Subunit-specific temporal and spatial patterns of AMPA receptor exocytosis in hippocampal neurons

Glutamate receptor ion channels

Mayer, M. L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.05.004 · Cited by 3,655

Optimized survival of hippocampal neurons in B27‐supplemented neurobasal™, a new serum‐free medium combination

Brewer, G. J., Torricelli, J. R., Evege, E. K., & Price, P. J. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490350513 · Cited by 2,325

Brefeldin A: insights into the control of membrane traffic and organelle structure.

Klausner, R. D., Donaldson, J. G., & Lippincott‐Schwartz, J. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.116.5.1071 · Cited by 1,843

Driving AMPA receptors into synapses by LTP and CaMKII: requirement for GluR1 and PDZ domain interaction

Hayashi, Y., Shi, S.-H., Esteban, J. A., Piccini, A., Poncer, J.-C., & Malinow, R. (2000) · Science · doi:10.1126/science.287.5461.2262 · Cited by 1,524

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

Shi, S.-H., Hayashi, Y., Petralia, R. S., Zaman, S. H., Wenthold, R. J., Svoboda, K., & Malinow, R. (1999) · Science · doi:10.1126/science.284.5421.1811 · Cited by 1,276

PDZ Domains and the Organization of Supramolecular Complexes

Sheng, M., & Sala, C. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1 · Cited by 1,211

Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms

Chen, L., Chetkovich, D. M., Petralia, R. S., Sweeney, N. T., Kawasaki, Y., Wenthold, R. J., Bredt, D. S., & Nicoll, R. A. (2000) · Nature · doi:10.1038/35050030 · Cited by 1,111

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

Subunit-Specific Rules Governing AMPA Receptor Trafficking to Synapses in Hippocampal Pyramidal Neurons

Shi, S.-H., Hayashi, Y., Esteban, J. A., & Malinow, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00321-x · Cited by 1,094

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

Inhibitory Receptor Diffusion Dynamics

Maynard, S. A., & Triller, A. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00313 · Cited by 31

Ca2+/calmodulin protein kinase II and memory: learning‐related changes in a localized region of the domestic chick brain

Solomonia, R. O., Kotorashvili, A., Kiguradze, T., McCabe, B. J., & Horn, G. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.098012 · Cited by 28

The role of endosomal-recycling in long-term potentiation

Kelly, E. E., Horgan, C. P., McCaffrey, M. W., & Young, P. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0516-2 · Cited by 27

Regulation of stargazin synaptic trafficking by C‐terminal PDZ ligand phosphorylation in bidirectional synaptic plasticity

Stein, E. L. A., & Chetkovich, D. M. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06529.x · Cited by 28

GluR2 protein-protein interactions and the regulation of AMPA receptors during synaptic plasticity

Duprat, F., Daw, M. I., Lim, W., Collingridge, G. L., & Isaac, J. T. R. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1215 · Cited by 28

Fluorescence imaging of synapse formation and remodeling

Okabe, S. (2013) · Microscopy · doi:10.1093/jmicro/dfs083 · Cited by 26

The SNARE Protein Syntaxin 3 Confers Specificity for Polarized Axonal Trafficking in Neurons

Hoo, L. S., Banna, C. D., Radeke, C. M., Sharma, N., Albertolle, M. E., Low, S. H., Weimbs, T., & Vandenberg, C. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0163671 · Cited by 27

Synaptic NR2A- but not NR2B-containing NMDA receptors increase with blockade of ionotropic glutamate receptors

von Engelhardt, J. (2009) · Frontiers in Molecular Neuroscience · doi:10.3389/neuro.02.019.2009 · Cited by 27

A Critical Role for the GluA1 Accessory Protein, SAP97, in Cocaine Seeking

White, S., Ortinski, P. I., Friedman, S. H., Zhang, L., Neve, R. L., Kalb, R. G., Schmidt, H. D., & Pierce, R. C. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.199 · Cited by 31

Permissive Role of Insulin in the Expression of Long-Term Potentiation in the Hippocampus of Immature Rats

