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

Endosomal sorting of readily releasable synaptic vesicles

Hoopmann, P., Punge, A., Barysch, S. V., Westphal, V., Bückers, J., Opazo, F., Bethani, I., Lauterbach, M. A., Hell, S. W., & Rizzoli, S. O. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007037107 · Cited by 168

Alternative Zippering as an On-Off Switch for SNARE-Mediated Fusion

Giraudo, C. G., Garcia-Diaz, A., Eng, W. S., Chen, Y., Hendrickson, W. A., Melia, T. J., & Rothman, J. E. (2009) · Science · doi:10.1126/science.1166500 · Cited by 168

Only a Fraction of Quantal Content is Released During Exocytosis as Revealed by Electrochemical Cytometry of Secretory Vesicles

Omiatek, D. M., Dong, Y., Heien, M. L., & Ewing, A. G. (2010) · ACS Chemical Neuroscience · doi:10.1021/cn900040e · Cited by 168

Munc18-1 binding to the neuronal SNARE complex controls synaptic vesicle priming

Deák, F., Xu, Y., Chang, W.-P., Dulubova, I., Khvotchev, M. V., Liu, X., Südhof, T. C., & Rizo, J. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200812026 · Cited by 167

UNC-13 and UNC-10/Rim Localize Synaptic Vesicles to Specific Membrane Domains

Weimer, R. M., Gracheva, E. O., Meyrignac, O., Miller, K. G., Richmond, J. E., & Bessereau, J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2350-06.2006 · Cited by 167

Selective Neuronal Degeneration in Huntington's Disease

Cowan, C. M., & Raymond, L. A. (2006) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(06)75002-5 · Cited by 166

Evidence for Anterograde Transport and Transcytosis of Botulinum Neurotoxin A (BoNT/A)

Restani, L., Antonucci, F., Gianfranceschi, L., Rossi, C., Rossetto, O., & Caleo, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2618-11.2011 · Cited by 166

DTNBP1, a schizophrenia susceptibility gene, affects kinetics of transmitter release

Chen, X.-W., Feng, Y., Hao, C., Guo, X., He, X., Zhou, Z.-Y., Guo, N., Huang, H.-P., Xiong, W., Zheng, H., et al. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200711021 · Cited by 166

Fluid Biomarkers for Synaptic Dysfunction and Loss

Camporesi, E., Nilsson, J., Brinkmalm, A., Becker, B., Ashton, N. J., Blennow, K., & Zetterberg, H. (2020) · Biomarker Insights · doi:10.1177/1177271920950319 · Cited by 165

Homotypic fusion of early endosomes: SNAREs do not determine fusion specificity

Brandhorst, D., Zwilling, D., Rizzoli, S. O., Lippert, U., Lang, T., & Jahn, R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511138103 · Cited by 165

Rab GTPases and their roles in brain neurons and glia

Ng, E. L., & Tang, B. L. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.04.006 · Cited by 165

Synapse loss in dementias

Clare, R., King, V. G., Wirenfeldt, M., & Vinters, H. V. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22392 · Cited by 163

Endocytosis, Recycling, and Regulated Exocytosis of Glucose Transporter 4

Foley, K. P., Boguslavsky, S., & Klip, A. (2011) · Biochemistry · doi:10.1021/bi2000356 · Cited by 163

A Vesicle Superpool Spans Multiple Presynaptic Terminals in Hippocampal Neurons

Staras, K., Branco, T., Burden, J. J., Pozo, K., Darcy, K., Marra, V., Ratnayaka, J. A., & Goda, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.020 · Cited by 163

A common molecular basis for membrane docking and functional priming of synaptic vesicles

Siksou, L., Varoqueaux, F., Pascual, O., Triller, A., Brose, N., & Marty, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06811.x · Cited by 160

Complexin Has Opposite Effects on Two Modes of Synaptic Vesicle Fusion

Martin, J. A., Hu, Z., Fenz, K. M., Fernandez, J., & Dittman, J. S. (2011) · Current Biology · doi:10.1016/j.cub.2010.12.014 · Cited by 159

SUR1: a unique ATP-binding cassette protein that functions as an ion channel regulator

Aittoniemi, J., Fotinou, C., Craig, T. J., de Wet, H., Proks, P., & Ashcroft, F. M. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0142 · Cited by 159

