The DOI matches its Crossref record; 40 of the 41 references it cites were found in a registry or an index.
Knockout of ERK1 MAP Kinase Enhances Synaptic Plasticity in the Striatum and Facilitates Striatal-Mediated Learning and Memory
Open accessAbstract
Extracellular signal-regulated kinases (ERK1 and 2) are synaptic signaling components necessary for several forms of learning. In mice lacking ERK1, we observe a dramatic enhancement of striatum-dependent long-term memory, which correlates with a facilitation of long-term potentiation in the nucleus accumbens. At the cellular level, we find that ablation of ERK1 results in a stimulus-dependent increase of ERK2 signaling, likely due to its enhanced interaction with the upstream kinase MEK. Consistently, such activity change is responsible for the hypersensitivity of ERK1 mutant mice to the rewarding properties of morphine. Our results reveal an unexpected complexity of ERK-dependent signaling in the brain and a critical regulatory role for ERK1 in the long-term adaptive changes underlying striatum-dependent behavioral plasticity and drug addiction.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“During development, ERK1 and ERK2 have divergent functions since ERK1 null mice are grossly viable and fertile while ERK2 null mice are embryonic lethal7–9.”
From Conditional loss of ERK1 and ERK2 results in abnormal placentation and delayed parturition in the mouse (2019) · cites this paper as [7]
Citations
Cites
LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444
Mitogen-Activated Protein (MAP) Kinase Pathways: Regulation and Physiological Functions*
Pearson, G. W., Robinson, F. L., Gibson, T. B., Xu, B.-E., Karandikar, M. S., Berman, K. S., & Cobb, M. H. (2001) · Endocrine Reviews · doi:10.1210/edrv.22.2.0428 · Cited by 4,111
Identification of a Novel Inhibitor of Mitogen-activated Protein Kinase Kinase
Favata, M. F., Horiuchi, K. Y., Manos, E. J., Daulerio, A. J., Stradley, D. A., Feeser, W. S., Dyk, D. E. V., Pitts, W. J., Earl, R. A., Hobbs, F. W., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.29.18623 · Cited by 3,016
Synaptic Plasticity and Memory: An Evaluation of the Hypothesis
Martin, S. J., Grimwood, P. D., & Morris, R. G. M. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.649 · Cited by 2,794
Molecular basis of long-term plasticity underlying addiction
Nestler, E. J. (2001) · Nature reviews. Neuroscience · doi:10.1038/35053570 · Cited by 1,893
Addiction and the brain: The neurobiology of compulsion and its persistence
Hyman, S. E., & Malenka, R. C. (2001) · Nature reviews. Neuroscience · doi:10.1038/35094560 · Cited by 1,337
Addiction, Dopamine, and the Molecular Mechanisms of Memory
Berke, J. D., & Hyman, S. E. (2000) · Neuron · doi:10.1016/s0896-6273(00)81056-9 · Cited by 1,184
Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens
Nicola, S. M., Surmeier, D. J., & Malenka, R. C. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.185 · Cited by 931
A Requirement for the Mitogen-activated Protein Kinase Cascade in Hippocampal Long Term Potentiation
English, J. D., & Sweatt, J. D. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.31.19103 · Cited by 860
Understanding Ras: ‘it ain’t over ’til it’s over’
Shields, J. M., Pruitt, K., McFall, A. J., Maddox, A. S., & Der, C. J. (2000) · Trends in Cell Biology · doi:10.1016/s0962-8924(00)01740-2 · Cited by 784
Research works printed but not linked: 1
- Pearson, 2001, Mitogen-activated protein (MAP) kinase pathways, Endocr. Rev., 22, 153
Cited by
Sorted by citations
Roles of the Raf/MEK/ERK pathway in cell growth, malignant transformation and drug resistance
McCubrey, J. A., Steelman, L. S., Chappell, W. H., Abrams, S. L., Wong, E. W. T., Chang, F., Lehmann, B. D., Terrian, D. M., Milella, M., Tafuri, A., et al. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.10.001 · Cited by 2,349
Mitogen-activated protein kinases in synaptic plasticity and memory
Sweatt, J. D. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.04.001 · Cited by 1,013
