The DOI matches its Crossref record; 48 of the 49 references it cites were found in a registry or an index.
Lateral Diffusion Drives Constitutive Exchange of AMPA Receptors at Dendritic Spines and Is Regulated by Spine Morphology
Open accessAbstract
Synapse specificity is a basic feature of synaptic plasticity, but it remains unclear how synapse-specific signaling is achieved if postsynaptic membrane proteins can diffuse laterally between synapses. We monitored movements of AMPA receptors (AMPARs) on the surface of mature neurons to investigate the role of lateral diffusion in constitutive AMPAR trafficking and to assess the influence of membrane architecture on the surface distribution of synaptic proteins. Our data show that lateral diffusion is responsible for the continual exchange of a substantial pool of AMPARs at the spine surface. Furthermore, we found that a general characteristic of membrane proteins is that their movement into and out of spines is slow compared with that in nonspiny membrane. This shows that lateral diffusion is dependent on spine morphology and is restricted at the spine neck. These results demonstrate the importance of lateral diffusion in trafficking of AMPAR protein population and provide new insight into how spine structure can maintain synapse specificity by compartmentalizing lateral diffusion and therefore increasing the residence time of membrane proteins near individual synapses.
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
“Studying the FRAP dynamics of a fusion of SEP with the AMPA receptor subunit GluA2 (SEP-GluA2) revealed that receptor turnover in spines is slower compared to non-spinal plasma membrane and that recovery in the spine neck and base is particularly slow (Ashby et al., 2006).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Ashby et al., 2006
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Furthermore, fluorescently-tagged plasma membrane probes in spines of different morphologies showed a faster recovery rate in stubby than in mushroom-shaped spines (Richards et al., 2004; Ashby et al., 2006), indicating that mushroom-shaped spines form a membrane compartment in which diffusion is slowed.”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Ashby et al., 2006
The cited source says what the claim attributes to it.
In the citing paper
“indicating that mushroom-shaped spines form a membrane compartment in which diffusion is slowed.”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Ashby et al., 2006
The cited source says what the claim attributes to it.
In the citing paper
“Mushroom shaped spines were found to retain AMPA receptors in the vicinity of the synapse for an increased period of time (Ashby et al., 2006; Ehlers et al., 2007; Opazo and Choquet, 2011, see Figure 3A).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Ashby et al., 2006
The cited source says what the claim attributes to it.
In the citing paper
“Several experiments have shown that two-dimensional diffusion of membrane markers and AMPA-type glutamate receptors is sensitive to the morphology of the dendritic spine (Ashby et al., 2006; Shim et al., 2012).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Ashby et al., 2006
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
Mobility measurement by analysis of fluorescence photobleaching recovery kinetics
Axelrod, D., Koppel, D. E., Schlessinger, J., Elson, E. L., & Webb, W. W. (1976) · Biophysical Journal · doi:10.1016/s0006-3495(76)85755-4 · Cited by 2,717
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
Structural 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
Structure and function of dendritic spines
Nimchinsky, E. A., Sabatini, B. L., & Svoboda, K. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.081501.160008 · Cited by 1,208
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
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
Shi, S.-H., Hayashi, Y., Esteban, J. A., & Malinow, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00321-x · Cited by 1,094
