scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | S. O. Rizzoli | |
P2860 | cites work | Long-term relationships between synaptic tenacity, synaptic remodeling, and network activity | Q21145818 |
Cholesterol binds to synaptophysin and is required for biogenesis of synaptic vesicles | Q22011017 | ||
The synaptic vesicle cycle | Q24297813 | ||
The neuron-specific kinesin superfamily protein KIF1A is a unique monomeric motor for anterograde axonal transport of synaptic vesicle precursors | Q24307447 | ||
Structure, function and regulation of the vacuolar (H+)-ATPase | Q24323225 | ||
External push and internal pull forces recruit curvature-sensing N-BAR domain proteins to the plasma membrane | Q24339419 | ||
Transport route for synaptobrevin via a novel pathway of insertion into the endoplasmic reticulum membrane | Q24568369 | ||
Superresolution imaging of chemical synapses in the brain | Q24599389 | ||
Synaptophysin, a major synaptic vesicle protein, is not essential for neurotransmitter release | Q24601743 | ||
Doc2b is a high-affinity Ca2+ sensor for spontaneous neurotransmitter release | Q24611697 | ||
Counting the number of releasable synaptic vesicles in a presynaptic terminal | Q24646074 | ||
Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs | Q24656954 | ||
Synaptic vesicle exocytosis captured by quick freezing and correlated with quantal transmitter release | Q24682015 | ||
Activation of endosomal dynein motors by stepwise assembly of Rab7-RILP-p150Glued, ORP1L, and the receptor betalll spectrin | Q24683555 | ||
RIM genes differentially contribute to organizing presynaptic release sites | Q26269874 | ||
RIM determines Ca²+ channel density and vesicle docking at the presynaptic active zone | Q26269881 | ||
CSPα knockout causes neurodegeneration by impairing SNAP-25 function | Q26269887 | ||
Doc2 supports spontaneous synaptic transmission by a Ca(2+)-independent mechanism | Q26269899 | ||
Piccolo and bassoon maintain synaptic vesicle clustering without directly participating in vesicle exocytosis | Q26269909 | ||
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 | ||
Synaptophysin is targeted to similar microvesicles in CHO and PC12 cells | Q26269968 | ||
rab3 is a small GTP-binding protein exclusively localized to synaptic vesicles | Q26269982 | ||
Molecular machines governing exocytosis of synaptic vesicles | Q26849286 | ||
Membrane curvature and its generation by BAR proteins | Q27006768 | ||
GTPase networks in membrane traffic | Q27015776 | ||
COPI budding within the Golgi stack | Q27021670 | ||
A high precision survey of the molecular dynamics of mammalian clathrin-mediated endocytosis | Q27322340 | ||
Ca2+ influx through distinct routes controls exocytosis and endocytosis at drosophila presynaptic terminals | Q44722207 | ||
The structural organization of the readily releasable pool of synaptic vesicles | Q44814913 | ||
The kinetics of synaptic vesicle pool depletion at CNS synaptic terminals | Q44815994 | ||
Developmental refinement of vesicle cycling at Schaffer collateral synapses | Q45210560 | ||
Vesicle endocytosis requires dynamin-dependent GTP hydrolysis at a fast CNS synapse. | Q45214894 | ||
An isolated pool of vesicles recycles at rest and drives spontaneous neurotransmission | Q45274254 | ||
Super-resolution imaging prompts re-thinking of cell biology mechanisms: selected cases using stimulated emission depletion microscopy | Q45348282 | ||
Synaptic PI(3,4,5)P3 is required for Syntaxin1A clustering and neurotransmitter release | Q45399289 | ||
Calcium dependence of exo- and endocytotic coupling at a glutamatergic synapse. | Q45916727 | ||
Synaptophysin is sorted from endocytotic markers in neuroendocrine PC12 cells but not transfected fibroblasts | Q46169848 | ||
A targeting signal in VAMP regulating transport to synaptic vesicles | Q46365410 | ||
Clathrin-dependent and clathrin-independent retrieval of synaptic vesicles in retinal bipolar cells | Q46543788 | ||
Single synaptic vesicle tracking in individual hippocampal boutons at rest and during synaptic activity. | Q46818707 | ||
Axonal translation of β-catenin regulates synaptic vesicle dynamics. | Q36837251 | ||
Activity-dependent control of bulk endocytosis by protein dephosphorylation in central nerve terminals | Q36856219 | ||
Inactivation of clathrin heavy chain inhibits synaptic recycling but allows bulk membrane uptake | Q36860399 | ||
Roles of calmodulin and calmodulin-binding proteins in synaptic vesicle recycling during regulated exocytosis at submicromolar Ca2+ concentrations | Q36865269 | ||
SNARE proteins synaptobrevin, SNAP-25, and syntaxin are involved in rapid and slow endocytosis at synapses | Q36902034 | ||
The neurotransmitter cycle and quantal size | Q36946152 | ||
Ca(2+) and calmodulin initiate all forms of endocytosis during depolarization at a nerve terminal. | Q36951925 | ||
The SNARE proteins SNAP25 and synaptobrevin are involved in endocytosis at hippocampal synapses | Q36954387 | ||
SNARE function is not involved in early endosome docking | Q36992967 | ||
Mu2 adaptin facilitates but is not essential for synaptic vesicle recycling in Caenorhabditis elegans | Q36993368 | ||
Most vesicles in a central nerve terminal participate in recycling | Q37010287 | ||
Alignment of synaptic vesicle macromolecules with the macromolecules in active zone material that direct vesicle docking | Q37033490 | ||
Reconstitution of the vital functions of Munc18 and Munc13 in neurotransmitter release | Q37071048 | ||
UNC-13L, UNC-13S, and Tomosyn form a protein code for fast and slow neurotransmitter release in Caenorhabditis elegans | Q37094524 | ||
Fos and Jun potentiate individual release sites and mobilize the reserve synaptic vesicle pool at the Drosophila larval motor synapse. | Q37103741 | ||
Formation of Golgi-derived active zone precursor vesicles. | Q37117339 | ||
Ultrafast endocytosis at Caenorhabditis elegans neuromuscular junctions | Q37145198 | ||
The synaptic vesicle cluster: a source of endocytic proteins during neurotransmitter release | Q37149042 | ||
