galactose has been researched along with Leigh Disease in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Beyrath, J; Iannetti, EF; Koopman, WJH; Smeitink, JAM; Willems, PHGM | 1 |
| Augustin, S; Bénit, P; Bonnet, C; Corral-Debrinski, M; Ellouze, S; Forster, V; Kaltimbacher, V; Rustin, P; Sahel, JA | 1 |
| Feigenbaum, A; Laframboise, R; Pitkänen, S; Robinson, BH | 1 |
| Belcher-Timme, CA; Gohil, VM; Luo, B; Mootha, VK; Nilsson, R; Root, DE | 1 |
4 other study(ies) available for galactose and Leigh Disease
| Article | Year |
|---|---|
Rescue from galactose-induced death of Leigh Syndrome patient cells by pyruvate and NAD
Topics: Adenosine Triphosphate; Aspartic Acid; Cell Death; Culture Media; Electron Transport Complex I; Fibroblasts; Galactose; Gene Expression; Glycolysis; Humans; Ketoglutaric Acids; Leigh Disease; Malates; Mitochondria; Mitochondrial Diseases; Mutation; NAD; NADH Dehydrogenase; Oxaloacetic Acid; Primary Cell Culture; Pyruvic Acid; Skin | 2018 |
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits.
Topics: Adenosine Triphosphatases; Carrier Proteins; Cell Division; Cells, Cultured; Culture Media; Cytosol; DNA, Mitochondrial; Electron Transport; Electron Transport Complex I; Fibroblasts; Galactose; Genetic Therapy; Humans; Infant; Leigh Disease; Membrane Proteins; Mitochondria; Mitochondrial Proton-Translocating ATPases; Mutation; NADH Dehydrogenase; Oxidative Phosphorylation; Plasmids; RNA, Messenger; Transfection | 2007 |
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings.
Topics: Acidosis, Lactic; Adenosine Triphosphate; Cardiomyopathies; Cataract; Cell Line; Child; Child, Preschool; Fibroblasts; Galactose; Hepatomegaly; Humans; Infant; Infant, Newborn; Kidney Diseases; Leigh Disease; NAD(P)H Dehydrogenase (Quinone); Phenotype; Vitamin K | 1996 |
Mitochondrial and nuclear genomic responses to loss of LRPPRC expression.
Topics: Cell Line, Transformed; DNA, Mitochondrial; Gene Expression Profiling; Gene Expression Regulation; Gene Silencing; Genome-Wide Association Study; Glycosphingolipids; Hexoses; Humans; Leigh Disease; Mitochondrial Proteins; Models, Biological; Mutation; Neoplasm Proteins; Prostaglandins; RNA, Messenger | 2010 |