Distribution and synaptic localization of immunocytochemically identified NMDA receptor subunit proteins in sensory-motor and visual cortices of monkey and human

A synaptic model of memory: long-term potentiation in the hippocampus

Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566 · see citing works

Glutamate neurotoxicity and diseases of the nervous system

Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,152 · see citing works

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 4,033 · see citing works

Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones

Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,906 · see citing works

Molecular diversity of glutamate receptors and implications for brain function

Nakanishi, S. (1992) · Science · doi:10.1126/science.1329206 · Cited by 2,543 · see citing works

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 · see citing works

Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry

Wong‐Riley, M. T. T. (1979) · Brain Research · doi:10.1016/0006-8993(79)90728-5 · Cited by 1,853 · see citing works

Excitatory amino acid neurotoxicity and neurodegenerative disease

Meldrum, B. S., & Garthwaite, J. (1990) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(90)90184-a · Cited by 1,774 · see citing works

Molecular cloning and characterization of the rat NMDA receptor

Moriyoshi, K., Masu, M., Ishii, T., Shigemoto, R., Mizuno, N., & Nakanishi, S. (1991) · Nature · doi:10.1038/354031a0 · Cited by 1,771 · see citing works

Anatomy and physiology of a color system in the primate visual cortex

Livingstone, M. S., & Hubel, D. H. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-01-00309.1984 · Cited by 1,637 · see citing works

Molecular diversity of the NMDA receptor channel

Kutsuwada, T., Kashiwabuchi, N., Mori, H., Sakimura, K., Kushiya, E., Araki, K., Meguro, H., Hisashi, M., Kumanishi, T., Arakawa, M., et al. (1992) · Nature · doi:10.1038/358036a0 · Cited by 1,346 · see citing works

Somatosensory cortical map changes following digit amputation in adult monkeys

Merzenich, M. M., Nelson, R. J., Stryker, M. P., Cynader, M. S., Schoppmann, A., & Zook, J. M. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902240408 · Cited by 1,326 · see citing works

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 1,174 · see citing works

Concurrent processing streams in monkey visual cortex

DeYoe, E. A., & Essen, D. C. V. (1988) · Trends in Neurosciences · doi:10.1016/0166-2236(88)90130-0 · Cited by 1,118 · see citing works

The Fine Structure of the Nervous System

Afifi, A. K. (1991) · Neurology · doi:10.1212/wnl.41.9.1535-b · Cited by 1,052 · see citing works

Topographic reorganization of somatosensory cortical areas 3b and 1 in adult monkeys following restricted deafferentation

Merzenich, M. M., Kaas, J. H., Wall, J., Nelson, R. J., Sur, M., & Felleman, D. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90024-6 · Cited by 1,042 · see citing works

Reshaping the Cortical Motor Map by Unmasking Latent Intracortical Connections

Jacobs, K. M., & Donoghue, J. P. (1991) · Science · doi:10.1126/science.2000496 · Cited by 1,014 · see citing works

Long-term potentiation and NMDA receptors in rat visual cortex

Artola, A., & Singer, W. (1987) · Nature · doi:10.1038/330649a0 · Cited by 966 · see citing works

Laminar and columnar distribution of geniculo‐cortical fibers in the macaque monkey

Hubel, D. H., & Wiesel, T. N. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901460402 · Cited by 945 · see citing works

Blockade of "NMDA" Receptors Disrupts Experience-Dependent Plasticity of Kitten Striate Cortex

Kleinschmidt, A. K., Bear, M. F., & Singer, W. (1987) · Science · doi:10.1126/science.2443978 · Cited by 906 · see citing works

Excitatory amino acid receptors and synaptic plasticity

Collingridge, G. L., & Singer, W. (1990) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(90)90011-v · Cited by 862 · see citing works

Functional characterization of a heteromeric NMDA receptor channel expressed from cloned cDNAs

Meguro, H., Mori, H., Araki, K., Kushiya, E., Kutsuwada, T., Yamazaki, M., Kumanishi, T., Arakawa, M., Sakimura, K., & Mishina, M. (1992) · Nature · doi:10.1038/357070a0 · Cited by 798 · see citing works

Patterned Activity, Synaptic Convergence, and the NMDA Receptor in Developing Visual Pathways

Constantine-Paton, M., Cline, H. T., & Debski, E. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.001021 · Cited by 784 · see citing works

Reorganization of Retinotopic Cortical Maps in Adult Mammals After Lesions of the Retina

Kaas, J. H., Krubitzer, L. A., Chino, Y. M., Langston, A., Polley, E. H., & Blair, N. P. (1990) · Science · doi:10.1126/science.2326637 · Cited by 647 · see citing works

Biochemical and immunochemical evidence that the "major postsynaptic density protein" is a subunit of a calmodulin-dependent protein kinase.

Kennedy, 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 · see citing works

Numbers and proportions of GABA-immunoreactive neurons in different areas of monkey cerebral cortex

Hendry, S., Schwark, H. D., Jones, E. G., & Yan, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-05-01503.1987 · Cited by 601 · see citing works

Varieties and distribution of non‐pyramidal cells in the somatic sensory cortex of the squirrel monkey

Jones, E. G. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901600204 · Cited by 593 · see citing works

Structures and properties of seven isoforms of the NMDA receptor generated by alternative splicing

Sugihara, H., Moriyoshi, K., Ishii, T. M., Masu, M., & Nakanishi, S. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(92)91701-q · Cited by 523 · see citing works

Two classes of cortical GABA neurons defined by differential calcium binding protein immunoreactivities

Hendry, S. H. C., Jones, E. G., Emson, P. C., Lawson, D. E. M., Heizmann, C. W., & Streit, P. (1989) · Experimental Brain Research · doi:10.1007/bf00247904 · Cited by 512 · see citing works

Excitatory Amino Acid Neurotransmission: NMDA Receptors and Hebb-Type Synaptic Plasticity

Cotman, C. W., & Monaghan, D. T. (1988) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.11.030188.000425 · Cited by 484 · see citing works

Excitatory amino acids and Alzheimer's disease

Greenamyre, J. T., & Young, A. B. (1989) · Neurobiology of Aging · doi:10.1016/0197-4580(89)90143-7 · Cited by 482 · see citing works

