| P2093 | author name string | Stephan J Sigrist | |
| | Tina Ghelani | |
| P2860 | cites work | Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons | Q22254603 |
| | A family of RIM-binding proteins regulated by alternative splicing: Implications for the genesis of synaptic active zones | Q24312023 |
| | Interaction of the ERC family of RIM-binding proteins with the liprin-alpha family of multidomain proteins | Q24316033 |
| | The LAR transmembrane protein tyrosine phosphatase and a coiled-coil LAR-interacting protein co-localize at focal adhesions | Q24324355 |
| | Liprins, a family of LAR transmembrane protein-tyrosine phosphatase-interacting proteins | Q24324506 |
| | Spontaneous subthreshold activity at motor nerve endings | Q24544018 |
| | Some features of the submicroscopic morphology of synapses in frog and earthworm | Q24641866 |
| | Cast: a novel protein of the cytomatrix at the active zone of synapses that forms a ternary complex with RIM1 and munc13-1 | Q24671839 |
| | Physical and functional interaction of the active zone proteins, CAST, RIM1, and Bassoon, in neurotransmitter release | Q24676624 |
| | Synaptic vesicle exocytosis captured by quick freezing and correlated with quantal transmitter release | Q24682015 |
| | The functional organization of motor nerve terminals | Q38600128 |
| | ELKS1 localizes the synaptic vesicle priming protein bMunc13-2 to a specific subset of active zones. | Q38713426 |
| | Mechanisms controlling assembly and plasticity of presynaptic active zone scaffolds | Q38821752 |
| | The Cerebellar Mossy Fiber Synapse as a Model for High-Frequency Transmission in the Mammalian CNS. | Q38988265 |
| | The readily releasable pool of synaptic vesicles | Q39095247 |
| | Presynaptic morphogenesis, active zone organization and structural plasticity in Drosophila | Q39226947 |
| | The Mechanisms and Functions of Synaptic Facilitation | Q39284166 |
| | Homeostatic Activity-Dependent Tuning of Recurrent Networks for Robust Propagation of Activity | Q39643564 |
| | RIM-binding protein, a central part of the active zone, is essential for neurotransmitter release | Q39754475 |
| | RIM3γ and RIM4γ are key regulators of neuronal arborization. | Q39754850 |
| | Fusion Competent Synaptic Vesicles Persist upon Active Zone Disruption and Loss of Vesicle Docking | Q39756941 |
| | RSY-1 is a local inhibitor of presynaptic assembly in C. elegans | Q39872809 |
| | Estimating synaptic parameters from mean, variance, and covariance in trains of synaptic responses | Q40191777 |
| | Molecular Remodeling of the Presynaptic Active Zone of Drosophila Photoreceptors via Activity-Dependent Feedback. | Q41042257 |
| | α2δ-3 Is Required for Rapid Transsynaptic Homeostatic Signaling | Q41065466 |
| | The liprin protein SYD-2 regulates the differentiation of presynaptic termini in C. elegans | Q41695648 |
| | An open form of syntaxin bypasses the requirement for UNC-13 in vesicle priming | Q41768196 |
| | What is Rate-Limiting during Sustained Synaptic Activity: Vesicle Supply or the Availability of Release Sites | Q41810022 |
| | Septins regulate developmental switching from microdomain to nanodomain coupling of Ca(2+) influx to neurotransmitter release at a central synapse | Q42066054 |
| | Super-resolution microscopy of the synaptic active zone | Q42116692 |
| | Teneurins instruct synaptic partner matching in an olfactory map | Q42149573 |
| | Naked dense bodies provoke depression. | Q42478978 |
| | Munc13-1 C1 domain activation lowers the energy barrier for synaptic vesicle fusion. | Q42507707 |
| | Ultrafast action potentials mediate kilohertz signaling at a central synapse. | Q42681944 |
| | RIM binding proteins (RBPs) couple Rab3-interacting molecules (RIMs) to voltage-gated Ca(2+) channels | Q42861890 |
