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

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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

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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

Correction: 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.0179296 · Cited by 13

Lipopolysaccharide induces neuroinflammation in a valproic acid male model of autism

Jiang, J., Zhang, L., Wu, D. A., Zhao, D., Ying, S., & Ding, S. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.111154 · Cited by 12

Mitochondrial specialization and signaling shape neuronal function

Tong, B. C., Gubinelli, F., Burbulla, L. F., & Harbauer, A. B. (2026) · Trends in Neurosciences · doi:10.1016/j.tins.2025.12.006 · Cited by 12

The role of nitric oxide in the regulation of neurotransmitter release and processes of exo- and endocytosis of synaptic vesicles in mouse motor nerve endings

Yakovleva, O. V., Ulfatovich, S. M., & Ситдикова, Г. Ф. (2013) · Neurochemical Journal · doi:10.1134/s1819712413020104 · Cited by 12

Concurrent administration of thyroxine and donepezil induces plastic changes in the prefrontal cortex of adult hypothyroid rats

Wang, F., Wu, Z., Zha, X., Cai, Y., Wu, B., Jia, X., & Zhu, D.-F. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.6977 · Cited by 12

Environmental Enrichment Enhances Cav 2.1 Channel-Mediated Presynaptic Plasticity in Hypoxic–Ischemic Encephalopathy

Song, S.-Y., Pyo, S., Choi, S.-C., Oh, H. S., Seo, J. H., Yu, J. H., Baek, A., Shin, Y., Lee, H. Y., Choi, J. Y., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073414 · Cited by 12

Development of synaptic fidelity and action potential robustness at an inhibitory sound localization circuit: effects of otoferlin‐related deafness

Müller, N. I. C., Paulußen, I., Hofmann, L. N., Fisch, J. O., Singh, A., & Friauf, E. (2022) · The Journal of Physiology · doi:10.1113/jp280403 · Cited by 12

SNARE mimicry by the CD225 domain of IFITM3 enables regulation of homotypic late endosome fusion

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Perinatal exposure to alcohol reduces the expression of complexins I and II

Zink, M., Araç, G., Frank, S. T., Gass, P., Gebicke‐Haerter, P. J., & Spanagel, R. (2009) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2009.08.001 · Cited by 12

The Number of Components of Enhancement Contributing to Short-Term Synaptic Plasticity at the Neuromuscular Synapse during Patterned Nerve Stimulation Progressively Decreases As Basal Release Probability Is Increased from Low to Normal Levels by Changing Extracellular Ca2+

Holohean, A. M., & Magleby, K. L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0392-11.2011 · Cited by 12

Acyl-Chain Correlation in Membrane Fusion Intermediates: X-Ray Diffraction from the Rhombohedral Lipid Phase

Weinhausen, B., Aeffner, S., Reusch, T., & Salditt, T. (2012) · Biophysical Journal · doi:10.1016/j.bpj.2012.03.069 · Cited by 12

Lipid–protein interactions in exocytotic release of hormones and neurotransmitters

Rituper, B., Davletov, B. A., & Zorec, R. (2010) · Clinical Lipidology · doi:10.2217/clp.10.61 · Cited by 12

Stable RNA interference of synaptotagmin I in PC12 cells results in differential regulation of transmitter release

Roden, W. H., Papke, J. B., Moore, J. M., Cahill, A. L., Macarthur, H., & Harkins, A. B. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00482.2006 · Cited by 12

The vesicle cycle in motor nerve endings of the mouse diaphragm

Zefirov, A. L., Zakharov, A., Mukhametzyanov, R. D., Petrov, A. M., & Ситдикова, Г. Ф. (2009) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-009-9122-x · Cited by 12

A Systematic RNAi Screen Reveals a Novel Role of a Spindle Assembly Checkpoint Protein BuGZ in Synaptic Transmission in C. elegans

Han, M., Zou, W., Chang, H., Yu, Y., Zhang, H., Li, S., Cheng, H., Wei, G., Chen, Y., Reinke, V., et al. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00141 · Cited by 12

A Stimulation Function of Synaptotagmin-1 in Ternary SNARE Complex Formation Dependent on Munc18 and Munc13

Li, Y., Wang, S., Li, T., Zhu, L., Xu, Y., & Ma, C. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00256 · Cited by 12

Interactions between amyloid precursor protein-like (APPL) and MAGUK scaffolding proteins contribute to appetitive long-term memory inDrosophila melanogaster

Silva, B., Niehage, C., Maglione, M., Hoflack, B., Sigrist, S. J., Wassmer, T., Pavlowsky, A., & Préat, T. (2020) · Journal of Neurogenetics · doi:10.1080/01677063.2020.1712597 · Cited by 12

Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degeneration

Hargrove-Grimes, P., Mondal, A. K., Gumerson, J., Nellissery, J. K., Aponte, A. M., Gieser, L. M., Qian, H., Fariss, R. N., Bonifacino, J. S., Li, T., et al. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1009259 · Cited by 12

Mitochondria-Endoplasmic Reticulum Interplay Regulates Exo-Cytosis in Human Neuroblastoma Cells

Dentoni, G., Naia, L., & Ankarcrona, M. (2022) · Cells · doi:10.3390/cells11030514 · Cited by 12

Sensory Influence on Homeostasis and Lifespan: Molecules and Circuits

Alcedo, J., Maier, W., & Ch'ng, Q.-L. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7002-2_14 · Cited by 12

Ultrastructural Basis for Craniofacial Sensory Processing in The Brainstem

Bae, Y. C., & Yoshida, A. (2011) · International review of neurobiology · doi:10.1016/b978-0-12-385198-7.00005-9 · Cited by 12

Effects of thienorphine on synaptic structure and synaptophysin expression in the rat nucleus accumbens

Yong, Z., Yan, L., Gao, X., Gong, Z., & Su, R. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.05.026 · Cited by 12

The development of benzo- and naphtho-fused quinoline-2,4-dicarboxylic acids as vesicular glutamate transporter (VGLUT) inhibitors reveals a possible role for neuroactive steroids

Carrigan, C. N., Patel, S. A., Cox, H. D., Bolstad, E. S. D., Gerdes, J. M., Smith, W. E., Bridges, R. J., & Thompson, C. M. (2013) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2013.12.086 · Cited by 12

Real-time imaging of single synaptic vesicles in live neurons

Yu, C., Zhang, M., Qin, X., Yang, X., & Park, H. (2016) · Frontiers in Biology · doi:10.1007/s11515-016-1397-z · Cited by 12

Polypyrrole-amphiphile blend electrodes: new reaction-driven structural processes with possible formation of vesicles

Otero, T. F., Valero, L., & Martínez, J. G. (2017) · Electrochimica Acta · doi:10.1016/j.electacta.2017.06.006 · Cited by 12

SV2 frustrating exocytosis at the semi‐diffusor synapse

Vautrin, J. (2009) · Synapse · doi:10.1002/syn.20610 · Cited by 12

Loss of laminin‐a4 results in pre‐ and postsynaptic modifications at the neuromuscular junction

Chand, K. K., Lee, K. M., Lavidis, N. A., & Noakes, P. G. (2016) · The FASEB Journal · doi:10.1096/fj.201600899r · Cited by 12

Rab26

Ward, H., Peterson, B., & Wandinger‐Ness, A. (2008) · AfCS-Nature Molecule Pages · doi:10.1038/mp.a001977.01 · Cited by 11

Mercury-induced excitotoxicity in presynaptic brain nerve terminals: modulatory effects of carbonaceous airborne particulate simulants

Krisanova, N., Pastukhov, A. O., Dekaliuk, M. O., Dudarenko, M., Pozdnyakova, N., Driuk, M., & Borisova, Т. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-31359-x · Cited by 11

Functional role of UNC13D in immune diseases and its therapeutic applications

Duong, V.-T., Lee, D., Kim, Y. H., & Oh, S. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460882 · Cited by 11

Serotonergic Mechanisms in Proteinoid-Based Protocells

Mougkogiannis, P., & Adamatzky, A. (2025) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00801 · Cited by 11

Molecular Machines Determining the Fate of Endocytosed Synaptic Vesicles in Nerve Terminals

Fassio, A., Fadda, M., & Benfenati, F. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00010 · Cited by 11

Spike Activity Regulates Vesicle Filling at a Glutamatergic Synapse

Li, D., Zhu, Y. F., & Huang, H. Y. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2945-19.2020 · Cited by 11

The Role of Vti1a in Biological Functions and Its Possible Role in Nervous System Disorders

Tang, F., Fan, J., Zhang, X., Zou, Z., Xiao, D., & Li, X. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.918664 · Cited by 11

Photons Induce Vesicular Exocytotic Release of Glutamate in a Power-Dependent Way

Cervetto, C., Amaroli, A., Amato, S., Gatta, E., Diaspro, A., Maura, G., Signore, A., Benedicenti, S., & Marcoli, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310977 · Cited by 11

Potential nervous threat of nanoplastics to Monopterus albus: Implications from a metabolomics study

