BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 10703974)

  • 1. Mass spectrometric (HPLC/ESI--MS/MS) quantification of pyrimido[1,3-a]purin-10(3H)-one, a guanine adduct formed by reaction of malondialdehyde with DNA.
    Hakala K; Auriola S; Koivisto A; Lönnberg H
    J Pharm Biomed Anal; 1999 Dec; 21(5):1053-61. PubMed ID: 10703974
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Kinetic and thermodynamic analysis of the hydrolytic ring-opening of the malondialdehyde-deoxyguanosine adduct, 3-(2'-deoxy-beta-D-erythro-pentofuranosyl)- pyrimido[1,2-alpha]purin-10(3H)-one.
    Riggins JN; Daniels JS; Rouzer CA; Marnett LJ
    J Am Chem Soc; 2004 Jul; 126(26):8237-43. PubMed ID: 15225065
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of a malondialdehyde-deoxyguanosine adduct in human leukocyte DNA by liquid chromatography nanoelectrospray-high-resolution tandem mass spectrometry.
    Ma B; Villalta PW; Balbo S; Stepanov I
    Chem Res Toxicol; 2014 Oct; 27(10):1829-36. PubMed ID: 25181548
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pyrimido[1,2-alpha]purin-10(3H)-one: a reactive electrophile in the genome.
    Schnetz-Boutaud N; Daniels JS; Hashim MF; Scholl P; Burrus T; Marnett LJ
    Chem Res Toxicol; 2000 Oct; 13(10):967-70. PubMed ID: 11080044
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Quantitative analysis of 1,3-butadiene-induced DNA adducts in vivo and in vitro using liquid chromatography electrospray ionization tandem mass spectrometry.
    Tretyakova NYu ; Chiang SY; Walker VE; Swenberg JA
    J Mass Spectrom; 1998 Apr; 33(4):363-76. PubMed ID: 9597770
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparison of DNA adduct levels associated with oxidative stress in human pancreas.
    Kadlubar FF; Anderson KE; Häussermann S; Lang NP; Barone GW; Thompson PA; MacLeod SL; Chou MW; Mikhailova M; Plastaras J; Marnett LJ; Nair J; Velic I; Bartsch H
    Mutat Res; 1998 Sep; 405(2):125-33. PubMed ID: 9748537
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Quantification of tamoxifen DNA adducts using on-line sample preparation and HPLC-electrospray ionization tandem mass spectrometry.
    Gamboa da Costa G; Marques MM; Beland FA; Freeman JP; Churchwell MI; Doerge DR
    Chem Res Toxicol; 2003 Mar; 16(3):357-66. PubMed ID: 12641436
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Development of a method for determination of the malondialdehyde-deoxyguanosine adduct in urine using liquid chromatography-tandem mass spectrometry.
    Otteneder M; Daniels JS; Voehler M; Marnett LJ
    Anal Biochem; 2003 Apr; 315(2):147-51. PubMed ID: 12689823
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High-performance liquid chromatography/electrospray mass spectrometry for the analysis of modified bases in DNA: 7-(2-hydroxyethyl)guanine, the major ethylene oxide-DNA adduct.
    Leclercq L; Laurent C; De Pauw E
    Anal Chem; 1997 May; 69(10):1952-5. PubMed ID: 9164163
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of adducts produced by the reaction of 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanol with deoxyguanosine and DNA.
    Upadhyaya P; Sturla SJ; Tretyakova N; Ziegel R; Villalta PW; Wang M; Hecht SS
    Chem Res Toxicol; 2003 Feb; 16(2):180-90. PubMed ID: 12588189
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multi-DNA Adduct and Abasic Site Quantitation In Vivo by Nano-Liquid Chromatography/High-Resolution Orbitrap Tandem Mass Spectrometry: Methodology for Biomonitoring Colorectal DNA Damage.
    Konorev D; Yao L; Turesky RJ
    Chem Res Toxicol; 2022 Sep; 35(9):1519-1532. PubMed ID: 36066083
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reaction of malondialdehyde-DNA adducts with hydrazines-development of a facile assay for quantification of malondialdehyde equivalents in DNA.
    Otteneder M; Plastaras JP; Marnett LJ
    Chem Res Toxicol; 2002 Mar; 15(3):312-8. PubMed ID: 11896677
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of M1G-dR in DNA by aldehyde reactive probe labeling and liquid chromatography tandem mass spectrometry.
    Jeong YC; Sangaiah R; Nakamura J; Pachkowski BF; Ranasinghe A; Gold A; Ball LM; Swenberg JA
    Chem Res Toxicol; 2005 Jan; 18(1):51-60. PubMed ID: 15651849
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pyrimido[1,2-a]-purin-10(3H)-one, M1G, is less prone to artifact than base oxidation.
    Jeong YC; Nakamura J; Upton PB; Swenberg JA
    Nucleic Acids Res; 2005; 33(19):6426-34. PubMed ID: 16282591
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of the Major Purine and Pyrimidine Adducts Formed after Incubations of 1-Chloro-3-buten-2-one with Single-/Double-Stranded DNA and Human Cells.
    Liu LY; Zheng J; Kong C; An J; Yu YX; Zhang XY; Elfarra AA
    Chem Res Toxicol; 2017 Feb; 30(2):552-563. PubMed ID: 27977153
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of O2-substituted pyrimidine adducts formed in reactions of 4-(acetoxymethylnitrosamino)- 1-(3-pyridyl)-1-butanone and 4-(acetoxymethylnitros- amino)-1-(3-pyridyl)-1-butanol with DNA.
    Hecht SS; Villalta PW; Sturla SJ; Cheng G; Yu N; Upadhyaya P; Wang M
    Chem Res Toxicol; 2004 May; 17(5):588-97. PubMed ID: 15144215
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 38(41):13491-501. PubMed ID: 10521256
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of 1,N2-ethenoguanine and 5,6,7,9-tetrahydro-7-hydroxy-9-oxoimidazo[1,2-a]purine in DNA treated with 2-chlorooxirane by high performance liquid chromatography/electrospray mass spectrometry and comparison of amounts to other DNA adducts.
    Müller M; Belas FJ; Blair IA; Guengerich FP
    Chem Res Toxicol; 1997 Feb; 10(2):242-7. PubMed ID: 9049437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.