Subunit-Specific NMDA Receptor Trafficking to Synapses

Cloned Glutamate Receptors

Hollmann, M., & Heinemann, S. F. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.000335 · Cited by 4,056

Glutamate receptor ion channels

Mayer, M. L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.05.004 · Cited by 3,655

The Glutamate Receptor Ion Channels

Dingledine, R., Borges, K., Bowie, D., & Traynelis, S. F. (1999) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01394-2 · Cited by 3,554

Developmental and regional expression in the rat brain and functional properties of four NMDA receptors

Monyer, H., Burnashev, N., Laurie, D. J., Sakmann, B., & Seeburg, P. H. (1994) · Neuron · doi:10.1016/0896-6273(94)90210-0 · Cited by 3,535

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 2,941

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

Quality control in the endoplasmic reticulum

Ellgaard, L., & Helenius, A. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1052 · Cited by 2,171

Domain Interaction Between NMDA Receptor Subunits and the Postsynaptic Density Protein PSD-95

Kornau, H., Schenker, L. T., Kennedy, M. B., & Seeburg, P. H. (1995) · Science · doi:10.1126/science.7569905 · Cited by 1,916

The molecular basis of CaMKII function in synaptic and behavioural memory

Lisman, J., Schulman, H., & Cline, H. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn753 · Cited by 1,860

Changing subunit composition of heteromeric NMDA receptors during development of rat cortex

Sheng, M., Cummings, J., Roldan, L. A., Jan, Y. N., & Jan, L. Y. (1994) · Nature · doi:10.1038/368144a0 · Cited by 1,377

Endogenous ion channel complexes: the NMDA receptor

Frank, R. (2011) · Biochemical Society Transactions · doi:10.1042/bst0390707 · Cited by 8

Translational Regulation of the N-Methyl-D-Aspartate Receptor Subunit NR1

Vazhappilly, R., & Sucher, N. J. (2004) · Neurosignals · doi:10.1159/000077525 · Cited by 8

Activity-Dependent Stabilization of Nascent Dendritic Spines Requires Nonenzymatic CaMKIIα Function

Claiborne, N., Anisimova, M., & Zito, K. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1393-22.2023 · Cited by 8

GluN2B-mediated regulation of silent synapses for receptor specification and addiction memory

Kim, H. J., Lee, S., Kim, G. H., Sung, K., Yoo, T., Pyo, J. H., Jo, H.-J., Lee, S., Lee, H. Y., Jung, J. H., et al. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01399-z · Cited by 8

SAP97 blocks the RXR ER retention signal of NMDA receptor subunit GluN1-3 through its SH3 domain

Hong, X., Avetisyan, M., Ronilo, M., & Standley, S. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2014.11.030 · Cited by 7

Cloning and phylogenetic analysis of NMDA receptor subunits NR1, NR2A and NR2B in Xenopus laevis tadpoles

Ewald, R. C. (2009) · Frontiers in Molecular Neuroscience · doi:10.3389/neuro.02.004.2009 · Cited by 8

The second PDZ domain of scaffold protein Frmpd2 binds to GluN2A of NMDA receptors

Lu, X., Zhang, Q., Tian, X., & Wang, X. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.05.087 · Cited by 8

Visualizing the triheteromeric N-methyl-D-aspartate receptor subunit composition

Beesley, S., Gunjan, A., & Kumar, S. S. (2023) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2023.1156777 · Cited by 6

Acute spinal cord injury diminishes silent synapses in the rat hippocampus

Jing, Y., Bai, F., Chen, H., & Dong, H. (2017) · Neuroreport · doi:10.1097/wnr.0000000000000885 · Cited by 6

Activity dependent localization of synaptic NMDA receptors in spinal neurons

Rosen, K. M., Moghekar, A., & O’Brien, R. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.12.008 · Cited by 6

NMDA Receptors

Petralia, R. S., & Wenthold, R. J. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-055-3_2 · Cited by 7

NMDA Receptors

Cull-Candy, S. G. (2007) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0000254.pub2 · Cited by 6

Single-cell synaptome mapping of endogenous protein subpopulations in mammalian brain

Uchigashima, M., Iguchi, R., Fujii, K., Shiku, K., Kumar, P., Liu, X.-Y., Isogai, M., Hoshino, C., Abe, M., Nozumi, M., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65813-w · Cited by 6