Mebratu, Y. A., & Tesfaigzi, Y. (2009) · Cell Cycle · doi:10.4161/cc.8.8.8147 · Cited by 989
The MEK/ERK cascade: From signaling specificity to diverse functions
Shaul, Y. D., & Seger, R. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.10.005 · Cited by 969
Translational Control by MAPK Signaling in Long-Term Synaptic Plasticity and Memory
Kelleher, R. J., Govindarajan, A., Jung, H.-Y., Kang, H., & Tonegawa, S. (2004) · Cell · doi:10.1016/s0092-8674(04)00115-1 · Cited by 845
Sex-specific transcriptional signatures in human depression
Labonté, B., Engmann, O., Purushothaman, I., Menard, C., Wang, J., Tan, C., Scarpa, J. R., Moy, G., Loh, Y.-H. E., Cahill, M., et al. (2017) · Nature Medicine · doi:10.1038/nm.4386 · Cited by 748
Recurrent 16p11.2 microdeletions in autism
Kumar, R. A., KaraMohamed, S., Sudi, J., Conrad, D. F., Brune, C., Badner, J. A., Gilliam, T. C., Nowak, N. J., Cook, E. H., Dobyns, W. B., et al. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm376 · Cited by 731
Chang, F., Steelman, L. S., Lee, J. T., Shelton, J. G., Navolanic, P. M., Blalock, W. L., Franklin, R. A., & McCubrey, J. A. (2003) · Leukemia · doi:10.1038/sj.leu.2402945 · Cited by 738
Microduplications of 16p11.2 are associated with schizophrenia
Wellcome Trust Case Control Consortium, McCarthy, S. E., Makarov, V., Kirov, G., Addington, A. M., McClellan, J., Yoon, S., Perkins, D. O., Dickel, D. E., Kusenda, M., et al. (2009) · Nature Genetics · doi:10.1038/ng.474 · Cited by 711
JAK/STAT, Raf/MEK/ERK, PI3K/Akt and BCR-ABL in cell cycle progression and leukemogenesis
Steelman, L. S., Pohnert, S. C., Shelton, J. G., Franklin, R. A., Bertrand, F. E., & McCubrey, J. A. (2004) · Leukemia · doi:10.1038/sj.leu.2403241 · Cited by 705
Roles of the RAF/MEK/ERK and PI3K/PTEN/AKT pathways in malignant transformation and drug resistance
McCubrey, J. A., Steelman, L. S., Abrams, S. L., Lee, J. T., Chang, F., Bertrand, F. E., Navolanic, P. M., Terrian, D. M., Franklin, R. A., D’Assoro, A. B., et al. (2006) · Advances in Enzyme Regulation · doi:10.1016/j.advenzreg.2006.01.004 · Cited by 656
ERK1/2 MAP kinases in cell survival and apoptosis
Lu, Z., & Xu, S. (2006) · IUBMB Life · doi:10.1080/15216540600957438 · Cited by 675
Moreno, S., Vecchioli, S. F., & Cerù, M. P. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.08.064 · Cited by 595
Shinawi, M., Liu, P., Kang, S.-H. L., Shen, J., Belmont, J. W., Scott, D. A., Probst, F. J., Craigen, W. J., Graham, B. H., Pursley, A., et al. (2010) · Journal of Medical Genetics · doi:10.1136/jmg.2009.073015 · Cited by 580
The role of MAPKs in adipocyte differentiation and obesity
Bost, F., Aouadi, M., Caron, L., & Binétruy, B. (2004) · Biochimie · doi:10.1016/j.biochi.2004.10.018 · Cited by 583
Targeting dual-specificity phosphatases: Manipulating MAP kinase signalling and immune responses
Jeffrey, K. L., Camps, M., Rommel, C., & Mackay, C. R. (2007) · Nature Reviews Drug Discovery · doi:10.1038/nrd2289 · Cited by 533
It could be habit forming: drugs of abuse and striatal synaptic plasticity
Gerdeman, G. L., Partridge, J. G., Lupica, C. R., & Lovinger, D. M. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00065-1 · Cited by 480
The Role of the Extracellular Signal-Regulated Kinase Signaling Pathway in Mood Modulation
Einat, H., Yuan, P., Gould, T. D., Li, J., Du, J., Zhang, L., Manji, H. K., & Chen, G. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07311.2003 · Cited by 475
Valjent, E., Pagès, C., Hervé, D., Girault, J., & Caboche, J. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03278.x · Cited by 453
MAPK signalling: ERK5 versus ERK1/2
Nishimoto, S., & Nishida, E. (2006) · EMBO Reports · doi:10.1038/sj.embor.7400755 · Cited by 431
Calcium signaling in neurodegeneration
Marambaud, P., Dreses‐Werringloer, U., & Vingtdeux, V. (2009) · Molecular Neurodegeneration · doi:10.1186/1750-1326-4-20 · Cited by 363
ERK2: a logical AND gate critical for drug-induced plasticity?
