Reduced hippocampal long-term potentiation and context-specific deficit in associative learning in mGluR1 mutant mice.

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

Chomczynski, P., & Sacchi, N. (1987) · Analytical Biochemistry · doi:10.1006/abio.1987.9999 · Cited by 65,515

Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.

Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376

Selective impairment of learning and blockade of long-term potentiation by an N-methyl-D-aspartate receptor antagonist, AP5

Morris, R. G. M., Anderson, E., Lynch, G. S., & Baudry, M. (1986) · Nature · doi:10.1038/319774a0 · Cited by 3,640

Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.

Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292

Molecular diversity of glutamate receptors and implications for brain function

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

Modality-Specific Retrograde Amnesia of Fear

Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483

Homosynaptic long-term depression in area CA1 of hippocampus and effects of N-methyl-D-aspartate receptor blockade.

Dudek, S. M., & Bear, M. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4363 · Cited by 1,708

Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice

Silva, A. J., Stevens, C. F., Tonegawa, S., & Wang, Y. (1992) · Science · doi:10.1126/science.1378648 · Cited by 1,472

Impaired Spatial Learning in α-Calcium-Calmodulin Kinase II Mutant Mice

Silva, A. J., Paylor, R. E., Wehner, J. M., & Tonegawa, S. (1992) · Science · doi:10.1126/science.1321493 · Cited by 1,366

Sequence and expression of a metabotropic glutamate receptor

Masu, M., Tanabe, Y., Tsuchida, K., Shigemoto, R., & Nakanishi, S. (1991) · Nature · doi:10.1038/349760a0 · Cited by 1,216

What behavioral benefit does stiffness control have? An elaboration of Smith's proposal

van Galen, G. P., Hendriks, A. W. C. J., & DeJong, W. P. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081917 · Cited by 4

Two separate pathways for cerebellar LTD: NO-dependent and NO-independent

Hartell, N. A. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081681 · Cited by 4

Protein Networks Associated with Native Metabotropic Glutamate 1 Receptors (mGlu1) in the Mouse Cerebellum

Mansouri, M., Kremser, L., Nguyen, T.-P., Kasugai, Y., Caberlotto, L., Gassmann, M., Sarg, B., Lindner, H., Bettler, B., Carboni, L., et al. (2023) · Cells · doi:10.3390/cells12091325 · Cited by 3

Ataxia and cerebellar hypoexcitability in a mouse model of SCN1B-linked Dravet syndrome

Yuan, Y., O’Malley, H. A., Winters, J. J., Lavado, A., Denomme, N., Bakshi, S., Hodges, S. L., Lopez‐Santiago, L. F., Chen, C., & Isom, L. L. (2025) · JCI Insight · doi:10.1172/jci.insight.187606 · Cited by 3

Is Purkinje Neuron Hyperpolarisation Important for Cerebellar Synaptic Plasticity? A Retrospective and Prospective Analysis

Canepari, M. (2020) · The Cerebellum · doi:10.1007/s12311-020-01164-0 · Cited by 4

Selective reduction in the expression of type‐1 metabotropic glutamate receptors in the hippocampus of adult rats born by caesarean section

Zuena, A. R., Casolini, P., Venerosi, A., Alemà, G., Nicoletti, F., & Calamandrei, G. (2021) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10105 · Cited by 3

Targeting mGlu1 Receptors in the Treatment of Motor and Cognitive Dysfunctions in Mice Modeling Type 1 Spinocerebellar Ataxia

Liberatore, F., Antenucci, N., Tortolani, D., Mascio, G., Fanti, F., Sergi, M., Battaglia, G., Bruno, V., Nicoletti, F., Maccarrone, M., et al. (2022) · Cells · doi:10.3390/cells11233916 · Cited by 3

[1] Optical measurements of calcium signals in mammalian presynaptic terminals

Saggau, P., Gray, R. G. F., & Dani, J. A. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)94004-1 · Cited by 3

