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Journal Abstract Search

151 related items for PubMed ID: 3345736

  • 1. Metabolism of 2-acetylaminofluorene in the Chinese hamster ovary cell mutation assay.
    Heflich RH, Djurić Z, Zhuo Z, Fullerton NF, Casciano DA, Beland FA.
    Environ Mol Mutagen; 1988; 11(2):167-81. PubMed ID: 3345736
    [Abstract] [Full Text] [Related]

  • 2. Association between DNA strand breaks and specific DNA adducts in murine hepatocytes following in vivo and in vitro exposure to N-hydroxy-2-acetylaminofluorene and N-acetoxy-2-acetylaminofluorene.
    Vu VT, Møller ME, Grantham PH, Wirth PJ, Thorgeirsson SS.
    Carcinogenesis; 1985 Jan; 6(1):45-52. PubMed ID: 4038475
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  • 3. The 32P-post-labeling method in quantitative DNA adduct dosimetry of 2-acetylaminofluorene-induced mutagenicity in Chinese hamster ovary cells and Salmonella typhimurium TA1538.
    Arce GT, Cline DT, Mead JE.
    Carcinogenesis; 1987 Apr; 8(4):515-20. PubMed ID: 3549038
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  • 4. Mutagenicity-enhancing effect of quercetin on the active metabolites of 2-acetylaminofluorene with mammalian metabolic activation systems.
    Ogawa S, Hirayama T, Tokuda M, Hirai K, Fukui S.
    Mutat Res; 1987 Apr; 190(4):241-6. PubMed ID: 3550450
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  • 5. The essential role of microsomal deacetylase activity in the metabolic activation, DNA-(deoxyguanosin-8-yl)-2-aminofluorene adduct formation and initiation of liver tumors by N-hydroxy-2-acetylaminofluorene in the livers of infant male B6C3F1 mice.
    Lai CC, Miller EC, Miller JA, Liem A.
    Carcinogenesis; 1988 Jul; 9(7):1295-302. PubMed ID: 3383346
    [Abstract] [Full Text] [Related]

  • 6. Quantification of adducts formed in DNA treated with N-acetoxy-2-acetylaminofluorene or N-hydroxy-2-aminofluorene: comparison of trifluoroacetic acid and enzymatic degradation.
    Tang M, Lieberman MW.
    Carcinogenesis; 1983 Aug; 4(8):1001-6. PubMed ID: 6307542
    [Abstract] [Full Text] [Related]

  • 7. Interaction of nucleophiles with the enzymatically-activated carcinogen, N-hydroxy-2-acetylaminofluorene, and with the model ester, N-acetoxy-2-acetylaminofluorene.
    Smith BA, Gutmann HR, Springfield JR.
    Carcinogenesis; 1985 Feb; 6(2):271-7. PubMed ID: 3971491
    [Abstract] [Full Text] [Related]

  • 8. Activation of N-acetoxy- and N-hydroxy-2-acetylaminofluorene to mutagenic and cytotoxic metabolites by V79 Chinese hamster cells.
    Glatt H, Oesch F.
    Mutat Res; 1985 Apr; 149(2):265-9. PubMed ID: 3885026
    [Abstract] [Full Text] [Related]

  • 9. Processing of 2-aminofluorene and 2-acetylaminofluorene DNA adducts in Chinese hamster ovary cells.
    Nairn RS, Tang MS, Wang RM, Adair GM, Humphrey RM.
    Carcinogenesis; 1988 Aug; 9(8):1369-75. PubMed ID: 3402033
    [Abstract] [Full Text] [Related]

  • 10. Initiation of hepatocarcinogenesis in infant male B6C3F1 mice by N-hydroxy-2-aminofluorene or N-hydroxy-2-acetylaminofluorene depends primarily on metabolism to N-sulfooxy-2-aminofluorene and formation of DNA-(deoxyguanosin-8-yl)-2-aminofluorene adducts.
    Lai CC, Miller EC, Miller JA, Liem A.
    Carcinogenesis; 1987 Mar; 8(3):471-8. PubMed ID: 3815742
    [Abstract] [Full Text] [Related]

  • 11. Interaction of the synthetic ultimate carcinogens, N-sulfonoxy- and N-acetoxy-2-acetylaminofluorene, and of enzymatically activated N-hydroxy-2-acetylaminofluorene with nucleophiles.
    Smith BA, Springfield JR, Gutmann HR.
    Carcinogenesis; 1986 Mar; 7(3):405-11. PubMed ID: 3512117
    [Abstract] [Full Text] [Related]

  • 12. Metabolic activation of 2-aminofluorene, 2-acetylaminofluorene and N-hydroxy-acetylaminofluorene to bacterial mutagens with mussel (Mytilus galloprovincialis) and carp (Cyprinus carpio) subcellular preparations.
    Kurelec B, Krca S.
    Comp Biochem Physiol C Comp Pharmacol Toxicol; 1987 Mar; 88(1):171-7. PubMed ID: 2890481
    [Abstract] [Full Text] [Related]

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  • 17. The role of specific DNA adducts in the induction of micronuclei by N-hydroxy-2-acetylaminofluorene in rat liver in vivo.
    van de Poll ML, van der Hulst DA, Tates AD, Mulder GJ, Meerman JH.
    Carcinogenesis; 1989 Apr; 10(4):717-22. PubMed ID: 2702720
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