The DOI matches its Crossref record; 64 of the 64 references it cites were found in a registry or an index.
The Role of NMDA Receptors in Information Processing
Abstract
In this review, we have concentrated on the parallels between the cellular properties of the NMDA receptor and a variety of functional properties within sensory and motor systems. Of course, the NMDA channel exists within the cell in conjunction with a variety of other channels, including non-NMDA channels. Although the NMDA receptor is unique in a cellular sense--it is the only ligand-gated channel that is also voltage dependent and calcium permeable--it is not unique in a functional sense. A cell that has non-NMDA receptors and voltage-sensitive channels will also exhibit nonlinear behavior. Moreover, Buhrle & Sonnhof (1983) demonstrated some time ago that calcium flows into frog motor neurons through more than one type of calcium channel. The contribution to the inflow of calcium from NMDA channels may vary from cell to cell and could easily be a minor proportion of the total. Many authors have pointed out that the NMDA channel has a low conductance at a resting potential of -70 mV. However, many cells in the nervous system are depolarized from -70 mV by excitatory input. Thus, as pointed out above. NMDA receptors make a contribution to the tonic or spontaneous activity of cells in both visual cortex and spinal cord. In practice, many cells are probably working in a range of membrane potentials where the NMDA channels are always open to some extent. Even in the hippocampal slice where a substantial amount of afferent input is removed, NMDA receptors contribute to spontaneous activity (Sah et al 1989). Does the NMDA receptor act as a switch? Does it act as an AND gate? The suggestion that it may act as a switch comes from work on LTP in the hippocampus, which is readily produced by high-frequency stimulation and is abolished by APV. However, activation of the NMDA receptor is only the first in a sequence of reactions leading to LTP: In theory, switch-like behavior could also be produced by calcium-buffering systems within dendritic spines, or by enzymatic processes (Lisman 1985; Zador et al 1990). Fox & Daw (1992) have modeled the action of NMDA and non-NMDA receptors that are activated in parallel with each other, and shown that the occurrence of switch-like behavior depends on the relative density of NMDA versus non-NMDA receptors. Switch-like behavior is not seen in the visual cortex, but might be seen in the hippocampus if the relative density of NMDA receptors there was higher than in the visual cortex.(ABSTRACT TRUNCATED AT 400 WORDS)
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
“Visual pathways within the brain use glutamate as their primary neurotransmitter, and N-methyl d-aspartate (NMDA) seems to have a central role in gain control.”
From Visual perception and its impairment in schizophrenia (2008) · cites this paper as [15]
In the citing paper
“For instance, NMDA receptors amplify responses to isolated stimuli as well as amplifying the effects of lateral inhibition (e.g., increase surround antagonism of center receptive field responses) (15).”
From Visual perception and its impairment in schizophrenia (2008) · cites this paper as [15]
Citations
Cites
Magnesium gates glutamate-activated channels in mouse central neurones
Nowak, L. M., Bregestovski, P. D., Ascher, P., Herbet, A., & Prochiantz, A. (1984) · Nature · doi:10.1038/307462a0 · Cited by 4,116
The Role Of Glutamate Neurotoxicity In Hypoxic-Ischemic Neuronal Death
Choi, D. W., & Rothman, S. M. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.001131 · Cited by 2,210
