| scholarly article | Q13442814 |
| P2093 | author name string | Nicolas Vitale | |
| Petra Tryoen-Toth | |||
| Alice D Lam | |||
| Edward L Stuenkel | |||
| Bill Tsai | |||
| P2860 | cites work | A conformational switch in syntaxin during exocytosis: role of munc18. | Q24534308 |
| SNAREpins: minimal machinery for membrane fusion | Q28131697 | ||
| Syntaxin: a synaptic protein implicated in docking of synaptic vesicles at presynaptic active zones | Q28211190 | ||
| Temperature-sensitive paralytic mutations demonstrate that synaptic exocytosis requires SNARE complex assembly and disassembly | Q28281473 | ||
| Characterization of two alternately spliced forms of phospholipase D1. Activation of the purified enzymes by phosphatidylinositol 4,5-bisphosphate, ADP-ribosylation factor, and Rho family monomeric GTP-binding proteins and protein kinase C-alpha | Q28302448 | ||
| SNAREs are concentrated in cholesterol-dependent clusters that define docking and fusion sites for exocytosis | Q28364095 | ||
| Phospholipase D1: a key factor for the exocytotic machinery in neuroendocrine cells | Q28364949 | ||
| Reconstituted syntaxin1a/SNAP25 interacts with negatively charged lipids as measured by lateral diffusion in planar supported bilayers | Q28367662 | ||
| Botulinum neurotoxin C1 blocks neurotransmitter release by means of cleaving HPC-1/syntaxin | Q28609203 | ||
| SNAREs--engines for membrane fusion | Q29547230 | ||
| Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin | Q29619130 | ||
| Insulin-stimulated plasma membrane fusion of Glut4 glucose transporter-containing vesicles is regulated by phospholipase D1. | Q33841346 | ||
| A role for phospholipase D1 in neurotransmitter release. | Q33953145 | ||
| Rapid fluctuations in transmitter release from single vesicles in bovine adrenal chromaffin cells | Q34017485 | ||
| Measured effects of diacylglycerol on structural and elastic properties of phospholipid membranes | Q34041052 | ||
| Fluorescence resonance energy transfer-based stoichiometry in living cells | Q34179589 | ||
| Protein-Lipid Interplay in Fusion and Fission of Biological Membranes | Q34267537 | ||
| Transmembrane segments of syntaxin line the fusion pore of Ca2+-triggered exocytosis. | Q34305380 | ||
| Analysis of exocytotic events recorded by amperometry | Q34445186 | ||
| Genetic evidence of a role for membrane lipid composition in the regulation of soluble NEM-sensitive factor receptor function in Saccharomyces cerevisiae | Q34643047 | ||
| Asymmetric phospholipid distribution drives in vitro reconstituted SNARE-dependent membrane fusion. | Q35075467 | ||
| Ca2+-dependent regulation of synaptic SNARE complex assembly via a calmodulin- and phospholipid-binding domain of synaptobrevin | Q35212588 | ||
| The energetics of membrane fusion from binding, through hemifusion, pore formation, and pore enlargement | Q35887194 | ||
| SNARE proteins are highly enriched in lipid rafts in PC12 cells: implications for the spatial control of exocytosis. | Q35888471 | ||
| Probing phosphoinositide functions in signaling and membrane trafficking. | Q36113257 | ||
| The physical chemistry of biological membranes | Q36628162 | ||
| The Caenorhabditis elegans unc-64 locus encodes a syntaxin that interacts genetically with synaptobrevin | Q36872521 | ||
| Receptor-mediated regulation of tomosyn-syntaxin 1A interactions in bovine adrenal chromaffin cells | Q40124894 | ||
| Stalk model of membrane fusion: solution of energy crisis | Q40201228 | ||
| Lipids in biological membrane fusion | Q40415555 | ||
| Spontaneous curvature of phosphatidic acid and lysophosphatidic acid. | Q40447703 | ||
| Fluorescence resonance energy transfer reports properties of syntaxin1a interaction with Munc18-1 in vivo | Q40503280 | ||
| Phospholipase D1 regulates secretagogue-stimulated insulin release in pancreatic beta-cells. | Q40566108 | ||
