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

Identification and characterization of SV31, a novel synaptic vesicle membrane protein and potential transporter

Burré, J., Zimmermann, H., & Volknandt, W. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04758.x · Cited by 40

A novel fast mechanism for GPCR-mediated signal transduction—control of neurotransmitter release

Kupchik, Y. M., Barchad-Avitzur, O., Wess, J., Ben-Chaim, Y., Parnas, I., & Parnas, H. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201007053 · Cited by 40

Volatile Anesthetic Effects on Glutamate versus GABA Release from Isolated Rat Cortical Nerve Terminals: 4-Aminopyridine-Evoked Release

Westphalen, R. I., & Hemmings, H. C. (2005) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.090662 · Cited by 40

Therapeutic hypothermia protects against ischemia-induced impairment of synaptic plasticity following juvenile cardiac arrest in sex-dependent manner

Dietz, R. M., Deng, G., Orfila, J. E., Xu, H., Traystman, R. J., & Herson, P. S. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.03.052 · Cited by 40

Structure determination of clathrin coats to subnanometer resolution by single particle cryo-electron microscopy

Fotin, A., Kirchhausen, T. L., Grigorieff, N., Harrison, S. C., Walz, T., & Cheng, Y. (2006) · Journal of Structural Biology · doi:10.1016/j.jsb.2006.07.001 · Cited by 40

Neurotransmitters and Integration in Neuronal-Astroglial Networks

Verkhratsky, A., Rodriguez, J. J., & Parpura, V. (2012) · Neurochemical Research · doi:10.1007/s11064-012-0765-6 · Cited by 39

Sharing vesicles between central presynaptic terminals: implications for synaptic function

Staras, K. (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00020 · Cited by 39

Synaptic vesicle recycling is enhanced by torsinA that harbors the DYT1 dystonia mutation

Kakazu, Y., Koh, J., Ho, K. W. D., Gonzalez‐Alegre, P., & Harata, N. C. (2011) · Synapse · doi:10.1002/syn.21534 · Cited by 39

Express assessment of neurotoxicity of particles of planetary and interstellar dust

Borisova, Т. (2019) · npj Microgravity · doi:10.1038/s41526-019-0062-7 · Cited by 39

Synaptopathies in Developmental and Epileptic Encephalopathies: A Focus on Pre-synaptic Dysfunction

Spoto, G., Valentini, G., Saia, M. C., Butera, A., Amore, G., Salpietro, V., Nicotera, A. G., & Rosa, G. D. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.826211 · Cited by 39

Stability of presynaptic vesicle pools and changes in synapse morphology in the amygdala following fear learning in adult rats

Ostroff, L. E., Cain, C. K., Jindal, N., Dar, N., & LeDoux, J. E. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22691 · Cited by 39

Dose-related gene expression changes in forebrain following acute, low-level chlorpyrifos exposure in neonatal rats

Ray, A., Liu, J., Ayoubi, P. J., & Pope, C. (2010) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2010.07.026 · Cited by 39

Asymmetric accumulation of hippocampal 7S SNARE complexes occurs regardless of kindling paradigm

Matveeva, E. A., VANAMAN, T. C., Whiteheart, S. W., & Slevin, J. T. (2006) · Epilepsy Research · doi:10.1016/j.eplepsyres.2006.11.003 · Cited by 39

De novo DNM1 mutations in two cases of epileptic encephalopathy

Nakashima, M., Kouga, T., Lourenço, C. M., Shiina, M., Goto, T., Tsurusaki, Y., Miyatake, S., Miyake, N., Saitsu, H., Ogata, K., et al. (2015) · Epilepsia · doi:10.1111/epi.13257 · Cited by 39

Early motor development is abnormal in complexin 1 knockout mice

Glynn, D., Sizemore, R. J., & Morton, A. J. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.10.011 · Cited by 39

