about
Comprehensive kinetic analysis of influenza hemagglutinin-mediated membrane fusion: role of sialate binding.Energetics of intermediates in membrane fusion: comparison of stalk and inverted micellar intermediate mechanismsMembrane fusion mediated by the influenza virus hemagglutinin requires the concerted action of at least three hemagglutinin trimers.Influenza virus-membrane fusion triggered by proton uncaging for single particle studies of fusion kineticsRole of hemagglutinin surface density in the initial stages of influenza virus fusion: lack of evidence for cooperativityConformational intermediates and fusion activity of influenza virus hemagglutinin.Cholesterol-dependent nanomechanical stability of phase-segregated multicomponent lipid bilayersMorphological changes and fusogenic activity of influenza virus hemagglutinin.Investigation of pathways for the low-pH conformational transition in influenza hemagglutinin.Kinetically differentiating influenza hemagglutinin fusion and hemifusion machines.Molecular mechanism underlying the action of a novel fusion inhibitor of influenza A virusSecretory and viral fusion may share mechanistic events with fusion between curved lipid bilayersThe initial fusion pore induced by baculovirus GP64 is large and forms quicklyCellular uptake mechanisms of novel anionic siRNA lipoplexes.Diacylglycerol and hexadecane increase divalent cation-induced lipid mixing rates between phosphatidylserine large unilamellar vesicles.Thermostability of reovirus disassembly intermediates (ISVPs) correlates with genetic, biochemical, and thermodynamic properties of major surface protein mu1.Minimal aggregate size and minimal fusion unit for the first fusion pore of influenza hemagglutinin-mediated membrane fusion.Membrane fusion mediated by coiled coils: a hypothesis.Stochastic simulation of hemagglutinin-mediated fusion pore formation.Measuring pKa of activation and pKi of inactivation for influenza hemagglutinin from kinetics of membrane fusion of virions and of HA expressing cells.Membrane fusion by single influenza hemagglutinin trimers. Kinetic evidence from image analysis of hemagglutinin-reconstituted vesicles.Membrane perturbation and fusion pore formation in influenza hemagglutinin-mediated membrane fusion. A new model for fusion.How many trimers? Modeling influenza virus fusion yields a minimum aggregate size of six trimers, three of which are fusogenic.Partial fusion activity of influenza virus toward liposomes and erythrocyte ghosts is distinct from viral inactivation.Influence of the spectrin network on fusion of influenza virus with red blood cells.Rotation-Activated and Cooperative Zipping Characterize Class I Viral Fusion Protein Dynamics.
P2860
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P2860
description
1992 nî lūn-bûn
@nan
1992 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Intermediates and kinetics of membrane fusion.
@ast
Intermediates and kinetics of membrane fusion.
@en
Intermediates and kinetics of membrane fusion.
@nl
type
label
Intermediates and kinetics of membrane fusion.
@ast
Intermediates and kinetics of membrane fusion.
@en
Intermediates and kinetics of membrane fusion.
@nl
prefLabel
Intermediates and kinetics of membrane fusion.
@ast
Intermediates and kinetics of membrane fusion.
@en
Intermediates and kinetics of membrane fusion.
@nl
P2860
P1433
P1476
Intermediates and kinetics of membrane fusion.
@en
P2093
P2860
P304
P356
10.1016/S0006-3495(92)81622-3
P407
P577
1992-08-01T00:00:00Z