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

Cryo-EM single-particle analysis expanding towards increasingly native samples

Moecking, J., & Zeev‐Ben‐Mordehai, T. (2025) · Acta Crystallographica Section D Structural Biology · doi:10.1107/s2059798325008332 · Cited by 6

Target Genes of MITF in Projection Neurons of the Olfactory Bulb—A Role for MITF in Defining Gene Expression of Middle Tufted Cells

Mechmet, F., José, A. S. S., Sigurðsson, S., Gautsson, I., Steingrímsson, E., & Petersen, P. H. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70293 · Cited by 6

Actin cage for the synaptic vesicle liquid phase

Brodin, L., & Shupliakov, O. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116630 · Cited by 6

Synaptic Vesicle Recycling: Genetic and Cell Biological Studies

Majumder, R., & Krishnan, K. S. (2010) · Journal of Neurogenetics · doi:10.3109/01677063.2010.506229 · Cited by 6

Probing Rotational Viscosity in Synaptic Vesicles

Zeigler, M. B., Allen, P. B., & Chiu, D. T. (2011) · Biophysical Journal · doi:10.1016/j.bpj.2011.04.042 · Cited by 6

Neuro at the Nanoscale

Castro, J. B., & Gould, T. J. (2015) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155415610169 · Cited by 6

Functional Magnetic Resonance Spectroscopy Study of Total Glutamate and Glutamine in the Human Visual Cortex Activated by a Short Stimulus

Yakovlev, A., Manzhurtsev, A. V., Menshchikov, P. E., Ublinskiy, M. V., Melnikov, I. A., Kupriyanov, D., Akhadov, T. A., & Семенова, Н. А. (2022) · BIOPHYSICS · doi:10.1134/s0006350922020245 · Cited by 6

Ca2+-dependent lipid preferences shape synaptotagmin-1 C2A and C2B dynamics: Insights from experiments and simulations

Bender, J., Kundlacz, T., Rudden, L. S. P., Frick, M., Bieber, J., Degiacomi, M. T., & Schmidt, C. (2024) · Structure · doi:10.1016/j.str.2024.07.017 · Cited by 6

NPT100-18A rescues mitochondrial oxidative stress and neuronal degeneration in human iPSC-based Parkinson’s model

Alecu, J. E., Sigutova, V., Brazdis, R.-M., Lörentz, S., Bogiongko, M., Nursaitova, A., Regensburger, M., Roybon, L., Galler, K. M., Wrasidlo, W., et al. (2025) · BMC Neuroscience · doi:10.1186/s12868-025-00926-y · Cited by 6

Synaptic vesicle fusion promotes phosphatidylinositol 4-phosphate synthesis for efficient synaptic transmission

Yoshida, T., Kawano, H., Omi, J., Hori, T., Kobayashi, Y., Saitoh, N., Aoki, J., & Takamori, S. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115634 · Cited by 6

Accumulation of SNAP25 in mouse gustatory and somatosensory cortices in response to food and chemical stimulation

Kawakami, S., Ohmoto, M., Itoh, S., Yuasa, R., Inagaki, H., Nishimura, E., Ito, T., & Misaka, T. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.045 · Cited by 6

Rab3a ablation related changes in morphology of secretory vesicles in major endocrine pancreatic cells, pituitary melanotroph cells and adrenal gland chromaffin cells in mice

Lipovšek, S., Janžekovič, F., Leitinger, G., & Rupnik, M. S. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2013.01.007 · Cited by 6

ATP dependence of the non-specific ion channel in Torpedo synaptic vesicles

Ahdut-HaCohen, R., Meiri, H., & Rahamimoff, R. (2006) · Neuroreport · doi:10.1097/00001756-200604240-00019 · Cited by 6

Role of phospholipase C in nuclear envelope assembly

Byrne, R. D., Poccia, D., & Larijani, B. (2009) · Clinical Lipidology · doi:10.2217/17584299.4.1.103 · Cited by 6