Identification of Soluble N-Ethylmaleimide-Sensitive Factor Attachment Protein Receptor Exocytotic Machinery in Human Plasma Cells: SNAP-23 Is Essential for Antibody Secretion

Reales, E., Mora‐López, F., Rivas, V., García-Poley, A., Brieva, J. A., & Campos‐Caro, A. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.10.6686 · Cited by 39

Distinct patterns of gene expression in the left and right hippocampal formation of developing rats

Moskal, J. R., Kroes, R. A., Otto, N. J., Rahimi, O. B., & Claiborne, B. J. (2006) · Hippocampus · doi:10.1002/hipo.20198 · Cited by 39

α-Synuclein oligomers and fibrils: partners in crime in synucleinopathies

Bigi, A., Cascella, R., & Cecchi, C. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.371345 · Cited by 38

A Highly Tilted Membrane Configuration for the Prefusion State of Synaptobrevin

Blanchard, A. E., Arcario, M. J., Schulten, K. J., & Tajkhorshid, E. (2014) · Biophysical Journal · doi:10.1016/j.bpj.2014.09.013 · Cited by 38

Cytosolic Transmitter Concentration Regulates Vesicle Cycling at Hippocampal GABAergic Terminals

Wang, L., Tu, P., Bonet, L., Aubrey, K. R., & Supplisson, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.021 · Cited by 38

Efficient Exploration of Membrane-Associated Phenomena at Atomic Resolution

Vermaas, J. V., Baylon, J. L., Arcario, M. J., Muller, M. P., Wu, Z., Pogorelov, T. V., & Tajkhorshid, E. (2015) · The Journal of Membrane Biology · doi:10.1007/s00232-015-9806-9 · Cited by 38

The where, what, and when of membrane protein degradation in neurons

Jin, E. J., Kiral, F. R., & Hiesinger, P. R. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22534 · Cited by 38

Plastic smoke aerosol: Nano-sized particle distribution, absorption/fluorescent properties, dysregulation of oxidative processes and synaptic transmission in rat brain nerve terminals

Borysov, A., Tarasenko, A. S., Krisanova, N. V., Pozdnyakova, N., Pastukhov, A. O., Dudarenko, M., Paliienko, K., & Borisova, Т. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.114502 · Cited by 38

Clathrin-independent endocytic retrieval of SV proteins mediated by the clathrin adaptor AP-2 at mammalian central synapses

López-Hernández, T., Takenaka, K.-I., Mori, Y., Kongpracha, P., Nagamori, S., Haucke, V., & Takamori, S. (2021) · eLife · doi:10.7554/elife.71198 · Cited by 38

Single Exosome Amperometric Measurements Reveal Encapsulation of Chemical Messengers for Intercellular Communication

Hu, K., Vo, K. L. L., Wang, F., Zhang, X., Gu, C., Fang, N., Phan, N. T. N., & Ewing, A. G. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c02844 · Cited by 38

Quantitative investigations of amperometric spike feet suggest different controlling factors of the fusion pore in exocytosis at chromaffin cells

Amatore, C. A., Arbault, S., Bonifas, I., & Guille‐Collignon, M. (2009) · Biophysical Chemistry · doi:10.1016/j.bpc.2009.04.007 · Cited by 38

Nerve Terminal GABAA Receptors Activate Ca2+/Calmodulin-dependent Signaling to Inhibit Voltage-gated Ca2+ Influx and Glutamate Release

Long, P., Mercer, A., Begum, R., Stephens, G. J., Sihra, T. S., & Jovanovic, J. N. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m805322200 · Cited by 38

Differential expression of synaptoporin and synaptophysin in primary sensory neurons and up-regulation of synaptoporin after peripheral nerve injury

Sun, T., Xiao, H., Zhou, P.-B., Lu, Y.-J., Bao, L., & Zhang, X. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.05.010 · Cited by 38

Regulated Exocytosis: Novel Insights from Intravital Microscopy

Masedunskas, A., Porat‐Shliom, N., & Weigert, R. (2012) · Traffic · doi:10.1111/j.1600-0854.2012.01328.x · Cited by 37

