The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
AMPA Receptor Incorporation into Synapses during LTP: The Role of Lateral Movement and Exocytosis
Open accessAbstract
The regulated trafficking of AMPA receptors (AMPARs) to synapses is thought to underlie the enhanced transmission in long-term potentiation (LTP), a cellular model of memory. However, there is controversy regarding the nonsynaptic site, either on the surface or intracellularly, from which AMPARs move into synapses during LTP. Using recombinant surface-fluorescent receptors in organotypic rat hippocampal slices, we show that the majority of AMPARs incorporated into synapses during LTP is from lateral diffusion of spine surface receptors containing GluR1, an AMPAR subunit. Following synaptic potentiation, AMPARs in intracellular pools containing GluR1 are driven to the surface primarily on dendrites. These exocytosed receptors likely serve to replenish the local extrasynaptic pool available for subsequent bouts of plasticity. These results clarify the role of intracellular and surface AMPARs during synaptic plasticity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Numerous studies have shown that blocking postsynaptic exocytosis by a variety of means blocks LTP/sLTP (195, 249, 250, 332–338).”
From Synaptic memory and CaMKII (2023) · cites this paper as [249]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Surface localized AMPARs are supplied by exocytosis from pools of intracellular receptors contained within endosomes (Lin et al., 2009, Makino and Malinow, 2009).”
From The AMPA Receptor Code of Synaptic Plasticity (2018) · cites this paper as Makino and Malinow, 2009
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Large packets of GluA1 are inserted into the dendritic shaft from intracellular recycling endosomes, containing an estimated fifty GluA1-containing receptors, in an activity-dependent manner (Lin et al., 2009, Makino and Malinow, 2009).”
From The AMPA Receptor Code of Synaptic Plasticity (2018) · cites this paper as Makino and Malinow, 2009
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Combining SEP-GluA1 photobleaching experiments with glutamate uncaging in organotypic slices revealed that synaptic potentiation of AMPA receptors is achieved by restricting their diffusion out of the synaptic membrane (Makino and Malinow, 2009).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Makino and Malinow, 2009
The cited source says what the claim attributes to it.
In the citing paper
“These synapses contain AMPARs, but LTP-inducing stimuli cause a rapid addition of AMPARs to the synapse (246–250).”
From Synaptic memory and CaMKII (2023) · cites this paper as [249]
The cited source says what the claim attributes to it.
In the citing paper
“These studies show that many synaptic proteins are remarkably dynamic, including AMPARs (237, 249, 327, 328), NMDARs (329), CaMKII (330), and scaffolding proteins, such as PSD-95 (331).”
From Synaptic memory and CaMKII (2023) · cites this paper as [249]
The cited source says what the claim attributes to it.
In the citing paper
“By tagging AMPARs with a pH-sensitive tag (SEP-GluA1), the insertion of AMPARs into the surface membrane can be directly visualized during LTP-inducing protocols (249, 250, 335, 337, 338, 340).”
From Synaptic memory and CaMKII (2023) · cites this paper as [249]
The cited source says what the claim attributes to it.
In the citing paper
“Fourth, in most cases the AMPARs are inserted via exocytosis into the dendritic shaft, some distance from the synapse (220, 249, 250, 337).”
From Synaptic memory and CaMKII (2023) · cites this paper as [249]
In the citing paper
“This form of plasticity shares many properties with Schaffer collateral LTP, including dependence on N-methyl-d-aspartate receptors (NMDARs), Rho GTPase signaling, Ca2+/calmodulin-dependent protein kinase II (CaMKII) phosphorylation, F-actin polymerization and synaptic AMPAR insertion (20–24).”
