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Inhibition of Cytochromes P4501A by Nitric Oxide

Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3559-3563

1994

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Flavonoids inhibit genetic toxicity produced by carcinogens in cells expressing CYP1A2 and CYP1A1

Mutagenesis, 2002-01, Vol.17 (1), p.45-53

2002

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Predicting Drug Metabolism-dependent Toxicity for Humans with a Genetically Engineered Cell Battery

Alternatives to laboratory animals, 2006-12, Vol.34 (6), p.561-575

Doehmer, J

2006

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Cytochrome P450 CYP1B1 Determines Susceptibility to 7,12-dimethylbenz[a]anthracene-induced Lymphomas

Proceedings of the National Academy of Sciences - PNAS, 1999-03, Vol.96 (5), p.1977-1982

1999

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Stable Expression of Rat Cytochrome P-450IIB1 cDNA in Chinese Hamster Cells (V79) and Metabolic Activation of Aflatoxin B1

Proceedings of the National Academy of Sciences - PNAS, 1988-08, Vol.85 (16), p.5769-5773

1988

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Assessment of extracts from mistletoe ( Viscum album) for herb–drug interaction by inhibition and induction of cytochrome P450 activities

Phytomedicine (Stuttgart), 2011-10, Vol.18 (13), p.S19-S19

2011

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Cytochrome P450 CYP1B1 protein expression:: A novel mechanism of anticancer drug resistance

Biochemical pharmacology, 2001-07, Vol.62 (2), p.207-212

2001

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Assessment of drug–drug interaction for silymarin

Toxicology in vitro, 2008-04, Vol.22 (3), p.610-617

2008

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Improved Determination of Drug Metabolism by Perifusion of Recombinant V79 Cells Carrying Human CYP3A4

Toxicology in vitro, 1999-08, Vol.13 (4), p.639-643

1999

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Competitive inhibition of carcinogen‐activating CYP1A1 and CYP1B1 enzymes by a standardized complex mixture of PAH extracted from coal tar

International journal of cancer, 2007-03, Vol.120 (6), p.1161-1168

2007

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MOLECULAR STUDIES ON THE TOXIFYING EFFECTS BY GENETICALLY ENGINEERED CYTOCHROMES P450

Drug metabolism reviews, 1999-01, Vol.31 (2), p.423-435

1999

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Stable expression and coexpression of human cytochrome P450 oxidoreductase and cytochrome P450 1A2 in V79 Chinese hamster cells: sensitivity to quinones and biotransformation of 7-alkoxyresorufins and triazines

Drug metabolism and disposition, 1996-12, Vol.24 (12), p.1314

1996

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Stable expression of rat cytochrome P-450IA1 cDNA in V79 Chinese hamster cells and their use in mutagenicity testing

Molecular pharmacology, 1990-05, Vol.37 (5), p.608-613

1990

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Molecular studies on the toxifying effects by genetically engineered cytochromes P450

Drug metabolism reviews, 1999-01, Vol.31 (2), p.423-435

1999

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Expression of human glutathione S-transferase P1 confers resistance to benzo[a]pyrene or benzo[a]pyrene-7,8-dihydrodiol mutagenesis, macromolecular alkylation and formation of stable N2-Gua-BPDE adducts in stably transfected V79MZ cells co-expressing hCYP1A1

Carcinogenesis (New York), 2007-01, Vol.28 (1), p.207-214

2007

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V79 Chinese hamster cells genetically engineered for cytochrome P450 and their use in mutagenicity and metabolism studies

Toxicology (Amsterdam), 1993-10, Vol.82 (1), p.105-118

1993

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Inhibition of cytochrome P450 enzymes by nitric oxide

Advances in experimental medicine and biology, 1996, Vol.387, p.187

1996

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Dual-colour FISH analysis to characterize a marker chromosome in cytochrome P450 2B1 recombinant V79 Chinese hamster cells

Mutagenesis, 1999, Vol.14 (1), p.57-61

1999

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Phytoalexin resveratrol attenuates the mutagenicity of the heterocyclic amines 2-amino-1-methyl-6-phenylimidazo[4,5- b]pyridine and 2-amino-3,8-dimethylimidazo[4,5- f]quinoxaline

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2004-03, Vol.802 (1), p.217-223

2004

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Protective Efficacy of hGSTM1-1 against B[a]P and (+)- or (−)-B[a]P-7,8-Dihydrodiol Cytotoxicity, Mutagenicity, and Macromolecular Adducts in V79 Cells Coexpressing hCYP1A1

Toxicological sciences, 2007-09, Vol.99 (1), p.51-57

2007

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Cytotoxicity and mutagenicity of 5-methylchrysene and its 1,2-dihydrodiol in V79MZ cells modified to express human CYP1A1 or CYP1B1, in the presence or absence of human GSTP1 coexpression

