The DOI matches its Crossref record; 154 of the 154 references it cites were found in a registry or an index.
The Postsynaptic Architecture of Excitatory Synapses: A More Quantitative View
Abstract
Excitatory (glutamatergic) synapses in the mammalian brain are usually situated on dendritic spines, a postsynaptic microcompartment that also harbors organelles involved in protein synthesis, membrane trafficking, and calcium metabolism. The postsynaptic membrane contains a high concentration of glutamate receptors, associated signaling proteins, and cytoskeletal elements, all assembled by a variety of scaffold proteins into an organized structure called the postsynaptic density (PSD). A complex machine made of hundreds of distinct proteins, the PSD dynamically changes its structure and composition during development and in response to synaptic activity. The molecular size of the PSD and the stoichiometry of many major constituents have been recently measured. The structures of some intact PSD proteins, as well as the spatial arrangement of several proteins within the PSD, have been determined at low resolution by electron microscopy. On the basis of such studies, a more quantitative and geometrically realistic view of PSD architecture is emerging.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Second, it is present in the brain at extraordinarily high levels, rivaling the levels of cytoskeletal proteins (63–67), suggesting that CaMKII may play a structural role (27, 68).”
From Synaptic memory and CaMKII (2023) · cites this paper as [66]
In the citing paper
“since there are roughly 20–30 NMDARs in the PSD (66, 143) and ∼100 holoenzymes [∼1,200 CaMKII subunits (65)], after NMDAR activation only a small fraction of subunits per holoenzyme would be directly bound to GluN2B.”
From Synaptic memory and CaMKII (2023) · cites this paper as [66]
In the citing paper
“However, actin is largely excluded from the core of the PSD, interacting with such proteins as Shank and SAPAP located in the deeper, cytoplasmic-facing layer of the PSD referred to as the pallium (66, 162, 322).”
From Synaptic memory and CaMKII (2023) · cites this paper as [66]
In the citing paper
“It should be pointed out that, although it is well established that CaMKII phosphorylates numerous synaptic proteins (66, 434–437), as reviewed here, despite intensive research an essential role for CaMKII phosphorylation of many of these targets largely remains elusive.”
From Synaptic memory and CaMKII (2023) · cites this paper as [66]
In the citing paper
“Actin is largely excluded from the core of the PSD (66, 322), and evidence suggests that, at least for the first hour, the changes in spine size are not accompanied by changes in the size of the PSD (56).”
From Synaptic memory and CaMKII (2023) · cites this paper as [66]
In the citing paper
“The geometry of the spine neck determines the rate of calcium efflux into the dendrite shaft and hence the degree of elevation of calcium concentrations within the spine head, following n-methyl-D-aspartate receptor (NMDAR) activation (Bloodgood and Sabatini, 2005; Alvarez and Sabatini, 2007; Sheng and Hoogenraad, 2007).”
From Human Brain/Cloud Interface (2019) · cites this paper as Sheng and Hoogenraad, 2007
In the citing paper
“Remarkably, recent evidence points toward the rapid exchange of PSD proteins, such as AMPARS and PSD-95, even between neighboring synapses under steady-state conditions (Sheng and Hoogenraad, 2007).”
From Human Brain/Cloud Interface (2019) · cites this paper as Sheng and Hoogenraad, 2007
In the citing paper
“Longer-term changes in the PSD structure and composition (from hours to days) involve altered protein synthesis, either within the neuronal cell body, or dendrites (Sheng and Hoogenraad, 2007).”
From Human Brain/Cloud Interface (2019) · cites this paper as Sheng and Hoogenraad, 2007
In the citing paper
“The PSD dynamically regulates its components through protein phosphorylation, palmitoylation, local protein translation, the ubiquitin-proteasome system for protein degradation, and redistribution of specific proteins (e.g., CaMKIIα, AMPARs) both entering and leaving the PSD (Kim and Ko, 2006; Sheng and Hoogenraad, 2007).”
From Human Brain/Cloud Interface (2019) · cites this paper as Sheng and Hoogenraad, 2007
In the citing paper
“For instance, the activity-dependent modification of PSD proteins occurring over timescales of seconds to hours is believed to underlie plasticity processes such as LTP and LTD (Sheng and Hoogenraad, 2007).”
