Regulation of Hepatocyte Nuclear Factor 4α-mediated Transcription
スポンサーリンク
概要
- 論文の詳細を見る
- 2008-02-25
著者
-
GONZALEZ Frank
Laboratory of Metabolism, National Cancer Institute, National Institutes of Health
-
Gonzalez Frank
Laboratory Of Metabolism National Cancer Institute National Instituted Of Health
-
Gonzalez Frank
Laboratory Of Metabolism Division Of Basic Science National Cancer Institute
関連論文
- Di(2-ethylhexyl)phthalate Induces Hepatic Tumorigenesis through a Peroxisome Proliferator-activated Receptor α-independent Pathway
- Different Mechanisms of DEHP-induced Hepatocellular Adenoma Tumorigenesis in Wild-type and Pparα-null Mice
- Regulation of Hepatocyte Nuclear Factor 4α-mediated Transcription
- Differential Effects of Aging, Drinking and Exercise on Serum Cholesterol Levels Dependent on the PPARA-V227A Polymorphism
- Bile Acid-Induced Elevated Oxidative Stress in the Absence of Farnesoid X Receptor(Biochemistry)
- Hydroxysteroid sulfotransferase (SULT2A) の発現はFXRにより抑制的に調節される
- Bile acid sulfates as a possible early marker of liver toxicity(Drug metabolism, Proceedings of the 32nd Annual Meeting)
- Expression of hydroxysteroid sulfotransferase involved in protection against bile acid-induced hepatotoxicity(Drug metabolism, Proceedings of the 32nd Annual Meeting)
- Protection from liver toxicity induced by lithocholic acid-feeding : Involvement of cyp3a and hydroxysteroid sulfotransferase(Drug metabolism, Proceedings of the 32nd Annual Meeting)
- Bile acid-induced liver toxicity and nuclear receptor FXR (LIVER/DIGESTIVE SYSTEM) (GENERAL SESSION BY POSTER PRESENTATION) (Proceedings of the 30th Annual Meeting)
- O11-03 Relative importance of maternal and embryonic microsomal epoxide hydrolase in 7, 12-dimethylbenz[a] anthracene : induced developmental toxicity
- Mechanism of 7,12-Dimethylbenz[α]anthracene-Induced Immunotoxicity: Role of Metabolic Activation at the Target Organ
- O-26 Difference between Spleen and Thymus in 7, 12-Dimethylbenz[a]anthracene-lnduced lmmunotoxicity.(Proceedings of the 27th Annual Meeting)
- AHR-mediated suppression of PPARα target gene expression caused by exposed polycyclic aromatic hydrocarbons (TOXICOGENOMICS AND TOXICOPROTEOMICS) (GENERAL SESSION BY POSTER PRESENTATION) (Proceedings of the 30th Annual Meeting)
- SUPPRESSION OF PPAR ALPHA SIGNAL CAUSED BY POLYCYCLIC AROMATIC HYDROCARBONS.(GENERAL SESSION BY POSTER PRESENTATION)(MOLECULAR TOXICITY & TOXICOGENOMICS)
- Expression of human CYP1A2 capable of activating heterocyclic amine in Bm 6 cells using baculovirus (BmNPV) system.
- Regulation of insulin-like growth factor binding protein-1 and lipoprotein lipase by the aryl hydrocarbon receptor
- SL1 The role of the aryl hydrocarbon receptor in animal development, physiological homeostasis and toxicity of TCDD
- Hepatic regeneration in peroxisome proliferator-activated receptor α-null mice after partial hepatectomy
- Regulation of peroxisome proliferator activated receptor α-mediated pathways in alcohol fed cytochrome P450 2E1 deficient mice
- Control of Constitutively-expressed Developmentally-activated Rat Hepatic Cytochrome P450 Genes
- Regulation of insulin-like growth factor binding protein-1 and lipoprotein lipase by the aryl hydrocarbon receptor
- Expression of Hepatic Fat-Specific Protein 27 Depends on the Specific Etiology of Fatty Liver