These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 7067041)

  • 1. Rapid release of carcinogen-guanine adducts from DNA after reaction with N-acetoxy-2-acetylaminofluorene or N-benzoyloxy-N-methyl-4-aminoazobenzene.
    Tarpley WG; Miller JA; Miller EC
    Carcinogenesis; 1982; 3(1):81-8. PubMed ID: 7067041
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Adducts from the reaction of N-benzoyloxy-N-methyl-4-aminoazobenzene with deoxyguanosine or DNA in vitro and from hepatic DNA of mice treated with N-methyl- or N,N-dimethyl-4-aminoazobenzene.
    Tarpley WG; Miller JA; Miller EC
    Cancer Res; 1980 Jul; 40(7):2493-9. PubMed ID: 7388806
    [TBL] [Abstract][Full Text] [Related]  

  • 4. N-substitution of carbon 8 in guanosine and deoxyguanosine by the carcinogen N-benzoyloxy-N-methyl-4-aminoazobenzene in vitro.
    Lin JK; Schmall B; Sharpe ID; Miura I; Miller JA; Miller EC
    Cancer Res; 1975 Mar; 35(3):832-43. PubMed ID: 1116138
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Formation of DNA adducts from N-acetoxy-2-acetylaminofluorene and N-hydroxy-2-acetylaminofluorene in rat hemopoietic tissues in vivo.
    Vu VT; Grantham PH; Roller PP; Hankins WD; Wirth PJ; Thorgeirsson SS
    Cancer Res; 1986 Jan; 46(1):233-8. PubMed ID: 3940194
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 4-aminoazobenzene and N,N-dimethyl-4-aminoazobenzene as equipotent hepatic carcinogens in male C57BL/6 X C3H/He F1 mice and characterization of N-(Deoxyguanosin-8-yl)-4-aminoazobenzene as the major persistent hepatic DNA-bound dye in these mice.
    Delclos KB; Tarpley WG; Miller EC; Miller JA
    Cancer Res; 1984 Jun; 44(6):2540-50. PubMed ID: 6426782
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization and properties of the DNA adducts formed from N-methyl-4-aminoazobenzene in rats during a carcinogenic treatment regimen.
    Tullis DL; Dooley KL; Miller DW; Baetcke KP; Kadlubar FF
    Carcinogenesis; 1987 Apr; 8(4):577-83. PubMed ID: 3829320
    [TBL] [Abstract][Full Text] [Related]  

  • 13. N-sulfoöxy-2-aminofluorene is the major ultimate electrophilic and carcinogenic metabolite of N-hydroxy-2-acetylaminofluorene in the livers of infant male C57BL/6J x C3H/HeJ F1 (B6C3F1) mice.
    Lai CC; Miller JA; Miller EC; Liem A
    Carcinogenesis; 1985 Jul; 6(7):1037-45. PubMed ID: 3860305
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Monoclonal antibodies to DNA modified by the carcinogen N-acetoxy-N-2 acetyl aminofluorene.
    Le Guern A; Leng M; Kourilsky P
    Dev Biol Stand; 1984; 57():409-14. PubMed ID: 6084621
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effect of pH on the ratio of substitution products in DNA after reaction with the carcinogen N-acetoxy-2-acetylaminofluorene.
    Kriek E
    Cancer Lett; 1979 Jul; 7(2-3):141-6. PubMed ID: 38901
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effects of adduct formation on the biological activity of single- and double-stranded øX174 DNA, modified by N-acetoxy-N-acetyl-2-aminofluorene.
    Lutgerink JT; Retèl J; Loman H
    Biochim Biophys Acta; 1984 Feb; 781(1-2):81-91. PubMed ID: 6230108
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DNA adducts formed from N-benzoyloxy-N-methyl-4-aminoazobenzene in vitro and from N, N-dimethyl-4-aminoazobenzene in mouse liver.
    Tarpley WG; Miller JA; Miller EC
    Natl Cancer Inst Monogr; 1981 Dec; (58):163-4. PubMed ID: 7341973
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of the DNA adducts formed in vitro from N-benzoyloxy-N-methyl-4-aminoazobenzene and in rat liver in vivo after administration of N-methyl-4-aminoazobenzene.
    Beland FA; Tullis DL; Kadlubar FF; Straub KM; Evans FE
    Natl Cancer Inst Monogr; 1981 Dec; (58):153-61. PubMed ID: 7341972
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel method for the small scale synthesis of N-acetoxy-2-acetylaminofluorene and its adducts.
    Van Roy FP; Moyer GH; Austin GE
    Cancer Lett; 1981 Mar; 12(1-2):147-52. PubMed ID: 7272998
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.