(Q37427023)

English

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

scientific article published on September 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

author name string

Andrew D Johnson

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Ying Zhang

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Audrey C Papp

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Julia K Pinsonneault

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Jeong-Eun Lim

5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

David Saffen

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Zunyan Dai

7

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Danxin Wang

8

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Wolfgang Sadée

9

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

publication date

1 September 2008

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Pharmacogenetics and Genomics

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

18

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

9

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

781-791

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

The role of a single-stranded nucleotide loop in transcriptional regulation of the human sod2 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Extreme context specificity in differential allelic expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Highly variable mRNA expression and splicing of L-type voltage-dependent calcium channel alpha subunit 1C in human heart tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

ACE polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Influence of human genome polymorphism on gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Analysis of allelic differential expression in human white blood cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Ancient and recent positive selection transformed opioid cis-regulation in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Allelic variation in gene expression in thyroid tissue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Allelic variation in gene expression identified through computational analysis of the dbEST database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Allelic variations in gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Mfold web server for nucleic acid folding and hybridization prediction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Abundant raw material for cis-regulatory evolution in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Transcriptional regulation of the human manganese superoxide dismutase gene: the role of specificity protein 1 (Sp1) and activating protein-2 (AP-2).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Polymorphisms in the SOD2 and HLA-DRB1 genes are associated with nonfamilial idiopathic dilated cardiomyopathy in Japanese

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

T-786-->C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Genetic instabilities in human cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Parental imprinting studied by allele-specific primer extension after PCR: paternal X chromosome-linked genes are transcribed prior to preferential paternal X chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

23 August 2017

Survey of allelic expression using EST mining

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

14 September 2017

A survey of genetic and epigenetic variation affecting human gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

14 September 2017

In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

14 September 2017

Decreased expression of manganese superoxide dismutase in transformed cells is associated with increased cytosine methylation of the SOD2 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

28 September 2017

The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

26 June 2018

In vitro assays fail to predict in vivo effects of regulatory polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

Monoallelic and unequal allelic expression of the HTR2A gene in human brain and peripheral lymphocytes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

Increased reactive oxygen species production and functional alterations in antioxidant enzymes in human failing myocardium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

Pharmacogenetic study of statin therapy and cholesterol reduction

1 reference

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2 September 2018

Genetic polymorphisms of MPO, COMT, MnSOD, NQO1, interactions with environmental exposures and bladder cancer risk

1 reference

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2 September 2018

M-CSF induces vascular endothelial growth factor production and angiogenic activity from human monocytes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

Cis-acting variation in the expression of a high proportion of genes in human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

Detection of regulatory variation in mouse genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

2 September 2018

Allelic Variation in Human Gene Expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2779843

3 December 2018

The cyclin D1 alternative transcripts [a] and [b] are expressed in normal and malignant lymphocytes and their relative levels are influenced by the polymorphism at codon 241

1 reference

https://pubmed.ncbi.nlm.nih.gov/18698231

12 December 2020

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inferred from PubMed ID database lookup

Natural variation in human gene expression assessed in lymphoblastoid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18698231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PKA-dependent binding of mRNA to the mitochondrial AKAP121 protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/18698231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Moments of the Boltzmann distribution for RNA secondary structures

1 reference

https://pubmed.ncbi.nlm.nih.gov/18698231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18698231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18698231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel polymorphism in the MCP-1 gene regulatory region that influences MCP-1 expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/18698231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/FPC.0B013E3283050107

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

release_o2cr5edi25hydo3l3ww6zhfh2i

1 reference

https://api.fatcat.wiki/v0/release/o2cr5edi25hydo3l3ww6zhfh2i

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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