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

Visualization of Rab3A dissociation during exocytosis: A study by total internal reflection microscopy

Lin, C., Huang, C., Lin, K., Cheng, K. ‐., Yang, D., Tsai, Y., Ong, R. ‐., Huang, Y. ‐., & Kao, L. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20938 · Cited by 24

Spontaneous vesicle recycling in the synaptic bouton

Truckenbrodt, S., & Rizzoli, S. O. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00409 · Cited by 24

The tail domain of tomosyn controls membrane fusion through tomosyn displacement by VAMP2

Yamamoto, Y., Fujikura, K., Sakaue, M., Okimura, K., Kobayashi, Y., Nakamura, T., & Sakisaka, T. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.07.026 · Cited by 24

Synip Arrests Soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (SNARE)-dependent Membrane Fusion as a Selective Target Membrane SNARE-binding Inhibitor

Yu, H., Rathore, S. S., & Shen, J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.465450 · Cited by 24

The importance of an asymmetric distribution of acidic lipids for synaptotagmin 1 function as a Ca2+ sensor

Lai, Y., & Shin, Y. (2012) · Biochemical Journal · doi:10.1042/bj20112044 · Cited by 24

Brpf1 Haploinsufficiency Impairs Dendritic Arborization and Spine Formation, Leading to Cognitive Deficits

Su, Y., Liu, J., Yu, B., Ba, R., & Zhao, C. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00249 · Cited by 24

A Hyperactive Form of unc-13 Enhances Ca2+ Sensitivity and Synaptic Vesicle Release Probability in C. elegans

Li, L., Liu, H., Hall, Q., Wang, W., Yu, Y., Kaplan, J. M., & Hu, Z. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.018 · Cited by 24

Inhibition of sigma-1 receptors substantially modulates GABA and glutamate transport in presynaptic nerve terminals

Pozdnyakova, N., Krisanova, N. V., Dudarenko, M., Vavers, E., Zvejniece, L., Dambrova, M., & Borisova, Т. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113434 · Cited by 24

Developmental expression of Synaptotagmin isoforms in single calyx of Held-generating neurons

Xiao, L., Han, Y., Runne, H., Murray, H., Kochubey, O., Luthi‐Carter, R., & Schneggenburger, R. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.05.002 · Cited by 24

Development- and activity-dependent regulation of SNAP-25 phosphorylation in rat brain

Kataoka, M., Kuwahara, R., Matsuo, R., Sekiguchi, M., Inokuchi, K., & Takahashi, M. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.08.055 · Cited by 24

Dynasore inhibits rapid endocytosis in bovine chromaffin cells

Tsai, C.-C., Lin, C.-L., Ohn, T., Chou, A., Chou, M.-Y., Lee, C., Peng, I.-W., Liao, J.-H., Chen, Y., & Pan, C. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00562.2008 · Cited by 24

Antidepressants differentially affect expression of complexin I and II RNA in rat hippocampus

Zink, M., Rapp, S., Gebicke‐Haerter, P. J., Henn, F. A., & Thome, J. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0017-4 · Cited by 24

Retrieval and Reuse of Pituitary Secretory GranuleProteins

Ferraro, F., Eipper, B. A., & Mains, R. E. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414156200 · Cited by 24

Activity-dependent calpain activation plays a critical role in synaptic facilitation and post-tetanic potentiationPreprint

Khoutorsky, A., & Spira, M. E. (2009) · Learning & Memory · doi:10.1101/lm.1275709 · Cited by 24

Vesicular Glutamate Transporter Expression Ensures High-Fidelity Synaptic Transmission at the Calyx of Held Synapses

Nakakubo, Y., Abe, S., Yoshida, T., Takami, C., Isa, M., Wojcik, S. M., Brose, N., Takamori, S., & Hori, T. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108040 · Cited by 23

Function of Drosophila Synaptotagmins in membrane trafficking at synapses

Quiñones-Frías, M. C., & Littleton, J. T. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03788-9 · Cited by 23

Amyloid pathology and synaptic loss in pathological aging

Gkanatsiou, E., Nilsson, J., Toomey, C. E., Vrillon, A., Kvartsberg, H., Portelius, E., Zetterberg, H., Blennow, K., Brinkmalm, A., Lashley, T., et al. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15487 · Cited by 23

Reduced synaptic proteins and SNARE complexes in Down syndrome with Alzheimer's disease and the Dp16 mouse Down syndrome model: Impact of APP gene dose

Chen, X., Zuo, X., Becker, A., Head, E., & Mobley, W. C. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12835 · Cited by 23

