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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Slow waves, synaptic plasticity and information processing: insights from transcranial magnetic stimulation and high‐density EEG experiments

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Mechanisms of induction and maintenance of spike-timing dependent plasticity in biophysical synapse models

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Current perspectives on the development of non-biogenic amine-based antidepressants

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Loss of Hyperdirect Pathway Cortico-Subthalamic Inputs Following Degeneration of Midbrain Dopamine Neurons

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Regulation of hippocampal long-term potentiation by p21-activated protein kinase 1 (PAK1)

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Bidirectional Changes in Spatial Dendritic Integration Accompanying Long-Term Synaptic Modifications

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Differential roles for NSF and GRIP/ABP in AMPA receptor cycling

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Ligand-Dependent Recruitment of the ErbB4 Signaling Complex into Neuronal Lipid Rafts

Ma, L., Huang, Y. Z., Pitcher, G. M., Valtschanoff, J. G., Ma, Y. H., Feng, L., Lu, B., Xiong, W., Salter, M. W., Weinberg, R. J., et al. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03164.2003 · Cited by 130

A neuroanatomically grounded Hebbian‐learning model of attention–language interactions in the human brain

Garagnani, M., Wennekers, T., & Friedemann Pulvermüller, A. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06015.x · Cited by 136

Theta Burst Firing Recruits BDNF Release and Signaling in Postsynaptic CA1 Neurons in Spike-Timing-Dependent LTP

Edelmann, E., Cepeda-Prado, E., Franck, M., Lichtenecker, P., Brigadski, T., & Leßmann, V. (2015) · Neuron · doi:10.1016/j.neuron.2015.04.007 · Cited by 132

Visual memory and visual perception recruit common neural substrates

Slotnick, S. D. (2004) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582304274070 · Cited by 130

Voluntary Ethanol Intake Enhances Excitatory Synaptic Strength in the Ventral Tegmental Area

Stuber, G. D., Hopf, F. W., Hahn, J., Cho, S. L., Guillory, A. M., & Bonci, A. (2008) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2008.00749.x · Cited by 130

Protein kinase A‐dependent enhanced NMDA receptor function in pain‐related synaptic plasticity in rat amygdala neurones

Bird, G. C., Lash, L. L., Han, J. S., Zou, X., Willis, W. D., & Neugebauer, V. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.084780 · Cited by 132

Serotonin 5-HT1A Receptors Regulate AMPA Receptor Channels through Inhibiting Ca2+/Calmodulin-dependent Kinase II in Prefrontal Cortical Pyramidal Neurons

Cai, X., Gu, Z., Zhong, P., Ren, Y., & Yan, Z. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203752200 · Cited by 129

Heterosynaptic Regulation of External Globus Pallidus Inputs to the Subthalamic Nucleus by the Motor Cortex

Chu, H., Atherton, J. F., Wokosin, D. L., Surmeier, D. J., & Bevan, M. D. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.022 · Cited by 127

A study on neuroinflammation and NMDA receptor function in STZ (ICV) induced memory impaired rats

Rai, S., Kamat, P. K., Nath, C., & Shukla, R. (2012) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2012.08.008 · Cited by 129

Dose-dependent reductions in spatial learning and synaptic function in the dentate gyrus of adult rats following developmental thyroid hormone insufficiency

Gilbert, M. E., & Sui, L. (2006) · Brain Research · doi:10.1016/j.brainres.2005.10.049 · Cited by 129

Novel presynaptic mechanisms for coincidence detection in synaptic plasticity

Duguid, I., & Sjöström, P. J. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.05.008 · Cited by 127

MAGUKs in synapse assembly and function: an emerging view

Montgomery, J. M., Zamorano, P. L., & Garner, C. C. (2004) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-003-3364-5 · Cited by 128

A Biophysically Based Neural Model of Matching Law Behavior: Melioration by Stochastic Synapses

Soltani, A., & Wang, X. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5159-05.2006 · Cited by 129

Unique domain anchoring of Src to synaptic NMDA receptors via the mitochondrial protein NADH dehydrogenase subunit 2

Gingrich, J. R., Pelkey, K. A., Fam, S. R., Huang, Y., Petralia, R. S., Wenthold, R. J., & Salter, M. W. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401413101 · Cited by 131

Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice

Yu, T., Liu, C., Belichenko, P., Clapcote, S. J., Li, S., Pao, A., Kleschevnikov, A., Bechard, A. R., Asrar, S., Chen, R., et al. (2010) · Brain Research · doi:10.1016/j.brainres.2010.09.107 · Cited by 127

Progesterone–estrogen interactions in synaptic plasticity and neuroprotection

Baudry, M., Bi, X., & Aguirre, C. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.10.051 · Cited by 130

Nanoscale channel organic ferroelectric synaptic transistor array for high recognition accuracy neuromorphic computing

Li, E., Wu, X., Chen, Q., Wu, S., He, L., Yu, R., Hu, Y., Chen, H., & Guo, T. (2021) · Nano Energy · doi:10.1016/j.nanoen.2021.106010 · Cited by 127

Postsynaptic Targeting of Alternative Postsynaptic Density-95 Isoforms by Distinct Mechanisms

Chetkovich, D. M., Bunn, R. C., Kuo, S., Kawasaki, Y., Kohwi, M., & Bredt, D. S. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06415.2002 · Cited by 126

Hippocampal long-term potentiation, memory, and longevity in mice that overexpress mitochondrial superoxide dismutase

Hu, D., Cao, P., Thiels, E., Chu, C. T., Wu, G., Oury, T. D., & Klann, E. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2006.10.003 · Cited by 127

Activation of Calcium/Calmodulin-dependent Protein Kinase IV in Long Term Potentiation in the Rat Hippocampal CA1 Region

Kasahara, J., Fukunaga, K., & Miyamoto, E. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100247200 · Cited by 128

Synaptic Influence of Hippocampus on Pyramidal Cells of the Rat Prefrontal Cortex: An In Vivo Intracellular Recording Study

Dégenètais, E. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.7.782 · Cited by 131

Retrograde Amnesia for Spatial Memory Induced by NMDA Receptor-Mediated Long-Term Potentiation

Brun, V. H., Ytterbø, K., Morris, R., Moser, M., & Moser, E. I. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00356.2001 · Cited by 132

Synaptic reentry reinforcement based network model for long‐term memory consolidation

Wittenberg, G. M., Sullivan, M. R., & Tsien, J. Z. (2002) · Hippocampus · doi:10.1002/hipo.10102 · Cited by 129

Spiking neurons can discover predictive features by aggregate-label learning

Gütig, R. (2016) · Science · doi:10.1126/science.aab4113 · Cited by 125

Regulation of ADF/cofilin phosphorylation and synaptic function by LIM-kinase

Meng, Y., Takahashi, H., Meng, J., Zhang, Y., Lu, G., Asrar, S., Nakamura, T., & Jia, Z. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.030 · Cited by 129

Nicotinic Acetylcholine Receptors at Glutamate Synapses Facilitate Long-Term Depression or Potentiation

Ge, S., & Dani, J. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0542-05.2005 · Cited by 132

Calcium-dependent regulation of exocytosis

Barclay, J. W., Morgan, A., & Burgoyne, R. D. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.06.012 · Cited by 130

Plasticity and pain: role of the dorsal horn

Woolf, C. J., & Salter, M. W. (2006) · Elsevier eBooks · doi:10.1016/b0-443-07287-6/50010-2 · Cited by 125

Analysis of knock-out mice to determine the role of HPC-1/syntaxin 1A in expressing synaptic plasticity

Fujiwara, T., Mishima, T., Kofuji, T., Chiba, T., Tanaka, K., Yamamoto, A., & Akagawa, K. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0289-06.2006 · Cited by 125

Neurotoxicants, Micronutrients, and Social Environments

Hubbs‐Tait, L., Nation, J. R., Krebs, N. F., & Bellinger, D. C. (2005) · Gothic.net · doi:10.1111/j.1529-1006.2005.00024.x · Cited by 127

Wnt-5a Modulates Recycling of Functional GABAA Receptors on Hippocampal Neurons

Cuitiño, L., Godoy, J. A., Farı́as, G. G., Couve, A., Bonansco, C., Fuenzalida, M., & Inestrosa, N. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5736-09.2010 · Cited by 125

