cysteine has been researched along with Encephalomyopathies, Mitochondrial 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 |
|---|---|
| Boczonadi, V; Chinnery, PF; Gomez-Duran, A; Horvath, R; Pyle, A; Schara, U; Smith, PM; Tulinius, M | 1 |
| Hassinen, IE; Hinttala, R; Majamaa, K; Rantala, H; Remes, AM; Uusimaa, J | 1 |
| Dimauro, S; Hirano, M; Naini, A; Navas, P; Quinzii, C; Salviati, L; Trevisson, E | 1 |
3 other study(ies) available for cysteine and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency.
Topics: Cell Line; Cysteine; Gene Expression Regulation; Humans; Mitochondria; Mitochondrial Diseases; Mitochondrial Encephalomyopathies; Mitochondrial Proteins; Muscle, Skeletal; Mutation; Myoblasts; Oxidative Phosphorylation; Protein Biosynthesis; RNA, Transfer; Thiouridine; tRNA Methyltransferases | 2013 |
Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathy.
Topics: Alleles; Amino Acid Substitution; Arginine; Child; Computational Biology; Conserved Sequence; Cysteine; Electron Transport Complex I; Genetic Variation; Humans; Mitochondrial Encephalomyopathies; Mutation; NAD(P)H Dehydrogenase (Quinone); NADH Dehydrogenase; Protein Subunits; Sequence Analysis, DNA; Transcription, Genetic | 2005 |
A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency.
Topics: Alkyl and Aryl Transferases; Amino Acid Sequence; Amino Acid Substitution; Child, Preschool; Coenzymes; Cysteine; Female; Fibroblasts; Humans; Infant; Male; Mitochondrial Encephalomyopathies; Molecular Sequence Data; Mutation; Mutation, Missense; Tyrosine; Ubiquinone | 2006 |