Glucose elicits serine/threonine kinase VRK1 to phosphorylate nuclear pregnane X receptor as a novel hepatic gluconeogenic signal
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Cell Biology
Reference22 articles.
1. An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway;Kliewer;Cell,1998
2. Ligand-activated pregnane X receptor interferes with HNF-4 signaling by targeting a common coactivator PGC-1alpha. Functional implications in hepatic cholesterol and glucose metabolism;Bhalla;J. Biol. Chem.,2004
3. Nuclear receptors CAR and PXR cross talk with FOXO1 to regulate genes that encode drug-metabolizing and gluconeogenic enzymes;Kodama;Mol. Cell. Biol.,2004
4. Nuclear pregnane X receptor cross-talk with FoxA2 to mediate drug-induced regulation of lipid metabolism in fasting mouse liver;Nakamura;J. Biol. Chem.,2007
5. Serum- and glucocorticoid-regulated kinase 2 determines drug-activated pregnane X receptor to induce gluconeogenesis in human liver cells;Gotoh;J. Pharmacol. Exp. Ther.,2014
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