Sensitivity of Intracellular Calcium-Binding Sites for Exo- and Endocytosis of Synaptic Vesicles to Sr, Ba, and Mg Ions

Zefirov, A. L., & Григорьев, П. Н. (2010) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-010-9269-5 · Cited by 6

Heterogeneous Presynaptic Distribution of Munc13 Isoforms at Retinal Synapses and Identification of an Unconventional Bipolar Cell Type with Dual Expression of Munc13 Isoforms: A Study Using Munc13-EXFP Knock-in Mice

Gierke, K., von Wittgenstein, J., Hemmerlein, M., Atorf, J., Joachimsthaler, A., Kremers, J., Cooper, B. H., Varoqueaux, F., Regus‐Leidig, H., & Brandstätter, J. H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217848 · Cited by 6

Imaging Single Synaptic Vesicles in Mammalian Central Synapses with Quantum Dots

Zhang, Q. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-468-5_5 · Cited by 6

Neurotransmitter uptake of synaptic vesicles studied by X-ray diffraction

Komorowski, K., Preobraschenski, J., Ganzella, M., Alfken, J., Neuhaus, C., Jahn, R., & Salditt, T. (2022) · European Biophysics Journal · doi:10.1007/s00249-022-01609-w · Cited by 6

Unusual retinal layer organization in HPC-1/syntaxin 1A knockout mice

Kaneko, Y., Suge, R., Fujiwara, T., Akagawa, K., & Watanabe, S. (2011) · Journal of Molecular Histology · doi:10.1007/s10735-011-9346-2 · Cited by 6

Organelle docking: R-SNAREs are late

Verhage, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911425106 · Cited by 6

Role of the cAMP cascade in the turnover of synaptic vesicles of the frog motor nerve terminal

Petrov, A. M., Giniatullin, А. R., & Zefirov, A. L. (2008) · Neurochemical Journal · doi:10.1134/s1819712408030069 · Cited by 6

Effects of hydrogen sulfide on the exo- and endocytosis of synaptic vesicles in frog motor nerve endings

Ситдикова, Г. Ф., Yakovlev, A. V., Odnoshivkina, Y. G., & Zefirov, A. L. (2011) · Neurochemical Journal · doi:10.1134/s1819712411040155 · Cited by 6

SNAP-25a/b Isoform Levels in Human Brain Dorsolateral Prefrontal Cortex and Anterior Cingulate Cortex

Thompson, P. M., Cruz, D. A., Fucich, E. A., Olukotun, D. Y., Takahashi, M., & Itakura, M. (2015) · Complex Psychiatry · doi:10.1159/000441224 · Cited by 6

Structural analysis of Ca2+-binding pocket of synaptotagmin 5 C2A domain

Qiu, X., Ge, J., Gao, Y., Teng, M., & Niu, L. (2016) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2016.10.083 · Cited by 6

Combined Application of Glutamate Transporter Inhibitors and Hypothermia Discriminates Principal Constituent Processes Involved in Glutamate Homo- and Heteroexchange in Brain Nerve Terminals

Pastukhov, A. O., & Borisova, Т. (2018) · Therapeutic Hypothermia and Temperature Management · doi:10.1089/ther.2017.0047 · Cited by 6

PnTx2-6 (or δ-CNTX-Pn2a), a toxin from Phoneutria nigriventer spider venom, releases l-glutamate from rat brain synaptosomes involving Na+ and Ca2+ channels and changes protein expression at the blood-brain barrier

da Silva, C. N., Lomeo, R. S., Torres, F. S., Borges, M. H., Nascimento, M. C., Britto, M. H. R. M., Rapôso, C., Pimenta, A. M. C., da Cruz‐Höfling, M. A., Gomes, D. A., et al. (2018) · Toxicon · doi:10.1016/j.toxicon.2018.06.073 · Cited by 6

