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PUBMED FOR HANDHELDS

Journal Abstract Search


210 related items for PubMed ID: 30819615

  • 1. 2-Alkenal modification of hemoglobin: Identification of a novel hemoglobin-specific alkanoic acid-histidine adduct.
    Yoshitake J, Shibata T, Shimayama C, Uchida K.
    Redox Biol; 2019 May; 23():101115. PubMed ID: 30819615
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  • 2. Quantitative analysis of acrolein-specific adducts generated during lipid peroxidation-modification of proteins in vitro: identification of N(τ)-(3-propanal)histidine as the major adduct.
    Maeshima T, Honda K, Chikazawa M, Shibata T, Kawai Y, Akagawa M, Uchida K.
    Chem Res Toxicol; 2012 Jul 16; 25(7):1384-92. PubMed ID: 22716039
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  • 5. Reactive aldehyde metabolites from the anti-HIV drug abacavir: amino acid adducts as possible factors in abacavir toxicity.
    Charneira C, Godinho AL, Oliveira MC, Pereira SA, Monteiro EC, Marques MM, Antunes AM.
    Chem Res Toxicol; 2011 Dec 19; 24(12):2129-41. PubMed ID: 22032494
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  • 6. 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 19; 37(12):1219-28. PubMed ID: 12489081
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  • 11. Abundance of DNA adducts of 4-oxo-2-alkenals, lipid peroxidation-derived highly reactive genotoxins.
    Kawai Y, Nuka E.
    J Clin Biochem Nutr; 2018 Jan 19; 62(1):3-10. PubMed ID: 29362517
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  • 12. Histidine and lysine as targets of oxidative modification.
    Uchida K.
    Amino Acids; 2003 Dec 19; 25(3-4):249-57. PubMed ID: 14661088
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  • 14. Identification of modification sites on human serum albumin and human hemoglobin adducts with houttuynin using liquid chromatography coupled with mass spectrometry.
    Deng Z, Zhong D, Chen X.
    Biomed Chromatogr; 2012 Nov 19; 26(11):1377-85. PubMed ID: 22334394
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  • 15. Protein modification by acrolein: formation and stability of cysteine adducts.
    Cai J, Bhatnagar A, Pierce WM.
    Chem Res Toxicol; 2009 Apr 19; 22(4):708-16. PubMed ID: 19231900
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  • 16. Formation of mono- and bis-Michael adducts by the reaction of nucleophilic amino acids with hydroxymethylvinyl ketone, a reactive metabolite of 1,3-butadiene.
    Barshteyn N, Elfarra AA.
    Chem Res Toxicol; 2009 May 19; 22(5):918-25. PubMed ID: 19317513
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  • 17. 16α-Hydroxyestrone: Mass Spectrometry-Based Methodologies for the Identification of Covalent Adducts Formed with Blood Proteins.
    Charneira C, Nunes J, Antunes AMM.
    Chem Res Toxicol; 2020 Aug 17; 33(8):2147-2156. PubMed ID: 32692160
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  • 18. Michael addition-type 4-hydroxy-2-nonenal adducts in modified low-density lipoproteins: markers for atherosclerosis.
    Uchida K, Toyokuni S, Nishikawa K, Kawakishi S, Oda H, Hiai H, Stadtman ER.
    Biochemistry; 1994 Oct 18; 33(41):12487-94. PubMed ID: 7918471
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  • 20. HNE Michael adducts to histidine and histidine-containing peptides as biomarkers of lipid-derived carbonyl stress in urines: LC-MS/MS profiling in Zucker obese rats.
    Orioli M, Aldini G, Benfatto MC, Facino RM, Carini M.
    Anal Chem; 2007 Dec 01; 79(23):9174-84. PubMed ID: 17979257
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