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
Shrinkage of dendritic spines associated with long-term depression of hippocampal synapses
Zhou, Q., Homma, K. J., & Poo, M.-M. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.011 · Cited by 1,025
Evidence for multiple AMPA receptor complexes in hippocampal CA1/CA2 neurons
Wenthold, R., Petralia, R., Blahos J, II, & Niedzielski, A. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-06-01982.1996 · Cited by 850
Flagged first, then by citations
1 of the 49 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- (2003), Nat Rev Neurosci, 4, 251
- (2003), Histol Histopathol, 18, 617
Cited by
Sorted by citations
Items 201–300 of 302
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
Padamsey, Z., & Emptage, N. J. (2011) · Molecular Brain · doi:10.1186/1756-6606-4-36 · Cited by 15
Lambert, L., Dubayle, D., Fafouri, A., Herzog, É., Csaba, Z., Dournaud, P., Mestikawy, S. E., & Bernard, V. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00450 · Cited by 14
Genetically encoded fluorescent sensors for studying healthy and diseased nervous systems
Tian, L., & Looger, L. L. (2008) · Drug Discovery Today Disease Models · doi:10.1016/j.ddmod.2008.07.003 · Cited by 14
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
Biophysical Modeling of Synaptic Plasticity
Lee, C. T., Bell, M. K., Bonilla-Quintana, M., & Rangamani, P. (2024) · Annual Review of Biophysics · doi:10.1146/annurev-biophys-072123-124954 · Cited by 16
How energy determines spatial localisation and copy number of molecules in neurons
Bergmann, C., Mousaei, K., Rizzoli, S. O., & Tchumatchenko, T. (2025) · Nature Communications · doi:10.1038/s41467-025-56640-0 · Cited by 13
Illuminating Relationships Between the Pre- and Post-synapse
Sanderson, T. M., Georgiou, J., & Collingridge, G. L. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00009 · Cited by 17
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
Malavasi, E. L. V., Ghosh, A., Booth, D. G., Zagnoni, M., Sherman, D. L., & Brophy, P. (2021) · eLife · doi:10.7554/elife.68089 · Cited by 13
Transient, nano-scale, liquid-like molecular assemblies coming of age
Kusumi, A., Tsunoyama, T. A., Suzuki, K. G. N., Fujiwara, T. K., & Aladağ, A. (2024) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2024.102394 · Cited by 12
Zhang, Y., Wei, J., & Yang, Z. R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.03.061 · Cited by 12
Interacting Partners of AMPA-Type Glutamate Receptors
Cheng, J., Dong, J., Cui, Y., Wang, L., Wu, B., & Zhang, C. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9724-6 · Cited by 12
Proposed Correction to Feder's Anomalous Diffusion FRAP Equations
Kang, M., DiBenedetto, E., & Kenworthy, A. K. (2011) · Biophysical Journal · doi:10.1016/j.bpj.2010.11.091 · Cited by 12
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
Erythropoietin Induces Homeostatic Plasticity at Hippocampal Synapses
Dias, R. B., Rodrigues, T. M., Rombo, D. M., Ribeiro, F. F., Rodrigues, J. S., McGarvey, J., Orcinha, C. R., Henley, J. M., & Sebastião, A. M. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx159 · Cited by 11
Self-citationСЕПТИНОВЫЕ КОМПЛЕКСЫ И?ДИНАМИКА ЦИТОСКЕЛЕТА, "Молекулярная биология"
Akhmetova, K., Chesnokov, I. N., & Fedorova, S. A. (2018) · Molecular Biology · doi:10.7868/s0026898418020015 · Cited by 12
Bell, M. K., & Rangamani, P. (2023) · The Journal of Physiology · doi:10.1113/jp284029 · Cited by 12
Kamiya, H. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0720-12.2012 · Cited by 12
Impact of morphology on diffusive dynamics on curved surfaces
Kusters, R., & Storm, C. (2014) · Physical Review E · doi:10.1103/physreve.89.032723 · Cited by 10
Fang, X.-Q., Qiao, H., Groveman, B. R., Feng, S., Pflueger, M., Xin, W.-K., Ali, M. K., Lin, S.-X., Xu, J., Duclot, F., et al. (2015) · Molecular Brain · doi:10.1186/s13041-015-0167-1 · Cited by 12
Liouta, K., Lubas, M., Venugopal, V., Chabbert, J., Jeannière, C., Diaz, C., Munier, M., Tessier, B., Claverol, S., Favereaux, A., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-53090-y · Cited by 9
