The ESCRT system is required for hepatitis C virus production. - Wikidata - wikimedia - TriplyDB

The ESCRT system is required for hepatitis C virus production.

The ESCRT system is required for hepatitis C virus production.

http://www.wikidata.org/entity/Q33802795

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Identification and targeting of an interaction between a tyrosine motif within hepatitis C virus core protein and AP2M1 essential for viral assembly A host YB-1 ribonucleoprotein complex is hijacked by hepatitis C virus for the control of NS3-dependent particle production Hepatitis C virus comes for dinner: How the hepatitis C virus interferes with autophagy The Phe105 Loop of Alix Bro1 Domain Plays a Key Role in HIV-1 Release A role for retromer in hepatitis C virus replication Hepatitis C virus hijacks P-body and stress granule components around lipid droplets Hepatitis C Virus Is Released via a Noncanonical Secretory Route.Nonstructural protein 5A is incorporated into hepatitis C virus low-density particle through interaction with core protein and microtubules during intracellular transport.NS2 is dispensable for efficient assembly of hepatitis C virus-like particles in a bipartite trans-encapsidation system.Focal adhesion kinase (FAK) mediates the induction of pro-oncogenic and fibrogenic phenotypes in hepatitis C virus (HCV)-infected cells.Specific acquisition of functional CD59 but not CD46 or CD55 by hepatitis C virus.Alix serves as an adaptor that allows human parainfluenza virus type 1 to interact with the host cell ESCRT system Mechanism of Ca²⁺-triggered ESCRT assembly and regulation of cell membrane repair.Role of phosphatidylinositol 4-phosphate (PI4P) and its binding protein GOLPH3 in hepatitis C virus secretion.Look who's talking-the crosstalk between oxidative stress and autophagy supports exosomal-dependent release of HCV particles.Cell Walls and the Convergent Evolution of the Viral Envelope.Short-range exosomal transfer of viral RNA from infected cells to plasmacytoid dendritic cells triggers innate immunity.Thioredoxin and thioredoxin target proteins: from molecular mechanisms to functional significance.Hepatitis C Virus Proteins Interact with the Endosomal Sorting Complex Required for Transport (ESCRT) Machinery via Ubiquitination To Facilitate Viral Envelopment.The ins and outs of hepatitis C virus entry and assembly.Understanding the interaction of hepatitis C virus with host DEAD-box RNA helicases.Virion assembly and release.Incorporation of hepatitis C virus E1 and E2 glycoproteins: the keystones on a peculiar virion.Multiple functions of DDX3 RNA helicase in gene regulation, tumorigenesis, and viral infection.Staphylococcus aureus Esx Factors Control Human Dendritic Cell Functions Conditioning Th1/Th17 Response.The Intracellular Cholesterol Transport Inhibitor U18666A Inhibits the Exosome-Dependent Release of Mature Hepatitis C Virus.Protein Interactions during the Flavivirus and Hepacivirus Life Cycle.The membrane on the surface of hepatitis E virus particles is derived from the intracellular membrane and contains trans-Golgi network protein 2.PI3K/SHIP2/PTEN pathway in cell polarity and hepatitis C virus pathogenesis.Cellular VPS4 is required for efficient entry and egress of budded virions of Autographa californica multiple nucleopolyhedrovirus.Release of Infectious Hepatitis C Virus from Huh7 Cells Occurs via a trans-Golgi Network-to-Endosome Pathway Independent of Very-Low-Density Lipoprotein Secretion.Molecular cloning, expression and characterization of a novel vacuolar protein sorting 4 gene in silkworm, Bombyx mori.Budding of Enveloped Viruses: Interferon-Induced ISG15-Antivirus Mechanisms Targeting the Release Process Pivotal role for the ESCRT-II complex subunit EAP30/SNF8 in IRF3-dependent innate antiviral defense.A role for domain I of the hepatitis C virus NS5A protein in virus assembly.The Arabidopsis Endosomal Sorting Complex Required for Transport III Regulates Internal Vesicle Formation of the Prevacuolar Compartment and Is Required for Plant Development.ESCRT machinery components are required for Orthobunyavirus particle production in Golgi compartments.Current and future targets of antiviral therapy in the hepatitis C virus life cycle

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P2860

The ESCRT system is required for hepatitis C virus production.

http://www.wikidata.org/entity/Q33802795

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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name

The ESCRT system is required for hepatitis C virus production.

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The ESCRT system is required for hepatitis C virus production.

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type

label

The ESCRT system is required for hepatitis C virus production.

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The ESCRT system is required for hepatitis C virus production.

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prefLabel

The ESCRT system is required for hepatitis C virus production.

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The ESCRT system is required for hepatitis C virus production.

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The ESCRT system is required for hepatitis C virus production.

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P2093

Hiromichi Dansako

http://www.w3.org/2001/XMLSchema#string

Masanori Ikeda

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Masatoshi Maki

http://www.w3.org/2001/XMLSchema#string

Misao Kuroki

http://www.w3.org/2001/XMLSchema#string

Nobuyuki Kato

http://www.w3.org/2001/XMLSchema#string

Takaji Wakita

http://www.w3.org/2001/XMLSchema#string

Yasuo Ariumi

http://www.w3.org/2001/XMLSchema#string

P2860

Tsg101 and the vacuolar protein sorting pathway are essential for HIV-1 budding

DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication

The ALG-2-interacting protein Alix associates with CHMP4b, a human homologue of yeast Snf7 that is involved in multivesicular body sorting

E6AP ubiquitin ligase mediates ubiquitylation and degradation of hepatitis C virus core protein

The DNA damage sensors ataxia-telangiectasia mutated kinase and checkpoint kinase 2 are required for hepatitis C virus RNA replication

Proteasome activator PA28gamma-dependent nuclear retention and degradation of hepatitis C virus core protein

The penta-EF-hand protein ALG-2 interacts directly with the ESCRT-I component TSG101, and Ca2+-dependently co-localizes to aberrant endosomes with dominant-negative AAA ATPase SKD1/Vps4B

Identification of Residues in the Hepatitis C Virus Core Protein That Are Critical for Capsid Assembly in a Cell-Free System

Compensatory Mutations in E1, p7, NS2, and NS3 Enhance Yields of Cell Culture-Infectious Intergenotypic Chimeric Hepatitis C Virus

Alanine Scanning of the Hepatitis C Virus Core Protein Reveals Numerous Residues Essential for Production of Infectious Virus

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1

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