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  1. 1.   Urethane and N-nitrosodiethylamine are mutagenic for the Syrian hamster fetus
  2. Donovan, P. J.; Smith, G. T.
  3. Mutation Research-Genetic Toxicology and Environmental Mutagenesis. 2008 657(2): 160-163.
  1. 2.   A Liquid Chromatography-Mass Spectrometry Method for the Simultaneous Measurement of 15 Urinary Estrogens and Estrogen Metabolites: Assay Reproducibility and Interindividual Variability
  2. Falk, R. T.; Xu, X.; Keefer, L.; Veenstra, T. D.; Ziegler, R. G.
  3. Cancer Epidemiology Biomarkers & Prevention. 2008 17(12): 3411-3418.
  1. 3.   Pharmacokinetics, pharmacodynamics and drug metabolism - Characterization of in vitro and in vivo metabolic pathways of the investigational anticancer agent, 2-methoxyestradiol
  2. Lakhani, N. J.; Sparreboom, A.; Xu, X.; Veenstra, T. D.; Venitz, J.; Dahut, W. L.; Figg, W. D.
  3. Journal of Pharmaceutical Sciences. 2007, Jul; 96(7): 1821-1831.
  1. 4.   Environmental genotoxicants/carcinogens and childhood cancer: Bridgeable gaps in scientific knowledge
  2. Anderson, L. M.
  3. Mutation Research-Genetic Toxicology and Environmental Mutagenesis. 2006, Sep; 608(2): 136-156.
  1. 5.   Differential metabolism of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in mice humanized for CYP1A1 and CYP1A2
  2. Cheung, C.; Ma, X. C.; Krausz, K. W.; Kimura, S.; Feigenbaum, L.; Dalton, T. P.; Nebert, D. W.; Idle, J. R.; Gonzalez, F. J.
  3. Chemical Research in Toxicology. 2005, SEP; 18(9): 1471-1478.
  1. 6.   Fluorinated 2-(4-amino-3-methylphenyl) benzothiazoles induce CYP1A1 expression, become metabolized, and bind to macromolecules in sensitive human cancer cells
  2. Brantley, E.; Trapani, V.; Alley, M. C.; Hose, C. D.; Bradshaw, T. D.; Stevens, M. F. G.; Sausville, E. A.; Stinson, S. F.
  3. Drug Metabolism and Disposition. 2004, DEC; 32(12): 1392-1401.
  1. 7.   7-hydroxystaurosporine (UCN-01) inhibition of Akt Thr(308) but not Ser(473) phosphorylation: A basis for decreased insulin-stimulated glucose transport
  2. Kondapaka, S. B.; Zarnowski, M. J.; Yver, D. R.; Sausville, E. A.; Cushman, S. W.
  3. Clinical Cancer Research. 2004, NOV 1; 10(21): 7192-7198.
  1. 8.   Proteomic investigation of natural killer cell microsomes using gas-phase fractionation by mass spectrometry
  2. Blonder, J.; Rodriguez-Galan, M. C.; Lucas, D. A.; Young, H. A.; Issaq, H. J.; Veenstra, T. D.; Conrads, T. P.
  3. Biochimica Et Biophysica Acta-Proteins and Proteomics. 2004 1698(1): 87-95.
  1. 9.   Constitutive expression and localization of the major drug metabolizing enzyme, cytochrome P4502D in human brain
  2. Chinta, S. J.; Pai, H. V.; Upadhya, S. C.; Boyd, M. R.; Ravindranath, V.
  3. Molecular Brain Research. 2002 103(1-2): 49-61.
  1. 10.   Enhancement of N-nitrosodiethylamine-initiated hepatocarcinogenesis by phenytoin in male F344/NCr rats at a dose causing maximal induction of CYP2B
  2. Diwan, B. A.; Henneman, J. R.; Nims, R. W.
  3. International Journal of Toxicology. 2001 20(2): 81-87.
  1. 11.   Role of CYP1A1 in modulation of antitumor properties of the novel agent 2-(4-amino-3-methylphenyl)benzothiazole (DF 203, NSC 674495) in human breast cancer cells
  2. Chua, M. S.; Kashiyama, E.; Bradshaw, T. D.; Stinson, S. F.; Brantley, E.; Sausville, E. A.; Stevens, M. F. G.
  3. Cancer Research. 2000 60(18): 5196-5203.
  1. 12.   Metabolism of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone by cultured monkey lung explants
  2. Hecht, S. S.; Trushin, N.; Chhabra, S. K.; Anderson, L. M.; Nerurkar, P. V.
  3. Drug Metabolism and Disposition. 2000 28(1): 5-9.
  1. 13.   Multiple forms of cytochrome P450 and associated monooxygenase activities in human brain mitochondria
  2. Bhagwat, S. V.; Boyd, M. R.; Ravindranath, V.
  3. Biochemical Pharmacology. 2000 59(5): 573-582.
  1. 14.   The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor
  2. Ciolino, H. P.; Yeh, G. C.
  3. British Journal of Cancer. 1999 79(9-10): 1340-1346.
  1. 15.   Comparative Pharmacodynamics of Cyp2b Induction By Ddt, Dde, and Ddd in Male Rat Liver and Cultured Rat Hepatocytes
  2. Nims, R. W.; Lubet, R. A.; Fox, S. D.; Jones, C. R.; Thomas, P. E.; Reddy, A. B.; Kocarek, T. A.
  3. Journal of Toxicology and Environmental Health. 1998 53(6): 455-477.
  1. 16.   Role of Cytochrome P450 Enzyme Induction in the Metabolic Activation of Benzo
  2. Einolf, H. J.; Story, W. T.; Marcus, C. B.; Larsen, M. C.; Jefcoate, C. R.; Greenlee, W. F.; Yagi, H.; Jerina, D. M.; Amin, S.; Park, S. S.; Gelboin, H. V.; Baird, W. M.
  3. Chemical Research in Toxicology. 1997 10(5): 609-617.
  1. 17.   Catalysis of the Cysteine Conjugation and Protein Binding of Acetaminophen By Microsomes From a Human Lymphoblast Line Transfected With the Cdnas of Various Forms of Human Cytochrome P450
  2. Zhou, L. X.; Erickson, R. R.; Hardwick, J. P.; Park, S. S.; Wrighton, S. A.; Holtzman, J. L.
  3. Journal of Pharmacology and Experimental Therapeutics. 1997 281(2): 785-790.
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