The DOI matches its Crossref record; 43 of the 45 references it cites were found in a registry or an index.
Synaptotagmin I: A major Ca2+ sensor for transmitter release at a central synapse
Open accessAbstract
Mice carrying a mutation in the synaptotagmin I gene were generated by homologous recombination. Mutant mice are phenotypically normal as heterozygotes, but die within 48 hr after birth as homozygotes. Studies of hippocampal neurons cultured from homozygous mutant mice reveal that synaptic transmission is severely impaired. The synchronous, fast component of Ca(2+)-dependent neurotransmitter release is decreased, whereas asynchronous release processes, including spontaneous synaptic activity (miniature excitatory postsynaptic current frequency) and release triggered by hypertonic solution or alpha-latrotoxin, are unaffected. Our findings demonstrate that synaptotagmin I function is required for Ca2+ triggering of synchronous neurotransmitter release, but is not essential for asynchronous or Ca(2+)-independent release. We propose that synaptotagmin I is the major low affinity Ca2+ sensor mediating Ca2+ regulation of synchronous neurotransmitter release in hippocampal neurons.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Among these isoforms, synaptotagmin-1 (Syt1) is a Ca2+ sensor for evoked synchronous neurotransmitter release7.”
From Architecture of the synaptotagmin–SNARE machinery for neuronal exocytosis (2015) · cites this paper as [7]
In the citing paper
“As expected7, removal of Syt1 abolished synchronous release monitored by recording evoked inhibitory postsynaptic currents (eIPSCs), a phenotype that can be rescued by re-introduction of WT but not mutant Syt1 cDNA (Figs. 4a, b).”
From Architecture of the synaptotagmin–SNARE machinery for neuronal exocytosis (2015) · cites this paper as [7]
Citations
Cites
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
Molecular cloning: A laboratory manual
Deininger, P. L. (1990) · Analytical Biochemistry · doi:10.1016/0003-2697(90)90595-z · Cited by 84,684
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
Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells
Thomas, K. R., & Capecchi, M. R. (1987) · Cell · doi:10.1016/0092-8674(87)90646-5 · Cited by 2,355
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
Soriano, P. M., Montgomery, C. A., Geske, R. S., & Bradley, A. (1991) · Cell · doi:10.1016/0092-8674(91)90499-o · Cited by 1,997
Spontaneous subthreshold activity at motor nerve endings
Fatt, P., & Katz, B. (1952) · The Journal of Physiology · doi:10.1113/jphysiol.1952.sp004735 · Cited by 1,835
Co‐operative action of calcium ions in transmitter release at the neuromuscular junction
Dodge, F. A., & Rahamimoff, R. (1967) · The Journal of Physiology · doi:10.1113/jphysiol.1967.sp008367 · Cited by 1,315
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
Synaptotagmin: a Calcium Sensor on the Synaptic Vesicle Surface
Brose, N., Petrenko, A. G., Südhof, T. C., & Jahn, R. (1992) · Science · doi:10.1126/science.1589771 · Cited by 979
Self-citation
Research works printed but not linked: 1
- Shirataki, 1993, Rabphillin-3A, a putative target protein for smg p25Arab3A small GTP-binding protein related to synaptotagmin, Mol. Cell. Biol., 13, 2061, 10.1128/MCB.13.4.2061 · DOI
Cited by
Sorted by citations
Items 101–200 of 1,005
Thyroid Hormone Action in Neural Development
Thompson, C. C. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.939 · Cited by 265
Synaptotagmin-1 Docks Secretory Vesicles to Syntaxin-1/SNAP-25 Acceptor Complexes
de Wit, H., Walter, A. M., Milošević, I., Gulyás-Kovács, A., Riedel, D., Sørensen, J. B., & Verhage, M. (2009) · Cell · doi:10.1016/j.cell.2009.07.027 · Cited by 267
TrkB and TrkC Signaling Are Required for Maturation and Synaptogenesis of Hippocampal Connections
Martínez, A., Alcántara, S., Borrell, V., del Río, J. A., Blasi, J., Otal, R., Campos, N., Boronat, A., Barbacid, M., Silos‐Santiago, I., et al. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-18-07336.1998 · Cited by 265
Unraveling the mechanisms of synaptotagmin and SNARE function in neurotransmitter release
Rizo, J., Chen, X., & Araç, D. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.04.006 · Cited by 262
Direct Interaction of a Ca2+-binding Loop of Synaptotagmin with Lipid Bilayers*
Chapman, E., & Davis, A. F. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.22.13995 · Cited by 252
Synaptotagmin I Functions as a Calcium Sensor to Synchronize Neurotransmitter Release
Yoshihara, M., & Littleton, J. T. (2002) · Neuron · doi:10.1016/s0896-6273(02)01065-6 · Cited by 285
Interactions of Presynaptic Ca2+ Channels and Snare Proteins in Neurotransmitter Release
Catterall, W. A. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb11284.x · Cited by 273
Reversal of synaptic vesicle docking at central synapses
Murthy, V. N., & Stevens, C. F. (1999) · Nature Neuroscience · doi:10.1038/9149 · Cited by 254
Self-citationRAB3 and synaptotagmin: the yin and yang of synaptic membrane fusion.