Calcium-channel number critically influences synaptic strength and plasticity at the active zone

Sheng, J., He, L., Zheng, H., Xue, L., Luo, F., Shin, W., Sun, T., Kuner, T., Yue, D. T., & Wu, L. (2012) · Nature Neuroscience · doi:10.1038/nn.3129 · Cited by 158

Immunoisolation of two synaptic vesicle pools from synaptosomes: a proteomics analysis

Morciano, M., Burré, J., Corvey, C., Karas, M., Zimmermann, H., & Volknandt, W. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03506.x · Cited by 158

Neurotransmitter Release at Central Synapses

Stevens, C. F. (2003) · Neuron · doi:10.1016/s0896-6273(03)00643-3 · Cited by 158

Rab3 Dynamically Controls Protein Composition at Active Zones

Graf, E. R., Daniels, R. W., Burgess, R. W., Schwarz, T. L., & DiAntonio, A. (2009) · Neuron · doi:10.1016/j.neuron.2009.11.002 · Cited by 157

Actin dynamics provides membrane tension to merge fusing vesicles into the plasma membrane

Wen, P. J., Grenklo, S., Arpino, G., Tan, X., Liao, H.-S., Heureaux, J., Peng, S.-Y., Chiang, H., Hamid, E., Zhao, W.-D., et al. (2016) · Nature Communications · doi:10.1038/ncomms12604 · Cited by 157

Synaptic vesicle recycling studied in transgenic mice expressing synaptopHluorin

Li, Z., Burrone, J., Tyler, W. J., Hartman, K. N., Albeanu, D. F., & Murthy, V. N. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501145102 · Cited by 157

Rapid structural alterations of the active zone lead to sustained changes in neurotransmitter release

Matz, J., Gilyan, A., Kolar, A., McCarvill, T., & Krueger, S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906087107 · Cited by 156

Synaptotagmin-1 drives synchronous Ca2+-triggered fusion by C2B-domain-mediated synaptic-vesicle-membrane attachment

Chang, S., Trimbuch, T., & Rosenmund, C. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0037-5 · Cited by 156

Regulatory Logic of Pan-Neuronal Gene Expression in C. elegans

Stefanakis, N., Carrera, I., & Hobert, O. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.031 · Cited by 155

NMDA and AMPA receptors dysregulation in Alzheimer's disease

Babaei, P. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174310 · Cited by 155

Double Patch Clamp Reveals That Transient Fusion (Kiss-and-Run) Is a Major Mechanism of Secretion in Calf Adrenal Chromaffin Cells: High Calcium Shifts the Mechanism from Kiss-and-Run to Complete Fusion

Elhamdani, A., Azizi, F., & Artalejo, C. R. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5275-05.2006 · Cited by 155

Augmenting neurotransmitter release by enhancing the apparent Ca 2+ affinity of synaptotagmin 1

Rhee, J.-S., Li, L. Y., Shin, O.-H., Rah, J.-C., Rizo, J., Südhof, T. C., & Rosenmund, C. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509153102 · Cited by 155

In vitro system capable of differentiating fast Ca 2+ -triggered content mixing from lipid exchange for mechanistic studies of neurotransmitter release

Kyoung, M., Srivastava, A., Zhang, Y., Diao, J., Vrljic, M., Grob, P., Nogales, E., Chu, S., & Brunger, A. T. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107900108 · Cited by 154

Calcium Channels and Short-term Synaptic Plasticity

Catterall, W. A., Leal, K., & Nanou, E. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.r112.411645 · Cited by 153

Development of Cortical Maps: Perspectives From the Barrel Cortex

Inan, M., & Crair, M. C. (2007) · The Neuroscientist · doi:10.1177/1073858406296257 · Cited by 152

Analyzing complex functional brain networks: Fusing statistics and network science to understand the brain

Simpson, S. L., Bowman, F. D., & Laurienti, P. J. (2013) · Statistics Surveys · doi:10.1214/13-ss103 · Cited by 152

Aging, Synaptic Dysfunction, and Insulin-Like Growth Factor (IGF)-1

Deák, F., & Sonntag, W. E. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls118 · Cited by 151