Yao, C., Liu, C., Hong, S., Zhou, J., Gao, Z., Li, Y., Lv, W., & Zhou, W. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.168482 · Cited by 11

A transcriptomics-based analysis of mechanisms involved in the sex-dependent effects of diazepam on zebrafish

Zhang, Y.-B., Shi, Y., Tang, J., Chen, K., Wu, M. C., Wu, X., & Qiu, X. (2024) · Aquatic Toxicology · doi:10.1016/j.aquatox.2024.107063 · Cited by 11

Rab3Gap1 mediates exocytosis of Claudin-1 and tight junction formation during epidermal barrier acquisition

Youssef, G., Gerner, L., Naeem, A. S., Ralph, O. G., Ono, M., O’Neill, C. A., & O’Shaughnessy, R. F. L. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.04.034 · Cited by 11

The effects of hydrogen sulfide on the processes of exo- and endocytosis of synaptic vesicles in the mouse motor nerve endings

Mitrukhina, O., Yakovlev, A. V., & Ситдикова, Г. Ф. (2013) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747812050121 · Cited by 11

Inhibition of Ca2+-regulated exocytosis by levetiracetam, a ligand for SV2A, in antral mucous cells of guinea pigs

Harada, S., Tanaka, S., Takahashi, Y., Matsumura, H., Shimamoto, C., Nakano, T., Kuwabara, H., Sawabe, Y., & Nakahari, T. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.09.037 · Cited by 11

Thalamic Proteome Changes and Behavioral Impairments in Thiamine-deficient Rats

Nunes, P. T., Gómez‐Mendoza, D. P., Rezende, C. P., Figueiredo, H. C. P., & Ribeiro, A. M. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.06.003 · Cited by 11

Therapeutic implications of the serotonin transporter gene in depression

El‐Mallakh, R. S., & Ali, Z. (2019) · Biomarkers in Neuropsychiatry · doi:10.1016/j.bionps.2019.100004 · Cited by 11

Transcriptome profiling of the Eriocheir sinensis thoracic ganglion under the Spiroplasma eriocheiris challenge

Hou, L., Ma, Y., Cao, X., Gu, W., Cheng, Y., Wu, X., Wang, W., & Meng, Q. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735257 · Cited by 11

Amphiphilic anti-SARS-CoV-2 drug remdesivir incorporates into the lipid bilayer and nerve terminal membranes influencing excitatory and inhibitory neurotransmission

Krisanova, N. V., Pozdnyakova, N., Pastukhov, A. O., Dudarenko, M., Shatursky, O. Y., Gnatyuk, O., Afonina, U., Pyrshev, K. A., Довбешко, Г. И., Yesylevskyy, S. O., et al. (2022) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2022.183945 · Cited by 11

Understanding the Role of ATP Release through Connexins Hemichannels during Neurulation

Tovar, L. M., Burgos, C. F., Yévenes, G. E., Moraga‐Cid, G., Fuentealba, J., Coddou, C., Bascuñán‐Godoy, L., Catrupay, C., Torres, A., & Castro, P. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032159 · Cited by 11

C2 Domains and Membrane Fusion

Martens, S., & McMahon, H. T. (2011) · Current topics in membranes · doi:10.1016/b978-0-12-385891-7.00006-4 · Cited by 11

Dual role of calbindin‐D 28K in vesicular catecholamine release from mouse chromaffin cells

Westerink, R. H. S., Rook, M. B., Beekwilder, J. P., & Wadman, W. J. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04099.x · Cited by 11

Ultrastructural readout of functional synaptic vesicle pools in hippocampal slices based on FM dye labeling and photoconversion

Marra, V., Burden, J. J., Crawford, F., & Staras, K. (2014) · Nature Protocols · doi:10.1038/nprot.2014.088 · Cited by 11

Analysis of organelles within the nervous system: impact on brain and organelle functions

Tribl, F., Meyer, H. E., & Marcus, K. (2008) · Expert Review of Proteomics · doi:10.1586/14789450.5.2.333 · Cited by 11

Two gigs of Munc18 in membrane fusion

Shin, Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313749110 · Cited by 11

Silence of Synaptotagmin VII inhibits release of dense core vesicles in PC12 cells

Li, J., Xiao, Y., Zhou, W., Wu, Z., Zhang, R., & Xu, T. (2009) · Science in China Series C Life Sciences · doi:10.1007/s11427-009-0160-y · Cited by 11

Antagonistic Effect of a Salivary Proline-Rich Peptide on the Cytosolic Ca2+ Mobilization Induced by Progesterone in Oral Squamous Cancer Cells

