The production of recombinant infectious DI-particles of a murine coronavirus in the absence of helper virus.
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Cooperation of an RNA packaging signal and a viral envelope protein in coronavirus RNA packagingMolecular mechanisms of severe acute respiratory syndrome (SARS)Coronavirus particle assembly: primary structure requirements of the membrane protein.Assembly of the coronavirus envelope: homotypic interactions between the M proteinsRole of the transmembrane domains of prM and E proteins in the formation of yellow fever virus envelope.Structure and inhibition of the SARS coronavirus envelope protein ion channelStructure of a conserved Golgi complex-targeting signal in coronavirus envelope proteinsHigh-Resolution Analysis of Coronavirus Gene Expression by RNA Sequencing and Ribosome Profiling.The 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.Virus-like particles of SARS-like coronavirus formed by membrane proteins from different origins demonstrate stimulating activity in human dendritic cells.RNase L-independent specific 28S rRNA cleavage in murine coronavirus-infected cellsInduction of apoptosis in murine coronavirus-infected cultured cells and demonstration of E protein as an apoptosis inducer.Identification of a novel coronavirus in bats.Analysis of constructed E gene mutants of mouse hepatitis virus confirms a pivotal role for E protein in coronavirus assemblyRetargeting of coronavirus by substitution of the spike glycoprotein ectodomain: crossing the host cell species barrierSelf-assembly of severe acute respiratory syndrome coronavirus membrane protein.Infectious bronchitis virus E protein is targeted to the Golgi complex and directs release of virus-like particles.Characterization of the coronavirus M protein and nucleocapsid interaction in infected cells.Identification of a novel structural protein of arteriviruses.Structural maturation of the transmissible gastroenteritis coronavirus.Model of a putative pore: the pentameric alpha-helical bundle of SARS coronavirus E protein in lipid bilayers.A major determinant for membrane protein interaction localizes to the carboxy-terminal domain of the mouse coronavirus nucleocapsid protein.A conserved domain in the coronavirus membrane protein tail is important for virus assembly.Genetic evidence for a structural interaction between the carboxy termini of the membrane and nucleocapsid proteins of mouse hepatitis virus.Evolved variants of the membrane protein can partially replace the envelope protein in murine coronavirus assembly.A novel severe acute respiratory syndrome coronavirus protein, U274, is transported to the cell surface and undergoes endocytosis.Coronaviruses: an overview of their replication and pathogenesis.Identification of functionally important negatively charged residues in the carboxy end of mouse hepatitis coronavirus A59 nucleocapsid protein.Nucleocapsid-independent specific viral RNA packaging via viral envelope protein and viral RNA signal.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.Suppression of coronavirus replication by inhibition of the MEK signaling pathway.Exceptional flexibility in the sequence requirements for coronavirus small envelope protein functionRole of the coronavirus E viroporin protein transmembrane domain in virus assembly.The Emerging Roles of Viroporins in ER Stress Response and Autophagy Induction during Virus InfectionImportance of the penultimate positive charge in mouse hepatitis coronavirus A59 membrane protein.Murine coronavirus packaging signal confers packaging to nonviral RNA.Assembled coronavirus from complementation of two defective interfering RNAs.Contributions of the structural proteins of severe acute respiratory syndrome coronavirus to protective immunity.Envelope protein palmitoylations are crucial for murine coronavirus assembly.
P2860
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P2860
The production of recombinant infectious DI-particles of a murine coronavirus in the absence of helper virus.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh
1996年學術文章
@zh-hant
name
The production of recombinant ...... n the absence of helper virus.
@en
type
label
The production of recombinant ...... n the absence of helper virus.
@en
prefLabel
The production of recombinant ...... n the absence of helper virus.
@en
P2093
P356
P1433
P1476
The production of recombinant ...... n the absence of helper virus.
@en
P2093
Koerten HK
van der Meulen HV
P356
10.1006/VIRO.1996.0165
P407
P577
1996-04-01T00:00:00Z