Zhao, W., Wu, X., Xie, H., Ke, Y., & Yung, W. (2010) · Neurosignals · doi:10.1159/000324040 · Cited by 28

Control of Cerebellar Long-Term Potentiation by P-Rex-Family Guanine-Nucleotide Exchange Factors and Phosphoinositide 3-Kinase

Jackson, C. L. M., Welch, H. C. E., & Bellamy, T. C. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011962 · Cited by 28

Distinct LIN-10 Domains Are Required for Its Neuronal Function, Its Epithelial Function, and Its Synaptic Localization

Glodowski, D. R., Wright, T. M., Martinowich, K., Chang, H. C.-H., Beach, D. F., & Rongo, C. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-10-0885 · Cited by 27

Psychostimulant-Induced Adaptations in Nucleus Accumbens Glutamatergic TransmissionPreprint

Wright, W. J., & Dong, Y. (2020) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a039255 · Cited by 29

The dendritic SNARE fusion machinery involved in AMPARs insertion during long-term potentiation

Jurado, S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00407 · Cited by 25

AMPA receptor subunit localization in schizophrenia anterior cingulate cortex

Benesh, J. L., Mueller, T., & Meador‐Woodruff, J. H. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.01.025 · Cited by 27

Brain insulin signaling as a potential mediator of early life adversity effects on physical and mental health

Alberry, B., & Silveira, P. P. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105350 · Cited by 28

The effect of cinnamaldehyde on passive avoidance memory and hippocampal Akt, ERK and GSK-3β in mice

SoukhakLari, R., Borhani‐Haghighi, A., Farsadrooh, A., Moezi, L., Pirsalami, F., Kazerouni, A., Safari, A., & Moosavi, M. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.172530 · Cited by 26

Dynamics of postsynaptic glutamate receptor targeting

Chen, L., Tracy, T. E., & Nam, C. I. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.11.001 · Cited by 25

Persistent synaptic scaling independent of AMPA receptor subunit composition

Altimimi, H. F., & Stellwagen, D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1102-13.2013 · Cited by 25

Distribution of the SynDIG4/proline-rich transmembrane protein 1 in rat brain

Kirk, L. M., Ti, S. W., Bishop, H. I., Orozco‐Llamas, M., Pham, M., Trimmer, J. S., & Díaz, E. (2016) · Journal of Comparative Neurology · doi:10.1002/cne.23945 · Cited by 26

AMPA receptor subunits define properties of state-dependent synaptic plasticity

Emond, M. R., Montgomery, J. M., Huggins, M. L., Hanson, J. E., Mao, L., Huganir, R. L., & Madison, D. V. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.187229 · Cited by 26

Transmembrane and Ubiquitin-Like Domain-Containing Protein 1 (Tmub1/HOPS) Facilitates Surface Expression of GluR2-Containing AMPA Receptors

Yang, H., Takagi, H., Konishi, Y., Ageta, H., Ikegami, K., Yao, I., Sato, S., Hatanaka, K., Inokuchi, K., Seog, D., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002809 · Cited by 25

Spine Modifications Associated with Long-Term Potentiation

Yang, Y., & Zhou, Q. (2009) · The Neuroscientist · doi:10.1177/1073858409340800 · Cited by 30

Physiology and pathology of NMDA receptors.

Petrović, M., Hořák, M., Sedlacek, M., & Vyklický, L. (2005) · PubMed · Cited by 24

AMPA receptor trafficking and its role in heterosynaptic plasticity

Antunes, G., & Simões-de-Souza, F. M. (2018) · Scientific Reports · doi:10.1038/s41598-018-28581-w · Cited by 28

Estrogen dissociates Tau and alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor subunit in postischemic hippocampus

Cardona‐Gómez, G. P., Arango-Dávila, C. A., Gallego-Gómez, J. C., Barrera-Ocampo, A. A., Pimienta, H. J., & García‐Segura, L. M. (2006) · Neuroreport · doi:10.1097/01.wnr.0000230508.78467.96 · Cited by 25

The extracellular fragment of GPNMB (Glycoprotein nonmelanosoma protein B, osteoactivin) improves memory and increases hippocampal GluA1 levels in mice

