The DOI matches its Crossref record; 64 of the 64 references it cites were found in a registry or an index.
Short-term forms of presynaptic plasticity
Open accessAbstract
Synapses exhibit several forms of short-term plasticity that play a multitude of computational roles. Short-term depression suppresses neurotransmitter release for hundreds of milliseconds to tens of seconds; facilitation and post-tetanic potentiation lead to synaptic enhancement lasting hundreds of milliseconds to minutes. Recent advances have provided insight into the mechanisms underlying these forms of plasticity. Vesicle depletion, as well as inactivation of both release sites and calcium channels, contribute to synaptic depression. Mechanisms of short-term enhancement include calcium channel facilitation, local depletion of calcium buffers, increases in the probability of release downstream of calcium influx, altered vesicle pool properties, and increases in quantal size. Moreover, there is a growing appreciation of the heterogeneity of vesicles and release sites and how they can contribute to use-dependent plasticity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Short-term synaptic plasticity can increase or decrease the strength of a synaptic signal several-fold (Fioravante and Regehr, 2011).”
From The Presynaptic Active Zone (2012) · cites this paper as Fioravante and Regehr, 2011
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Self-citationThe role of calcium in neuromuscular facilitation
Katz, B., & Miledi, R. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008469 · Cited by 1,347
Neher, E. (1998) · Neuron · doi:10.1016/s0896-6273(00)80983-6 · Cited by 1,010
Rizzoli, S. O., & Betz, W. J. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1583 · Cited by 975
Multiple Roles of Calcium Ions in the Regulation of Neurotransmitter Release
Neher, E., & Sakaba, T. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.019 · Cited by 966
Newton, A. C. (2001) · Chemical Reviews · doi:10.1021/cr0002801 · Cited by 963
The synapsins: Key actors of synapse function and plasticity
Cesca, F., Baldelli, P., Valtorta, F., & Benfenati, F. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.04.006 · Cited by 654
Calcium Channel Regulation and Presynaptic Plasticity
Catterall, W. A., & Few, A. P. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.005 · Cited by 647
RIM proteins tether Ca2+ channels to presynaptic active zones via a direct PDZ-domain interaction
Kaeser, P. S., Deng, L., Wang, Y., Dulubova, I., Liu, X., Rizo, J., & Südhof, T. C. (2011) · Cell · doi:10.1016/j.cell.2010.12.029 · Cited by 607
RIM1α forms a protein scaffold for regulating neurotransmitter release at the active zone
Schoch, S., Castillo, P. E., Jo, T., Mukherjee, K., Geppert, M., Wang, Y., Schmitz, F., Malenka, R. C., & Südhof, T. C. (2002) · Nature · doi:10.1038/415321a · Cited by 579
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 383
Maheu, M., & Ressler, K. J. (2017) · Learning & Memory · doi:10.1101/lm.044271.116 · Cited by 17
Integrated Opto-Synaptic IGZO Transistors for Image Recognition Fabricated at Room Temperature
Qi, S. M., Li, J. C., Xia, Y. H., Liu, Z. C., Dai, D., Song, T. L., Yang, H., Ma, Y. X., & Wang, Y. (2025) · ACS Photonics · doi:10.1021/acsphotonics.4c01809 · Cited by 13
The M domain in UNC-13 regulates the probability of neurotransmitter release
Liu, H., Li, L., Sheoran, S., Yu, Y., Richmond, J. E., Xia, J., Tang, J., Liu, J., & Hu, Z. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108828 · Cited by 12
