Cited by 1,602Visual perception and processing mechanismsMotor Control and AdaptationFace Recognition and Perception

The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.

The connections of the middle temporal visual area (MT) and their relationship to a cortical hierarchy in the macaque monkey

Open access

Maunsell, JH, van Essen, DC·1983·The Journal of Neuroscience

DOI 10.1523/jneurosci.03-12-02563.1983PMC PMC6564662

Open this paper in CoChat — free account Open PDF

Abstract

The cortical and subcortical connections of the middle temporal visual area (MT) of the macaque monkey were investigated using combined injections of [3H]proline and horseradish peroxidase within MT. Cortical connections were assigned to specific visual areas on the basis of their relationship to the pattern of interhemispheric connections, revealed by staining for degeneration following callosal transection. MT was shown to be reciprocally connected with many topographically organized cortical visual areas, including V1, V2, V3, and V4. These pathways link regions representing corresponding portions of the visual field in the different areas. In addition, MT has reciprocal connections with two previously unidentified cortical areas, which we have designated the medial superior temporal area (MST) and the ventral intraparietal area (VIP). The laminar distribution of terminals and cell bodies in cortical areas connected with MT follows a consistent pattern. In areas V1, V2, and V3, the projections to MT arise largely or exclusively from cells in supragranular layers, and the reciprocal connections from MT terminate mainly in supragranular and infragranular layers. In contrast, the projections to MST and VIP terminate mainly in layer IV, and the reciprocal pathways originate from cells in both superficial and deep layers. On the basis of this pattern, each connection can be designated as forward or feedback in nature, and a hierarchical arrangement of visual areas can be determined. In this hierarchy, MT is at a higher level than V1, V2, and V3, and at a lower level than MST and VIP. Subcortical projections were seen from MT to the claustrum, the putamen, the caudate nucleus, the inferior and lateral subdivisions of the pulvinar complex, the ventral lateral geniculate nucleus, the reticular nucleus of the thalamus, the superior colliculus, and the pontine nuclei.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1523/jneurosci.03-12-02563.1983

Cites

52 of 52 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
Receptive fields and functional architecture of monkey striate cortex
Hubel, D. H., & Wiesel, T. N. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008455 · Cited by 6,685
Tetramethyl benzidine for horseradish peroxidase neurohistochemistry: a non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents.
Mesulam, M. M. (1978) · Journal of Histochemistry & Cytochemistry · doi:10.1177/26.2.24068 · Cited by 4,303
The autoradiographic demonstration of axonal connections in the central nervous system
Cowan, W. M., Gottlieb, D. I., Hendrickson, A. E., Price, J. L., & Woolsey, T. A. (1972) · Brain Research · doi:10.1016/0006-8993(72)90344-7 · Cited by 1,610
Functional properties of neurons in middle temporal visual area of the macaque monkey. I. Selectivity for stimulus direction, speed, and orientation
Maunsell, J. H. R., & Essen, D. C. V. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1127 · Cited by 1,462
Self-citation
The representation of the visual field on the cerebral cortex in monkeys
Daniel, P. M., & Whitteridge, D. (1961) · The Journal of Physiology · doi:10.1113/jphysiol.1961.sp006803 · Cited by 1,147
Functional organization of a visual area in the posterior bank of the superior temporal sulcus of the rhesus monkey
Zeki, S. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010452 · Cited by 982
Intracortical connectivity of architectonic fields in the somatic sensory, motor and parietal cortex of monkeys
Jones, E. G., Coulter, J. D., & Hendry, S. H. C. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810206 · Cited by 977
Silver Staining of Myelin by Means of Physical Development
Gallyas, F. (1979) · Neurological Research · doi:10.1080/01616412.1979.11739553 · Cited by 936
Functional properties of neurons in middle temporal visual area of the macaque monkey. II. Binocular interactions and sensitivity to binocular disparity
Maunsell, J. H. R., & Essen, D. C. V. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1148 · Cited by 746
Self-citation

Show all 52 references

Research works printed but not linked: 1

Olszewski, J. (1952) The Thalamus of the Macaca mulatta, S. Karger AG, Basel.