Proteasome inhibition triggers activity-dependent increase in the size of the recycling vesicle pool in cultured hippocampal neurons | Q37149682 | ||
Synaptic vesicle protein trafficking at the glutamate synapse. | Q37160079 | ||
Influence of synaptic vesicle position on release probability and exocytotic fusion mode | Q37180772 | ||
Mechanical tension contributes to clustering of neurotransmitter vesicles at presynaptic terminals | Q37268796 | ||
Position of UNC-13 in the active zone regulates synaptic vesicle release probability and release kinetics | Q37290090 | ||
Think locally: control of ubiquitin-dependent protein degradation in neurons | Q37349687 | ||
A distributed set of interactions controls mu2 functionality in the role of AP-2 as a sorting adaptor in synaptic vesicle endocytosis. | Q37432138 | ||
Tilting the balance between facilitatory and inhibitory functions of mammalian and Drosophila Complexins orchestrates synaptic vesicle exocytosis. | Q37464966 | ||
Rab3 dynamically controls protein composition at active zones. | Q37484962 | ||
The little we know on the structure and machinery of V-ATPase | Q37485461 | ||
The balance between capture and dissociation of presynaptic proteins controls the spatial distribution of synapses | Q37503931 | ||
Ultrafast endocytosis at mouse hippocampal synapses. | Q37642826 | ||
Intersectin 1: a versatile actor in the synaptic vesicle cycle | Q37674793 | ||
Membrane protein clusters at nanoscale resolution: more than pretty pictures | Q37739708 | ||
The synapsins: key actors of synapse function and plasticity. | Q37741320 | ||
Rab7: Role of its protein interaction cascades in endo-lysosomal traffic | Q37790159 | ||
Vesicular sterols are essential for synaptic vesicle cycling. | Q42792578 | ||
Two-color far-field fluorescence nanoscopy | Q42908511 | ||
Role of Drosophila Rab5 during endosomal trafficking at the synapse and evoked neurotransmitter release | Q42917089 | ||
V-ATPase Membrane Sector Associates with Synaptobrevin to Modulate Neurotransmitter Release | Q42952232 | ||
Morphological correlates of functionally defined synaptic vesicle populations | Q43558103 | ||
Visualization of changes in presynaptic function during long-term synaptic plasticity | Q43653565 | ||
Visualizing postendocytic traffic of synaptic vesicles at hippocampal synapses | Q43730142 | ||
A membrane marker leaves synaptic vesicles in milliseconds after exocytosis in retinal bipolar cells | Q44158659 | ||
Effects of 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one on synaptic vesicle cycling at the frog neuromuscular junction. | Q44251927 | ||
The ubiquitin proteasome system acutely regulates presynaptic protein turnover and synaptic efficacy | Q44461744 | ||
Auxilin-dynamin interactions link the uncoating ATPase chaperone machinery with vesicle formation. | Q44468554 | ||
Synaptic vesicle mobility in mouse motor nerve terminals with and without synapsin. | Q46852222 | ||
Constitutive sharing of recycling synaptic vesicles between presynaptic boutons | Q46931398 | ||
Fast synaptic fatigue in shibire mutants reveals a rapid requirement for dynamin in synaptic vesicle membrane trafficking | Q47070147 | ||
Bruchpilot promotes active zone assembly, Ca2+ channel clustering, and vesicle release | Q47070593 | ||
Drosophila synaptotagmin I null mutants survive to early adulthood | Q47072128 | ||
Inactivity produces increases in neurotransmitter release and synapse size | Q47198414 | ||
Development of tonic firing behavior in rat soleus muscle | Q47928653 | ||
A complete genetic analysis of neuronal Rab3 function. | Q47952687 | ||
Rapid and intermittent cotransport of slow component-b proteins | Q48232827 | ||
Comparing video-rate STED nanoscopy and confocal microscopy of living neurons | Q48242975 | ||
Kinetics of synaptic vesicle refilling with neurotransmitter glutamate | Q48301483 | ||
Synaptic vesicles recycling spontaneously and during activity belong to the same vesicle pool | Q48311376 | ||
Synaptosomes possess an exocytotic pool of glutamate | Q48332236 | ||
Endocytic structures and synaptic vesicle recycling at a central synapse in awake rats | Q48378968 | ||
Actin has a molecular scaffolding, not propulsive, role in presynaptic function | Q48405526 | ||
Proteasome inhibition alleviates SNARE-dependent neurodegeneration | Q48407910 | ||
Reliability and precision of the mouse calyx of Held synapse | Q48416953 | ||
Comment on "The dynamic control of kiss-and-run and vesicular reuse probed with single nanoparticles". | Q48456444 | ||
Dynamic control of synaptic vesicle replenishment and short-term plasticity by Ca(2+)-calmodulin-Munc13-1 signaling | Q48461386 | ||
Single and multiple vesicle fusion induce different rates of endocytosis at a central synapse | Q48592708 | ||
Rab3 superprimes synaptic vesicles for release: implications for short-term synaptic plasticity. | Q48673213 | ||
Independent vesicle pools underlie different modes of release during neuronal development. | Q48677274 | ||
Synapsin dispersion and reclustering during synaptic activity | Q48726387 | ||
Post-transcriptional regulation of synaptic vesicle protein expression and the developmental control of synaptic vesicle formation. | Q48757809 | ||
Site-specific phosphorylation of synapsin I by mitogen-activated protein kinase and Cdk5 and its effects on physiological functions | Q48939390 | ||
A small GTP-binding protein dissociates from synaptic vesicles during exocytosis | Q50337421 | ||
Helical extension of the neuronal SNARE complex into the membrane | Q27646399 | ||
Phosphatidylinositol 4,5-bisphosphate clusters act as molecular beacons for vesicle recruitment | Q27678096 | ||
Functional rafts in cell membranes | Q27860768 | ||
Rab proteins as membrane organizers | Q27860861 | ||
Phosphoinositides in cell regulation and membrane dynamics | Q27861051 | ||
Synaptotagmin activates membrane fusion through a Ca2+-dependent trans interaction with phospholipids | Q27863371 | ||
Rab GTPases as coordinators of vesicle traffic | Q28131746 | ||
