Meyer UA - Search Results

1

Daly AK, Brockmöller J, Broly F, Eichelbaum M, Evans WE, Gonzalez FJ, Huang JD, Idle JR, Ingelman-Sundberg M, Ishizaki T, Jacqz-Aigrain E, Meyer UA, Nebert DW, Steen VM, Wolf CR, Zanger UM. Daly AK, et al. Among authors: meyer ua. Pharmacogenetics. 1996 Jun;6(3):193-201. doi: 10.1097/00008571-199606000-00001. Pharmacogenetics. 1996. PMID: 8807658

2

Debrisoquine oxidation polymorphism: phenotypic consequences of a 3-base-pair deletion in exon 5 of the CYP2D6 gene.

Broly F, Meyer UA. Broly F, et al. Among authors: meyer ua. Pharmacogenetics. 1993 Jun;3(3):123-30. Pharmacogenetics. 1993. PMID: 8101460

3

Identification of a new variant CYP2D6 allele lacking the codon encoding Lys-281: possible association with the poor metabolizer phenotype.

Tyndale R, Aoyama T, Broly F, Matsunaga T, Inaba T, Kalow W, Gelboin HV, Meyer UA, Gonzalez FJ. Tyndale R, et al. Among authors: meyer ua. Pharmacogenetics. 1991 Oct;1(1):26-32. doi: 10.1097/00008571-199110000-00005. Pharmacogenetics. 1991. PMID: 1844820

4

An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis.

Broly F, Marez D, Sabbagh N, Legrand M, Millecamps S, Lo Guidice JM, Boone P, Meyer UA. Broly F, et al. Among authors: meyer ua. Pharmacogenetics. 1995 Dec;5(6):373-84. doi: 10.1097/00008571-199512000-00006. Pharmacogenetics. 1995. PMID: 8747409

5

Polymorphism of the cytochrome P450 CYP2D6 gene in a European population: characterization of 48 mutations and 53 alleles, their frequencies and evolution.

Marez D, Legrand M, Sabbagh N, Lo Guidice JM, Spire C, Lafitte JJ, Meyer UA, Broly F. Marez D, et al. Among authors: meyer ua. Pharmacogenetics. 1997 Jun;7(3):193-202. doi: 10.1097/00008571-199706000-00004. Pharmacogenetics. 1997. PMID: 9241659

6

Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.

Kalman LV, Agúndez J, Appell ML, Black JL, Bell GC, Boukouvala S, Bruckner C, Bruford E, Caudle K, Coulthard SA, Daly AK, Del Tredici A, den Dunnen JT, Drozda K, Everts RE, Flockhart D, Freimuth RR, Gaedigk A, Hachad H, Hartshorne T, Ingelman-Sundberg M, Klein TE, Lauschke VM, Maglott DR, McLeod HL, McMillin GA, Meyer UA, Müller DJ, Nickerson DA, Oetting WS, Pacanowski M, Pratt VM, Relling MV, Roberts A, Rubinstein WS, Sangkuhl K, Schwab M, Scott SA, Sim SC, Thirumaran RK, Toji LH, Tyndale RF, van Schaik R, Whirl-Carrillo M, Yeo K, Zanger UM. Kalman LV, et al. Among authors: meyer ua. Clin Pharmacol Ther. 2016 Feb;99(2):172-85. doi: 10.1002/cpt.280. Epub 2015 Nov 20. Clin Pharmacol Ther. 2016. PMID: 26479518 Free PMC article. Review.

7

Debrisoquine/sparteine hydroxylation genotype and phenotype: analysis of common mutations and alleles of CYP2D6 in a European population.

Broly F, Gaedigk A, Heim M, Eichelbaum M, Morike K, Meyer UA. Broly F, et al. Among authors: meyer ua. DNA Cell Biol. 1991 Oct;10(8):545-58. doi: 10.1089/dna.1991.10.545. DNA Cell Biol. 1991. PMID: 1681816

8

The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene.

Kimura S, Umeno M, Skoda RC, Meyer UA, Gonzalez FJ. Kimura S, et al. Among authors: meyer ua. Am J Hum Genet. 1989 Dec;45(6):889-904. Am J Hum Genet. 1989. PMID: 2574001 Free PMC article.

9

The human CYP2D locus associated with a common genetic defect in drug oxidation: a G1934----A base change in intron 3 of a mutant CYP2D6 allele results in an aberrant 3' splice recognition site.

Hanioka N, Kimura S, Meyer UA, Gonzalez FJ. Hanioka N, et al. Among authors: meyer ua. Am J Hum Genet. 1990 Dec;47(6):994-1001. Am J Hum Genet. 1990. PMID: 1978565 Free PMC article.

10

Molecular mechanisms of genetic polymorphisms of drug metabolism.

Meyer UA, Zanger UM. Meyer UA, et al. Annu Rev Pharmacol Toxicol. 1997;37:269-96. doi: 10.1146/annurev.pharmtox.37.1.269. Annu Rev Pharmacol Toxicol. 1997. PMID: 9131254 Review.

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