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

Intestinal signaling to GABAergic neurons regulates a rhythmic behavior in Caenorhabditis elegans

Mahoney, T. R., Luo, S., Round, E. K., Brauner, M., GOTTSCHALK, A. R., Thomas, J. H., & Nonet, M. L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803617105 · Cited by 99

The synaptic vesicle proteome

Burré, J., & Volknandt, W. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04453.x · Cited by 99

Flexibility in a Gene Network Affecting a Simple Behavior in Drosophila melanogaster

van Swinderen, B., & Greenspan, R. J. (2005) · Genetics · doi:10.1534/genetics.104.032631 · Cited by 99

Reversal of ApoE4-induced recycling block as a novel prevention approach for Alzheimer’s disease

Xian, X., Pohlkamp, T., Durakoglugil, M. S., Wong, C. H., Beck, J. K., Lane-Donovan, C., Plattner, F., & Herz, J. (2018) · eLife · doi:10.7554/elife.40048 · Cited by 98

Homocysteinylation of neuronal proteins contributes to folate deficiency‐associated alterations of differentiation, vesicular transport, and plasticity in hippocampal neuronal cells

Akchiche, N., Bossenmeyer‐Pourié, C., Kerek, R., Martin, N., Pourié, G., Koziel, V., Helle, D., Alberto, J., Ortiou, S., Camadro, J., et al. (2012) · The FASEB Journal · doi:10.1096/fj.12-205757 · Cited by 98

SNARE bundle and syntaxin N-peptide constitute a minimal complement for Munc18-1 activation of membrane fusion

Shen, J., Rathore, S. S., Khandan, L., & Rothman, J. E. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201003148 · Cited by 98

Modulation of Synaptic Plasticity by Glutamatergic Gliotransmission: A Modeling Study

Pittà, M. D., & Brunel, N. (2016) · Neural Plasticity · doi:10.1155/2016/7607924 · Cited by 98

Role of the Wnt receptor Frizzled-1 in presynaptic differentiation and function

Varela-Nallar, L., Grabowski, C. P., Alfaro, I. E., Alvarez, A. R., & Inestrosa, N. C. (2009) · Neural Development · doi:10.1186/1749-8104-4-41 · Cited by 97

Synaptic function is modulated by LRRK2 and glutamate release is increased in cortical neurons of G2019S LRRK2 knock-in mice

Beccano-Kelly, D. A., Kuhlmann, N., Tatarnikov, I., Volta, M., Munsie, L. N., Chou, P., Cao, L.-P., Han, H., Tapia, L., Farrer, M. J., et al. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00301 · Cited by 97

Cell Adhesion, the Backbone of the Synapse: "Vertebrate" and "Invertebrate" Perspectives

Giagtzoglou, N., Ly, C. V., & Bellen, H. J. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003079 · Cited by 97

Cholesterol and synaptic transmitter release at crayfish neuromuscular junctions

Zamir, O., & Charlton, M. P. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.098319 · Cited by 97

Cdc42 and Actin Control Polarized Expression of TI-VAMP Vesicles to Neuronal Growth Cones and Their Fusion with the Plasma Membrane

Alberts, P., Rudge, R., Irinopoulou, T., Danglot, L., Gauthier‐Rouvière, C., & Galli, T. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-07-0643 · Cited by 97

Complexin arrests a pool of docked vesicles for fast Ca2+‐dependent release

Malsam, J., Parisotto, D. A., Bharat, T. A. M., Scheutzow, A., Krause, J. M., Briggs, J. A. G., & Söllner, T. H. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.164 · Cited by 96

Neurotransmitter Release at the Thalamocortical Synapse Instructs Barrel Formation But Not Axon Patterning in the Somatosensory Cortex

Narboux‐Nême, N., Evrard, A., Férézou, I., Erzurumlu, R. S., Kaeser, P. S., Lainé, J., Rossier, J., Ropert, N., Südhof, T. C., & Gaspar, P. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0343-12.2012 · Cited by 96

Visualizing long-term single-molecule dynamics in vivo by stochastic protein labeling

Liu, H., Dong, P., Ioannou, M. S., Li, L., Shea, J., Pasolli, H. A., Grimm, J. B., Rivlin, P. K., Lavis, L. D., Koyama, M., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1713895115 · Cited by 95

Vesicle Clustering in a Living Synapse Depends on a Synapsin Region that Mediates Phase Separation

