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  1. 1.   Nitric oxide donor, V-PROLI/NO, provides protection against arsenical induced toxicity in rat liver cells: Requirement for Cyp1a1
  2. Qu, W.; Cheng, L. D.; Dill, A. L.; Saavedra, J. E.; Hong, S. Y.; Keefer, L. K.; Waalkes, M. P.
  3. Chemico-Biological Interactions. 2011, Aug; 193(1): 88-96.
  1. 2.   Sulindac regulates the aryl hydrocarbon receptor-mediated expression of Phase 1 metabolic enzymes in vivo and in vitro
  2. Ciolino, H. P.; MacDonald, C. J.; Memon, O. S.; Bass, S. E.; Yeh, G. C.
  3. Carcinogenesis. 2006, Aug; 27(8): 1586-1592.
  1. 3.   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. 4.   CYP1A1 Val(462) and NQO1 Ser(187) polymorphisms, cigarette use, and risk for colorectal adenoma
  2. Hou, L. F.; Chatterjee, N.; Huang, W. Y.; Baccarelli, A.; Yadavalli, S.; Yeager, M.; Bresalier, R. S.; Chanock, S. J.; Caporaso, N. E.; Ji, B. T.; Weissfeld, J. L.; Hayes, R. B.
  3. Carcinogenesis. 2005, JUN; 26(6): 1122-1128.
  1. 5.   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. 6.   CYP1A1 and GSTM1 polymorphisms in relation to lung cancer risk in Chinese women
  2. Yang, X. H. R.; Wacholder, S.; Xu, Z. Y.; Dean, M.; Clark, V.; Gold, B.; Brown, L. M.; Stone, B. J.; Fraumeni, J. F.; Caporaso, N. E.
  3. Cancer Letters. 2004, OCT 28; 214(2): 197-204.
  1. 7.   The experimental antitumor agents Phortress and Doxorubicin are equiactive against human-derived breast carcinoma xenograft models
  2. Fichtner, I.; Monks, A.; Hose, C.; Stevens, M. F. G.; Bradshaw, T. D.
  3. Breast Cancer Research and Treatment. 2004, SEP; 87(1): 97-107.
  1. 8.   Sensitivity of renal cell carcinoma to aminoflavone: Role of CYP1A1
  2. Loaiza-Perez, A. I.; Kenney, S.; Boswell, J.; Hollingshead, M.; Hose, C.; Linehan, W. M.; Worrell, R.; Rubinstein, L.; Sausville, A.; Vistica, D. T.
  3. Journal of Urology. 2004 171(4): 1688-1697.
  1. 10.   Aryl hydrocarbon receptor activation of an antitumor aminoflavone: Basis of selective toxicity for MCF-7 breast tumor cells
  2. Loaiza-Perez, A. I.; Kenney, S.; Boswell, J.; Hollingshead, M.; Alley, M. C.; Hose, C.; Ciolino, H. P.; Yeh, G. C.; Trepel, J. B.; Vistica, D. T.; Sausville, E. A.
  3. Molecular Cancer Therapeutics. 2004 3(6): 715-725.
  1. 11.   DNA damage and cell cycle arrest induced by 2-(4-amino-3- methylphenyl)-5-fluorobenzothiazole (5F 203, NSC 703786) is attenuated in aryl hydrocarbon receptor deficient MCF-7 cells
  2. Trapani, V.; Patel, V.; Leong, C. O.; Ciolino, H. P.; Yeh, G. C.; Hose, C.; Trepel, J. B.; Stevens, M. F. G.; Sausville, E. A.; Loaiza-Perez, A. I.
  3. British Journal of Cancer. 2003 88(4): 599-605.
  1. 12.   Induction of CYP1A1 in tumor cells by the antitumor agent 2-[4- amino-3-methylphenyl]-5-fluoro-benzothiazole: A potential surrogate marker for patient sensitivity
  2. Hose, C. D.; Hollingshead, M.; Sausville, E. A.; Monks, A.
  3. Molecular Cancer Therapeutics. 2003 2(12): 1265-1272.
  1. 13.   Resistance of MCF-7 cells to dimethylbenz(a)anthracene-induced apoptosis is due to reduced CYP1A1 expression
  2. Ciolino, H. P.; Dankwah, M.; Yeh, G. C.
  3. International Journal of Oncology. 2002 21(2): 385-391.
  1. 14.   Dibenzoylmethane modulates aryl hydrocarbon receptor function and expression of cytochromes P450 1A1, 1A2, and 1B1
  2. MacDonald, C. J.; Ciolino, H. P.; Yeh, G. C.
  3. Cancer Research. 2001 61(10): 3919-3924.
  1. 15.   Influence of antioxidants and the CYP1A1 isoleucine to valine polymorphism on the Smoking Lung Cancer Association
  2. Ratnasinghe, D.; Tangrea, J. A.; Stewart, C.; Bhat, N. K.; Virtamo, J.; Albanes, D.; Taylor, P. R.
  3. Anticancer Research. 2001 21(2B): 1295-1299.
  1. 16.   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. 17.   Effect of Curcumin On the Aryl Hydrocarbon Receptor and Cytochrome P450 1a1 in Mcf-7 Human Breast Carcinoma Cells
  2. Ciolino, H. P.; Daschner, P. J.; Wang, T. T. Y.; Yeh, G. C.
  3. Biochemical Pharmacology. 1998 56(2): 197-206.
  1. 18.   The effect of flavonoids on DMBA-DNA adduct formation in MCF-7 human breast cancer cells
  2. Ciolino, H. P.; Yeh, G. C.
  3. Annual Meeting of the American Association for Cancer Research. 1997, 38 A3890.
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