From Synaptic evidence for the efficacy of spaced learning (2012) · cites this paper as [23]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Self-citationStructural basis of long-term potentiation in single dendritic spines
Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483
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
Self-citationRapid 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
Self-citationAMPA 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
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
Shi, S.-H., Hayashi, Y., Esteban, J. A., & Malinow, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00321-x · Cited by 1,094
Self-citationReceptor 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
Petralia, R. S., & Wenthold, R. J. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903180309 · Cited by 1,003
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
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 500
Localising Receptors and Channels Across the Dendritic Arbour
Bikbaev, A. F., Duménieu, M., Lopez‐Rojas, J., & Heine, M. (2016) · Springer eBooks · doi:10.1007/978-4-431-56050-0_16 · Cited by 1
Запара, Т. А., Proskura, A. L., Malakhin, I. A., Vechkapova, S. O., & Ratushnyak, A. S. (2017) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-017-0430-2 · Cited by 1
Wong, V. C., Houlihan, P. R., Liu, H., Walpita, D., DeSantis, M. C., Liu, Z. J., & O’Shea, E. K. (2024) · eLife · doi:10.7554/elife.80622 · Cited by 2
Monitoring Synaptic Plasticity by Imaging AMPA Receptor Content and Dynamics on Dendritic Spines
Makino, H., & Li, B. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-444-9_25 · Cited by 1
Self-citationVogel III, E. W. (2017) · doi:10.7916/d8p273tk · Cited by 1
Bui, T. A., Shatto, J., Cuppens, T., Droit, A., & Bolduc, F. V. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.730987 · Cited by 1
Electrophysiological and Visual Tags
Graziane, N., & Dong, Y. (2022) · Neuromethods · doi:10.1007/978-1-0716-2589-7_21 · Cited by 1
Nayak, P. K. (2013) · Otago University Research Archive (University of Otago) · Cited by 1
Vadakkan, K. I. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/085589 · Cited by 1
Sound encoding in mutant mice with disrupted action potential generation
Yamanbaeva, G. (2018) · doi:10.53846/goediss-7005 · Cited by 1
Compans, B., Martineau, M., Klaassen, R. V., Bartol, T. M., Butler, C., Kechkar, A., Perrais, D., B, T. J. S. A., Sibarita, J., Smit, A. B., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/759191 · Cited by 1
The Role of Synaptic Plasticity in the Pathophysiology of Cocaine Addiction
Daneff, M., & Jadavji, N. M. (2019) · doi:10.22186/jyi.37.4.33-38 · Cited by 1
Protein Kinase D promotes activity-dependent AMPA receptor endocytosis in hippocampal neuronsPreprint
Morales, C. O. O., Ignácz, A., Bencsik, N., Rátkai, A. E., Lieb, W. S., Eisler, S. A., Szűcs, A. L., Schlett, K., & Hausser, A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.09.033514 · Cited by 1
Synaptic Organization of Surface AMPARs Changes by Brain Region and TauopathyPreprint
Vaidya, R. M., Zhang, J., Nall, D., Pendharkar, R., Lee, Y., Kim, E. C., Ma, D., Huang, F., Nonaka, H., Kiyonaka, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.22.604547 · Cited by 1
Role of vSNAREs in post-synaptic AMPAR trafficking, glutamatergic transmisson and plasticity
Bakr, M. (2020) · theses.fr (ABES) · doi:10.70675/32528bd6ze209z428fzbe94z1a44fc665a82 · Cited by 1
The role of Wnt signalling in excitatory hippocampal synapse formation and function
Anane, D. (2012) · UCL Discovery (University College London)
Sourial-Bassillious, N. (2010) · Figshare
Mishra, D. (2013) · Figshare
Neto, H. C. F. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2014.tde-19022015-143700
Luchkina, N. V. (2015) · Työväentutkimus Vuosikirja
Huupponen, J. (2013) · Työväentutkimus Vuosikirja
Stress, emotional learning and AMPA receptors: from behavior to molecule
Mengyuan, Z. (2011) · UvA-DARE (University of Amsterdam)
Spatiotemporal Kinetics of AMPAR Trafficking in Single Spines
Patterson, M. (2010) · DukeSpace (Duke University)
Characterisation of transgenic mouse models of Alzheimer's disease
Graham, L. (2011) · OpenGrey (Institut de l'Information Scientifique et Technique)