Michaluk, P., & Rusakov, D. A. (2022) · Nature Protocols · doi:10.1038/s41596-022-00732-4 · Cited by 9
Fluorescence lifetime imaging of AMPA receptor endocytosis in living neurons: effects of Aβ and PP1
Prinkey, K., Thompson, E., Saikia, J. M., Cid, T., & Doré, K. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1409401 · 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
Septin 6 localizes to microtubules in neuronal dendrites
Moon, I. S., Lee, H., & Walikonis, R. S. (2012) · Cytotechnology · doi:10.1007/s10616-012-9477-7 · Cited by 8
Więckowska‐Gacek, A., Gajewska‐Woźniak, O., Głowacka, A., Ji, B., Grycz, K., Czarkowska‐Bauch, J., & Skup, M. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14567 · Cited by 8
Validity of pHluorin-tagged GluA2 as a reporter for AMPA receptor surface expression and endocytosis
Wilkinson, K. A., Ashby, M. C., & Henley, J. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1319322111 · Cited by 8
Self-citationChen, Y., Liu, S., Jacobi, A. A., Jeng, G., Ulrich, J. D., Stein, I. S., Patriarchi, T., & Hell, J. W. (2024) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2024.1291262 · Cited by 9
Structural plasticity of dendritic spines
Zhang, S., Wang, J., & Wang, L. (2010) · Frontiers in Biology · doi:10.1007/s11515-010-0011-z · Cited by 7
Schumm, R. D., & Bressloff, P. C. (2022) · Physical review. E · doi:10.1103/physreve.105.064407 · Cited by 7
Seewald, A., Schönherr, S., Hörtnagl, H., Ehrlich, I., Schmuckermair, C., & Ferraguti, F. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.634558 · Cited by 7
Hildick, K. L., González‐González, I. M., Jaskolski, F., & Henley, J. M. (2012) · Journal of Visualized Experiments · doi:10.3791/3747-v · Cited by 6
Self-citationTwo-dimensional interfacial diffusion model of inhibitory synaptic receptor dynamics
Bressloff, P. C. (2023) · Proceedings of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rspa.2022.0831 · Cited by 6
A Multiscale Analysis of Diffusions on Rapidly Varying Surfaces
Duncan, A., Elliott, C. M., Pavliotis, G. A., & Stuart, A. M. (2015) · Journal of Nonlinear Science · doi:10.1007/s00332-015-9237-x · Cited by 6
Ashby, M. C., Daw, M. I., & Isaac, J. T. R. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-055-3_1 · Cited by 7
Self-citationMolecular Composition of Developing Glutamatergic Synapses
Barrow, S. L., & McAllister, A. K. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00102-2 · Cited by 5
It Is Time to Move: Role of Lateral Diffusion in AMPA Receptor Trafficking: Figure 1.
Yang, G., Huang, A., Zhu, S., & Xiong, W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3018-06.2006 · Cited by 5
Trafficking of Glutamate Receptors and Associated Proteins in Synaptic Plasticity
Hořák, M., Seabold, G. K., & Petralia, R. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00008-0 · Cited by 4
Lateral diffusions: The influence of geometry fluctuations
Chevalier, C., & Debbasch, F. (2010) · Europhysics Letters (EPL) · doi:10.1209/0295-5075/89/38001 · Cited by 4
A computational approach to the study of AMPA receptor clustering at Purkinje cell synapses.
Launey, T. (2007) · PubMed · Cited by 4
AMPA Receptor Cell Biology/Trafficking
Hastie, P. G. R., & Henley, J. M. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01222-5 · Cited by 3
Self-citationA spike-timing-dependent plasticity rule for single, clustered and distributed dendritic spinesPreprint
Tazerart, S., Mitchell, D. E., Miranda‐Rottmann, S., & Araya, R. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/397323 · Cited by 3
Dendritic spine neck plasticity controls synaptic expression of long-term potentiationPreprint
Gupta, R., & O’Donnell, C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.27.525952 · Cited by 3
Soga, K., Fujiwara, T., Nakagawa, M., Shibata, A., Adriel, H., Yatsuzuka, K., Kakegawa, W., Yuzaki, M., Hamachi, I., Nango, E., et al. (2025) · Science Advances · doi:10.1126/sciadv.adt6683 · Cited by 3
"Cowboy's belt with revolver" scleroderma caused by vitamin K1 injections.