Why homocysteine is a risk factor of neurodegenerative diseases mini review

Болдырев, А. А. (2007) · Neurochemical Journal · doi:10.1134/s1819712407010023 · Cited by 3

Molecular Recognition of Metabotropic Glutamate Receptor Type 1 (mGluR1): Synergistic Understanding with Free Energy Perturbation and Linear Response Modeling

Kang, S.-G., Das, P., McGrane, S. J., Martin, A. J., Huynh, T., Royyuru, A. K., TAYLOR, A. J., Jones, P. G., & Zhou, R. (2014) · The Journal of Physical Chemistry B · doi:10.1021/jp410232j · Cited by 3

Spanning the levels in cerebellar function

Arbib, M. A. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081516 · Cited by 3

Cannabinoids and Synaptic Transmission in the Cerebellum

Myoga, M. H., & Regehr, W. G. (2012) · Springer eBooks · doi:10.1007/978-3-030-23810-0_39 · Cited by 3

Long-term changes of synaptic transmission: A topic of long-term interest

Calabresi, P., Pisani, A., & Bernardi, G. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081565 · Cited by 3

Direct radiolabeling by [3H]quisqualic acid of group I metabotropic glutamate receptor in rat brain synaptic membranes

Hinoi, E., Ogita, K., Takeuchi, Y., Ohashi, H., Maruyama, T., & Yoneda, Y. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02809-2 · Cited by 3

Metabotropic glutamate receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database

Acher, F., Battaglia, G., Bräuner‐Osborne, H., Conn, P. J., Duvoisin, R. M., Ferraguti, F., Flor, P. J., Goudet, C., Gregory, K. J., Hampson, D. R., et al. (2019) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f40/2019.4 · Cited by 3

Cerebellar rhythms: Exploring another metaphor

Roberts, P. D., McCollum, G., & Holly, J. E. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0008184x · Cited by 3

Gene targeting approaches to the autonomic nervous system

Fritz, J. D., & Robertson, D. (1996) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(96)00055-0 · Cited by 3

More models of the cerebellum

Houk, J. C., & Barto, A. G. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0008198x · Cited by 3

Catecholamines in Post-Traumatic Stress Disorder

THOMAS, S. A. (2012) · doi:10.21236/ada585061 · Cited by 3

Positive cerebellar feedback loops

Hesslow, G. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0008170x · Cited by 3

Metabotropic Glutamate Receptor-Dependent Synaptic Plasticity

Fitzjohn, S. M., & Bashir, Z. I. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-055-3_13 · Cited by 2

Assessing cognitive function in animal models of mental retardation

Strupp, B. J., & Diamond, A. D. (1996) · Mental Retardation and Developmental Disabilities Research Reviews · doi:10.1002/(sici)1098-2779(1996)2:4 · Cited by 12

LONG TERM POTENTIATION AS A MECHANISM FOR LEARNING AND MEMORY

Talaei, S. A., Gh.A., H., & Masoud, S. S. (2009) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 2

Role of the Cerebellum in the Acquisition and Consolidation of Memory of Motor Learning

Nagao, S. (2021) · Contemporary clinical neuroscience · doi:10.1007/978-3-030-75817-2_14 · Cited by 3

Potential of olfactory neuroepithelial cells as a model to study schizophrenia: A focus on GPCRs (Review)

Sánchez-Florentino, Z. A., Romero-Martínez, B. S., Flores‐Soto, E., Serrano, H., Montaño, L., Valdés‐Tovar, M., Calixto, E., Aquino‐Gálvez, A., López-Riquelme, G. O., Alvarado, R., et al. (2023) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2023.5331 · Cited by 2

Cognition in Rodents

Janus, C., Galsworthy, M. J., Wolfer, D. P., & Welzl, H. (2009) · Springer eBooks · doi:10.1007/978-0-387-76727-7_11 · Cited by 2

A polymorphism (rs2073287) of glutamate receptor, metabotropic 1 (GRM1) is associated with an increased risk of stroke in Korean population