From Human Brain/Cloud Interface (2019) · cites this paper as Sheng and Hoogenraad, 2007
Citations
Cites
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
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
Heteromeric NMDA receptors: molecular and functional distinction of subtypes
Monyer, H., Sprengel, R., Schoepfer, R., Herb, A., Higuchi, M., Lomeli, H., Burnashev, N., Sakmann, B., & Seeburg, P. H. (1992) · Science · doi:10.1126/science.256.5060.1217 · Cited by 2,541
Südhof, T. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131412 · Cited by 2,491
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
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
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
Chan, D. C. (2006) · Cell · doi:10.1016/j.cell.2006.06.010 · Cited by 1,987
Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex
Trachtenberg, J. T., Chen, B. E., Knott, G. W., Feng, G., Sanes, J. R., Welker, E., & Svoboda, K. (2002) · Nature · doi:10.1038/nature01273 · Cited by 1,927
Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study.
Eg, G. (1959) · PubMed · Cited by 1,768
Extrasynaptic NMDARs oppose synaptic NMDARs by triggering CREB shut-off and cell death pathways
Hardingham, G. E., Fukunaga, Y., & Bading, H. (2002) · Nature Neuroscience · doi:10.1038/nn835 · Cited by 1,686
PDZ domain proteins of synapses
Kim, E., & Sheng, M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1517 · Cited by 1,630
Self-citationThe importance of dendritic mitochondria in the morphogenesis and plasticity of spines and synapses
Li, Z., Okamoto, K.-I., Hayashi, Y., & Sheng, M. (2004) · Cell · doi:10.1016/j.cell.2004.11.003 · Cited by 1,498
Self-citationMorphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity
Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269
Long-term dendritic spine stability in the adult cortex
Grutzendler, J., Kasthuri, N., & Gan, W.-B. (2002) · Nature · doi:10.1038/nature01276 · Cited by 1,198
Proteomic analysis of NMDA receptor–adhesion protein signaling complexes
Husi, H., Ward, M. A., Choudhary, J. S., Blackstock, W. P., & Grant, S. G. N. (2000) · Nature Neuroscience · doi:10.1038/76615 · Cited by 1,194
Cho, K.-O., Hunt, C. A., & Kennedy, M. B. (1992) · Neuron · doi:10.1016/0896-6273(92)90245-9 · Cited by 1,188
AMPA receptor trafficking at excitatory synapses
Bredt, D. S., & Nicoll, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00640-8 · Cited by 1,150
Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity
Liu, L., Wong, T. P., Pozza, M. F., Lingenhoehl, K., Wang, Y., Sheng, M., Auberson, Y. P., & Wang, Y. T. (2004) · Science · doi:10.1126/science.1096615 · Cited by 1,131
Self-citationReinsertion 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
Coupling of mGluR/Homer and PSD-95 Complexes by the Shank Family of Postsynaptic Density Proteins
Tu, J. C., Xiao, B., Naisbitt, S. R., Yuan, J. P., Petralia, R. S., Brakeman, P., Doan, A., Aakalu, V. K., Lanahan, A. A., Sheng, M., et al. (1999) · Neuron · doi:10.1016/s0896-6273(00)80810-7 · Cited by 1,079
Self-citationAn adaptive coding model of neural function in prefrontal cortex
Sanes, J., & Lichtman, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35097557 · Cited by 1,056
Activity level controls postsynaptic composition and signaling via the ubiquitin-proteasome system
Ehlers, M. D. (2003) · Nature Neuroscience · doi:10.1038/nn1013 · Cited by 977
Colonnier, M. (1968) · Brain Research · doi:10.1016/0006-8993(68)90234-5 · Cited by 946
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
Baude, A., Nusser, Z., Roberts, J. D. B., Mulvihill, E., Jeffrey Mcllhinney, R. A., & Somogyi, P. (1993) · Neuron · doi:10.1016/0896-6273(93)90086-7 · Cited by 927
Cerebellar Long-Term Depression: Characterization, Signal Transduction, and Functional Roles
Ito, M. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.3.1143 · Cited by 855
Structure-stability-function relationships of dendritic spines
Kasai, H., Matsuzaki, M., Noguchi, J., Yasumatsu, N., & Nakahara, H. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00162-0 · Cited by 847
Cell Type and Pathway Dependence of Synaptic AMPA Receptor Number and Variability in the Hippocampus
Nusser, Z., Lujan, R., Laube, G., Roberts, J. D. B., Molnar, E., & Somogyi, P. (1998) · Neuron · doi:10.1016/s0896-6273(00)80565-6 · Cited by 804
