staurosporine has been researched along with kinetin in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 7 (70.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Patzlaff, JS; Paulson, JR; Vallis, AJ | 1 |
| Cassimeris, L; Howell, B; Odde, DJ | 1 |
| Cruz, M; Eneroth, P; Idoyaga Vargas, V; Sidén, A; Yakisich, JS | 1 |
| Meijer, L | 1 |
| Martin, WH; Peterson, MF; Spencer, RW; Tate, BF | 1 |
| Elbaum, D; Lydon, NB; Toledo, LM | 1 |
| Détivaud, L; Doerig, C; Gray, N; Meijer, L | 1 |
| Alemany, C; Ciudad, CJ; Noé, V; Peñuelas, S | 1 |
| Bentke, A; Laidler, P; Małecki, JM; Ostrowska, B | 1 |
| Havlicek, L; Hyun, TK; Roitsch, T; Strnad, M | 1 |
3 review(s) available for staurosporine and kinetin
| Article | Year |
|---|---|
Chemical inhibitors of cyclin-dependent kinases.
Topics: 4-Butyrolactone; Animals; Cell Cycle; Cyclin-Dependent Kinases; Enzyme Inhibitors; Flavonoids; Humans; Kinetin; Piperidines; Purines; Staurosporine; Suramin | 1995 |
The structure-based design of ATP-site directed protein kinase inhibitors.
Topics: Adenosine Triphosphate; Adenylyl Imidodiphosphate; Anthraquinones; Binding Sites; Catalytic Domain; Cyclin-Dependent Kinases; Drug Design; Enzyme Inhibitors; Humans; Kinetin; Piperazines; Protein-Tyrosine Kinases; Purines; Pyridines; Pyrimidines; Pyrroles; Quinazolines; Receptors, Growth Factor; Roscovitine; Staurosporine; Structure-Activity Relationship | 1999 |
ATP-site directed inhibitors of cyclin-dependent kinases.
Topics: Adenine; Adenosine Triphosphate; Amino Acid Sequence; Antineoplastic Agents; Binding Sites; Cell Cycle; Cyclin-Dependent Kinases; Drug Design; Enzyme Inhibitors; Flavonoids; Humans; Isopentenyladenosine; Kinetin; Molecular Sequence Data; Piperidines; Purines; Roscovitine; Sequence Alignment; Sequence Homology, Amino Acid; Staurosporine; Suramin | 1999 |
7 other study(ies) available for staurosporine and kinetin
| Article | Year |
|---|---|
Evidence that the endogenous histone H1 phosphatase in HeLa mitotic chromosomes is protein phosphatase 1, not protein phosphatase 2A.
Topics: Cell Nucleus; Chromatin; Enzyme Inhibitors; HeLa Cells; Histones; Humans; Kinetin; Marine Toxins; Metaphase; Microcystins; Mitosis; Okadaic Acid; Oxazoles; Peptides, Cyclic; Phosphoprotein Phosphatases; Phosphorylation; Protein Kinase Inhibitors; Protein Phosphatase 1; Protein Phosphatase 2; Purines; Staurosporine | 1996 |
Kinase and phosphatase inhibitors cause rapid alterations in microtubule dynamic instability in living cells.
Topics: Animals; Cells, Cultured; Enzyme Inhibitors; Epithelium; Kinetin; Lung; Microscopy, Interference; Microtubules; Okadaic Acid; Phosphorylases; Phosphotransferases; Purines; Salamandridae; Staurosporine; Time Factors | 1997 |
Early inhibition of DNA synthesis in the developing rat cerebral cortex by the purine analogues olomoucine and roscovitine.
Topics: Animals; Cell Cycle; Cerebral Cortex; Cyclin-Dependent Kinases; DNA; Enzyme Inhibitors; Etoposide; Kinetin; Nucleic Acid Synthesis Inhibitors; Purines; Rats; Rats, Sprague-Dawley; Roscovitine; Staurosporine; Thymidine; Tritium | 1998 |
The use of beta, gamma-methyleneadenosine 5'-triphosphate to determine ATP competition in a scintillation proximity kinase assay.
Topics: Adenosine Triphosphate; Binding, Competitive; Calcium-Calmodulin-Dependent Protein Kinases; Enzyme Inhibitors; Glycogen Synthase Kinase 3; Glycogen Synthase Kinases; Indoles; Kinetics; Kinetin; Protein Kinase Inhibitors; Purines; Scintillation Counting; Staurosporine | 1999 |
The expression of retinoblastoma and Sp1 is increased by low concentrations of cyclin-dependent kinase inhibitors.
Topics: Animals; Blotting, Western; Cell Division; Cell Nucleus; CHO Cells; Cloning, Molecular; Cricetinae; Cyclin-Dependent Kinases; Dose-Response Relationship, Drug; Flow Cytometry; HeLa Cells; Humans; Indoles; K562 Cells; Kinetin; Luciferases; Maleimides; Phosphorylation; Promoter Regions, Genetic; Protein Kinase C; Protein Synthesis Inhibitors; Purines; Retinoblastoma Protein; RNA, Messenger; Roscovitine; Sp1 Transcription Factor; Staurosporine; Tetrahydrofolate Dehydrogenase; Time Factors; Transcription, Genetic; Transfection | 2003 |
Cytochalasin D, LY294002 and olomoucine synergize in promoting death of melanoma cells through activation of caspase-3 and apoptosis.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Caspase 3; Cell Growth Processes; Cell Line, Tumor; Cell Survival; Chromones; Cytochalasin D; Drug Synergism; Enzyme Activation; Humans; In Situ Nick-End Labeling; Kinetin; Melanoma; Morpholines; Skin Neoplasms; Staurosporine; Up-Regulation | 2010 |
Trisubstituted purines are useful tools for developing potent plant mitogen-activated protein kinase inhibitors.
Topics: Benzyl Compounds; Cells, Cultured; Imidazoles; Kinetin; Mitogen-Activated Protein Kinases; Plants; Protein Kinase Inhibitors; Purines; Pyridines; Signal Transduction; Solanaceae; Staurosporine; Structure-Activity Relationship | 2010 |