Gregory B. Stanton
Howard University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Gregory B. Stanton.
Neuroscience Letters | 1977
Gregory B. Stanton; William L.R. Cruce; Michael E. Goldberg; David Lee Robinson
Abstract Projections to the inferior parietal lobule were studied by retrograde axonal transport of horseradish peroxidase (HRP). Several cortical and subcortical areas projected to both areas PF and PG including the cingulate and periarcuate cortex, the basal nucleus of Meynert, several intralaminar nuclei of the thalamus, and the ventral lateral thalamic nucleus. However, area PF received afferents from the second somatosensory area of the parietal operculum, the oral pulvinar nucleus, and ventral parts of the medial pulvinar nucleus, whereas area PG received imputs from the banks of the superior temporal and occipitotemporal sulci and from the dorsal parts of the medial pulvinar and lateral posterior nuclei.
Experimental Brain Research | 2005
Gregory B. Stanton; Harriet R. Friedman; Elisa C. Dias; Charles J. Bruce
In primates, the frontal eye field (FEF) contains separate representations of saccadic and smooth-pursuit eye movements. The smooth-pursuit region (FEFsem) in macaque monkeys lies principally in the fundus and deep posterior wall of the arcuate sulcus, between the FEF saccade region (FEFsac) in the anterior wall and somatomotor areas on the posterior wall and convexity. In this study, cortical afferents to FEFsem were mapped by injecting retrograde tracers (WGA-HRP and fast blue) into electrophysiologically identified FEFsem sites in two monkeys. In the frontal lobe, labeled neurons were found mostly on the ipsilateral side in the (1) supplementary eye field region and lateral area F7; (2) area F2 along the superior limb of the arcuate sulcus; and (3) in the buried cortex of the arcuate sulcus extending along the superior and inferior limbs and including FEFsac and adjacent areas 8, 45, and PMv. Labeled cells were also found in the caudal periprincipal cortex (area 46) in one monkey. Labeled cells were found bilaterally in the frontal lobe in the deep posterior walls of the arcuate sulcus and postarcuate spurs and in cingulate motor areas 24 and 24c. In postcentral cortical areas all labeling was ipsilateral and there were two major foci of labeled cells: (1) the depths of the intraparietal sulcus including areas VIP, LIP, and PEa, and (2) the anterior wall and fundus of the superior temporal sulcus including areas PP and MST. Smaller numbers of labeled cells were found in superior temporal sulcal areas FST, MT, and STP, posterior cingulate area 23b, area 3a within the central sulcus, areas SII, RI, Tpt in the lateral sulcus, and parietal areas 7a, 7b, PEc, MIP, DP, and V3A. Many of these posterior afferent cortical areas code visual-motion (MT, MST, and FST) or visual-motion and vestibular (PP, VIP) signals, consistent with the responses of neurons in FEFsem and with the overall physiology and anatomy of the smooth-pursuit eye movement system.
Experimental Brain Research | 1981
Gregory B. Stanton; R. W. Greene
SummarySix injections of HRP were placed in the periabducens reticular formation (PARF). Two were placed ventromedial to the caudal half of the abducend nucleus (VIn), two were placed further laterally and ventral to the rostral half of the nucleus, and two were placed rostral to the nucleus. Most injections in PARF produced cell labeling in the vestibular and perihypoglossal nuclei bilaterally and labeled cells in the reticularis gigantocellularis (Rgc) and reticularis pontis caudalis (Rpc) nuclei contralateral to the injection site. Few labeled neurons were found in the caudal part of the paramedian pontine reticular formation (PPRF). In the mesencephalon, bilateral but more numerous ipsilateral labeled cells were found in the medial mesodiencephalic region including the nuclei of Cajal, Darkschewitsch and the posterior commissure. Injections placed caudomedial to VIn resulted in a characteristic concentration of labeled cells in the ipsilateral nucleus cuneiformis and rostral half of the contralateral superior colliculus (SC). Injections placed rostral to VIn in PARF produced cell labeling in the nucleus campi Foreli. The results are related to physiological evidence which suggests that PARF is an important premotor center for coordination of oculomotor, head and body movements.
The Journal of Comparative Neurology | 2001
Gregory B. Stanton
Axonal projections to the nucleus reticularis tegmenti pontis (RTP) were studied in 11 macaque monkeys by mapping axonal degeneration from lesions centered in the dentate and interpositus anterior (IA) nuclei and by mapping anterograde transport of tritiated amino acid precursors injected into the dentate nucleus. Projections from the dentate and IA nuclei overlap in central parts of the body of RTP, but the terminal field of dentate axons extends dorsomedial and rostral to the terminal field of IA axons, and IA terminal fields extend more ventrolaterally. A caudal to rostral topography of projections from each nucleus onto dorsal to ventral parts of RTP was seen. Projections from rostral parts of both nuclei terminate in a sublemniscal part of the nucleus. The topography of dentate and IA projections onto central to ventrolateral RTP appears to match somatotopic maps of these cerebellar nuclei with the somatotopic map of projections to RTP from primary motor cortex. Projections from caudal and ventral parts of the dentate nucleus appear to overlap oculomotor inputs to rostral, dorsal, and medial RTP from the frontal and supplementary eye fields, the superior colliculus, and the oculomotor region of the caudal fastigial nucleus. Projections to the paramedian part of RTP from vestibular area “y” were also found in two cases that correlated with projections to vertical oculomotor motoneurons. The maps of dentate and IA projections onto RTP correlate predictably with maps of dentate and IA projections to the ventrolateral thalamus and subnuclei of the red nucleus that were made from these same cases (Stanton [1980b] J. Comp. Neurol. 192:377–385). J. Comp. Neurol. 432:169–183, 2001.
The Journal of Comparative Neurology | 1988
Gregory B. Stanton; M. E. Goldberg; C. J. Bruce
The Journal of Comparative Neurology | 1995
Gregory B. Stanton; Charles J. Bruce; M. E. Goldberg
The Journal of Comparative Neurology | 1988
Gregory B. Stanton; M. E. Goldberg; C. J. Bruce
The Journal of Comparative Neurology | 1993
Gregory B. Stanton; Charles J. Bruce; M. E. Goldberg
The Journal of Comparative Neurology | 1989
Gregory B. Stanton; S.-Y. Deng; E. M. Goldberg; Nathaniel T. McMullen
The Journal of Comparative Neurology | 1980
Gregory B. Stanton