Electrophysiological studies of NMDA receptors

Ascher, P., & Nowak, L. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90174-3 · Cited by 474 · see citing works

Molecular Neurobiology Of Glutamate Receptors

Gasic, G. P., & Hollmann, M. (1992) · Annual Review of Physiology · doi:10.1146/annurev.ph.54.030192.002451 · Cited by 450 · see citing works

NMDA receptors in the visual cortex of young kittens are more effective than those of adult cats

Tsumoto, T., Hagihara, K., Sato, H., & Hata, Y. (1987) · Nature · doi:10.1038/327513a0 · Cited by 440 · see citing works

Targets of horizontal connections in macaque primary visual cortex

McGuire, B. A., Gilbert, C. D., Rivlin, P. K., & Wiesel, T. N. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903050303 · Cited by 432 · see citing works

Excitatory amino acid receptors in the brain: membrane binding and receptor autoradiographic approaches

Young, A. B., & Fagg, G. E. (1990) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(90)90199-i · Cited by 392 · see citing works

The role of NMDA and non-NMDA excitatory amino acid receptors in the excitation of primate spinothalamic tract neurons by mechanical, chemical, thermal, and electrical stimuli

Dougherty, P. M., Paleček, J., Palečková, V., Sorkin, L. S., & Willis, W. H. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-08-03025.1992 · Cited by 367 · see citing works

Dynamic organization of primary motor cortex output to target muscles in adult rats II. Rapid reorganization following motor nerve lesions

Donoghue, J. P., Suner, S., & Sanes, J. N. (1990) · Experimental Brain Research · doi:10.1007/bf00229319 · Cited by 350 · see citing works

Long-Term Potentiation in the Motor Cortex

Iriki, A., Pavlides, C., Keller, A., & Asanuma, H. (1989) · Science · doi:10.1126/science.2551038 · Cited by 343 · see citing works

Visualization of chandelier cell axons by parvalbumin immunoreactivity in monkey cerebral cortex.

DeFelipe, J., Hendry, S. H. C., & Jones, E. G. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.6.2093 · Cited by 338 · see citing works

Glutamate decarboxylase-immunoreactive terminals of Golgi-impregnated axoaxonic cells and of presumed basket cells in synaptic contact with pyramidal neurons of the cat’s visual cortex

Freund, T. F., Martin, K. A. C., Smith, A. D., & Somogyi, P. (1983) · Journal of Comparative Neurology · doi:10.1002/cne.902210303 · Cited by 329 · see citing works

Immunocytochemical localization of glutamic acid decarboxylase in monkey striate cortex

Hendrickson, A. E., Hunt, S. P., & Wu, J. (1981) · Nature · doi:10.1038/292605a0 · Cited by 321 · see citing works

Synaptic targets of HRP-filled layer III pyramidal cells in the cat striate cortex

Kisvárday, Z. F., Martin, K. A. C., Freund, T. F., Maglóczky, Z., Whitteridge, D., & Somogyi, P. (1986) · Experimental Brain Research · doi:10.1007/bf00340492 · Cited by 313 · see citing works

The location and function of NMDA receptors in cat and kitten visual cortex

Fox, K., Sato, H., & Daw, N. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-07-02443.1989 · Cited by 307 · see citing works

Calcium‐binding proteins as markers for subpopulations of GABAergic neurons in monkey striate cortex

van Brederode, J. F. M., Mulligan, K. A., & Hendrickson, A. E. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902980102 · Cited by 284 · see citing works

Repetitive Microstimulation Alters the Cortical Representation of Movements in Adult Rats

Nudo, R. J., Jenkins, W. M., & Merzenieh, M. M. (1990) · Somatosensory & Motor Research · doi:10.3109/08990229009144720 · Cited by 274 · see citing works

Activity-dependent regulation of GABA expression in the visual cortex of adult monkeys

Hendry, S. H. C. (1988) · Neuron · doi:10.1016/0896-6273(88)90169-9 · Cited by 273 · see citing works

A magnesium‐sensitive post‐synaptic potential in rat cerebral cortex resembles neuronal responses to N‐methylaspartate.

Thomson, A. M. (1986) · The Journal of Physiology · doi:10.1113/jphysiol.1986.sp015949 · Cited by 246 · see citing works

A specialized type of neuron in the visual cortex of cat: A Golgi and electron microscope study of chandelier cells

Fairén, A. G., & Valverde, F. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901940405 · Cited by 239 · see citing works

A microcolumnar structure of monkey cerebral cortex revealed by immunocytochemical studies of double bouquet cell axons

DeFelipe, J., Hendry, S. H. C., Hashikawa, T., Molinari, M., & Jones, E. G. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90097-n · Cited by 231 · see citing works

Variability in the terminations of GABAergic chandelier cell axons on initial segments of pyramidal cell axons in the monkey sensory‐motor cortex

DeFelipe, J., Hendry, S. H. C., Jones, E. G., & Schmechel, D. E. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902310307 · Cited by 229 · see citing works

Heterogeneity of chandelier neurons in monkey neocortex: Corticotropin‐releasing factor‐and parvalbumin‐immunoreactive populations

Lewis, D. A., & Lund, J. S. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930406 · Cited by 220 · see citing works

Cellular components of the cerebral cortex

Peters, A., & Jones, E. G. (1984) · Plenum Press eBooks · Cited by 190 · see citing works

Visual responses in adult cat visual cortex depend on N-methyl-D-aspartate receptors.

Miller, K. D., Chapman, B., & Stryker, M. P. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.13.5183 · Cited by 181 · see citing works

The distribution and morphological characteristics of the intracortical VIP-positive cell: an immunohistochemical analysis.

Morrison, J., Magistretti, P., Benoit, R., & Bloom, F. (1984) · Brain Research · doi:10.1016/0006-8993(84)90763-7 · Cited by 176 · see citing works

Both NMDA and non-NMDA subtypes of glutamate receptors are concentrated at synapses on cerebral cortical neurons in culture

JONES, K. A., & Baughman, R. W. (1991) · Neuron · doi:10.1016/0896-6273(91)90372-7 · Cited by 172 · see citing works

The contribution of NMDA and non-NMDA receptors to fast and slow transmission of sensory information in the rat SI barrel cortex

Armstrong‐James, M., Welker, E., & Callahan, C. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-05-02149.1993 · Cited by 171 · see citing works

NMDA receptor-mediated currents are prominent in the thalamocortical synaptic response before maturation of inhibition

Agmon, A., & O’Dowd, D. K. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.68.1.345 · Cited by 166 · see citing works

Distribution of GABAergic neurons and axon terminals in the macaque striate cortex

Fitzpatrick, D., Lund, J. S., Schmechel, D. E., & Towles, A. C. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902640107 · Cited by 166 · see citing works

Immunoreactivity for a calmodulin-dependent protein kinase is selectively increased in macaque striate cortex after monocular deprivation.

