Cortico-basal ganglia networks subserving goal-directed behavior mediated by conditional visuo-goal association

Frontiers in Neural Circuits

Volumn 7, Issue OCT, 2013, Pages

  Hoshi, Eiji ^a,b  

^a TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Action; Executive function; Globus pallidus; Goal; Sensorimotor integration; Visuomotor integration

Indexed keywords

ARTICLE; BASAL GANGLION; BRAIN BLOOD FLOW; BRAIN FUNCTION; BRAIN MAPPING; CONCEPTUAL FRAMEWORK; CONDITIONAL VISUO GOAL ASSOCIATION; CORPUS STRIATUM; FUNCTIONAL MAGNETIC RESONANCE IMAGING; FUNCTIONAL NEUROIMAGING; HUMAN; INFORMATION PROCESSING; NERVE CELL NETWORK; NEUROPHYSIOLOGY; NONHUMAN; PERCEPTION; PREFRONTAL CORTEX; PREMOTOR CORTEX; SACCADIC EYE MOVEMENT; SENSORIMOTOR FUNCTION; SENSORIMOTOR INTEGRATION; SIGNAL PROCESSING; SIGNAL TRANSDUCTION; SUBSTANTIA NIGRA PARS RETICULATA; SUBTHALAMIC NUCLEUS; SYNAPSE; VENTROLATERAL PREFRONTAL CORTEX; VISUAL STIMULATION; VISUOMOTOR COORDINATION; VISUOMOTOR INTEGRATION; ACTION; ACTION POTENTIAL; ANIMAL; ANIMAL BEHAVIOR; BRAIN CORTEX; EXECUTIVE FUNCTION; GLOBUS PALLIDUS; GOAL; MOTIVATION; NERVE TRACT; PHYSIOLOGY; PROBLEM SOLVING; PSYCHOMOTOR PERFORMANCE; REVIEW; VISION;

ACTION; EXECUTIVE FUNCTION; GLOBUS PALLIDUS; GOAL; SENSORIMOTOR INTEGRATION; VISUOMOTOR INTEGRATION;

ACTION POTENTIALS; ANIMALS; BASAL GANGLIA; BEHAVIOR, ANIMAL; CEREBRAL CORTEX; EXECUTIVE FUNCTION; GOALS; NEURAL PATHWAYS; PROBLEM SOLVING; PSYCHOMOTOR PERFORMANCE; VISUAL PERCEPTION;

EID: 84886993565     PISSN: 16625110     EISSN: None     Source Type: Journal    
DOI: 10.3389/fncir.2013.00158     Document Type: Article

References (211)

1. Abe, M., and Hanakawa, T. (2009). Functional coupling underlying motor and cognitive functions of the dorsal premotor cortex. Behav. Brain Res. 198, 13-23. doi: 10.1016/j.bbr.2008.10.046
2. Alexander, G. E., and Crutcher, M. D. (1990a). Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci. 13, 266-271. doi: 10.1016/0166-2236(90)90107-L
3. Alexander, G. E., and Crutcher, M. D. (1990b). Neural representations of the target (goal) of visually guided arm movements in three motor areas of the monkey. J. Neurophysiol. 64, 164-178.
4. Alexander, G. E., and Crutcher, M. D. (1990c). Preparation for movement: neural representations of intended direction in three motor areas of the monkey. J. Neurophysiol. 64, 133-150.
5. Alexander, G. E., Delong, M. R., and Strick, P. L. (1986). Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu. Rev. Neurosci. 9, 357-381. doi: 10.1146/annurev.ne.09.030186.002041
6. Amiez, C., Hadj-Bouziane, F., and Petrides, M. (2012). Response selection versus feedback analysis in conditional visuo-motor learning. Neuroimage 59, 3723-3735. doi: 10.1016/j.neuroimage.2011.10.058
7. Amiez, C., Kostopoulos, P., Champod, A. S., and Petrides, M. (2006). Local morphology predicts functional organization of the dorsal premotor region in the human brain. J. Neurosci. 26, 2724-2731. doi: 10.1523/JNEUROSCI.4739-05.2006
8. Antzoulatos, E. G., and Miller, E. K. (2011). Differences between neural activity in prefrontal cortex and striatum during learning of novel abstract categories. Neuron 71, 243-249. doi: 10.1016/j.neuron.2011.05.040
9. Arimura, N., Nakayama, Y., Yamagata, T., Tanji, J., and Hoshi, E. (2013). Involvement of the globus pallidus in behavioral goal determination and action specification. J. Neurosci. 33, 13639-13653. doi: 10.1523/JNEUROSCI.1620-13.2013
10. Asaad, W. F., Rainer, G., and Miller, E. K. (1998). Neural activity in the primate prefrontal cortex during associative learning. Neuron 21, 1399-1407. doi: 10.1016/S0896-6273(00)80658-3
11. Averbeck, B. B., Chafee, M. V., Crowe, D. A., and Georgopoulos, A. P. (2002). Parallel processing of serial movements in prefrontal cortex. Proc. Natl. Acad. Sci. U.S.A. 99, 13172-13177. doi: 10.1073/pnas.162485599
12. Averbeck, B. B., Chafee, M. V., Crowe, D. A., and Georgopoulos, A. P. (2003). Neural activity in prefrontal cortex during copying geometrical shapes. I. Single cells encode shape, sequence, and metric parameters. Exp. Brain Res. 150, 127-141.
13. Barbas, H., and Pandya, D. N. (1987). Architecture and frontal cortical connections of the premotor cortex (area 6) in the rhesus monkey. J. Comp. Neurol. 256, 211-228. doi: 10.1002/cne.902560203
14. Barbas, H., and Pandya, D. N. (1989). Architecture and intrinsic connections of the prefrontal cortex in the rhesus monkey. J. Comp. Neurol. 286, 353-375. doi: 10.1002/cne.902860306
15. Barraclough, D. J., Conroy, M. L., and Lee, D. (2004). Prefrontal cortex and decision making in a mixed-strategy game. Nat. Neurosci. 7, 404-410. doi: 10.1038/nn1209
16. Bastian, A., Schoner, G., and Riehle, A. (2003). Preshaping and continuous evolution of motor cortical representations during movement preparation. Eur. J. Neurosci. 18, 2047-2058. doi: 10.1046/j.1460-9568.2003.02906.x
17. Beurze, S. M., De Lange, F. P., Toni, I., and Medendorp, W. P. (2007). Integration of target and effector information in the human brain during reach planning. J. Neurophysiol. 97, 188-199. doi: 10.1152/jn.00456.2006
18. Boussaoud, D. (2001). Attention versus intention in the primate premotor cortex. Neuroimage 14, S40-S45. doi: 10.1006/nimg.2001.0816
19. Boussaoud, D., and Wise, S. P. (1993a). Primate frontal cortex: effects of stimulus and movement. Exp. Brain Res. 95, 28-40. doi: 10.1007/BF00229651
20. Boussaoud, D., and Wise, S. P. (1993b). Primate frontal cortex: neuronal activity following attentional versus intentional cues. Exp. Brain Res. 95, 15-27. doi: 10.1007/BF00229650
21. Brasted, P. J., and Wise, S. P. (2004). Comparison of learning-related neuronal activity in the dorsal premotor cortex and striatum. Eur. J. Neurosci. 19, 721-740. doi: 10.1111/j.0953-816X.2003.03181.x
22. Brown, V. J., Desimone, R., and Mishkin, M. (1995). Responses of cells in the tail of the caudate nucleus during visual discrimination learning. J. Neurophysiol. 74, 1083-1094.
