review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Pascal S Kaeser | Q87912637 |
P2093 | author name string | Richard G Held | |
P2860 | cites work | The small GTPase Rab6B, a novel Rab6 subfamily member, is cell-type specifically expressed and localised to the Golgi apparatus | Q22254605 |
ELKS1 and Ca(2+) channel subunit β4 interact and colocalize at cerebellar synapses | Q24298132 | ||
An HMM model for coiled-coil domains and a comparison with PSSM-based predictions. | Q52040275 | ||
RIM-BPs Mediate Tight Coupling of Action Potentials to Ca(2+)-Triggered Neurotransmitter Release. | Q52148887 | ||
Synaptotagmin-1 Docks Secretory Vesicles to Syntaxin-1/SNAP-25 Acceptor Complexes | Q56992446 | ||
Local routes revisited: the space and time dependence of the Ca2+ signal for phasic transmitter release at the rat calyx of Held | Q78872717 | ||
Membrane fusion | Q81623456 | ||
Rab6, Rab8, and MICAL3 cooperate in controlling docking and fusion of exocytotic carriers | Q84149697 | ||
[Synaptic vesicles and pouches at the level of "active zones" of the neuromuscular junction] | Q93821507 | ||
Topographic Mapping of the Synaptic Cleft into Adhesive Nanodomains. | Q41863255 | ||
A post-docking role for active zone protein Rim. | Q41977207 | ||
Loss of the calcium channel β4 subunit impairs parallel fibre volley and Purkinje cell firing in cerebellum of adult ataxic mice | Q42414256 | ||
Naked dense bodies provoke depression. | Q42478978 | ||
RIM binding proteins (RBPs) couple Rab3-interacting molecules (RIMs) to voltage-gated Ca(2+) channels | Q42861890 | ||
UNC-13 is required for synaptic vesicle fusion in C. elegans | Q43240851 | ||
Binding to Rab3A-interacting molecule RIM regulates the presynaptic recruitment of Munc13-1 and ubMunc13-2. | Q45345777 | ||
Redundant localization mechanisms of RIM and ELKS in Caenorhabditis elegans. | Q46564659 | ||
A minimal domain responsible for Munc13 activity | Q46755751 | ||
Bruchpilot promotes active zone assembly, Ca2+ channel clustering, and vesicle release | Q47070593 | ||
Bruchpilot, a protein with homology to ELKS/CAST, is required for structural integrity and function of synaptic active zones in Drosophila | Q47072025 | ||
Deletion of the presynaptic scaffold CAST reduces active zone size in rod photoreceptors and impairs visual processing. | Q47288747 | ||
The active zone protein CAST regulates synaptic vesicle recycling and quantal size in the mouse hippocampus | Q47289037 | ||
Transcellular Nanoalignment of Synaptic Function | Q47990307 | ||
Physical and functional interaction of the active zone protein CAST/ERC2 and the β-subunit of the voltage-dependent Ca(2+) channel | Q48519130 | ||
How to Make an Active Zone: Unexpected Universal Functional Redundancy between RIMs and RIM-BPs | Q48564188 | ||
Contribution to the problem of structural organization of the presynaptic area | Q49116549 | ||
Dopamine Secretion Is Mediated by Sparse Active Zone-like Release Sites. | Q49344579 | ||
Liprin-α3 controls vesicle docking and exocytosis at the active zone of hippocampal synapses | Q50035046 | ||
A 1.5Mb terminal deletion of 12p associated with autism spectrum disorder | Q50308424 | ||
CLASPs link focal-adhesion-associated microtubule capture to localized exocytosis and adhesion site turnover | Q24298210 | ||
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 | ||
A conformational switch in syntaxin during exocytosis: role of munc18. | Q24534308 | ||
Membrane fusion: grappling with SNARE and SM proteins | Q24633113 | ||
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 | ||
RIM1 and RIM2 redundantly determine Ca2+ channel density and readily releasable pool size at a large hindbrain synapse | Q26269826 | ||
The active zone protein family ELKS supports Ca2+ influx at nerve terminals of inhibitory hippocampal neurons | Q26269841 | ||
Neurotransmitter release: the last millisecond in the life of a synaptic vesicle | Q26269845 | ||
The presynaptic active zone | Q26269863 | ||
RIM genes differentially contribute to organizing presynaptic release sites | Q26269874 | ||
RIM determines Ca²+ channel density and vesicle docking at the presynaptic active zone | Q26269881 | ||
