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Debio 025, a Cyclophilin Binding Molecule, Is Highly Efficient in Clearing Hepatitis C Virus (HCV) Replicon-Containing Cells When Used Alone or in Combination with Specifically Targeted Antiviral Therapy for HCV (STAT-C) Inhibitors

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Published in:Antimicrobial Agents and Chemotherapy 2009-03, Vol.53 (3), p.967-976
Main Authors: Coelmont, Lotte, Kaptein, Suzanne, Paeshuyse, Jan, Vliegen, Inge, Dumont, Jean-Maurice, Vuagniaux, Grégoire, Neyts, Johan
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cited_by cdi_FETCH-LOGICAL-a472t-b25d2b939d94f50b4be136142896eb58f4143cdddf15b94d23d33b7f38bb64593
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creator Coelmont, Lotte
Kaptein, Suzanne
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Dumont, Jean-Maurice
Vuagniaux, Grégoire
Neyts, Johan
description Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to AAC .asm.org, visit: AAC       
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identifier ISSN: 0066-4804
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source American Society for Microbiology Journals; PubMed Central
subjects Antiviral Agents
Antiviral Agents - pharmacology
Clinical Trials as Topic
Cyclophilins - metabolism
Cyclosporine
Cyclosporine - pharmacology
Dose-Response Relationship, Drug
Drug Combinations
Drug Synergism
Hepacivirus
Hepacivirus - drug effects
Hepacivirus - genetics
Hepacivirus - metabolism
Hepatitis C
Hepatitis C - drug therapy
Hepatitis C - genetics
Hepatitis C virus
Humans
Replicon - drug effects
Ribavirin - pharmacology
Viral Nonstructural Proteins
Viral Nonstructural Proteins - antagonists & inhibitors
Viral Nonstructural Proteins - genetics
title Debio 025, a Cyclophilin Binding Molecule, Is Highly Efficient in Clearing Hepatitis C Virus (HCV) Replicon-Containing Cells When Used Alone or in Combination with Specifically Targeted Antiviral Therapy for HCV (STAT-C) Inhibitors
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