Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules. - Wikidata - wikimedia - TriplyDB

Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules.

Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules.

http://www.wikidata.org/entity/Q36501665

about

Who Regulates Whom? An Overview of RNA Granules and Viral Infections Interplay between Inflammation and Cellular Stress Triggered by Flaviviridae Viruses N6-Methyladenosine in Flaviviridae Viral RNA Genomes Regulates Infection Hepatitis C Virus Exploitation of Processing Bodies Viral activation of MK2-hsp27-p115RhoGEF-RhoA signaling axis causes cytoskeletal rearrangements, p-body disruption and ARE-mRNA stabilization XRN1 stalling in the 5' UTR of Hepatitis C virus and Bovine Viral Diarrhea virus is associated with dysregulated host mRNA stability Hepatitis C virus subverts liver-specific miR-122 to protect the viral genome from exoribonuclease Xrn2.Modulation of hepatitis C virus RNA accumulation and translation by DDX6 and miR-122 are mediated by separate mechanisms The stress granule protein G3BP1 recruits protein kinase R to promote multiple innate immune antiviral responses.Hepatitis C Virus. Strategies to Evade Antiviral Responses Dynamic Interaction of Stress Granules, DDX3X, and IKK-α Mediates Multiple Functions in Hepatitis C Virus Infection Stress granules regulate double-stranded RNA-dependent protein kinase activation through a complex containing G3BP1 and Caprin1.Virus-induced translational arrest through 4EBP1/2-dependent decay of 5'-TOP mRNAs restricts viral infection.Supporting Role for GTPase Rab27a in Hepatitis C Virus RNA Replication through a Novel miR-122-Mediated Effect Regulation of Hepatitis C Virus Genome Replication by Xrn1 and MicroRNA-122 Binding to Individual Sites in the 5' Untranslated Region.Hepatitis C-like viruses are produced in cells from rabbit and hare DNA IFN-β-inducing, unusual viral RNA species produced by paramyxovirus infection accumulated into distinct cytoplasmic structures in an RNA-type-dependent manner Movements of HIV-1 genomic RNA-APOBEC3F complexes and PKR reveal cytoplasmic and nuclear PKR defenses and HIV-1 evasion strategies.Interaction of host cell microRNAs with the HCV RNA genome during infection of liver cells.Regulation of stress granules and P-bodies during RNA virus infection.Cytoplasmic RNA Granules and Viral Infection.Understanding the interaction of hepatitis C virus with host DEAD-box RNA helicases.miR-122 promotion of the hepatitis C virus life cycle: sound in the silence.DDX6 and its orthologs as modulators of cellular and viral RNA expression.RNA helicase DDX3: at the crossroad of viral replication and antiviral immunity.Cellular DEAD-box RNA helicase DDX6 modulates interaction of miR-122 with the 5' untranslated region of hepatitis C virus RNA.The P body protein LSm1 contributes to stimulation of hepatitis C virus translation, but not replication, by microRNA-122 miR-122 and the Hepatitis C RNA genome: more than just stability.Ultrastructural and biochemical basis for hepatitis C virus morphogenesis.Stress out the LINEs Hepatitis C virus plays with fire and yet avoids getting burned. A review for clinicians on processing bodies and stress granules.DDX6 Represses Aberrant Activation of Interferon-Stimulated Genes.Manipulation of cellular processing bodies and their constituents by viruses.Plant RNA Regulatory Network and RNA Granules in Virus Infection.Positive-sense RNA viruses reveal the complexity and dynamics of the cellular and viral epitranscriptomes during infection.Conflict in the Intracellular Lives of Endosymbionts and Viruses: A Mechanistic Look at Wolbachia-Mediated Pathogen-blocking.

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P2860

Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules.

http://www.wikidata.org/entity/Q36501665

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Modulation of hepatitis C viru ...... enrichment of stress granules.

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Modulation of hepatitis C viru ...... enrichment of stress granules.

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Modulation of hepatitis C viru ...... enrichment of stress granules.

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Modulation of hepatitis C viru ...... enrichment of stress granules.

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Modulation of hepatitis C viru ...... enrichment of stress granules.

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Modulation of hepatitis C viru ...... enrichment of stress granules.

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Modulation of hepatitis C viru ...... enrichment of stress granules.

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Cara T Pager

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Guangxiang Luo

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Peter Sarnow

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Sylvia Schütz

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Teresa M Abraham

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P2860

The DEAD-box RNA helicase DDX6 is required for efficient encapsidation of a retroviral genome

USP10 regulates p53 localization and stability by deubiquitinating p53

Multiple processing body factors and the ARE binding protein TTP activate mRNA decapping

Subproteomic study of hepatitis C virus replicon reveals Ras-GTPase-activating protein binding protein 1 as potential HCV RC component

Identification of major proteins in the lipid droplet-enriched fraction isolated from the human hepatocyte cell line HuH7

Y-box-binding protein 1 interacts with hepatitis C virus NS3/4A and influences the equilibrium between viral RNA replication and infectious particle production

The human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci.

Human Dcp2: a catalytically active mRNA decapping enzyme located in specific cytoplasmic structures

OGFOD1, a novel modulator of eukaryotic translation initiation factor 2alpha phosphorylation and the cellular response to stress

DDX6 (Rck/p54) is required for efficient hepatitis C virus replication but not for internal ribosome entry site-directed translation

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