Murata, K., Yoshino, Y., Tsuruma, K., Moriguchi, S., Oyagi, A., Tanaka, H., Ishisaka, M., Shimazawa, M., Fukunaga, K., & Hara, H. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.13010 · Cited by 24

PTEN Activity Defines an Axis for Plasticity at Cortico-Amygdala Synapses and Influences Social Behavior

Sánchez‐Puelles, C., Calleja-Felipe, M., Ouro, A., Bougamra, G., Arroyo, A., Diez, I. P., Erramuzpe, A., Cortés, J. M., Hernández, J. M., Luján, R., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz103 · Cited by 26

Novel toxicity of the unedited GluR2 AMPA receptor subunit dependent on surface trafficking and increased Ca2+-permeability

Mahajan, S. S., & Ziff, E. B. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.04.006 · Cited by 24

State-Dependent AMPA Receptor Trafficking in the Mammalian Retina

Xia, Y., Carroll, R. C., & Nawy, S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0169-06.2006 · Cited by 24

Analysis of Rab Protein Function in Neurotransmitter Receptor Trafficking at Hippocampal Synapses

Gerges, N. Z., Brown, T. C., Correia, S. S., & Esteban, J. A. (2005) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)03013-2 · Cited by 24

Cytosolic tail sequences and subunit interactions are critical for synaptic localization of glutamate receptors

Chang, H. C.-H., & Rongo, C. (2005) · Journal of Cell Science · doi:10.1242/jcs.02320 · Cited by 24

Primary Cilia and Dendritic Spines: Different but Similar Signaling Compartments

Nechipurenko, I. V., Doroquez, D. B., & Sengupta, P. (2013) · Molecules and Cells · doi:10.1007/s10059-013-0246-z · Cited by 23

A Fully Integrated Spintip-Based Approach for Sensitive and Quantitative Profiling of Region-Resolved in Vivo Brain Glycoproteome

Huang, P., Li, H., Gao, W., Cai, Z., & Tian, R. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b01930 · Cited by 23

Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome

Mehmood, T., Schneider‐Anthony, A., Sibille, J., Pereira, P. M., Pannetier, S., Ammar, M. R., Dembélé, D., Thibault-Carpentier, C., Rouach, N., & Hanauer, A. (2010) · Human Genetics · doi:10.1007/s00439-010-0918-0 · Cited by 22

MAP1B Light Chain Modulates Synaptic Transmission via AMPA Receptor Intracellular Trapping

Palenzuela, R., Gutiérrez, Y., Draffin, J. E., Lario, A., Benoist, M., & Esteban, J. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0505-17.2017 · Cited by 22

Development of GABAB subunits and functional GABAB receptors in rat cultured hippocampal neurons

Corrêa, S. A. L., Munton, R., Nishimune, A., Fitzjohn, S. M., & Henley, J. M. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.04.021 · Cited by 22

AMPAR exocytosis through NO modulation of PICK1

Sossa, K. G., Beattie, J. B., & Carroll, R. C. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2007.04.005 · Cited by 22

Proteomic Analysis of an Interactome for Long-Form AMPA Receptor Subunits

Santos, S. D., Manadas, B. J., Duarte, C. B., & Carvalho, A. L. (2010) · Journal of Proteome Research · doi:10.1021/pr900766r · Cited by 22

Secreted Amyloid Precursor Protein-Alpha Enhances LTP Through the Synthesis and Trafficking of Ca2+-Permeable AMPA Receptors

Livingstone, R. W., Elder, M. K., Singh, A., Westlake, C. M., Tate, W. P., Abraham, W. C., & Williams, J. M. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.660208 · Cited by 24

Metazoan evolution and diversity of glutamate receptors and their auxiliary subunits

Ramos-Vicente, D., Grant, S. G. N., & Bayés, À. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108640 · Cited by 21

Neuroadaptive changes in the mesocortical glutamatergic system during chronic nicotine self‐administration and after extinction in rats

Wang, F., Chen, H., & Sharp, B. M. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05456.x · Cited by 21

Changes in Synaptic Plasticity and Glutamate Receptors in Type 2 Diabetic KK-Ay Mice