Carlin, R. K., Grab, D. J., Cohen, R. S., & Siekevitz, P. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.86.3.831 · Cited by 788
Signal-Processing Machines at the Postsynaptic Density
Kennedy, M. B. (2000) · Science · doi:10.1126/science.290.5492.750 · Cited by 788
Tovar, K. R., & Westbrook, G. L. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-04180.1999 · Cited by 777
An adaptive coding model of neural function in prefrontal cortex
Duncan, J. (2001) · UCL Discovery (University College London) · Cited by 738
Postsynaptic signaling and plasticity mechanisms
Sheng, M., & Kim, M. J. (2002) · Science · doi:10.1126/science.1075333 · Cited by 731
Self-citationRecycling Endosomes Supply AMPA Receptors for LTP
Park, M., Penick, E. C., Edwards, J. G., Kauer, J. A., & Ehlers, M. D. (2004) · Science · doi:10.1126/science.1102026 · Cited by 730
Physiology and Pathophysiology of the Calcium Store in the Endoplasmic Reticulum of Neurons
Verkhratsky, A. (2004) · Physiological Reviews · doi:10.1152/physrev.00004.2004 · Cited by 718
Cortical rewiring and information storage
Chklovskii, D. B., Mel, B. W., & Svoboda, K. (2004) · Nature · doi:10.1038/nature03012 · Cited by 717
Regulation of Dendritic Spine Morphology and Synaptic Function by Shank and Homer
Sala, C., Piëch, V., Wilson, N. R., Passafaro, M., Liu, G., & Sheng, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00339-7 · Cited by 716
Self-citationNMDA Receptor Subunit Composition Controls Synaptic Plasticity by Regulating Binding to CaMKII
Barria, A., & Malinow, R. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.034 · Cited by 709
Unusual spectral energy distribution of a galaxy previously reported to be at redshift 6.68
Chen, H., Lanzetta, K. M., Pascarelle, S. M., & Yahata, N. (2000) · RePEc: Research Papers in Economics · Cited by 680
Different modes of expression of AMPA and NMDA receptors in hippocampal synapses
Takumi, Y., Ramírez-León, V., Laake, P., Rinvik, E., & Ottersen, O. P. (1999) · Nature Neuroscience · doi:10.1038/10172 · Cited by 675
Functional and Pharmacological Differences Between Recombinant N -Methyl- d -Aspartate Receptors
Vicini, S., Wang, J. F., Li, J. H., Zhu, W. J., Wang, Y. H., Luo, J. H., Wolfe, B. B., & Grayson, D. R. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.2.555 · Cited by 674
Subunit-specific temporal and spatial patterns of AMPA receptor exocytosis in hippocampal neurons
Passafaro, M., Piëch, V., & Sheng, M. (2001) · Nature Neuroscience · doi:10.1038/nn0901-917 · Cited by 655
Self-citationMolecular mechanisms of glutamate-dependent neurodegeneration in ischemia and traumatic brain injury
Arundine, M., & Tymianski, M. (2004) · Cellular and Molecular Life Sciences (CMLS) · doi:10.1007/s00018-003-3319-x · Cited by 647
Experience-dependent and cell-type-specific spine growth in the neocortex
Holtmaat, A., Wilbrecht, L., Knott, G. W., Welker, E., & Svoboda, K. (2006) · Nature · doi:10.1038/nature04783 · Cited by 631
Molecular mechanisms of dendritic spine morphogenesis
Tada, T., & Sheng, M. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.12.001 · Cited by 615
Self-citationKennedy, M. B., Bennett, M. K., & Erondu, N. E. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.23.7357 · Cited by 610
Spacek, J., & Harris, K. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00190.1997 · Cited by 599
Ubiquitination Regulates PSD-95 Degradation and AMPA Receptor Surface Expression
Colledge, M., Snyder, E. M., Crozier, R. A., Soderling, J. A., Jin, Y., Langeberg, L. K., Lu, H., Bear, M. F., & Scott, J. D. (2003) · Neuron · doi:10.1016/s0896-6273(03)00687-1 · Cited by 567
Regulation of AMPA receptor lateral movements
Borgdorff, A. J., & Choquet, D. (2002) · Nature · doi:10.1038/nature00780 · Cited by 542
Activity-dependent regulation of dendritic synthesis and trafficking of AMPA receptors
Ju, W. H., Morishita, W., Tsui, J., Gaietta, G. M., Deerinck, T. J., Adams, S., Garner, C. C., Tsien, R. Y., Ellisman, M. H., & Malenka, R. C. (2004) · Nature Neuroscience · doi:10.1038/nn1189 · Cited by 541
A developmental change in NMDA receptor-associated proteins at hippocampal synapses
Sans, N., Petralia, R. S., Wang, Y.-X., Blahos, J., Hell, J. W., & Wenthold, R. J. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-03-01260.2000 · Cited by 537
