(Q46800469)

25 December 2017

title

Identification of CYP2D6 impaired functional alleles in Mexican Americans (English)

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25 December 2017

author name string

Huai-Rong Luo

1

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25 December 2017

Andrea Gaedigk

2

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25 December 2017

Vasileios Aloumanis

3

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25 December 2017

Yu-Jui Yvonne Wan

4

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25 December 2017

publication date

8 November 2005

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25 December 2017

European Journal of Clinical Pharmacology

published in

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25 December 2017

volume

61

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25 December 2017

page(s)

797-802

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25 December 2017

issue

11

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25 December 2017

https://scigraph.springernature.com/pub.10.1007/s00228-005-0044-4

exact match

0 references

cites work

Clinical implications of genetic polymorphism of CYP2D6 in Mexican Americans

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00228-005-0044-4

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

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Impact of CYP2D6 intermediate metabolizer alleles on single-dose desipramine pharmacokinetics.

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Cloning and sequencing of a new non-functional CYP2D6 allele: deletion of T1795 in exon 3 generates a premature stop codon

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CYP2D6 poor metabolizer status can be ruled out by a single genotyping assay for the -1584G promoter polymorphism.

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Molecular genetics of CYP2D6: clinical relevance with focus on psychotropic drugs

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Simultaneous determination of dextromethorphan and three metabolites in plasma and urine using high-performance liquid chromatography with application to their disposition in man.

1 reference

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Analysis of the CYP2D6 gene polymorphism and enzyme activity in African-Americans in southern California

1 reference

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Characterization of the common genetic defect in humans deficient in debrisoquine metabolism

1 reference

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Optimization of cytochrome P4502D6 (CYP2D6) phenotype assignment using a genotyping algorithm based on allele frequency data

1 reference

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Unique CYP2D6 activity distribution and genotype-phenotype discordance in black Americans

1 reference

12 December 2020

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

1 reference

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Elucidation of the genetic basis of the common 'intermediate metabolizer' phenotype for drug oxidation by CYP2D6

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Characterization of the CYP2D6*29 allele commonly present in a black Tanzanian population causing reduced catalytic activity

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A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiency

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Genetic polymorphisms of CYP2D6, CYP1A1 and CYP2E1 in the South-Amerindian population of Chile

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Origins of U.S. Hispanics. Implications for diabetes

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The frequency of candidate alleles for CYP2D6 genotyping in the Japanese population with an additional respect to the -1584C to G substitution

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Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans

1 reference

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Genetic polymorphism of CYP2D6 in Chinese subjects in Malaysia.

1 reference

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

1 reference

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ADH1B*1, ADH1C*2, DRD2 (-141C Ins), and 5-HTTLPR are associated with alcoholism in Mexican American men living in Los Angeles

1 reference

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Limited association of the 2988g > a single nucleotide polymorphism with CYP2D641 in black subjects

1 reference

12 December 2020

A novel CYP2D6 allele with an abolished splice recognition site associated with the poor metabolizer phenotype

1 reference

12 December 2020

Comparison of two CYP2D6 genotyping methods and assessment of genotype-phenotype relationships

1 reference

12 December 2020

10.1007/S00228-005-0044-4

Identifiers

DOI

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25 December 2017

PubMed ID

16283274

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25 December 2017