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Critical Reviews™ in Neurobiology

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ISSN Печать: 0892-0915

ISSN Онлайн: 2375-0014

SJR: 0.121

The Frontal Cortex-Basal Ganglia System in Primates

Том 10, Выпуск 3-4, 1996, pp. 317-356
DOI: 10.1615/CritRevNeurobiol.v10.i3-4.30
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Краткое описание

The primate basal ganglia receives information from most of the cerebrum, including the frontal cortex, but projects (via the dorsal thalamus) primarily to the frontal lobe, perhaps in its entirety. As such, the frontal cortex and basal ganglia constitute an integrated, distributed neuronal architecture. We review evidence that the frontal lobe and basal ganglia specialize in different, but related, aspects of response learning. Frontal cortex acts when new rules need to be learned and older ones rejected, whereas the basal ganglia potentiate previously learned rules based on environmental context and reinforcement history. Such potentiation increases the probability that the central nervous system will select a particular rule to guide behavior.
We outline a possible mechanism for the basal ganglia's proposed role in rule potentiation, one that involves both the direct and indirect striatal output pathways and their dopaminergic input. It has previously been proposed that direct-pathway neurons recognize a pattern of corticostriatal inputs, which promotes activity in recurrent, positive-feedback modules (or loops) of which they are an integral part. We propose that this recurrent activity potentiates a rule associated with those modules. If so, then the dopaminergic system is well situated and organized to modulate rule potentiation in both the short and long term. Dopaminergic neurons of the midbrain increase activity during learning and other periods of relatively unpredictable reinforcement. Dopamine enhances gene expression and other forms of activity in striatal neurons of the direct pathway, while suppressing neurons of the indirect pathway. In the short term, then, dopamine may augment the activity of modules triggered by a recognized context, whereas in the long term it may promote context-dependent activation of the same modules. Together, these modulatory influences could support both rule potentiation and learning the context for potentiating that rule.

Ключевые слова: striatum, pallidum, prefrontal, premotor, dopamine
ЦИТИРОВАНО В
  1. Groenewegen Henk, Uylings Harry, Het enigma van de nucleus subthalamicus: implicaties voor neurologische en psychiatrische ziektebeelden, Neuropraxis, 14, 6, 2010. Crossref

  2. Schneider Mary L., Moore Colleen F., Kraemer Gary W., Moderate Alcohol During Pregnancy: Learning and Behavior in Adolescent Rhesus Monkeys, Alcoholism: Clinical and Experimental Research, 25, 9, 2001. Crossref

  3. Mian M. K., Sheth S. A., Patel S. R., Spiliopoulos K., Eskandar E. N., Williams Z. M., Encoding of Rules by Neurons in the Human Dorsolateral Prefrontal Cortex, Cerebral Cortex, 24, 3, 2014. Crossref

  4. Burkett James P., Young Larry J., The behavioral, anatomical and pharmacological parallels between social attachment, love and addiction, Psychopharmacology, 224, 1, 2012. Crossref

  5. UYS JOACHIM D. K., NIESINK RAYMOND J. M., Pharmacological aspects of the combined use of 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) and gamma-hydroxybutyric acid (GHB): a review of the literature, Drug and Alcohol Review, 24, 4, 2005. Crossref

  6. HABER SUZANNE N., GDOWSKI MARTHA JOHNSON, The Basal Ganglia, in The Human Nervous System, 2004. Crossref

  7. Nitschke Jack B., Mackiewicz Kristen L., Prefrontal and Anterior Cingulate Contributions to Volition in Depression, in Neuroimaging, Part B, 67, 2005. Crossref

  8. Kelley Ann E., Baldo Brian A., Pratt Wayne E., A proposed hypothalamic-thalamic-striatal axis for the integration of energy balance, arousal, and food reward, The Journal of Comparative Neurology, 493, 1, 2005. Crossref

  9. Glimcher Paul W, Lau Brian, Rethinking the thalamus, Nature Neuroscience, 8, 8, 2005. Crossref

  10. Marshall D. F., Strutt A. M., Williams A. E., Simpson R. K., Jankovic J., York M. K., Alternating verbal fluency performance following bilateral subthalamic nucleus deep brain stimulation for Parkinson's disease, European Journal of Neurology, 19, 12, 2012. Crossref

  11. Meck W.H., N'Diaye K., Un modèle neurobiologique de la perception et de l'estimation du temps, Psychologie Française, 50, 1, 2005. Crossref

  12. Cohen M. Michael, Perspectives on asymmetry: The erickson lecture, American Journal of Medical Genetics Part A, 158A, 12, 2012. Crossref

  13. Murray G.K., Veijola J., Moilanen K., Miettunen J., Glahn D.C., Cannon T.D., Jones P.B., Isohanni M., Infant motor development is associated with adult cognitive categorisation in a longitudinal birth cohort study, Journal of Child Psychology and Psychiatry, 47, 1, 2006. Crossref

  14. MINAMI Tetsuto, INUI Toshio, A NEURAL ARCHITECTURE FOR RULE-GUIDED BEHAVIOR: A SIMULATION OF PHYSIOLOGICAL EXPERIMENTS, PSYCHOLOGIA, 46, 4, 2003. Crossref

  15. Tseng Po-He, Cameron Ian G. M., Pari Giovanna, Reynolds James N., Munoz Douglas P., Itti Laurent, High-throughput classification of clinical populations from natural viewing eye movements, Journal of Neurology, 260, 1, 2013. Crossref

  16. Chesselet Marie-Francoise, Mapping the Basal Ganglia, in Brain Mapping: The Systems, 2000. Crossref

  17. Haber Suzanne N., Adler Avital, Bergman Hagai, The Basal Ganglia, in The Human Nervous System, 2012. Crossref

  18. Nauczyciel C., Drapier D., Stimulation magnétique transcrânienne répétée dans le traitement du trouble obsessionnel compulsif résistant, Revue Neurologique, 168, 8-9, 2012. Crossref

  19. Groenewegen Henk J., Uylings Harry B.M., The prefrontal cortex and the integration of sensory, limbic and autonomic information, in Cognition, emotion and autonomic responses: The integrative role of the prefrontal cortex and limbic structures, 126, 2000. Crossref

  20. Baker Phillip M., Thompson Jennifer L., Sweeney John A., Ragozzino Michael E., Differential effects of 5-HT2A and 5-HT2C receptor blockade on strategy-switching, Behavioural Brain Research, 219, 1, 2011. Crossref

  21. Anderson John R., Human Symbol Manipulation Within an Integrated Cognitive Architecture, Cognitive Science, 29, 3, 2005. Crossref

  22. Bussey Timothy J., Wise Steven P., Murray Elisabeth A., Interaction of ventral and orbital prefrontal cortex with inferotemporal cortex in conditional visuomotor learning., Behavioral Neuroscience, 116, 4, 2002. Crossref

  23. McDonald R. J., Foong N., Ray C., Rizos Z., Hong N. S., The role of medial prefrontal cortex in context-specific inhibition during reversal learning of a visual discrimination, Experimental Brain Research, 177, 4, 2007. Crossref

  24. Nicola Saleem M., The nucleus accumbens as part of a basal ganglia action selection circuit, Psychopharmacology, 191, 3, 2007. Crossref

  25. Yeshenko Oxana, Guazzelli Alex, Mizumori Sheri J. Y., Context-Dependent Reorganization of Spatial and Movement Representations by Simultaneously Recorded Hippocampal and Striatal Neurons During Performance of Allocentric and Egocentric Tasks., Behavioral Neuroscience, 118, 4, 2004. Crossref

  26. Brasted Peter, Wise Steven, The Arbitrary Mapping of Sensory Inputs to Voluntary and Involuntary Movement, in Motor Cortex in Voluntary Movements, 20044553, 2004. Crossref

  27. Shohamy D., Myers C. E., Onlaor S., Gluck M. A., Role of the Basal Ganglia in Category Learning: How Do Patients With Parkinson's Disease Learn?, Behavioral Neuroscience, 118, 4, 2004. Crossref

  28. Graham Kim S., Lee Andy C.H., Barense Morgan D., Chapter 5.1 Memory and perceptual impairments in amnesia and dementia, in Handbook of Episodic Memory, 18, 2008. Crossref

  29. Wallis J. D., Dias R., Robbins T. W., Roberts A. C., Dissociable contributions of the orbitofrontal and lateral prefrontal cortex of the marmoset to performance on a detour reaching task, European Journal of Neuroscience, 13, 9, 2001. Crossref

  30. Takada M., Tokuno H., Hamada I., Inase M., Ito Y., Imanishi M., Hasegawa N., Akazawa T., Hatanaka N., Nambu A., Organization of inputs from cingulate motor areas to basal ganglia in macaque monkey, European Journal of Neuroscience, 14, 10, 2001. Crossref

  31. Cain Christopher K., LeDoux Joseph E., Chapter 3.1 Brain mechanisms of Pavlovian and instrumental aversive conditioning, in Handbook of Anxiety and Fear, 17, 2008. Crossref

