Two novel mutations of the IRX4 gene in patients with congenital heart disease (Q84040828)

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30 January 2020

title

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

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30 January 2020

main subject

congenital heart disease

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Zhi Cheng

1

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30 January 2020

Jing Wang

2

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30 January 2020

Dongmei Su

3

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30 January 2020

Hong Pan

4

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30 January 2020

Guoying Huang

5

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30 January 2020

Xiaotian Li

6

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30 January 2020

Zhongzhi Li

7

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30 January 2020

Adong Shen

8

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30 January 2020

Xiaodong Xie

9

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30 January 2020

Binbin Wang

10

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30 January 2020

Xu Ma

11

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30 January 2020

publication date

5 May 2011

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volume

130

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issue

5

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page(s)

657-662

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

30 January 2020

cites work

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12 December 2020

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

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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.

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Transcriptional regulation of vertebrate cardiac morphogenesis

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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

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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