Regulation of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor trafficking through PKA phosphorylation of the Glu receptor 1 subunit

Glutamate neurotoxicity and diseases of the nervous system

Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,188

AMPA Receptor Trafficking and Synaptic Plasticity

Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588

MAPK cascade signalling and synaptic plasticity

Thomas, G. M., & Huganir, R. L. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1346 · Cited by 1,454

AMPA receptor trafficking at excitatory synapses

Bredt, D. S., & Nicoll, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00640-8 · Cited by 1,150

Reinsertion or Degradation of AMPA Receptors Determined by Activity-Dependent Endocytic Sorting

Ehlers, M. D. (2000) · Neuron · doi:10.1016/s0896-6273(00)00129-x · Cited by 1,096

Receptor trafficking and synaptic plasticity

Collingridge, G. L., Isaac, J. T. R., & Wang, Y. T. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1556 · Cited by 1,046

Activation of Synaptic NMDA Receptors Induces Membrane Insertion of New AMPA Receptors and LTP in Cultured Hippocampal Neurons

Lu, W.-Y., Man, H., Ju, W. H., Trimble, W. S., MacDonald, J. F., & Wang, Y. T. (2001) · Neuron · doi:10.1016/s0896-6273(01)00194-5 · Cited by 935

PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticity

Esteban, J. A., Shi, S.-H., Wilson, C., Nuriya, M., Huganir, R. L., & Malinow, R. (2003) · Nature Neuroscience · doi:10.1038/nn997 · Cited by 894

Phosphorylation of the AMPA Receptor GluR1 Subunit Is Required for Synaptic Plasticity and Retention of Spatial Memory

Lee, H.-K., Takamiya, K., Han, J.-S., Man, H., Kim, C.-H., Rumbaugh, G., Yu, S., Ding, L., He, C., Petralia, R. S., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00122-3 · Cited by 802

Regulation of AMPA receptors during synaptic plasticity

Song, I., & Huganir, R. L. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02270-1 · Cited by 798

Central sensitization: a generator of pain hypersensitivity by central neural plasticity

Latremoliere, A., & Woolf, C. J. (2009) · The Journal of Pain · doi:10.1016/j.jpain.2009.06.012 · Cited by 3,913

Glutamate Receptor Ion Channels: Structure, Regulation, and Function

Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568

The cell biology of synaptic plasticity: AMPA receptor trafficking

Shepherd, J. D., & Huganir, R. L. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123516 · Cited by 978

The AMPA Receptor Code of Synaptic Plasticity

Diering, G. H., & Huganir, R. L. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.018 · Cited by 844

Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels

Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686

Seminars in Cell & Developmental Biology

Lee, H., & Kirkwood, A. (2011) · Cited by 692

The Cell Biology of Synaptic Plasticity

Ho, V. M., Lee, J.-A., & Martin, K. C. (2011) · Science · doi:10.1126/science.1209236 · Cited by 573

Activation of estrogen receptor-β regulates hippocampal synaptic plasticity and improves memory

Liu, F., Day, M., Muñiz, L., Bitran, D., Arias, R. L., Revilla-Sanchez, R., Grauer, S. M., Zhang, G., Kelley, C., Pulito, V. L., et al. (2008) · Nature Neuroscience · doi:10.1038/nn2057 · Cited by 517

Regulation of AMPA receptor extrasynaptic insertion by 4.1N, phosphorylation and palmitoylation

Lin, D.-T., Makino, Y., Sharma, K., Hayashi, T., Neve, R., Takamiya, K., & Huganir, R. L. (2009) · Nature Neuroscience · doi:10.1038/nn.2351 · Cited by 347

AMPA receptor plasticity in the nucleus accumbens after repeated exposure to cocaine

Wolf, M. E., & Ferrario, C. R. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.01.013 · Cited by 271

Specific Roles of AMPA Receptor Subunit GluR1 (GluA1) Phosphorylation Sites in Regulating Synaptic Plasticity in the CA1 Region of Hippocampus

Lee, H.-K., Takamiya, K., He, K., Song, L., & Huganir, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00835.2009 · Cited by 261

IL-6 regulation of synaptic function in the CNS

Gruol, D. L. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.023 · Cited by 254

NMDA Receptor-Dependent LTD Requires Transient Synaptic Incorporation of Ca 2+ -Permeable AMPARs Mediated by AKAP150-Anchored PKA and Calcineurin

