(Q36055234)

English

Frequencies of CYP2D6 mutant alleles in a normal Japanese population and metabolic activity of dextromethorphan O-demethylation in different CYP2D6 genotypes

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Frequencies of CYP2D6 mutant alleles in a normal Japanese population and metabolic activity of dextromethorphan O-demethylation in different CYP2D6 genotypes (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

author name string

Kubota T

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Yamaura Y

2

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Ohkawa N

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Hara H

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Chiba K

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

language of work or name

0 references

publication date

1 July 2000

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

British Journal of Clinical Pharmacology

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

50

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

31-34

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

2 October 2017

Formation of morphine from codeine in Chinese subjects of different CYP2D6 genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

2 October 2017

A novel mutant variant of the CYP2D6 gene (CYP2D6*17) common in a black African population: association with diminished debrisoquine hydroxylase activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

11 July 2018

Nomenclature for human CYP2D6 alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

23 September 2018

Dextromethorphan polymorphic hepatic oxidation (CYP2D6) in healthy black American adult subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

23 September 2018

Genetic analysis of the CYP2D locus in relation to debrisoquine hydroxylation capacity in Korean, Japanese and Chinese subjects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

23 September 2018

Assessment of the predictive power of genotypes for the in-vivo catalytic function of CYP2D6 in a German population

2 references

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2000.00209.X

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

21 October 2018

Detection of the poor metabolizer-associated CYP2D6(D) gene deletion allele by long-PCR technology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014971

21 October 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10886115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the CYP2D6 gene in relation to dextromethorphan O-demethylation capacity in a Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/10886115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic dextromethorphan metabolism: co-segregation of oxidative O-demethylation with debrisoquin hydroxylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10886115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of genetic variation in debrisoquin hydroxylation in Chinese subjects: polymorphism in RFLP and DNA sequence of CYP2D6

1 reference

https://pubmed.ncbi.nlm.nih.gov/10886115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/10886115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new CYP2D6 allele with a nine base insertion in exon 9 in a Japanese population associated with poor metabolizer phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/10886115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An additional allelic variant of the CYP2D6 gene causing impaired metabolism of sparteine

1 reference

https://pubmed.ncbi.nlm.nih.gov/10886115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1046/J.1365-2125.2000.00209.X

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

ResearchGate publication ID

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