Woolf, C. J., & Thompson, S. (1991) · Pain · doi:10.1016/0304-3959(91)90100-c · Cited by 1,985
The physiology of excitatory amino acids in the vertebrate central nervous system
Mayer, M. L., & Westbrook, G. L. (1987) · Progress in Neurobiology · doi:10.1016/0301-0082(87)90011-6 · Cited by 1,711
McDonald, J. W., & Johnston, M. V. (1990) · Brain Research Reviews · doi:10.1016/0165-0173(90)90011-c · Cited by 1,403
NMDA receptors - their role in long-term potentiation
Collingridge, G. L., & Bliss, T. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90175-5 · Cited by 1,178
Physiological properties of unmyelinated fiber projection to the spinal cord
Mendell, L. M. (1966) · Experimental Neurology · doi:10.1016/0014-4886(66)90068-9 · Cited by 844
Dickenson, A. H., & Sullivan, A. F. (1987) · Neuropharmacology · doi:10.1016/0028-3908(87)90275-9 · Cited by 843
Bekkers, J. M., & Stevens, C. F. (1989) · Nature · doi:10.1038/341230a0 · Cited by 660
Laminar Organization of Thalamic Projections to the Rat Neocortex
Herkenham, M. A. (1980) · Science · doi:10.1126/science.7352263 · Cited by 595
Cited by
Sorted by citations
Items 101–200 of 311
Durand, J. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00925.x · Cited by 43
Thalamocortical Synaptic Connections: Efficacy, Modulation, Inhibition and Plasticity
Amitai, Y. (2001) · Reviews in the Neurosciences · doi:10.1515/revneuro.2001.12.2.159 · Cited by 43
Effects of MK-801 on recognition and neurodegeneration in an MPTP-induced Parkinson's rat model
Hsieh, M., Gu, S.-L., Ho, S.-C., Pawlak, C. R., Lin, C., Ho, Y., Lai, T., & Wu, F.-Y. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.12.035 · Cited by 42
Differential expression of N-methyl-d-aspartate receptor in the cochlear nucleus of the mouse
Bilak, M. M., Bilak, S. R., & Morest, D. K. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00197-2 · Cited by 42
van Vugt, B., van Kerkoerle, T., Vartak, D., & Roelfsema, P. R. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2121-19.2020 · Cited by 44
Boettiger, C. A., & Doupe, A. J. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.5.2615 · Cited by 41
Silent Synapses in a Thalamo-Cortical Circuit Necessary for Song Learning in Zebra Finches
Bottjer, S. W. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00282.2005 · Cited by 42
Spiro, J. E. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.2.835 · Cited by 40
Richter, R. M., & Weiss, F. (1999) · Synapse · doi:10.1002/(sici)1098-2396(19990615)32:4 · Cited by 210
Siddiqui, A. J., Badraoui, R., Jahan, S., Alshahrani, M. M., Siddiqui, M. A., Khan, A., & Adnan, M. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1208968 · Cited by 39
Ueno, K., Naganos, S., Hirano, Y., Horiuchi, J., & Saitoe, M. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.242909 · Cited by 39
Alvarez, E. O., & Ruarte, M. B. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.10.012 · Cited by 39
Heterogeneous glutamatergic receptor mRNA expression across phrenic motor neurons in rats
Rana, S. D., Sieck, G. C., & Mantilla, C. B. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14881 · Cited by 38
Activity-dependent structural changes during neuronal development
Hockfield, S. J., & Kalb, R. G. (1993) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(93)90040-6 · Cited by 38
Robol, V., Tibber, M. S., Anderson, E. J., Bobin, T., Carlin, P., Shergill, S. S., & Dakin, S. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060951 · Cited by 37
NMDA Receptor Gating of Information Flow through the Striatum In Vivo
Pomata, P. E., Belluscio, M., Riquelme, L. A., & Murer, M. G. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4343-08.2008 · Cited by 39