Quantitative Synaptic Biology: A Perspective on Techniques, Numbers and Expectations

Reshetniak, S., Fernández‐Busnadiego, R., Müller, M., Rizzoli, S. O., & Tetzlaff, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197298 · Cited by 6

Dynamics of the clinical state of patients with peri-implantitis under conditions of complex application of physiotherapy technologies

Лившиц, В. И., Nagornev, S. N., Фролков, В. К., & Gvetadze, R. S. (2021) · Fizioterapevt (Physiotherapist) · doi:10.33920/med-14-2108-05 · Cited by 6

Multiscale modeling of presynaptic dynamics from molecular to mesoscale

Garcia, J. W., Bartol, T. M., & B, T. J. S. A. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010068 · Cited by 6

Hauling t-SNAREs on the microtubule highway

Zhai, R. G., & Bellen, H. J. (2004) · Nature Cell Biology · doi:10.1038/ncb1004-918 · Cited by 6

Synaptic Vesicle Associated Proteins and Schizophrenia

Kao, H., & Porton, B. (2009) · Springer eBooks · doi:10.1007/978-0-387-30410-6_7 · Cited by 6

Assay and Functional Interactions of Rim2 with Rab3

Fukuda, M. (2005) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)03040-5 · Cited by 6

Creative or Not? Birds and Ants Draw with Muscles

al‐Rifaie, M. M., Bishop, M. T., & Aber, A. (2011) · Goldsmiths (University of London) · Cited by 6

[Experimental and modelling investigation of the mechanism of synaptic vesicles recycling].

Zakharov, A., Petrov, A. M., Nv, K., & Zefirov, A. L. (2012) · PubMed · Cited by 6

Is replenishment of the readily releasable pool associated with vesicular movement?

Bui, L., & Glavinović, M. I. (2013) · Cognitive Neurodynamics · doi:10.1007/s11571-013-9264-y · Cited by 6

Age-Related Remodeling of Neuromuscular Junctions

Mantilla, C. B., & Sieck, G. C. (2010) · Springer eBooks · doi:10.1007/978-90-481-9713-2_3 · Cited by 6

Presynaptic NMDA Receptors

Smart, T. G., & Duguid, I. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch14 · Cited by 6

Correction: Neuron Specific Rab4 Effector GRASP-1 Coordinates Membrane Specialization and Maturation of Recycling Endosomes

Hoogenraad, C. C., Popa, I., Futai, K., Martínez-Sanchez, E., Wulf, P. S., van Vlijmen, T., Dortland, B. R., Oorschot, V. M. J., Govers, R., Monti, M., et al. (2010) · PLoS Biology · doi:10.1371/annotation/b17dfb99-8809-4c5a-86c2-c2a0f7ca7f5e · Cited by 6

Measurement of intact quantal packet of transmitters released from single nerve terminal by loose-patch amperometry

Chen, P., Shen, X., Zhao, S., Liu, Z., Zhu, Q., Zhu, T., Zhang, S., Li, Y., Mao, L., & Sun, J. (2021) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2021.113143 · Cited by 5

Epigoitrin decreases synaptosomal glutamate release and protects neurons from glutamate excitotoxicity in rats

Chang, Y., Pan, W., & Wang, S. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177654 · Cited by 5

Genome‐wide DNA methylation profiles in the raphe nuclei of patients with autism spectrum disorder

Iwata, K., Nakabayashi, K., Ishiwata, K., Nakamura, K., Kameno, Y., Hata, K., & Matsuzaki, H. (2025) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13830 · Cited by 5

Endophilin A1 and synaptojanin 1-dependent endocytosis of synaptic vesicles in nociceptive spinal circuits maintains postoperative and cancer pain

Fialho, M. F. P., Arasu, G. S. T., Shen, C., Imlach, W. L., Bunnett, N. W., & Tonello, R. (2025) · Pain · doi:10.1097/j.pain.0000000000003657 · Cited by 5

