THE SYNAPTIC VESICLE CYCLE

Short-Term Synaptic Plasticity

Zucker, R. S., & Regehr, W. G. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.092501.114547 · Cited by 5,068

SNAP receptors implicated in vesicle targeting and fusion

Söllner, T. H., Whiteheart, S. W., Brunner, M., Erdjument‐Bromage, H., Geromanos, S. J., Tempst, P., & Rothman, J. E. (1993) · Nature · doi:10.1038/362318a0 · Cited by 3,239

EVIDENCE FOR RECYCLING OF SYNAPTIC VESICLE MEMBRANE DURING TRANSMITTER RELEASE AT THE FROG NEUROMUSCULAR JUNCTION

Heuser, J. E., & Reese, T. S. (1973) · The Journal of Cell Biology · doi:10.1083/jcb.57.2.315 · Cited by 2,147

The synaptic vesicle cycle: a cascade of protein–protein interactions

Südhof, T. C. (1995) · Nature · doi:10.1038/375645a0 · Cited by 1,991

Synaptotagmin I: A major Ca2+ sensor for transmitter release at a central synapse

Geppert, M., Goda, Y., Hammer, R. E., Li, C., Rosahl, T. W., Stevens, C. F., & Südhof, T. C. (1994) · Cell · doi:10.1016/0092-8674(94)90556-8 · Cited by 1,483

Synaptic assembly of the brain in the absence of neurotransmitter secretion.

Verhage, M., Maia, A., Plomp, J., Brussaard, A., Heeroma, J., Vermeer, H., Toonen, R., Hammer, R., van den Berg, T. K., Missler, M., et al. (2000) · Science · doi:10.1126/science.287.5454.864 · Cited by 1,387

Membrane Fusion

Jahn, R., Lang, T., & Südhof, T. C. (2003) · Cell · doi:10.1016/s0092-8674(03)00112-0 · Cited by 1,364

Syntaxin: A Synaptic Protein Implicated in Docking of Synaptic Vesicles at Presynaptic Active Zones

Bennett, M. K., Calakos, N., & Scheller, R. H. (1992) · Science · doi:10.1126/science.1321498 · Cited by 1,263

SNARE-mediated membrane fusion

Chen, Y. A., & Scheller, R. H. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35052017 · Cited by 1,133

Definition of the readily releasable pool of vesicles at hippocampal synapses.

Rosenmund, C., & Stevens, C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80146-4 · Cited by 1,084

Etude de l’interaction neuro-cardiaque sur puce microfluidique à partir de cellules souches pluripotentes induites humaines

Bernardin, A. A. (2022) · theses.fr (ABES) · doi:10.70675/4ad7be3ez4ba9z4af7z83aez54963d263fc2

Prévention de l’obésité alimentaire : impact des acides gras polyinsaturés en n-3 sur le microbiote intestinal et l’intégrité et le processus autophagique en lien avec la sécrétion du mucus colique

Bourragat, A. (2023) · theses.fr (ABES) · doi:10.70675/3b3b969dz44b9z4105z8818z615b5feee249

All-optical interrogation of the role of interneurons in CA1 cell assemblies

Vorobyev, A. (2023) · theses.fr (ABES) · doi:10.70675/eb10a4e1za595z4f16z9e3bz115344f3d87a

Rôles différentiels des composants pré- et postsynaptiques dans le contrôle de la plasticité synaptique à court terme à haute fréquence

Nowacka, A. (2023) · theses.fr (ABES) · doi:10.70675/c98153caz1fb7z4e28zba68z9e92eca244d3

Membranes remodeling by proteins in intracellular trafficking : a bottom up approach of the roles of golgins for Golgi structuration and of SNAREs for synaptic fusion

Mion, D. (2025) · theses.fr (ABES) · doi:10.70675/f85cd0f1z1db3z410dzb8a2zc76237cc43fc

Physiological implications of phase separation in vesicle organization and trafficking

Liu, C., Cheng, J., & Wu, X. (2026) · BMC Biology · doi:10.1186/s12915-026-02607-6

Temporal tracking of Synaptobrevin-1 trafficking reveals SAM-4/BORC-dependent trafficking routes in C. elegans neuronsPreprint

Chauhan, B. S., Kunwar, A., & Koushika, S. P. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.29.721573

Tracking Synaptic Vesicles in Live Neurons Using Single-Molecule Super-resolution Microscopy

Longfield, S. F., & Meunier, F. A. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5268-8_9

Hypoxia‐induced vulnerability of the somatosensory nervous system

Corbett, J., & Hulse, R. P. (2026) · The Journal of Physiology · doi:10.1113/jp290625

Activation in vesicle-mediated signaling shaped by batch arrival statistics

Hauke, J., Voits, J. B., & Schwarz, U. S. (2026) · New Journal of Physics · doi:10.1088/1367-2630/ae98a6

