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

Myosin phosphatase and RhoA-activated kinase modulate neurotransmitter release by regulating SNAP-25 of SNARE complex

Horváth, D., Tamás, I., Sipos, A., Darula, Z., Bécsi, B., Nagy, D., Iván, J., Erdődi, F., & Lontay, B. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177046 · Cited by 20

Regional differences in nerve terminal Na+ channel subtype expression and Na+ channel‐dependent glutamate and GABA release in rat CNS

Westphalen, R. I., Yu, J., Krivitski, M., Jih, T., & Hemmings, H. C. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06722.x · Cited by 20

A Central Kinase Domain of Type I Phosphatidylinositol Phosphate Kinases Is Sufficient to Prime Exocytosis

Wang, L., Li, G., & Sugita, S. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413263200 · Cited by 20

Action Potential Modulates Ca2+-Dependent and Ca2+-Independent Secretion in a Sensory Neuron

Zheng, H., Fan, J., Xiong, W., Zhang, C., Wang, X., Liu, H., Liu, H.-J., Sun, L., Wang, Y., Zheng, L. G., et al. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2008.11.037 · Cited by 20

Depressed excitability and ion currents linked to slow exocytotic fusion pore in chromaffin cells of the SOD1G93A mouse model of amyotrophic lateral sclerosis

Calvo‐Gallardo, E., de Pascual, R., Fernández‐Morales, J., Arranz-Tagarro, J.-A., Maroto, M., Nanclares, C., Gandía, L., de Diego, A. M. G., Padín, J. F., & de Diego, A. M. G. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00272.2014 · Cited by 20

Sequential onset of presynaptic molecules during olfactory sensory neuron maturation

Marcucci, F., Zou, D., & Firestein, S. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22094 · Cited by 20

Mechanisms of ATP Release and Inactivation

Burnstock, G., & Verkhratsky, A. (2012) · Springer eBooks · doi:10.1007/978-3-642-28863-0_4 · Cited by 20

The Regulation of Synaptic Vesicle Recycling by cGMP-Dependent Protein Kinase Type II in Cerebellar Granule Cells under Strong and Sustained Stimulation

Collado‐Alsina, A., Ramírez‐Franco, J., Sánchez‐Prieto, J., & Torres, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0103-14.2014 · Cited by 20

Delta Opioid Receptor Expression and Function in Primary Afferent Somatosensory Neurons

François, A., & Scherrer, G. (2017) · Handbook of experimental pharmacology · doi:10.1007/164_2017_58 · Cited by 20

MERCs. The Novel Assistant to Neurotransmission?

Shirokova, O. M., Pchelin, P. V., & Mukhina, I. V. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.589319 · Cited by 20

Rab3A deletion selectively reduces spontaneous neurotransmitter release at the mouse neuromuscular synapse

Sons, M. S., & Plomp, J. J. (2006) · Brain Research · doi:10.1016/j.brainres.2006.03.055 · Cited by 20

FM Dye Photo-Oxidation as a Tool for Monitoring Membrane Recycling in Inner Hair Cells

Kamin, D., Revelo, N. H., & Rizzoli, S. O. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088353 · Cited by 19

Phosphatidylserine-dependent structure of synaptogyrin remodels the synaptic vesicle membrane

Yu, T., Flores‐Solis, D., Eastep, G. N., Becker, S., & Zweckstetter, M. (2023) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-01004-9 · Cited by 19

Synapses without tension fail to fire in an in vitro network of hippocampal neurons

Joy, M. S. H., Nall, D., Emon, B., Lee, K. Y., Barishman, A., Ahmed, M., Rahman, S., Selvin, P. R., & Saif, M. T. A. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2311995120 · Cited by 19

Visualizing dopamine released from living cells using a nanoplasmonic probe

Qin, W., Wang, S. P., Li, J., Peng, T., Xu, Y., Wang, K. K., Shi, J., Fan, C., & Li, D. (2015) · Nanoscale · doi:10.1039/c5nr04433b · Cited by 19