Subcellular localization and putative role of VPS13A/chorein in dopaminergic neuronal cells

Hayashi, T., Kishida, M., Nishizawa, Y., Iijima, M., Koriyama, C., Nakamura, M., Sano, A., & Kishida, S. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.02.047 · Cited by 23

Rabx-5 Regulates RAB-5 Early Endosomal Compartments and Synaptic Vesicles in C. elegans

Sann, S. B., Crane, M. M., Lu, H., & Jin, Y. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037930 · Cited by 23

Signaling role of the voltage-gated calcium channel as the molecular on/off-switch of secretion

Atlas, D. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.04.003 · Cited by 23

Allelic variants of SNAP25 in a family-based sample of ADHD

Renner, T., Walitza, S., Dempfle, A., Eckert, L., Romanos, M., Gerlach, M., Schäfer, H., Warnke, A., Lesch, K., & Jacob, C. (2008) · Journal of Neural Transmission · doi:10.1007/s00702-007-0840-3 · Cited by 23

Enlightening molecular mechanisms through study of protein interactions

Rizo, J., Rosen, M. K., & Gardner, K. H. (2012) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjs036 · Cited by 23

Protein fingerprints of cultured CA3-CA1 hippocampal neurons: comparative analysis of the distribution of synaptosomal and cytosolic proteins

Corti, V., Sánchez-Ruíz, Y., Piccoli, G., Bergamaschi, A., Cannistraci, C. V., Pattini, L., Cerutti, S., Bachi, A., Alessio, M., & Malgaroli, A. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-36 · Cited by 23

α-Synuclein Regulates Development and Function of Cholinergic Enteric Neurons in the Mouse Colon

Swaminathan, M., Fung, C., Finkelstein, D. I., Bornstein, J. C., & Foong, J. P. P. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.10.029 · Cited by 23

Brain Pathogenesis and Potential Therapeutic Strategies in Myotonic Dystrophy Type 1

Liu, J., Guo, Z., Yan, X., Yang, Y., & Huang, S. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.755392 · Cited by 23

Molecular mechanisms that control initiation and termination of physiological depolarization-evoked transmitter release

Kupchik, Y. M., Rashkovan, G., Ohana, L., Raifman, T. K., Dascal, N., Parnas, H., & Parnas, I. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708540105 · Cited by 23

Nicotinic cholinergic intercellular communication: Implications for the developing auditory system

Morley, B. J. (2005) · Hearing Research · doi:10.1016/j.heares.2005.02.012 · Cited by 23

The Role of Phosphoinositides in Synapse Function

Ueda, Y. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8768-8 · Cited by 23

Synaptotagmin I is involved in the regulation of cortical granule exocytosis in the sea urchin

Leguía, M., Conner, S. D., Berg, L. K., & Wessel, G. M. (2006) · Molecular Reproduction and Development · doi:10.1002/mrd.20454 · Cited by 23

Presynaptic Serotonergic Gating of the Subthalamonigral Glutamatergic Projection

Ding, S., Li, L., & Zhou, F.-M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4111-12.2013 · Cited by 23

Crystal Structure of the RIM1α C2B Domain at 1.7 Å Resolution,

Guan, R. J., Dai, H., Tomchick, D. R., Dulubova, I., Machius, M., Südhof, T. C., & Rizo, J. (2007) · Biochemistry · doi:10.1021/bi700698a · Cited by 23

Therapeutic benefits of ACTH and levetiracetam in STXBP1 encephalopathy with a de novo mutation

Liu, S., Wang, L., Cai, X. T., Zhou, H., Yu, D., & Wang, Z. (2018) · Medicine · doi:10.1097/md.0000000000010663 · Cited by 23

Synaptic Density and Neuronal Metabolic Function Measured by Positron Emission Tomography in the Unilateral 6-OHDA Rat Model of Parkinson’s Disease

Raval, N. R., Gudmundsen, F., Juhl, M., Andersen, I. V., Speth, N., Videbæk, A., Petersen, I. N., Mikkelsen, J. D., Fisher, P. M., Herth, M. M., et al. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.715811 · Cited by 22

Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice

Okamoto, Y., Lipstein, N., Hua, Y., Lin, K., Brose, N., Sakaba, T., & Midorikawa, M. (2016) · eLife · doi:10.7554/elife.14643 · Cited by 22

circRNA Acbd6 promotes neural stem cell differentiation into cholinergic neurons via the miR-320-5p-Osbpl2 axis

Li, W., Shan, B., Cheng, X., He, H., Qin, J., Zhao, H., Tian, M., Zhang, X., & Jin, G. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.101828 · Cited by 22