Sanderson, J. L., Gorski, J. A., & Dell’Acqua, M. L. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.043 · Cited by 210

Chapter 6 Regulation of hippocampus-dependent memory by cyclic AMP-dependent protein kinase

Abel, T., & Nguyen, P. V. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(07)00006-4 · Cited by 198

A three-step model for the synaptic recruitment of AMPA receptors

Opazo, P., & Choquet, D. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.014 · Cited by 190

Stabilization of Ca 2+ -permeable AMPA receptors at perisynaptic sites by GluR1-S845 phosphorylation

He, K., Song, L., Cummings, L. W., Goldman, J. W., Huganir, R. L., & Lee, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910338106 · Cited by 194

Enhanced AMPA Receptor Trafficking Mediates the Anorexigenic Effect of Endogenous Glucagon-like Peptide-1 in the Paraventricular Hypothalamus

Liu, J., Conde, K., Zhang, P., Lilascharoen, V., Xu, Z., Lim, B. K., Seeley, R. J., Zhu, J. J., Scott, M. M., & Pang, Z. P. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.042 · Cited by 192

FMRP Acts as a Key Messenger for Dopamine Modulation in the Forebrain

Wang, H., Wu, L.-J., Kim, S. S., Lee, F. J. S., Gong, B., Toyoda, H., Ren, M., Shang, Y.-Z., Xu, H., Liu, F., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.06.027 · Cited by 186

AKAP signaling complexes in regulation of excitatory synaptic plasticity

Sanderson, J. L., & Dell'Acqua, M. L. (2011) · The Neuroscientist · doi:10.1177/1073858410384740 · Cited by 185

The developmental stages of synaptic plasticity

Löhmann, C., & Kessels, H. W. H. G. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.235119 · Cited by 195

Early Alterations of AMPA Receptors Mediate Synaptic Potentiation Induced by Neonatal Seizures

Rakhade, S. N., Zhou, C., Aujla, P. K., Fishman, R. E., Sucher, N. J., & Jensen, F. E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1734-08.2008 · Cited by 182

Homeostatic regulation of AMPA receptor expression at single hippocampal synapses

Hou, Q., Zhang, D., Jarzylo, L., Huganir, R. L., & Man, H.-Y. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706447105 · Cited by 179

Age‐dependent requirement of AKAP150‐anchored PKA and GluR2‐lacking AMPA receptors in LTP

Lü, Y., Allen, M., Halt, A. R., Weisenhaus, M., Dallapiazza, R. F., Hall, D. D., Usachev, Y. M., McKnight, G. S., & Hell, J. W. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601884 · Cited by 170

Agonist- and Ca2+-dependent Desensitization of TRPV1 Channel Targets the Receptor to Lysosomes for Degradation

Sanz-Salvador, L., Andrés-Bordería, A., Ferrer-Montiel, A. V., & Planells‐Cases, R. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.289751 · Cited by 167

Peripheral inflammation induces tumor necrosis factor dependent AMPA receptor trafficking and Akt phosphorylation in spinal cord in addition to pain behavior

Choi, J. I., Svensson, C. I., Koehrn, F. J., Bhuskute, A. A., & Sorkin, L. S. (2010) · Pain · doi:10.1016/j.pain.2010.02.008 · Cited by 163

β-Adrenergic receptor signaling and modulation of long-term potentiation in the mammalian hippocampus

O'Dell, T. J., Connor, S. A., Guglietta, R., & Nguyen, P. V. (2015) · Learning & Memory · doi:10.1101/lm.031088.113 · Cited by 163

Neural functions of calcineurin in synaptic plasticity and memory: Figure 1.Preprint

Baumgärtel, K., & Mansuy, I. M. (2012) · Learning & Memory · doi:10.1101/lm.027201.112 · Cited by 163

Nedd4‐mediated AMPA receptor ubiquitination regulates receptor turnover and trafficking

Lin, A. W., Hou, Q., Jarzylo, L. A., Amato, S., Gilbert, J. P., Shang, F., & Man, H. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07221.x · Cited by 161

PKA-GluA1 coupling via AKAP5 controls AMPA receptor phosphorylation and cell-surface targeting during bidirectional homeostatic plasticity

Diering, G. H., Gustina, A. S., & Huganir, R. L. (2014) · Neuron · doi:10.1016/j.neuron.2014.09.024 · Cited by 153