  32. Hatanaka Nobuhiko, Tokuno Hironobu, Hamada Ikuma, Inase Masahiko, Ito Yumi, Imanishi Michiko, Hasegawa Naomi, Akazawa Toshikazu, Nambu Atsushi, Takada Masahiko, Thalamocortical and intracortical connections of monkey cingulate motor areas, The Journal of Comparative Neurology, 462, 1, 2003. Crossref

  33. Van Dyke Julie A., The role of memory in language and communication, in Cognition and Acquired Language Disorders, 2012. Crossref

  34. Cabrera Sara M., Chavez Candice M., Corley Sean R., Kitto Michael R., Butt Allen E., Selective lesions of the nucleus basalis magnocellularis impair cognitive flexibility., Behavioral Neuroscience, 120, 2, 2006. Crossref

  35. Petanjek Z., Judas M., Kostovic I., Uylings H. B. M., Lifespan Alterations of Basal Dendritic Trees of Pyramidal Neurons in the Human Prefrontal Cortex: A Layer-Specific Pattern, Cerebral Cortex, 18, 4, 2008. Crossref

  36. Rinaldi Arianna, Mandillo Silvia, Oliverio Alberto, Mele Andrea, D1 and D2 Receptor Antagonist Injections in the Prefrontal Cortex Selectively Impair Spatial Learning in Mice, Neuropsychopharmacology, 32, 2, 2007. Crossref

  37. Ragozzino Michael E., Kim Jenna, Hassert Derrick, Minniti Nancy, Kiang Charlene, The contribution of the rat prelimbic-infralimbic areas to different forms of task switching., Behavioral Neuroscience, 117, 5, 2003. Crossref

  38. Wallis Jonathan D., Anderson Kathleen C., Miller Earl K., Single neurons in prefrontal cortex encode abstract rules, Nature, 411, 6840, 2001. Crossref

  39. Tsujimoto Satoshi, Genovesio Aldo, Wise Steven P., Transient Neuronal Correlations Underlying Goal Selection and Maintenance in Prefrontal Cortex, Cerebral Cortex, 18, 12, 2008. Crossref

  40. Collins P., Wilkinson L. S., Everitt B. J., Robbins T. W., Roberts A. C., The effect of dopamine depletion from the caudate nucleus of the common marmoset (Callithrix jacchus) on tests of prefrontal cognitive function., Behavioral Neuroscience, 114, 1, 2000. Crossref

  41. Anderson John R., Bothell Daniel, Byrne Michael D., Douglass Scott, Lebiere Christian, Qin Yulin, An Integrated Theory of the Mind., Psychological Review, 111, 4, 2004. Crossref

  42. Redgrave Peter, Gurney Kevin, The short-latency dopamine signal: a role in discovering novel actions?, Nature Reviews Neuroscience, 7, 12, 2006. Crossref

  43. Haber Suzanne N., Integrative Networks Across Basal Ganglia Circuits, in Handbook of Basal Ganglia Structure and Function, 20, 2010. Crossref

  44. Cragg Stephanie J., Baufreton Jerome, Xue Yi, Bolam J. Paul, Bevan Mark D., Synaptic release of dopamine in the subthalamic nucleus, European Journal of Neuroscience, 20, 7, 2004. Crossref

  45. Holroyd Clay B., Yeung Nick, Coles Michael G. H., Cohen Jonathan D., A Mechanism for Error Detection in Speeded Response Time Tasks., Journal of Experimental Psychology: General, 134, 2, 2005. Crossref

  46. DelParigi A, Chen K, Salbe A D, Hill J O, Wing R R, Reiman E M, Tataranni P A, Successful dieters have increased neural activity in cortical areas involved in the control of behavior, International Journal of Obesity, 31, 3, 2007. Crossref

  47. Miller Earl K., Wallis Jonathan D., The Prefrontal Cortex and Executive Brain Functions, in Fundamental Neuroscience, 2013. Crossref

  48. Groenewegen Henk J., Uylings Harry B.M., Organization of Prefrontal-Striatal Connections, in Handbook of Basal Ganglia Structure and Function, 20, 2010. Crossref

  49. Lebedev Mikhail A, Messinger Adam, Kralik Jerald D, Wise Steven P, Wolfram Schultz , Representation of Attended Versus Remembered Locations in Prefrontal Cortex, PLoS Biology, 2, 11, 2004. Crossref

  50. Pasupathy Anitha, Miller Earl K., Different time courses of learning-related activity in the prefrontal cortex and striatum, Nature, 433, 7028, 2005. Crossref

  51. Khan Zafar U., Muly E. Chris, Molecular mechanisms of working memory, Behavioural Brain Research, 219, 2, 2011. Crossref

  52. Ambesi-Impiombato Alberto, Panariello Fabio, Dell'aversano Carmela, Tomasetti Carmine, Muscettola Giovanni, de Bartolomeis Andrea, Differential expression ofHomer 1 gene by acute and chronic administration of antipsychotics and dopamine transporter inhibitors in the rat forebrain, Synapse, 61, 6, 2007. Crossref

  53. Graham Kim S., Barense Morgan D., Lee Andy C.H., Going beyond LTM in the MTL: A synthesis of neuropsychological and neuroimaging findings on the role of the medial temporal lobe in memory and perception, Neuropsychologia, 48, 4, 2010. Crossref

  54. Ragozzino Michael E., Ragozzino Katharine E., Mizumori Sheri J. Y., Kesner Raymond P., Role of the dorsomedial striatum in behavioral flexibility for response and visual cue discrimination learning., Behavioral Neuroscience, 116, 1, 2002. Crossref

  55. Erik Ween Jon, Functional Imaging of Stroke Recovery: An Ecological Review from a Neural Network Perspective with an Emphasis on Motor Systems, Journal of Neuroimaging, 18, 3, 2008. Crossref

  56. Epstein Russell A., Higgins J. Stephen, Thompson-Schill Sharon L., Learning Places from Views: Variation in Scene Processing as a Function of Experience and Navigational Ability, Journal of Cognitive Neuroscience, 17, 1, 2005. Crossref

  57. Bihel Ebeline, Pro-Sistiaga Palma, Letourneur Annelise, Toutain Jerome, Saulnier Romaric, Insausti Ricardo, Bernaudin Myriam, Roussel Simon, Touzani Omar, Permanent or Transient Chronic Ischemic Stroke in the Non-Human Primate: Behavioral, Neuroimaging, Histological, and Immunohistochemical Investigations, Journal of Cerebral Blood Flow & Metabolism, 30, 2, 2010. Crossref

  58. Yanike Marianna, Ferrera Vincent P, Interpretive monitoring in the caudate nucleus, eLife, 3, 2014. Crossref

  59. Praamstra P., Plat F. M., Failed Suppression of Direct Visuomotor Activation in Parkinson's Disease, Journal of Cognitive Neuroscience, 13, 1, 2001. Crossref

  60. Engin Elif, Bakhurin Konstantin I, Smith Kiersten S, Hines Rochelle M, Reynolds Lauren M, Tang Wannan, Sprengel Rolf, Moss Stephen J, Rudolph Uwe, Neural Basis of Benzodiazepine Reward: Requirement for α2 Containing GABAA Receptors in the Nucleus Accumbens, Neuropsychopharmacology, 39, 8, 2014. Crossref

  61. Devan Bryan D., Hong Nancy S., McDonald Robert J., Parallel associative processing in the dorsal striatum: Segregation of stimulus–response and cognitive control subregions, Neurobiology of Learning and Memory, 96, 2, 2011. Crossref

  62. Andrzejewski M.E., Spencer R.C., Kelley A.E., Instrumental learning, but not performance, requires dopamine D1-receptor activation in the amygdala, Neuroscience, 135, 2, 2005. Crossref

  63. Nieoullon André, Coquerel Antoine, Dopamine, Current Opinion in Neurology, 16, 2003. Crossref

  64. Hornak J., O'Doherty J., Bramham J., Rolls E. T., Morris R. G., Bullock P. R., Polkey C. E., Reward-related Reversal Learning after Surgical Excisions in Orbito-frontal or Dorsolateral Prefrontal Cortex in Humans, Journal of Cognitive Neuroscience, 16, 3, 2004. Crossref

  65. Wang Min, Zhang Hui, Li Bao-Ming, Deficit in conditional visuomotor learning by local infusion of bicuculline into the ventral prefrontal cortex in monkeys, European Journal of Neuroscience, 12, 10, 2000. Crossref

  66. Gabriele Amanda, See Ronald E., Reversible inactivation of the basolateral amygdala, but not the dorsolateral caudate putamen, attenuates consolidation of cocaine-cue associative learning in a reinstatement model of drug-seeking, European Journal of Neuroscience, 32, 6, 2010. Crossref

  67. Hans Miller William, The Symbolic Species: The Co-Evolution of Language and the Brain, Neuropsychoanalysis, 1, 1, 1999. Crossref

