Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
about
MicroRNAs as Important Players in Host-hepatitis B Virus InteractionsRoles of hepatocyte nuclear factors in hepatitis B virus infectionHepatitis B virus molecular biology and pathogenesisMicroRNAs as therapeutic strategy for hepatitis B virus-associated hepatocellular carcinoma: current status and future prospectsPrevalent HBV point mutations and mutation combinations at BCP/preC region and their association with liver disease progression.Limited effects of bile acids and small heterodimer partner on hepatitis B virus biosynthesis in vivo.Nuclear receptor variants in liver disease.Synthesis and biological evaluations of chalcones, flavones and chromenes as farnesoid x receptor (FXR) antagonists.Independent activation of hepatitis B virus biosynthesis by retinoids, peroxisome proliferators, and bile acids.Epigenetically regulated miR-449a enhances hepatitis B virus replication by targeting cAMP-responsive element binding protein 5 and modulating hepatocytes phenotype.Multiple nuclear receptors may regulate hepatitis B virus biosynthesis during development.Peroxisome proliferator-activated receptor gamma Coactivator 1alpha and small heterodimer partner differentially regulate nuclear receptor-dependent hepatitis B virus biosynthesis.Transforming growth factor β-activated kinase 1 transcriptionally suppresses hepatitis B virus replication.CRTC2 enhances HBV transcription and replication by inducing PGC1α expression.Hepatocyte metabolic signalling pathways and regulation of hepatitis B virus expression.An unhealthy relationship: viral manipulation of the nuclear receptor superfamily.Interactions of Hepatitis B Virus Infection with Nonalcoholic Fatty Liver Disease: Possible Mechanisms and Clinical Impact.Resveratrol, sirtuins, and viruses.Epigallocatechin gallate inhibits hepatitis B virus via farnesoid X receptor alpha.Virus-host interplay in hepatitis B virus infection and epigenetic treatment strategies.Inhibition of interferon-α-induced signaling by hyperosmolarity and hydrophobic bile acids.Bile Acids Act as Soluble Host Restriction Factors Limiting Cytomegalovirus Replication in Hepatocytes.Bile acids increase hepatitis B virus gene expression and inhibit interferon-alpha activity.Hepatitis B virus: the "metabolovirus" highjacks cholesterol and bile acid metabolism.Bile acid-induced modulation of virus replication.Silencing Retinoid X Receptor Alpha Expression Enhances Early-stage Hepatitis B Virus Infection In Cell Cultures.Anti-inflammatory consequences of bile acid accumulation in virus-infected bile duct ligated mice.Host functions used by hepatitis B virus to complete its life cycle: Implications for developing host-targeting agents to treat chronic hepatitis B
P2860
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P2860
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
@en
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
@nl
type
label
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
@en
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
@nl
prefLabel
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
@en
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
@nl
P2093
P2860
P356
P1433
P1476
Transactivation of the hepatitis B virus core promoter by the nuclear receptor FXRalpha.
@en
P2093
Caroline Scholtès
Christophe Ramière
Laure Perrin-Cocon
Mary-Anne Trabaud
Olivier Diaz
Patrice André
Vinca Icard
Vincent Lotteau
P2860
P304
10832-10840
P356
10.1128/JVI.00883-08
P407
P577
2008-09-03T00:00:00Z