Regulation of NMDA receptor Ca2+ signalling and synaptic plasticity

Lau, C. G., Takeuchi, K., Rodenas-Ruano, A., Takayasu, Y., Murphy, J., Bennett, M. V. L., & Zukin, R. S. (2009) · Biochemical Society Transactions · doi:10.1042/bst0371369 · Cited by 138

Adaptations in AMPA receptor transmission in the nucleus accumbens contributing to incubation of cocaine craving

Loweth, J. A., Tseng, K. Y., & Wolf, M. E. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.04.061 · Cited by 142

AKAP150-Anchored Calcineurin Regulates Synaptic Plasticity by Limiting Synaptic Incorporation of Ca2+-Permeable AMPA Receptors

Sanderson, J. L., Gorski, J. A., Gibson, E. S., Lam, P., Freund, R. K., Chick, W. S., & Dell'Acqua, M. L. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3326-12.2012 · Cited by 137

Subcellular Dynamics of Type II PKA in Neurons

Zhong, H., Sia, G.-M., Sato, T., Gray, N. W., Mao, T., Khuchua, Z. A., Huganir, R. L., & Svoboda, K. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.013 · Cited by 126

Regulation of Nucleus Accumbens Activity by the Hypothalamic Neuropeptide Melanin-Concentrating Hormone

Sears, R. M., Liu, R.-J., Narayanan, N. S., Sharf, R., Yeckel, M. F., Laubach, M., Aghajanian, G. K., & Dileone, R. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5858-09.2010 · Cited by 130

Na,K-ATPase Activity Regulates AMPA Receptor Turnover through Proteasome-Mediated Proteolysis

Zhang, D., Hou, Q., Wang, M., Lin, A. W., Jarzylo, L. A., Navis, A., Raissi, A. J., Liu, F., & Man, H. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6094-08.2009 · Cited by 122

Phosphorylation-Dependent Regulation of Ca2+-Permeable AMPA Receptors During Hippocampal Synaptic Plasticity

Purkey, A., & Dell’Acqua, M. L. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00008 · Cited by 120

Acute and Chronic Dopamine Receptor Stimulation Modulates AMPA Receptor Trafficking in Nucleus Accumbens Neurons Cocultured with Prefrontal Cortex Neurons

Sun, X., Milovanovic, M., Zhao, Y., & Wolf, M. E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0258-08.2008 · Cited by 111

Sex Differences in Psychiatric Disease: A Focus on the Glutamate System

Wickens, M. M., Bangasser, D. A., & Briand, L. A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00197 · Cited by 117

Amyloid-β-Induced Dysregulation of AMPA Receptor Trafficking

Guntupalli, S., Widagdo, J., & Anggono, V. (2016) · Neural Plasticity · doi:10.1155/2016/3204519 · Cited by 110

Alterations in AMPA receptor subunits and TARPs in the rat nucleus accumbens related to the formation of Ca2+-permeable AMPA receptors during the incubation of cocaine craving

Ferrario, C. R., Loweth, J. A., Milovanovic, M., Ford, K. A., Galiñanes, G. L., Heng, L., Tseng, K. Y., & Wolf, M. E. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.01.021 · Cited by 113

O-GlcNAcylation of AMPA Receptor GluA2 Is Associated with a Novel Form of Long-Term Depression at Hippocampal Synapses

Taylor, E. W., Wang, K., Nelson, A. R., Bredemann, T. M., Fraser, K. B., Clinton, S. M., Puckett, R. E., Marchase, R. B., Chatham, J. C., & McMahon, L. L. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4761-12.2014 · Cited by 112

Palmitoylation of A-Kinase Anchoring Protein 79/150 Regulates Dendritic Endosomal Targeting and Synaptic Plasticity Mechanisms

Keith, D. J., Sanderson, J. L., Gibson, E. S., Woolfrey, K. M., Robertson, H. R., Olszewski, K., Kang, R., El-Husseini, A., & Dell'Acqua, M. L. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0784-12.2012 · Cited by 108

Cellular, molecular, and epigenetic mechanisms in non-associative conditioning: Implications for pain and memory

Rahn, E. J., Karlsson, M. G., & Sweatt, J. D. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.06.008 · Cited by 113

