1970
DOI: 10.1093/brain/93.4.793
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An Anatomical Study of Converging Sensory Pathways Within the Cerebral Cortex of the Monkey

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Cited by 1,612 publications
(684 citation statements)
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“…Thus, it is tempting to conclude that highly complex pyramidal cells in the dorsolateral gPFC is a characteristic of the latter species, which may differ from that in other primates that diverged earlier, such as New World monkeys and the great apes. Alternatively, the apparent species differences may reflect regional variation in neuronal maturation rates (Jacobs and Scheibel, 1993; Jacobs et al, 1995, 1997; Page et al, 2002; Duan et al, 2003; Elston et al, 2009, 2010a,b) or arise through sampling different subsets of projection neurons in the different cortical areas, which have been shown to differ in both their morphology (Schofield et al, 1987; Hallman et al, 1988; Hübener and Bolz, 1988; de Lima et al, 1990; Hübener et al, 1990; Einstein, 1996; Matsubara et al, 1996; Duan et al, 2002; Soloway et al, 2002; Elston and Rosa, 2006) and density (Jones and Powell, 1970; Barbas, 1992; Young, 1992; Pandya and Yeterian, 2000; Petrides, 2000; Collins et al, 2005) in different cortical areas. In either case, the result is consistent with our main conclusion that pyramidal cells develop differently among cortical areas and mature into specialized circuits.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, it is tempting to conclude that highly complex pyramidal cells in the dorsolateral gPFC is a characteristic of the latter species, which may differ from that in other primates that diverged earlier, such as New World monkeys and the great apes. Alternatively, the apparent species differences may reflect regional variation in neuronal maturation rates (Jacobs and Scheibel, 1993; Jacobs et al, 1995, 1997; Page et al, 2002; Duan et al, 2003; Elston et al, 2009, 2010a,b) or arise through sampling different subsets of projection neurons in the different cortical areas, which have been shown to differ in both their morphology (Schofield et al, 1987; Hallman et al, 1988; Hübener and Bolz, 1988; de Lima et al, 1990; Hübener et al, 1990; Einstein, 1996; Matsubara et al, 1996; Duan et al, 2002; Soloway et al, 2002; Elston and Rosa, 2006) and density (Jones and Powell, 1970; Barbas, 1992; Young, 1992; Pandya and Yeterian, 2000; Petrides, 2000; Collins et al, 2005) in different cortical areas. In either case, the result is consistent with our main conclusion that pyramidal cells develop differently among cortical areas and mature into specialized circuits.…”
Section: Discussionmentioning
confidence: 99%
“…Input from the premotor (area 6) cortex reaches both banks of the caudal two-thirds of the principalis and is also preferentially directed to the mid-ventral principalis region, to the same site which receives the somatosensory input. The premotor cortex, with its known reciprocal connections with the motor cortex, 28 -69 may provide a link underlying the execution phase of tasks supported by the principalis cortex. Indeed a distinct class of neurons in the caudalhalf of the principalis fires in association with the motor aspect of a task.…”
Section: Discussionmentioning
confidence: 99%
“…In support of this view was the absence of strong anatomical links between the areas of different modalities at the level of the first stages of sensory processing (see Jones and Powell, 1970). Recent anatomical and electrophysiological studies in non-human primates as well as human functional brain studies led to a reappraisal of this concept (see Ghazanfar and Schroeder, 2006;Driver and Noesselt, 2008 for recent reviews) and highlight that the mechanisms for multisensory interplay are believed to include several levels of brain processing, from the thalamus to the primary sensory areas and higher stages of sensory processing.…”
Section: Introductionmentioning
confidence: 96%