Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease.
|
27154817 |
2016 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Variants in the GATA4 gene have been implicated in several congenital heart diseases (CHD), such as the tetralogy of Fallot (ToF), atrial septal defect (ASD), ventricular septal defect (VSD), atrioventricular septal defect (AVSD), and dilated cardiomyopathy (DCM).
|
26376067 |
2016 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Using induced pluripotent stem cells, Ang et al. elucidate how a mutation in the transcription factor GATA4 causes congenital heart disease.
|
27984717 |
2016 |
Congenital heart disease
|
0.200 |
Biomarker
|
group |
BEFREE |
Results showed that NKX2.5, GATA4, and FOG2 were susceptibility genes of congenital heart disease.
|
27118988 |
2016 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Dominant GATA4 mutations cause congenital heart disease (CHD), specifically atrial and atrioventricular septal defects (ASDs and AVSDs).
|
28167794 |
2017 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Identification of intronic-splice site mutations in GATA4 gene in Indian patients with congenital heart disease.
|
28843068 |
2017 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Three GATA4 gene mutations, 99 G>T, 487 C>T, and 354 A>C, have been reported in congenital heart disease (CHD).
|
28471988 |
2017 |
Congenital heart disease
|
0.200 |
CausalMutation
|
group |
CLINVAR |
Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
|
27426723 |
2017 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Familial ASDs and other forms of congenital heart disease may be seen with mutations in associated myocardial transcription factors NKX2.5, GATA4, TBX6, along with conduction disorders such as AV block.
|
30305954 |
2018 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Functional mutant GATA4 identification and potential application in preimplantation diagnosis of congenital heart diseases.
|
29111206 |
2018 |
Congenital heart disease
|
0.200 |
Biomarker
|
group |
BEFREE |
GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease.
|
31115957 |
2019 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease.
|
30121862 |
2019 |
Congenital heart disease
|
0.200 |
Biomarker
|
group |
BEFREE |
NKX2-5 and GATA4 were the first congenital heart disease-causing genes identified by linkage analysis.
|
30834692 |
2019 |
Congenital heart disease
|
0.200 |
Biomarker
|
group |
BEFREE |
GATA4 is an important transcription factor involved in cardiac development and a well-known candidate gene associated with congenital heart disease (CHD).
|
30590232 |
2019 |
Congenital heart disease
|
0.200 |
GeneticVariation
|
group |
BEFREE |
Functional analysis of the congenital heart disease‑associated GATA4 H436Y mutation in vitro.
|
31322241 |
2019 |