selenocysteine has been researched along with Atrophy in 2 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baxa, U; French, RL; Matthies, D; Puppala, AK; Simonović, M; Subramaniam, S | 1 |
| Agamy, O; Ben Zeev, B; Birk, OS; Fine, D; Flusser, H; Hoffmann, C; Lerman-Sagie, T; Leshinsky-Silver, E; Lev, D; Marcus, B; Narkis, G; Ofir, R; Sivan, S; Söll, D; Su, D | 1 |
2 other study(ies) available for selenocysteine and Atrophy
| Article | Year |
|---|---|
Structural basis for early-onset neurological disorders caused by mutations in human selenocysteine synthase.
Topics: Age of Onset; Amino Acid Substitution; Amino Acyl-tRNA Synthetases; Ataxia; Atrophy; Binding Sites; Cerebellum; Cerebral Cortex; Crystallography, X-Ray; Humans; Irritable Mood; Models, Molecular; Muscle Spasticity; Mutation; Protein Binding; Protein Conformation, alpha-Helical; Protein Conformation, beta-Strand; Protein Folding; Protein Interaction Domains and Motifs; Protein Stability; Recombinant Proteins; RNA, Transfer; Seizures; Selenocysteine; Substrate Specificity | 2016 |
Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy.
Topics: Amino Acyl-tRNA Synthetases; Atrophy; Base Sequence; Cerebellum; Cerebral Cortex; Chromosome Mapping; Genes, Recessive; Heredodegenerative Disorders, Nervous System; Humans; Iraq; Jews; Molecular Sequence Data; Morocco; Mutation; Pedigree; Selenocysteine; Sequence Alignment; Sequence Analysis, DNA | 2010 |