Myosin Va-dependent Transport of NMDA Receptors in Hippocampal Neurons

Gong, R., Qin, L., Chen, L., Wang, N., Bao, Y., & Lu, W. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-023-01174-y · Cited by 5

Aβ1-42 Oligomer Injection Model: Understanding Neural Dysfunction and Contextual Memory Deficits in Dorsal CA1

Min-Kaung-Wint-Mon, & Mitsushima, D. (2025) · Journal of dementia and Alzheimer's disease · doi:10.3390/jdad2030025 · Cited by 5

Regulation of glutamate signaling in the extended amygdala by adolescent alcohol exposure

Holmgren, E. B., & Wills, T. A. (2021) · International review of neurobiology · doi:10.1016/bs.irn.2021.08.004 · Cited by 6

Meeting report: Flux-independent signaling by ionotropic receptors: Unforeseen roles, complexities, and challenges

Balderas, P. M. D. O. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102330 · Cited by 5

Uncovering the Significance of STEP61 in Alzheimer’s Disease: Structure, Substrates, and Interactome

Bagwe, P. V., Deshpande, R. D., Juhász, G., Sathaye, S. S., & Joshi, S. V. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01364-2 · Cited by 5

Rescuing tri-heteromeric NMDA receptor function: the potential of pregnenolone-sulfate in loss-of-function GRIN2B variants

Kellner, S., & Berlin, S. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05243-x · Cited by 5

Over-expression of the GluN2B subunit in the forebrain facilitates the acquisition of morphine-related positive and aversive memory in rats

Li, Y., Ping, X., Yu, P., Liang, J., Shen, F., Han, J., & Cui, C. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.05.039 · Cited by 5

Molecular Properties and Cell Biology of the NMDA Receptor

Wenthold, R. J., Al‐Hallaq, R. A., Swanwick, C. C., & Petralia, R. S. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_12 · Cited by 5

Expression of GFP-tagged neuronal glutamate transporters in cerebellar Purkinje neurons

Meera, P., Dodson, P. D., Karakossian, M. H., & Otis, T. S. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.08.015 · Cited by 5

Increasing Synaptic GluN2B levels within the Basal and Lateral Amygdala Enables the Modification of Strong Reconsolidation Resistant Fear MemoriesPreprint

de Solis, C. A., Gonzalez, C. U., Galdamez, M., Perish, J. M., Woodard, S. W., Salinas, C. E., Miller, J. N., Elahi, H., Pineda, O. H., Oad, S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/537142 · Cited by 5

ABCA7 deficiency exacerbates glutamate excitotoxicity in Alzheimer’s disease mice – A new pharmacological target for Glu-related neurotoxicity

Górska, A. M., Santos‐García, I., Kvasnička, A., Dobešová, D., Friedecký, D., Gildenblat, J., & Pahnke, J. (2026) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2026.102891 · Cited by 6

Trafficking of Glutamate Receptors and Associated Proteins in Synaptic Plasticity

Hořák, M., Seabold, G. K., & Petralia, R. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00008-0 · Cited by 4

Significance of NMDA receptor-targeting compounds in neuropsychological disorders: An in-depth review

Forouzanfar, F., Ahmadzadeh, A. M., Pourbagher‐Shahri, A. M., & Gorji, A. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177690 · Cited by 4

D‐Serine‐induced Inactivation of NMDA Receptors in Cultured Rat Hippocampal Neurons Expressing NR 2A Subunits is Ca2+‐Dependent

Li, X., Zhang, Y., Chen, Z., Jiang, Z., Sun, L., Xu, L., Yang, Y. L., & Zhang, Y. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12308 · Cited by 4

Synaptic and Extra-Synaptic NMDA Receptors in the CNS

Papouin, T., & Oliet, S. H. R. (2017) · Springer eBooks · doi:10.1007/978-3-319-49795-2_2 · Cited by 4

Effects of morphine and NeuroAid on the expression levels of GluN2A and GluN3A in the hippocampus and striatum of rats.

