| Item Type | Name |
|
Concept
|
Actins
|
|
Concept
|
Action Potentials
|
|
Concept
|
Adenosine
|
|
Concept
|
Antigens, Neoplasm
|
|
Concept
|
Arrhythmias, Cardiac
|
|
Concept
|
Animals
|
|
Concept
|
Animals, Newborn
|
|
Concept
|
Anti-Arrhythmia Agents
|
|
Concept
|
Anal Canal
|
|
Concept
|
Aortic Valve
|
|
Concept
|
Cleft Lip
|
|
Concept
|
Base Sequence
|
|
Concept
|
Cell Movement
|
|
Concept
|
Atrial Fibrillation
|
|
Concept
|
Atrioventricular Node
|
|
Concept
|
Binding Sites
|
|
Concept
|
Biopsy
|
|
Concept
|
Bundle of His
|
|
Concept
|
Embryonic Induction
|
|
Concept
|
Bradycardia
|
|
Concept
|
Chromosomes, Human, Pair 1
|
|
Concept
|
Cell Transformation, Neoplastic
|
|
Concept
|
Chromosome Deletion
|
|
Concept
|
Cleft Palate
|
|
Concept
|
Coronary Artery Disease
|
|
Concept
|
DNA Nucleotidyltransferases
|
|
Concept
|
DNA-Binding Proteins
|
|
Concept
|
Cysteine Endopeptidases
|
|
Concept
|
Immunosuppressive Agents
|
|
Concept
|
DNA, Bacterial
|
|
Concept
|
Down Syndrome
|
|
Concept
|
DNA, Recombinant
|
|
Concept
|
Heart Septum
|
|
Concept
|
Heart Valves
|
|
Concept
|
Lac Operon
|
|
Concept
|
Electrophysiology
|
|
Concept
|
Esophagus
|
|
Concept
|
DNA, Superhelical
|
|
Concept
|
Infant, Newborn
|
|
Concept
|
Mice, Inbred C3H
|
|
Concept
|
Multienzyme Complexes
|
|
Concept
|
Atrial Natriuretic Factor
|
|
Concept
|
Glycogen Storage Disease
|
|
Concept
|
Fibroblast Growth Factors
|
|
Concept
|
Genetic Complementation Test
|
|
Concept
|
DNA (Cytosine-5-)-Methyltransferases
|
|
Concept
|
Heart
|
|
Concept
|
Heart Septal Defects, Atrial
|
|
Concept
|
Heart Ventricles
|
|
Concept
|
Endocardium
|
|
Concept
|
Fluorescent Antibody Technique
|
|
Concept
|
Heart Atria
|
|
Concept
|
Membrane Glycoproteins
|
|
Concept
|
Microfilament Proteins
|
|
Concept
|
Mice, Transgenic
|
|
Concept
|
Purpura, Thrombocytopenic
|
|
Concept
|
Mesoderm
|
|
Concept
|
Mice, Inbred C57BL
|
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
|
Concept
|
Myocardial Contraction
|
|
Concept
|
Nucleic Acid Conformation
|
|
Concept
|
Mediastinal Neoplasms
|
|
Concept
|
Embryonic and Fetal Development
|
|
Concept
|
Fibrosis
|
|
Concept
|
Procainamide
|
|
Concept
|
Poliomyelitis
|
|
Concept
|
Heart Septal Defects, Ventricular
|
|
Concept
|
Receptors, Cell Surface
|
|
Concept
|
Risk Factors
|
|
Concept
|
Xenopus
|
|
Concept
|
Cohort Studies
|
|
Concept
|
Regulatory Sequences, Nucleic Acid
|
|
Concept
|
Sarcomeres
|
|
Concept
|
Sinoatrial Node
|
|
Concept
|
Sodium
|
|
Concept
|
Risk
|
|
Concept
|
Humans
|
|
Concept
|
Single-Blind Method
|
|
Concept
|
Truncus Arteriosus
|
|
Concept
|
United States
|
|
Concept
|
Trisomy
|
|
Concept
|
Caenorhabditis elegans
|
|
Concept
|
Tamoxifen
|
|
Concept
|
Xenopus laevis
|
|
Concept
|
Sodium Channels
|
|
Concept
|
Reverse Transcriptase Polymerase Chain Reaction
|
|
Concept
|
Models, Animal
|
|
Concept
|
Ventricular Fibrillation
