Construction of a severe acute respiratory syndrome coronavirus infectious cDNA clone and a replicon to study coronavirus RNA synthesis.
about
Viral bacterial artificial chromosomes: generation, mutagenesis, and removal of mini-F sequencesCoronavirus reverse genetic systems: infectious clones and repliconsFunctional screen reveals SARS coronavirus nonstructural protein nsp14 as a novel cap N7 methyltransferaseReverse Genetics Approaches for the Development of Influenza VaccinesGenome-wide analysis of protein-protein interactions and involvement of viral proteins in SARS-CoV replicationIn vitro reconstitution of SARS-coronavirus mRNA cap methylationA novel porcine reproductive and respiratory syndrome virus vector system that stably expresses enhanced green fluorescent protein as a separate transcription unitMolecular mapping of the RNA Cap 2'-O-methyltransferase activation interface between severe acute respiratory syndrome coronavirus nsp10 and nsp16.Infidelity of SARS-CoV Nsp14-exonuclease mutant virus replication is revealed by complete genome sequencing.Pathogenicity of severe acute respiratory coronavirus deletion mutants in hACE-2 transgenic mice.Achieving a golden mean: mechanisms by which coronaviruses ensure synthesis of the correct stoichiometric ratios of viral proteins.Mechanisms of severe acute respiratory syndrome pathogenesis and innate immunomodulation.The PDZ-binding motif of severe acute respiratory syndrome coronavirus envelope protein is a determinant of viral pathogenesis.Severe acute respiratory syndrome coronavirus envelope protein regulates cell stress response and apoptosis.The SARS-coronavirus-host interactome: identification of cyclophilins as target for pan-coronavirus inhibitorsSevere acute respiratory syndrome coronavirus replication inhibitor that interferes with the nucleic acid unwinding of the viral helicaseCoronavirus non-structural protein 16: evasion, attenuation, and possible treatments.Novel inhibitors of severe acute respiratory syndrome coronavirus entry that act by three distinct mechanismsThe nsp3 macrodomain promotes virulence in mice with coronavirus-induced encephalitisA simplified positive-sense-RNA virus construction approach that enhances analysis throughput.Efficient generation of recombinant RNA viruses using targeted recombination-mediated mutagenesis of bacterial artificial chromosomes containing full-length cDNA.Severe acute respiratory syndrome coronaviruses with mutations in the E protein are attenuated and promising vaccine candidates.RNA-RNA and RNA-protein interactions in coronavirus replication and transcriptionA severe acute respiratory syndrome coronavirus that lacks the E gene is attenuated in vitro and in vivo.Molecular characterization of feline infectious peritonitis virus strain DF-2 and studies of the role of ORF3abc in viral cell tropism.A G-quadruplex-binding macrodomain within the "SARS-unique domain" is essential for the activity of the SARS-coronavirus replication-transcription complex.RNA 3'-end mismatch excision by the severe acute respiratory syndrome coronavirus nonstructural protein nsp10/nsp14 exoribonuclease complex.Identification of the Mechanisms Causing Reversion to Virulence in an Attenuated SARS-CoV for the Design of a Genetically Stable Vaccine.Severe acute respiratory syndrome coronavirus nsp1 facilitates efficient propagation in cells through a specific translational shutoff of host mRNA.High fidelity of murine hepatitis virus replication is decreased in nsp14 exoribonuclease mutants.Engineering infectious cDNAs of coronavirus as bacterial artificial chromosomes.Subcellular location and topology of severe acute respiratory syndrome coronavirus envelope proteinInterference of ribosomal frameshifting by antisense peptide nucleic acids suppresses SARS coronavirus replication.SARS-CoV replication and pathogenesis in an in vitro model of the human conducting airway epitheliumBacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses.A review of genetic methods and models for analysis of coronavirus-induced severe pneumonitis.Severe acute respiratory syndrome coronavirus protein 6 accelerates murine hepatitis virus infections by more than one mechanism.Complete protection against severe acute respiratory syndrome coronavirus-mediated lethal respiratory disease in aged mice by immunization with a mouse-adapted virus lacking E protein.Regulation of cell death during infection by the severe acute respiratory syndrome coronavirus and other coronaviruses.SARS coronavirus accessory proteins.
P2860
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P2860
Construction of a severe acute respiratory syndrome coronavirus infectious cDNA clone and a replicon to study coronavirus RNA synthesis.
description
2006 nî lūn-bûn
@nan
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Construction of a severe acute ...... udy coronavirus RNA synthesis.
@ast
Construction of a severe acute ...... udy coronavirus RNA synthesis.
@en
type
label
Construction of a severe acute ...... udy coronavirus RNA synthesis.
@ast
Construction of a severe acute ...... udy coronavirus RNA synthesis.
@en
prefLabel
Construction of a severe acute ...... udy coronavirus RNA synthesis.
@ast
Construction of a severe acute ...... udy coronavirus RNA synthesis.
@en
P2093
P2860
P50
P356
P1433
P1476
Construction of a severe acute ...... tudy coronavirus RNA synthesis
@en
P2093
Carmen Capiscol
Carmen Galán
David Escors
Jose L Moreno
Marta L Dediego
Sara Alonso
P2860
P304
10900-10906
P356
10.1128/JVI.00385-06
P407
P577
2006-08-23T00:00:00Z