23. Buckley, M. J., Mansouri, F. A., Hoda, H., Mahboubi, M., Browning, P. G., Kwok, S. C., et al. (2009). Dissociable components of rule-guided behavior depend on distinct medial and prefrontal regions. Science 325, 52-58. doi: 10.1126/science.1172377
24. Bunge, S. A., and Wallis, J. D. (2008). Neuroscience of Rule-Guided Behavior. New York: Oxford University Press.
25. Bunge, S. A., Wallis, J. D., Parker, A., Brass, M., Crone, E. A., Hoshi, E., et al. (2005). Neural circuitry underlying rule use in humans and nonhuman primates. J. Neurosci. 25, 10347-10350. doi: 10.1523/JNEUROSCI.2937-05.2005
26. Buschman, T. J., Denovellis, E. L., Diogo, C., Bullock, D., and Miller, E. K. (2012). Synchronous oscillatory neural ensembles for rules in the prefrontal cortex. Neuron 76, 838-846. doi: 10.1016/j.neuron.2012.09.029
27. Bussey, T. J., Wise, S. P., and Murray, E. A. (2001). The role of ventral and orbital prefrontal cortex in conditional visuomotor learning and strategy use in rhesus monkeys (Macaca mulatta). Behav. Neurosci. 115, 971-982. doi: 10.1037/0735-7044.115.5.971
28. Bussey, T. J., Wise, S. P., and Murray, E. A. (2002). Interaction of ventral and orbital prefrontal cortex with inferotemporal cortex in conditional visuomotor learning. Behav. Neurosci. 116, 703-715. doi: 10.1037/0735-7044.116.4.703
29. Caan, W., Perrett, D. I., and Rolls, E. T. (1984). Responses of striatal neurons in the behaving monkey. 2. Visual processing in the caudal neostriatum. Brain Res. 290, 53-65. doi: 10.1016/0006-8993(84)90735-2
30. Chen, L. L., and Wise, S. P. (1995a). Neuronal activity in the supplementary eye field during acquisition of conditional oculomotor associations. J. Neurophysiol. 73, 1101-1121.
31. Chen, L. L., and Wise, S. P. (1995b). Supplementary eye field contrasted with the frontal eye field during acquisition of conditional oculomotor associations. J. Neurophysiol. 73, 1122-1134.
32. Cheng, K., Saleem, K. S., and Tanaka, K. (1997). Organization of corticostriatal and corticoamygdalar projections arising from the anterior inferotemporal area TE of the macaque monkey: a Phaseolus vulgaris leucoagglutinin study. J. Neurosci. 17, 7902-7925.
33. Cisek, P., and Kalaska, J. F. (2002). Simultaneous encoding of multiple potential reach directions in dorsal premotor cortex. J. Neurophysiol. 87, 1149-1154.
34. Cisek, P., and Kalaska, J. F. (2004). Neural correlates of mental rehearsal in dorsal premotor cortex. Nature 431, 993-996. doi: 10.1038/nature03005
35. Cisek, P., and Kalaska, J. F. (2005). Neural correlates of reaching decisions in dorsal premotor cortex: specification of multiple direction choices and final selection of action. Neuron 45, 801-814. doi: 10.1016/j.neuron.2005.01.027
36. Cisek, P., and Kalaska, J. F. (2010). Neural Mechanisms for Interacting with a world full of action choices. Annu. Rev. Neurosci. 33, 269-298. doi: 10.1146/annurev.neuro.051508.135409
37. Colby, C. L., and Goldberg, M. E. (1999). Space and attention in parietal cortex. Annu. Rev. Neurosci. 22, 319-349. doi: 10.1146/annurev.neuro.22.1.319
38. Crucian, G. P., and Okun, M. S. (2003). Visual-spatial ability in Parkinson's disease. Front. Biosci. 8:s992-s997. doi: 10.2741/1171
39. Diedrichsen, J., Grafton, S., Albert, N., Hazeltine, E., and Ivry, R. B. (2006). Goal-selection and movement-related conflict during bimanual reaching movements. Cereb. Cortex 16, 1729-1738. doi: 10.1093/cercor/bhj108
40. di Pellegrino, G., and Wise, S. P. (1993). Visuospatial versus visuomotor activity in the premotor and prefrontal cortex of a primate. J. Neurosci. 13, 1227-1243.
41. Doya, K. (2000). Complementary roles of basal ganglia and cerebellum in learning and motor control. Curr. Opin. Neurobiol. 10, 732-739. doi: 10.1016/S0959-4388(00)00153-7
42. Dubois, B., and Pillon, B. (1997). Cognitive deficits in Parkinson's disease. J. Neurol. 244, 2-8. doi: 10.1007/PL00007725
43. Eacott, M. J., and Gaffan, D. (1992). Inferotemporal-frontal disconnection: the uncinate fascicle and visual associative learning in monkeys. Eur. J. Neurosci. 4, 1320-1332. doi: 10.1111/j.1460-9568.1992.tb00157.x
44. Everling, S., Tinsley, C. J., Gaffan, D., and Duncan, J. (2002). Filtering of neural signals by focused attention in the monkey prefrontal cortex. Nat. Neurosci. 5, 671-676. doi: 10.1038/nn874
45. Flaherty, A. W., and Graybiel, A. M. (1994). Input-output organization of the sensorimotor striatum in the squirrel monkey. J. Neurosci. 14, 599-610.