Hendry, S. H. C., & Kennedy, M. B. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.5.1536 · Cited by 166 · see citing works

NMDA- and non-NMDA-receptor components of excitatory synaptic potentials recorded from cells in layer V of rat visual cortex

Jones, K., & Baughman, R. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-09-03522.1988 · Cited by 165 · see citing works

An electron microscopic study of the laminar pattern and mode of termination of afferent fibre pathways in the somatic sensory cortex of the cat

Jones, E. G., & Powell, T. P. S. (1970) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1970.0007 · Cited by 162 · see citing works

Large-scale functional reorganization in adult monkey cortex after peripheral nerve injury.

Garraghty, P. E., & Kaas, J. H. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.16.6976 · Cited by 154 · see citing works

Long-term potentiation of thalamic input to the motor cortex induced by coactivation of thalamocortical and corticocortical afferents

Iriki, A., Pavlides, C., Keller, A., & Asanuma, H. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.6.1435 · Cited by 148 · see citing works

Alpha calcium/calmodulin-dependent protein kinase II selectively expressed in a subpopulation of excitatory neurons in monkey sensory- motor cortex: comparison with GAD-67 expression

Jones, E. G., Huntley, G. W., & Benson, D. L. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-02-00611.1994 · Cited by 141 · see citing works

The synaptology of parvalbumin‐immunoreactive neurons in the primate prefrontal cortex

Williams, S. M., Goldman, P. S., & Leranth, C. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903200307 · Cited by 139 · see citing works

Organization of adult motor cortex representation patterns following neonatal forelimb nerve injury in rats

Donoghue, J. P., & Sanes, J. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-09-03221.1988 · Cited by 127 · see citing works

Do NMDA receptors have a critical function in visual cortical plasticity?

Fox, K. D., & Daw, N. W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90136-a · Cited by 127 · see citing works

Control of NMDA receptor-mediated activity by GABAergic mechanisms in mature and developing rat neocortex

Luhmann, H. J., & Prince, D. A. (1990) · Developmental Brain Research · doi:10.1016/0165-3806(90)90152-o · Cited by 121 · see citing works

High‐Resolution Light and Electron Microscopic Immunocytochemistry of Colocalized GABA and Calbindin D‐28k in Somata and Double Bouquet Cell Axons of Monkey Somatosensory Cortex

DeFelipe, J., & Jones, E. G. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00108.x · Cited by 121 · see citing works

Sensory-Motor Areas and Aspects of Cortical Connectivity

(1986) · Cerebral cortex · doi:10.1007/978-1-4613-2149-1 · Cited by 115 · see citing works

Combinatorial RNA splicing alters the surface charge on the NMDA receptor

Anantharam, V., Panchal, R. G., Wilson, A., Koltchine, V. V., Treistman, S. N., & Bayley, H. (1992) · FEBS Letters · doi:10.1016/0014-5793(92)80648-z · Cited by 108 · see citing works

Plasticity in the barrel cortex of the adult mouse: transient increase of GAD-immunoreactivity following sensory stimulation

Welker, E., Soriano, E., Dörfl, J., & der Loos, H. V. (1989) · Experimental Brain Research · doi:10.1007/bf00230256 · Cited by 106 · see citing works

Changes in Neurotransmitters during Development

Parnavelas, J. G., Papadopoulos, G. C., & Cavanagh, M. E. (1988) · Cerebral cortex · doi:10.1007/978-1-4615-6619-9_6 · Cited by 84 · see citing works

The morphology and synaptic connections of spiny stellate neurons in monkey visual cortex (area 17): A golgi‐electron microscopic study

Marie, R. L. S., & Peters, A. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902330205 · Cited by 81 · see citing works

Actions of excitatory amino acid antagonists on synaptic potentials of layer II/III neurons of the cat's visual cortex

Shirokawa, T., Nishigori, A., Kimura, F., & Tsumoto, T. (1989) · Experimental Brain Research · doi:10.1007/bf00230237 · Cited by 78 · see citing works

The role of the anterior intralaminar nuclei and N-methyl D-aspartate receptors in the generation of spontaneous bursts in rat neocortical neurones

Fox, K. D., & Armstrong‐James, M. (1986) · Experimental Brain Research · doi:10.1007/bf00237474 · Cited by 78 · see citing works

Functional reorganization of adult cat somatosensory cortex is dependent on NMDA receptors

Kano, M., lino, K., & Kano, M. (1991) · Neuroreport · doi:10.1097/00001756-199102000-00003 · Cited by 74 · see citing works

Blockade of inhibition in a pathway with dual excitatory and inhibitory action unmasks a capability for LTP that is otherwise not expressed

Steward, O., Tomasulo, R. A., & Levy, W. B. (1990) · Brain Research · doi:10.1016/0006-8993(90)90930-a · Cited by 72 · see citing works

Patterned Activity, Synaptic Convergence, And The NMDA Receptor In Developing Visual Pathways

Constantine‐Paton, M. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.13.1.129 · Cited by 68 · see citing works

Function of non-NMDA receptors and NMDA receptors in synaptic responses to natural somatosensory stimulation in the ventrobasal thalamus

Salt, T. E., & Eaton, S. A. (1989) · Experimental Brain Research · doi:10.1007/bf00249618 · Cited by 67 · see citing works

Primary afferent depolarization in the rat spinal cord is mediated by pathways utilising NMDA and non-NMDA receptors

Evans, R. H., & Long, S. K. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90690-3 · Cited by 56 · see citing works

Synapses made by axons of callosal projection neurons in mouse somatosensory cortex: Emphasis on intrinsic connections

White, E. L., & Czeiger, D. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903030206 · Cited by 53 · see citing works

Organization and quantitative analysis of kainate receptor subunit GluR5-7 immunoreactivity in monkey hippocampus

