Long-Term Potentiation--A Decade of Progress?

A synaptic model of memory: long-term potentiation in the hippocampus

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Synaptic Activity and the Construction of Cortical Circuits

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Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice

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Developmental mechanisms that generate precise patterns of neuronal connectivity

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Dendritic spine changes associated with hippocampal long-term synaptic plasticity

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Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice

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Synaptic plasticity: LTP and LTD

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Inhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP

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Rapid Spine Delivery and Redistribution of AMPA Receptors After Synaptic NMDA Receptor Activation

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Alternative splicing modulates the frequency‐dependent response of CaMKII to Ca2+ oscillations

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Long-Term Potentiation in the Rat Hippocampus Is Reversibly Depressed by Chronic Intermittent Ethanol Exposure

Roberto, M., Nelson, T. E., Ur, C. L., & Gruol, D. L. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.87.5.2385 · Cited by 112

Protein kinase C potentiation of N -methyl- d -aspartate receptor activity is not mediated by phosphorylation of N -methyl- d -aspartate receptor subunits

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Astrocytes and Synaptic Plasticity

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Neurons involved in the exteroceptive function of pain

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Mechanisms and State of the Art of Transcranial Magnetic Stimulation

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On the Importance of Inhibition: Central and Peripheral Manifestations of Nonlinear Inhibitory Processes in Neural Systems

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Developmental regulation of the NMDA receptor subunits, NR3A and NR1, in human prefrontal cortex

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Spine loss and other dendritic abnormalities in epilepsy

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Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits

Ramakers, G. J. A., Wolfer, D. P., Rosenberger, G., Kuchenbecker, K., Kreienkamp, H., Prange‐Kiel, J., Rune, G. M., Richter, K., Langnaese, K., Masneuf, S., et al. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr457 · Cited by 108

Flavonoids as modulators of memory and learning: molecular interactions resulting in behavioural effects

Rendeiro, C., Guerreiro, J. D. T., Williams, C. M., & Spencer, J. P. E. (2012) · Proceedings of The Nutrition Society · doi:10.1017/s0029665112000146 · Cited by 114

Modeling Synaptic Dynamics Driven by Receptor Lateral Diffusion

Holcman, D., & Triller, A. (2006) · Biophysical Journal · doi:10.1529/biophysj.106.081935 · Cited by 113

Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin-Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning

Zeniou, M. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.23.2929 · Cited by 110

NMDA receptors are essential for the acquisition, but not expression, of conditional fear and associative spike firing in the lateral amygdala

Goosens, K. A., & Maren, S. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03513.x · Cited by 108

Transient and sustained types of long‐term potentiation in the CA1 area of the rat hippocampus

Volianskis, A., & Jensen, M. S. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.044214 · Cited by 107

Correlated network activity enhances synaptic efficacy via BDNF and the ERK pathway at immature CA3–CA1 connections in the hippocampus

Mohajerani, M. H., Sivakumaran, S., Zacchi, P., Aguilera, P. A., & Cherubini, E. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704533104 · Cited by 113

Adenylyl cyclase I regulates AMPA receptor trafficking during mouse cortical 'barrel' map development

Lu, H., She, W.-C., Plas, D. T., Neumann, P. E., Janz, R., & Crair, M. C. (2003) · Nature Neuroscience · doi:10.1038/nn1106 · Cited by 109

Activity-Dependent Dendritic Spine Structural Plasticity Is Regulated by Small GTPase Rap1 and Its Target AF-6

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Origins of altered reinforcement effects in ADHD

Johansen, E., Killeen, P. R., Russell, V. A., Tripp, G., Wickens, J. R., Tannock, R., Williams, J., & Sagvolden, T. (2009) · Behavioral and Brain Functions · doi:10.1186/1744-9081-5-7 · Cited by 108

ERK and mTOR Signaling Couple β-Adrenergic Receptors to Translation Initiation Machinery to Gate Induction of Protein Synthesis-dependent Long-term Potentiation

Gelinas, J. N., Banko, J. L., Hou, L., Sonenberg, N., Weeber, E. J., Klann, E., & Nguyen, P. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701077200 · Cited by 108

Mitogen-Activated Protein Kinase Regulates Early Phosphorylation and Delayed Expression of Ca2+/Calmodulin-Dependent Protein Kinase II in Long-Term Potentiation

