N-methyl-D-aspartate receptor-dependent plasticity within a distributed corticostriatal network mediates appetitive instrumental learning.

The amygdala: vigilance and emotion

Davis, M., & Whalen, P. J. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000812 · Cited by 2,882 · see citing works

Addiction motivation reformulated: an affective processing model of negative reinforcement

Baker, T. B., Piper, M. E., McCarthy, D. E., Majeskie, M. R., & Fiore, M. C. (2004) · Psychological Review · doi:10.1037/0033-295x.111.1.33 · Cited by 2,162 · see citing works

Ventral striatal control of appetitive motivation: role in ingestive behavior and reward-related learning

Kelley, A. E. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2003.11.015 · Cited by 942 · see citing works

The neuropsychological basis of addictive behaviour

Everitt, B. J., Dickinson, A., & Robbins, T. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00088-1 · Cited by 808 · see citing works

Multiple neural systems controlling food intake and body weight

Berthoud, H.-R. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00014-3 · Cited by 725 · see citing works

Parallel and interactive learning processes within the basal ganglia: relevance for the understanding of addiction

Belin, D., Jonkman, S., Dickinson, A., Robbins, T. W., & Everitt, B. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.027 · Cited by 520 · see citing works

The role of prelimbic cortex in instrumental conditioning

Corbit, L. H., & Balleine, B. W. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.023 · Cited by 423 · see citing works

Selective inactivation of the dorsomedial prefrontal cortex and the basolateral amygdala attenuates conditioned-cued reinstatement of extinguished cocaine-seeking behavior in rats

McLaughlin, J., & See, R. E. (2002) · Psychopharmacology · doi:10.1007/s00213-002-1196-x · Cited by 392 · see citing works

The effect of lesions of the basolateral amygdala on instrumental conditioning

Balleine, B. W., Killcross, A. S., & Dickinson, A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00666.2003 · Cited by 355 · see citing works

Coincident Activation of NMDA and Dopamine D1Receptors within the Nucleus Accumbens Core Is Required for Appetitive Instrumental Learning

Smith‐Roe, S. L., & Kelley, A. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-20-07737.2000 · Cited by 321 · see citing works

Discrete neurochemical coding of distinguishable motivational processes: insights from nucleus accumbens control of feeding

Baldo, B. A., & Kelley, A. E. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0741-z · Cited by 312 · see citing works

Optical activation of lateral amygdala pyramidal cells instructs associative fear learning

Johansen, J. P., Hamanaka, H., Monfils, M. H., Behnia, R., Deisseroth, K., Blair, H. T., & LeDoux, J. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002418107 · Cited by 308 · see citing works

Functional Interaction Between NMDA and mGlu5 Receptors: Effects on Working Memory, Instrumental Learning, Motor Behaviors, and Dopamine Release

Homayoun, H., Stefani, M. R., Adams, B. W., Tamagan, G. D., & Moghaddam, B. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300417 · Cited by 252 · see citing works

Rapid strengthening of thalamo-amygdala synapses mediates cue–reward learning

Tye, K. M., Stuber, G. D., de Ridder, B., Bonci, A., & Janak, P. H. (2008) · Nature · doi:10.1038/nature06963 · Cited by 216 · see citing works

Interactions of the basolateral amygdala with the dorsal hippocampus and dorsomedial prefrontal cortex regulate drug context‐induced reinstatement of cocaine‐seeking in rats

Fuchs, R. A., Eaddy, J. L., Su, Z., & Bell, G. H. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05674.x · Cited by 212 · see citing works

Modulation of Long-Term Depression by Dopamine in the Mesolimbic System

Thomas, M. J., Malenka, R. C., & Bonci, A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-15-05581.2000 · Cited by 212 · see citing works

Functional Specificity of Ventral Striatal Compartments in Appetitive Behaviors

KELLEY, A. E. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09262.x · Cited by 198 · see citing works

Neural integrative activities of nucleus accumbens subregions in relation to learning and motivation

Kelley, A. E. (1999) · Psychobiology · doi:10.3758/bf03332114 · Cited by 195 · see citing works

Appetitive Instrumental Learning Requires Coincident Activation of NMDA and Dopamine D1 Receptors within the Medial Prefrontal Cortex

Baldwin, A. E., Sadeghian, K., & Kelley, A. E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-03-01063.2002 · Cited by 191 · see citing works