Palmerini, C. A., Mazzoni, M., Radicioni, G., Marzano, V., Granieri, L., Iavarone, F., Longhi, R., Messana, I., Cabras, T., Sanna, M. T., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147925 · Cited by 11

Synaptic Vesicle Protein 2A as a Novel Pharmacological Target with Broad Potential for New Antiepileptic Drugs

Pichardo‐Macías, L. A., Contreras‐García, I. J., Zamudio, S., Mixcoha, E., & Mendoza‐Torreblanca, J. G. (2016) · Methods in pharmacology and toxicology · doi:10.1007/978-1-4939-6355-3_4 · Cited by 11

Limited proteolysis as a tool to probe the tertiary conformation of dysferlin and structural consequences of patient missense variant L344P

Woolger, N., Bournazos, A., Sophocleous, R. A., Evesson, F. J., Lek, A., Driemer, B., Sutton, R. B., & Cooper, S. T. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.790014 · Cited by 11

Impaired synaptic vesicle recycling contributes to presynaptic dysfunction in lipoprotein lipase-deficient mice

Liu, X., Zhang, B., Yang, H., Wang, H., Liu, Y., Huang, A., Liu, T., Tian, X., Tong, Y., Zhou, T., et al. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.080 · Cited by 11

Exploiting Microelectrode Geometry for Comprehensive Detection of Individual Exocytosis Events at Single Cells

Alwis, C. D., Denison, J. D., Shah, R., McCarty, G. S., & Sombers, L. A. (2023) · ACS Sensors · doi:10.1021/acssensors.3c00884 · Cited by 10

Single-molecule two- and three-colour FRET studies reveal a transition state in SNARE disassembly by NSF

Cheppali, S. K., Li, C., Xing, W., Sun, R., Yang, M., Xue, Y., Lu, S., Yao, J., Sun, S., Chen, C., et al. (2025) · Nature Communications · doi:10.1038/s41467-024-55531-0 · Cited by 10

Decoding crosstalk between neurotransmitters and α-synuclein in Parkinson’s disease: pathogenesis and therapeutic implications

Guan, L., Lin, L., Ma, C., & Qiu, L. (2025) · Therapeutic Advances in Neurological Disorders · doi:10.1177/17562864251339895 · Cited by 10

Unraveling the mechanism of brain damage in Carassius auratus by polypropylene microplastics and oxytetracycline via the brain-gut-microbiota axis

Zhang, P., Lu, G., Zhang, L., Yan, Z., Zhang, J., & Ding, K. (2025) · Journal of Environmental Management · doi:10.1016/j.jenvman.2025.126711 · Cited by 10

Mitochondrial Ca2+ Signaling at the Tripartite Synapse: A Unifying Framework for Glutamate Homeostasis, Metabolic Coupling, and Network Vulnerability

Mancuso, M., Mezzalira, F., Vignoli, B., & Greotti, E. (2026) · Biomolecules · doi:10.3390/biom16010171 · Cited by 10

Investigating the Effect of Oxaliplatin on Vesicular Dopamine Cargo and Release Dynamics in Brain with Single-Vesicle Electrochemistry

Chen, J., Liu, Y. L., Cao, L., Zhou, J., Nan, X., Li, C., Liu, W., Xiong, M., Jiang, Y., Dai, Q., et al. (2026) · Analytical Chemistry · doi:10.1021/acs.analchem.5c07278 · Cited by 10

Molecular sabotage of hippocampal synaptic plasticity by amyloid-β in Alzheimer's disease: A narrative review

Behroozi, Z., Askarpour, H., & Baghcheghi, Y. (2026) · Journal of Alzheimer s Disease Reports · doi:10.1177/25424823261415807 · Cited by 10

Molecular Machines in the Synapse: Overlapping Protein Sets Control Distinct Steps in Neurosecretion

Cornelisse, L. N., Tsivtsivadze, E., Meijer, M., Dijkstra, T. M. H., Heskes, T., & Verhage, M. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002450 · Cited by 10

Required improvements for cerebrospinal fluid-based biomarker tests of Alzheimer’s disease

Gaetani, L., Chiasserini, D., Paoletti, F. P., Bellomo, G., & Parnetti, L. (2023) · Expert Review of Molecular Diagnostics · doi:10.1080/14737159.2023.2276918 · Cited by 10

α-Synuclein is the major platelet isoform but is dispensable for activation, secretion, and thrombosis

Smith, A. N., Joshi, S., Chanzu, H. A., Alfar, H. R., Prakhya, K. S., & Whiteheart, S. W. (2023) · Platelets · doi:10.1080/09537104.2023.2267147 · Cited by 10