From gene to therapy in MODY: β-cell mechanisms and precision treatment

Wang, T., Tan, M., Zhou, H., Chen, C., Zhong, M., Dai, Y., Zeng, J., & Song, S. (2026) · Academia molecular biology and genomics. · doi:10.20935/acadmolbiogen8301

Genetic Rescue of a Lethal Wasting Mutation ( Syb1 lew/lew ) by Neuron-Specific Expression of ECFP-Syb2Preprint

Lin, W., Ye, Q., & Lin, W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.22.727260

Biology and physiology of synaptic vesicle clusters

Brodin, L., & Shupliakov, O. (2026) · Trends Open · doi:10.1016/j.treopn.2026.04.006

Spontaneous neurotransmitter release is regulated by Unc-5Preprint

Vernon, S. W., Ruchti, E., Paolantoni, C., Smith, R. C., Campenhoudt, M. V., & McCabe, B. D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.02.729526

Genetic modifiers of psychiatric, motor, and cognitive symptoms in Huntington’s diseasePreprint

Li, Q. S., 곽승, Sampaio, C., Vogt, T., & Rosinski, J. (2026) · medRxiv · doi:10.64898/2026.06.16.26355789

Munc18-1 is crucial for photoreceptor function, survival and regulation of syntaxin-3 localization and expression

Huang, M., Chow, C. H., Noworolski, R., Charish, J., Indrawinata, K., Harada, H., Wallace, V. A., Monnier, P. P., & Sugita, S. (2026) · Scientific Reports · doi:10.1038/s41598-026-57827-1

Glutamate, Immune Cells and Alzheimer’s Disease: An Attempt to Link the Triad

Chinas, N. A., & Alexopoulos, H. (2026) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-026-01784-w

LUHMES-derived 3D organoids as an enhanced platform for modelling dopaminergic neurodegeneration in Parkinson's disease

Keighron, C. N., Casas-Martinez, J. C., Barral, S., & Quinlan, L. R. (2026) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2026.1807358

X-linked SYTL4 missense variant disrupts RAB27A-dependent vesicle trafficking and synaptic transmission in autism

Liao, Y., Zhang, S., Zhang, X., Tan, S., Luo, Y., Wan, Y., Lyu, Y., Xie, B., Zhan, R., Zhang, Y., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2605483123

Impaired NADH-linked mitochondrial respiration disrupts ventral midbrain neuronal programs in POLG disease

Chen, A., Yangzom, T., Sullivan, G. J., & Liang, K. X. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-08706-w

Development of Calcium Signaling in Postsynaptic Neurons of the Medial Nucleus of the Trapezoid Body in the Mouse

Tanmy, T. T., Wang, H., & Lu, Y. (2026) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-026-01066-8

A microfluidics platform for studying ion and solute transport by isolated synaptic vesicles

Upmanyu, N., Olsthoorn, L., Leon, S., Sambandan, S., Perego, E., Mimoso, T., Socrier, L., Cretich, M., Chiari, M., Steinem, C., et al. (2026) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2026.116020

“Dynamic protein changes in aversive taste conditioning: insights from GAP-43 and synaptophysin in memory retrieval and extinction”

Grijalva-Contreras, L. E., & Paredes, R. G. (2026) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2026.108204

Neurotoxins As Tools for Studying Neuromuscular Transmission in Cholinergic Synapses

Bukharaeva, E. A., & Petrov, A. M. (2026) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747826700157

Paralog-specific roles of GSK-3 in synaptic plasticity and behaviour in the adult mouse hippocampus

Kang, S. (2026) · TSpace (University of Toronto)

Energy distribution in memristive neuronal networks with unidirectional chemical synapses

Xie, Y., Jia, Y., & Yang, L. (2026) · Physica A Statistical Mechanics and its Applications · doi:10.1016/j.physa.2026.132002

Advances in electrochemical methods for exocytosis analysis

Chu, P., Pan, C., & Yu, P. (2026) · Journal of Electroanalytical Chemistry · doi:10.1016/j.jelechem.2026.120571

Экспериментальная биология и биотехнология. – 2023. – № 3

(2023) · Digital Library of the Belarusian State University (Belarusian State University)

Rabies Virus Glycoprotein G Variation Is Associated with Neurovirulence and Reduced Vamp2 Abundance in a Mouse Model of Direct CNS Infection

Liu, C., Guo, H., Yin, K., Sun, Y., Ma, Z., Wang, F., Niu, Y., & 温永俊 (2026) · Veterinary Sciences · doi:10.3390/vetsci13090919

Cross-omics profiling reveals cortical neuronal dysfunction following neonatal intraventricular haemorrhage that is attenuated by decorin treatmentPreprint

Hewitt, B. J., García‐Bonilla, M., McAllister, J. P., Pahuja, S., Pellowe, G. A., Newman, M. S., Roberts, L., Roberts, J. A., Kitchen, P., Bill, R. M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.07.749813

Neuroplasticity after traumatic brain injury: mechanisms and clinical implications