Good, P. F., Huntley, G. W., Rogers, S. W., Heinemann, S. F., & Morrison, J. H. (1993) · Brain Research · doi:10.1016/0006-8993(93)90102-s · Cited by 50 · see citing works

Thalamic inputs to cytochrome oxidase-rich regions in monkey visual cortex

(1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.23.7604-d · Cited by 38 · see citing works

Differential vulnerability, connectivity, and cell typology

Morrison, J. H. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90021-3 · Cited by 36 · see citing works

Contribution of quisqualate/ kainate and NMDA receptors to excitatory synaptic transmission in the rat's visual cortex

Nishigori, A., Tsumoto, T., & Kimura, F. (1990) · Visual Neuroscience · doi:10.1017/s0952523800000754 · Cited by 35 · see citing works

Excitatory Amino Acid Neurotransmission: NMDA Receptors And Hebb-Type Synaptic Plasticity

Cotman, C. W. (1988) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.11.1.61 · Cited by 30 · see citing works

Common Forms of Synaptic Plasticity in the Hippocampus and Neocortex in Vitro

Kirkwood, A., Dudek, S. M., Gold, J. T., Aizenman, C. D., & Bear, M. F. (1995) · World Scientific series in 20th century physics · doi:10.1142/9789812795885_0014 · Cited by 25 · see citing works

EPSPs in rat neocortical pyramidal neurones in vitro are prolonged by NMDA receptor-mediated currents

Nicoll, A. J., Larkman, A. U., & Blakemore, C. B. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90220-2 · Cited by 16 · see citing works

Involvement of NMDA and NonNMDA Receptors in Motor Task—related Activity in the Primary and Secondary Cortical Motor Areas of the Monkey

Shima, K., & Tanji, J. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.4.330 · Cited by 15 · see citing works

Molecular Neurobiology Of Glutamate Receptors

Gasic, G. (1992) · Annual Review of Physiology · doi:10.1146/annurev.physiol.54.1.507 · Cited by 15 · see citing works

Long-Term Potentiation of Synaptic Transmission in Kitten Visual Cortex

Komatsu, Y., Fujii, K., Maeda, J. E. M. S., Sakaguchi, H., & Toyama, K. (1988) · Journal of Neurophysiology · doi:10.1152/jn.1988.59.1.1-a · Cited by 6 · see citing works

Types of neurons, synaptic connections and chemical characteristics of cells immunoreactive for calbindin-D28K, parvalbumin and calretinin in the neocortex

DeFelipe, J. (1997) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(97)10013-8 · Cited by 550 · see citing works

PSD-95 Assembles a Ternary Complex with theN-Methyl-d-aspartic Acid Receptor and a Bivalent Neuronal NO Synthase PDZ Domain

Christopherson, K. S., Hillier, B. J., Lim, W. A., & Bredt, D. S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.39.27467 · Cited by 536 · see citing works

Axons, but not cell bodies, are activated by electrical stimulation in cortical gray matter

Nowak, L. G., & Bullier, J. (1998) · Experimental Brain Research · doi:10.1007/s002210050304 · Cited by 492 · see citing works

Activity Regulates the Synaptic Localization of the NMDA Receptor in Hippocampal Neurons

Rao, A., & Craig, A. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80962-9 · Cited by 492 · see citing works

Alterations in GABA-related transcriptome in the dorsolateral prefrontal cortex of subjects with schizophrenia

Hashimoto, T., Arion, D., Unger, T., Maldonado-Avilés, J. G., Morris, H. M., Volk, D. W., Mirnics, K., & Lewis, D. A. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002011 · Cited by 490 · see citing works

Selective alterations in gene expression for NMDA receptor subunits in prefrontal cortex of schizophrenics

Akbarian, S., Sucher, N. J., Bradley, D., Tafazzoli, A., Trinh, D., Hetrick, W. P., Potkin, S. G., Sandman, C., Bunney, W. E., & Jones, E. G. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-01-00019.1996 · Cited by 440 · see citing works

SAP97 Is Associated with the α-Amino-3-hydroxy-5-methylisoxazole-4-propionic Acid Receptor GluR1 Subunit

Leonard, A. S., Davare, M. A., Horne, M. C., Garner, C. C., & Hell, J. W. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.31.19518 · Cited by 374 · see citing works

Increased spontaneous MEG signal diversity for psychoactive doses of ketamine, LSD and psilocybin

Schartner, M. M., Carhart-Harris, R. L., Barrett, A. B., Seth, A. K., & Muthukumaraswamy, S. D. (2017) · Scientific Reports · doi:10.1038/srep46421 · Cited by 410 · see citing works

Presynaptic glutamate receptors: physiological functions and mechanisms of action

Pinheiro, P. S., & Mulle, C. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2379 · Cited by 368 · see citing works

Neurofilaments: neurobiological foundations for biomarker applications

Gafson, A., Barthélemy, N. R., Bomont, P., Carare, R. O., Durham, H. D., Julien, J., Kühle, J., Leppert, D., Nixon, R. A., Weller, R. O., et al. (2020) · Brain · doi:10.1093/brain/awaa098 · Cited by 327 · see citing works

Axons, but not cell bodies, are activated by electrical stimulation in cortical gray matter

Nowak, L. G., & Bullier, J. (1998) · Experimental Brain Research · doi:10.1007/s002210050305 · Cited by 324 · see citing works

Pathophysiologically based treatment interventions in schizophrenia

Lewis, D. A., & González‐Burgos, G. (2006) · Nature Medicine · doi:10.1038/nm1478 · Cited by 320 · see citing works

Synapse-specific localization of NMDA and GABAA receptor subunits revealed by antigen-retrieval immunohistochemistry

Fritschy, J., Weinmann, O., Wenzel, A., & Benke, D. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980112)390:2 · Cited by 321 · see citing works

Selective scarcity of NMDA receptor channel subunits in the stratum lucidum (mossy fibre‐recipient layer) of the mouse hippocampal CA3 subfield

Watanabe, M., Fukaya, M., Sakimura, K., Manabe, T., Mishina, M., & Inoue, Y. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00063.x · Cited by 292 · see citing works

Regulated Subcellular Distribution of the NR1 Subunit of the NMDA Receptor

Ehlers, M., Tingley, W. G., & Huganir, R. L. (1995) · Science · doi:10.1126/science.7569904 · Cited by 293 · see citing works

