staurosporine has been researched along with Leigh Disease in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Carrozzo, R; Malorni, W; Matarrese, P; Mormone, E; Pierini, R; Rizza, T; Santorelli, FM; Stringaro, A | 1 |
1 other study(ies) available for staurosporine and Leigh Disease
Article | Year |
---|---|
Maternally-inherited Leigh syndrome-related mutations bolster mitochondrial-mediated apoptosis.
Topics: Adenosine Triphosphatases; Antioxidants; Apoptosis; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Cells, Cultured; Child; Clone Cells; Enzyme Inhibitors; Extrachromosomal Inheritance; Fibroblasts; Genetic Predisposition to Disease; Humans; Hybrid Cells; Intracellular Membranes; Ionophores; Leigh Disease; Membrane Potentials; Mitochondria; Mitochondrial Proton-Translocating ATPases; Mutation; Osteosarcoma; Oxidative Phosphorylation; Staurosporine; Tumor Necrosis Factor-alpha; Uncoupling Agents | 2004 |