Heshmatzad, K., Nasehi, M., & Vaseghi, S. (2021) · PubMed Central · doi:10.22038/ijbms.2021.52004.11787 · Cited by 4

Molecular and anatomical evidence for the input pathway- and target cell type-dependent regulation of glutamatergic synapses

Yamasaki, M. (2015) · Anatomical Science International · doi:10.1007/s12565-015-0303-0 · Cited by 4

NMDA receptor mobility: cultures versus acute brain slices or neonatal versus mature synapses?

Köhr, G. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.144865 · Cited by 4

Properties of glutamatergic synapses in immature layer Vb pyramidal neurons: coupling of pre- and postsynaptic maturational states

Walz, C., Elßner-Beyer, B., Schubert, D., & Gottmann, K. (2009) · Experimental Brain Research · doi:10.1007/s00221-009-2051-7 · Cited by 4

Subunit-Specific NMDA Receptor Trafficking to Synapses

Barría, A. (2007) · Elsevier eBooks · doi:10.1016/b978-012369437-9/50015-3 · Cited by 4

Endogenous Pigment Mimicking Engineered Nanovesicle Targets Extrasynaptic NMDA Receptors against Ca2+-Mediated Excitotoxicity in Alzheimer’s Disease

Roy, R., Khatua, M. M., Ghosh, S., Nandi, S., Ram, H., & Ghosh, S. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5c08303 · Cited by 3

NMDAR and glutamate control axon growth by regulating Rac1-dependent actin dynamics and H2O2 production

Muñoz-Palma, E., Acosta-Tapia, N., Villablanca, C., Wilson, C., Hidalgo, C., & González-Billault, C. E. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104027 · Cited by 4

Wnt-5a induces the conversion of silent to functional synapses in the hippocampus

Álvarez‐Ferradas, C., Wellmann, M., Morales-Weil, K., Fuenzalida, M., Cerpa, W. F., Inestrosa, N. C., & Bonansco, C. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1024034 · Cited by 3

Synaptogenesis by Cholinergic Stimulation of Astrocytes

Roqué, P. J., Barría, A., Zhang, X., Hashimoto, J. G., Costa, L. G., & Guizzetti, M. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03979-9 · Cited by 3

Disease-associated nonsense and frame-shift variants resulting in the truncation of the GluN2A or GluN2B C-terminal domain decrease NMDAR surface expression and reduce potentiating effects of neurosteroids

Kysilov, B., Kuchtiak, V., Krausová, B. H., Balík, A., Kořı́nek, M., Fili, K., Dobrovolski, M., Abramova, V., Chodounská, H., Kudová, E., et al. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05062-6 · Cited by 4

GluN2A- and GluN2B-containing pre-synaptic N -methyl- d -aspartate receptors differentially regulate action potential-evoked Ca 2+ influx via modulation of SK channels

Schmidt, C. C., Tong, R., & Emptage, N. J. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0222 · Cited by 4

Adverse Outcome Pathway on chronic binding of antagonist to N-methyl-D-aspartate receptors during brain development leading to neurodegeneration with impairment in learning and memory in aging

Monnet‐Tschudi, F., & FitzGerald, R. (2018) · OECD series on adverse outcome pathways · doi:10.1787/95f569ad-en · Cited by 4

The polyamine naphthyl-acetyl spermine trihydrochloride (NASPM) lacks specificity for Ca 2+ -permeable AMPA receptors and suppresses seizure like activity in human brain tissue by inhibition of NMDA receptorsPreprint

Podestà, A., Monni, L., Arnold, F., Arnold, J., Bertelli, S., Xu, R., Onken, J., Thomale, U., Kalbhenn, T., Simon, M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.14.653650 · Cited by 3

AN IN VITRO MODEL OF ASPARTAME CYTOTOXICITY VIA HETEROLOGOUS EXPRESSION OF NMDA RECEPTORS

SHAHER, S. A. A. (2023) · FARMACIA · doi:10.31925/farmacia.2023.3.17 · Cited by 2

GluN2A–NMDAR mediated neuronal NFκB activation plays a key role in exacerbating ischemic brain injury under hyperhomocysteinemic conditions

Seelig, S., Paramasivam, P., Gomez, M., Smith, A., Miller, J. W., Paul, S., & Poddar, R. (2025) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x251399012 · Cited by 2