High-resolution immunogold localization of AMPA type glutamate receptor subunits at synaptic and non-synaptic sites in rat hippocampus

Baude, A., Nusser, Z., Molnár, E., McIlhinney, R. A. J., & Somogyi, P. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00350-r · Cited by 291 · see citing works

Splice Variant-Specific Interaction of the NMDA Receptor Subunit NR1 with Neuronal Intermediate Filaments

Ehlers, M., Fung, E. T., O’Brien, R., & Huganir, R. L. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-02-00720.1998 · Cited by 267 · see citing works

Molecular mechanisms of glutamate receptor clustering at excitatory synapses

O’Brien, R., Lau, L., & Huganir, R. L. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80062-7 · Cited by 270 · see citing works

Glutamate Receptors and Nociception: Implications for the Drug Treatment of Pain

Fundytus, M. E. (2001) · CNS Drugs · doi:10.2165/00023210-200115010-00004 · Cited by 250 · see citing works

Cortical dysplasia

Spreafico, R., Battaglia, G. S., Arcelli, P., Andermann, F., Dubeau, F., Palmini, A., Olivier, A., Villemure, J., Tampieri, D. I., AVANZINI, G., et al. (1998) · Neurology · doi:10.1212/wnl.50.1.27 · Cited by 221 · see citing works

Parvalbumin interneuron vulnerability and brain disorders

Ruden, J. B., Dugan, L. L., & Konradi, C. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-0778-9 · Cited by 194 · see citing works

Numbers of Meynert and layer IVB cells in area V1: A stereologic analysis in young and aged macaque monkeys

Hof, P. R., Nimchinsky, E. A., Young, W. G., & Morrison, J. H. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000424)420:1 · Cited by 71 · see citing works

Dissociation of broadband high-frequency activity and neuronal firing in the neocortex

Leszczyński, M., Barczak, A., Kajikawa, Y., Ulbert, I., Falchier, A. Y., Tal, I., Haegens, S., Melloni, L., Knight, R. T., & Schroeder, C. E. (2020) · Science Advances · doi:10.1126/sciadv.abb0977 · Cited by 188 · see citing works

Differential localization of NMDA and AMPA receptor subunits in the lateral and basal nuclei of the amygdala: A light and electron microscopic study

Farb, C. R., Aoki, C. J., & LeDoux, J. E. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903620106 · Cited by 171 · see citing works

Patterns of cell death in mouse anteroventral cochlear nucleus neurons after unilateral cochlea removal

Mostafapour, S. P., Cochran, S. L., del Puerto, N. M., & Rubel, E. W. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001030)426:4 · Cited by 156 · see citing works

The neurobiology of methamphetamine induced psychosis

Hsieh, J. H., Stein, D. J., & Howells, F. M. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00537 · Cited by 158 · see citing works

Relationship between N-Methyl-D-aspartate Receptor NR1 Splice Variants and NR2 Subunits

Blahoš, J., & Wenthold, R. J. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.26.15669 · Cited by 157 · see citing works

Gonadotropin-Releasing Hormone and NMDA Receptor Gene Expression and Colocalization Change during Puberty in Female Rats

Gore, A. C., Wu, T. J., Rosenberg, J. J., & Roberts, J. L. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05281.1996 · Cited by 152 · see citing works

Cellular and synaptic localization of NMDA and non-NMDA receptor subunits in neocortex: organizational features related to cortical circuitry, function and disease

Huntley, G. W., Vickers, J. C., & Morrison, J. H. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90158-9 · Cited by 149 · see citing works

Dopamine innervation of a subclass of local circuit neurons in monkey prefrontal cortex: ultrastructural analysis of tyrosine hydroxylase and parvalbumin immunoreactive structures

Sesack, S. R. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.7.614 · Cited by 149 · see citing works

Expression of NR1 and NR2A/B subunits of the NMDA receptor in cortical astrocytes

Conti, F., Debiasi, S., Minelli, A., & Melone, M. (1996) · Glia · doi:10.1002/(sici)1098-1136(199607)17:3 · Cited by 143 · see citing works

Essential Role of thefosB Gene in Molecular, Cellular, and Behavioral Actions of Chronic Electroconvulsive Seizures

Hiroi, N., Marek, G. J., Brown, J. R., Ye, H., Saudou, F., Vaidya, V. A., Duman, R. S., Greenberg, M. E., & Nestler, E. J. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-17-06952.1998 · Cited by 139 · see citing works

Electron microscopic immunocytochemical detection of PSD‐95, PSD‐93, SAP‐102, and SAP‐97 at postsynaptic, presynaptic, and nonsynaptic sites of adult and neonatal rat visual cortex

Aoki, C. J., Miko, I. J., Oviedo, H. V., Mikeladze‐Dvali, T., Alexandre, L. C., Sweeney, N. T., & Bredt, D. S. (2001) · Synapse · doi:10.1002/syn.1047 · Cited by 138 · see citing works

Immunohistochemical localization of metabotropic glutamate receptors mGluR1a and mGluR2/3 in the rat basal ganglia

Testa, C. M., Friberg, I. K., Weiss, S. W., & Standaert, D. G. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980105)390:1 · Cited by 237 · see citing works

Glutamatergic deficits and parvalbumin-containing inhibitory neurons in the prefrontal cortex in schizophrenia

Bitanihirwe, B., Lim, M., Kelley, J., Kaneko, T., & Woo, T. (2009) · BMC Psychiatry · doi:10.1186/1471-244x-9-71 · Cited by 137 · see citing works

Roles of Presynaptic NMDA Receptors in Neurotransmission and Plasticity

Banerjee, A., Larsen, R. S., Philpot, B. D., & Paulsen, O. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.11.001 · Cited by 131 · see citing works

Memantine Protects Neurons From Shrinkage in the Lateral Geniculate Nucleus in Experimental Glaucoma

Yücel, Y. H. (2006) · Archives of Ophthalmology · doi:10.1001/archopht.124.2.217 · Cited by 117 · see citing works

Neuronal calcium-binding proteins and schizophrenia

Eyles, D. W., McGrath, J. J., & Reynolds, G. P. (2002) · Schizophrenia Research · doi:10.1016/s0920-9964(01)00299-7 · Cited by 113 · see citing works

