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

Drosophila synaptotagmin Inull mutants show severe alterations in vesicle populations but calcium-binding motif mutants do not

Loewen, C. A., Royer, S. M., & Reist, N. E. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20868 · Cited by 16

AP180 and CALM

Koo, S. J., Puchkov, D., & Haucke, V. (2011) · Cellular Logistics · doi:10.4161/cl.1.4.18897 · Cited by 16

Synapsin is required to “boost” memory strength for highly salient eventsPreprint

Kleber, J., Chen, Y., Michels, B., Saumweber, T., Schleyer, M. H., Kähne, T., Buchner, E., & Gerber, B. (2015) · Learning & Memory · doi:10.1101/lm.039685.115 · Cited by 16

Neurotransmitter Release

Ting, J. T., & Phillips, P. E. M. (2008) · Wiley eBooks · doi:10.1002/9780470048672.wecb385 · Cited by 16

Cerebrospinal Fluid Synaptosomal-Associated Protein 25 Levels in Patients with Alzheimer’s Disease: A Meta-Analysis

Liu, Q., Liu, H., Zhang, S., Yang, Q., Shen, L. H., & Jiao, B. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-215696 · Cited by 15

Fluoxetine Enhances Synaptic Vesicle Trafficking and Energy Metabolism in the Hippocampus of Socially Isolated Rats

Filipović, D., Costina, V., Findeisen, P., & Inta, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315351 · Cited by 15

Phase Separation–Mediated Compartmentalization Underlies Synapse Formation and Plasticity

Wu, X., Shen, Z., & Zhang, M. (2025) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-112723-040159 · Cited by 15

Mutational Analysis of Rab3 Function for Controlling Active Zone Protein Composition at the Drosophila Neuromuscular Junction

Chen, S., Gendelman, H. K., Roche, J. P., Alsharif, P., & Graf, E. R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136938 · Cited by 15

Cayman Ataxia-Related Protein is a Presynapse-Specific Caspase-3 Substrate

Itoh, M., Li, S., Ohta, K., Yamada, A., Hayakawa‐Yano, Y., Ueda, M., Hida, Y., Suzuki, Y., Ohta, E., Mizuno, A., et al. (2011) · Neurochemical Research · doi:10.1007/s11064-011-0430-5 · Cited by 15

Expression and regulation of reelin and its receptors in the enteric nervous system

Böttner, M., Fidkouhi, P. G., Harde, J., Barrenschee, M., Hellwig, I., Vogel, I., Ebsen, M., Förster, E., & Wedel, T. (2014) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2014.05.001 · Cited by 15

Ectopic release sites lack fast vesicle recycling mechanisms, causing long‐term depression of neuron‐glial transmission in rat cerebellum

Balakrishnan, S., Jackson, C. L. M., Russell, N. A., & Bellamy, T. C. (2010) · Glia · doi:10.1002/glia.21078 · Cited by 15

Distinct Localization of SNAP47 Protein in GABAergic and Glutamatergic Neurons in the Mouse and the Rat Hippocampus

Münster‐Wandowski, A., Heilmann, H., Bolduan, F., Trimbuch, T., Yanagawa, Y., & Vida, I. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00056 · Cited by 15

Gliotransmitter Exocytosis and Its Consequences on Synaptic Transmission

Pittà, M. D. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_10 · Cited by 15

Quantitative Immunoblotting Analyses Reveal that the Abundance of Actin, Tubulin, Synaptophysin and EEA1 Proteins is Altered in the Brains of Aged Mice

Ve, H., Cabana, V. C., Gouspillou, G., & Lussier, M. P. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.06.044 · Cited by 15

miR-128 as a Regulator of Synaptic Properties in 5xFAD Mice Hippocampal Neurons

Shvarts-Serebro, I., Sheinin, A., Gottfried, I., Adler, L., Schottlender, N., Ashery, U., & Barak, B. (2021) · Journal of Molecular Neuroscience · doi:10.1007/s12031-021-01862-2 · Cited by 15

Deficiency of ER Ca2+ sensor STIM1 in AgRP neurons confers protection against dietary obesity

Chen, Z., Pan, S., Yin, K., Zhang, Y., Yuan, X., Wang, S., Yang, S., Shen, Q. X., Tang, Y., Li, J., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109868 · Cited by 15

Single vesicle tracking for studying synaptic vesicle dynamics in small central synapses

Park, C., Jung, S., & Park, H. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102596 · Cited by 15

Amyloid pathology disrupts gliotransmitter release in astrocytes

Pillai, A. G., & Nadkarni, S. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010334 · Cited by 15