Pechstein, A., Tomilin, N. V., Fredrich, K., Vorontsova, O. V., Sopova, E., Evergren, E., Haucke, V., Brodin, L., & Shupliakov, O. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.092 · Cited by 95

Mechanical Characterization of Liposomes and Extracellular Vesicles, a Protocol

Vorselen, D., Piontek, M. C., Roos, W. H., & Wuite, G. J. L. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00139 · Cited by 95

The functional organization of motor nerve terminals

Slater, C. R. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.09.004 · Cited by 95

SNAP25 is a pre‐synaptic target for the depressant action of reactive oxygen species on transmitter release

Giniatullin, А. R., Darios, F. D., Shakirzyanova, A., Davletov, B. A., & Giniatullin, R. A. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03997.x · Cited by 94

The proteome of the presynaptic active zone: from docked synaptic vesicles to adhesion molecules and maxi‐channels

Morciano, M., Beckhaus, T., Karas, M., Zimmermann, H., & Volknandt, W. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05824.x · Cited by 94

Synapse Geometry and Receptor Dynamics Modulate Synaptic Strength

Freche, D., Pannasch, U., Rouach, N., & Holcman, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025122 · Cited by 94

TRPM7 facilitates cholinergic vesicle fusion with the plasma membrane

Brauchi, S., Krapivinsky, G. B., Krapivinsky, L., & Clapham, D. E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800881105 · Cited by 94

A Programmable DNA Origami Platform to Organize SNAREs for Membrane Fusion

Xu, W., Nathwani, B., Lin, C., Wang, J., Karatekin, E., Pincet, F., Shih, W. M., & Rothman, J. E. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b13107 · Cited by 94

Scribble Interacts with β-Catenin to Localize Synaptic Vesicles to Synapses

Sun, Y., Aiga, M., Yoshida, E., Humbert, P. O., & Bamji, S. X. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-12-1172 · Cited by 93

Genetic analysis of synaptotagmin-7 function in synaptic vesicle exocytosis

Maximov, A., Lao, Y., Li, H., Chen, X., Rizo, J., Sørensen, J. B., & Südhof, T. C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712372105 · Cited by 93

Profiling Synaptic Proteins Identifies Regulators of Insulin Secretion and Lifespan

Ch'ng, Q.-L., Sieburth, D., & Kaplan, J. M. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000283 · Cited by 93

In Vivo and in Vitro Characterization of Novel Neuronal Plasticity Factors Identified following Spinal Cord Injury

Giovanni, S. D., Biase, A. D., Yakovlev, A. G., Finn, T. P., Beers, J. K., Hoffman, E. P., & Faden, A. I. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m411975200 · Cited by 93

Ca2+Influx Slows Single Synaptic Vesicle Endocytosis

Leitz, J., & Kavalali, E. T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3358-11.2011 · Cited by 93

Vesicular Neurotransmitter Transporters as Targets for Endogenous and Exogenous Toxic Substances

Chaudhry, F. A., Edwards, R. H., & Fonnum, F. (2007) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.46.120604.141146 · Cited by 93

Regulation of transmitter release by Ca2+ and synaptotagmin: insights from a large CNS synapse

Kochubey, O., Lou, X., & Schneggenburger, R. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.02.006 · Cited by 92

An overview of the synaptic vesicle lipid composition

Binotti, B., Jahn, R., & Pérez-Lara, Á. (2021) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2021.108966 · Cited by 92

Post-fusion structural changes and their roles in exocytosis and endocytosis of dense-core vesicles

Chiang, H., Shin, W., Zhao, W.-D., Hamid, E., Sheng, J., Baydyuk, M., Wen, P. J., Jin, A. J., Momboisse, F., & Wu, L. (2014) · Nature Communications · doi:10.1038/ncomms4356 · Cited by 92

Herpes Simplex Virus Utilizes the Large Secretory Vesicle Pathway for Anterograde Transport of Tegument and Envelope Proteins and for Viral Exocytosis from Growth Cones of Human Fetal Axons

Saksena, M. M., Boadle, R. A., Aggarwal, A., Tijono, B., Rixon, F. J., Diefenbach, R. J., & Cunningham, A. L. (2009) · Journal of Virology · doi:10.1128/jvi.01579-08 · Cited by 92