Neuronal and Glial Localization of NR1 and NR2A/B Subunits of the NMDA Receptor in the Human Cerebral Cortex

Conti, F. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.2.110 · Cited by 110 · see citing works

Synaptic targeting of glutamate receptors

Ehlers, M., Mammen, A. L., Lau, L., & Huganir, R. L. (1996) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(96)80024-x · Cited by 110 · see citing works

Deciphering the Disease Process of Schizophrenia: The Contribution of Cortical Gaba Neurons

Lewis, D. A., & Hashimoto, T. (2007) · International review of neurobiology · doi:10.1016/s0074-7742(06)78004-7 · Cited by 105 · see citing works

Systemic ketamine attenuates nociceptive behaviors in a rat model of peripheral neuropathy

Qian, J., Brown, S. D., & Carlton, S. M. (1996) · Brain Research · doi:10.1016/0006-8993(95)01452-7 · Cited by 105 · see citing works

Differential Subcellular Regulation of NMDAR1 Protein and mRNA in Dendrites of Dentate Gyrus Granule Cells after Perforant Path Transection

Gazzaley, A. H., Benson, D. L., Huntley, G. W., & Morrison, J. H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-06-02006.1997 · Cited by 104 · see citing works

Deficiency of the Mre11 DNA repair complex in Alzheimer's disease brains

Jacobsen, E. A., Beach, T. G., Shen, Y., Li, R., & Chang, Y. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.05.023 · Cited by 102 · see citing works

A re‐examination of adult mouse nicotinic acetylcholine receptor channel activation kinetics

Salamone, F. N., Zhou, M., & Auerbach, A. L. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0315v.x · Cited by 102 · see citing works

Colocalization of synapse marker proteins evaluated by STED-microscopy reveals patterns of neuronal synapse distribution in vitro

Dzyubenko, E., Rozenberg, A., Hermann, D. M., & Faissner, A. (2016) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2016.09.001 · Cited by 98 · see citing works

The Development of Excitatory Synapses in Cultured Spinal Neurons

O’Brien, R., Mammen, A. L., Blackshaw, S., Ehlers, M., Rothstein, J. D., & Huganir, R. L. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-19-07339.1997 · Cited by 100 · see citing works

Histone methylation at gene promoters is associated with developmental regulation and region‐specific expression of ionotropic and metabotropic glutamate receptors in human brain

Stadler, F. J., Kolb, G., Rubusch, L., Baker, S. P., Jones, E. G., & Akbarian, S. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03190.x · Cited by 98 · see citing works

NMDA and AMPA receptors on neocortical neurons are differentially distributed

Dodt, H., Frick, A., Kampe, K. K. W., & Zieglgänsberger, W. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00338.x · Cited by 96 · see citing works

Transplanted Neuroblasts Differentiate Appropriately into Projection Neurons with Correct Neurotransmitter and Receptor Phenotype in Neocortex Undergoing Targeted Projection Neuron Degeneration

Shin, J. J., Fricker‐Gates, R. A., Perez, F. A., Leavitt, B. R., Zurakowski, D., & Macklis, J. D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07404.2000 · Cited by 88 · see citing works

EM colocalization of AMPA and NMDA receptor subunits at synapses in rat cerebral cortex

Kharazia, V., Phend, K. D., Rustioni, A., & Weinberg, R. J. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(96)12658-6 · Cited by 90 · see citing works

Serotonin-1A antagonists attenuate the effects of nicotine withdrawal on the auditory startle response

Rasmussen, K., Kallman, M. J., & Helton, D. R. (1997) · Synapse · doi:10.1002/(sici)1098-2396(199710)27:2 · Cited by 43 · see citing works

Comparative ultrastructural localization of the NMDAR1 glutamate receptor in the rat basolateral amygdala and bed nucleus of the stria terminalis

Gracy, K. N., & Pickel, V. M. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903620105 · Cited by 87 · see citing works

Neuronal and glial localization of NMDA receptors in the cerebral cortex

Conti, F., Minelli, A., Debiasi, S., & Melone, M. (1997) · Molecular Neurobiology · doi:10.1007/bf02740618 · Cited by 86 · see citing works

Age-related changes in GluR2 and NMDAR1 glutamate receptor subunit protein immunoreactivity in corticocortically projecting neurons in macaque and patas monkeys

Hof, P. R., Duan, H., Page, T. L., Einstein, M. C., Wicinski, B. A., He, Y., ERWIN, J. M., & Morrison, J. H. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03345-5 · Cited by 85 · see citing works

Contributions of Voltage-Gated Ca2+Channels in the Proximal versus Distal Dendrites to Synaptic Integration in Prefrontal Cortical Neurons

Seamans, J. K., Gorelova, N. A., & Yang, C. R. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05936.1997 · Cited by 85 · see citing works

The Human Temporal Cortex: Characterization of Neurons Expressing Nitric Oxide Synthase, Neuropeptides and Calcium-binding Proteins, and their Glutamate Receptor Subunit Profiles

Gonzalez-Albo, M. C. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.12.1170 · Cited by 77 · see citing works

NMDAR1 Glutamate Receptor Subunit Isoforms in Neostriatal, Neocortical, and Hippocampal Nitric Oxide Synthase Neurons

Weiss, S. W., Albers, D. S., Iadarola, M. J., Dawson, V. L., Dawson, V. L., & Standaert, D. G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-05-01725.1998 · Cited by 76 · see citing works

Glutamatergic synaptic responses and long-term potentiation are impaired in the CA1 hippocampal area of calbindin D28k-deficient mice

Jouvenceau, A., Potier, B., Battini, R., Ferrari, S. M., Dutar, P., & Billard, J. (1999) · Synapse · doi:10.1002/(sici)1098-2396(19990901)33:3 · Cited by 52 · see citing works

Glutamate and nicotinic receptor interactions in working memory: importance for the cognitive impairment of schizophrenia

Timofeeva, O. A., & Levin, E. D. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.038 · Cited by 74 · see citing works

Compartmentation of alpha-internexin and neurofilament triplet proteins in cultured hippocampal neurons

Benson, D. L., Mandell, J. W., Shaw, G., & Banker, G. A. (1996) · Journal of Neurocytology · doi:10.1007/bf02284795 · Cited by 70 · see citing works

Neuroendocrine Aging in the Female Rat: The Changing Relationship of Hypothalamic Gonadotropin-Releasing Hormone Neurons and N-Methyl-d-Aspartate Receptors**Preliminary versions of this work were presented at the 28th and 29th Annual Meetings of the Society for Neuroscience (Abstracts 110.11 and 777.10). This work was supported by the Brookdale Foundation (to A.C.G.), NIH Grant 1-PO1-AG16765–01 (to A.C.G. and J.H.M.).

