(Q45731906)

15 December 2017

title

Genetic analysis of the TBX1 gene promoter in ventricular septal defects (English)

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15 December 2017

7

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15 December 2017

Haihua Wang

1

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15 December 2017

Dongfeng Chen

2

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15 December 2017

Liming Ma

3

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15 December 2017

Haihong Meng

4

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15 December 2017

Yumei Liu

5

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15 December 2017

Wen Xie

6

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15 December 2017

Bo Yan

8

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15 December 2017

publication date

17 July 2012

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Molecular and Cellular Biochemistry

15 December 2017

published in

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15 December 2017

volume

370

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15 December 2017

issue

1-2

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15 December 2017

page(s)

53-58

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https://scigraph.springernature.com/pub.10.1007/s11010-012-1397-5

15 December 2017

exact match

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Making or breaking the heart: from lineage determination to morphogenesis

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Epigenetic factors and cardiac development

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T-box genes in vertebrate development

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Mechanisms of T-box gene function in the developing heart

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Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract

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Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

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The del22q11.2 candidate gene Tbx1 controls regional outflow tract identity and coronary artery patterning

21 January 2018

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Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development

21 January 2018

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Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm

21 January 2018

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22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development

21 January 2018

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Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

21 January 2018

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Role of TBX1 in human del22q11.2 syndrome

21 January 2018

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

21 January 2018

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Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects

21 January 2018

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Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.

21 January 2018

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Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.

21 January 2018

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DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

21 January 2018

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

21 January 2018

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

21 January 2018

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In vivo response to high-resolution variation of Tbx1 mRNA dosage

21 January 2018

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Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

21 January 2018

1 reference

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Gain of function of Tbx1 affects pharyngeal and heart development in the mouse

21 January 2018

1 reference

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Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

21 January 2018

1 reference

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Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development

21 January 2018

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Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle

21 January 2018

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Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer

21 January 2018

1 reference

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Tbx1 regulates proliferation and differentiation of multipotent heart progenitors

21 January 2018

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Retracted: Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner

21 January 2018

1 reference

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Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Identification of downstream genetic pathways of Tbx1 in the second heart field

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Tbx1 is a negative modulator of Mef2c

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Loss of Gbx2 results in neural crest cell patterning and pharyngeal arch artery defects in the mouse embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Role of mesodermal FGF8 and FGF10 overlaps in the development of the arterial pole of the heart and pharyngeal arch arteries

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Hes1 is expressed in the second heart field and is required for outflow tract development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-012-1397-5

10.1007/S11010-012-1397-5

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

15 December 2017

1042406220

0 references

1 reference