Association of the kinesin motor KIF1A with the multimodular protein liprin-alpha | Q28202542 | ||
The molecular motor toolbox for intracellular transport | Q28211349 | ||
Vesicular proteins exocytosed and subsequently retrieved by compensatory endocytosis are nonidentical | Q28252426 | ||
Changes in muscle contractile properties and neural control during human muscular fatigue | Q28259787 | ||
Video-rate far-field optical nanoscopy dissects synaptic vesicle movement | Q28269663 | ||
Molecular anatomy of a trafficking organelle | Q28274481 | ||
Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins | Q28276992 | ||
Synaptic vesicles position complexin to block spontaneous fusion | Q28284213 | ||
Alternative zippering as an on-off switch for SNARE-mediated fusion | Q28307492 | ||
Recruitment of endophilin to clathrin-coated pit necks is required for efficient vesicle uncoating after fission | Q28505115 | ||
SCRAPPER-dependent ubiquitination of active zone protein RIM1 regulates synaptic vesicle release | Q28505380 | ||
Snapin facilitates the synchronization of synaptic vesicle fusion | Q28508747 | ||
Spatiotemporal control of endocytosis by phosphatidylinositol-3,4-bisphosphate | Q28511509 | ||
Essential role of phosphoinositide metabolism in synaptic vesicle recycling | Q28511682 | ||
Synaptophysin regulates the kinetics of synaptic vesicle endocytosis in central neurons | Q28512527 | ||
Overlapping role of dynamin isoforms in synaptic vesicle endocytosis | Q28513338 | ||
A function for the AP3 coat complex in synaptic vesicle formation from endosomes | Q28567917 | ||
Stonin 2 is a major adaptor protein for clathrin-mediated synaptic vesicle retrieval | Q28570743 | ||
The involvement of the small GTP-binding protein Rab5a in neuronal endocytosis | Q28571235 | ||
Visualization of synaptic vesicle movement in intact synaptic boutons using fluorescence fluctuation spectroscopy | Q28571700 | ||
Assembling the presynaptic active zone: a characterization of an active one precursor vesicle | Q28571859 | ||
Molecular in situ topology of Aczonin/Piccolo and associated proteins at the mammalian neurotransmitter release site | Q28576284 | ||
Synaptic vesicle recycling at CNS snapses without AP-2 | Q28577663 | ||
Evidence for early endosome-like fusion of recently endocytosed synaptic vesicles | Q28579652 | ||
The V0 sector of the V-ATPase, synaptobrevin, and synaptophysin are associated on synaptic vesicles in a Triton X-100-resistant, freeze-thawing sensitive, complex | Q28583592 | ||
SNARE protein recycling by αSNAP and βSNAP supports synaptic vesicle priming | Q28589671 | ||
Kainate modulates presynaptic GABA release from two vesicle pools | Q33592144 | ||
Synapsins as regulators of neurotransmitter release | Q33598970 | ||
Regulation of endosome fusion. | Q33637955 | ||
Acute dynamin inhibition dissects synaptic vesicle recycling pathways that drive spontaneous and evoked neurotransmission | Q33661188 | ||
Preferred sites of exocytosis and endocytosis colocalize during high- but not lower-frequency stimulation in mouse motor nerve terminals. | Q33693767 | ||
Structure of clathrin coat with bound Hsc70 and auxilin: mechanism of Hsc70-facilitated disassembly | Q33697076 | ||
Mechanisms of synaptic vesicle recycling illuminated by fluorescent dyes. | Q33785262 | ||
Synaptic vesicle biogenesis | Q33804355 | ||
Cotrafficking of SV2 and synaptotagmin at the synapse. | Q33835261 | ||
Activity-dependent bulk endocytosis and clathrin-dependent endocytosis replenish specific synaptic vesicle pools in central nerve terminals | Q33929652 | ||
Molecular determinants of presynaptic active zones | Q33941567 | ||
Activity-dependent augmentation of spontaneous neurotransmission during endoplasmic reticulum stress | Q33942946 | ||
SNARE-complex disassembly by NSF follows synaptic-vesicle fusion | Q33947145 | ||
Dynamin I phosphorylation by GSK3 controls activity-dependent bulk endocytosis of synaptic vesicles. | Q33948657 | ||
Synaptic vesicle pools | Q33983958 | ||
SV2 acts via presynaptic calcium to regulate neurotransmitter release. | Q34034957 | ||
A heterogeneous "resting" pool of synaptic vesicles that is dynamically interchanged across boutons in mammalian CNS synapses | Q34076862 | ||
A comprehensive comparison of transmembrane domains reveals organelle-specific properties | Q34083658 | ||
Structure and dynamics of a two-helix SNARE complex in live cells | Q34087501 | ||
The Rab7 effector protein RILP controls lysosomal transport by inducing the recruitment of dynein-dynactin motors | Q34100590 | ||
Limited intermixing of synaptic vesicle components upon vesicle recycling | Q34104085 | ||
Safety factor at the neuromuscular junction | Q34199050 | ||
Three modes of synaptic vesicular recycling revealed by single-vesicle imaging | Q34203451 | ||
Regulation of synaptic vesicle docking by different classes of macromolecules in active zone material | Q34206193 | ||
Depletion of vesicles from frog neuromuscular junctions by prolonged tetanic stimulation | Q34207075 | ||
Evidence for recycling of synaptic vesicle membrane during transmitter release at the frog neuromuscular junction | Q34207383 | ||
Turnover of transmitter and synaptic vesicles at the frog neuromuscular junction | Q34207387 | ||
Membrane protein sequestering by ionic protein-lipid interactions | Q34226601 | ||
Endocytosis of synaptic vesicle membrane at the frog neuromuscular junction | Q34264377 | ||
The first five seconds in the life of a clathrin-coated pit. | Q34292187 | ||
Single reconstituted neuronal SNARE complexes zipper in three distinct stages | Q34294781 | ||
Super-resolution imaging reveals the internal architecture of nano-sized syntaxin clusters | Q34304810 | ||
Actin, spectrin, and associated proteins form a periodic cytoskeletal structure in axons | Q34317568 | ||
Probing vesicle dynamics in single hippocampal synapses | Q34351915 | ||
A new ticket for entry into budding vesicles-ubiquitin | Q34365247 | ||
