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Journal Abstract Search

268 related items for PubMed ID: 7955105

  • 1. 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(11):2553-8. PubMed ID: 7955105
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  • 2. Reaction of the N2-acetoxy derivative of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) with 2'-deoxyguanosine and DNA. Synthesis and identification of N2-(2'-deoxyguanosin-8-yl)-PhIP.
    Frandsen H, Grivas S, Andersson R, Dragsted L, Larsen JC.
    Carcinogenesis; 1992 Apr; 13(4):629-35. PubMed ID: 1576716
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  • 3. 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
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  • 4. 32-P-HPLC analysis of DNA adducts formed in vitro and in vivo by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine and 2-amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline, utilizing an improved adduct enrichment procedure.
    Wohlin P, Zeisig M, Gustafsson JA, Möller L.
    Chem Res Toxicol; 1996 Sep; 9(6):1050-6. PubMed ID: 8870995
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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 Sep; 5(4):479-90. PubMed ID: 1391614
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  • 6. 32P-post-labelling analysis of DNA adducts formed by food-derived heterocyclic amines: evidence for incomplete hydrolysis and a procedure for adduct pattern simplification.
    Pfau W, Brockstedt U, Söhren KD, Marquardt H.
    Carcinogenesis; 1994 May; 15(5):877-82. PubMed ID: 8200090
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  • 7. Antibodies to the food mutagens, 2-amino-1-methyl-6-phenylimidazo [4,5-b]pyridine and 2-amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline: useful for immunoassay and immunoaffinity chromatography of biological samples.
    Dragsted LO, Grivas S, Frandsen H, Larsen JC.
    Carcinogenesis; 1995 Nov; 16(11):2795-806. PubMed ID: 7586201
    [Abstract] [Full Text] [Related]

  • 8. DNA adduct formation of the food carcinogen 2-amino-3-methylimidazo[4,5- f]quinoline at the C-8 and N2 atoms of guanine.
    Turesky RJ, Markovic J.
    Chem Res Toxicol; 1994 Nov; 7(6):752-61. PubMed ID: 7696529
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  • 15. Reaction of N-hydroxylamine and N-acetoxy derivatives of 2-amino-3-methylimidazolo[4,5-f]quinoline with DNA. Synthesis and identification of N-(deoxyguanosin-8-yl)-IQ.
    Snyderwine EG, Roller PP, Adamson RH, Sato S, Thorgeirsson SS.
    Carcinogenesis; 1988 Jun; 9(6):1061-5. PubMed ID: 3370750
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  • 17. Characterization of the major DNA adduct formed by the food mutagen 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeAalphaC) in primary rat hepatocytes.
    Pfau W, Brockstedt U, Schulze C, Neurath G, Marquardt H.
    Carcinogenesis; 1996 Dec; 17(12):2727-32. PubMed ID: 9006112
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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; 10(10):1192-7. PubMed ID: 9348443
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