GATA2 is associated with familial early-onset coronary artery disease. - Test2 - elhamkhani - TriplyDB

GATA2 is associated with familial early-onset coronary artery disease.

GATA2 is associated with familial early-onset coronary artery disease.

http://www.wikidata.org/entity/Q33255348

about

Over-expression of DSCAM and COL6A2 cooperatively generates congenital heart defects Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking Molecular mechanism of monoamine oxidase A gene regulation under inflammation and ischemia-like conditions: key roles of the transcription factors GATA2, Sp1 and TBP Molecular hallmarks of endogenous chromatin complexes containing master regulators of hematopoiesis A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.Genetic and functional association of FAM5C with myocardial infarction Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies.Expression of a retinoic acid signature in circulating CD34 cells from coronary artery disease patients.The critical role of SENP1-mediated GATA2 deSUMOylation in promoting endothelial activation in graft arteriosclerosis Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.Evaluation and application of modularly assembled zinc-finger nucleases in zebrafish.Calling sample mix-ups in cancer population studies.Integrative bioinformatics analysis of genomic and proteomic approaches to understand the transcriptional regulatory program in coronary artery disease pathways.Genetic framework for GATA factor function in vascular biology.Evaluation of Hs-CRP levels and interleukin 18 (-137G/C) promoter polymorphism in risk prediction of coronary artery disease in first degree relatives.Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.GATA2 is required for lymphatic vessel valve development and maintenance.Genetic and genomic insights into the molecular basis of atherosclerosis.Cis-element mutated in GATA2-dependent immunodeficiency governs hematopoiesis and vascular integrity A Guide for a Cardiovascular Genomics Biorepository: the CATHGEN Experience.An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery disease The mitochondrial paradigm for cardiovascular disease susceptibility and cellular function: a complementary concept to Mendelian genetics.Common dysfunctional variants in ABCG2 are a major cause of early-onset gout.Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.The genetic basis for survivorship in coronary artery disease.Mitochondrial genetic background modulates bioenergetics and susceptibility to acute cardiac volume overload.A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease Atherosclerosis and transit of HDL through the lymphatic vasculature.Interleukin 6(-174G/C) variant and its circulating levels in coronary artery disease patients and their first degree relatives.GATA2 gene analysis in several forms of hematological malignancies including familial aggregations.Intraluminal valves: development, function and disease.Genome and epigenome analysis of monozygotic twins discordant for congenital heart disease.

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P2860

GATA2 is associated with familial early-onset coronary artery disease.

http://www.wikidata.org/entity/Q33255348

description

2006 nî lūn-bûn

@nan

2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հուլիսին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

GATA2 is associated with familial early-onset coronary artery disease.

@ast

GATA2 is associated with familial early-onset coronary artery disease.

@en

GATA2 is associated with familial early-onset coronary artery disease.

@nl

type

label

GATA2 is associated with familial early-onset coronary artery disease.

@ast

GATA2 is associated with familial early-onset coronary artery disease.

@en

GATA2 is associated with familial early-onset coronary artery disease.

@nl

prefLabel

GATA2 is associated with familial early-onset coronary artery disease.

@ast

GATA2 is associated with familial early-onset coronary artery disease.

@en

GATA2 is associated with familial early-onset coronary artery disease.

@nl

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JOURNAL.PGEN.0020139

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GATA2 is associated with familial early-onset coronary artery disease.

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A Brent Hale

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Carol Haynes

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Christopher J H Jones

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David C Crossman

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David R Crosslin

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Elizabeth R Hauser

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Jessica J Connelly

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Julie E Cox

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Liyong Wang

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Pascal J Goldschmidt-Clermont

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P2860

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Haploview: analysis and visualization of LD and haplotype maps

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study

Functional analysis of the human endothelial nitric oxide synthase promoter. Sp1 and GATA factors are necessary for basal transcription in endothelial cells

An early haematopoietic defect in mice lacking the transcription factor GATA-2

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

Score tests for association between traits and haplotypes when linkage phase is ambiguous

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2

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Jeffery M. Vance

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Jonathan L Haines

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2006-07-20T00:00:00Z

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