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136 related items for PubMed ID: 11123963

  • 1. Identification of fluorescent 2'-deoxyadenosine adducts formed in reactions of conjugates of malonaldehyde and acetaldehyde, and of malonaldehyde and formaldehyde.
    Le Curieux F, Pluskota D, Munter T, Sjöholm R, Kronberg L.
    Chem Res Toxicol; 2000 Dec; 13(12):1228-34. PubMed ID: 11123963
    [Abstract] [Full Text] [Related]

  • 2. Identification of conjugate adducts formed in the reactions of malonaldehyde-acetaldehyde and malonaldehyde-formaldehyde with cytidine.
    Pluskota-Karwatka D, Le Curieux F, Munter T, Sjöholm R, Kronberg L.
    Chem Res Toxicol; 2002 Feb; 15(2):110-7. PubMed ID: 11849036
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  • 4. 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; 11(9):989-94. PubMed ID: 9760272
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  • 6. Formation of malonaldehyde-acetaldehyde conjugate adducts in calf thymus DNA.
    Pluskota-Karwatka D, Pawłowicz AJ, Kronberg L.
    Chem Res Toxicol; 2006 Jul; 19(7):921-6. PubMed ID: 16841960
    [Abstract] [Full Text] [Related]

  • 7. Identification of adducts formed in reactions of 2-deoxyadenosine and calf thymus DNA with the bacterial mutagen 3-chloro-4-(chloromethyl)-5-hydroxy-2(5H)-furanone.
    Munter T, Le Curieux F, Sjöholm R, Kronberg L.
    Chem Res Toxicol; 1999 Dec; 12(12):1205-12. PubMed ID: 10604870
    [Abstract] [Full Text] [Related]

  • 8. Reaction of the potent bacterial mutagen 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) with 2'-deoxyadenosine and calf thymus DNA: identification of fluorescent propenoformyl derivatives.
    Munter T, Le Curieux F, Sjöholm R, Kronberg L.
    Chem Res Toxicol; 1998 Mar; 11(3):226-33. PubMed ID: 9544621
    [Abstract] [Full Text] [Related]

  • 9. Reactions of malonaldehyde and acetaldehyde with calf thymus DNA: formation of conjugate adducts.
    Pluskota-Karwatka D, Pawlowicz AJ, Kronberg L.
    Nucleosides Nucleotides Nucleic Acids; 2007 Mar; 26(6-7):567-71. PubMed ID: 18066857
    [Abstract] [Full Text] [Related]

  • 10. Identification of adducts formed in the reactions of malonaldehyde-glyoxal and malonaldehyde-methylglyoxal with adenosine and calf thymus DNA.
    Pluskota-Karwatka D, Pawłowicz AJ, Bruszyńska M, Greszkiewicz A, Latajka R, Kronberg L.
    Chem Biodivers; 2010 Apr; 7(4):959-74. PubMed ID: 20397229
    [Abstract] [Full Text] [Related]

  • 11. Reactions of formaldehyde plus acetaldehyde with deoxyguanosine and DNA: formation of cyclic deoxyguanosine adducts and formaldehyde cross-links.
    Cheng G, Shi Y, Sturla SJ, Jalas JR, McIntee EJ, Villalta PW, Wang M, Hecht SS.
    Chem Res Toxicol; 2003 Feb; 16(2):145-52. PubMed ID: 12588185
    [Abstract] [Full Text] [Related]

  • 12. Large scale synthesis of p-benzoquinone-2'-deoxycytidine and p-benzoquinone-2'-deoxyadenosine adducts and their site-specific incorporation into DNA oligonucleotides.
    Chenna A, Singer B.
    Chem Res Toxicol; 1995 Sep; 8(6):865-74. PubMed ID: 7492736
    [Abstract] [Full Text] [Related]

  • 13. Identification and characterization of novel stable deoxyguanosine and deoxyadenosine adducts of benzo[a]pyrene-7,8-quinone from reactions at physiological pH.
    Balu N, Padgett WT, Lambert GR, Swank AE, Richard AM, Nesnow S.
    Chem Res Toxicol; 2004 Jun; 17(6):827-38. PubMed ID: 15206904
    [Abstract] [Full Text] [Related]

  • 14. New nucleoside analogs from 2-amino-9-(beta-D-ribofuranosyl)purine.
    Virta P, Holmström T, Roslund MU, Mattjus P, Kronberg L, Sjöholm R.
    Org Biomol Chem; 2004 Mar 21; 2(6):821-7. PubMed ID: 15007409
    [Abstract] [Full Text] [Related]

  • 15. Identification of a Fused-Ring 2'-Deoxyadenosine Adduct Formed in Human Cells Incubated with 1-Chloro-3-buten-2-one, a Potential Reactive Metabolite of 1,3-Butadiene.
    Zeng FM, Liu LY, Zheng J, Kong C, An J, Yu YX, Zhang XY, Elfarra AA.
    Chem Res Toxicol; 2016 Jun 20; 29(6):1041-50. PubMed ID: 27161607
    [Abstract] [Full Text] [Related]

  • 16. Adducts of chlorohydroxyfuranones and of aldehyde conjugates.
    Kronberg L, Munter T, Mäki J, Le Curieux F, Pluskota D, Sjöholm R.
    IARC Sci Publ; 1999 Jun 20; (150):115-21. PubMed ID: 10626213
    [Abstract] [Full Text] [Related]

  • 17. Formation of 1,N6-etheno-2'-deoxyadenosine adducts by trans,trans-2, 4-Decadienal.
    Carvalho VM, Di Mascio P, de Arruda Campos IP, Douki T, Cadet J, Medeiros MH.
    Chem Res Toxicol; 1998 Sep 20; 11(9):1042-7. PubMed ID: 9760278
    [Abstract] [Full Text] [Related]

  • 18. Identification of DNA adducts of acetaldehyde.
    Wang M, McIntee EJ, Cheng G, Shi Y, Villalta PW, Hecht SS.
    Chem Res Toxicol; 2000 Nov 20; 13(11):1149-57. PubMed ID: 11087437
    [Abstract] [Full Text] [Related]

  • 19. DNA oligomers containing site-specific and stereospecific exocyclic deoxyadenosine adducts of 1,2,3,4-diepoxybutane: synthesis, characterization, and effects on DNA structure.
    Seneviratne U, Antsypovich S, Dorr DQ, Dissanayake T, Kotapati S, Tretyakova N.
    Chem Res Toxicol; 2010 Oct 18; 23(10):1556-67. PubMed ID: 20873715
    [Abstract] [Full Text] [Related]

  • 20. Characterization of adducts formed in the reaction of glutaraldehyde with 2'-deoxyadenosine.
    Olsen R, Backman J, Molander P, Øvrebø S, Thorud S, Lundanes E, Greibrokk T, Kronberg L.
    Chem Res Toxicol; 2007 Jun 18; 20(6):965-74. PubMed ID: 17518482
    [Abstract] [Full Text] [Related]

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