Regulation of anti-atherogenic apolipoprotein M gene expression by the orphan nuclear receptor LRH-1. (Q38296796)

1 September 2017

Regulation of anti-atherogenic apolipoprotein M gene expression by the orphan nuclear receptor LRH-1. (English)

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1 September 2017

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Nicolas Venteclef

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Iannis Talianidis

object named as

Iannis Talianidis

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author name string

Anna Haroniti

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1 September 2017

Jean-Jacques Tousaint

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1 September 2017

Philippe Delerive

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1 September 2017

language of work or name

English

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publication date

31 October 2007

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Journal of Biological Chemistry

1 September 2017

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1 September 2017

283

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1 September 2017

7

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1 September 2017

3694-3701

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LRH-1: an orphan nuclear receptor involved in development, metabolism and steroidogenesis

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Structural analyses reveal phosphatidyl inositols as ligands for the NR5 orphan receptors SF-1 and LRH-1.

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The crystal structures of human steroidogenic factor-1 and liver receptor homologue-1.

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Phosphorylation of the hinge domain of the nuclear hormone receptor LRH-1 stimulates transactivation

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SUMO-dependent compartmentalization in promyelocytic leukemia protein nuclear bodies prevents the access of LRH-1 to chromatin

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Orphan nuclear receptor LRH-1 is required to maintain Oct4 expression at the epiblast stage of embryonic development

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The fetoprotein transcription factor (FTF) gene is essential to embryogenesis and cholesterol homeostasis and is regulated by a DR4 element

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The nuclear receptor LRH-1 critically regulates extra-adrenal glucocorticoid synthesis in the intestine

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Alpha 1-fetoprotein transcription factor is required for the expression of sterol 12alpha -hydroxylase, the specific enzyme for cholic acid synthesis. Potential role in the bile acid-mediated regulation of gene transcription

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The orphan nuclear receptor LRH-1 activates the ABCG5/ABCG8 intergenic promoter

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The orphan nuclear receptor LRH-1 potentiates the sterol-mediated induction of the human CETP gene by liver X receptor

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Liver receptor homolog 1 controls the expression of carboxyl ester lipase

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Molecular characterization of the role of orphan receptor small heterodimer partner in development of fatty liver

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A key role for orphan nuclear receptor liver receptor homologue-1 in activation of fatty acid synthase promoter by liver X receptor

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Activation of the promoter of the orphan receptor SHP by orphan receptors that bind DNA as monomers

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Apolipoprotein M is required for prebeta-HDL formation and cholesterol efflux to HDL and protects against atherosclerosis

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Regulation of apolipoprotein M gene expression by MODY3 gene hepatocyte nuclear factor-1alpha: haploinsufficiency is associated with reduced serum apolipoprotein M levels

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Regulation of hepatic metabolic pathways by the orphan nuclear receptor SHP.

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The role of alpha1-fetoprotein transcription factor/LRH-1 in bile acid biosynthesis: a known nuclear receptor activator that can act as a suppressor of bile acid biosynthesis

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A regulatory cascade of the nuclear receptors FXR, SHP-1, and LRH-1 represses bile acid biosynthesis

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Bile acids reduce SR-BI expression in hepatocytes by a pathway involving FXR/RXR, SHP, and LRH-1.

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LXXLL motifs in Dax-1 have target specificity for the orphan nuclear receptors Ad4BP/SF-1 and LRH-1.

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Apolipoprotein M--a novel player in high-density lipoprotein metabolism and atherosclerosis

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A novel human apolipoprotein (apoM)

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Isolation and characterization of human apolipoprotein M-containing lipoproteins

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Molecular regulation of HDL metabolism and function: implications for novel therapies

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Liver receptor homologue-1 mediates species- and cell line-specific bile acid-dependent negative feedback regulation of the apical sodium-dependent bile acid transporter

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Both leptin and leptin-receptor are essential for apolipoprotein M expression in vivo

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Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis

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Hepatocyte nuclear factor-1alpha is an essential regulator of bile acid and plasma cholesterol metabolism

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Clinical utility of bile acid sequestrants in the treatment of dyslipidemia: a scientific review

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Plasticity and expanding complexity of the hepatic transcription factor network during liver development

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Histone modifications defining active genes persist after transcriptional and mitotic inactivation

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Identifiers

DOI

10.1074/JBC.M706382200

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1 September 2017

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