Calcium-sensing beyond neurotransmitters: functions of synaptotagmins in neuroendocrine and endocrine secretion

Gustavsson, N., & Han, W. (2009) · Bioscience Reports · doi:10.1042/bsr20090031 · Cited by 91

Fusion-activated Ca 2+ entry via vesicular P2X 4 receptors promotes fusion pore opening and exocytotic content release in pneumocytes

Miklavc, P., Mair, N., Wittekindt, O. H., Haller, T., Dietl, P., Felder, E., Timmler, M., & Frick, M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1101039108 · Cited by 91

Glutaminase in microglia: A novel regulator of neuroinflammation

Ding, L., Xu, X., Li, C., Wang, Y., Xia, X., & Zheng, J. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.11.038 · Cited by 91

Vesicle pools and synapsins: New insights into old enigmas

Fdez, E., & Hilfiker, S. (2007) · Journal of Neurocytology · doi:10.1007/s11068-007-9013-4 · Cited by 91

A Preferentially Segregated Recycling Vesicle Pool of Limited Size Supports Neurotransmission in Native Central Synapses

Marra, V., Burden, J. J., Thorpe, J. R., Smith, I. T., Smith, S. L., Häusser, M., Branco, T., & Staras, K. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.042 · Cited by 91

Compromised fidelity of endocytic synaptic vesicle protein sorting in the absence of stonin 2

Kononenko, N. L., Diril, M. K., Puchkov, D., Kintscher, M., Koo, S. J., Pfuhl, G., Winter, Y., Wienisch, M., Klingauf, J., Breustedt, J., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1218432110 · Cited by 91

Binding of calcium ions and SNAP-25 to the hexa EF-hand protein secretagogin

Rogstam, A., Linse, S. S., Lindqvist, A., James, P., Wagner, L., & Berggård, T. (2006) · Biochemical Journal · doi:10.1042/bj20060918 · Cited by 91

Presynaptic Ca2+ dynamics, Ca2+ buffers and synaptic efficacy

Burnashev, N., & Rozov, A. V. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.01.003 · Cited by 91

Regulation of synaptic vesicle recycling by complex formation between intersectin 1 and the clathrin adaptor complex AP2

Pechstein, A., Bacetic, J., Vahedi‐Faridi, A., Gromova, K. V., Sundborger, A., Tomlin, N., Krainer, G., Vorontsova, O. V., Schäfer, J. G., Owe, S. G., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911073107 · Cited by 91

Acute Cocaine Induces Fast Activation of D1 Receptor and Progressive Deactivation of D2 Receptor Striatal Neurons:In Vivo Optical Microprobe [Ca2+]iImaging

Luo, Z., Volkow, N. D., Heintz, N., Pan, Y., & Du, C. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2369-11.2011 · Cited by 90

Unique Luminal Localization of VGAT-C Terminus Allows for Selective Labeling of Active Cortical GABAergic Synapses

Martens, H., Weston, M. C., Boulland, J., Grønborg, M., Grosche, J., Kacza, J., Hoffmann, A., Matteoli, M., Takamori, S., Harkany, T., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3887-08.2008 · Cited by 90

Comparative studies of Munc18c and Munc18-1 reveal conserved and divergent mechanisms of Sec1/Munc18 proteins

Yu, H., Rathore, S. S., Lopez, J. A., Davis, E. M., James, D. E., Martin, J. L., & Shen, J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311232110 · Cited by 90

High- and Low-Mobility Stages in the Synaptic Vesicle Cycle

Kamin, D., Lauterbach, M. A., Westphal, V., Keller‐Findeisen, J., Schönle, A., Hell, S. W., & Rizzoli, S. O. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.04.054 · Cited by 90

CSPα-deficiency causes massive and rapid photoreceptor degeneration

Schmitz, F., Tabares, L., Khimich, D., Strenzke, N., de la Villa, P., Castellano-Muñoz, M., Bulankina, A. V., Moser, T., Fernández‐Chacón, R., & Südhof, T. C. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510060103 · Cited by 90

Ethanol-enhanced GABA release: A focus on G protein-coupled receptors

Kelm, M. K., Criswell, H. E., & Breese, G. R. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.09.003 · Cited by 90

Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline

Hardies, K., Cai, Y., Jardel, C., Jansen, A., Cao, M., May, P., Djémié, T., Camus, C. H. L., Keymolen, K., Deconinck, T., et al. (2016) · Brain · doi:10.1093/brain/aww180 · Cited by 90

