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Temodal Reference List
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1.
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Newlands, E.S., M.F.G. Stevens, S.R. Wedge, R.T. Wheelhouse, and C. Brock. |
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Temozolomide: A review of its discovery, chemical properties, pre-clinical development and clinical trials. Cancer Treatment Reviews 23: 35-61, 1997. |
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Krauseneck, P. |
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Standards and recent advances in neuro-oncology. Aktuelle Neurologie 25: 219-226, 1998. |
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3.
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Beijnen, J.H., K.P. Flora, G.W. Halbert, R.E. Henrar, and J.A. Slack. |
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CRC/EORTC/NCI Joint Formulation Working Party: experiences in the formulation of investigational cytotoxic drugs. British Journal of Cancer 72: 210-218, 1995. |
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Weiss, G.R., H.A. Burris, S.G. Eckhardt, G.I. Rodriguez, S. Sharma, and A. Valley. |
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New anticancer agents. [Review] [89 refs]. Cancer Chemotherapy & Biological Response Modifiers 17: 178-194, 1997. |
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Armand, J.P. |
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New anticancer drugs in Europe. [Review] [120 refs]. Gan to Kagaku Ryoho [Japanese Journal of Cancer & Chemotherapy] 24 Suppl 1: 70-93, 1997. |
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6.
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Workman, P., S.B. Kaye, and G. Schwartsmann. |
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Laboratory and phase I studies of new cancer drugs [published erratum appears in Curr Opin Oncol 1993 Mar;5(2):434]. [Review] [60 refs]. Current Opinion in Oncology 4: 1065-1072, 1992. |
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Berger, N.A. |
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Alkylating agents. [Review] [55 refs]. Cancer Chemotherapy & Biological Response Modifiers 15: 32-43, 1994. |
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Stevens, M.F.G. and E.S. Newlands. |
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From triazines and triazenes to temozolomide. European Journal of Cancer 29A: 1045-1047, 1993. |
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9.
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Wang, W.F. and M.F.G. Stevens. |
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Antitumor imidazotetrazines .35. New synthetic routes to the antitumor drug temozolomide. Journal of Organic Chemistry 62: 7288-7294, 1997. |
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10.
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Wang, W.F., P.R. Lowe, W.T. Thomson, J. Clark, and M.F.G. Stevens. |
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A new route to the antitumour drug temozolomide, but not thiotemozolomide. Chemical Communications 363-364, 1997. |
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11.
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Wheelhouse, R.T., D.E.V. Wilman, W. Thomson, and M.F.G. Stevens. |
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Antitumor imidazotetrazines.31. The synthesis of isotopically labelled temozolomide and a multinuclear (H-1,C-13,N-15) magnetic-resonance investigation of temozolomide and mitozolomide. Journal of the Chemical Society - Perkin Transactions 249-252, 1995. |
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12.
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Wang, W.F., M.F.G. Stevens, W.T. Thomson, and B.P. Shutts. |
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Antitumour imidazotetrazines .33.New syntheses of the antitumour drug temozolomide using masked methyl isocyanates. Journal of the Chemical Society - Perkin Transactions 2783-2787, 1995. |
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13.
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Wang, Y.F., R.T. Wheelhouse, L.X. Zhao, D.F. Langnel, and M.F.G. Stevens. |
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Antitumour imidazotetrazines. Part 36. Conversion of 5- aminoimidazole-4-carboxamide to imidazo[5,1-d][1,2,3,5]tetrazin- 4(3H)-ones and imidazo[1,5-a][1,3,5]triazin-4(3H)-ones related in structure to the antitumour agents temozolomide and mitozolomide. Journal of the Chemical Society - Perkin Transactions 1669-1675, 1998. |
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14.
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Peori, M.B., K. Vaughan, and D.L. Hooper. |
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Synthesis and characterization of novel bis-triazenes: 3,8-di[2-aryl- 1-azenyl]-1,3,6,8-tetraazabicyclo[4.4.1]undecanes and 1,3-di-2-[(4- methoxyphenyl)-1-diazenyl]imidazolidine. The reaction of diazonium ions with ethylenediamine/formaldehyde mixtures. Journal of Organic Chemistry 63: 7437-7444, 1998. |
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15.
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Clark, A.S., B. Deans, M.F.G. Stevens, M.J. Tisdale, R.T. Wheelhouse, B.J. Denny, and J.A. Hartley. |
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. Antitumor imidazotetrazines. 32. Synthesis of novel imidazotetrazinones and related bicyclic heterocycles to probe the mode of action of the antitumor drug temozolomide. Journal of Medicinal Chemistry 38: 1493-1504, 1995. |
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16.
