(Q84040828)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

title

Two novel mutations of the IRX4 gene in patients with congenital heart disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

main subject

congenital heart disease

1 reference

Zhi Cheng

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Jing Wang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Dongmei Su

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Hong Pan

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Guoying Huang

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Xiaotian Li

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Zhongzhi Li

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Adong Shen

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Xiaodong Xie

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Binbin Wang

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Xu Ma

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

publication date

5 May 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

volume

130

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

page(s)

657-662

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21544582%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00439-011-0996-7

30 January 2020

exact match

0 references

cites work

Developmental expression of the Xenopus Iroquois-family homeobox genes, Irx4 and Irx5.

1 reference

12 December 2020

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

1 reference

12 December 2020

Irx4 forms an inhibitory complex with the vitamin D and retinoic X receptors to regulate cardiac chamber-specific slow MyHC3 expression.

1 reference

12 December 2020

The Iroquois family of genes: from body building to neural patterning.

1 reference

12 December 2020

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

1 reference

12 December 2020

Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2.

1 reference

12 December 2020

Transcriptional regulation of vertebrate cardiac morphogenesis

1 reference

12 December 2020

Regulation of chamber-specific gene expression in the developing heart by Irx4.

1 reference

12 December 2020

An analysis of the syndrome of malformations induced by maternal vitamin A deficiency. Effects of restoration of vitamin A at various times during gestation

1 reference

12 December 2020

RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis.

1 reference

12 December 2020

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

1 reference

12 December 2020

Essential roles of the bHLH transcription factor Hrt2 in repression of atrial gene expression and maintenance of postnatal cardiac function

1 reference

12 December 2020

Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand

1 reference

12 December 2020

Atrial-like phenotype is associated with embryonic ventricular failure in retinoid X receptor alpha -/- mice.

1 reference

12 December 2020

1 reference

12 December 2020

Hey genes: a novel subfamily of hairy- and Enhancer of split related genes specifically expressed during mouse embryogenesis

1 reference

12 December 2020

A genetic blueprint for cardiac development

1 reference

12 December 2020

Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expression

1 reference

12 December 2020

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

1 reference

12 December 2020