histidine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial 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 |
|---|---|
| Anderson, KS; Bailey, CM; Copeland, WC; Spell, D; Stillwagon, M; Stumpf, JD | 1 |
| Finnilä, S; Hassinen, I; Hinttala, R; Kärppä, M; Komulainen, T; Majamaa, K; Pajunen, L; Rantala, H; Tuominen, H; Uusimaa, J | 1 |
2 other study(ies) available for histidine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae.
Topics: Age Factors; DNA Polymerase gamma; DNA Polymerase I; DNA Primers; DNA Replication; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Histidine; Humans; Mitochondrial Diseases; Models, Molecular; Mutation; Phenotype; Plasmids; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins | 2010 |
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
Topics: Aged, 80 and over; Arginine; Brain; Deglutition Disorders; Diabetes Mellitus, Type 2; Disease Progression; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Histidine; Humans; Male; Mitochondrial Diseases; Mutation; Ophthalmoplegia; Phenotype | 2010 |