(Q35637464)

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Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries

scientific article published on 2 April 2015

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scholarly article

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Europe PubMed Central

PubMed publication ID

9 August 2017

Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries (English)

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Europe PubMed Central

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9 August 2017

Sekar Kathiresan

11

object named as

Sekar Kathiresan

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Europe PubMed Central

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9 August 2017

object named as

Hong-Hee Won

3

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ORCID Public Data File 2021

Jean-Claude Tardif

12

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Jean-Claude Tardif

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Europe PubMed Central

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9 August 2017

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Mélissa Beaudoin

1

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Europe PubMed Central

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9 August 2017

Rajat M Gupta

2

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9 August 2017

Ken Sin Lo

4

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Europe PubMed Central

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9 August 2017

Ron Do

5

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9 August 2017

Christopher A Henderson

6

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9 August 2017

Claire Lavoie-St-Amour

7

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9 August 2017

Simon Langlois

8

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9 August 2017

Daniel Rivas

9

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9 August 2017

Stephanie Lehoux

10

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9 August 2017

Kiran Musunuru

13

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9 August 2017

Guillaume Lettre

14

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9 August 2017

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2 April 2015

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9 August 2017

Arteriosclerosis, Thrombosis, and Vascular Biology

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Europe PubMed Central

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9 August 2017

35

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Europe PubMed Central

PubMed publication ID

9 August 2017

6

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Europe PubMed Central

PubMed publication ID

9 August 2017

1472-1479

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes

1 reference

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MicroRNA-584 and the protein phosphatase and actin regulator 1 (PHACTR1), a new signaling route through which transforming growth factor-β Mediates the migration and actin dynamics of breast cancer cells

1 reference

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Large-scale association analysis identifies new risk loci for coronary artery disease

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Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

1 reference

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1 reference

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Depletion of the novel protein PHACTR-1 from human endothelial cells abolishes tube formation and induces cell death receptor apoptosis

1 reference

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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

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A map of human genome variation from population-scale sequencing

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27 July 2018

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

1 reference

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Biological, clinical and population relevance of 95 loci for blood lipids

1 reference

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LocusZoom: regional visualization of genome-wide association scan results

1 reference

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Cervical-artery dissections: predisposing factors, diagnosis, and outcome

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Shared and distinct genetic variants in type 1 diabetes and celiac disease

1 reference

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MEF2: a central regulator of diverse developmental programs

1 reference

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Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data

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Lack of MEF2A mutations in coronary artery disease

1 reference

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

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A genetic risk variant for myocardial infarction on chromosome 6p24 is associated with impaired central hemodynamic indexes

1 reference

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12 December 2020

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10.1161/ATVBAHA.115.305534

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PMC publication ID

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Europe PubMed Central

PubMed publication ID

9 August 2017

PubMed publication ID

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Europe PubMed Central

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9 August 2017

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