  68. Hélie Sébastien, Ell Shawn W., Ashby F. Gregory, Learning robust cortico-cortical associations with the basal ganglia: An integrative review, Cortex, 64, 2015. Crossref

  69. Kane Michael J., Engle Randall W., The role of prefrontal cortex in working-memory capacity, executive attention, and general fluid intelligence: An individual-differences perspective, Psychonomic Bulletin & Review, 9, 4, 2002. Crossref

  70. Mariano T. Y., Bannerman D. M., McHugh S. B., Preston T. J., Rudebeck P. H., Rudebeck S. R., Rawlins J. N. P., Walton M. E., Rushworth M. F. S., Baxter M. G., Campbell T. G., Impulsive choice in hippocampal but not orbitofrontal cortex-lesioned rats on a nonspatial decision-making maze task, European Journal of Neuroscience, 30, 3, 2009. Crossref

  71. Saint-Cyr Jean A., Neuropsychology for Movement Disorders Neurosurgery, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 30, S1, 2003. Crossref

  72. WICHMANN THOMAS, DeLONG MAHLON R., Pathophysiology of Parkinson's Disease: The MPTP Primate Model of the Human Disorder, Annals of the New York Academy of Sciences, 991, 1, 2006. Crossref

  73. Barter Joseph W., Castro Stephen, Sukharnikova Tatyana, Rossi Mark A., Yin Henry H., The role of the substantia nigra in posture control, European Journal of Neuroscience, 39, 9, 2014. Crossref

  74. Moody Sohie Lee, Wise Steven P., A Model that Accounts for Activity Prior to Sensory Inputs and Responses During Matching-to-Sample Tasks, Journal of Cognitive Neuroscience, 12, 3, 2000. Crossref

  75. Baxter Mark G., Gaffan David, Kyriazis Diana A., Mitchell Anna S., Ventrolateral prefrontal cortex is required for performance of a strategy implementation task but not reinforcer devaluation effects in rhesus monkeys, European Journal of Neuroscience, 29, 10, 2009. Crossref

  76. Hadj-Bouziane Fadila, Frankowska Hélène, Meunier Martine, Coquelin Pierre-Arnaud, Boussaoud Driss, Conditional visuo-motor learning and dimension reduction, Cognitive Processing, 7, 2, 2006. Crossref

  77. Van Golf Racht-Delatour B., Massioui N. El, Alleviation of overtraining reversal effect by transient inactivation of the dorsal striatum, European Journal of Neuroscience, 12, 9, 2000. Crossref

  78. Pell Marc D., Leonard Carol L., Processing emotional tone from speech in Parkinson’s disease: A role for the basal ganglia, Cognitive, Affective, & Behavioral Neuroscience, 3, 4, 2003. Crossref

  79. Ball Kevin T., Budreau Daniel, Rebec George V., Context-dependent behavioural and neuronal sensitization in striatum to MDMA (ecstasy) administration in rats, European Journal of Neuroscience, 24, 1, 2006. Crossref

  80. Narita Minoru, Matsushima Yuki, Niikura Keiichi, Narita Michiko, Takagi Shigemi, Nakahara Kae, Kurahashi Kana, Abe Minako, Saeki Mai, Asato Megumi, Imai Satoshi, Ikeda Kazutaka, Kuzumaki Naoko, Suzuki Tsutomu, Implication of dopaminergic projection from the ventral tegmental area to the anterior cingulate cortex in μ-opioid-induced place preference, Addiction Biology, 15, 4, 2010. Crossref

  81. Dias R., Aggleton J. P., Effects of selective excitotoxic prefrontal lesions on acquisition of nonmatching- and matching-to-place in the T-maze in the rat: differential involvement of the prelimbic-infralimbic and anterior cingulate cortices in providing behavioural flexibility, European Journal of Neuroscience, 12, 12, 2000. Crossref

  82. Khemlani Sangeet S., Barbey Aron K., Johnson-Laird Philip N., Causal reasoning with mental models, Frontiers in Human Neuroscience, 8, 2014. Crossref

  83. Papadopoulou Marianna, Evdokimidis Ioannis, Tsoukas Evangelos, Mantas Asimakis, Smyrnis Nikolaos, Event-related potentials before saccades and antisaccades and their relation to reaction time, Experimental Brain Research, 205, 4, 2010. Crossref

  84. REFERENCES, Monographs of the Society for Research in Child Development, 68, 3, 2003. Crossref

  85. Troche S. J., Trenkwalder C., Morelli-Canelo M., Gibbons H., Rammsayer T. H., To the influence of general slowing and medication on identity- and location-based priming effects in patients with Parkinson's disease, Journal of Neuropsychology, 3, 2, 2009. Crossref

  86. McDonald Robert J., King Amy L., Foong Natalie, Rizos Zoe, Hong Nancy S., Neurotoxic lesions of the medial prefrontal cortex or medial striatum impair multiple-location place learning in the water task: evidence for neural structures with complementary roles in behavioural flexibility, Experimental Brain Research, 187, 3, 2008. Crossref

  87. Grol Meike J., Toni Ivan, Lock Mireille, Verstraten Frans A. J., Spatial representation of overlearned arbitrary visuomotor associations, Experimental Brain Research, 192, 4, 2009. Crossref

  88. Parker Amanda, Wilding Edward, Akerman Colin, The von Restorff Effect in Visual Object Recognition Memory in Humans and Monkeys: The Role of Frontal/Perirhinal Interaction, Journal of Cognitive Neuroscience, 10, 6, 1998. Crossref

  89. Lavigne Frédéric, Avnaïm Francis, Dumercy Laurent, Inter-synaptic learning of combination rules in a cortical network model, Frontiers in Psychology, 5, 2014. Crossref

  90. Kesner Raymond P., Churchwell John C., An analysis of rat prefrontal cortex in mediating executive function, Neurobiology of Learning and Memory, 96, 3, 2011. Crossref

  91. Lee Ya-Yun, Winstein Carolee J., Gordon James, Petzinger Giselle M., Zelinski Elizabeth M., Fisher Beth E., Context-Dependent Learning in People With Parkinson's Disease, Journal of Motor Behavior, 48, 3, 2016. Crossref

  92. Erixon-Lindroth Nina, Farde Lars, Robins Wahlin Tarja-Brita, Sovago Judit, Halldin Christer, Bäckman Lars, The role of the striatal dopamine transporter in cognitive aging, Psychiatry Research: Neuroimaging, 138, 1, 2005. Crossref

  93. Ragozzino Michael E, Jih Jane, Tzavos Arianna, Involvement of the dorsomedial striatum in behavioral flexibility: role of muscarinic cholinergic receptors, Brain Research, 953, 1-2, 2002. Crossref

  94. Van Golf Racht-Delatour Barbara, El Massioui Nicole, Rule-Based Learning Impairment in Rats with Lesions to the Dorsal Striatum, Neurobiology of Learning and Memory, 72, 1, 1999. Crossref

  95. Hale James B., Fitzer Kim R., Evaluating Orbital-Ventral Medial System Regulation of Personal Attention: A Critical Need for Neuropsychological Assessment and Intervention, Applied Neuropsychology: Child, 4, 2, 2015. Crossref

  96. Berke Joshua D., Hyman Steven E., Addiction, Dopamine, and the Molecular Mechanisms of Memory, Neuron, 25, 3, 2000. Crossref

  97. Krishnan Gopee, Tiwari Shivani, Revisiting the acquired neurogenic stuttering in the light of developmental stuttering, Journal of Neurolinguistics, 24, 3, 2011. Crossref

  98. Pally Regina, Non-Conscious Prediction and a Role for Consciousness in Correcting Prediction Errors, Cortex, 41, 5, 2005. Crossref

  99. Ullman Michael T., Pierpont Elizabeth I., Specific Language Impairment is not Specific to Language: the Procedural Deficit Hypothesis, Cortex, 41, 3, 2005. Crossref

  100. Murray Elisabeth A, Wise Steven P, Interactions between orbital prefrontal cortex and amygdala: advanced cognition, learned responses and instinctive behaviors, Current Opinion in Neurobiology, 20, 2, 2010. Crossref

  101. Raghanti Mary Ann, Edler Melissa K., Stephenson Alexa R., Wilson Lakaléa J., Hopkins William D., Ely John J., Erwin Joseph M., Jacobs Bob, Hof Patrick R., Sherwood Chet C., Human-specific increase of dopaminergic innervation in a striatal region associated with speech and language: A comparative analysis of the primate basal ganglia, Journal of Comparative Neurology, 524, 10, 2016. Crossref

  102. Hadj-Bouziane Fadila, Meunier Martine, Boussaoud Driss, Conditional visuo-motor learning in primates: a key role for the basal ganglia, Journal of Physiology-Paris, 97, 4-6, 2003. Crossref

  103. Gengler Simon, Mallot Hanspeter A, Hölscher Christian, Inactivation of the rat dorsal striatum impairs performance in spatial tasks and alters hippocampal theta in the freely moving rat, Behavioural Brain Research, 164, 1, 2005. Crossref

