The Hepatitis C Virus Replicon Presents a Higher Barrier to Resistance to Nucleoside Analogs than to Nonnucleoside Polymerase or Protease Inhibitors
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Virologic Tools for HCV Drug Resistance TestingChutes and ladders in hepatitis C nucleoside drug developmentSelection and Characterization of Hepatitis C Virus Replicons Dually Resistant to the Polymerase and Protease Inhibitors HCV-796 and Boceprevir (SCH 503034)Naturally occurring dominant resistance mutations to hepatitis C virus protease and polymerase inhibitors in treatment-naïve patientsGT-1a or GT-1b Subtype-Specific Resistance Profiles for Hepatitis C Virus Inhibitors Telaprevir and HCV-796The Octadecyloxyethyl Ester of (S)-9-[3-Hydroxy-2-(Phosphonomethoxy) Propyl]Adenine Is a Potent and Selective Inhibitor of Hepatitis C Virus Replication in Genotype 1A, 1B, and 2A RepliconsSlow Binding Inhibition and Mechanism of Resistance of Non-nucleoside Polymerase Inhibitors of Hepatitis C VirusProanthocyanidin from Blueberry Leaves Suppresses Expression of Subgenomic Hepatitis C Virus RNADevelopment of a Cell-Based Hepatitis C Virus Infection Fluorescent Resonance Energy Transfer Assay for High-Throughput Antiviral Compound ScreeningScreening for hepatitis C virus non-nucleotide resistance mutations in treatment-naive womenHepatitis C: recent successes and continuing challenges in the development of improved treatment modalitiesAnalysis of the virus dynamics model reveals that early treatment of HCV infection may lead to the sustained virological responseArtemisinin analogues as potent inhibitors of in vitro hepatitis C virus replicationMechanisms of activity and inhibition of the hepatitis C virus RNA-dependent RNA polymerase.Inhibitors of the tick-borne, hemorrhagic fever-associated flaviviruses.Treatment of hepatitis C virus infection with interferon and small molecule direct antivirals: viral kinetics and modelingPSI-7851, a pronucleotide of beta-D-2'-deoxy-2'-fluoro-2'-C-methyluridine monophosphate, is a potent and pan-genotype inhibitor of hepatitis C virus replicationTelaprevir: an NS3/4A protease inhibitor for the treatment of chronic hepatitis C.Therapeutic implications of hepatitis C virus resistance to antiviral drugs.Safety and pharmacokinetics of IDX184, a liver-targeted nucleotide polymerase inhibitor of hepatitis C virus, in healthy subjects.Comparison of the Mechanisms of Drug Resistance among HIV, Hepatitis B, and Hepatitis C.Efficacy and tolerability of telaprevir for chronic hepatitis virus C genotype 1 infection: a meta-analysisRapid emergence of protease inhibitor resistance in hepatitis C virus.Hepatitis C virus RNA elimination and development of resistance in replicon cells treated with BMS-790052INX-08189, a phosphoramidate prodrug of 6-O-methyl-2'-C-methyl guanosine, is a potent inhibitor of hepatitis C virus replication with excellent pharmacokinetic and pharmacodynamic properties.Hepatitis C virus drug resistance and immune-driven adaptations: relevance to new antiviral therapy.Inhibition of hepatitis C virus replicon RNA synthesis by PSI-352938, a cyclic phosphate prodrug of β-D-2'-deoxy-2'-α-fluoro-2'-β-C-methylguanosine.Review article: adherence to medication for chronic hepatitis C - building on the model of human immunodeficiency virus antiretroviral adherence researchActivity and the metabolic activation pathway of the potent and selective hepatitis C virus pronucleotide inhibitor PSI-353661.Synthesis and antiviral evaluation of 9-(S)-[3-alkoxy-2-(phosphonomethoxy)propyl]nucleoside alkoxyalkyl esters: inhibitors of hepatitis C virus and HIV-1 replicationAntiviral efficacy upon administration of a HepDirect prodrug of 2'-C-methylcytidine to hepatitis C virus-infected chimpanzees.Inhibitors of the Hepatitis C Virus RNA-Dependent RNA Polymerase NS5B.New developments in small molecular compounds for anti-hepatitis C virus (HCV) therapy.Use of illumina deep sequencing technology to differentiate hepatitis C virus variants.Modeling quasispecies and drug resistance in hepatitis C patients treated with a protease inhibitorShort-term monotherapy with IDX184, a liver-targeted nucleotide polymerase inhibitor, in patients with chronic hepatitis C virus infection.NTP-mediated nucleotide excision activity of hepatitis C virus RNA-dependent RNA polymerase.Sofosbuvir and ABT-450: terminator of hepatitis C virus?Anti-HCV drugs in the pipeline.Avoiding therapeutic pitfalls: the rational use of specifically targeted agents against hepatitis C infection.
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P2860
The Hepatitis C Virus Replicon Presents a Higher Barrier to Resistance to Nucleoside Analogs than to Nonnucleoside Polymerase or Protease Inhibitors
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@ast
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@en
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@nl
type
label
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@ast
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@en
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@nl
prefLabel
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@ast
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@en
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@nl
P2093
P2860
P356
P1476
The Hepatitis C Virus Replicon ...... ymerase or Protease Inhibitors
@en
P2093
Hyunsoon Kang
Isabel Najera
Julian Symons
Matthew F McCown
Nick Cammack
Sonal Rajyaguru
Sophie Le Pogam
Wen-Rong Jiang
P2860
P304
P356
10.1128/AAC.01317-07
P407
P577
2008-05-01T00:00:00Z