Viral protein synthesis in mouse hepatitis virus strain A59-infected cells: effect of tunicamycin.
about
Cooperation of an RNA packaging signal and a viral envelope protein in coronavirus RNA packagingRegulation of Stress Responses and Translational Control by CoronavirusCoronavirus particle assembly: primary structure requirements of the membrane protein.Assembly of the coronavirus envelope: homotypic interactions between the M proteinsLocalization and Membrane Topology of Coronavirus Nonstructural Protein 4: Involvement of the Early Secretory Pathway in ReplicationCryo-electron tomography of mouse hepatitis virus: Insights into the structure of the coronavirion.Retargeting of coronavirus by substitution of the spike glycoprotein ectodomain: crossing the host cell species barrierCharacterization of the coronavirus M protein and nucleocapsid interaction in infected cells.Dissecting virus entry: replication-independent analysis of virus binding, internalization, and penetration using minimal complementation of β-galactosidaseVirus maturation by budding.Genetic evidence for a structural interaction between the carboxy termini of the membrane and nucleocapsid proteins of mouse hepatitis virus.Coronaviruses maintain viability despite dramatic rearrangements of the strictly conserved genome organizationDeficient incorporation of spike protein into virions contributes to the lack of infectivity following establishment of a persistent, non-productive infection in oligodendroglial cell culture by murine coronavirus.Nucleocapsid-independent specific viral RNA packaging via viral envelope protein and viral RNA signal.Supramolecular architecture of severe acute respiratory syndrome coronavirus revealed by electron cryomicroscopy.Incorporation of spike and membrane glycoproteins into coronavirus virions.Membrane protein molecules of transmissible gastroenteritis coronavirus also expose the carboxy-terminal region on the external surface of the virion.Nucleocapsid-independent assembly of coronavirus-like particles by co-expression of viral envelope protein genes.Assembled coronavirus from complementation of two defective interfering RNAs.Site of addition of N-acetyl-galactosamine to the E1 glycoprotein of mouse hepatitis virus-A59Assembly in vitro of a spanning membrane protein of the endoplasmic reticulum: the E1 glycoprotein of coronavirus mouse hepatitis virus A59.Envelope glycoprotein interactions in coronavirus assemblyCoronavirus M proteins accumulate in the Golgi complex beyond the site of virion budding.Proteolytic cleavage of the E2 glycoprotein of murine coronavirus: activation of cell-fusing activity of virions by trypsin and separation of two different 90K cleavage fragments.Characterization and translation of transmissible gastroenteritis virus mRNAs.Coronavirus E1 glycoprotein expressed from cloned cDNA localizes in the Golgi region.Coronavirus multiplication: locations of genes for virion proteins on the avian infectious bronchitis virus genomeCell-free translation of murine coronavirus RNA.Coronavirus proteins: biogenesis of avian infectious bronchitis virus virion proteins.Coronavirus proteins: structure and function of the oligosaccharides of the avian infectious bronchitis virus glycoproteinsCoronavirus genetically redirected to the epidermal growth factor receptor exhibits effective antitumor activity against a malignant glioblastomaGenetic analysis of determinants for spike glycoprotein assembly into murine coronavirus virions: distinct roles for charge-rich and cysteine-rich regions of the endodomain.Characterization of the budding compartment of mouse hepatitis virus: evidence that transport from the RER to the Golgi complex requires only one vesicular transport step.Analyses of Coronavirus Assembly Interactions with Interspecies Membrane and Nucleocapsid Protein ChimerasMapping of the coronavirus membrane protein domains involved in interaction with the spike protein.The viral spike protein is not involved in the polarized sorting of coronaviruses in epithelial cells.Assembly of spikes into coronavirus particles is mediated by the carboxy-terminal domain of the spike protein.Characterization of two temperature-sensitive mutants of coronavirus mouse hepatitis virus strain A59 with maturation defects in the spike proteinCoronaviruses as vectors: position dependence of foreign gene expressionThe function of the spike protein of mouse hepatitis virus strain A59 can be studied on virus-like particles: cleavage is not required for infectivity.
P2860
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P2860
Viral protein synthesis in mouse hepatitis virus strain A59-infected cells: effect of tunicamycin.
description
1981 nî lūn-bûn
@nan
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
1981年论文
@zh
1981年论文
@zh-cn
name
Viral protein synthesis in mou ...... cells: effect of tunicamycin.
@en
type
label
Viral protein synthesis in mou ...... cells: effect of tunicamycin.
@en
prefLabel
Viral protein synthesis in mou ...... cells: effect of tunicamycin.
@en
P2093
P2860
P1433
P1476
Viral protein synthesis in mou ...... cells: effect of tunicamycin.
@en
P2093
Horzinek MC
Rottier PJ
van der Zeijst BA
P2860
P304
P407
P577
1981-11-01T00:00:00Z