253 related articles for article (PubMed ID: 23898916)
1. DNA adducts of the tobacco carcinogens 2-amino-9H-pyrido[2,3-b]indole and 4-aminobiphenyl are formed at environmental exposure levels and persist in human hepatocytes.
Nauwelaërs G; Bellamri M; Fessard V; Turesky RJ; Langouët S
Chem Res Toxicol; 2013 Sep; 26(9):1367-77. PubMed ID: 23898916
[TBL] [Abstract][Full Text] [Related]
2. DNA adduct formation of 4-aminobiphenyl and heterocyclic aromatic amines in human hepatocytes.
Nauwelaers G; Bessette EE; Gu D; Tang Y; Rageul J; Fessard V; Yuan JM; Yu MC; Langouët S; Turesky RJ
Chem Res Toxicol; 2011 Jun; 24(6):913-25. PubMed ID: 21456541
[TBL] [Abstract][Full Text] [Related]
3. Bioactivation of the tobacco carcinogens 4-aminobiphenyl (4-ABP) and 2-amino-9H-pyrido[2,3-b]indole (AαC) in human bladder RT4 cells.
Bellamri M; Yao L; Bonala R; Johnson F; Von Weymarn LB; Turesky RJ
Arch Toxicol; 2019 Jul; 93(7):1893-1902. PubMed ID: 31203411
[TBL] [Abstract][Full Text] [Related]
4. Quantification of Hemoglobin and White Blood Cell DNA Adducts of the Tobacco Carcinogens 2-Amino-9H-pyrido[2,3-b]indole and 4-Aminobiphenyl Formed in Humans by Nanoflow Liquid Chromatography/Ion Trap Multistage Mass Spectrometry.
Cai T; Bellamri M; Ming X; Koh WP; Yu MC; Turesky RJ
Chem Res Toxicol; 2017 Jun; 30(6):1333-1343. PubMed ID: 28493705
[TBL] [Abstract][Full Text] [Related]
5. Metabolism of the Tobacco Carcinogen 2-Amino-9H-pyrido[2,3-b]indole (AαC) in Primary Human Hepatocytes.
Bellamri M; Le Hegarat L; Turesky RJ; Langouët S
Chem Res Toxicol; 2017 Feb; 30(2):657-668. PubMed ID: 27976871
[TBL] [Abstract][Full Text] [Related]
6. 2-Amino-9H-pyrido[2,3-b]indole (AαC) Adducts and Thiol Oxidation of Serum Albumin as Potential Biomarkers of Tobacco Smoke.
Pathak KV; Bellamri M; Wang Y; Langouët S; Turesky RJ
J Biol Chem; 2015 Jun; 290(26):16304-18. PubMed ID: 25953894
[TBL] [Abstract][Full Text] [Related]
7. Biomonitoring DNA Adducts of Cooked Meat Carcinogens in Human Prostate by Nano Liquid Chromatography-High Resolution Tandem Mass Spectrometry: Identification of 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine DNA Adduct.
Xiao S; Guo J; Yun BH; Villalta PW; Krishna S; Tejpaul R; Murugan P; Weight CJ; Turesky RJ
Anal Chem; 2016 Dec; 88(24):12508-12515. PubMed ID: 28139123
[TBL] [Abstract][Full Text] [Related]
8. Targeted and Untargeted Detection of DNA Adducts of Aromatic Amine Carcinogens in Human Bladder by Ultra-Performance Liquid Chromatography-High-Resolution Mass Spectrometry.
Guo J; Villalta PW; Weight CJ; Bonala R; Johnson F; Rosenquist TA; Turesky RJ
Chem Res Toxicol; 2018 Dec; 31(12):1382-1397. PubMed ID: 30387604
[TBL] [Abstract][Full Text] [Related]
9. The impact of NAT2 acetylator genotype on mutagenesis and DNA adducts from 2-amino-9H-pyrido[2,3-b]indole.
Turesky RJ; Bendaly J; Yasa I; Doll MA; Hein DW
Chem Res Toxicol; 2009 Apr; 22(4):726-33. PubMed ID: 19243127
[TBL] [Abstract][Full Text] [Related]
10. Methemoglobin Formation and Characterization of Hemoglobin Adducts of Carcinogenic Aromatic Amines and Heterocyclic Aromatic Amines.