Single vesicle biochips for ultra-miniaturized nanoscale fluidics and single molecule bioscience

Christensen, A. L., Lohr, C., Christensen, S. M., & Stamou, D. G. (2013) · Lab on a Chip · doi:10.1039/c3lc50492a · Cited by 19

Role of presynaptic phosphoprotein synapsin II in schizophrenia

Molinaro, L., Hui, P., Tan, M. L., & Mishra, R. K. (2015) · World Journal of Psychiatry · doi:10.5498/wjp.v5.i3.260 · Cited by 19

Botulinum Toxin A for Controlling Obesity

Pero, R., Coretti, L., & Lembo, F. (2016) · Toxins · doi:10.3390/toxins8100281 · Cited by 19

Calcium Assists Dopamine Release by Preventing Aggregation on the Inner Leaflet of Presynaptic Vesicles

Mokkila, S., Postila, P. A., Rissanen, S., Juhola, H., Vattulainen, I., & Róg, T. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00395 · Cited by 19

Activity-Dependence of Synaptic Vesicle Dynamics

Forte, L. A., Gramlich, M. W., & Klyachko, V. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0383-17.2017 · Cited by 19

Haploinsufficiency of STXBP1 and Ohtahara Syndrome

Saitsu, H., Kato, M., & Matsumoto, N. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0064 · Cited by 19

Solvatochromic and pH-Sensitive Fluorescent Membrane Probes for Imaging of Live Cells

Thomas, D. M., Rubio, V., Iragavarapu‐Charyulu, V., Guzmán, E. A., Pelletier, O. B., Alamgir, S., Zhang, Q., & Stawikowski, M. J. (2021) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00732 · Cited by 19

Investigation of neuromuscular abnormalities in neurotrophin‐3‐deficient mice

Sheard, P. W., Bewick, G. S., Woolley, A. G., Shaw, J., Fisher, L. C., Fong, S. W., & Duxson, M. J. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07032.x · Cited by 19

Proteomic analysis reveals differentially expressed proteins in the rat frontal cortex after methamphetamine treatment

Faure, J., Hattingh, S., Stein, D. J., & Daniels, W. M. U. (2009) · Metabolic Brain Disease · doi:10.1007/s11011-009-9167-0 · Cited by 19

Neuron-Specific Expression of Tomosyn1 in the Mouse Hippocampal Dentate Gyrus Impairs Spatial Learning and Memory

Barak, B., Okun, E., Ben‐Simon, Y., Lavi, A., Shapira, R., Madar, R., Wang, Y., Norman, E. D., Sheinin, A., Pita, M. A., et al. (2013) · NeuroMolecular Medicine · doi:10.1007/s12017-013-8223-4 · Cited by 19

Role of the ubiquitin–proteasome system in nervous system function and disease: using C. elegans as a dissecting tool

Baptista, M. S., Duarte, C. B., & Maciel, P. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0946-0 · Cited by 19

AcuteIn VivoGenetic Rescue Demonstrates That Phosphorylation of RIM1α Serine 413 Is Not Required for Mossy Fiber Long-Term Potentiation

Yang, Y., & Calakos, N. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4285-09.2010 · Cited by 19

Paracrine Role of GABA in Adrenal Chromaffin Cells

Inoue, M., Harada, K., Matsuoka, H., & Warashina, A. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9569-x · Cited by 19

Imaging of Ca2+ responses mediated by presynaptic L-type channels on GABAergic boutons of cultured hippocampal neurons

Holmgaard, K., Jensen, K., & Lambert, J. D. C. (2008) · Brain Research · doi:10.1016/j.brainres.2008.10.033 · Cited by 19

Correlative electron and confocal microscopy assessment of synapse localization in the central nervous system of an insect

Hohensee, S., Bleiß, W., & Duch, C. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.09.018 · Cited by 19