Mice carrying a GluN2B protein-truncating variant have altered NMDA receptor subunit composition and their behavior recapitulates patient phenotypes

Fili, K., Kuchtiak, V., Tomović, E., Candelas, M., Kubik‐Zahorodna, A., Harant, K., Božíková, P., Černý, J., Kořı́nek, M., Krausová, B. H., et al. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-06057-1 · Cited by 2

Linear ubiquitination of the NMDA receptor GluN2A subunit facilitates the GluN2B-to-GluN2A switch and synaptic maturation

Chu, Y., Xu, Y., Huang, M., Fang, X., Huang, X., Yao, Z., Wu, J., Zhou, N., He, K., Liu, Y., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2515389123 · Cited by 3

Behind the scenes: Are latent memories supported by calcium independent plasticity?

Keith, R. E., Ogoe, R. H., & Dumas, T. C. (2021) · Hippocampus · doi:10.1002/hipo.23332 · Cited by 2

Pharmacological characterization and differential expression of NMDA receptor subunits in the chicken vestibular system during development

Ramírez, A., Monjaraz, E., Manjarrez, E., Moyaho, A., Cebada, J., & Flores, A. (2022) · Synapse · doi:10.1002/syn.22252 · Cited by 2

Roles and Sources of Calcium in Synaptic Exocytosis

Wang, Z., Chen, B., & Ge, Q. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-481-0_4 · Cited by 2

Synaptic accumulation of GluN2B-containing NMDA receptors mediates the effects of BDNF-TrkB signalling on synaptic plasticity and in epileptogenesisPreprint

Luca, P. D., Mele, M., Tanqueiro, S. R., Napoli, F., Butkevičiūtė, U., Souto, A. C., Costa, R. O., Schwarz, A. P., Drexel, M., Sebastião, A. M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.21.618702 · Cited by 2

Homeostasis of dendritic spines in hippocampal CA1 cells

Mestrallet, C. A. (2011) · UCL Discovery (University College London) · Cited by 2

Increased NMDAR activity and GluN2A-NMDAR silent synapse expansion induced by chronic benzodiazepine treatment

Chapman, C. A., Povysheva, N. V., Johnson, J. W., & Jacob, T. C. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110624 · Cited by 1

GluN2A-mediated currents and calcium signal in human iPSC-derived neurons

Escamilla, S., Avilés-Granados, C., Peralta, F. A., Paternain, A. V., Cortés‐Gómez, M., Zetterberg, H., de la Peña, E., Salas-Lucia, F., Sáez‐Valero, J., & Cuchillo‐Ibáñez, I. (2026) · Scientific Reports · doi:10.1038/s41598-026-38482-y · Cited by 1

Pathophysiological mechanisms of development of epilepsy and special features of epileptogenesis in the immature brain

Martyniuk, V. Y., Знаменська, Т. К., & Shveikina, V. B. (2021) · Modern pediatrics Ukraine · doi:10.15574/sp.2021.114.26 · Cited by 1

Roles and Sources of Calcium in Synaptic Exocytosis

Wang, Z., Riaz, S., & Niu, L. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-34229-5_6 · Cited by 1

Tonic NMDAR Currents of NR2A-Containing NMDARs Represent Altered Ambient Glutamate Concentration in the Supraoptic Nucleus

Shin, H., Sharma, R., Neupane, C., Phạm, T. L., Park, S. E., Lee, S. Y., Kim, H., Bae, Y. M., Stern, J. E., & Park, J. B. (2024) · eNeuro · doi:10.1523/eneuro.0279-23.2023 · Cited by 1

Glutamate Signaling and Neuroligin/Neurexin Adhesion Play Opposing Roles That Are Mediated by Major Histocompatibility Complex I Molecules in Cortical Synapse Formation

Sell, G. L., Barrow, S. L., & McAllister, A. K. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0797-24.2024 · Cited by 1

Nature and Nurture Converge in the Nucleus to Regulate Activity-Dependent Neuronal Development

Thompson, J. R., & Lin, Y. (2024) · Springer eBooks · doi:10.1007/978-3-031-68550-7_10 · Cited by 1

Synaptic and extrasynaptic NMDA receptors: Problems and prospects

Kudryashova, I. V. (2007) · Neurochemical Journal · doi:10.1134/s1819712407040022 · Cited by 1

