Infectious RNA transcribed in vitro from a cDNA copy of the human coronavirus genome cloned in vaccinia virus.
about
Targeting membrane-bound viral RNA synthesis reveals potent inhibition of diverse coronaviruses including the middle East respiratory syndrome virusReverse genetics system for the avian coronavirus infectious bronchitis virusEngineering the transmissible gastroenteritis virus genome as an expression vector inducing lactogenic immunityCoronavirus reverse genetic systems: infectious clones and repliconsTransmissible Gastroenteritis Coronavirus Packaging Signal Is Located at the 5' End of the Virus GenomeCoronaviruses and the human airway: a universal system for virus-host interaction studiesCoronavirus non-structural protein 1 is a major pathogenicity factor: implications for the rational design of coronavirus vaccines.Selective replication of coronavirus genomes that express nucleocapsid proteinRecombinant mouse hepatitis virus strain A59 from cloned, full-length cDNA replicates to high titers in vitro and is fully pathogenic in vivoDevelopment of a transgenic mouse model susceptible to human coronavirus 229E.Humanized mice develop coronavirus respiratory disease.RNA virus reverse genetics and vaccine design.Reverse genetics of SARS-related coronavirus using vaccinia virus-based recombination.Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus.Genetic evidence for a structural interaction between the carboxy termini of the membrane and nucleocapsid proteins of mouse hepatitis virus.Systematic assembly of a full-length infectious cDNA of mouse hepatitis virus strain A59.Recovery of a neurovirulent human coronavirus OC43 from an infectious cDNA clone.Discovery of an RNA virus 3'->5' exoribonuclease that is critically involved in coronavirus RNA synthesisAttenuation of mouse hepatitis virus by deletion of the LLRKxGxKG region of Nsp1.Infectious Bronchitis Virus as a Vector for the Expression of Heterologous Genes.Switching species tropism: an effective way to manipulate the feline coronavirus genome.Manipulation of the porcine epidemic diarrhea virus genome using targeted RNA recombination.Construction of a severe acute respiratory syndrome coronavirus infectious cDNA clone and a replicon to study coronavirus RNA synthesis.Complete genome sequence of a Chinese virulent porcine epidemic diarrhea virus strain.RNA-RNA and RNA-protein interactions in coronavirus replication and transcriptionHuman coronavirus 229E encodes a single ORF4 protein between the spike and the envelope genesHuman coronavirus 229E papain-like proteases have overlapping specificities but distinct functions in viral replication.Comparison of SARS and NL63 papain-like protease binding sites and binding site dynamics: inhibitor design implicationsCross-species transfer of viruses: implications for the use of viral vectors in biomedical research, gene therapy and as live-virus vaccines.Early endonuclease-mediated evasion of RNA sensing ensures efficient coronavirus replicationGenome organization and reverse genetic analysis of a type I feline coronavirusEngineering infectious cDNAs of coronavirus as bacterial artificial chromosomes.Enhanced virulence mediated by the murine coronavirus, mouse hepatitis virus strain JHM, is associated with a glycine at residue 310 of the spike glycoprotein.Human respiratory coronavirus OC43: genetic stability and neuroinvasion.Reverse genetics with a full-length infectious cDNA of severe acute respiratory syndrome coronavirus.A review of genetic methods and models for analysis of coronavirus-induced severe pneumonitis.Isolation and characterization of current human coronavirus strains in primary human epithelial cell cultures reveal differences in target cell tropismSystematic assembly of a full-length infectious clone of human coronavirus NL63Mouse hepatitis virus liver pathology is dependent on ADP-ribose-1''-phosphatase, a viral function conserved in the alpha-like supergroup.Organ-specific attenuation of murine hepatitis virus strain A59 by replacement of catalytic residues in the putative viral cyclic phosphodiesterase ns2.
P2860
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P2860
Infectious RNA transcribed in vitro from a cDNA copy of the human coronavirus genome cloned in vaccinia virus.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Infectious RNA transcribed in ...... nome cloned in vaccinia virus.
@en
Infectious RNA transcribed in ...... nome cloned in vaccinia virus.
@nl
type
label
Infectious RNA transcribed in ...... nome cloned in vaccinia virus.
@en
Infectious RNA transcribed in ...... nome cloned in vaccinia virus.
@nl
prefLabel
Infectious RNA transcribed in ...... nome cloned in vaccinia virus.
@en
Infectious RNA transcribed in ...... nome cloned in vaccinia virus.
@nl
P2093
P1476
Infectious RNA transcribed in ...... enome cloned in vaccinia virus
@en
P2093
P304
P356
10.1099/0022-1317-82-6-1273
P407
P50
P577
2001-06-01T00:00:00Z