Probing the Lateral Diffusion of Individual Neurotransmitter Receptors
Petrini, E. M., & Barberis, A. (2014) · Advances in atom and single molecule machines · doi:10.1007/978-3-662-43367-6_11
Paulo, S., Humana, F., & Antunes, R. D. A. (2014)
Dynamics and function of nicotinic acetylcholine receptors in the nervous system
Fernandes, C. D. C. (2011) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
The Role of LMO4 in the Regulation of Hippocampal and Amygdalar Synaptic Function
Qin, Z. (2013) · uO Research (University of Ottawa) · doi:10.20381/ruor-2709
Electrophysiological and Visual Tags
Graziane, N., & Dong, Y. (2015) · Neuromethods · doi:10.1007/978-1-4939-3274-0_21
The organization of proteins involved in synaptic plasticity
Jacob, A. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/6mpm-0w63
Storage of spatiotemporal input sequences in dendrites of pyramidal neurons
Macak, M. (2016) · UCL Discovery (University College London)
Fulopova, B. (2015) · UTAS Research Repository · doi:10.25959/23238728
NOVEL APPROACHES TO THE STUDY OF SYNAPTIC PLASTICITY IN THE RAT HIPPOCAMPUS
Podor, B. (2017) · DalSpace (Dalhousie University)
Yin, S., Schulze, C., & Oertner, T. G. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/435446
Labrecque, S. (2012) · Corpus Université Laval (Université Laval)
The Development of Spatial Memory Processes and Associated Cellular Correlates in Juvenile Rats
Tzakis, N. (2020) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2020-13967
AMPA receptor trafficking in the developing and mature glutamatergic synapse
Catsburg, L. A. E., & MacGillavry, H. D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00023-5
Exciting inhibition: Local regulation of synapse formation and plasticity
Kruijssen, D. L. H. (2020) · Utrecht University Repository (Utrecht University) · doi:10.33540/296
Barberis, A., & Benfenati, F. (2014) · Springer eBooks · doi:10.1007/978-3-319-04924-3_9
Theoretical model of postsynaptic AMPA receptor trafficking during synaptic plasticity
Huang, H., & Yinyun, L. (2020) · Neurology and Neuroscience · doi:10.33425/2692-7918.1007
β-amyloid−driven synaptic depression requires PDZ protein interaction at AMPA-receptor subunit GluA3Preprint
Reinders, N. R., van der Spek, S. J. F., Klaassen, R. V., Koymans, K. J., Li, K. W., Smit, A. B., & Kessels, H. W. H. G. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.03.462970
Udeh‐Momoh, C. T., Yi, J. H., Piers, T. M., Waite, E., Whitehead, G., Whitcomb, D. J., Lightman, S. L., Cho, K. K., & Conway-Campbell, B. L. (2021) · Research Square · doi:10.21203/rs.3.rs-923210/v1
Hell, J. W. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.740118999.793586183
Santamarı́a, F., & Marinov, T. M. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_186-3
Santamarı́a, F., & Marinov, T. M. (2015) · Springer eBooks · doi:10.1007/978-1-4614-6675-8_186
Udeh‐Momoh, C. T., Piers, T. M., Yi, J. H., Waite, E., Whitehead, G., Whitcomb, D. J., Lightman, S. L., Cho, K. K., & Conway-Campbell, B. L. (2021) · Research Square · doi:10.21203/rs.3.rs-244813/v1
Natural Brains and Motivated, Emotional Mind
(2020) · Advances in human and social aspects of technology book series · doi:10.4018/978-1-7998-5653-5.ch004
Rab10 inactivation promotes AMPAR trafficking and spine enlargement during long-term potentiation
Wang, J., Nishiyama, J., Parra-Bueno, P., Okaz, E., Oz, G., Liu, X., Watabe, T., Suponitsky-Kroyter, I., McGraw, T. E., Szatmari, E. M., et al. (2025) · eLife · doi:10.7554/elife.103879.3
Disinhibition of Rab10 gates AMPAR insertion and spine enlargement during long-term potentiationPreprint
Wang, J., Nishiyama, J., Parra-Bueno, P., Okaz, E., Oz, G., Liu, X., Suponitsky-Kroyter, I., McGraw, T. E., Szatmari, E. M., & Yasuda, R. (2022) · Research Square · doi:10.21203/rs.3.rs-1691042/v1
AMPA Receptor Number and Dynamics on a Synapse-to-Synapse Basis During Maintenance of Chemical LTPPreprint
Jin, C., Jang, S.-S., Ge, P., Chung, H. J., & Selvin, P. R. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4112547
Santamarı́a, F., & Marinov, T. M. (2022) · Springer eBooks · doi:10.1007/978-1-0716-1006-0_186
Scheefhals, N. (2022) · Utrecht University Repository (Utrecht University) · doi:10.33540/1224
Modulação da plasticidade sináptica por TREK-1 e 5HT>sub<1A>/sub< no estresse crônico pós-natal.