Kreimeyer, A., Laube, B., Sturgess, M., Goeldner, M. P., & Foucaud, B. (1999) · Journal of Medicinal Chemistry · doi:10.1021/jm9910730 · Cited by 36
Fukushima, Y., Tsukada, M., Tsuda, I., Yamaguti, Y., & Kuroda, S. (2007) · Cognitive Neurodynamics · doi:10.1007/s11571-007-9026-9 · Cited by 36
Klein, T., Magerl, W., Hanschmann, A., Althaus, M., & Treede, R. (2007) · European Journal of Pain · doi:10.1016/j.ejpain.2007.02.002 · Cited by 36
Spuhler‐Phillips, K., Lee, Y. H., Hughes, P., Randoll, L., & Leslie, S. W. (1997) · Alcoholism Clinical and Experimental Research · doi:10.1097/00000374-199702000-00010 · Cited by 36
Treadmill exercise enhances NMDA receptor expression in schizophrenia mice
Park, J.-K., Lee, S., & Kim, T. (2014) · Journal of Exercise Rehabilitation · doi:10.12965/jer.140088 · Cited by 35
Summers, M. J., Crowe, S. F., & Ng, K. T. (1997) · Cognitive Brain Research · doi:10.1016/s0926-6410(97)00007-4 · Cited by 35
Ferretti, V., Sargolini, F., Oliverio, A., Mele, A., & Roullet, P. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.009 · Cited by 34
Central pattern generators in the turtle spinal cord: selection among the forms of motor behaviors
Stein, P. S. G. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00602.2017 · Cited by 35
Memory retrieval in the day-old chick: a psychobiological approach
Summers, M. J., Crowe, S. F., & Ng, K. T. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(03)00032-0 · Cited by 34
Galehdari, H. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9148-5 · Cited by 33
Pussinen, R., & Sirviö, J. (1999) · Journal of Psychopharmacology · doi:10.1177/026988119901300210 · Cited by 33
Bottai, D., Maler, L., & Dunn, R. J. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-14-05191.1998 · Cited by 32
The Cortical Neuron as an Electrophysiological Unit
Gutnick, M. J., & Crill, W. E. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0003 · Cited by 32
Neuroligin1 Drives Synaptic and Behavioral Maturation through Intracellular Interactions
Hoy, J. L., Haeger, P. A., Constable, J. R. L., Arias, R. J., McCallum, R., Kyweriga, M., Davis, L., Schnell, E., Wehr, M., Castillo, P. E., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4660-12.2013 · Cited by 30
Effects of MK-801 on rough-and-tumble play in juvenile rats
Sivity, S. M., Line, B. S., & Darcy, E. A. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(94)00361-8 · Cited by 30
Ernst, A. F., Jurney, W. M., & McLoon, S. C. (1998) · Progress in brain research · doi:10.1016/s0079-6123(08)63204-5 · Cited by 30
Functions of Local Circuits in Neocortex: Synchrony and Laminae
Connors, B. W., & Amitai, Y. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0009 · Cited by 30
Vega-Villar, M., Horvitz, J. C., & Nicola, S. M. (2019) · Nature Communications · doi:10.1038/s41467-019-12387-z · Cited by 30
Plasticity Mechanisms of Memory Consolidation and Reconsolidation in the Perirhinal Cortex
Miranda, M., & Bekinschtein, P. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.06.002 · Cited by 31
Voluntary wheel running ameliorates symptoms of MK-801-induced schizophrenia in mice
Kim, T.-W., Kang, H., Park, J.-K., Lee, S., Baek, S.-B., & Kim, C. (2014) · Molecular Medicine Reports · doi:10.3892/mmr.2014.2644 · Cited by 27
Functional diversity of central glutamate synapses‐pre‐ and post‐synaptic mechanisms
Brodin, L., & Shupliakov, O. (1994) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1994.tb09653.x · Cited by 28
Dynamics of spiking neurons: between homogeneity and synchrony
Rangan, A. V., & Young, L.-S. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0429-1 · Cited by 25
