Regulation of AMPA receptor lateral movements

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

Calcium Signaling in Neurons: Molecular Mechanisms and Cellular Consequences

Ghosh, A., & Greenberg, M. E. (1995) · Science · doi:10.1126/science.7716515 · Cited by 1,411

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

Regulation of distinct AMPA receptor phosphorylation sites during bidirectional synaptic plasticity

Lee, H.-K., Barbarosie, M., Kameyama, K., Bear, M. F., & Huganir, R. L. (2000) · Nature · doi:10.1038/35016089 · Cited by 1,116

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

Regulation of AMPA receptor endocytosis by a signaling mechanism shared with LTD

Beattie, E. C., Carroll, R. C., Yu, X., Morishita, W., Yasuda, H., von Zastrow, M., & Malenka, R. C. (2000) · Nature Neuroscience · doi:10.1038/81823 · Cited by 745

Regulation of AMPA Receptor–Mediated Synaptic Transmission by Clathrin-Dependent Receptor Internalization

Man, H., Lin, J., Ju, W. H., Ahmadian, G., Liu, L., Becker, L. E., Sheng, M., & Wang, Y. T. (2000) · Neuron · doi:10.1016/s0896-6273(00)81067-3 · Cited by 711

Role of AMPA Receptor Cycling in Synaptic Transmission and Plasticity

Lüscher, C., Xia, H., Beattie, E. C., Carroll, R. C., von Zastrow, M., Malenka, R. C., & Nicoll, R. A. (1999) · Neuron · doi:10.1016/s0896-6273(00)81119-8 · Cited by 692

Distinct molecular mechanisms and divergent endocytotic pathways of AMPA receptor internalization

Lin, J., Ju, W. H., Foster, K. A., Lee, S. H., Ahmadian, G., Wyszynski, M. W., Wang, Y. T., & Sheng, M. (2000) · Nature Neuroscience · doi:10.1038/81814 · Cited by 562

The role of PKMζ in the maintenance of long-term memory: a review

Patel, H., & Zamani, R. (2021) · Reviews in the Neurosciences · doi:10.1515/revneuro-2020-0105 · Cited by 23

The role of molecular diffusion within dendritic spines in synaptic function

Obashi, K., Taraska, J. W., & Okabe, S. (2021) · The Journal of General Physiology · doi:10.1085/jgp.202012814 · Cited by 24

AMPA Receptors: A Key Piece in the Puzzle of Memory Retrieval

Pereyra, M., & Medina, J. H. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.729051 · Cited by 26

Brownian Motion in Dire Straits

Holcman, D., & Schuss, Z. (2012) · Multiscale Modeling and Simulation · doi:10.1137/110857519 · Cited by 22

Phospho-dependent Accumulation of GABABRs at Presynaptic Terminals after NMDAR Activation

Hannan, S. B., Gerrow, K., Triller, A., & Smart, T. G. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.021 · Cited by 21

Quantum dot conjugated nanobodies for multiplex imaging of protein dynamics at synapses

Modi, S., Higgs, N., Sheehan, D. F., Griffin, L. D., & Kittler, J. T. (2018) · Nanoscale · doi:10.1039/c7nr09130c · Cited by 21

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

The role of dendritic spine morphology in the compartmentalization and delivery of surface receptors

Simon, C. M., Hepburn, I., Chen, W., & Schutter, E. D. (2013) · Journal of Computational Neuroscience · doi:10.1007/s10827-013-0482-4 · Cited by 21

Auxiliary subunits provide new insights into regulation of AMPA receptor trafficking

Sumioka, A. (2013) · The Journal of Biochemistry · doi:10.1093/jb/mvt015 · Cited by 21

A role for the cytoskeleton in heat‐shock–mediated thermoprotection of locust neuromuscular junctions

Klose, M. K., Armstrong, G. A. B., & Robertson, R. M. (2004) · Journal of Neurobiology · doi:10.1002/neu.20058 · Cited by 21

Inhibiting Hippo pathway kinases releases WWC1 to promote AMPAR-dependent synaptic plasticity and long-term memory in mice

Stepan, J., Heinz, D. E., Dethloff, F., Wiechmann, S., Martinelli, S., Hafner, K., Ebert, T., Junglas, E., Häusl, A. S., Pöhlmann, M. L., et al. (2024) · Science Signaling · doi:10.1126/scisignal.adj6603 · Cited by 20