Increased presynaptic excitability in a migraine with aura mutation
Suryavanshi, P. S., Sawant-Pokam, P., Clair, S., & Brennan, K. C. (2023) · Brain · doi:10.1093/brain/awad326 · Cited by 14
Sex Differences in Central Amygdala Glutamate Responses to Calcitonin Gene-Related Peptide
Lorsung, R. M., Cramer, N., Alipio, J. B., Ji, Y., Han, S., Masri, R. M., & Keller, A. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1898-24.2024 · Cited by 13
Li, Y., Tao, R., He, W., Chang, C., Zou, Z., Zhang, Y., Wang, D., Wang, J., Fan, Z. H., Zhou, G., et al. (2021) · Journal of Applied Physics · doi:10.1063/5.0043016 · Cited by 13
Marchionni, I., Pilati, N., Forli, A., Sessolo, M., Tottene, A., & Pietrobon, D. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0228-22.2022 · Cited by 15
Lithium: An Old Drug for New Therapeutic Strategy for Alzheimer’s Disease and Related Dementia
Shim, S. S., Berglund, K., & Yu, S. P. (2023) · Neurodegenerative Diseases · doi:10.1159/000533797 · Cited by 14
Neuronal dynamics and pain perception modeling based on the SMM-HR model
Xu, Y., Gao, S., Xu, X., Banerjee, S., Mou, J., & Cao, Y. (2025) · Chinese Journal of Physics · doi:10.1016/j.cjph.2025.10.010 · Cited by 12
Cai, C., Wang, L., Li, S., Lou, S.-C., Luo, J., Fu, D., & Chen, T. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1989-21.2022 · Cited by 13
Zhang, F., Yang, X., Qi, Y., Tian, S.-Y., & Huang, W. (2024) · Chemical Science · doi:10.1039/d4sc01664e · Cited by 12
Perrier, S. P., Gleizes, M., Fonta, C., & Nowak, L. G. (2019) · Physiological Reports · doi:10.14814/phy2.13992 · Cited by 12
Short-term plasticity as a mechanism to regulate and retain multistability
Zhou, X., Tian, C., Zhang, X., Zheng, M., & Xu, K. (2022) · Chaos Solitons & Fractals · doi:10.1016/j.chaos.2022.112891 · Cited by 12
Cortical Presynaptic Control of Dorsal Horn C–Afferents in the Rat
Moreno-López, Y., Pérez-Sánchez, J., Martı́nez-Lorenzana, G., Condés‐Lara, M., & Rojas‐Piloni, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069063 · Cited by 12
Laminar‐specific encoding of texture elements in rat barrel cortex
Allitt, B. J., Alwis, D. S., & Rajan, R. (2017) · The Journal of Physiology · doi:10.1113/jp274865 · Cited by 12
Real-time imaging of single synaptic vesicles in live neurons
Yu, C., Zhang, M., Qin, X., Yang, X., & Park, H. (2016) · Frontiers in Biology · doi:10.1007/s11515-016-1397-z · Cited by 12
Srikimkaew, O., Azhari, S., Banerjee, D., Usami, Y., & Tanaka, H. (2024) · Advanced Electronic Materials · doi:10.1002/aelm.202400360 · Cited by 13
Mechanisms underlying CSD initiation implicated by genetic mouse models of migraine
Pietrobon, D., & Brennan, K. C. (2025) · The Journal of Headache and Pain · doi:10.1186/s10194-025-01948-x · Cited by 11
Martin, L., Sándor, B., & Gros, C. (2016) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2016.00012 · Cited by 12
von Engelhardt, J. (2021) · The Journal of Physiology · doi:10.1113/jp280878 · Cited by 11
Neonatal NMDA blockade alters the LTP, LTD and cognitive functions in male and female Wistar rats
Golitabari, N., Mohammadian, F., Salari, A., & Amani, M. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108896 · Cited by 11
Wang, W., Deng, D., Jenkins, K., Zinsmaier, A. K., Zhou, Q., & Bao, S. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.12.006 · Cited by 10
Fioravante, D., Myoga, M. H., Leitges, M., & Regehr, W. G. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0683-12.2012 · Cited by 10
Self-citationSong, C., Xu, X.-B., He, Y., Liu, Z.-P., Wang, M., Zhang, X., Li, B., & Pan, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060154 · Cited by 10