Sorted by citations

Items 601–700 of 1,001

Morphology and connections of neurons in area 17 projecting to the extrastriate areas mt and 19DM and to the superior colliculus in the monkey Callithrix jacchus
Weisenhorn, D. M. V., Ilung, R. B., & Spatz, W. B. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903620207 · Cited by 59
Connection from cortical area V2 to MT in macaque monkey
Anderson, J. C., & Martin, K. A. C. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.10100 · Cited by 59
Clustering of ipsilateral cortico-cortical projection neurons to area 7 in the rhesus monkey
Hiorns, R. W., Neal, J., Pearson, R. C. A., & Powell, T. P. S. (1991) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1991.0117 · Cited by 59
The emotion–action link? Naturalistic emotional stimuli preferentially activate the human dorsal visual stream
Goldberg, H., Preminger, S., & Malach, R. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.032 · Cited by 58
Can Ophthalmologists Repair the Brain in Infantile Esotropia? Early Surgery, Stereopsis, Monofixation Syndrome, and the Legacy of Marshall Parks
Tychsen, L. (2005) · Journal of American Association for Pediatric Ophthalmology and Strabismus · doi:10.1016/j.jaapos.2005.06.007 · Cited by 58
Encoding of Smooth Pursuit Direction and Eye Position by Neurons of Area MSTd of Macaque Monkey
Squatrito, S., & Maioli, M. G. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03847.1997 · Cited by 58
NMDA, AMPA, and benzodiazepine binding site changes in Alzheimer's disease visual cortex
Carlson, M. D., Penney, J. B., & Young, A. B. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90120-z · Cited by 58
Asymmetrical access to color and location in visual working memory
Rajsic, J., & Wilson, D. E. (2014) · Attention Perception & Psychophysics · doi:10.3758/s13414-014-0723-2 · Cited by 60
Updating working memory for words: A PET activation study
Clark, C. R., Egan, G. F., McFARLANE, A. C., Morris, P. E., Weber, D. L., Sonkkilla, C., Marcina, J., & Tochon‐Danguy, H. (2000) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(2000)9:1 · Cited by 79
Laminar origin of direct projection from cortex area V1 to V4 in the rhesus monkey
Yukie, M., & Iwai, E. (1985) · Brain Research · doi:10.1016/0006-8993(85)90875-3 · Cited by 57
Computational Methods for the Analysis of Brain Connectivity
Hilgetag, C. C., Kötter, R., Stephan, K. E., & Sporns, O. (2002) · Humana Press eBooks · doi:10.1007/978-1-59259-275-3_14 · Cited by 60
Two rules for callosal connectivity in striate cortex of the rat
Lewis, J. W., & Olavarría, J. F. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903610110 · Cited by 57
Organization of individual afferent axons in layer IV of striate cortex in a primate
Florence, S. L., & Casagrande, V. A. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-12-03850.1987 · Cited by 57
Differential Patterns of Dysconnectivity in Mirror Neuron and Mentalizing Networks in Schizophrenia
Schilbach, L., Derntl, B., Aleman, A., Caspers, S., Clos, M., Diederen, K. M. J., Gruber, O., Kogler, L., Liemburg, E. J., Sommer, I. E., et al. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw015 · Cited by 58
Functional Segregation and Development of Mouse Higher Visual Areas
Murakami, T., Matsui, T., & Ohki, K. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0731-17.2017 · Cited by 59
Coordination of Head and Eyes during the Performance of Natural (and Unnatural) Visual Tasks
Kowler, E., Pizlo, Z., Zhu, G.-L., Erkelens, C. J., Steinman, R. M., & Collewijn, H. (1992) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195068207.003.0065 · Cited by 56
Vestibular response kinematics in posterior parietal cortex neurons of macaque monkeys
Klam, F., & Graf, W. M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02813.x · Cited by 55
