(Q24317048)

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0035922

T-box transcription factor 20

1 reference

atrial septum morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

12

André Mégarbané

André

Mégarbané

1 reference

20 October 2023

Georges Nemer

11

Georges

Nemer

1 reference

20 October 2023

Margaret Sunde

3

Margaret

Sunde

1 reference

20 October 2023

Richard P Harvey

16

Richard P

Harvey

1 reference

20 October 2023

Felix Berger

15

Felix

Berger

1 reference

20 October 2023

Maximilian G Posch

1

Maximilian G

Posch

1 reference

20 October 2023

Michael Gramlich

2

Michael

Gramlich

1 reference

20 October 2023

Katharina R Schmitt

4

Katharina R

Schmitt

1 reference

20 October 2023

Stella H Y Lee

5

Stella H Y

Lee

1 reference

20 October 2023

Silke Richter

6

Silke

Richter

1 reference

20 October 2023

Andrea Kersten

7

Andrea

Kersten

1 reference

20 October 2023

Andreas Perrot

8

Andreas

Perrot

1 reference

20 October 2023

Anna N Panek

9

Anna N

Panek

1 reference

20 October 2023

Iman H Al Khatib

10

Iman H

Al Khatib

1 reference

20 October 2023

Rainer Dietz

13

Rainer

Dietz

1 reference

20 October 2023

Brigitte Stiller

14

Brigitte

Stiller

1 reference

20 October 2023

Cemil Ozcelik

17

Cemil

Ozcelik

1 reference

Journal of Medical Genetics

20 October 2023

language of work or name

English

0 references

publication date

April 2010

0 references

published in

0 references

volume

47

0 references

issue

4

0 references

page(s)

230-5

0 references

cites work

T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Characterization of TBX20 in human hearts and its regulation by TFAP2

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Role of TBX1 in human del22q11.2 syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Predicting deleterious amino acid substitutions

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Structure of the DNA-bound T-box domain of human TBX3, a transcription factor responsible for ulnar-mammary syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Human non-synonymous SNPs: server and survey

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Transcription factor neuromancer/TBX20 is required for cardiac function in Drosophila with implications for human heart disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

The developmental genetics of congenital heart disease.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

T-box transcription factors and their roles in regulatory hierarchies in the developing heart

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Inheritance of persistent foramen ovale and atrial septal defects and the relation to familial migraine with aura

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Is patent foramen ovale a family trait? A transcranial Doppler sonographic study

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Incidence and size of patent foramen ovale during the first 10 decades of life: an autopsy study of 965 normal hearts

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Conformational stability and DNA binding specificity of the cardiac T-box transcription factor Tbx20.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981023

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5

29 November 2018

1 reference

12 December 2020

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect

1 reference

12 December 2020

Quantitative trait loci modifying cardiac atrial septal morphology and risk of patent foramen ovale in the mouse

1 reference

12 December 2020

A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.2009.069997

1 reference

release_u4k7k5iv55akfi45bdbtttggba

Fatcat ID

0 references

1 reference

1 reference

1 reference