Cross-talk between peroxisome proliferator-activated receptor (PPAR) alpha and liver X receptor (LXR) in nutritional regulation of fatty acid metabolism. II. LXRs suppress lipid degradation gene promoters through inhibition of PPAR signaling.
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The Deep Correlation between Energy Metabolism and Reproduction: A View on the Effects of Nutrition for Women FertilityMitochondrial dysfunction in obesity: potential benefit and mechanism of Co-enzyme Q10 supplementation in metabolic syndromeThe inhibition of the human cholesterol 7alpha-hydroxylase gene (CYP7A1) promoter by fibrates in cultured cells is mediated via the liver x receptor alpha and peroxisome proliferator-activated receptor alpha heterodimerSystems analysis of small signaling modules relevant to eight human diseasesLarge scale gene expression profiles of regenerating inner ear sensory epithelia.Liver X receptor alpha is a transcriptional repressor of the uncoupling protein 1 gene and the brown fat phenotype.Ligand modulated antagonism of PPARgamma by genomic and non-genomic actions of PPARdelta.Susceptibility of pancreatic beta cells to fatty acids is regulated by LXR/PPARalpha-dependent stearoyl-coenzyme A desaturase.Metabolic syndrome without obesity: Hepatic overexpression of 11beta-hydroxysteroid dehydrogenase type 1 in transgenic miceRegulation of insulin resistance and adiponectin signaling in adipose tissue by liver X receptor activation highlights a cross-talk with PPARγ.Metabolic switching of human myotubes is improved by n-3 fatty acidsMacrophage fatty-acid synthase deficiency decreases diet-induced atherosclerosisTranscriptional regulation of human and rat hepatic lipid metabolism by the grapefruit flavonoid naringenin: role of PPARalpha, PPARgamma and LXRalpha.Peroxisome proliferator-activated receptors (PPARs)-independent functions of fish oil on glucose and lipid metabolism in diet-induced obese mice.Ligand-binding regulation of LXR/RXR and LXR/PPAR heterodimerizations: SPR technology-based kinetic analysis correlated with molecular dynamics simulation.Both liver-X receptor (LXR) isoforms control energy expenditure by regulating brown adipose tissue activity.Concurrent activation of liver X receptor and peroxisome proliferator-activated receptor alpha exacerbates hepatic steatosis in high fat diet-induced obese mice.Ligand-activated PPARbeta efficiently represses the induction of LXR-dependent promoter activity through competition with RXRL-carnitine and PPARα-agonist fenofibrate are involved in the regulation of Carnitine Acetyltransferase (CrAT) mRNA levels in murine liver cells.Genome-wide profiling of liver X receptor, retinoid X receptor, and peroxisome proliferator-activated receptor α in mouse liver reveals extensive sharing of binding sitesSea lampreys elicit strong transcriptomic responses in the lake trout liver during parasitismActivation of liver X receptor inhibits osteopontin and ameliorates diabetic nephropathyTreatment with PPARα Agonist Clofibrate Inhibits the Transcription and Activation of SREBPs and Reduces Triglyceride and Cholesterol Levels in Liver of Broiler Chickens.Genomic profiling in nuclear receptor-mediated toxicity.Liver lipid metabolism.Flavonoids as dietary regulators of nuclear receptor activityFenofibrate inhibits adipocyte hypertrophy and insulin resistance by activating adipose PPARalpha in high fat diet-induced obese miceRegulation of bile acid and cholesterol metabolism by PPARsOn the mechanism for PPAR agonists to enhance ABCA1 gene expression.The mechanistic basis for the induction of hepatic steatosis by xenobiotics.Effect of short-chain fatty acids on triacylglycerol accumulation, lipid droplet formation and lipogenic gene expression in goat mammary epithelial cells.n-3 fatty acids ameliorate hepatic steatosis and dysfunction after LXR agonist ingestion in mice.Tipping the Balance: Hepatotoxicity and the 4 Apical Key Events of Hepatic Steatosis.RIP140 triggers foam-cell formation by repressing ABCA1/G1 expression and cholesterol efflux via liver X receptor.Ligand-regulated heterodimerization of peroxisome proliferator-activated receptor α with liver X receptor α.G0S2: A small giant controller of lipolysis and adipose-liver fatty acid flux.Inflammatory stress exacerbates hepatic cholesterol accumulation via disrupting cellular cholesterol export.Selective action of human sera differing in fatty acids and cholesterol content on in vitro gene expression.Cross-Talk between PPARs and the Partners of RXR: A Molecular Perspective.The Niemann-Pick C1 gene interacts with a high-fat diet to promote weight gain through differential regulation of central energy metabolism pathways.
P2860
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P2860
Cross-talk between peroxisome proliferator-activated receptor (PPAR) alpha and liver X receptor (LXR) in nutritional regulation of fatty acid metabolism. II. LXRs suppress lipid degradation gene promoters through inhibition of PPAR signaling.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Cross-talk between peroxisome ...... inhibition of PPAR signaling.
@en
type
label
Cross-talk between peroxisome ...... inhibition of PPAR signaling.
@en
prefLabel
Cross-talk between peroxisome ...... inhibition of PPAR signaling.
@en
P2093
P356
P1476
Cross-talk between peroxisome ...... inhibition of PPAR signaling.
@en
P2093
Akimitsu Takahashi
Hitoshi Shimano
Jun-ichi Osuga
Ken Ohashi
Masanori Nakakuki
Michiyo Amemiya-Kudo
Nobuhiro Yamada
Sachiko Tomita
Shigeru Yatoh
Shun Ishibashi
P304
P356
10.1210/ME.2002-0191
P577
2003-05-01T00:00:00Z