Page last updated: 2024-08-17

taurocholic acid and gw 4064

taurocholic acid has been researched along with gw 4064 in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Claudel, T; Duval, C; Fruchart, JC; Kosykh, V; Pineda Torra, I; Staels, B1
Eigner, K; Fruhwürth, S; Röhrl, C; Stangl, H1
Anitha, M; Gao, X; Gonzalez, FJ; Jiang, C; Krausz, KW; Patterson, AD; Shi, J; Sun, D; Sun, L; Takahashi, S; Wang, T; Xie, C1
Adeli, K; Anakk, S; Baker, C; Dean, AE; Farr, S; Hoffman, S; Masoudpoor, H; Stankovic, B; Taher, J1

Other Studies

4 other study(ies) available for taurocholic acid and gw 4064

ArticleYear
Bile acids induce the expression of the human peroxisome proliferator-activated receptor alpha gene via activation of the farnesoid X receptor.
    Molecular endocrinology (Baltimore, Md.), 2003, Volume: 17, Issue:2

    Topics: Animals; Base Sequence; Bile Acids and Salts; Cells, Cultured; Chenodeoxycholic Acid; DNA-Binding Proteins; Gene Expression Regulation; Hepatocytes; Humans; Isoxazoles; Liver Neoplasms, Experimental; Male; Mice; Mice, Inbred C57BL; Molecular Sequence Data; Promoter Regions, Genetic; Receptor Cross-Talk; Receptors, Cytoplasmic and Nuclear; Receptors, Retinoic Acid; Response Elements; Retinoid X Receptors; RNA, Messenger; Species Specificity; Taurocholic Acid; Transcription Factors; Tumor Cells, Cultured

2003
Bile acids reduce endocytosis of high-density lipoprotein (HDL) in HepG2 cells.
    PloS one, 2014, Volume: 9, Issue:7

    Topics: Bile Acids and Salts; CD36 Antigens; Chenodeoxycholic Acid; Endocytosis; Hep G2 Cells; Humans; Isoxazoles; Lipoproteins, HDL; Receptors, Cytoplasmic and Nuclear; Scavenger Receptors, Class B; Taurocholic Acid; Transferrin

2014
An Intestinal Farnesoid X Receptor-Ceramide Signaling Axis Modulates Hepatic Gluconeogenesis in Mice.
    Diabetes, 2017, Volume: 66, Issue:3

    Topics: Acetyl Coenzyme A; Amidohydrolases; Animals; Body Weight; Caffeic Acids; Ceramides; Diet, High-Fat; Gastrointestinal Microbiome; Gluconeogenesis; Ileum; Insulin; Intestinal Mucosa; Intestines; Isoxazoles; Liver; Male; Mice; Mice, Inbred C57BL; Mitochondria, Liver; Phenylethyl Alcohol; Pyruvate Carboxylase; Receptors, Cytoplasmic and Nuclear; Signal Transduction; Taurocholic Acid

2017
Bile acid treatment and FXR agonism lower postprandial lipemia in mice.
    American journal of physiology. Gastrointestinal and liver physiology, 2020, 04-01, Volume: 318, Issue:4

    Topics: Animals; Bile Acids and Salts; Cholesterol 7-alpha-Hydroxylase; Deoxycholic Acid; Exenatide; Gastric Emptying; Gene Expression Regulation; Hyperlipidemias; Insulin; Intestinal Mucosa; Intestines; Isoxazoles; Lipid Metabolism; Male; Mice; Mice, Inbred C57BL; Postprandial Period; Receptors, Cytoplasmic and Nuclear; Receptors, G-Protein-Coupled; Taurocholic Acid

2020