Toxicology letters, 2008-12, Vol.183 (1), p.99-104

2008

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Cytochrome P450-mediated metabolism of tumour promoters modifies the inhibition of intercellular communication: a modified assay for tumour promotion

Carcinogenesis (New York), 1993-11, Vol.14 (11), p.2365-2371

1993

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Cytotoxicity and mutagenicity of dibenzo[ a,l]pyrene and (±)-dibenzo[ a,l]pyrene-11,12-dihydrodiol in V79MZ cells co-expressing either hCYP1A1 or hCYP1B1 together with human glutathione- S-transferase A1

Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis, 2007-11, Vol.624 (1), p.80-87

2007

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Genetically Engineered V79 Chinese Hamster Cells Metabolically Activate the Cytostatic Drugs Cyclophosphamide and Ifosfamide

Environmental health perspectives, 1990-08, Vol.88, p.63-65

1990

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Heterologous co-expression of human cytochrome P450 1A2 and polymorphic forms of N-acetyltransferase 2 for studies on aromatic amines in V79 Chinese hamster cells

Alternatives to laboratory animals, 2005-12, Vol.33 (6), p.561-577

2005

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Inhibition of Cytochromes P4501A by Nitric Oxide

Flavonoids inhibit genetic toxicity produced by carcinogens in cells expressing CYP1A2 and CYP1A1

Predicting Drug Metabolism-dependent Toxicity for Humans with a Genetically Engineered Cell Battery

Cytochrome P450 CYP1B1 Determines Susceptibility to 7,12-dimethylbenz[a]anthracene-induced Lymphomas

Stable Expression of Rat Cytochrome P-450IIB1 cDNA in Chinese Hamster Cells (V79) and Metabolic Activation of Aflatoxin B1

Assessment of extracts from mistletoe ( Viscum album) for herb–drug interaction by inhibition and induction of cytochrome P450 activities

Cytochrome P450 CYP1B1 protein expression:: A novel mechanism of anticancer drug resistance

Assessment of drug–drug interaction for silymarin

Improved Determination of Drug Metabolism by Perifusion of Recombinant V79 Cells Carrying Human CYP3A4

Competitive inhibition of carcinogen‐activating CYP1A1 and CYP1B1 enzymes by a standardized complex mixture of PAH extracted from coal tar

MOLECULAR STUDIES ON THE TOXIFYING EFFECTS BY GENETICALLY ENGINEERED CYTOCHROMES P450

Stable expression and coexpression of human cytochrome P450 oxidoreductase and cytochrome P450 1A2 in V79 Chinese hamster cells: sensitivity to quinones and biotransformation of 7-alkoxyresorufins and triazines

Stable expression of rat cytochrome P-450IA1 cDNA in V79 Chinese hamster cells and their use in mutagenicity testing

Molecular studies on the toxifying effects by genetically engineered cytochromes P450

Expression of human glutathione S-transferase P1 confers resistance to benzo[a]pyrene or benzo[a]pyrene-7,8-dihydrodiol mutagenesis, macromolecular alkylation and formation of stable N2-Gua-BPDE adducts in stably transfected V79MZ cells co-expressing hCYP1A1

V79 Chinese hamster cells genetically engineered for cytochrome P450 and their use in mutagenicity and metabolism studies

Inhibition of cytochrome P450 enzymes by nitric oxide

Dual-colour FISH analysis to characterize a marker chromosome in cytochrome P450 2B1 recombinant V79 Chinese hamster cells

Phytoalexin resveratrol attenuates the mutagenicity of the heterocyclic amines 2-amino-1-methyl-6-phenylimidazo[4,5- b]pyridine and 2-amino-3,8-dimethylimidazo[4,5- f]quinoxaline

Protective Efficacy of hGSTM1-1 against B[a]P and (+)- or (−)-B[a]P-7,8-Dihydrodiol Cytotoxicity, Mutagenicity, and Macromolecular Adducts in V79 Cells Coexpressing hCYP1A1

Cytotoxicity and mutagenicity of 5-methylchrysene and its 1,2-dihydrodiol in V79MZ cells modified to express human CYP1A1 or CYP1B1, in the presence or absence of human GSTP1 coexpression

Cytochrome P450-mediated metabolism of tumour promoters modifies the inhibition of intercellular communication: a modified assay for tumour promotion

Cytotoxicity and mutagenicity of dibenzo[ a,l]pyrene and (±)-dibenzo[ a,l]pyrene-11,12-dihydrodiol in V79MZ cells co-expressing either hCYP1A1 or hCYP1B1 together with human glutathione- S-transferase A1

Genetically Engineered V79 Chinese Hamster Cells Metabolically Activate the Cytostatic Drugs Cyclophosphamide and Ifosfamide

Heterologous co-expression of human cytochrome P450 1A2 and polymorphic forms of N-acetyltransferase 2 for studies on aromatic amines in V79 Chinese hamster cells

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