Pages that link to "Q34182668"
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The following pages link to A new mechanism of model membrane fusion determined from Monte Carlo simulation (Q34182668):
Displaying 50 items.
- Control of membrane fusion mechanism by lipid composition: predictions from ensemble molecular dynamics (Q21145657) (← links)
- Cell entry of enveloped viruses (Q26863682) (← links)
- Distinct initial SNARE configurations underlying the diversity of exocytosis (Q26866150) (← links)
- Molecular mechanism of the synaptotagmin–SNARE interaction in Ca2 -triggered vesicle fusion (Q27659974) (← links)
- Prm1 prevents contact-dependent lysis of yeast mating pairs (Q27933298) (← links)
- Membrane fusion: a structural perspective on the interplay of lipids and proteins (Q30311181) (← links)
- The plasma membrane proteins Prm1 and Fig1 ascertain fidelity of membrane fusion during yeast mating. (Q30478914) (← links)
- Rapid membrane fusion of individual virus particles with supported lipid bilayers. (Q30479669) (← links)
- High Transmembrane Voltage Raised by Close Contact Initiates Fusion Pore. (Q30831345) (← links)
- Lipid mixing and content release in single-vesicle, SNARE-driven fusion assay with 1-5 ms resolution (Q33446904) (← links)
- The yeast cell fusion protein Prm1p requires covalent dimerization to promote membrane fusion (Q33582274) (← links)
- Atomic-resolution simulations predict a transition state for vesicle fusion defined by contact of a few lipid tails (Q33619201) (← links)
- Single-molecule studies of the neuronal SNARE fusion machinery (Q33789507) (← links)
- Expansion of the fusion stalk and its implication for biological membrane fusion (Q34002261) (← links)
- Field theoretic study of bilayer membrane fusion. I. Hemifusion mechanism (Q34187706) (← links)
- Mitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusion (Q34277591) (← links)
- Line-tension controlled mechanism for influenza fusion (Q34325691) (← links)
- Field theoretic study of bilayer membrane fusion: II. Mechanism of a stalk-hole complex (Q34353236) (← links)
- SNARE-mediated lipid mixing depends on the physical state of the vesicles (Q34418818) (← links)
- Persistent voids: a new structural metric for membrane fusion. (Q34626588) (← links)
- Mechanics of surface area regulation in cells examined with confined lipid membranes (Q35022066) (← links)
- General hydrophobic interaction potential for surfactant/lipid bilayers from direct force measurements between light-modulated bilayers (Q35229420) (← links)
- Field theoretic study of bilayer membrane fusion III: membranes with leaves of different composition (Q35794563) (← links)
- The energetics of membrane fusion from binding, through hemifusion, pore formation, and pore enlargement (Q35887194) (← links)
- Cardiomyocyte deletion of mitofusin-1 leads to mitochondrial fragmentation and improves tolerance to ROS-induced mitochondrial dysfunction and cell death (Q35906435) (← links)
- Activation thermodynamics of poly(ethylene glycol)-mediated model membrane fusion support mechanistic models of stalk and pore formation (Q36045509) (← links)
- Energetics of stalk intermediates in membrane fusion are controlled by lipid composition (Q36056533) (← links)
- Biological implications of cell fusion. (Q36163604) (← links)
- Cooperative elastic stresses, the hydrophobic effect, and lipid tilt in membrane remodeling (Q36189199) (← links)
- Trans-SNARE interactions elicit Ca2 efflux from the yeast vacuole lumen (Q36322360) (← links)
- Calculation of free energy barriers to the fusion of small vesicles (Q36459141) (← links)
- Calculating Transition Energy Barriers and Characterizing Activation States for Steps of Fusion (Q36678687) (← links)
- Domain formation in membranes caused by lipid wetting of protein (Q36833434) (← links)
- Interactions of membrane-active peptides with thick, neutral, nonzwitterionic bilayers. (Q36868899) (← links)
- Mechanics of membrane fusion (Q36901510) (← links)
- Mechanisms of receptor/coreceptor-mediated entry of enveloped viruses (Q37263225) (← links)
- Membrane lysis during biological membrane fusion: collateral damage by misregulated fusion machines (Q37292928) (← links)
- Fructan and its relationship to abiotic stress tolerance in plants. (Q37416046) (← links)
- Size-dependent protein segregation at membrane interfaces (Q37495024) (← links)
- Low amounts of sucrose are sufficient to depress the phase transition temperature of dry phosphatidylcholine, but not for lyoprotection of liposomes (Q38316330) (← links)
- Rupturing the hemi-fission intermediate in membrane fission under tension: Reaction coordinates, kinetic pathways, and free-energy barriers. (Q40082309) (← links)
- All-or-none versus graded: single-vesicle analysis reveals lipid composition effects on membrane permeabilization (Q41152752) (← links)
- Molecular dynamics simulation analysis of membrane defects and pore propensity of hemifusion diaphragms (Q41767241) (← links)
- A novel assay for detecting fusion pore formation: implications for the fusion mechanism. (Q41851592) (← links)
- Direct Simulation of Protein-Mediated Vesicle Fusion: Lung Surfactant Protein B (Q42140827) (← links)
- pH Alters PEG-mediated fusion of phosphatidylethanolamine-containing vesicles (Q42187111) (← links)
- Wild-type and mutant hemagglutinin fusion peptides alter bilayer structure as well as kinetics and activation thermodynamics of stalk and pore formation differently: mechanistic implications. (Q42250651) (← links)
- Molecular dynamics simulations of lipid vesicle fusion in atomic detail (Q42773706) (← links)
- Analysis of membrane fusion as a two-state sequential process: evaluation of the stalk model. (Q42790862) (← links)
- Stabilization of model membranes during drying by compatible solutes involved in the stress tolerance of plants and microorganisms (Q42808450) (← links)