(Q43902374)

27 November 2017

title

How many trimers? Modeling influenza virus fusion yields a minimum aggregate size of six trimers, three of which are fusogenic (English)

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27 November 2017

Maria Pamela Dobay

1

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27 November 2017

Akos Dobay

series ordinal

2

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27 November 2017

Johnrob Bantang

series ordinal

3

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27 November 2017

Eduardo Mendoza

series ordinal

4

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27 November 2017

language of work or name

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8 July 2011

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27 November 2017

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27 November 2017

volume

7

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27 November 2017

issue

10

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27 November 2017

page(s)

2741-2749

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Intracellular and viral membrane fusion: a uniting mechanism.

27 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Receptor binding and membrane fusion in virus entry: the influenza hemagglutinin

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Distribution of viral RNA, sialic acid receptor, and pathology in H5N1 avian influenza patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Minimal aggregate size and minimal fusion unit for the first fusion pore of influenza hemagglutinin-mediated membrane fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Nanoparticle delivery systems in cancer vaccines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Kinetics of influenza hemagglutinin-mediated membrane fusion as a function of technique.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Membrane fusion mediated by the influenza virus hemagglutinin requires the concerted action of at least three hemagglutinin trimers

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Single-particle kinetics of influenza virus membrane fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Membrane fusion by single influenza hemagglutinin trimers. Kinetic evidence from image analysis of hemagglutinin-reconstituted vesicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Role of hemagglutinin surface density in the initial stages of influenza virus fusion: lack of evidence for cooperativity

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

The fusion kinetics of influenza hemagglutinin expressing cells to planar bilayer membranes is affected by HA density and host cell surface

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Dilation of the influenza hemagglutinin fusion pore revealed by the kinetics of individual cell-cell fusion events

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

21 January 2018

Executable cell biology

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Organization of influenza A virus envelope at neutral and low pH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Quantitative relationships between an influenza virus and neutralizing antibody

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Comprehensive kinetic analysis of influenza hemagglutinin-mediated membrane fusion: role of sialate binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Stochastic simulation of hemagglutinin-mediated fusion pore formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Fusion of influenza hemagglutinin-expressing fibroblasts with glycophorin-bearing liposomes: role of hemagglutinin surface density

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Membrane fusion by surrogate receptor-bound influenza haemagglutinin

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Fusion of influenza virus with sialic acid-bearing target membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Hemifusion between cells expressing hemagglutinin of influenza virus and planar membranes can precede the formation of fusion pores that subsequently fully enlarge

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Intermediates and kinetics of membrane fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Influenza hemagglutinins outside of the contact zone are necessary for fusion pore expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Dynamic clustered distribution of hemagglutinin resolved at 40 nm in living cell membranes discriminates between raft theories

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

Incorporating output variance in local sensitivity analysis for stochastic models

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1MB05060E

21 January 2018

Identifiers

DOI

10.1039/C1MB05060E

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27 November 2017

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