MeSH term
Frequency | Condition_Probility | Eye Proteins/genetics | 3 | 6.0 |
Humans | 24 | 0.0 |
Mutation | 6 | 0.0 |
Research Support, Non-U.S. Gov't | 23 | 0.0 |
Carrier Proteins/genetics/*metabolism | 3 | 0.0 |
Immunohistochemistry | 3 | 0.0 |
Microscopy, Confocal | 3 | 0.0 |
Genotype | 5 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 12 | 0.0 |
Animals | 10 | 0.0 |
Carrier Proteins/*genetics | 6 | 0.0 |
Disease Models, Animal | 2 | 0.0 |
Mice | 6 | 0.0 |
Mice, Knockout | 2 | 0.0 |
Optic Atrophy, Hereditary, Leber/*genetics | 6 | 54.0 |
Exons | 2 | 0.0 |
Mutation/*genetics | 2 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Cell Line, Tumor | 2 | 0.0 |
Protein Structure, Tertiary | 2 | 0.0 |
Amino Acid Sequence | 2 | 0.0 |
Cattle | 3 | 0.0 |
Comparative Study | 3 | 0.0 |
DNA Mutational Analysis | 6 | 0.0 |
DNA Primers/chemistry | 2 | 0.0 |
Molecular Sequence Data | 3 | 0.0 |
Optic Atrophies, Hereditary/*genetics | 2 | 10.0 |
Phenotype | 8 | 0.0 |
Retinal Degeneration/*genetics | 3 | 7.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Proteins/metabolism | 2 | 0.0 |
Transcription Factors/metabolism | 2 | 0.0 |
Homeodomain Proteins/genetics | 2 | 0.0 |
*Mutation | 8 | 0.0 |
Nerve Tissue Proteins/genetics | 3 | 1.0 |
Prevalence | 2 | 0.0 |
Trans-Activators/genetics | 2 | 0.0 |
Variation (Genetics) | 2 | 0.0 |
Female | 8 | 0.0 |
Male | 7 | 0.0 |
Pedigree | 7 | 0.0 |
Polymorphism, Single-Stranded Conformational | 3 | 0.0 |
Adolescent | 3 | 0.0 |
Adult | 6 | 0.0 |
Blindness/congenital/*genetics/pathology | 2 | 100.0 |
Child | 5 | 0.0 |
Child, Preschool | 2 | 0.0 |
Electroretinography | 3 | 1.0 |
Infant | 2 | 0.0 |
Middle Aged | 2 | 0.0 |
Retinal Degeneration/congenital/*genetics/pathology | 2 | 100.0 |
*Disease Models, Animal | 2 | 0.0 |
Homozygote | 3 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
COS Cells | 5 | 0.0 |
Cercopithecus aethiops | 2 | 0.0 |
Two-Hybrid System Techniques | 2 | 0.0 |
Eye Proteins/*genetics | 2 | 1.0 |
Membrane Proteins/genetics | 2 | 0.0 |
Proteins/genetics | 3 | 0.0 |
Aged | 2 | 0.0 |
Blotting, Western | 2 | 0.0 |
Microscopy, Fluorescence | 2 | 0.0 |
Blindness/congenital/*genetics | 3 | 42.0 |
Carrier Proteins/genetics | 2 | 0.0 |
Guanylate Cyclase/genetics | 2 | 50.0 |
Carrier Proteins/*genetics/*metabolism | 2 | 2.0 |
Cell Line | 3 | 0.0 |
Cloning, Molecular | 2 | 0.0 |
Transfection | 2 | 0.0 |
Mutation/genetics | 2 | 0.0 |