de Oliveira, J. F. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2020.tde-23092021-134813
Montecinos-Oliva, C. (2018) · theses.fr (ABES) · doi:10.70675/1cb0a505zb904z4045z83b4z7ec8f3bc62b9
2D materials ratchet up biorealism in computing
Koppens, F. H. L., Aimone, J. B., & Chance, F. S. (2023) · Nature · doi:10.1038/d41586-023-03791-z
Synaptic Tagging and Metaplasticity as Mediators of Neuronal Consciousness
Maity, S., & Connor, S. A. (2024) · Springer eBooks · doi:10.1007/978-3-031-54864-2_11
Demystifying Narp in the context of stroke
Lau, G. L. (2024) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2024-15949
The Role of Elevated Glucocorticoid Levels in Alzheimer’s Disease PathologiesPreprint
Woo, S. (2024) · doi:10.58445/rars.1693
Rab10 inactivation promotes AMPAR trafficking and spine enlargement during long-term potentiationPreprint
Wang, J., Nishiyama, J., Parra-Bueno, P., Okaz, E., Oz, G., Liu, X., Watabe, T., Suponitsky-Kroyter, I., McGraw, T. E., Szatmari, E. M., et al. (2024) · eLife · doi:10.7554/elife.103879
Rab10 inactivation promotes AMPAR insertion and spine enlargement during long-term potentiationPreprint
Wang, J., Nishiyama, J., Parra-Bueno, P., Okaz, E., Oz, G., Liu, X., Watabe, T., Suponitsky-Kroyter, I., McGraw, T. E., Szatmari, E. M., et al. (2024) · eLife · doi:10.7554/elife.103879.1
Retrodictive Evidence for the Structure of Memory EngramPreprint
Vadakkan, K. I. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5072253
Rab10 inactivation promotes AMPAR trafficking and spine enlargement during long-term potentiationPreprint
Wang, J., Nishiyama, J., Parra-Bueno, P., Okaz, E., Oz, G., Liu, X., Watabe, T., Suponitsky-Kroyter, I., McGraw, T. E., Szatmari, E. M., et al. (2025) · eLife · doi:10.7554/elife.103879.2 · Cited by 1
Ryzhova, I. V., Vershinina, E. A., Markov, A. G., & Tobias, T. V. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl38852
Shontell, R. M., Araki, D., Ormsbee, K. M., Delgado, D. D., & Nichols, R. A. (2025) · eNeuro · doi:10.1523/eneuro.0044-25.2025
Intracellular regulation of a serotonin-gated ion channel links receptor trafficking to memory
Cesar, L. C., Zabeo, D., Cellini, A., Aspholm, E. E., Kolsrud, A., Panagaki, D., Höög, J. L., & Morud, J. (2026) · iScience · doi:10.1016/j.isci.2026.117309
Intercellular Communication and Heterosynaptic Metaplasticity in the Rodent Hippocampus
Jones, O. D. (2014) · Otago University Research Archive (University of Otago)
Hippocampal plasticity underlying learning and memory processes in healthy and diseased conditions
Petsophonsakul, P. (2017) · theses.fr (ABES) · doi:10.70675/5fdda64ez871dz42c8za517zf44c3618705e
Mécanisme d’activation neuronale de mTORC1 et de son altération par le peptide amyloïde β
Khamsing, D. (2017) · theses.fr (ABES) · doi:10.70675/8081dbf0zf76bz43bdza502z6c0c6c419856
Contribution of the potassium / chloride cotransporter KCC2 to hippocampal rhythmopathy
Goutierre, M. (2018) · theses.fr (ABES) · doi:10.70675/0e53b3d1zc373z40d8za27dz4bca44dc7555
Stimulation électrique transcrânienne multisite dans l'épilepsie pharmaco-résistante
Denoyer, Y. (2019) · theses.fr (ABES) · doi:10.70675/0c55a83dz3729z4ee8zb7c9zd03118d26e81
Computational modeling of calcium diffusion reveals nanoscale biophysics in neuronal spines
Basnayake, K. (2020) · theses.fr (ABES) · doi:10.70675/ef684abdz7e9dz4d29z9f2ezbc8a568b5d20
Transport intracellulaire des récepteurs AMPA et régulation par leurs protéines associées
