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142 related items for PubMed ID: 9806154

  • 1.
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  • 3. DNA adduct formation of the food-derived mutagen 2-amino-3-methylimidazo[4,5-f]quinoline in nonhuman primates undergoing carcinogen bioassay.
    Turesky RJ, Gremaud E, Markovic J, Snyderwine EG.
    Chem Res Toxicol; 1996 Mar; 9(2):403-8. PubMed ID: 8839042
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  • 4. Formation and differential removal of C-8 and N2-guanine adducts of the food carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline in the liver, kidney, and colorectum of the rat.
    Turesky RJ, Markovic J, Aeschlimann JM.
    Chem Res Toxicol; 1996 Mar; 9(2):397-402. PubMed ID: 8839041
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  • 5. Characterization of DNA adducts formed in vitro by reaction of N-hydroxy-2-amino-3-methylimidazo[4,5-f]quinoline and N-hydroxy-2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline at the C-8 and N2 atoms of guanine.
    Turesky RJ, Rossi SC, Welti DH, Lay JO, Kadlubar FF.
    Chem Res Toxicol; 1992 Mar; 5(4):479-90. PubMed ID: 1391614
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  • 6. Formation and persistence of DNA adducts of 2-amino-3-methylimidazo[4,5-f]quinoline in the rat and nonhuman primates.
    Turesky RJ, Box RM, Markovic J, Gremaud E, Snyderwine EG.
    Mutat Res; 1997 May 12; 376(1-2):235-41. PubMed ID: 9202760
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  • 7. Analysis of mutations induced by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in human lymphoblastoid cells.
    Morgenthaler PM, Holzhäuser D.
    Carcinogenesis; 1995 Apr 12; 16(4):713-8. PubMed ID: 7728948
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  • 8. Mutagenic specificity of 2-amino-3-methylimidazo[4,5-f]quinoline and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in the supF shuttle vector system.
    Endo H, Schut HA, Snyderwine EG.
    Cancer Res; 1994 Jul 15; 54(14):3745-51. PubMed ID: 8033094
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  • 9. 2-Nitrosoamino-3-methylimidazo[4,5-f]quinoline activated by the inflammatory response forms nucleotide adducts.
    Lakshmi VM, Schut HA, Zenser TV.
    Food Chem Toxicol; 2005 Nov 15; 43(11):1607-17. PubMed ID: 15964673
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  • 10. Mutational specificity of 2-amino-3-methylimidazo-[4,5-f]quinoline in the hprt locus of CHO-K1 cells.
    Lee H, Shih MK.
    Mol Carcinog; 1995 Jun 15; 13(2):122-7. PubMed ID: 7605580
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  • 11. Effect of rapid human N-acetyltransferase 2 haplotype on DNA damage and mutagenesis induced by 2-amino-3-methylimidazo-[4,5-f]quinoline (IQ) and 2-amino-3,8-dimethylimidazo-[4,5-f]quinoxaline (MeIQx).
    Metry KJ, Neale JR, Doll MA, Howarth AL, States JC, McGregor WG, Pierce WM, Hein DW.
    Mutat Res; 2010 Feb 03; 684(1-2):66-73. PubMed ID: 20004212
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  • 12. 32P-postlabeling analysis of IQ, MeIQx and PhIP adducts formed in vitro in DNA and polynucleotides and found in vivo in hepatic DNA from IQ-, MeIQx- and PhIP-treated monkeys.
    Snyderwine EG, Davis CD, Nouso K, Roller PP, Schut HA.
    Carcinogenesis; 1993 Jul 03; 14(7):1389-95. PubMed ID: 8330355
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  • 13. Biochemical basis of genotoxicity of heterocyclic arylamine food mutagens: Human DNA polymerase eta selectively produces a two-base deletion in copying the N2-guanyl adduct of 2-amino-3-methylimidazo[4,5-f]quinoline but not the C8 adduct at the NarI G3 site.
    Choi JY, Stover JS, Angel KC, Chowdhury G, Rizzo CJ, Guengerich FP.
    J Biol Chem; 2006 Sep 01; 281(35):25297-306. PubMed ID: 16835218
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  • 14. DNA adduct formation of the food carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) in liver, kidney and colo-rectum of rats.
    Turesky RJ, Markovic J.
    Carcinogenesis; 1995 Sep 01; 16(9):2275-9. PubMed ID: 7554091
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  • 15. Base-Displaced Intercalated Conformation of the 2-Amino-3-methylimidazo[4,5-f]quinoline N(2)-dG DNA Adduct Positioned at the Nonreiterated G(1) in the NarI Restriction Site.
    Stavros KM, Hawkins EK, Rizzo CJ, Stone MP.
    Chem Res Toxicol; 2015 Jul 20; 28(7):1455-68. PubMed ID: 26083477
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  • 16. Quantification of the heterocyclic aromatic amine DNA adduct N-(deoxyguanosin-8-yl)-2-amino-3-methylimidazo[4,5-f]quinoline in livers of rats using capillary liquid chromatography/microelectrospray mass spectrometry: a dose-response study.
    Soglia JR, Turesky RJ, Paehler A, Vouros P.
    Anal Chem; 2001 Jul 01; 73(13):2819-27. PubMed ID: 11467522
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  • 17. The C8-2'-deoxyguanosine adduct of 2-amino-3-methylimidazo[1,2-d]naphthalene, a carbocyclic analogue of the potent mutagen 2-amino-3-methylimidazo[4,5-f]quinoline, is a block to replication in vitro.
    Christov PP, Chowdhury G, Garmendia CA, Wang F, Stover JS, Elmquist CE, Kozekova A, Angel KC, Turesky RJ, Stone MP, Guengerich FP, Rizzo CJ.
    Chem Res Toxicol; 2010 Jun 21; 23(6):1076-88. PubMed ID: 20377178
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  • 18. Quantification of N-(deoxyguanosin-8-yl)-4-aminobiphenyl adducts in human lymphoblastoid TK6 cells dosed with N-hydroxy-4-acetylaminobiphenyl and their relationship to mutation, toxicity, and gene expression profiling.
    Ricicki EM, Luo W, Fan W, Zhao LP, Zarbl H, Vouros P.
    Anal Chem; 2006 Sep 15; 78(18):6422-32. PubMed ID: 16970317
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  • 19. DNA sequence modulates the conformation of the food mutagen 2-amino-3-methylimidazo[4,5-f]quinoline in the recognition sequence of the NarI restriction enzyme.
    Wang F, Elmquist CE, Stover JS, Rizzo CJ, Stone MP.
    Biochemistry; 2007 Jul 24; 46(29):8498-516. PubMed ID: 17602664
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  • 20. Translesion synthesis past the C8- and N2-deoxyguanosine adducts of the dietary mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline in the NarI recognition sequence by prokaryotic DNA polymerases.
    Stover JS, Chowdhury G, Zang H, Guengerich FP, Rizzo CJ.
    Chem Res Toxicol; 2006 Nov 24; 19(11):1506-17. PubMed ID: 17112239
    [Abstract] [Full Text] [Related]

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