Diverse organization of voltage-gated calcium channels at presynaptic active zones

Zhang, W., Jiang, H.-H., & Luo, F. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2022.1023256 · Cited by 15

Behavioral and Proteomic Studies Reveal Methylglyoxal Activate Pathways Associated with Alzheimer’s Disease

Patil, G. V., Kulsange, S. E., Kazi, R. S., Chirmade, T., Kale, V., Mote, C., Aswar, M. K., Koratkar, S., Agawane, S. B., & Kulkarni, M. J. (2022) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.2c00143 · Cited by 15

Targeting BACE1-mediated production of amyloid beta improves hippocampal synaptic function in an experimental model of ischemic stroke

Basak, J. M., Falk, M., Mitchell, D. N., Coakley, K. A., Quillinan, N., Orfila, J. E., & Herson, P. S. (2023) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x231159597 · Cited by 15

cAMP−EPAC−PKCε−RIM1α signaling regulates presynaptic long-term potentiation and motor learning

Wang, X., Zhou, L., Dong, B.-B., Xu, F., Wang, D., Shen, E.-W., Cai, X., Wang, Y., Wang, N., Ji, S., et al. (2023) · eLife · doi:10.7554/elife.80875 · Cited by 15

New effects of GABAB receptor allosteric modulator rac-BHFF on ambient GABA, uptake/release, Em and synaptic vesicle acidification in nerve terminals

Pozdnyakova, N., Dudarenko, M., & Borisova, Т. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.07.037 · Cited by 15

The Cooperative Response of Synaptotagmin I C2A. A Hypothesis for a Ca2+-Driven Molecular Hammer

Kertz, J. A., Almeida, P. F. F., Frazier, A. A., Berg, A. K., & Hinderliter, A. K. (2006) · Biophysical Journal · doi:10.1529/biophysj.106.087197 · Cited by 15

Enrichment of Inorganic Martian Dust Simulant with Carbon Component can Provoke Neurotoxicity

Pozdnyakova, N., Pastukhov, A. O., Dudarenko, M., Borysov, A., Krisanova, N. V., Nazarova, A., & Borisova, Т. (2017) · Microgravity Science and Technology · doi:10.1007/s12217-016-9533-6 · Cited by 15

Suo Quan Wan Protects Mouse From Early Diabetic Bladder Dysfunction by Mediating Motor Protein Myosin Va and Transporter Protein SLC17A9

Wang, J., Lian, D., Yang, X., Xu, Y., Chen, F., Lin, W.-J., Wang, R., Tang, L., Ren, W., Fu, L.-J., et al. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00552 · Cited by 15

Spatiotemporal organization and protein dynamics involved in regulated exocytosis of MMP-9 in breast cancer cells

Stephens, D. C., Osunsanmi, N., Sochacki, K. A., Powell, T. W., Taraska, J. W., & Harris, D. A. (2019) · The Journal of General Physiology · doi:10.1085/jgp.201812299 · Cited by 15

Synergistic Neuroprotective Effect of Endogenously-Produced Hydroxytyrosol and Synaptic Vesicle Proteins on Pheochromocytoma Cell Line against Salsolinol

Manzoor, R., Rasool, A., Ahmed, M., Ullah, K., Duru, L. N., Ma, H., & Deng, Y. (2020) · Molecules · doi:10.3390/molecules25071715 · Cited by 15

Differential Regulation of the Serotonin Transporter by Vesicle-Associated Membrane Protein 2 in Cells of Neuronal versus Non-Neuronal Origin

Müller, H. K., Kragballe, M., Fjorback, A. W., & Wiborg, O. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097540 · Cited by 15

New insights into the molecular mechanisms of priming of insulin exocytosis

Kwan, E. P., & Gaisano, H. Y. (2007) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2007.00788.x · Cited by 15

Neuronal dysfunction with aging and its amelioration

Susumu, A. N. D. O. (2012) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.88.266 · Cited by 15

Pituitary adenylate cyclase activating polypeptide induces long-term, transcription-dependent plasticity and remodeling at autonomic synapses

Starr, E. R., & Margiotta, J. F. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.10.002 · Cited by 15

Development of the Vertebrate Neuromuscular Junction

Fox, M. A. (2009) · Springer eBooks · doi:10.1007/978-0-387-92708-4_3 · Cited by 15

Molecular mechanism of nur77 gene expression and downstream target genes in the early stage of forskolin-induced differentiation in PC12 cells

Maruoka, H., Yamazoe, R., Takahashi, R., Yatsuo, K., Ido, D., Fuchigami, Y., Hoshikawa, F., & Shimoke, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-62968-y · Cited by 14

