arginine 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 | 0 (0.00) | 29.6817 |
| 2010's | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Harris, DC; Mangoni, AA; McEvoy, M; Sarant, JZ | 1 |
| Dittrich, M; Doll, J; Eslahi, A; Grimm, C; Haaf, T; Hofrichter, MAH; Hosseini, NS; Maroofian, R; Mojarad, M; Müller, T; Rajati, M; Vona, B | 1 |
| Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V | 1 |
3 other study(ies) available for arginine and Hearing Loss
| Article | Year |
|---|---|
Serum Methylarginines and Hearing Loss in a Population-based Cohort of Older Adults.
Topics: Aged; Arginine; Biomarkers; Cohort Studies; Cross-Sectional Studies; Female; Hearing Loss; Humans; Male; Middle Aged | 2018 |
The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family.
Topics: Adolescent; Amino Acid Substitution; Arginine; Consanguinity; Exome Sequencing; Female; Hearing Loss; Humans; Iran; Male; Models, Molecular; Pedigree; Protein Binding; Receptors, Lysosphingolipid; Sphingosine-1-Phosphate Receptors | 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 |