Page last updated: 2024-08-21

isoxazoles and pyrazolanthrone

isoxazoles has been researched along with pyrazolanthrone in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Billin, AN; Bisi, J; Donahee, M; Goodwin, B; Holt, JA; Jones, SA; Kliewer, SA; Kozarsky, KF; Luo, G; Mansfield, TA; McNeill, YY; Wang, DY1
Edwards, PA; Kast-Woelbern, HR; Lusis, AJ; Shih, DM; Wong, J; Xia, YR1
Beerheide, W; Boelsterli, UA; Latchoumycandane, C; Sattabongkot, J; Seah, QM; Tan, RC1
Chen, LW; Chen, PH; Hsu, CM; Tseng, HT1

Other Studies

4 other study(ies) available for isoxazoles and pyrazolanthrone

ArticleYear
Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis.
    Genes & development, 2003, Jul-01, Volume: 17, Issue:13

    Topics: Animals; Anthracenes; Bile Acids and Salts; Cell Line; Cells, Cultured; Chenodeoxycholic Acid; Cholesterol 7-alpha-Hydroxylase; DNA-Binding Proteins; Enzyme Repression; Fibroblast Growth Factors; Gene Expression Regulation; Hepatocytes; Humans; Isoxazoles; JNK Mitogen-Activated Protein Kinases; Mice; Mitogen-Activated Protein Kinases; Phosphorylation; Proto-Oncogene Proteins c-jun; Receptors, Cytoplasmic and Nuclear; Recombinant Proteins; Response Elements; Signal Transduction; Transcription Factors; Transfection

2003
A role for FXR and human FGF-19 in the repression of paraoxonase-1 gene expression by bile acids.
    Journal of lipid research, 2006, Volume: 47, Issue:2

    Topics: Administration, Oral; Animals; Anthracenes; Aryldialkylphosphatase; Bile Acids and Salts; Cell Line, Tumor; Chenodeoxycholic Acid; Cholesterol 7-alpha-Hydroxylase; Cholesterol, Dietary; Cholic Acid; Dietary Fats; DNA-Binding Proteins; Enzyme Inhibitors; Female; Fibroblast Growth Factors; Gene Expression; Humans; Isoxazoles; JNK Mitogen-Activated Protein Kinases; Mice; Mice, Inbred C57BL; Mice, Knockout; Mutation; Phospholipid Transfer Proteins; Promoter Regions, Genetic; Receptors, Cytoplasmic and Nuclear; Sterol Regulatory Element Binding Protein 1; Transcription Factors

2006
Leflunomide or A77 1726 protect from acetaminophen-induced cell injury through inhibition of JNK-mediated mitochondrial permeability transition in immortalized human hepatocytes.
    Toxicology and applied pharmacology, 2006, Nov-15, Volume: 217, Issue:1

    Topics: Acetaminophen; Aniline Compounds; Anthracenes; Antirheumatic Agents; Caspase 3; Cell Death; Cell Line; Crotonates; Cytochromes c; Dose-Response Relationship, Drug; Enzyme Activation; Glutathione; Hepatocytes; Humans; Hydroxybutyrates; Isoxazoles; JNK Mitogen-Activated Protein Kinases; Leflunomide; Mitochondria, Liver; Mitochondrial Membrane Transport Proteins; Mitochondrial Permeability Transition Pore; Mitogen-Activated Protein Kinase 8; Mitogen-Activated Protein Kinase 9; Nitriles; Phosphorylation; Protein Carbonylation; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-bcl-2; Toluidines

2006
Peritonitis-induced peroxynitrite and lung damage depends on c-Jun NH2-terminal kinase signaling of hematopoietic cells.
    Critical care medicine, 2010, Volume: 38, Issue:4

    Topics: Animals; Anthracenes; Blotting, Western; Dimethyl Sulfoxide; Disease Models, Animal; Hematopoiesis; Isoxazoles; JNK Mitogen-Activated Protein Kinases; Leflunomide; Lung Injury; Male; Mice; Mice, Inbred C57BL; Myeloid Cells; NF-kappa B; Nitric Oxide Synthase; Peritonitis; Peroxynitrous Acid; Rhodamines; Signal Transduction; Transcription Factor AP-1

2010