Motion-onset visual-evoked potentials as a function of retinal eccentricity in man
Schlykowa, L., van Dijk, B. W., & Ehrenstein, W. H. (1993) · Cognitive Brain Research · doi:10.1016/0926-6410(93)90024-y · Cited by 56
Directional defects in pursuit and motion perception in humans with unilateral cerebral lesions
Barton, J. J. S., Sharpe, J. A., & Raymond, J. E. (1996) · Brain · doi:10.1093/brain/119.5.1535 · Cited by 56
Motion perception: a review of developmental changes and the role of early visual experience
Hadad, B., Schwartz, S., Maurer, D. M., & Lewis, T. L. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00049 · Cited by 55
Processing of Coherent Visual Motion in Topographically Organized Visual Areas in Human Cerebral Cortex
Helfrich, R. F., Becker, H. G. T., & Haarmeier, T. (2012) · Brain Topography · doi:10.1007/s10548-012-0226-1 · Cited by 55
Parietal Area VIP Causally Influences Heading Perception during Pursuit Eye Movements
Zhang, T., & Britten, K. H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5520-10.2011 · Cited by 55
Visual cortical areas of the mouse: comparison of parcellation and network structure with primates
Laramée, M., & Boire, D. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00149 · Cited by 61
Comparison of the Spatial Limits on Direction Selectivity in Visual Areas MT and V1
Churchland, M. M., Priebe, N. J., & Lisberger, S. G. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00767.2004 · Cited by 60
Neural bases of peri-hand space plasticity through tool-use: Insights from a combined computational–experimental approach
Magosso, E., Ursino, M., di Pellegrino, G., Làdavas, E., & Serino, A. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.09.037 · Cited by 55
Real and Imaginary Rotary Motion Processing: Functional Parcellation of the Human Parietal Lobe Revealed by fMRI
Podzebenko, K., Egan, G. F., & Watson, J. D. G. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/0898929052879996 · Cited by 55
Response of MSTd Neurons to Simulated 3D Orientation of Rotating Planes
杉原, 弘., Murakami, I., Shenoy, K. V., Andersen, R. A., & Komatsu, H. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00900.2000 · Cited by 55
Stages of Self-Motion Processing in Primate Posterior Parietal Cortex
Bremmer, F., Duhamel, J., Hamed, S. B., & Graf, W. M. (2000) · International review of neurobiology · doi:10.1016/s0074-7742(08)60742-4 · Cited by 55
Anatomical organization of the visual system of the mink, Mustela vison
McConnell, S. K., & LeVay, S. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902500110 · Cited by 55
Convergence of processing channels in the extrastriate cortex of monkeys
Krubitzer, L. A., & Kaas, J. H. (1990) · Visual Neuroscience · doi:10.1017/s0952523800000778 · Cited by 55
Fellow Eye Deficits in Amblyopia
Birch, E. E., Kelly, K. R., & Giaschi, D. E. (2019) · Journal of Binocular Vision and Ocular Motility · doi:10.1080/2576117x.2019.1624440 · Cited by 54
Amygdalar activation alters the hippocampal GABA system: ?Partial? modelling for postmortem changes in schizophrenia
Berretta, S., Munno, D. W., & Benes, F. M. (2001) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20010305)431:2 · Cited by 68
The role of human ventral visual cortex in motion perception
Gilaie‐Dotan, S., Saygın, A. P., Lorenzi, L. J., Egan, R., Rees, G. E., & Behrmann, M. (2013) · Brain · doi:10.1093/brain/awt214 · Cited by 59
The Perception of Hierarchical Structure
Kimchi, R. (2014) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780199686858.013.025 · Cited by 54
Pattern motion is present in V1 of awake but not anaesthetized monkeys
Guo, K., Benson, P. J., & Blakemore, C. B. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03212.x · Cited by 54
Connectional Evidence for Dorsal and Ventral V3, and Other Extrastriate Areas in the Prosimian Primate, Galago garnetti