Cellular and System Biology of Memory: Timing, Molecules, and Beyond

Körte, M., & Schmitz, D. (2016) · Physiological Reviews · doi:10.1152/physrev.00010.2015 · Cited by 132

Calcium Input Frequency, Duration and Amplitude Differentially Modulate the Relative Activation of Calcineurin and CaMKII

Li, L., Stefan, M. I., & Novère, N. G. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043810 · Cited by 124

Generalized Bienenstock–Cooper–Munro rule for spiking neurons that maximizes information transmission

Toyoizumi, T., Pfister, J.-P., Aihara, K., & Gerstner, W. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500495102 · Cited by 124

Visual input induces long-term potentiation of developing retinotectal synapses

Zhang, L. I., Tao, H. W., & Poo, M. (2000) · Nature Neuroscience · doi:10.1038/76665 · Cited by 124

Neuroplasticity in children

Mundkur, N. (2005) · The Indian Journal of Pediatrics · doi:10.1007/bf02731115 · Cited by 123

Genetic Enhancement of Memory and Long-Term Potentiation but Not CA1 Long-Term Depression in NR2B Transgenic Rats

Wang, D., Cui, Z., Zeng, Q., Kuang, H., Wang, L. P., Tsien, J. Z., & Cao, X. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007486 · Cited by 123

Functional inactivation of orexin 1 receptors in CA1 region impairs acquisition, consolidation and retrieval in Morris water maze task

Akbari, E., Naghdi, N., & Motamedi, F. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.05.028 · Cited by 126

Homeostatic Synapse-Driven Membrane Plasticity in Nucleus Accumbens Neurons

Ishikawa, M., Mu, P., Moyer, J. T., Wolf, J. A., Quock, R. M., Davies, N. M., Hu, X., Schlüter, O. M., & Dong, Y. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5703-08.2009 · Cited by 121

Metacognitive monkeys or associative animals? Simple reinforcement learning explains uncertainty in nonhuman animals.

Pelley, M. E. L. (2012) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/a0026478 · Cited by 131

CaMKII Phosphorylation of TARPγ-8 Is a Mediator of LTP and Learning and Memory

Park, J., Chávez, A. E., Mineur, Y. S., Morimoto-Tomita, M., Lutzu, S., Kim, K. S., Picciotto, M. R., Castillo, P. E., & Tomita, S. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.002 · Cited by 121

Augmentation Treatment of Psychotherapy for Anxiety Disorders with D‐Cycloserine

Hofmann, S. G., Pollack, M. H., & Otto, M. W. (2006) · CNS Drug Reviews · doi:10.1111/j.1527-3458.2006.00208.x · Cited by 123

Presynaptic kainate receptors impart an associative property to hippocampal mossy fiber long-term potentiation

Schmitz, D., Mellor, J. R., Breustedt, J., & Nicoll, R. A. (2003) · Nature Neuroscience · doi:10.1038/nn1116 · Cited by 129

Induction of LTP in the human auditory cortex by sensory stimulation

Clapp, W. C., Kirk, I. J., Hamm, J. P., Shepherd, D., & Teyler, T. J. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04293.x · Cited by 122

Molecular regulation of dendritic spine dynamics and their potential impact on synaptic plasticity and neurological diseases

Maiti, P., Manna, J., Ilavazhagan, G., Rossignol, J., & Dunbar, G. L. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.09.020 · Cited by 128

Chronic Psychosocial Stress Exacerbates Impairment of Cognition and Long-Term Potentiation in β-Amyloid Rat Model of Alzheimer's Disease

Srivareerat, M., Tran, T. T., Alzoubi, K. H., & Alkadhi, K. A. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.08.021 · Cited by 128

Gestational and Neonatal Iron Deficiency Alters Apical Dendrite Structure of CA1 Pyramidal Neurons in Adult Rat Hippocampus

Brunette, K. E., Tran, P. V., Wobken, J. D., Carlson, E. S., & Georgieff, M. (2010) · Developmental Neuroscience · doi:10.1159/000314341 · Cited by 122

Remodelling of synaptic morphology but unchanged synaptic density during late phase long-term potentiation(ltp): A serial section electron micrograph study in the dentate gyrus in the anaesthetised rat