Protein-lipid interactions and phosphoinositide metabolism in membrane traffic: insights from vesicle recycling in nerve terminals | Q34374331 | ||
Rapid Ca2+-dependent decrease of protein ubiquitination at synapses | Q34388074 | ||
Impaired recycling of synaptic vesicles after acute perturbation of the presynaptic actin cytoskeleton | Q34394543 | ||
The dephosphins: dephosphorylation by calcineurin triggers synaptic vesicle endocytosis | Q34416249 | ||
Phosphatidylinositol-(4,5)-bisphosphate regulates sorting signal recognition by the clathrin-associated adaptor complex AP2. | Q34421459 | ||
NCAM and vesicle cycling: the importance of good glue in the long run. | Q34459742 | ||
Secretory vesicles are preferentially targeted to areas of low molecular SNARE density | Q34482442 | ||
STED microscopy reveals that synaptotagmin remains clustered after synaptic vesicle exocytosis | Q34513459 | ||
Distinct endocytic pathways control the rate and extent of synaptic vesicle protein recycling | Q34568799 | ||
Clathrin-mediated endocytosis at synapses | Q34634168 | ||
Three-dimensional architecture of presynaptic terminal cytomatrix. | Q34642485 | ||
Kiss-and-run, collapse and 'readily retrievable' vesicles | Q34654997 | ||
Single-molecule analysis of a molecular disassemblase reveals the mechanism of Hsc70-driven clathrin uncoating | Q34665652 | ||
Synaptic vesicles retain their identity through the endocytic cycle | Q34746833 | ||
Protein quantification at the single vesicle level reveals that a subset of synaptic vesicle proteins are trafficked with high precision | Q34807735 | ||
Use-dependent AMPA receptor block reveals segregation of spontaneous and evoked glutamatergic neurotransmission | Q34911758 | ||
Spontaneous glutamate release is independent of calcium influx and tonically activated by the calcium-sensing receptor | Q34989736 | ||
A synaptic vesicle-associated Ca2+ channel promotes endocytosis and couples exocytosis to endocytosis. | Q35001595 | ||
Synaptic tetraspan vesicle membrane proteins are conserved but not needed for synaptogenesis and neuronal function in Caenorhabditis elegans. | Q35039350 | ||
Physical and functional connection between auxilin and dynamin during endocytosis | Q35040012 | ||
Signals involved in targeting membrane proteins to synaptic vesicles | Q35065820 | ||
SNARE motif-mediated sorting of synaptobrevin by the endocytic adaptors clathrin assembly lymphoid myeloid leukemia (CALM) and AP180 at synapses | Q35170795 | ||
Two synaptobrevin molecules are sufficient for vesicle fusion in central nervous system synapses | Q35180827 | ||
Why do worms need cholesterol? | Q35190121 | ||
Synaptophysin is required for synaptobrevin retrieval during synaptic vesicle endocytosis | Q35281762 | ||
The reserve pool of synaptic vesicles acts as a buffer for proteins involved in synaptic vesicle recycling | Q35344955 | ||
A small pool of vesicles maintains synaptic activity in vivo | Q35345585 | ||
Regulation of vesicular neurotreansmitter transporters | Q35546785 | ||
Doc2 is a Ca2+ sensor required for asynchronous neurotransmitter release. | Q35562324 | ||
Ca²⁺ influx slows single synaptic vesicle endocytosis | Q35605344 | ||
Loading and recycling of synaptic vesicles in the Torpedo electric organ and the vertebrate neuromuscular junction | Q35617857 | ||
Maintenance of transmitter release from neuromuscular junctions with different patterns of usage "in vivo". | Q35700662 | ||
The role of extracellular calcium in exo- and endocytosis of synaptic vesicles at the frog motor nerve terminals | Q79135046 | ||
Synaptic vesicles interchange their membrane proteins with a large surface reservoir during recycling | Q79921374 | ||
Mobility of synaptic vesicles in different pools in resting and stimulated frog motor nerve terminals | Q80034619 | ||
The body temperature in rats on normal and deficient diets: Preliminary report | Q80327636 | ||
Synapsins contribute to the dynamic spatial organization of synaptic vesicles in an activity-dependent manner | Q84899754 | ||
Kinesin-1/Hsc70-dependent mechanism of slow axonal transport and its relation to fast axonal transport | Q28594088 | ||
SNAREs--engines for membrane fusion | Q29547230 | ||
Molecular mechanism and physiological functions of clathrin-mediated endocytosis | Q29615660 | ||
Membrane curvature and mechanisms of dynamic cell membrane remodelling | Q29617321 | ||
Membrane fusion | Q29618140 | ||
Endophilin drives the fast mode of vesicle retrieval in a ribbon synapse | Q30010485 | ||
Sorting in early endosomes reveals connections to docking- and fusion-associated factors | Q30047766 | ||
Endophilin functions as a membrane-bending molecule and is delivered to endocytic zones by exocytosis. | Q30155977 | ||
Targeting of the synaptic vesicle protein synaptobrevin in the axon of cultured hippocampal neurons: evidence for two distinct sorting steps. | Q30442138 | ||
Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons | Q30477482 | ||
Cell- and stimulus-dependent heterogeneity of synaptic vesicle endocytic recycling mechanisms revealed by studies of dynamin 1-null neurons | Q30483551 | ||
Differential requirements for clathrin in receptor-mediated endocytosis and maintenance of synaptic vesicle pools | Q30485732 | ||
Cytoskeletal requirements in axonal transport of slow component-b | Q30486187 | ||
The dynamic control of kiss-and-run and vesicular reuse probed with single nanoparticles | Q30488206 | ||
Coordinated actions of actin and BAR proteins upstream of dynamin at endocytic clathrin-coated pits | Q30494265 | ||
Rapid structural alterations of the active zone lead to sustained changes in neurotransmitter release. | Q30494986 | ||
Endosomal sorting of readily releasable synaptic vesicles | Q30497264 | ||
Single secretory granules of live cells recruit syntaxin-1 and synaptosomal associated protein 25 (SNAP-25) in large copy numbers | Q30497544 | ||
Syntaxin clusters assemble reversibly at sites of secretory granules in live cells | Q30497547 | ||
Mechanistic logic underlying the axonal transport of cytosolic proteins | Q30500273 | ||