Park, H., Kim, S. K., Lim, S. H., Ahn, W. Y., Gwak, G.-H., & Jo, D. J. (2011) · Molecular & Cellular Toxicology · doi:10.1007/s13273-011-0030-0 · Cited by 2

Algebraic Method for the Analysis of Signaling Crosstalk

Matsubara, Y. J., Kikuchi, S., Sugimoto, M., Oka, K., & Tomita, M. (2008) · Artificial Life · doi:10.1162/artl.2008.14.1.81 · Cited by 2

Cerebellum does more than recalibration of movements after perturbations

Gielen, C. C. A. M. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081632 · Cited by 2

No more news from the cerebellum

Vincent, S. R. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081978 · Cited by 2

Cerebellar arm ataxia: Theories still have a lot to explain

Hore, J. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081723 · Cited by 2

How and what does the cerebellum learn?

Gilbert, P. F. C. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081644 · Cited by 2

Saccades and the adjustable pattern generator

Dean, P. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081589 · Cited by 2

A bridge between cerebellar long-term depression and discrete motor learning: Studies on gene knockout mice

Kano, M. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081966 · Cited by 2

Metabotropic glutamate receptors (mGluRs): structure and function

BOCKAERT, L. F. A. J.-P. P. J. (2001) · CRC Press eBooks · doi:10.1201/9780203299388-10 · Cited by 2

Transgenic models for glutamate receptor function

Doherty, A., & Collingridge, G. (2001) · CRC Press eBooks · doi:10.1201/9780203299388-23 · Cited by 2

The G protein-Coupled Metabotropic Glutamate Receptor 1 controls neuronal macroautophagyPreprint

Donoso, M., Speranza, L., Kalinowska, M., Castillo, C., Sanctis, C. D., & Francesconi, A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.02.365783 · Cited by 2

Enhanced mGluR1 function causes motor deficits and region-specific Purkinje cell dysfunction

Ibrahim, M. F., Boyanova, S. T., Cheng, Y. C., Ligneul, C., Bains, R. S., Johnpulle, T. C., Lerch, J. P., Mann, E. O., Oliver, P. L., & Becker, E. B. E. (2026) · Brain · doi:10.1093/brain/awaf477 · Cited by 1

mGluR1 Negative Allosteric Modulators: An Alternative Metabotropic Approach for the Treatment of Schizophrenia

Ohta, H., Kawamoto, H., & Suzuki, G. (2010) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0346-0241-9_7 · Cited by 1

Path to understanding the pathophysiology of Fragile X syndrome

Mulle, J. G., Peñagarikano, O., & Warren, S. T. (2007) · Future Neurology · doi:10.2217/14796708.2.5.567 · Cited by 1

Glutamatergic Pathways and Receptors

Tomita, S. (2016) · Springer eBooks · doi:10.1007/978-3-319-24551-5_29 · Cited by 1

Class C GPCRs: Metabotropic Glutamate Receptors

Hlaváčková, V., Prézeau, L., Pin, J., & Blahoš, J. (2017) · Springer eBooks · doi:10.1007/978-3-319-60174-8_13 · Cited by 1

Metabotropic glutamate receptors (mGluRs)

Pin, J., Fagni, L., & Bockaert, J. (2001) · Pharmaceutical science series · doi:10.1201/9780203299388.pt2 · Cited by 1

Metabotropic Glutamate Receptors in Anxiety Disorder

Xu, J., & Zhu, Y. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.1002630 · Cited by 2

Neurotransmitter Release and Synaptic Plasticity

Huang, E. P., & Stevens, C. F. (1997) · Advances in organ biology · doi:10.1016/s1569-2590(08)60185-8 · Cited by 1

Purkinje Neurons: Synaptic Plasticy

Daniel, H., & Crépel, F. (2012) · Springer eBooks · doi:10.1007/978-3-030-23810-0_32 · Cited by 1

Learning Paradigms and Genetic Tools for the Study of Cerebellum-Dependent Learning and Memory