Cell biology of Ca2+-triggered exocytosis | Q26269905 | ||
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 | ||
RIM1alpha and RIM1beta are synthesized from distinct promoters of the RIM1 gene to mediate differential but overlapping synaptic functions | Q26269937 | ||
A Munc13/RIM/Rab3 tripartite complex: from priming to plasticity? | Q26269969 | ||
Molecular machines governing exocytosis of synaptic vesicles | Q26849286 | ||
Liprin-α1 and ERC1 control cell edge dynamics by promoting focal adhesion turnover | Q27347496 | ||
Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 A resolution | Q27765619 | ||
Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles | Q27863297 | ||
Drosophila UNC-13 is essential for synaptic transmission | Q28145978 | ||
Functional interaction of the active zone proteins Munc13-1 and RIM1 in synaptic vesicle priming | Q28188061 | ||
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 | ||
CLASPs attach microtubule plus ends to the cell cortex through a complex with LL5beta | Q28250713 | ||
Mammalian homologues of Caenorhabditis elegans unc-13 gene define novel family of C2-domain proteins | Q28289561 | ||
Total arrest of spontaneous and evoked synaptic transmission but normal synaptogenesis in the absence of Munc13-mediated vesicle priming | Q28504670 | ||
The calcium sensor synaptotagmin 7 is required for synaptic facilitation | Q28505395 | ||
ELKS controls the pool of readily releasable vesicles at excitatory synapses through its N-terminal coiled-coil domains. | Q37071725 | ||
Formation of Golgi-derived active zone precursor vesicles. | Q37117339 | ||
Maturation of active zone assembly by Drosophila Bruchpilot | Q37267704 | ||
RIM-binding protein 2 regulates release probability by fine-tuning calcium channel localization at murine hippocampal synapses. | Q37346952 | ||
Hierarchical assembly of presynaptic components in defined C. elegans synapses | Q37566924 | ||
Ultrafast endocytosis at mouse hippocampal synapses. | Q37642826 | ||
Synaptic Ribbons Require Ribeye for Electron Density, Proper Synaptic Localization, and Recruitment of Calcium Channels | Q37678588 | ||
Ca(2+) channels and transmitter release at the active zone | Q38017465 | ||
Structure and function of the β subunit of voltage-gated Ca²⁺ channels | Q38043712 | ||
CAST: functional scaffold for the integrity of the presynaptic active zone | Q38091781 | ||
Multiple roles for the active zone protein RIM1alpha in late stages of neurotransmitter release | Q38339903 | ||
A novel region in the CaV2.1 α1 subunit C-terminus regulates fast synaptic vesicle fusion and vesicle docking at the mammalian presynaptic active zone. | Q38429364 | ||
Neurosecretion: what can we learn from chromaffin cells | Q38628008 | ||
ELKS1 localizes the synaptic vesicle priming protein bMunc13-2 to a specific subset of active zones. | Q38713426 | ||
Liprin-α1, ERC1 and LL5 define polarized and dynamic structures that are implicated in cell migration. | Q38979205 | ||
Bassoon specifically controls presynaptic P/Q-type Ca(2+) channels via RIM-binding protein | Q39008473 | ||
The readily releasable pool of synaptic vesicles | Q39095247 | ||
Linking cortical microtubule attachment and exocytosis | Q39297068 | ||
Organization of the presynaptic active zone by ERC2/CAST1-dependent clustering of the tandem PDZ protein syntenin-1. | Q39751775 | ||
RIM-binding protein, a central part of the active zone, is essential for neurotransmitter release | Q39754475 | ||
Molecular profiling of synaptic vesicle docking sites reveals novel proteins but few differences between glutamatergic and GABAergic synapses | Q39755046 | ||
Fusion Competent Synaptic Vesicles Persist upon Active Zone Disruption and Loss of Vesicle Docking | Q39756941 | ||
Rab6 regulates transport and targeting of exocytotic carriers | Q40097541 | ||
Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy | Q40528552 | ||
Synaptotagmins: C2-domain proteins that regulate membrane traffic | Q41118335 | ||
Mechanisms of short-term plasticity at neuromuscular active zones of Drosophila | Q41788883 | ||
Impaired membrane resealing and autoimmune myositis in synaptotagmin VII-deficient mice | Q28511824 | ||
