MeSH term
Frequency | Condition_Probility | Abnormalities, Multiple/*genetics | 7 | 2.0 |
Amino Acid Sequence | 13 | 0.0 |
Animals | 38 | 0.0 |
Binding Sites | 5 | 0.0 |
Humans | 48 | 0.0 |
Molecular Sequence Data | 18 | 0.0 |
Protein Binding | 6 | 0.0 |
Research Support, Non-U.S. Gov't | 40 | 0.0 |
Sequence Alignment | 6 | 0.0 |
Syndrome | 17 | 0.0 |
Gene Expression Regulation, Developmental | 9 | 0.0 |
Dogs | 3 | 0.0 |
*Gene Expression Regulation, Developmental | 4 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 5 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 29 | 0.0 |
Transcription Factors/genetics/*metabolism | 2 | 0.0 |
Cell Nucleus/metabolism | 3 | 0.0 |
DNA/metabolism | 2 | 0.0 |
Electrophoretic Mobility Shift Assay | 2 | 0.0 |
Female | 10 | 0.0 |
Genotype | 2 | 0.0 |
Male | 11 | 0.0 |
Pedigree | 5 | 0.0 |
Phenotype | 7 | 0.0 |
Trans-Activation (Genetics) | 2 | 0.0 |
Embryonic and Fetal Development | 3 | 0.0 |
Gestational Age | 3 | 0.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Middle Aged | 2 | 0.0 |
T-Box Domain Proteins/*genetics | 8 | 24.0 |
Atrial Natriuretic Factor/*genetics | 2 | 16.0 |
Base Sequence | 11 | 0.0 |
Cell Differentiation | 3 | 0.0 |
Heart/embryology | 2 | 3.0 |
Heart Defects, Congenital/*genetics/physiopathology | 2 | 100.0 |
Mice | 21 | 0.0 |
Mice, Knockout | 2 | 0.0 |
Promoter Regions (Genetics) | 3 | 0.0 |
Cell Line | 6 | 0.0 |
Heart/*embryology | 8 | 15.0 |
Immunohistochemistry | 4 | 0.0 |
In Situ Hybridization | 5 | 0.0 |
Mice, Transgenic | 2 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Genes, Reporter | 2 | 0.0 |
Heart Defects, Congenital/genetics | 2 | 5.0 |
Homeodomain Proteins/*metabolism | 2 | 1.0 |
Limb Deformities, Congenital/genetics | 2 | 16.0 |
Mutation | 9 | 0.0 |
Myocardium/*cytology | 2 | 9.0 |
T-Box Domain Proteins/*metabolism | 2 | 50.0 |
*Xenopus Proteins | 3 | 0.0 |
Cloning, Molecular | 5 | 0.0 |
Exons | 3 | 0.0 |
Introns | 2 | 0.0 |
Sequence Homology, Amino Acid | 5 | 0.0 |
T-Box Domain Proteins/genetics | 2 | 20.0 |
Myocardium/*metabolism | 2 | 0.0 |
Animals, Genetically Modified | 2 | 0.0 |
Chick Embryo | 8 | 1.0 |
Mutagenesis, Site-Directed | 2 | 0.0 |
Mutation, Missense | 2 | 0.0 |
T-Box Domain Proteins/chemistry/genetics/*metabolism | 2 | 100.0 |
Transfection | 6 | 0.0 |
Tumor Cells, Cultured | 2 | 0.0 |
Adult | 4 | 0.0 |
Heart Defects, Congenital/*genetics | 8 | 20.0 |
Morphogenesis | 3 | 1.0 |
Recombinant Fusion Proteins | 2 | 0.0 |
Multigene Family | 3 | 0.0 |
English Abstract | 2 | 0.0 |
Limb Deformities, Congenital/*genetics | 4 | 20.0 |
*Mutation | 5 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Child | 2 | 0.0 |
Infant | 3 | 0.0 |
Infant, Newborn | 2 | 0.0 |
Mutation/*genetics | 2 | 0.0 |
DNA, Complementary | 2 | 0.0 |
*T-Box Domain Proteins | 9 | 30.0 |
Transcription Factors/chemistry/*genetics | 3 | 3.0 |
*Avian Proteins | 2 | 2.0 |
Electroporation | 2 | 3.0 |
Green Fluorescent Proteins | 3 | 0.0 |
Homeodomain Proteins/genetics/physiology | 2 | 10.0 |
Child, Preschool | 2 | 0.0 |
DNA-Binding Proteins/*genetics | 3 | 0.0 |
Transcription Factors/*genetics | 5 | 0.0 |
Gene Expression | 2 | 0.0 |
Transcription Factors/genetics/*physiology | 2 | 1.0 |
Cell Line, Tumor | 3 | 0.0 |
Transcription Factors/genetics | 2 | 0.0 |
*Zebrafish Proteins | 2 | 0.0 |
Arm/*abnormalities | 2 | 66.0 |
Chromosomes, Human, Pair 12 | 3 | 1.0 |
DNA Mutational Analysis | 4 | 0.0 |
*Gene Expression Regulation | 2 | 0.0 |
Binding Sites/genetics | 2 | 0.0 |
Microscopy, Fluorescence | 2 | 0.0 |
Recombinant Fusion Proteins/genetics/metabolism | 2 | 0.0 |
T-Box Domain Proteins/*genetics/physiology | 3 | 60.0 |
DNA | 2 | 0.0 |
Heart Defects, Congenital/embryology/*genetics | 2 | 40.0 |
T-Box Domain Proteins/genetics/*metabolism | 3 | 37.0 |
DNA-Binding Proteins/metabolism | 2 | 0.0 |
Homeodomain Proteins/metabolism | 2 | 2.0 |
Transcription Factors/metabolism | 2 | 0.0 |
Active Transport, Cell Nucleus | 2 | 0.0 |
COS Cells | 2 | 0.0 |
Heart Defects, Congenital/pathology | 2 | 20.0 |
Models, Molecular | 2 | 0.0 |
DNA/genetics/metabolism | 2 | 0.0 |
*Promoter Regions (Genetics) | 2 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Hela Cells | 2 | 0.0 |
