Miotic action of tramadol is determined by CYP2D6 genotype von Slanar, O, Nobilis, M, Kvetina, J, Mikoviny, R, Zima, T, Idle, J R, Perlík, F

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Rifampicin-Activated Human Pregnane X Receptor and CYP3A4 Induction Enhance Acetaminophen-Induced Toxicity von Cheng, Jie, Ma, Xiaochao, Krausz, Kristopher W., Idle, Jeffrey R., Gonzalez, Frank J.

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Identification of Novel Toxicity-associated Metabolites by Metabolomics and Mass Isotopomer Analysis of Acetaminophen Metabolism in Wild-type and Cyp2e1-null Mice von Chen, Chi, Krausz, Kristopher W., Idle, Jeffrey R., Gonzalez, Frank J.

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Comparative aromatic hydroxylation and N-demethylation of MPTP neurotoxin and its analogs, N-methylated β-carboline and isoquinoline alkaloids, by human cytochrome P450 2D6 von Herraiz, Tomás, Guillén, Hugo, Arán, Vicente J., Idle, Jeffrey R., Gonzalez, Frank J.

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Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene von Løvlie, Roger, Daly, Ann K., Molven, Anders, Idle, Jeffrey R., Steen, Vidar M.

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CYP2D6 polymorphism, tramadol pharmacokinetics and pupillary response von Slanar, Ondrej, Nobilis, Milan, Kvetina, Jaroslav, Idle, Jeffrey R, Perlík, Frantisek

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Pharmacokinetics of tramadol is affected by MDR1 polymorphism C3435T von Slanar, Ondrej, Nobilis, Milan, Kvétina, Jaroslav, Matousková, Olga, Idle, Jeffrey R, Perlík, Frantisek

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Antipsychotic drug-induced movement disorders in schizophrenics in relation to CYP2D6 genotype von Armstrong, Martin, Daly, Ann K., Blennerhassett, Richard, Ferrier, Nicol, Idle, Jeffrey R.

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Serum metabolomics reveals irreversible inhibition of fatty acid beta-oxidation through the suppression of PPARalpha activation as a contributing mechanism of acetaminophen-induced... von Chen, Chi, Krausz, Kristopher W, Shah, Yatrik M, Idle, Jeffrey R, Gonzalez, Frank J

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Nomenclature for human CYP2D6 alleles von DALY, A. K, BROCKMÖLLER, J, JACQZ-AIGRAIN, E, MEYER, U. A, NEBERT, D. W, STEEN, V. M, WOLF, C. R, ZANGER, U. M, BROLY, F, EICHELBAUM, M, EVANS, W. E, GONZALEZ, F. J, HUANG, J.-D, IDLE, J. R, INGELMAN-SUNDBERG, M, ISHIZAKI, T

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The effect of pregnane X receptor (PXR)‐mediated CYP3A induction on acetaminophen hepatotoxicity von MA, XIAOCHAO, CHEN, CHI, Shah, Yatrik, Morimura, Keiichirou, Krausz, Kristopher W., Idle, Jeffrey R., GONZALEZ, FRANK J

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Genetically determined oxidation capacity and the disposition of debrisoquine von Sloan, TP, Lancaster, R, Shah, RR, Idle, JR, Smith, RL

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A phase I study on the reversal of multidrug resistance (MDR) in vivo : nifedipine plus etoposide von PHILIP, P. A, JOEL, S, MONKMAN, S. C, DOLEGA-OSSOWSKI, E, TONKIN, K, CARMICHAEL, J, IDLE, J. R, HARRIS, A. L

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The N‐oxidation of trimethylamine in a Jordanian population von Hadidi, HF, Cholerton, S, Atkinson, S, Irshaid, YM, Rawashdeh, NM, Idle, JR

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Genetic aspects of the polymodally distributed sulphoxidation of S‐ carboxymethyl‐L‐cysteine in man von Mitchell, SC, Waring, RH, Haley, CS, Idle, JR, Smith, RL

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The rationale for case‐control methodology in epidemiological studies of cancer risk (response to Speirs et al., 1990) [see comments] von Caporaso, N, Idle, JR

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Detection of the poor metabolizer-associated CYP2D6(D) gene deletion allele by long-PCR technology von Steen, V M, Andreassen, O A, Daly, A K, Tefre, T, Børresen, A L, Idle, J R, Gulbrandsen, A K

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CYP2D6 phenotype : genotype relationships in African-Americans and Caucasians in Los Angeles von LEATHART, J. B. S, LONDON, S. J, STEWARD, A, ADAMS, J. D, IDLE, J. R, DALY, A. K

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The influence of food on the pharmacokinetics of ‘biphasic’ nifedipine at steady state in normal subjects von Rimoy, GH, Idle, JR, Bhaskar, NK, Rubin, PC

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A phase I study on the reversal of multidrug resistance (MDR) in vivo: nifedipine plus etoposide: Clinical Oncology/Epidemiology von Philip, PA, Joel, S, Monkman, SC, Dolega-Ossowski, E, Tonkin, K, Carmichael, J, Idle, JR, Harris, AL

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