Enhanced synaptic protein visualization by multicolor super-resolution expansion microscopy

Eilts, J., Reinhard, S., Michetschläger, N., Werner, C. D., & Sauer, M. (2023) · Neurophotonics · doi:10.1117/1.nph.10.4.044412 · Cited by 14

External and circadian inputs modulate synaptic protein expression in the visual system of Drosophila melanogaster

Krzeptowski, W., Górska‐Andrzejak, J., Kijak, E., Görlich, A., Guzik, E. ⁄. B., Moore, G., & Pyza, E. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00102 · Cited by 14

Calcium near the release site is essential for basal ACh release in Xenopus

Li, R., Lei, Q., Song, G., He, X., & Xie, Z. (2008) · Cell Biology International · doi:10.1016/j.cellbi.2008.05.001 · Cited by 14

The connectomics challenge.

Silvestri, L., Sacconi, L., & Pavone, F. S. (2013) · Europe PMC (PubMed Central) · doi:10.11138/fneur/2013.28.3.167 · Cited by 14

Levetiracetam-mediated improvement of decreased NMDA-induced glutamate release from nerve terminals during hypothermia

Pastukhov, A. O., & Borisova, Т. (2018) · Brain Research · doi:10.1016/j.brainres.2018.06.032 · Cited by 14

Botulinum Toxin as a Biological Warfare Agent: Poisoning, Diagnosis and Countermeasures

Pohanka, M. (2020) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557520666200228105312 · Cited by 14

The regulatory role of endoplasmic reticulum chaperone proteins in neurodevelopment

Sun, H., Wu, M., Wang, M., Zhang, X., & Zhu, J. Z. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1032607 · Cited by 14

Neuronal Exosomes as a New Signaling System

Yakovlev, A. A. (2023) · Biochemistry (Moscow) · doi:10.1134/s0006297923040028 · Cited by 14

Marine Toxins Potently Affecting Neurotransmitter Release

Meunier, F. A., Mattei, C., & Molgó, J. (2009) · Progress in molecular and subcellular biology · doi:10.1007/978-3-540-87895-7_6 · Cited by 14

Peroxynitrite induces tyrosine residue modifications in synaptophysin C‐terminal domain, affecting its interaction with src

Mallozzi, C., Ceccarini, M., Camerini, S., Macchia, G., Crescenzi, M., Petrucci, T. C., & Stasi, A. M. M. D. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06378.x · Cited by 14

Differential distribution of synaptotagmin-1, -4, -7, and -9 in rat adrenal chromaffin cells

Matsuoka, H., Harada, K., Nakamura, J., Fukuda, M., & Inoue, M. (2011) · Cell and Tissue Research · doi:10.1007/s00441-011-1131-8 · Cited by 14

Glutamatergic neurotransmission in the synapsin I and II double knock-out mouse

Bogen, I. L., Jensen, V., Hvalby, Ø., & Walaas, S. I. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.07.004 · Cited by 14

Calcium-induced exocytosis from actomyosin-driven, motile varicosities formed by dynamic clusters of organelles

Malkinson, G., Fridman, Z. M., Kamber, D., Dormann, A., Shapira, E., & Spira, M. E. (2007) · Journal of Neurocytology · doi:10.1007/s11068-006-9007-7 · Cited by 14

Intraneuronal accumulation of Aβ42 induces age-dependent slowing of neuronal transmission in Drosophila

Lin, J., Wang, W.-A., Zhang, X., Liu, H., Zhao, X., & Huang, F.-D. (2014) · Neuroscience Bulletin · doi:10.1007/s12264-013-1409-9 · Cited by 14

Control of Neuronal Ryanodine Receptor-Mediated Calcium Signaling by Calsenilin

Grillo, M. A., Grillo, S. L., Gerdes, B. C., Kraus, J. G., & Koulen, P. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1080-2 · Cited by 14

Metabolic pathways in the periphery and brain: Contribution to mental disorders?