Katoh, A. (2022) · Neuromethods · doi:10.1007/978-1-0716-2026-7_6 · Cited by 1

Moonwalker Mouse

Becker, E. B. E. (2020) · Springer eBooks · doi:10.1007/978-3-319-97911-3_107-1 · Cited by 1

An Overview of Mouse Models in Neuroscience Research

Popko, B. (1999) · Springer eBooks · doi:10.1007/978-1-4615-4887-4_1 · Cited by 1

Further evidence for the involvement of nitric oxide in trans-ACPD-induced suppression of AMPA responses in cultured chick Purkinje neurons

Mori-Okamoto, J., & Okamoto, K. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081802 · Cited by 1

The notions of joint stiffness and synaptic plasticity in motor memory

Latash, L. P., & Latash, M. L. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081784 · Cited by 1

How to link the specificity of cerebellar anatomy to motor learning?

Sultan, F. R., Heck, D. H., & Harold Bekkering, A. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081863 · Cited by 1

We know a lot about the cerebellum, but do we know what motor learning is?

Swinnen, S. P., Walter, C. B., & Dounskaia, N. V. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081875 · Cited by 1

A cerebellar long-term depression update

Linden, D. J. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081942 · Cited by 1

Cellular mechanisms of long-term depression: From consensus to open questions

Crépel, F. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081954 · Cited by 1

Nitric oxide is involved in cerebellar long-term depression

Okada, D. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081814 · Cited by 1

Resilient cerebellar theory complies with stiff opposition

Smith, A. M. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00082005 · Cited by 1

The cerebellum and cerebral cortex: Contrasting and converging contributions to spatial navigation and memory

O’Mara, S. M. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081826 · Cited by 1

How can the cerebellum match “error signal” and “error correction”?

Dufossé, M. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081590 · Cited by 1

Sensorimotor learning in structures “upstream” from the cerebellum

van Donkelaar, P. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081905 · Cited by 1

Plasticity of cerebro-cerebellar interactions in patients with cerebellar dysfunction

Wessel, K. (1996) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00081930 · Cited by 1

LTP Does Not Equal Memory

Sweatt, J. D. (2003) · Elsevier eBooks · doi:10.1016/b978-012678957-7/50011-6 · Cited by 1

Mouse Mutations in the Study of Cerebellar Development

Karagogeos, D., & Pavlou, O. (1999) · Springer eBooks · doi:10.1007/978-1-4615-4887-4_4 · Cited by 1

New animal models in target discovery.

Oosting, R. S., Stark, K. L., Hen, R., & Scharrenburg, G. J. M. V. (1998) · Pharmacochemistry library · doi:10.1016/s0165-7208(98)80058-5

Using Transgenic Mice to Probe the Role of Specific Genes in Behavior

Gingrich, J. A., & Hen, R. (2001) · Springer eBooks · doi:10.1007/978-3-642-59519-6_5

G Protein-Mediated Signalling Pathways

Offermanns, S. (2004) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-18934-0_6

Genetically Altered Mice as Models for Understanding Brain Disorders

Caron, M. G., & Gainetdinov, R. R. (2003) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-55543-5_5

Cellular mechanisms of synaptic plasticity in hippocampal area CA1

Guire, E. S. (2006) · doi:10.6083/m4mw2fdw

Neural Circuit Development and Plasticity Shaped by Glutamate Transporters

Miyazaki, T., Takasaki, C., & Watanabe, M. (2009) · Springer eBooks · doi:10.1007/978-4-431-98074-2_22

Chapter 3.2.7 Protein targeting in the functional analysis of EphA receptors: the use of immunoadhesins

Gerlai, R. T., Shinsky, N., Shih, A., Williams, P., Winer, J., Armanini, M. P., Moran, P., Cairns, B., Winslow, J. W., Gao, W., et al. (1999) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(99)80039-x

Short- and long-term neuronal plasticity in hippocampal CA1 region of rat

Huang, F. (2010) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Redundant Neuromodulatory Mechanisms That Control Fear Memory Consolidation