Geppert, M., & Südhof, T. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.75 · Cited by 278
Self-citationMultiple palmitoylation of synaptotagmin and the t‐SNARE SNAP‐25
Veit, M., Söllner, T. H., & Rothman, J. E. (1996) · FEBS Letters · doi:10.1016/0014-5793(96)00362-6 · Cited by 251
Synaptotagmin VII as a Plasma Membrane Ca2+ Sensor in Exocytosis
Sugita, S., Han, W., Butz, S., Liu, X., Fernández‐Chacón, R., Lao, Y., & Südhof, T. C. (2001) · Neuron · doi:10.1016/s0896-6273(01)00290-2 · Cited by 245
Self-citationDelayed Release of Neurotransmitter from Cerebellar Granule Cells
Atluri, P. P., & Regehr, W. G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08214.1998 · Cited by 250
Synaptic vesicle pools: an update
Denker (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00135 · Cited by 248
The Coupling between Synaptic Vesicles and Ca2+ Channels Determines Fast Neurotransmitter Release
Wadel, K., Neher, E., & Sakaba, T. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.021 · Cited by 256
The sequence of events that underlie quantal transmission at central glutamatergic synapses
Lisman, J. E., Raghavachari, S., & Tsien, R. W. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2191 · Cited by 260
Synaptotagmin-syntaxin interaction: the C2 domain as a Ca2+-dependent electrostatic switch.
Shao, X., Li, C., Fernández, I., Zhang, X., Südhof, T., & Rizo, J. (1997) · Neuron · doi:10.1016/s0896-6273(01)80052-0 · Cited by 229
Self-citationCa2+-dependent synaptotagmin binding to SNAP-25 is essential for Ca2+-triggered exocytosis.
Zhang, X.-D., Kim-Miller, M., Fukuda, M., Kowalchyk, J., & Martin, T. (2002) · Neuron · doi:10.1016/s0896-6273(02)00671-2 · Cited by 239
Munc13 C2B domain is an activity-dependent Ca2+ regulator of synaptic exocytosis
Shin, O.-H., Lu, J., Rhee, J.-S., Tomchick, D. R., Pang, Z. P., Wojcik, S. M., Camacho-Perez, M., Brose, N., Machius, M., Rizo, J., et al. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1758 · Cited by 243
Self-citationThe C Terminus of SNAP25 Is Essential for Ca2+-dependent Binding of Synaptotagmin to SNARE Complexes
Gerona, R. R. L., Larsen, E. C., Kowalchyk, J. A., & Martin, T. F. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.9.6328 · Cited by 244
Voets, T. (2000) · Neuron · doi:10.1016/s0896-6273(00)00131-8 · Cited by 242
Furie, B., Flaumenhaft, R. C., & Furie, B. (2001) · Thrombosis and Haemostasis · doi:10.1055/s-0037-1616219 · Cited by 238
Schneggenburger, R., & Forsythe, I. D. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0272-7 · Cited by 241
Routh, V. H. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00761-8 · Cited by 237
Molecular Mechanisms of Synaptic Vesicle Priming by Munc13 and Munc18
Lai, Y., Choi, U. B., Leitz, J., Rhee, H. J., Lee, C., Altas, B., Zhao, M., Pfuetzner, R. A., Wang, A. L., Brose, N., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.004 · Cited by 235
Protein phosphorylation and the regulation of synaptic membrane traffic
Turner, K. M., Burgoyne, R. D., & Morgan, A. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01436-8 · Cited by 240
Synaptic transmission at retinal ribbon synapses
