Core protein-coding sequence, but not core protein, modulates the efficiency of cap-independent translation directed by the internal ribosome entry site of hepatitis C virus
about
DDX6 (Rck/p54) is required for efficient hepatitis C virus replication but not for internal ribosome entry site-directed translationA cis-acting replication element in the sequence encoding the NS5B RNA-dependent RNA polymerase is required for hepatitis C virus RNA replicationCis-acting RNA elements in human and animal plus-strand RNA virusesEvidence for a functional RNA element in the hepatitis C virus core geneCharacterizing the function and structural organization of the 5' tRNA-like motif within the hepatitis C virus quasispeciesGenetic analysis of a poliovirus/hepatitis C virus chimera: new structure for domain II of the internal ribosomal entry site of hepatitis C virusSequences in the 5' nontranslated region of hepatitis C virus required for RNA replication.Mutation Master: profiles of substitutions in hepatitis C virus RNA of the core, alternate reading frame, and NS2 coding regions.Long-range RNA-RNA interaction between the 5' nontranslated region and the core-coding sequences of hepatitis C virus modulates the IRES-dependent translationInhibition of the protein kinase PKR by the internal ribosome entry site of hepatitis C virus genomic RNATriple Decoding of Hepatitis C Virus RNA by Programmed Translational FrameshiftingThe major form of hepatitis C virus alternate reading frame protein is suppressed by core protein expressionEfficient trans-Encapsidation of Hepatitis C Virus RNAs into Infectious Virus-Like ParticlesRole of the Hepatitis C Virus Core+1 Open Reading Frame and Core cis-Acting RNA Elements in Viral RNA Translation and ReplicationNaturally Occurring Hepatitis C Virus Subgenomic Deletion Mutants Replicate Efficiently in Huh-7 Cells and Are trans-Packaged In Vitro To Generate Infectious Defective ParticlesA long-range RNA-RNA interaction between the 5' and 3' ends of the HCV genomeIdentification of basic amino acids at the N-terminal end of the core protein that are crucial for hepatitis C virus infectivity.Structural analysis of hepatitis C RNA genome using DNA microarraysInhibition of Hepatitis C Virus in Mice by a Small Interfering RNA Targeting a Highly Conserved Sequence in Viral IRES Pseudoknot.Enhancement of the expression of HCV core gene does not enhance core-specific immune response in DNA immunization: advantages of the heterologous DNA prime, protein boost immunization regimenA two-pronged strategy to suppress host protein synthesis by SARS coronavirus Nsp1 protein.Inhibition of hepatitis C virus in chimeric mice by short synthetic hairpin RNAs: sequence analysis of surviving virus shows added selective pressure of combination therapy.Hepatitis C viral protein translation: mechanisms and implications in developing antivirals.Unmasking the information encoded as structural motifs of viral RNA genomes: a potential antiviral target.Understanding the potential of hepatitis C virus internal ribosome entry site domains to modulate translation initiation via their structure and function.Interfering with hepatitis C virus IRES activity using RNA molecules identified by a novel in vitro selection method.A twist in the tail: SHAPE mapping of long-range interactions and structural rearrangements of RNA elements involved in HCV replication.The functional RNA domain 5BSL3.2 within the NS5B coding sequence influences hepatitis C virus IRES-mediated translation.Hepatitis C virus internal ribosome entry site-mediated translation is stimulated by cis-acting RNA elements and trans-acting viral factors.p21-activated kinase 1 is activated through the mammalian target of rapamycin/p70 S6 kinase pathway and regulates the replication of hepatitis C virus in human hepatoma cells.RNA self-cleavage activated by ultraviolet light-induced oxidation.Correlation between translation efficiency and outcome of combination therapy in chronic hepatitis C genotype 3.Post-translational modification of the hepatitis C virus core protein by tissue transglutaminase.Conserved RNA secondary structures and long-range interactions in hepatitis C viruses.The acidic domain of hepatitis C virus NS4A contributes to RNA replication and virus particle assembly.End-to-end crosstalk within the hepatitis C virus genome mediates the conformational switch of the 3'X-tail region.Hepatitis C virus core protein acts as a trans-modulating factor on internal translation initiation of the viral RNA.Roles of the 5' untranslated region of non-primate hepacivirus in translation initiation and viral replication.Signals Involved in Regulation of Hepatitis C Virus RNA Genome Translation and Replication.
P2860
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P2860
Core protein-coding sequence, but not core protein, modulates the efficiency of cap-independent translation directed by the internal ribosome entry site of hepatitis C virus
description
2000 nî lūn-bûn
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2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
@zh-hant
2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@ast
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@en
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@nl
type
label
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@ast
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@en
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@nl
prefLabel
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@ast
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@en
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@nl
P2093
P2860
P1433
P1476
Core protein-coding sequence, ...... ntry site of hepatitis C virus
@en
P2093
R C Rijnbrand
P2860
P304
P356
10.1128/JVI.74.23.11347-11358.2000
P577
2000-12-01T00:00:00Z