  104. van den Heuvel Odile A, Groenewegen Henk J, Barkhof Frederik, Lazeron Richard H.C, van Dyck Richard, Veltman Dick J, Frontostriatal system in planning complexity: a parametric functional magnetic resonance version of tower of london task, NeuroImage, 18, 2, 2003. Crossref

  105. Liang Q., Situation Understanding Based on Heterogeneous Sensor Networks and Human-Inspired Favor Weak Fuzzy Logic System, 2009 IEEE International Conference on Communications, 2009. Crossref

  106. Apicella Paul, Leading tonically active neurons of the striatum from reward detection to context recognition, Trends in Neurosciences, 30, 6, 2007. Crossref

  107. Ullman Michael T., Is Broca's Area Part of a Basal Ganglia Thalamocortical Circuit?, Cortex, 42, 4, 2006. Crossref

  108. Prasad B.M, Hochstatter T, Sorg B.A, Expression of cocaine sensitization: regulation by the medial prefrontal cortex, Neuroscience, 88, 3, 1999. Crossref

  109. McDonald R.J, Hong N.S, A dissociation of dorso-lateral striatum and amygdala function on the same stimulus–response habit task, Neuroscience, 124, 3, 2004. Crossref

  110. Tanji Jun, Shima Keisetsu, Mushiake Hajime, Concept-based behavioral planning and the lateral prefrontal cortex, Trends in Cognitive Sciences, 11, 12, 2007. Crossref

  111. Ragozzino Michael E., Acetylcholine actions in the dorsomedial striatum support the flexible shifting of response patterns, Neurobiology of Learning and Memory, 80, 3, 2003. Crossref

  112. White Norman M., The role of stimulus ambiguity and movement in spatial navigation: A multiple memory systems analysis of location discrimination, Neurobiology of Learning and Memory, 82, 3, 2004. Crossref

  113. Mushiake Hajime, Saito Naohiro, Sakamoto Kazuhiro, Itoyama Yasuto, Tanji Jun, Activity in the Lateral Prefrontal Cortex Reflects Multiple Steps of Future Events in Action Plans, Neuron, 50, 4, 2006. Crossref

  114. Ashby F. Gregory, Turner Benjamin O., Horvitz Jon C., Cortical and basal ganglia contributions to habit learning and automaticity, Trends in Cognitive Sciences, 14, 5, 2010. Crossref

  115. Kerr Aurora, Zelazo Philip David, Development of “hot” executive function: The children’s gambling task, Brain and Cognition, 55, 1, 2004. Crossref

  116. Hackney Madeleine E., Nocera Joe R., Bowers Dawn, Altmann Lori J.P., Hass Chris J., The Chronic Exercise–Cognition Interaction and Parkinson Disease, in Exercise-Cognition Interaction, 2016. Crossref

  117. Hazy T.E., Frank M.J., O’Reilly R.C., Banishing the homunculus: Making working memory work, Neuroscience, 139, 1, 2006. Crossref

  118. Groenewegen Henk J., van den Heuvel Odile A., Cath Danielle C., Voorn P., Veltman Dick J., Does an imbalance between the dorsal and ventral striatopallidal systems play a role in Tourette's syndrome? A neuronal circuit approach, Brain and Development, 25, 2003. Crossref

  119. Moore Tara L., Killiany Ronald J., Herndon James G., Rosene Douglas L., Moss Mark B., Executive system dysfunction occurs as early as middle-age in the rhesus monkey, Neurobiology of Aging, 27, 10, 2006. Crossref

  120. Patrick Christopher J., Durbin C. Emily, Moser Jason S., Reconceptualizing antisocial deviance in neurobehavioral terms, Development and Psychopathology, 24, 3, 2012. Crossref

  121. Opris Ioan, Bruce Charles J., Neural circuitry of judgment and decision mechanisms, Brain Research Reviews, 48, 3, 2005. Crossref

  122. DeCoteau William E., McElvaine Daniel, Smolentzov Linnea, Kesner Raymond P., Effects of rodent prefrontal lesions on object-based, visual scene memory, Neurobiology of Learning and Memory, 92, 4, 2009. Crossref

  123. Berke J.D., Procedural Learning: Striatum, in Encyclopedia of Neuroscience, 2009. Crossref

  124. Ragozzino Michael E., Mohler Eric G., Prior Margaret, Palencia Carlos A., Rozman Suzanne, Acetylcholine activity in selective striatal regions supports behavioral flexibility, Neurobiology of Learning and Memory, 91, 1, 2009. Crossref

  125. Monchi Oury, Taylor John G., A hard wired model of coupled frontal working memories for various tasks, Information Sciences, 113, 3-4, 1999. Crossref

  126. Kesner Raymond P., Gilbert Paul E., The role of the agranular insular cortex in anticipation of reward contrast, Neurobiology of Learning and Memory, 88, 1, 2007. Crossref

  127. Marcos Encarni, Duff Armin, Sanchez-Fibla Marti, Verschure Paul F. M. J., The neuronal substrate underlying order and interval representations in sequential tasks: A biologically based robot study, The 2010 International Joint Conference on Neural Networks (IJCNN), 2010. Crossref

  128. Deschênes Annie, Goulet Sonia, Doré François Y., Rule shift under long-term PCP challenge in rats, Behavioural Brain Research, 167, 1, 2006. Crossref

  129. Brasted Peter J, Dunnett Stephen B, Robbins Trevor W, Unilateral lesions of the medial agranular cortex impair responding on a lateralised reaction time task, Behavioural Brain Research, 111, 1-2, 2000. Crossref

  130. Gilbert Peter F.C., An outline of brain function, Cognitive Brain Research, 12, 1, 2001. Crossref

  131. Gill Kathryn M., Bernstein Ilene L., Mizumori Sheri J.Y., Immediate early gene activation in hippocampus and dorsal striatum: Effects of explicit place and response training, Neurobiology of Learning and Memory, 87, 4, 2007. Crossref

  132. Burk Joshua A, Mair Robert G, Effects of dorsal and ventral striatal lesions on delayed matching trained with retractable levers, Behavioural Brain Research, 122, 1, 2001. Crossref

  133. Mullette-Gillman O'Dhaniel A., Detwiler Jacqueline M., Winecoff Amy, Dobbins Ian, Huettel Scott A., Infrequent, task-irrelevant monetary gains and losses engage dorsolateral and ventrolateral prefrontal cortex, Brain Research, 1395, 2011. Crossref

  134. Schiller D., Weiner I., Lesions to the basolateral amygdala and the orbitofrontal cortex but not to the medial prefrontal cortex produce an abnormally persistent latent inhibition in rats, Neuroscience, 128, 1, 2004. Crossref

  135. Melcher Tobias, Gruber Oliver, Oddball and incongruity effects during Stroop task performance: A comparative fMRI study on selective attention, Brain Research, 1121, 1, 2006. Crossref

  136. Biundo Roberta, Weis Luca, Facchini Silvia, Formento-Dojot Patrizia, Vallelunga Annamaria, Pilleri Manuela, Weintraub Daniel, Antonini Angelo, Patterns of cortical thickness associated with impulse control disorders in Parkinson's disease, Movement Disorders, 30, 5, 2015. Crossref

  137. Graham Kim S., Lee Andy C. H., Barense Morgan D., Invited Address at the Occasion of the Bertelson Award 2005 Impairments in visual discrimination in amnesia: Implications for theories of the role of medial temporal lobe regions in human memory, European Journal of Cognitive Psychology, 20, 4, 2008. Crossref

  138. Adam Jos J., van Houdt Hanna, Scholtissen Bart, Visser-Vandewalle Veerle, Winogrodzka Ania, Duits Annelien, Executive control in Parkinson's disease: Effects of dopaminergic medication and deep brain stimulation on anti-cue keypress performance, Neuroscience Letters, 500, 2, 2011. Crossref

  139. Gardner Eliot L., Vorel S.Robert, Cannabinoid Transmission and Reward-Related Events, Neurobiology of Disease, 5, 6, 1998. Crossref

  140. Kim Yong Kyun, Choi Jung-Hwa, Yoon Jeong-Gyu, Lee Jang-Won, Cho Sung Sik, Improved Dysphagia After Decannulation of Tracheostomy in Patients With Brain Injuries, Annals of Rehabilitation Medicine, 39, 5, 2015. Crossref

  141. Monchi O., Taylor J.G., Dagher A., A neural model of working memory processes in normal subjects, Parkinson's disease and schizophrenia for fMRI design and predictions, Neural Networks, 13, 8-9, 2000. Crossref

  142. Swinnen Stephan P, Steyvers Maarten, Van Den Bergh Lynn, Stelmach George E, Motor learning and Parkinson’s disease: refinement of within-limb and between-limb coordination as a result of practice, Behavioural Brain Research, 111, 1-2, 2000. Crossref