Multifunctional calcium and calmodulin-dependent kinase II in neuronal function and disease
Churn, S. B. (1995) · Advances in Neuroimmunology · doi:10.1016/0960-5428(95)00016-u · Cited by 26
Cain, D. P., Ighanian, K., & Boon, F. H. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00150-9 · Cited by 26
Self-organized dynamics in plastic neural networks: bistability and coherence
Kalitzin, S., van Dijk, B. W., & Spekreijse, H. (2000) · Biological Cybernetics · doi:10.1007/s004220000157 · Cited by 25
Nonlinear EEG analysis during sleep in premature and full-term newborns
Ferri, R., Chiaramonti, R., Elia, M., Musumeci, S. A., Ragazzoni, A., & Stam, C. J. (2003) · Clinical Neurophysiology · doi:10.1016/s1388-2457(03)00089-0 · Cited by 25
NMDAR-Dependent Control of Call Duration in Xenopus laevis
Zornik, E., Katzen, A. W., Rhodes, H. J., & Yamaguchi, A. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00155.2010 · Cited by 24
Pharmacology of sensory gating in the ascending auditory system of the pigeon ( Columba livia )
Schall, U., Keysers, C., & Kast, B. (1999) · Psychopharmacology · doi:10.1007/s002130051059 · Cited by 24
Johnson, F. A., Dawson, A. J., & Meyer, R. L. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990419)406:4 · Cited by 23
Light deprivation improves melatonin related suppression of hippocampal plasticity
Talaei, S. A., Sheibani, V., & Salami, M. (2010) · Hippocampus · doi:10.1002/hipo.20650 · Cited by 27
The modification of NMDA receptors by visual experience in the rat retina is age dependent
Xue, J., & Cooper, N. G. F. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00141-3 · Cited by 22
Kouvaros, S., & Papatheodoropoulos, C. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2015.12.059 · Cited by 24
Gating Information by Two-State Membrane Potential Fluctuations
Kepecs, Á., & Raghavachari, S. (2007) · Journal of Neurophysiology · doi:10.1152/jn.01242.2006 · Cited by 22
Synapse Models for Neural Networks: From Ion Channel Kinetics to Multiplicative Coefficient wij
Chapeau‐Blondeau, F., & Chambet, N. (1995) · Neural Computation · doi:10.1162/neco.1995.7.4.713 · Cited by 22
Sestito, R. S., Trindade, L. B., de Souza, R. G., Kerbauy, L. N., Iyomasa-Pilon, M. M., & Rosa, M. L. N. M. (2010) · Journal of Psychopharmacology · doi:10.1177/0269881110385595 · Cited by 22
Schizophrenia: Putting context in context
Park, S., Lee, J., Folley, B. S., & Kim, J. (2003) · Behavioral and Brain Sciences · doi:10.1017/s0140525x03380021 · Cited by 21
Oestreich, J., Dembrow, N. C., George, A. A., & Zakon, H. H. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.027 · Cited by 20
Multi-directional representation of spatial working memory in a model prefrontal cortical circuit
Tanaka, S. (2002) · Neurocomputing · doi:10.1016/s0925-2312(02)00503-9 · Cited by 21
Curti, S., Falconi, A., Morales, F. R., & Borde, M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-09133.1999 · Cited by 22
L-trans-2,3-Pyrrolidine Dicarboxylate: Characterization of a Novel Excitotoxin
Willis, C. L., Humphrey, J. M., Koch, H. P., Hart, J. A., Blakely, T. N., Ralston, L., BAKER, C. A., SHIM, S., Kadri, M. M., Chamberlin, A. R., et al. (1996) · Neuropharmacology · doi:10.1016/0028-3908(96)84623-5 · Cited by 21
Fukuda, M., Hata, Y., Ohshima, M., & Tsumoto, T. (1998) · Neuroscience Research · doi:10.1016/s0168-0102(98)00018-2 · Cited by 20
Excitatory and inhibitory neurotransmitters in the nucleus rotundus of pigeons
Gao, H., Wu, G., Frost, B. J., & Wang, S. (1995) · Visual Neuroscience · doi:10.1017/s095252380000938x · Cited by 20
Alvarez, E. O., & Ruarte, M. B. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00190-5 · Cited by 19
Why do schizophrenic patients hallucinate?
