| P50 | author | Ludger Johannes | Q33116275 |
| | Christian Wunder | Q40393802 |
| | Patricia Bassereau | Q43295944 |
| P2860 | cites work | Imaging coexisting fluid domains in biomembrane models coupling curvature and line tension | Q51808476 |
| | Elastic curvature constants of lipid monolayers and bilayers. | Q51930944 |
| | Formation and Interaction of Membrane Tubes | Q57252588 |
| | Domain-induced budding of vesicles | Q57252607 |
| | Effect of Line Tension on the Lateral Organization of Lipid Membranes | Q57372754 |
| | Fission of a Multiphase Membrane Tube | Q57958285 |
| | GM1 structure determines SV40-induced membrane invagination and infection | Q58830543 |
| | Line tension at fluid membrane domain boundaries measured by micropipette aspiration | Q80742387 |
| | Induced domain formation in endocytic invagination, lipid sorting, and scission | Q84772653 |
| | Structural basis of membrane invagination by F-BAR domains | Q24308717 |
| | FCHo proteins are nucleators of clathrin-mediated endocytosis | Q24310377 |
| | GTP-dependent twisting of dynamin implicates constriction and tension in membrane fission | Q24322874 |
| | A pseudoatomic model of the dynamin polymer identifies a hydrolysis-dependent powerstroke | Q24338959 |
| | Effect of chain length and unsaturation on elasticity of lipid bilayers | Q24537369 |
| | Membrane curvature and its generation by BAR proteins | Q27006768 |
| | Function and regulation of the endosomal fusion and fission machineries | Q27015677 |
| | A feedback loop between dynamin and actin recruitment during clathrin-mediated endocytosis | Q27319900 |
| | A high precision survey of the molecular dynamics of mammalian clathrin-mediated endocytosis | Q27322340 |
| | The mechanochemistry of endocytosis | Q27327832 |
| | Curvature of clathrin-coated pits driven by epsin | Q27639716 |
| | BAR domains as sensors of membrane curvature: the amphiphysin BAR structure | Q27642663 |
| | Structure and analysis of FCHo2 F-BAR domain: a dimerizing and membrane recruitment module that effects membrane curvature | Q27645108 |
| | A modular design for the clathrin- and actin-mediated endocytosis machinery | Q27934608 |
| | Membrane proteins of the endoplasmic reticulum induce high-curvature tubules | Q27939309 |
| | Structural characteristics of BAR domain superfamily to sculpt the membrane | Q27967668 |
| | Progressive ordering with decreasing temperature of the phospholipids of influenza virus | Q28270891 |
| | Mechanisms of membrane curvature sensing | Q28307953 |
| | Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice | Q28510217 |
| | Mechanisms of endocytosis | Q29547609 |
| | Molecular mechanism and physiological functions of clathrin-mediated endocytosis | Q29615660 |
| | Membrane curvature and mechanisms of dynamic cell membrane remodelling | Q29617321 |
| | Harnessing actin dynamics for clathrin-mediated endocytosis | Q29620544 |
| | The BAR domain superfamily: membrane-molding macromolecules | Q30014845 |
| | Membrane fission is promoted by insertion of amphipathic helices and is restricted by crescent BAR domains | Q30461258 |
| | Role of curvature and phase transition in lipid sorting and fission of membrane tubules | Q30475946 |
| | Curvature-driven lipid sorting needs proximity to a demixing point and is aided by proteins | Q30486937 |
| | Membrane curvature controls dynamin polymerization | Q30493714 |
| | Generation of coated intermediates of clathrin-mediated endocytosis on protein-free liposomes | Q47802787 |
| | Reconstitution of clathrin-coated bud and vesicle formation with minimal components. | Q51377286 |
| | Coordinated actions of actin and BAR proteins upstream of dynamin at endocytic clathrin-coated pits | Q30494265 |
| | Actin dynamics counteract membrane tension during clathrin-mediated endocytosis | Q30503955 |
| | Steric confinement of proteins on lipid membranes can drive curvature and tubulation | Q33842718 |
| | On soliton propagation in biomembranes and nerves | Q33896003 |
| | Sterol structure determines the separation of phases and the curvature of the liquid-ordered phase in model membranes | Q33927396 |
| | Inhibition of retrograde transport protects mice from lethal ricin challenge | Q34022109 |
| | A minimal system allowing tubulation with molecular motors pulling on giant liposomes | Q34024836 |
| | The first five seconds in the life of a clathrin-coated pit. | Q34292187 |
| | COP and clathrin-coated vesicle budding: different pathways, common approaches | Q34334300 |
| | Molecular model for a complete clathrin lattice from electron cryomicroscopy | Q34361610 |
| | Plasma membrane reshaping during endocytosis is revealed by time-resolved electron tomography. | Q34365825 |
| | Retromer: a master conductor of endosome sorting | Q34401990 |
| | Membrane deformations induced by the matrix protein of vesicular stomatitis virus in a minimal system | Q34468953 |
| | Cells respond to mechanical stress by rapid disassembly of caveolae | Q34588611 |
| | Shiga toxin induces tubular membrane invaginations for its uptake into cells | Q34719609 |