Heidelberger, R., Thoreson, W. B., & Witkovsky, P. (2005) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2005.04.002 · Cited by 239
A resting pool of vesicles is responsible for spontaneous vesicle fusion at the synapse
Fredj, N. B., & Burrone, J. (2009) · Nature Neuroscience · doi:10.1038/nn.2317 · Cited by 231
Inhibitory Transmission Mediated by Asynchronous Transmitter Release
Lu, T., & Trussell, L. O. (2000) · Neuron · doi:10.1016/s0896-6273(00)81204-0 · Cited by 223
Glycosylated SV2A and SV2B Mediate the Entry of Botulinum Neurotoxin E into Neurons
Dong, M., Liu, H., Tepp, W. H., Johnson, E. A., Janz, R., & Chapman, E. R. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-07-0765 · Cited by 230
Distinct domains of complexin I differentially regulate neurotransmitter release
Xue, M., Reim, K., Chen, X., Chao, H., Deng, H., Rizo, J., Brose, N., & Rosenmund, C. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1292 · Cited by 229
Chaperoning SNARE assembly and disassembly
Baker, R. W., & Hughson, F. M. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.65 · Cited by 231
Pang, Z. P., Melicoff, E., Padgett, D., Liu, Y., Teich, A. F., Dickey, B. F., Lin, W., Adachi, R., & Südhof, T. C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3519-06.2006 · Cited by 228
Self-citationAnderson, G. R., Galfin, T., Xu, W., Aoto, J. N., Malenka, R. C., & Südhof, T. C. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1216398109 · Cited by 234
Self-citationThe schizophrenia risk gene product miR-137 alters presynaptic plasticity
Siegert, S., Seo, J., Kwon, E. J., Rudenko, A., Cho, S., Wang, W., Flood, Z., Martorell, A. J., Ericsson, M., Mungenast, A. E., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4023 · Cited by 221
Synaptotagmins I and IV promote transmitter release independently of Ca2+ binding in the C2A domain
Robinson, I. M., Ranjan, R., & Schwarz, T. (2002) · Nature · doi:10.1038/nature00915 · Cited by 232
Synaptotagmin I, a Ca2+ sensor for neurotransmitter release
Koh, T., & Bellen, H. J. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00195-4 · Cited by 224
Doc2 Is a Ca2+ Sensor Required for Asynchronous Neurotransmitter Release
Yao, J., Gaffaney, J. D., Kwon, S. E., & Chapman, E. R. (2011) · Cell · doi:10.1016/j.cell.2011.09.046 · Cited by 218
Schapire, A. L., Voigt, B., Jásik, J., Rosado, A., López-Cobollo, R., Menzel, D., Salinas, J., Mancuso, S., Valpuesta, V., Baluška, F., et al. (2008) · The Plant Cell · doi:10.1105/tpc.108.063859 · Cited by 220
Huynh, D. P. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg269 · Cited by 216
SV2 modulates the size of the readily releasable pool of secretory vesicles
Xu, T., & Bajjalieh, S. M. (2001) · Nature Cell Biology · doi:10.1038/35087000 · Cited by 212
Littleton, J. T., Chapman, E. R., Kreber, R. A., Garment, M. B., Carlson, S. D., & Ganetzky, B. (1998) · Neuron · doi:10.1016/s0896-6273(00)80549-8 · Cited by 211
Vesicle Docking in Regulated Exocytosis
Verhage, M., & Sørensen, J. B. (2008) · Traffic · doi:10.1111/j.1600-0854.2008.00759.x · Cited by 213
Membrane trafficking in the presynaptic nerve terminal.