  143. Fielding Joanne, Georgiou-Karistianis Nellie, Bradshaw John, Millist Lynette, White Owen, No sequence dependent modulation of the Simon effect in Parkinson's disease, Cognitive Brain Research, 25, 1, 2005. Crossref

  144. Teichmann Marc, Rosso Charlotte, Martini Jean-Baptiste, Bloch Isabelle, Brugières Pierre, Duffau Hugues, Lehéricy Stéphane, Bachoud-Lévi Anne-Catherine, A cortical-subcortical syntax pathway linking Broca's area and the striatum, Human Brain Mapping, 36, 6, 2015. Crossref

  145. Meyer Martin, Steinhauer Karsten, Alter Kai, Friederici Angela D., von Cramon D.Yves, Brain activity varies with modulation of dynamic pitch variance in sentence melody, Brain and Language, 89, 2, 2004. Crossref

  146. Meck Warren H, Benson Aimee M, Dissecting the Brain's Internal Clock: How Frontal–Striatal Circuitry Keeps Time and Shifts Attention, Brain and Cognition, 48, 1, 2002. Crossref

  147. Hannesson D.K, Vacca G, Howland J.G, Phillips A.G, Medial prefrontal cortex is involved in spatial temporal order memory but not spatial recognition memory in tests relying on spontaneous exploration in rats, Behavioural Brain Research, 153, 1, 2004. Crossref

  148. Tomasetti C., Dell’Aversano C., Iasevoli F., de Bartolomeis A., Homer splice variants modulation within cortico-subcortical regions by dopamine D2 antagonists, a partial agonist, and an indirect agonist: Implication for glutamatergic postsynaptic density in antipsychotics action, Neuroscience, 150, 1, 2007. Crossref

  149. Histed Mark H., Pasupathy Anitha, Miller Earl K., Learning Substrates in the Primate Prefrontal Cortex and Striatum: Sustained Activity Related to Successful Actions, Neuron, 63, 2, 2009. Crossref

  150. Miller Earl K, The Prefrontal Cortex, Neuron, 22, 1, 1999. Crossref

  151. Ghods-Sharifi Sarvin, Haluk Desirae M., Floresco Stan B., Differential effects of inactivation of the orbitofrontal cortex on strategy set-shifting and reversal learning, Neurobiology of Learning and Memory, 89, 4, 2008. Crossref

  152. Floresco Stan B., Block Annie E., Tse Maric T.L., Inactivation of the medial prefrontal cortex of the rat impairs strategy set-shifting, but not reversal learning, using a novel, automated procedure, Behavioural Brain Research, 190, 1, 2008. Crossref

  153. Bezard Erwan, Gross Christian E., Brotchie Jonathan M., Presymptomatic compensation in Parkinson's disease is not dopamine-mediated, Trends in Neurosciences, 26, 4, 2003. Crossref

  154. den Heuvel Odile A. van, der Werf Ysbrand D. van, Verhoef Kim M.W., de Wit Stella, Berendse Henk W., Wolters Erik Ch., Veltman Dick J., Groenewegen Henk J., Frontal–striatal abnormalities underlying behaviours in the compulsive–impulsive spectrum, Journal of the Neurological Sciences, 289, 1-2, 2010. Crossref

  155. Tzavos Arianna, Jih Jane, Ragozzino Michael E., Differential effects of M1 muscarinic receptor blockade and nicotinic receptor blockade in the dorsomedial striatum on response reversal learning, Behavioural Brain Research, 154, 1, 2004. Crossref

  156. Liang Qilian, Situation Understanding Based on Heterogeneous Sensor Networks and Human-Inspired Favor Weak Fuzzy Logic System, IEEE Systems Journal, 5, 2, 2011. Crossref

  157. Atmaca Murad, Aydin Ayşe, Tezcan Ertan, Poyraz A. Kursad, Kara Bilge, Volumetric investigation of brain regions in patients with conversion disorder, Progress in Neuro-Psychopharmacology and Biological Psychiatry, 30, 4, 2006. Crossref

  158. Surmeier D.James, Bevan Mark D, “The Little Engine that Could”, Neuron, 39, 1, 2003. Crossref

  159. Otani Satoru, Prefrontal cortex function, quasi-physiological stimuli, and synaptic plasticity, Journal of Physiology-Paris, 97, 4-6, 2003. Crossref

  160. Hallworth Nicholas E., Bland Brian H., Basal ganglia–hippocampal interactions support the role of the hippocampal formation in sensorimotor integration, Experimental Neurology, 188, 2, 2004. Crossref

  161. Gibbs Marie E, Summers Roger J, α2-adrenoceptors in the basal ganglia have a role in memory consolidation and reinforcement, Neuropharmacology, 45, 3, 2003. Crossref

  162. Kesner Raymond P, Ragozzino Michael E, The role of the prefrontal cortex in object–place learning: a test of the attribute specificity model, Behavioural Brain Research, 146, 1-2, 2003. Crossref

  163. White Norman M., McDonald Robert J., Multiple Parallel Memory Systems in the Brain of the Rat, Neurobiology of Learning and Memory, 77, 2, 2002. Crossref

  164. Matell Matthew S., Meck Warren H., Lustig Cindy, Not “just” a coincidence: Frontal‐striatal interactions in working memory and interval timing, Memory, 13, 3-4, 2005. Crossref

  165. Dias Flávia Regina Cruz, Carey Robert J., Carrera Marinete Pinheiro, Conditioned locomotion induced by unilateral intrastriatal administration of Apomorphine: D2 receptor activation is critical but not the expression of the unconditioned response, Brain Research, 1083, 1, 2006. Crossref

  166. Matsumoto Kenji, Matsumoto Madoka, Abe Hiroshi, Goal-based action selection and utility-based action bias, Neural Networks, 19, 8, 2006. Crossref

  167. Schoenbaum Geoffrey, Setlow Barry, Ramus Seth J., A systems approach to orbitofrontal cortex function: recordings in rat orbitofrontal cortex reveal interactions with different learning systems, Behavioural Brain Research, 146, 1-2, 2003. Crossref

  168. Ullman Michael T, Contributions of memory circuits to language: the declarative/procedural model, Cognition, 92, 1-2, 2004. Crossref

  169. Wagner Amy K., Arenth Patricia M., Kwasnica Christina, Rogers Emily H., Traumatic Brain Injury, in Physical Medicine and Rehabilitation, 2011. Crossref

  170. Anderson John R., Qin Yulin, Sohn Myeong-Ho, Stenger V. Andrew, Carter Cameron S., An information-processing model of the BOLD response in symbol manipulation tasks, Psychonomic Bulletin & Review, 10, 2, 2003. Crossref

  171. Chong Raymond K.Y, Horak Fay B, Woollacott Marjorie H, Parkinson’s disease impairs the ability to change set quickly, Journal of the Neurological Sciences, 175, 1, 2000. Crossref

  172. Woolgar Alexandra, Afshar Soheil, Williams Mark A., Rich Anina N., Flexible Coding of Task Rules in Frontoparietal Cortex: An Adaptive System for Flexible Cognitive Control, Journal of Cognitive Neuroscience, 27, 10, 2015. Crossref

  173. Rauch Scott L., Savage Cary R., NEUROIMAGING AND NEUROPSYCHOLOGY OF THE STRIATUM, Psychiatric Clinics of North America, 20, 4, 1997. Crossref

  174. Manrique Héctor Marín, Call Josep, Age-dependent cognitive inflexibility in great apes, Animal Behaviour, 102, 2015. Crossref

  175. Peterson Bradley S., Clinical neuroscience and imaging studies of core psychoanalytic constructs, Clinical Neuroscience Research, 4, 5-6, 2005. Crossref

  176. White Norman M, Mnemonic functions of the basal ganglia, Current Opinion in Neurobiology, 7, 2, 1997. Crossref

  177. Savage Cary R., NEUROPSYCHOLOGY OF SUBCORTICAL DEMENTIAS, Psychiatric Clinics of North America, 20, 4, 1997. Crossref

  178. Moro Sara Basso, Carrieri Marika, Avola Danilo, Brigadoi Sabrina, Lancia Stefania, Petracca Andrea, Spezialetti Matteo, Ferrari Marco, Placidi Giuseppe, Quaresima Valentina, A novel semi-immersive virtual reality visuo-motor task activates ventrolateral prefrontal cortex: a functional near-infrared spectroscopy study, Journal of Neural Engineering, 13, 3, 2016. Crossref

  179. Anderson John R., Qin Yulin, Using Brain Imaging to Extract the Structure of Complex Events at the Rational Time Band, Journal of Cognitive Neuroscience, 20, 9, 2008. Crossref

  180. Stephenson Alexa R., Edler Melissa K., Erwin Joseph M., Jacobs Bob, Hopkins William D., Hof Patrick R., Sherwood Chet C., Raghanti Mary Ann, Cholinergic innervation of the basal ganglia in humans and other anthropoid primates, Journal of Comparative Neurology, 525, 2, 2017. Crossref

