(Q34134235)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

Identification of GATA6 sequence variants in patients with congenital heart defects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

0 references

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Vidu Garg

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

author name string

Meenakshi Maitra

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Deepak Srivastava

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

language of work or name

English

0 references

publication date

1 October 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

volume

68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

page(s)

281-285

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1203/pdr.0b013e3181ed17e4

6 February 2020

exact match

0 references

cites work

A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac 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=2940936

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

Loss of both GATA4 and GATA6 blocks cardiac myocyte differentiation and results in acardia in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

The developmental genetics of 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=2940936

GATA4 sequence variants in patients with 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=2940936

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=2940936

Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

The genetics of cardiac birth 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=2940936

Making or breaking the heart: from lineage determination to 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=2940936

Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

A threshold of GATA4 and GATA6 expression is required for cardiovascular 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=2940936

Insights into the genetic basis of 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=2940936

GATA-6 regulates semaphorin 3C and is required in cardiac neural crest for cardiovascular 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=2940936

Mutation in myosin heavy chain 6 causes atrial septal defect

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

GATA4 is essential for formation of the proepicardium and regulates cardiogenesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

GATA-4 and GATA-6 modulate tissue-specific transcription of the human gene for P450c17 by direct interaction with Sp1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

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=2940936

The incidence of 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=2940936

The zinc finger-containing transcription factors GATA-4, -5, and -6. Ubiquitously expressed regulators of tissue-specific gene expression.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

Requirement of the transcription factor GATA4 for heart tube formation and ventral 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=2940936

GATA4 transcription factor is required for ventral morphogenesis and heart tube formation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

Over-expression of GATA-6 in Xenopus embryos blocks differentiation of heart precursors

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

GATA-6: a zinc finger transcription factor that is expressed in multiple cell lineages derived from lateral mesoderm

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

Functional domains of the Drosophila Engrailed protein

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

GATA-4 activates transcription via two novel domains that are conserved within the GATA-4/5/6 subfamily

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181ED17E4

NKX2.5mutations in patients with congenital heart disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2940936

A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20581743

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The transcription factor GATA6 is essential for early extraembryonic development

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20581743

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20581743

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1203/PDR.0B013E3181ED17E4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

6 February 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581743%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

PubMed publication ID

20581743

1 reference