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Advances in the genetic basis of coronary artery disease
scientific article
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instance of
scholarly article
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review article
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stated in
Europe PubMed Central
title
Advances in the genetic basis of coronary artery disease
(English)
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main subject
coronary artery disease
1 reference
based on heuristic
inferred from title
author name string
Qing Wang
series ordinal
1
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language of work or name
English
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publication date
May 2005
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published in
Current Atherosclerosis Reports
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volume
7
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page(s)
235-41
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issue
3
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exact match
https://scigraph.springernature.com/pub.10.1007/s11883-005-0012-6
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cites work
5-Lipoxygenase Pathway, Dendritic Cells, and Adaptive Immunity
1 reference
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PubMed Central
reference URL
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retrieved
7 April 2017
Mutation of MEF2A in an inherited disorder with features of coronary artery disease
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
retrieved
7 April 2017
Localization of a susceptibility gene for common forms of stroke to 5q12
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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7 April 2017
hMEF2C gene encodes skeletal muscle- and brain-specific transcription factors
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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7 April 2017
A fourth human MEF2 transcription factor, hMEF2D, is an early marker of the myogenic lineage
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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7 April 2017
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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7 April 2017
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
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PubMed Central
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7 April 2017
A new myocyte-specific enhancer-binding factor that recognizes a conserved element associated with multiple muscle-specific genes
1 reference
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PubMed Central
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7 April 2017
Human myocyte-specific enhancer factor 2 comprises a group of tissue-restricted MADS box transcription factors
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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7 April 2017
Arachidonate 5-lipoxygenase promoter genotype, dietary arachidonic acid, and atherosclerosis
1 reference
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PubMed Central
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7 April 2017
Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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7 April 2017
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
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7 April 2017
Human SRF-related proteins: DNA-binding properties and potential regulatory targets
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7 April 2017
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28 September 2017
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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7 April 2017
Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
Transcription factor MEF2A mutations in patients with coronary artery disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
retrieved
28 September 2017
The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
Coronary artery disease in the developing world
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
Lipoxygenase genes and their targeted disruption
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 September 2017
A trio family study showing association of the lymphotoxin-alpha N26 (804A) allele with coronary artery disease.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 November 2018
Lack of association of polymorphisms of the lymphotoxin alpha gene with myocardial infarction in Japanese.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 November 2018
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 November 2018
Tumor necrosis factor-α, lymphotoxin-α, and interleukin-10 gene polymorphisms and restenosis after coronary artery stenting
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 November 2018
The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 November 2018
Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 November 2018
Identification of 5-lipoxygenase as a major gene contributing to atherosclerosis susceptibility in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
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28 November 2018
Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
retrieved
28 November 2018
A comprehensive linkage analysis for myocardial infarction and its related risk factors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
retrieved
28 November 2018
A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783687
retrieved
28 November 2018
Interleukin-10 and tumor necrosis factor gene polymorphisms and risk of coronary artery disease and myocardial infarction
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15811259
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S11883-005-0012-6
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1547613
Dimensions Publication ID
1017250092
0 references
OpenCitations bibliographic resource ID
1547613
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1547613
PMCID
1783687
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1547613
PubMed ID
15811259
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1547613
ResearchGate publication ID
7925654
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