Calcium-Permeable AMPA Receptors Mediate the Induction of the Protein Kinase A-Dependent Component of Long-Term Potentiation in the Hippocampus

Park, P., Sanderson, T. M., Amici, M., Choi, S.-L., Bortolotto, Z. A., Zhuo, M., Kaang, B., & Collingridge, G. L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3625-15.2016 · Cited by 109

Role of nucleus accumbens glutamatergic plasticity in drug addiction

Garzola, G. C. Q. (2013) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s45963 · Cited by 116

Intracellular oligomeric amyloid-beta rapidly regulates GluA1 subunit of AMPA receptor in the hippocampus

Whitcomb, D. J., Hogg, E. L., Regan, P. L., Piers, T. M., Narayan, P. S., Whitehead, G., Winters, B. L., Kim, D.-H., Kim, E., George‐Hyslop, P. S., et al. (2015) · Scientific Reports · doi:10.1038/srep10934 · Cited by 108

Homeostatic Regulation of AMPA Receptor Trafficking and Degradation by Light-Controlled Single-Synaptic Activation

Hou, Q., Gilbert, J. P., & Man, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.011 · Cited by 107

Soluble Oligomers of Amyloid-β Peptide Disrupt Membrane Trafficking of α-Amino-3-hydroxy-5-methylisoxazole-4-propionic Acid Receptor Contributing to Early Synapse Dysfunction

Miñano-Molina, A. J., España, J., Martín, E., Barneda‐Zahonero, B., Fadó, R., Solé, M., Trullás, R., Saura, C. A., & Rodrı́guez-Álvarez, J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.227504 · Cited by 114

Assembly of a β2‐adrenergic receptor—GluR1 signalling complex for localized cAMP signalling

Joiner, M.-L. A., Lisé, M.-F., Yuen, E. Y., Kam, A. Y. F., Zhang, M., Hall, D. D., Malik, Z. A., Qian, H., Chen, Y., Ulrich, J. D., et al. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.344 · Cited by 105

Protein Kinases and Addiction

Lee, A. M., & Messing, R. O. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1441.022 · Cited by 103

The Role of Calcium-Permeable AMPARs in Long-Term Potentiation at Principal Neurons in the Rodent Hippocampus

Park, P., Kang, H., Sanderson, T. M., Bortolotto, Z. A., Georgiou, J., Zhuo, M., Kaang, B., & Collingridge, G. L. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00042 · Cited by 103

AMPA Receptors as Therapeutic Targets for Neurological Disorders

Lee, K., Goodman, L., Fourie, C., Schenk, S., Leitch, B., & Montgomery, J. M. (2015) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2015.10.004 · Cited by 106

Integration of GPCR Signaling and Sorting from Very Early Endosomes via Opposing APPL1 Mechanisms

Sposini, S., Jean‐Alphonse, F., Ayoub, M. A., Oqua, A. I., West, C., Lavery, S. A., Brosens, J. J., Reiter, É., & Hanyaloglu, A. C. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.11.023 · Cited by 100

GluA1 Phosphorylation Contributes to Postsynaptic Amplification of Neuropathic Pain in the Insular Cortex

Qiu, S., Zhang, M., Liu, Y., Guo, Y., Zhao, H., Song, Q., Zhao, M., Huganir, R. L., Luo, J., Xu, H., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1431-14.2014 · Cited by 97

Melanocortin-4 Receptor Regulates Hippocampal Synaptic Plasticity through a Protein Kinase A-Dependent Mechanism

Shen, Y., Fu, W., Cheng, E. Y. L., Fu, A. K. Y., & Ip, N. Y. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3282-12.2013 · Cited by 97

Synaptic targeting of AMPA receptors is regulated by a CaMKII site in the first intracellular loop of GluA1

Lü, W., Isozaki, K., Roche, K. W., & Nicoll, R. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016289107 · Cited by 97

Aptamers selected against the unglycosylated EGFRvIII ectodomain and delivered intracellularly reduce membrane-bound EGFRvIII and induce apoptosis

Liu, Y., Kuan, C., Mi, J., Zhang, X., Clary, B. M., Bigner, D. D., & Sullenger, B. A. (2008) · Biological Chemistry · doi:10.1515/bc.2009.022 · Cited by 92

Extensive phosphorylation of AMPA receptors in neurons

Diering, G. H., Heo, S., Hussain, N. K., Liu, B., & Huganir, R. L. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610631113 · Cited by 100

