(Q35654120)

9 August 2017

1 reference

title

Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapy (English)

1 reference

9 August 2017

1 reference

1

W Sadee

1 reference

9 August 2017

D Wang

2

1 reference

9 August 2017

A C Papp

3

1 reference

9 August 2017

J K Pinsonneault

4

1 reference

9 August 2017

R M Smith

5

1 reference

9 August 2017

R A Moyer

6

1 reference

9 August 2017

A D Johnson

7

1 reference

9 August 2017

language of work or name

English

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publication date

2 February 2011

1 reference

Clinical Pharmacology & Therapeutics

9 August 2017

published in

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9 August 2017

volume

89

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9 August 2017

issue

3

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9 August 2017

page(s)

355-365

1 reference

Effect of CYP2B6, ABCB1, and CYP3A5 polymorphisms on efavirenz pharmacokinetics and treatment response: an AIDS Clinical Trials Group study

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Intronic polymorphism in CYP3A4 affects hepatic expression and response to statin drugs

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Transcriptome-wide identification of RNA-binding protein and microRNA target sites by PAR-CLIP

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Genetic polymorphism in N-Acetyltransferase (NAT): Population distribution of NAT1 and NAT2 activity

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Regulation of alternative splicing by histone modifications

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Alternative splicing and extensive RNA editing of human TPH2 transcripts

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Measuring cis-acting regulatory variants genome-wide: new insights into expression genetics and disease susceptibility

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

microRNAs and genetic diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Finding the missing heritability of complex diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Expansion of the human mu-opioid receptor gene architecture: novel functional variants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Aberrant splicing caused by single nucleotide polymorphism c.516G>T [Q172H], a marker of CYP2B6*6, is responsible for decreased expression and activity of CYP2B6 in liver

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Polymorphisms in human dopamine D2 receptor gene affect gene expression, splicing, and neuronal activity during working memory.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Haplotype of N-acetyltransferase 1 and 2 and risk of pancreatic cancer

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Splicing in disease: disruption of the splicing code and the decoding machinery

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

A "silent" polymorphism in the MDR1 gene changes substrate specificity

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Allelic expression imbalance of human mu opioid receptor (OPRM1) caused by variant A118G.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Polymorphisms affecting gene regulation and mRNA processing: broad implications for pharmacogenetics

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Genetics and beyond--the transcriptome of human monocytes and disease susceptibility

27 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Allelic expression of serotonin transporter (SERT) mRNA in human pons: lack of correlation with the polymorphism SERTLPR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Subcellular mRNA localization in animal cells and why it matters

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Protective effect of the CYP2C19 *17 polymorphism with increased activation of clopidogrel on cardiovascular events

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Significant effect of polymorphisms in CYP2D6 and ABCC2 on clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Impaired expression of CYP2D6 in intermediate metabolizers carrying the *41 allele caused by the intronic SNP 2988G>A: evidence for modulation of splicing events.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Response to antiretroviral treatment in HIV-1-infected individuals with allelic variants of the multidrug resistance transporter 1: a pharmacogenetics study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

C825T polymorphism in the human G protein beta3 subunit gene is associated with long-term clozapine treatment-induced body weight change in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Dopamine D2 receptor gene variants and quantitative measures of positive and negative symptom response following clozapine treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Effect of SNP at position 40237 in exon 7 of the TPH2 gene on susceptibility to suicide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Common genetic variations in human brain-specific tryptophan hydroxylase-2 and response to antidepressant treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Meta-analysis of the relevance of the OPRM1 118A>G genetic variant for pain treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

A functional polymorphism of the mu-opioid receptor gene is associated with naltrexone response in alcohol-dependent patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Induction of CYP1A2 by heavy coffee consumption is associated with the CYP1A2 -163C>A polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

A common polymorphism decreases low-density lipoprotein receptor exon 12 splicing efficiency and associates with increased cholesterol.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Effects of DRD2/ANKK1 gene variations and clinical factors on aripiprazole efficacy in schizophrenic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Intronic polymorphisms affecting alternative splicing of human dopamine D2 receptor are associated with cocaine abuse

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3251919

Association of genetic polymorphism in ABCC2 with hepatic multidrug resistance-associated protein 2 expression and pravastatin pharmacokinetics

25 September 2018

1 reference

https://api.crossref.org/works/10.1038%2FCLPT.2010.314

Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21289622

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21289622

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C>T affects mRNA stability

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21289622

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/CLPT.2010.314

1 reference

9 August 2017

1 reference

9 August 2017

1 reference