Actin-dependent rapid recruitment of reluctant synaptic vesicles into a fast-releasing vesicle pool | Q30512960 | ||
Readily releasable pool of synaptic vesicles measured at single synaptic contacts | Q30528334 | ||
Rapid feedback regulation of synaptic efficacy during high-frequency activity at the Drosophila larval neuromuscular junction | Q30540256 | ||
Glutamate induces the rapid formation of spine head protrusions in hippocampal slice cultures | Q30856843 | ||
The architecture of active zone material at the frog's neuromuscular junction | Q30981051 | ||
Phosphoinositides in membrane traffic at the synapse | Q32066953 | ||
Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons | Q32129557 | ||
Structure and function of neuromuscular junctions in the vastus lateralis of man. A motor point biopsy study of two groups of patients | Q33189587 | ||
Macromolecular-scale resolution in biological fluorescence microscopy | Q33251616 | ||
3D reconstruction of high-resolution STED microscope images | Q33338854 | ||
How does synaptotagmin trigger neurotransmitter release? | Q33345212 | ||
Macromolecular connections of active zone material to docked synaptic vesicles and presynaptic membrane at neuromuscular junctions of mouse | Q33410405 | ||
Evaluation of the heterogeneous reactivity of the syntaxin molecules on the inner leaflet of the plasma membrane | Q33507761 | ||
Structural determinants of the reliability of synaptic transmission at the vertebrate neuromuscular junction | Q35700679 | ||
Reduced release probability prevents vesicle depletion and transmission failure at dynamin mutant synapses | Q35779287 | ||
Stick-and-diffuse and caged diffusion: a comparison of two models of synaptic vesicle dynamics | Q35781192 | ||
Neuropeptide delivery to synapses by long-range vesicle circulation and sporadic capture. | Q35803998 | ||
Determinants of synaptobrevin regulation in membranes | Q35810575 | ||
A membrane pool retrieved via endocytosis overshoot at nerve terminals: a study of its retrieval mechanism and role | Q35888943 | ||
Identification of CSPα clients reveals a role in dynamin 1 regulation. | Q35893528 | ||
VAMP4 directs synaptic vesicles to a pool that selectively maintains asynchronous neurotransmission | Q35916627 | ||
Release probability of hippocampal glutamatergic terminals scales with the size of the active zone. | Q36068532 | ||
Quantum dots provide an optical signal specific to full collapse fusion of synaptic vesicles | Q36140639 | ||
ER-to-Golgi transport: form and formation of vesicular and tubular carriers. | Q36175436 | ||
Mechanisms of vertebrate synaptogenesis | Q36196530 | ||
Structural changes after transmitter release at the frog neuromuscular junction | Q36208626 | ||
The cytoskeletal architecture of the presynaptic terminal and molecular structure of synapsin 1. | Q36219796 | ||
Redistribution of synaptophysin and synapsin I during alpha-latrotoxin-induced release of neurotransmitter at the neuromuscular junction | Q36222565 | ||
The synaptic vesicle cycle: a single vesicle budding step involving clathrin and dynamin | Q36237077 | ||
Minireview: recent developments in the regulation of glucose transporter-4 traffic: new signals, locations, and partners | Q36252775 | ||
ADP ribosylation factor 1 is required for synaptic vesicle budding in PC12 cells. | Q36276374 | ||
Single-vesicle imaging reveals that synaptic vesicle exocytosis and endocytosis are coupled by a single stochastic mode | Q36300120 | ||
Botulinum neurotoxin A blocks synaptic vesicle exocytosis but not endocytosis at the nerve terminal | Q36313397 | ||
Colocalization of synapsin and actin during synaptic vesicle recycling | Q36381468 | ||
Differences in synaptic efficacy at neuromuscular junctions in frog twitch muscles | Q36414984 | ||
RIM promotes calcium channel accumulation at active zones of the Drosophila neuromuscular junction. | Q36450432 | ||
Quantitative fine-structural analysis of olfactory cortical synapses | Q36459259 | ||
RIM controls homeostatic plasticity through modulation of the readily-releasable vesicle pool | Q36469214 | ||
Synaptic vesicle membrane proteins interact to form a multimeric complex | Q36530918 | ||
Colocalization of synaptophysin with transferrin receptors: implications for synaptic vesicle biogenesis | Q36532901 | ||
Vesicle formation at the plasma membrane and trans-Golgi network: the same but different | Q36594583 | ||
Compromised fidelity of endocytic synaptic vesicle protein sorting in the absence of stonin 2 | Q36598109 | ||
Protein sorting in the synaptic vesicle life cycle | Q36639159 | ||
AP2 hemicomplexes contribute independently to synaptic vesicle endocytosis | Q36666714 | ||
Sorting of synaptophysin into special vesicles in nonneuroendocrine epithelial cells | Q36709683 | ||
Emerging roles for ubiquitin and protein degradation in neuronal function | Q36747899 | ||
Molecular motors in neurons: transport mechanisms and roles in brain function, development, and disease. | Q37811131 | ||
Protein scaffolds in the coupling of synaptic exocytosis and endocytosis | Q37838259 | ||
Vesicular neurotransmitter transporter: bioenergetics and regulation of glutamate transport | Q37879648 | ||
Structural insights into dynamin-mediated membrane fission | Q38051857 | ||
Perspectives on kiss-and-run: role in exocytosis, endocytosis, and neurotransmission | Q38067906 | ||
Presynaptic regulation of quantal size: K+/H+ exchange stimulates vesicular glutamate transport | Q38592365 | ||
Estimates of quantal content during 'chemical potentiation' of transmitter release | Q39284298 | ||
Synapsin I senses membrane curvature by an amphipathic lipid packing sensor motif. | Q39430082 | ||
ELP3 controls active zone morphology by acetylating the ELKS family member Bruchpilot | Q39431404 | ||
Ca2+ induces clustering of membrane proteins in the plasma membrane via electrostatic interactions | Q39583577 | ||
Clathrin-mediated endocytosis is the dominant mechanism of vesicle retrieval at hippocampal synapses. | Q39751968 | ||