Schaller, R. (1995) · Neuron · doi:10.1016/0896-6273(95)90328-3 · Cited by 38
Direct Interaction of the Rab3 Effector RIM with Ca2+Channels, SNAP-25, and Synaptotagmin*
Coppola, T., Magnin-Lüthi, S., Perret-Menoud, V., Gattesco, S., Schiavo, G., & Regazzi, R. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100929200 · Cited by 216
Synaptic vesicle protein 2 enhances release probability at quiescent synapses
Custer, K. L., Austin, N. S., Sullivan, J. M., & Bajjalieh, S. M. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2699-05.2006 · Cited by 211
Mechanism of neurotransmitter release coming into focus
Rizo, J. (2018) · Protein Science · doi:10.1002/pro.3445 · Cited by 210
Fusion Pore Dynamics Are Regulated by Synaptotagmin•t-SNARE Interactions
Bai, J., Wang, C., Richards, D. A., Jackson, M. B., & Chapman, E. R. (2004) · Neuron · doi:10.1016/s0896-6273(04)00117-5 · Cited by 207
Membrane traffic in the secretory pathway
Malsam, J., Kreye, S., & Söllner, T. H. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8352-3 · Cited by 216
Synaptotagmin IV regulates glial glutamate release
Zhang, Q., Fukuda, M., Bockstaele, E. V., Pascual, O., & Haydon, P. G. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401960101 · Cited by 209
Membrane Curvature in Synaptic Vesicle Fusion and Beyond
McMahon, H. T., Kozlov, M. M., & Martens, S. (2010) · Cell · doi:10.1016/j.cell.2010.02.017 · Cited by 210
Munc18-1 in secretion: lonely Munc joins SNARE team and takes control.
Toonen, R., & Verhage, M. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.08.008 · Cited by 231
TRANSPORT VESICLE DOCKING: SNAREs and Associates
Pfeffer, S. R. (1996) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.12.1.441 · Cited by 204
Maximov, A., & Südhof, T. C. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.006 · Cited by 238
Self-citationalpha-Latrotoxin and its receptors: neurexins and CIRL/latrophilins.
Südhof, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.933 · Cited by 215
Self-citationA molecular machine for neurotransmitter release: synaptotagmin and beyond
Südhof, T. C. (2013) · Nature Medicine · doi:10.1038/nm.3338 · Cited by 213
Self-citationChicka, M. C., Hui, E., Liu, H., & Chapman, E. R. (2008) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1463 · Cited by 198
Voets, T., Moser, T., Lund, P.-E., Chow, R. H.-P., Geppert, M., Südhof, T. C., & Neher, E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.201398798 · Cited by 204
Self-citationAtasoy, D., Ertunç, M., Moulder, K., Blackwell, J., Chung, C.-Y., Su, J.-Z., & Kavalali, E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2432-08.2008 · Cited by 201
Kee, Y., Lin, R. C.-S., Hsu, S.-C., & Scheller, R. H. (1995) · Neuron · doi:10.1016/0896-6273(95)90337-2 · Cited by 199
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Guerrini, R., Conti, V., Mantegazza, M., Balestrini, S., Galanopoulou, A. S., & Benfenati, F. (2023) · Physiological Reviews · doi:10.1152/physrev.00063.2021 · Cited by 196
Regulation of Membrane Fusion in Synaptic Excitation-Secretion Coupling: Speed and Accuracy Matter
Wojcik, S. M., & Brose, N. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.013 · Cited by 194
Postsynaptic synaptotagmins mediate AMPA receptor exocytosis during LTP
Wu, D., Bacaj, T., Morishita, W., Goswami, D., Arendt, K. L., Xu, W., Chen, L., Malenka, R. C., & Südhof, T. C. (2017) · Nature · doi:10.1038/nature21720 · Cited by 195
Self-citationGlutamate and GABA synthesis, release, transport and metabolism as targets for seizure control
Rowley, N. M., Madsen, K. K., Schousboe, A., & White, H. S. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.02.013 · Cited by 211
Johnson, S. L., Marcotti, W., & Kros, C. J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.074740 · Cited by 193
A Novel Function for the Second C2 Domain of Synaptotagmin
Chapman, E. R., An, S. J., Edwardson, J., & Jahn, R. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.10.5844 · Cited by 191
Functional properties of multiple synaptotagmins in brain.