Roelfsema, P. R., & Supèr, H. (2003) · Behavioral and Brain Sciences · doi:10.1017/s0140525x03410029 · Cited by 18
Impact of calcium-activated potassium channels on NMDA spikes in cortical layer 5 pyramidal neurons
Bock, T., & Stuart, G. J. (2016) · Journal of Neurophysiology · doi:10.1152/jn.01047.2015 · Cited by 19
Synaptic Runaway in Associative Networks and the Pathogenesis of Schizophrenia
Greenstein‐Messica, A., & Ruppin, E. (1998) · Neural Computation · doi:10.1162/089976698300017836 · Cited by 18
Laminar circuit organization and response modulation in mouse visual cortex
Olivas, N. D., Quintanar-Zilinskas, V., Nenadic, Z., & Xu, X. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00070 · Cited by 17
NMDA receptor expression in the mouse cerebellar cortex
Bilak, S. R., Bilak, M. M., & Morest, D. K. (1995) · Synapse · doi:10.1002/syn.890200310 · Cited by 17
Inhibition in the Cortical Network
Benardo, L. S., & Wong, R. K. S. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0010 · Cited by 19
(1995) · doi:10.1093/acprof:oso/9780195083309.001.0001 · Cited by 18
Nicotine recruits glutamate receptors to postsynaptic sites
Duan, J.-J., Lozada, A. F., Gou, C., Xu, J., Chen, Y., & Berg, D. K. (2015) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.09.002 · Cited by 20
Burtoloso, A. C. B., & Correia, C. R. D. (2008) · Tetrahedron · doi:10.1016/j.tet.2008.08.001 · Cited by 16
Catts, S. V., Ward, P. B., Lloyd, A. R., Huang, X., Dixon, G., Chahl, L. A., Harper, C. G., & Wakefield, D. (1997) · Australian & New Zealand Journal of Psychiatry · doi:10.3109/00048679709073795 · Cited by 17
Yang, B., Wang, Y., & Cynader, M. S. (1996) · Brain Research · doi:10.1016/0006-8993(96)00047-9 · Cited by 16
Overview: Basic Elements of the Cortical Network
Jones, E. G. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0008 · Cited by 17
Redistribution of NMDA receptors in the cochlear nucleus following cochleotomy
Förster, C. R., & Illing, R. (1998) · Neuroreport · doi:10.1097/00001756-199810260-00036 · Cited by 15
Stimulus Selectivity Is Enhanced by Voltage-Dependent Conductances in Combination-Sensitive Neurons
Carlson, B. A., & Kawasaki, M. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00839.2006 · Cited by 15
The complexity of pain: part 2. Pain as a complex adaptive system
Stephenson, R. (1999) · Physical Therapy Reviews · doi:10.1179/108331999786821753 · Cited by 15
Ouardouz, M., & Durand, J. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00558.x · Cited by 15
Dinse, H. R. (1994) · Physica D Nonlinear Phenomena · doi:10.1016/0167-2789(94)90279-8 · Cited by 15
Long-term effects of excitatory amino acid antagonists NBQX and MK-801 on the developing brain
Tandon, P., Liu, Z., Stafstrom, C. E., Sarkisian, M. R., Werner, S. J., Mikati, M. A., Yang, Y., & Holmes, G. L. (1996) · Developmental Brain Research · doi:10.1016/0165-3806(96)00094-6 · Cited by 14
Gattuso, J. J., Wilson, C., Hannan, A. J., & Renoir, T. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109689 · Cited by 14
Network, Cellular, and Molecular Mechanisms Underlying Long-Term Memory Formation
Carasatorre, M., & Ramı́rez-Amaya, V. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_229 · Cited by 14
Effects of ketamine anesthesia on central nociceptive processing in the rat: a 2-deoxyglucose study
Porro, C. A., Cavazzuti, M., Giuliani, D., Vellani, V., Lui, F., & Baraldi, P. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.01.039 · Cited by 13
Ma, X., Kohashi, T., & Carlson, B. A. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00145.2013 · Cited by 13
Pinaud, R. (2006) · Springer eBooks · doi:10.1007/0-387-28190-8_8 · Cited by 13
García, P. S., Whalin, M. K., & Sebel, P. S. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4377-1679-5.00009-0 · Cited by 12
Spatial Suppression and Sensitivity for Motion in Schizophrenia
Linares, D., Amoretti, S., Marin-Campos, R., Sousa, A., Prades, L., Dalmau, J. O., Bernardo, M., & Compte, A. (2020) · Schizophrenia Bulletin Open · doi:10.1093/schizbullopen/sgaa045 · Cited by 10
Two Affinity States of N-Methyl-d-Aspartate Recognition Sites: Modulation by Cations
Mukhin, A. G., Kovaleva, E. S., & London, E. D. (1997) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36883-1 · Cited by 12
Large-Scale Computational Modeling of the Primary Visual Cortex
Rangan, A. V., Tao, L., Kovačič, G., & Cai, D. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0389-1_14 · Cited by 12
No blind schizophrenics: Are NMDA-receptor dynamics involved?