Girault, J., Valjent, E., Caboche, J., & Hervé, D. (2006) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2006.08.012 · Cited by 348
Mu opioid receptor: a gateway to drug addiction
Contet, C., Kieffer, B. L., & Befort, K. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.05.005 · Cited by 340
Bost, F., Aouadi, M., Caron, L., Even, P. C., Belmonte, N., Prot, M., Dani, C., Hofman, P. M., Pagès, G., Pouysségur, J., et al. (2005) · Diabetes · doi:10.2337/diabetes.54.2.402 · Cited by 351
Self-citationExtracellular signal-regulated kinase 2 is necessary for mesoderm differentiation
Yao, Y., Li, W., Wu, J., Germann, U. A., Su, M. S. S., Kuida, K., & Boucher, D. M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2134254100 · Cited by 323
Hébert, S. S., Papadopoulou, A. S., Smith, P. Y., Galas, M., Planel, E., Silahtaroglu, A., Sergeant, N., Buée, L., & Strooper, B. D. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq311 · Cited by 334
Neurotrophic factors and axonal growth
Markus, A., Patel, T. D., & Snider, W. D. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00372-0 · Cited by 315
MicroRNA-128 governs neuronal excitability and motor behavior in mice
Tan, C. L., Plotkin, J. L., Venø, M. T., von Schimmelmann, M., Feinberg, P., Mann, S., Handler, A., Kjems, J., Surmeier, D. J., O’Carroll, D., et al. (2013) · Science · doi:10.1126/science.1244193 · Cited by 301
Essential role for ERK2 mitogen‐activated protein kinase in placental development
Hatano, N., Mori, Y., Oh‐hora, M., Kosugi, A., Fujikawa, T., Nakai, N., Niwa, H., Miyazaki, J., Hamaoka, T., & Ogata, M. (2003) · Genes to Cells · doi:10.1046/j.1365-2443.2003.00680.x · Cited by 296
Brami‐Cherrier, K., Valjent, E., Hervé, D., Darragh, J., Corvol, J., Pagès, C., Simon, A. J., Girault, J., & Caboche, J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1711-05.2005 · Cited by 307
Gourley, S. L., Wu, F. J., Kiraly, D. D., Ploski, J. E., Kedves, A. T., Duman, R. S., & Taylor, J. R. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.07.016 · Cited by 287
ERK1 and ERK2 Map Kinases: Specific Roles or Functional Redundancy?
