propionyl-coenzyme a 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 | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hinz, A; Hoffmann, GF; Hörster, F; Kölker, S; Mayatepek, E; Okun, JG; Sauer, S; Schwab, M; Smeitink, JA; Wolf, NI | 1 |
| Brandt, U; Dröse, S; Hoffmann, GF; Kölker, S; Nijtmans, LG; Okun, JG; Rodenburg, RJ; Sauer, SW; Schwab, MA; Smeitink, JA; Ter Laak, H; van den Heuvel, LP | 1 |
2 other study(ies) available for propionyl-coenzyme a and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Methylmalonic acid, a biochemical hallmark of methylmalonic acidurias but no inhibitor of mitochondrial respiratory chain.
Topics: Acyl Coenzyme A; Adenosine Triphosphate; Aging; Amino Acid Metabolism, Inborn Errors; Animals; Cattle; Citrates; Citric Acid Cycle; Dose-Response Relationship, Drug; Electron Transport; Female; Hydrogen-Ion Concentration; Male; Malonates; Methylmalonic Acid; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Muscles; Myocardium; Oxygen; Phosphorylation; Pyruvates; Spectrophotometry; Time Factors | 2003 |
Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins.
Topics: Acetyl Coenzyme A; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Animals; Cattle; Energy Metabolism; Fatty Acids; Female; Fibroblasts; Humans; Infant, Newborn; Male; Mitochondrial Diseases; Oxidative Phosphorylation; Propionates; Pyruvate Dehydrogenase Complex; Quadriceps Muscle; Skin; Swine; Toxins, Biological | 2006 |