Popov, V. I., Davies, H. A., Rogachevsky, V. V., Patrushev, I., Errington, M. L., Gabbott, P. L. A., Bliss, T. V. P., & Stewart, M. G. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.029 · Cited by 121

Glutamate mediated signaling in the pathophysiology of autism spectrum disorders

Choudhury, P. R., Lahiri, S., & Rajamma, U. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.06.023 · Cited by 121

Absence of metabotropic glutamate receptor-mediated plasticity in the neocortex of fragile X mice

Wilson, B. M., & Cox, C. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610875104 · Cited by 121

Inhibition of the cAMP Pathway Decreases Early Long-Term Potentiation at CA1 Hippocampal Synapses

Otmakhova, N. A., Otmakhov, N., Mortenson, L. H., & Lisman, J. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-12-04446.2000 · Cited by 124

Effect of varied gestational stress on acquisition of spatial memory, hippocampal LTP and synaptic proteins in juvenile male rats

Yaka, R., Salomon, S., Matzner, H., & Weinstock, M. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.018 · Cited by 120

Neural plasticity and stress coping in teleost fishes

Sørensen, C., Johansen, I. B., & Øverli, Ø. (2012) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2012.12.003 · Cited by 124

On the Hypes and Falls in Neuroprotection: Targeting the NMDA Receptor

Villmann, C., & Becker, C. (2007) · The Neuroscientist · doi:10.1177/1073858406296259 · Cited by 121

Two Forms of Synaptic Plasticity with Distinct Dependence on Age, Experience, and NMDA Receptor Subtype in Rat Visual Cortex

Yoshimura, Y., Ohmura, T., & Komatsu, Y. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-16-06557.2003 · Cited by 120

Integrin signaling cascades are operational in adult hippocampal synapses and modulate NMDA receptor physiology

Bernard‐Trifilo, J. A., Kramár, E. A., Torp, R., Lin, C., Pineda, E. A., LYNCH, G. S., & Gall, C. M. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03062.x · Cited by 120

Dominant role of the GluR2 subunit in regulation of AMPA receptors by CaMKII

Oh, M. C., & Derkach, V. A. (2005) · Nature Neuroscience · doi:10.1038/nn1476 · Cited by 120

Neuroprotection by nicotine in mouse primary cortical cultures involves activation of calcineurin and L-type calcium channel inactivation

Stevens, T. R., Krueger, S. R., Fitzsimonds, R. M., & Picciotto, M. R. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10093.2003 · Cited by 119

A Learning and Memory Area in the Octopus Brain Manifests a Vertebrate-Like Long-Term Potentiation

Hochner, B., Brown, E. R., Langella, M., Shomrat, T., & Fiorito, G. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00645.2003 · Cited by 118

Role of Egr1 in Hippocampal Synaptic Enhancement Induced by Tetanic Stimulation and Amputation

Wei, F., Xu, Z. C., Qu, Z., Milbrandt, J., & Zhuo, M. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.7.1325 · Cited by 119

Stress and excitatory synapses: From health to disease

Timmermans, W., Xiong, H., Hoogenraad, C. C., & Krugers, H. J. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.05.043 · Cited by 120

Increased phosphorylation of the neuronal L-type Ca 2+ channel Ca v 1.2 during aging

Davare, M. A., & Hell, J. W. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2236970100 · Cited by 121

Roles of CaMKII, PKA, and PKC in the Induction and Maintenance of LTP of C-Fiber-Evoked Field Potentials in Rat Spinal Dorsal Horn

Yang, H.-W., Hu, X.-D., Zhang, H., Xin, W., Li, M.-T., Zhang, T., Zhou, L., & Liu, X. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00735.2003 · Cited by 116

Neuroprotection by the NR3A Subunit of the NMDA Receptor

Nakanishi, N., Tu, S., Shin, Y., Cui, J., Kurokawa, T., Zhang, D., Chen, H.-S. V., Tong, G., & Lipton, S. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1067-09.2009 · Cited by 118

Intracellular Calcium Regulation by Burst Discharge Determines Bidirectional Long-Term Synaptic Plasticity at the Cerebellum Input Stage

Gall, D., Prestori, F., Sola, E., D’Errico, A., Roussel, C., Forti, L., Rossi, P., & D'Angelo, E. U. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0410-05.2005 · Cited by 117

