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Journal Abstract Search

105 related items for PubMed ID: 2131822

  • 1. Investigation of the adducts formed by reaction of malondialdehyde with adenosine.
    Stone K, Ksebati MB, Marnett LJ.
    Chem Res Toxicol; 1990; 3(1):33-8. PubMed ID: 2131822
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  • 3. Identification of adducts formed by reaction of guanine nucleosides with malondialdehyde and structurally related aldehydes.
    Basu AK, O'Hara SM, Valladier P, Stone K, Mols O, Marnett LJ.
    Chem Res Toxicol; 1988; 1(1):53-9. PubMed ID: 2979712
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  • 4. Studies of the reaction of malondialdehyde with cytosine nucleosides.
    Stone K, Uzieblo A, Marnett LJ.
    Chem Res Toxicol; 1990; 3(5):467-72. PubMed ID: 2133098
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  • 5. A novel synthesis of malondialdehyde adducts of deoxyguanosine, deoxyadenosine, and deoxycytidine.
    Wang H, Marnett LJ, Harris TM, Rizzo CJ.
    Chem Res Toxicol; 2004 Feb; 17(2):144-9. PubMed ID: 14967001
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  • 6. Characterization of N1- and N6-adenosine adducts and N1-inosine adducts formed by the reaction of butadiene monoxide with adenosine: evidence for the N1-adenosine adducts as major initial products.
    Selzer RR, Elfarra AA.
    Chem Res Toxicol; 1996 Feb; 9(5):875-81. PubMed ID: 8828924
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  • 8. Formation of conjugate adducts in the reactions of malonaldehyde-acetaldehyde and malonaldehyde-formaldehyde with guanosine.
    Pluskota-Karwatka D, Le Curieux F, Munter T, Sjöholm R, Kronberg L.
    Chem Res Toxicol; 2005 Feb; 18(2):300-7. PubMed ID: 15720136
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  • 9. Reaction of mucochloric and mucobromic acids with adenosine and cytidine: formation of chloro- and bromopropenal derivatives.
    Kronberg L, Asplund D, Mäki J, Sjöholm R.
    Chem Res Toxicol; 1996 Dec; 9(8):1257-63. PubMed ID: 8951227
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  • 10. Solution structure of an oligodeoxynucleotide containing the malondialdehyde deoxyguanosine adduct N2-(3-oxo-1-propenyl)-dG (ring-opened M1G) positioned in a (CpG)3 frameshift hotspot of the Salmonella typhimurium hisD3052 gene.
    Mao H, Reddy GR, Marnett LJ, Stone MP.
    Biochemistry; 1999 Oct 12; 38(41):13491-501. PubMed ID: 10521256
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  • 11. Formation of a fluorescent adduct in the reaction of 2'-deoxyadenosine with a malonaldehyde-acetaldehyde condensation product.
    Le Curieux F, Pluskota D, Munter T, Sjöholm R, Kronberg L.
    Chem Res Toxicol; 1998 Sep 12; 11(9):989-94. PubMed ID: 9760272
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  • 12. Characterization of an N6-oxopropenyl-2'-deoxyadenosine adduct in malondialdehyde-modified DNA using liquid chromatography/electrospray ionization tandem mass spectrometry.
    Chaudhary AK, Reddy GR, Blair IA, Marnett LJ.
    Carcinogenesis; 1996 May 12; 17(5):1167-70. PubMed ID: 8640930
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  • 14. Reaction of malondialdehyde (MDA) with alpha-N-acetylhistidine in the presence of alkanal.
    Ohya T.
    Biol Pharm Bull; 1994 Apr 12; 17(4):554-6. PubMed ID: 8069270
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  • 15. Quantification of malondialdehyde and 4-hydroxynonenal adducts to lysine residues in native and oxidized human low-density lipoprotein.
    Requena JR, Fu MX, Ahmed MU, Jenkins AJ, Lyons TJ, Baynes JW, Thorpe SR.
    Biochem J; 1997 Feb 15; 322 ( Pt 1)(Pt 1):317-25. PubMed ID: 9078279
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  • 18. Site specific N6-(2-hydroxy-3,4-epoxybut-1-yl)adenine oligodeoxynucleotide adducts of 1,2,3,4-diepoxybutane: synthesis and stability at physiological pH.
    Antsypovich S, Quirk-Dorr D, Pitts C, Tretyakova N.
    Chem Res Toxicol; 2007 Apr 15; 20(4):641-9. PubMed ID: 17355152
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  • 19. Mechanisms of formation of adducts from reactions of glycidaldehyde with 2'-deoxyguanosine and/or guanosine.
    Golding BT, Slaich PK, Kennedy G, Bleasdale C, Watson WP.
    Chem Res Toxicol; 1996 Apr 15; 9(1):147-57. PubMed ID: 8924584
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  • 20. Duplex DNA catalyzes the chemical rearrangement of a malondialdehyde deoxyguanosine adduct.
    Mao H, Schnetz-Boutaud NC, Weisenseel JP, Marnett LJ, Stone MP.
    Proc Natl Acad Sci U S A; 1999 Jun 08; 96(12):6615-20. PubMed ID: 10359760
    [Abstract] [Full Text] [Related]

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