Synaptic changes induced by melanocortin signalling

Caruso, V., Lagerström, M. C., Olszewski, P. K., Fredriksson, R., & Schiöth, H. B. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3657 · Cited by 90

Emerging Link between Alzheimer’s Disease and Homeostatic Synaptic Plasticity

Jang, S.-S., & Chung, H. J. (2016) · Neural Plasticity · doi:10.1155/2016/7969272 · Cited by 93

Activation of D1/D5 Dopamine Receptors Protects Neurons from Synapse Dysfunction Induced by Amyloid-β Oligomers

Jürgensen, S., Antonio, L. L., Mussi, G. E. A., Brito-Moreira, J., Bomfim, T. R., De Felice, F. G., Garrido-Sanabria, E. R., Cavalheiro, É. A., & Ferreira, S. T. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.177790 · Cited by 88

Psychostimulant-Induced Neuroadaptations in Nucleus Accumbens AMPA Receptor TransmissionPreprint

Pierce, R. C., & Wolf, M. E. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a012021 · Cited by 90

Signaling pathway adaptations and novel protein kinase A substrates related to behavioral sensitization to cocaine

Boudreau, A. C., Ferrario, C. R., Glucksman, M., & Wolf, M. E. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06140.x · Cited by 86

Homeostatic synaptic plasticity as a metaplasticity mechanism — a molecular and cellular perspective

Li, J., Park, E., Zhong, L. R., & Chen, L. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.08.010 · Cited by 84

Wnt Signaling Mediates LTP-Dependent Spine Plasticity and AMPAR Localization through Frizzled-7 Receptors

McLeod, F., Bossio, A., Marzo, A., Ciani, L., Sibilla, S., Hannan, S. B., Wilson, G. A., Palomer, E., Smart, T. G., Gibb, A. J., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.119 · Cited by 80

Amyloid-β Induces AMPA Receptor Ubiquitination and Degradation in Primary Neurons and Human Brains of Alzheimer’s Disease

Zhang, Y., Guo, O., Huo, Y., Wang, G., & Man, H. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-170879 · Cited by 84

Mechanisms of postsynaptic localization of AMPA-type glutamate receptors and their regulation during long-term potentiation

Buonarati, O. R., Hammes, E. A., Watson, J. F., Greger, I. H., & Hell, J. W. (2019) · Science Signaling · doi:10.1126/scisignal.aar6889 · Cited by 86

Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth

Maldergem, L. V., Hou, Q., Kalscheuer, V. M., Rio, M., Doco‐Fenzy, M., Medeira, A., de Brouwer, A. P. M., Cabrol, C., Haas, S. A., Cacciagli, P., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt187 · Cited by 80

β2-Adrenergic receptor supports prolonged theta tetanus-induced LTP

Qian, H., Matt, L., Zhang, M., Nguyen, M., Patriarchi, T., Koval, O. M., Anderson, M. E., He, K., Lee, H., & Hell, J. W. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00374.2011 · Cited by 85

Regulation of AMPA receptor localization in lipid rafts

Hou, Q., Huang, Y., Amato, S., Snyder, S. H., Huganir, R. L., & Man, H. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.02.010 · Cited by 79

cAMP-PKA cascade: An outdated topic for depression?

Gao, F., Yang, S., Wang, J., & Zhu, G. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113030 · Cited by 83

AMPA receptor regulation during synaptic plasticity in hippocampus and neocortex

Lee, H., & Kirkwood, A. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.06.007 · Cited by 772

Enhanced synaptic plasticity in mice with phosphomimetic mutation of the GluA1 AMPA receptor

Makino, Y., Johnson, R. C., Yu, Y., Takamiya, K., & Huganir, R. L. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105261108 · Cited by 77

Regulation of AMPA Receptor Trafficking in the Nucleus Accumbens by Dopamine and Cocaine

Wolf, M. E. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9176-0 · Cited by 80

Synaptic plasticity through activation of GluA3-containing AMPA-receptors

Renner, M. C., Albers, E. H., Gutierrez-Castellanos, N., Reinders, N. R., van Huijstee, A. N., Xiong, H., Lodder, T. R., & Kessels, H. W. (2017) · eLife · doi:10.7554/elife.25462 · Cited by 75