Buscà, R., Pouysségur, J., & Lenormand, P. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00053 · Cited by 303
Self-citationMolecular and cellular cognitive studies of the role of synaptic plasticity in memory
Silva, A. J. (2002) · Journal of Neurobiology · doi:10.1002/neu.10169 · Cited by 285
Samuels, I. S., Karlo, J. C., Faruzzi, A. N., Pickering, K., Herrup, K., Sweatt, J. D., Saitta, S. C., & Landreth, G. E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0679-08.2008 · Cited by 278
Westin, J. E., Vercammen, L., Strome, E. M., Konradi, C. L., & Cenci, M. A. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.11.032 · Cited by 281
MAPK signaling in inflammation-associated cancer development
Huang, P., Han, J., & Hui, L. (2010) · Protein & Cell · doi:10.1007/s13238-010-0019-9 · Cited by 273
Fernandez, S. M., Lewis, M. C., Pechenino, A. S., Harburger, L. L., Orr, P. T., Gresack, J. E., Schafe, G. E., & Frick, K. M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1968-08.2008 · Cited by 289
Role of ERK in cocaine addiction
Lü, L., Koya, E., Zhai, H., Hope, B. T., & Shaham, Y. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.10.005 · Cited by 269
GnRH signaling, the gonadotrope and endocrine control of fertility
Bliss, S. P., Navratil, A. M., Xie, J., & Roberson, M. S. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.04.002 · Cited by 259
ERK in Learning and Memory: A Review of Recent Research
Peng, S., Zhang, Y., Zhang, J., Wang, H., & Ren, B. (2010) · International Journal of Molecular Sciences · doi:10.3390/ijms11010222 · Cited by 254
NMDA receptor mediates tau-induced neurotoxicity by calpain and ERK/MAPK activation
Amadoro, G., Ciotti, M. T., Costanzi, M., Cestari, V., Calissano, P., & Canu, N. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511065103 · Cited by 243
Self-citationDickey, C. A., Loring, J. F., Montgomery, J., Gordon, M. N., Eastman, P. S., & Morgan, D. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05219.2003 · Cited by 242
Sun, J., & Nan, G. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.2962 · Cited by 245
Albert‐Gascó, H., Ros‐Bernal, F., Castillo-Gómez, E., & Olucha-Bordonau, F. E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124471 · Cited by 248
Functions of the MAPK family in vertebrate‐development
Krens, G., Spaink, H. P., & Snaar-Jagalska, E. B. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.08.025 · Cited by 248
McCubrey, J. A., Steelman, L. S., Abrams, S. L., Bertrand, F. E., Ludwig, D. E., Bäsecke, J., Libra, M., Stivala, F., Milella, M., Tafuri, A., et al. (2008) · Leukemia · doi:10.1038/leu.2008.27 · Cited by 234
Ohori, M., Kinoshita, T., Okubo, M., Sato, K., Yamazaki, A., Arakawa, H., Nishimura, S., Inamura, N., Nakajima, H., Neya, M., et al. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.08.082 · Cited by 236
Zhang, L., Lou, D., Jiao, H., Zhang, D., Wang, X., Xia, Y., Zhang, J., & Xu, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0060-04.2004 · Cited by 228
The beneficial effects of fruit polyphenols on brain aging
Lau, F. C., Shukitt-Hale, B., & Joseph, J. A. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.08.007 · Cited by 217
Neurodevelopmental effects of insulin-like growth factor signaling
OʼKusky, J. R., & Ye, P. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2012.06.002 · Cited by 219
Intracellular signaling pathway regulation of myelination and remyelination in the CNS
Gaesser, J. M., & Fyffe-Maricich, S. L. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.03.008 · Cited by 217
Yoshimura, Y., Yamauchi, Y., Shinkawa, T., Taoka, M., Donai, H., Takahashi, N., Isobe, T., & Yamauchi, T. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02136.x · Cited by 208
ERK1 and ERK2 mitogen-activated protein kinases affect Ras-dependent cell signaling differentially
