Item Type | Name |
Concept
|
Actins
|
Concept
|
Action Potentials
|
Concept
|
Age Factors
|
Concept
|
Aortic Coarctation
|
Concept
|
Aortic Valve Stenosis
|
Concept
|
Arteries
|
Concept
|
Arrhythmias, Cardiac
|
Concept
|
Alleles
|
Concept
|
Cardiomyopathy, Hypertrophic
|
Concept
|
Animals, Newborn
|
Concept
|
Anal Canal
|
Concept
|
Cleft Lip
|
Concept
|
Base Sequence
|
Concept
|
Cations, Divalent
|
Concept
|
Cell Nucleus
|
Concept
|
Atrial Fibrillation
|
Concept
|
Chimera
|
Concept
|
Blastomeres
|
Concept
|
Biopsy
|
Concept
|
Bundle of His
|
Concept
|
Embryonic Induction
|
Concept
|
Bradycardia
|
Concept
|
Chromosomes, Human, Pair 1
|
Concept
|
Cardiomyopathy, Dilated
|
Concept
|
Chromosome Deletion
|
Concept
|
Cleft Palate
|
Concept
|
Coronary Artery Disease
|
Concept
|
Cysteine Endopeptidases
|
Concept
|
DNA, Bacterial
|
Concept
|
Down Syndrome
|
Concept
|
Cell Fusion
|
Concept
|
Echocardiography
|
Concept
|
Ductus Arteriosus, Patent
|
Concept
|
Cardiomegaly
|
Concept
|
Lac Operon
|
Concept
|
Electrophysiology
|
Concept
|
Cilia
|
Concept
|
DNA, Superhelical
|
Concept
|
Electrocardiography
|
Concept
|
Glycogen Storage Disease
|
Concept
|
Genes, Lethal
|
Concept
|
Fibroblast Growth Factors
|
Concept
|
Genetic Complementation Test
|
Concept
|
Heart Diseases
|
Concept
|
Heart Failure
|
Concept
|
Heart Septal Defects, Atrial
|
Concept
|
Embryo, Mammalian
|
Concept
|
Escherichia coli
|
Concept
|
Fluorescent Antibody Technique
|
Concept
|
Microfilament Proteins
|
Concept
|
Molecular Sequence Data
|
Concept
|
Pre-Excitation Syndromes
|
Concept
|
Procainamide
|
Concept
|
Tetralogy of Fallot
|
Concept
|
Poliomyelitis
|
Concept
|
Heart Defects, Congenital
|
Concept
|
Heart Septal Defects, Ventricular
|
Concept
|
Repressor Proteins
|
Concept
|
Risk Factors
|
Concept
|
Wolff-Parkinson-White Syndrome
|
Concept
|
Cohort Studies
|
Concept
|
Sarcomeres
|
Concept
|
Sodium
|
Concept
|
Spine
|
Concept
|
Transcription, Genetic
|
Concept
|
Truncus Arteriosus
|
Concept
|
Trisomy
|
Concept
|
Caenorhabditis elegans
|
Concept
|
Sodium Channels
|
Concept
|
Trans-Activators
|
Concept
|
Chromosomes, Artificial, Bacterial
|
Concept
|
Ventricular Fibrillation
|
Concept
|
Transforming Growth Factor beta
|
Concept
|
Vacuolar Proton-Translocating ATPases
|
Concept
|
Antigens, CD
|
Concept
|
Mortality
|
Concept
|
Gene Expression
|
Concept
|
Chromosomes, Mammalian
|
Concept
|
Connexins
|
Concept
|
Genes, Reporter
|
Concept
|
Cardiomyopathies
|
Concept
|
Myocarditis
|
Concept
|
Hypertrophy, Left Ventricular
|
Concept
|
Connexin 43
|
Concept
|
Cell Proliferation
|
Concept
|
Ventricular Dysfunction
|
Concept
|
Disease Progression
|
Concept
|
Basic-Leucine Zipper Transcription Factors
|
Concept
|
Transgenes
|
Concept
|
Chemokines, CC
|
Concept
|
Cardiomyopathy, Hypertrophic, Familial
|
Concept
|
Myosin Heavy Chains
|
Concept
|
In Situ Hybridization, Fluorescence
|
Concept
|
Fatal Outcome
|
Concept
|
Single-Cell Analysis
|
Concept
|
Peripheral Blood Stem Cell Transplantation
|
Concept
|
Chromatin Assembly and Disassembly