Glutamate as a therapeutic target in psychiatric disorders
Javitt, D. C. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001551 · Cited by 534
Self- and actin-templated assembly of Mammalian septins
Kinoshita, M., Field, C. M., Coughlin, M. L., Straight, A. F., & Mitchison, T. J. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00366-0 · Cited by 526
Cheng, D., Hoogenraad, C. C., Rush, J., Ramm, E., Schlager, M. A., Duong, D. M., Xu, P., Wijayawardana, S. R., Hanfelt, J., Nakagawa, T., et al. (2006) · Molecular & Cellular Proteomics · doi:10.1074/mcp.d500009-mcp200 · Cited by 510
Self-citationShepherd, G. M. G., & Harris, K. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08300.1998 · Cited by 502
Petralia, R. S., Esteban, J. A., Wang, Y. –., Partridge, J. G., Zhao, H. –., Wenthold, R. J., & Malinow, R. (1999) · Nature Neuroscience · doi:10.1038/4532 · Cited by 496
Kim, M. J., Dunah, A. W., Wang, Y. T., & Sheng, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.031 · Cited by 494
Self-citationMEMBRANE-ASSOCIATED GUANYLATE KINASES REGULATE ADHESION AND PLASTICITY AT CELL JUNCTIONS
Funke, L., Dakoji, S., & Bredt, D. S. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.74.082803.133339 · Cited by 482
Rapid turnover of actin in dendritic spines and its regulation by activity
Star, E. N., Kwiatkowski, D. J., & Murthy, V. N. (2002) · Nature Neuroscience · doi:10.1038/nn811 · Cited by 481
Peng, J., Kim, M. J., Cheng, D., Duong, D. M., Gygi, S. P., & Sheng, M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m400103200 · Cited by 473
Self-citationConstructing inhibitory synapses
Moss, S. J., & Smart, T. G. (2001) · Nature reviews. Neuroscience · doi:10.1038/35067500 · Cited by 467
Targeting of PKA to Glutamate Receptors through a MAGUK-AKAP Complex
Colledge, M., Dean, R. A., Scott, G. K., Langeberg, L. K., Huganir, R. L., & Scott, J. D. (2000) · Neuron · doi:10.1016/s0896-6273(00)00013-1 · Cited by 467
Ostroff, L. E., Fiala, J. C., Allwardt, B., & Harris, K. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00785-7 · Cited by 461
Importance of the Intracellular Domain of NR2 Subunits for NMDA Receptor Function In Vivo
Sprengel, R., Suchanek, B., Amico, C., Brusa, R., Burnashev, N., Rozov, A. V., Hvalby, Ø., Jensen, V., Paulsen, O., Andersen, P. N., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)80921-6 · Cited by 460
Collins, M. O., Husi, H., Yu, L., Brandon, J. M., Anderson, C. N. G., Blackstock, W. P., Choudhary, J. S., & Grant, S. G. N. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03507.x · Cited by 448
Mobile NMDA Receptors at Hippocampal Synapses
Tovar, K. R., & Westbrook, G. L. (2002) · Neuron · doi:10.1016/s0896-6273(02)00658-x · Cited by 448
Unusual spectral energy distribution of a galaxy previously reported to be at redshift 6.68
Chen, H., Lanzetta, K. M., Pascarelle, S., & Yahata, N. (2000) · Nature · doi:10.1038/35046031 · Cited by 447
Lee, S. H., Liu, L., Wang, Y. T., & Sheng, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)01024-3 · Cited by 441
Self-citationThe role of receptor diffusion in the organization of the postsynaptic membrane
Choquet, D., & Triller, A. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1077 · Cited by 427
Spine-Neck Geometry Determines NMDA Receptor-Dependent Ca2+ Signaling in Dendrites
Noguchi, J., Matsuzaki, M., Ellis-Davies, G. C. R., & Kasai, H. (2005) · Neuron · doi:10.1016/j.neuron.2005.03.015 · Cited by 419
Chicurel, M. E., & Harris, K. M. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903250204 · Cited by 417
Nusser, Z., Mulvihill, E. R., Streit, P., & Somogyi, P. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90421-9 · Cited by 416
Kistner, U., Wenzel, B., Veh, R. W., Cases-Langhoff, C., Garner, A. M., APPELTAUER, U., Voss, B., Gundelfinger, E. D., & Garner, C. C. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)53433-5 · Cited by 414
Identification of Proteins in the Postsynaptic Density Fraction by Mass Spectrometry
Walikonis, R. S., Jensen, O. N., Mann, M., Provance, D. W., Mercer, J. A., & Kennedy, M. B. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04069.2000 · Cited by 395
Dynamics and Regulation of Clathrin Coats at Specialized Endocytic Zones of Dendrites and Spines
Blanpied, T. A., Scott, D. B., & Ehlers, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00979-0 · Cited by 392