Lembo, S., Megna, M., Balato, A., & Balato, N. (2012) · PubMed · Cited by 2
Antunes, M. G., Sanial, M., Contremoulins, V., Carvalho, S., Plessis, A., & Bécam, I. (2022) · eLife · doi:10.7554/elife.79843 · Cited by 2
Mobilité des récepteurs du glutamate
Choquet, D., & Lounis, B. (2008) · médecine/sciences · doi:10.1051/medsci/2008245548 · Cited by 2
Diffusion on rapidly-varying surfaces
Duncan, A. (2026) · Warwick Research Archive Portal (University of Warwick) · doi:10.82444/warw.33641101 · Cited by 2
Using p H luorins to Investigate Synaptic Function
Grubb, M. S., & Burrone, J. (2009) · Wiley eBooks · doi:10.1002/9780470015902.a0021387 · Cited by 2
Bell, M. K., & Rangamani, P. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.23.473965 · Cited by 2
Villanueva, C. B., Stephensen, H. J. T., Mokso, R., Benraiss, A., Jon Sporring, A., & Goldman, S. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.06.519168 · Cited by 2
Homeostasis of dendritic spines in hippocampal CA1 cells
Mestrallet, C. A. (2011) · UCL Discovery (University College London) · Cited by 2
Role of the different domains of PSD-95 in basal synaptic transmission
Bonnet, A. D. S. (2011) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-509 · Cited by 2
Elementary Theory of Stochastic Narrow Escape
Holcman, D., & Schuss, Z. (2015) · Springer eBooks · doi:10.1007/978-1-4939-3103-3_1 · Cited by 1
Crestani, A. P., Zacharias, L. R., Marques, D. B., Fonseca, F. F. F., Ruggiero, R. N., & Leite, J. P. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05254-0 · Cited by 1
NET in Molecular and Cellular Biology
Holcman, D., & Schuss, Z. (2015) · Springer eBooks · doi:10.1007/978-1-4939-3103-3_3 · Cited by 1
Accelerators, Brakes, and Gears of Actin Dynamics in Dendritic Spines
Pontrello, C. G., & Ethell, I. M. (2014) · The Open Neuroscience Journal · doi:10.2174/1874082000903010067 · Cited by 1
Dendritic Organelles for Postsynaptic Trafficking
Hanus, C., & Ehlers, M. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_8 · Cited by 1
Recovery of function after lesions of the anterior thalamic nuclei: CA1 neuromorphology
Harland, B. C. (2013) · doi:10.26021/5935 · Cited by 1
Piña, J. A. T. (2015) · doi:10.5821/dissertation-2117-95842 · Cited by 1
Wagle, S., Kracht, M. K., Bührke, A., Acker‐Palmer, A., Kraynyukova, N., Hafner, A., Schuman, E. M., & Tchumatchenko, T. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.08.637220 · Cited by 1
Synapses, spines, zinc and pathology of Alzheimer's disease.
Familtsev, D. (2013) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/420 · Cited by 1
Surface Trafficking of Membrane Proteins at Excitatory and Inhibitory Synapses
Choquet, D., & Triller, A. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_13
Jansson, L. C. (2013) · Työväentutkimus Vuosikirja
Sourial-Bassillious, N. (2010) · Figshare
Quantitative Imaging of Receptor Trafficking
James, A. R., Awaji, T., Stephenson, F. A., & Hartell, N. A. (2010) · doi:10.1002/9780470749210.ch4
Huupponen, J. (2013) · Työväentutkimus Vuosikirja
Effective large-scale description of lateral diffusions on fluctuating interfaces
Chevalier, C., & Debbasch, F. (2010) · Journal of Physics Conference Series · doi:10.1088/1742-6596/246/1/012027
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)
Involvement of neuroligins and associated proteins in synapse development
Levinson, J. N. (2010) · cIRcle (University of British Columbia) · doi:10.14288/1.0071424
Role of the Septin Cytoskeleton for the Functional Organization of the Plasma Membrane
Kinoshita, M. (2010) · Pan Stanford Publishing eBooks · doi:10.1201/b11671-20
Fernandez, N. A. (2010) · TSpace (University of Toronto)
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)
Dubes, S., Soula, A., Benquet, S., Tessier, B., Poujol, C., Favereaux, A., Thoumine, O. R., & Letellier, M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.30.442089