Lyon, D. C., & Kaas, J. H. (2002) · Brain Behavior and Evolution · doi:10.1159/000064159 · Cited by 54
Dopamine D1 and D5 Receptors Are Localized to Discrete Populations of Interneurons in Primate Prefrontal Cortex
Glausier, J. R., Khan, Z. U., & Muly, E. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn212 · Cited by 58
Inferior frontal eye field projections to the pursuit-related dorsolateral pontine nucleus and middle temporal area (MT) in the monkey
Leichnetz, G. R. (1989) · Visual Neuroscience · doi:10.1017/s0952523800004478 · Cited by 54
Parietal maps of visual signals for bodily action planning
Orban, G. A., Sepe, A., & Bonini, L. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02378-6 · Cited by 57
Delayed Reentrant Processing Impairs Visual Awareness
Dux, P. E., Visser, T. A. W., Goodhew, S. C., & Lipp, O. V. (2010) · Psychological Science · doi:10.1177/0956797610379866 · Cited by 53
An Attention-Sensitive Memory Trace in Macaque MT Following Saccadic Eye Movements
Yao, T., Treue, S., & Krishna, B. S. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002390 · Cited by 53
Does the Middle Temporal Area Carry Vestibular Signals Related to Self-Motion?
Chowdhury, S. A., Takahashi, K., DeAngelis, G. C., & Angelaki, D. E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0004-09.2009 · Cited by 52
Organization of the posterior parietal cortex in galagos: II. Ipsilateral cortical connections of physiologically identified zones within anterior sensorimotor region
Stepniewska, I., Cerkevich, C. M., Fang, P. Y., & Kaas, J. H. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22190 · Cited by 53
Complex dendritic fields of pyramidal cells in the frontal eye field of the macaque monkey
Elston, G. N., & Rosa, M. G. P. (1998) · Neuroreport · doi:10.1097/00001756-199801050-00025 · Cited by 53
Projections from Areas 18 and 19 to Cat Striate Cortex: Divergence and Laminar Specificity
Henry, G. H., Salin, P. A., & Bullier, J. (1991) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1991.tb00079.x · Cited by 53
Functional projections from striate cortex and superior temporal sulcus to the nucleus of the optic tract (NOT) and dorsal terminal nucleus of the accessory optic tract (DTN) of macaque monkeys
Hoffmann, K. ‐., Distler, C., & Erickson, R. G. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903130413 · Cited by 53
Why is “blindsight” blind? A new perspective on primary visual cortex, recurrent activity and visual awareness
Silvanto, J. (2014) · Consciousness and Cognition · doi:10.1016/j.concog.2014.08.001 · Cited by 56
Neural Representations Observed
Thomson, E. E., & Piccinini, G. (2018) · Minds and Machines · doi:10.1007/s11023-018-9459-4 · Cited by 62
The oculomotor role of the pontine nuclei and the nucleus reticularis tegmenti pontis
Thier, P., & Möck, M. (2005) · Progress in brain research · doi:10.1016/s0079-6123(05)51010-0 · Cited by 52
Ovarian hormones differentially influence immunoreactivity for dopamine ?- hydroxylase, choline acetyltransferase, and serotonin in the dorsolateral prefrontal cortex of adult rhesus monkeys
Kritzer, M. F., & Kohama, S. G. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990705)409:3 · Cited by 126
Activity-dependent refinement in the goldfish retinotectal system is mediated by the dynamic regulation of processes withdrawal: An in vivo imaging study
Johnson, F. A., Dawson, A. J., & Meyer, R. L. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990419)406:4 · Cited by 23
Specificity of Projections from Wide-Field and Local Motion-Processing Regions within the Middle Temporal Visual Area of the Owl Monkey
Berezovskii, V. K., & Born, R. T. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-03-01157.2000 · Cited by 52
Altered responses to cutaneous stimuli in the second somatosensory cortex following lesions of the postcentral gyrus in infant and juvenile macaques