| Site of docking and fusion of insulin secretory granules in live MIN6 beta cells analyzed by TAT-conjugated anti-syntaxin 1 antibody and total internal reflection fluorescence microscopy | Q40607328 | ||
| Chromaffin granule-associated phosphatidylinositol 4-kinase activity is required for stimulated secretion. | Q41064785 | ||
| Transient transfection studies of secretion in bovine chromaffin cells and PC12 cells. Generation of kainate-sensitive chromaffin cells. | Q41552954 | ||
| Syntaxin and synaptobrevin function downstream of vesicle docking in Drosophila | Q41666993 | ||
| Evidence that the inositol phospholipids are necessary for exocytosis. Loss of inositol phospholipids and inhibition of secretion in permeabilized cells caused by a bacterial phospholipase C and removal of ATP. | Q41882249 | ||
| Role of the position of unsaturation on the phase behavior and intrinsic curvature of phosphatidylethanolamines | Q42016351 | ||
| Regulation of neuronal SNARE assembly by the membrane | Q44436595 | ||
| The activation of exocytotic sites by the formation of phosphatidylinositol 4,5-bisphosphate microdomains at syntaxin clusters | Q45291363 | ||
| Progesterone regulation of catecholamine secretion from chromaffin cells | Q46464441 | ||
| Distinct domains of syntaxin are required for synaptic vesicle fusion complex formation and dissociation | Q46887153 | ||
| Type I phosphatidylinositol 4-phosphate 5-kinase isoforms are specifically stimulated by phosphatidic acid. | Q48139459 | ||
| Botulinum neurotoxin type C cleaves a single Lys-Ala bond within the carboxyl-terminal region of syntaxins | Q49164892 | ||
| Clostridial neurotoxins and substrate proteolysis in intact neurons: botulinum neurotoxin C acts on synaptosomal-associated protein of 25 kDa. | Q52202304 | ||
| Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells | Q52423917 | ||
| Lysolipids reversibly inhibit Ca(2+)-, GTP- and pH-dependent fusion of biological membranes. | Q52545773 | ||
| PIP2 increases the speed of response of synaptotagmin and steers its membrane-penetration activity toward the plasma membrane. | Q55038004 | ||
| ATP-dependent inositide phosphorylation required for Ca2+-activated secretion | Q56689852 | ||
| Botulinum neurotoxin A selectively cleaves the synaptic protein SNAP-25 | Q57979097 | ||
| Phospholipase D1 Production of Phosphatidic Acid at the Plasma Membrane Promotes Exocytosis of Large Dense-core Granules at a Late Stage | Q58025406 | ||
| Vesicular restriction of synaptobrevin suggests a role for calcium in membrane fusion | Q58979943 | ||
| Novel function of phosphatidylinositol 4,5-bisphosphate as a cofactor for brain membrane phospholipase D | Q72135980 | ||
| Membrane topologies of neuronal SNARE folding intermediates | Q74702117 | ||
| A model for structural similarity between different SNARE complexes based on sequence relationships | Q77135305 | ||
| Insertion of the membrane-proximal region of the neuronal SNARE coiled coil into the membrane | Q78799372 | ||
| Lipidic antagonists to SNARE-mediated fusion | Q80057614 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 485-497 | |
| P577 | publication date | 2007-11-14 | |
| P1433 | published in | Molecular Biology of the Cell | Q2338259 |
| P1476 | title | SNARE-catalyzed fusion events are regulated by Syntaxin1A-lipid interactions | |
| P478 | volume | 19 |
| Q35867388 | A Coarse Grained Model for a Lipid Membrane with Physiological Composition and Leaflet Asymmetry |
| Q35876833 | A dual role for diacylglycerol kinase generated phosphatidic acid in autoantibody-induced neutrophil exocytosis. |
| Q30408604 | A molecular toggle after exocytosis sequesters the presynaptic syntaxin1a molecules involved in prior vesicle fusion |
| Q35011226 | A new role for the dynamin GTPase in the regulation of fusion pore expansion |