Bonnet, C. (2021) · theses.fr (ABES) · doi:10.70675/a51a45f6zee8cz4c6az85a5z8b01dfd87159
Interaction between synaptic and structural plasticity
Camus, C. (2021) · theses.fr (ABES) · doi:10.70675/6340fbbaz26d9z40d5zade8z917b9d9fd531
Case Study: Illuminating the Nanoscale World of Microbiology
Syed, P., Schembri, M. A., McCann, A. J., & Meunier, F. A. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5268-8_14
Woodard, G. E., & Julien, C. (2026) · Behavioural Brain Research · doi:10.1016/j.bbr.2026.116267
Structures, toxicity and internalization of cell-penetrating peptides
Eiríksdóttir, E. (2010) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Distinct roles of AMPA receptor subunits as potential therapeutic targets in Alzheimer’s disease
Seo, J., Kim, K., & Park, M. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108394
PTPRO Governs Synaptic Density, Long-Term Potentiation and Cognitive Function In Vivo
Wang, X., Wu, J., Liu, M., Zhang, K., Yuan, X., 邢方婷, Xu, W., Zheng, Y., Wu, Y., Luo, L., et al. (2026) · Neuroscience Bulletin · doi:10.1007/s12264-026-01704-4
Saito, M., & Saito, M. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.25.754367
Synaptic Organization of Surface AMPARs Changes by Brain Region and TauopathyPreprint
Vaidya, R. M., Zhang, J., Nall, D., Pendharkar, R., Lee, Y., Kim, E. C., Donghan, 马. M., Huang, F., Nonaka, H., Kiyonaka, S., et al. (2026) · eLife · doi:10.7554/elife.112632
Synaptic Organization of Surface AMPARs Changes by Brain Region and TauopathyPreprint
Vaidya, R. M., Zhang, J., Nall, D., Pendharkar, R., Lee, Y., Kim, E. C., Donghan, 马. M., Huang, F., Nonaka, H., Kiyonaka, S., et al. (2026) · eLife · doi:10.7554/elife.112632.1
Author response: Synaptic Organization of Surface AMPARs Changes by Brain Region and Tauopathy
Vaidya, R. M., Zhang, J., Nall, D., Pendharkar, R., Lee, Y., Kim, E. C., Donghan, 马. M., Huang, F., Nonaka, H., Kiyonaka, S., et al. (2026) · eLife · doi:10.7554/elife.112632.1.sa0
The Importance of Glia-Synapse Interactions in Synaptic Connectivity
Haider, T. (2014) · Utrecht University Repository (Utrecht University)
Metadata
- Authors
- Makino, H., & Malinow, R.
- Affiliations
- Cold Spring Harbor Laboratory (US)
- Corresponding author
- Malinow, Roberto
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2009-11
- Volume
- 64
- Issue
- 3
- Pages
- 381-390
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2999463
- OpenAlex
- W2058113433
- Cited by
- 501
- References
- 41
- Citations by year
- 2026: 16 · 2025: 18 · 2024: 20 · 2023: 12 · 2022: 22 · 2021: 38 · 2020: 39 · 2019: 27 · 2018: 34 · 2017: 35 · 2016: 26 · 2015: 22 · 2014: 41 · 2013: 52 · 2012: 38
- FWCI
- 13.72
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1354 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Funders
- National Institute on Aging (R01AG032132)
- National Institute of Mental Health (R01MH049159, R37MH049159)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- AMPA receptors, long-term potentiation, receptor trafficking, synaptic plasticity, GluR1, lateral diffusion, exocytosis, hippocampus, memory
- MeSH terms
- Animals, Cell Membrane, Dendrites, Diffusion, Exocytosis, Fluorescence, Hippocampus, Neurons, Synapses, Video Recording, Long-Term Potentiation, Pyramidal Cells, Receptors, AMPA, Intracellular Space, Dendritic Spines, Rats, CA1 Region, Hippocampal, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