| | Drosophila neuroligin 1 promotes growth and postsynaptic differentiation at glutamatergic neuromuscular junctions | Q43024195 |
| | Nanodomain coupling at an excitatory cortical synapse. | Q43730440 |
| | Calcium secretion coupling at calyx of Held governed by nonuniform channel-vesicle topography. | Q43906979 |
| | Hair cell synaptic ribbons are essential for synchronous auditory signalling. | Q50473698 |
| | The spatial pattern of exocytosis and post-exocytic mobility of synaptopHluorin in mouse motor nerve terminals. | Q50605937 |
| | Delayed synaptic transmission in Drosophila cacophonynull embryos. | Q50619967 |
| | Loose coupling between Ca2+ channels and release sensors at a plastic hippocampal synapse. | Q50690277 |
| | RIM-BPs Mediate Tight Coupling of Action Potentials to Ca(2+)-Triggered Neurotransmitter Release. | Q52148887 |
| | Active Zone Scaffold Protein Ratios Tune Functional Diversity across Brain Synapses. | Q52803563 |
| | ELKS active zone proteins as multitasking scaffolds for secretion. | Q53840590 |
| | Properties of synaptic transmission at single hippocampal synaptic boutons | Q59080676 |
| | Quantal mechanism of neural transmitter release | Q68625734 |
| | The nature of the neuromuscular block produced by magnesium | Q73536420 |
| | [Synaptic vesicles and pouches at the level of "active zones" of the neuromuscular junction] | Q93821507 |
| | The active zone protein family ELKS supports Ca2+ influx at nerve terminals of inhibitory hippocampal neurons | Q26269841 |
| | The presynaptic active zone | Q26269863 |
| | RIM determines Ca²+ channel density and vesicle docking at the presynaptic active zone | Q26269881 |
| | Munc13 C2B domain is an activity-dependent Ca2+ regulator of synaptic exocytosis | Q26269911 |
| | RIM proteins activate vesicle priming by reversing autoinhibitory homodimerization of Munc13 | Q26269920 |
| | RIM proteins tether Ca2+ channels to presynaptic active zones via a direct PDZ-domain interaction | Q26269921 |
| | ELKS2alpha/CAST deletion selectively increases neurotransmitter release at inhibitory synapses | Q26269927 |
| | A Munc13/RIM/Rab3 tripartite complex: from priming to plasticity? | Q26269969 |
| | Role of Bassoon and Piccolo in Assembly and Molecular Organization of the Active Zone | Q26770446 |
| | Molecular machines governing exocytosis of synaptic vesicles | Q26849286 |
| | Deep molecular diversity of mammalian synapses: why it matters and how to measure it | Q26998700 |
| | Presynaptic spinophilin tunes neurexin signalling to control active zone architecture and function | Q27322542 |
| | Merits and Limitations of Vesicle Pool Models in View of Heterogeneous Populations of Synaptic Vesicles | Q28081497 |
| | Association of the kinesin motor KIF1A with the multimodular protein liprin-alpha | Q28202542 |
| | RIM1alpha forms a protein scaffold for regulating neurotransmitter release at the active zone | Q28215837 |
| | CAST2: identification and characterization of a protein structurally related to the presynaptic cytomatrix protein CAST | Q28238737 |
| | Subcellular distribution of docking/fusion proteins in neutrophils, secretory cells with multiple exocytic compartments | Q28285149 |
| | Total arrest of spontaneous and evoked synaptic transmission but normal synaptogenesis in the absence of Munc13-mediated vesicle priming | Q28504670 |
| | Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis | Q28506181 |
| | The morphological and molecular nature of synaptic vesicle priming at presynaptic active zones | Q28506683 |
| | Beta phorbol ester- and diacylglycerol-induced augmentation of transmitter release is mediated by Munc13s and not by PKCs | Q28511979 |
| | Identification of a Munc13-sensitive step in chromaffin cell large dense-core vesicle exocytosis | Q28564812 |
| | Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex | Q28569612 |
| | The RIM/NIM family of neuronal C2 domain proteins. Interactions with Rab3 and a new class of Src homology 3 domain proteins | Q28570571 |
| | Definition of Munc13-homology-domains and characterization of a novel ubiquitously expressed Munc13 isoform | Q28576630 |
| | Neurexin mediates the assembly of presynaptic terminals | Q28585766 |
| | Elfn1 regulates target-specific release probability at CA1-interneuron synapses | Q28592199 |
| | Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis | Q28593220 |
| | The Munc13 proteins differentially regulate readily releasable pool dynamics and calcium-dependent recovery at a central synapse | Q28593555 |
| | Relating structure and function of inner hair cell ribbon synapses | Q30407369 |
| | Bassoon and the synaptic ribbon organize Ca²+ channels and vesicles to add release sites and promote refilling | Q30497701 |
| | The Bruchpilot cytomatrix determines the size of the readily releasable pool of synaptic vesicles | Q30543185 |
| | Quantitative super-resolution imaging of Bruchpilot distinguishes active zone states | Q30586285 |
| | Drosophila liprin-alpha and the receptor phosphatase Dlar control synapse morphogenesis | Q43946448 |
| | Different Munc13 isoforms function as priming factors in lytic granule release from murine cytotoxic T lymphocytes | Q44359640 |
| | The BMP homolog Gbb provides a retrograde signal that regulates synaptic growth at the Drosophila neuromuscular junction. | Q44520391 |
| | wishful thinking encodes a BMP type II receptor that regulates synaptic growth in Drosophila | Q45121632 |
| | SYD-2 Liprin-alpha organizes presynaptic active zone formation through ELKS. | Q45958930 |
| | Synaptic vesicles in mature calyx of Held synapses sense higher nanodomain calcium concentrations during action potential-evoked glutamate release | Q46178156 |
| | Drosophila Syd-1 Has RhoGAP Activity That Is Required for Presynaptic Clustering of Bruchpilot/ELKS but Not Neurexin-1. | Q46245687 |
| | Developmental transformation of the release modality at the calyx of Held synapse. | Q46448188 |
| | SYD-1, a presynaptic protein with PDZ, C2 and rhoGAP-like domains, specifies axon identity in C. elegans | Q46453307 |
| | Redundant localization mechanisms of RIM and ELKS in Caenorhabditis elegans. | Q46564659 |
| | Activity-dependent site-specific changes of glutamate receptor composition in vivo | Q46602691 |
| | Glutamate receptor dynamics organizing synapse formation in vivo | Q46682134 |
| | Nanodomain coupling between Ca2+ channels and Ca2+ sensors promotes fast and efficient transmitter release at a cortical GABAergic synapse | Q46730437 |
| | A minimal domain responsible for Munc13 activity | Q46755751 |
| | Fast vesicle reloading and a large pool sustain high bandwidth transmission at a central synapse. | Q46958777 |
| | Role of efficient neurotransmitter release in barrel map development. | Q46981392 |
| | Synaptic calcium-channel function in Drosophila: analysis and transformation rescue of temperature-sensitive paralytic and lethal mutations of cacophony. | Q47071378 |
| | Bruchpilot, a protein with homology to ELKS/CAST, is required for structural integrity and function of synaptic active zones in Drosophila | Q47072025 |
| | Cooperation of Syd-1 with Neurexin synchronizes pre- with postsynaptic assembly. | Q47072312 |
| | Active zone localization of presynaptic calcium channels encoded by the cacophony locus of Drosophila. | Q47072697 |
| | The Drosophila BMP type II receptor Wishful Thinking regulates neuromuscular synapse morphology and function | Q47072727 |
| | Clarinet (CLA-1), a novel active zone protein required for synaptic vesicle clustering and release. | Q47163565 |