Hell, J. W. (2007) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1091502.554769
AMPA Receptor Cell Biology/Trafficking☆
Wilkinson, K. A., Hastie, P. G. R., & Henley, J. M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.04494-9
Self-citationWartman, B. C. (2014) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2014-10457
Baker, K., & Dalley, J. W. (2023) · Brain and Neuroscience Advances · doi:10.1177/23982128231199006
Soga, K., Fujiwara, T., Nakagawa, M., Shibata, A., Adriel, H., Yatsuzuka, K., Kakegawa, W., Yuzaki, M., Hamachi, I., Nango, E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.21.608930
Chen, K. Y., Yang, J., Liu, B., Jiang, C., Koylass, N., Zhang, Z., Sun, S., Huganir, R. L., & Qiu, Z. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.27.615471
Biophysically plausible models of synaptic plasticity
Shouval, H. Z. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00071-7
Mátyás, D., Tukacs, V., Tóth, V., Baracskay, P., Pap, S. K., Stráner, P., Hiền, T. M., Hunyadi‐Gulyás, É., Darula, Z., Perczel, A., et al. (2025) · Brain Sciences · doi:10.3390/brainsci15080881
Ducrot, C., Lemoigne, C., Saint-Jean, P. L., Cloâtre, T., Daburon, S., Seiling, K., Mohrmann, L., Rohlmann, A., Missler, M., Fronzes, R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.08.681152
Intercellular Communication and Heterosynaptic Metaplasticity in the Rodent Hippocampus
Jones, O. D. (2014) · Otago University Research Archive (University of Otago)
Jézéquel, J. (2016) · theses.fr (ABES) · doi:10.70675/a7276087zc049z442fz8b5bzab9e03d034cb
The Scrib1 Interactome and its relevance for synaptic plasticity & neurodevelopmental disorders
Pinheiro, V. L. M. (2014) · theses.fr (ABES) · doi:10.70675/b1c2e418zac9cz44c5zb050z72f9b6a47586
Simonnet, C. (2019) · theses.fr (ABES) · doi:10.70675/dcc67be7z8c6dz47b5z92e8z4d75367bfd48
Contribution of the potassium / chloride cotransporter KCC2 to hippocampal rhythmopathy
Goutierre, M. (2018) · theses.fr (ABES) · doi:10.70675/0e53b3d1zc373z40d8za27dz4bca44dc7555
Montecinos-Oliva, C. (2018) · theses.fr (ABES) · doi:10.70675/1cb0a505zb904z4045z83b4z7ec8f3bc62b9
Antunes, M. G. (2022) · theses.fr (ABES) · doi:10.70675/0257f25ez6da2z4e32z9ca1z211c99cec280
Mechanical Properties of Septins and Their Role in Establishing Diffusion Barriers
Chauvin, B. (2022) · theses.fr (ABES) · doi:10.70675/3d3cb268z6531z496dz8ebcz9c81b8f85871
Molecular impact of anti-NMDA receptor autoantibodies
Jamet, Z. (2023) · theses.fr (ABES) · doi:10.70675/87243db0za802z49e1zbd1ez607bb3d60120
Metadata
- Authors
- Ashby, M. C., Maier, S. R., Nishimune, A., & Henley, J. M.
- Affiliations
- University of Bristol (GB)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2006-06-28
- Volume
- 26
- Issue
- 26
- Pages
- 7046-7055
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6673929
- OpenAlex
- W1982726026
- Cited by
- 302
- References
- 49
- Citations by year
- 2026: 2 · 2025: 7 · 2024: 11 · 2023: 8 · 2022: 12 · 2021: 16 · 2020: 8 · 2019: 6 · 2018: 13 · 2017: 14 · 2016: 8 · 2015: 15 · 2014: 26 · 2013: 19 · 2012: 20
- FWCI
- 8.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Bristol Research (University of Bristol) (submittedVersion)
- Funders
- Wellcome Trust
- European Commission
- Medical Research Council
- 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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
- Keywords
- lateral diffusion, AMPA receptors, dendritic spines, dendritic spine morphology, receptor trafficking, synapse specificity, membrane protein diffusion, synaptic plasticity, postsynaptic membrane
- MeSH terms
- Animals, Biological Transport, Cell Membrane, Cells, Cultured, Diffusion, Neurons, Tissue Distribution, Receptors, AMPA, Protein Transport, Photobleaching, Dendritic Spines, Green Fluorescent Proteins, Rats
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