Hippo-released WWC1 facilitates AMPA receptor regulatory complexes for hippocampal learning

Stepan, J., Heinz, D. E., Dethloff, F., Bajaj, T., Zellner, A., Hafner, K., Wiechmann, S., Mackert, S., Mecdad, Y., Rabenstein, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111766 · Cited by 20

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

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

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

Proton-triggered rearrangement of the AMPA receptor N-terminal domains impacts receptor kinetics and synaptic localization

Ivica, J., Kejzar, N., Ho, H., Stockwell, I., Kuchtiak, V., Scrutton, A. M., Nakagawa, T., & Greger, I. H. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01369-5 · Cited by 20

Functional differences between D1 and D5 revealed by high resolution imaging on live neurons

Kruusmägi, M., Kumar, S., Zelenin, S. M., Brismar, H., Aperia, A. C., & Scott, L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.052 · Cited by 19

Targeting cell surface trafficking of pain-facilitating receptors to treat chronic pain conditions

Ma, W., & Quirion, R. (2014) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2014.887683 · Cited by 19

N‐terminal SAP97 isoforms differentially regulate synaptic structure and postsynaptic surface pools of AMPA receptors

Goodman, L., Baddeley, D., Ambroziak, W., Waites, C. L., Garner, C. C., Soeller, C., & Montgomery, J. M. (2017) · Hippocampus · doi:10.1002/hipo.22723 · Cited by 20

zapERtrap: A light-regulated ER release system reveals unexpected neuronal trafficking pathways

Bourke, A. M., Schwartz, S. L., Bowen, A. B., Kleinjan, M. S., Winborn, C. S., Kareemo, D. J., Gutnick, A., Schwarz, T. L., & Kennedy, M. J. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202103186 · Cited by 19

Synaptic Basis of Behavioral Timescale PlasticityPreprint

Gonzalez, K. C., Negrean, A., Liao, Z., Polleux, F., & Losonczy, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.04.560848 · Cited by 20

Alteration in the Synaptic and Extrasynaptic Organization of AMPA Receptors in the Hippocampus of P301S Tau Transgenic Mice

Alfaro‐Ruiz, R., Aguado, C., Martín‐Belmonte, A., Moreno‐Martínez, A. E., Merchán‐Rubira, J., Hernández, F., Ávila, J., Fukazawa, Y., & Luján, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113527 · Cited by 19

Mobility of NMDA autoreceptors but not postsynaptic receptors at glutamate synapses in the rat entorhinal cortex

Yang, J. F., Chamberlain, S. E. L., Woodhall, G. L., & Jones, R. S. G. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.157974 · Cited by 18

Molecular membrane dynamics: Insights into synaptic function and neuropathological disease

Bannai, H. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.07.007 · Cited by 18

Lateral Diffusion of the GABAB Receptor Is Regulated by the GABAB2 C Terminus

Pooler, A. M., & McIlhinney, R. A. J. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702358200 · Cited by 18

Non-canonical interplay between glutamatergic NMDA and dopamine receptors shapes synaptogenesis

Bénac, N., Saraceno, G. E., Butler, C., Kuga, N., Nishimura, Y., Yokoi, T., Su, P., Sasaki, T., Petit‐Pedrol, M., Galland, R., et al. (2024) · Nature Communications · doi:10.1038/s41467-023-44301-z · Cited by 17

Developmental perfluorooctane sulfonate exposure inhibits long-term potentiation by affecting AMPA receptor trafficking

Zhang, Q., Liu, W., Zhao, H., Zhang, Z., Qin, H., Luo, F., & Niu, Q. L. (2018) · Toxicology · doi:10.1016/j.tox.2018.11.015 · Cited by 18

Dynamics of surface neurotransmitter receptors and transporters in glial cells: Single molecule insights

Ciappelloni, S., Murphy‐Royal, C., Dupuis, J. P., Oliet, S. H. R., & Groc, L. (2017) · Cell Calcium · doi:10.1016/j.ceca.2017.08.009 · Cited by 16

How Receptor Surface Diffusion and Cell Rotation Increase Association Rates

Lawley, S. D., & Miles, C. E. (2019) · SIAM Journal on Applied Mathematics · doi:10.1137/18m1217188 · 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

Postsynaptic Targeting and Mobility of Membrane Surface-Localized hASIC1a

Song, X.-L., Liu, D.-S., Qiang, M., Li, Q., Liu, M., Li, W., Qi, X., Xu, N., Yang, G., Zhu, M. X., et al. (2020) · Neuroscience Bulletin · doi:10.1007/s12264-020-00581-9 · Cited by 17

