Correlation of the Tight Junction-like Distribution of Claudin-1 to the Cellular Tropism of Hepatitis C Virus - Test2 - elhamkhani - TriplyDB

Correlation of the Tight Junction-like Distribution of Claudin-1 to the Cellular Tropism of Hepatitis C Virus

Correlation of the Tight Junction-like Distribution of Claudin-1 to the Cellular Tropism of Hepatitis C Virus

http://www.wikidata.org/entity/Q27486250

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Mechanisms of viral entry: sneaking in the front door Phospholipid scramblase 1 mediates hepatitis C virus entry into host cells Listeria monocytogenes internalin B activates junctional endocytosis to accelerate intestinal invasion The CD81 Partner EWI-2wint Inhibits Hepatitis C Virus Entry CD81 and Claudin 1 Coreceptor Association: Role in Hepatitis C Virus Entry Protein Kinase A-Dependent Step(s) in Hepatitis C Virus Entry and Infectivity CD81 Is a Central Regulator of Cellular Events Required for Hepatitis C Virus Infection of Human Hepatocytes Fatty acid synthase is up-regulated during hepatitis C virus infection and regulates hepatitis C virus entry and production Tight Junction Proteins Claudin-1 and Occludin Control Hepatitis C Virus Entry and Are Downregulated during Infection To Prevent Superinfection Residues in a Highly Conserved Claudin-1 Motif Are Required for Hepatitis C Virus Entry and Mediate the Formation of Cell-Cell Contacts Polarization Restricts Hepatitis C Virus Entry into HepG2 Hepatoma Cells Hepatoma Cell Density Promotes Claudin-1 and Scavenger Receptor BI Expression and Hepatitis C Virus Internalization Mouse-Specific Residues of Claudin-1 Limit Hepatitis C Virus Genotype 2a Infection in a Human Hepatocyte Cell Line Claudin association with CD81 defines hepatitis C virus entry.Hepatitis C virus induces CD81 and claudin-1 endocytosis.Adaptation of hepatitis C virus to mouse CD81 permits infection of mouse cells in the absence of human entry factors.The SR-BI partner PDZK1 facilitates hepatitis C virus entry.Host-derived apolipoproteins play comparable roles with viral secretory proteins Erns and NS1 in the infectious particle formation of Flaviviridae Growth differentiation factor 15 is induced by hepatitis C virus infection and regulates hepatocellular carcinoma-related genes.A human claudin-1-derived peptide inhibits hepatitis C virus entry.Species-specific regions of occludin required by hepatitis C virus for cell entry.Discovery of cellular proteins required for the early steps of HCV infection using integrative genomics.Impenetrable barriers or entry portals? The role of cell-cell adhesion during infection A novel small-molecule inhibitor of hepatitis C virus replication acts by suppressing signal transducer and activator of transcription 3.Identification of a Potent and Broad-Spectrum Hepatitis C Virus Fusion Inhibitory Peptide from the E2 Stem Domain Selection of a hepatitis C virus with altered entry factor requirements reveals a genetic interaction between the E1 glycoprotein and claudins Expression of microRNA miR-122 facilitates an efficient replication in nonhepatic cells upon infection with hepatitis C virus.Targeting of tetraspanin proteins--potential benefits and strategies A Novel Class of Small Molecule Compounds that Inhibit Hepatitis C Virus Infection by Targeting the Prohibitin-CRaf Pathway.Screening and rational design of hepatitis C virus entry inhibitory peptides derived from GB virus A NS5A.High-throughput profiling of alpha interferon- and interleukin-28B-regulated microRNAs and identification of let-7s with anti-hepatitis C virus activity by targeting IGF2BP1.Primary hepatocytes as targets for hepatitis C virus replication.Cellular and molecular biology of HCV infection and hepatitis.CD81 and hepatitis C virus (HCV) infection.CD81-receptor associations--impact for hepatitis C virus entry and antiviral therapies.Know your enemy: translating insights about the molecular biology of hepatitis C virus into novel therapeutic approaches.Hepatitis C virus entry and the tetraspanin CD81.Roles of the two distinct proteasome pathways in hepatitis C virus infection.Claudins in viral infection: from entry to spread.The second extracellular loop dictates Occludin-mediated HCV entry

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Correlation of the Tight Junction-like Distribution of Claudin-1 to the Cellular Tropism of Hepatitis C Virus

http://www.wikidata.org/entity/Q27486250

description

2008 nî lūn-bûn

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2008 թուականի Մարտին հրատարակուած գիտական յօդուած

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2008 թվականի մարտին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Journal of Biological Chemistry

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Correlation of the Tight Junct ...... r Tropism of Hepatitis C Virus

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Chao Qiu

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Jing Jin

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Nabanita Biswas

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Ronald C Montelaro

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Simon C Watkins

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Tianyi Wang

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Wei Yang

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P2860

Binding of hepatitis C virus to CD81

Adenovirus fiber disrupts CAR-mediated intercellular adhesion allowing virus escape

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

A small rab GTPase is distributed in cytoplasmic vesicles in non polarized cells but colocalizes with the tight junction marker ZO-1 in polarized epithelial cells

Structure-function analysis of hepatitis C virus envelope-CD81 binding

Coxsackievirus entry across epithelial tight junctions requires occludin and the small GTPases Rab34 and Rab5

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

Claudin-1 and -2: novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin

The transmembrane domain of hepatitis C virus glycoprotein E1 is a signal for static retention in the endoplasmic reticulum.

A retention signal necessary and sufficient for endoplasmic reticulum localization maps to the transmembrane domain of hepatitis C virus glycoprotein E2.

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8643-53

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2027377

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10.1074/JBC.M709824200

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13

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283

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2008-03-28T00:00:00Z

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18211898

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2417170

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