| | Synaptic weight set by Munc13-1 supramolecular assemblies. | Q47174177 |
| | How to maintain active zone integrity during high-frequency transmission. | Q47314041 |
| | Creating diverse synapses from the same molecules | Q47850254 |
| | Stable Positioning of Unc13 Restricts Synaptic Vesicle Fusion to Defined Release Sites to Promote Synchronous Neurotransmission | Q47862604 |
| | Quantal Fluctuations in Central Mammalian Synapses: Functional Role of Vesicular Docking Sites | Q48142509 |
| | Developmental tightening of cerebellar cortical synaptic influx-release coupling. | Q48228732 |
| | The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina | Q48368679 |
| | Dynamic control of synaptic vesicle replenishment and short-term plasticity by Ca(2+)-calmodulin-Munc13-1 signaling | Q48461386 |
| | Neurotransmission: spontaneous and evoked release filing for divorce | Q48543921 |
| | Actin- and Myosin-Dependent Vesicle Loading of Presynaptic Docking Sites Prior to Exocytosis | Q48564179 |
| | How to Make an Active Zone: Unexpected Universal Functional Redundancy between RIMs and RIM-BPs | Q48564188 |
| | Active zone protein CAST is a component of conventional and ribbon synapses in mouse retina | Q48646131 |
| | Developmental changes in Ca2+ channel subtypes regulating endocytosis at the calyx of Held | Q48728279 |
| | Munc13-3 Is Required for the Developmental Localization of Ca2+ Channels to Active Zones and the Nanopositioning of Cav2.1 Near Release Sensors. | Q50422450 |
| | Vesicle docking in regulated exocytosis. | Q37150432 |
| | Spontaneous and evoked release are independently regulated at individual active zones | Q37266482 |
| | Maturation of active zone assembly by Drosophila Bruchpilot | Q37267704 |
| | Multiple roles of calcium ions in the regulation of neurotransmitter release | Q37279408 |
| | Position of UNC-13 in the active zone regulates synaptic vesicle release probability and release kinetics | Q37290090 |
| | RIM-binding protein 2 regulates release probability by fine-tuning calcium channel localization at murine hippocampal synapses. | Q37346952 |
| | Liprin-α/SYD-2 determines the size of dense projections in presynaptic active zones in C. elegans | Q37379005 |
| | UNC-13 and UNC-10/rim localize synaptic vesicles to specific membrane domains. | Q37417587 |
| | Assembling the presynaptic active zone | Q37460406 |
| | Rab3 dynamically controls protein composition at active zones. | Q37484962 |
| | Hierarchical assembly of presynaptic components in defined C. elegans synapses | Q37566924 |
| | Action potential evoked transmitter release in central synapses: insights from the developing calyx of Held | Q37638786 |
| | The active zone T-bar--a plasticity module? | Q37765592 |
| | CAST and ELKS proteins: structural and functional determinants of the presynaptic active zone | Q37767955 |
| | Molecular organization and plasticity of the cytomatrix at the active zone | Q37949766 |
| | Short-term presynaptic plasticity | Q38023125 |
| | Theoretical models of synaptic short term plasticity | Q38102690 |
| | Seeing the forest tree by tree: super-resolution light microscopy meets the neurosciences | Q38116904 |
| | Pushing synaptic vesicles over the RIM. | Q38437297 |
| | Ca2+ channel to synaptic vesicle distance accounts for the readily releasable pool kinetics at a functionally mature auditory synapse. | Q38445469 |
| | The architecture of active zone material at the frog's neuromuscular junction | Q30981051 |
| | Electron microscopy of basophilic structures of some invertebrate oocytes. I. Periodic lamellane and the nuclear envelope | Q30984793 |
| | Differential expression of multiple isoforms of the ELKS mRNAs involved in a papillary thyroid carcinoma | Q31106255 |
