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An intricately patterned prefronto‐caudate projection in the rhesus monkey
Abstract
The distribution of prefronto‐caudate fibers in the caudate nucleus was studied autoradiographically in monkeys of various ages in which tritiated amino acids had been injected into the middle one‐third of the length of the dorsal bank of the principal sulcus. The results indicate that, contrary to previous reports which had suggested a projection to only the head of the caudate nucleus, area 9 of Brodmann projects to the entire length of the nucleus. In the head of the caudate nucleus the cortico‐caudate fibers are distributed in a pattern which is remarkable in two respects. First, the grains are not uniformly distributed but rather are segregated into clusters separated from one another by territories in which grain density does not exceed background. Second, individual clusters of grains, circular or elliptical in shape, surround grain free cores. These patterns of fiber distribution within the head of the nucleus are more sharply defined in newborn than in older monkeys. Our findings suggest that the caudate nucleus is organized more as an anatomic and functional mosaic than as the homogeneously organized structure that it is commonly considered to be.
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Cited by
Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop
Parent, A., & Hazrati, L.-N. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(94)00007-c · Cited by 2,161
(1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62678-3 · Cited by 1,961
Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory
Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960
Sesack, S. R., Deutch, A. Y., Roth, R. H., & Bunney, B. S. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902900205 · Cited by 1,568
Anatomical evidence for cerebellar and basal ganglia involvement in higher cognitive function
Middleton, F. A., & Strick, P. L. (1994) · Science · doi:10.1126/science.7939688 · Cited by 1,356
Schmahmann, J. D., & Pandya, D. N. (2006) · doi:10.1093/acprof:oso/9780195104233.001.0001 · Cited by 1,157
Neuropsychological studies of the frontal lobes.
Stuss, D. T., & Benson, D. F. (1984) · Psychological Bulletin · doi:10.1037/0033-2909.95.1.3 · Cited by 1,073
Haber, S. N. (2016) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2016.18.1/shaber · Cited by 922
Graybiel, A. M., & Ragsdale, C. W. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.11.5723 · Cited by 784
Swerdlow, N. R., & Koob, G. F. (1987) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00047488 · Cited by 674
Development of Cortical Circuitry and Cognitive Function
Goldman-Rakic, P. S. (1987) · Child Development · doi:10.2307/1130201 · Cited by 655
Physiology and pharmacology of striatal neurons
Kreitzer, A. C. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135422 · Cited by 530
Differential Innervation of Direct- and Indirect-Pathway Striatal Projection Neurons
Wall, N. R., De La Parra, M., Callaway, E. M., & Kreitzer, A. C. (2013) · Neuron · doi:10.1016/j.neuron.2013.05.014 · Cited by 489
The nucleus accumbens: a comprehensive review
Salgado, S., & Kaplitt, M. G. (2015) · Stereotactic and Functional Neurosurgery · doi:10.1159/000368279 · Cited by 489
Arnsten, A. F. T. (1996) · Archives of General Psychiatry · doi:10.1001/archpsyc.1996.01830050084013 · Cited by 458
Organization of the nigrothalamocortical system in the rhesus monkey
Ilinsky, I. A., Jouandet, M. L., & Goldman‐Rakic, P. S. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902360304 · Cited by 406
The amygdalostriatal projections in the monkey. An anterograde tracing study
Russchen, F. T., Bakst, I., Amaral, D. G., & Price, J. L. (1985) · Brain Research · doi:10.1016/0006-8993(85)90530-x · Cited by 395
Anatomy of the Prefrontal Cortex
Fuster, J. M. (2008) · The Prefrontal Cortex · doi:10.1016/b978-0-12-373644-4.00002-5 · Cited by 364
Ernst, M., & Fudge, J. L. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.10.009 · Cited by 358
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Yeterian, E. H., & Pandya, D. N. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903120105 · Cited by 351
Levy, R., Friedman, H. R., Davachi, L., & Goldman-Rakic, P. S. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03870.1997 · Cited by 279
Afferent and Efferent Relationships of the Basal Ganglia
Nauta, W. J. H., & Domesick, V. B. (1984) · Novartis Foundation Symposia · doi:10.1002/9780470720882.ch2 · Cited by 272
Self-citationLeichnetz, G. R. (1986) · Journal of Comparative Neurology · doi:10.1002/cne.902540403 · Cited by 234
Lynd-Balta, E., & Haber, S. N. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90182-1 · Cited by 233
Morecraft, R. J., & van Hoesen, G. W. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903370411 · Cited by 203
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Makris, N., Biederman, J., Monuteaux, M. C., & Seidman, L. J. (2009) · Developmental Neuroscience · doi:10.1159/000207492 · Cited by 178
Pan, W. X., Mao, T., & Dudman, J. T. (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00147 · Cited by 150
“It was observed in the earliest tract tracing studies that axons from subregions and lamina of the neocortex were inhomogeneously distributed in the dorsal striatum of rats (Gerfen, 1984) or the caudate–putamen (CPu) of primates (Goldman and Nauta, 1977).”
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Smaers, J. B., Schleicher, A., Zilles, K., & Vinicius, L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009123 · Cited by 81
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DeLong, M. R., & Georgopoulos, A. P. (1981) · Comprehensive Physiology · doi:10.1002/j.2040-4603.1981.tb00859.x · Cited by 1
Metadata
- Authors
- Goldman, P. S., & Nauta, W. J. H.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1977-02
- Volume
- 171
- Issue
- 3
- Pages
- 369-385
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2034577726
- Cited by
- 517
- References
- 0
- FWCI
- 7.51
- Type
- journal article
- Language
- en
- Open access
- closed
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