lysine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alkhater, RA; Carroll, CJ; Christen, S; Civiletto, G; Euro, L; Gut, P; He, W; Isohanni, P; Jackson, CB; Liu, X; Locasale, JW; Matilainen, S; Meyer, JG; Minassian, BA; Moco, S; Newman, JC; Nishida, Y; Pällijeff, P; Parisi, A; Rardin, MJ; Richard, J; Schilling, B; Suomalainen, A; Thevenet, J; Verdin, E; Østergaard, E | 1 |
| García-Villoria, J; Girós, M; Ribes, A; Ruiz, A; Torres, MA; Tort, F; Ugarteburu, O | 1 |
| Lee, WY; Wei, YH; Wu, SB; Wu, YT | 1 |
| Ahari, SE; Bahar, M; Banoei, MM; Houshmand, M; Kasraie, S; Moin, M; Panahi, MS; Shariati, P | 1 |
1 review(s) available for lysine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Mitochondrial respiratory dysfunction-elicited oxidative stress and posttranslational protein modification in mitochondrial diseases.
Topics: Acetylation; Animals; Disease Progression; DNA, Mitochondrial; Electron Transport; Humans; Lysine; Mitochondria; Mitochondrial Diseases; Mutation; Oxidative Stress; Phosphorylation; Protein Processing, Post-Translational; Syndrome; Ubiquitin | 2010 |
3 other study(ies) available for lysine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease.
Topics: Acyl Coenzyme A; Animals; Cells, Cultured; Female; Humans; Infant; Lysine; Male; Mice; Mice, Knockout; Mitochondria; Mitochondrial Diseases; Mutation; Proteomics; Sirtuins; Succinate-CoA Ligases; Survival Analysis; Zebrafish | 2020 |
Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient.
Topics: Child; Diet; Epilepsies, Myoclonic; Female; Homozygote; Humans; Hyperlysinemias; Lactic Acid; Lysine; Mitochondrial Diseases; Mitochondrial Proteins; Mutation; Nervous System Malformations; Phosphotransferases (Alcohol Group Acceptor); Pipecolic Acids; Pyridoxal Phosphate; RNA, Messenger; Vitamin B Complex | 2016 |
Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's disease.
Topics: Adenosine Triphosphatases; Amino Acid Substitution; DNA Damage; DNA Mutational Analysis; DNA, Mitochondrial; Genetic Predisposition to Disease; Genetic Testing; Humans; Huntington Disease; Leucine; Lysine; Mitochondrial Diseases; Mutation; RNA, Transfer | 2008 |