The Ca2+ Affinity of Synaptotagmin 1 Is Markedly Increased by a Specific Interaction of Its C2B Domain with Phosphatidylinositol 4,5-Bisphosphate

Radhakrishnan, A., Stein, A., Jahn, R., & Fasshauer, D. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.042499 · Cited by 151

Theoretical models of synaptic short term plasticity

Hennig, M. H. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00154 · Cited by 151

Omega-3 fatty acids and brain resistance to ageing and stress: body of evidence and possible mechanisms

Denis, I., Potier, B., Vancassel, S., Heberden, C., & Lavialle, M. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.01.007 · Cited by 150

Lipid imbalance in the neurological disorder, Niemann‐Pick C disease

Vance, J. E. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.06.008 · Cited by 150

A fast, single-vesicle fusion assay mimics physiological SNARE requirements

Karatekin, E., Giovanni, J. D., Iborra, C., Coleman, J., O’Shaughnessy, B., SEAGAR, M. J., & Rothman, J. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914723107 · Cited by 149

Ribbon synapses of the retina

Dieck, S. T., & Brandstätter, J. H. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0234-0 · Cited by 149

Factors regulating the abundance and localization of synaptobrevin in the plasma membrane

Dittman, J. S., & Kaplan, J. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600784103 · Cited by 149

Identification of the minimal protein domain required for priming activity of Munc13-1

Stevens, D. R., Wu, Z.-X., Matti, U., Junge, H. J., Schirra, C., Becherer, U., Wojcik, S. M., Brose, N., & Rettig, J. (2005) · Current Biology · doi:10.1016/j.cub.2005.10.055 · Cited by 149

Adverse Drug Reactions in Patients with Phaeochromocytoma

Eisenhofer, G., Rivers, G., Rosas, A. L., Quezado, Z., Manger, W. M., & Pacák, K. (2007) · Drug Safety · doi:10.2165/00002018-200730110-00004 · Cited by 148

Vesicle-Mediated Steroid Hormone Secretion in Drosophila melanogaster

Yamanaka, N., Marqués, G., & O’Connor, M. B. (2015) · Cell · doi:10.1016/j.cell.2015.10.022 · Cited by 147

Presynaptic long-term plasticity

Yang, Y., & Calakos, N. (2013) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2013.00008 · Cited by 147

Core Proteins of the Secretory Machinery

Lang, T., & Jahn, R. (2007) · Handbook of experimental pharmacology · doi:10.1007/978-3-540-74805-2_5 · Cited by 147

Complexin Clamps Asynchronous Release by Blocking a Secondary Ca2+ Sensor via Its Accessory α Helix

Yang, X., Kaeser‐Woo, Y. J., Pang, Z. P., Xu, W., & Südhof, T. C. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.001 · Cited by 146

Dynamic of Ion Channel Expression at the Plasma Membrane of Cardiomyocytes

Balse, E., Steele, D. F., Abriel, H., Coulombe, A., Fedida, D., & Hatem, S. N. (2012) · Physiological Reviews · doi:10.1152/physrev.00041.2011 · Cited by 145

Extended synaptotagmins are Ca 2+ -dependent lipid transfer proteins at membrane contact sites

Yu, H., Liu, Y., Gulbranson, D. R., Paine, A. R., Rathore, S. S., & Shen, J. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1517259113 · Cited by 145

Evidence for CALM in Directing VAMP2 Trafficking

Harel, A., Wu, F., Mattson, M. P., Morris, C. M., & Yao, P. J. (2008) · Traffic · doi:10.1111/j.1600-0854.2007.00694.x · Cited by 144

Solar-blind SnO2 nanowire photo-synapses for associative learning and coincidence detection

Chen, Y., Qiu, W., Wang, X., Liu, W., Wang, J., Dai, G., Yuan, Y., Gao, Y., & Sun, J. (2019) · Nano Energy · doi:10.1016/j.nanoen.2019.05.064 · Cited by 144

Dynamin 3 is a component of the postsynapse, where it interacts with mGluR5 and Homer

Gray, N. W., Fourgeaud, L., Huang, B., Chen, J., Cao, H., Oswald, B. J., Hémar, A., & McNiven, M. A. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00136-2 · Cited by 143

Brain Human Monoclonal Autoantibody from Sydenham Chorea Targets Dopaminergic Neurons in Transgenic Mice and Signals Dopamine D2 Receptor: Implications in Human Disease

