Forkhead box transcription factor O1 inhibits cholesterol 7α-hydroxylase in human hepatocytes and in high fat diet-fed mice
- 31 October 2009
- journal article
- Published by Elsevier BV in Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
- Vol. 1791 (10), 991-996
- https://doi.org/10.1016/j.bbalip.2009.05.004
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Arginine Methylation of FOXO Transcription Factors Inhibits Their Phosphorylation by AktMolecular Cell, 2008
- O-GlcNAc Regulates FoxO Activation in Response to GlucoseOnline Journal of Public Health Informatics, 2008
- Impaired Regulation of Hepatic Glucose Production in Mice Lacking the Forkhead Transcription Factor Foxo1 in LiverCell Metabolism, 2007
- Aberrant Forkhead Box O1 Function Is Associated with Impaired Hepatic MetabolismEndocrinology, 2006
- Insulin Regulation of Cholesterol 7α-Hydroxylase Expression in Human HepatocytesOnline Journal of Public Health Informatics, 2006
- Dual role of transcription factor FoxO1 in controlling hepatic insulin sensitivity and lipid metabolismJCI Insight, 2006
- Bile acids and cytokines inhibit the human cholesterol 7α-hydroxylase gene via the JNK/c-jun pathway in human liver cellsHepatology, 2006
- Farnesoid X receptor is essential for normal glucose homeostasisJCI Insight, 2006
- Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasisCell Metabolism, 2005
- Regulation of bile acid synthesis: pathways, nuclear receptors, and mechanismsJournal of Hepatology, 2004