New approaches for solving old problems in neuronal protein trafficking

Bourke, A. M., Bowen, A. B., & Kennedy, M. J. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.04.004 · Cited by 17

Ultra-sensitive detection of individual gold nanoparticles: spectroscopy and applications to biology

Cognet, L., & Lounis, B. (2008) · Gold bulletin · doi:10.1007/bf03216591 · Cited by 16

Live-cell imaging of receptors around postsynaptic membranes

Tanaka, H., Fujii, S., & Hirano, T. (2013) · Nature Protocols · doi:10.1038/nprot.2013.171 · 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

Ligand-Induced Dynamics of Neurotrophin Receptors Investigated by Single-Molecule Imaging Approaches

Marchetti, L., Luin, S., Bonsignore, F., Nadai, T. D., Beltram, F., & Cattaneo, A. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16011949 · 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

Pin1 Binding to Phosphorylated PSD-95 Regulates the Number of Functional Excitatory Synapses

Delgado, J. Y., Nall, D., & Selvin, P. R. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00010 · Cited by 15

Intracellular Ca 2+ and not the extracellular matrix determines surface dynamics of AMPA-type glutamate receptors on aspiny neurons

Klueva, J., Gundelfinger, E. D., Frischknecht, R., & Heine, M. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0605 · Cited by 15

Imaging synaptic plasticity

Padamsey, Z., & Emptage, N. J. (2011) · Molecular Brain · doi:10.1186/1756-6606-4-36 · Cited by 15

Organization and dynamics of AMPA receptors inside synapses—nano-organization of AMPA receptors and main synaptic scaffolding proteins revealed by super-resolution imaging

Hosy, E., Butler, C., & Sibarita, J. (2014) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2014.05.017 · Cited by 18

A Revised View on the Role of Surface AMPAR Mobility in Tuning Synaptic Transmission: Limitations, Tools, and Alternative Views

Delgado, J. Y., & Selvin, P. R. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00021 · Cited by 16

Cell biochemistry studied by single-molecule imaging

Mashanov, G. I., Nenasheva, T. A., Peckham, M., & Molloy, J. E. (2006) · Biochemical Society Transactions · doi:10.1042/bst0340983 · Cited by 15

Spatial patterns and cell surface clusters in perineuronal nets

Arnst, N., Kuznetsova, S., Lipachev, N., Shaikhutdinov, N., Melnikova, A., Олегович, М. М., Uvarov, P., Baltina, T., Rauvala, H., Osin, Y. N., et al. (2016) · Brain Research · doi:10.1016/j.brainres.2016.07.020 · Cited by 15

APPsα rescues impaired Ca 2+ homeostasis in APP- and APLP2-deficient hippocampal neurons

Ludewig, S., Herrmann, U., Michaelsen‐Preusse, K., Metzdorf, K., Just, J., Bold, C. S., Müller, U., & Körte, M. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2011506118 · Cited by 14

Rapid non-classical effects of steroids on the membrane receptor dynamics and downstream signaling in neurons

Barabás, K., Godó, S., Lengyel, F., Ernszt, D., Pál, J., & Ábrahám, I. M. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.05.008 · Cited by 18

Overuse of high stability antibiotics and its consequences in public and environmental health.

Zdziarski, P., Simon, K. A., & Majda, J. (2003) · PubMed · Cited by 14

The enigma of transmitter-selective receptor accumulation at developing inhibitory synapses

Meier, J. C. (2003) · Cell and Tissue Research · doi:10.1007/s00441-002-0694-9 · Cited by 14

Syngap1Disruption Induced by Recombination between Inverted loxP Sites Is Associated with Hippocampal Interneuron Dysfunction

Khlaifia, A., Jadhav, V., Danik, M., Badra, T., Berryer, M. H., Dionne‐Laporte, A., Chattopadhyaya, B., Cristo, G. D., Lacaille, J., & Michaud, J. L. (2023) · eNeuro · doi:10.1523/eneuro.0475-22.2023 · Cited by 13

Learning complex temporal patterns with resource-dependent spike timing-dependent plasticity

Hunzinger, J. F., Chan, V. H., & Froemke, R. C. (2012) · Journal of Neurophysiology · doi:10.1152/jn.01150.2011 · Cited by 13