Young, M. B. (2013) · Scholarly Commons (University of Pennsylvania)

Plasticidad del sistema glutamatérgico en la vía olfatoria de roedores sometidos a deprivación sensorial. Estudio del receptor mGluR1a en el bulbo olfatorio

González, M. V. B. (2011) · doi:10.14201/gredos.110642

Protein Kinases in Spinal Plasticity: A Role for Metabotropic Glutamate Receptors

Russell, J. A., & Adam, R. (2012) · InTech eBooks · doi:10.5772/37788

Die Rolle metabotroper Glutamatrezeptoren der Gruppe I beim Lernen und Gedächtnis der Ratte

Karls, E. (2006)

Cerebellar Grafting and the Recovery of Function

Triarhou, L. C. (1997) · Neuroscience intelligence unit · doi:10.1007/978-3-662-22213-3_8

Analysis of Long-Term Depression in the Purkinje Cell Circuit (a Model Study)

Zhang, X. C., Liu, S. Q., Ren, H., Zeng, Y., & Zhan, G. X. (2014) · Neurophysiology · doi:10.1007/s11062-014-9402-0

Ligand-Induced Dimeric Rearrangement of the Metabotropic Glutamate Receptor 1

Tateyama, M., & Kubo, Y. (2005) · Seibutsu Butsuri · doi:10.2142/biophys.45.90

mGlu1 Metabotropic Glutamate Receptor

Alexander, S. P. H. (2007) · Elsevier eBooks · doi:10.1016/b978-008055232-3.60140-0

Efectos de la administracion de MPEP, un antagonista selectivo de los receptors de glutamato mGlu5, sobre la memoria especial en ratones

Blanco, E., Martín‐López, M., Cavas, M., Arias, J. L., & Navarro, J. F. (2008) · Psiquiatría Biológica · doi:10.1016/s1134-5934(08)71120-5

Modulation of Synaptic Transmission by Metabotropic Glutamate Receptors and Endocannabinoid Signaling

Nagaraja, R. Y. (2006) · EUR Research Repository (Erasmus University Rotterdam)

Signal Transduction Cascade from mGluR1 to PKCγ Is Involved in Climbing Fiber Synapse Elimination During Postnatal Cerebellar Development

Kano, M., & Hashimoto, K. (2000) · Springer eBooks · doi:10.1007/978-4-431-66973-9_44

Transgene Mäuse zur molekularbiologischen Untersuchung spezifisch genetischer Einflüsse auf das Verhalten

Gingrich, J. A., & Hen, R. (1999) · Springer eBooks · doi:10.1007/978-3-642-60174-3_5

Septohippocampal Cholinergic Neurons Produces a Direct Excitation of Identified Group I Metabotropic Glutamate Receptor Activation

Hajszán, T., Xu, C., Léránth, C., Alreja, M., Kim, Y. S., Watanabe, M., Shin, H., Shin, J., Gangadharan, G., Kim, S.-W., et al. (2015)

Introductory Review: Synaptic Plasticity and Modulation

Yoshioka, T., & Kuba, K. (2000) · Springer eBooks · doi:10.1007/978-4-431-66973-9_36

Long Term Depression in the Granule Cell-Purkinje Cell Synapse

Tanaka, K. (2014) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_472-1

Regulatory Crosstalk Analysis of Biochemical Networks in the Hippocampus and Nucleus Accumbens

Kikuchi, S., & Voit, E. O. (2013) · Springer eBooks · doi:10.1007/978-94-007-6803-1_4

Regulation of AMPA Receptors by Metabotropic Receptors and Receptor Tyrosine Kinases: Mechanisms and Physiological Roles

Carvalho, A. L., Caldeira, M. V., Gomes, A. R., Carvalho, A. P., & Duarte, C. B. (2008) · Springer eBooks · doi:10.1007/978-0-387-30382-6_12

Phänotypische und molekulare Analyse einer Maus mit Insertionsmutation und axonaler Reorganisation im Hippocampus

