selenocysteine has been researched along with Cochlear Hearing Loss in 1 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Agostini, M; Aitken, S; Baguley, D; Beck-Peccoz, P; Blount, M; Brierley, C; Burton, H; Campi, I; Castanet, M; Castets, P; Ceron-Gutierrez, L; Chatterjee, K; Clemons, N; Coles, A; Cooke, M; Dattani, M; Dean, A; Dixon, A; Doffinger, R; Fitzgerald, R; Gaston, H; Grasso, L; Groeneveld, M; Guicheney, P; Gurnell, M; Halsall, D; Holmgren, A; Karbaschi, M; Khanna, KK; Lu, J; Luan, J; Mitchell, C; Montano, S; Muntoni, F; O'Donovan, D; Ogunko, A; Padidela, R; Papp, L; Prevosto, C; Rajanayagam, O; Schoenmakers, E; Schoenmakers, N; Schwabe, J; Semple, R; Todd, P; Wareham, N; Warren, A; Williams, J | 1 |
1 other study(ies) available for selenocysteine and Cochlear Hearing Loss
| Article | Year |
|---|---|
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans.
Topics: Adult; Aged; Amino Acid Sequence; Animals; Azoospermia; Base Sequence; Child; Child, Preschool; Codon, Nonsense; DNA; Female; Hearing Loss, Sensorineural; Humans; Insulin Resistance; Male; Mice; Middle Aged; Models, Molecular; Molecular Sequence Data; Muscular Dystrophies; Mutation; Mutation, Missense; Pedigree; Photosensitivity Disorders; Reactive Oxygen Species; RNA-Binding Proteins; Selenocysteine; Selenoproteins; Sequence Homology, Amino Acid; Spermatogenesis; T-Lymphocytes | 2010 |