Mechanical strength and biomechanics of extracellular vesicles

Zhai, Y., Ji, F., He, F., Qin, Z., Liu, J., & Li, S. (2025) · Nano Today · doi:10.1016/j.nantod.2025.102905 · Cited by 5

HSV-1 strain H129 co-opts neuronal synaptic transmission machinery for its transsynaptic spread

Qin, H.-B., Zhou, Y., Wu, Y., Ji, T.-X., Du, A.-N., Gao, D., Sun, J.-Y., Jiang, X., Xu, Z. S., Liu, Z.-Y., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02254-8 · Cited by 5

GABA release provoked by disturbed Na+, K+ and Ca2+ homeostasis in cerebellar nerve endings: Roles of Ca2+ channels, Na+/Ca2+ exchangers and GAT1 transporter reversal

Romei, C., Sabolla, C., & Raiteri, L. (2014) · Neurochemistry International · doi:10.1016/j.neuint.2014.04.003 · Cited by 5

FM1-43 Photoconversion and Electron Microscopy Analysis at the Drosophila Neuromuscular Junction

Sabeva, N. S., & Bykhovskaia, M. (2017) · BIO-PROTOCOL · doi:10.21769/bioprotoc.2523 · Cited by 5

High‐Precision Mapping of Membrane Proteins on Synaptic Vesicles using Spectrally Encoded Super‐Resolution Imaging

Jiang, Y., Zhang, J., Jung, S., Chen, H., Xu, S., & Chiu, D. T. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202217889 · Cited by 5

Synaptic boutons are smaller in chandelier cell cartridges in autism

Hong, T., McBride, E., Dufour, B. D., Falcone, C., Doan, M., Noctor, S. C., & Martínez‐Cerdeño, V. (2023) · PLoS ONE · doi:10.1371/journal.pone.0281477 · Cited by 5

Alterations in Synaptic Connectivity and Synaptic Transmission in Alzheimer’s Disease with High Physical Activity

Wu, C., Ruan, T., Yuan, Y., Xu, C., Du, L., Wang, F., & Xu, S. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-240123 · Cited by 5

Characterization of neuronal differentiation in human adipose-derived stromal cells: morphological, molecular, and ultrastructural insights

Yuan, X., Li, W., Yuan, Y., Zhu, X., Meng, Y., Wu, Q., Qi, Y., & Zhang, P. (2024) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2024.110296 · Cited by 5

Crystal Structure of the Central Coiled-Coil Domain from Human Liprin-β2

Stafford, R., Tang, M.-Y., Sawaya, M. R., Phillips, M. L., & Bowie, J. U. (2011) · Biochemistry · doi:10.1021/bi200141e · Cited by 5

Orthogonal Sensing of Small Molecules Using a Modular Nanoparticle‐Based Assay

Neri, S., Pinalli, R., Dalcanale, E., & Prins, L. J. (2016) · ChemNanoMat · doi:10.1002/cnma.201600075 · Cited by 5

Genetics of X-Linked Intellectual Disability

Schwartz, C. E., & Boccuto, L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800109-7.00003-0 · Cited by 5

Retrograde Axonal Transport of Liposomes from Peripheral Tissue to Spinal Cord and DRGs by Optimized Phospholipid and CTB Modification

Fukui, T., Tateno, H., Nakamura, T., Yamada, Y., Sato, Y., Iwasaki, N., Harashima, H., & Kadoya, K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126661 · Cited by 5

Triose-phosphate isomerase deficiency is associated with a dysregulation of synaptic vesicle recycling in Drosophila melanogaster

Stone, A., Cujic, O., Rowlett, A., Aderhold, S., Savage, E., Graham, B. P., & Steinert, J. R. (2023) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2023.1124061 · Cited by 5

Hypoxia releases S-nitrosocysteine from carotid body glomus cells—relevance to expression of the hypoxic ventilatory response

