DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
about
Cyclosporin A associated helicase-like protein facilitates the association of hepatitis C virus RNA polymerase with its cellular cyclophilin BExpression of DDX3 is directly modulated by hypoxia inducible factor-1 alpha in breast epithelial cellsHepatitis B virus polymerase blocks pattern recognition receptor signaling via interaction with DDX3: implications for immune evasionThe DEAD-box RNA helicase DDX6 is required for efficient encapsidation of a retroviral genomeDEAD/H BOX 3 (DDX3) helicase binds the RIG-I adaptor IPS-1 to up-regulate IFN-beta-inducing potentialDDX3 regulates cell growth through translational control of cyclin E1Hepatitis C virus core-derived peptides inhibit genotype 1b viral genome replication via interaction with DDX3XA motif unique to the human DEAD-box protein DDX3 is important for nucleic acid binding, ATP hydrolysis, RNA/DNA unwinding and HIV-1 replicationThe DEAD-box helicase DDX3 supports the assembly of functional 80S ribosomesHuman DDX3 interacts with the HIV-1 Tat protein to facilitate viral mRNA translationHuman DDX3 functions in translation and interacts with the translation initiation factor eIF3Viral targeting of DEAD box protein 3 reveals its role in TBK1/IKKepsilon-mediated IRF activationThe DNA damage sensors ataxia-telangiectasia mutated kinase and checkpoint kinase 2 are required for hepatitis C virus RNA replicationA host YB-1 ribonucleoprotein complex is hijacked by hepatitis C virus for the control of NS3-dependent particle productionModulation of the type I interferon pathways by culture-adaptive hepatitis C virus core mutantsThe DEAD-box helicase DDX3X is a critical component of the TANK-binding kinase 1-dependent innate immune responseThe variable N-terminal region of DDX5 contains structural elements and auto-inhibits its interaction with NS5B of hepatitis C virusCritical roles of RNA helicase DDX3 and its interactions with eIF4E/PABP1 in stress granule assembly and stress responseDDX6 (Rck/p54) is required for efficient hepatitis C virus replication but not for internal ribosome entry site-directed translationWho Regulates Whom? An Overview of RNA Granules and Viral InfectionsFoamy virus assembly with emphasis on pol encapsidationAutophagy in hepatitis C virus-host interactions: potential roles and therapeutic targets for liver-associated diseasesHepatitis B virus reverse transcriptase: diverse functions as classical and emerging targets for antiviral interventionArsenic Trioxide Inhibits Hepatitis C Virus RNA Replication through Modulation of the Glutathione Redox System and Oxidative StressA Functional Genomic Screen Identifies Cellular Cofactors of Hepatitis C Virus ReplicationThe DEAD-box protein Ded1 modulates translation by the formation and resolution of an eIF4F-mRNA complex.Host factors that interact with the pestivirus N-terminal protease, Npro, are components of the ribonucleoprotein complexEngineered Aedes aegypti JAK/STAT Pathway-Mediated Immunity to Dengue VirusAn integrated transcriptomic and meta-analysis of hepatoma cells reveals factors that influence susceptibility to HCV infectionHepatitis C virus hijacks P-body and stress granule components around lipid dropletsDHX9 pairs with IPS-1 to sense double-stranded RNA in myeloid dendritic cellsHepatitis C virus core protein abrogates the DDX3 function that enhances IPS-1-mediated IFN-beta induction.The ESCRT system is required for hepatitis C virus production.Gene expression profiling indicates the roles of host oxidative stress, apoptosis, lipid metabolism, and intracellular transport genes in the replication of hepatitis C virus.Translational regulation of HIV-1 replication by HIV-1 Rev cellular cofactors Sam68, eIF5A, hRIP, and DDX3.Requirement of cellular DDX3 for hepatitis C virus replication is unrelated to its interaction with the viral core protein.RNA helicases: emerging roles in viral replication and the host innate response.Intracellular innate immune cascades and interferon defenses that control hepatitis C virusHIV-1 Gag co-opts a cellular complex containing DDX6, a helicase that facilitates capsid assemblyDDX3 DEAD-box RNA helicase is a host factor that restricts hepatitis B virus replication at the transcriptional level
P2860
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P2860
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@ast
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@en
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@en-gb
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@nl
type
label
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@ast
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@en
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@en-gb
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@nl
altLabel
DDX3 DEAD-Box RNA Helicase Is Required for Hepatitis C Virus RNA Replication
@en
prefLabel
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@ast
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@en
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@en-gb
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@nl
P2093
P2860
P3181
P356
P1433
P1476
DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication
@en
P2093
Hiromichi Dansako
Ken-ichi Abe
Masanori Ikeda
Misao Kuroki
Nobuyuki Kato
Yasuo Ariumi
P2860
P304
P3181
P356
10.1128/JVI.01517-07
P407
P577
2007-12-01T00:00:00Z