Giovannini, M. G., Blitzer, R. D., Wong, T., Asoma, K., Tsokas, P., Morrison, J. H., Iyengar, R., & Landau, E. M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07053.2001 · Cited by 108

Molecular mechanisms for activity-regulated protein synthesis in the synapto-dendritic compartment

Wells, D. G., Richter, J. D., & Fallon, J. R. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)00050-1 · Cited by 108

Suppression of synaptic plasticity by cerebrospinal fluid from anti-NMDA receptor encephalitis patients

Zhang, Q., Tanaka, K., Sun, P., Nakata, M., Yamamoto, R., Sakimura, K., Matsui, M., & Kato, N. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.09.019 · Cited by 110

The possible mechanism of silver nanoparticle impact on hippocampal synaptic plasticity and spatial cognition in rats

Liu, Y., Guan, W., Ren, G., & Yang, Z. R. (2012) · Toxicology Letters · doi:10.1016/j.toxlet.2012.01.001 · Cited by 107

Early Stage Drug Treatment That Normalizes Proinflammatory Cytokine Production Attenuates Synaptic Dysfunction in a Mouse Model That Exhibits Age-Dependent Progression of Alzheimer's Disease-Related Pathology

Bachstetter, A. D., Norris, C. M., Sompol, P. M., Wilcock, D. M., Goulding, D. S., Neltner, J. H., Clair, D. K. S., Watterson, D. M., & Eldik, L. J. V. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1496-12.2012 · Cited by 106

Radiation Induces Acute Alterations in Neuronal Function

Wu, P. H., Coultrap, S. J., Pinnix, C. C., Davies, K. D., Tailor, R. C., Ang, K. K., Browning, M. D., & Grosshans, D. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037677 · Cited by 109

Transient synaptic activation of NMDA receptors leads to the insertion of native AMPA receptors at hippocampal neuronal plasma membranes

Pickard, L., Noël, J., Duckworth, J. K., Fitzjohn, S. M., Henley, J. M., Collingridge, G. L., & Molnár, E. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00127-7 · Cited by 109

Regional changes in the hippocampal density of AMPA and NMDA receptors across the lifespan of the rat

Wenk, G. L., & Barnes, C. A. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02792-x · Cited by 108

Early remodeling of the neocortex upon episodic memory encoding

Bero, A. W., Meng, J., Cho, S., Shen, A. H., Canter, R. G., Ericsson, M., & Tsai, L. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1408378111 · Cited by 116

Plasticity, Synaptic Strength, and Epilepsy: What Can We Learn from Ultrastructural Data?

Leite, J. P., Neder, L., Arisi, G. M., Carlotti, C. G., Assirati, J. A., & Moreira, J. E. (2005) · Epilepsia · doi:10.1111/j.1528-1167.2005.01021.x · Cited by 107

Regulation of BDNF expression in primary neuron culture by LY392098, a novel AMPA receptor potentiator

Legutko, B., Li, X., & Skolnick, P. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00006-5 · Cited by 106

Dendritic Transport and Localization of Protein Kinase Mζ mRNA

Muslimov, I. A., Nimmrich, V., Hernandez, A. I., Tcherepanov, A., Sacktor, T. C., & Tiedge, H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m409240200 · Cited by 106

Progress in Understanding the Factors Regulating Reversibility of Long-term Potentiation

Huang, C.-C., & Hsu, K.-S. (2001) · Reviews in the Neurosciences · doi:10.1515/revneuro.2001.12.1.51 · Cited by 105

Mitochondria-Targeted Antioxidants as Promising Drugs for Treatment of Age-Related Brain Diseases

Skulachev, V. P. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-111391 · Cited by 109

Regulation of Signal Transduction by Protein Targeting: The Case for CaMKII

Bayer, K. U., & Schulman, H. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.6063 · Cited by 104

Coincident Pre- and Postsynaptic Activation Induces Dendritic Filopodia via Neurotrypsin-Dependent Agrin Cleavage

Matsumoto, K., Sokolowska, E., Zurlinden, A., Gee, C. E., Lüscher, D., Hettwer, S., Wölfel, J., Ladner, A. P., Ster, J., Gerber, U. R., et al. (2009) · Cell · doi:10.1016/j.cell.2009.02.034 · Cited by 104