Lesions of mediodorsal thalamus and anterior thalamic nuclei produce dissociable effects on instrumental conditioning in rats

Corbit, L. H., Muir, J. L., & Balleine, B. W. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02833.x · Cited by 186 · see citing works

Early consolidation of instrumental learning requires protein synthesis in the nucleus accumbens

Hernandez, P. J., Sadeghian, K., & Kelley, A. E. (2002) · Nature Neuroscience · doi:10.1038/nn973 · Cited by 186 · see citing works

NMDA receptors, cognition and schizophrenia – Testing the validity of the NMDA receptor hypofunction hypothesis

Gilmour, G., Dix, S. L., Fellini, L., Gastambide, F., Plath, N., Steckler, T., Talpos, J. C., & Tricklebank, M. D. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.03.015 · Cited by 183 · see citing works

Using Pavlovian Higher-Order Conditioning Paradigms to Investigate the Neural Substrates of Emotional Learning and MemoryPreprint

Gewirtz, J. C., & Davis, M. E. (2000) · Learning & Memory · doi:10.1101/lm.35200 · Cited by 168 · see citing works

The Amygdala as a Neurobiological Target for Ghrelin in Rats: Neuroanatomical, Electrophysiological and Behavioral Evidence

Álvarez-Crespo, M., Skibicka, K. P., Farkas, I., Molnár, C. S., Egecioglu, E., Hrabovszky, E., Liposits, Z., & Dickson, S. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046321 · Cited by 166 · see citing works

Glutamate Receptor-Dependent Modulation of Dopamine Efflux in the Nucleus Accumbens by Basolateral, But Not Central, Nucleus of the Amygdala in Rats

Howland, J. G., Taepavarapruk, P., & Phillips, A. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-03-01137.2002 · Cited by 155 · see citing works

Dopamine D1and NMDA Receptors Mediate Potentiation of Basolateral Amygdala-Evoked Firing of Nucleus Accumbens Neurons

Floresco, S., Blaha, C. D., Yang, C. R., & Phillips, A. G. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06370.2001 · Cited by 142 · see citing works

Disconnection of the basolateral amygdala complex and nucleus accumbens impairs appetitive pavlovian second-order conditioned responses

Setlow, B., Holland, P. C., & Gallagher, M. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.2.267 · Cited by 160 · see citing works

Dissociable regulation of instrumental action within mouse prefrontal cortex

Gourley, S. L., Lee, A. S., Howell, J. L., Pittenger, C., & Taylor, J. R. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07438.x · Cited by 117 · see citing works

Long-term memory for instrumental responses does not undergo protein synthesis-dependent reconsolidation upon retrievalPreprint

Hernandez, P. J., & Kelley, A. E. (2004) · Learning & Memory · doi:10.1101/lm.84904 · Cited by 120 · see citing works

Systemic and Prefrontal Cortical NMDA Receptor Blockade Differentially Affect Discrimination Learning and Set-Shift Ability in Rats.

Stefani, M. R., & Moghaddam, B. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.2.420 · Cited by 106 · see citing works

Induction of the learning and plasticity‐associated gene Zif268 following exposure to a discrete cocaine‐associated stimulus

Thomas, K. L., Arroyo, M., & Everitt, B. J. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02617.x · Cited by 104 · see citing works

Psychostimulants and motivated behavior: Arousal and cognition

Berridge, C. W., & Arnsten, A. F. T. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.005 · Cited by 104 · see citing works

Dorsal striatum and stimulus–response learning: lesions of the dorsolateral, but not dorsomedial, striatum impair acquisition of a simple discrimination task

Featherstone, R. E., & McDonald, R. J. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00218-3 · Cited by 98 · see citing works

Appetitive Instrumental Learning Is Impaired by Inhibition of cAMP-Dependent Protein Kinase within the Nucleus Accumbens

Baldwin, A. E., Sadeghian, K., Holahan, M. R., & Kelley, A. E. (2002) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2000.4002 · Cited by 98 · see citing works

Selective responding of nucleus accumbens core and shell dopamine to aversively conditioned contextual and discrete stimuli

Pezze, M. A., Heidbreder, C. A., Feldon, J., & Murphy, C. A. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00403-1 · Cited by 96 · see citing works

Learning-related changes in response patterns of prefrontal neurons during instrumental conditioning.

