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Evidence for novel hepaciviruses in rodentsStructure and functionality in flavivirus NS-proteins: perspectives for drug designThe crystal structure of coxsackievirus B3 RNA-dependent RNA polymerase in complex with its protein primer VPg confirms the existence of a second VPg binding site on Picornaviridae polymerasesmRNA Capping by Venezuelan Equine Encephalitis Virus nsP1: Functional Characterization and Implications for Antiviral ResearchThe hexamer structure of Rift Valley fever virus nucleoprotein suggests a mechanism for its assembly into ribonucleoprotein complexesA second, non-canonical RNA-dependent RNA polymerase in SARS CoronavirusPreliminary crystallographic characterization of an RNA helicase from Kunjin virusPreliminary characterization of (nucleoside-2′-O-)-methyltransferase crystals from Meaban and Yokose flavivirusesPurification and crystallization of Kokobera virus helicaseFunctional Characterization of the Cleavage Specificity of the Sapovirus Chymotrypsin-Like ProteaseThe Crystal Structures of Chikungunya and Venezuelan Equine Encephalitis Virus nsP3 Macro Domains Define a Conserved Adenosine Binding PocketCrystal structure and activity of Kunjin virus NS3 helicase; protease and helicase domain assembly in the full length NS3 proteinStructure and biochemical analysis of Kokobera virus helicaseRecognition of RNA cap in the Wesselsbron virus NS5 methyltransferase domain: implications for RNA-capping mechanisms in FlavivirusStructural and biochemical analysis of human pathogenic astrovirus serine protease at 2.0 A resolutionStructure of the methyltransferase domain from the Modoc virus, a flavivirus with no known vectorStructure of the C-terminal domain of nsp4 from feline coronavirusStructure of the X (ADRP) domain of nsp3 from feline coronavirusThe N-Terminal Domain of the Arenavirus L Protein Is an RNA Endonuclease Essential in mRNA TranscriptionCrystal Structure and Functional Analysis of the SARS-Coronavirus RNA Cap 2′-O-Methyltransferase nsp10/nsp16 ComplexStructural Basis for Antiviral Inhibition of the Main Protease, 3C, from Human Enterovirus 933C Protease of Enterovirus 68: Structure-Based Design of Michael Acceptor Inhibitors and Their Broad-Spectrum Antiviral Effects against PicornavirusesThe Crystal Structure of a Cardiovirus RNA-Dependent RNA Polymerase Reveals an Unusual Conformation of the Polymerase Active SiteAssessment of Dengue virus helicase and methyltransferase as targets for fragment-based drug discoveryStructural characterization of the N-terminal part of the MERS-CoV nucleocapsid by X-ray diffraction and small-angle X-ray scatteringDiscovery of novel dengue virus NS5 methyltransferase non-nucleoside inhibitors by fragment-based drug designThe Zika virus methyltransferase: structure and functions for drug design perspectivesFlavivirus NS3 and NS5 proteins interaction network: a high-throughput yeast two-hybrid screenThe RNA template channel of the RNA-dependent RNA polymerase as a target for development of antiviral therapy of multiple genera within a virus familyScreening of a Library of FDA-Approved Drugs Identifies Several Enterovirus Replication Inhibitors That Target Viral Protein 2C
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Bruno Coutard
@ast
Bruno Coutard
@en
Bruno Coutard
@es
Bruno Coutard
@sl
type
label
Bruno Coutard
@ast
Bruno Coutard
@en
Bruno Coutard
@es
Bruno Coutard
@sl
prefLabel
Bruno Coutard
@ast
Bruno Coutard
@en
Bruno Coutard
@es
Bruno Coutard
@sl