Role of activation of PIP5Kγ661 by AP‐2 complex in synaptic vesicle endocytosis

Nakano-Kobayashi, A., Yamazaki, M., Unoki, T., Hongu, T., Murata, C., Taguchi, R., Katada, T., Frohman, M. A., Yokozeki, T., & Kanaho, Y. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601573 · Cited by 89

Piccolo Regulates the Dynamic Assembly of Presynaptic F-Actin

Waites, C. L., Leal‐Ortiz, S., Andlauer, T. F. M., Sigrist, S. J., & Garner, C. C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1835-11.2011 · Cited by 89

Pathophysiological actions of neuropathy‐related anti‐ganglioside antibodies at the neuromuscular junction

Plomp, J. J., & Willison, H. J. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.171702 · Cited by 89

A New Component in Synaptic Plasticity: Upregulation of Kinesin in the Neurons of the Gill-Withdrawal Reflex

Puthanveettil, S. V., Monje, F. J., Miniaci, M. C., Choi, Y., Karl, K. A., Khandros, E., Gawinowicz, M. A., Sheetz, M. P., & Kandel, E. R. (2008) · Cell · doi:10.1016/j.cell.2008.11.003 · Cited by 89

Phosphorylation of Synapsin I by cAMP-Dependent Protein Kinase Controls Synaptic Vesicle Dynamics in Developing Neurons

Bonanomi, D., Menegon, A., Miccio, A., Ferrari, G., Corradi, A. M., Kao, H., Benfenati, F., & Valtorta, F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1573-05.2005 · Cited by 89

Desynchronization of Neocortical Networks by Asynchronous Release of GABA at Autaptic and Synaptic Contacts from Fast-Spiking Interneurons

Manseau, F., Marinelli, S., Méndez, P., Schwaller, B., Prince, D. A., Huguenard, J. R., & Bacci, A. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000492 · Cited by 89

Cochlear Inner Hair Cell Ribbon Synapse is the Primary Target of Ototoxic Aminoglycoside Stimuli

Liu, K., Jiang, X., Shi, C., Shi, L., Yang, B., Shi, L., Xu, Y., Wei–yan, Y., & Yang, S. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8454-2 · Cited by 89

SNARE Protein Recycling by αSNAP and βSNAP Supports Synaptic Vesicle Priming

Burgalossi, A., Jung, S., Meyer, G., Jockusch, W. J., Jahn, O., Taschenberger, H., O'Connor, V. M., Nishiki, T., Takahashi, M., Brose, N., et al. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.019 · Cited by 89

Differential expression of the regulated catecholamine secretory pathway in different hereditary forms of pheochromocytoma

Eisenhofer, G., Huynh, T., ELKAHLOUN, A. G., Morris, J. C., Bratslavsky, G., Linehan, W. M., Zhuang, Z., Balgley, B. M., Lee, C. S., Mannelli, M., et al. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90591.2008 · Cited by 89

Short-distance vesicle transport via phase separation

Qiu, H., Wu, X., Ma, X., Li, S., Cai, Q., Ganzella, M., Ge, L., Zhang, H., & Zhang, M. (2024) · Cell · doi:10.1016/j.cell.2024.03.003 · Cited by 88

Slit1a Inhibits Retinal Ganglion Cell Arborization and Synaptogenesis via Robo2-Dependent and -Independent Pathways

Campbell, D. S., Stringham, S. A., Timm, A., Xiao, T., Law, M.-Y., Baier, H., Nonet, M. L., & Chien, C.-B. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.034 · Cited by 88

Molecular Dynamics of a Presynaptic Active Zone Protein Studied in Munc13-1–Enhanced Yellow Fluorescent Protein Knock-In Mutant Mice

Kalla, S., Stern, M., Basu, J., Varoqueaux, F., Reim, K., Rosenmund, C., Ziv, N. E., & Brose, N. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4330-06.2006 · Cited by 88

Snapin Facilitates the Synchronization of Synaptic Vesicle Fusion

Pan, P., Tian, J.-H., & Sheng, Z. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.029 · Cited by 88

Hippocampal Drebrin Loss in Mild Cognitive Impairment

Counts, S., He, B., Nadeem, M., Wuu, J., Scheff, S. W., & Mufson, E. J. (2012) · Neurodegenerative Diseases · doi:10.1159/000333122 · Cited by 88