The mechanism of mitochondrial autophagy regulating Clathrin‐mediated endocytosis in epilepsy

Zhou, X., Xu, J., Yang, J., Zhang, H., Yang, J., Luo, Z. Y., Tai, Z., Yu, C., & Xu, Z. (2024) · Epilepsia Open · doi:10.1002/epi4.12945 · Cited by 10

Synergistic neurological threat from Сu and wood smoke particulate matter

Krisanova, N., Pozdnyakova, N., Pastukhov, A. O., Dudarenko, M., Tarasenko, A. S., Borysov, A., Driuk, M., Tolochko, A., Bezkrovnyi, O. S., Paliienko, K., et al. (2024) · Food and Chemical Toxicology · doi:10.1016/j.fct.2024.115009 · Cited by 10

Chapter 8 Compartmentalization and Regulation of Insulin Signaling to GLUT4 by the Cytoskeleton

Eyster, C. A., & Olson, A. L. (2009) · Vitamins and hormones · doi:10.1016/s0083-6729(08)00608-0 · Cited by 10

Impact of Delays and Noise on Dopamine Signal Transduction

Wu, J., Qi, Z., & Voit, E. O. (2010) · In Silico Biology · doi:10.3233/isb-2010-0413 · Cited by 10

Regulation of vesicular trafficking by Parkinson's disease-associated genes

Imai, Y., & Inoshita, T. (2015) · AIMS molecular science · doi:10.3934/molsci.2015.4.461 · Cited by 10

Shaping Neuronal Network Activity by Presynaptic Mechanisms

Lavi, A., Perez, O., & Ashery, U. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004438 · Cited by 10

Use‐dependent control of presynaptic calcium signalling at central synapses

Scott, R. S. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00728.x · Cited by 10

The specific and rapid labeling of cell surface proteins with recombinant FKBP-fused fluorescent proteins

Zhang, X., Deng, Y., Chang, H., Ji, C. F., Zhang, M., Peng, J., Xu, T., & Xu, P. (2014) · Protein & Cell · doi:10.1007/s13238-014-0090-8 · Cited by 10

Rab3 GTPase Lands Bruchpilot

Γιαγτζόγλου, Ν., Mahoney, T. R., Yao, C., & Bellen, H. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.11.029 · Cited by 10

Structure/function assessment of synapses at motor nerve terminals

Johnstone, A. F. M., Viele, K., & Cooper, R. L. (2010) · Synapse · doi:10.1002/syn.20847 · Cited by 10

A Phenomenological Synapse Model for Asynchronous Neurotransmitter Release

Wang, T., Yin, L., Zou, X., Shu, Y., Rasch, M. J., & Wu, S. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2015.00153 · Cited by 10

Presynaptic Calmodulin targets: lessons from structural proteomics

Lipstein, N., Göth, M., Piotrowski, C., Pagel, K., Sinz, A., & Jahn, O. (2017) · Expert Review of Proteomics · doi:10.1080/14789450.2017.1275966 · Cited by 10

Multiscale models and stochastic simulation methods for computing rare but key binding events in cell biology

Guerrier, C., & Holcman, D. (2017) · Journal of Computational Physics · doi:10.1016/j.jcp.2017.03.058 · Cited by 10

Millisecond Ca2+ dynamics activate multiple protein cascades for synaptic vesicle control

Mochida, S. (2017) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.93.050 · Cited by 10

Comparative Analysis of Neurotoxic Potential of Synthesized, Native, and Physiological Nanoparticles

Borysov, A., Pozdnyakova, N., Pastukhov, A. O., & Borisova, Т. (2018) · Neuromethods · doi:10.1007/978-1-4939-7584-6_13 · Cited by 10

Modulation of neurosecretion and approaches for its multistep analysis

Kasatkina, L. A., Gumenyuk, V. P., Sturm, E. M., Heinemann, Á., Bernaś, T., & Trikash, I. O. (2018) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2018.08.004 · Cited by 10

Dipolar Janus liposomes: formation, electrokinetic motion and self-assembly

Liu, Z., Cui, J., & Zhan, W. (2020) · Soft Matter · doi:10.1039/c9sm02254f · Cited by 10

Activity and Cytosolic Na + Regulate Synaptic Vesicle Endocytosis

Zhu, Y. F., Li, D., & Huang, H. Y. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0119-20.2020 · Cited by 10

Loss of Dysbindin Implicates Synaptic Vesicle Replenishment Dysregulation as a Potential Pathogenic Mechanism in Schizophrenia

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Ca2+/Calmodulin and Presynaptic Short-Term Plasticity

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