Mulder, A. B., Nordquist, R. E., Örgüt, O., & Pennartz, C. M. A. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.016 · Cited by 84 · see citing works

Effects of nicotinic and NMDA receptor channel blockers on intravenous cocaine and nicotine self-administration in mice

Blokhina, E. A., Кашкин, В. А., Zvartau, E. E., Danysz, W., & Bespalov, A. (2004) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2004.07.005 · Cited by 85 · see citing works

The role of different subregions of the basolateral amygdala in cue-induced reinstatement and extinction of food-seeking behavior

McLaughlin, R. J., & Floresco, S. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.03.025 · Cited by 85 · see citing works

Developmental regulation of excitatory-inhibitory synaptic balance in the prefrontal cortex during adolescence

Caballero, A., Orozco, A., & Tseng, K. Y. (2021) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2021.02.008 · Cited by 83 · see citing works

Increased Expression of 5-HT6 Receptors in the Rat Dorsomedial Striatum Impairs Instrumental Learning

Mitchell, E. S., Sexton, T. J., & Neumaier, J. F. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301284 · Cited by 76 · see citing works

Involvement of Amygdala Dopamine and Nucleus Accumbens NMDA Receptors in Ethanol-Seeking Behavior in Mice

Gremel, C. M., & Cunningham, C. L. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.179 · Cited by 76 · see citing works

Glutamate‐Mediated Plasticity in Corticostriatal Networks

Kelley, A. E., Andrzejewski, M. E., Baldwin, A. E., Hernandez, P. J., & Pratt, W. E. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.061 · Cited by 77 · see citing works

The NMDA-receptor antagonist MK-801 selectively disrupts reversal learning in rats

van der Meulen, J. A. J., Bilbija, L., Joosten, R. N. J. M. A., de Bruin, J. P. C., & Feenstra, M. G. P. (2003) · Neuroreport · doi:10.1097/00001756-200312020-00018 · Cited by 65 · see citing works

5-hydroxytryptamine 2C receptors in the dorsal striatum mediate stress-induced interference with negatively reinforced instrumental escape behavior

Strong, P. V., Christianson, J. P., Loughridge, A. B., Amat, J., Maier, S. F., Fleshner, M., & Greenwood, B. N. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.09.041 · Cited by 61 · see citing works

A within-subject cognitive battery in the rat: differential effects of NMDA receptor antagonists

Dix, S. L., Gilmour, G., Potts, S., Smith, J. W., & Tricklebank, M. D. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1945-1 · Cited by 61 · see citing works

Instrumental learning, but not performance, requires dopamine D1-receptor activation in the amygdala

Andrzejewski, M. E., Spencer, R. C., & Kelley, A. E. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.06.038 · Cited by 59 · see citing works

Parabrachial nucleus lesions block taste and attenuate flavor preference and aversion conditioning in rats.

Sclafani, A. J., Azzara, A. V., Touzani, K., Grigson, P. S., & Norgren, R. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.4.920 · Cited by 60 · see citing works

Dopamine D1‐like receptor antagonism in amygdala impairs the acquisition of glucose‐conditioned flavor preference in rats

Touzani, K., Bodnar, R. J., & Sclafani, A. J. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06829.x · Cited by 53 · see citing works

Amygdalostriatal projections in the neurocircuitry for motivation: a neuroanatomical thread through the career of Ann Kelley

Zorrilla, E. P., & Koob, G. F. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.019 · Cited by 57 · see citing works

Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions

Smith, A. C. W., Jonkman, S., DiFeliceantonio, A. G., O’Connor, R. M., Ghoshal, S., Romano, M. F., Everitt, B. J., & Kenny, P. J. (2021) · Nature Communications · doi:10.1038/s41467-021-25460-3 · Cited by 44 · see citing works

GABA-Mediated Inactivation of Medial Prefrontal and Agranular Insular Cortex in the Rat: Contrasting Effects on Hunger- and Palatability-Driven Feeding

Baldo, B. A., Spencer, R. C., Sadeghian, K., & Mena, J. D. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.222 · Cited by 46 · see citing works

Differential representation of Pavlovian–instrumental transfer by prefrontal cortex subregions and striatum

Homayoun, H., & Moghaddam, B. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06679.x · Cited by 45 · see citing works

INVOLVEMENT OF NMDA RECEPTORS IN MORPHINE STATE–DEPENDENT LEARNING IN MICE

Zarrindast, M., Jafari‐Sabet, M., Rezayat, S. M., et al. (2006) · International Journal of Neuroscience · doi:10.1080/00207450600675068 · Cited by 44 · see citing works

Facilitation of appetitive Pavlovian conditioning by d-amphetamine in the shell, but not the core, of the nucleus accumbens.