Synaptic Capture of Laterally Diffusing AMPA Receptors – An Idea That Stuck

Hastings, M. H., & Man, H. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.03.016 · Cited by 13

Fast Regulation of GABAAR Diffusion Dynamics by Nogo-A Signaling

Fricke, S., Metzdorf, K., Ohm, M., Haak, S., Heine, M., Körte, M., & Zagrebelsky, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.015 · Cited by 13

Nonchannel Functions of the Calcium Channel γ Subunit: Insight from Research on the Stargazer Mutant

Qiao, X., & Meng, H. (2003) · Journal of Bioenergetics and Biomembranes · doi:10.1023/b:jobb.0000008030.79380.fb · Cited by 13

Regulation of the Stability and Localization of Post-synaptic Membrane Proteins by Liquid-Liquid Phase Separation

Hosokawa, T., & Liu, P.-W. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.795757 · Cited by 12

Molecular mechanisms of AMPAR reversible stabilization at synapses

Bessa‐Neto, D., & Choquet, D. (2023) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2023.103856 · Cited by 12

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

Subdiffusion-limited fractional reaction-subdiffusion equations with affine reactions: Solution, stochastic paths, and applications

Lawley, S. D. (2020) · Physical review. E · doi:10.1103/physreve.102.042125 · Cited by 12

Surface Traffic in Synaptic Membranes

Heine, M. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-3-7091-0932-8_9 · Cited by 13

Molecular remodeling mechanisms of the neural somatodendritic compartment

Moore, F. B., & Baleja, J. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.06.006 · Cited by 12

Glutamate receptors on the move

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

AMPA receptor diffusional trapping machinery as an early therapeutic target in neurodegenerative and neuropsychiatric disorders

Choquet, D., Opazo, P., & Zhang, H. (2025) · Translational Neurodegeneration · doi:10.1186/s40035-025-00470-z · Cited by 11

Lateral diffusion of inositol 1,4,5‐trisphosphate receptor type 1 in Purkinje cells is regulated by calcium and actin filaments

Fukatsu, K., Bannai, H., Inoue, T., & Mikoshiba, K. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06885.x · Cited by 11

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

Abl2:Cortactin Interactions Regulate Dendritic Spine Stability via Control of a Stable Filamentous Actin Pool

Shaw, J. E., Kilander, M. B. C., Lin, Y., & Koleske, A. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2472-20.2021 · Cited by 12

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

AMPA Receptor Subunits Get Their Share of the Pie

Béïque, J.-C., & Huganir, R. L. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.016 · Cited by 11

Cellular diffusion processes in singularly perturbed domains

Bressloff, P. C. (2024) · Journal of Mathematical Biology · doi:10.1007/s00285-024-02160-2 · Cited by 10

NMDA and AMPA receptor physiology and role in visceral hypersensitivity: a review

Cheng, F., Du, L., Kim, J. J., Zhu, F., He, H., & Dai, N. (2022) · European Journal of Gastroenterology & Hepatology · doi:10.1097/meg.0000000000002351 · Cited by 10

Photochemical Inactivation Analysis of Temporal Dynamics of Postsynaptic Native AMPA Receptors in Hippocampal Slices

Kamiya, H. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0720-12.2012 · Cited by 12

Self-crowding of AMPA receptors in the excitatory postsynaptic density can effectuate anomalous receptor sub-diffusion

Gupta, R. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005984 · Cited by 10

Ubiquitination, Protein Turnover, and Long-Term Synaptic Plasticity

Schwartz, J. H. (2003) · Science Signaling · doi:10.1126/stke.2003.190.pe26 · Cited by 10

Synapse-specific and plasticity-regulated AMPA receptor mobility tunes synaptic integration

Nowacka, A., Getz, A. M., Zieger, H. L., Malivert, M., Bessa‐Neto, D., Augusto, E., Breillat, C., Daburon, S., Lemoigne, C., Marais, S., et al. (2026) · Neuron · doi:10.1016/j.neuron.2025.12.004 · Cited by 10

Dysregulation of AMPA Receptor Trafficking and Intracellular Vesicular Sorting in the Prefrontal Cortex of Dopamine Transporter Knock-Out Rats

Targa, G., Mottarlini, F., Rizzi, B., Leo, D., Caffino, L., & Fumagalli, F. (2023) · Biomolecules · doi:10.3390/biom13030516 · Cited by 9

Loss of the proton-activated chloride channel in neurons impairs AMPA receptor endocytosis and LTD via endosomal hyper-acidification