A selective activity-dependent requirement for dynamin 1 in synaptic vesicle endocytosis | Q39752213 | ||
KIF1Bbeta- and KIF1A-mediated axonal transport of presynaptic regulator Rab3 occurs in a GTP-dependent manner through DENN/MADD. | Q39752721 | ||
Quantitative analysis of synaptic vesicle Rabs uncovers distinct yet overlapping roles for Rab3a and Rab27b in Ca2+-triggered exocytosis | Q39753923 | ||
Bassoon speeds vesicle reloading at a central excitatory synapse. | Q39754011 | ||
Loss of skywalker reveals synaptic endosomes as sorting stations for synaptic vesicle proteins | Q39754179 | ||
RIM-binding protein, a central part of the active zone, is essential for neurotransmitter release | Q39754475 | ||
Vesicle hypothesis of the release of quanta of acetylcholine | Q40284776 | ||
Synaptophysin I controls the targeting of VAMP2/synaptobrevin II to synaptic vesicles. | Q40286914 | ||
Stonin 2 is an AP-2-dependent endocytic sorting adaptor for synaptotagmin internalization and recycling | Q40320414 | ||
The SNARE motif is essential for the formation of syntaxin clusters in the plasma membrane | Q40323730 | ||
Vti1a identifies a vesicle pool that preferentially recycles at rest and maintains spontaneous neurotransmission | Q40442647 | ||
Activity-dependent control of slow synaptic vesicle endocytosis by cyclin-dependent kinase 5. | Q40803584 | ||
Newly synthesized synaptophysin is transported to synaptic-like microvesicles via constitutive secretory vesicles and the plasma membrane. | Q41083206 | ||
Mice lacking synaptophysin reproduce and form typical synaptic vesicles | Q41264671 | ||
The movement of membranous organelles in axons. Electron microscopic identification of anterogradely and retrogradely transported organelles | Q41264903 | ||
Clathrin dependence of synaptic-vesicle formation at the Drosophila neuromuscular junction | Q41334894 | ||
Motor-unit discharge rates in maximal voluntary contractions of three human muscles | Q41590650 | ||
A v-SNARE participates in synaptic vesicle formation mediated by the AP3 adaptor complex | Q41644775 | ||
Assembly of presynaptic active zones from cytoplasmic transport packets | Q41730812 | ||
A vesicle superpool spans multiple presynaptic terminals in hippocampal neurons. | Q41786614 | ||
What is Rate-Limiting during Sustained Synaptic Activity: Vesicle Supply or the Availability of Release Sites | Q41810022 | ||
CDK5 serves as a major control point in neurotransmitter release. | Q41862687 | ||
SNARE proteins: one to fuse and three to keep the nascent fusion pore open | Q41920045 | ||
Vesicular ATPase inserted into the plasma membrane of motor terminals by exocytosis alkalinizes cytosolic pH and facilitates endocytosis | Q41957038 | ||
Axonal transport of synapsin I-like proteins in rabbit retinal ganglion cells | Q41964022 | ||
Two pathways of synaptic vesicle retrieval revealed by single-vesicle imaging | Q41997492 | ||
A preferentially segregated recycling vesicle pool of limited size supports neurotransmission in native central synapses | Q42022259 | ||
Synaptic vesicle retrieval time is a cell-wide rather than individual-synapse property. | Q42090946 | ||
The t-SNAREs syntaxin 1 and SNAP-25 are present on organelles that participate in synaptic vesicle recycling | Q42117532 | ||
High- and low-mobility stages in the synaptic vesicle cycle | Q42125696 | ||
A general model of synaptic transmission and short-term plasticity | Q42136692 | ||
Synaptic vesicle pools: an update | Q42140979 | ||
v-SNARE composition distinguishes synaptic vesicle pools. | Q42142233 | ||
A role for the ubiquitin-proteasome system in activity-dependent presynaptic silencing | Q42153361 | ||
Synaptobrevin N-terminally bound to syntaxin-SNAP-25 defines the primed vesicle state in regulated exocytosis | Q42176873 | ||
Defect in synaptic vesicle precursor transport and neuronal cell death in KIF1A motor protein-deficient mice. | Q42243086 | ||
Metabolic control of vesicular glutamate transport and release. | Q42370957 | ||
The fate of synaptic vesicle components upon fusion | Q42380550 | ||
Abnormal synaptic vesicle biogenesis in Drosophila synaptogyrin mutants | Q42429487 | ||
Optical quantal analysis of synaptic transmission in wild-type and rab3-mutant Drosophila motor axons | Q42484876 | ||
Use dependence of presynaptic tenacity. | Q42497470 | ||
One SNARE complex is sufficient for membrane fusion | Q42531466 | ||
A resting pool of vesicles is responsible for spontaneous vesicle fusion at the synapse | Q42547280 | ||
Quantitative proteomics analysis of detergent-resistant membranes from chemical synapses: evidence for cholesterol as spatial organizer of synaptic vesicle cycling | Q42692486 | ||
Hair cell synaptic ribbons are essential for synchronous auditory signalling. | Q50473698 | ||
Fast vesicle fusion in living cells requires at least three SNARE complexes. | Q50541149 | ||
Anatomy and dynamics of a supramolecular membrane protein cluster. | Q50668558 | ||
Intracellular transport of single-headed molecular motors KIF1A. | Q50740212 | ||
The small GTPase Rab7 controls the endosomal trafficking and neuritogenic signaling of the nerve growth factor receptor TrkA. | Q50747092 | ||
Fatigue of maintained voluntary muscle contraction in man | Q51108545 | ||
The same synaptic vesicles drive active and spontaneous release. | Q52712414 | ||
Effects of enhanced activity on synaptic transmission in mouse extensor digitorum longus muscle | Q54298017 | ||
CSPα promotes SNARE-complex assembly by chaperoning SNAP-25 during synaptic activity. | Q54397791 | ||
Real-time measurements of vesicle-SNARE recycling in synapses of the central nervous system. | Q55033831 | ||
Neurotransmitter release: fusion or 'kiss-and-run'? | Q55038012 | ||
Synaptotagmin-1 Docks Secretory Vesicles to Syntaxin-1/SNAP-25 Acceptor Complexes | Q56992446 | ||
A readily retrievable pool of synaptic vesicles | Q57949867 | ||
Endosomal Fusion upon SNARE Knockdown is Maintained by Residual SNARE Activity and Enhanced Docking | Q57978902 | ||