Phillips, G. D., Setzu, E., & Hitchcott, P. K. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.4.675 · Cited by 43 · see citing works

Functional interaction between the basolateral amygdala and the nucleus accumbens underlies incentive motivation for food reward on a fixed ratio schedule

Simmons, D. A., & Neill, D. B. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.01.026 · Cited by 47 · see citing works

Central amygdalar and dorsal striatal NMDA receptor involvement in instrumental learning and spontaneous behavior.

Andrzejewski, M. E., Sadeghian, K., & Kelley, A. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.4.715 · Cited by 36 · see citing works

Individual differences in dopamine efflux in nucleus accumbens shell and core during instrumental learningPreprint

Cheng, J., & Feenstra, M. G. P. (2006) · Learning & Memory · doi:10.1101/lm.1806 · Cited by 34 · see citing works

Heterogeneity of Reward Mechanisms

Lajtha, Á., & Sershen, H. W. (2009) · Neurochemical Research · doi:10.1007/s11064-009-0096-4 · Cited by 32 · see citing works

NMDA Receptors Control Cue-Outcome Selectivity and Plasticity of Orbitofrontal Firing Patterns during Associative Stimulus-Reward Learning

van Wingerden, M., Vinck, M. A., Tijms, V., Ferreira, I. R. S., Jonker, A. J., & Pennartz, C. M. A. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.039 · Cited by 31 · see citing works

Neuronal connections of the central amygdalar nucleus with refeeding-activated brain areas in rats

Zséli, G., Vida, B., Szilvásy‐Szabó, A., Tóth, M., Lechan, R. M., & Fekete, C. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1501-4 · Cited by 30 · see citing works

Ghrelin-containing neurons in the olfactory bulb send collateralized projections into medial amygdaloid and arcuate hypothalamic nuclei: neuroanatomical study

Russo, C., Russo, A., Pellitteri, R., & Stanzani, S. (2018) · Experimental Brain Research · doi:10.1007/s00221-018-5298-z · Cited by 24 · see citing works

Dissociating ventral and dorsal subicular dopamine D₁ receptor involvement in instrumental learning, spontaneous motor behavior, and motivation.

Andrzejewski, M. E., Spencer, R. C., & Kelley, A. E. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.3.542 · Cited by 24 · see citing works

External incentives and internal states guide goal-directed behavior via the differential recruitment of the nucleus accumbens and the medial prefrontal cortex

Moscarello, J. M., Ben‐Shahar, O., & Ettenberg, A. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.07.002 · Cited by 21 · see citing works

Neuroadaptive changes in the mesocortical glutamatergic system during chronic nicotine self‐administration and after extinction in rats

Wang, F., Chen, H., & Sharp, B. M. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05456.x · Cited by 21 · see citing works

Glucose-conditioned flavor preference learning requires co-activation of NMDA and dopamine D1-like receptors within the amygdala

Touzani, K., Bodnar, R. J., & Sclafani, A. J. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.07.016 · Cited by 20 · see citing works

Maintenance in working memory or response selection?

Lissek, S., & Güntürkün, O. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.01.007 · Cited by 20 · see citing works

Distinct recruitment of basolateral amygdala-medial prefrontal cortex pathways across Pavlovian appetitive conditioning

Keefer, S. E., & Petrovich, G. D. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.03.006 · Cited by 19 · see citing works

NMDA receptors in the avian amygdala and the premotor arcopallium mediate distinct aspects of appetitive extinction learning

Gao, M., Lengersdorf, D., Stüttgen, M. C., & Güntürkün, O. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.01.026 · Cited by 16 · see citing works

Differential effects of calcineurin inhibition and protein kinase A activation on nucleus accumbens amphetamine‐produced conditioned place preference in rats

Gerdjikov, T. V., & Beninger, R. J. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04256.x · Cited by 19 · see citing works