Sprengers, M., Raedt, R., Larsen, L. E., Delbeke, J., Wadman, W. J., Boon, P., & Vonck, K. E. J. (2020) · Epilepsia · doi:10.1111/epi.16498 · Cited by 10
(M)Unc13s in Active Zone Diversity: A Drosophila Perspective
Piao, C., & Sigrist, S. J. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.798204 · Cited by 8
Bosco, F., Valente, P., Milanese, M., Piccini, A., Messa, M., Bonanno, G., Lombroso, P. J., Baldelli, P., Benfenati, F., & Giovedı̀, S. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-0980-5 · Cited by 9
Presynaptic Calmodulin targets: lessons from structural proteomics
Lipstein, N., Göth, M., Piotrowski, C., Pagel, K., Sinz, A., & Jahn, O. (2017) · Expert Review of Proteomics · doi:10.1080/14789450.2017.1275966 · Cited by 10
Efferent Innervation to the Cochlea
Elgoyhen, A. B., Wedemeyer, C., & Guilmi, M. N. D. (2018) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190849061.013.3 · Cited by 9
Glutamate receptor interacting protein acts within the prefrontal cortex to blunt cocaine seeking
Wickens, M. M., Deutschmann, A. U., McGrath, A. G., Parikh, V., & Briand, L. A. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107672 · Cited by 10
Synaptic plasticity of inhibitory synapses onto medial olivocochlear efferent neurons
Cadenas, L. T., Cheng, H., & Weisz, C. J. C. (2022) · The Journal of Physiology · doi:10.1113/jp282815 · Cited by 9
A review of hafnium-based ferroelectrics for advanced computing
Xu, X., Luo, Z., Sun, H., Xu, Y., Gao, L., & Yu, Z. (2025) · Solid-State Electronics · doi:10.1016/j.sse.2024.109053 · Cited by 8
Yang, Y., Hu, C.-C., & Lai, Y. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00060 · Cited by 8
Short-Term Plasticity at Olfactory Cortex to Granule Cell Synapses Requires CaV2.1 Activation
Zhou, F., Puché, A. C., & Shipley, M. T. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00387 · Cited by 8
Church, E., Hamid, E., & Alford, S. T. (2019) · eNeuro · doi:10.1523/eneuro.0343-19.2019 · Cited by 8
Biomimetic Neuromorphic Sensory System via Electrolyte Gated Transistors
Li, S., Gao, L., Liu, C., Guo, H., & Yu, J. (2024) · Sensors · doi:10.3390/s24154915 · Cited by 10
Cerebellar pathology contributes to neurodevelopmental deficits in spinal muscular atrophy
Gerstner, F., Wittig, S., Menedo, C., Ruwald, S., Carlini, M. J., Vankova, A., Sowoidnich, L., Martín-López, G., Dreilich, V., Alonso-Collado, A., et al. (2025) · Brain · doi:10.1093/brain/awaf336 · Cited by 10
Short-Term Synaptic Plasticity: Microscopic Modelling and (Some) Computational Implications
Barri, A., & Mongillo, G. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-89439-9_5 · Cited by 6
Blitz, D. M., Pritchard, A. E., Latimer, J. K., & Wakefield, A. T. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.148908 · Cited by 7
Young DAPK1 knockout mice have altered presynaptic function
Goodell, D. J., Tullis, J. E., & Bayer, K. U. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00055.2021 · Cited by 7
Concentration of stimulant regulates initial exocytotic molecular plasticity at single cells
He, X., & Ewing, A. G. (2022) · Chemical Science · doi:10.1039/d1sc05278k · Cited by 7
Multiscale modeling of presynaptic dynamics from molecular to mesoscale
Garcia, J. W., Bartol, T. M., & B, T. J. S. A. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010068 · Cited by 6
Factors Influencing Short-term Synaptic Plasticity in the Avian Cochlear Nucleus Magnocellularis
Sanchez, J. T., Karla, Q., & Sebastian, O.-M. (2015) · Journal of Experimental Neuroscience · doi:10.4137/jen.s25472 · Cited by 7