Yin, H., Wang, W., Yu, W., Li, J., Feng, N., Wang, L., & Wang, X. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-160858 · Cited by 21

Elastic Properties of the Cell Surface and Trafficking of Single AMPA Receptors in Living Hippocampal Neurons

Yersin, A., Hirling, H., Kasas, S., Roduit, C., Kulangara, K., Dietler, G., Lafont, F., Catsicas, S., & Steiner, P. (2007) · Biophysical Journal · doi:10.1529/biophysj.106.092742 · Cited by 21

Neuronal enriched endosomal protein of 21 kDa colocalizes with glutamate receptor subunit GLUR2/3 at the postsynaptic membrane

Utvik, J. K., Haglerød, C., Mylonakou, M. N., Holen, T., Kropf, M., Hirling, H., Skare, Ø., Laake, P., Ottersen, O. P., Haug, F. Š., et al. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.11.030 · Cited by 20

P2X7 receptors exert a permissive effect on the activation of presynaptic AMPA receptors in rat trigeminal caudal nucleus glutamatergic nerve terminals

Currò, D., Navarra, P., Samengo, I., & Martire, M. (2020) · The Journal of Headache and Pain · doi:10.1186/s10194-020-01153-y · Cited by 18

Biophysical mechanisms regulating AMPA receptor accumulation at synapses

Czöndör, K., & Thoumine, O. R. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2012.11.001 · Cited by 28

Neurodegenerative disorders share common features of “loss of function” states of a proposed mechanism of nervous system functions

Vadakkan, K. I. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.06.042 · Cited by 21

Two mutations preventing PDZ–protein interactions of GluR1 have opposite effects on synaptic plasticityPreprint

Boehm, J., Ehrlich, I., Hsieh, H. V., & Malinow, R. (2006) · Learning & Memory · doi:10.1101/lm.253506 · Cited by 20

Optogenetic Control of Spine-Head JNK Reveals a Role in Dendritic Spine Regression

Hollós, P., John, J., Lehtonen, J. V., & Coffey, E. T. (2020) · eNeuro · doi:10.1523/eneuro.0303-19.2019 · Cited by 18

Cable theory of protein receptor trafficking in a dendritic tree

Bressloff, P. C. (2009) · Physical Review E · doi:10.1103/physreve.79.041904 · Cited by 18

The biophysical basis underlying the maintenance of early phase long-term potentiation

Becker, M., & Tetzlaff, C. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008813 · Cited by 22

Regulation of the intracellular distribution, cell surface expression, and protein levels of AMPA receptor GluR2 subunits by the monocarboxylate transporter MCT2 in neuronal cells

Maekawa, F., Tsuboi, T., & Pellerin, L. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06100.x · Cited by 19

Molecular Characterization of AMPA-Receptor-Containing Vesicles

Peters, J. J., Leitz, J., Oses-Prieto, J. A., Burlingame, A. L., & Brunger, A. T. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.754631 · Cited by 18

Activity-dependent diffusion trapping of AMPA receptors as a key step for expression of early LTP

Nowacka, A., Getz, A. M., Bessa‐Neto, D., & Choquet, D. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0220 · Cited by 21

TSPAN7

Bassani, S., & Passafaro, M. (2012) · BioArchitecture · doi:10.4161/bioa.20829 · Cited by 22

APPL1 gates long-term potentiation through its plekstrin homology domain

Fernández‐Monreal, M., Sánchez‐Castillo, C., & Esteban, J. A. (2016) · Journal of Cell Science · doi:10.1242/jcs.183475 · Cited by 17

Impaired synaptic scaling in mouse hippocampal neurones expressing NMDA receptors with reduced calcium permeability

Pawlak, V., Schupp, B. J., Single, F. N., Seeburg, P. H., & Köhr, G. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.076794 · Cited by 18

Trafficking of calcium-permeable and calcium-impermeable AMPA receptors in nucleus accumbens medium spiny neurons co-cultured with prefrontal cortex neurons

