[1] H. Bagci, J. H. Stuy, Bromouracil-induced mutagenesis in a mismatch-repair-deficient strain of Haemophilus influenzae, Mutat. Res. 73 (1994), 15-19.
[2] P. Quillardet and M. Hofnung, The SOS Chromotest, a colorimetric bacterial assay for geno-toxins: procedures, Mutat. Res. 147 (1985), 65-78.
[3] D. Forman, Ames, the Ames test, and the causes of cancer, BMJ 303 (1991), 428-429.
[4] B. N. Ames, Mutagenesis and carcinogenesis: Endogenous and exogenous factors, Environ. Mol. Mutagen. 14 (1989), 66-77.
[5] P. Einistoü, M. Watanabe, M. Jr. Ishidate, T. Nohmi, Mutagenicity of 30 chemicals in Salmonella typhimurium strains possessing different nitroreductase or O-acetyltransferase activities, Mutat. Res. 259 (1991), 95-102.
[6] R. Vikse, A. Knapstad, L. Klungs0yr and S. Grivas, Mutagenic activity of the methyl and phenyl derivatives of the food mutagen 2-amino-3-methylimidazo[4,5-f]quinoxaline (IQx) in the Ames test, Mutat. Res. 298 (1993), 207-214.
[7] M. Manneberg, W. Lahm and M. Fountoulakis, Quantification of cysteine residues following oxidation to cysteic acid in the presence of sodium azide, Anal. Biochem. 231 (1995), 349-353.
[8] J. S. Fisherman, B. L. Osborn, H. G. Chun, J. Plowman, A. C. Smith, M. C. Christian, D. S. Zaharko and R. H. Shoemaker, Chloroquinoxaline sulfonamide: A sulfanilamide antitumor agent entering clinical trials, Invest. New Drugs 11 (1993), 1-9.
[9] N. S. Habib and S. A. el-Hawash, Synthesis and antimicrobial testing of thiazolinyl-, thiazolidinonyl-quinoxalines and 1,2,4-triazolo[4,3-a]quinoxalines, Pharmazie 52 (1997), 594¬598.
[10] J. B. Sutherland, F. E. Evans, J. P. Freeman and A. J. Williams, Biotransformation of quinox-aline by Streptomyces badius, Lett. Appl. Microbiol. 22 (1996), 199-201.
[11] Y. Oda, H. Yamazaki, M. Watanabe, T. Nohmi and T. Shimada, Highly sensitive umu test system for the detection of mutagenic nitroarenes in Salmonella typhimurium NM3009 having high O-acetyltransferase and nitroreductase activities, Environ. Mol. Mutagen. 21 (1993),
357-364.
[12] Y. Oda, H. Yamazaki and T. Shimada, Role of human N-acetyltransferases, NAT1 or NAT2, in genotoxicity of nitroarenes and aromatic amines in Salmonella typhimurium NM6001 and NM6002, Carcinogenesis 20 (1999), 1079-1083.
86
Çeyhan et al.
[13] Y. Oda, H. Yamazaki, M. Watanabe, T. Nohmi and T. Shimada, Development of high sen¬sitive umu test system: rapid detection of genotoxicity of promutagenic aromatic amines by Salmonella typhimurium strain NM2009 possessing high O-acetyltransferase activity, Mutat. Res. 334 (1995), 145-156.
[14] G. Reifferscheid and J. Heil, Validation of the SOS/umu test using test results of 486 chemicals and comparison with the Ames test and carcinogenicity data, Mutat. Res. 369 (1996), 129¬145.
[15] D. W. Hein, M. Hirata, I. B. Glowinski and W. W. Weber, Biochemical evidence for the coexistence of monomorphic and polymorphic N-acetyltransferase activities on a common protein in rabbit liver, J. Pharmacol. Exp. Ther. 220 (1982), 1-7.
[16] O. H. Lowry, N. J. Rosenbrough, A. L. Farr and R. J. Randall, Protein measurement with the Folin phenol reagent, J. Biol. Chem. 193 (1951), 265-275.
[17] K. T. Bogen, Applicability of alternative models of revertant variance to Ames-test data for
121 mutagenic carcinogens, Mutat. Res. 322 (1994), 265-273.
[18] L. Dalgaard, R. K. Hjortkjaer, B. Regnier and L. Nordholm, Pharmacokinetics of the neuro-protective glutamate antagonist NBQX (6-nitro-7-sulfamoyl-benzo(f)quinoxaline-2,3-dione) in mice, rats, and dogs. Interactions with probenecid, Drug Metab. Dispos. 22 (1994), 289-293.
[19] C. Sengstag C and F. E. Würgler, DNA recombination induced by aflatoxin B1 activated by cytochrome P450 1A enzymes, Mol. Carcinog. 11 (1994), 227-235.
[20] N. Shibuya, T. Ohta, H. Nakadaira, H. Mano, K. Endoh and M. Yamamoto, Mutagenicity of activated carbon adsorbate of drinking water in the Ames assay, Tohoku J. Exp. Med. 171 (1993), 89-95.
[21] L. D. Claxton, J. Creason, B. Leroux, E. Agurell, S. Bagley, D. W. Bryant, Y. A. Courtois, G. Douglas, C. B. Clare, S. Goto, P. Quillardet, D. R. Jagannath, K. Kataoka, G. Mohn, P.
A. Nielsen, T. Ong, T. C. Pederson, H. Shimizu, L. Nylund, H. Tokiwa, G. J. Vink, Y. Wang
and D. Warshawsky, Results of the IPCS collaborative study on complex mixtures, Mutat.
Res. 276 (1992), 23-32.
[22] S. Monarca, R. Pasquini and P. Arcaleni, Detection of mutagens in unconcentrated and con¬centrated drinking water supplies before and after treatment using a microscale fluctuation test, Chemosphere 14 (1985), 1069-1080.
[23] M. Font, A. Monge, E. Alvarez, A. Cuartero, M. J. Losa, M. J. Fidalgo, C. SanMartın, E. Nadal, I. Ruiz, I. Merino, J. J. Martmez-Irujo, E. Alberdi, E. Santiago, I. Prieto, J. J. Lasarte, P. Sarobe and F. Borras, Synthesis and evaluation of new Reissert analogs as HIV-1 reverse transcriptase inhibitors. 1. Quinoline and quinoxaline derivatives, Drug Des. Discov.
14 (1997), 305-332.
Thank you for copying data from http://www.arastirmax.com