UA Meyer
UA Meyer
Professor of Pharmacology, Biozentrum, University of Basel, Switzerland
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Cited by
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The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans.
SM De Morais, GR Wilkinson, J Blaisdell, K Nakamura, UA Meyer, ...
Journal of Biological Chemistry 269 (22), 15419-15422, 1994
Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese.
SM De Morais, GR Wilkinson, J Blaisdell, UA Meyer, K Nakamura, ...
Molecular pharmacology 46 (4), 594-598, 1994
Characterization of the common genetic defect in humans deficient in debrisoquine metabolism
FJ Gonzalez, RC Skodat, S Kimura, M Umeno, UM Zanger, DW Nebert, ...
Nature 331 (6155), 442-446, 1988
Pharmacogenetics and adverse drug reactions
UA Meyer
The Lancet 356 (9242), 1667-1671, 2000
Molecular mechanisms of genetic polymorphisms of drug metabolism
UA Meyer, UM Zanger
Annual review of pharmacology and toxicology 37 (1), 269-296, 1997
Cyclosporine metabolism in human liver: identification of a cytochrome P‐450III gene family as the major cyclosporine‐metabolizing enzyme explains interactions of cyclosporine …
T Kronbach, V Fischer, UA Meyer
Clinical Pharmacology & Therapeutics 43 (6), 630-635, 1988
Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4.
T Kronbach, D Mathys, M Umeno, FJ Gonzalez, UA Meyer
Molecular pharmacology 36 (1), 89-96, 1989
Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification
M Heim, UA Meyer
The Lancet 336 (8714), 529-532, 1990
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 …
T Aoyama, S Yamano, DJ Waxman, DP Lapenson, UA Meyer, V Fischer, ...
Journal of Biological Chemistry 264 (18), 10388-10395, 1989
Human Arylamine N-Acetyltransferase Genes: Isolation, Chromosomal Localization, and Functional Expression
M Blum, DM Grant, W McBride, M Heim, UA Meyer
DNA and cell biology 9 (3), 193-203, 1990
Induction of drug metabolism: the role of nuclear receptors
C Handschin, UA Meyer
Pharmacological reviews 55 (4), 649-673, 2003
Nomenclature for human CYP2D6 alleles.
AK Daly, J Brockmöller, F Broly, M Eichelbaum, WE Evans, FJ Gonzalez, ...
Pharmacogenetics 6 (3), 193-201, 1996
The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene.
S Kimura, M Umeno, RC Skoda, UA Meyer, FJ Gonzalez
American journal of human genetics 45 (6), 889, 1989
Parenchymal cells from adult rat liver in nonproliferating monolayer culture: I. functional studies
D Montgomery Bissell, LE Hammaker, UA Meyer
The Journal of cell biology 59 (3), 722-734, 1973
Polymorphism of the cytochrome P450 CYP2D6 gene in a European population: characterization of 48 mutations and 53 alleles, their frequencies and evolution.
D Marez, M Legrand, N Sabbagh, LG JM, C Spire, JJ Lafitte, UA Meyer, ...
Pharmacogenetics 7 (3), 193-202, 1997
Nomenclature for N-acetyltransferases.
KP Vatsis, WW Weber, DA Bell, JM Dupret, DA Evans, DM Grant, ...
Pharmacogenetics 5 (1), 1-17, 1995
Molecular mechanism of slow acetylation of drugs and carcinogens in humans.
M Blum, A Demierre, DM Grant, M Heim, UA Meyer
Proceedings of the National Academy of Sciences 88 (12), 5237-5241, 1991
Pharmacogenetics–five decades of therapeutic lessons from genetic diversity
UA Meyer
Nature Reviews Genetics 5 (9), 669-676, 2004
Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by …
M Kagimoto, M Heim, K Kagimoto, T Zeugin, UA Meyer
Journal of Biological Chemistry 265 (28), 17209-17214, 1990
Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism.
A Gaedigk, M Blum, R Gaedigk, M Eichelbaum, UA Meyer
American journal of human genetics 48 (5), 943, 1991
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