Identification of GATA6 sequence variants in patients with congenital heart defects.
about
Of mice and men: molecular genetics of congenital heart diseaseToying with fate: Redirecting the differentiation of adrenocortical progenitor cells into gonadal-like tissueEmbryonic Development of the Bicuspid Aortic Valve.GATA6 haploinsufficiency causes pancreatic agenesis in humans.Novel and functional DNA sequence variants within the GATA6 gene promoter in ventricular septal defects.GATA4 and GATA6 control mouse pancreas organogenesis.GATA factors in endocrine neoplasiaNovel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallotGATA5 loss-of-function mutations underlie tetralogy of fallot.Novel GATA4 mutations in patients with congenital ventricular septal defects.GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiencyConditional mutagenesis of Gata6 in SF1-positive cells causes gonadal-like differentiation in the adrenal cortex of mice.Transcription factor pathways and congenital heart disease.Cardiac outflow tract anomalies.Genetics of Congenital Heart Disease: Past and Present.GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis.Genetic insights into bicuspid aortic valve formation.A novel GATA6 mutation in a child with congenital heart malformation and neonatal diabetes.GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect.Elevated methylation of the RXRA promoter region may be responsible for its downregulated expression in the myocardium of patients with TOF.Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve.Genome-wide association scan suggests basis for microtia in Awassi sheep.Zinc-finger proteins in health and disease.Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes.Cardiac manifestations of Pallister-Killian syndrome.
P2860
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P2860
Identification of GATA6 sequence variants in patients with congenital heart defects.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Identification of GATA6 sequence variants in patients with congenital heart defects.
@ast
Identification of GATA6 sequence variants in patients with congenital heart defects.
@en
Identification of GATA6 sequence variants in patients with congenital heart defects.
@nl
type
label
Identification of GATA6 sequence variants in patients with congenital heart defects.
@ast
Identification of GATA6 sequence variants in patients with congenital heart defects.
@en
Identification of GATA6 sequence variants in patients with congenital heart defects.
@nl
prefLabel
Identification of GATA6 sequence variants in patients with congenital heart defects.
@ast
Identification of GATA6 sequence variants in patients with congenital heart defects.
@en
Identification of GATA6 sequence variants in patients with congenital heart defects.
@nl
P2860
P1433
P1476
Identification of GATA6 sequence variants in patients with congenital heart defects
@en
P2093
Deepak Srivastava
Meenakshi Maitra
P2860
P2888
P304
P356
10.1203/PDR.0B013E3181ED17E4
P407
P577
2010-10-01T00:00:00Z
P6179
1015914656