(Q34193363)

31 July 2017

Heterogeneity of genetic modifiers ensures normal cardiac development (English)

1 reference

31 July 2017

1 reference

Julia B Winston

1

1 reference

31 July 2017

Jonathan M Erlich

2

1 reference

31 July 2017

Courtney A Green

3

1 reference

31 July 2017

Ashley Aluko

4

1 reference

31 July 2017

Kristine A Kaiser

5

1 reference

31 July 2017

Mai Takematsu

6

1 reference

31 July 2017

Robert S Barlow

7

1 reference

31 July 2017

Ashish O Sureka

8

1 reference

31 July 2017

Martin J LaPage

9

1 reference

31 July 2017

Luc L Janss

10

1 reference

31 July 2017

Patrick Y Jay

11

1 reference

31 July 2017

language of work or name

English

0 references

publication date

8 March 2010

1 reference

31 July 2017

1 reference

31 July 2017

121

1 reference

31 July 2017

11

1 reference

31 July 2017

1313-1321

1 reference

Genetic analysis of blood pressure in 8 mouse intercross populations

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Decanalization and the origin of complex disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Spectrum of heart disease associated with murine and human GATA4 mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

The genetic dissection of essential hypertension

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Uncovering cryptic genetic variation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Development gone awry: congenital heart disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Transcriptional regulation of vertebrate cardiac morphogenesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Congenital heart disease caused by mutations in the transcription factor NKX2-5

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

The prostaglandin receptor EP4 triggers remodelling of the cardiovascular system at birth.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Congenital heart disease among spontaneous abortuses and stillborn fetuses: prevalence and associations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Cardiovascular phenotyping of fetal mice by noninvasive high-frequency ultrasound facilitates recovery of ENU-induced mutations causing congenital cardiac and extracardiac defects

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

NKX2.5mutations in patients with congenital heart disease

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Patterns of recurrence of congenital heart disease: an analysis of 6,640 consecutive pregnancies evaluated by detailed fetal echocardiography

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953850

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5

28 October 2018

1 reference

12 December 2020

A mouse model of congenital heart disease: cardiac arrhythmias and atrial septal defect caused by haploinsufficiency of the cardiac transcription factor Csx/Nkx2.5.

1 reference

12 December 2020

Significance of cardiac defects in the developing fetus: a study of spontaneous abortuses

1 reference

12 December 2020

A second-generation study of 427 probands with congenital heart defects and their 837 children

1 reference

12 December 2020

From generational studies to a multilevel genetic-environmental interaction

1 reference

12 December 2020

Spontaneous closure of atrial septal defects within the oval fossa

1 reference

12 December 2020

The spectrum of cardiovascular anomalies in CHF1/Hey2 deficient mice reveals roles in endocardial cushion, myocardial and vascular maturation

1 reference

12 December 2020

10.1161/CIRCULATIONAHA.109.887687

Identifiers

DOI

1 reference

31 July 2017

1 reference

31 July 2017

1 reference