Pages that link to "Q35887194"
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The following pages link to The energetics of membrane fusion from binding, through hemifusion, pore formation, and pore enlargement (Q35887194):
Displaying 50 items.
- IFITM proteins restrict viral membrane hemifusion (Q21558779) (← links)
- SERINC3 and SERINC5 restrict HIV-1 infectivity and are counteracted by Nef (Q24338889) (← links)
- HIV-1 Nef promotes infection by excluding SERINC5 from virion incorporation (Q24338895) (← links)
- Viral and developmental cell fusion mechanisms: conservation and divergence (Q24631787) (← links)
- Membrane fusion: grappling with SNARE and SM proteins (Q24633113) (← links)
- Predicted protein interactions of IFITMs which inhibit Zika virus infection (Q26247786) (← links)
- Remodeling of the Host Cell Plasma Membrane by HIV-1 Nef and Vpu: A Strategy to Ensure Viral Fitness and Persistence (Q26767362) (← links)
- Membrane tension and membrane fusion (Q26797464) (← links)
- Distinct initial SNARE configurations underlying the diversity of exocytosis (Q26866150) (← links)
- IFITM3 restricts influenza A virus entry by blocking the formation of fusion pores following virus-endosome hemifusion (Q27329190) (← links)
- Cholesterol Alters the Dynamics of Release in Protein Independent Cell Models for Exocytosis (Q27347074) (← links)
- Characterization of a Structural Intermediate of Flavivirus Membrane Fusion (Q27478061) (← links)
- A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins (Q27485479) (← links)
- Closing the door on flaviviruses: Entry as a target for antiviral drug design (Q27487953) (← links)
- Structures and Mechanisms of Viral Membrane Fusion Proteins: Multiple Variations on a Common Theme (Q27487974) (← links)
- Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin (Q27681363) (← links)
- The polybasic juxtamembrane region of Sso1p is required for SNARE function in vivo (Q27931683) (← links)
- Fusion of Enveloped Viruses in Endosomes (Q28073406) (← links)
- Receptor-induced thiolate couples Env activation to retrovirus fusion and infection (Q28471846) (← links)
- Reovirus FAST Proteins Drive Pore Formation and Syncytiogenesis Using a Novel Helix-Loop-Helix Fusion-Inducing Lipid Packing Sensor (Q28548068) (← links)
- Docking and fast fusion of synaptobrevin vesicles depends on the lipid compositions of the vesicle and the acceptor SNARE complex-containing target membrane (Q30429848) (← links)
- SCAMP2 interacts with Arf6 and phospholipase D1 and links their function to exocytotic fusion pore formation in PC12 cells (Q30437458) (← links)
- Liposome reconstitution of a minimal protein-mediated membrane fusion machine (Q30476143) (← links)
- Multiple intermediates in SNARE-induced membrane fusion (Q30478481) (← links)
- Rapid membrane fusion of individual virus particles with supported lipid bilayers. (Q30479669) (← links)
- The role of lateral tension in calcium-induced DPPS vesicle rupture (Q31073179) (← links)
- Identification of the HIV-1 gp41 core-binding motif--HXXNPF. (Q33253687) (← links)
- Membrane interaction and structure of the transmembrane domain of influenza hemagglutinin and its fusion peptide complex (Q33314968) (← links)
- Enhanced fusion pore expansion mediated by the trans-acting Endodomain of the reovirus FAST proteins (Q33415477) (← links)
- Pulling force generated by interacting SNAREs facilitates membrane hemifusion. (Q33519916) (← links)
- Single Molecule Measurements of Interaction Free Energies Between the Proteins Within Binary and Ternary SNARE Complexes (Q33526994) (← links)
- An electrostatically preferred lateral orientation of SNARE complex suggests novel mechanisms for driving membrane fusion (Q33529109) (← links)
- Investigation of SNARE-Mediated Membrane Fusion Mechanism Using Atomic Force Microscopy (Q33540688) (← links)
- SERINC5 protein inhibits HIV-1 fusion pore formation by promoting functional inactivation of envelope glycoproteins. (Q33567639) (← links)
- The Surprising Role of Amyloid Fibrils in HIV Infection (Q33570363) (← links)
- Dilation of fusion pores by crowding of SNARE proteins (Q33603031) (← links)
- Atomic-resolution simulations predict a transition state for vesicle fusion defined by contact of a few lipid tails (Q33619201) (← links)
- Minimum membrane bending energies of fusion pores (Q33708251) (← links)
- The three lives of viral fusion peptides (Q33770459) (← links)
- Negative potentials across biological membranes promote fusion by class II and class III viral proteins (Q33907054) (← links)
- Membrane bridging and hemifusion by denaturated Munc18. (Q33963890) (← links)
- The fusion pores of Ca2+ -triggered exocytosis (Q34037133) (← links)
- Effect of surfaces on amyloid fibril formation (Q34053378) (← links)
- Line tension and interaction energies of membrane rafts calculated from lipid splay and tilt (Q34188903) (← links)
- Single reconstituted neuronal SNARE complexes zipper in three distinct stages (Q34294781) (← links)
- The membrane fusion enigma: SNAREs, Sec1/Munc18 proteins, and their accomplices--guilty as charged? (Q34305507) (← links)
- Mechanistic study of broadly neutralizing human monoclonal antibodies against dengue virus that target the fusion loop (Q34306877) (← links)
- Investigating Hydrophilic Pores in Model Lipid Bilayers Using Molecular Simulations: Correlating Bilayer Properties with Pore-Formation Thermodynamics (Q34459308) (← links)
- A structural role for the synaptobrevin 2 transmembrane domain in dense-core vesicle fusion pores (Q34470858) (← links)
- Persistent voids: a new structural metric for membrane fusion. (Q34626588) (← links)