Feuerriegel, D., Churches, O. F., Coussens, S. W., & Keage, H. A. D. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.11.010 · Cited by 7
Mango, D., Caruso, A., Saidi, A., Nisticò, R., & Scaccianoce, S. (2019) · Synapse · doi:10.1002/syn.22101 · Cited by 7
Differential Distribution of Ca2+Channel Subtypes at Retinofugal Synapses
Govindaiah, G., Campbell, P. W., & Guido, W. (2020) · eNeuro · doi:10.1523/eneuro.0293-20.2020 · Cited by 9
Mondal, Y., Pena, R. F. O., & Rotstein, H. G. (2022) · Journal of Computational Neuroscience · doi:10.1007/s10827-022-00822-y · Cited by 7
Shan, K., Tian, C., Zheng, Z., Zheng, M., & Xu, K. (2025) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/5.0243837 · Cited by 6
Daur, N., Farzan Nadim, A., & Bucher, D. M. (2021) · eNeuro · doi:10.1523/eneuro.0351-21.2021 · Cited by 6
Malkinson, G., & Spira, M. E. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00165 · Cited by 6
Hajizadeh, A., Matysiak, A., Wolfrum, M., May, P., & König, R. (2022) · Biological Cybernetics · doi:10.1007/s00422-022-00936-7 · Cited by 6
Postnatal GABAA Receptor Activation Alters Synaptic Plasticity and Cognition in Adult Wistar Rats
Amani, M., Mohammadian, F., Golitabari, N., & Salari, A. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02805-7 · Cited by 6
Recent progress in neuromorphic computing based on spin–orbit torque devices
Liang, Q., Huang, Y., Tan, Y., Tang, Y., & Xie, X. (2025) · Journal of Physics D Applied Physics · doi:10.1088/1361-6463/ae1241 · Cited by 7
Nassiri, I., Masoudi‐Nejad, A., Jalili, M., & Moeini, A. (2013) · Genomics · doi:10.1016/j.ygeno.2013.07.012 · Cited by 5
Robinson, B. S., Yu, G. J., Hendrickson, P. J., Song, D. B., & Berger, T. (2012) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2012.6346192 · Cited by 5
Modulation of the plasticity of an all-metal oxide synaptic transistor via laser irradiation
Yang, Q., Lv, D., Huang, J., Chen, J., Chen, H., & Guo, T. (2020) · Nanotechnology · doi:10.1088/1361-6528/ab7252 · Cited by 5
Dlg Is Required for Short-Term Memory and Interacts with NMDAR in the Drosophila Brain
Bertin, F., Moya‐Alvarado, G., Quiroz-Manríquez, E., Ibacache, A., Köhler-Solís, A., Oliva, C., & Sierralta, J. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169187 · Cited by 5
The Influence of the Number of Spiking Neurons on Synaptic Plasticity
Uleru, G., Hulea, M. G., & Barleanu, A. (2023) · Biomimetics · doi:10.3390/biomimetics8010028 · Cited by 5
Yang, D., Zhang, Y., Wang, H., & Chen, Y. H. (2024) · Communications in Nonlinear Science and Numerical Simulation · doi:10.1016/j.cnsns.2024.108127 · Cited by 5
Caspase-3 and calpain: Differently directed involvement in presynaptic long-term plasticity
Kudryashova, I. V., Onufriev, M. V., & Gulyaeva, N. V. (2014) · Neurochemical Journal · doi:10.1134/s181971241403009x · Cited by 5
Imaging Glutamate with Genetically Encoded Fluorescent Sensors
Broussard, G. J., Unger, E. K., Liang, R., McGrew, B. P., & Tian, L. (2017) · Neuromethods · doi:10.1007/978-1-4939-7228-9_5 · Cited by 5
Data Driven Models of Short-Term Synaptic Plasticity
Mokhtari, E. B., Lawrence, J. J., & Stone, E. F. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00032 · Cited by 5
Ma, R., Xiao, M., & Gustafsson, B. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.09.008 · Cited by 5
Kawaguchi, S. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00269 · Cited by 5
Ferrante, D., Parisi, B., Marte, A., Marianna, D., Prestigio, C., Benzi, A., Bruzzone, S., Benfenati, F., Onofri, F., Valente, P., et al. (2025) · The Journal of Physiology · doi:10.1113/jp288763 · Cited by 4
