Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 241 checked references that resolve
resolves10.1111/jnc.13865C2‐domain containing calcium sensors in neuroendocrine secretion
resolves10.1016/0092-8674(93)90376-2A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion
resolves10.1038/1799The synaptic SNARE complex is a parallel four-stranded helical bundle
resolves10.1038/26412Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolution
resolves10.1016/S0092-8674(00)80512-7Structure and Conformational Changes in NSF and Its Membrane Receptor Complexes Visualized by Quick-Freeze/Deep-Etch Electron Microscopy
resolves10.1038/362318a0SNAP receptors implicated in vesicle targeting and fusion
resolves10.1073/pnas.95.26.15781Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs
resolves10.1038/sj.emboj.7601003Sequential N‐ to C‐terminal SNARE complex assembly drives priming and fusion of secretory vesicles
resolves10.1073/pnas.0812356106Effects of linker sequences on vesicle fusion mediated by lipid-anchored DNA oligonucleotides
resolves10.1073/pnas.96.22.12571Content mixing and membrane integrity during membrane fusion driven by pairing of isolated v-SNAREs and t-SNAREs
resolves10.1073/pnas.1107900108In vitro system capable of differentiating fast Ca
<sup>2+</sup>
-triggered content mixing from lipid exchange for mechanistic studies of neurotransmitter release
resolves10.1042/BJ20131668Multiple conformations of a single SNAREpin between two nanodisc membranes reveal diverse pre-fusion states
resolves10.1126/science.1221976Membrane Fusion Intermediates via Directional and Full Assembly of the SNARE Complex
resolves10.1073/pnas.1101818108Two synaptobrevin molecules are sufficient for vesicle fusion in central nervous system synapses
resolves10.1038/ncomms2692Mechanical unzipping and rezipping of a single SNARE complex reveals hysteresis as a force-generating mechanism
resolves10.1016/j.neuron.2013.09.010Lipid-Anchored SNAREs Lacking Transmembrane Regions Fully Support Membrane Fusion during Neurotransmitter Release
resolves10.1038/nature24469A tethering complex drives the terminal stage of SNARE-dependent membrane fusion
resolves10.7554/eLife.22567Mechanistic insights into neurotransmitter release and presynaptic plasticity from the crystal structure of Munc13-1 C1C2BMUN
resolves10.1074/jbc.271.34.20223N-Ethylmaleimide-sensitive Factor Acts at a Prefusion ATP-dependent Step in Ca2+-activated Exocytosis
resolves10.1038/11097Crystal structure of the amino-terminal domain of N-ethylmaleimide-sensitive fusion protein
resolves10.1074/jbc.270.49.29182Each Domain of the N-Ethylmaleimide-sensitive Fusion Protein Contributes to Its Transport Activity
resolves10.1038/1843Structure of the ATP-dependent oligomerization domain of N-ethylmaleimide sensitive factor complexed with ATP
resolves10.1083/jcb.126.4.945N-ethylmaleimide-sensitive fusion protein: a trimeric ATPase whose hydrolysis of ATP is required for membrane fusion.
resolves10.1038/nature14148Mechanistic insights into the recycling machine of the SNARE complex
resolves10.1074/jbc.M109.045286A Conserved Membrane Attachment Site in α-SNAP Facilitates N-Ethylmaleimide-sensitive Factor (NSF)-driven SNARE Complex Disassembly
resolves10.1038/emboj.2010.97HOPS prevents the disassembly of trans‐SNARE complexes by Sec17p/Sec18p during membrane fusion
resolves10.1038/emboj.2008.139Reconstituted membrane fusion requires regulatory lipids, SNAREs and synergistic SNARE chaperones
resolves10.1093/emboj/17.12.3269Vam7p, a vacuolar SNAP‐25 homolog, is required for SNARE complex integrity and vacuole docking and fusion
resolves10.1083/jcb.200811082Capture and release of partially zipped trans-SNARE complexes on intact organelles
resolves10.7554/eLife.26646Sec17/Sec18 act twice, enhancing membrane fusion and then disassembling cis-SNARE complexes
resolves10.7554/eLife.27396Sec17 (α-SNAP) and an SM-tethering complex regulate the outcome of SNARE zippering in vitro and in vivo
resolves10.1126/science.1230473Reconstitution of the Vital Functions of Munc18 and Munc13 in Neurotransmitter Release