Burton, H., Sathian, K., & Dian‐hua, S. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902910307 · Cited by 55
Intrinsic connections of layer III of striate cortex in squirrel monkey and bush baby: Correlations with patterns of cytochrome oxidase
Lachica, E. A., Beck, P. D., & Casagrande, V. A. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903290203 · Cited by 52
Dissociating distinct cortical networks associated with subregions of the human medial temporal lobe using precision neuroimaging
Reznik, D., Trampel, R., Weiskopf, N., Witter, M. P., & Doeller, C. F. (2023) · Neuron · doi:10.1016/j.neuron.2023.05.029 · Cited by 52
Widespread correlation patterns of fMRI signal across visual cortex reflect eccentricity organization
Arcaro, M. J., Honey, C. J., Mruczek, R. E. B., Kästner, S., & Hasson, U. (2015) · eLife · doi:10.7554/elife.03952 · Cited by 53
Grasping the non-conscious: Preserved grip scaling to unseen objects for immediate but not delayed grasping following a unilateral lesion to primary visual cortex
Whitwell, R. L., Striemer, C. L., Nicolle, D. A., & Goodale, M. A. (2011) · Vision Research · doi:10.1016/j.visres.2011.02.005 · Cited by 51
Topographic organization of areas V3 and V4 and its relation to supra-areal organization of the primate visual system
Arcaro, M. J., & Kästner, S. (2015) · Visual Neuroscience · doi:10.1017/s0952523815000115 · Cited by 49
A direct interareal feedback-to-feedforward circuit in primate visual cortex
Siu, C. R., Balsor, J. L., Merlin, S., Federer, F., & Angelucci, A. (2021) · Nature Communications · doi:10.1038/s41467-021-24928-6 · Cited by 51
The Superior Temporal Polysensory Region in Monkeys
Cusick, C. G. (1997) · Cerebral cortex · doi:10.1007/978-1-4757-9625-4_10 · Cited by 51
Distribution and morphology of area 17 neurons that project to the cat's extrastriate cortex
Einstein, G., & Fitzpatrick, D. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903030112 · Cited by 51
Cytochrome oxidase activity in the striate cortex and lateral geniculate nucleus of the newborn and adult macaque monkey
Kennedy, H., Bullier, J., & Dehay, C. (1985) · Experimental Brain Research · doi:10.1007/bf00235636 · Cited by 51
Peripersonal space : a multisensory interface for body-objects interactions
Brozzoli, C. (2009) · theses.fr (ABES) · doi:10.70675/076b34fezd0d1z4b1czb627zed5a1652e4fa · Cited by 53
Robot-centric Activity Recognition from First-Person RGB-D Videos
Xia, L., Gori, I., Aggarwal, J. K., & Ryoo, M. S. (2015) · IEEE Winter Conference on Applications of Computer Vision · doi:10.1109/wacv.2015.54 · Cited by 50
Juggling revisited — A voxel–based morphometry study with expert jugglers
Gerber, P. A., Schlaffke, L., Heba, S., Greenlee, M. W., Schultz, T., & Schmidt‐Wilcke, T. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.04.023 · Cited by 52
Functional Plasticity in Somatosensory Cortex Supports Motor Learning by Observing
McGregor, H. E., Cashaback, J. G. A., & Gribble, P. L. (2016) · Current Biology · doi:10.1016/j.cub.2016.01.064 · Cited by 50
Motion perception as a model for perceptual aging
Billino, J., & Pilz, K. S. (2019) · Journal of Vision · doi:10.1167/19.4.3 · Cited by 51
Comparison of Head Movement Strategies among Mammals
Fuller, J. H. (1992) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195068207.003.0013 · Cited by 51
Visual perception and memory systems: from cortex to medial temporal lobe
Khan, Z. U., Martín‐Montañez, E., & Baxter, M. G. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0641-6 · Cited by 53
Organization of extrastriate and temporal cortex in chimpanzees compared to humans and macaques
Bryant, K., Glasser, M. F., Li, L., Bae, J. J.-C., Jacquez, N. J., Alarcón, L., Fields, A., & Preuss, T. M. (2019) · Cortex · doi:10.1016/j.cortex.2019.02.010 · Cited by 53