Cox, C. J., Sharma, M., Leckman, J. F., Zuccolo, J., Zuccolo, A., Kovoor, A., Swedo, S. E., & Cunningham, M. W. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1102592 · Cited by 143

Retrograde regulation of motoneuron differentiation by muscle β-catenin

Li, X. M., Dong, X., Luo, S.-W., Zhang, B., Lee, D.-H., Ting, A. K. L., Neiswender, H., Kim, C., Carpenter‐Hyland, E. P., Gao, T. M., et al. (2008) · Nature Neuroscience · doi:10.1038/nn2053 · Cited by 143

UNC-51/ATG1 kinase regulates axonal transport by mediating motor–cargo assemblyPreprint

Toda, H., Mochizuki, H., Flores, R., Josowitz, R., Krasieva, T. B., LaMorte, V. J., Suzuki, E., Gindhart, J. G., Furukubo-Tokunaga, K., & Tomoda, T. (2008) · Genes & Development · doi:10.1101/gad.1734608 · Cited by 143

Phosphoinositide-3-Kinase Activation Controls Synaptogenesis and Spinogenesis in Hippocampal Neurons

Cuesto, G., Enríquez-Barreto, L., Caramés, C., Cantarero, M., Gasull, X., Sandi, C., Ferrús, A., Acebes, Á., & Morales, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4477-10.2011 · Cited by 142

Fast, Temperature-Sensitive and Clathrin-Independent Endocytosis at Central Synapses

Delvendahl, I., Vyleta, N. P., von Gersdorff, H., & Hallermann, S. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.013 · Cited by 141

BDNF-mediated neurotransmission relies upon a myosin VI motor complex

Yano, H., Ninan, I., Zhang, H., Milner, T. A., Arancio, O., & Chao, M. V. (2006) · Nature Neuroscience · doi:10.1038/nn1730 · Cited by 141

Chapter 2 Synapse Formation in Developing Neural Circuits

Colón‐Ramos, D. A. (2009) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(09)01202-2 · Cited by 141

Loss-of-Function Mutations in TBC1D20 Cause Cataracts and Male Infertility in blind sterile Mice and Warburg Micro Syndrome in Humans

Liegel, R. P., Handley, M. T., Ronchetti, A., Brown, S. D. M., Langemeyer, L., Linford, A., Chang, B., Morris-Rosendahl, D. J., Carpanini, S. M., Posmyk, R., et al. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.10.011 · Cited by 140

Dysbindin deficiency in sandy mice causes reduction of snapin and displays behaviors related to schizophrenia

FENG, Y., ZHOU, Z., HE, X., WANG, H., Guo, X. W., HAO, C., GUO, Y., Zhen, X., & Li, W. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.07.018 · Cited by 140

A Tale of Two Stories: Astrocyte Regulation of Synaptic Depression and Facilitation

Pittà, M. D., Volman, V., Berry, H., & Ben‐Jacob, E. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002293 · Cited by 140

Homeostatic plasticity at the Drosophila neuromuscular junction

Frank, C. A. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.06.015 · Cited by 140

Synaptobrevin N-terminally bound to syntaxin–SNAP-25 defines the primed vesicle state in regulated exocytosis

Walter, A. M., Wiederhold, K., Bruns, D., Fasshauer, D., & Sørensen, J. B. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200907018 · Cited by 140

Differential Abilities of SNAP-25 Homologs to Support Neuronal Function

Delgado-Martínez, I., Nehring, R. B., & Sørensen, J. B. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5092-06.2007 · Cited by 140

Molecular organization and plasticity of the cytomatrix at the active zone

Gundelfinger, E. D., & Fejtová, A. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.10.005 · Cited by 139

The Vesicular Acetylcholine Transporter Is Required for Neuromuscular Development and Function

de Castro, B. M., Jaeger, X. D., Martins-Silva, C., Lima, R. D. F., Amaral, E. A., Menezes, C. A. S., Lima, P., Neves, C. M. L., Pires, R. G. W., Gould, T. W., et al. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00245-09 · Cited by 139

Functions of SNAREs in intracellular membrane fusion and lipid bilayer mixing

Ungermann, C., & Langosch, D. (2005) · Journal of Cell Science · doi:10.1242/jcs.02561 · Cited by 139