Human neuronal changes in brain edema and increased intracranial pressure

Faragó, N., Kocsis, Á. K., Braskó, C., Lovas, S., Rózsa, M., Baka, J., Kovács, B., Mikite, K., Szemenyei, V., Molnár, G., et al. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0356-x · Cited by 19

Effects of Metabolic Energy on Synaptic Transmission and Dendritic Integration in Pyramidal Neurons

Yuan, Y., Huo, H., & Fang, T. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00079 · Cited by 19

Regulation of Gastric Acid Secretion

Shulkes, A., Baldwin, G. S., & Giraud, A. S. (2006) · Elsevier eBooks · doi:10.1016/b978-012088394-3/50052-0 · Cited by 19

Characterization of the localization and function of NECAP 1 in neurons

Murshid, A., Srivastava, A., Kumar, R., & Presley, J. F. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04066.x · Cited by 19

The fate of synaptic vesicle components upon fusion

Opazo, F., & Rizzoli, S. O. (2010) · Communicative & Integrative Biology · doi:10.4161/cib.3.5.12132 · Cited by 19

Synaptic vesicle-omics in mice captures signatures of aging and synucleinopathy

Gao, V., Chlebowicz, J., Gaskin, K., Briano, J. A., Komer, L. E., Pineda, A., Jhalani, S., Ahmad, S., Uwaifo, E., Black, L. S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59441-7 · Cited by 18

Presynaptic Precursor Vesicles—Cargo, Biogenesis, and Kinesin-Based Transport across Species

Petzoldt, A. G. (2023) · Cells · doi:10.3390/cells12182248 · Cited by 18

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

Paul, M. S., Michener, S. L., Pan, H., Chan, H., Pfliger, J. M., Rosenfeld, J. A., Lerma, V. C., Tran, A. A., Longley, M. A., Lewis, R. A., et al. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2023.12.004 · Cited by 18

Non-ionotropic voltage-gated calcium channel signaling

Trus, M., & Atlas, D. (2024) · Channels · doi:10.1080/19336950.2024.2341077 · Cited by 18

Quantal amplitude at the cone ribbon synapse can be adjusted by changes in cytosolic glutamate.

Bartoletti, T. M., & Thoreson, W. B. (2011) · PubMed · Cited by 18

Imaging of kiss-and-run exocytosis of surface receptors in neuronal cultures

Román‐Vendrell, C., Chevalier, M. W., Acevedo‐Canabal, A., Delgado‐Peraza, F., Flores‐Otero, J., & Yudowski, G. A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00363 · Cited by 18

The regulation and packaging of synaptic vesicles as related to recruitment within glutamatergic synapses

Wu, W., & Cooper, R. L. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.037 · Cited by 18

Intracellular Parcel Service: Current Issues in Intracellular Membrane Trafficking

Herrmann, J. M., & Spang, A. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-2309-0_1 · Cited by 18

Genome-wide DNA methylation changes associated with olfactory learning and memory in Apis mellifera

Li, Y., Zhang, L.-Z., Yi, Y., Hu, W.-W., Guo, Y.-J., Zeng, Z., Huang, Z.-Y., & Wang, Z. (2017) · Scientific Reports · doi:10.1038/s41598-017-17046-1 · Cited by 18

Calcium-Independent Exo-endocytosis Coupling at Small Central Synapses

Orlando, M., Schmitz, D., Rosenmund, C., & Herman, M. A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.060 · Cited by 18

Real-time three-dimensional tracking of single vesicles reveals abnormal motion and pools of synaptic vesicles in neurons of Huntington's disease mice

Chen, S., Yoo, H., Li, C. H., Park, C., Park, G., Tan, L. Y., Jung, S., & Park, H. (2021) · iScience · doi:10.1016/j.isci.2021.103181 · Cited by 18

Comprehensive Analysis of Mouse Hippocampal Lysine Acetylome Mediated by Sea Cucumber Peptides Preventing Memory Impairment

