(Q35897778)

English

The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C1935 and CYP2C192 Alleles

scientific article published on 28 May 2015

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C19*35 and CYP2C19*2 Alleles (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

object named as

Eleni Aklillu

9

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author name string

Amarjit S Chaudhry

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Bhagwat Prasad

2

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Yoshiyuki Shirasaka

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Alison Fohner

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

David Finkelstein

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Yiping Fan

6

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Shuoguo Wang

7

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Gang Wu

8

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Sarah C Sim

10

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Kenneth E Thummel

11

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Europe PubMed Central

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11 August 2017

Erin G Schuetz

12

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Europe PubMed Central

PMC publication ID

11 August 2017

publication date

28 May 2015

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Europe PubMed Central

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11 August 2017

Drug Metabolism and Disposition

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Europe PubMed Central

PMC publication ID

11 August 2017

43

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Europe PubMed Central

PMC publication ID

11 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

1226-1235

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

HTSeq--a Python framework to work with high-throughput sequencing data

1 reference

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Optimized approaches for quantification of drug transporters in tissues and cells by MRM proteomics

1 reference

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Inactive alleles of cytochrome P450 2C19 may be positively selected in human evolution

1 reference

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CYP2C19 polymorphisms and therapeutic drug monitoring of voriconazole: are we ready for clinical implementation of pharmacogenomics?

1 reference

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Clinical Pharmacogenetics Implementation Consortium guidelines for CYP2C19 genotype and clopidogrel therapy: 2013 update.

1 reference

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1 reference

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1 reference

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Clinical Pharmacogenetics Implementation Consortium guideline for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants

1 reference

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Impact of genetic polymorphisms in CYP2C9 and CYP2C19 on the pharmacokinetics of clinically used drugs

1 reference

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STAR: ultrafast universal RNA-seq aligner

1 reference

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Large-scale mapping of branchpoints in human pre-mRNA transcripts in vivo

1 reference

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The Pediatric Cancer Genome Project

1 reference

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1 reference

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Cytochrome P450 variations in different ethnic populations

1 reference

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Integrative genomics viewer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4518065

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Genome-wide association between branch point properties and alternative splicing

1 reference

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Pharmacogenetics of CYP2C19: functional and clinical implications of a new variant CYP2C19*17

1 reference

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Human Splicing Finder: an online bioinformatics tool to predict splicing signals

1 reference

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11 July 2018

Sequence features responsible for intron retention in human

1 reference

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11 July 2018

Minigene reporter for identification and analysis of cis elements and trans factors affecting pre-mRNA splicing

1 reference

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11 July 2018

A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants

1 reference

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11 July 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

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Detecting recent positive selection in the human genome from haplotype structure

1 reference

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The CYP2C19 enzyme polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4518065

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The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans

1 reference

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Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese

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Exome sequencing identifies a branch point variant in Aarskog-Scott syndrome.

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A class of human exons with predicted distant branch points revealed by analysis of AG dinucleotide exclusion zones

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Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression

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Evidence for environmental influence on CYP2D6-catalysed debrisoquine hydroxylation as demonstrated by phenotyping and genotyping of Ethiopians living in Ethiopia or in Sweden

1 reference

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Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression

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S-mephenytoin hydroxylation phenotype and CYP2C19 genotype among Ethiopians

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S-mephenytoin hydroxylation phenotypes in a Swedish population determined after coadministration with debrisoquin

1 reference

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1 reference

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1124/DMD.115.064428

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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