histidine has been researched along with Hearing Loss in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Garza-Lopez, E; Hagen, J; Lee, A; Lopez, JA; Meiner, V; Sheffer, R | 1 |
| Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V | 1 |
| Cunningham, JM; Dyck, PJ; Kilfoyle, DH; Klein, CJ; Klein, DM; Kumar, N; Litchy, WJ; Wu, Y | 1 |
3 other study(ies) available for histidine and Hearing Loss
| Article | Year |
|---|---|
Role of a conserved glutamine in the function of voltage-gated Ca
Topics: Amino Acid Sequence; Calcium Channels, L-Type; Calcium Signaling; Conserved Sequence; Exome Sequencing; Glutamine; Glycine; Hearing Loss; Histidine; Humans; Intellectual Disability; Ion Channel Gating; Mutation; Sequence Homology, Amino Acid; Synaptic Transmission | 2018 |
Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.
Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine | 2013 |
Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis.
Topics: Adult; Age of Onset; Child, Preschool; DNA Mutational Analysis; Female; Hearing Loss; Hereditary Sensory and Autonomic Neuropathies; Histidine; Humans; Male; Middle Aged; Multiple Sclerosis; Myelin P0 Protein; Pedigree; Phenotype; Proline; Restless Legs Syndrome | 2006 |