  181. Johnston Kevin, Everling Stefan, Neural Activity in Monkey Prefrontal Cortex Is Modulated by Task Context and Behavioral Instruction during Delayed-match-to-sample and Conditional Prosaccade—Antisaccade Tasks, Journal of Cognitive Neuroscience, 18, 5, 2006. Crossref

  182. Dickson P.E., Cairns J., Goldowitz D., Mittleman G., Cerebellar contribution to higher and lower order rule learning and cognitive flexibility in mice, Neuroscience, 345, 2017. Crossref

  183. Nagypál Tamás, Gombkötő Péter, Barkóczi Balázs, Benedek György, Nagy Attila, Chacron Maurice J., Activity of Caudate Nucleus Neurons in a Visual Fixation Paradigm in Behaving Cats, PLOS ONE, 10, 11, 2015. Crossref

  184. Lee Y.-Y., Winstein C. J., Fisher B. E., Foxe John, Role of the dorsolateral prefrontal cortex in context-dependent motor performance, European Journal of Neuroscience, 43, 7, 2016. Crossref

  185. Villarreal Mirta F., Cerquetti Daniel, Caruso Silvina, Schwarcz López Aranguren Violeta, Gerschcovich Eliana Roldán, Frega Ana Lucía, Leiguarda Ramón C., Maurits Natasha M., Neural Correlates of Musical Creativity: Differences between High and Low Creative Subjects, PLoS ONE, 8, 9, 2013. Crossref

  186. Groenewegen H.J., Wouterlood F.G., Uylings H.B.M., Organization of Prefrontal-Striatal Connections, in Handbook of Basal Ganglia Structure and Function, Second Edition, 24, 2016. Crossref

  187. Schneider Mary L., Moore Colleen F., Roberts Andrew D., Dejesus Onofre, Prenatal Stress Alters Early Neurobehavior, Stress Reactivity and Learning in Non-human Primates: A Brief Review, Stress, 4, 3, 2001. Crossref

  188. Kesner Raymond P., Exploration of the Neurobiological Basis for a Three-System, Multiattribute Model of Memory, in Behavioral Neuroscience of Learning and Memory, 37, 2016. Crossref

  189. Lee Shu-Hui, Walker Zachary M., Hale James B., Chen S.H. Annabel, Frontal-subcortical circuitry in social attachment and relationships: A cross-sectional fMRI ALE meta-analysis, Behavioural Brain Research, 325, 2017. Crossref

  190. Izquierdo Alicia, Murray Elisabeth A., Combined Unilateral Lesions of the Amygdala and Orbital Prefrontal Cortex Impair Affective Processing in Rhesus Monkeys, Journal of Neurophysiology, 91, 5, 2004. Crossref

  191. Marcos Encarni, Nougaret Simon, Tsujimoto Satoshi, Genovesio Aldo, Outcome Modulation Across Tasks in the Primate Dorsolateral Prefrontal Cortex, Neuroscience, 371, 2018. Crossref

  192. Swainson R., Rogers R.D., Sahakian B.J., Summers B.A., Polkey C.E., Robbins T.W., Probabilistic learning and reversal deficits in patients with Parkinson’s disease or frontal or temporal lobe lesions: possible adverse effects of dopaminergic medication, Neuropsychologia, 38, 5, 2000. Crossref

  193. Shadlen Michael N., Newsome William T., Neural Basis of a Perceptual Decision in the Parietal Cortex (Area LIP) of the Rhesus Monkey, Journal of Neurophysiology, 86, 4, 2001. Crossref

  194. Sobotka Stanislaw, Diltz Mark D., Ringo James L., Can Delay-Period Activity Explain Working Memory?, Journal of Neurophysiology, 93, 1, 2005. Crossref

  195. DeSouza Joseph F. X., Menon Ravi S., Everling Stefan, Preparatory Set Associated With Pro-Saccades and Anti-Saccades in Humans Investigated With Event-Related fMRI, Journal of Neurophysiology, 89, 2, 2003. Crossref

  196. Lawrence A.D, Sahakian B.J, Rogers R.D, Hodges J.R, Robbins T.W, Discrimination, reversal, and shift learning in Huntington’s disease: mechanisms of impaired response selection, Neuropsychologia, 37, 12, 1999. Crossref

  197. Schneider Mary L, Moore Colleen F, Kraemer Gary W, Roberts Andrew D, DeJesus Onofre T, The impact of prenatal stress, fetal alcohol exposure, or both on development: perspectives from a primate model, Psychoneuroendocrinology, 27, 1-2, 2002. Crossref

  198. Bullock Kelly R., Pieper Florian, Sachs Adam J., Martinez-Trujillo Julio C., Visual and presaccadic activity in area 8Ar of the macaque monkey lateral prefrontal cortex, Journal of Neurophysiology, 118, 1, 2017. Crossref

  199. Dagher Alain, Owen Adrian M., Boecker Henning, Brooks David J., Mapping the network for planning: a correlational PET activation study with the Tower of London task, Brain, 122, 10, 1999. Crossref

  200. Baker Phillip M., Mizumori Sheri J.Y., Control of behavioral flexibility by the lateral habenula, Pharmacology Biochemistry and Behavior, 162, 2017. Crossref

  201. Wallis Jonathan D., Miller Earl K., From Rule to Response: Neuronal Processes in the Premotor and Prefrontal Cortex, Journal of Neurophysiology, 90, 3, 2003. Crossref

  202. Asaad Wael F., Rainer Gregor, Miller Earl K., Task-Specific Neural Activity in the Primate Prefrontal Cortex, Journal of Neurophysiology, 84, 1, 2000. Crossref

  203. Lebedev Mikhail A., Douglass Diana K., Moody Sohie Lee, Wise Steven P., Prefrontal Cortex Neurons Reflecting Reports of a Visual Illusion, Journal of Neurophysiology, 85, 4, 2001. Crossref

  204. Opris Ioan, Casanova Manuel F., Lebedev Mikhail A., Popescu Aurel I., Prefrontal Cortical Microcircuits Support the Emergence of Mind, in The Physics of the Mind and Brain Disorders, 11, 2017. Crossref

  205. Deiber M.-P., Wise S. P., Honda M., Catalan M. J., Grafman J., Hallett M., Frontal and Parietal Networks for Conditional Motor Learning: A Positron Emission Tomography Study, Journal of Neurophysiology, 78, 2, 1997. Crossref

  206. Adams Barbara W., Bradberry Charles W., Moghaddam Bita, NMDA antagonist effects on striatal dopamine release: Microdialysis studies in awake monkeys, Synapse, 43, 1, 2002. Crossref

  207. Noga Brian R., Opris Ioan, The Hierarchical Circuit for Executive Control of Movement, in The Physics of the Mind and Brain Disorders, 11, 2017. Crossref

  208. Lebedev Mikhail A., Wise Steven P., Insights into Seeing and Grasping: Distinguishing the Neural Correlates of Perception and Action, Behavioral and Cognitive Neuroscience Reviews, 1, 2, 2002. Crossref

  209. Haber Suzanne, Mcfarland Nikolaus R., The Place of the Thalamus in Frontal Cortical-Basal Ganglia Circuits, The Neuroscientist, 7, 4, 2001. Crossref

  210. Hoshi Eiji, Tanji Jun, Area-Selective Neuronal Activity in the Dorsolateral Prefrontal Cortex for Information Retrieval and Action Planning, Journal of Neurophysiology, 91, 6, 2004. Crossref

  211. Tanji Jun, Hoshi Eiji, Role of the Lateral Prefrontal Cortex in Executive Behavioral Control, Physiological Reviews, 88, 1, 2008. Crossref

  212. Mazlan Mazlina, Traumatic Brain Injury, in Braddom's Rehabilitation Care: A Clinical Handbook, 2018. Crossref

  213. Suzuki Wendy A., Brown Emery N., Behavioral and Neurophysiological Analyses of Dynamic Learning Processes, Behavioral and Cognitive Neuroscience Reviews, 4, 2, 2005. Crossref

  214. Hoshi Eiji, Shima Keisetsu, Tanji Jun, Neuronal Activity in the Primate Prefrontal Cortex in the Process of Motor Selection Based on Two Behavioral Rules, Journal of Neurophysiology, 83, 4, 2000. Crossref

  215. Yang Shun-nan, Hwang Helen, Ford Joel, Heinen Stephen, Supplementary Eye Field Activity Reflects a Decision Rule Governing Smooth Pursuit but not the Decision, Journal of Neurophysiology, 103, 5, 2010. Crossref

  216. Will Matthew J., Vanderheyden William M., Kelley Ann E., Striatal opioid peptide gene expression differentially tracks short-term satiety but does not vary with negative energy balance in a manner opposite to hypothalamic NPY, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 292, 1, 2007. Crossref

  217. Dal-Pan Alexandre, Pifferi Fabien, Marchal Julia, Picq Jean-Luc, Aujard Fabienne, Chapouthier Georges, Cognitive Performances Are Selectively Enhanced during Chronic Caloric Restriction or Resveratrol Supplementation in a Primate, PLoS ONE, 6, 1, 2011. Crossref