Ethanol-Mediated Facilitation of AMPA Receptor Function in the Dorsomedial Striatum: Implications for Alcohol Drinking Behavior

Wang, J., Hamida, S. B., Darcq, E., Zhu, W., Gibb, S. L., Lanfranco, M. F., Carnicella, S., & Dorit Ron, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2783-12.2012 · Cited by 102

An Electronic Synapse Based on 2D Ferroelectric CuInP 2 S 6

Li, B., Li, S., Wang, H., Chen, L., Liu, L., Feng, X., Li, Y., Chen, J., Gong, X., & Ang, K. (2020) · Advanced Electronic Materials · doi:10.1002/aelm.202000760 · Cited by 104

Slow Presynaptic and Fast Postsynaptic Components of Compound Long-Term Potentiation

Bayazitov, I. T., Richardson, R. J., Fricke, R. G., & Zakharenko, S. S. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3077-07.2007 · Cited by 102

Interaction of transmembrane AMPA receptor regulatory proteins with multiple membrane associated guanylate kinases

Dakoji, S., Tomita, S., Karimzadegan, S., Nicoll, R. A., & Bredt, D. S. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(03)00267-3 · Cited by 104

PKCλ is critical in AMPA receptor phosphorylation and synaptic incorporation during LTP

Ren, S., Yan, J., Zhang, X., Bu, Y.-F., Pan, W.-W., Yao, W., Tian, T., & Lü, W. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.60 · Cited by 113

Synapse‐specific mGluR1‐dependent long‐term potentiation in interneurones regulates mouse hippocampal inhibition

Lapointe, V., Morin, F., Ratté, S., Croce, A., Conquet, F., & Lacaille, J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.053603 · Cited by 103

Injury-induced alterations in CNS electrophysiology

Cohen, A. S., Pfister, B. J., Schwarzbach, E., Grady, M. S., Goforth, P. B., & Satin, L. S. (2007) · Progress in brain research · doi:10.1016/s0079-6123(06)61010-8 · Cited by 104

Neuronal and Vascular Oxidative Stress in Alzheimers Disease

Massaad, C. A. (2011) · Current Neuropharmacology · doi:10.2174/157015911798376244 · Cited by 102

Metal Toxicity at the Synapse: Presynaptic, Postsynaptic, and Long-Term Effects

Sadiq, S., Ghazala, Z., Chowdhury, A., & Büsselberg, D. (2012) · Journal of Toxicology · doi:10.1155/2012/132671 · Cited by 106

Assembly and plasticity of the glutamatergic postsynaptic specialization

McGee, A. W., & Bredt, D. S. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00008-4 · Cited by 102

CaMKII Autonomy Is Substrate-dependent and Further Stimulated by Ca2+/Calmodulin

Coultrap, S. J., Buard, I., Kulbe, J. R., Dell’Acqua, M. L., & Bayer, K. U. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.069351 · Cited by 105

Auditory Fear Conditioning and Long-Term Potentiation in the Lateral Amygdala Require ERK/MAP Kinase Signaling in the Auditory Thalamus: A Role for Presynaptic Plasticity in the Fear System

Apergis-Schoute, A. M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0096-05.2005 · Cited by 101

Cocaine-induced metaplasticity in the nucleus accumbens: Silent synapse and beyond

Lee, B. R., & Dong, Y. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.12.033 · Cited by 103

Reversal of Synaptic Memory by Ca2+/Calmodulin-Dependent Protein Kinase II Inhibitor

Sanhueza, M., McIntyre, C., & Lisman, J. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5049-06.2007 · Cited by 101

Modulation of Top-Down Control of Visual Attention by Cathodal tDCS over Right IPS

Moos, K., Vossel, S., Weidner, R., Sparing, R., & Fink, G. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6233-11.2012 · Cited by 102

AMPA receptor trafficking for postsynaptic potentiation

Park, M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00361 · Cited by 77

Cognitive remediation: a promising tool for the treatment of schizophrenia

Demily, C., & Nicolas Franck, B. (2008) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.8.7.1029 · Cited by 102

Improving Hand Function in Stroke Survivors: A Pilot Study of Contralaterally Controlled Functional Electric Stimulation in Chronic Hemiplegia

Knutson, J. S., Harley, M. Y., Hisel, T. Z., & Chae, J. (2007) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2007.01.003 · Cited by 102