SOMATIC INJURY PRECEDES DISTAL ATROPHY FOLLOWING EXCITOTOXIC HIPPOCAMPAL INSULT

Sharrett-Field, L. J. (2010) · UKnowledge (University of Kentucky) · Cited by 1

NMDA Receptors, Cell Biology and Trafficking

Wenthold, R. J., & Petralia, R. S. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01224-9 · Cited by 1

Possible Role of Neuroprotectants and Natural Products in Epilepsy: Clinical Aspects and Mode of Action

Kumar, A., Bhardwaj, M., & Kaur, H. (2017) · doi:10.1002/9783527803781.ch9 · Cited by 1

Glutamate and early functional NMDA Receptors promote axonal elongation modulating both actin cytoskeleton dynamics and H 2 O 2 production dependent on Rac1 activityPreprint

Muñoz-Palma, E., Wilson, C., Hidalgo, C., & González-Billault, C. E. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.18.638875 · Cited by 1

Neuroligins and Neurexins in Alzheimer’s disease

Sindi, I. A. (2014) · The University of Queensland · doi:10.14264/uql.2015.176

Coordination between presynaptic and postsynaptic properties measured at single terminals in hippocampal cultures

Murnick, J. G. (2003) · DSpace@MIT (Massachusetts Institute of Technology)

Plasticity of the developing glutamate synapse in the hippocampus

Abrahamsson, T. (2007) · Gothenburg University Publications Electronic Archive (Gothenburg University)

FUNCTIONAL PLASTICITY OF HIPPOCAMPAL GLUTAMATERGIC SYNAPSES IN DEVELOPMENT AND DISEASE

Peng, X. (2011) · ScholarlyCommons (University of Pennsylvania)

Experimental studies of N-methyl-D- aspartate receptor NR3 subunits

Öhman, A. (2008) · Figshare

CONTRIBUTION OF NUCLEUS ACCUMBENS CORE TO IMPULSIVE CHOICE: ROLE OF DOPAMINE AND GLUTAMATE SYSTEMS

Yates, J. R. (2014) · UKnowledge (University of Kentucky)

Role of Reelin in synaptogenesis and synaptic stabilization in the adult brain

Piñol, C. B. (2014) · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)

Input-Specific Metaplasticity by a Local Switch in NMDA Receptors

Lee, M. (2009) · DukeSpace (Duke University)

The N-Methyl-D-Aspartate Receptor in Cerebral Ischemia

Tan, T. Y. L., Albert, M. S., & Sun, Y. (2009) · North American Journal of Medicine and Science

Neuronal synapse formation regulated by intercellular adhesion molecules-5 (ICAM-5)

Lin, N. (2013) · Työväentutkimus Vuosikirja

EXAMINATION OF NMDA RECEPTOR SUBUNIT PREVALENCE AND DISTRIBUTION IN CRUDE SYNAPTIC MEMBRANES PURIFIED FROM A MOUSE MODEL OF RETT SYNDROME.

Maliszewska‐Cyna, E. (2010) · TSpace (University of Toronto)

Coupling extrasynaptic NMDA receptors to aberrant intracellular signaling in Huntington disease

Dau, A. (2013) · cIRcle (University of British Columbia) · doi:10.14288/1.0073889

Insulin signaling and synaptic physiology: Insights into the pathogenesis of Alzheimer's disease

Shonesy, B. C. (2009)

Leptin Induces a Novel Form of NMDA Receptor- Dependent LTP at Hippocampal Temporoammonic-

Luo, X. M., McGregor, G., Irving, A. J., & Harvey, J. (2015)

Wędrówki receptorów jonotropowych — do synapsy i z powrotem

Nenckiego, M. (2006)

Electrophysiological Tagging of Ionotropic Glutamate Receptors

Barría, A. (2015) · Neuromethods · doi:10.1007/978-1-4939-2812-5_4

Exzitotoxizität im ZNS bei Mausmutanten mit veränderten Glutamatrezeptoren

Coserea, I. (2005) · heiDOK (Heidelberg University) · doi:10.11588/heidok.00005439

Review Article Differential roles of GluN2A- and GluN2B-containing NMDA receptors in neuronal survival and death