Pathak KV; Chiu TL; Amin EA; Turesky RJ
Chem Res Toxicol; 2016 Mar; 29(3):255-69. PubMed ID: 26824300
[TBL] [Abstract][Full Text] [Related]
11. UDP-glucuronosyltransferase-mediated metabolic activation of the tobacco carcinogen 2-amino-9H-pyrido[2,3-b]indole.
Tang Y; LeMaster DM; Nauwelaërs G; Gu D; Langouët S; Turesky RJ
J Biol Chem; 2012 Apr; 287(18):14960-72. PubMed ID: 22393056
[TBL] [Abstract][Full Text] [Related]
12. Human T lymphocytes bioactivate heterocyclic aromatic amines by forming DNA adducts.
Bellamri M; Le Hegarat L; Vernhet L; Baffet G; Turesky RJ; Langouët S
Environ Mol Mutagen; 2016 Dec; 57(9):656-667. PubMed ID: 27801952
[TBL] [Abstract][Full Text] [Related]
13. Effect of Cytochrome P450 Reductase Deficiency on 2-Amino-9H-pyrido[2,3-b]indole Metabolism and DNA Adduct Formation in Liver and Extrahepatic Tissues of Mice.
Turesky RJ; Konorev D; Fan X; Tang Y; Yao L; Ding X; Xie F; Zhu Y; Zhang QY
Chem Res Toxicol; 2015 Dec; 28(12):2400-10. PubMed ID: 26583703
[TBL] [Abstract][Full Text] [Related]
14. DNA adduct formation of 14 heterocyclic aromatic amines in mouse tissue after oral administration and characterization of the DNA adduct formed by 2-amino-9H-pyrido[2,3-b]indole (AalphaC), analysed by 32P_HPLC.
Baranczewski P; Gustafsson JA; Moller L
Biomarkers; 2004; 9(3):243-57. PubMed ID: 15764290
[TBL] [Abstract][Full Text] [Related]
15. Comparative DNA adduct formation and induction of colonic aberrant crypt foci in mice exposed to 2-amino-9H-pyrido[2,3-b]indole, 2-amino-3,4-dimethylimidazo[4,5-f]quinoline, and azoxymethane.
Kim S; Guo J; O'Sullivan MG; Gallaher DD; Turesky RJ
Environ Mol Mutagen; 2016 Mar; 57(2):125-36. PubMed ID: 26734915
[TBL] [Abstract][Full Text] [Related]
16. Screening for DNA adducts by data-dependent constant neutral loss-triple stage mass spectrometry with a linear quadrupole ion trap mass spectrometer.
Bessette EE; Goodenough AK; Langouët S; Yasa I; Kozekov ID; Spivack SD; Turesky RJ
Anal Chem; 2009 Jan; 81(2):809-19. PubMed ID: 19086795
[TBL] [Abstract][Full Text] [Related]
17. Syntheses of DNA adducts of two heterocyclic amines, 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeAalphaC) and 2-amino-9H-pyrido[2,3-b]indole (AalphaC) and identification of DNA adducts in organs from rats dosed with MeAalphaC.
Frederiksen H; Frandsen H; Pfau W
Carcinogenesis; 2004 Aug; 25(8):1525-33. PubMed ID: 15059926
[TBL] [Abstract][Full Text] [Related]
18. DNA adduct formation of 2-amino-9H-pyrido[2,3-b]indole and 2-amino-3,4-dimethylimidazo[4,5-f]quinoline in mouse liver and extrahepatic tissues during a subchronic feeding study.
Tang Y; Kassie F; Qian X; Ansha B; Turesky RJ
Toxicol Sci; 2013 Jun; 133(2):248-58. PubMed ID: 23535364
[TBL] [Abstract][Full Text] [Related]
19. Identification of carcinogen DNA adducts in human saliva by linear quadrupole ion trap/multistage tandem mass spectrometry.
Bessette EE; Spivack SD; Goodenough AK; Wang T; Pinto S; Kadlubar FF; Turesky RJ
Chem Res Toxicol; 2010 Jul; 23(7):1234-44. PubMed ID: 20443584
[TBL] [Abstract][Full Text] [Related]
20. Analysis and quantification of DNA adducts of 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline in liver of rats by liquid chromatography/electrospray tandem mass spectrometry.
Paehler A; Richoz J; Soglia J; Vouros P; Turesky RJ
Chem Res Toxicol; 2002 Apr; 15(4):551-61. PubMed ID: 11952342
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