Developmental Easing of Short-Term Depression in “Winner” Climbing Fibers
Pätz, C., Brachtendorf, S., & Eilers, J. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00183 · Cited by 4
Specific presynaptic functions require distinct Drosophila Cav2 splice isoforms
Bell, C., Kilo, L., Gottschalk, D., Arian, J., Deneke, L., Kern, H. B., Rickert, C., Kobler, O., Strauß, J., Heine, M., et al. (2024) · eLife · doi:10.7554/elife.100394.3 · Cited by 6
Level of M1 GABAB predicts micro offline consolidation of motor learning during wakefulness
Cardellicchio, P., & Borgomaneri, S. (2025) · npj Science of Learning · doi:10.1038/s41539-025-00299-1 · Cited by 4
Error correction and fast detectors implemented by ultrafast neuronal plasticity
Vardi, R., Marmari, H., & Kanter, I. (2014) · Physical Review E · doi:10.1103/physreve.89.042712 · Cited by 4
Snow, W. M., Oikawa, K., Djordjevic, J., & Albensi, B. C. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.10.005 · Cited by 4
Gaydukov, A. E., Bogacheva, P. O., & Balezina, O. P. (2019) · Neurochemical Journal · doi:10.1134/s1819712419010082 · Cited by 4
Rahy, R., Asari, H., & Gross, C. T. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.964634 · Cited by 4
Gleizes, M., Perrier, S. P., Fonta, C., & Nowak, L. G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0183246 · Cited by 4
Optical Dissection of Synaptic Plasticity for Early Adaptation in Caenorhabditis elegans
Ashida, K., Shidara, H., Hotta, K., & Oka, K. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2019.12.026 · Cited by 4
The Reorganization of the Actin Matrix as a Factor of Presynaptic Plasticity
Kudryashova, I. V. (2021) · Neurochemical Journal · doi:10.1134/s1819712421030089 · Cited by 4
Mohammadian, F., Golitabari, N., Abedi, A. J., Saadati, H., Milan, H. S., Salari, A., & Amani, M. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.174992 · Cited by 4
Slow-wave sleep : generation and propagation of slow waves, role in long-term plasticity and gating
Chauvette, S. (2013) · Corpus Université Laval (Université Laval) · Cited by 4
Song, C., Xu, X.-B., He, Y., Liu, Z., Wang, M., Zhang, X., Li, B., & Pan, B. (2013) · PLoS ONE · doi:10.1371/annotation/3bc30ead-f84a-434a-8314-4aa1c9fcdcc0 · Cited by 4
Adaptation in the Visual System: Networked Fatigue or Suppressed Prediction Error Signalling?Preprint
Feuerriegel, D. (2023) · doi:10.31234/osf.io/73hb4 · Cited by 4
Synaptic Theory of Working Memory for Serial OrderPreprint
Mongillo, G., & Tsodyks, M. V. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.11.575157 · Cited by 6
Ketogenic diet dampens excitatory neurotransmission by shrinking synaptic vesicle pools
Stunault, M. I., Deng, P.-Y., Yadav, A., Periandri, E. M., Vitorino, F. N. D. L., Thomsen, M. B., Sponagel, J., Barfield, A. J., Ponce, R. J., Foroughi, L., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.116945 · Cited by 3
Ranjan, M., Lin, K., Mueller, B. D., Wojcik, S. M., Lohse, M., Südhof, T. C., Jørgensen, E. M., Neher, E., Lipstein, N., Brose, N., et al. (2026) · Science Advances · doi:10.1126/sciadv.aea0449 · Cited by 3
Ferrati, G., Martini, F. J., & Maravall, M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00009 · Cited by 3
The Slow Depolarization Following Individual Spikes in Thin, Unmyelinated Axons in Mammalian Cortex
Raastad, M. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00203 · Cited by 3
A missense mutation in Kcnc3 causes hippocampal learning deficits in mice