Auxiliary Subunits Assist AMPA-Type Glutamate Receptors
Nicoll, R. A., Tomita, S., & Bredt, D. S. (2006) · Science · doi:10.1126/science.1123339 · Cited by 390
Quinlan, E. M., Olstein, D. H., & Bear, M. F. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12876 · Cited by 382
Penzes, P., Johnson, R. C., Sattler, R., Zhang, X., Huganir, R. L., Kambampati, V., Mains, R. E., & Eipper, B. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00193-3 · Cited by 378
Neuroligins and neurexins: linking cell adhesion, synapse formation and cognitive function
Dean, C., & Dresbach, T. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.11.003 · Cited by 376
Yamagata, M., Sanes, J. R., & Weiner, J. A. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(03)00107-8 · Cited by 374
Molecular mechanisms of dendritic spine development and remodeling
Ethell, I. M., & Pasquale, E. B. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.02.003 · Cited by 367
Ligand-Gated Ion Channel Interactions with Cytoskeletal and Signaling Proteins
Sheng, M., & Pak, D. T. S. (2000) · Annual Review of Physiology · doi:10.1146/annurev.physiol.62.1.755 · Cited by 349
Self-citationActivity-dependent dynamics and sequestration of proteasomes in dendritic spines
Bingol, B., & Schuman, E. M. (2006) · Nature · doi:10.1038/nature04769 · Cited by 347
Neuronal activity regulates diffusion across the neck of dendritic spines
Bloodgood, B. L., & Sabatini, B. L. (2005) · Science · doi:10.1126/science.1114816 · Cited by 344
Proteomic Analysis of in Vivo Phosphorylated Synaptic Proteins
Collins, M. O., Yu, L., Coba, M. P., Husi, H., Campuzano, I., Blackstock, W. P., Choudhary, J. S., & Grant, S. G. N. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m411220200 · Cited by 320
C ELL -C ELL S IGNALING D URING S YNAPSE F ORMATION IN THE CNS
Scheiffele, P. (2003) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.043002.094940 · Cited by 316
Calcium/calmodulin-dependent protein kinase II and synaptic plasticity
Colbran, R. J., & Brown, A. M. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.05.008 · Cited by 311
Targeted Protein Degradation and Synapse Remodeling by an Inducible Protein Kinase
Pak, D. T. S., & Sheng, M. (2003) · Science · doi:10.1126/science.1082475 · Cited by 305
Self-citationNMDA Receptor Content of Synapses in Stratum Radiatum of the Hippocampal CA1 Area
Racca, C., Stephenson, F. A., Streit, P., Roberts, J. D. B., & Somogyi, P. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02512.2000 · Cited by 304
Ashby, M. C., Maier, S. R., Nishimune, A., & Henley, J. M. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1235-06.2006 · Cited by 302
Laminar Organization of the NMDA Receptor Complex within the Postsynaptic Density
Valtschanoff, J. G., & Weinberg, R. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01211.2001 · Cited by 301
Identification and Verification of Novel Rodent Postsynaptic Density Proteins
Jordan, B. A., Fernholz, B. D., Boussac, M., Xu, C., Grigorean, G., Ziff, E. B., & Neubert, T. A. (2004) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m400045-mcp200 · Cited by 296
An Architectural Framework That May Lie at the Core of the Postsynaptic Density
Baron, M. K., Boeckers, T. M., Vaida, B., Faham, S., Gingery, M., Sawaya, M. R., Salyer, D., Gundelfinger, E. D., & Bowie, J. U. (2006) · Science · doi:10.1126/science.1118995 · Cited by 292
Synaptopodin-deficient mice lack a spine apparatus and show deficits in synaptic plasticity
Deller, T., Körte, M., Chabanis, S., Drakew, A., Schwegler, H., Stefani, G. G., Zúñiga, A., Schwarz, K., Bonhoeffer, T., Zeller, R., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1832384100 · Cited by 291
Glutamate receptors at atomic resolution
Mayer, M. L. (2006) · Nature · doi:10.1038/nature04709 · Cited by 290
Integration of biochemical signalling in spines
Kennedy, M. B., Beale, H. C., Carlisle, H. J., & Washburn, L. R. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1685 · Cited by 286
Synaptic and Extrasynaptic NMDA Receptor NR2 Subunits in Cultured Hippocampal Neurons
Thomas, C. G., Miller, A., & Westbrook, G. L. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00771.2005 · Cited by 286
Surface trafficking of receptors between synaptic and extrasynaptic membranes: and yet they do move!