Werner, C. T., Murray, C. H., Reimers, J. M., Chauhan, N. M., Woo, K., Molla, H. M., Loweth, J. A., & Wolf, M. E. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.12.014 · Cited by 15

Localizing Proton-Mediated Inhibitory Feedback at the Retinal Horizontal Cell–Cone Synapse with Genetically-Encoded pH Probes

Beckwith‐Cohen, B., Holzhausen, L. C., Wang, T.-M., Rajappa, R., & Krämer, R. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1541-18.2018 · Cited by 16

Prenatal Nutritional Intervention Reduces Autistic-Like Behavior Rates Among Mthfr-Deficient Mice

Orenbuch, A., Fortis, K., Taesuwan, S., Yaffe, R., Caudill, M. A., & Golan, H. M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00383 · Cited by 16

Trafficking and Activity of Glutamate and GABA Receptors: Regulation by Cell Adhesion Molecules

Keable, R., Leshchyns’ka, I., & Sytnyk, V. (2020) · The Neuroscientist · doi:10.1177/1073858420921117 · Cited by 16

Insulin-Dependent Maturation of Newly Generated Olfactory Sensory Neurons after Injury

Kuboki, A., Kikuta, S., Otori, N., Kojima, H., Matsumoto, I., Reisert, J., & Yamasoba, T. (2021) · eNeuro · doi:10.1523/eneuro.0168-21.2021 · Cited by 16

AMPA Receptor Regulation and the Reversal of Synaptic Plasticity – LTP, LTD, Depotentiation, and Dedepression

Lee, H., & Huganir, R. L. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00035-8 · Cited by 15

Subunit-specific surface mobility of differentially labeled AMPA receptor subunits

Kropf, M., Rey, G., Glauser, L., Kulangara, K., Johnsson, K., & Hirling, H. (2008) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2008.02.014 · Cited by 15

Social isolation perturbs experience‐driven synaptic glutamate receptor subunit 4 delivery in the developing rat barrel cortex

Miyazaki, T., Kunii, M., Jitsuki, S., Sano, A., Kuroiwa, Y., & Takahashi, T. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12188 · Cited by 15

Contextual fear memory modulates PSD95 phosphorylation, AMPAr subunits, PKMζ and PI3K differentially between adult and juvenile rats

Zanca, R. M., Sanay, S., Avila, J. A., Rodriguez, E., Shair, H. N., & Serrano, P. A. (2018) · Neurobiology of Stress · doi:10.1016/j.ynstr.2018.11.002 · Cited by 16

AMPA Receptor Phosphorylation in Synaptic Plasticity: Insights from Knockin Mice

Kittler, J. T., & Moss, S. J. (2006) · CRC Press eBooks · doi:10.1201/9780203486283-17 · Cited by 16

Sustained treatment with an α5 GABA A receptor negative allosteric modulator delays excitatory circuit development while maintaining GABAergic neurotransmission

Nuwer, J. L., Brady, M. L., Povysheva, N. V., Coyne, A., & Jacob, T. C. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108724 · Cited by 14

Involvement of AMPA Receptor GluR2 and GluR3 Trafficking in Trigeminal Spinal Subnucleus Caudalis and C1/C2 Neurons in Acute-Facial Inflammatory Pain

Miyamoto, M., Tsuboi, Y., Honda, K., Kobayashi, M., Takamiya, K., Huganir, R., Kondo, M., Shinoda, M., Sessle, B., Katagiri, A., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044055 · Cited by 15

Distributed interfacing by nanoscale photodiodes enables single-neuron light activation and sensory enhancement in 3D spinal explants

Thalhammer, A., Fontanini, M., Shi, J., Scaini, D., Recupero, L., Evtushenko, A. S., Fu, Y., Pavagada, S., Bistrović, A., Fruk, L., et al. (2022) · Science Advances · doi:10.1126/sciadv.abp9257 · Cited by 14

AMPA Receptor Activation Causes Silencing of AMPA Receptor-Mediated Synaptic Transmission in the Developing Hippocampus

Wasling, P., Strandberg, J., & Hanse, E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034474 · Cited by 14

Rapid visual stimulation increases extrasynaptic glutamate receptor expression but not visual‐evoked potentials in the adult rat primary visual cortex