| Q37849817 | A role for V-ATPase subunits in synaptic vesicle fusion? |
| Q46156003 | ARF6 regulates the synthesis of fusogenic lipids for calcium-regulated exocytosis in neuroendocrine cells |
| Q37372099 | Abrogating Munc18-1-SNARE complex interaction has limited impact on exocytosis in PC12 cells |
| Q41844831 | Basic motifs target PSGL-1, CD43, and CD44 to plasma membrane sites where HIV-1 assembles. |
| Q35294357 | Butanol isomers exert distinct effects on voltage-gated calcium channel currents and thus catecholamine secretion in adrenal chromaffin cells. |
| Q42001037 | Calcium-dependent regulation of SNARE-mediated membrane fusion by calmodulin |
| Q36281699 | Characterization of P4 ATPase Phospholipid Translocases (Flippases) in Human and Rat Pancreatic Beta Cells: THEIR GENE SILENCING INHIBITS INSULIN SECRETION |
| Q35536327 | Characterization of phospholipids in insulin secretory granules and mitochondria in pancreatic beta cells and their changes with glucose stimulation |
| Q30435941 | Clustering of syntaxin-1A in model membranes is modulated by phosphatidylinositol 4,5-bisphosphate and cholesterol |
| Q37447913 | Complex lipid requirements for SNARE- and SNARE chaperone-dependent membrane fusion |
| Q33761303 | Differential interaction of tomosyn with syntaxin and SNAP25 depends on domains in the WD40 β-propeller core and determines its inhibitory activity |
| Q30429848 | Docking and fast fusion of synaptobrevin vesicles depends on the lipid compositions of the vesicle and the acceptor SNARE complex-containing target membrane |
| Q35211011 | Evidence for a fence that impedes the diffusion of phosphatidylinositol 4,5-bisphosphate out of the forming phagosomes of macrophages |
| Q42684322 | Evidence that electrostatic interactions between vesicle-associated membrane protein 2 and acidic phospholipids may modulate the fusion of transport vesicles with the plasma membrane |
| Q37508152 | Exocytosis and cell polarity in plants - exocyst and recycling domains. |
| Q39123295 | Fusion pores and their control of neurotransmitter and hormone release. |
| Q35185536 | Groundnut bud necrosis virus encoded NSm associates with membranes via its C-terminal domain |
| Q37313544 | HIV-1 Tat protein perturbs diacylglycerol production at the plasma membrane of neurosecretory cells during exocytosis |
| Q27646399 | Helical extension of the neuronal SNARE complex into the membrane |
| Q37851547 | How important are Rho GTPases in neurosecretion? |
| Q92242558 | Intracellular Vesicle Fusion Requires a Membrane-Destabilizing Peptide Located at the Juxtamembrane Region of the v-SNARE |
| Q37814211 | Links between lipid homeostasis, organelle morphodynamics and protein trafficking in eukaryotic and plant secretory pathways |
| Q37809768 | Lipid dynamics in exocytosis. |
| Q36786543 | Lipid molecules influence early stages of yeast SNARE-mediated membrane fusion. |
| Q47727421 | Lipid remodelling in neuroendocrine secretion |
| Q38560548 | Lipids implicated in the journey of a secretory granule: from biogenesis to fusion |
| Q37178033 | Lipids in Regulated Exocytosis: What are They Doing? |
| Q33990912 | Lumenal protein within secretory granules affects fusion pore expansion |
| Q33880350 | Membrane bending energy and fusion pore kinetics in Ca(2+)-triggered exocytosis |
| Q34226601 | Membrane protein sequestering by ionic protein-lipid interactions |
| Q85392206 | Membrane-proximal tryptophans of synaptobrevin II stabilize priming of secretory vesicles |
| Q30424426 | Molecular mechanism of cholesterol- and polyphosphoinositide-mediated syntaxin clustering |
| Q24315878 | Munc18/Syntaxin interaction kinetics control secretory vesicle dynamics |
| Q34571498 | Neuronal porosome lipidome |
| Q38256514 | PI(4,5)P₂-binding effector proteins for vesicle exocytosis |