46. Freedman, D. J., and Assad, J. A. (2006). Experience-dependent representation of visual categories in parietal cortex. Nature 443, 85-88. doi: 10.1038/nature05078
47. Freedman, D. J., Riesenhuber, M., Poggio, T., and Miller, E. K. (2001). Categorical representation of visual stimuli in the primate prefrontal cortex. Science 291, 312-316. doi: 10.1126/science.291.5502.312
48. Frith, C. D., Friston, K., Liddle, P. F., and Frackowiak, R. S. (1991). Willed action and the prefrontal cortex in man: a study with PET. Proc. Biol. Sci. 244, 241-246. doi: 10.1098/rspb.1991.0077
49. Funahashi, S., Bruce, C. J., and Goldman-Rakic, P. S. (1989). Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex. J. Neurophysiol. 61, 331-349.
50. Funahashi, S., Chafee, M. V., and Goldman-Rakic, P. S. (1993). Prefrontal neuronal activity in rhesus monkeys performing a delayed anti-saccade task. Nature 365, 753-756. doi: 10.1038/365753a0
51. Fuster, J. (2008). The Prefrontal Cortex. London: Academic Press.
52. Galletti, C., Fattori, P., Kutz, D. F., and Battaglini, P. P. (1997). Arm movement-related neurons in the visual area V6A of the macaque superior parietal lobule. Eur. J. Neurosci. 9, 410-413. doi: 10.1111/j.1460-9568.1997.tb01410.x
53. Genovesio, A., Brasted, P. J., Mitz, A. R., and Wise, S. P. (2005). Prefrontal cortex activity related to abstract response strategies. Neuron 47, 307-320. doi: 10.1016/j.neuron.2005.06.006
54. Genovesio, A., Tsujimoto, S., and Wise, S. P. (2012). Encoding goals but not abstract magnitude in the primate prefrontal cortex. Neuron 74, 656-662. doi: 10.1016/j.neuron.2012.02.023
55. Godschalk, M., Lemon, R. N., Nijs, H. G., and Kuypers, H. G. (1981). Behaviour of neurons in monkey peri-arcuate and precentral cortex before and during visually guided arm and hand movements. Exp. Brain Res. 44, 113-116. doi: 10.1007/BF00238755
56. Goel, V., and Grafman, J. (1995). Are the frontal lobes implicated in "planning" functions? Interpreting data from the Tower of Hanoi. Neuropsychologia 33, 623-642. doi: 10.1016/0028-3932(95)90866-P
57. Goldman-Rakic, P. S. (1988). Topography of cognition: parallel distributed networks in primate association cortex. Annu. Rev. Neurosci. 11, 137-156. doi: 10.1146/ annurev.ne.11.030188.001033
58. Goodwin, S. J., Blackman, R. K., Sakellaridi, S., and Chafee, M. V. (2012). Executive control over cognition: stronger and earlier rule-based modulation of spatial category signals in prefrontal cortex relative to parietal cortex. J. Neurosci. 32, 3499-3515. doi: 10.1523/JNEUROSCI.3585-11.2012
59. Grafton, S. T., Fagg, A. H., and Arbib, M. A. (1998). Dorsal premotor cortex and conditional movement selection: A PET functional mapping study. J. Neurophysiol. 79, 1092-1097.
60. Graybiel, A. M. (2008). Habits, rituals, and the evaluative brain. Annu. Rev. Neurosci. 31, 359-387. doi: 10.1146/annurev.neuro.29.051605.112851
61. Graybiel, A. M., Aosaki, T., Flaherty, A. W., and Kimura, M. (1994). The basal ganglia and adaptive motor control. Science 265, 1826-1831. doi: 10.1126/science.8091209
62. Haber, S., Kim, K.-S., Mailly, P., and Calzavara, R. (2006). Reward-related cortical inputs define a large striatal region in primates that interface with associative cortical connections, providing a substrate for incentive-based learning. J. Neurosci. 26, 8368-8376. doi: 10.1523/JNEUROSCI.0271-06.2006
63. Hadj-Bouziane, F., and Boussaoud, D. (2003). Neuronal activity in the monkey striatum during conditional visuomotor learning. Exp. Brain Res. 153, 190-196. doi: 10.1007/s00221-003-1592-4
64. Hahnloser, R. H., Kozhevnikov, A. A., and Fee, M. S. (2002). An ultra-sparse code underlies the generation of neural sequences in a songbird. Nature 419, 65-70. doi: 10.1038/nature00974
65. Halsband, U., and Freund, H. J. (1990). Premotor cortex and conditional motor learning in man. Brain 113(Pt 1), 207-222. doi: 10.1093/brain/113.1.207
66. Halsband, U., and Passingham, R. E. (1982). The role of premotor and parietal cortex in the direction of action. Brain Res. 240, 368-372. doi: 10.1016/0006-8993(82)90239-6
67. Halsband, U., and Passingham, R. E. (1985). Premotor cortex and the conditions for movement in monkeys (Macaca fascicularis). Behav. Brain Res. 18, 269-277. doi: 10.1016/0166-4328(85)90035-X
68. Hanakawa, T., Honda, M., Sawamoto, N., Okada, T., Yonekura, Y., Fukuyama, H., et al. (2002). The role of rostral Brodmann area 6 in mental-operation tasks: an integrative neuroimaging approach. Cereb. Cortex 12, 1157-1170. doi: 10.1093/cercor/12.11.1157
69. Hasegawa, I., Fukushima, T., Ihara, T., and Miyashita, Y. (1998). Callosal window between prefrontal cortices: cognitive interaction to retrieve long-term memory. Science 281, 814-818. doi: 10.1126/science.281.5378.814
70. Haynes, W., and Haber, S. (2013). The organization of prefrontal-subthalamic inputs in primates provides an anatomical substrate for both functional specificity and integration: implications for Basal Ganglia models and deep brain stimulation. J. Neurosci. 33, 4804-4814. doi: 10.1523/ JNEUROSCI.4674-12.2013
71. Hernández, A., Zainos, A., and Romo, R. (2002). Temporal evolution of a decision-making process in medial premotor cortex. Neuron 33, 959-972. doi: 10.1016/S0896-6273(02)00613-X
72. Hikosaka, O., Nakahara, H., Rand, M. K., Sakai, K., Lu, X., Nakamura, K., et al. (1999). Parallel neural networks for learning sequential procedures. Trends Neurosci. 22, 464-471. doi: 10.1016/S0166-2236(99)01439-3
73. Hirabayashi, T., Takeuchi, D., Tamura, K., and Miyashita, Y. (2013a). Functional microcircuit recruited during retrieval of object association memory in monkey perirhinal cortex. Neuron 77, 192-203. doi: 10.1016/j.neuron.2012.10.031
74. Hirabayashi, T., Takeuchi, D., Tamura, K., and Miyashita, Y. (2013b). Microcircuits for hierarchical elaboration of object coding across primate temporal areas. Science 341, 191-195. doi: 10.1126/science.1236927
75. Hollerman, J. R., Tremblay, L., and Schultz, W. (2000). Involvement of basal ganglia and orbitofrontal cortex in goal-directed behavior. Prog. Brain Res. 126, 193-215. doi: 10.1016/S0079-6123(00)26015-9
76. Hoshi, E., Shima, K., and Tanji, J. (1998). Task-dependent selectivity of movement-related neuronal activity in the primate prefrontal cortex. J. Neurophysiol. 80, 3392-3397.