Triller, A., & Choquet, D. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.01.001 · Cited by 285
Activity-Dependent Redistribution and Essential Role of Cortactin in Dendritic Spine Morphogenesis
Hering, H., & Sheng, M. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-37-11759.2003 · Cited by 269
Self-citationCooney, J. R., Hurlburt, J. L., Selig, D. K., Harris, K. M., & Fiala, J. C. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02215.2002 · Cited by 269
Subunit Rules Governing the Sorting of Internalized AMPA Receptors in Hippocampal Neurons
Lee, S. H., Simonetta, A., & Sheng, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.015 · Cited by 268
Self-citationSpine loss and other dendritic abnormalities in epilepsy
Swann, J. W., Al‐Noori, S., Jiang, M., & Lee, C. L. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:5 · Cited by 268
Zuber, B., Nikonenko, I., Klauser, P., Müller, D., & Dubochet, J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509527102 · Cited by 263
SynGAP regulates synaptic strength and mitogen-activated protein kinases in cultured neurons
Rumbaugh, G., Adams, J. P., Kim, J. H., & Huganir, R. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600084103 · Cited by 260
Nakagawa, T., Futai, K., Lashuel, H. A., Lo, I., Okamoto, K., Walz, T., Hayashi, Y., & Sheng, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.012 · Cited by 250
Self-citationComprehensive Identification of Phosphorylation Sites in Postsynaptic Density Preparations
Trinidad, J. C., Specht, C. G., Thalhammer, A., Schoepfer, R., & Burlingame, A. L. (2006) · Molecular & Cellular Proteomics · doi:10.1074/mcp.t500041-mcp200 · Cited by 246
Structure and different conformational states of native AMPA receptor complexes
Nakagawa, T., Cheng, Y., Ramm, E. I., Sheng, M., & Walz, T. (2005) · Nature · doi:10.1038/nature03328 · Cited by 242
Self-citationDendritic spine geometry: functional implication and regulation
Hayashi, Y., & Majewska, A. K. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.006 · Cited by 237
Lateral organization of endocytic machinery in dendritic spines
Rácz, B., Blanpied, T. A., Ehlers, M., & Weinberg, R. J. (2004) · Nature Neuroscience · doi:10.1038/nn1303 · Cited by 236
Ontogeny of postsynaptic density proteins at glutamatergic synapses
Petralia, R. S., Sans, N., Wang, Y.-X., & Wenthold, R. J. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.03.013 · Cited by 236
Mass of the postsynaptic density and enumeration of three key molecules
Chen, X., Vinade, L., Leapman, R. D., Petersen, J. D., Nakagawa, T., Phillips, T. M., Sheng, M., & Reese, T. S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505359102 · Cited by 236
Self-citationPhotoinactivation of native AMPA receptors reveals their real-time trafficking
Adesnik, H., Nicoll, R. A., & England, P. M. (2005) · Neuron · doi:10.1016/j.neuron.2005.11.030 · Cited by 234
Brown, T. C., Tran, I. C., Backos, D. S., & Esteban, J. A. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.023 · Cited by 234
Choi, J., Ko, J., Rácz, B., Burette, A., Lee, J.-R., Kim, S.-H., Na, M., Lee, H. W., Kim, K., Weinberg, R. J., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3212-04.2005 · Cited by 232
Synaptic regulation of translation of dendritic mRNAs
Schuman, E. M., Dynes, J. L., & Steward, O. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1796-06.2006 · Cited by 230
Dendritic and Postsynaptic Protein Synthetic Machinery
Gardiol, A., Racca, C., & Triller, A. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00168.1999 · Cited by 230
The Number of Glutamate Receptors Opened by Synaptic Stimulation in Single Hippocampal Spines
Nimchinsky, E. A., Yasuda, R., Oertner, T. G., & Svoboda, K. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5066-03.2004 · Cited by 219
Petersen, J. D., Chen, X., Vinadé, L., Döṣemeci, A., Lisman, J. E., & Reese, T. S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11270.2003 · Cited by 212
A Preformed Complex of Postsynaptic Proteins Is Involved in Excitatory Synapse Development
Gerrow, K., Romorini, S., Nabi, S., Colicos, M. A., Sala, C., & El-Husseini, A. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.015 · Cited by 211
Yoshimura, Y., Yamauchi, Y., Shinkawa, T., Taoka, M., Donai, H., Takahashi, N., Isobe, T., & Yamauchi, T. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02136.x · Cited by 208
The postsynaptic density: a possible role in long-lasting effects in the central nervous system.