Xu, P., Shimomura, K., Lee, C., Gao, X., Simpson, E. H., Huang, G., Joseph, C., Kumar, V., Ge, W., Pawlowski, K. S., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2204901119 · Cited by 4
Presynaptic Plasticity Is Associated with Actin Polymerization
Kudryashova, I. V. (2023) · Biochemistry (Moscow) · doi:10.1134/s0006297923030082 · Cited by 3
Neuroimmune Modulation of Synaptic Function
Pribiag, H., & Stellwagen, D. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4729-0_3 · Cited by 4
Etherington, S. J., Johnstone, V., & Everett, A. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087174 · Cited by 3
Satake, S., Inoue, T., & Imoto, K. (2015) · The Cerebellum · doi:10.1007/s12311-015-0677-5 · Cited by 3
Short-Term Synaptic Plasticity in Central Pattern Generators
Martínez, D., Matveev, V., & Nadim, F. (2014) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_467-1 · Cited by 3
Dorgans, K., Demais, V., Bailly, Y. J. R., Poulain, B., Isope, P., & Doussau, F. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/338152 · Cited by 3
Koppensteiner, P., Bhandari, P., Önal, C., Borges-Merjane, C., Monnier, E. L., Nakamura, Y., Sadakata, T., Sanbo, M., Hirabayashi, M., Brose, N., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.28.514202 · Cited by 3
A Model of the CA1 Field Rhythms.
Mysin, I. E. (2021) · PubMed Central · doi:10.1523/eneuro.0192-21.2021 · Cited by 2
Synaptic models of Working Memory
Mongillo, G. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00075-4 · Cited by 2
Mechanisms that regulate the C1-C2B mutual inhibition control functional switch of UNC-13
Liu, H., Li, L., Wang, J., Hu, J., Xia, J., Yu, X.-C., Tang, J., Liu, H., Yang, X., Ma, C., et al. (2025) · eLife · doi:10.7554/elife.105199.3 · Cited by 2
Faingold, C. L. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102770 · Cited by 2
Auditory Efferent System: New Insights from Cortex to Cochlea
(2016) · Frontiers research topics · doi:10.3389/978-2-88919-935-8 · Cited by 2
Hageman, K. N., Stypulkowski, P. H., & Stanslaski, S. R. (2024) · Brain Research · doi:10.1016/j.brainres.2024.149233 · Cited by 2
Glutamate Signaling in the Auditory Brainstem
Sanchez, J. T., & Lu, Y. (2017) · Springer handbook of auditory research · doi:10.1007/978-3-319-21530-3_4 · Cited by 2
Short-term synaptic plasticity across topographic maps in the electrosensory system
Mileva, G., Kozak, I. J., & Lewis, J. E. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.01.014 · Cited by 2
Metadata
- Authors
- Fioravante, D., & Regehr, W. G.
- Affiliations
- Harvard University (US)
- Corresponding author
- Regehr, Wade G
- Venue
- Current Opinion in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2011-04
- Volume
- 21
- Issue
- 2
- Pages
- 269-274
- ISSN
- 0959-4388 (ISSN-L)
- PMC
- PMC3599780
- OpenAlex
- W1975727393
- Cited by
- 375
- References
- 64
- Citations by year
- 2026: 12 · 2025: 22 · 2024: 22 · 2023: 16 · 2022: 26 · 2021: 26 · 2020: 23 · 2019: 37 · 2018: 34 · 2017: 25 · 2016: 26 · 2015: 29 · 2014: 28 · 2013: 22 · 2012: 24
- FWCI
- 2.38
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (R37 NS032405)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- short-term plasticity, short-term depression, short-term facilitation, post-tetanic potentiation, neurotransmitter release, vesicle depletion, calcium buffers, quantal size, release sites, vesicle heterogeneity, use-dependent plasticity
- MeSH terms
- Animals, Humans, Neuronal Plasticity, Synaptic Vesicles, Calcium Channels, Presynaptic Terminals
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