Pharmacogenetics and adverse drug reactions von Meyer, Urs A

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The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans von de Morais, S M, Wilkinson, G R, Blaisdell, J, Nakamura, K, Meyer, U A, Goldstein, J A

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Personalized Medicine: A Personal View von Meyer, U A

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Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese von De Morais, S M, Wilkinson, G R, Blaisdell, J, Meyer, U A, Nakamura, K, Goldstein, J A

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Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification von Heim, M, Meyer, U.A

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Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4 von KRONBACH, T, MATHYS, D, UMENO, M, GONZALEZ, F. J, MEYER, U. A

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Molecular Mechanism of Slow Acetylation of Drugs and Carcinogens in Humans von Blum, Martin, Demierre, Anne, Grant, Denis M., Heim, Markus, Meyer, Urs A.

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Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by expression o... von Kagimoto, M, Heim, M, Kagimoto, K, Zeugin, T, Meyer, U A

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Metabolic interactions of the proton-pump inhibitors lansoprazole, omeprazole and pantoprazole with other drugs von Meyer, Urs A

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The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene von KIMURA, S, UMENO, M, SKODA, R. C, MEYER, U. A, GONZALEZ, F. J

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Pharmacogenetics: The Slow, The Rapid, and the Ultrarapid von Meyer, Urs A.

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Cytochrome P-450 hPCN3, a novel cytochrome P-450 IIIA gene product that is differentially expressed in adult human liver. cDNA and deduced amino acid sequence and distinct specific... von AOYAMA, T, YAMAMO, S, GONZALEZ, F. J, WAXMAN, D. J, LAPENSON, D. P, MEYER, U. A, FISCHER, V, TYNDALE, R, INABA, T, KALOW, W, GELBOIN, H. V

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Monomorphic and polymorphic human arylamine N-acetyltransferases: a comparison of liver isozymes and expressed products of two cloned genes von GRANT, D. M, BLUM, M, BEER, M, MEYER, U. A

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Site-directed mutation studies of human liver cytochrome P-450 isoenzymes in the CYP2C subfamily von VERONESE, M. E, DOECKE, C. J, MACKENZIE, P. I, MCMANUS, M. E, MINERS, J. O, REES, D. L. P, GASSER, R, MEYER, U. A, BIRKETT, D. J

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Debrisoquine/sparteine hydroxylation genotype and phenotype : analysis of common mutations and alleles of CYP2D6 in a european population von BROLY, F, GAEDICK, A, HEIM, M, EICHELBAUM, M, MORIKE, K, MEYER, U. A

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Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria von Lindberg, Raija L.P, Porcher, Catherine, Grandchamp, Bernard, Ledermann, Birgit, Bürki, Kurt, Brandner, Sebastian, Aguzzi, Adriano, Meyer, Urs A

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Antibodies against Human Cytochrome P-450db1 in Autoimmune Hepatitis Type II von Zanger, Ulrich M., Hauri, Hans-Peter, Loeper, Jacqueline, Homberg, Jean-Claude, Meyer, Urs A.

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Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism von GAEDIGK, A, BLUM, M, GAEDIGK, R, EICHELBAUM, M, MEYER, U. A

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Identification of human liver cytochrome P450 isoforms mediating omeprazole metabolism von ANDERSSON, TOMMY, MINERS, JOHN O., VERONESE, MAURICE E., TASSANEEYAKUL, WICHITTRA, TASSANEEYAKUL, WONGWIWAT, MEYER, URS A., BIRKETT, DONALD J.

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Regulatory network of lipid-sensing nuclear receptors: roles for CAR, PXR, LXR, and FXR von Handschin, Christoph, Meyer, Urs A.

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