bromodeoxyuridine has been researched along with okadaic acid in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 6 (75.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rieber, M; Rieber, MS | 2 |
| Nagao, M; Oikawa, A; Sugimura, T; Tohda, H | 1 |
| Iwata, H; Nakanishi, H; Suganuma, M; Tatematsu, M; Yoshida, K; Yuasa, H | 1 |
| Dzau, VJ; Hayashida, W; Horiuchi, M | 1 |
| Kopf, GS; Moos, J; Schultz, RM | 1 |
| Everett, AD; Stoops, TD; Taylor, BK | 1 |
| Higuchi, S; Ikekita, M; Matsuoka, Y; Nagahara, Y; Saito, K; Shinomiya, T | 1 |
8 other study(ies) available for bromodeoxyuridine and okadaic acid
| Article | Year |
|---|---|
UV radiation induces DNA fragmentation and cell death in B16 melanoma sensitized by bromodeoxyuridine: impaired c-jun induction and defective tyrosine phosphorylation signalling.
Topics: Animals; Bromodeoxyuridine; Cell Death; Cell Survival; DNA Damage; DNA, Neoplasm; Ethers, Cyclic; Genes, jun; Immunoblotting; Melanoma, Experimental; Mice; Okadaic Acid; Phosphorylation; Phosphotyrosine; Protein Tyrosine Phosphatases; Proto-Oncogene Proteins c-jun; Radiation-Sensitizing Agents; Signal Transduction; Tumor Cells, Cultured; Tyrosine; Ultraviolet Rays; Vanadates | 1994 |
Okadaic acid, a protein phosphatase inhibitor, induces sister-chromatid exchanges depending on the presence of bromodeoxyuridine.
Topics: Animals; Benzamides; Bromodeoxyuridine; Camptothecin; Cell Line; CHO Cells; Cricetinae; Cricetulus; DNA Replication; DNA Topoisomerases, Type I; Drug Synergism; Enzyme Activation; Ethers, Cyclic; Humans; Lymphocytes; Okadaic Acid; Phosphoprotein Phosphatases; Phosphorylation; Poly(ADP-ribose) Polymerases; Protein Phosphatase 1; Sister Chromatid Exchange | 1993 |
Increase of labeling indices in gastrointestinal mucosae of mice and rats by compounds of the okadaic acid type.
Topics: Administration, Oral; Animals; Antifungal Agents; Bromodeoxyuridine; Carcinogens; Cell Division; Dose-Response Relationship, Drug; Ethers, Cyclic; Intestinal Mucosa; Male; Marine Toxins; Mice; Mice, Inbred ICR; Okadaic Acid; Oxazoles; Pyrans; Rats; Rats, Sprague-Dawley; Spiro Compounds; Time Factors | 1994 |
Intracellular third loop domain of angiotensin II type-2 receptor. Role in mediating signal transduction and cellular function.
Topics: Amino Acid Sequence; Animals; Bromodeoxyuridine; Calcium-Calmodulin-Dependent Protein Kinases; Cell Division; DNA, Complementary; Ethers, Cyclic; Microscopy, Fluorescence; Mitogen-Activated Protein Kinase 3; Mitogen-Activated Protein Kinases; Molecular Sequence Data; Okadaic Acid; Pertussis Toxin; Protein Conformation; Protein Structure, Tertiary; Rats; Receptor, Angiotensin, Type 2; Receptors, Angiotensin; Signal Transduction; Thymidine; Transfection; Vanadates; Virulence Factors, Bordetella | 1996 |
Cycloheximide-induced activation of mouse eggs: effects on cdc2/cyclin B and MAP kinase activities.
Topics: Animals; Bromodeoxyuridine; Calcium-Calmodulin-Dependent Protein Kinases; Chromatin; Cyclin B; Cyclin B1; Cyclins; Cycloheximide; DNA Replication; Egg Proteins; Electrophoresis, Polyacrylamide Gel; Enzyme Inhibitors; Female; Half-Life; Maturation-Promoting Factor; Membrane Glycoproteins; Mice; Nocodazole; Okadaic Acid; Oocytes; Phosphorylation; Receptors, Cell Surface; Zona Pellucida Glycoproteins | 1996 |
Sensitization to DNA damage by okadaic acid or bromodeoxyuridine involves unequal effects on melanoma cell adhesion and differentiation.
Topics: Animals; Antimetabolites, Antineoplastic; Arsenicals; Bromodeoxyuridine; Cell Adhesion; Cell Differentiation; Cycloheximide; DNA Damage; DNA Fragmentation; Enzyme Inhibitors; Melanoma; Mice; Okadaic Acid; Phosphoprotein Phosphatases; Pigmentation; Protein Synthesis Inhibitors; Radiation-Sensitizing Agents; Tumor Cells, Cultured; Ultraviolet Rays | 1997 |
Protein phosphatase inhibitors arrest cell cycle and reduce branching morphogenesis in fetal rat lung cultures.
Topics: Animals; Antimetabolites; Apoptosis; Blotting, Northern; Bromodeoxyuridine; Calcineurin; Calcineurin Inhibitors; Cantharidin; Cell Differentiation; Cell Division; Cells, Cultured; Enzyme Inhibitors; Fetus; Gene Expression Regulation, Developmental; Gene Expression Regulation, Enzymologic; Insecticides; Lung; Nitriles; Okadaic Acid; Phosphoprotein Phosphatases; Protein Phosphatase 2; Proteolipids; Pulmonary Surfactants; Pyrethrins; Rats; Respiratory Mucosa; RNA, Messenger | 2000 |
Coordinate involvement of cell cycle arrest and apoptosis strengthen the effect of FTY720.
Topics: Antineoplastic Agents; Apoptosis; Blotting, Western; Bromodeoxyuridine; Cell Cycle; Cell Division; DNA Fragmentation; Down-Regulation; Enzyme Activation; Fingolimod Hydrochloride; HL-60 Cells; Humans; Immunosuppressive Agents; Jurkat Cells; Okadaic Acid; Phosphoprotein Phosphatases; Phosphorylation; Precipitin Tests; Propylene Glycols; Retinoblastoma Protein; Signal Transduction; Sphingosine; Time Factors | 2001 |