Identification of network-level coding units for real-time representation of episodic experiences in the hippocampus

Lin, L., Osan, R. M., Shoham, S., Jin, W., Zuo, W., & Tsien, J. Z. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408233102 · Cited by 118

Neural substrates of memory: From synapse to system

Dubnau, J., Chiang, A., & Tully, T. (2002) · Journal of Neurobiology · doi:10.1002/neu.10170 · Cited by 118

Neural Plasticity After Spinal Cord Injury

Ding, Y., Kastin, A. J., & Pan, W. (2005) · Current Pharmaceutical Design · doi:10.2174/1381612053507855 · Cited by 117

Enhancement of Associative Long-Term Potentiation by Activation of β-Adrenergic Receptors at CA1 Synapses in Rat Hippocampal Slices

Lin, Y., Min, M., Chiu, T., & Yang, H. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04173.2003 · Cited by 116

Dynamical model of long-term synaptic plasticity

Abarbanel, H. D. I., Huerta, R., & Rabinovich, M. I. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.132651299 · Cited by 116

Postsynaptic signaling networks: Cellular cogwheels underlying long-term plasticity

Blitzer, R. D., Iyengar, R., & Landau, E. M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.02.031 · Cited by 117

Thalamocortical Assemblies

Alain Destexhe, A., & Sejknowski, T. (2023) · doi:10.1093/oso/9780198864998.001.0001 · Cited by 115

The role of synaptic morphology in neural plasticity: structural interactions underlying synaptic power

Marrone, D. F. (2002) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00147-3 · Cited by 116

Modulating the brain at work using noninvasive transcranial stimulation

McKinley, R. A., Bridges, N. R., Walters, C. M., & Nelson, J. T. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.075 · Cited by 120

Endoplasmic reticulum stress/autophagy pathway is involved in diabetes-induced neuronal apoptosis and cognitive decline in mice

Kong, F., Ma, L., Guo, J., Xu, L., Li, Y., & Qu, S. (2017) · Clinical Science · doi:10.1042/cs20171432 · Cited by 115

Nicotine regulates multiple synaptic proteins by inhibiting proteasomal activity

Rezvani, K., Teng, Y., Shim, D., & De Biasi, M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3353-07.2007 · Cited by 113

Lamina-specific abnormalities of AMPA receptor trafficking and signaling molecule transcripts in the prefrontal cortex in schizophrenia

Beneyto, M., & Meador‐Woodruff, J. H. (2006) · Synapse · doi:10.1002/syn.20329 · Cited by 113

Shisa6 traps AMPA receptors at postsynaptic sites and prevents their desensitization during synaptic activity

Klaassen, R. V., Stroeder, J., Coussen, F., Hafner, A., Petersen, J. D., Renancio, C., Schmitz, L. J. M., Normand, E., Lodder, J. C., Rotaru, D. C., et al. (2016) · Nature Communications · doi:10.1038/ncomms10682 · Cited by 117

Altered response to rTMS in patients with Alzheimer's disease

Inghilleri, M., Conte, A., Frasca, V., Scaldaferri, N., Gilio, F., Santini, M., Fabbrini, G., Prencipe, M., & Berardelli, A. (2005) · Clinical Neurophysiology · doi:10.1016/j.clinph.2005.09.016 · Cited by 113

Long-Term Depression of NMDA Receptor-Mediated Synaptic Transmission Is Dependent on Activation of Metabotropic Glutamate Receptors and Is Altered to Long-Term Potentiation by Low Intracellular Calcium Buffering

Harney, S. C., Rowan, M. J., & Anwyl, R. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2753-05.2006 · Cited by 119

Orexins/hypocretins cause sharp wave- and θ-related synaptic plasticity in the hippocampus via glutamatergic, gabaergic, noradrenergic, and cholinergic signaling

Selbach, O., Doreulee, N., Bohla, C., Eriksson, K. S., Sergeeva, O. A., Poelchen, W., Brown, R. E., & Haas, H. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.05.012 · Cited by 113

α 1E -Containing Ca 2+ channels are involved in synaptic plasticity

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CaMKIIβ Association with the Actin Cytoskeleton Is Regulated by Alternative Splicing

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