Sanders, G. S., Platek, S. M., & Gallup, G. G. (2003) · Behavioral and Brain Sciences · doi:10.1017/s0140525x03420025 · Cited by 13
The Neural Basis of Learning with Particular Reference to the Role of Synaptic Plasticity
Morris, R. (1994) · Elsevier eBooks · doi:10.1016/b978-0-08-057169-0.50012-7 · Cited by 12
Neural Correlates of Sensitive Periods in Avian Song Learning
Nordeen, K. W. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb51934.x · Cited by 11
Synaptic Plasticity in Hippocampus and Neocortex: A Comparison
Malenka, R. C. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0007 · Cited by 11
Optical imaging of intrinsic signals in somatosensory cortex
Tommerdahl, M., & Whitsel, B. L. (1996) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-9016-8_31 · Cited by 11
Wang, S., Liao, C., Meng, W., Huang, Q. D., & Li, D. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.01.032 · Cited by 10
Effects of Uncontrolled Seizures
Stafstrom, C. E., & Holmes, G. L. (2002) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-1335-3_17 · Cited by 10
The complexity of pain: part 1. No pain without gain: the augmentation of nociception in the CNS
Stephenson, R. (1999) · Physical Therapy Reviews · doi:10.1179/108331999786822121 · Cited by 10
Learning Invariance from Natural Images Inspired by Observations in the Primary Visual Cortex
Teichmann, M., Wiltschut, J., & Hamker, F. H. (2012) · Neural Computation · doi:10.1162/neco_a_00268 · Cited by 10
Frau, R., Pardu, A., Godar, S. C., Bini, V., & Bortolato, M. (2022) · Pharmaceuticals · doi:10.3390/ph15020213 · Cited by 9
Doriat, J., Koziel, V., Humbert, A., & Daval, J. (1999) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(99)00033-7 · Cited by 9
Mechanisms of disrupted language comprehension in schizophrenia
Condray, R., & Steinhauer, S. R. (2003) · Behavioral and Brain Sciences · doi:10.1017/s0140525x03270023 · Cited by 9
A MULTI-DISCIPLINARY SURVEY OF BIOCOMPUTING: 1. MOLECULAR AND CELLULAR LEVELS
Hong, F. T. (2005) · Series on advances in bioinformatics and computational biology · doi:10.1142/9781860946882_0001 · Cited by 8
Effects of uncontrolled seizures. Neural changes in animal models.
Stafstrom, C. E., & Holmes, G. L. (2002) · PubMed · Cited by 8
Metadata
- Authors
- Daw, N. W., Stein, P. S. G., & Fox, K.
- Affiliations
- Yale University (US)
- ORCID
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 1993-03
- Volume
- 16
- Issue
- 1
- Pages
- 207-222
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- OpenAlex
- W2179166911
- Cited by
- 311
- References
- 64
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 7 · 2023: 8 · 2022: 1 · 2021: 4 · 2020: 3 · 2019: 3 · 2018: 4 · 2017: 4 · 2016: 2 · 2015: 5 · 2014: 4 · 2013: 11 · 2012: 17
- FWCI
- 8.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5p01ns029343-02)
- National Eye Institute (R01EY000053, EY-00053)
- National Institute of Neurological Disorders and Stroke (NS27759, NS29343)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- NMDA receptor, synaptic plasticity, long-term potentiation, switch-like behavior, non-NMDA receptors, calcium influx, spontaneous neuronal activity, hippocampus, visual cortex, motor neurons, dendritic spines, calcium buffering, APV, glutamate receptors, dendritic integration
- MeSH terms
- Animals, Brain, Mental Processes, Neurons, Nociceptors, Spinal Cord, Synapses, Visual Cortex, Receptors, N-Methyl-D-Aspartate, N-Methylaspartate
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