|
Concept
|
Smad4 Protein
|
Concept
|
Genomic Imprinting
|
Concept
|
Response Elements
|
Concept
|
Bone Morphogenetic Proteins
|
Concept
|
Small Ubiquitin-Related Modifier Proteins
|
Concept
|
Platelet Count
|
Concept
|
SUMO-1 Protein
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Hedgehog Proteins
|
Concept
|
Sarcoplasmic Reticulum
|
Concept
|
Brugada Syndrome
|
Concept
|
HEK293 Cells
|
Concept
|
E2F3 Transcription Factor
|
Concept
|
GATA4 Transcription Factor
|
Concept
|
GATA6 Transcription Factor
|
Concept
|
Wnt2 Protein
|
Concept
|
Kruppel-Like Transcription Factors
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Insulin-Secreting Cells
|
Concept
|
Regulatory Elements, Transcriptional
|
Concept
|
Chemokine CCL4
|
Concept
|
Zebrafish
|
Concept
|
Fibroblast Growth Factor 4
|
Concept
|
Fibroblast Growth Factor 8
|
Concept
|
Heart Transplantation
|
Concept
|
Axonemal Dyneins
|
Concept
|
Cyclosporine
|
Concept
|
Mice, 129 Strain
|
Concept
|
Death, Sudden, Cardiac
|
Concept
|
Ventricular Outflow Obstruction
|
Concept
|
Genes, Helminth
|
Concept
|
Survival Rate
|
Concept
|
DNA Methylation
|
Concept
|
Troponin T
|
Concept
|
Stroke
|
Concept
|
T-Box Domain Proteins
|
Concept
|
Gene Silencing
|
Concept
|
Homeodomain Proteins
|
Concept
|
Cardiac Myosins
|
Concept
|
Ventricular Dysfunction, Left
|
Concept
|
Cell Lineage
|
Concept
|
Macrophage Inflammatory Proteins
|
Concept
|
Electrophysiologic Techniques, Cardiac
|
Concept
|
Transcriptome
|
Concept
|
Genome-Wide Association Study
|
Concept
|
Haploinsufficiency
|
Concept
|
Forkhead Transcription Factors
|
Concept
|
Atrial Septum
|
Concept
|
Calcium
|
Concept
|
Cell Line
|
Concept
|
Cells, Cultured
|
Concept
|
Brain Ischemia
|
Concept
|
Chromatin
|
Concept
|
Disease Models, Animal
|
Concept
|
Endothelium
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Epidermis
|
Concept
|
Genetic Testing
|
Concept
|
Heart Septal Defects
|
Concept
|
Heart Valve Diseases
|
Concept
|
Hydrocephalus
|
Concept
|
Intercellular Junctions
|
Concept
|
Staining and Labeling
|
Concept
|
Translocation, Genetic
|
Concept
|
Regulon
|
Concept
|
Computational Biology
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Genomics
|
Concept
|
Potassium Channels, Voltage-Gated
|
Concept
|
Sarcoplasmic Reticulum Calcium-Transporting ATPases
|
Concept
|
Genetic Loci
|
Concept
|
Cytoplasmic Dyneins
|
Academic Article
|
Comparison of two murine models of familial hypertrophic cardiomyopathy.
|
Academic Article
|
Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C gene.
|
Academic Article
|
Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice.
|
Academic Article
|
The T-Box transcription factor Tbx5 is required for the patterning and maturation of the murine cardiac conduction system.
|
Academic Article
|
Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome.
|
Academic Article
|
Repression of cell-cell fusion by components of the C. elegans vacuolar ATPase complex.
|
Academic Article
|
A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development.
