Generation of a replication-competent, propagation-deficient virus vector based on the transmissible gastroenteritis coronavirus genome.
about
Engineering the transmissible gastroenteritis virus genome as an expression vector inducing lactogenic immunityDevelopment of next-generation respiratory virus vaccines through targeted modifications to viral immunomodulatory genesRelevance of Viroporin Ion Channel Activity on Viral Replication and PathogenesisCoronavirus virulence genes with main focus on SARS-CoV envelope geneCoronavirus reverse genetic systems: infectious clones and repliconsTransmissible Gastroenteritis Coronavirus Packaging Signal Is Located at the 5' End of the Virus GenomeStructure and inhibition of the SARS coronavirus envelope protein ion channelStructure of a conserved Golgi complex-targeting signal in coronavirus envelope proteinsThe M, E, and N structural proteins of the severe acute respiratory syndrome coronavirus are required for efficient assembly, trafficking, and release of virus-like particles.Coronavirus non-structural protein 1 is a major pathogenicity factor: implications for the rational design of coronavirus vaccines.Severe acute respiratory syndrome coronavirus envelope protein ion channel activity promotes virus fitness and pathogenesisPalmitoylation of SARS-CoV S protein is necessary for partitioning into detergent-resistant membranes and cell-cell fusion but not interaction with M protein.Severe acute respiratory syndrome coronavirus envelope protein regulates cell stress response and apoptosis.A major determinant for membrane protein interaction localizes to the carboxy-terminal domain of the mouse coronavirus nucleocapsid protein.Contribution of trafficking signals in the cytoplasmic tail of the infectious bronchitis virus spike protein to virus infection.Dendritic cell-specific antigen delivery by coronavirus vaccine vectors induces long-lasting protective antiviral and antitumor immunity.Intracellular targeting signals contribute to localization of coronavirus spike proteins near the virus assembly site.Culturing the unculturable: human coronavirus HKU1 infects, replicates, and produces progeny virions in human ciliated airway epithelial cell cultures.Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus.Evolved variants of the membrane protein can partially replace the envelope protein in murine coronavirus assembly.Identification of functionally important negatively charged residues in the carboxy end of mouse hepatitis coronavirus A59 nucleocapsid protein.The small envelope protein E is not essential for murine coronavirus replication.Identification of a Golgi complex-targeting signal in the cytoplasmic tail of the severe acute respiratory syndrome coronavirus envelope protein.A severe acute respiratory syndrome coronavirus that lacks the E gene is attenuated in vitro and in vivo.The cytoplasmic tail of the severe acute respiratory syndrome coronavirus spike protein contains a novel endoplasmic reticulum retrieval signal that binds COPI and promotes interaction with membrane protein.Exceptional flexibility in the sequence requirements for coronavirus small envelope protein functionRole of the coronavirus E viroporin protein transmembrane domain in virus assembly.Coronavirus envelope (E) protein remains at the site of assemblyComparison of SARS and NL63 papain-like protease binding sites and binding site dynamics: inhibitor design implicationsCoronavirus E protein forms ion channels with functionally and structurally-involved membrane lipids.Kunjin virus replicons: an RNA-based, non-cytopathic viral vector system for protein production, vaccine and gene therapy applications.Envelope protein palmitoylations are crucial for murine coronavirus assembly.Importance of conserved cysteine residues in the coronavirus envelope protein.Subcellular location and topology of severe acute respiratory syndrome coronavirus envelope proteinHosting the severe acute respiratory syndrome coronavirus: specific cell factors required for infection.Reverse genetics with a full-length infectious cDNA of severe acute respiratory syndrome coronavirus.Vaccines to prevent severe acute respiratory syndrome coronavirus-induced disease.Systematic assembly of a full-length infectious clone of human coronavirus NL63Effects of infection with transmissible gastroenteritis virus on concomitant immune responses to dietary and injected antigens.Accommodation of large cargo within Golgi cisternae
P2860
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P2860
Generation of a replication-competent, propagation-deficient virus vector based on the transmissible gastroenteritis coronavirus genome.
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
name
Generation of a Replication-Co ...... roenteritis Coronavirus Genome
@nl
Generation of a replication-co ...... oenteritis coronavirus genome.
@ast
Generation of a replication-co ...... oenteritis coronavirus genome.
@en
type
label
Generation of a Replication-Co ...... roenteritis Coronavirus Genome
@nl
Generation of a replication-co ...... oenteritis coronavirus genome.
@ast
Generation of a replication-co ...... oenteritis coronavirus genome.
@en
prefLabel
Generation of a Replication-Co ...... roenteritis Coronavirus Genome
@nl
Generation of a replication-co ...... oenteritis coronavirus genome.
@ast
Generation of a replication-co ...... oenteritis coronavirus genome.
@en
P2093
P2860
P921
P1433
P1476
Generation of a replication-co ...... oenteritis coronavirus genome.
@en
P2093
David Escors
Hubert Laude
Javier Ortego
P2860
P304
11518-11529
P356
10.1128/JVI.76.22.11518-11529.2002
P577
2002-11-01T00:00:00Z