Vantaggiato, C., Formentini, I., Bondanza, A., Bonini, C., Naldini, L., & Brambilla, R. (2006) · Journal of Biology · doi:10.1186/jbiol38 · Cited by 210
Self-citationLeFloch, R., Pouysségur, J., & Lenormand, P. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00800-07 · Cited by 212
Self-citationMAP'ing CNS Development and Cognition: An ERKsome Process
Samuels, I. S., Saitta, S. C., & Landreth, G. E. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.001 · Cited by 200
Mitogen-activated protein kinases in hepatocellular carcinoma development
Min, L., He, B., & Hui, L. (2010) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2010.10.011 · Cited by 179
Shaltiel, G., Maeng, S., Malkesman, O., Pearson, B., Schloesser, R. J., Tragon, T., Rogawski, M., Gasior, M., Luckenbaugh, D., Chen, G., et al. (2008) · Molecular Psychiatry · doi:10.1038/mp.2008.20 · Cited by 173
Role of the ERK pathway in psychostimulant-induced locomotor sensitization
Valjent, E., Corvol, J., Trzăskos, J. M., Girault, J., & Hervé, D. (2006) · BMC Neuroscience · doi:10.1186/1471-2202-7-20 · Cited by 173
Fidelity and spatio‐temporal control in MAP kinase (ERKs) signalling
Pouysségur, J., & Lenormand, P. (2003) · European Journal of Biochemistry · doi:10.1046/j.1432-1033.2003.03707.x · Cited by 171
Self-citationCalcium Activation of ERK Mediated by Calmodulin Kinase I
Schmitt, J., Wayman, G. A., Nozaki, N., & Soderling, T. R. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401501200 · Cited by 168
Davis, S., & Laroche, S. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00230.x · Cited by 168
Satoh, Y., Endo, S., Ikeda, T., Yamada, K., Ito, M., Kuroki, M., Hiramoto, T., Imamura, O., Kobayashi, Y., Watanabe, Y., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0117-07.2007 · Cited by 165
Yuan, P., Zhou, R., Wang, Y., Li, X., Li, J., Chen, G., Guitart, X., & Manji, H. K. (2009) · Journal of Affective Disorders · doi:10.1016/j.jad.2009.10.017 · Cited by 160
The ERK2 Mitogen-Activated Protein Kinase Regulates the Timing of Oligodendrocyte Differentiation
Fyffe-Maricich, S. L., Karlo, J. C., Landreth, G. E., & Miller, R. H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3239-10.2011 · Cited by 164
Role of MAPKs in development and differentiation: lessons from knockout mice
Aouadi, M., Binétruy, B., Caron, L., MARCHAND‐BRUSTEL, Y. L., & Bost, F. (2006) · Biochimie · doi:10.1016/j.biochi.2006.06.003 · Cited by 158
Proteomic and genomic evidence implicates the postsynaptic density in schizophrenia
Föcking, M., Lopez, L. M., English, J. A., Dicker, P., Wolff, A., Brindley, E., Wynne, K. J., Cagney, G., & Cotter, D. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.63 · Cited by 156
A Role for ERK MAP Kinase in Physiologic Temporal Integration in Hippocampal Area CA1Preprint
Selcher, J. C., Weeber, E. J., Christian, J., Nekrasova, T., Landreth, G. E., & Sweatt, J. D. (2003) · Learning & Memory · doi:10.1101/lm.51103 · Cited by 158
Cellular Plasticity Cascades: Genes-To-Behavior Pathways in Animal Models of Bipolar Disorder
Einat, H., & Manji, H. K. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.11.004 · Cited by 156
ERK2 Contributes to the Control of Social Behaviors in Mice
Satoh, Y., Endo, S., Nakata, T., Kobayashi, Y., Yamada, K., Ikeda, T., Takeuchi, A., Hiramoto, T., Watanabe, Y., & Kazama, T. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2349-11.2011 · Cited by 145
ERK activation causes epilepsy by stimulating NMDA receptor activity
Nateri, A. S., Raivich, G., Gebhardt, C., Costa, C. D., Naumann, H., Vreugdenhil, M., Makwana, M., Brandner, S., Adams, R. H., Jefferys, J. G. R., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601911 · Cited by 145
ERK2 is required for efficient terminal differentiation of skeletal myoblasts
Li, J., & Johnson, S. E. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.05.051 · Cited by 137
Nascent Proteome Remodeling following Homeostatic Scaling at Hippocampal Synapses