Gore, A. C., Yeung, G., Morrison, J. H., & Oung, T. (2000) · Endocrinology · doi:10.1210/endo.141.12.7841 · Cited by 69 · see citing works

Potential role of synaptopodin in spine motility by coupling actin to the spine apparatus

Deller, T., Mundel, P. H., & Frotscher, M. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:5 · Cited by 61 · see citing works

Synaptic localization of ionotropic glutamate receptors in the rat substantia nigra

Chatha, B. T., Bernard, V., Streit, P., & Bolam, J. P. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00432-2 · Cited by 67 · see citing works

Age-Related Changes in Estrogen Receptor β in Rat Hypothalamus: A Quantitative Analysis

Chakraborty, T. R., Ng, L., & Gore, A. C. (2003) · Endocrinology · doi:10.1210/en.2003-0052 · Cited by 66 · see citing works

A unified model of ketamine’s dissociative and psychedelic properties

Marguilho, M., Figueiredo, I., & Castro-Rodrigues, P. (2022) · Journal of Psychopharmacology · doi:10.1177/02698811221140011 · Cited by 65 · see citing works

Synapse restructuring associated with the maintenance phase of hippocampal long-term potentiation

Geinisman, Y., deToledo‐Morrell, L., Morrell, F., Persina, I. S., & Beatty, M. A. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960506)368:3 · Cited by 140 · see citing works

Architectural and synaptic mechanisms underlying coherent spontaneous activity in V1

Cai, D., Rangan, A. V., & McLaughlin, D. W. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501913102 · Cited by 63 · see citing works

Neurochemical organization of the macaque striate cortex: Correlation of cytochrome oxidase with Na+K+ATPase, NADPH-diaphorase, nitric oxide synthase, and N-methyl-d-aspartate receptor subunit 1

Wong‐Riley, M. T. T., Anderson, B. D., Liebl, W., & Huang, Z. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00432-6 · Cited by 63 · see citing works

Laminar distribution and co-distribution of neurotransmitter receptors in early human visual cortex

Eickhoff, S. B., Rottschy, C., & Zilles, K. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0156-y · Cited by 59 · see citing works

Human retinohypothalamic tract as revealed by in vitro postmortem tracing

Dai, J., van der Vliet, J., Swaab, D. F., & Buijs, R. M. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980803)397:3 · Cited by 83 · see citing works

Modeling the spatiotemporal cortical activity associated with the line-motion illusion in primary visual cortex

Rangan, A. V., Cai, D., & McLaughlin, D. W. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509481102 · Cited by 58 · see citing works

Dendrite plasticity in the lateral geniculate nucleus in primate glaucoma

Ly, T., Gupta, N., Weinreb, R. N., Kaufman, P. L., & Yücel, Y. H. (2010) · Vision Research · doi:10.1016/j.visres.2010.08.003 · Cited by 54 · see citing works

Neurochemical organization of the macaque retina: effect of TTX on levels and gene expression of cytochrome oxidase and nitric oxide synthase and on the immunoreactivity of Na+K+ATPase and NMDA receptor subunit I

Wong‐Riley, M. T. T., Huang, Z., Liebl, W., Nie, F., Xu, H., & Zhang, C. (1998) · Vision Research · doi:10.1016/s0042-6989(98)00001-7 · Cited by 52 · see citing works

CART peptide-immunoreactive neurones in the nucleus accumbens in monkeys: Ultrastructural analysis, colocalization studies, and synaptic interactions with dopaminergic afferents

Smith, Y., Kieval, J. Z., Couceyro, P. R., & Kuhar, M. J. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990517)407:4 · Cited by 122 · see citing works

Ionotropic glutamate receptors: Which ones, when, and where in the mammalian neocortex

Hadzic, M., Jäck, A., & Wahle, P. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24103 · Cited by 49 · see citing works

Expression of N-methyl-D-aspartate receptor subunits in the rat parabrachial and K�lliker-Fuse nuclei and in selected pontomedullary brainstem nuclei

Guthmann, A., & Herbert, H. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991227)415:4 · Cited by 1 · see citing works

Perinatal Changes in Hypothalamic N-Methyl-D-Aspartate Receptors and Their Relationship to Gonadotropin-Releasing Hormone Neurons

Adams, M. M., Flagg, R. A., & Gore, A. C. (1999) · Endocrinology · doi:10.1210/en.140.5.2288 · Cited by 49 · see citing works

Quantitative localization of NMDAR1 receptor subunit immunoreactivity in inferotemporal and prefrontal association cortices of monkey and human

Huntley, G. W., Vickers, J. C., & Morrison, J. H. (1997) · Brain Research · doi:10.1016/s0006-8993(96)00847-5 · Cited by 47 · see citing works

Kinetic theory for neuronal networks with fast and slow excitatory conductances driven by the same spike train

Rangan, A. V., Kovačič, G., & Cai, D. (2008) · Physical Review E · doi:10.1103/physreve.77.041915 · Cited by 47 · see citing works

Effect of monocular deprivation on NMDAR1 immunostaining in ocular dominance columns of the marmoset Callithrix jacchus

Fonta, C., Chappert, C., & Imbert, M. (2000) · Visual Neuroscience · doi:10.1017/s0952523800173031 · Cited by 47 · see citing works

Chapter 13 Dynamic modulation of cerebral cortex synaptic function by nitric oxide

Kara, P., & Friedlander, M. J. (1998) · Progress in brain research · doi:10.1016/s0079-6123(08)63208-2 · Cited by 44 · see citing works

Excitatory responses evoked in prefrontal cortex by mediodorsal thalamic nucleus stimulation: influence of anaesthesia

Pirot, S., Glowinski, J., & Thierry, A. M. (1995) · European Journal of Pharmacology · doi:10.1016/0014-2999(95)00377-w · Cited by 43 · see citing works