Böhm, D. (2002) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-97

Structural Rearrangement and Functional Regulation of the Metabotropic Glutamate Receptor

Kubo, Y., & Tateyama, M. (2009) · Springer eBooks · doi:10.1007/978-0-387-30370-3_17

Cerebellum and Classical Conditioning

Thompson, R. F. (2011) · Neuromethods · doi:10.1007/978-1-61779-301-1_15

Modulation of N-methyl-D-aspartate receptors by Gαs- and Gαi/o-coupled receptors

Trepanier, C. H. (2013) · TSpace (University of Toronto)

IP3 Receptor and Ca2+ Signaling

Hisatsune, C., & Mikoshiba, K. (2009) · Springer eBooks · doi:10.1007/978-0-387-30370-3_31

Metabotropic glutamate receptors in GtoPdb v.2021.3

Acher, F., Battaglia, G., Bräuner‐Osborne, H., Conn, P. J., Duvoisin, R. M., Ferraguti, F., Flor, P. J., Goudet, C., Gregory, K. J., Hampson, D. R., et al. (2021) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f40/2021.3

mGluR1 Is a Molecular “Hub” for Synapse Elimination in the Developing Cerebellum

Kano, M., Watanabe, T., & Uesaka, N. (2021) · Contemporary clinical neuroscience · doi:10.1007/978-3-030-75817-2_4

Role of LTD in Cerebellar Motor Learning: The 75th FUJIHARA Seminar “The Cerebellum as a CNS Hub”

Yamaguchi, K. (2021) · Contemporary clinical neuroscience · doi:10.1007/978-3-030-75817-2_17 · Cited by 2

AMPA Receptor

Tomita, S. (2009) · Springer eBooks · doi:10.1007/978-0-387-30370-3_18

mGluR1

Mak, T. W., Penninger, J. M., Roder, J., Rossant, J., & Saunders, M. E. (1998) · Elsevier eBooks · doi:10.1016/b978-012466044-1/50407-5

Long Term Depression in the Granule Cell-Purkinje Cell Synapse

Tanaka, K. (2022) · Springer eBooks · doi:10.1007/978-1-0716-1006-0_472

Long Term Depression in the Granule Cell-Purkinje Cell Synapse

Tanaka, K. (2015) · Springer eBooks · doi:10.1007/978-1-4614-6675-8_472

Involvement of the mGluR1 Receptor in Hippocampal Synaptic Plasticity and Associative Learning in Behaving Mice

Gil, C., Delgado-García, J. M., Fairén, A. G., & Gruart, A. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm193 · Cited by 67

Motor deficit and impairment of synaptic plasticity in mice lacking mGluR1

Conquet, F., Bashir, Z. I., Davies, C. H., Daniel, H., Ferraguti, F., Bordi, F., Franz-Bacon, K., Reggiani, A., Matarese, V., Condé, F., et al. (1994) · Nature · doi:10.1038/372237a0 · Cited by 743

Mice Lacking Metabotropic Glutamate Receptor 5 Show Impaired Learning and Reduced CA1 Long-Term Potentiation (LTP) But Normal CA3 LTP

Lu, Y.-M., Jia, Z., Janus, C., Henderson, J. T., Gerlai, R., Wojtowicz, J. M., & Roder, J. C. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-13-05196.1997 · Cited by 634

Pharmacological antagonism of metabotropic glutamate receptor 1 regulates long‐term potentiation and spatial reference memory in the dentate gyrus of freely moving rats via N‐methyl‐ d ‐aspartate and metabotropic glutamate receptor‐dependent mechanisms

Naie, K., & Manahan‐Vaughan, D. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03864.x · Cited by 74

Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice

Aiba, A., Kano, M., Chen, C., Stanton, M. E., Fox, G. D., Herrup, K., Zwingman, T. A., & Tonegawa, S. (1994) · Cell · doi:10.1016/0092-8674(94)90205-4 · Cited by 930