Nagalski, A., Koziński, K., & Wisniewska, M. B. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.09.012 · Cited by 14

Synapsin II Regulation of GABAergic Synaptic Transmission Is Dependent on Interneuron Subtype

Feliciano‐Ramos, P. A., Matos, H. Y., Andrade, R., & Bykhovskaia, M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0844-16.2016 · Cited by 14

SNAP-25 Puts SNAREs at Center Stage in Metabolic Disease

Irfan, M., Daraio, T., & Bark, C. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.07.035 · Cited by 14

Intracellular Trafficking

Pigino, G. F., Morfini, G. A., & Brady, S. T. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374947-5.00007-9 · Cited by 14

A Computational Model to Investigate GABA-Activated Astrocyte Modulation of Neuronal Excitation

Li, L., Zhou, J., Sun, H., Liu, J., Wang, H., Liu, X., & Wang, C. (2020) · Computational and Mathematical Methods in Medicine · doi:10.1155/2020/8750167 · Cited by 14

In-depth quantitative proteomic characterization of organotypic hippocampal slice culture reveals sex-specific differences in biochemical pathways

Weis, S. N., de Souza, J. M. F., Hoppe, J. B., Firmino, M., Auer, M., Ataii, N. N., da Silva, L. A., Gaelzer, M. M., Klein, C. P., Mól, A. R., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-82016-7 · Cited by 14

Physiological involvement of presynaptic L-type voltage dependent calcium channels in GABA release of cerebellar molecular layer interneurons

Rey, S. A., Maton, G., Satake, S., Llano, I., Kang, S., Surmeier, D. J., Silverman, R. B., & Collin, T. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.15100 · Cited by 14

Storage of GABA in chromaffin granules and not in synaptic‐like microvesicles in rat adrenal medullary cells

Harada, K., Matsuoka, H., Nakamura, J., Fukuda, M., & Inoue, M. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06792.x · Cited by 14

Nerve growth factor‐induced phosphorylation of amphiphysin‐1 by casein kinase 2 regulates clathrin–amphiphysin interactions

Döring, M., Loos, A., Schrader, N., Pfander, B., & Bauerfeind, R. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04037.x · Cited by 14

In Vivo Analysis of Conserved C. elegans Tomosyn Domains

Burdina, A. O., Klosterman, S. M., Shtessel, L., Ahmed, S. C., & Richmond, J. E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026185 · Cited by 14

Numerical simulation for a neurotransmitter transport model in the axon terminal of a presynaptic neuron

Bielecki, A., Kalita, P., Lewandowski, M. H., & Siwek, B. (2010) · Biological Cybernetics · doi:10.1007/s00422-010-0380-z · Cited by 14

Overexpression of complexin in PC12 cells inhibits exocytosis by preventing SNARE complex recycling

Liu, J., Guo, T., Wu, J., Bai, X., Zhou, Q., & Sui, S. (2007) · Biochemistry (Moscow) · doi:10.1134/s0006297907040116 · Cited by 14

Decoding Ca2+ signals

Muallem, S. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200506047 · Cited by 14

Reduced expression of complexins I and II in rats bred for learned helplessness

Zink, M., Vollmayr, B., Gebicke‐Haerter, P. J., Henn, F. A., & Thome, J. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.066 · Cited by 14

Influence of Integrin-blocking Peptide on Gadolinium- and Hypertonic Shrinking-induced Neurotransmitter Release in Rat Brain Synaptosomes

Waseem, T. V., Lapatsina, L. P., & Fedorovich, S. V. (2008) · Neurochemical Research · doi:10.1007/s11064-007-9585-5 · Cited by 14

Stochastic models for the in silico simulation of synaptic processes

Bracciali, A., Brunelli, M., Cataldo, E., & Degano, P. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-s4-s7 · Cited by 14

Regulation of resident and newcomer insulin granules by calcium and SNARE proteins

Aoyagi, K. (2010) · Frontiers in bioscience · doi:10.2741/3784 · Cited by 14

Substance P plays a critical role in synaptic transmission in striatal neurons

He, Z., Liu, T., Yin, Y.-Y., Song, H., & Zhu, X. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.02.055 · Cited by 14

Enhancement of synaptic transmission and nociceptive behaviour in HPC‐1/syntaxin 1A knockout mice following peripheral nerve injury

Takasusuki, T., Fujiwara, T., Yamaguchi, S., Fukushima, T., Akagawa, K., & Hori, Y. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05830.x · Cited by 14

Synaptic Vesicles Studied by SAXS: Derivation and Validation of a Model Form Factor

Castorph, S., Arleth, L., Sztucki, M., Vainio, U., Ghosh, S. K., Holt, M. G., Jahn, R., & Salditt, T. (2010) · Journal of Physics Conference Series · doi:10.1088/1742-6596/247/1/012015 · Cited by 14

Silence of synaptotagmin I in INS-1 cells inhibits fast exocytosis and fast endocytosis

Xiong, X., Zhou, K.-M., Wu, Z., & Xu, T. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.06.045 · Cited by 14

A Role for Soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor Complex Dimerization during Neurosecretion