Localization of Rab5 to synaptic vesicles identifies endosomal intermediate in synaptic vesicle recycling pathway | Q57979066 | ||
Syntaxin1A Lateral Diffusion Reveals Transient and Local SNARE Interactions | Q58052095 | ||
Topogenesis and sorting of synaptophysin: Synthesis of a synaptic vesicle protein from a gene transfected into nonneuroendocrine cells | Q58438839 | ||
Firing patterns of motor units in normal rats | Q59062044 | ||
A common origin of synaptic vesicles undergoing evoked and spontaneous fusion | Q62089125 | ||
The absence of neuromuscular transmission failure in sustained maximal voluntary contractions | Q67247592 | ||
Influence of spinal cord transection on the presence and axonal transport of CGRP-, chromogranin A-, VIP-, synapsin I-, and synaptophysin-like immunoreactivities in rat motor nerve | Q67465442 | ||
Muscle injury, cross-sectional area and fibre type distribution in mouse soleus after intermittent wheel-running | Q68589262 | ||
Muscle damage and repair in voluntarily running mice: strain and muscle differences | Q69419124 | ||
Contractile speed and EMG changes during fatigue of sustained maximal voluntary contractions | Q70154300 | ||
Monitoring of black widow spider venom (BWSV) induced exo- and endocytosis in living frog motor nerve terminals with FM1-43 | Q71014073 | ||
Axonal transport of synaptic vesicle proteins in the rat optic nerve | Q73071990 | ||
Transmitter release differs at snake twitch and tonic endplates during potassium-induced nerve terminal depolarization | Q73145371 | ||
Endocytic vesicles move at the tips of actin tails in cultured mast cells | Q73177693 | ||
The contribution of postsynaptic folds to the safety factor for neuromuscular transmission in rat fast- and slow-twitch muscles | Q73211955 | ||
Voluntary strength and fatigue | Q73466180 | ||
Action, and spontaneous release, of acetylcholine at an inexcitable nerve-muscle junction | Q73689914 | ||
Synaptic vesicle pools at the frog neuromuscular junction | Q73744519 | ||
Cdk5/p25(nck5a) interaction with synaptic proteins in bovine brain | Q73748003 | ||
Three-dimensional comparison of ultrastructural characteristics at depressing and facilitating synapses onto cerebellar Purkinje cells | Q74411621 | ||
Synaptic vesicle dynamics in rat fast and slow motor nerve terminals | Q74624725 | ||
Spontaneous electromyographic activity in adult rat soleus muscle | Q74765936 | ||
Alterations in transmission, vesicle dynamics, and transmitter release machinery at NCAM-deficient neuromuscular junctions | Q77334872 | ||
Synaptic physiology and ultrastructure in comatose mutants define an in vivo role for NSF in neurotransmitter release | Q77679760 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell | Q7868 |
nervous system | Q9404 | ||
synaptic vesicle uncoating | Q21135065 | ||
synaptic vesicle budding from endosome | Q22291791 | ||
P304 | page(s) | 788-822 | |
P577 | publication date | 2014-04-16 | |
P1433 | published in | The EMBO Journal | Q1278554 |
P1476 | title | Synaptic vesicle recycling: steps and principles | |
P478 | volume | 33 |
Q64768758 | Q64768758 |
Q104064467 | A minimalist model to measure interactions between proteins and synaptic vesicles |
Q83226085 | A model of neuronal ceroid lipofuscinosis reveals a hypermorphic gain of function mechanism |
Q36585916 | APP and APLP2 interact with the synaptic release machinery and facilitate transmitter release at hippocampal synapses |
Q28543167 | APP is cleaved by Bace1 in pre-synaptic vesicles and establishes a pre-synaptic interactome, via its intracellular domain, with molecular complexes that regulate pre-synaptic vesicles functions |
Q48130645 | ATP binding to synaspsin IIa regulates usage and clustering of vesicles in terminals of hippocampal neurons. |
Q40256866 | An essential role of acetylcholine-glutamate synergy at habenular synapses in nicotine dependence |
Q28828903 | Analysis of protein phosphorylation in nerve terminal reveals extensive changes in active zone proteins upon exocytosis |
Q48398553 | Analyzing Endosomal Docking, Fusion, Sorting, and Budding Mechanisms in Isolated Organelles |
Q30847138 | Anterograde Transport of Rab4-Associated Vesicles Regulates Synapse Organization in Drosophila |
Q93024949 | Antibody-driven capture of synaptic vesicle proteins on the plasma membrane enables the analysis of their interactions with other synaptic proteins |
Q39313571 | Autophagy in the presynaptic compartment in health and disease |
Q36778750 | Calcium Promotes the Formation of Syntaxin 1 Mesoscale Domains through Phosphatidylinositol 4,5-Bisphosphate |
Q64088611 | Cholesterol and the Safety Factor for Neuromuscular Transmission |
Q57031999 | Comparative synaptosome imaging: a semi-quantitative method to obtain copy numbers for synaptic and neuronal proteins |
Q37592135 | Complexin Mutants Reveal Partial Segregation between Recycling Pathways That Drive Evoked and Spontaneous Neurotransmission |
Q28574891 | Composition of isolated synaptic boutons reveals the amounts of vesicle trafficking proteins |
Q37718249 | Correlated optical and isotopic nanoscopy |
Q42503281 | Descending projections from the basal forebrain to the orexin neurons in mice. |
Q48041957 | Dissipative self-assembly of vesicular nanoreactors. |
Q64072134 | Dysregulation of Microglial Function Contributes to Neuronal Impairment in Mcoln1a-Deficient Zebrafish |
Q36495013 | Effects of exercise training on neuromuscular junction morphology and pre- to post-synaptic coupling in young and aged rats. |
Q55379225 | Endophilin A and B Join Forces With Clathrin to Mediate Synaptic Vesicle Recycling in Caenorhabditis elegans. |
Q40442566 | Entry of Botulinum Neurotoxin Subtypes A1 and A2 into Neurons |
Q48184232 | Functional role of ATP binding to synapsin I in synaptic vesicle trafficking and release dynamics. |
Q38651168 | Functionally heterogeneous synaptic vesicle pools support diverse synaptic signalling |
Q64996883 | GFP nanobodies reveal recently-exocytosed pHluorin molecules. |
Q89355524 | Genetic dissection of neuropeptide cell biology at high and low activity in a defined sensory neuron |
