Pages that link to "Q40380573"

The following pages link to Structure and function of fusion pores in exocytosis and ectoplasmic membrane fusion (Q40380573):

Displaying 50 items.

• The new anti-actin agent dihydrohalichondramide reveals fenestrae-forming centers in hepatic endothelial cells (Q24805588) ‎ (← links)
• X-ray structure of a neuronal complexin-SNARE complex from squid (Q27638957) ‎ (← links)
• Membrane fusion mechanisms: the influenza hemagglutinin paradigm and its implications for intracellular fusion (Q27863691) ‎ (← links)
• The V-ATPase proteolipid cylinder promotes the lipid-mixing stage of SNARE-dependent fusion of yeast vacuoles. (Q27931031) ‎ (← links)
• The Vtc proteins in vacuole fusion: coupling NSF activity to V(0) trans-complex formation. (Q27932292) ‎ (← links)
• Prm1 prevents contact-dependent lysis of yeast mating pairs (Q27933298) ‎ (← links)
• SNAREpins: minimal machinery for membrane fusion (Q28131697) ‎ (← links)
• Synaptotagmin: a Ca(2+) sensor that triggers exocytosis? (Q28208303) ‎ (← links)
• Delineation of the oligomerization, AP-2 binding, and synprint binding region of the C2B domain of synaptotagmin (Q28577061) ‎ (← links)
• Evidence that the transition of HIV-1 gp41 into a six-helix bundle, not the bundle configuration, induces membrane fusion (Q28646673) ‎ (← links)
• Membrane fusion and exocytosis (Q29614426) ‎ (← links)
• Membrane fusion (Q29618140) ‎ (← links)
• Supramolecular SNARE assembly precedes hemifusion in SNARE-mediated membrane fusion. (Q30369961) ‎ (← links)
• The pathway of membrane fusion catalyzed by influenza hemagglutinin: restriction of lipids, hemifusion, and lipidic fusion pore formation (Q30442120) ‎ (← links)
• Membrane fusion mediated by the influenza virus hemagglutinin requires the concerted action of at least three hemagglutinin trimers (Q30442203) ‎ (← links)
• Amino acid sequence requirements of the transmembrane and cytoplasmic domains of influenza virus hemagglutinin for viable membrane fusion (Q30454311) ‎ (← links)
• The lipid-anchored ectodomain of influenza virus hemagglutinin (GPI-HA) is capable of inducing nonenlarging fusion pores (Q30454458) ‎ (← links)
• Exocytosis in plants. (Q32021045) ‎ (← links)
• Atomic force microscope spectroscopy reveals a hemifusion intermediate during soluble N-ethylmaleimide-sensitive factor-attachment protein receptors-mediated membrane fusion (Q33299157) ‎ (← links)
• Investigation of SNARE-Mediated Membrane Fusion Mechanism Using Atomic Force Microscopy (Q33540688) ‎ (← links)
• Minimum membrane bending energies of fusion pores (Q33708251) ‎ (← links)
• The cytomegalovirus-encoded chemokine receptor US28 can enhance cell-cell fusion mediated by different viral proteins (Q33783347) ‎ (← links)
• Membrane bending energy and fusion pore kinetics in Ca(2+)-triggered exocytosis (Q33880350) ‎ (← links)
• Fusion pore expansion in horse eosinophils is modulated by Ca2+ and protein kinase C via distinct mechanisms (Q33889198) ‎ (← links)
• Poly(ethylene glycol) (PEG)-mediated fusion between pure lipid bilayers: a mechanism in common with viral fusion and secretory vesicle release? (Q33892321) ‎ (← links)
• Protein machines and lipid assemblies: current views of cell membrane fusion (Q33922435) ‎ (← links)
• Role of the N-terminal peptides of viral envelope proteins in membrane fusion. (Q33933461) ‎ (← links)
• The fusion pores of Ca2+ -triggered exocytosis (Q34037133) ‎ (← links)
• Signalling mechanisms: a decade of signalling. (Q34085522) ‎ (← links)
• Duration of fusion pore opening and the amount of hormone released are regulated by myosin II during kiss-and-run exocytosis. (Q34119438) ‎ (← links)
• Model systems for membrane fusion. (Q34154703) ‎ (← links)
• Greasing membrane fusion and fission machineries (Q34156718) ‎ (← links)
• Lipid flow through fusion pores connecting membranes of different tensions (Q34170566) ‎ (← links)
• Hemifusion between cells expressing hemagglutinin of influenza virus and planar membranes can precede the formation of fusion pores that subsequently fully enlarge (Q34171963) ‎ (← links)
• Lipid intermediates in membrane fusion: formation, structure, and decay of hemifusion diaphragm (Q34179155) ‎ (← links)
• Membrane permeability changes at early stages of influenza hemagglutinin-mediated fusion (Q34182695) ‎ (← links)
• Electrostatic interactions between the syntaxin membrane anchor and neurotransmitter passing through the fusion pore (Q34189535) ‎ (← links)
• Protein-Lipid Interplay in Fusion and Fission of Biological Membranes (Q34267537) ‎ (← links)
• The v-ATPase V0 subunit a1 is required for a late step in synaptic vesicle exocytosis in Drosophila. (Q34420273) ‎ (← links)
• Imaging direct, dynamin-dependent recapture of fusing secretory granules on plasma membrane lawns from PC12 cells (Q34430018) ‎ (← links)
• Secretion: dense-core vesicles can kiss-and-run too. (Q34452053) ‎ (← links)
• What drives membrane fusion in eukaryotes? (Q34460159) ‎ (← links)
• A structural role for the synaptobrevin 2 transmembrane domain in dense-core vesicle fusion pores (Q34470858) ‎ (← links)
• The timing of endocytosis after activation of a G-protein-coupled receptor in a sensory neuron (Q34546941) ‎ (← links)
• Role of synaptotagmin in Ca2+-triggered exocytosis (Q34669186) ‎ (← links)
• Rab3D, a small GTPase, is localized on mast cell secretory granules and translocates to the plasma membrane upon exocytosis. (Q34756187) ‎ (← links)
• Visualization of synaptotagmin I oligomers assembled onto lipid monolayers. (Q34763458) ‎ (← links)
• Cell and molecular biology of myoblast fusion (Q35107552) ‎ (← links)
• Live cell imaging of in vitro human trophoblast syncytialization. (Q35150866) ‎ (← links)
• The fusion pore (Q35197986) ‎ (← links)