Page last updated: 2024-08-26

22-hydroxycholesterol and gw 3965

22-hydroxycholesterol has been researched along with gw 3965 in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gao, X; Gong, H; Khadem, S; Lee, JH; Li, S; Lu, Y; Xie, W; Zhang, J1
Bussolino, F; Morello, F; Mulatero, P; Noghero, A; Saglio, E; Schiavone, D; Veglio, F; Verhovez, A; Williams, TA1
Asavapanumas, N; Chatsudthipong, V; Kittayaruksakul, S; Muanprasat, C; Soodvilai, S1
Chatsudthipong, V; Fongsupa, S; Jia, Z; Soodvilai, S; Yang, T1
Asgarova, A; Biichlé, S; Ceroi, A; Delettre, FA; Duperrier, A; Gauthier, T; Lagrost, L; Marotel, C; Masson, D; Mourey, G; Perruche, S; Saas, P1

Other Studies

5 other study(ies) available for 22-hydroxycholesterol and gw 3965

ArticleYear
Androgen deprivation by activating the liver X receptor.
    Endocrinology, 2008, Volume: 149, Issue:8

    Topics: Androgens; Animals; Benzoates; Benzylamines; Cells, Cultured; DNA-Binding Proteins; Drug Resistance, Neoplasm; Gene Expression Regulation, Enzymologic; Humans; Hydroxycholesterols; Liver X Receptors; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Neoplasms, Hormone-Dependent; Orphan Nuclear Receptors; Prostate; Prostatic Neoplasms; Receptors, Cytoplasmic and Nuclear; Regeneration; Sulfotransferases; Testosterone

2008
LXR-activating oxysterols induce the expression of inflammatory markers in endothelial cells through LXR-independent mechanisms.
    Atherosclerosis, 2009, Volume: 207, Issue:1

    Topics: Anticholesteremic Agents; Benzoates; Benzylamines; Cells, Cultured; Chemokines; Cholesterol; E-Selectin; Endothelial Cells; Gene Expression Profiling; Gene Expression Regulation; Humans; Hydrocarbons, Fluorinated; Hydroxycholesterols; Inflammation Mediators; Intercellular Adhesion Molecule-1; Lipopolysaccharides; Liver X Receptors; Orphan Nuclear Receptors; RNA Interference; RNA, Messenger; Signal Transduction; Sulfonamides; Transcription Factors; Transfection; Tumor Necrosis Factor-alpha; Vascular Cell Adhesion Molecule-1

2009
Liver X receptor activation downregulates organic anion transporter 1 (OAT1) in the renal proximal tubule.
    American journal of physiology. Renal physiology, 2012, Mar-01, Volume: 302, Issue:5

    Topics: Animals; Benzoates; Benzylamines; Cell Line; Cells, Cultured; Down-Regulation; Humans; Hydrocarbons, Fluorinated; Hydroxycholesterols; Kidney Tubules, Proximal; Liver X Receptors; Mice; Organic Anion Transport Protein 1; Orphan Nuclear Receptors; Sulfonamides

2012
Liver X receptor agonists decrease ENaC-mediated sodium transport in collecting duct cells.
    American journal of physiology. Renal physiology, 2012, Dec-15, Volume: 303, Issue:12

    Topics: Animals; Anticholesteremic Agents; Benzoates; Benzylamines; Biological Transport; Cells, Cultured; Epithelial Sodium Channels; Hydrocarbons, Fluorinated; Hydroxycholesterols; Kidney Tubules, Collecting; Ligands; Liver X Receptors; Mice; Orphan Nuclear Receptors; Sodium; Sodium-Potassium-Exchanging ATPase; Sulfonamides

2012
The anti-inflammatory effects of platelet-derived microparticles in human plasmacytoid dendritic cells involve liver X receptor activation.
    Haematologica, 2016, Volume: 101, Issue:3

    Topics: Angiogenic Proteins; ATP Binding Cassette Transporter 1; Benzoates; Benzylamines; Blood Platelets; Cell-Derived Microparticles; Dendritic Cells; Endothelial Cells; Gene Expression Regulation; Humans; Hydrocarbons, Fluorinated; Hydroxycholesterols; Imidazoles; Immunity, Innate; Liver X Receptors; NF-kappa B; Oligodeoxyribonucleotides; Phenylenediamines; Primary Cell Culture; Receptors, G-Protein-Coupled; Signal Transduction; Sterol Regulatory Element Binding Protein 1; Sulfonamides; Toll-Like Receptor 7; Tumor Necrosis Factor-alpha

2016