77. Hoshi, E., Shima, K., and Tanji, J. (2000). Neuronal activity in the primate prefrontal cortex in the process of motor selection based on two behavioral rules. J. Neurophysiol. 83, 2355-2373.
78. Hoshi, E., and Tanji, J. (2000). Integration of target and body-part information in the premotor cortex when planning action. Nature 408, 466-470. doi: 10.1038/35044075
79. Hoshi, E., and Tanji, J. (2002). Contrasting neuronal activity in the dorsal and ventral premotor areas during preparation to reach. J. Neurophysiol. 87, 1123-1128.
80. Hoshi, E., and Tanji, J. (2004a). Area-selective neuronal activity in the dorsolateral prefrontal cortex for information retrieval and action planning. J. Neurophysiol. 91, 2707-2722. doi: 10.1152/jn.00904.2003
81. Hoshi, E., and Tanji, J. (2004b). Differential roles of neuronal activity in the supplementary and presupplementary motor areas: from information retrieval to motor planning and execution. J. Neurophysiol. 92, 3482-3499. doi: 10.1152/jn.00547.2004
82. Hoshi, E., and Tanji, J. (2006). Differential involvement of neurons in the dorsal and ventral premotor cortex during processing of visual signals for action planning. J. Neurophysiol. 95, 3596-3616. doi: 10.1152/jn.01126.2005
83. Hoshi, E., and Tanji, J. (2007). Distinctions between dorsal and ventral premotor areas: anatomical connectivity and functional properties. Curr. Opin. Neurobiol. 17, 234-242. doi: 10.1016/j.conb.2007.02.003
84. Houk, J. C., and Wise, S. P. (1995). Distributed modular architectures linking basal ganglia, cerebellum, and cerebral cortex: their role in planning and controlling action. Cereb. Cortex 5, 95-110. doi: 10.1093/cercor/5.2.95
85. Huerta, M. F., and Kaas, J. H. (1990). Supplementary eye field as defined by intracortical microstimulation: connections in macaques. J. Comp. Neurol. 293, 299-330. doi: 10.1002/cne.902930211
86. Hussar, C. R., and Pasternak, T. (2009). Flexibility of sensory representations in prefrontal cortex depends on cell type. Neuron 64, 730-743. doi: 10.1016/j.neuron.2009.11.018
87. Inase, M., Li, B. M., Takashima, I., and Iijima, T. (2001). Pallidal activity is involved in visuomotor association learning in monkeys. Eur. J. Neurosci. 14, 897-901. doi: 10.1046/j.0953-816x.2001.01701.x
88. Inase, M., and Tanji, J. (1994). Projections from the globus pallidus to the thalamic areas projecting to the dorsal area 6 of the macaque monkey: a multiple tracing study. Neurosci. Lett. 180, 135-137. doi: 10.1016/0304-3940(94)90505-3
89. Johnson, P. B., Ferraina, S., and Caminiti, R. (1993). Cortical networks for visual reaching. Exp. Brain Res. 97, 361-365. doi: 10.1007/BF00228707
90. Kalaska, J. F., Sergio, L. E., and Cisek, P. (1998). Cortical control of whole-arm motor tasks. Novartis Found. Symp. 218, 176-190.
91. Kamigaki, T., Fukushima, T., and Miyashita, Y. (2009). Cognitive set reconfiguration signaled by macaque posterior parietal neurons. Neuron 61, 941-951. doi: 10.1016/j.neuron.2009.01.028
92. Kim, J. N., and Shadlen, M. N. (1999). Neural correlates of a decision in the dorsolateral prefrontal cortex of the macaque. Nat. Neurosci. 2, 176-185. doi: 10.1038/5739
93. Konishi, S., Nakajima, K., Uchida, I., Kameyama, M., Nakahara, K., Sekihara, K., et al. (1998). Transient activation of inferior prefrontal cortex during cognitive set shifting. Nat. Neurosci. 1, 80-84. doi: 10.1038/283
94. Kurata, K. (1993). Premotor cortex of monkeys: set-and movement-related activity reflecting amplitude and direction of wrist movements. J. Neurophysiol. 69, 187-200.
95. Kurata, K., and Hoffman, D. S. (1994). Differential effects of muscimol microinjection into dorsal and ventral aspects of the premotor cortex of monkeys. J. Neurophysiol. 71, 1151-1164.
96. Kurata, K., and Wise, S. P. (1988). Premotor cortex of rhesus monkeys: set-related activity during two conditional motor tasks. Exp. Brain Res. 69, 327-343. doi: 10.1007/BF00247578
97. Lebedev, M. A., and Wise, S. P. (2001). Tuning for the orientation of spatial attention in dorsal premotor cortex. Eur. J. Neurosci. 13, 1002-1008. doi: 10.1046/j.0953-816x.2001.01457.x
98. Lee, D., Seo, H., and Jung, M. W. (2012). Neural basis of reinforcement learning and decision making. Annu. Rev. Neurosci. 35, 287-308. doi: 10.1146/annurev-neuro-062111-150512
99. Lu, M. T., Preston, J. B., and Strick, P. L. (1994). Interconnections between the prefrontal cortex and the premotor areas in the frontal lobe. J. Comp. Neurol. 341, 375-392. doi: 10.1002/cne.903410308
100. Luk, C. H., and Wallis, J. D. (2013). Choice coding in frontal cortex during stimulus-guided or action-guided decision-making. J. Neurosci. 33, 1864-1871. doi: 10.1523/JNEUROSCI.4920-12.2013
101. Luppino, G., Matelli, M., Camarda, R., and Rizzolatti, G. (1993). Corticocortical connections of area F3 (SMA-proper) and area F6 (pre-SMA) in the macaque monkey. J. Comp. Neurol. 338, 114-140. doi: 10.1002/cne.903380109
102. Luppino, G., Rozzi, S., Calzavara, R., and Matelli, M. (2003). Prefrontal and agranular cingulate projections to the dorsal premotor areas F2 and F7 in the macaque monkey. Eur. J. Neurosci. 17, 559-578. doi: 10.1046/j.1460-9568.2003.02476.x