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Wang, Y.F. and M.F.G. Stevens. |
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Synthetic studies of 8-carbamoylimidazo-[5,1-d]1,2,3,5-tetrazin- 4(3H)-one: A key derivative of antitumour drug temozolomide. Bioorganic & Medicinal Chemistry Letters 6: 185-188, 1996. |
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17.
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Lowe, P.R., C.E. Sansom, C.H. Schwalbe, M.F.G. Stevens, and A.S. Clark. |
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Antitumor imidazotetrazines. 25. Crystal structure of 8-carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one (temozolomide) and structural comparisons with the related drugs mitozolomide and DTIC. Journal of Medicinal Chemistry 35: 3377-3382, 1992. |
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18.
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Clark, A.S., M.F.G. Stevens, C.E. Sansom, and C.H. Schwalbe. |
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Anti-tumour imidazotetrazines. Part XXI. Mitozolomide and temozolomide: probes for the major groove of DNA. Anti-Cancer Drug Design 5: 63-68, 1990. |
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19.
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Williams, C.I., M.A. Whitehead, and B.J. JeanClaude. |
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Equilibrium geometries and enantiomeric interconversions in tetrazepinone ring systems - A molecular mechanics, semiempirical and ab initio treatment. Theochem-Journal of Molecular Structure 392: 27-42, 1997. |
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20.
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Mizuno, N.S. and R.W. Decker. |
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Alteration of DNA by 5-(3-methyl-1-triazeno)imidazole-4-carboxamide(NSC-407347). Biochem Pharmacol 25: 2643-2647, 1976. |
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21.
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Denny, B.J., R.T. Wheelhouse, M.F.G. Stevens, L.L. Tsang, and J.A. Slack. |
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. NMR and molecular modeling investigation of the mechanism of activation of the antitumor drug temozolomide and its interaction with DNA. Biochemistry 33: 9045-9051, 1994. |
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22.
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Tsang, L.L., C.P. Quarterman, A. Gescher, and J.A. Slack. |
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Comparison of the cytotoxicity in vitro of temozolomide and dacarbazine, prodrugs of 3-methyl-(triazen-1-yl)imidazole-4-carboxamide. Cancer Chemotherapy & Pharmacology 27: 342-346, 1991. |
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23.
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Williams, C.I., M.A. Whitehead, and B.J. JeanClaude. |
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A semiempirical PM3 treatment of benzotetrazepinone decomposition in acid media. Journal of Organic Chemistry 62: 7006-7014, 1997. |
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24.
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Wilman, D.E. |
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Prodrugs in cancer chemotherapy. Biochemical Society Transactions 14: 375-382, 1986. |
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25.
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Shen, F., L.A. Decosterd, M. Gander, S. Leyvraz, J. Biollax, and F. Lejeune. |
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. Determination of temozolomide in human plasma and urine by high-performance liquid chromatography after solid-phase extraction. Journal of Chromatography B: Biomedical Applications 667: 291-300, 1995. |
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26.
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Kim, H.K., C.C. Lin, D. Parker, J. Veals, J. Lim, P. Likhari, P. Statkevich, A. Marco, and A.A. Nomeir. |
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High-performance liquid chromatographic determination and stability of 5-(3-methyltriazen-1-yl)-imidazo-4-carboximide, the biologically active product of the antitumor agent temozolomide, in human plasma. Journal of Chromatography B, Biomedical Sciences & Applications. 703: 225-233, 1997. |
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27.
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Artemov, D., Z.M. Bhujwalla, R.J. Maxwell, J.R. Griffiths, I.R. Judson, M.O. Leach, and J.D. Glickson. |
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. Pharmacokinetics of the 13C labeled anticancer agent temozolomide detected in vivo by selective cross-polarization transfer. Magnetic Resonance in Medicine 34: 338-342, 1995. |
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28.
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Ma, J. and J.M. Gallo. |
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Delivery of cytotoxic drugs from carrier cells to tumour cells by apoptosis. Apoptosis 3: 195-202, 1998. |
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29.
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Meikle, S.R., J.C. Matthews, C.S. Brock, P. Wells, R.J. Harte, V.J. Cunningham, T. Jones, and P. Price. |
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. Pharmacokinetic assessment of novel anti-cancer drugs using spectral analysis and positron emission tomography: a feasibility study. Cancer Chemotherapy & Pharmacology 42: 183-193, 1998. |
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30.