Lujan, B., Liu, X., & Wan, Q. (2012)

Efecto del Estrés crónico sobre la remodelación dendrítica en la región CA3 del hipocampo Effect of chronic stress on the dendritic remodeling in the region CA3 hippocampal

Meraz, M. T., & Bañuelos, P. J. (2009)

Regulation of System Xc-by the Neuropeptide PACAP: Implications for Glutamate Transmission in Drug Addiction

Kong, L. (2017) · ProQuest Demo Repository

Role of DLG-MAGUKs in surface NMDAR localization and its patho-physiological functions

Samaddar, T. (2014) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4742

Functional and molecular approaches to study mu and delta opioid receptor hetero-oligomerization in a model of neuropathic pain

Sutherland, K. R. (2009) · QSpace (Queen's University Library)

Modulation of the Astrocytic Influence on Synapse Structure and Function by Ethanol and Cholinergic Stimulation

Roqué, P. J. (2013) · ResearchWorks at the University of Washington (University of Washington)

Neuromodulatory and metaplastic regulation of long-term synaptic plasticity in the primary visual cortex of adult rats.

Gagolewicz, P. J. (2018) · QSpace (Queen's University Library)

Preparation of Organotypic Slice Cultures for the Study of Glutamate Receptor Function

Barría, A. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9077-1_5

Role of the NMDA receptor subunit, NR3A, in glutamatergic synapse development

Henson, M. A. (2010) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/s4z0-fd80

Sensory experience-dependent synaptic modifications in the visual cortex

Yashiro, K. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/02ds-km68

Oligomerization of Dopamine D1 and Glutamate NMDA Receptors: A New Mechanism Regulating Striatal Function

Fiorentini, C., Busi, C., Bontempi, S., Spano, P., & Missale, C. (2005) · Springer eBooks · doi:10.1007/0-387-28066-9_13

The role of Ca2+/calmodulin-dependent kinase II in normal and abnormal early postnatal development

Gustin, R. M. (2010)

Faculty Opinions recommendation of Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice.

Geschwind, D. H. (2007) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1090653.545891

Faculty Opinions recommendation of Metaplasticity at single glutamatergic synapses.

Littleton, J. T., & Cho, R. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.4275956.4077054

Activity-Dependent Induction of Younger Molecular, Cellular and Organism PhenotypesPreprint

Lissek, T. (2022) · Preprints.org · doi:10.20944/preprints202204.0055.v1

The role of auditory sensory input during functional pre- and postsynaptic maturation of the calyx of Held synapse

Erazo-Fischer, E. (2006) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-164

NMDA Receptors, Cell Biology and Trafficking ☆

Wenthold, R. J., & Petralia, R. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.04700-0

Neuroadaptive Changes in the Mesocortical Glutamatergic System during Nicotine Self-administration and after Extinction in Rats

Wang, F. (2007) · doi:10.21007/etd.cghs.2007.0340

NMDA Receptors

Gibb, A. J. (2019) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0000254.pub3

Faculty Opinions recommendation of REST-dependent epigenetic remodeling promotes the developmental switch in synaptic NMDA receptors.

Hell, J. W. (2012) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.717959572.793462834

Faculty Opinions recommendation of CD47 Protects Synapses from Excess Microglia-Mediated Pruning during Development.

Kano, M., & Watanabe, T. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734198247.793562677

P.2.086 Atypical antipsychotics and time of hospitalization

Mahía, M. G., Millares, M. V., Ramos, R. G., Molino, C. P., & Borrás, C. (2003) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(03)92039-6

Trafficking and Targeting of NMDA Receptors

Petralia, R. S., Wenthold, R. J., & Al‐Hallaq, R. A. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch8 · Cited by 45

NMDA receptor subunit composition controls synaptogenesis and synapse stabilization

Gambrill, A. C., & Barría, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1012676108 · Cited by 240

Functional contributions of synaptically localized NR2B subunits of the NMDA receptor to synaptic transmission and long‐term potentiation in the adult mouse CNS

Miwa, H., Fukaya, M., Watabe, A. M., Watanabe, M., & Manabe, T. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2007.147652 · Cited by 66

Receptor Trafficking

Stornetta, R. L., & Zhu, J. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00352-1