103. Luria, A. R. (1966). Higher Cortical Functions in Man. New York: Basic Book.
104. Mann, S. E., Thau, R., and Schiller, P. H. (1988). Conditional task-related responses in monkey dorsomedial frontal cortex. Exp. Brain Res. 69, 460-468. doi: 10.1007/BF00247300
105. Mansouri, F. A., Buckley, M. J., and Tanaka, K. (2007). Mnemonic function of the dorsolateral prefrontal cortex in conflict-induced behavioral adjustment. Science 318, 987-990. doi: 10.1126/science.1146384
106. Marsden, C. D. (1982). The mysterious motor function of the basal ganglia: the Robert Wartenberg Lecture. Neurology 32, 514-539. doi: 10.1212/WNL.32.5.514
107. Matelli, M., Govoni, P., Galletti, C., Kutz, D. F., and Luppino, G. (1998). Superior area 6 afferents from the superior parietal lobule in the macaque monkey. J. Comp. Neurol. 402, 327-352. doi: 10.1002/(SICI)1096-9861(19981221)402:3<327::AID-CNE4>3.0.CO;2-Z
108. Matelli, M., Luppino, G., and Rizzolatti, G. (1985). Patterns of cytochrome oxidase activity in the frontal agranular cortex of the macaque monkey. Behav. Brain Res. 18, 125-136. doi: 10.1016/0166-4328(85)90068-3
109. Matsumoto, K., Suzuki, W., and Tanaka, K. (2003). Neuronal correlates of goal-based motor selection in the prefrontal cortex. Science 301, 229-232. doi: 10.1126/science.1084204
110. Matsuzaka, Y., Aizawa, H., and Tanji, J. (1992). A motor area rostral to the supplementary motor area (presupplementary motor area) in the monkey: neuronal activity during a learned motor task. J. Neurophysiol. 68, 653-662.
111. Matsuzaka, Y., and Tanji, J. (1996). Changing directions of forthcoming arm movements: neuronal activity in the presupplementary and supplementary motor area of monkey cerebral cortex. J. Neurophysiol. 76, 2327-2342.
112. Mendez, M. F., Adams, N. L., and Lewandowski, K. S. (1989). Neurobehavioral changes associated with caudate lesions. Neurology 39, 349-354. doi: 10.1212/WNL.39.3.349
113. Meyers, E. M., Qi, X. L., and Constantinidis, C. (2012). Incorporation of new information into prefrontal cortical activity after learning working memory tasks. Proc. Natl. Acad. Sci. U.S.A. 109, 4651-4656. doi: 10.1073/pnas.1201022109
114. Middleton, F. A., and Strick, P. L. (1994). Anatomical evidence for cerebellar and basal ganglia involvement in higher cognitive function. Science 266, 458-461. doi: 10.1126/science.7939688
115. Middleton, F. A., and Strick, P. L. (2000). Basal ganglia and cerebellar loops: motor and cognitive circuits. Brain Res. Brain Res. Rev. 31, 236-250. doi: 10.1016/S0165-0173(99)00040-5
116. Miller, E. K. (2000). The prefrontal cortex and cognitive control. Nat. Rev. Neurosci. 1, 59-65. doi: 10.1038/35036228
117. Miller, E. K., and Cohen, J. D. (2001). An integrative theory of prefrontal cortex function. Annu. Rev. Neurosci. 24, 167-202. doi: 10.1146/annurev.neuro.24.1.167
118. Milner, B. (1963). Effects of different brain lesions on card sorting. Arch. Neurol. 9, 90-100. doi: 10.1001/archneur.1963.00460070100010
119. Mink, J. W. (1996). The basal ganglia: focused selection and inhibition of competing motor programs. Prog. Neurobiol. 50, 381-425. doi: 10.1016/S0301-0082(96)00042-1
120. Mitchell, S. J., Richardson, R. T., Baker, F. H., and Delong, M. R. (1987). The primate globus pallidus: neuronal activity related to direction of movement. Exp. Brain Res. 68, 491-505. doi: 10.1007/BF00249793
121. Mitz, A. R., Godschalk, M., and Wise, S. P. (1991). Learning-dependent neuronal activity in the premotor cortex: activity during the acquisition of conditional motor associations. J. Neurosci. 11, 1855-1872.
122. Morecraft, R., Stilwell-Morecraft, K., Cipolloni, P., Ge, J., Mcneal, D., and Pandya, D. (2012). Cytoarchitecture and cortical connections of the anterior cingulate and adjacent somatomotor fields in the rhesus monkey. Brain Res. Bull. 87, 457-497. doi: 10.1016/j.brainresbull.2011.12.005
123. Muhammad, R., Wallis, J. D., and Miller, E. K. (2006). A comparison of abstract rules in the prefrontal cortex, premotor cortex, inferior temporal cortex, and striatum. J. Cogn. Neurosci. 18, 974-989. doi: 10.1162/jocn.2006.18.6.974
124. Murray, E. A., Bussey, T. J., and Wise, S. P. (2000). Role of prefrontal cortex in a network for arbitrary visuomotor mapping. Exp. Brain Res. 133, 114-129. doi: 10.1007/s002210000406
125. Mushiake, H., Saito, N., Sakamoto, K., Itoyama, Y., and Tanji, J. (2006). Activity in the lateral prefrontal cortex reflects multiple steps of future events in action plans. Neuron 50, 631-641. doi: 10.1016/j.neuron.2006.03.045
126. Nakayama, Y., Yamagata, T., Tanji, J., and Hoshi, E. (2008). Transformation of a virtual action plan into a motor plan in the premotor cortex. J. Neurosci. 28, 10287-10297. doi: 10.1523/JNEUROSCI.2372-08.2008
127. Nambu, A., Tokuno, H., Inase, M., and Takada, M. (1997). Corticosubthalamic input zones from forelimb representations of the dorsal and ventral divisions of the premotor cortex in the macaque monkey: comparison with the input zones from the primary motor cortex and the supplementary motor area. Neurosci. Lett. 239, 13-16. doi: 10.1016/S0304-3940(97)00877-X
128. Nambu, A., Tokuno, H., and Takada, M. (2002). Functional significance of the cortico-subthalamo-pallidal 'hyperdirect' pathway. Neurosci. Res. 43, 111-117. doi: 10.1016/S0168-0102(02)00027-5
129. Naya, Y., Yoshida, M., and Miyashita, Y. (2001). Backward spreading of memory-retrieval signal in the primate temporal cortex. Science 291, 661-664. doi: 10.1126/science.291.5504.661
130. Nieder, A., Freedman, D. J., and Miller, E. K. (2002). Representation of the quantity of visual items in the primate prefrontal cortex. Science 297, 1708-1711. doi: 10.1126/science.1072493
131. Nixon, P. D., Mcdonald, K. R., Gough, P. M., Alexander, I. H., and Passingham, R. E. (2004). Cortico-basal ganglia pathways are essential for the recall of well-established visuomotor associations. Eur. J. Neurosci. 20, 3165-3178. doi: 10.1111/j.1460-9568.2004.03788.x
132. Olshausen, B. A., and Field, D. J. (2004). Sparse coding of sensory inputs. Curr. Opin. Neurobiol. 14, 481-487. doi: 10.1016/j.conb.2004.07.007
133. Olson, C. R., and Tremblay, L. (2000). Macaque supplementary eye field neurons encode object-centered locations relative to both continuous and discontinuous objects. J. Neurophysiol. 83, 2392-2411.