AKAP150‐anchored PKA activity is important for LTD during its induction phase

Lü, Y., Zhang, M., Lim, I. A., Hall, D. D., Allen, M., Medvedeva, Y. V., McKnight, G. S., Usachev, Y. M., & Hell, J. W. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.151662 · Cited by 73

The Autism Protein Ube3A/E6AP Remodels Neuronal Dendritic Arborization via Caspase-Dependent Microtubule Destabilization

Khatri, N., Gilbert, J. P., Huo, Y., Sharaflari, R., Nee, M., Qiao, H., & Man, H. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1511-17.2017 · Cited by 73

Chronic Stress Induces Maladaptive Behaviors by Activating Corticotropin-Releasing Hormone Signaling in the Mouse Oval Bed Nucleus of the Stria Terminalis

Hu, P., Liu, J., Maita, I., Kwok, C., Gu, E., Gergues, M. M., Kelada, F., Phan, M., Zhou, J.-N., Swaab, D. F., et al. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.2410-19.2020 · Cited by 71

GluA1 subunit ubiquitination mediates amyloid-β-induced loss of surface α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors

Guntupalli, S., Jang, S. E., Zhu, T., Huganir, R. L., Widagdo, J., & Anggono, V. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.774554 · Cited by 70

Leptin reverses long‐term potentiation at hippocampal CA1 synapses

Moult, P. R., Milojkovic, B. A., & Harvey, J. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05810.x · Cited by 68

Postsynaptic localization and regulation of AMPA receptors and Cav1.2 by β2 adrenergic receptor/PKA and Ca2+/CaMKII signaling

Patriarchi, T., Buonarati, O. R., & Hell, J. W. (2018) · The EMBO Journal · doi:10.15252/embj.201899771 · Cited by 68

Viagra for your synapses: Enhancement of hippocampal long-term potentiation by activation of beta-adrenergic receptors

O’Dell, T. J., Connor, S. A., Gelinas, J. N., & Nguyen, P. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2009.12.004 · Cited by 71

Regulation of Postsynaptic Structure and Function by an A-Kinase Anchoring Protein-Membrane-Associated Guanylate Kinase Scaffolding Complex

Robertson, H. R., Gibson, E. S., Benke, T. A., & Dell’Acqua, M. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6093-08.2009 · Cited by 70

Emerging role of AMPA receptor subunit GluA1 in synaptic plasticity: Implications for Alzheimer's disease

Qu, W., Yuan, B., Li, R., Liu, Q., Zhang, X., Cui, R., Yang, W., & Li, B. (2020) · Cell Proliferation · doi:10.1111/cpr.12959 · Cited by 65

Adenylyl Cyclase Anchoring by a Kinase Anchor Protein AKAP5 (AKAP79/150) Is Important for Postsynaptic β-Adrenergic Signaling

Zhang, M., Patriarchi, T., Stein, I. S., Qian, H., Matt, L., Nguyen, M., Xiang, Y. K., & Hell, J. W. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.449462 · Cited by 68

miR-501-3p mediates the activity-dependent regulation of the expression of AMPA receptor subunit GluA1

Hu, Z., Zhao, J. W., Hu, T., Luo, Y., Zhu, J., & Li, Z. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201404092 · Cited by 65

Glutamate Receptor 1 Phosphorylation at Serine 831 and 845 Modulates Seizure Susceptibility and Hippocampal Hyperexcitability after Early Life Seizures

Rakhade, S. N., Fitzgerald, E. F., Klein, P., Zhou, C., Sun, H., Huganir, R. L., & Jensen, F. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6121-11.2012 · Cited by 65

Rescue of NMDAR-Dependent Synaptic Plasticity in Fmr1 Knock-Out Mice

Bostrom, C. A., Majaess, N. M., Morch, K., White, E. R., Eadie, B. D., & Christie, B. R. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht237 · Cited by 67

AKAP150 Palmitoylation Regulates Synaptic Incorporation of Ca2+-Permeable AMPA Receptors to Control LTP

Purkey, A., Woolfrey, K. M., Crosby, K. C., Stich, D., Chick, W. S. H., Aoto, J. N., & Dell’Acqua, M. L. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.085 · Cited by 67

A-Kinase Anchoring Protein 150 and Protein Kinase A Complex in the Basolateral Amygdala Contributes to Depressive-like Behaviors Induced by Chronic Restraint Stress