|
Academic Article
|
Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia.
|
Academic Article
|
Characterization of sinoatrial node in four conduction system marker mice.
|
Academic Article
|
Complex genomic rearrangement in CCS-LacZ transgenic mice.
|
Academic Article
|
The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
|
Academic Article
|
A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines.
|
Academic Article
|
Genome-wide identification of mouse congenital heart disease loci.
|
Academic Article
|
A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus.
|
Academic Article
|
Tbx5-hedgehog molecular networks are essential in the second heart field for atrial septation.
|
Academic Article
|
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
|
Academic Article
|
TBX5 drives Scn5a expression to regulate cardiac conduction system function.
|
Academic Article
|
E2F3 plays an essential role in cardiac development and function.
|
Academic Article
|
Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development. [corrected]
|
Academic Article
|
Complex interactions between genes controlling trafficking in primary cilia.
|
Academic Article
|
Defective sumoylation pathway directs congenital heart disease.
|
Academic Article
|
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
|
Academic Article
|
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
|
Academic Article
|
Ventricular fibrillation following autologous intramyocardial cell therapy for inherited cardiomyopathy.
|
Academic Article
|
sonic hedgehog is required in pulmonary endoderm for atrial septation.
|
Academic Article
|
DNMT3B7, a truncated DNMT3B isoform expressed in human tumors, disrupts embryonic development and accelerates lymphomagenesis.
|
Academic Article
|
Inducible recombination in the cardiac conduction system of minK: CreERT² BAC transgenic mice.
|
Academic Article
|
The emerging genetic landscape underlying cardiac conduction system function.
|
Academic Article
|
Giant cell myocarditis in a 12-year-old girl with common variable immunodeficiency.
|
Academic Article
|
Enhanced desumoylation in murine hearts by overexpressed SENP2 leads to congenital heart defects and cardiac dysfunction.
|
Academic Article
|
Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis.
|
Academic Article
|
Low-dose cyclosporin A therapy in children with refractory immune thrombocytopenic purpura.
|
Academic Article
|
Tetralogy of Fallot with congenital aortic valvar stenosis: the tetralogy-truncus interrelationship.
|
Academic Article
|
Expression of sumoylation deficient Nkx2.5 mutant in Nkx2.5 haploinsufficient mice leads to congenital heart defects.
|
Academic Article
|
Foxf genes integrate tbx5 and hedgehog pathways in the second heart field for cardiac septation.
|
Academic Article
|
MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus.
|
Academic Article
|
Maternal and zygotic Zfp57 modulate NOTCH signaling in cardiac development.
|
Academic Article
|
A common genetic variant within SCN10A modulates cardiac SCN5A expression.
|
Academic Article
|
The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model.
|
Academic Article
|
Many ways to break a heart.
|
Academic Article
|
The Cardiac TBX5 Interactome Reveals a Chromatin Remodeling Network Essential for Cardiac Septation.
|
Academic Article
|
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
|
Academic Article
|
Pitx2 modulates a Tbx5-dependent gene regulatory network to maintain atrial rhythm.
|
Academic Article
|
Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.
|
Academic Article
|
TBX5: A Key Regulator of Heart Development.
|
Academic Article
|
Correction: Foxf Genes Integrate Tbx5 and Hedgehog Pathways in the Second Heart Field for Cardiac Septation.
|
Academic Article
|
Gata4 potentiates second heart field proliferation and Hedgehog signaling for cardiac septation.
|
Academic Article
|
Chromatin-enriched lncRNAs can act as cell-type specific activators of proximal gene transcription.
|
Academic Article
|
Transcription-factor-dependent enhancer transcription defines a gene regulatory network for cardiac rhythm.
|
Academic Article
|
A promoter interaction map for cardiovascular disease genetics.
|
Academic Article
|
Evolutionarily conserved Tbx5-Wnt2/2b pathway orchestrates cardiopulmonary development.
|
Academic Article
|
A conserved HH-Gli1-Mycn network regulates heart regeneration from newt to human.
