Page last updated: 2024-08-23

staurosporine and Leigh Disease

staurosporine has been researched along with Leigh Disease in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Carrozzo, R; Malorni, W; Matarrese, P; Mormone, E; Pierini, R; Rizza, T; Santorelli, FM; Stringaro, A1

Other Studies

1 other study(ies) available for staurosporine and Leigh Disease

ArticleYear
Maternally-inherited Leigh syndrome-related mutations bolster mitochondrial-mediated apoptosis.
    Journal of neurochemistry, 2004, Volume: 90, Issue:2

    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