Zhou, H.-Y., He, J., Hu, Z., Xue, S.-G., Xu, J., Cui, Q., Gao, S., Zhou, B., Wu, P., Long, L., et al. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.03.967 · Cited by 63

Role of cyclic nucleotides and their downstream signaling cascades in memory function: Being at the right time at the right spot

Argyrousi, E. K., Heckman, P. R. A., & Prickaerts, J. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.02.004 · Cited by 64

ERβ in CNS: New Roles in Development and Function

Fan, X., Xu, H., Warner, M. N., & Gustafsson, J.-Å. (2010) · Progress in brain research · doi:10.1016/s0079-6123(08)81013-8 · Cited by 65

Norepinephrine triggers metaplasticity of LTP by increasing translation of specific mRNAsPreprint

Maity, S., Rah, S. S., Sonenberg, N., Gkogkas, C. G., & Nguyen, P. (2015) · Learning & Memory · doi:10.1101/lm.039222.115 · Cited by 61

Overnight neuronal plasticity and adaptation to emotional distress

Cabrera, Y., Koymans, K. J., Poe, G. R., Kessels, H. W. H. G., Someren, E. J. W. V., & Wassing, R. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00799-w · Cited by 68

Presynaptic Type III Neuregulin1-ErbB signaling targets α7 nicotinic acetylcholine receptors to axons

Hancock, M., Canetta, S., Role, L. W., & Talmage, D. A. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200710037 · Cited by 62

Calcineurin mediates homeostatic synaptic plasticity by regulating retinoic acid synthesis

Arendt, K. L., Zhang, Z., Ganesan, S., Hintze, M., Shin, M. M., Tang, Y., Cho, A., Graef, I. A., & Chen, L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510239112 · Cited by 64

STIM2 regulates PKA-dependent phosphorylation and trafficking of AMPARs

García-Alvarez, G., Lu, B., Yap, K. A. F., Wong, L. C., Thevathasan, J. V., Lim, L., Ji, F., Tan, K. W., Mancuso, J. J., Tang, W., et al. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-07-1222 · Cited by 59

Involvement of pGluR1, EAAT2 and EAAT3 in offspring depression induced by prenatal stress

Zhang, X., Jia, N., Zhao, X. Y., Tang, G. K., Guan, L. X., Wang, D., Sun, H., Li, H., & Zhu, Z. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.04.031 · Cited by 61

Critical role of inflammatory cytokines in impairing biochemical processes for learning and memory after surgery in rats

Tan, H., Cao, J., Zhang, J., & Zuo, Z. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-93 · Cited by 60

‘Silent’ priming of translation-dependent LTP by β-adrenergic receptors involves phosphorylation and recruitment of AMPA receptorsPreprint

Tenorio, G., Connor, S. A., Guévremont, D., Abraham, W. C., Williams, J., O’Dell, T. J., & Nguyen, P. (2010) · Learning & Memory · doi:10.1101/lm.1974510 · Cited by 60

PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticity

Esteban, J. A., Shi, S.-H., Wilson, C., Nuriya, M., Huganir, R. L., & Malinow, R. (2003) · Nature Neuroscience · doi:10.1038/nn997 · Cited by 894

Enhancement of AMPA currents and GluR1 membrane expression through PKA‐coupled adenosine A2Areceptors

Dias, R. B., Ribeiro, J. A., & Sebastião, A. M. (2010) · Hippocampus · doi:10.1002/hipo.20894 · Cited by 84

Regulation of AMPA receptor extrasynaptic insertion by 4.1N, phosphorylation and palmitoylation

Lin, D.-T., Makino, Y., Sharma, K., Hayashi, T., Neve, R., Takamiya, K., & Huganir, R. L. (2009) · Nature Neuroscience · doi:10.1038/nn.2351 · Cited by 347

Phosphorylation of AMPA Receptors: Mechanisms and Synaptic Plasticity

Wang, J. Q., Arora, A. K., Yang, L., Parelkar, N. K., Zhang, G., Liu, X., Choe, E. S., & Mao, L. (2005) · Molecular Neurobiology · doi:10.1385/mn:32:3:237 · Cited by 135

Regulation of AMPA receptor subunit GluA1 surface expression by PAK3 phosphorylation

Hussain, N. K., Thomas, G. M., Luo, J., & Huganir, R. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1518382112 · Cited by 73