Siekevitz, P. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.10.3494 · Cited by 197
Gaertner, T. R., Kolodziej, S. J., Wang, D., Kobayashi, R., Koomen, J. M., Stoops, J. K., & Waxham, M. N. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313597200 · Cited by 193
Citron binds to PSD-95 at glutamatergic synapses on inhibitory neurons in the hippocampus
Zhang, W., Vazquez, L., Apperson, M., & Kennedy, M. B. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00096.1999 · Cited by 190
Determination of absolute protein numbers in single synapses by a GFP-based calibration technique
Sugiyama, Y., Kawabata, I., Sobue, K., & Okabe, S. (2005) · Nature Methods · doi:10.1038/nmeth783 · Cited by 189
Glutamate-induced transient modification of the postsynaptic density
Dosemeci, A., Tao-Cheng, J.-H., Vinade, L., Winters, C. A., Pozzo-Miller, L., & Reese, T. S. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.181336998 · Cited by 184
Synaptic contact dynamics controlled by cadherin and catenins
Takeichi, M., & Abe, K. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.02.002 · Cited by 176
Apperson, M., Moon, I. S., & Kennedy, M. B. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-21-06839.1996 · Cited by 166
Karpova, A., Mikhaylova, M., Thomas, U., Knöpfel, T., & Behnisch, T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4573-05.2006 · Cited by 162
Assembly of Proteins to Postsynaptic Densities after Transient Cerebral Ischemia
Hu, B. R., Park, M., Martone, M. E., Fischer, W. H., Ellisman, M. H., & Zivin, J. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-02-00625.1998 · Cited by 160
Activity-driven postsynaptic translocation of CaMKII
Merrill, M. A., Chen, Y., Strack, S., & Hell, J. W. (2005) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2005.10.003 · Cited by 155
Secretory trafficking in neuronal dendrites
Horton, A. C., & Ehlers, M. (2004) · Nature Cell Biology · doi:10.1038/ncb0704-585 · Cited by 154
Ryan, X. P., Alldritt, J., Svenningsson, P., Allen, P. B., Wu, G.-Y., Nairn, A. C., & Greengard, P. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.013 · Cited by 142
Proteomics of the nervous system
Husi, H., & Grant, S. G. N. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01792-6 · Cited by 134
Robison, A. J., Bass, M. A., Jiao, Y., MacMillan, L. B., Carmody, L. C., Bartlett, R. K., & Colbran, R. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502191200 · Cited by 134
Walsh, M. J., & Kuruc, N. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb09421.x · Cited by 123
Submicroscopic Morphology of the Synapse
Robertis, E. D. P. D. (1959) · International review of cytology · doi:10.1016/s0074-7696(08)62728-x · Cited by 114
Morphological Characterization of Molecular Complexes Present in the Synaptic Cleft
́, V. L., Yang, T., Schweikert, G., Förster, F. G., & Baumeister, W. P. (2005) · Structure · doi:10.1016/j.str.2005.02.005 · Cited by 109
Tangential synaptic distribution of NMDA and AMPA receptors in rat neocortex
Kharazia, V. N., & Weinberg, R. J. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)00846-x · Cited by 104
Assembly and plasticity of the glutamatergic postsynaptic specialization
McGee, A. W., & Bredt, D. S. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00008-4 · Cited by 102
Tetrameric Hub Structure of Postsynaptic Scaffolding Protein Homer
Hayashi, M. K., Ames, H. M., & Hayashi, Y. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2731-06.2006 · Cited by 101
A role for zinc in postsynaptic density asSAMbly and plasticity?