Schanzenbächer, C. T., Sambandan, S., Langer, J. D., & Schuman, E. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.058 · Cited by 138
Synaptic plasticity in the mesolimbic dopamine system
Thomas, M. J., & Malenka, R. C. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1236 · Cited by 137
Frielingsdorf, H., Bath, K. G., Soliman, F., Difede, J., Casey, B. J., & Lee, F. S. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05722.x · Cited by 139
Mizoguchi, H., Yamada, K., Mizuno, M., Mizuno, T., Nitta, A., Noda, Y., & Nabeshima, T. (2004) · Molecular Pharmacology · doi:10.1124/mol.65.5.1293 · Cited by 130
Erk1 Positively Regulates Osteoclast Differentiation and Bone Resorptive Activity
He, Y., Staser, K. W., Rhodes, S. D., Liu, Y., Wu, X., Park, S.-J., Yuan, J., Yang, X., Li, X., Jiang, L., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024780 · Cited by 130
Mitogen-Activated Protein Kinases in Cell-Cycle Control
MacCorkle, R. A., & Tan, T. (2005) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:43:3:451 · Cited by 130
do Prado, C. H., Rizzo, L. B., Wieck, A., Lopes, R. P., Teixeira, A. L., Grassi‐Oliveira, R., & Bauer, M. E. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.08.005 · Cited by 131
The extracellular signal-regulated kinase pathway: an emerging promising target for mood stabilizers
Chen, G., & Manji, H. K. (2006) · Current Opinion in Psychiatry · doi:10.1097/01.yco.0000218604.63463.cd · Cited by 126
Sharma, S. K., Sherff, C. M., Shobe, J., Bagnall, M. W., Sutton, M. A., & Carew, T. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-09-03899.2003 · Cited by 125
Impact of the BDNF Val66Met Polymorphism on Cognition
Dincheva, I., Glatt, C. E., & Lee, F. S. (2012) · The Neuroscientist · doi:10.1177/1073858411431646 · Cited by 133
Knockout of ERK1 Enhances Cocaine-Evoked Immediate Early Gene Expression and Behavioral Plasticity
Ferguson, S. M., Fasano, S., Yang, P., Brambilla, R., & Robinson, T. E. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301014 · Cited by 130
Self-citationGerdjikov, T. V., Ross, G. M., & Beninger, R. J. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.4.740 · Cited by 124
Bevilaqua, L. R., Kerr, D. S., Medina, J. H., Izquierdo, I., & Cammarota, M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02524.x · Cited by 124
BDNF Val66Met and cognition: all, none, or some? A meta‐analysis of the genetic association
Mandelman, S. D., & Grigorenko, E. L. (2012) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2011.00738.x · Cited by 122
Impact of Genetic Variant BDNF (Val66Met) on Brain Structure and Function
Chen, Z., Bath, K., McEwen, B., Hempstead, B., & Lee, F. (2008) · Novartis Foundation Symposia · doi:10.1002/9780470751251.ch14 · Cited by 119
Engel, S. R., Creson, T. K., Hao, Y., Shen, Y., Maeng, S., Nekrasova, T., Landreth, G. E., Manji, H. K., & Chen, G. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002135 · Cited by 124
Smith, B., Burton, L. J., Henderson, V., Randle, D. D., Morton, D. J., Smith, B. A., Taliaferro-Smith, L. D., Nagappan, P., Yates, C. C., Zayzafoon, M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104987 · Cited by 117
Cunha, C., Angelucci, A., D'Antoni, A., Döbrössy, M. D., Dunnett, S. B., Berardi, N., & Brambilla, R. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2008.11.004 · Cited by 120
Self-citationGrueter, B. A., Gosnell, H., Olsen, C. M., Schramm‐Sapyta, N. L., Nekrasova, T., Landreth, G. E., & Winder, D. G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0170-06.2006 · Cited by 115
Nuclear Calcium/Calmodulin Regulates Memory Consolidation
Limbäck-Stokin, K., Korzus, E., Nagaoka-Yasuda, R., & Mayford, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1022-04.2004 · Cited by 122
Deviance-related electrophysiological activity in mice: is there mismatch negativity in mice?