Atomoxetine affects transcription/translation of the NMDA receptor and the norepinephrine transporter in the rat brain – an in vivo study

Ludolph, A. G., Udvardi, P. T., Föhr, K. J., Henes, C., Liebau, S., Dreyhaupt, J., & Boeckers (2013) · Drug Design Development and Therapy · doi:10.2147/dddt.s50448 · Cited by 37

New Insights Into Interactions of Presynaptic Calcium Channel Subtypes and SNARE Proteins in Neurotransmitter Release

He, R., Zhang, J., Yu, Y., Jizi, L., Wang, W., & Li, M. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00213 · Cited by 37

Relationship of SNAP25 variants with schizophrenia and antipsychotic-induced weight change in large-scale schizophrenia patients

Guan, F., Zhang, T., Han, W., Zhu, L., Ni, T., Lin, H., Liu, D., Chen, G., Xiao, J., & Li, T. (2019) · Schizophrenia Research · doi:10.1016/j.schres.2019.09.015 · Cited by 37

Vaccines against botulism

Karalewitz, A., & Barbieri, J. T. (2012) · Current Opinion in Microbiology · doi:10.1016/j.mib.2012.05.009 · Cited by 37

A role for vesicular glutamate transporter 1 in synaptic vesicle clustering and mobility

Siksou, L., Silm, K., Biesemann, C., Nehring, R. B., Wojcik, S. M., Triller, A., Mestikawy, S. E., Marty, S., & Herzog, É. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12199 · Cited by 37

Signaling at the vertebrate synapse: New roles for embryonic morphogens?

Salinas, P. C. (2005) · Journal of Neurobiology · doi:10.1002/neu.20159 · Cited by 37

Robust syntaxin-4 immunoreactivity in mammalian horizontal cell processes

Hirano, A. A., Brandstätter, J. H., VILA, A., & Brecha, N. C. (2007) · Visual Neuroscience · doi:10.1017/s0952523807070198 · Cited by 37

Ca2+ Triggers a Novel Clathrin‐Independent but Actin‐Dependent Fast Endocytosis in Pancreatic Beta Cells

He, Z., Fan, J., Kang, L., Lu, J., Xue, Y., Xu, P., Xu, T., & Chen, L. (2008) · Traffic · doi:10.1111/j.1600-0854.2008.00730.x · Cited by 37

N type Ca2+ channels and RIM scaffold protein covary at the presynaptic transmitter release face but are components of independent protein complexes

Khanna, R., Li, Q., Sun, L., Collins, T. J., & Stanley, E. F. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.04.053 · Cited by 37

Some Selective Serotonin Reuptake Inhibitors Inhibit Dynamin I Guanosine Triphosphatase (GTPase)

Otomo, M., Takahashi, K., Miyoshi, H., Osada, K., Nakashima, H., & Yamaguchi, N. (2008) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.31.1489 · Cited by 37

Dynamic presenilin 1 and synaptotagmin 1 interaction modulates exocytosis and amyloid β production

Zoltowska, K. M., Maesako, M., Lushnikova, I., Takeda, S., Keller, L. J., Skibo, G., Hyman, B. T., & Berezovska, O. (2017) · Molecular Neurodegeneration · doi:10.1186/s13024-017-0159-y · Cited by 36

Distinct roles of Drosophila cacophony and Dmca1D Ca2+ channels in synaptic homeostasis: Genetic interactions with slowpoke Ca2+‐activated BK channels in presynaptic excitability and postsynaptic response

Lee, J., Ueda, A., & Wu, C. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22120 · Cited by 36

Protective Effects of Testosterone on Presynaptic Terminals against Oligomeric β -Amyloid Peptide in Primary Culture of Hippocampal Neurons