  218. Szabo Birgit, Noble Daniel W.A., Byrne Richard W., Tait David S., Whiting Martin J., Subproblem learning and reversal of a multidimensional visual cue in a lizard: evidence for behavioural flexibility?, Animal Behaviour, 144, 2018. Crossref

  219. Constantinidis Christos, Franowicz Matthew N., Goldman-Rakic Patricia S., The sensory nature of mnemonic representation in the primate prefrontal cortex, Nature Neuroscience, 4, 3, 2001. Crossref

  220. Rice D, Barone S, Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models., Environmental Health Perspectives, 108, suppl 3, 2000. Crossref

  221. Lovell Peter V., Huizinga Nicole A., Friedrich Samantha R., Wirthlin Morgan, Mello Claudio V., The constitutive differential transcriptome of a brain circuit for vocal learning, BMC Genomics, 19, 1, 2018. Crossref

  222. Praamstra P, Kleine B.-U, Schnitzler A, Magnetic stimulation of the dorsal premotor cortex modulates the Simon effect, NeuroReport, 10, 17, 1999. Crossref

  223. Miller Earl K., The prefontral cortex and cognitive control, Nature Reviews Neuroscience, 1, 1, 2000. Crossref

  224. OTANI SATORU, Memory trace in prefrontal cortex: theory for the cognitive switch, Biological Reviews of the Cambridge Philosophical Society, 77, 4, 2002. Crossref

  225. Christoff Kalina, Ream Justin M., Geddes Leo P. T., Gabrieli John D. E., Evaluating Self-Generated Information: Anterior Prefrontal Contributions to Human Cognition., Behavioral Neuroscience, 117, 6, 2003. Crossref

  226. La Camera Giancarlo, Bouret Sebastien, Richmond Barry J., Contributions of Lateral and Orbital Frontal Regions to Abstract Rule Acquisition and Reversal in Monkeys, Frontiers in Neuroscience, 12, 2018. Crossref

  227. Procyk E., Tanaka Y. L., Joseph J. P., Anterior cingulate activity during routine and non-routine sequential behaviors in macaques, Nature Neuroscience, 3, 5, 2000. Crossref

  228. Parker Andrew, Derrington Andrew, Blakemore Colin, Miller Earl K., Freedman David J., Wallis Jonathan D., The prefrontal cortex: categories, concepts and cognition, Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 357, 1424, 2002. Crossref

  229. Parker Andrew, Derrington Andrew, Blakemore Colin, Gaffan David, Against memory systems, Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 357, 1424, 2002. Crossref

  230. Raichle M. E., The neural correlates of consciousness: an analysis of cognitive skill learning, Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 353, 1377, 1998. Crossref

  231. Nougaret Simon, Genovesio Aldo, Learning the meaning of new stimuli increases the cross-correlated activity of prefrontal neurons, Scientific Reports, 8, 1, 2018. Crossref

  232. Frank Michael J., Claus Eric D., Anatomy of a decision: Striato-orbitofrontal interactions in reinforcement learning, decision making, and reversal., Psychological Review, 113, 2, 2006. Crossref

  233. Wirthlin Morgan, Chang Edward F., Knörnschild Mirjam, Krubitzer Leah A., Mello Claudio V., Miller Cory T., Pfenning Andreas R., Vernes Sonja C., Tchernichovski Ofer, Yartsev Michael M., A Modular Approach to Vocal Learning: Disentangling the Diversity of a Complex Behavioral Trait, Neuron, 104, 1, 2019. Crossref

  234. Strominger Norman L., Demarest Robert J., Laemle Lois B., Basal Ganglia and Extrapyramidal System, in Noback's Human Nervous System, Seventh Edition, 2012. Crossref

  235. Troche S.J., Trenkwalder C., Morelli-Canelo M., Gibbons H., Rammsayer T.H., Unimpaired negative but enhanced positive priming in Parkinson's disease: Evidence from an identity and a location priming task, Neuropsychologia, 44, 10, 2006. Crossref

  236. Lee Ya-Yun, Tai Chun-Hwei, Fisher Beth E., Context-Dependent Behavior in Parkinson’s Disease With Freezing of Gait, Neurorehabilitation and Neural Repair, 33, 12, 2019. Crossref

  237. Reischies F. M., Psychopathologie des Frontalhirns, in Frontalhirn, 2002. Crossref

  238. Reischiesc F. M., Psychopathologie, in Frontalhirn, 2005. Crossref

  239. Zeng Guanxiong, Chen Yang, Cui Bo, Yu Shan, Continual learning of context-dependent processing in neural networks, Nature Machine Intelligence, 1, 8, 2019. Crossref

  240. Seamans Jeremy K., Working Memory in Prefrontal Cortex and its Neuromodulation, in Prefrontal Cortex: From Synaptic Plasticity to Cognition, 2004. Crossref

  241. Feenstra Matthijs G. P., de Bruin Jan P. C., Strategy Switching and the Rat Prefrontal Cortex, in Prefrontal Cortex: From Synaptic Plasticity to Cognition, 2004. Crossref

  242. Mitchell Rachel L.C., Phillips Louise H., The psychological, neurochemical and functional neuroanatomical mediators of the effects of positive and negative mood on executive functions, Neuropsychologia, 45, 4, 2007. Crossref

  243. White Norman M., How independent are parallel memory systems? A theoretical comment on Gibson and Shettleworth (2005)., Behavioral Neuroscience, 119, 4, 2005. Crossref

  244. Christoff Kalina, Human Thought and the Lateral Prefrontal Cortex, in Neural Correlates of Thinking, 1, 2009. Crossref

  245. Kuatsjah Eunice, Khoshnam Mahta, Menon Carlo, Murphy Bernadette Ann, Investigation on the effect of noisy galvanic vestibular stimulation on fine motor skills during a visuomotor task in healthy participants, PLOS ONE, 14, 5, 2019. Crossref

  246. Chiu Yu-Chin, Egner Tobias, Cortical and subcortical contributions to context-control learning, Neuroscience & Biobehavioral Reviews, 99, 2019. Crossref

  247. Bonnavion Patricia, Fernández Elisa Pozuelo, Varin Christophe, de Kerchove d’Exaerde Alban, It takes two to tango: Dorsal direct and indirect pathways orchestration of motor learning and behavioral flexibility, Neurochemistry International, 124, 2019. Crossref

  248. Murray Elisabeth A., Bussey Timothy J., Wise Steven P., Role of prefrontal cortex in a network for arbitrary visuomotor mapping, in Executive Control and the Frontal Lobe: Current Issues, 2000. Crossref

  249. Haber Suzanne N., Functional Anatomy and Physiology of the Basal Ganglia: Non-motor Functions, in Deep Brain Stimulation in Neurological and Psychiatric Disorders, 2008. Crossref

  250. Pally Regina, The Predicting Brain: Psychoanalysis and Repeating the Past in the Present, in Psychoanalysis and Neuroscience, 2006. Crossref

  251. Bussey Timothy J., Wise Steven P., Murray Elisabeth A., The role of ventral and orbital prefrontal cortex in conditional visuomotor learning and strategy use in rhesus monkeys (Macaca mulatta)., Behavioral Neuroscience, 115, 5, 2001. Crossref

  252. Weiner I., Joel D., Dopamine in Schizophrenia Dysfunctional Information Processing in Basal Ganglia — Thalamocortical Split Circuits, in Dopamine in the CNS II, 154 / 2, 2002. Crossref

  253. Filoteo J. Vincent, Maddox W. Todd, Salmon David P., Song David D., Information-Integration Category Learning in Patients With Striatal Dysfunction., Neuropsychology, 19, 2, 2005. Crossref

  254. Basal Ganglia and Extrapyramidal System, in The Human Nervous System, 2005. Crossref

  255. Badgaiyan Rajendra D., Nonconscious mind: smart or dumb?, in Neuroscience of the Nonconscious Mind, 2019. Crossref

  256. Castellanos F. Xavier, The Psychobiology of Attention-Deficit/Hyperactivity Disorder, in Handbook of Disruptive Behavior Disorders, 1999. Crossref

  257. Kesner Raymond P., Exploration of the Neurobiological Basis for a Three-System, Multi-attribute Model of Memory, in The Neurobiological Basis of Memory, 2016. Crossref

  258. Haddon J. E., Killcross A. S., MEDIAL PREFRONTAL CORTEX LESIONS ABOLISH CONTEXTUAL CONTROL OF COMPETING RESPONSES, Journal of the Experimental Analysis of Behavior, 84, 3, 2005. Crossref

  259. Ragozzino Michael E., Baker Phillip M., Prefrontal Cortex and Basal Ganglia Attributes Underlying Behavioral Flexibility, in The Neurobiological Basis of Memory, 2016. Crossref

