staurosporine has been researched along with Autosomal Dominant Optic Atrophy 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 |
|---|---|
| Amati-Bonneau, P; Belenguer, P; Bonneau, D; Bonnemains, C; Calvas, P; Dollfus, H; Guichet, A; Lenaers, G; Malecaze, F; Malinge, MC; Malthièry, Y; Olichon, A; Pelletier, JB; Reynier, P; Simard, G; Verny, C | 1 |
| Amati-Bonneau, P; Arnauné-Pelloquin, L; Belenguer, P; Bonneau, D; Delettre, C; Emorine, LJ; Guichet, A; Hamel, C; Landes, T; Lenaers, G; Mils, V; Olichon, A; Reynier, P | 1 |
2 other study(ies) available for staurosporine and Autosomal Dominant Optic Atrophy
| Article | Year |
|---|---|
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Sequence; Apoptosis; Cataract; Child; DNA Mutational Analysis; Female; Fibroblasts; France; Genes, Dominant; Humans; Infant; Lod Score; Male; Membrane Potentials; Middle Aged; Mitochondria; Molecular Sequence Data; Mutation, Missense; Optic Atrophy, Autosomal Dominant; Pedigree; Proteins; Staurosporine | 2004 |
Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis.
Topics: Apoptosis; Blotting, Western; Fibroblasts; Gene Deletion; GTP Phosphohydrolases; HeLa Cells; Humans; Microscopy, Fluorescence; Mitochondria; Mutation; Mutation, Missense; Optic Atrophy, Autosomal Dominant; Phenotype; Skin; Staurosporine; Transfection | 2007 |