Umbricht, D., Vyssotki, D., Латанов, А. В., Nitsch, R. M., & Lipp, H. (2004) · Clinical Neurophysiology · doi:10.1016/j.clinph.2004.08.015 · Cited by 112
Self-citationWang, J. Q., Tang, Q., Parelkar, N. K., Liu, Z., Samdani, S., Choe, E. S., Yang, L., & Mao, L. (2004) · Molecular Neurobiology · doi:10.1385/mn:29:1:01 · Cited by 113
Shiflett, M. W., Brown, R. A., & Balleine, B. W. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1778-09.2010 · Cited by 119
NF-κB/Rel Regulates Inhibitory and Excitatory Neuronal Function and Synaptic Plasticity
O'Mahony, A., Raber, J., Montano, M., Foehr, E., Han, V., Lu, S.-M., Kwon, H., LeFevour, A., Chakraborty-Sett, S., & Greene, W. C. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00510-06 · Cited by 110
Shimizu, K., Phan, T., Mansuy, I. M., & Storm, D. R. (2007) · Cell · doi:10.1016/j.cell.2006.12.047 · Cited by 112
Frémin, C., Ezan, F., Boisselier, P., Bessard, A., Pagès, G., Pouysségur, J., & Baffet, G. (2007) · Hepatology · doi:10.1002/hep.21551 · Cited by 99
Self-citationThe vestibular–basal ganglia connection: Balancing motor control
Stiles, L., & Smith, P. F. (2014) · Brain Research · doi:10.1016/j.brainres.2014.11.063 · Cited by 108
Molecular substrates of action control in cortico-striatal circuits
Shiflett, M. W., & Balleine, B. W. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.05.007 · Cited by 120
Fasano, S., D'Antoni, A., Orban, P. C., Valjent, E., Putignano, E., Vara, H., Pizzorusso, T., Giustetto, M., Yoon, B.-J., Soloway, P. D., et al. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.03.014 · Cited by 107
Self-citation
Metadata
- Authors
- Mazzucchelli, C., Vantaggiato, C., Ciamei, A., Fasano, S., Pakhotin, P., Krezel, W., Welzl, H., Wolfer, D. P., Pagès, G., Valverde, O., Marowsky, A., Porrazzo, A., Orban, P. C., Maldonado, R., Ehrengruber, M. U., Cestari, V., Lipp, H.-P., Chapman, P. F., Pouysségur, J., & Brambilla, R.
- Affiliations
- National Research Council (IT)
- Cardiff University (GB)
- University of Zurich (CH)
- Centre National de la Recherche Scientifique (FR)
- Universitat Pompeu Fabra (ES)
- Corresponding author
- Brambilla, Riccardo
- ORCID
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2002-05
- Volume
- 34
- Issue
- 5
- Pages
- 807-820
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W1967318257
- Cited by
- 456
- References
- 41
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 4 · 2023: 3 · 2022: 8 · 2021: 8 · 2020: 11 · 2019: 14 · 2018: 17 · 2017: 15 · 2016: 22 · 2015: 18 · 2014: 23 · 2013: 20 · 2012: 31
- FWCI
- 9.18
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 4095 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- ERK1, ERK2, MEK, MAPK signaling, striatum, synaptic plasticity, long-term potentiation, nucleus accumbens, learning and memory, morphine reward, drug addiction, behavioral plasticity, knockout mice
- MeSH terms
- Amygdala, Animals, Avoidance Learning, Behavior, Animal, Cognition Disorders, Corpus Striatum, Female, Hippocampus, Male, Memory, Morphine, Motor Activity, Mutation, Nerve Net, Nervous System Malformations, Synaptic Transmission, Nucleus Accumbens, Up-Regulation, Presynaptic Terminals, Long-Term Potentiation, Mice, Knockout, Mitogen-Activated Protein Kinase 1, Mitogen-Activated Protein Kinases, MAP Kinase Kinase Kinases, Mitogen-Activated Protein Kinase 3, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review