Lau, C. G., Ho, J. Y. S., Hung, C. H.-L., Wuwongse, S., Poon, C.-H., Chiu, K., Yang, X., Chu, L., & Chang, R. C. (2014) · BioMed Research International · doi:10.1155/2014/103906 · Cited by 36

Near-Membrane Dynamics and Capture of TRPM8 Channels within Transient Confinement Domains

Veliz, L., Toro, C. A., Vivar, J. P., Arias-Darraz, L., Villegas, J., Castro, M. A., & Brauchi, S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013290 · Cited by 36

Cholesterol and regulated exocytosis: A requirement for unitary exocytotic events

Rituper, B., Flašker, A., Guček, A., Chowdhury, H. H., & Zorec, R. (2012) · Cell Calcium · doi:10.1016/j.ceca.2012.05.009 · Cited by 36

Resolving the Function of Distinct Munc18-1/SNARE Protein Interaction Modes in a Reconstituted Membrane Fusion Assay

Schollmeier, Y., Krause, J. M., Kreye, S., Malsam, J., & Söllner, T. H. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.269886 · Cited by 36

Nitric oxide-mediated posttranslational modifications control neurotransmitter release by modulating complexin farnesylation and enhancing its clamping ability

Robinson, S. W., Bourgognon, J.-M., Spiers, J. G., Breda, C., Campesan, S., Butcher, A. J., Mallucci, G. R., Dinsdale, D. D., Morone, N., Mistry, R., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2003611 · Cited by 36

GPCR regulation of secretion

Yim, Y. Y., Zurawski, Z., & Hamm, H. E. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.07.005 · Cited by 36

A Novel ELISA for the Measurement of Cerebrospinal Fluid SNAP-25 in Patients with Alzheimer’s Disease

Öhrfelt, A., Brinkmalm, A., Dumurgier, J., Zetterberg, H., Bouaziz-Amar, É., Hugon, J., Paquet, C., & Blennow, K. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.11.038 · Cited by 36

Glutamatergic signaling between neurons and oligodendrocyte lineage cells: Is it synaptic or non‐synaptic?

Kula, B., Chen, T., & Kukley, M. (2019) · Glia · doi:10.1002/glia.23617 · Cited by 36

Critical Analysis of Neuronal Cell and the Mouse Bioassay for Detection of Botulinum Neurotoxins

Pellett, S., Tepp, W. H., & Johnson, E. A. (2019) · Toxins · doi:10.3390/toxins11120713 · Cited by 36

Polarized sorting of Patched enables cytoneme‐mediated Hedgehog reception in the Drosophila wing disc

González‐Méndez, L., Gradilla, A., Sánchez‐Hernández, D., González, E., Aguirre‐Tamaral, A., Jiménez‐Jiménez, C., Guerra, M., Aguilar, G., Andrés, G., Falcón‐Pérez, J. M., et al. (2020) · The EMBO Journal · doi:10.15252/embj.2019103629 · Cited by 36

Mdivi-1 alleviates brain damage and synaptic dysfunction after intracerebral hemorrhage in mice

Zhang, Y., Rui, T., Luo, C., & Li, Q. (2021) · Experimental Brain Research · doi:10.1007/s00221-021-06089-6 · Cited by 36

Exercise protects synaptic density in a rat model of Parkinson's disease

Binda, K. H., Lillethorup, T. P., Real, C. C., Bærentzen, S. L., Nielsen, M. N., Orłowski, D., Brooks, D. J., Chacur, M., & Landau, A. M. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113741 · Cited by 36

A comparative study of neurotoxic potential of synthesized polysaccharide-coated and native ferritin-based magnetic nanoparticles

Borysov, A., Krisanova, N. V., Chunikhin, О. Y., Остапченко, Л. І., Pozdnyakova, N., & Borisova, Т. (2014) · Croatian Medical Journal · doi:10.3325/cmj.2014.55.195 · Cited by 36

Share and share alike: trading of presynaptic elements between central synapses

Staras, K. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.04.005 · Cited by 36