Memory deficits are associated with impaired ability to modulate neuronal excitability in middle-aged micePreprint

Kaczorowski, C. C., & Disterhoft, J. F. (2009) · Learning & Memory · doi:10.1101/lm.1365609 · Cited by 101

Regulation of Spine Morphology and Synaptic Function by LIMK and the Actin Cytoskeleton

Meng, Y., Zhang, Y., Tregoubov, V., Falls, D. L., & Jia, Z. (2003) · Reviews in the Neurosciences · doi:10.1515/revneuro.2003.14.3.233 · Cited by 101

The selective orexin 1 receptor antagonist SB-334867-A impairs acquisition and consolidation but not retrieval of spatial memory in Morris water maze

Akbari, E., Naghdi, N., & Motamedi, F. (2006) · Peptides · doi:10.1016/j.peptides.2006.11.002 · Cited by 100

Synaptic plasticity: A molecular memory switch

Lisman, J. E., & McIntyre, C. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00472-9 · Cited by 106

Structure and function of dendritic spines within the hippocampus

Halbach, O. V. B. U. (2009) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2009.08.006 · Cited by 112

Signaling Cascade Regulating Long-Term Potentiation of GABAAReceptor Responsiveness in Cerebellar Purkinje Neurons

Kawaguchi, S., & Hirano, T. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-10-03969.2002 · Cited by 99

Mechanisms involved in systemic nicotine-induced glutamatergic synaptic plasticity on dopamine neurons in the ventral tegmental area

Gao, M., Jin, Y., Yang, K., Zhang, D., Lukas, R. J., & Wu, J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1943-10.2010 · Cited by 99

The neurophysiology of language: Insights from non-invasive brain stimulation in the healthy human brain.

Hartwigsen, G. (2015) · Brain and Language · doi:10.1016/j.bandl.2014.10.007 · Cited by 90

Oxytocin receptor signaling in the hippocampus: Role in regulating neuronal excitability, network oscillatory activity, synaptic plasticity and social memory

Lin, Y.-T., & Hsu, K. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.10.003 · Cited by 102

Activity Shapes Neural Circuit Form and Function: A Historical Perspective

Pan, Y., & Monje, M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0740-19.2019 · Cited by 98

Modulation of NMDA Receptor Properties and Synaptic Transmission by the NR3A Subunit in Mouse Hippocampal and Cerebrocortical Neurons

Tong, G., Takahashi, H., Tu, S., Shin, Y., Talantova, M. V., Zago, W. M., Xia, P., Nie, Z., Goetz, T., Zhang, D., et al. (2007) · Journal of Neurophysiology · doi:10.1152/jn.01044.2006 · Cited by 98

Role of the Neurogranin Concentrated in Spines in the Induction of Long-Term Potentiation

Zhabotinsky, A. M., Camp, R. N., Epstein, I. R., & Lisman, J. E. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0729-06.2006 · Cited by 96

Long-Term Potentiation Induced by θ Frequency Stimulation Is Regulated by a Protein Phosphatase-1-Operated Gate

Brown, G. P., Blitzer, R. D., Connor, J. H., Wong, T., Shenolikar, S., Iyengar, R., & Landau, E. M. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-21-07880.2000 · Cited by 98

Neurofeedback treatment of epilepsy: from basic rationale to practical application

Egner, T., & Sterman, M. B. (2006) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.6.2.247 · Cited by 102

Tactile Stimulation Evokes Long-Term Synaptic Plasticity in the Granular Layer of Cerebellum

Roggeri, L., Rivieccio, B., Rossi, P., & D'Angelo, E. U. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5709-07.2008 · Cited by 99

A critical role of Rho-kinase ROCK2 in the regulation of spine and synaptic function

Zhou, Z., Meng, Y., Asrar, S., Todorovski, Z., & Jia, Z. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.031 · Cited by 97

Protective Effects of Exogenous Hydrogen Sulfide on Neurons of Hippocampus in a Rat Model of Brain Ischemia

Li, Z., Wang, Y., Xie, Y., Yang, Z. R., & Zhang, T. (2011) · Neurochemical Research · doi:10.1007/s11064-011-0502-6 · Cited by 95

Altered dendritic development of cerebellar Purkinje cells in slice cultures from protein kinase Cγ-deficient mice

