P-body components LSM1, GW182, DDX3, DDX6 and XRN1 are recruited to WNV replication sites and positively regulate viral replication
about
Who Regulates Whom? An Overview of RNA Granules and Viral InfectionsUse of Cellular Decapping Activators by Positive-Strand RNA VirusesComprehensive Protein Interactome Analysis of a Key RNA Helicase: Detection of Novel Stress Granule ProteinsViral activation of MK2-hsp27-p115RhoGEF-RhoA signaling axis causes cytoskeletal rearrangements, p-body disruption and ARE-mRNA stabilizationXRN1 Is a Species-Specific Virus Restriction Factor in YeastsIRAV (FLJ11286), an Interferon Stimulated Gene with Antiviral Activity Against Dengue Virus, Interacts with MOV10In-Cell Western Assays to Evaluate Hantaan Virus Replication as a Novel Approach to Screen Antiviral Molecules and Detect Neutralizing Antibody Titers.Flaviviral RNAs: weapons and targets in the war between virus and host.Modulation of hepatitis C virus RNA accumulation and translation by DDX6 and miR-122 are mediated by separate mechanismsVirus-induced translational arrest through 4EBP1/2-dependent decay of 5'-TOP mRNAs restricts viral infection.A Polymorphism in the Processing Body Component Ge-1 Controls Resistance to a Naturally Occurring Rhabdovirus in DrosophilaStanding your ground to exoribonucleases: Function of Flavivirus long non-coding RNAs.Movements of HIV-1 genomic RNA-APOBEC3F complexes and PKR reveal cytoplasmic and nuclear PKR defenses and HIV-1 evasion strategies.Diversion of stress granules and P-bodies during viral infection.Regulation of stress granules and P-bodies during RNA virus infection.Cytoplasmic RNA Granules and Viral Infection.Human DDX3 protein is a valuable target to develop broad spectrum antiviral agents.Spatial control of translation repression and polarized growth by conserved NDR kinase Orb6 and RNA-binding protein Sts5mRNA decapping enzyme 1a (Dcp1a)-induced translational arrest through protein kinase R (PKR) activation requires the N-terminal enabled vasodilator-stimulated protein homology 1 (EVH1) domain.Attacked from All Sides: RNA Decay in Antiviral Defense.The role of the DEAD-box RNA helicase DDX3 in mRNA metabolism.miR-122 promotion of the hepatitis C virus life cycle: sound in the silence.Regulation of flavivirus RNA synthesis and capping.Noncoding subgenomic flavivirus RNA: multiple functions in West Nile virus pathogenesis and modulation of host responses.The Ded1/DDX3 subfamily of DEAD-box RNA helicases.Multiple functions of DDX3 RNA helicase in gene regulation, tumorigenesis, and viral infection.RNA helicase DDX3: at the crossroad of viral replication and antiviral immunity.The ATP-Dependent RNA Helicase DDX3X Modulates Herpes Simplex Virus 1 Gene Expression.DDX3 Interacts with Influenza A Virus NS1 and NP Proteins and Exerts Antiviral Function through Regulation of Stress Granule Formation.Simultaneous detection of the subcellular localization of RNAs and proteins in cultured cells by combined multicolor RNA-FISH and IF.DEAD-Box Helicase DDX25 Is a Negative Regulator of Type I Interferon Pathway and Facilitates RNA Virus Infection.The P body protein LSm1 contributes to stimulation of hepatitis C virus translation, but not replication, by microRNA-122Hepatitis C virus plays with fire and yet avoids getting burned. A review for clinicians on processing bodies and stress granules.The cellular decapping activators LSm1, Pat1, and Dhh1 control the ratio of subgenomic to genomic Flock House virus RNAsManipulation of cellular processing bodies and their constituents by viruses.The Lsm1-7-Pat1 complex promotes viral RNA translation and replication by differential mechanisms.Dengue Virus Capsid Interacts with DDX3X-A Potential Mechanism for Suppression of Antiviral Functions in Dengue Infection.The DEAD-Box RNA Helicase DDX3 Interacts with m6A RNA Demethylase ALKBH5.Biochemistry and Molecular Biology of Flaviviruses.DDX3 suppresses type I interferons and favors viral replication during Arenavirus infection
P2860
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P2860
P-body components LSM1, GW182, DDX3, DDX6 and XRN1 are recruited to WNV replication sites and positively regulate viral replication
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
P-body components LSM1, GW182, ...... ely regulate viral replication
@en
P-body components LSM1, GW182, ...... ly regulate viral replication.
@nl
type
label
P-body components LSM1, GW182, ...... ely regulate viral replication
@en
P-body components LSM1, GW182, ...... ly regulate viral replication.
@nl
prefLabel
P-body components LSM1, GW182, ...... ely regulate viral replication
@en
P-body components LSM1, GW182, ...... ly regulate viral replication.
@nl
P2093
P2860
P1433
P1476
P-body components LSM1, GW182, ...... ely regulate viral replication
@en
P2093
Harendra S Chahar
N Manjunath
Shuiping Chen
P2860
P356
10.1016/J.VIROL.2012.09.041
P407
P577
2012-10-24T00:00:00Z