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Journal Abstract Search


185 related items for PubMed ID: 3070292

  • 1. In vitro reaction of hydroxyamino derivatives of MeIQx, Glu-P-1 and Trp-P-1 with DNA: 32P-postlabelling analysis of DNA adducts formed in vivo by the parent amines and in vitro by their hydroxyamino derivatives.
    Yamashita K, Umemoto A, Grivas S, Kato S, Sugimura T.
    Mutagenesis; 1988 Nov; 3(6):515-20. PubMed ID: 3070292
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  • 2. Chemical modification of DNA with muta-carcinogens. I. 3-Amino-1-methyl-5H-pyrido[4,3-b]indole and 2-amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole: metabolic activation and structure of the DNA adducts.
    Hashimoto Y, Shudo K.
    Environ Health Perspect; 1985 Oct; 62():209-14. PubMed ID: 4085425
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  • 3. The formation of heart DNA adducts in F344 rat following dietary administration of heterocyclic amines.
    Overvik E, Ochiai M, Hirose M, Sugimura T, Nagao M.
    Mutat Res; 1991 Jan; 256(1):37-43. PubMed ID: 1944385
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  • 6. 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
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  • 9. N-oxidative metabolism of 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) in humans: excretion of the N2-glucuronide conjugate of 2-hydroxyamino-MeIQx in urine.
    Stillwell WG, Turesky RJ, Sinha R, Tannenbaum SR.
    Cancer Res; 1999 Oct 15; 59(20):5154-9. PubMed ID: 10537291
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  • 10. 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 15; 25(8):1525-33. PubMed ID: 15059926
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  • 11. Syntheses of hydroxyamino, nitroso and nitro derivatives of Trp-P-2 and Glu-P-1, amino acid pyrolysate mutagens, and their direct mutagenicities towards Salmonella typhimurium TA98 and TA98NR.
    Saito K, Yamazoe Y, Kamataki T, Kato R.
    Carcinogenesis; 1983 Dec 15; 4(12):1547-50. PubMed ID: 6360404
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  • 12. In vitro binding of potent mutagenic pyrolysates to intestinal bacteria.
    Morotomi M, Mutai M.
    J Natl Cancer Inst; 1986 Jul 15; 77(1):195-201. PubMed ID: 3014197
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  • 13. Formation of DNA adducts by the food mutagen 2-amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline (4,8-DiMeIQx) in vitro and in vivo. Identification of a N2-(2'-deoxyguanosin-8-yl)-4,8-DiMeIQx adduct.
    Frandsen H, Grivas S, Turesky RJ, Andersson R, Dragsted LO, Larsen JC.
    Carcinogenesis; 1994 Nov 15; 15(11):2553-8. PubMed ID: 7955105
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  • 14. Effects of lactic acid bacteria on binding and absorption of mutagenic heterocyclic amines.
    Terahara M, Meguro S, Kaneko T.
    Biosci Biotechnol Biochem; 1998 Feb 15; 62(2):197-200. PubMed ID: 9532774
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  • 16. Enzymatic phase II activation of the N-hydroxylamines of IQ, MeIQx and PhIP by various organs of monkeys and rats.
    Davis CD, Schut HA, Snyderwine EG.
    Carcinogenesis; 1993 Oct 15; 14(10):2091-6. PubMed ID: 8222059
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  • 18. Identification of the major hepatic DNA adduct formed by the food mutagen 2-amino-9H-pyrido[2,3-b]indole (A alpha C).
    Pfau W, Schulze C, Shirai T, Hasegawa R, Brockstedt U.
    Chem Res Toxicol; 1997 Oct 15; 10(10):1192-7. PubMed ID: 9348443
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  • 19. Identification of N2-(deoxyguanosin-8-yl)-2-amino-3,8-dimethyl-imidazo[4,5- f]quinoxaline 3',5'-diphosphate, a major DNA adduct, detected by nuclease P1 modification of the 32P-postlabeling method, in the liver of rats fed MeIQx.
    Ochiai M, Nagaoka H, Wakabayashi K, Tanaka Y, Kim SB, Tada A, Nukaya H, Sugimura T, Nagao M.
    Carcinogenesis; 1993 Oct 15; 14(10):2165-70. PubMed ID: 8222070
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  • 20. The contribution of N-oxidation to the metabolism of the food-borne carcinogen 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline in rat hepatocytes.
    Turesky RJ, Bracco-Hammer I, Markovic J, Richli U, Kappeler AM, Welti DH.
    Chem Res Toxicol; 1990 Oct 15; 3(6):524-35. PubMed ID: 2103323
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