(Q41593701)

4 October 2017

Effect of the CYP2D6*10 genotype on venlafaxine pharmacokinetics in healthy adult volunteers (English)

1 reference

4 October 2017

1 reference

Fukuda T

1

1 reference

4 October 2017

Yamamoto I

2

1 reference

4 October 2017

Nishida Y

3

1 reference

4 October 2017

Zhou Q

4

1 reference

4 October 2017

Ohno M

5

1 reference

4 October 2017

Takada K

6

1 reference

4 October 2017

Azuma J

7

1 reference

4 October 2017

language of work or name

English

0 references

publication date

1 April 1999

1 reference

British Journal of Clinical Pharmacology

4 October 2017

1 reference

4 October 2017

47

1 reference

4 October 2017

4

1 reference

4 October 2017

450-453

1 reference

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

4 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

Genetic analysis of the Chinese cytochrome P4502D locus: characterization of variant CYP2D6 genes present in subjects with diminished capacity for debrisoquine hydroxylation.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

Venlafaxine: a heterocyclic antidepressant.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

Venlafaxine oxidation in vitro is catalysed by CYP2D6.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

Nomenclature for human CYP2D6 alleles.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

Evidence for a new variant CYP2D6 allele CYP2D6J in a Japanese population associated with lower in vivo rates of sparteine metabolism.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

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

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification

19 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1046%2FJ.1365-2125.1999.00913.X

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014246

Metoprolol and mephenytoin oxidation polymorphisms in Far Eastern Oriental subjects: Japanese versus mainland Chinese

2 December 2018

1 reference

12 December 2020

Debrisoquine and S-mephenytoin hydroxylation phenotypes and genotypes in a Korean population

1 reference

12 December 2020

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

1 reference

12 December 2020

Metabolic disposition of 14C-venlafaxine in mouse, rat, dog, rhesus monkey and man

1 reference

12 December 2020

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

1 reference

12 December 2020

The cytochrome P450 CYP2D6 allelic variant CYP2D6J and related polymorphisms in a European population

1 reference

12 December 2020

Propranolol disposition in Chinese subjects of different CYP2D6 genotypes

1 reference

12 December 2020

10.1046/J.1365-2125.1999.00913.X

Identifiers

DOI

1 reference

4 October 2017

1 reference

4 October 2017

PubMed publication ID

10233212

1 reference