Fdez, E., Jowitt, T. A., Wang, M.-C., Rajebhosale, M., Foster, K., Bella, J., Baldock, C., Woodman, P. G., & Hilfiker, S. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-01-0010 · Cited by 14

Rab3 mediates cyclic AMP-dependent presynaptic plasticity and olfactory learningPreprint

Sachidanandan, D., Aravamudhan, A., Mrestani, A., Nerlich, J., Lamberty, M., Hasenauer, N., Ehmann, N., Pauls, D., Seubert, T., Maiellaro, I., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.21.572589 · Cited by 14

Challenges and rewards of in vivo synaptic density imaging, and its application to the study of depression

Asch, R. H., Abdallah, C. G., Carson, R. E., & Esterlis, I. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-024-01913-3 · Cited by 13

Synaptotagmin IV Acts as a Multi-Functional Regulator of Ca2+-Dependent Exocytosis

Mori, Y., & Fukuda, M. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0352-7 · Cited by 13

Real-Time Study of the Modification of the Peptide Bond by Atomic Calcium

Kummer, K., Vyalikh, D. V., Blüher, A., Sivkov, V. N., Maslyuk, V. V., Bredow, T., Mertig, I., Mertig, M., & Molodtsov, S. L. (2011) · The Journal of Physical Chemistry B · doi:10.1021/jp109555j · Cited by 13

Downregulation of serum RAB27B confers improved prognosis and is associated with hepatocellular carcinoma progression through PI3K-AKT-P21 signaling

Yang, X., Ye, X., Sun, L., Gao, F., Li, Y., Ji, X., Wang, X., Feng, Y., & Wang, X. (2017) · Oncotarget · doi:10.18632/oncotarget.18010 · Cited by 13

Nano-Precision Tweezers for Mechanosensitive Proteins and Beyond

Yang, T., Park, C., Rah, S.-H., & Shon, M. J. (2022) · Molecules and Cells · doi:10.14348/molcells.2022.2026 · Cited by 13

Exploration of the Shared Molecular Mechanisms between COVID-19 and Neurodegenerative Diseases through Bioinformatic Analysis

Shi, Y., Liu, W., Yang, Y., Ci, Y., & Shi, L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054839 · Cited by 13

Synapse-Specific Defects in Synaptic Transmission in the Cerebellum of W246G Mutant ELOVL4 Rats–a Model of Human SCA34

Nagaraja, R. Y., Stiles, M. A., Sherry, D. M., Agbaga, M., & Ahmad, M. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0378-23.2023 · Cited by 13

Mutations in Wnt2 Alter Presynaptic Motor Neuron Morphology and Presynaptic Protein Localization at the Drosophila Neuromuscular Junction

Liebl, F. L. W., McKeown, C. L., Yao, Y., & Hing, H. K. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012778 · Cited by 13

Caenorhabditis elegans Rab escort protein (REP‐1) differently regulates each Rab protein function and localization in a tissue‐dependent manner

Tanaka, D., Kameyama, K., Okamoto, H., & Doi, M. (2008) · Genes to Cells · doi:10.1111/j.1365-2443.2008.01232.x · Cited by 13

Antinociceptive effects of A1 and A2 type botulinum toxins on carrageenan-induced hyperalgesia in rat

Shin, M.-C., Yukihira, T., Ito, Y., & Akaike, N. (2012) · Toxicon · doi:10.1016/j.toxicon.2012.12.011 · Cited by 13

Glucose-induced translocation of coronin 3 regulates the retrograde transport of the secretory membrane in the pancreatic β-cells

Kimura, T., Taniguchi, S., Toya, K., & Niki, I. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.03.173 · Cited by 13

Label-Free Detection of G Protein–SNARE Interactions and Screening for Small Molecule Modulators

Wells, C. A., Betke, K. M., Lindsley, C. W., & Hamm, H. E. (2011) · ACS Chemical Neuroscience · doi:10.1021/cn200102d · Cited by 13

Behavioral effects of non-viral mediated RNA interference of synapsin II in the medial prefrontal cortex of the rat

Dyck, B. A., Tan, M. L., Daya, R. P., Basu, D., Sookram, C. D., Thomas, N., & Mishra, R. K. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.01.029 · Cited by 13

Activation of m1 muscarinic acetylcholine receptor induces surface transport of KCNQ channel via CRMP-2 mediated pathway

Jiang, L., Kosenko, A., Yu, C., Huang, L., Li, X., & Hoshi, N. (2015) · Journal of Cell Science · doi:10.1242/jcs.175547 · Cited by 13

Multiple roles of afadin in the ultrastructural morphogenesis of mouse hippocampal mossy fiber synapses

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