MeSH term
Frequency | Condition_Probility | Animals | 10 | 0.0 |
Comparative Study | 5 | 0.0 |
Humans | 20 | 0.0 |
Male | 8 | 0.0 |
Mice | 9 | 0.0 |
Mice, Nude | 5 | 0.0 |
Neoplasm Transplantation | 3 | 0.0 |
Research Support, Non-U.S. Gov't | 11 | 0.0 |
Disease Models, Animal | 2 | 0.0 |
Female | 7 | 0.0 |
*Membrane Transport Proteins | 2 | 0.0 |
Middle Aged | 2 | 0.0 |
*Neuropeptides | 2 | 1.0 |
Transplantation, Heterologous | 2 | 0.0 |
Tumor Cells, Cultured/metabolism | 2 | 1.0 |
Karyotyping | 3 | 0.0 |
Mice, Inbred BALB C | 2 | 0.0 |
Aspartate Aminotransferases/*genetics | 4 | 44.0 |
Base Sequence | 2 | 0.0 |
Chromosomes, Human, Pair 10/*genetics | 3 | 2.0 |
Molecular Sequence Data | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Chromosome Banding | 4 | 0.0 |
*Chromosome Mapping | 3 | 0.0 |
Genetic Markers | 4 | 0.0 |
Alleles | 2 | 0.0 |
Phenotype | 4 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Japan | 3 | 0.0 |
Hamsters | 2 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 3 | 0.0 |
Adult | 2 | 0.0 |
*Variation (Genetics) | 2 | 0.0 |
*Chromosomes, Human, 6-12 and X | 4 | 2.0 |
*Trisomy | 2 | 1.0 |
Infant | 2 | 0.0 |
Chromosome Mapping | 4 | 0.0 |
Chromosomes/*ultrastructure | 2 | 9.0 |
Child, Preschool | 2 | 0.0 |
Chromosome Deletion | 2 | 0.0 |