Eckert, M. J., Guévremont, D., Williams, J. M., & Abraham, W. C. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12053 · Cited by 13

A neurochemical signature of visual recovery after extrastriate cortical damage in the adult cat

Huxlin, K. R., Williams, J. M., & Price, T. A. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21658 · Cited by 14

Glutamate receptors on the move

Sheng, M., & Nakagawa, T. (2002) · Nature · doi:10.1038/417601a · Cited by 12

RNA interference of Xenopus NMDAR NR1 in vitro and in vivo

Miskevich, F., Doench, J. G., Townsend, M., Sharp, P. A., & Constantine‐Paton, M. (2005) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2005.08.010 · Cited by 13

Long-Term Potentiation

Lisman, J. E., & Hell, J. W. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_17 · Cited by 12

The functional role of all postsynaptic potentials examined from a first-person frame of reference

Vadakkan, K. I. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2015-0036 · Cited by 13

Protein kinase D promotes activity‐dependent AMPA receptor endocytosis in hippocampal neurons

Morales, C. O. O., Ignácz, A., Bencsik, N., Szíber, Z., Rátkai, A. E., Lieb, W. S., Eisler, S. A., Szűcs, A. L., Schlett, K., & Haußer, A. (2021) · Traffic · doi:10.1111/tra.12819 · Cited by 10

Inhibiting PTEN Protects Hippocampal Neurons against Stretch Injury by Decreasing Membrane Translocation of AMPA Receptor GluR2 Subunit

Liu, Y., Wang, L., Long, Z.-Y., Wu, Y., Wan, Q., Jiang, J., & Wang, Z. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065431 · Cited by 12

The tetraspanin TSPAN5 regulates AMPAR exocytosis by interacting with the AP4 complex

Moretto, E., Longatti, A., Miozzo, F., Bonnet, C., Coussen, F., Jaudon, F., Cingolani, L. A., & Passafaro, M. (2023) · eLife · doi:10.7554/elife.76425 · Cited by 11

Evidence of Glutamatergic Dysfunction in the Pathophysiology of Schizophrenia

Hammond, J. C., Shan, D., Meador‐Woodruff, J. H., & McCullumsmith, R. E. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1056-4_15 · Cited by 12

Brownian diffusion of AMPA receptors is sufficient to explain fast onset of LTP

Tölle, D., & Novère, N. G. L. (2010) · BMC Systems Biology · doi:10.1186/1752-0509-4-25 · Cited by 12

Proteins Involved in the Trafficking and Functional Synaptic Expression of AMPA and KA Receptors

Rue, S. A. D. L., & Henley, J. M. (2002) · The Scientific World JOURNAL · doi:10.1100/tsw.2002.97 · Cited by 10

Acute inhibition of AMPA receptors by perampanel reduces amyloid β‐protein levels by suppressing β‐cleavage of APP in Alzheimer's disease models

Ueda, S., Kuzuya, A., Kawata, M., Okawa, K., Honjo, C., Wada, T., Matsumoto, M., Goto, K., Miyamoto, M., Yonezawa, A., et al. (2023) · The FASEB Journal · doi:10.1096/fj.202300837r · Cited by 10

Differences in AMPA and GABAA/B receptor subunit expression between the chronically reorganized cortex and brainstem of adult squirrel monkeys

Mowery, T. M., Sarin, R. M., Kostylev, P. V., & Garraghty, P. E. (2015) · Brain Research · doi:10.1016/j.brainres.2015.03.010 · Cited by 11

Spatial dynamics of the insulin receptor in living neurons

Gralle, M., Labrecque, S., Salesse, C., & Koninck, P. D. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14950 · Cited by 10

PKA-Dependent Membrane Surface Recruitment of CI-AMPARs Is Crucial for BCP-Mediated Protection Against Post-acute Ischemic Stroke Cognitive Impairment

Chen, S., Wang, Y., Wang, X., He, M. Q., Zhang, L., & Dong, Z. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.566067 · Cited by 10