Dopamine-Glutamate Interactions in Reward-Related Incentive Learning

Beninger, R. J., & Gerdjikov, T. V. (2005) · Humana Press eBooks · doi:10.1007/978-1-59259-852-6_14 · Cited by 17 · see citing works

Ventral tegmental area-basolateral amygdala-nucleus accumbens shell neurocircuitry controls the expression of heroin-conditioned immunomodulation

Szczytkowski, J. L., Fuchs, R. A., & Lysle, D. T. (2011) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2011.06.002 · Cited by 17 · see citing works

Effects of disconnection of amygdala dopamine and nucleus accumbens N‐methyl‐ d ‐aspartate receptors on ethanol‐seeking behavior in mice

Gremel, C. M., & Cunningham, C. L. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07044.x · Cited by 17 · see citing works

Dopamine Preferentially Inhibits NMDA Receptor-Mediated EPSCs by Acting on Presynaptic D1 Receptors in Nucleus Accumbens during Postnatal Development

Zhang, L., Bose, P., & Warren, R. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086970 · Cited by 16 · see citing works

Local N-Methyl-D-Aspartate Receptor Antagonism in the Prefrontal Cortex Attenuates Spatial Cognitive Deficits Induced by Gonadectomy in Adult Male Rats

Locklear, M., Bhamidipaty, S., & Kritzer, M. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.12.032 · Cited by 16 · see citing works

A Proteomics Approach to Identify Long-Term Molecular Changes in Rat Medial Prefrontal Cortex Resulting from Sucrose Self-Administration

van den Oever, M. C., Spijker, S., Li, K. W., et al. (2005) · Journal of Proteome Research · doi:10.1021/pr050303y · Cited by 15 · see citing works

Orexin decreases mRNA expressions of NMDA and AMPA receptor subunits in rat primary neuron cultures

Yamada, N., Katsuura, G., Tatsuno, I., Asaki, T., Kawahara, S., Ebihara, K., Saitō, Y., & Nakao, K. (2008) · Peptides · doi:10.1016/j.peptides.2008.05.002 · Cited by 14 · see citing works

C-fos activation patterns in rat prefrontal cortex during acquisition of a cued classical conditioning task.

Nordquist, R., Pennartz, C., Uylings, H., Joosten, R., Jonker, A., Groenewegen, H., & Voorn, P. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.014 · Cited by 17 · see citing works

The clinical relevance of neuroplasticity in corticostriatal networks during operant learning

Andrzejewski, M. E., McKee, B. L., Baldwin, A. E., Burns, L. H., & Hernandez, P. J. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.03.019 · Cited by 13 · see citing works

Amygdalar glutamatergic neuronal systems play a key role on the hibernating state of hamsters

Alò, R., Avolio, E., Carelli, A., Facciolo, R. M., & Canonaco, M. (2011) · BMC Neuroscience · doi:10.1186/1471-2202-12-10 · Cited by 12 · see citing works

Role of CA1 GABAA and GABAB receptors on learning deficit induced by D-AP5 in passive avoidance step-through task

Ebrahimi-Ghiri, M., Rostampour, M., Jamshidi-Mehr, M., Nasehi, M., & Zarrindast, M. (2017) · Brain Research · doi:10.1016/j.brainres.2017.10.004 · Cited by 12 · see citing works

Identifying non-toxic doses of manganese for manganese-enhanced magnetic resonance imaging to map brain areas activated by operant behavior in trained rats

Gálosi, R., Szalay, C., Aradi, M., Perlaki, G., Pál, J., Steier, R., Lénárd, L., & Karádi, Z. (2016) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2016.11.017 · Cited by 11 · see citing works

The subiculum role on learning and memory tasks using rats and mice: A scoping review

de Melo, M. B., Daldegan‐Bueno, D., Favaro, V. M., & Oliveira, M. G. M. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105460 · Cited by 9 · see citing works

Acquisition and expression of fat-conditioned flavor preferences are differentially affected by NMDA receptor antagonism in BALB/c and SWR mice

Kraft, T. T., Huang, D., LaMagna, S., Warshaw, D., Natanova, E., Sclafani, A. J., & Bodnar, R. J. (2017) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2017.01.034 · Cited by 10 · see citing works