Chen, K. H., Yang, J., Liu, B., Jiang, C., Koylass, N., Zhang, Z., Sun, S., Huganir, R. L., & Qiu, Z. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115302 · Cited by 10

Activation-Dependent Rapid Postsynaptic Clustering of Glycine Receptors in Mature Spinal Cord Neurons

Nakahata, Y., Eto, K., Murakoshi, H., Watanabe, M., Kuriu, T., Hirata, H., Moorhouse, A. J., Ishibashi, H., & Nabekura, J. (2017) · eNeuro · doi:10.1523/eneuro.0194-16.2017 · Cited by 9

Glutamatergic Receptor Trafficking and Delivery: Role of the Exocyst Complex

Lira, M., Mira, R. G., Carvajal, F. J., Zamorano, P. L., Inestrosa, N. C., & Cerpa, W. F. (2020) · Cells · doi:10.3390/cells9112402 · Cited by 9

Spot patterns of the Schnakenberg reaction–diffusion system on a curved torus

Tzou, J. C., & Tzou, L. (2019) · Nonlinearity · doi:10.1088/1361-6544/ab5161 · Cited by 9

Energetics of stochastic BCM type synaptic plasticity and storing of accurate information

Karbowski, J. (2021) · Journal of Computational Neuroscience · doi:10.1007/s10827-020-00775-0 · Cited by 8

Molecular composition of developing glutamatergic synapses

Sell, G. L., Barrow, S. L., & McAllister, A. K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00001-6 · Cited by 8

Stochastic lattice model of synaptic membrane protein domains

Li, Y., Kahraman, O., & Haselwandter, C. A. (2017) · Physical review. E · doi:10.1103/physreve.95.052406 · Cited by 8

The M3/M4 cytoplasmic loop of the α1 subunit restricts GABAARs lateral mobility: A study using fluorescence recovery after photobleaching

Perán, M., Hooper, H., Boulaiz, H., Marchal, J. A., Aránega, A., & Salas, R. (2006) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20156 · Cited by 8

Neurochemical Basis for an Epigenetic Vision of Synaptic Organization

Costa, E., Grayson, D. R., Veldić, M., & Guidotti, A. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59004-9 · Cited by 8

Paradigm Shift of the Molecular Dynamics Concept in the Cell Membrane: High‐Speed Single‐Molecule Tracking Revealed the Partitioning of the Cell Membrane

Kusumi, A., Umemura, Y. M., Morone, N., & Fujiwara, T. K. (2008) · Wiley eBooks · doi:10.1002/9783527622979.ch19 · Cited by 8

Modification of the synaptic cleft under excitatory conditions

Tao-Cheng, J.-H., Moreira, S. L., Winters, C. A., Reese, T. S., & Döṣemeci, A. (2023) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2023.1239098 · Cited by 7

On the cause of sleep: Protein fragments, the concept of sentinels, and links to epilepsy

Varshavsky, A. J. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1904709116 · Cited by 8

Enhanced apoptosis and decreased ampa receptors are involved in deficit in fear memory in rin1 knockout rats

Ma, L., Chen, X., Zhao, B., Shi, Y., & Han, F. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.02.040 · Cited by 7

Local accumulation times in a diffusion-trapping model of receptor dynamics at proximal axodendritic synapses

Schumm, R. D., & Bressloff, P. C. (2022) · Physical review. E · doi:10.1103/physreve.105.064407 · Cited by 7

Disuse plasticity limits spinal cord injury recovery

Morioka, K., Tazoe, T., Huie, J. R., Hayakawa, K., Okazaki, R., Guandique, C. F., de Almeida, C., Haefeli, J., Hamanoue, M., Endoh, T., et al. (2025) · iScience · doi:10.1016/j.isci.2025.112180 · Cited by 6

Postsynaptic Machinery for Receptor Trafficking

Condon, K. H., & Ehlers, M. (2007) · Elsevier eBooks · doi:10.1016/b978-012369437-9/50013-x · Cited by 6

Long and short distance movements of β2-adrenoceptor in cell membrane assessed by photoconvertible fluorescent protein dendra2–β2-adrenoceptor fusion

Kaya, A. İ., Uğur, Ö., Altuntaş, O., Sayar, K., & Onaran, H. O. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.05.008 · Cited by 6

A Multiscale Analysis of Diffusions on Rapidly Varying Surfaces

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