|
Academic Article
|
Genetic variant at coronary artery disease and ischemic stroke locus 1p32.2 regulates endothelial responses to hemodynamics.
|
Academic Article
|
Functional Assays to Screen and Dissect Genomic Hits: Doubling Down on the National Investment in Genomic Research.
|
Academic Article
|
A calcium transport mechanism for atrial fibrillation in Tbx5-mutant mice.
|
Academic Article
|
Gata4 regulates hedgehog signaling and Gata6 expression for outflow tract development.
|
Academic Article
|
Atrial fibrillation risk loci interact to modulate Ca2+-dependent atrial rhythm homeostasis.
|
Academic Article
|
Enhancer transcription identifies cis-regulatory elements for photoreceptor cell types.
|
Academic Article
|
Chromatin-enriched RNAs mark active and repressive cis-regulation: An analysis of nuclear RNA-seq.
|
Academic Article
|
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria.
|
Academic Article
|
Transcriptional Patterning of the Ventricular Cardiac Conduction System.
|
Academic Article
|
ZO-1 Regulates Intercalated Disc Composition and Atrioventricular Node Conduction.
|
Academic Article
|
Hedgehog-FGF signaling axis patterns anterior mesoderm during gastrulation.
|
Academic Article
|
Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation.
|
Academic Article
|
Chamber-specific transcriptional responses in atrial fibrillation.
|
Academic Article
|
Enhancer transcription identifies cis-regulatory elements for photoreceptor cell types.
|
Academic Article
|
Control of cardiomyocyte differentiation timing by intercellular signaling pathways.
|
Academic Article
|
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
|
Academic Article
|
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
|
Academic Article
|
Identification of direct transcriptional targets of NFATC2 that promote ß cell proliferation.
|
Academic Article
|
Tbx5 drives Aldh1a2 expression to regulate a RA-Hedgehog-Wnt gene regulatory network coordinating cardiopulmonary development.
|
Academic Article
|
Differential Etv2 threshold requirement for endothelial and erythropoietic development.
|
Academic Article
|
Detecting critical transition signals from single-cell transcriptomes to infer lineage-determining transcription factors.
|
Academic Article
|
Hedgehog signaling activates a mammalian heterochronic gene regulatory network controlling differentiation timing across lineages.
|
Academic Article
|
Frem1 activity is regulated by Sonic hedgehog signaling in the cranial neural crest mesenchyme during midfacial morphogenesis.
|
Academic Article
|
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.
|
Concept
|
N-Myc Proto-Oncogene Protein
|
Concept
|
Zinc Finger Protein GLI1
|
Concept
|
Homeobox Protein Nkx-2.5
|
Concept
|
Zinc Finger Protein Gli3
|
Concept
|
NAV1.5 Voltage-Gated Sodium Channel
|
Concept
|
NAV1.8 Voltage-Gated Sodium Channel
|
Concept
|
Filamins
|
Grant
|
Genetic and Molecular Analysis of Congenital Heart Disease
|
Grant
|
Gene Expression Networks for Human Cardiac Differentiation in Down Syndrome
|
Grant
|
Etiology of Congenital Heart Disease in Down Syndrome
|
Academic Article
|
Tbx5 maintains atrial identity by regulating an atrial enhancer network.
|
Academic Article
|
ETV2 primes hematoendothelial gene enhancers prior to hematoendothelial fate commitment.
|
Academic Article
|
Single-cell genomics improves the discovery of risk variants and genes of atrial fibrillation.
|
Academic Article
|
The cGAS-STING pathway is dispensable in a mouse model of LMNA-cardiomyopathy despite nuclear envelope rupture.
|
Academic Article
|
An Anterior Second Heart Field Enhancer Regulates the Gene Regulatory Network of the Cardiac Outflow Tract.
|
Academic Article
|
A Genomic Link From Heart Failure to Atrial Fibrillation Risk: FOG2 Modulates a TBX5/GATA4-Dependent Atrial Gene Regulatory Network.
|
Academic Article
|
Tbx5 maintains atrial identity in post-natal cardiomyocytes by regulating an atrial-specific enhancer network.
|