Item Type | Name |
Concept
|
Arrhythmias, Cardiac
|
Concept
|
Alleles
|
Concept
|
Basal Metabolism
|
Concept
|
Base Sequence
|
Concept
|
Body Weight
|
Concept
|
Cell Adhesion
|
Concept
|
Chromosomes, Human, Pair 12
|
Concept
|
Diabetes Mellitus, Type 2
|
Concept
|
Diet
|
Concept
|
Insulysin
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 9
|
Concept
|
Introns
|
Concept
|
Electrocardiography
|
Concept
|
Genes, Dominant
|
Concept
|
Heart Failure
|
Concept
|
Heart Septal Defects, Atrial
|
Concept
|
Multigene Family
|
Concept
|
Myocardial Infarction
|
Concept
|
Molecular Sequence Data
|
Concept
|
Oxidation-Reduction
|
Concept
|
Heart Defects, Congenital
|
Concept
|
Risk Factors
|
Concept
|
Body Mass Index
|
Concept
|
Incidence
|
Concept
|
Oxo-Acid-Lyases
|
Concept
|
Urokinase-Type Plasminogen Activator
|
Concept
|
Sodium Channels
|
Concept
|
Prevalence
|
Concept
|
Chi-Square Distribution
|
Concept
|
Gene Expression
|
Concept
|
Case-Control Studies
|
Concept
|
Connexins
|
Concept
|
Genes, Reporter
|
Concept
|
Cardiomyopathies
|
Concept
|
Amyloid beta-Protein Precursor
|
Concept
|
alpha Catenin
|
Concept
|
Parkinson Disease
|
Concept
|
Catenins
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Zebrafish
|
Concept
|
Amyloid beta-Peptides
|
Concept
|
T-Box Domain Proteins
|
Concept
|
Homeodomain Proteins
|
Concept
|
Cell Line, Tumor
|
Concept
|
Alzheimer Disease
|
Concept
|
Cell Line
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Genetic Testing
|
Concept
|
Hypothalamus
|
Concept
|
Age of Onset
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Molecular Dynamics Simulation
|
Academic Article
|
A multi-incident, Old-Order Amish family with PD.
|
Academic Article
|
Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.
|
Academic Article
|
Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease.
|
Academic Article
|
Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme.
|
Academic Article
|
A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
|
Academic Article
|
Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease.
|
Academic Article
|
Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms.
|
Academic Article
|
DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.
|
Academic Article
|
Redundancy in genotyping arrays.
|
Academic Article
|
TBX5 drives Scn5a expression to regulate cardiac conduction system function.
|
Academic Article
|
Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function.
|
Academic Article
|
Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP).
|
Academic Article
|
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
|
Academic Article
|
Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family.
|
Academic Article
|
FTO-mediated formation of N6-hydroxymethyladenosine and N6-formyladenosine in mammalian RNA.
|
Academic Article
|
A common genetic variant within SCN10A modulates cardiac SCN5A expression.
|
Academic Article
|
Obesity-associated variants within FTO form long-range functional connections with IRX3.
|
Academic Article
|
Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors.
|
Concept
|
Alpha-Ketoglutarate-Dependent Dioxygenase FTO
|
Concept
|
NAV1.5 Voltage-Gated Sodium Channel
|
Concept
|
NAV1.8 Voltage-Gated Sodium Channel
|