| | The coupling between synaptic vesicles and Ca2+ channels determines fast neurotransmitter release | Q33273491 |
| | Evoked and spontaneous transmission favored by distinct sets of synapses | Q33598497 |
| | Immunocytochemical localization of synaptic proteins to photoreceptor synapses of Drosophila melanogaster | Q33644628 |
| | Two pools of vesicles associated with the presynaptic cytosolic projection in Drosophila neuromuscular junctions | Q33647528 |
| | Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices | Q33688834 |
| | A Syd-1 homologue regulates pre- and postsynaptic maturation in Drosophila | Q33689606 |
| | Presynaptic LRP4 promotes synapse number and function of excitatory CNS neurons | Q33793623 |
| | The presynaptic dense projection of the Caenorhabditis elegans cholinergic neuromuscular junction localizes synaptic vesicles at the active zone through SYD-2/liprin and UNC-10/RIM-dependent interactions | Q33853608 |
| | Numbers of presynaptic Ca2+ channel clusters match those of functionally defined vesicular docking sites in single central synapses | Q33865652 |
| | Quantal currents at single-site central synapses | Q33957012 |
| | The calyx of Held synapse: from model synapse to auditory relay | Q34228357 |
| | The membrane fusion enigma: SNAREs, Sec1/Munc18 proteins, and their accomplices--guilty as charged? | Q34305507 |
| | Active zone scaffolds differentially accumulate Unc13 isoforms to tune Ca(2+) channel-vesicle coupling | Q34537376 |
| | Neurexin-1 is required for synapse formation and larvae associative learning in Drosophila. | Q34627866 |
| | Three-dimensional architecture of presynaptic terminal cytomatrix. | Q34642485 |
| | Nanodomain coupling explains Ca²⁺ independence of transmitter release time course at a fast central synapse | Q34729496 |
| | Nanoscale distribution of presynaptic Ca(2+) channels and its impact on vesicular release during development. | Q35008556 |
| | Presynaptic nanodomains: a tale of two synapses | Q35012672 |
| | Neurexin-neuroligin transsynaptic interaction mediates learning-related synaptic remodeling and long-term facilitation in aplysia | Q35104642 |
| | Synaptic diversity enables temporal coding of coincident multisensory inputs in single neurons | Q35549622 |
| | An Exclusion Zone for Ca2+ Channels around Docked Vesicles Explains Release Control by Multiple Channels at a CNS Synapse | Q35624301 |
| | Orchestrating development and function: retrograde BMP signaling in the Drosophila nervous system | Q35704573 |
| | The architecture of the active zone in the presynaptic nerve terminal | Q35894403 |
| | Presynaptic active zones in invertebrates and vertebrates | Q36004250 |
| | Crucial role of Drosophila neurexin in proper active zone apposition to postsynaptic densities, synaptic growth, and synaptic transmission | Q36087830 |
| | RIM promotes calcium channel accumulation at active zones of the Drosophila neuromuscular junction. | Q36450432 |
| | RIM controls homeostatic plasticity through modulation of the readily-releasable vesicle pool | Q36469214 |
| | Active zone assembly and synaptic release. | Q36628647 |
| | Nanodomain coupling between Ca²⁺ channels and sensors of exocytosis at fast mammalian synapses | Q36742868 |
| | ELKS controls the pool of readily releasable vesicles at excitatory synapses through its N-terminal coiled-coil domains. | Q37071725 |
| | UNC-13L, UNC-13S, and Tomosyn form a protein code for fast and slow neurotransmitter release in Caenorhabditis elegans | Q37094524 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 81 | |
| P577 | publication date | 2018-01-01 | |
| P1433 | published in | Frontiers in Neuroanatomy | Q1893158 |
| P1476 | title | Coupling the Structural and Functional Assembly of Synaptic Release Sites | |
| P478 | volume | 12 | |