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Stevens, M.F.G., J.A. Hickman, S.P. Langdon, D. Chubb, L. Vickers, R. Stone, Baig, C. Goddard, N.W. Gibson, and J.A. Slack. |
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Antitumor activity and pharmacokinetics in mice of 8-carbamoyl-3-methyl-imidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one (CCRG 81045; M & B 39831), a novel drug with potential as an alternative to dacarbazine. Cancer Research 47: 5846-5852, 1987. |
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31.
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Reid, J.M., D.C. Stevens, J. Rubin, and M.M. Ames. |
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Pharmacokinetics of 3-methyl-(triazen-1-yl)imidazole-4-carboximide following administration of temozolomide to patients with advanced cancer. Clinical Cancer Research 3: 2393-2398, 1997. |
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32.
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Tsang, L.L., P.B. Farmer, A. Gescher, and J.A. Slack. |
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. Characterisation of urinary metabolites of temozolomide in humans and mice and evaluation of their cytotoxicity. Cancer Chemotherapy & Pharmacology 26: 429-436, 1990. |
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33.
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Lowe, P.R. and C.H. Schwalbe. |
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DCMCIT, an analogue of the antitumour drugs mitozolomide and temozolomide. Acta Crystallographica - Section C - Crystal Structure Communications 50: 1629-1631, 1994. |
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34.
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Jean-Claude, B.J., A. Mustafa, N.D. Cetateanu, Z. Damian, M.J. De, R. Yen, D. Vasilescu, T.H. Chan, and B. Leyland-Jones . |
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Design and mechanism of action of a novel cytotoxic 1,2,3-triazene-containing heterocycle, 3,5-dimethyl-pyrido-1,2,3,5-tetrazepin-4-one (PYRZ), in the human epithelial ovarian cancer cell line NIH:OVCAR-3 in vitro. British Journal of Cancer 76: 467-473, 1997. |
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35.
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Jean-Claude, B.J., A. Mustafa, Z. Damian, J. DeMarte, D.E. Vasilescu, R. Yen, T.H. Chan, and B. LeylandJones. |
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. Comparative studies between the effects of mitozolomide and two novel tetrazepinones PYRCL and QUINCL on NIH:OVCAR-3 cells. Cancer Chemotherapy and Pharmacology 42: 59-67, 1998. |
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36.
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D'Incalci, M., P. Taverna, E. Erba, S. Filippeschi, D. Potenza, L. Mariani, L. Citti, and C.V. Catapano. |
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O6-methylguanine and temozolomide can reverse the resistance to chloroethylnitrosoureas of a mouse L1210 leukemia. Anticancer Research 11: 115-121, 1991. |
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37.
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Marzolini, C., L.A. Decosterd, F. Shen, M. Gander, S. Leyvraz, J. Bauer, T. Buclin, J. Biollaz, and F. Lejeune. |
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Pharmacokinetics of temozolomide in association with fotemustine in malignant melanoma and malignant glioma patients: comparison of oral, intravenous, and hepatic intra-arterial administration. Cancer Chemotherapy and Pharmacology 42: 433-440, 1998. |
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38.
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Chinnasamy, N., J.A. Rafferty, I. Hickson, J. Ashby, H. Tinwell, G.P. Margison, T.M. Dexter, and L.J. Fairbairn. |
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O6-benzylguanine potentiates the in vivo toxicity and clastogenicity of temozolomide and BCNU in mouse bone marrow. Blood 89: 1566-1573, 1997. |
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39.
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Statkevich, P., I. Judson, D. Cutler, M. Dugan, M. Salfi, V. Batra, and P. Reidenberg |
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Effect of ranitidine (R) on the pharmacokinetics (PK) of temozolomide (T). Clin Pharm & Ther 61: I47- (Abstract PI-39)1997. |
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40.
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Dive, C., P. Workman, and J.V. Watson. |
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Inhibition of cellular esterases by the antitumour imidazotetrazines mitozolomide and temozolomide: demonstration by flow cytometry and conventional spectrofluorimetry. Cancer Chemotherapy & Pharmacology 25: 149-155, 1989. |
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41.
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Hooper, N.I., M.J. Tisdale, and P.J. Thornalley. |
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Glyoxalase activity during differentiation of human leukaemia cells in vitro. Leukemia Research 11: 1141-1148, 1987. |
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42.