Ullrich, B., Li, C., Zhang, J. Z., McMahon, H., Anderson, R. G. W., Geppert, M., & Südhof, T. (1994) · Neuron · doi:10.1016/0896-6273(94)90415-4 · Cited by 199
Self-citationThe Molecular Machinery of Neurotransmitter Release (Nobel Lecture)
Südhof, T. C. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201406359 · Cited by 196
Self-citationThompson, C. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-07832.1996 · Cited by 209
Chamberlain, L. H., Roth, D., Morgan, A., & Burgoyne, R. D. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.130.5.1063 · Cited by 191
Thoreson, W. B., Rábl, K., Townes‐Anderson, E., & Heidelberger, R. (2004) · Neuron · doi:10.1016/s0896-6273(04)00254-5 · Cited by 190
Local Ca2+ Release from Internal Stores Controls Exocytosis in Pituitary Gonadotrophs
Tse, F. W., Tse, A., Hille, B., Horstmann, H., & Almers, W. (1997) · Neuron · doi:10.1016/s0896-6273(01)80051-9 · Cited by 190
Xu, W., Morishita, W., Buckmaster, P. S., Pang, Z. P., Malenka, R. C., & Südhof, T. C. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.036 · Cited by 195
Self-citationHui, E., Bai, J., Wang, P., Sugimori, M., Llinás, R. R., & Chapman, E. R. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500941102 · Cited by 188
Novel Ca2+-binding protein (CAPS) related to UNC-31 required for Ca2+-activated exocytosis
Ann, K., Kowalchyk, J. A., Loyet, K. M., & Martin, T. F. J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.32.19637 · Cited by 182
Using Knockout and Transgenic Mice to Study Neurophysiology and Behavior
Picciotto, M. R., & Wickman, K. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.4.1131 · Cited by 189
Continuous Vesicle Cycling in the Synaptic Terminal of Retinal Bipolar Cells
Lagnado, L., Gomis, A., & Job, C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80226-3 · Cited by 186
Schonn, J., Maximov, A., Lao, Y., Südhof, T. C., & Sørensen, J. B. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712373105 · Cited by 186
Self-citationThe Biochemistry of Neurotransmitter Secretion(*)
Bajjalieh, S., & Scheller, R. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.5.1971 · Cited by 188
The pre-synaptic vesicle protein synaptotagmin is a novel biomarker for Alzheimer’s disease
Öhrfelt, A., Brinkmalm, A., Dumurgier, J., Brinkmalm, G., Hansson, O., Zetterberg, H., Bouaziz-Amar, E., Hugon, J., Paquet, C., & Blennow, K. (2016) · Alzheimer's Research & Therapy · doi:10.1186/s13195-016-0208-8 · Cited by 184
Molecular determinants of regulated exocytosis.
Gerber, S. H., & Südhof, T. (2002) · Diabetes · doi:10.2337/diabetes.51.2007.s3 · Cited by 179
Self-citationThe protein machinery of vesicle budding and fusion
Rothman, J. E. (1996) · Protein Science · doi:10.1002/pro.5560050201 · Cited by 190
GENETICS OF SYNAPTIC VESICLE FUNCTION: Toward the Complete Functional Anatomy of an Organelle
Fernández‐Chacón, R., & Südhof, T. C. (1999) · Annual Review of Physiology · doi:10.1146/annurev.physiol.61.1.753 · Cited by 184
Self-citationLeenders, A. G. M., & SHENG, Z. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.10.012 · Cited by 181
Ca2+ and secretory-vesicle dynamics
Burgoyne, R. D., & Morgan, A. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93900-i · Cited by 182
Kümmel, D., Krishnakumar, S. S., Radoff, D., Li, F., Giraudo, C., Pincet, F., Rothman, J., & Reinisch, K. (2011) · Nature Structural &Molecular Biology · doi:10.1038/nsmb.2101 · Cited by 133
Molecular mechanisms of platelet exocytosis: insights into the "secrete" life of thrombocytes.
Reed, G. L., Fitzgerald, M. L., & Polgár, J. (2000) · PubMed · Cited by 181
Interaction of the synprint site of N-type Ca2+ channels with the C2B domain of synaptotagmin I.
