Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection. - sprookjes - yvandenbroek - TriplyDB

Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

http://www.wikidata.org/entity/Q34742966

about

Tight Junctions Go Viral!New hepatitis C virus drug discovery strategies and model systems Tree shrew (Tupaia belangeri) as a novel laboratory disease animal model Interferon-lambda3 (IFN-λ3) and its cognate receptor subunits in tree shrews (Tupaia belangeri): genomic sequence retrieval, molecular identification and expression analysis Determination of the human antibody response to the neutralization epitopes encompassing amino acids 313-327 and 432-443 of hepatitis C virus E1E2 glycoproteins An interferon-beta promoter reporter assay for high throughput identification of compounds against multiple RNA viruses.Hepatitis C virus and antiviral innate immunity: who wins at tug-of-war?A Schisandra-Derived Compound Schizandronic Acid Inhibits Entry of Pan-HCV Genotypes into Human Hepatocytes Identification and Characterization of Liver MicroRNAs of the Chinese Tree Shrew via Deep Sequencing.Three different functional microdomains in the hepatitis C virus hypervariable region 1 (HVR1) mediate entry and immune evasion.CD36 is a co-receptor for hepatitis C virus E1 protein attachment.Metabolomic analysis of key regulatory metabolites in hepatitis C virus-infected tree shrews.Detection and analysis of tupaia hepatocytes via mAbs against tupaia serum albumin.An Ebola Virus-Like Particle-Based Reporter System Enables Evaluation of Antiviral Drugs In Vivo under Non-Biosafety Level 4 Conditions.CXCL10 decreases GP73 expression in hepatoma cells at the early stage of hepatitis C virus (HCV) infection.CD81 and hepatitis C virus (HCV) infection.How hepatitis C virus invades hepatocytes: the mystery of viral entry Complete definition of immunological correlates of protection and clearance of hepatitis C virus infection: a relevant pending task for vaccine development.Animal models for the study of hepatitis C virus infection and replication.Hepatitis C virus infection and related liver disease: the quest for the best animal model Functional Analysis of Hepatitis C Virus (HCV) Envelope Protein E1 Using a trans-Complementation System Reveals a Dual Role of a Putative Fusion Peptide of E1 in both HCV Entry and Morphogenesis.Exosomal MicroRNAs Derived From Umbilical Mesenchymal Stem Cells Inhibit Hepatitis C Virus Infection.Impact of intra- and interspecies variation of occludin on its function as coreceptor for authentic hepatitis C virus particles.Single amino acid mutation of SR-BI decreases infectivity of hepatitis C virus derived from cell culture in a cell culture model.Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo.Insilico modeling and molecular dynamic simulation of claudin-1 point mutations in HCV infection.Interaction of L-SIGN with hepatitis C virus envelope protein E2 up-regulates Raf-MEK-ERK pathway.Genome of the Chinese tree shrew.Scavenger receptor B type 1: expression, molecular regulation, and cholesterol transport function

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

http://www.wikidata.org/entity/Q34742966

description

2010 nî lūn-bûn

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2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

@yue

name

Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

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Tupaia CD81, SR-BI, claudin-1, and occludin support hepatitis C virus infection.

@en

P2093

Hui Ding

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

Li Gao

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

Mark A Feitelson

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

Ping Zhao

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

Xian Hua

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

Xueshan Xia

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

Yimin Tong

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

Yongzhe Zhu

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

Yongzhi Wang

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

Yuan Liu

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

P2860

Binding of hepatitis C virus to CD81

Characterization of hepatitis C virus E2 glycoprotein interaction with a putative cellular receptor, CD81.

The human scavenger receptor class B type I is a novel candidate receptor for the hepatitis C virus.

Regulating intracellular antiviral defense and permissiveness to hepatitis C virus RNA replication through a cellular RNA helicase, RIG-I

Scavenger receptor BI and BII expression levels modulate hepatitis C virus infectivity

Infectious hepatitis C virus pseudo-particles containing functional E1-E2 envelope protein complexes

Scavenger receptor class B type I and hepatitis C virus infection of primary tupaia hepatocytes.

Functional characterization of intracellular and secreted forms of a truncated hepatitis C virus E2 glycoprotein

Robust hepatitis C virus infection in vitro.

Identification of the hepatitis C virus E2 glycoprotein binding site on the large extracellular loop of CD81

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2793-2802

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10.1128/JVI.01818-10

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2010-12-22T00:00:00Z

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