Requirement for GP64 to drive efficient budding of Autographa californica multicapsid nucleopolyhedrovirus.
about
Baculovirus nuclear import: open, nuclear pore complex (NPC) sesameSurface displaying of swine IgG1 Fc enhances baculovirus-vectored vaccine efficacy by facilitating viral complement escape and mammalian cell transduction.The membrane-proximal stem region of vesicular stomatitis virus G protein confers efficient virus assembly.Identification of the lymantria dispar nucleopolyhedrovirus envelope fusion protein provides evidence for a phylogenetic division of the BaculoviridaeA cellular Drosophila melanogaster protein with similarity to baculovirus F envelope fusion proteins.A GP64-null baculovirus pseudotyped with vesicular stomatitis virus G proteinProteomics of the Autographa californica nucleopolyhedrovirus budded virionsDirect interaction of baculovirus capsid proteins VP39 and EXON0 with kinesin-1 in insect cells determined by fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy.Partial functional rescue of Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus infectivity by replacement of F protein with GP64 from Autographa californica multicapsid nucleopolyhedrovirus.Genome sequence of Erinnyis ello granulovirus (ErelGV), a natural cassava hornworm pesticide and the first sequenced sphingid-infecting betabaculovirus.Furin is involved in baculovirus envelope fusion protein activation.Characterization of the role of very late expression factor 1 in baculovirus capsid structure and DNA processingAnalysis of an Autographa californica multicapsid nucleopolyhedrovirus lef-6-null virus: LEF-6 is not essential for viral replication but appears to accelerate late gene transcription.Analysis of BmNPV orf101 disruption: orf101 is essential for mediating budded virus productionThe baculovirus GP64 protein mediates highly stable infectivity of a human respiratory syncytial virus lacking its homologous transmembrane glycoproteinsInfectivity of a human respiratory syncytial virus lacking the SH, G, and F proteins is efficiently mediated by the vesicular stomatitis virus G protein.Class III viral membrane fusion proteins.A new theraphosid spider toxin causes early insect cell death by necrosis when expressed in vitro during recombinant baculovirus infection.Abrogation of contaminating RNA activity in HIV-1 Gag VLPs.The FP25K Acts as a Negative Factor for the Infectivity of AcMNPV Budded Virus.Baculovirus GP64-mediated entry into mammalian cellsCharacterization of baculovirus constructs lacking either the Ac 101, Ac 142, or the Ac 144 open reading frameEstablishment of insect cell lines expressing green fluorescent protein on cell surface based on AcMNPV GP64 membrane fusion characteristic.Baculovirus as a vaccine vectorAutographa californica multiple nucleopolyhedrovirus nucleocapsid protein BV/ODV-C42 mediates the nuclear entry of P78/83.Mutagenesis and nuclear magnetic resonance analyses of the fusion peptide of Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus F protein.The F-like protein Ac23 enhances the infectivity of the budded virus of gp64-null Autographa californica multinucleocapsid nucleopolyhedrovirus pseudotyped with baculovirus envelope fusion protein F.The Autographa californica multiple nucleopolyhedrovirus ORF78 is essential for budded virus production and general occlusion body formationGene transduction in mammalian cells using Bombyx mori nucleopolyhedrovirus assisted by glycoprotein 64 of Autographa californica multiple nucleopolyhedrovirusBaculovirus FP25K Localization: Role of the Coiled-Coil Domain.Unraveling the entry mechanism of baculoviruses and its evolutionary implications.Baculovirus-mediated gene delivery and RNAi applications.Roles of cellular NSF protein in entry and nuclear egress of budded virions of Autographa californica multiple nucleopolyhedrovirus.Immediate-early protein ME53 forms foci and colocalizes with GP64 and the major capsid protein VP39 at the cell membranes of Autographa californica multiple nucleopolyhedrovirus-infected cells.Trichoplusia ni Kinesin-1 Associates with Autographa californica Multiple Nucleopolyhedrovirus Nucleocapsid Proteins and Is Required for Production of Budded Virus.Autographa californica multiple nucleopolyhedrovirus GP64 protein: roles of histidine residues in triggering membrane fusion and fusion pore expansion.Functional role of the cytoplasmic tail domain of the major envelope fusion protein of group II baculoviruses.Functional analysis of the Autographa californica multiple nucleopolyhedrovirus GP64 terminal fusion loops and interactions with membranesSeamless replacement of Autographa californica multiple nucleopolyhedrovirus gp64 with each of five novel type II alphabaculovirus fusion sequences generates pseudotyped virus that fails to transduce mammalian cells.Novel baculovirus expression vectors that provide sialylation of recombinant glycoproteins in lepidopteran insect cells.
P2860
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P2860
Requirement for GP64 to drive efficient budding of Autographa californica multicapsid nucleopolyhedrovirus.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Requirement for GP64 to drive ...... ticapsid nucleopolyhedrovirus.
@en
Requirement for GP64 to drive ...... ticapsid nucleopolyhedrovirus.
@nl
type
label
Requirement for GP64 to drive ...... ticapsid nucleopolyhedrovirus.
@en
Requirement for GP64 to drive ...... ticapsid nucleopolyhedrovirus.
@nl
prefLabel
Requirement for GP64 to drive ...... ticapsid nucleopolyhedrovirus.
@en
Requirement for GP64 to drive ...... ticapsid nucleopolyhedrovirus.
@nl
P356
P1433
P1476
Requirement for GP64 to drive ...... ticapsid nucleopolyhedrovirus.
@en
P2093
A G Oomens
P304
P356
10.1006/VIRO.1998.9523
P407
P577
1999-02-01T00:00:00Z