The Role of NMDA Receptors in Human Eating Behavior

Perogamvros, L., Schnider, A., & Leemann, B. (2012) · Cognitive and Behavioral Neurology · doi:10.1097/wnn.0b013e31825921a6 · Cited by 9 · see citing works

Scientific and conceptual flaws of coercive treatment models in addiction

Uusitalo, S., & van der Eijk, Y. (2015) · Journal of Medical Ethics · doi:10.1136/medethics-2015-102910 · Cited by 8 · see citing works

Dissociable hippocampal and amygdalar D1-like receptor contribution to discriminated Pavlovian conditioned approach learning

Andrzejewski, M. E., & Ryals, C. D. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.11.034 · Cited by 6 · see citing works

Case for raising the minimum legal age of tobacco sale to 25

van der Eijk, Y., & Chen, J. I. (2021) · Tobacco Control · doi:10.1136/tobaccocontrol-2020-055964 · Cited by 6 · see citing works

Activation of the basolateral or the central amygdala dampened the incentive motivation for food reward on high fixed-ratio schedules

Shih, C.-C., & Chang, C. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114682 · Cited by 4 · see citing works

Removal of reinforcement improves instrumental performance in humans by decreasing a general action bias rather than unmasking learnt associations

Kurtenbach, H., Ort, E., Froböse, M. I., & Jocham, G. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010201 · Cited by 3 · see citing works

The Contribution of the Amygdala to Reward-Related Learning and Extinction

Chesworth, R., & Corbit, L. H. (2017) · InTech eBooks · doi:10.5772/67831 · Cited by 4 · see citing works

Differential effects of clozapine, metoclopramide, haloperidol and risperidone on acquisition and performance of operant responding in rats

Baker, T. W., Florczynski, M. M., & Beninger, R. J. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3789-6 · Cited by 4 · see citing works

An aversive diet as thiamine‐free food blocks food‐induced release of excitatory amino acids in the accumbens

Monda, M., Viggiano, A., & Luca, V. D. (2003) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2003.01136.x · Cited by 2 · see citing works

Strategy Switching and the Rat Prefrontal Cortex

Feenstra, M. G. P., & de Bruin, J. P. C. (2004) · Springer eBooks · doi:10.1007/1-4020-7949-4_8 · Cited by 1 · see citing works

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

Alcohol and Cannabinoid Binges and Daily Exposure to Nicotine in Adolescent/Young Adult Rats induce Sex-Dependent Long-Term Learning and Motivation AlterationsPreprint

Abela, N., Haywood, K., & Giovanni, G. D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.20.521255

Ventral Hippocampus and NAc Core, but not Shell activity is required for well-learned instrumental memory destabilizationPreprint

Lima, R. H., Cheng, C., & Lee, J. L. C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.21.654887

Ventral hippocampus and NAc core, but not shell activity is required for well-learned instrumental memory destabilisation

Lima, R. H., Cheng, C., & Lee, J. L. C. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115868

AMPA receptor activation in dorsal medial prefrontal cortex–to–nucleus accumbens neurons regulates the expression of conditioned approach

Nisanov, R., Patel, N., Persaud, K., Chowdhury, S., Safier, G., & Ranaldi, R. (2026) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2026.178823

DETERMINING QUALITY REQUIREMENTS AT THE UNIVERSITIES TO IMPROVE THE QUALITY OF EDUCATION

Mustafa, N. H., Kelesbayev, D., & Alibekova, Z. D. (2018) · The Journal of Economic Research & Business Administration · doi:10.26577/be-2018-2-2141

Susquehanna Chorale Spring Concert "Roots and Wings"

Hawkins, D. (2017)

A NEUROPLASTICITY AND FUNCTIONAL RESTORATION AFTER STROKE

Кадыков, А. С., Шахпаронова, Н. В., Belopasova, A. V., et al. (2019) · Physical and rehabilitation medicine medical rehabilitation · doi:10.36425/2658-6843-19184 · Cited by 6 · see citing works

A NEUROPLASTICITY AND FUNCTIONAL RESTORATION AFTER STROKE

(2019) · Physical and rehabilitation medicine medical rehabilitation · doi:10.36425/2658-6843-2019-2-32-36 · Cited by 1 · see citing works

Personality correlates and utilitarian judgments in the everyday context: Psychopathic traits and differential effects of empathy, social dominance orientation, and dehumanization beliefs

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