Lu, Z., Xu, X., Li, D., Sun, N., & Lin, S. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c05155 · Cited by 18

Protein phosphatase‐1M and Rho‐kinase affect exocytosis from cortical synaptosomes and influence neurotransmission at a glutamatergic giant synapse of the rat auditory system

Lontay, B., Pál, B. Z., Serfözö, Z., Kőszeghy, Á., Szűcs, G., Rusznák, Z., & Erdődi, F. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07882.x · Cited by 18

Inhibition of exocytosis or endocytosis blocks activity‐dependent redistribution of synapsin

Orenbuch, A., Shulman, Y., Lipstein, N., Bechar, A., Lavy, Y., Brumer, E., Vasileva, M., Kahn, J., Barki‐Harrington, L., Kuner, T., et al. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07579.x · Cited by 18

Kindling‐induced asymmetric accumulation of hippocampal 7S SNARE complexes correlates with enhanced glutamate release

Matveeva, E. A., Davis, V. A., Whiteheart, S. W., VANAMAN, T. C., Gerhardt, G. A., & Slevin, J. T. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03345.x · Cited by 18

Identification of reproduction-related proteins and characterization of the protein disulfide isomerase A6 cDNA in ovaries of the giant tiger shrimp Penaeus monodon

Talakhun, W., Roytrakul, S., Phaonakrop, N., Kittisenachai, S., Khamnamtong, B., Klinbunga, S., & Menasveta, P. (2012) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2012.02.003 · Cited by 18

Depletion of Complexin II does not affect disease progression in a mouse model of Huntington's disease (HD); support for role for complexin II in behavioural pathology in a mouse model of HD

Glynn, D., Reim, K., Brose, N., & Morton, A. J. (2006) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.10.017 · Cited by 18

Phylogenetic Analysis of the NEEP21/Calcyon/P19 Family of Endocytic Proteins: Evidence for Functional Evolution in the Vertebrate CNS

Muthusamy, N., Ahmed, S. A., Rana, B. K., Navarre, S., Kozlowski, D. J., Liberles, D. A., & Bergson, C. M. (2009) · Journal of Molecular Evolution · doi:10.1007/s00239-009-9273-y · Cited by 18

Synaptotagmin 1 directs repetitive release by coupling vesicle exocytosis to the Rab3 cycle

Cheng, Y., Wang, J., Wang, Y., & Ding, M. (2015) · eLife · doi:10.7554/elife.05118 · Cited by 18

The C2H2 zinc-finger protein SYD-9 is a putative posttranscriptional regulator for synaptic transmission

Wang, Y., Gracheva, E. O., Richmond, J. E., Kawano, T., Couto, J. M., Calarco, J. A., Vijayaratnam, V., Jin, Y., & Zhen, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602073103 · Cited by 18

Temperature-sensitive paralytic mutants: insights into the synaptic vesicle cycle

Vijayakrishnan, N., & Broadie, K. S. (2006) · Biochemical Society Transactions · doi:10.1042/bst0340081 · Cited by 18

Muscle fibers and their synapses differentially adapt to aging and endurance training

Deschenes, M. R., Li, S., Adan, M. A., Oh, J. J., & Ramsey, H. C. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.03.010 · Cited by 18

An updated investigation on the dromedary camel cerebellum (Camelus dromedarius) with special insight into the distribution of calcium-binding proteins

Attaai, A., Noreldin, A. E., Abdel‐Maksoud, F. M., & Hussein, M. T. (2020) · Scientific Reports · doi:10.1038/s41598-020-78192-7 · Cited by 18

Stimulus-Dependent Alterations in Quantal Neurotransmitter Release

Grabner, C. P., & Fox, A. P. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00017.2006 · Cited by 18

The C2A-C2B Linker Defines the High Affinity Ca2+ Binding Mode of Rabphilin-3A

Montaville, P., Schlicker, C., Leonov, A., Zweckstetter, M., Sheldrick, G. M., & Becker, S. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606746200 · Cited by 18