Large-Scale Profiling of Rab GTPase Trafficking Networks: The Membrome

Gürkan, C., Lapp, H., Alory, C., Su, A. I., Hogenesch, J. B., & Balch, W. E. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-01-0062 · Cited by 139

Myosin IIA is required for cytolytic granule exocytosis in human NK cells

Andzelm, M. M., Chen, X., Krzewski, K., Orange, J. S., & Strominger, J. L. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20071143 · Cited by 138

Dual‐Color STED Microscopy at 30‐nm Focal‐Plane Resolution

Meyer, L., Wildanger, D., Medda, R., Punge, A., Rizzoli, S. O., Donnert, G., & Hell, S. W. (2008) · Small · doi:10.1002/smll.200800055 · Cited by 138

A small pool of vesicles maintains synaptic activity in vivo

Denker, A., Bethani, I., Kröhnert, K., Körber, C., Horstmann, H., Wilhelm, B. G., Barysch, S. V., Kuner, T., Neher, E., & Rizzoli, S. O. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112688108 · Cited by 137

Surface-based lipid vesicle reactor systems: fabrication and applications

Christensen, S. M., & Stamou, D. G. (2007) · Soft Matter · doi:10.1039/b702849k · Cited by 137

BDNF increases release probability and the size of a rapidly recycling vesicle pool within rat hippocampal excitatory synapses

Tyler, W. J., Zhang, X., Hartman, K. N., Winterer, J., Müller, W. S., Stanton, P. K., & Pozzo‐Miller, L. D. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.111310 · Cited by 137

Functional Compartmentalization of Endosomal Trafficking for the Synaptic Delivery of AMPA Receptors during Long-Term Potentiation

Brown, T. C., Correia, S. S., Petrok, C. N., & Esteban, J. A. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4258-07.2007 · Cited by 136

Gene Expression in Temporal Lobe Epilepsy is Consistent with Increased Release of Glutamate by Astrocytes

Lee, T.-S. W., Mane, S., Eid, T., Zhao, H., Lin, A., Guan, Z., Kim, J. H., Schweitzer, J., King-Stevens, D., Weber, P. B., et al. (2007) · Molecular Medicine · doi:10.2119/2006-00079.lee · Cited by 136

Postsynaptic Complexin Controls AMPA Receptor Exocytosis during LTP

Ahmad, M., Polepalli, J. S., Goswami, D., Yang, X., Kaeser-Woo, Y. J., Südhof, T. C., & Malenka, R. C. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.020 · Cited by 133

Current concepts in neuromuscular transmission

Fagerlund, M. J., & Eriksson, L. I. (2009) · British Journal of Anaesthesia · doi:10.1093/bja/aep150 · Cited by 133

Structural Basis for a Munc13–1 Homodimer to Munc13–1/RIM Heterodimer Switch

Lu, J., Machius, M., Dulubova, I., Dai, H., Südhof, T. C., Tomchick, D. R., & Rizo, J. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040192 · Cited by 132

Mechanisms and Function of Dendritic Exocytosis

Kennedy, M. J., & Ehlers, M. D. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.032 · Cited by 132

Compound vesicle fusion increases quantal size and potentiates synaptic transmission

He, L., Xue, L., Xu, J., McNeil, B. D., Bai, L., Melicoff, E., Adachi, R., & Wu, L. (2009) · Nature · doi:10.1038/nature07860 · Cited by 132

Botulinum Neurotoxin D Uses Synaptic Vesicle Protein SV2 and Gangliosides as Receptors

Peng, L., Tepp, W. H., Johnson, E. A., & Dong, M. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002008 · Cited by 132

Cryo–electron tomography reveals a critical role of RIM1α in synaptic vesicle tethering

Fernández‐Busnadiego, R., Asano, S. M., Oprişoreanu, A., Sakata, E., Doengi, M., Kochovski, Z., Zürner, M., Stein, V., Schoch, S., Baumeister, W. P., et al. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201206063 · Cited by 132

Cryo-electron Tomography of Clathrin-coated Vesicles: Structural Implications for Coat Assembly

Cheng, Y., Boll, W., Kirchhausen, T. L., Harrison, S. C., & Walz, T. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.10.036 · Cited by 132

