staurosporine has been researched along with Cataract 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 |
|---|---|
| Andersson, M; Honarvar, A; Karlsson, JO; Peterson, A; Sjöstrand, J | 1 |
| 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 |
2 other study(ies) available for staurosporine and Cataract
| Article | Year |
|---|---|
Decreased caspase-3 activity in human lens epithelium from posterior subcapsular cataracts.
Topics: Apoptosis; Caspase 3; Caspases; Cataract; Cell Culture Techniques; Dose-Response Relationship, Drug; Enzyme Inhibitors; Epithelial Cells; Female; Humans; Lens Capsule, Crystalline; Male; Staurosporine | 2003 |
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 |