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Journal Abstract Search

114 related items for PubMed ID: 2155662

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  • 3. Oxidation of 20-hydroxyleukotriene B4 to 20-carboxyleukotriene B4 by human neutrophil microsomes. Role of aldehyde dehydrogenase and leukotriene B4 omega-hydroxylase (cytochrome P-450LTB omega) in leukotriene B4 omega-oxidation.
    Sumimoto H, Minakami S.
    J Biol Chem; 1990 Mar 15; 265(8):4348-53. PubMed ID: 2155225
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  • 4. Purification and characterization of 20-hydroxy-leukotriene B4 dehydrogenase in human neutrophils.
    Gotoh Y, Sumimoto H, Minakami S.
    Eur J Biochem; 1989 Feb 01; 179(2):315-21. PubMed ID: 2537206
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  • 5. Identification of an aldehyde dehydrogenase in the microsomes of human polymorphonuclear leukocytes that metabolizes 20-aldehyde leukotriene B4.
    Sutyak J, Austen KF, Soberman RJ.
    J Biol Chem; 1989 Sep 05; 264(25):14818-23. PubMed ID: 2549038
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  • 6. Mechanism for the formation of dihydro metabolites of 12-hydroxyeicosanoids. Conversion of leukotriene B4 and 12-hydroxy-5,8,10,14-eicosatetraenoic acid to 12-oxo intermediates.
    Wainwright SL, Powell WS.
    J Biol Chem; 1991 Nov 05; 266(31):20899-906. PubMed ID: 1657938
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  • 7. NAD+-dependent oxidation of 20-hydroxyleukotriene B4 to 20-carboxyleukotriene B4 by rat liver cytosol.
    Gotoh Y, Sumimoto H, Takeshige K, Minakami S.
    Biochim Biophys Acta; 1988 Jun 15; 960(3):342-50. PubMed ID: 2838090
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  • 8. NAD+-dependent conversion of 20-OH-LTB4 to 20-COOH-LTB4 by a cell-free system of human polymorphonuclear leukocytes.
    Sumimoto H, Takeshige K, Minakami S.
    Biochem Biophys Res Commun; 1985 Nov 15; 132(3):864-70. PubMed ID: 3000366
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  • 9. Isocratic determination of arachidonic acid 5-lipoxygenase products in human neutrophils by high-performance liquid chromatography.
    Mita H, Yui Y, Yasueda H, Shida T.
    J Chromatogr; 1988 Sep 09; 430(2):299-308. PubMed ID: 2853166
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  • 10. Linoleic acid and dihomogammalinolenic acid inhibit leukotriene B4 formation and stimulate the formation of their 15-lipoxygenase products by human neutrophils in vitro. Evidence of formation of antiinflammatory compounds.
    Iversen L, Fogh K, Bojesen G, Kragballe K.
    Agents Actions; 1991 Jul 09; 33(3-4):286-91. PubMed ID: 1659156
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  • 11. Omega-hydroxylation of lipoxin B4 by human neutrophil microsomes: identification of omega-hydroxy metabolite of lipoxin B4 and catalysis by leukotriene B4 omega-hydroxylase (cytochrome P-450LTB omega).
    Mizukami Y, Sumimoto H, Isobe R, Minakami S.
    Biochim Biophys Acta; 1993 May 20; 1168(1):87-93. PubMed ID: 8389204
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  • 12. Metabolism of 12(S)-hydroxy-5,8,10,14-eicosatetraenoic acid and other hydroxylated fatty acids by the reductase pathway in porcine polymorphonuclear leukocytes.
    Wainwright S, Falck JR, Yadagiri P, Powell WS.
    Biochemistry; 1990 Oct 30; 29(43):10126-35. PubMed ID: 2176862
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  • 13. Metabolism of 5(S)-hydroxy-6,8,11,14-eicosatetraenoic acid and other 5(S)-hydroxyeicosanoids by a specific dehydrogenase in human polymorphonuclear leukocytes.
    Powell WS, Gravelle F, Gravel S.
    J Biol Chem; 1992 Sep 25; 267(27):19233-41. PubMed ID: 1326548
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  • 14. Effects of exogenous arachidonic, eicosapentaenoic, and docosahexaenoic acids on the generation of 5-lipoxygenase pathway products by ionophore-activated human neutrophils.
    Lee TH, Mencia-Huerta JM, Shih C, Corey EJ, Lewis RA, Austen KF.
    J Clin Invest; 1984 Dec 25; 74(6):1922-33. PubMed ID: 6096400
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  • 15. Stereochemistry of leukotriene B4 metabolites formed by the reductase pathway in porcine polymorphonuclear leukocytes: inversion of stereochemistry of the 12-hydroxyl group.
    Wainwright S, Falck JR, Yadagiri P, Powell WS.
    Biochemistry; 1990 Feb 06; 29(5):1180-5. PubMed ID: 2157486
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  • 16. Stereospecificity of leukotriene B4 and structure-function relationships for chemotaxis of human neutrophils.
    Dahinden CA, Clancy RM, Hugli TE.
    J Immunol; 1984 Sep 06; 133(3):1477-82. PubMed ID: 6086758
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  • 17. Intracellular retention of the 5-lipoxygenase pathway product, leukotriene B4, by human neutrophils activated with unopsonized zymosan.
    Williams JD, Lee TH, Lewis RA, Austen F.
    J Immunol; 1985 Apr 06; 134(4):2624-30. PubMed ID: 2982947
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  • 18. Stereochemical analysis and biological activity of 3-hydroxy-leukotriene B4: a metabolite from ethanol-treated rat hepatocytes.
    Wheelan P, Sala A, Folco G, Nicosia S, Falck JR, Bhatt RK, Murphy RC.
    J Pharmacol Exp Ther; 1994 Dec 06; 271(3):1514-9. PubMed ID: 7996465
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