In vivo and in vitro regulation of sterol 27-hydroxylase in the liver during the acute phase response. potential role of hepatocyte nuclear factor-1.
about
Roles of infection, inflammation, and the immune system in cholesterol gallstone formationXenobiotic and Endobiotic Mediated Interactions Between the Cytochrome P450 System and the Inflammatory Response in the LiverMyeloperoxidase and serum amyloid A contribute to impaired in vivo reverse cholesterol transport during the acute phase response but not group IIA secretory phospholipase A(2)Nuclear receptors: mediators and modifiers of inflammation-induced cholestasis.Innate and acquired immunity intersect in a global view of the acute-phase response.Zymosan-mediated inflammation impairs in vivo reverse cholesterol transport.Bile acids and cytokines inhibit the human cholesterol 7 alpha-hydroxylase gene via the JNK/c-jun pathway in human liver cellsThe interaction between metabolism, cancer and cardiovascular disease, connected by 27-hydroxycholesterol.Tetradecylthioacetic acid increases hepatic mitochondrial β-oxidation and alters fatty acid composition in a mouse model of chronic inflammationDistinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis.Regulation of reverse cholesterol transport - a comprehensive appraisal of available animal studies.Impact of a cafeteria diet and daily physical training on the rat serum metabolome.Re-adopting classical nuclear receptors by cholesterol metabolites.Decreased plasma concentrations of apolipoprotein M in sepsis and systemic inflammatory response syndromes.Opposite regulation of the human apolipoprotein M gene by hepatocyte nuclear factor 1 and Jun transcription factors.The acute phase response inhibits reverse cholesterol transport.Marked upregulation of cholesterol 25-hydroxylase expression by lipopolysaccharide.Cytokine regulation of human sterol 12alpha-hydroxylase (CYP8B1) gene.Hormonal regulation of the human sterol 27-hydroxylase gene CYP27A1.Acrolein-induced dyslipidemia and acute-phase response are independent of HMG-CoA reductase.Suppression of cholesterol 7alpha-hydroxylase transcription and bile acid synthesis by an alpha1-antitrypsin peptide via interaction with alpha1-fetoprotein transcription factor.Repression of farnesoid X receptor during the acute phase response.Gene expression analysis of the acute phase response using a canine microarray.Endothelial lipase is synthesized by hepatic and aorta endothelial cells and its expression is altered in apoE-deficient mice.Suppression of DHEA sulfotransferase (Sult2A1) during the acute-phase response.Deficiency of interleukin-1 receptor antagonist deteriorates fatty liver and cholesterol metabolism in hypercholesterolemic mice.Is the effect of high fat diet on lipid and carbohydrate metabolism related to inflammation?
P2860
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P2860
In vivo and in vitro regulation of sterol 27-hydroxylase in the liver during the acute phase response. potential role of hepatocyte nuclear factor-1.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
In vivo and in vitro regulatio ...... f hepatocyte nuclear factor-1.
@en
In vivo and in vitro regulatio ...... f hepatocyte nuclear factor-1.
@nl
type
label
In vivo and in vitro regulatio ...... f hepatocyte nuclear factor-1.
@en
In vivo and in vitro regulatio ...... f hepatocyte nuclear factor-1.
@nl
prefLabel
In vivo and in vitro regulatio ...... f hepatocyte nuclear factor-1.
@en
In vivo and in vitro regulatio ...... f hepatocyte nuclear factor-1.
@nl
P2093
P2860
P356
P1476
In vivo and in vitro regulatio ...... f hepatocyte nuclear factor-1.
@en
P2093
C Grunfeld
J K Shigenaga
K R Feingold
P2860
P304
30118-30126
P356
10.1074/JBC.M102516200
P407
P577
2001-06-13T00:00:00Z