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Journal Abstract Search

269 related items for PubMed ID: 11325611

  • 1. Aldehydic lipid peroxidation products derived from linoleic acid.
    Spiteller P, Kern W, Reiner J, Spiteller G.
    Biochim Biophys Acta; 2001 Apr 30; 1531(3):188-208. PubMed ID: 11325611
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  • 5. Previously unknown aldehydic lipid peroxidation compounds of arachidonic acid.
    Mlakar A, Spiteller G.
    Chem Phys Lipids; 1996 Jan 25; 79(1):47-53. PubMed ID: 8907242
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  • 8. Two distinct pathways of formation of 4-hydroxynonenal. Mechanisms of nonenzymatic transformation of the 9- and 13-hydroperoxides of linoleic acid to 4-hydroxyalkenals.
    Schneider C, Tallman KA, Porter NA, Brash AR.
    J Biol Chem; 2001 Jun 15; 276(24):20831-8. PubMed ID: 11259420
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  • 9. Reduction of 13-hydroperoxy-9,11-octadecadienoic acid by dopamine-melanin.
    Stepień K, Zajdel A, Swierczek G, Wilczok A, Wilczok T.
    Biochem Biophys Res Commun; 1998 Mar 27; 244(3):781-4. PubMed ID: 9535742
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  • 10. Mechanism of linoleic acid hydroperoxide reaction with alkali.
    Gardner HW, Simpson TD, Hamberg M.
    Lipids; 1996 Oct 27; 31(10):1023-8. PubMed ID: 8898300
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  • 11. Gas chromatographic-electron impact mass spectrometric screening procedure for unknown hydroxyaldehydic lipid peroxidation products after pentafluorobenzyloxime derivatization.
    Loidl-Stahlhofen A, Kern W, Spiteller G.
    J Chromatogr B Biomed Appl; 1995 Nov 03; 673(1):1-14. PubMed ID: 8925062
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  • 12. Linoleic acid oxidation in the presence of amino compounds produces pyrroles by carbonyl amine reactions.
    Zamora R, Hidalgo FJ.
    Biochim Biophys Acta; 1995 Oct 05; 1258(3):319-27. PubMed ID: 7548203
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  • 13. Effect of 4-hydroxy-2(E)-nonenal on soybean lipoxygenase-1.
    Gardner HW, Deighton N.
    Lipids; 2001 Jun 05; 36(6):623-8. PubMed ID: 11485167
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  • 14. Strong dependence of the lipid peroxidation product spectrum whether Fe2+/O2 or Fe3+/O2 is used as oxidant.
    Spiteller P, Spiteller G.
    Biochim Biophys Acta; 1998 May 20; 1392(1):23-40. PubMed ID: 9593808
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  • 15. Liquid chromatography/mass spectrometry analysis of bifunctional electrophiles and DNA adducts from vitamin C mediated decomposition of 15-hydroperoxyeicosatetraenoic acid.
    Williams MV, Lee SH, Blair IA.
    Rapid Commun Mass Spectrom; 2005 May 20; 19(6):849-58. PubMed ID: 15723435
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  • 16. alpha-Hydroxyaldehydes, products of lipid peroxidation.
    Loidl-Stahlhofen A, Spiteller G.
    Biochim Biophys Acta; 1994 Mar 03; 1211(2):156-60. PubMed ID: 8117742
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  • 17. Formation of Aldehydic Phosphatidylcholines during the Anaerobic Decomposition of a Phosphatidylcholine Bearing the 9-Hydroperoxide of Linoleic Acid.
    Onyango AN.
    Biomed Res Int; 2016 Mar 03; 2016():8218439. PubMed ID: 27366754
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  • 18. Vitamin C conjugates of genotoxic lipid peroxidation products: structural characterization and detection in human plasma.
    Sowell J, Frei B, Stevens JF.
    Proc Natl Acad Sci U S A; 2004 Dec 28; 101(52):17964-9. PubMed ID: 15608056
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  • 19. Formation of ketodienoic fatty acids by the pure pea lipoxygenase-1.
    Kühn H, Wiesner R, Rathmann J, Schewe T.
    Eicosanoids; 1991 Dec 28; 4(1):9-14. PubMed ID: 1905562
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  • 20. Lipid peroxidation in aging and age-dependent diseases.
    Spiteller G.
    Exp Gerontol; 2001 Sep 28; 36(9):1425-57. PubMed ID: 11525868
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