O’Connor, M., Sankar, S., Sharma, S., Alghazi, D., Chundru, V., Al-Alem, Z. Y. M. Z., Lukin, R., & Banjo, E. (2026) · Irish Journal of Medical Science (1971 -) · doi:10.1007/s11845-026-04624-4

Dynamic remodeling of the transcriptional landscape drives Merkel cell specification and mechanosensory differentiation

Zhang, Y., Yuan, H., Jiang, Y., Wang, T., Rui, C., Ding, Y., Wang, T., Wang, C., & Xiao, Y. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2603770123

Targeted Restoration of the Microbial Tryptophan Oxidative Pathway Ameliorates Autism‐Like Behavioral and Synaptic Deficits

Guo, R., He, C., Xiao, X., Li, J., Zhang, Z., He, Y., Wang, C., Zhao, J., Gong, J., Liang, J., et al. (2026) · Advanced Science · doi:10.1002/advs.202522265

PAK4 exacerbates melanoma immunosuppression by promoting exosome release

Zhou, R., Xu, T., Shen, Z., Zhang, Y., Li, S., Liu, C., Li, J., Wang, H., Ren, M., Gao, X., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2536086123

The medicinal plant Sutherlandia Frutescens regulates gene expression to reverse insulin resistace in rats

Fortuin, M. (2013) · Nelson Mandela University Research Repository

Humanin attenuates neuronal cellular senescence and preserves neurotransmitter release in differentiated PC12 cells

棚橋美紀, Kozuka, A., Sasakawa, N., & Niikura, T. (2026) · Neuroscience · doi:10.1016/j.neuroscience.2026.10.017

Interaction of the vesicle membrane and cell membrane

Wu, M., Feng, S., Li, Y., & Lai, Y. (2026) · Advances in biomembranes and lipid self-assembly · doi:10.1016/bs.abl.2026.10.001

Phospholipid Monolayers and Vesicular Membranes Show Only Minor Structural Changes After Interaction With α$\alpha$‐Synuclein at Low and Physiological Concentrations

Major, A., von Campenhausen, E., Hilger, R., Bruns, H., Czajka, T., Pontoni, D., Rosenthal, M., Pérez, G. A., Hoffmann, C., Al‐Azzani, M., et al. (2026) · ChemPhysChem · doi:10.1002/cphc.70589

Synaptic transmission and plasticity: molecular mechanisms, biological functions and therapeutic opportunities in neurodegenerative diseases

Sun, J., Gao, G., Wang, S., Li, S., Tang, J., Liu, H., & Tang, T.-S. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02776-4

Conservation of a synaptic blueprint across the animal kingdom

Houcek, A., & Kavalali, E. T. (2026) · The Journal of Physiology · doi:10.1113/jp291096

An analysis of fatty acid metabolism's role in the development of acute functional tolerance to ethanol in Caenorhabditis elegans

Raabe, R. (2014) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/r9rc-gz34

Mécanismes cellulaires sous-tendant le raffinement des projections rétiniennes

Assali, A. (2014) · theses.fr (ABES) · doi:10.70675/1fe553f7zd7caz4470za801z41712c488de4

L’organisation spatiale des canaux calciques cav1.3 détermine l’efficacité de l’exocytose des synapses à ruban dans les cellules ciliées de l’oreille interne

Vincent, P. (2015) · theses.fr (ABES) · doi:10.70675/d6640df4zd5b5z4c26z8029zca84c46a7615

Parkin mediated mitochondrial quality control in central dopamine neurons

Hawong, H.-Y. (2014) · Michigan State University Libraries · doi:10.25335/m5ph73

Synaptic Plasticity: Short-Term Mechanisms

Dittman, J. S., & Kreitzer, A. C. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01386-3

Studien zu den biochemischen und strukturellen Eigenschaften von Snapin und zu seiner Rolle in der neuronalen Exozytose

Vites, O. (2005) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-172

Clinical and functional studies of autoimmune disorders of neuromuscular transmission

Spillane, J. E. (2015) · UCL Discovery (University College London)

On the chloride dependence of vesicular glutamate transport

Schenck, S. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-362

A single molecular study of the regulation of SNARE-mediated membrane fusion

Song, J. (2014) · Iowa State University Digital Repository (Iowa State University)

Snares and Munc18 in synaptic vesicle fusion

Rizo, J., & Südhof, T. C. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn898 · Cited by 539

Molecular machines governing exocytosis of synaptic vesicles

Jahn, R., & Fasshauer, D. (2012) · Nature · doi:10.1038/nature11320 · Cited by 1,004

The molecular machinery of synaptic vesicle exocytosis

Li, L., & Chin, L. (2003) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-003-2240-7 · Cited by 129

Mechanism of neurotransmitter release coming into focus

Rizo, J. (2018) · Protein Science · doi:10.1002/pro.3445 · Cited by 210

3. Molecular analysis of neurotransmitter release

Schiavo, G., & Stenbeck, G. (2017) · Princeton University Press eBooks · doi:10.2307/j.ctv3hh4x0.8