Alzheimer’s Disease beyond Calcium Dysregulation: The Complex Interplay between Calmodulin, Calmodulin-Binding Proteins and Amyloid Beta from Disease Onset through Progression

O’Day, D. H. (2023) · Current Issues in Molecular Biology · doi:10.3390/cimb45080393 · Cited by 22

The Complex Interplay between Toxic Hallmark Proteins, Calmodulin-Binding Proteins, Ion Channels, and Receptors Involved in Calcium Dyshomeostasis in Neurodegeneration

O’Day, D. H. (2024) · Biomolecules · doi:10.3390/biom14020173 · Cited by 22

Inositol hexakisphosphate suppresses excitatory neurotransmission via synaptotagmin-1 C2B domain in the hippocampal neuron

Yang, S.-N., Shi, Y., Yang, G., Li, Y., Yu, L., Shin, O., Bacaj, T., Südhof, T. C., Yu, J. H., & Berggren, P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1115070109 · Cited by 22

Presynaptic Inhibitory Terminals Are Functionally Abnormal in a Rat Model of Posttraumatic Epilepsy

Faria, L. C., & Prince, D. A. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00351.2010 · Cited by 22

SNAP-25 is abundantly expressed in enteric neuronal networks and upregulated by the neurotrophic factor GDNF

Barrenschee, M., Böttner, M., Harde, J., Lange, C., Cossais, F., Ebsen, M., Vogel, I., & Wedel, T. (2015) · Histochemistry and Cell Biology · doi:10.1007/s00418-015-1310-x · Cited by 22

Rescue of tau-induced synaptic transmission pathology by paclitaxel

Erez, H., Shemesh, O. A., & Spira, M. E. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00034 · Cited by 22

Synaptotagmin 1 and Ca2+ drive trans SNARE zippering

Lai, Y., Lou, X., Wang, C., Xia, T., & Tong, J. (2014) · Scientific Reports · doi:10.1038/srep04575 · Cited by 22

Differentiation and neural integration of hippocampal neuronal progenitors: Signaling pathways sequentially involved

Akchiche, N., Bossenmeyer‐Pourié, C., Pourié, G., Koziel, V., Nédélec, E., Guéant, J., & Daval, J. (2009) · Hippocampus · doi:10.1002/hipo.20690 · Cited by 22

Lysophosphatidylcholine Drives Neuroblast Cell Fate

Paoletti, L., Domizi, P., Marcucci, H., Montaner, A., Krapf, D., Salvador, G. A., & Banchio, C. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9528-0 · Cited by 22

Revealing Clusters of Connected Pathways Through Multisource Data Integration in Huntington's Disease and Spastic Ataxia

Kakouri, A. C., Christodoulou, C. C., Zachariou, M., Oulas, A., Minadakis, G., Demetriou, C. A., Votsi, C., Zamba‐Papanicolaou, E., Christodoulou, K., & Spyrou, G. M. (2018) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2018.2865569 · Cited by 22

Comparative synaptosome imaging: a semi-quantitative method to obtain copy numbers for synaptic and neuronal proteins

Richter, K. N., Wildhagen, H., Helm, M. S., Ußling, J., Schikorski, T., & Rizzoli, S. O. (2018) · Scientific Reports · doi:10.1038/s41598-018-33130-6 · Cited by 22

Ubiquitin and Ubiquitin-Like Proteins in the Critical Equilibrium between Synapse Physiology and Intellectual Disability

Folci, A., Mirabella, F., & Fossati, M. (2020) · eNeuro · doi:10.1523/eneuro.0137-20.2020 · Cited by 22

Botulinum Neurotoxins Can Enter Cultured Neurons Independent of Synaptic Vesicle Recycling

Pellett, S., Tepp, W. H., Scherf, J. M., & Johnson, E. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133737 · Cited by 22

Thinking about Visual Behavior; Learning about Photoreceptor Function

Choe, K., & Clandinin, T. R. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)69007-2 · Cited by 22

Synaptic vesicles studied by dynamic light scattering

Castorph, S., Henriques, S. S. G., Holt, M. G., Riedel, D., Jahn, R., & Salditt, T. (2011) · The European Physical Journal E · doi:10.1140/epje/i2011-11063-2 · Cited by 22

Matrix metalloproteinase-7 modulates synaptic vesicle recycling and induces atrophy of neuronal synapses

Szklarczyk, A., Conant, K. E., Owens, D. F., Ravin, R., McKay, R. D. G., & Gerfen, C. R. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.032 · Cited by 22