NMDA receptor blockade in intact adult cortex increases trafficking of NR2A subunits into spines, postsynaptic densities, and axon terminals

Aoki, C. J., Fujisawa, S., Mahadomrongkul, V., Shah, P. J., Nader, K., & Erişir, A. (2003) · Brain Research · doi:10.1016/s0006-8993(02)03962-8 · Cited by 43 · see citing works

Microzonal decreases in the immunostaining for non-NMDA ionotropic excitatory amino acid receptor subunits GluR 2/3 and GluR 5/6/7 in the human epileptogenic neocortex

DeFelipe, J., Huntley, G. W., del Rı́o, M. R., de Sola, R. G., & Morrison, J. H. (1994) · Brain Research · doi:10.1016/0006-8993(94)90962-8 · Cited by 43 · see citing works

Anatomical evidence supporting the potential for modulation by multiple neurotrophins in the majority of adult lumbar sensory neurons

Karchewski, L. A., Kim, F. A., Johnston, J. M., McKnight, R. M., & Verge, V. M. K. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991018)413:2 · Cited by 81 · see citing works

N-cadherin regulates molecular organization of excitatory and inhibitory synaptic circuits in adult hippocampus in vivo

Nikitczuk, J. S., Patil, S. B., Matikainen‐Ankney, B. A., Scarpa, J. R., Shapiro, M. L., Benson, D. L., & Huntley, G. W. (2014) · Hippocampus · doi:10.1002/hipo.22282 · Cited by 42 · see citing works

Sensory Regulation of Immediate-early Genes c-fos and zif268 in Monkey Visual Cortex at Birth and Throughout the Critical Period

Kaczmarek, L. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.2.179 · Cited by 41 · see citing works

Glutamate Receptors Form Hot Spots on Apical Dendrites of Neocortical Pyramidal Neurons

Frick, A., Zieglgänsberger, W., & Dodt, H. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.3.1412 · Cited by 41 · see citing works

Chronic haloperidol and clozapine administration increases the number of cortical NMDA receptors in rats

Ossowska, K., Pietraszek, M., Wardas, J., Nowak, G., & Wolfarth, S. (1999) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/pl00005353 · Cited by 41 · see citing works

Identification of an N-Methyl-d-aspartate Receptor in Isolated Nervous System Mitochondria

Korde, A. S., & Maragos, W. F. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.322032 · Cited by 38 · see citing works

Chronic hypoxia induces modification of the N-methyl-d-aspartate receptor in rat brain

Pichiule, P., Chavez, J. C., Boero, J., & Arregui, A. (1996) · Neuroscience Letters · doi:10.1016/s0304-3940(96)13113-x · Cited by 35 · see citing works

Topographic organization in the retinocollicular pathway of the fetal cat demonstrated by retrograde labeling of ganglion cells

Chalupa, L. M., Snider, C. J., & Kirby, M. A. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960429)368:2 · Cited by 22 · see citing works

Dissociation of broadband high-frequency activity and neuronal firing in the neocortexPreprint

Leszczyński, M., Barczak, A., Kajikawa, Y., Ulbert, I., Falchier, A., Tal, I., Haegens, S., Melloni, L., Knight, R. T., & Schroeder, C. E. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/531368 · Cited by 37 · see citing works

Properties of single NMDA receptor channels in human dentate gyrus granule cells.

Lieberman, D. N., & Módy, I. (1999) · PubMed Central · doi:10.1111/j.1469-7793.1999.0055r.x · Cited by 36 · see citing works

c-Fos proteins, induced by the serotonin receptor agonist DOI, are not expressed in 5-HT2A positive cortical neurons

Maćkowiak, M., Chocyk, A., Fijał, K., Czyrak, A., & Wędzony, K. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00195-3 · Cited by 36 · see citing works

Novel localization of NMDA receptors within neuroendocrine gonadotropin-releasing hormone terminals.

Yin, W., Mendenhall, J. M., Bratton, S. B., Oung, T., Janssen, W. G. M., Morrison, J. H., & Gore, A. C. (2007) · PubMed · Cited by 36 · see citing works

Cortical Neuropathology in Aging and Dementing Disorders

Hof, P. R., Bouras, C., & Morrison, J. H. (1999) · Cerebral cortex · doi:10.1007/978-1-4615-4885-0_8 · Cited by 35 · see citing works

Localization of NMDA receptors in the cerebral cortex: a schematic overview

Conti, F. (1997) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1997000500001 · Cited by 33 · see citing works

N-methyl-d-aspartate enhancement of phasic responses in primate neocortex

Schroeder, C. E., Javitt, D. C., Steinschneider, M., Mehta, A. D., Givre, S. J., Vaughan, H. G., & Arezzo, J. C. (1997) · Experimental Brain Research · doi:10.1007/pl00005635 · Cited by 33 · see citing works

Quantitative localization of NMDAR1 receptor subunit immunoreactivity in inferotemporal and prefrontal association cortices of monkey and human

Huntley, G. W., Vickers, J. C., & Morrison, J. H. (1997) · Brain Research · doi:10.1016/s0006-8993(96)00847-5 · Cited by 47 · see citing works

CART peptide-immunoreactive neurones in the nucleus accumbens in monkeys: Ultrastructural analysis, colocalization studies, and synaptic interactions with dopaminergic afferents

Smith, Y., Kieval, J. Z., Couceyro, P. R., & Kuhar, M. J. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990517)407:4 · Cited by 122 · see citing works

Regional, cellular, and ultrastructural distribution of N-methyl-D-aspartate receptor subunit 1 in monkey hippocampus.

Siegel, S. J., Brose, N., Janssen, W. G. M., Gasic, G. P., Jahn, R., Heinemann, S., & Morrison, J. H. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.2.564 · Cited by 339 · see citing works

Neuronal and Glial Localization of NR1 and NR2A/B Subunits of the NMDA Receptor in the Human Cerebral Cortex

Conti, F. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.2.110 · Cited by 110 · see citing works

Cellular and subcellular localization of NMDA-R1 subunit immunoreactivity in the visual cortex of adult and neonatal rats

Aoki, C. J., Venkatesan, C., Go, C. G., Mong, J., & Dawson, T. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-09-05202.1994 · Cited by 255 · see citing works