Low energy cost for optimal speed and control of membrane fusion

François-Martin, C., Rothman, J. E., & Pincet, F. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1621309114 · Cited by 88

Neurotransmitter Release

Südhof, T. C. (2007) · Handbook of experimental pharmacology · doi:10.1007/978-3-540-74805-2_1 · Cited by 88

Coupling exo- and endocytosis: An essential role for PIP2 at the synapse

Koch, M., & Holt, M. G. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2012.02.008 · Cited by 87

Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission

Rothman, J. E., Krishnakumar, S. S., Grushin, K. S., & Pincet, F. (2017) · FEBS Letters · doi:10.1002/1873-3468.12874 · Cited by 87

Brain Pyroglutamate Amyloid-β is Produced by Cathepsin B and is Reduced by the Cysteine Protease Inhibitor E64d, Representing a Potential Alzheimer's Disease Therapeutic

Hook, G., Yu, J., Toneff, T., Kindy, M. S., & HOOK, V. Y. H. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-131370 · Cited by 87

Rapid Upregulation of α7 Nicotinic Acetylcholine Receptors by Tyrosine Dephosphorylation

Cho, C.-H., Song, W., Leitzell, K., Teo, E., Meleth, A. D., Quick, M. W., & Lester, R. A. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5389-03.2005 · Cited by 87

In vivo single-molecule imaging of syntaxin1A reveals polyphosphoinositide- and activity-dependent trapping in presynaptic nanoclusters

Bademosi, A. T., Lauwers, E., Padmanabhan, P., Odierna, G. L., Chai, Y. J., Papadopulos, A., Goodhill, G. J., Verstreken, P., van Swinderen, B., & Meunier, F. A. (2016) · Nature Communications · doi:10.1038/ncomms13660 · Cited by 87

Presynaptic Signaling by Heterotrimeric G-Proteins

Brown, D. A., & Sihra, T. S. (2007) · Handbook of experimental pharmacology · doi:10.1007/978-3-540-74805-2_8 · Cited by 86

Distribution of plasma membrane-associated syntaxins 1 through 4 indicates distinct trafficking functions in the synaptic layers of the mouse retina

Sherry, D. M., Mitchell, R., Standifer, K. M., & du Plessis, B. (2006) · BMC Neuroscience · doi:10.1186/1471-2202-7-54 · Cited by 86

SNARE Proteins Synaptobrevin, SNAP-25, and Syntaxin Are Involved in Rapid and Slow Endocytosis at Synapses

Xu, J., Luo, F., Zhang, Z., Xue, L., Wu, X., Chiang, H., Shin, W., & Wu, L. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.03.010 · Cited by 86

Evidence for Early Endosome‐like Fusion of Recently Endocytosed Synaptic Vesicles

Rizzoli, S. O., Bethani, I., Zwilling, D., Wenzel, D., Siddiqui, T. J., Brandhorst, D., & Jahn, R. (2006) · Traffic · doi:10.1111/j.1600-0854.2006.00466.x · Cited by 86

Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour

Hernández‐Hernández, Ó., Guiraud-Dogan, C., Sicot, G., Huguet-Lachon, A., Luilier, S., Steidl, E., Saenger, S., Marciniak, E., Obriot, H., Chevarin, C., et al. (2013) · Brain · doi:10.1093/brain/aws367 · Cited by 86

Sodium channels and the synaptic mechanisms of inhaled anaesthetics

Hemmings, H. C. (2009) · British Journal of Anaesthesia · doi:10.1093/bja/aep144 · Cited by 86

A secretagogin locus of the mammalian hypothalamus controls stress hormone release

Romanov, R. A., Alpár, A., Zhang, M., Zeisel, A., Calas, A., Landry, M., Fuszard, M., Shirran, S. L., Schnell, R., Dobolyi, Á., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201488977 · Cited by 85

CAST and ELKS proteins: structural and functional determinants of the presynaptic active zone

Hida, Y., & Ohtsuka, T. (2010) · The Journal of Biochemistry · doi:10.1093/jb/mvq065 · Cited by 85

Neuromodulator Signaling Bidirectionally Controls Vesicle Numbers in Human Synapses

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Long latency of evoked quantal transmitter release from somata of locus coeruleus neurons in rat pontine slices

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