A lysolecithin/fatty acid mixture promotes and then blocks neurotransmitter release at the Drosophila melanogaster larval neuromuscular junction

Megighian, A., Rigoni, M., Caccin, P., Zordan, M. A., & Montecucco, C. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.01.040 · Cited by 18

Progress in understanding the neuronal SNARE function and its regulation

Yoon, T., & Shin, Y.-K. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8372-z · Cited by 18

The t-SNARE Complex: A Close Up

Dun, A. R., Rickman, C., & Duncan, R. R. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9599-4 · Cited by 17

Effects of lipophilic phycotoxin okadaic acid on the early development and transcriptional expression of marine medaka Oryzias melastigma

Yang, Y., Li, A., Qiu, J., Yan, W., Han, L., Li, D., & Yin, C. (2023) · Aquatic Toxicology · doi:10.1016/j.aquatox.2023.106576 · Cited by 17

The Na+/H+ Exchanger Nhe1 Modulates Network Excitability via GABA Release

Bocker, H. T., Heinrich, T., Liebmann, L., Hennings, J. C., Seemann, E. A., Gerth, M., Jakovčevski, I., Preobraschenski, J., Kessels, M. M., Westermann, M., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy308 · Cited by 17

Energetic substrate availability regulates synchronous activity in an excitatory neural network

Tourigny, D. S., Karim, M. K. A., Echeveste, R., Kotter, M., & O'Neill, J. S. (2019) · PLoS ONE · doi:10.1371/journal.pone.0220937 · Cited by 17

The CHD Protein, Kismet, is Important for the Recycling of Synaptic Vesicles during Endocytosis

Latcheva, N. K., Delaney, T. L., Viveiros, J. M., Smith, R. A., Bernard, K. M., Harsin, B., Marenda, D. R., & Liebl, F. L. W. (2019) · Scientific Reports · doi:10.1038/s41598-019-55900-6 · Cited by 17

Expansion tomography for large volume tissue imaging with nanoscale resolution

Chen, R., Cheng, X., Zhang, Y., Yang, X., Wang, Y., Liu, X., & Zeng, S. (2021) · Biomedical Optics Express · doi:10.1364/boe.431696 · Cited by 17

Serum calcium levels are associated with cognitive function in hypoparathyroidism: a neuropsychological and biochemical study in an Italian cohort of patients with chronic post-surgical hypoparathyroidism

Saponaro, F., Alfì, G., Cetani, F., Matrone, A., Mazoni, L., Apicella, M., Pardi, E., Borsari, S., Laurino, M., Lai, E. Y., et al. (2022) · Journal of Endocrinological Investigation · doi:10.1007/s40618-022-01822-6 · Cited by 17

A search for synthetic peptides that inhibit soluble N‐ethylmaleimide sensitive‐factor attachment receptor‐mediated membrane fusion

Jung, C. H., Yang, Y., Kim, J., Shin, J., Jin, Y., Shin, J., Lee, J. H., Chung, K. M., Hwang, J. S., Oh, J. M., et al. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06458.x · Cited by 17

The pre‐synaptic motor nerve terminal as a site for antibody‐mediated neurotoxicity in autoimmune neuropathies and synaptopathies

Fewou, S. N., Plomp, J. J., & Willison, H. J. (2013) · Journal of Anatomy · doi:10.1111/joa.12088 · Cited by 17

Cyclic AMP potentiates Ca2+-dependent exocytosis in pancreatic duct epithelial cells

Jung, S., Hille, B., Nguyen, T. D., & Koh, D. (2010) · The Journal of General Physiology · doi:10.1085/jgp.200910355 · Cited by 17

Ropren® treatment reverses anxiety-like behavior and monoamines levels in gonadectomized rat model of Alzheimer’s disease

Fedotova, J., Soultanov, V., Nikitina, T. V., Roschin, V., Ordyan, N., & Hriţcu, L. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.08.065 · Cited by 17