Schrenk, K., Kapfhammer, J. P., & Metzger, F. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00559-0 · Cited by 97

Glutamatergic Plasticity by Synaptic Delivery of GluR-Blong-Containing AMPA Receptors

Kolleker, A., Zhu, J., Schupp, B. J., Qin, Y., Mack, V., Borchardt, T., Köhr, G., Malinow, R., Seeburg, P. H., & Osten, P. (2003) · Neuron · doi:10.1016/s0896-6273(03)00722-0 · Cited by 97

Mutation at the TrkB PLCγ-docking site affects hippocampal LTP and associative learning in conscious micePreprint

Gruart, A., Sciarretta, C., Valenzuela‐Harrington, M., Delgado-Garcia, J. M., & Minichiello, L. (2007) · Learning & Memory · doi:10.1101/lm.428307 · Cited by 95

ARG1-expressing microglia show a distinct molecular signature and modulate postnatal development and function of the mouse brain

Stratoulias, V., Ruiz, R., Kanatani, S., Osman, A. M., Keane, L., Armengol, J. A., Rodríguez-Moreno, A., Murgoci, A.-N., García-Domínguez, I., Alonso-Bellido, I., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01326-3 · Cited by 96

Pre- and postnatal exposure to glyphosate-based herbicide causes behavioral and cognitive impairments in adult mice: evidence of cortical ad hippocampal dysfunction

Ait-Bali, Y., Ba-M’hamed, S., Gambarotta, G., Sassoé‐Pognetto, M., Giustetto, M., & Bennis, M. (2020) · Archives of Toxicology · doi:10.1007/s00204-020-02677-7 · Cited by 102

The role of TRPV1 receptors in pain evoked by noxious thermal and chemical stimuli

Willis, W. D. (2009) · Experimental Brain Research · doi:10.1007/s00221-009-1760-2 · Cited by 96

Long-Term Depression of Presynaptic Release from the Readily Releasable Vesicle Pool Induced by NMDA Receptor-Dependent Retrograde Nitric Oxide

Stanton, P. K., Winterer, J., Bailey, C. P., Kyrozis, A., Рагинов, И. С., Laube, G., Veh, R. W., Nguyen, C. Q., & Müller, W. S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05936.2003 · Cited by 102

Fast AMPAR trafficking for a high‐frequency synaptic transmission

Choquet, D. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07350.x · Cited by 101

Complexity of calcium signaling in synaptic spines

Franks, K. M., & B, T. J. S. A. (2002) · BioEssays · doi:10.1002/bies.10193 · Cited by 98

TRPV1 activation alleviates cognitive and synaptic plasticity impairments through inhibiting AMPAR endocytosis in APP23/PS45 mouse model of Alzheimer’s disease

Du, Y., Fu, M., Huang, Z., Tian, X., Li, J., Pang, Y., Song, W., Tian Wang, Y., & Dong, Z. (2020) · Aging Cell · doi:10.1111/acel.13113 · Cited by 95

Dendritic synapse location and neocortical spike-timing-dependent plasticity

Froemke, R. C. (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00029 · Cited by 99

Translational control by eIF2α kinases in long-lasting synaptic plasticity and long-term memory

Trinh, M. A., & Klann, E. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.04.013 · Cited by 98

Protective Effects of Prenatal Choline Supplementation on Seizure-Induced Memory Impairment

Yang, Y., Liu, Z., Cermak, J. M., Tandon, P., Sarkisian, M. R., Stafstrom, C. E., Neill, J. C., Blusztajn, J. K., & Holmes, G. L. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-j0006.2000 · Cited by 95

A Review on the Role of the Neuroscience of Flow States in the Modern World

Gold, J., & Ciorciari, J. (2020) · Behavioral Sciences · doi:10.3390/bs10090137 · Cited by 99

Rapid, Bidirectional Remodeling of Synaptic NMDA Receptor Subunit Composition by A-type K+ Channel Activity in Hippocampal CA1 Pyramidal Neurons

Jung, S., Kim, J., & Hoffman, D. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.029 · Cited by 94

Multiple forms of long-term plasticity at unitary neocortical layer 5 synapses

Sjöström, P. J., Turrigiano, G. G., & Nelson, S. B. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.021 · Cited by 90

To spike, or when to spike?

Gütig, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.004 · Cited by 93

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