coenzyme a has been researched along with Electron Transport Chain Deficiencies, 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 | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Ando, M; Hashiguchi, A; Higuchi, Y; Hiramatsu, Y; Ishiura, H; Kumada, T; Matsui, N; Matsuura, E; Mitsui, J; Miyazaki, Y; Morishita, S; Murayama, K; Nishino, I; Nozaki, F; Okamoto, Y; Suzuki, M; Suzuki, Y; Takashima, H; Tanaka, M; Tsuji, S; Yamaguchi, M; Yamamoto, Y; Yoshimura, A; Yuan, JH | 1 |
| Ayciriex, S; Cavestro, C; Di Meo, I; Fu, T; Lavermicocca, L; Levi, S; Ligorio, S; Manocchio, A; Mitro, N; Pedretti, S; Ripamonti, M; Santambrogio, P; Tiranti, V | 1 |
| Abramov, AY; Angelova, PR; Arber, C; Bhatia, KP; Duce, JA; Gout, I; Hardy, J; Houlden, H; Mazzacuva, F; Mills, K; Preza, E; Tsuchiya, Y; Wiethoff, S; Wray, S | 1 |
3 other study(ies) available for coenzyme a and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes.
Topics: Charcot-Marie-Tooth Disease; Coenzyme A; DNA, Mitochondrial; Humans; Mitochondrial Diseases; Mutation; Oxidoreductases | 2022 |
Neuronal Ablation of CoA Synthase Causes Motor Deficits, Iron Dyshomeostasis, and Mitochondrial Dysfunctions in a CoPAN Mouse Model.
Topics: Animals; Coenzyme A; Coenzyme A Ligases; Female; Hemochromatosis; Homeostasis; Iron; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mitochondria; Mitochondrial Diseases; Motor Disorders; Pantothenate Kinase-Associated Neurodegeneration; Synapsins | 2020 |
iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early disease.
Topics: Acetyl Coenzyme A; Adolescent; Biopsy; Brain; Cell Differentiation; Child; Coenzyme A; Female; Fibroblasts; Humans; Induced Pluripotent Stem Cells; Iron; Karyotyping; Lipid Peroxidation; Male; Membrane Potential, Mitochondrial; Mitochondria; Mitochondrial Diseases; Mutation; NAD; Neurons; Pantothenate Kinase-Associated Neurodegeneration; Pantothenic Acid; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Plasmids; Reactive Oxygen Species | 2017 |