Magnetic response of human extrastriate cortex in the detection of coherent and incoherent motion
Lam, K., Kaneoke, Y., Gunji, A., Yamasaki, H. R., Matsumoto, E., Naito, T., & Kakigi, R. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00037-3 · Cited by 50
Relative Sensitivities to Large-Field Optic-Flow Patterns Varying in Direction and Speed
Edwards, M., & Ibbotson, M. R. (2007) · Perception · doi:10.1068/p5626 · Cited by 47
The role of terminators and occlusion cues in motion integration and segmentation: a neural network model
Lidén, L., & Pack, C. C. (1999) · Vision Research · doi:10.1016/s0042-6989(99)00055-3 · Cited by 49
The Effect of Removing Superior Temporal Cortical Motion Areas in the Macaque Monkey: II. Motion Discrimination Using Random Dot Displays
Marcar, V. L., & Cowey, A. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00148.x · Cited by 49
Chapter 14: The patchy intrinsic projections of visual cortex
LeVay, S. (1988) · Progress in brain research · doi:10.1016/s0079-6123(08)60474-4 · Cited by 49
Computational Studies on Acquisition and Adaptation of Ocular Following Responses Based on Cerebellar Synaptic Plasticity
Yamamoto, K., Kobayashi, Y., Takemura, A., Kawano, K., & Kawato, M. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00166.2001 · Cited by 49
Predictive processing models and affective neuroscience
Lee, K. M., Ferreira‐Santos, F., & Satpute, A. B. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.009 · Cited by 53
Temporal Relation of Population Activity in Visual Areas MT/MST and in Primary Motor Cortex during Visually Guided Tracking Movements
Kruse, W. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.5.466 · Cited by 48
Cortical connections to single digit representations in area 3b of somatosensory cortex in squirrel monkeys and prosimian galagos
Liao, C., Gharbawie, O. A., Qi, H., & Kaas, J. H. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23377 · Cited by 49
Somatosensory System
Kaas, J. H. (2004) · Elsevier eBooks · doi:10.1016/b978-012547626-3/50029-6 · Cited by 49
Area 17 lesions deactivate area MT in owl monkeys
Kaas, J. H., & Krubitzer, L. A. (1992) · Visual Neuroscience · doi:10.1017/s0952523800010804 · Cited by 48
Segregation of callosal and association pathways during development in the visual cortex of the primate
Meissirel, C., Dehay, C., Berland, M., & Kennedy, H. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-11-03297.1991 · Cited by 48
Short-latency ocular following in humans: sensitivity to binocular disparity
Masson, G. S., Busettini, C., Yang, D., & Miles, F. A. (2001) · Vision Research · doi:10.1016/s0042-6989(01)00029-3 · Cited by 48
Projections from visual cortical areas of the superior temporal sulcus to the lateral terminal nucleus of the accessory optic system in macaque monkeys
Maioli, M. G., Squatrito, S., & Domeniconi, R. (1989) · Brain Research · doi:10.1016/0006-8993(89)91123-2 · Cited by 48
Higher and deeper: Bringing layer fMRI to association cortex
Finn, E. S., Huber, L., & Bandettini, P. A. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101930 · Cited by 47
The ipsilateral cortico-cortical connections of area 7b, PF, in the parietal and tempral lobes of the monkey
Neal, J., Pearson, R. C. A., & Powell, T. P. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)90500-b · Cited by 46
Occipital network for figure/ground organization
Likova, L. T., & Tyler, C. W. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1417-6 · Cited by 46
Chemoarchitecture of the middle temporal visual area in the marmoset monkey (Callithrix jacchus): Laminar distribution of calcium‐binding proteins (calbindin, parvalbumin) and nonphosphorylated neurofilament
Bourne, J. A., Warner, C. E., Upton, D. J., & Rosa, M. G. P. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21190 · Cited by 47