Seckler, J. M., Getsy, P. M., May, W. J., Gaston, B. M., Baby, S. M., Lewis, T. H. J., Bates, J. N., & Lewis, S. J. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1250154 · Cited by 5

Serum proteomic biomarker investigation of vascular depression using data-independent acquisition: a pilot study

Lan, L., Peng, S., Zhang, R., He, H., Yang, Y., Xi, B., & Zhang, J. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1341374 · Cited by 5

Cyclic AMP and Epac Contribute to the Genesis of the Positive Interaction Between Hypoxia and Hypercapnia in the Carotid Body

Ramirez, M., Almaraz, L., González, C., & Rocher, A. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-4584-1_30 · Cited by 5

Expression of synaptogyrin-1 in T1R2-expressing type II taste cells and type III taste cells of rat circumvallate taste buds

Kotani, T., Toyono, T., Seta, Y., Kitou, A., Kataoka, S., & Toyoshima, K. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1629-3 · Cited by 5

An Inhibitory Effect of Extracellular Ca2+ on Ca2+-Dependent Exocytosis

Xiong, W., Liu, T., Wang, Y., Chen, X., Sun, L., Guo, N., Zheng, H., Zheng, L., Ruat, M., Han, W., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024573 · Cited by 5

Deletion 1q43‐44 in a patient with clinical diagnosis of Warburg–Micro syndrome

Carrera, I. A., Tristancho, M. S. D. Z., Bermejo, E., Martínez‐Fernández, M. L., Lafuente, A. L., MacDonald, A., Zúñiga, Á., Gómez-Skármeta, J. L., & Martínez‐Frías, M. L. (2015) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.36878 · Cited by 5

Molecular Composition of Developing Glutamatergic Synapses

Barrow, S. L., & McAllister, A. K. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00102-2 · Cited by 5

Morphine Antidependence ofErythroxylum cuneatum(Miq.) Kurz in Neurotransmission ProcessesIn Vitro

Suliman, N. A., Moklas, M. A. M., Taib, C. N. M., Adenan, M. I., Baharuldin, M. T. H., Basir, R., & Amom, Z. (2016) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2016/3517209 · Cited by 5

Neuronal vacuolation and spinocerebellar degeneration associated with altered neurotransmission

Giannakopoulou, A. (2017) · Folia Neuropathologica · doi:10.5114/fn.2017.68580 · Cited by 5

Photoconversion of FM1-43 Reveals Differences in Synaptic Vesicle Recycling and Sensitivity to Pharmacological Disruption of Actin Dynamics in Individual Synapses

Rampérez, A., Bartolomé‐Martín, D., García-Pascual, Á., Sánchez‐Prieto, J., & Torres, M. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00712 · Cited by 5

Doc2b Ca2+ binding site mutants enhance synaptic release at rest at the expense of sustained synaptic strength

Bourgeois-Jaarsma, Q., Verhage, M., & Groffen, A. J. A. (2019) · Scientific Reports · doi:10.1038/s41598-019-50684-1 · Cited by 5

GABAA receptor agonist cinazepam and its active metabolite 3-hydroxyphenazepam act differently at the presynaptic site

Borisova, Т., Pozdnyakova, N., Dudarenko, M., Krisanova, N. V., & Andronati, S. A. (2021) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2021.03.013 · Cited by 5

Hyperglycemia-Induced Dysregulated Fusion Intermediates in Insulin-Secreting Cells Visualized by Super-Resolution Microscopy

Yang, G., Li, L., Liu, Y., Liang, K., Wei, L., & Chen, L. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.650167 · Cited by 5

Specificities of Gβγ subunits for the SNARE complex before and after stimulation of α 2a -adrenergic receptors

Yim, Y. Y., McDonald, W. H., Betke, K. M., Kaya, A. İ., Hyde, K., Erreger, K., Gilsbach, R., Hein, L., & Hamm, H. E. (2021) · Science Signaling · doi:10.1126/scisignal.abc4970 · Cited by 5

