manganese 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 |
|---|---|
| Berndtsson, J; Broeskamp, F; Büttner, S; Diessl, J; Drobysheva, S; Habernig, L; Kohler, V; Nandy, A; Ott, M; Pelosi, L; Peselj, C; Pierrel, F; Vazquez-Calvo, C; Vögtle, FN | 1 |
| Choi, EK; Gupta, N; Iwase, S; Nguyen, TT; Seo, YA | 1 |
| Bahlo, M; Balasubramaniam, S; Christodoulou, J; Cowley, MJ; Gayevskiy, V; Prelog, K; Riley, LG; Roscioli, T; Sue, CM; Thorburn, DR | 1 |
| Wilson, RB | 1 |
1 review(s) available for manganese and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Iron dysregulation in Friedreich ataxia.
Topics: Amino Acid Sequence; Animals; Frataxin; Friedreich Ataxia; Heme; Humans; Iron; Iron Metabolism Disorders; Iron-Binding Proteins; Manganese; Mice; Mice, Knockout; Mitochondria; Mitochondrial Diseases; Molecular Sequence Data; Oxygen Consumption; Sulfur; Superoxide Dismutase | 2006 |
3 other study(ies) available for manganese and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Manganese-driven CoQ deficiency.
Topics: Ataxia; Humans; Manganese; Mitochondrial Diseases; Mixed Function Oxygenases; Muscle Weakness; Ubiquinone | 2022 |
Functional analysis of SLC39A8 mutations and their implications for manganese deficiency and mitochondrial disorders.
Topics: Amino Acid Sequence; Biological Transport; Cation Transport Proteins; Gene Expression Regulation; HeLa Cells; Humans; Manganese; Mitochondrial Diseases; Mutation; Oxidative Phosphorylation; Vesicular Transport Proteins | 2018 |
A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders.
Topics: Cation Transport Proteins; Child; Congenital Disorders of Glycosylation; Female; Genetic Variation; Glycosylation; Humans; Infant; Leigh Disease; Manganese; Mitochondrial Diseases | 2017 |