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Karran, P. and R. Hampson. |
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Genomic instability and tolerance to alkylating agents. [Review] [38 refs]. Cancer Surveys 28: 69-85, 1996. |
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43.
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Bull, V.L. and M.J. Tisdale |
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Antitumour imidazotetrazines--XVI. Macromolecular alkylation by 3-substituted imidazotetrazinones. Biochemical Pharmacology 36: 3215-3220, 1987. |
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44.
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Imperatori, L., G. Damia, P. Taverna, E. Garattini, L. Citti, L. Boldrini, and M. D'Incalci. |
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3T3 NIH murine fibroblasts and B78 murine melanoma cells expressing the Escherichia coli N3-methyladenine-DNA glycosylase I do not become resistant to alkylating agents. Carcinogenesis 15: 533-537, 1994. |
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45.
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Zucchetti, M., C.V. Catapano, S. Filippeschi, E. Erba, and M. D'Incalci. |
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. Temozolomide induced differentiation of K562 leukemia cells is not mediated by gene hypomethylation. Biochemical Pharmacology 38: 2069-2075, 1989. |
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46.
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Tisdale, M.J. |
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Antitumour imidazotetrazines--XVIII. Modification of the level of 5-methylcytosine in DNA by 3-substituted imidazotetrazinones. Biochemical Pharmacology 38: 1097-1101, 1989. |
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47.
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Tisdale, M.J. |
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Antitumour imidazotetrazines-X. Effect of 8-carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4-(3H)-one (CCRG 81045; M & B 39831; NSC 362856) on DNA methylation during induction of haemoglobin synthesis in human leukaemia cell line K562. Biochemical Pharmacology 35: 311-316, 1986. |
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48.
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Tisdale, M.J. |
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Antitumour imidazotetrazines and gene expression. Acta Oncologica 27: 511-516, 1988. |
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49.
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Catapano, C.V., M. Broggini, E. Erba, M. Ponti, L. Mariani, L. Citti, and D'Incalci. |
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In vitro and in vivo methazolastone-induced DNA damage and repair in L-1210 leukemia sensitive and resistant to chloroethylnitrosoureas. Cancer Research 47: 4884-4889, 1987. |
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50.
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Tisdale, M.J. |
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Antitumor imidazotetrazines--XV. Role of guanine O6 alkylation in the mechanism of cytotoxicity of imidazotetrazinones. Biochemical Pharmacology 36: 457-462, 1987. |
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51.
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Taverna, P., C.V. Catapano, L. Citti, M. Bonfanti, and M. D'Incalci. |
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Influence of O6-methylguanine on DNA damage and cytotoxicity of temozolomide in L1210 mouse leukemia sensitive and resistant to chloroethylnitrosoureas. Anti-Cancer Drugs 3: 401-405, 1992. |
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52.
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Lee, S.M., N. Thatcher, D. Crowther, and G.P. Margison. |
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Inactivation of O6-alkylguanine-DNA alkyltransferase in human peripheral blood mononuclear cells by temozolomide. Brit Journal of Cancer 69: 452-456, 1994. |
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53.
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Baer, J.C., A.A. Freeman, E.S. Newlands, A.J. Watson, J.A. Rafferty, and G.P. Margison. |
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Depletion of O6-alkylguanine-DNA alkyltransferase correlates with potentiation of temozolomide and CCNU toxicity in human tumour cells. British Journal of Cancer 67: 1299-1302, 1993. |
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54.
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Mitchell, R.B. and M.E. Dolan. |
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Effect of temozolomide and dacarbazine on O6-alkylguanine-DNA alkyltransferase activity and sensitivity of human tumor cells and xenografts to 1,3-bis(2-chloroethyl)-1-nitrosourea. Cancer Chemotherapy & Pharmacology 32: 59-63, 1993. |
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55.
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Lacal, P.M., S. D'Atri, L. Orlando, E. Bonmassar, and G. Graziani. |
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In vitro inactivation of human O6-alkylguanine DNA alkyltransferase by antitumor triazene compounds. J Pharm & Expt Ther 279: 416-422, 1996. |
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56.
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Tentori, L., L. Orlando, P.M. Lacal, E. Benincasa, I. Faraoni, E. Bonmassar, S. D'Atri, and G. Graziani. |
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Inhibition of O6-alkylguanine DNA-alkyltransferase or poly(ADP-ribose) polymerase increases susceptibility of leukemic cells to apoptosis induced by temozolomide. Molecular Pharm 52: 249-258, 1997. |
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57.
