Production of a dominant-negative fragment due to G3BP1 cleavage contributes to the disruption of mitochondria-associated protective stress granules during CVB3 infection - Wikidata - wikimedia - TriplyDB

Production of a dominant-negative fragment due to G3BP1 cleavage contributes to the disruption of mitochondria-associated protective stress granules during CVB3 infection

Production of a dominant-negative fragment due to G3BP1 cleavage contributes to the disruption of mitochondria-associated protective stress granules during CVB3 infection

http://www.wikidata.org/entity/Q30009523

about

A novel function of human Pumilio proteins in cytoplasmic sensing of viral infection Who Regulates Whom? An Overview of RNA Granules and Viral Infections Enterovirus Control of Translation and RNA Granule Stress Responses Roles of the Picornaviral 3C Proteinase in the Viral Life Cycle and Host Cells Regulation of antiviral innate immune signaling by stress-induced RNA granules Innate Immunity Evasion by Enteroviruses: Insights into Virus-Host Interaction Diverse Strategies Used by Picornaviruses to Escape Host RNA Decay Pathways Feline Calicivirus Infection Disrupts Assembly of Cytoplasmic Stress Granules and Induces G3BP1 Cleavage Stress granule components G3BP1 and G3BP2 play a proviral role early in Chikungunya virus replication.The stress granule protein G3BP1 recruits protein kinase R to promote multiple innate immune antiviral responses.Stress granules regulate double-stranded RNA-dependent protein kinase activation through a complex containing G3BP1 and Caprin1.Enhanced enteroviral infectivity via viral protease-mediated cleavage of Grb2-associated binder 1.Cleavage of DAP5 by coxsackievirus B3 2A protease facilitates viral replication and enhances apoptosis by altering translation of IRES-containing genes.Cytoplasmic RNA Granules and Viral Infection.Porcine Reproductive and Respiratory Syndrome Virus Infection Induces Stress Granule Formation Depending on Protein Kinase R-like Endoplasmic Reticulum Kinase (PERK) in MARC-145 Cells.Integration of PKR-dependent translation inhibition with innate immunity is required for a coordinated anti-viral response.Cytoplasmic translocation, aggregation, and cleavage of TDP-43 by enteroviral proteases modulate viral pathogenesis CpG and UpA dinucleotides in both coding and non-coding regions of echovirus 7 inhibit replication initiation post-entry.Dominant-negative function of the C-terminal fragments of NBR1 and SQSTM1 generated during enteroviral infection.Phosphorylation and degradation of αB-crystallin during enterovirus infection facilitates viral replication and induces viral pathogenesis.N-Terminomics TAILS identifies host cell substrates of poliovirus and coxsackievirus B3 3C proteinases that modulate virus infection.Foot-and-Mouth Disease Virus Counteracts on Internal Ribosome Entry Site Suppression by G3BP1 and Inhibits G3BP1-Mediated Stress Granule Assembly via Post-Translational Mechanisms.

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P2860

Production of a dominant-negative fragment due to G3BP1 cleavage contributes to the disruption of mitochondria-associated protective stress granules during CVB3 infection

http://www.wikidata.org/entity/Q30009523

description

2013 nî lūn-bûn

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2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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Production of a dominant-negat ...... granules during CVB3 infection

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Production of a dominant-negat ...... granules during CVB3 infection

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Chen Seng Ng

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Eric Jan

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Fanny Chu

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Gabriel Fung

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Honglin Luo

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Jerry Wong

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Jingchun Zhang

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Julienne Jagdeo

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Junyan Shi

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Lillian Han

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P2860

A novel phosphorylation-dependent RNase activity of GAP-SH3 binding protein: a potential link between signal transduction and RNA stability.

Stress granule assembly is mediated by prion-like aggregation of TIA-1

Stress granules and processing bodies are dynamically linked sites of mRNP remodeling

A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly

Mammalian stress granules represent sites of accumulation of stalled translation initiation complexes

Stress granules: the Tao of RNA triage

RNA-binding proteins TIA-1 and TIAR link the phosphorylation of eIF-2 alpha to the assembly of mammalian stress granules

Eukaryotic stress granules: the ins and outs of translation

Encephalomyocarditis virus disrupts stress granules, the critical platform for triggering antiviral innate immune responses.

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