Sub-Cellular Distribution and Translocation of TRP Channels

Toro, C. A., Arias-Darraz, L., & Brauchi, S. (2010) · Current Pharmaceutical Biotechnology · doi:10.2174/138920111793937899 · Cited by 22

Immunohistochemical Characterisation of Classical Scrapie Neuropathology in Sheep

Vidal, E., Acín, C., Foradada, L., Monzón, M., Márquez, M., Monleón, E., Pumarola, M. B., Badiola, J. J., & Bolea, R. (2009) · Journal of Comparative Pathology · doi:10.1016/j.jcpa.2009.04.002 · Cited by 22

Molecular origins of synaptotagmin 1 activities on vesicle docking and fusion pore opening

Lai, Y., Lou, X., Diao, J., & Shin, Y. (2015) · Scientific Reports · doi:10.1038/srep09267 · Cited by 22

Polarized targeting of ion channels in neurons

Arnold, D. B. (2006) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-006-0155-5 · Cited by 22

Temporal evolution of neurophysiological and behavioral features of synapsin I/II/III triple knock-out mice

Cambiaghi, M., Cursi, M., Monzani, E., Benfenati, F., Comı, G., Minicucci, F., Valtorta, F., & Leocani, L. (2012) · Epilepsy Research · doi:10.1016/j.eplepsyres.2012.07.012 · Cited by 22

Different mechanisms of Ca2+regulation that influence synaptic transmission: Comparison between crayfish and Drosophila neuromuscular junctions

Desai-Shah, M., & Cooper, R. L. (2009) · Synapse · doi:10.1002/syn.20695 · Cited by 22

Measuring Ca2+-Induced Structural Changes in Lipid Monolayers: Implications for Synaptic Vesicle Exocytosis

Ghosh, S. K., Castorph, S., Konovalov, O., Salditt, T., Jahn, R., & Holt, M. G. (2012) · Biophysical Journal · doi:10.1016/j.bpj.2012.01.006 · Cited by 22

Cloning and functional expression of voltage-gated ion channel subunits from cnidocytes of the Portuguese Man O'War Physalia physalis

Bouchard, C., Price, R. B., Moneypenny, C. G., Thompson, L. F., Zillhardt, M., Stalheim, L., & Anderson, P. A. V. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02314 · Cited by 22

PCR-verified microarray analysis and functionalin vitrostudies indicate a role of α-tocopherol in vesicular transport

Nell, S., Bahtz, R., Boßecker, A., Kipp, A. P., Landes�, N., Bumke‐Vogt, C., Halligan, E. P., Lunec, J., & Brigelius‐Flohé, R. (2007) · Free Radical Research · doi:10.1080/10715760701416988 · Cited by 22

5-HT4 receptor activation facilitates recovery from synaptic rundown and increases transmitter release from single varicosities of myenteric neurons

Ren, J., Zhou, X., & Galligan, J. J. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00078.2008 · Cited by 22

Synaptic protein dysregulation in myotonic dystrophy type 1

Hernández‐Hernández, Ó., Sicot, G., Dincã, D. M., Huguet-Lachon, A., Nicole, A., Buée, L., Münnich, A., Sergeant, N., Gourdon, G., & Gomes-Pereira, M. (2013) · Rare Diseases · doi:10.4161/rdis.25553 · Cited by 22

The beginning and the end of SNARE ‐induced membrane fusion

Mion, D., Bunel, L., Heo, P., & Pincet, F. (2022) · FEBS Open Bio · doi:10.1002/2211-5463.13447 · Cited by 21

The contribution of endocytosis to sensitization of nociceptors and synaptic transmission in nociceptive circuits

Tonello, R., Anderson, W. B., Davidson, S., Escriou, V., Yang, L., Schmidt, B. L., Imlach, W. L., & Bunnett, N. W. (2022) · Pain · doi:10.1097/j.pain.0000000000002826 · Cited by 21

Compartmentalization of soluble endocytic proteins in synaptic vesicle clusters by phase separation

Yoshida, T., Takenaka, K.-I., Sakamoto, H., Kojima, Y., Sakano, T., Shibayama, K., Nakamura, K., Hanawa‐Suetsugu, K., Mori, Y., Hirabayashi, Y., et al. (2023) · iScience · doi:10.1016/j.isci.2023.106826 · Cited by 21

A comparative multi-level toxicity assessment of carbon-based Gd-free dots and Gd-doped nanohybrids from coffee waste: hematology, biochemistry, histopathology and neurobiology study

Kuznietsova, H. M., Dziubenko, N., Paliienko, K., Pozdnyakova, N., Krisanova, N. V., Pastukhov, A. O., Lysenko, T., Dudarenko, M., Skryshevsky, V. A., Lysenko, V., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-36496-4 · Cited by 21