resolves10.1074/jbc.RA118.003313Arrest of trans-SNARE zippering uncovers loosely and tightly docked intermediates in membrane fusion
resolves10.1038/35006120Three-dimensional structure of the neuronal-Sec1–syntaxin 1a complex
resolves10.1038/nsmb.3038Syntaxin opening by the MUN domain underlies the function of Munc13 in synaptic-vesicle priming
resolves10.1073/pnas.122623799Total arrest of spontaneous and evoked synaptic transmission but normal synaptogenesis in the absence of Munc13-mediated vesicle priming
resolves10.1038/14755UNC-13 is required for synaptic vesicle fusion in C. elegans
resolves10.1038/14764Drosophila Unc-13 is essential for synaptic transmission
resolves10.1038/emboj.2008.37Munc18a controls SNARE assembly through its interaction with the syntaxin N‐peptide
resolves10.1038/nsmb.2047Munc13 mediates the transition from the closed syntaxin–Munc18 complex to the SNARE complex
resolves10.1074/jbc.272.4.2520Direct Interaction of the Rat unc-13 Homologue Munc13-1 with the N Terminus of Syntaxin
resolves10.1038/35085583An open form of syntaxin bypasses the requirement for UNC-13 in vesicle priming
resolves10.1083/jcb.200812026Munc18-1 binding to the neuronal SNARE complex controls synaptic vesicle priming
resolves10.7554/eLife.09580Munc18-1-regulated stage-wise SNARE assembly underlying synaptic exocytosis
resolves10.1021/bi9021878Binding of Munc18-1 to Synaptobrevin and to the SNARE Four-Helix Bundle
resolves10.1073/pnas.1012997108Syntaxin N-terminal peptide motif is an initiation factor for the assembly of the SNARE–Sec1/Munc18 membrane fusion complex
resolves10.1038/emboj.2012.307Syntaxin‐1 N‐peptide and Habc‐domain perform distinct essential functions in synaptic vesicle fusion
resolves10.1091/mbc.E09-08-0712Rescue of Munc18-1 and -2 Double Knockdown Reveals the Essential Functions of Interaction between Munc18 and Closed Syntaxin in PC12 Cells
resolves10.1038/emboj.2012.72Munc18‐1 mutations that strongly impair SNARE‐complex binding support normal synaptic transmission
resolves10.1126/science.aac7906A direct role for the Sec1/Munc18-family protein Vps33 as a template for SNARE assembly
resolves10.1074/jbc.M113.514273An Extended Helical Conformation in Domain 3a of Munc18-1 Provides a Template for SNARE (Soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor) Complex Assembly
resolves10.1073/pnas.0914906108Possible roles for Munc18-1 domain 3a and Syntaxin1 N-peptide and C-terminal anchor in SNARE complex formation
resolves10.7554/eLife.24278Autoinhibition of Munc18-1 modulates synaptobrevin binding and helps to enable Munc13-dependent regulation of membrane fusion
resolves10.15252/embj.201696270An activated Q‐SNARE/SM protein complex as a possible intermediate in SNARE assembly
resolves10.15252/embj.201695775Conformational change of syntaxin linker region induced by Munc13s initiates SNARE complex formation in synaptic exocytosis
resolves10.1021/bi702345mBinding of the Munc13-1 MUN Domain to Membrane-Anchored SNARE Complexes
resolves10.1016/j.str.2007.12.010Accessory Proteins Stabilize the Acceptor Complex for Synaptobrevin, the 1:1 Syntaxin/SNAP-25 Complex
resolves10.1038/ncomms15915Munc13-1 and Munc18-1 together prevent NSF-dependent de-priming of synaptic vesicles
resolves10.1523/JNEUROSCI.0338-17.2017UNC-18 and Tomosyn Antagonistically Control Synaptic Vesicle Priming Downstream of UNC-13 in <i>Caenorhabditis elegans</i>
resolves10.1016/S0092-8674(01)00635-3β Phorbol Ester- and Diacylglycerol-Induced Augmentation of Transmitter Release Is Mediated by Munc13s and Not by PKCs
resolves10.1021/bi0476127Intramolecular Occlusion of the Diacylglycerol-Binding Site in the C<sub>1</sub> Domain of Munc13-1<sup>,</sup>
resolves10.1038/nsmb.1758Munc13 C2B domain is an activity-dependent Ca2+ regulator of synaptic exocytosis
resolves10.1038/ncomms15293Heterodimerization of Munc13 C2A domain with RIM regulates synaptic vesicle docking and priming
