(Q34985920)

5 August 2017

Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population (English)

1 reference

5 August 2017

0 references

1 reference

congenital heart disease

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Jing Xu

1

1 reference

5 August 2017

Zhibin Hu

2

1 reference

5 August 2017

Zhengfeng Xu

3

1 reference

5 August 2017

Haiyong Gu

4

1 reference

5 August 2017

Long Yi

5

1 reference

5 August 2017

Hailong Cao

6

1 reference

5 August 2017

Jiaping Chen

7

1 reference

5 August 2017

Tian Tian

8

1 reference

5 August 2017

Jie Liang

9

1 reference

5 August 2017

Ying Lin

10

1 reference

5 August 2017

Wanshan Qiu

11

1 reference

5 August 2017

Hongxia Ma

12

1 reference

5 August 2017

Hongbing Shen

13

1 reference

5 August 2017

Yijiang Chen

14

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5 August 2017

1 August 2009

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5 August 2017

1 reference

5 August 2017

30

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5 August 2017

8

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5 August 2017

1231-1236

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

5 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

The developmental genetics of congenital heart disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Expression of homeobox genes Msx-1 (Hox-7) and Msx-2 (Hox-8) during cardiac development in the chick

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

An SNP-guided microRNA map of fifteen common human disorders identifies a consensus disease phenocode aiming at principal components of the nuclear import pathway

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Independent requirements for Hedgehog signaling by both the anterior heart field and neural crest cells for outflow tract development.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Intracardiac septation requires hedgehog-dependent cellular contributions from outside the heart

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Congenital abnormalities of body patterning: embryology revisited

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

The microRNA Registry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

The incidence of congenital heart disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

The microRNA miR-196 acts upstream of Hoxb8 and Shh in limb development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Hox genes in vertebrate development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

MicroRNA-responsive 'sensor' transgenes uncover Hox-like and other developmentally regulated patterns of vertebrate microRNA expression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Steroid-dependent modification of Hox function drives myocyte reprogramming in the Drosophila heart

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

A decade of discoveries in cardiac biology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Gene regulatory networks in the evolution and development of the heart

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

MicroRNA expression profiling of single whole embryonic stem cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

MicroRNAs in the human heart: a clue to fetal gene reprogramming in heart failure

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

MicroRNAs: powerful new regulators of heart disease and provocative therapeutic targets

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

VEGF C-634G polymorphism is associated with protection from isolated ventricular septal defect: case-control and TDT studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

MicroRNA-directed cleavage of HOXB8 mRNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Dysregulation of cardiogenesis, cardiac conduction, and cell cycle in mice lacking miRNA-1-2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21044

7 January 2021

Identifiers

DOI

10.1002/HUMU.21044

1 reference

5 August 2017

1 reference