| | Endocytic vesicle scission by lipid phase boundary forces | Q34772048 |
| | Membrane tube formation from giant vesicles by dynamic association of motor proteins | Q34789539 |
| | Membrane texture induced by specific protein binding and receptor clustering: active roles for lipids in cellular function | Q34879991 |
| | Influenza virus assembly and budding | Q34913111 |
| | Membrane shape at the edge of the dynamin helix sets location and duration of the fission reaction | Q34915566 |
| | Actin polymerization serves as a membrane domain switch in model lipid bilayers | Q35129016 |
| | Spatiotemporal regulation of chemical reactions by active cytoskeletal remodeling | Q35202675 |
| | Kinetics of Hole Nucleation in Biomembrane Rupture | Q35237611 |
| | Endocytic accessory factors and regulation of clathrin-mediated endocytosis | Q35548941 |
| | Nature of curvature coupling of amphiphysin with membranes depends on its bound density. | Q35657648 |
| | Chirality-induced budding: a raft-mediated mechanism for endocytosis and morphology of caveolae? | Q35751504 |
| | Seeing is believing: imaging actin dynamics at single sites of endocytosis. | Q35832636 |
| | Ultrastructural dynamics of proteins involved in endocytic budding | Q36300807 |
| | Ultrastructural identification of uncoated caveolin-independent early endocytic vehicles | Q36321371 |
| | Dynamin, a membrane-remodelling GTPase | Q36460251 |
| | Structural design of cage and coat scaffolds that direct membrane traffic | Q36774855 |
| | Plasma membranes are poised for activation of raft phase coalescence at physiological temperature | Q36786913 |
| | More than one door - Budding of enveloped viruses through cellular membranes | Q36791778 |
| | Curvature sorting of proteins on a cylindrical lipid membrane tether connected to a reservoir | Q36920650 |
| | Biophysical approaches to protein-induced membrane deformations in trafficking | Q37186230 |
| | Sorting of lipids and proteins in membrane curvature gradients | Q37263234 |
| | Effect of cholesterol on structural and mechanical properties of membranes depends on lipid chain saturation | Q37374180 |
| | GTPase cycle of dynamin is coupled to membrane squeeze and release, leading to spontaneous fission | Q37401393 |
| | Molecular mechanisms of clathrin-independent endocytosis. | Q37491917 |
| | Conserved functions of membrane active GTPases in coated vesicle formation. | Q37591700 |
| | Dissecting dynamin's role in clathrin-mediated endocytosis. | Q37597372 |
| | Membrane shape modulates transmembrane protein distribution. | Q37638252 |
| | A unifying mechanism accounts for sensing of membrane curvature by BAR domains, amphipathic helices and membrane-anchored proteins. | Q37652795 |
| | Endocytosis unplugged: multiple ways to enter the cell | Q37686075 |
| | Geometric catalysis of membrane fission driven by flexible dynamin rings | Q37693589 |
| | Molecules, mechanisms, and cellular roles of clathrin-independent endocytosis | Q37741519 |
| | Dynamin: functional design of a membrane fission catalyst. | Q37877698 |
| | Membrane trafficking and signaling: two sides of the same coin | Q37956473 |
| | Membrane fission: the biogenesis of transport carriers | Q37998566 |
| | Mechanical feedback between membrane tension and dynamics | Q38037852 |
| | Molecular mechanisms of the membrane sculpting ESCRT pathway | Q38134065 |
| | Rapid constriction of lipid bilayers by the mechanochemical enzyme dynamin | Q38516317 |
| | Active remodeling of cortical actin regulates spatiotemporal organization of cell surface molecules. | Q39334584 |
| | Correlated fluorescence and 3D electron microscopy with high sensitivity and spatial precision | Q39612822 |
| | Missing-in-metastasis and IRSp53 deform PI(4,5)P2-rich membranes by an inverse BAR domain-like mechanism | Q39734937 |
| | Cholesterol-sensitive Cdc42 activation regulates actin polymerization for endocytosis via the GEEC pathway | Q40140638 |
| | Possible role of deep tubular invaginations of the plasma membrane in MHC-I trafficking | Q40426114 |
| | The hydrophobic insertion mechanism of membrane curvature generation by proteins | Q41908234 |
| | Domain-induced budding of fluid membranes | Q42088826 |
| | Lipid cosorting mediated by shiga toxin induced tubulation. | Q42871726 |
| | Real-time visualization of dynamin-catalyzed membrane fission and vesicle release | Q43141309 |
| | Actin dynamics drive membrane reorganization and scission in clathrin-independent endocytosis | Q43152766 |
| | Membrane bending by protein-protein crowding | Q44017551 |
| | Elastic properties of lipid bilayers: theory and possible experiments | Q44282845 |
| | Nanoclusters of GPI-anchored proteins are formed by cortical actin-driven activity. | Q46205813 |
| P433 | issue | 1 | |
| P577 | publication date | 2014-01-01 | |
| P1433 | published in | Cold Spring Harbor Perspectives in Biology | Q3927509 |
| P1476 | title | Bending "on the rocks"--a cocktail of biophysical modules to build endocytic pathways | |
| P478 | volume | 6 | |