134. Ongur, D., and Price, J. L. (2000). The organization of networks within the orbital and medial prefrontal cortex of rats, monkeys and humans. Cereb. Cortex 10, 206-219. doi: 10.1093/cercor/10.3.206
135. Orban, G. A. (2008). Higher order visual processing in macaque extrastriate cortex. Physiol. Rev. 88, 59-89. doi: 10.1152/physrev.00008.2007
136. O'Scalaidhe, S. P., Wilson, F. A., and Goldman-Rakic, P. S. (1997). Areal segregation of face-processing neurons in prefrontal cortex. Science 278, 1135-1138. doi: 10.1126/science.278.5340.1135
137. O'Scalaidhe, S. P., Wilson, F. A., and Goldman-Rakic, P. S. (1999). Face-selective neurons during passive viewing and working memory performance of rhesus monkeys: evidence for intrinsic specialization of neuronal coding. Cereb. Cortex 9, 459-475. doi: 10.1093/cercor/9.5.459
138. Packard, M. G., and Knowlton, B. J. (2002). Learning and memory functions of the Basal Ganglia. Annu. Rev. Neurosci. 25, 563-593. doi: 10.1146/annurev.neuro.25.112701.142937
139. Passingham, R., and Wise, S. P. (2012). The Neurobiology of the Prefrontal Cortex: Anatomy, Evolution, and the Origin of Insight. Oxford: Oxford University Press.
140. Passingham, R. E. (1993). The Frontal Lobes and Voluntary Action. Oxford: Oxford University Press.
141. Pasupathy, A., and Miller, E. K. (2005). Different time courses of learning-related activity in the prefrontal cortex and striatum. Nature 433, 873-876. doi: 10.1038/nature03287
142. Pesaran, B., Nelson, M. J., and Andersen, R. A. (2008). Free choice activates a decision circuit between frontal and parietal cortex. Nature 453, 406-409. doi: 10.1038/nature06849
143. Petrides, M. (1982). Motor conditional associative-learning after selective prefrontal lesions in the monkey. Behav. Brain Res. 5, 407-413. doi: 10.1016/0166-4328(82)90044-4
144. Petrides, M. (1986). The effect of periarcuate lesions in the monkey on the performance of symmetrically and asymmetrically reinforced visual and auditory go, no-go tasks. J. Neurosci. 6, 2054-2063.
145. Petrides, M., and Pandya, D. N. (1999). Dorsolateral prefrontal cortex: comparative cytoarchitectonic analysis in the human and the macaque brain and corticocortical connection patterns. Eur. J. Neurosci. 11, 1011-1036. doi: 10.1046/j.1460-9568.1999.00518.x
146. Petrides, M., and Pandya, D. N. (2002). Comparative cytoarchitectonic analysis of the human and the macaque ventrolateral prefrontal cortex and corticocortical connection patterns in the monkey. Eur. J. Neurosci. 16, 291-310. doi: 10.1046/j.1460-9568.2001.02090.x
147. Picard, N., and Strick, P. L. (2001). Imaging the premotor areas. Curr. Opin. Neurobiol. 11, 663-672. doi: 10.1016/S0959-4388(01)00266-5
148. Rainer, G., Asaad, W. F., and Miller, E. K. (1998). Selective representation of relevant information by neurons in the primate prefrontal cortex. Nature 393, 577-579. doi: 10.1038/31235
149. Rainer, G., Rao, S. C., and Miller, E. K. (1999). Prospective coding for objects in primate prefrontal cortex. J. Neurosci. 19, 5493-5505.
150. Riehle, A., and Requin, J. (1989). Monkey primary motor and premotor cortex: single-cell activity related to prior information about direction and extent of an intended movement. J. Neurophysiol. 61, 534-549.
151. Rizzolatti, G., and Luppino, G. (2001). The cortical motor system. Neuron 31, 889-901. doi: 10.1016/S0896-6273(01)00423-8
152. Rowe, J. B., Toni, I., Josephs, O., Frackowiak, R. S., and Passingham, R. E. (2000). The prefrontal cortex: response selection or maintenance within working memory? Science 288, 1656-1660. doi: 10.1126/science.288.5471.1656
153. Rozzi, S., Calzavara, R., Belmalih, A., Borra, E., Gregoriou, G. G., Matelli, M., et al. (2006). Cortical connections of the inferior parietal cortical convexity of the macaque monkey. Cereb. Cortex 16, 1389-1417. doi: 10.1093/cercor/bhj076
154. Rushworth, M. F., Buckley, M. J., Gough, P. M., Alexander, I. H., Kyriazis, D., Mcdonald, K. R., et al. (2005). Attentional selection and action selection in the ventral and orbital prefrontal cortex. J. Neurosci. 25, 11628-11636. doi: 10.1523/JNEUROSCI.2765-05.2005
155. Rushworth, M. F., Nixon, P. D., Eacott, M. J., and Passingham, R. E. (1997). Ventral prefrontal cortex is not essential for working memory. J. Neurosci. 17, 4829-4838.