Enrichment of integral membrane proteins from small amounts of brain tissue

Schindler, J., Jung, S.-Y., Niedner‐Schatteburg, G., Friauf, E., & Nothwang, H. G. (2006) · Journal of Neural Transmission · doi:10.1007/s00702-006-0508-4 · Cited by 36

Increasing small conductance Ca2+‐activated potassium channel activity reverses ischemia‐induced impairment of long‐term potentiation

Orfila, J. E., Shimizu, K., Garske, A. K., Deng, G., Maylie, J., Traystman, R. J., Quillinan, N., Adelman, J. P., & Herson, P. S. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12683 · Cited by 36

Sequence and Membrane Determinants of the Random Coil–Helix Transition of α-Synuclein

Lokappa, S. B., Suk, J.-E., Balasubramanian, A., Samanta, S., Situ, A. J., & Ulmer, T. S. (2014) · Journal of Molecular Biology · doi:10.1016/j.jmb.2014.02.024 · Cited by 36

C-terminal ECFP Fusion Impairs Synaptotagmin 1 Function

Han, W., Rhee, J., Maximov, A., Lin, W., Hammer, R. E., Rosenmund, C., & Südhof, T. C. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408757200 · Cited by 36

Functional Heterogeneity at Dopamine Release Sites

Daniel, J. A., Galbraith, S., Iacovitti, L., Abdipranoto, A., & Vissel, B. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1349-09.2009 · Cited by 36

Exocytosis, dependent on Ca2+ release from Ca2+ stores, is regulated by Ca2+ microdomains

Low, J. T., Shukla, A., Behrendorff, N., & Thorn, P. (2010) · Journal of Cell Science · doi:10.1242/jcs.071225 · Cited by 36

Abnormalities in α/β-CaMKII and related mechanisms suggest synaptic dysfunction in hippocampus of LPA1 receptor knockout mice

Musazzi, L., Daniel, E. D., Maycox, P. R., Racagni, G., & Popoli, M. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710001240 · Cited by 36

Autocrine signaling involved in cell volume regulation: The role of released transmitters and plasma membrane receptors

Franco, R., Panayiotidis, M. I., & la Paz, L. D. O.-D. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21406 · Cited by 36

Biochemical, molecular and behavioral phenotypes of Rab3A mutations in the mouse

Yang, S., Farias, M. L. C., Kapfhamer, D., Tobias, J. W., Grant, G. R., Abel, T. G., & Bućan, M. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00235.x · Cited by 36

Development of SV2A Ligands for Epilepsy Treatment: A Review of Levetiracetam, Brivaracetam, and Padsevonil

Wu, P.-P., Cao, B.-R., Tian, F.-Y., & Gao, Z.-B. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-023-01138-2 · Cited by 35

Synaptic vesicle glycoprotein 2A modulates vesicular release and calcium channel function at peripheral sympathetic synapses

Vogl, C., Tanifuji, S., Danis, B., Daniels, V., Foerch, P., Wolff, C., Whalley, B. J., Mochida, S., & Stephens, G. J. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12799 · Cited by 35

Imaging Neurotransmitters with Small‐Molecule Fluorescent Probes

Bade, A., Yadav, P., Zhang, L., Bypaneni, R. N., Xu, M., & Glass, T. E. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202406401 · Cited by 35

Direct interaction of SNARE complex binding protein synaphin/complexin with calcium sensor synaptotagmin 1

Tokumaru, H., Shimizu‐Okabe, C., & Abe, T. (2008) · Journal of Neurocytology · doi:10.1007/s11068-008-9032-9 · Cited by 35

Beyond the cytoskeleton: The emerging role of organelles and membrane remodeling in the regulation of axon collateral branches

Winkle, C. C., Taylor, K. L., Dent, E. W., Gallo, G., Greif, K. F., & Gupton, S. L. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22398 · Cited by 35