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Wang, G., C. Weiss, P. Sheng, and E. Bresnick. |
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Retrovirus-mediated transfer of the human O6-methylguanine-DNA methyltransferase gene into a murine hematopoietic stem cell line and resistance to the toxic effects of certain alkylating agents. Biochemical Pharmacology 51: 1221-1228, 1996. |
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58.
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Graziani, G., I. Faraoni, U. Grohmann, R. Bianchi, L. Binaglia, G.P. Margison, A.J. Watson, L. Orlando, E. Bonmassar, and S. D'Atri. |
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O6-alkylguanine-DNA alkyltransferase attenuates triazene-induced cytotoxicity and tumor cell immunogenicity in murine L1210 leukemia. Cancer Research 55: 6231-6236, 1995. |
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59.
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Tentori, L., G. Graziani, S. Gilberti, P.M. Lacal, E. Bonmassar, and S. D'Atri. |
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Triazene compounds induce apoptosis in O6-alkylguanine-DNA alkyltransferase deficient leukemia cell lines. Leukemia 9: 1888-1895, 1995. |
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60.
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Jackson, P.E., C.N. Hall, P.J. OConnor, D.P. Cooper, G.P. Margison, and A.C. Povey. |
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Low O-6-alkylguanine DNA-alkyltransferase activity in normal colorectal tissue is associated with colorectal tumours containing a GC->AT transition in the K-ras oncogene. Carcinogenesis 18: 1299-1302, 1997. |
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Bianchi, R., L. Citti, R. Beghetti, L. Romani, M. D'Incalci, P. Puccetti, and M.C. Fioretti. |
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O6-methylguanine-DNA methyltransferase activity and induction of novel immunogenicity in murine tumor cells treated with methylating agents. Cancer Chemotherapy & Pharmacology 29: 277-282, 1992. |
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63.
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Gerson, S.L., W. Phillips, M. Kastan, L.L. Dumenco, and C. Donovan. |
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Human CD34(+) hematopoietic progenitors have low, cytokine- unresponsive O-6-alkylguanine-DNA alkyltransferase and are sensitive to O-6-benzylguanine plus BCNU. Blood 88: 1649-1655, 1996. |
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Chemoprotective gene transfer II: multilineage in vivo protection of haemopoiesis against the effects of an antitumour agent by expression of a mutant human O6-alkylguanine-DNA alkyltransferase. Gene Therapy 5: 842-847, 1998. |
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Hickson, I., L.J. Fairbairn, N. Chinnasamy, L.S. Lashford, N. Thatcher, Margison, GP, T.M. Dexter, and J.A. Rafferty. |
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Chemoprotective gene transfer I: transduction of human haemopoietic progenitors with O6-benzylguanine-resistant O6-alkylguanine-DNA alkyltransferase attenuates the toxic effects of O6-alkylating agents in vitro. Gene Therapy 5: 835-841, 1998. |
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67.
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Fairbairn, L.J., A.J. Watson, J.A. Rafferty, R.H. Elder, and G.P. Margison. |
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O6-benzylguanine increases the sensitivity of human primary bone marrow cells to the cytotoxic effects of temozolomide. Experimental Hematology 23: 112-116, 1995. |
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68.
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Hickson, I., L.J. Fairbairn, N. Chinnasamy, T.M. Dexter, G.P. Margison, and J.A. Rafferty. |
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69.
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Berg, S.L., D.J. Murry, C.L. McCully, K. Godwin, and F.M. Balis. |
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Wedge, S.R., J.K. Porteous, and E.S. Newlands. |
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3-aminobenzamide and/or O6-benzylguanine evaluated as an adjuvant to temozolomide or BCNU treatment in cell lines of variable mismatch repair status and O6-alkylguanine-DNA alkyltransferase activity. British Journal of Cancer 74: 1030-1036, 1996. |
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73.
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Liu, L., S. Markowitz, and S.L. Gerson. |
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Mismatch repair mutations override alkyltransferase in conferring resistance to temozolomide but not to 1,3-bis(2-chloroethyl)nitrosourea. Cancer Research 56: 5375-5379, 1996. |
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74.
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DNA mismatch repair and O-6-alkylguanine-DNA alkyltransferase analysis and response to temodal in newly diagnosed malignant glioma. Journal of Clinical Oncology 16: 3851-3857, 1998. |
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