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Hepatitis C virus entry into hepatocytes: Molecular mechanisms and targets for antiviral therapies

Data up to Jan 2025

Published2010
Citations178
References151

Total Citations Per Year

Abstract

References (151)

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Serum Amyloid A Binding to CLA-1 (CD36 and LIMPII Analogous-1) Mediates Serum Amyloid A Protein-induced Activation of ERK1/2 and p38 Mitogen-activated Protein Kinases

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Characterization of Fusion Determinants Points to the Involvement of Three Discrete Regions of Both E1 and E2 Glycoproteins in the Membrane Fusion Process of Hepatitis C Virus

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Inhibition of hepatitis C virus infection by anti-claudin-1 antibodies is mediated by neutralization of E2-CD81-Claudin-1 associations

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Identification of a Residue in Hepatitis C Virus E2 Glycoprotein That Determines Scavenger Receptor BI and CD81 Receptor Dependency and Sensitivity to Neutralizing Antibodies

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Serum Amyloid A Is a Ligand for Scavenger Receptor Class B Type I and Inhibits High Density Lipoprotein Binding and Selective Lipid Uptake

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Monoclonal Anti-Claudin 1 Antibodies Prevent Hepatitis C Virus Infection of Primary Human Hepatocytes

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The Tight Junction-Associated Protein Occludin Is Required for a Postbinding Step in Hepatitis C Virus Entry and Infection

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Hepatitis C Virus Glycoproteins Mediate Low pH-dependent Membrane Fusion with Liposomes

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Viral entry and escape from antibody-mediated neutralization influence hepatitis C virus reinfection in liver transplantation

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Residues in a Highly Conserved Claudin-1 Motif Are Required for Hepatitis C Virus Entry and Mediate the Formation of Cell-Cell Contacts

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Amphipathic DNA Polymers Inhibit Hepatitis C Virus Infection by Blocking Viral Entry

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Phosphorothioate Oligonucleotides Inhibit Human Immunodeficiency Virus Type 1 Fusion by Blocking gp41 Core Formation

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Hepatitis C virus entry into hepatocytes: Molecular mechanisms and targets for antiviral… (2010) – Journal of Hepatology | Metascience Observatory Explorer