nocodazole has been researched along with 8-((4-chlorophenyl)thio)cyclic-3',5'-amp in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bennett, MV; Dermietzel, R; Gregory, WA; Hertzberg, EL; Reid, L; Sáez, JC; Spray, DC; Watanabe, T | 1 |
| Phillips, ME; Taylor, A | 1 |
| Farinelli, SE; Greene, LA | 1 |
| Cassiman, JJ; Segal, A; Simaels, J; Van Driessche, W; Vankeerberghen, A; Weber, WM | 1 |
4 other study(ies) available for nocodazole and 8-((4-chlorophenyl)thio)cyclic-3',5'-amp
| Article | Year |
|---|---|
cAMP delays disappearance of gap junctions between pairs of rat hepatocytes in primary culture.
Topics: 8-Bromo Cyclic Adenosine Monophosphate; Amanitins; Animals; Benzimidazoles; Bucladesine; Cells, Cultured; Connexins; Cyclic AMP; Cycloheximide; Immunohistochemistry; Intercellular Junctions; Liver; Membrane Proteins; Microscopy, Electron; Microtubules; Nocodazole; Rats; Rats, Inbred Strains; RNA, Messenger; Thionucleotides; Transcription, Genetic | 1989 |
Effect of nocodazole on the water permeability response to vasopressin in rabbit collecting tubules perfused in vitro.
Topics: Animals; Cell Membrane Permeability; Cyclic AMP; Dose-Response Relationship, Drug; Female; In Vitro Techniques; Kidney Tubules; Kidney Tubules, Collecting; Male; Microtubules; Nocodazole; Rabbits; Thionucleotides; Time Factors; Vasopressins; Water | 1989 |
Cell cycle blockers mimosine, ciclopirox, and deferoxamine prevent the death of PC12 cells and postmitotic sympathetic neurons after removal of trophic support.
Topics: Animals; Aphidicolin; Apoptosis; Cell Cycle; Cell Division; Ciclopirox; Cyclic AMP; Deferoxamine; G1 Phase; Mimosine; Mitosis; Nerve Growth Factors; Neurons; Nocodazole; PC12 Cells; Pyridones; Rats; Superior Cervical Ganglion; Teniposide; Thionucleotides | 1996 |
Functional integrity of the vesicle transporting machinery is required for complete activation of cFTR expressed in xenopus laevis oocytes.
Topics: 1-Methyl-3-isobutylxanthine; Animals; Antimalarials; Antineoplastic Agents; Brefeldin A; Calcium; Chelating Agents; Cyclic AMP; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Egtazic Acid; Electric Conductivity; Enzyme Inhibitors; Exocytosis; Gene Expression; Membrane Potentials; Nocodazole; Oocytes; Patch-Clamp Techniques; Phosphodiesterase Inhibitors; Primaquine; Protein Kinase C; Protein Synthesis Inhibitors; Protein Transport; Thionucleotides; Transport Vesicles; Xenopus laevis | 2001 |