Gundelfinger, E. D., Boeckers, T. M., Baron, M. K., & Bowie, J. U. (2006) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2006.05.007 · Cited by 98
Yoshimura, Y., Shinkawa, T., Taoka, M., Kobayashi, K., Isobe, T., & Yamauchi, T. (2002) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.6320 · Cited by 94
Drake, C. T., Bausch, S. B., Milner, T. A., & Chavkin, C. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.3.1007 · Cited by 93
Svoboda, K., & Mainen, Z. F. (1999) · Neuron · doi:10.1016/s0896-6273(00)80698-4 · Cited by 91
Hsueh, Y., & Sheng, M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.1.532 · Cited by 86
Self-citationIdentification of activity‐regulated proteins in the postsynaptic density fraction
Satoh, K., Takeuchi, M., Oda, Y., Deguchi‐Tawarada, M., Sakamoto, Y., Matsubara, K., Nagasu, T., & Takai, Y. (2002) · Genes to Cells · doi:10.1046/j.1356-9597.2001.00505.x · Cited by 85
Steinberg, J. P., Huganir, R. L., & Linden, D. J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408278102 · Cited by 73
Preparation of postsynaptic density fraction from hippocampal slices and proteomic analysis
Döṣemeci, A., Tao-Cheng, J.-H., Vinadé, L., & Jaffe, H. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.11.069 · Cited by 72
Christopherson, K. S., Sweeney, N. T., Craven, S. E., Kang, R., El-Husseini, A., & Bredt, D. S. (2003) · Journal of Cell Science · doi:10.1242/jcs.00617 · Cited by 70
Inoue, A., & Okabe, S. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00077-1 · Cited by 62
Pierce, J. P., van Leyen, K., & McCarthy, J. B. (2000) · Nature Neuroscience · doi:10.1038/74908 · Cited by 57
Structural basis for developmentally regulated changes in cadherin function at synapses
Elste, A. M., & Benson, D. L. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20876 · Cited by 50
NSF interaction is important for direct insertion of GluR2 at synaptic sites
Beretta, F., Sala, C., Saglietti, L., Hirling, H., Sheng, M., & Passafaro, M. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.11.008 · Cited by 48
Self-citationIdentification of novel phosphorylation sites on postsynaptic density proteins
Jaffe, H., Vinadé, L., & Döṣemeci, A. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.06.122 · Cited by 48
Research works printed but not linked: 3
- Gray EG, 1959, J. Anat., 93, 420
- Collins MO, 2005, J. Neurochem., 97, 16
- Tsuriel S, 2006, PLoS Biol., 15, 4(9)
Cited by
Sorted by citations
The physiology, signaling, and pharmacology of dopamine receptors
Beaulieu, J.-M., & Gainetdinov, R. R. (2011) · Pharmacological Reviews · doi:10.1124/pr.110.002642 · Cited by 2,763
Neuroligins and neurexins link synaptic function to cognitive disease
Südhof, T. C. (2008) · Nature · doi:10.1038/nature07456 · Cited by 1,849
How the Timing and Quality of Early Experiences Influence the Development of Brain Architecture
Fox, S. E., Levitt, P., & Nelson, C. A. (2010) · Child Development · doi:10.1111/j.1467-8624.2009.01380.x · Cited by 1,088
Brain Glucose Metabolism: Integration of Energetics with Function
Dienel, G. A. (2018) · Physiological Reviews · doi:10.1152/physrev.00062.2017 · Cited by 911
Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy.
Cingolani, L. A., & Goda, Y. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2373 · Cited by 831
Metadata
- Authors
- Sheng, M., & Hoogenraad, C. C.
- Affiliations
- Howard Hughes Medical Institute (US)
- Erasmus MC (NL)
- Venue
- Annual Review of Biochemistry
- Publisher
- Annual Reviews
- Published
- 2007-06-07
- Volume
- 76
- Issue
- 1
- Pages
- 823-847
- ISSN
- 0066-4154 (ISSN-L)
- 1545-4509
- OpenAlex
- W2071318481
- Cited by
- 1,003
- References
- 154
- Citations by year
- 2026: 27 · 2025: 37 · 2024: 32 · 2023: 42 · 2022: 41 · 2021: 51 · 2020: 64 · 2019: 58 · 2018: 52 · 2017: 39 · 2016: 58 · 2015: 42 · 2014: 62 · 2013: 68 · 2012: 65
- FWCI
- 5.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- postsynaptic density, excitatory synapses, glutamatergic synapses, dendritic spines, synaptic structure, glutamate receptors, synaptic scaffolds, protein stoichiometry, postsynaptic membrane, synaptic plasticity, electron microscopy of synapses
- MeSH terms
- Animals, Brain, Cell Membrane, Models, Molecular, Nerve Tissue Proteins, Synapses, Receptors, Glutamate, Dendritic Spines
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