|
|
Concept
|
Transforming Growth Factor beta
|
|
Concept
|
Vacuolar Proton-Translocating ATPases
|
|
Concept
|
Giant Cells
|
|
Concept
|
Mutagenesis
|
|
Concept
|
Antigens, CD
|
|
Concept
|
Lymphoma
|
|
Concept
|
Mortality
|
|
Concept
|
Chromosomes, Mammalian
|
|
Concept
|
Myocardium
|
|
Concept
|
Lower Extremity Deformities, Congenital
|
|
Concept
|
Sequence Analysis, DNA
|
|
Concept
|
Connexins
|
|
Concept
|
Limb Deformities, Congenital
|
|
Concept
|
Point Mutation
|
|
Concept
|
Connexin 43
|
|
Concept
|
Sequence Deletion
|
|
Concept
|
Mice, Knockout
|
|
Concept
|
Disease Progression
|
|
Concept
|
Chemokines, CC
|
|
Concept
|
Cardiomyopathy, Hypertrophic, Familial
|
|
Concept
|
Calcium Signaling
|
|
Concept
|
Mutation, Missense
|
|
Concept
|
Xenopus Proteins
|
|
Concept
|
Myosin Heavy Chains
|
|
Concept
|
In Situ Hybridization, Fluorescence
|
|
Concept
|
Fatal Outcome
|
|
Concept
|
Peripheral Blood Stem Cell Transplantation
|
|
Concept
|
Intercellular Signaling Peptides and Proteins
|
|
Concept
|
Embryonic Development
|
|
Concept
|
Smad4 Protein
|
|
Concept
|
Genomic Imprinting
|
|
Concept
|
Response Elements
|
|
Concept
|
Bone Morphogenetic Proteins
|
|
Concept
|
Myocytes, Cardiac
|
|
Concept
|
Retinal Dehydrogenase
|
|
Concept
|
Platelet Count
|
|
Concept
|
SUMO-1 Protein
|
|
Concept
|
Progeria
|
|
Concept
|
Animals, Genetically Modified
|
|
Concept
|
Postoperative Complications
|
|
Concept
|
Promoter Regions, Genetic
|
|
Concept
|
Mice
|
|
Concept
|
Receptors, Notch
|
|
Concept
|
Hedgehog Proteins
|
|
Concept
|
Sarcoplasmic Reticulum
|
|
Concept
|
Laser Therapy
|
|
Concept
|
RNA, Messenger
|
|
Concept
|
Lamin Type A
|
|
Concept
|
Mechanotransduction, Cellular
|
|
Concept
|
Wnt2 Protein
|
|
Concept
|
Kruppel-Like Transcription Factors
|
|
Concept
|
Inhibitor of Differentiation Protein 2
|
|
Concept
|
Adaptor Proteins, Signal Transducing
|
|
Concept
|
Chemokine CCL4
|
|
Concept
|
Zebrafish
|
|
Concept
|
Fibroblast Growth Factor 4
|
|
Concept
|
Fibroblast Growth Factor 8
|
|
Concept
|
Axonemal Dyneins
|
|
Concept
|
Cyclosporine
|
|
Concept
|
Mice, 129 Strain
|
|
Concept
|
Death, Sudden, Cardiac
|
|
Concept
|
Reproducibility of Results
|
|
Concept
|
Genes, Helminth
|
|
Concept
|
Survival Rate
|
|
Concept
|
DNA Methylation
|
|
Concept
|
Integrases
|
|
Concept
|
Troponin T
|
|
Concept
|
Cardiac Myosins
|
|
Concept
|
Ubiquitin
|
|
Concept
|
Cell Lineage
|
|
Concept
|
Macrophage Inflammatory Proteins
|
|
Concept
|
Body Patterning
|
|
Concept
|
Phosphatidylinositol 3-Kinases
|
|
Concept
|
Caenorhabditis elegans Proteins
|
|
Concept
|
Ventricular Septum
|
|
Concept
|
Genome-Wide Association Study
|
|
Concept
|
Haploinsufficiency
|
|
Concept
|
Upper Extremity Deformities, Congenital
|
|
Concept
|
Organogenesis
|
|
Concept
|
Atrial Septum
|
|
Concept
|
Gastrulation
|
|
Concept
|
National Heart, Lung, and Blood Institute (U.S.)
