<tei>
    <teiHeader>
        <fileDesc xml:id="0"/>
    </teiHeader>
    <text xml:lang="en">
        <listBibl><bibl><label>[35]</label>Y. Saito, N. Hanioka, K. Maekawa, T. Isobe, Y. Tsuneto, R. Nakamura, A. Soyama, S. Ozawa, T. Tanaka-Kagawa, H. Jinno, S. Narimatsu, J. Sawada, Functional analysis of three CYP1A2 variants found in a Japanese population, Drug Metab. Dispos. 12 (2005) 1905–1910.</bibl>
            <bibl> <label>[36]</label>Z. Jiang, T.P. Dalton, L. Jin, X.B. Wang, Y. Tsuneoka, H.G. Shertzer, R. Deka, D.W. Nebert, Toward evaluation of function in genetic variability: characterizing human SNP frequencies and establishing BAC transgenic mice carrying the human CYP1A1 CYP1A2 locus, Hum. Mutat. 25 (2005) 196–206.</bibl>
            <bibl> <label>[37]</label>H. Zhou, P.D. Josephy, D. Kim, F.P. Guengerich, Functional characterization of four allelic variants of human cytochrome P450 1A2, Arch. Biochem. Biophys. 422 (2004) 23–30.</bibl>
            <bibl> <label>[38]</label>B.B. Palma, E. Silva, M. Sousa, C.R. Vosmeer, J. Lastdrager, J. Rueff, N.P. Vermeulen, M. Kranendonk, Functional characterization of eight human cytochrome P450 1A2 gene variants by recombinant protein expression, Phar- macogen. J. 10 (2010) 478–488.</bibl>
            <bibl> <label>[39]</label>S. Sansen, J.K. Yano, R.L. Reynald, G.A. Schoch, K.J. Grifﬁn, C.D. Stout, E.F. Johnson, Adaptations for the oxidation of polycyclic aromatic hydrocarbons exhibited by the structure of human P450 1A2, J. Biol. Chem. 282 (2007) 14348–14355.</bibl>
            <bibl> <label>[40]</label>C. Sengstag, B. Weibel, M. Fasullo, Genotoxicity of aﬂatoxin B1: evidence for a recombination-mediated mechanism in Saccharomyces cerevisiae, Cancer Res. 56 (1996) 5457–5465.</bibl>
            <bibl> <label>[41]</label>M. Keller-Seitz, U. Certa, C. Sengstag, F. Wurgler, M. Sun, M. Fasullo, Transcrip- tional response of the yeast to the carcinogen aﬂatoxin B1: recombinational repair involving RAD51 and RAD1, Mol. Biol. Cell 15 (2004) 4321–4336.</bibl>
            <bibl> <label>[42]</label>M. Fasullo, M. Sun, P. Egner, Stimulation of sister chromatid exchanges and mutation by aﬂatoxin B1-DNA adducts in Saccharomyces cerevisiae requires MEC1 (ATR), RAD53, and DUN1, Mol. Carcinog. 47 (2008) 608–615.</bibl>
            <bibl> <label>[43]</label>M. Fasullo, Y. Chen, W. Bortcosh, M. Sun, P.A. Egner, Aﬂatoxin B1-associated DNA adducts stall S phase and stimulate Rad51 foci in Saccharomyces cerevisiae, J. Nucleic Acids 1 (2010) 456487.</bibl>
            <bibl> <label>[44]</label>D. Burke, D. Dawson, T. Stearns, Methods in yeast genetics: A Cold Spring Harbor Laboratory Course Manual, Cold Spring Harbor Press, New York, NY, 2000.</bibl>
            <bibl> <label>[45]</label>R.S. Sikorski, P. Hieter, A system of shuttle vectors and yeast host strains designed for efﬁcient manipulation of DNA in Saccharomyces cerevisiae, Genet- ics 122 (1989) 19–27.</bibl>
            <bibl> <label>[46]</label>F.M. Ausubel, R. Brent, R.E. Kingston, D.D. Moore, J.G. Seidman, J.A. Smith, K. Struhl, Short Protocols in Molecular Biology, fourth ed., Wiley, New York, NY, 1999.</bibl>
            <bibl> <label>[47]</label>M.T. Fasullo, T. Bennett, P. AhChing, J. Koudelik, The Saccharomyces cerevisiae RAD9 checkpoint reduces the DNA damage-associated stimulation of directed reciprocal translocations, Mol. Cell. Biol. 18 (1998) 1190–2000.</bibl>
            <bibl> <label>[48]</label>M.T. Fasullo, R.W. Davis, Recombination substrates designed to study recom- bination between unique and repetitive sequences in vivo, PNAS 84 (1987) 6215–6219.</bibl>
            <bibl> <label>[49]</label>M. Fasullo, P. Dave, R. Rothstein, DNA-damaging agents stimulate the formation of directed reciprocal translocations in Saccharomyces cerevisiae, Mutat. Res. 314 (1994) 121–133.</bibl>
        </listBibl>
    </text>
</tei>
