about
A molecular pathway revealing a genetic basis for human cardiac and craniofacial defectsGATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5Mutations in NOTCH1 cause aortic valve diseaseChromosomal haplotypes by genetic phasing of human familiesGenetics of valvular heart diseaseSpectrum of heart disease associated with murine and human GATA4 mutationTbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch developmentInteraction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac developmentA unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.Identification of GATA6 sequence variants in patients with congenital heart defects.Disruption of myocardial Gata4 and Tbx5 results in defects in cardiomyocyte proliferation and atrioventricular septation.Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve.Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.MicroRNA miR145 regulates TGFBR2 expression and matrix synthesis in vascular smooth muscle cellsPharmacological inhibitor of notch signaling stabilizes the progression of small abdominal aortic aneurysm in a mouse model.Impact of Mendelian inheritance in cardiovascular disease.Insights into the genetic basis of congenital heart disease.Percutaneous Patent Ductus Arteriosus (PDA) Closure in Very Preterm Infants: Feasibility and Complications.Lifetime prevalence of sexual intercourse and contraception use at last sex among adolescents and young adults with congenital heart diseaseEndothelial Notch1 Is Required for Proper Development of the Semilunar Valves and Cardiac Outflow Tract.GATA4 sequence variants in patients with congenital heart disease.Early versus delayed umbilical cord clamping in infants with congenital heart disease: a pilot, randomized, controlled trial.Measuring genetic knowledge: a brief survey instrument for adolescents and adults.Etiology of valvular heart disease-genetic and developmental origins.Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.Nestin expression is dynamically regulated in cardiomyocytes during embryogenesis.Genetic basis of aortic valvular disease.Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease.A common cis-acting sequence in the DiGeorge critical region regulates bi-directional transcription of UFD1L and CDC45L.Genetics of congenital heart disease.A rare human sequence variant reveals myocardin autoinhibition.Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve.Compacting the heart with Notch.Genetic abnormalities in FOXP1 are associated with congenital heart defects.The Role of Lipoprotein(a) in Calcific Aortic Valve Disease: Insights From a Large-Cohort Genetic Study.Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association.Heredity of bicuspid aortic valve: is family screening indicated?Erratum: Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral developmentSubmicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart SyndromeCryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease
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description
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հետազոտող
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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Vidu Garg
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P244
P1053
D-8240-2012
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P1153
7201574939
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P214
5091151002115030280007
P244
no2017140460
P31
P3829
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0000-0002-3778-5927
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lccn-no2017140460