Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve
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Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart DiseaseHypoplastic left heart syndrome: current considerations and expectationsMyocardial alternative RNA splicing and gene expression profiling in early stage hypoplastic left heart syndromeInterrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen.Congenital heart disease linked to maternal autoimmunity against cardiac myosin.Rare copy number variants contribute to congenital left-sided heart disease.Genome-wide association study of maternal and inherited effects on left-sided cardiac malformationsDirected differentiation of patient-specific induced pluripotent stem cells identifies the transcriptional repression and epigenetic modification of NKX2-5, HAND1, and NOTCH1 in hypoplastic left heart syndrome.Loss of Gata5 in mice leads to bicuspid aortic valve.Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic NetworksAorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve.A roadmap to investigate the genetic basis of bicuspid aortic valve and its complications: insights from the International BAVCon (Bicuspid Aortic Valve Consortium).The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesions.New Genetic Insights into Congenital Heart Disease.Hypoplastic left heart syndrome is associated with structural and vascular placental abnormalities and leptin dysregulation.Bicuspid aortic valve and thoracic aortic aneurysm: three patient populations, two disease phenotypes, and one shared genotype.The complex genetics of hypoplastic left heart syndrome.Transcriptional Impact of Rare and Private Copy Number Variants in Hypoplastic Left Heart SyndromeA genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.Heart valve development: regulatory networks in development and diseasePersistent left superior vena cava: does it have a role in the pathogenesis of hypoplastic left heart syndrome?Molecular and developmental mechanisms of congenital heart valve disease.Hypoplastic left heart syndrome and other left heart disease: evolution of understanding from population-based analysis to molecular biology and back again--a brief overview.Family-based studies to identify genetic variants that cause congenital heart defects.Mendelian forms of structural cardiovascular disease.Comparative transcriptome profiling in human bicuspid aortic valve disease using RNA sequencing.Concise Review: Cardiac Disease Modeling Using Induced Pluripotent Stem Cells.The myocardial and coronary histopathology and pathogenesis of hypoplastic left heart syndrome.An induced pluripotent stem cell model of hypoplastic left heart syndrome (HLHS) reveals multiple expression and functional differences in HLHS-derived cardiac myocytes.Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.Impact of MYH6 variants in hypoplastic left heart syndrome.Microcephaly is associated with early adverse neurologic outcomes in hypoplastic left heart syndrome.Left atrial ligation alters intracardiac flow patterns and the biomechanical landscape in the chick embryo.Factors other than genotype account largely for the phenotypic variation of the pulmonary valve in Syrian hamsters.Chromosomal Abnormalities Affect the Surgical Outcome in Infants with Hypoplastic Left Heart Syndrome: A Large Cohort Analysis.Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach.NOTCH1-Dependent Nitric Oxide Signaling Deficiency in Hypoplastic Left Heart Syndrome Revealed Through Patient-Specific Phenotypes Detected in Bioengineered Cardiogenesis.Genetically alike Syrian hamsters display both bifoliate and trifoliate aortic valves.6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathy.
P2860
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P2860
Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve
description
2009 nî lūn-bûn
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2009 թուականի Մարտին հրատարակուած գիտական յօդուած
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2009 թվականի մարտին հրատարակված գիտական հոդված
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2009年の論文
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2009年論文
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2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
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2009年論文
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2009年论文
@wuu
name
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@ast
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@en
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@nl
type
label
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@ast
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@en
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@nl
prefLabel
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@ast
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@en
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@nl
P2093
P2860
P1476
Hypoplastic left heart syndrom ...... lated to bicuspid aortic valve
@en
P2093
D Woodrow Benson
Linda H Cripe
Meredith E Tabangin
Robert B Hinton
Smitha Rame-Gowda
P2860
P304
P356
10.1016/J.JACC.2008.12.023
P407
P577
2009-03-01T00:00:00Z