Sheng, Z.-H., Yokoyama, C., & Catterall, W. (1997) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.94.10.5405 · Cited by 185
Phosphorylation of Snapin by PKA modulates its interaction with the SNARE complex
Chheda, M. G., Ashery, U., Thakur, P., Rettig, J., & Sheng, Z. (2001) · Nature Cell Biology · doi:10.1038/35070000 · Cited by 183
FUSION PORES AND FUSION MACHINES IN CA2+-TRIGGERED EXOCYTOSIS
Jackson, M. B., & Chapman, E. R. (2006) · Annual Review of Biophysics and Biomolecular Structure · doi:10.1146/annurev.biophys.35.040405.101958 · Cited by 182
Tick salivary glands: function, physiology and future
Bowman, A. S., & Sauer, J. R. (2004) · Parasitology · doi:10.1017/s0031182004006468 · Cited by 178
Molecular Mechanisms of Fast Neurotransmitter Release
Brünger, A. T., Choi, U. B., Lai, Y., Leitz, J., & Zhou, Q. (2018) · Annual Review of Biophysics · doi:10.1146/annurev-biophys-070816-034117 · Cited by 180
Formation, stabilisation and fusion of the readily releasable pool of secretory vesicles
S∅rensen, J. C. (2004) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-004-1247-8 · Cited by 177
A Novel Ubiquitous Form of Munc-18 Interacts with Multiple Syntaxins.
Hata, Y., & Südhof, T. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.22.13022 · Cited by 188
Self-citationMorphologically Docked Synaptic Vesicles Are Reduced insynaptotagminMutants ofDrosophila
Reist, N. E., Buchanan, J., Li, J., DiAntonio, A., Buxton, E. M., & Schwarz, T. L. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-19-07662.1998 · Cited by 176
Synaptotagmin I and II are present in distinct subsets of central synapses
Fox, M. A., & Sanes, J. R. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21381 · Cited by 176
LRRK2 functions in synaptic vesicle endocytosis through a kinase-dependent mechanism
Arranz, A. M., Delbroek, L., Van Kolen, K., Guimarães, M. R., Mandemakers, W., Daneels, G., Matta, S., Calafate, S., Shaban, H., Baatsen, P., et al. (2014) · Journal of Cell Science · doi:10.1242/jcs.158196 · Cited by 111
Hagler, D., & Goda, Y. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.6.2324 · Cited by 167
Self-citationA possible docking and fusion particle for synaptic transmission
Schiavo, G., Gmachl, M., Stenbeck, G., Söllner, T. H., & Rothman, J. E. (1995) · Nature · doi:10.1038/378733a0 · Cited by 175
Clare, R., King, V. G., Wirenfeldt, M., & Vinters, H. V. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22392 · Cited by 163
Genetic analysis of synaptotagmin 2 in spontaneous and Ca2+‐triggered neurotransmitter release
Pang, Z. P., Sun, J., Rizo, J., Maximov, A., & Südhof, T. C. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601103 · Cited by 174
Self-citation
Metadata
- Authors
- Geppert, M., Goda, Y., Hammer, R. E., Li, C., Rosahl, T. W., Stevens, C. F., & Südhof, T. C.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Salk Institute for Biological Studies (US)
- Howard Hughes Medical Institute (US)
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1994-11
- Volume
- 79
- Issue
- 4
- Pages
- 717-727
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2165302477
- Cited by
- 1,483
- References
- 45
- Citations by year
- 2026: 17 · 2025: 24 · 2024: 34 · 2023: 36 · 2022: 41 · 2021: 42 · 2020: 47 · 2019: 49 · 2018: 43 · 2017: 41 · 2016: 31 · 2015: 41 · 2014: 51 · 2013: 33 · 2012: 59
- FWCI
- 20.67
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- National Institutes of Health (5r01ns012961-22)
- National Institute of Neurological Disorders and Stroke (R0 NS 12961-17)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- synaptotagmin-1, calcium sensor, asynchronous release, calcium-independent release, hippocampal neurons, synaptic transmission, mouse mutants, alpha-latrotoxin, spontaneous synaptic activity
- MeSH terms
- Animals, Animals, Newborn, Base Sequence, Brain, Calcium, Calcium-Binding Proteins, Exons, Hippocampus, Homozygote, Hypertonic Solutions, Membrane Glycoproteins, Mice, Neurologic Mutants, Molecular Sequence Data, Mutation, Nerve Tissue Proteins, Synaptic Transmission, Neurons, Reference Values, Spider Venoms, Synapses, Restriction Mapping, Polymerase Chain Reaction, Mutagenesis, DNA Primers, Neurotransmitter Agents, Synaptotagmins, Synaptotagmin I, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review