Solution structure of the RIM1alpha PDZ domain in complex with an ELKS1b C-terminal peptide | Q28564444 | ||
The proteome of the presynaptic active zone: from docked synaptic vesicles to adhesion molecules and maxi-channels | Q28567071 | ||
Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex | Q28569612 | ||
Differential expression of two novel Munc13 proteins in rat brain | Q28572369 | ||
Munc18-1 promotes large dense-core vesicle docking | Q28587706 | ||
Characterization of novel Rab6-interacting proteins involved in endosome-to-TGN transport | Q28592027 | ||
Differential control of vesicle priming and short-term plasticity by Munc13 isoforms | Q28592163 | ||
Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit | Q28592875 | ||
A protein interaction node at the neurotransmitter release site: domains of Aczonin/Piccolo, Bassoon, CAST, and rim converge on the N-terminal domain of Munc13-1 | Q28595053 | ||
Rab6 coordinates a novel Golgi to ER retrograde transport pathway in live cells | Q28609753 | ||
GTP-bound forms of rab6 induce the redistribution of Golgi proteins into the endoplasmic reticulum | Q28609828 | ||
Membrane fusion | Q29618140 | ||
12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech | Q30529890 | ||
The Bruchpilot cytomatrix determines the size of the readily releasable pool of synaptic vesicles | Q30543185 | ||
The architecture of active zone material at the frog's neuromuscular junction | Q30981051 | ||
Differential expression of multiple isoforms of the ELKS mRNAs involved in a papillary thyroid carcinoma | Q31106255 | ||
Quantitative analysis of the native presynaptic cytomatrix by cryoelectron tomography | Q33523242 | ||
Heterodimerization of Munc13 C2A domain with RIM regulates synaptic vesicle docking and priming | Q33702262 | ||
Routing of the RAB6 secretory pathway towards the lysosome related organelle of melanocytes | Q33810200 | ||
Fusion of a novel gene, ELKS, to RET due to translocation t(10;12)(q11;p13) in a papillary thyroid carcinoma | Q33862909 | ||
Quantitative proteomics of the Cav2 channel nano-environments in the mammalian brain. | Q34093833 | ||
Fusion of cells by flipped SNAREs | Q34205790 | ||
Timing of neurotransmission at fast synapses in the mammalian brain | Q34406384 | ||
Synaptic computation | Q35918051 | ||
The small GTP-binding protein rab6 functions in intra-Golgi transport | Q36235031 | ||
RIM controls homeostatic plasticity through modulation of the readily-releasable vesicle pool | Q36469214 | ||
Molecular organization of the presynaptic active zone | Q36545836 | ||
Syntaxin opening by the MUN domain underlies the function of Munc13 in synaptic-vesicle priming | Q36734003 | ||
Nanodomain coupling between Ca²⁺ channels and sensors of exocytosis at fast mammalian synapses | Q36742868 | ||
Regulation of membrane fusion in synaptic excitation-secretion coupling: speed and accuracy matter | Q36870246 | ||
How to make a synaptic ribbon: RIBEYE deletion abolishes ribbons in retinal synapses and disrupts neurotransmitter release | Q36906425 | ||
Calcium channels link the muscle-derived synapse organizer laminin β2 to Bassoon and CAST/Erc2 to organize presynaptic active zones | Q37044607 | ||
Reconstitution of the vital functions of Munc18 and Munc13 in neurotransmitter release | Q37071048 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 2 | |
P921 | main subject | peptide | Q172847 |
nerve tissue protein | Q6996861 | ||
P577 | publication date | 2018-02-01 | |
P1433 | published in | Open Biology | Q7095958 |
P1476 | title | ELKS active zone proteins as multitasking scaffolds for secretion | |
P478 | volume | 8 |
Q58553974 | Coupling the Structural and Functional Assembly of Synaptic Release Sites |
Q90246164 | Presynaptic calcium channels: specialized control of synaptic neurotransmitter release |
Q89999397 | Role of the active zone protein, ELKS, in insulin secretion from pancreatic β-cells |
Q98188948 | Synapse development and maturation at the drosophila neuromuscular junction |
Q103756649 | Tissue distribution and subcellular localization of the family of Kidney Ankyrin Repeat Domain (KANK) proteins |
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