(Q43100237)

13 November 2017

0 references

The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction (English)

1 reference

13 November 2017

myocardial infarction

1 reference

P González

1

1 reference

13 November 2017

M García-Castro

2

1 reference

13 November 2017

J R Reguero

3

1 reference

13 November 2017

A Batalla

4

1 reference

13 November 2017

A G Ordóñez

5

1 reference

13 November 2017

R L Palop

6

1 reference

13 November 2017

I Lozano

7

1 reference

13 November 2017

M Montes

8

1 reference

13 November 2017

V Alvarez

9

1 reference

13 November 2017

E Coto

10

1 reference

13 November 2017

language of work or name

English

0 references

publication date

15 June 2005

1 reference

Journal of Medical Genetics

13 November 2017

1 reference

13 November 2017

43

1 reference

13 November 2017

2

1 reference

13 November 2017

167-169

1 reference

Lack of MEF2A mutations in coronary artery disease

13 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Advances in the genetic basis of coronary artery disease

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Coronary heart disease and polymorphisms in genes affecting lipid metabolism and inflammation

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Polyglutamine expansion diseases: failing to deliver

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Transcription factor MEF2A mutations in patients with coronary artery disease

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Roles of cardiac transcription factors in cardiac hypertrophy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Mitochondrial deficiency and cardiac sudden death in mice lacking the MEF2A transcription factor

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathies

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

A simple salting out procedure for extracting DNA from human nucleated cells

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564638

Myocyte enhancer binding factor-2 expression and activity in vascular smooth muscle cells. Association with the activated phenotype

25 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15958500

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.2005.035071

1 reference

13 November 2017

1 reference

13 November 2017

PubMed publication ID

15958500

1 reference