resolves10.1038/emboj.2009.373Modular architecture of Munc13/calmodulin complexes: dual regulation by Ca2+ and possible function in short‐term synaptic plasticity
resolves10.1016/j.cell.2004.06.029Calmodulin and Munc13 Form a Ca2+ Sensor/Effector Complex that Controls Short-Term Synaptic Plasticity
resolves10.1038/415321aRIM1α forms a protein scaffold for regulating neurotransmitter release at the active zone
resolves10.1038/nn732A post-docking role for active zone protein Rim
resolves10.1016/j.cell.2010.12.029RIM Proteins Tether Ca2+ Channels to Presynaptic Active Zones via a Direct PDZ-Domain Interaction
resolves10.1038/415327aRIM1α is required for presynaptic long-term potentiation
resolves10.1038/41580Rim is a putative Rab3 effector in regulating synaptic-vesicle fusion
resolves10.1038/41574Rab3A is essential for mossy fibre long-term potentiation in the hippocampus
resolves10.1073/pnas.0803012105Complexins facilitate neurotransmitter release at excitatory and inhibitory synapses in mammalian central nervous system
resolves10.1038/nrn.2015.16Should I stop or should I go? The role of complexin in neurotransmitter release
resolves10.1073/pnas.1321367110Deconstructing complexin function in activating and clamping Ca
<sup>2+</sup>
-triggered exocytosis by comparing knockout and knockdown phenotypes
resolves10.1038/nsmb.1791Binding of the complexin N terminus to the SNARE complex potentiates synaptic-vesicle fusogenicity
resolves10.1038/nsmb1124Hemifusion arrest by complexin is relieved by Ca2+–synaptotagmin I
resolves10.1038/nn1980A complexin fusion clamp regulates spontaneous neurotransmitter release and synaptic growth
resolves10.1038/nsmb1292Distinct domains of complexin I differentially regulate neurotransmitter release
resolves10.1038/ncomms5955Membrane curvature sensing by the C-terminal domain of complexin
resolves10.3389/fnmol.2017.00146Evolutionary Divergence of the C-terminal Domain of Complexin Accounts for Functional Disparities between Vertebrate and Invertebrate Complexins
resolves10.1016/j.neuron.2009.09.043Tilting the Balance between Facilitatory and Inhibitory Functions of Mammalian and Drosophila Complexins Orchestrates Synaptic Vesicle Exocytosis
resolves10.1523/JNEUROSCI.3360-11.2012C-Terminal Complexin Sequence Is Selectively Required for Clamping and Priming But Not for Ca<sup>2+</sup>Triggering of Synaptic Exocytosis
resolves10.1038/nature23484The primed SNARE–complexin–synaptotagmin complex for neuronal exocytosis
resolves10.1021/ja407392nComplexin-1 Enhances the On-Rate of Vesicle Docking via Simultaneous SNARE and Membrane Interactions
resolves10.1038/nsmb.2103A conformational switch in complexin is required for synaptotagmin to trigger synaptic fusion
resolves10.1038/nsmb.2102Complexin activates and clamps SNAREpins by a common mechanism involving an intermediate energetic state
resolves10.7554/eLife.30286Reconciling isothermal titration calorimetry analyses of interactions between complexin and truncated SNARE complexes
resolves10.1073/pnas.1409311111Genetic analysis of the Complexin trans-clamping model for cross-linking SNARE complexes in vivo
resolves10.7554/eLife.04553The accessory helix of complexin functions by stabilizing central helix secondary structure
resolves10.7554/eLife.16886Complexin induces a conformational change at the membrane-proximal C-terminal end of the SNARE complex
resolves10.1016/j.neuron.2013.10.026Synaptotagmin-1 and Synaptotagmin-7 Trigger Synchronous and Asynchronous Phases of Neurotransmitter Release
resolves10.1038/nn.2320Synaptotagmin-1 functions as a Ca2+ sensor for spontaneous release
resolves10.1371/journal.pbio.1002267Synaptotagmin-1 and -7 Are Redundantly Essential for Maintaining the Capacity of the Readily-Releasable Pool of Synaptic Vesicles
resolves10.1038/s41593-017-0037-5Synaptotagmin-1 drives synchronous Ca2+-triggered fusion by C2B-domain-mediated synaptic-vesicle-membrane attachment
resolves10.1021/bi981789hSolution Structures of the Ca<sup>2+</sup>-free and Ca<sup>2+</sup>-bound C<sub>2</sub>A Domain of Synaptotagmin I: Does Ca<sup>2+</sup> Induce a Conformational Change?