MUNC18–1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Hamada, N., Iwamoto, I., Tabata, H., & Nagata, K. (2017) · Acta Neuropathologica Communications · doi:10.1186/s40478-017-0498-5 · Cited by 35

Saikosaponin D suppresses enterovirus A71 infection by inhibiting autophagy

Li, C., Huang, L., Sun, W., Chen, Y., He, M., Yue, J., & Ballard, H. J. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0037-x · Cited by 35

Role of Cofilin in Alzheimer’s Disease

Wang, Q., Yuan, W., Yang, X., Wang, Y., Li, Y., & Qiao, H. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.584898 · Cited by 35

Structural Analysis of Botulinum Neurotoxin Type G Receptor Binding,

Schmitt, J., Karalewitz, A., Benefield, D. A., Mushrush, D. J., Pruitt, R. N., Spiller, B. W., Barbieri, J. T., & Lacy, D. B. (2010) · Biochemistry · doi:10.1021/bi100412v · Cited by 35

Synaptotagmin‐1 promotes the formation of axonal filopodia and branches along the developing axons of forebrain neurons

Greif, K. F., Asabere, N., Lutz, G. J., & Gallo, G. (2012) · Developmental Neurobiology · doi:10.1002/dneu.22033 · Cited by 35

Mechanisms of constitutive and ATP-evoked ATP release in neonatal mouse olfactory epithelium

Hayoz, S., Jia, C., & Hegg, C. C. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-53 · Cited by 35

Increased Synaptophysin Is Involved in Inflammation-Induced Heat Hyperalgesia Mediated by Cyclin-Dependent Kinase 5 in Rats

Zhang, H., Zhang, X., Wang, W., Xue, Q., Han, L., Huang, J., Gui, T., & Yu, B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046666 · Cited by 35

The Cystic Fibrosis Transmembrane Conductance Regulator's Expanding SNARE Interactome

Tang, B. L., Gee, H. Y., & Lee, M. G. (2011) · Traffic · doi:10.1111/j.1600-0854.2011.01161.x · Cited by 35

Exocytosis of a Single Bovine Adrenal Chromaffin Cell: The Electrical and Morphological Studies

Tsai, C., Yang, C.-C. B., Shih, P.-Y., Wu, C.-S., Chen, C., Pan, C., & Chen, Y. (2008) · The Journal of Physical Chemistry B · doi:10.1021/jp803000a · Cited by 35

New Model of Action for Mood Stabilizers: Phosphoproteome from Rat Pre-Frontal Cortex Synaptoneurosomal Preparations

Corena-McLeod, M. D. P., Walss‐Bass, C., Oliveros, A., Villegas, A. G., Ceballos, C., Charlesworth, C. M., Madden, B. J., Linser, P. J., Ekeris, L. V., Smith, K., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0052147 · Cited by 35

Depolarization‐induced differentiation of PC12 cells is mediated by phospholipase D2 through the transcription factor CREB pathway

Banno, Y., Nemoto, S., Murakami, M., Kimura, M., Ueno, Y., Ohguchi, K., Hara, A., Okano, Y., Kitade, Y., Onozuka, M., et al. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05085.x · Cited by 35

Computer Modeling of Mild Axonal Injury: Implications for Axonal Signal Transmission

Volman, V., & Ng, L. J. (2013) · Neural Computation · doi:10.1162/neco_a_00491 · Cited by 35

Tomosyn-dependent regulation of synaptic transmission is required for a late phase of associative odor memory

Chen, K., Richlitzki, A., Featherstone, D. E., Schwärzel, M., & Richmond, J. E. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1110184108 · Cited by 35

Transsynaptic modulation of the synaptic vesicle cycle by cell‐adhesion molecules

Gottmann, K. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21484 · Cited by 35

Dynamic Gradient of Glutamate Across the Membrane: Glutamate/Aspartate-Induced Changes in the Ambient Level of l-[14C]glutamate and d-[3H]aspartate in Rat Brain Nerve Terminals

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