Q58729447 | Interdependency Between Autophagy and Synaptic Vesicle Trafficking: Implications for Dopamine Release |
Q37268523 | Ion mobility-enhanced MS(E)-based label-free analysis reveals effects of low-dose radiation post contextual fear conditioning training on the mouse hippocampal proteome. |
Q51167256 | Lipid Head Group Charge and Fatty Acid Configuration Dictate Liposome Mobility in Neurofilament Networks. |
Q36199834 | M30 Antagonizes Indoleamine 2,3-Dioxygenase Activation and Neurodegeneration Induced by Corticosterone in the Hippocampus |
Q26744736 | Molecular Machines Determining the Fate of Endocytosed Synaptic Vesicles in Nerve Terminals |
Q26766019 | Molecular Machines Regulating the Release Probability of Synaptic Vesicles at the Active Zone |
Q36083087 | Molecular underpinnings of synaptic vesicle pool heterogeneity |
Q36101948 | Monitoring Synaptic Vesicle Protein Sorting with Enhanced Horseradish Peroxidase in the Electron Microscope |
Q48110129 | Mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities |
Q57462279 | Myosin V functions as a vesicle tether at the plasma membrane to control neurotransmitter release in central synapses |
Q60956587 | NGF-Dependent Changes in Ubiquitin Homeostasis Trigger Early Cholinergic Degeneration in Cellular and Animal AD-Model |
Q93352899 | Nanobodies reveal an extra-synaptic population of SNAP-25 and Syntaxin 1A in hippocampal neurons |
Q90359231 | Neurodegenerative diseases: model organisms, pathology and autophagy |
Q47625210 | New tools for "hot-wiring" clathrin-mediated endocytosis with temporal and spatial precision. |
Q64982621 | Newly produced synaptic vesicle proteins are preferentially used in synaptic transmission. |
Q28085042 | Organization and dynamics of SNARE proteins in the presynaptic membrane |
Q38583424 | Permanent dynamic transporter-mediated turnover of glutamate across the plasma membrane of presynaptic nerve terminals: arguments in favor and against |
Q57038657 | Postnatal Restriction of Activity-Induced Ca Responses to Schwann Cells at the Neuromuscular Junction Are Caused by the Proximo-Distal Loss of Axonal Synaptic Vesicles during Development |
Q48269998 | Presynaptic clathrin levels are a limiting factor for synaptic transmission |
Q57175515 | Presynaptic disorders: a clinical and pathophysiological approach focused on the synaptic vesicle |
Q40607068 | Proteome Analysis of Potential Synaptic Vesicle Cycle Biomarkers in the Cerebrospinal Fluid of Patients with Sporadic Creutzfeldt-Jakob Disease. |
Q39224304 | Proton electrochemical gradient: Driving and regulating neurotransmitter uptake. |
Q39210221 | Putting a brake on synaptic vesicle endocytosis. |
Q30401163 | Quantitative analysis of vesicle recycling at the calyx of Held synapse |
Q52804356 | Rab GTPases and Membrane Trafficking in Neurodegeneration. |
Q92702531 | Rab GTPases: Switching to Human Diseases |
Q36000841 | Regulation of synaptic activity by snapin-mediated endolysosomal transport and sorting |
Q64902305 | Robo2 regulates synaptic oxytocin content by affecting actin dynamics. |
Q91280711 | Role of actin in organelle trafficking in neurons |
Q35126563 | Septin dynamics are essential for exocytosis |
Q89535702 | Significance of chromogranin A and synaptophysin in pancreatic neuroendocrine tumors |
Q64996479 | Slow presynaptic mechanisms that mediate adaptation in the olfactory pathway of Drosophila. |
Q28085061 | Spontaneous vesicle recycling in the synaptic bouton |
Q47171795 | Stimulation of synapse formation between stem cell-derived neurons and native brainstem auditory neurons |
Q90024357 | Stromalin Constrains Memory Acquisition by Developmentally Limiting Synaptic Vesicle Pool Size |
Q51673629 | Super-resolution Microscopy of Clickable Amino Acids Reveals the Effects of Fluorescent Protein Tagging on Protein Assemblies. |
Q48051171 | Synapsin Isoforms Regulating GABA Release from Hippocampal Interneurons |
Q40132068 | Synapsins Are Downstream Players of the BDNF-Mediated Axonal Growth |
Q33790158 | Synaptic Impairment and Robustness of Excitatory Neuronal Networks with Different Topologies |
Q90012237 | Synaptic Vesicle Endocytosis in Different Model Systems |
Q98513674 | Systems biology reveals reprogramming of the S-nitroso-proteome in the cortical and striatal regions of mice during aging process |
Q38895201 | The BLOC-1 Subunit Pallidin Facilitates Activity-Dependent Synaptic Vesicle Recycling. |
Q41109238 | The Calcineurin-Binding, Activity-Dependent Splice Variant Dynamin1xb Is Highly Enriched in Synapses in Various Regions of the Central Nervous System. |
Q91583364 | The Calmodulin Binding Region of the Synaptic Vesicle Protein Mover Is Required for Homomeric Interaction and Presynaptic Targeting |
Q33905778 | The LRRK2 G2385R variant is a partial loss-of-function mutation that affects synaptic vesicle trafficking through altered protein interactions. |
Q47124943 | The Nanoworld of the Tripartite Synapse: Insights from Super-Resolution Microscopy. |
Q38603413 | The Regulation of Synaptic Protein Turnover |
Q26768185 | The Roles of Microtubule-Based Transport at Presynaptic Nerve Terminals |
Q47405859 | The axonal endoplasmic reticulum: One organelle-many functions in development, maintenance, and plasticity |
Q47880463 | The impact of cytoskeletal organization on the local regulation of neuronal transport. |
Q47342203 | The presynaptic scaffolding protein Piccolo organizes the readily releasable pool at the calyx of Held |
Q92598532 | The role of PDLIM1, a PDZ-LIM domain protein, at the ribbon synapses in the chicken retina |
Q64083779 | The temporal profile of activity-dependent presynaptic phospho-signalling reveals long-lasting patterns of poststimulus regulation |
Q47836274 | The where, what, and when of membrane protein degradation in neurons. |
Q48227076 | Tight temporal coupling between synaptic rewiring of olfactory glomeruli and the emergence of odor-guided behavior in Xenopus tadpoles |
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