resolves10.1021/bi9807512Mechanism of Phospholipid Binding by the C<sub>2</sub>A-Domain of Synaptotagmin I
resolves10.1038/35065004Synaptotagmin I functions as a calcium regulator of release probability
resolves10.1073/pnas.0509153102Augmenting neurotransmitter release by enhancing the apparent Ca
<sup>2+</sup>
affinity of synaptotagmin 1
resolves10.1038/nature00846The C2B Ca2+-binding motif of synaptotagmin is required for synaptic transmission in vivo
resolves10.1523/JNEUROSCI.2545-04.2004Dual Roles of the C<sub>2</sub>B Domain of Synaptotagmin I in Synchronizing Ca<sup>2+</sup>-Dependent Neurotransmitter Release
resolves10.1073/pnas.0908798106Differential but convergent functions of Ca
<sup>2+</sup>
binding to synaptotagmin-1 C
<sub>2</sub>
domains mediate neurotransmitter release
resolves10.1523/JNEUROSCI.4652-11.2012Calcium Binding by Synaptotagmin's C<sub>2</sub>A Domain is an Essential Element of the Electrostatic Switch That Triggers Synchronous Synaptic Transmission
resolves10.1038/nature21720Postsynaptic synaptotagmins mediate AMPA receptor exocytosis during LTP
resolves10.1073/pnas.1710708114Exceptionally tight membrane-binding may explain the key role of the synaptotagmin-7 C
<sub>2</sub>
A domain in asynchronous neurotransmitter release
resolves10.1038/nsmb709PIP2 increases the speed of response of synaptotagmin and steers its membrane-penetration activity toward the plasma membrane
resolves10.1074/jbc.M600888200Phosphatidylinositol Phosphates as Co-activators of Ca2+ Binding to C2 Domains of Synaptotagmin 1
resolves10.1038/nsmb1056Close membrane-membrane proximity induced by Ca2+-dependent multivalent binding of synaptotagmin-1 to phospholipids
resolves10.1038/nsmb.1508The Janus-faced nature of the C2B domain is fundamental for synaptotagmin-1 function
resolves10.1038/nsmb.3035Dynamic binding mode of a Synaptotagmin-1–SNARE complex in solution
resolves10.1038/nature14975Architecture of the synaptotagmin–SNARE machinery for neuronal exocytosis
resolves10.1083/jcb.200203135Calcium-independent stimulation of membrane fusion and SNAREpin formation by synaptotagmin I
resolves10.1126/science.1097196Reconstitution of Ca
<sup>2+</sup>
-Regulated Membrane Fusion by Synaptotagmin and SNAREs
resolves10.1126/science.1187722Dynamic Ca
<sup>2+</sup>
-Dependent Stimulation of Vesicle Fusion by Membrane-Anchored Synaptotagmin 1
resolves10.1038/nsmb.2075Mechanism and function of synaptotagmin-mediated membrane apposition
resolves10.1038/nsmb.2061Synaptotagmin-1 may be a distance regulator acting upstream of SNARE nucleation
resolves10.1038/nsmb.2375Controlling synaptotagmin activity by electrostatic screening
resolves10.1038/emboj.2012.57Solution single‐vesicle assay reveals PIP2‐mediated sequential actions of synaptotagmin‐1 on SNAREs
resolves10.1021/bi400230uAnalysis of SNARE Complex/Synaptotagmin-1 Interactions by One-Dimensional NMR Spectroscopy
resolves10.1038/nsmb.3097Synaptotagmin-1 binds to PIP2-containing membrane but not to SNAREs at physiological ionic strength
resolves10.7554/eLife.00109Synaptic proteins promote calcium-triggered fast transition from point contact to full fusion
resolves10.1038/nsmb.1763Single-molecule FRET–derived model of the synaptotagmin 1–SNARE fusion complex
resolves10.1523/JNEUROSCI.1011-16.2016Interactions Between SNAP-25 and Synaptotagmin-1 Are Involved in Vesicle Priming, Clamping Spontaneous and Stimulating Evoked Neurotransmission
resolves10.7554/eLife.28409A synaptotagmin suppressor screen indicates SNARE binding controls the timing and Ca2+ cooperativity of vesicle fusion
resolves10.1038/10076Structure of the Janus-faced C2B domain of rabphilin
resolves10.1038/ncomms10971Different states of synaptotagmin regulate evoked versus spontaneous release
resolves10.1002/1873-3468.12874Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission
resolves10.1083/jcb.200908082Quantitative analysis of the native presynaptic cytomatrix by cryoelectron tomography
resolves10.3389/fnmol.2017.00380Productive and Non-productive Pathways for Synaptotagmin 1 to Support Ca2+-Triggered Fast Exocytosis
resolves10.1021/cn5002667Amperometric Detection of Single Vesicle Acetylcholine Release Events from an Artificial Cell
resolves10.15252/embj.201796484Tyrosine phosphorylation of Munc18‐1 inhibits synaptic transmission by preventing SNARE assembly
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