| Q61811029 | Phosphatidic Acid: From Pleiotropic Functions to Neuronal Pathology |
| Q38965341 | Phosphatidic acid and neurotransmission |
| Q47685834 | Phosphatidic acid-producing enzymes regulating the synaptic vesicle cycle: Role for PLD? |
| Q36292164 | Phosphatidylinositol 4,5-biphosphate (PIP(2)) lipids regulate the phosphorylation of syntaxin N-terminus by modulating both its position and local structure |
| Q39034153 | Phosphatidylinositol 4,5-biphosphate (PIP2) modulates interaction of syntaxin-1A with sulfonylurea receptor 1 to regulate pancreatic β-cell ATP-sensitive potassium channels |
| Q52652446 | Phosphatidylinositol 4,5-biphosphate (PIP2) modulates syntaxin-1A binding to sulfonylurea receptor 2A to regulate cardiac ATP-sensitive potassium (KATP) channels. |
| Q36790508 | Phosphatidylinositol 4,5-bisphosphate regulates SNARE-dependent membrane fusion |
| Q40308075 | Phosphatidylinositol 4,5-bisphosphate regulation of SNARE function in membrane fusion mediated by CAPS. |
| Q27936601 | Phosphatidylinositol-4,5-bisphosphate and phospholipase D-generated phosphatidic acid specify SNARE-mediated vesicle fusion for prospore membrane formation |
| Q37475313 | Phosphatidylserine regulation of Ca2+-triggered exocytosis and fusion pores in PC12 cells. |
| Q27931924 | Phosphoinositides and SNARE chaperones synergistically assemble and remodel SNARE complexes for membrane fusion |
| Q38980009 | Porosome in Cystic Fibrosis |
| Q26861207 | Real-time imaging of plasma membrane deformations reveals pre-fusion membrane curvature changes and a role for dynamin in the regulation of fusion pore expansion |
| Q64886187 | Regulation of Membrane Turnover by Phosphatidic Acid: Cellular Functions and Disease Implications. |
| Q30432882 | Requirement for Golgi-localized PI(4)P in fusion of COPII vesicles with Golgi compartments |
| Q37374904 | Rescuing the subprime meltdown in insulin exocytosis in diabetes |
| Q37989033 | Role of PI(4,5)P(2) in vesicle exocytosis and membrane fusion |
| Q36528090 | Role of phosphoinositides at the neuronal synapse |
| Q41871108 | SNARE complex zipping as a driving force in the dilation of proteinaceous fusion pores |
| Q34482442 | Secretory vesicles are preferentially targeted to areas of low molecular SNARE density |
| Q34190825 | Solution single-vesicle assay reveals PIP2-mediated sequential actions of synaptotagmin-1 on SNAREs |
| Q28475365 | Synaptic vesicle docking: sphingosine regulates syntaxin1 interaction with Munc18 |
| Q27936803 | The Central Polybasic Region of the Soluble SNARE (Soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor) Vam7 Affects Binding to Phosphatidylinositol 3-Phosphate by the PX (Phox Homology) Domain |
| Q34391853 | The Coffin-Lowry syndrome-associated protein RSK2 regulates neurite outgrowth through phosphorylation of phospholipase D1 (PLD1) and synthesis of phosphatidic acid. |
| Q47407123 | The Dual Function of the Polybasic Juxtamembrane Region of Syntaxin 1A in Clamping Spontaneous Release and Stimulating Ca2+-Triggered Release in Neuroendocrine Cells. |
| Q64277232 | The Membrane Proximal Domain of TRPV1 and TRPV2 Channels Mediates Protein⁻Protein Interactions and Lipid Binding In Vitro |
| Q38837981 | The Molecules of Sperm Exocytosis |
| Q39121037 | The Multifaceted Role of SNARE Proteins in Membrane Fusion. |
| Q34164934 | The eukaryotic signal sequence, YGRL, targets the chlamydial inclusion |
| Q89110786 | The fusion pore, 60 years after the first cartoon |
| Q36864226 | The lipid composition and physical properties of the yeast vacuole affect the hemifusion-fusion transition |
| Q35594101 | The synaptotagmin juxtamembrane domain is involved in neuroexocytosis. |
| Q37806681 | The t-SNARE complex: a close up. |
| Q30494220 | t-SNARE protein conformations patterned by the lipid microenvironment |
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