HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

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HOXA1 binds RBCK1/HOIL-1 and TRAF2 and modulates the TNF/NF-κB pathway in a transcription-independent manner.

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Q37228895-A3618749-5651-4676-9CF1-66BE305B9015

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HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

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http://www.wikidata.org/entity/Q43830126

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

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2012年學術文章

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2012年學術文章

@zh-hant

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HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

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HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

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Item

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HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

@en

HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

@nl

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HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

@en

HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

@nl

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HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

@en

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Binbin Wang

http://www.w3.org/2001/XMLSchema#string

Bingren Gao

http://www.w3.org/2001/XMLSchema#string

Hang Li

http://www.w3.org/2001/XMLSchema#string

Jiangyan Liu

http://www.w3.org/2001/XMLSchema#string

Jing Wang

http://www.w3.org/2001/XMLSchema#string

Longfei Cheng

http://www.w3.org/2001/XMLSchema#string

Xu Ma

http://www.w3.org/2001/XMLSchema#string

Xuehong Chen

http://www.w3.org/2001/XMLSchema#string

P2860

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

Structure and function of the HOX A1 human homeobox gene cDNA

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

The clinical spectrum of homozygous HOXA1 mutations

The incidence of congenital heart disease

Hoxa1 lineage tracing indicates a direct role for Hoxa1 in the development of the inner ear, the heart, and the third rhombomere

Genomics of the HOX gene cluster.

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

Hox genes define distinct progenitor sub-domains within the second heart field.

Cardiovascular defects in a mouse model of HOXA1 syndrome.

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s00246-012-0418-1

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226-230

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scholarly article

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10.1007/S00246-012-0418-1

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http://www.w3.org/2001/XMLSchema#string

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2012-07-10T00:00:00Z

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1043436284

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22777240

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HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

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P2860

P2860

HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P6179

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P6179

P698