Effect of O-methyl-β-cyclodextrin-modified magnetic nanoparticles on the uptake and extracellular level of l-glutamate in brain nerve terminals

Horák, D., Beneš, M. J., Procházková, Z., Trchová, M., Borysov, A., Pastukhov, A. O., Paliienko, K., & Borisova, Т. (2016) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2016.10.007 · Cited by 17

Accelerating SNARE‐Mediated Membrane Fusion by DNA–Lipid Tethers

Xu, W., Wang, J., Rothman, J. E., & Pincet, F. (2015) · Angewandte Chemie · doi:10.1002/ange.201506844 · Cited by 17

Synthesis of new fluorinated analogs of GABA, Pregabalin bioisosteres, and their effects on [3H]GABA uptake by rat brain nerve terminals

Borisova, Т., Pozdnyakova, N., Shaitanova, E. N., Gerus, I. I., Dudarenko, M., Mironets, R. V., Haufe, G., & Kukhar, V. P. (2015) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2015.06.038 · Cited by 17

Ideal observer analysis of signal quality in retinal circuits

Smith, R. G., & Dhingra, N. K. (2009) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2009.05.001 · Cited by 17

Nonhomogeneous distribution of filamentous actin in the presynaptic terminals on the spinal motoneurons

Li, Y., Bai, W., Zhou, L., Sun, L., & Hashikawa, T. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22374 · Cited by 17

Synaptic Vesicles: An Organelle Comes of Age

Südhof, T. C. (2006) · Cell · doi:10.1016/j.cell.2006.10.033 · Cited by 17

Mso1 Is a Novel Component of the Yeast Exocytic SNARE Complex

Castillo-Flores, A., Weinberger, A., Robinson, M., & Gerst, J. E. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507142200 · Cited by 17

Linking differences in membrane tension with the requirement for a contractile actomyosin scaffold during exocytosis in salivary glands

Masedunskas, A., Porat‐Shliom, N., & Weigert, R. (2012) · Communicative & Integrative Biology · doi:10.4161/cib.18258 · Cited by 17

Exocytosis is impaired in mucopolysaccharidosis IIIA mouse chromaffin cells

Keating, D. J., Winter, M. A., Hemsley, K. M., Mackenzie, K., Teo, E. H., Hopwood, J. J., Brooks, D. A., & Parkinson-Lawrence, E. J. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.034 · Cited by 16

Proteomic investigations of the synaptic vesicle interactome

Barth, J., & Volknandt, W. (2011) · Expert Review of Proteomics · doi:10.1586/epr.11.7 · Cited by 16

Mechanism for Calcium Ion Sensing by the C2A Domain of Synaptotagmin I

Gauer, J. W., Sisk, R. M., Murphy, J., Jacobson, H., Sutton, R. B., Gillispie, G. D., & Hinderliter, A. K. (2012) · Biophysical Journal · doi:10.1016/j.bpj.2012.05.051 · Cited by 16

Negative Coupling as a Mechanism for Signal Propagation between C2 Domains of Synaptotagmin I

Fealey, M. E., Gauer, J. W., Kempka, S. C., Miller, K. M., Nayak, K., Sutton, R. B., & Hinderliter, A. K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046748 · Cited by 16

Personalized approach in brain protection by hypothermia: individual changes in non-pathological and ischemia-related glutamate transport in brain nerve terminals

Pastukhov, A. O., Krisanova, N. V., Maksymenko, V., & Borisova, Т. (2016) · The EPMA Journal · doi:10.1186/s13167-016-0075-1 · Cited by 16

Trafficking of synaptic vesicles is changed at the hypothalamus by exposure to an 835 MHz radiofrequency electromagnetic field

Kim, J. H., Huh, Y. H., & Kim, H. R. (2019) · General Physiology and Biophysics · doi:10.4149/gpb_2019020 · Cited by 16