|
|
Concept
|
Induced Pluripotent Stem Cells
|
|
Concept
|
Sumoylation
|
|
Concept
|
Calcium
|
|
Concept
|
Disease Models, Animal
|
|
Concept
|
Enhancer Elements, Genetic
|
|
Concept
|
Ethylnitrosourea
|
|
Concept
|
Genetic Testing
|
|
Concept
|
Heart Conduction System
|
|
Concept
|
Heart Rate
|
|
Concept
|
Heart Septal Defects
|
|
Concept
|
Hysteria
|
|
Concept
|
Mice, Mutant Strains
|
|
Concept
|
Models, Biological
|
|
Concept
|
Salamandridae
|
|
Concept
|
Staining and Labeling
|
|
Concept
|
Translocation, Genetic
|
|
Concept
|
Mutagenesis, Insertional
|
|
Concept
|
Receptors, Platelet-Derived Growth Factor
|
|
Concept
|
Genetic Predisposition to Disease
|
|
Concept
|
Polymorphism, Single Nucleotide
|
|
Concept
|
Potassium Channels, Voltage-Gated
|
|
Concept
|
Databases, Nucleic Acid
|
|
Concept
|
Sarcoplasmic Reticulum Calcium-Transporting ATPases
|
|
Academic Article
|
Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice.
|
|
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
|
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
|
A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines.
|
|
Academic Article
|
Complex interactions between genes controlling trafficking in primary cilia.
|
|
Academic Article
|
Defective sumoylation pathway directs congenital heart disease.
|
|
Academic Article
|
DNMT3B7, a truncated DNMT3B isoform expressed in human tumors, disrupts embryonic development and accelerates lymphomagenesis.
|
|
Academic Article
|
The emerging genetic landscape underlying cardiac conduction system function.
|
|
Academic Article
|
Configuration of DNA strands and mechanism of strand exchange in the Hin invertasome as revealed by analysis of recombinant knots.
|
|
Academic Article
|
Alignment of recombination sites in Hin-mediated site-specific DNA recombination.
|
|
Academic Article
|
Hysteria in poliomyelitis.
|
|
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
|
MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus.
|
|
Academic Article
|
A common genetic variant within SCN10A modulates cardiac SCN5A expression.
|
|
Academic Article
|
Chromatin-enriched lncRNAs can act as cell-type specific activators of proximal gene transcription.
|
|
Academic Article
|
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria.
|
|
Academic Article
|
Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation.
|
|
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.
|
|
Concept
|
N-Myc Proto-Oncogene Protein
|
|
Concept
|
Smoothened Receptor
|
|
Concept
|
Zinc Finger Protein Gli3
|
|
Concept
|
Receptor, Notch4
|
|
Concept
|
NAV1.5 Voltage-Gated Sodium Channel
|
|
Concept
|
NAV1.8 Voltage-Gated Sodium Channel
|
|
Concept
|
Zonula Occludens-1 Protein
|
|
Concept
|
Filamins
|
|
Concept
|
Atrial Remodeling
|
|
Grant
|
Gene Regulatory Networks for Cardiac Morphogenesis
|
|
Grant
|
Genetic and Molecular Analysis of Congenital Heart Disease
|
|
Grant
|
Functional Assays to Screen Genomic Hits
|
|
Grant
|
Functional Assays to Screen Genomic Hits
|