156. Saga, Y., Hashimoto, M., Tremblay, L., Tanji, J., and Hoshi, E. (2013). Representation of spatial-and object-specific behavioral goals in the dorsal globus pallidus of monkeys during reaching movement. J. Neurosci. 33, 16360-16371. doi: 10.1523/JNEUROSCI.1187-13.2013
157. Saga, Y., Hirata, Y., Takahara, D., Inoue, K., Miyachi, S., Nambu, A., et al. (2011). Origins of multisynaptic projections from the basal ganglia to rostrocaudally distinct sectors of the dorsal premotor area in macaques. Eur. J. Neurosci. 33, 285-297. doi: 10.1111/j.1460-9568.2010.07492.x
158. Saint-Cyr, J. A., Ungerleider, L. G., and Desimone, R. (1990). Organization of visual cortical inputs to the striatum and subsequent outputs to the pallido-nigral complex in the monkey. J. Comp. Neurol. 298, 129-156. doi: 10.1002/cne.902980202
159. Saito, N., Mushiake, H., Sakamoto, K., Itoyama, Y., and Tanji, J. (2005). Representation of immediate and final behavioral goals in the monkey prefrontal cortex during an instructed delay period. Cereb. Cortex 15, 1535-1546. doi: 10.1093/cercor/bhi032
160. Sakagami, M., and Pan, X. (2007). Functional role of the ventrolateral prefrontal cortex in decision making. Curr. Opin. Neurobiol. 17, 228-233. doi: 10.1016/j.conb.2007.02.008
161. Sakai, K. (2008). Task set and prefrontal cortex. Annu. Rev. Neurosci. 31, 219-245. doi: 10.1146/annurev.neuro.31.060407.125642
162. Sakai, K., Hikosaka, O., Miyauchi, S., Sasaki, Y., Fujimaki, N., and Putz, B. (1999). Presupplementary motor area activation during sequence learning reflects visuo-motor association. J. Neurosci. 19, RC1.
163. Sakai, K., and Miyashita, Y. (1991). Neural organization for the long-term memory of paired associates. Nature 354, 152-155. doi: 10.1038/354152a0
164. Samejima, K., Ueda, Y., Doya, K., and Kimura, M. (2005). Representation of action-specific reward values in the striatum. Science 310, 1337-1340. doi: 10.1126/science.1115270
165. Schall, J. D. (2001). Neural basis of deciding, choosing and acting. Nat. Rev. Neurosci. 2, 33-42. doi: 10.1038/35049054
166. Schall, J. D., Morel, A., King, D. J., and Bullier, J. (1995). Topography of visual cortex connections with frontal eye field in macaque: convergence and segregation of processing streams. J. Neurosci. 15, 4464-4487.
167. Schlag, J., and Schlag, R. M. (1987). Evidence for a supplementary eye field. J. Neurophysiol. 57, 179-200.
168. Schluter, N. D., Rushworth, M. F., Passingham, R. E., and Mills, K. R. (1998). Temporary interference in human lateral premotor cortex suggests dominance for the selection of movements. A study using transcranial magnetic stimulation. Brain 121(Pt 5), 785-799. doi: 10.1093/brain/121.5.785
169. Schultz, W., Dayan, P., and Montague, P. R. (1997). A neural substrate of prediction and reward. Science 275, 1593-1599. doi: 10.1126/science.275.5306.1593
170. Selemon, L. D., and Goldman-Rakic, P. S. (1985). Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey. J. Neurosci. 5, 776-794.
171. Seo, M., Lee, E., and Averbeck, B. B. (2012). Action selection and action value in frontal-striatal circuits. Neuron 74, 947-960. doi: 10.1016/j.neuron.2012.03.037
172. Serrien, D. J., Ivry, R. B., and Swinnen, S. P. (2007). The missing link between action and cognition. Prog. Neurobiol. 82, 95-107. doi: 10.1016/j.pneurobio.2007.02.003
173. Shallice, T. (1982). Specific impairments of planning. Philos. Trans. R. Soc. Lond. B Biol. Sci. 298, 199-209. doi: 10.1098/rstb.1982.0082
174. Snyder, L. H., Batista, A. P., and Andersen, R. A. (1997). Coding of intention in the posterior parietal cortex. Nature 386, 167-170. doi: 10.1038/386167a0
175. Stoet, G., and Snyder, L. H. (2004). Single neurons in posterior parietal cortex of monkeys encode cognitive set. Neuron 42, 1003-1012. doi: 10.1016/j.neuron.2004.06.003
176. Swaminathan, S. K., and Freedman, D. J. (2012). Preferential encoding of visual categories in parietal cortex compared with prefrontal cortex. Nat. Neurosci. 15, 315-320. doi: 10.1038/nn.3016
177. Tachibana, Y., Nambu, A., Hatanaka, N., Miyachi, S., and Takada, M. (2004). Input-output organization of the rostral part of the dorsal premotor cortex, with special reference to its corticostriatal projection. Neurosci. Res. 48, 45-57. doi: 10.1016/j.neures.2003.09.006
178. Takada, M., Tokuno, H., Nambu, A., and Inase, M. (1998). Corticostriatal projections from the somatic motor areas of the frontal cortex in the macaque monkey: segregation versus overlap of input zones from the primary motor cortex, the supplementary motor area, and the premotor cortex. Exp. Brain Res. 120, 114-128. doi: 10.1007/s002210050384
179. Takahara, D., Inoue, K., Hirata, Y., Miyachi, S., Nambu, A., Takada, M., et al. (2012). Multisynaptic projections from the ventrolateral prefrontal cortex to the dorsal premotor cortex in macaques-anatomical substrate for conditional visuomotor behavior. Eur. J. Neurosci. 36, 3365-3375. doi: 10.1111/j.1460-9568.2012.08251.x
180. Takeda, K., and Funahashi, S. (2002). Prefrontal task-related activity representing visual cue location or saccade direction in spatial working memory tasks. J. Neurophysiol. 87, 567-588.
181. Tanaka, K. (1996). Inferotemporal cortex and object vision. Annu. Rev. Neurosci. 19, 109-139. doi: 10.1146/annurev.ne.19.030196.000545
182. Tanji, J., and Hoshi, E. (2001). Behavioral planning in the prefrontal cortex. Curr. Opin. Neurobiol. 11, 164-170. doi: 10.1016/S0959-4388(00)00192-6
183. Tanji, J., and Hoshi, E. (2008). Role of the lateral prefrontal cortex in executive behavioral control. Physiol. Rev. 88, 37-57. doi: 10.1152/physrev.00014.2007
184. Toni, I., Rowe, J., Stephan, K. E., and Passingham, R. E. (2002). Changes of cortico-striatal effective connectivity during visuomotor learning. Cereb. Cortex 12, 1040-1047. doi: 10.1093/cercor/12.10.1040
185. Toni, I., Rushworth, M. F., and Passingham, R. E. (2001). Neural correlates of visuomotor associations. Spatial rules compared with arbitrary rules. Exp. Brain Res. 141, 359-369. doi: 10.1007/s002210100877
186. Tremblay, L., Gettner, S. N., and Olson, C. R. (2002). Neurons with object-centered spatial selectivity in macaque SEF: do they represent locations or rules? J. Neurophysiol. 87, 333-350.