Cortical and subcortical connections of V1 and V2 in early postnatal macaque monkeys
Baldwin, M. K. L., Kaskan, P. M., Zhang, B., Chino, Y. M., & Kaas, J. H. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22732 · Cited by 46
Attention-biased multi-stable surface perception in three-dimensional structure-from-motion
Hol, K., Koene, A. R., & van Ee, R. (2003) · Journal of Vision · doi:10.1167/3.7.3 · Cited by 49
Representation of Head-Centric Flow in the Human Motion Complex
Goossens, J., Dukelow, S. P., Menon, R. S., Vilis, T., & van den Berg, A. V. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0730-06.2006 · Cited by 47
The Representation of Movement in Near Extra-Personal Space in the Macaque Ventral Intraparietal Area (VIP)
Bremmer, F., Duhamel, J., Hamed, S. B., & Graf, W. M. (1997) · Springer eBooks · doi:10.1007/978-3-642-60661-8_33 · Cited by 47
Activation of Human Extrageniculostriate Pathways after Damage to Area V1
Ptito, M., Johannsen, P., Faubert, J., & GJEDDE, A. H. (1999) · NeuroImage · doi:10.1006/nimg.1998.0390 · Cited by 46
The connections of area PG, 7a, with cortex in the parietal, occipital and temporal lobes of the monkey
Neal, J., Pearson, R. C. A., & Powell, T. P. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)91767-b · Cited by 46
Change in Neuronal Firing Patterns in the Process of Motor Command Generation for the Ocular Following Response
Takemura, A., Inoue, Y., Gomi, H., Kawato, M., & Kawano, K. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.1750 · Cited by 46
Ontogeny of somatostatin in cerebral cortex of macaque monkey: an immunohistochemical study
Yamashita, A., Hayashi, M., Shimizu, K., & Oshima, K. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90012-6 · Cited by 47
Visual Processing in Macaque Area MT/V5 and Its Satellites (MSTd and MSTv)
Orban, G. A. (1997) · Cerebral cortex · doi:10.1007/978-1-4757-9625-4_9 · Cited by 46
Responses in the First or Second Somatosensory Cortical Area in Cats during Transient Inactivation of the Other Ipsilateral Area with Lidocaine Hydrochloride
Burton, H., & Robinson, C. J. (1987) · Somatosensory Research · doi:10.3109/07367228709144608 · Cited by 46
N‐acetylaspartylglutamate immunoreactivity in neurons of the monkey's visual pathway
Tieman, S. B., Neale, J. H., & Tieman, D. G. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903130105 · Cited by 46
Somatosensory System
Kaas, J. H. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10030-6 · Cited by 48

Authors: Maunsell, J., & van Essen, D.
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 1983-12-01
Volume: 3
Issue: 12
Pages: 2563-2586
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.03-12-02563.1983
PMC: PMC6564662
OpenAlex: W2145439642
Cited by: 1,602
References: 52
Citations by year: 2026: 14 · 2025: 19 · 2024: 16 · 2023: 17 · 2022: 21 · 2021: 31 · 2020: 52 · 2019: 30 · 2018: 33 · 2017: 34 · 2016: 30 · 2015: 31 · 2014: 40 · 2013: 49 · 2012: 39
FWCI: 30.40
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Eye Institute (R01EY002091)
National Institute of General Medical Sciences (T32GM007737)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
Keywords: middle temporal area, MT, cortical hierarchy, visual cortex, interhemispheric connections, medial superior temporal area, ventral intraparietal area, visual area V1, visual area V2, area V4, subcortical projections, pulvinar, superior colliculus, macaque
MeSH terms: Animals, Brain Mapping, Horseradish Peroxidase, Macaca, Macaca fascicularis, Thalamus, Visual Cortex, Visual Fields, Visual Pathways

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

The connections of the middle temporal visual area (MT) and their relationship to a cortical hierarchy in the macaque monkey

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks