The molecular physiology of hepatic nuclear factor 3 in the regulation of gluconeogenesis.
about
The forkhead transcription factor Foxo1 (Fkhr) confers insulin sensitivity onto glucose-6-phosphatase expressionThe nuclear receptor cofactor, receptor-interacting protein 140, is required for the regulation of hepatic lipid and glucose metabolism by liver X receptorInhibition of Foxo1 function is associated with improved fasting glycemia in diabetic miceFoxa2 (HNF3beta ) controls multiple genes implicated in metabolism-secretion coupling of glucose-induced insulin releasec-Myc is required for the glucose-mediated induction of metabolic enzyme genesFoxa3 (hepatocyte nuclear factor 3gamma ) is required for the regulation of hepatic GLUT2 expression and the maintenance of glucose homeostasis during a prolonged fastCompensatory roles of Foxa1 and Foxa2 during lung morphogenesisAn integrated functional genomics screening program reveals a role for BMP-9 in glucose homeostasis.Insulin and epidermal growth factor suppress basal glucose-6-phosphatase catalytic subunit gene transcription through overlapping but distinct mechanisms.FoxOs function synergistically to promote glucose production.Novel concepts in insulin regulation of hepatic gluconeogenesis.Functional analyses of the mutation nt-128 T→G in the hepatocyte nuclear factor-1α promoter region in Chinese diabetes pedigrees.Prediction of CYP3A4 enzyme activity using haplotype tag SNPs in African Americans.Hepatocyte metabolic signalling pathways and regulation of hepatitis B virus expression.Minireview: new molecular mediators of glucocorticoid receptor activity in metabolic tissues.Role of accessory factors and steroid receptor coactivator 1 in the regulation of phosphoenolpyruvate carboxykinase gene transcription by glucocorticoids.Distinct mechanisms of glucose lowering by specific agonists for peroxisomal proliferator activated receptor gamma and retinoic acid X receptors.Glucocorticoids repress transcription of phosphoenolpyruvate carboxykinase (GTP) gene in adipocytes by inhibiting its C/EBP-mediated activation.Characterization of a novel Foxa (hepatocyte nuclear factor-3) site in the glucagon promoter that is conserved between rodents and humans.Tumour necrosis factor alpha decreases glucose-6-phosphatase gene expression by activation of nuclear factor kappaB.Adenovirus-mediated increase in HNF-3beta or HNF-3alpha shows differences in levels of liver glycogen and gene expression.Insulin inhibits hepatocellular glucose production by utilizing liver-enriched transcriptional inhibitory protein to disrupt the association of CREB-binding protein and RNA polymerase II with the phosphoenolpyruvate carboxykinase gene promoter.Glucocorticoids regulate transcription of the gene for phosphoenolpyruvate carboxykinase in the liver via an extended glucocorticoid regulatory unit.
P2860
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P2860
The molecular physiology of hepatic nuclear factor 3 in the regulation of gluconeogenesis.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
The molecular physiology of he ...... regulation of gluconeogenesis.
@en
type
label
The molecular physiology of he ...... regulation of gluconeogenesis.
@en
prefLabel
The molecular physiology of he ...... regulation of gluconeogenesis.
@en
P2093
P2860
P356
P1476
The molecular physiology of he ...... regulation of gluconeogenesis.
@en
P2093
P2860
P304
14717-14721
P356
10.1074/JBC.275.19.14717
P407
P577
2000-05-01T00:00:00Z