These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 14680375)

  • 1. Identification and characterization of a series of nucleoside adducts formed by the reaction of 2'-deoxyguanosine and 1,2,3,4-diepoxybutane under physiological conditions.
    Zhang XY; Elfarra AA
    Chem Res Toxicol; 2003 Dec; 16(12):1606-15. PubMed ID: 14680375
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of the reaction products of 2'-deoxyguanosine and 1,2,3,4-diepoxybutane after acid hydrolysis: formation of novel guanine and pyrimidine adducts.
    Zhang XY; Elfarra AA
    Chem Res Toxicol; 2004 Apr; 17(4):521-8. PubMed ID: 15089094
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Reaction of 1,2,3,4-diepoxybutane with 2'-deoxyguanosine: initial products and their stabilities and decomposition patterns under physiological conditions.
    Zhang XY; Elfarra AA
    Chem Res Toxicol; 2005 Aug; 18(8):1316-23. PubMed ID: 16097805
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of 1,2,3,4-diepoxybutane-2'-deoxyguanosine cross-linking products formed at physiological and nonphysiological conditions.
    Zhang XY; Elfarra AA
    Chem Res Toxicol; 2006 Apr; 19(4):547-55. PubMed ID: 16608166
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structural characterization of adducts formed in the reaction of 2,3-epoxy-4-hydroxynonanal with deoxyguanosine.
    Sodum RS; Chung FL
    Chem Res Toxicol; 1989; 2(1):23-8. PubMed ID: 2519227
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kinetics and mechanism of the general-acid-catalyzed ring-closure of the malondialdehyde-DNA adduct, N2-(3-oxo-1-propenyl)deoxyguanosine (N2OPdG-), to 3-(2'-Deoxy-beta-D-erythro-pentofuranosyl)pyrimido[1,2-alpha]purin- 10(3H)-one (M1dG).
    Riggins JN; Pratt DA; Voehler M; Daniels JS; Marnett LJ
    J Am Chem Soc; 2004 Sep; 126(34):10571-81. PubMed ID: 15327313
    [TBL] [Abstract][Full Text] [Related]  

  • 7. N
    Groehler AS; Najjar D; Pujari SS; Sangaraju D; Tretyakova NY
    Chem Res Toxicol; 2018 Sep; 31(9):885-897. PubMed ID: 30016111
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis, characterization, and in vitro quantitation of N-7-guanine adducts of diepoxybutane.
    Tretyakova NYu ; Sangaiah R; Yen TY; Swenberg JA
    Chem Res Toxicol; 1997 Jul; 10(7):779-85. PubMed ID: 9250412
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Formation of fused-ring 2'-deoxycytidine adducts from 1-chloro-3-buten-2-one, an in vitro 1,3-butadiene metabolite, under in vitro physiological conditions.
    Sun L; Pelah A; Zhang DP; Zhong YF; An J; Yu YX; Zhang XY; Elfarra AA
    Chem Res Toxicol; 2013 Oct; 26(10):1545-53. PubMed ID: 24020501
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Butadiene diolepoxide- and diepoxybutane-derived DNA adducts at N7-guanine: a high occurrence of diolepoxide-derived adducts in mouse lung after 1,3-butadiene exposure.
    Koivisto P; Kilpeläinen I; Rasanen I; Adler ID; Pacchierotti F; Peltonen K
    Carcinogenesis; 1999 Jul; 20(7):1253-9. PubMed ID: 10383898
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DEB-FAPy-dG Adducts of 1,3-Butadiene: Synthesis, Structural Characterization, and Formation in 1,2,3,4-Diepoxybutane Treated DNA.
    Pujari SS; Jokipii Krueger CC; Chao C; Hutchins S; Hurben AK; Boysen G; Tretyakova N
    Chemistry; 2022 Jan; 28(3):e202103245. PubMed ID: 34767297
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel adducts from the reaction of 1-chloro-3-buten-2-one with 2'-deoxyguanosine. Structural characterization and potential as tools to investigate 1,3-butadiene carcinogenicity.
    Zheng J; Li Y; Yu YX; An J; Zhang XY; Elfarra AA
    Chem Biol Interact; 2015 Jan; 226():40-8. PubMed ID: 25500269
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Formation of adducts in the reaction of glyoxal with 2'-deoxyguanosine and with calf thymus DNA.
    Pluskota-Karwatka D; Pawłowicz AJ; Tomas M; Kronberg L
    Bioorg Chem; 2008 Apr; 36(2):57-64. PubMed ID: 18078668
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel DNA adduct, originating from 1,2-epoxy-3,4-butanediol, is the major DNA adduct after exposure to [2,3-(14)C]-1,3-butadiene,[4-(14)C]-1,2-epoxy-3-butane.
    Boogaard PJ; van Sittert NJ; Watson WP; de Kloe KP
    Chem Biol Interact; 2001 Jun; 135-136():687-93. PubMed ID: 11397423
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Quantitative analysis of the oxidative DNA lesion, 2,2-diamino-4-(2-deoxy-beta-D-erythro-pentofuranosyl)amino]-5(2H)-oxazolone (oxazolone), in vitro and in vivo by isotope dilution-capillary HPLC-ESI-MS/MS.
    Matter B; Malejka-Giganti D; Csallany AS; Tretyakova N
    Nucleic Acids Res; 2006; 34(19):5449-60. PubMed ID: 17020926
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 9(1):147-57. PubMed ID: 8924584
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Coupling products of nucleosides with the glyoxal adduct of deoxyguanosine.
    Brock AK; Kozekov ID; Rizzo CJ; Harris TM
    Chem Res Toxicol; 2004 Aug; 17(8):1047-56. PubMed ID: 15310236
    [TBL] [Abstract][Full Text] [Related]  

  • 19. trans,trans-2,4-decadienal-induced 1,N(2)-etheno-2'-deoxyguanosine adduct formation.
    Loureiro AP; Di Mascio P; Gomes OF; Medeiros MH
    Chem Res Toxicol; 2000 Jul; 13(7):601-9. PubMed ID: 10898592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reactions of alpha-acetoxy-N-nitrosopyrrolidine and alpha-acetoxy-N-nitrosopiperidine with deoxyguanosine: formation of N2-tetrahydrofuranyl and N2-tetrahydropyranyl adducts.
    Young-Sciame R; Wang M; Chung FL; Hecht SS
    Chem Res Toxicol; 1995 Jun; 8(4):607-16. PubMed ID: 7548742
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.