MeSH term
Frequency | Condition_Probility | Humans | 29 | 0.0 |
Animals | 21 | 0.0 |
Base Sequence | 6 | 0.0 |
Gene Expression Regulation | 2 | 0.0 |
Kidney Glomerulus/*cytology/physiology | 2 | 100.0 |
Molecular Sequence Data | 7 | 0.0 |
Cell Differentiation | 3 | 0.0 |
Mice | 14 | 0.0 |
Mice, Knockout | 6 | 0.0 |
Models, Animal | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 22 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 14 | 0.0 |
Animals, Newborn | 2 | 0.0 |
Cell Differentiation/physiology | 3 | 0.0 |
Collagen Type IV/genetics | 2 | 40.0 |
Gene Expression | 4 | 0.0 |
Mutation | 6 | 0.0 |
Nail-Patella Syndrome/genetics/pathology | 2 | 66.0 |
Phenotype | 8 | 0.0 |
RNA, Messenger/genetics/metabolism | 2 | 0.0 |
Heterozygote | 2 | 0.0 |
In Situ Hybridization | 2 | 0.0 |
Transcription, Genetic | 2 | 0.0 |
Adolescent | 4 | 0.0 |
Homeodomain Proteins/*genetics | 4 | 0.0 |
Male | 8 | 0.0 |
Patella/abnormalities | 2 | 66.0 |
Homeodomain Proteins/genetics/metabolism | 2 | 2.0 |
DNA Mutational Analysis | 3 | 0.0 |
Homeodomain Proteins/chemistry/*genetics | 6 | 26.0 |
Mutation/*genetics | 2 | 0.0 |
Nail-Patella Syndrome/*genetics | 8 | 50.0 |
Homeodomain Proteins/*metabolism | 2 | 1.0 |
Mice, Mutant Strains | 3 | 0.0 |
Base Sequence/genetics | 2 | 0.0 |
Cloning, Molecular | 3 | 0.0 |
Genes, Dominant | 4 | 0.0 |
Immunohistochemistry | 2 | 0.0 |
Age Factors | 2 | 0.0 |
Amino Acid Sequence | 4 | 0.0 |
Dopamine/*physiology | 4 | 4.0 |
Rats | 2 | 0.0 |
Chick Embryo | 2 | 0.0 |
Female | 6 | 0.0 |
*Mutation | 4 | 0.0 |
Pedigree | 3 | 0.0 |
Point Mutation | 2 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
Sequence Deletion | 2 | 0.0 |
Transcription Factors/chemistry/genetics | 2 | 14.0 |
Family Health | 2 | 0.0 |
Adult | 4 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Middle Aged | 4 | 0.0 |
Neurons/*metabolism | 2 | 0.0 |
Gene Expression Regulation, Developmental | 3 | 0.0 |
Signal Transduction | 2 | 0.0 |
Cell Differentiation/genetics | 2 | 0.0 |
Homeodomain Proteins/genetics | 3 | 1.0 |
Aged | 2 | 0.0 |
Child | 2 | 0.0 |
Child, Preschool | 2 | 0.0 |
Infant | 2 | 0.0 |
Nails/abnormalities | 2 | 25.0 |
Genotype | 2 | 0.0 |
