(Q34266144)

1 August 2017

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot (English)

1 reference

1 August 2017

1 reference

12

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1 August 2017

Francesca Amati

7

0 references

Merlin Crossley

object named as

Merlin Crossley

11

0 references

Antonio Pizzuti

object named as

Antonio Pizzuti

1

0 references

Emanuela Conti

4

object named as

Emanuela Conti

1 reference

1 August 2017

3

Anthea L Newton

1 reference

1 August 2017

5

Elisabetta Flex

1 reference

1 August 2017

8

Debora Gianni

1 reference

1 August 2017

9

Caterina Tandoi

1 reference

1 August 2017

Anna Sarkozy

2

1 reference

PubMed ID

14517948

1 August 2017

Maria Cristina Digilio

6

1 reference

PubMed ID

14517948

1 August 2017

Bruno Marino

10

1 reference

1 August 2017

1 November 2003

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1 August 2017

1 reference

1 August 2017

22

1 reference

1 August 2017

5

1 reference

1 August 2017

372-377

1 reference

FOG-2, a heart- and brain-enriched cofactor for GATA transcription factors

1 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Distinct domains of the GATA-1 cofactor FOG-1 differentially influence erythroid versus megakaryocytic maturation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Key residues characteristic of GATA N-fingers are recognized by FOG.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Transcriptional cofactors of the FOG family interact with GATA proteins by means of multiple zinc fingers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

San Luis Valley Recombinant chromosome 8 and tetralogy of Fallot: A review of chromosome 8 anomalies and congenital heart disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

NKX2.5 mutations in patients with tetralogy of fallot

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

hFOG-2, a novel zinc finger protein, binds the co-repressor mCtBP2 and modulates GATA-mediated activation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Molecular cloning of FOG-2: a modulator of transcription factor GATA-4 in cardiomyocytes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

A functionally conserved N-terminal domain of the friend of GATA-2 (FOG-2) protein represses GATA4-dependent transcription

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10261

7 January 2021

Identifiers

DOI

10.1002/HUMU.10261

1 reference

1 August 2017

1 reference

PubMed ID

14517948