187. Tsujimoto, S., Genovesio, A., and Wise, S. P. (2009). Monkey orbitofrontal cortex encodes response choices near feedback time. J. Neurosci. 29, 2569-2574. doi: 10.1523/JNEUROSCI.5777-08.2009
188. Tsujimoto, S., Genovesio, A., and Wise, S. P. (2010). Evaluating self-generated decisions in frontal pole cortex of monkeys. Nat. Neurosci. 13, 120-126. doi: 10.1038/nn.2453
189. Tsujimoto, S., Genovesio, A., and Wise, S. P. (2011). Comparison of strategy signals in the dorsolateral and orbital prefrontal cortex. J. Neurosci. 31, 4583-4592. doi: 10.1523/JNEUROSCI.5816-10.2011
190. Uc, E. Y., Rizzo, M., Anderson, S. W., Qian, S., Rodnitzky, R. L., and Dawson, J. D. (2005). Visual dysfunction in Parkinson disease without dementia. Neurology 65, 1907-1913. doi: 10.1212/01.wnl.0000191565.11065.11
191. Ungerleider, L. G., Mishkin, M., Ingle, D. J., Goodale, M. A., and Mansfield, R. J. W. (1982). "Two cortical visual systems, " in Analysis of Visual Behavior, eds D. J. Ingle, M. A. Goodale, and R. J. W. Mansfield (Cambridge: MIT press), 549-586.
192. Wallis, J. D., Anderson, K. C., and Miller, E. K. (2001). Single neurons in prefrontal cortex encode abstract rules. Nature 411, 953-956. doi: 10.1038/35082081
193. Wallis, J. D., and Miller, E. K. (2003). From rule to response: neuronal processes in the premotor and prefrontal cortex. J. Neurophysiol. 90, 1790-1806. doi: 10.1152/jn.00086.2003
194. Wang, M., Zhang, H., and Li, B. M. (2000). Deficit in conditional visuomotor learning by local infusion of bicuculline into the ventral prefrontal cortex in monkeys. Eur. J. Neurosci. 12, 3787-3796. doi: 10.1046/j.1460-9568.2000.00238.x
195. Webster, M. J., Bachevalier, J., and Ungerleider, L. G. (1993). Subcortical connections of inferior temporal areas TE and TEO in macaque monkeys. J. Comp. Neurol. 335, 73-91. doi: 10.1002/cne.903350106
196. Webster, M. J., Bachevalier, J., and Ungerleider, L. G. (1994). Connections of inferior temporal areas TEO and TE with parietal and frontal cortex in macaque monkeys. Cereb. Cortex 4, 470-483. doi: 10.1093/cercor/4.5.470
197. Weinrich, M., and Wise, S. P. (1982). The premotor cortex of the monkey. J. Neurosci. 2, 1329-1345.
198. Weinrich, M., Wise, S. P., and Mauritz, K. H. (1984). A neurophysiological study of the premotor cortex in the rhesus monkey. Brain 107 (Pt 2), 385-414. doi: 10.1093/brain/107.2.385
199. White, I. M., and Wise, S. P. (1999). Rule-dependent neuronal activity in the prefrontal cortex. Exp. Brain Res. 126, 315-335. doi: 10.1007/s002210050740
200. Wilson, F. A., Scalaidhe, S. P., and Goldman-Rakic, P. S. (1993). Dissociation of object and spatial processing domains in primate prefrontal cortex. Science 260, 1955-1958. doi: 10.1126/science.8316836
201. Wise, S. P., Boussaoud, D., Johnson, P. B., and Caminiti, R. (1997). Premotor and parietal cortex: corticocortical connectivity and combinatorial computations. Annu. Rev. Neurosci. 20, 25-42. doi: 10.1146/annurev.neuro.20.1.25
202. Wise, S. P., and Mauritz, K. H. (1985). Set-related neuronal activity in the premotor cortex of rhesus monkeys: effects of changes in motor set. Proc. R. Soc. Lond. B Biol. Sci. 223, 331-354. doi: 10.1098/rspb.1985.0005
203. Wise, S. P., and Murray, E. A. (2000). Arbitrary associations between antecedents and actions. Trends Neurosci. 23, 271-276. doi: 10.1016/S0166-2236(00)01570-8
204. Wise, S. P., Murray, E. A., and Gerfen, C. R. (1996). The frontal cortex-basal ganglia system in primates. Crit. Rev. Neurobiol. 10, 317-356. doi: 10.1615/CritRevNeurobiol.v10.i3-4.30
205. Wise, S. P., Weinrich, M., and Mauritz, K. H. (1983). Motor aspects of cue-related neuronal activity in premotor cortex of the rhesus monkey. Brain Res. 260, 301-305. doi: 10.1016/0006-8993(83)90685-6
206. Yamagata, T., Nakayama, Y., Tanji, J., and Hoshi, E. (2009). Processing of visual signals for direct specification of motor targets and for conceptual representation of action targets in the dorsal and ventral premotor cortex. J. Neurophysiol. 102, 3280-3294. doi: 10.1152/jn.00452.2009
207. Yamagata, T., Nakayama, Y., Tanji, J., and Hoshi, E. (2012). Distinct information representation and processing for goal-directed behavior in the dorsolateral and ventrolateral prefrontal cortex and the dorsal premotor cortex. J. Neurosci. 32, 12934-12949. doi: 10.1523/JNEUROSCI.2398-12.2012
208. Yamamoto, S., Kim, H. F., and Hikosaka, O. (2013). Reward value-contingent changes of visual responses in the primate caudate tail associated with a visuomotor skill. J. Neurosci. 33, 11227-11238. doi: 10.1523/JNEUROSCI.0318-13.2013
209. Yamamoto, S., Monosov, I. E., Yasuda, M., and Hikosaka, O. (2012). What and where information in the caudate tail guides saccades to visual objects. J. Neurosci. 32, 11005-11016. doi: 10.1523/JNEUROSCI.0828-12.2012
210. Yasuda, M., Yamamoto, S., and Hikosaka, O. (2012). Robust representation of stable object values in the oculomotor Basal Ganglia. J. Neurosci. 32, 16917-16932. doi: 10.1523/JNEUROSCI.3438-12.2012
211. Yoshida, A., and Tanaka, M. (2009). Enhanced modulation of neuronal activity during antisaccades in the primate globus pallidus. Cereb. Cortex 19, 206-217. doi: 10.1093/cercor/bhn069