Farnesoid X receptor inhibits the transcriptional activity of carbohydrate response element binding protein in human hepatocytes. - Wikidata - wikimedia - TriplyDB

Farnesoid X receptor inhibits the transcriptional activity of carbohydrate response element binding protein in human hepatocytes.

Farnesoid X receptor inhibits the transcriptional activity of carbohydrate response element binding protein in human hepatocytes.

http://www.wikidata.org/entity/Q39175545

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Estrogen and Estrogen Receptor-α-Mediated Transrepression of Bile Salt Export Pump O-GlcNAcylation and the Metabolic Shift in High-Proliferating Cells: All the Evidence Suggests that Sugars Dictate the Flux of Lipid Biogenesis in Tumor Processes Energy metabolism in the liver The role of dietary sugars and de novo lipogenesis in non-alcoholic fatty liver disease Farnesoid X receptor inhibits glucagon-like peptide-1 production by enteroendocrine L cells Crosstalk of HNF4α with extracellular and intracellular signaling pathways in the regulation of hepatic metabolism of drugs and lipids Bile acid signaling in metabolic disease and drug therapy Farnesoid X receptor: a master regulator of hepatic triglyceride and glucose homeostasis Coordinated Actions of FXR and LXR in Metabolism: From Pathogenesis to Pharmacological Targets for Type 2 Diabetes Epigenetic modification of histone 3 lysine 27: mediator subunit MED25 is required for the dissociation of polycomb repressive complex 2 from the promoter of cytochrome P450 2C9 Upregulation of microRNA-122 by farnesoid X receptor suppresses the growth of hepatocellular carcinoma cells.The transcriptional activity of hepatocyte nuclear factor 4 alpha is inhibited via phosphorylation by ERK1/2.Pharmacology of bile acid receptors: Evolution of bile acids from simple detergents to complex signaling molecules.Soaping up type 2 diabetes with bile acids?: the link between glucose and bile acid metabolism in humans tightens: quality matters!SEURAT-1 liver gold reference compounds: a mechanism-based review.O-GlcNAcylation Links ChREBP and FXR to Glucose-Sensing Immortalized Human Hepatic Cell Lines for In Vitro Testing and Research Purposes.Identification of potential dual agonists of FXR and TGR5 using e-pharmacophore based virtual screening.A dynamic CTCF chromatin binding landscape promotes DNA hydroxymethylation and transcriptional induction of adipocyte differentiation Intestinal bile acid receptors are key regulators of glucose homeostasis.Bacterial bile salt hydrolase: an intestinal microbiome target for enhanced animal health.The regulation and role of carbohydrate response element binding protein in metabolic homeostasis and disease.The RBM14/CoAA-interacting, long intergenic non-coding RNA Paral1 regulates adipogenesis and coactivates the nuclear receptor PPARγ.Bile acid metabolism in liver pathobiology.The bile acid-sequestering resin sevelamer eliminates the acute GLP-1 stimulatory effect of endogenously released bile acids in patients with type 2 diabetes.Glucose sensing O-GlcNAcylation pathway regulates the nuclear bile acid receptor farnesoid X receptor (FXR).ChREBP Rather Than SHP Regulates Hepatic VLDL Secretion.Bile acid receptors link nutrient sensing to metabolic regulation

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P2860

Farnesoid X receptor inhibits the transcriptional activity of carbohydrate response element binding protein in human hepatocytes.

http://www.wikidata.org/entity/Q39175545

description

2013 nî lūn-bûn

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2013年の論文

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name

Farnesoid X receptor inhibits ...... protein in human hepatocytes.

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Farnesoid X receptor inhibits ...... protein in human hepatocytes.

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type

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Farnesoid X receptor inhibits ...... protein in human hepatocytes.

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Farnesoid X receptor inhibits ...... protein in human hepatocytes.

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Molecular and Cellular Biology

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Farnesoid X receptor inhibits ...... g protein in human hepatocytes

@en

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Bertrand Cariou

http://www.w3.org/2001/XMLSchema#string

Carolina Huaman Samanez

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Emilie Dorchies

http://www.w3.org/2001/XMLSchema#string

Fleur Lien

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Olivier Briand

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Philippe Lefebvre

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Sandrine Caron

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P2860

Identification of a nuclear receptor for bile acids

Bile acids: natural ligands for an orphan nuclear receptor

WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog

The Cellular Fate of Glucose and Its Relevance in Type 2 Diabetes

Glucose and cAMP regulate the L-type pyruvate kinase gene by phosphorylation/dephosphorylation of the carbohydrate response element binding protein

Carbohydrate response element binding protein directly promotes lipogenic enzyme gene transcription

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Endogenous bile acids are ligands for the nuclear receptor FXR/BAR

Deficiency of carbohydrate response element-binding protein (ChREBP) reduces lipogenesis as well as glycolysis

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2202-2211

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scholarly article

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10.1128/MCB.01004-12

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11

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33

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Catherine Postic

Hélène Dehondt

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2013-03-25T00:00:00Z

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23530060

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3648076

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