proline has been researched along with Deafness, Transitory 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 | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Iida, M; Kato, M; Kumasaka, MY; Li, X; Ohgami, N; Oshino, R; Yajima, I | 1 |
| Cunningham, JM; Dyck, PJ; Kilfoyle, DH; Klein, CJ; Klein, DM; Kumar, N; Litchy, WJ; Wu, Y | 1 |
| Cuajungco, MP; Grimm, C; Heller, S; Jörs, S; Kros, CJ; Ricci, AJ; Schnee, M; van Aken, AF | 1 |
3 other study(ies) available for proline and Deafness, Transitory
| Article | Year |
|---|---|
Manganese-mediated acceleration of age-related hearing loss in mice.
Topics: Aging; Animals; Disease Models, Animal; Hearing Loss; Hydroxylation; Hypoxia-Inducible Factor 1, alpha Subunit; Manganese; Mice; Mice, Transgenic; Nerve Degeneration; Phosphorylation; Proline; Proto-Oncogene Proteins c-ret; Spiral Ganglion; Up-Regulation | 2016 |
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 |
A helix-breaking mutation in TRPML3 leads to constitutive activity underlying deafness in the varitint-waddler mouse.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Apoptosis; Cell Line; Hearing Loss; Mice; Molecular Sequence Data; Proline; Protein Structure, Secondary; Protein Structure, Tertiary; Transient Receptor Potential Channels; TRPM Cation Channels | 2007 |