MeSH term
Frequency | Condition_Probility | Adult | 3 | 0.0 |
Female | 9 | 0.0 |
Gene Expression | 2 | 0.0 |
Humans | 28 | 0.0 |
Neuregulin-1/genetics | 5 | 71.0 |
Oligonucleotide Array Sequence Analysis | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 18 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Transcription Factors/genetics | 3 | 0.0 |
Tumor Cells, Cultured | 2 | 0.0 |
Signal Transduction/physiology | 2 | 0.0 |
Transcription Factors/*metabolism | 2 | 0.0 |
Amino Acid Sequence | 3 | 0.0 |
Animals | 14 | 0.0 |
Base Sequence | 3 | 0.0 |
Genotype | 4 | 0.0 |
Molecular Sequence Data | 6 | 0.0 |
Transcription, Genetic | 2 | 0.0 |
DNA-Binding Proteins/genetics | 2 | 0.0 |
*Gene Expression Regulation, Fungal | 2 | 4.0 |
Research Support, U.S. Gov't, P.H.S. | 11 | 0.0 |
Asian Continental Ancestry Group/genetics | 2 | 0.0 |
Case-Control Studies | 2 | 0.0 |
Family | 2 | 0.0 |
Male | 6 | 0.0 |
Neuregulin-1/*genetics | 6 | 100.0 |
Polymorphism, Genetic | 2 | 0.0 |
Schizophrenia/*genetics | 8 | 3.0 |
Carrier Proteins/genetics | 4 | 1.0 |
Linkage (Genetics)/genetics | 2 | 0.0 |
Comparative Study | 3 | 0.0 |
*Genetic Predisposition to Disease | 2 | 0.0 |
Schizophrenia/epidemiology/*genetics | 3 | 14.0 |
Chromosome Mapping | 6 | 0.0 |
Chromosomes, Human, Pair 8/*genetics | 2 | 1.0 |
Nerve Tissue Proteins/*genetics | 2 | 0.0 |
Animals, Newborn | 3 | 0.0 |
Cloning, Molecular | 4 | 0.0 |
Gene Expression Regulation, Developmental | 2 | 0.0 |
Ligands | 3 | 0.0 |
RNA, Messenger/analysis | 2 | 0.0 |
Rats | 4 | 0.0 |
Signal Transduction/*physiology | 2 | 0.0 |
*Intracellular Signaling Peptides and Proteins | 2 | 0.0 |
Mice | 9 | 0.0 |
Immunohistochemistry | 2 | 0.0 |
China/epidemiology | 2 | 1.0 |
Haplotypes | 3 | 0.0 |
Risk Factors | 2 | 0.0 |
Gene Frequency/genetics | 2 | 0.0 |
Genetic Markers/genetics | 2 | 0.0 |
Genetic Predisposition to Disease/*genetics | 3 | 0.0 |
Linkage Disequilibrium | 3 | 0.0 |
Polymorphism, Single Nucleotide | 2 | 0.0 |
Phenotype | 2 | 0.0 |
Signal Transduction/genetics/*physiology | 2 | 5.0 |
Genetic Predisposition to Disease | 2 | 0.0 |
Catechol O-Methyltransferase/genetics | 2 | 6.0 |
D-Amino-Acid Oxidase/genetics | 2 | 66.0 |
Proline Oxidase/genetics | 2 | 66.0 |
RGS Proteins/genetics | 2 | 100.0 |
Haplotypes/genetics | 2 | 0.0 |
Disease Models, Animal | 2 | 0.0 |
Polymorphism, Single Nucleotide/genetics | 2 | 0.0 |
