Pages that link to "Q40793734"

The following pages link to The 1-127 HA2 construct of influenza virus hemagglutinin induces cell-cell hemifusion (Q40793734):

Displaying 33 items.

• Reovirus FAST Proteins Drive Pore Formation and Syncytiogenesis Using a Novel Helix-Loop-Helix Fusion-Inducing Lipid Packing Sensor (Q28548068) (← links)
• Hypothesis: spring-loaded boomerang mechanism of influenza hemagglutinin-mediated membrane fusion (Q30311060) (← links)
• Viral envelope protein folding and membrane hemifusion are enhanced by the conserved loop region of HIV‐1 gp41 (Q30426201) (← links)
• Reversible stages of the low-pH-triggered conformational change in influenza virus hemagglutinin (Q30453331) (← links)
• Microscopic observations reveal that fusogenic peptides induce liposome shrinkage prior to membrane fusion (Q30542283) (← links)
• Membrane permeability changes at early stages of influenza hemagglutinin-mediated fusion (Q34182695) (← links)
• Oligomeric beta-structure of the membrane-bound HIV-1 fusion peptide formed from soluble monomers (Q34187142) (← links)
• Protein-Lipid Interplay in Fusion and Fission of Biological Membranes (Q34267537) (← links)
• Cytosol-dependent membrane fusion in ER, nuclear envelope and nuclear pore assembly: biological implications (Q34521574) (← links)
• The Final Conformation of the Complete Ectodomain of the HA2 Subunit of Influenza Hemagglutinin Can by Itself Drive Low pH-dependent Fusion (Q34787116) (← links)
• Early steps of the conformational change of influenza virus hemagglutinin to a fusion active state: stability and energetics of the hemagglutinin (Q35182219) (← links)
• Are fusion peptides a good model to study viral cell fusion? (Q35182239) (← links)
• Fusion peptides and the mechanism of viral fusion (Q35182242) (← links)
• Viral fusion proteins: multiple regions contribute to membrane fusion (Q35182246) (← links)
• The energetics of membrane fusion from binding, through hemifusion, pore formation, and pore enlargement (Q35887194) (← links)
• Class II fusion protein of alphaviruses drives membrane fusion through the same pathway as class I proteins. (Q36321675) (← links)
• Full-length trimeric influenza virus hemagglutinin II membrane fusion protein and shorter constructs lacking the fusion peptide or transmembrane domain: Hyperthermostability of the full-length protein and the soluble ectodomain and fusion peptide ma (Q36385125) (← links)
• The Interaction between Influenza HA Fusion Peptide and Transmembrane Domain Affects Membrane Structure (Q36426451) (← links)
• Conserved glycine residues in the fusion peptide of the paramyxovirus fusion protein regulate activation of the native state (Q37683548) (← links)
• Influenza virus entry (Q37980627) (← links)
• Tight binding of influenza virus hemagglutinin to its receptor interferes with fusion pore dilation (Q38360836) (← links)
• Molecular dynamics simulation of the evolution of hydrophobic defects in one monolayer of a phosphatidylcholine bilayer: relevance for membrane fusion mechanisms (Q40213545) (← links)
• Measuring pKa of activation and pKi of inactivation for influenza hemagglutinin from kinetics of membrane fusion of virions and of HA expressing cells. (Q40217289) (← links)
• The conserved glycine residues in the transmembrane domain of the Semliki Forest virus fusion protein are not required for assembly and fusion. (Q40468559) (← links)
• A nonfusogenic antigen mimic of influenza hemagglutinin glycoproteins constituted with soluble full-length HA1 and truncated HA2 proteins expressed in E. coli (Q42184367) (← links)
• Hairpin folding of HIV gp41 abrogates lipid mixing function at physiologic pH and inhibits lipid mixing by exposed gp41 constructs (Q42667010) (← links)
• Thermal denaturation of influenza virus and its relationship to membrane fusion (Q43002057) (← links)
• Ca(2+) and Mg(2+)/ATP independently trigger homotypic membrane fusion in gastric secretory membranes (Q43910877) (← links)
• Efficient Fusion at Neutral pH by Human Immunodeficiency Virus gp41 Trimers containing the Fusion Peptide and Transmembrane Domain. (Q47551930) (← links)
• Influenza hemagglutinins outside of the contact zone are necessary for fusion pore expansion (Q47780558) (← links)
• The Stabilities of the Soluble Ectodomain and Fusion Peptide Hairpins of the Influenza Virus Hemagglutinin Subunit II Protein Are Positively Correlated with Membrane Fusion (Q59353970) (← links)
• The protein coat in membrane fusion: lessons from fission (Q77869246) (← links)
• Hydrogen-Deuterium Exchange Supports Independent Membrane-Interfacial Fusion Peptide and Transmembrane Domains in Subunit 2 of Influenza Virus Hemagglutinin Protein, a Structured and Aqueous-Protected Connection between the Fusion Peptide and Solubl (Q90126245) (← links)