A catalytically and genetically optimized beta-lactamase-matrix based assay for sensitive, specific, and higher throughput analysis of native henipavirus entry characteristics.
about
The β-Lactamase Assay: Harnessing a FRET Biosensor to Analyse Viral Fusion MechanismsA broad-spectrum antiviral targeting entry of enveloped virusesInterferon-inducible cholesterol-25-hydroxylase broadly inhibits viral entry by production of 25-hydroxycholesterolEndothelial galectin-1 binds to specific glycans on nipah virus fusion protein and inhibits maturation, mobility, and function to block syncytia formation.Novel method of cell-free in vitro synthesis of the human fibroblast growth factor 1 geneDissecting virus entry: replication-independent analysis of virus binding, internalization, and penetration using minimal complementation of β-galactosidaseVirus particle release from glycosphingolipid-enriched microdomains is essential for dendritic cell-mediated capture and transfer of HIV-1 and henipavirus.Timing of galectin-1 exposure differentially modulates Nipah virus entry and syncytium formation in endothelial cells.Hendra and nipah infection: pathology, models and potential therapies.Nipah virus envelope-pseudotyped lentiviruses efficiently target ephrinB2-positive stem cell populations in vitro and bypass the liver sink when administered in vivoDevelopment of novel entry inhibitors targeting emerging viruses.Detection of receptor-induced glycoprotein conformational changes on enveloped virions by using confocal micro-Raman spectroscopy.Strategies for in vivo imaging of enzyme activity: an overview and recent advances.A combination HIV reporter virus system for measuring post-entry event efficiency and viral outcome in primary CD4+ T cell subsetsC-Terminal DxD-Containing Sequences within Paramyxovirus Nucleocapsid Proteins Determine Matrix Protein Compatibility and Can Direct Foreign Proteins into Budding Particles.Nipah virion entry kinetics, composition, and conformational changes determined by enzymatic virus-like particles and new flow virometry tools.A quantitative and kinetic fusion protein-triggering assay can discern distinct steps in the nipah virus membrane fusion cascadeThe V4 and V5 Variable Loops of HIV-1 Envelope Glycoprotein Are Tolerant to Insertion of Green Fluorescent Protein and Are Useful Targets for Labeling.HIV-1 Fusion Assay.
P2860
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P2860
A catalytically and genetically optimized beta-lactamase-matrix based assay for sensitive, specific, and higher throughput analysis of native henipavirus entry characteristics.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
A catalytically and geneticall ...... pavirus entry characteristics.
@en
A catalytically and geneticall ...... pavirus entry characteristics.
@nl
type
label
A catalytically and geneticall ...... pavirus entry characteristics.
@en
A catalytically and geneticall ...... pavirus entry characteristics.
@nl
altLabel
A catalytically and geneticall ...... ipavirus entry characteristics
@en
prefLabel
A catalytically and geneticall ...... pavirus entry characteristics.
@en
A catalytically and geneticall ...... pavirus entry characteristics.
@nl
P2093
P2860
P356
P1433
P1476
A catalytically and geneticall ...... pavirus entry characteristics.
@en
P2093
Alexander N Freiberg
Hector C Aguilar
Michael R Holbrook
Mike C Wolf
P2860
P2888
P356
10.1186/1743-422X-6-119
P407
P50
P577
2009-07-31T00:00:00Z
P5875
P6179
1030030464