Developmental Time Course of SNAP-25 Isoforms Regulate Hippocampal Long-Term Synaptic Plasticity and Hippocampus-Dependent Learning

Gopaul, K. R., Irfan, M., Miry, O., Vose, L. R., Moghadam, A. A., Subah, G., Hökfelt, T. G. M., Bark, C., & Stanton, P. K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041448 · Cited by 16

Hippocampal network dysfunction as a mechanism of early-onset dementia after preeclampsia and eclampsia

Johnson, A. C., Li, Z., Orfila, J. E., Herson, P. S., & Cipolla, M. J. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101938 · Cited by 16

Neurexins play a crucial role in cerebellar granule cell survival by organizing autocrine machinery for neurotrophins

Uemura, T., Suzuki‐Kouyama, E., Kawase, S., Kurihara, T., Yasumura, M., Yoshida, T., Fukai, S., Yamazaki, M., Fei, P., Abe, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110624 · Cited by 16

Involvement of calpain and synaptotagmin Ca2+ sensors in hormone secretion from excitable endocrine cells

Aganna, E., Burrin, J. M., Hitman, G. A., & Turner, M. D. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06737 · Cited by 16

Optical control of calcium-regulated exocytosis

Izquierdo-Serra, M., Trauner, D. H., Llobet, A., & Gorostiza, P. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.11.003 · Cited by 16

Developmental and spatial expression pattern of α‐Taxilin in the rat central nervous system

Sakakibara, S., Nakadate, K., Tanaka‐Nakadate, S., Yoshida, K., Nogami, S., Shirataki, H., & Ueda, S. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21817 · Cited by 16

Protein kinase C modulates synaptic vesicle acidification in a ribbon type nerve terminal in the retina

Abreu, B. J., Guimarães, M. D. S., Jácome, L. U., Vígh, J., VonGersdorff, H., Prado, M. A. M., & Guatimosim, C. (2008) · Neurochemistry International · doi:10.1016/j.neuint.2008.07.004 · Cited by 16

Manipulation of isolated brain nerve terminals by an external magnetic field using D-mannose-coated γ-Fe2O3 nano-sized particles and assessment of their effects on glutamate transport

Borisova, Т., Krisanova, N. V., Borуsov, A., Sivko, R., Остапченко, Л. І., Babič, M., & Horák, D. (2014) · Beilstein Journal of Nanotechnology · doi:10.3762/bjnano.5.90 · Cited by 16

Quantitative proteomics reveals olfactory input-dependent alterations in the mouse olfactory bulb proteome

Zeng, H., Rao, X., Zhang, L., Zhao, X., Zhang, W.-P., Wang, J., Xu, F., & Guo, L. (2014) · Journal of Proteomics · doi:10.1016/j.jprot.2014.06.023 · Cited by 16

A minimalist model to measure interactions between proteins and synaptic vesicles

Perego, E., Reshetniak, S., Lorenz, C., Hoffmann, C., Milovanović, D., Rizzoli, S. O., & Köster, S. (2020) · Scientific Reports · doi:10.1038/s41598-020-77887-1 · Cited by 16

Neuroprotective Role of the B Vitamins in the Modulation of the Central Glutamatergic Neurotransmission

Huang, S.-K., Lü, C.-W., Lin, T., & Wang, S. (2021) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527320666210902165739 · Cited by 16

Identification of a novel herpes simplex virus type 1 transcript and protein (AL3) expressed during latency

Jaber, T., Henderson, G., Li, S., Perng, G., Carpenter, D., Wechsler, S. L., & Jones, C. (2009) · Journal of General Virology · doi:10.1099/vir.0.013318-0 · Cited by 16

Motifs and cis-regulatory modules mediating the expression of genes co-expressed in presynaptic neurons

Liu, R. R., Hannenhalli, S. S., & Bućan, M. (2009) · Genome biology · doi:10.1186/gb-2009-10-7-r72 · Cited by 16

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

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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

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3. Molecular analysis of neurotransmitter release

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