Direct Interaction of Otoferlin with Syntaxin 1A, SNAP-25, and the L-type Voltage-gated Calcium Channel CaV1.3

Ramakrishnan, N. A., Drescher, M. J., & Drescher, D. G. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m803605200 · Cited by 132

The reserve pool of synaptic vesicles acts as a buffer for proteins involved in synaptic vesicle recycling

Denker, A., Kröhnert, K., Bückers, J., Neher, E., & Rizzoli, S. O. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112690108 · Cited by 132

CART: An Hrs/Actinin-4/BERP/Myosin V Protein Complex Required for Efficient Receptor Recycling

Yan, Q., Sun, W., Kujala, P., Lotfi, Y., Vida, T. A., & Bean, A. J. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-11-1014 · Cited by 131

Somatodendritic dopamine release: recent mechanistic insights

Rice, M. E., & Patel, J. C. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0185 · Cited by 131

The Janus-faced nature of the C2B domain is fundamental for synaptotagmin-1 function

Xue, M., Ma, C., Craig, T. K., Rosenmund, C., & Rizo, J. (2008) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1508 · Cited by 131

Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segments

Mazelova, J., Ransom, N. L., Astuto-Gribble, L. M., Wilson, M. C., & Deretic, D. (2009) · Journal of Cell Science · doi:10.1242/jcs.039982 · Cited by 130

Sr2+ Binding to the Ca2+ Binding Site of the Synaptotagmin 1 C2B Domain Triggers Fast Exocytosis without Stimulating SNARE Interactions

Shin, O., Rhee, J., Tang, J., Sugita, S., Rosenmund, C., & Südhof, T. C. (2003) · Neuron · doi:10.1016/s0896-6273(02)01145-5 · Cited by 129

Neurotransmitter release regulated by a MALS-liprin-α presynaptic complex

Olsen, O., Moore, K. A., Fukata, M., Kazuta, T., Trinidad, J. C., Kauer, F. W., Streuli, M., Misawa, H., Burlingame, A. L., Nicoll, R. A., et al. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200503011 · Cited by 128

Distinctive Profiles of Gene Expression in the Human Nucleus Accumbens Associated with Cocaine and Heroin Abuse

Albertson, D. N., Schmidt, C. J., Kapatos, G., & Bannon, M. J. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301089 · Cited by 128

Two‐Photon Fluorescent Probes for Acidic Vesicles in Live Cells and Tissue

Kim, H. M., An, M. J., Hong, J. H., Jeong, B. H., Kwon, O., Hyon, J., Hong, S., Lee, K. J., & Cho, B. R. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200704586 · Cited by 128

Synaptic tau: A pathological or physiological phenomenon?

Robbins, M., Clayton, E. L., & Schierle, G. S. K. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01246-y · Cited by 128

Phosphatidylinositol Phosphates as Co-activators of Ca2+ Binding to C2 Domains of Synaptotagmin 1

Li, L., Shin, O., Rhee, J., Araç, D., Rah, J., Rizo, J., Südhof, T. C., & Rosenmund, C. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600888200 · Cited by 128

Zinc Is Required for FcεRI-Mediated Mast Cell Activation

Kabu, K., Yamasaki, S., Kamimura, D., Ito, Y., Hasegawa, A., Sato, E., Kitamura, H., Nishida, K., & Hirano, T. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.1296 · Cited by 128

A Quaternary SNARE–Synaptotagmin–Ca2+–Phospholipid Complex in Neurotransmitter Release

Dai, H., Shen, N., Araç, D., & Rizo, J. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.01.040 · Cited by 127

Complexin and Ca2+ stimulate SNARE-mediated membrane fusion

Yoon, T., Lu, X., Diao, J., Lee, S.-M., Ha, T., & Shin, Y. (2008) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1446 · Cited by 127

Membrane transporters as mediators of synaptic dopamine dynamics: implications for disease

Lohr, K. M., Masoud, S. T., Salahpour, A., & Miller, G. W. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13357 · Cited by 127

Snares and Munc18 in synaptic vesicle fusion

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

Molecular machines governing exocytosis of synaptic vesicles

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

The molecular machinery of synaptic vesicle exocytosis

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

Mechanism of neurotransmitter release coming into focus

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

3. Molecular analysis of neurotransmitter release

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