepatic circulation of these byproducts of lipid peroxidation.
    Laurent A; Alary J; Debrauwer L; Cravedi JP
    Chem Res Toxicol; 1999 Oct; 12(10):887-94. PubMed ID: 10525263
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Formation and export of the glutathione conjugate of 4-hydroxy-2, 3-E-nonenal (4-HNE) in hepatoma cells.
    Tjalkens RB; Cook LW; Petersen DR
    Arch Biochem Biophys; 1999 Jan; 361(1):113-9. PubMed ID: 9882435
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Metabolism of 4-hydroxynonenal, a cytotoxic product of lipid peroxidation, in rat precision-cut liver slices.
    Laurent A; Perdu-Durand E; Alary J; Debrauwer L; Cravedi JP
    Toxicol Lett; 2000 Apr; 114(1-3):203-14. PubMed ID: 10713486
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The fate of diastereomeric glutathione conjugates of alpha-bromoisovalerylurea in blood in the rat in vivo and in the perfused liver. Stereoselectivity in biliary and urinary excretion.
    Polhuijs M; Meijer DK; Mulder GJ
    J Pharmacol Exp Ther; 1991 Feb; 256(2):458-61. PubMed ID: 1993989
    [TBL] [Abstract][Full Text] [Related]  

  • 11. alpha-Bromoisovalerylurea as model substrate for studies on pharmacokinetics of glutathione conjugation in the rat. II. Pharmacokinetics and stereoselectivity of metabolism and excretion in vivo and in the perfused liver.
    te Koppele JM; Dogterom P; Vermeulen NP; Meijer DK; van der Gen A; Mulder GJ
    J Pharmacol Exp Ther; 1986 Dec; 239(3):905-14. PubMed ID: 3795049
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat.
    Alary J; Bravais F; Cravedi JP; Debrauwer L; Rao D; Bories G
    Chem Res Toxicol; 1995; 8(1):34-9. PubMed ID: 7703364
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Metabolism of the lipid peroxidation product, 4-hydroxy-trans-2-nonenal, in isolated perfused rat heart.
    Srivastava S; Chandra A; Wang LF; Seifert WE; DaGue BB; Ansari NH; Srivastava SK; Bhatnagar A
    J Biol Chem; 1998 May; 273(18):10893-900. PubMed ID: 9556565
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lack of glutathione conjugation of melphalan in the isolated in situ liver perfusion in humans.
    Vahrmeijer AL; Snel CA; Steenvoorden DP; Beijnen JH; Pang KS; Schutrups J; Tirona R; Keizer HJ; van Dierendonck JH; van de Velde CJ; Mulder GJ
    Cancer Res; 1996 Oct; 56(20):4709-14. PubMed ID: 8840988
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of metabolic pathways of the lipid peroxidation product 4-hydroxynonenal in in situ perfused rat kidney.
    Grune T; Siems WG; Petras T
    J Lipid Res; 1997 Aug; 38(8):1660-5. PubMed ID: 9300788
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detoxification of cytotoxic alpha,beta-unsaturated aldehydes by carnosine: characterization of conjugated adducts by electrospray ionization tandem mass spectrometry and detection by liquid chromatography/mass spectrometry in rat skeletal muscle.
    Aldini G; Granata P; Carini M
    J Mass Spectrom; 2002 Dec; 37(12):1219-28. PubMed ID: 12489081
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Enantioselective metabolism of (R)- and (S)-4-hydroxy-2-nonenal in rat.
    Guéraud F; Crouzet F; Alary J; Rao D; Debrauwer L; Laurent F; Cravedi JP
    Biofactors; 2005; 24(1-4):97-104. PubMed ID: 16403968
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitogenic responses of vascular smooth muscle cells to lipid peroxidation-derived aldehyde 4-hydroxy-trans-2-nonenal (HNE): role of aldose reductase-catalyzed reduction of the HNE-glutathione conjugates in regulating cell growth.
    Ramana KV; Bhatnagar A; Srivastava S; Yadav UC; Awasthi S; Awasthi YC; Srivastava SK
    J Biol Chem; 2006 Jun; 281(26):17652-60. PubMed ID: 16648138
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The hepatocellular metabolism of 4-hydroxynonenal by alcohol dehydrogenase, aldehyde dehydrogenase, and glutathione S-transferase.
    Hartley DP; Ruth JA; Petersen DR
    Arch Biochem Biophys; 1995 Jan; 316(1):197-205. PubMed ID: 7840616
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Low glutathione level favors formation of DNA adducts to 4-hydroxy-2(E)-nonenal, a major lipid peroxidation product.
    Falletti O; Douki T
    Chem Res Toxicol; 2008 Nov; 21(11):2097-105. PubMed ID: 18847228
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.