  260. Schlund Michael W., Cataldo Michael F., INTEGRATING FUNCTIONAL NEUROIMAGING AND HUMAN OPERANT RESEARCH: BRAIN ACTIVATION CORRELATED WITH PRESENTATION OF DISCRIMINATIVE STIMULI, Journal of the Experimental Analysis of Behavior, 84, 3, 2005. Crossref

  261. Duggan Emily C., Garcia-Barrera Mauricio A., Executive Functioning and Intelligence, in Handbook of Intelligence, 2015. Crossref

  262. Pally Regina, Il cervello che predice: psicoanalisi e ripetizione del passato nel presente, in Psicoanalisi e Neuroscienze, 2007. Crossref

  263. Hatz Florian, Meyer Antonia, Roesch Anne, Taub Ethan, Gschwandtner Ute, Fuhr Peter, Quantitative EEG and Verbal Fluency in DBS Patients: Comparison of Stimulator-On and -Off Conditions, Frontiers in Neurology, 9, 2019. Crossref

  264. Ducharme Simon, Dougherty Darin D., Drevets Wayne C., Neuroimaging and Neurocircuitry of Obsessive-Compulsive Disorder and Major Depressive Disorder, in Psychiatric Neurotherapeutics, 2016. Crossref

  265. Guirado Ramon, Perez-Rando Marta, Ferragud Antonio, Gutierrez-Castellanos Nicolas, Umemori Juzoh, Carceller Hector, Nacher Juan, Castillo-Gómez Esther, A Critical Period for Prefrontal Network Configurations Underlying Psychiatric Disorders and Addiction, Frontiers in Behavioral Neuroscience, 14, 2020. Crossref

  266. Boonstra E.A, van Schouwenburg M.R, Seth A.K, Bauer M, Zantvoord J.B, Kemper E.M, Lansink C.S, Slagter H.A, Conscious perception and the modulatory role of dopamine: no effect of the dopamine D2 agonist cabergoline on visual masking, the attentional blink, and probabilistic discrimination, Psychopharmacology, 237, 9, 2020. Crossref

  267. Lee Moon-Soo, Anumagalla Purnima, Pavuluri Mani N., Individuals with the post-traumatic stress disorder process emotions in subcortical regions irrespective of cognitive engagement: a meta-analysis of cognitive and emotional interface, Brain Imaging and Behavior, 15, 2, 2021. Crossref

  268. Bittmann Frank, Dech Silas, Aehle Markus, Schaefer Laura, Manual Muscle Testing—Force Profiles and Their Reproducibility, Diagnostics, 10, 12, 2020. Crossref

  269. Anderson John R., Carter Cameron S., Fincham Jon M., Qin Yulin, Ravizza Susan M., Rosenberg-Lee Miriam, Using fMRI to Test Models of Complex Cognition, Cognitive Science, 32, 8, 2008. Crossref

  270. Ahmari Susanne E., Rauch Scott L., The prefrontal cortex and OCD, Neuropsychopharmacology, 47, 1, 2022. Crossref

  271. Ragozzino Michael E., Choi Daniel, Dynamic Changes in Acetylcholine Output in the Medial Striatum During Place Reversal Learning, Learning & Memory, 11, 1, 2004. Crossref

  272. Schaefer Laura V., Dech Silas, Aehle Markus, Bittmann Frank N., Disgusting odours affect the characteristics of the Adaptive Force in contrast to neutral and pleasant odours, Scientific Reports, 11, 1, 2021. Crossref

  273. Chiba A A, Kesner R P, Gibson C J, Memory for temporal order of new and familiar spatial location sequences: role of the medial prefrontal cortex., Learning & Memory, 4, 4, 1997. Crossref

  274. Oualian Catherine, Gisquet-Verrier Pascale, The differential involvement of the prelimbic and infralimbic cortices in response conflict affects behavioral flexibility in rats trained in a new automated strategy-switching task, Learning & Memory, 17, 12, 2010. Crossref

  275. Jaffe Russell J., Constantinidis Christos, Working Memory: From Neural Activity to the Sentient Mind, in Comprehensive Physiology, 2021. Crossref

  276. Packard Mark G., Knowlton Barbara J., Learning and Memory Functions of the Basal Ganglia, Annual Review of Neuroscience, 25, 1, 2002. Crossref

  277. Schoenbaum Geoffrey, Setlow Barry, Integrating Orbitofrontal Cortex into Prefrontal Theory: Common Processing Themes across Species and Subdivisions, Learning & Memory, 8, 3, 2001. Crossref

  278. Gunaydin Lisa A., Kreitzer Anatol C., Cortico–Basal Ganglia Circuit Function in Psychiatric Disease, Annual Review of Physiology, 78, 1, 2016. Crossref

  279. Miller Earl K., Cohen Jonathan D., An Integrative Theory of Prefrontal Cortex Function, Annual Review of Neuroscience, 24, 1, 2001. Crossref

  280. Perez-Rando Marta, Guirado Ramón, The Medial Prefrontal Cortex (mPFC) and Addictions, in Handbook of Substance Misuse and Addictions, 2022. Crossref

  281. Cui Qiaoling, Li Qian, Geng Hongyan, Chen Lei, Ip Nancy Y., Ke Ya, Yung Wing-Ho, Dopamine receptors mediate strategy abandoning via modulation of a specific prelimbic cortex–nucleus accumbens pathway in mice, Proceedings of the National Academy of Sciences, 115, 21, 2018. Crossref

  282. Baxter Mark G., Murray Elisabeth A., The amygdala and reward, Nature Reviews Neuroscience, 3, 7, 2002. Crossref

  283. Buckley Mark J., Mansouri Farshad A., Hoda Hassan, Mahboubi Majid, Browning Philip G. F., Kwok Sze C., Phillips Adam, Tanaka Keiji, Dissociable Components of Rule-Guided Behavior Depend on Distinct Medial and Prefrontal Regions, Science, 325, 5936, 2009. Crossref

  284. Mizumori Sheri J. Y., Ragozzino Katharine E., Cooper Brenton G., Location and head direction representation in the dorsal striatum of rats, Psychobiology, 28, 4, 2000. Crossref

  285. Kesner Raymond P., Subregional analysis of mnemonic functions of the prefrontal cortex in the rat, Psychobiology, 28, 2, 2000. Crossref

  286. Ardid Salva, Sherfey Jason S., McCarthy Michelle M., Hass Joachim, Pittman-Polletta Benjamin R., Kopell Nancy, Biased competition in the absence of input bias revealed through corticostriatal computation, Proceedings of the National Academy of Sciences, 116, 17, 2019. Crossref

  287. Andalman Aaron S., Fee Michale S., A basal ganglia-forebrain circuit in the songbird biases motor output to avoid vocal errors, Proceedings of the National Academy of Sciences, 106, 30, 2009. Crossref

  288. Rainer Gregor, Asaad Wael F., Miller Earl K., Memory fields of neurons in the primate prefrontal cortex, Proceedings of the National Academy of Sciences, 95, 25, 1998. Crossref

  289. Hoshi Eiji, Functional specialization within the dorsolateral prefrontal cortex: A review of anatomical and physiological studies of non-human primates, Neuroscience Research, 54, 2, 2006. Crossref

  290. Kelley Ann E., Neural integrative activities of nucleus accumbens subregions in relation to learning and motivation, Psychobiology, 27, 2, 1999. Crossref

  291. Zelazo Philip David, Müller Ulrich, Executive Function in Typical and Atypical Development, in The Wiley‐Blackwell Handbook of Childhood Cognitive Development, 2010. Crossref

  292. Mizumori Sheri J. Y., Pratt Wayne E., Ragozzino Kay E., Function of the nucleus accumbens within the context of the larger striatal system, Psychobiology, 27, 2, 1999. Crossref

  293. Schaefer Laura V., Dech Silas, Bittmann Frank N., Adaptive Force and emotionally related imaginations – preliminary results suggest a reduction of the maximal holding capacity as reaction to disgusting food imagination, Heliyon, 7, 8, 2021. Crossref

  294. Vaštík Kateřina Menšíková Sandra Kurčová Miroslav, Kaiserová Zuzana Matejčíková Petr Kaňovský Michaela, Functional basal ganglia interconnection, Neurologie pro praxi, 18, 4, 2017. Crossref

  295. Touzani K., Puthanveettil S. V., Kandel E. R., Consolidation of learning strategies during spatial working memory task requires protein synthesis in the prefrontal cortex, Proceedings of the National Academy of Sciences, 104, 13, 2007. Crossref

  296. Gagnon Anthony, Grenier Gabrielle, Bocti Christian, Gillet Virginie, Lepage Jean-François, Baccarelli Andrea A, Posner Jonathan, Descoteaux Maxime, Takser Larissa, White matter microstructural variability linked to differential attentional skills and impulsive behavior in a pediatric population, Cerebral Cortex, 2022. Crossref

  297. Perez-Rando Marta, Guirado Ramón, The Medial Prefrontal Cortex (mPFC) and Addictions, in Handbook of Substance Misuse and Addictions, 2022. Crossref

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