Neuromodulation by selective angiotensin-converting enzyme 2 inhibitors

Pozdnyakova, N., Krisanova, N. V., Pastukhov, A. O., Tarasenko, A. S., Dudarenko, M., Chernykh, A. V., Pashenko, A. E., Ryabukhin, S. V., Tolstanova, G. M., Volochnyuk, D. M., et al. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.07.003 · Cited by 5

Electrophysiological and Molecular Properties of the Oxytocin- and Vasopressin-Secreting Systems in Mammals

Yamashita, H., Ueta, Y., & Dyball, R. E. J. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50062-7 · Cited by 5

Auditory fidelity

Parsons, T. D. (2006) · Nature · doi:10.1038/4441013a · Cited by 5

Acute phencyclidine administration reduces extracellular glutamate levels and the expression of synaptophysin and SNAP-25 in rat frontal cortex

Fattorini, G., Bragina, L., Candiracci, C., Melone, M., Cozzi, A., Pellegrini-Giampietro, D. E., & Conti, F. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.11.022 · Cited by 5

The many faces of egg activation at fertilization

Leguía, M., & Wessel, G. M. (2007) · Signal Transduction · doi:10.1002/sita.200600122 · Cited by 5

Axonal transport of neuropeptides: Retrograde tracing study in live cell cultures of rat sympathetic cervical ganglia

Li, J., & Dahlström, A. B. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21285 · Cited by 5

Automated analysis of secretory vesicle distribution at the ultrastructural level

van Weering, J. R. T., Wijntjes, R., de Wit, H., Wortel, J., Cornelisse, L. N., Veldkamp, W. J. H., & Verhage, M. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2008.05.022 · Cited by 5

Molecular Aspects of Memory Dysfunction in Alzheimer’s Disease

Chin, J., Roberson, E. D., & Mucke, L. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00015-2 · Cited by 5

Analysis on the Emerging Role of Rab3 GTPase‐Activating Protein in Warburg Micro and Martsolf Syndrome

Sakane, A., Miyoshi, J., Takai, Y., & Sasaki, T. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(07)38009-9 · Cited by 5

Lysosomal Disorders of the Nervous System

Walkley, S. U. (2007) · Elsevier eBooks · doi:10.1016/b978-012088592-3/50003-7 · Cited by 5

Imaging Fast SNARE Mediated-Membrane Fusion in Planar-Supported Bilayers

Kiessling, V. (2005) · Biophysical Journal · doi:10.1529/biophysj.105.068460 · Cited by 5

Quantification of exocytosis kinetics by DIC image analysis of cortical lawns

Mooney, J., Thakur, S., Kahng, P. W., Trapani, J. G., & Poccia, D. (2013) · Journal of Chemical Biology · doi:10.1007/s12154-013-0104-7 · Cited by 5

Can the ‘neuron theory’ be complemented by a universal mechanism for generic neuronal differentiation

Ernsberger, U. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-2049-8 · Cited by 5

Fluctuations of hippocampal neuronal protein levels over the estrous cycle in the rat

Diao, W., Chen, W., Höger, H., Pollak, A. J., & Lübec, G. (2007) · Neurochemistry International · doi:10.1016/j.neuint.2007.10.013 · Cited by 5

The phenomenon of synaptic vesicle clustering as the prefusion state in the model system of exocytosis

Gumenyuk, V. P., Chunikhin, A. J., Himmelreich, N. H., & Trikash, I. O. (2013) · General Physiology and Biophysics · doi:10.4149/gpb_2013037 · Cited by 5

FRAP Analysis of Secretory Granule Lipids and Proteins in the Sea Urchin Egg

Wong, J. L., & Wessel, G. M. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-178-9_5 · Cited by 5

Oxidant-induced increase in norepinephrine secretion from PC12 cells is dependent on TRPM8 channel-mediated intracellular calcium elevation

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