Molecularly and structurally distinct synapses mediate reliable encoding and processing of auditory information

Wichmann, C. (2015) · Hearing Research · doi:10.1016/j.heares.2015.07.008 · Cited by 21

Loss of Photoreceptors Results in Upregulation of Synaptic Proteins in Bipolar Cells and Amacrine Cells

Dagar, S., Nagar, S., Goel, M., Cherukuri, P., & Dhingra, N. K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090250 · Cited by 21

Motor neuropathy‐associated mutation impairs Seipin functions in neurotransmission

Wei, S., Soh, S. L., Xia, J., Ong, W., Pang, Z. P., & Han, W. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12638 · Cited by 21

Intranasal Vaccination with an Engineered Influenza Virus Expressing the Receptor Binding Subdomain of Botulinum Neurotoxin Provides Protective Immunity Against Botulism and Influenza

Li, J., Díaz-Arévalo, D., Chen, Y., & Zeng, M. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00170 · Cited by 21

A unique SNARE machinery for exocytosis of cytotoxic granules and platelets granules

Tang, B. L. (2015) · Molecular Membrane Biology · doi:10.3109/09687688.2015.1079934 · Cited by 21

Synaptic vesicle pool‐specific modification of neurotransmitter release by intravesicular free radical generation

Afuwape, O. A., Wasser, C. R., Schikorski, T., & Kavalali, E. T. (2016) · The Journal of Physiology · doi:10.1113/jp273115 · Cited by 21

Release activity-dependent control of vesicle endocytosis by the synaptic adhesion molecule N-cadherin

van Stegen, B., Dagar, S., & Gottmann, K. (2017) · Scientific Reports · doi:10.1038/srep40865 · Cited by 21

Presynaptic NMDA Receptors

Duguid, I., & Smart, T. G. (2009) · Europe PMC (PubMed Central) · Cited by 21

Chapter 20 Regulated Exocytosis from Astrocytes

Calì, C., Marchaland, J., Spagnuolo, P., Gremion, J., & Bezzi, P. (2009) · International review of neurobiology · doi:10.1016/s0074-7742(09)85020-4 · Cited by 21

PKA-mediated phosphorylation is a novel mechanism for levetiracetam, an antiepileptic drug, activating ROMK1 channels

Lee, C., Lee, C.-Y., Tsai, T.-S., & Liou, H. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.04.012 · Cited by 21

Distinct roles of the C2A and the C2B domain of the vesicular Ca2+ sensor synaptotagmin 9 in endocrine β-cells

Grise, F., Taib-Maamar, N., Monterrat, C., Lagrée, V., & Lang, J. (2007) · Biochemical Journal · doi:10.1042/bj20061182 · Cited by 21

Influence of Intra- and Extracellular Acidification on Free Radical Formation and Mitochondria Membrane Potential in Rat Brain Synaptosomes

Pekun, T. G., Lemeshchenko, V. V., Lyskova, T. I., Waseem, T. V., & Fedorovich, S. V. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9913-3 · Cited by 21

Activity-Dependent Potentiation of Large Dense-Core Vesicle Release Modulated by Mitogen-Activated Protein Kinase/Extracellularly Regulated Kinase Signaling

Park, Y., Jun, D., Hur, E., Lee, S., Suh, B.-S., & Kim, K. (2005) · Endocrinology · doi:10.1210/en.2005-0959 · Cited by 21

The Complex Secretions of the Salivary Glands of Drosophila melanogaster, A Model System

Farkas, R. (2016) · Springer eBooks · doi:10.1007/978-3-319-40740-1_15 · Cited by 21

Trafficking mechanisms of synaptogenic cell adhesion molecules

Ribeiro, L. F., Verpoort, B., & de Wit, J. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.04.003 · Cited by 21

Spike-Mediated and Graded Inhibitory Synaptic Transmission Between Leech Interneurons: Evidence for Shared Release Sites

Ivanov, A. I., & Calabrese, R. L. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01094.2005 · Cited by 21

Influence of cholesterol depletion in plasma membrane of rat brain synaptosomes on calcium-dependent and calcium-independent exocytosis

Waseem, T. V., Kolos, V. A., Lapatsina, L. P., & Fedorovich, S. V. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.06.029 · Cited by 21

Rab11 as a modulator of synaptic transmission

Giorgini, F., & Steinert, J. R. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.26807 · Cited by 21

Splotch: Robust estimation of aligned spatial temporal gene expression dataPreprint

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PTPRM Is Critical for Synapse Formation Regulated by Zinc Ion

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