Pharmacological Investigation of Fluoro-Gold Entry into Spinal Neurons

Falgairolle, M., & O'Donovan, M. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0131430 · Cited by 11

Analysis of the Potential Role of GluA4 Carboxyl-Terminus in PDZ Interactions

Coleman, S. K., Cai, C., Kalkkinen, N., Korpi, E. R., & KEINÄNEN, K. P. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008715 · Cited by 10

Molecular Organization and Regulation of Glutamate Receptors in Developing and Adult Mammalian Central Nervous Systems

Molnár, E. (2008) · Springer eBooks · doi:10.1007/978-0-387-30382-6_17 · Cited by 11

Proteasomal-Mediated Degradation of AKAP150 Accompanies AMPAR Endocytosis during cLTD

Cheng, W., Siedlecki‐Wullich, D., Català-Solsona, J., Fábregas, C., Fadó, R., Casals, N., Solé, M., Unzeta, M., Saura, C. A., Rodrı́guez-Álvarez, J., et al. (2020) · eNeuro · doi:10.1523/eneuro.0218-19.2020 · Cited by 10

AMPA receptors in the evolving synapse: structure, function, and disease implications

Francis, F., Chettri, D., & Nair, D. K. (2025) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2025.1661342 · Cited by 9

Monitoring cell membrane recycling dynamics of proteins using whole-cell fluorescence recovery after photobleaching of pH-sensitive genetic tags

Michaluk, P., & Rusakov, D. A. (2022) · Nature Protocols · doi:10.1038/s41596-022-00732-4 · Cited by 9

Increased insulin receptor expression in anterior temporal neocortex of patients with intractable epilepsy

Wang, L., Liu, G., He, M., Shen, L., Shen, D., Lü, Y., & Wang, X. (2010) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2010.06.005 · Cited by 9

PI 3-kinase and PKCζ mediate insulin-induced potentiation of NMDA receptor currents in Xenopus oocytes

Jones, M. L., Liao, G., Malecki, R., Li, M., Salazar, N. M., & Leonard, J. P. (2011) · Brain Research · doi:10.1016/j.brainres.2011.11.020 · Cited by 9

GABAA receptor membrane insertion rates are specified by their subunit composition

Joshi, S., Keith, K. J., Ilyas, A., & Kapur, J. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.05.003 · Cited by 9

The Insulin/IGF Signaling Regulators Cytohesin/GRP-1 and PIP5K/PPK-1 Modulate Susceptibility to Excitotoxicity in C. elegans

Tehrani, N., Rosario, J. S. D., Dominguez, M., Kalb, R. G., & Mano, I. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113060 · Cited by 9

Visualization of Exo- and Endocytosis of AMPA Receptors During Hippocampal Synaptic Plasticity Around Postsynaptic-Like Membrane Formed on Glass Surface

Hirano, T. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00442 · Cited by 10

Endocytosis of AMPA receptors: Role in neurological conditions

Bencsik, N., Morales, C. O. O., Haußer, A., & Schlett, K. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.09.007 · Cited by 9

Regulated delivery of AMPA receptor subunits to the presynaptic membrane

Schenk, U., Verderio, C., Benfenati, F., & Matteoli, M. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg059 · Cited by 48

Real-Time Imaging of Discrete Exocytic Events Mediating Surface Delivery of AMPA Receptors

Yudowski, G. A., Puthenveedu, M. A., Leonoudakis, D., Panicker, S., Thorn, K. S., Beattie, E. C., & von Zastrow, M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2465-07.2007 · Cited by 197

Separate Paths to the Surface

(2001) · Science s STKE · doi:10.1126/stke.2001.82.tw4

Trafficking of AMPA Receptors at Plasma Membranes of Hippocampal Neurons

Tao-Cheng, J.-H., Crocker, V. T., Winters, C. A., Azzam, R., Chludzinski, J., & Reese, T. S. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4745-10.2011 · Cited by 82

Subunit-Specific Rules Governing AMPA Receptor Trafficking to Synapses in Hippocampal Pyramidal Neurons

Shi, S.-H., Hayashi, Y., Esteban, J. A., & Malinow, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00321-x · Cited by 1,094