Significance and mechanism of CYP7a1 gene regulation during the acute phase of liver regeneration. - Wikidata - wikimedia - TriplyDB

Significance and mechanism of CYP7a1 gene regulation during the acute phase of liver regeneration.

Significance and mechanism of CYP7a1 gene regulation during the acute phase of liver regeneration.

http://www.wikidata.org/entity/Q37302363

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Promotion of liver regeneration/repair by farnesoid X receptor in both liver and intestine in mice Bile acids: regulation of synthesis Bile Acid Metabolism and Signaling in Cholestasis, Inflammation, and Cancer The role of bile salts in liver regeneration FXR regulates liver repair after CCl4-induced toxic injury Bile acid flux is necessary for normal liver regeneration.Recent advances in the development of farnesoid X receptor agonists Enhanced expression of G-protein coupled estrogen receptor (GPER/GPR30) in lung cancer Bile acid signaling and liver regeneration.Current research on the treatment of primary sclerosing cholangitis.GPBAR1/TGR5 mediates bile acid-induced cytokine expression in murine Kupffer cells.FXR protects lung from lipopolysaccharide-induced acute injury Hepatocarcinogenesis in FXR-/- mice mimics human HCC progression that operates through HNF1α regulation of FXR expression FXR and liver carcinogenesis Farnesoid X receptor, the bile acid sensing nuclear receptor, in liver regeneration.Downregulation of nuclear receptor FXR is associated with multiple malignant clinicopathological characteristics in human hepatocellular carcinoma.Bile Acid Receptors and Liver Cancer.Significant lethality following liver resection in A20 heterozygous knockout mice uncovers a key role for A20 in liver regeneration FGF19 functions as autocrine growth factor for hepatoblastoma Cholesterol: recapitulation of its active role during liver regeneration.Bile acid transporters and regulatory nuclear receptors in the liver and beyond FXR agonists as therapeutic agents for non-alcoholic fatty liver disease.MicroRNA-657 promotes tumorigenesis in hepatocellular carcinoma by targeting transducin-like enhancer protein 1 through nuclear factor kappa B pathways.Kinetic analysis of bile acid sulfation by stably expressed human sulfotransferase 2A1 (SULT2A1).Long-term Administration of Nuclear Bile Acid Receptor FXR Agonist Prevents Spontaneous Hepatocarcinogenesis in Abcb4-/- Mice.Cholestyramine alters bile acid amounts and the expression of cholesterol-related genes in rabbit intestinal and hepatic tissues.

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Significance and mechanism of CYP7a1 gene regulation during the acute phase of liver regeneration.

http://www.wikidata.org/entity/Q37302363

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 04 December 2008

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Significance and mechanism of ...... e phase of liver regeneration.

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Significance and mechanism of ...... e phase of liver regeneration.

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Significance and mechanism of ...... e phase of liver regeneration.

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Significance and mechanism of ...... e phase of liver regeneration.

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Molecular Endocrinology

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Significance and mechanism of ...... e phase of liver regeneration.

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Bingning Dong

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David D Moore

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Lisheng Zhang

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Steven Shiah

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Wendong Huang

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Xiongfei Huang

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Zhipeng Meng

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P2860

Bile acids: natural ligands for an orphan nuclear receptor

Molecular basis for feedback regulation of bile acid synthesis by nuclear receptors

Vitamin D receptor as an intestinal bile acid sensor

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

Identification of membrane-type receptor for bile acids (M-BAR)

A G protein-coupled receptor responsive to bile acids

The nuclear receptor PXR is a lithocholic acid sensor that protects against liver toxicity

CPF: an orphan nuclear receptor that regulates liver-specific expression of the human cholesterol 7alpha-hydroxylase gene

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

Overexpression of cholesterol transporter StAR increases in vivo rates of bile acid synthesis in the rat and mouse

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137-145

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scholarly article

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10.1210/ME.2008-0198

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23

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