The DOI matches its Crossref record; 108 of the 108 references it cites were found in a registry or an index.
Pathways for motion analysis: Cortical connections of the medial superior temporal and fundus of the superior temporal visual areas in the macaque
Abstract
To identify the cortical connections of the medial superior temporal (MST) and fundus of the superior temporal (FST) visual areas in the extrastriate cortex of the macaque, we injected multiple tracers, both anterograde and retrograde, in each of seven macaques under physiological control. We found that, in addition to connections with each other, both MST and FST have widespread connections with visual and polysensory areas in posterior prestriate, parietal, temporal, and frontal cortex. In prestriate cortex, both areas have connections with area V3A. MST alone has connections with the far peripheral field representations of V1 and V2, the parieto-occipital (PO) visual area, and the dorsal prelunate area (DP), whereas FST alone has connections with area V4 and the dorsal portion of area V3. Within the caudal superior temporal sulcus, both areas have extensive connections with the middle temporal area (MT), MST alone has connections with area PP, and FST alone has connections with area V4t. In the rostral superior temporal sulcus, both areas have extensive connections with the superior temporal polysensory area (STP) in the upper bank of the sulcus and with area IPa in the sulcal floor. FST also has connections with the cortex in the lower bank of the sulcus, involving area TEa. In the parietal cortex, both the central field representation of MST and FST have connections with the ventral intraparietal (VIP) and lateral intraparietal (LIP) areas, whereas MST alone has connections with the inferior parietal gyrus. In the temporal cortex, the central field representation of MST as well as FST has connections with visual area TEO and cytoarchitectonic area TF. In the frontal cortex, both MST and FST have connections with the frontal eye field. On the basis of the laminar pattern of anterograde and retrograde label, it was possible to classify connections as forward, backward, or intermediate and thereby place visual areas into a cortical hierarchy. In general, MST and FST receive forward inputs from prestriate visual areas, have intermediate connections with parietal areas, and project forward to the frontal eye field and areas in the rostral superior temporal sulcus. Because of the strong inputs to MST and FST from area MT, an area known to play a role in the analysis of visual motion, and because MST and FST themselves have high proportions of directionally selective cells, they appear to be important stations in a cortical motion processing system.
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Meng, Y., Hu, X. P., Bachevalier, J., & Zhang, X. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.04.003 · Cited by 24
“Such maintenance of stimulus information is likely to be mediated in part by feedback projections from prefrontal cortex (PFC) to posterior association cortices, through reciprocal connections between these visual areas (Boussaoud et al., 1990; Chafee et al., 1998; Miller et al., 1996; Ungerleider et al., 1989; Webste…”
Axonal Projections From the Middle Temporal Area in the Common Marmoset
Abe, H., Tani, T., Mashiko, H., Kitamura, N., Hayami, T., Watanabe, S., Sakai, K., Suzuki, W., Mizukami, H., Watakabe, A., et al. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00089 · Cited by 24
A MULTILAYER IN-PLACE LEARNING NETWORK FOR DEVELOPMENT OF GENERAL INVARIANCES
Weng, J., Luwang, T., Lu, H., & Xue, X. (2007) · International Journal of Humanoid Robotics · doi:10.1142/s0219843607001072 · Cited by 24
“(6) is nearly optimal given the observations.”
La perception visuelle des orientations et« l'effet de l'oblique »
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Savaki, H. E., Raos, V., & Dalezios, Y. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00439-3 · Cited by 23
Smith, A. T. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02325-5 · Cited by 22
“A study of several cases involving tracer injections in MST (Boussaoud et al. 1990) showed no labelling in the cingulate sulcus.”
BackgroundMeasuring the response to visually presented faces in the human lateral prefrontal cortex
Nikel, L., Sliwinska, M. W., Küçük, E., Ungerleider, L. G., & Pitcher, D. (2022) · Cerebral Cortex Communications · doi:10.1093/texcom/tgac036 · Cited by 25
“For example, the functional and anatomical connections from primary visual cortex into the STS have been extensively mapped in macaques (Boussaoud et al., 1990; Desimone & Ungerleider, 1986; Ungerleider & Desimone, 1986).”
BackgroundLinear Responses to Stochastic Motion Signals in Area MST
Heuer, H. W., & Britten, K. H. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00083.2007 · Cited by 23
“This is consistent with observations in extrastriate area MT, a major source of input to MST (Baizer et al. 1991; Boussaoud et al. 1990; Maunsell and Van Essen 1983).”
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Gregoriou, G. G., & Savaki, H. E. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200106000-00005 · Cited by 21
“Area VIP receives visual input from areas MT, MST, FST (Maunsell and Van Essen, 1983; Ungerleider and Desimone, 1986; Boussaoud et al., 1990), and PO (Colby et al., 1988), and projects to the ventral premotor cortex (Luppino et al., 1999).”
BackgroundConstruction and Representation of Visual Space in the Inferior Parietal Lobule
Siegel, R. M., & Read, H. L. (1997) · Cerebral cortex · doi:10.1007/978-1-4757-9625-4_12 · Cited by 21
“It has projections to and from memory and limbic structures via the cingulate (LC in von Bonin and Bailey’s (1947) terminology) and the parahippocampal gyrus (TFi) and sparse, although consistent, projections to the temporal lobule, in particular to the polysensory area (STPa) and inferotemporal cortex (Mesulam et al.…”
BackgroundThe macaque ventral intraparietal area has expanded into three homologue human parietal areas
Foster, C., Sheng, W.-A., Heed, T., & Ben Hamed, S. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102185 · Cited by 20
Becker, H. G. T., Haarmeier, T., Tatagiba, M., & Gharabaghi, A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0556-13.2013 · Cited by 20
“At least as far as monkey studies are concerned there is convincing evidence for both claims (Maunsell and van Essen, 1983; Ungerleider and Desimone, 1986; Boussaoud et al., 1990; Kaas and Morel, 1993; Tolias et al., 2005; Logothetis et al., 2010; Sultan et al., 2011).”
BackgroundGoto, T., Uno, A., Haruhara, N., Kaneko, M., Awaya, N., Kozuka, J., & Katano, S. (2010) · The Japan Journal of Logopedics and Phoniatrics · doi:10.5112/jjlp.51.38 · Cited by 20
Rushmore, J., Sylvain Bouix, A., Kubicki, M. R., Yogesh Rathi, A., Rosene, D. L., Yeterian, E. H., & Makris, N. (2020) · Brain Imaging and Behavior · doi:10.1007/s11682-020-00357-9 · Cited by 19
Optic flow direction coding in area PEc of the behaving monkey
Raffi, M., Maioli, M. G., & Squatrito, S. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.07.036 · Cited by 19
Distinct fMRI Responses to Self-Induced versus Stimulus Motion during Free Viewing in the Macaque
Russ, B. E., Kaneko, T., Saleem, K. S., Berman, R. A., & Leopold, D. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1152-16.2016 · Cited by 19
“…stream, anatomical and functional studies indicate the existence of multiple parallel pathways within the ventral stream, including a motion-sensitive ventral pathway originating in the caudal motion-sensitive areas (Boussaoud et al., 1990; Kravitz et al., 2013; Fisher and Freiwald, 2015).”
BackgroundKovacs-Balint, Z., Feczko, E., Pincus, M., Earl, E., Miranda-Domínguez, Ó., Howell, B., Morin, E. L., Maltbie, E. A., Li, L., Steele, J., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy222 · Cited by 19
“Although the brain networks supporting early developing visual social skills are still unknown, work in adult monkeys have demonstrated at least 3 cortical networks: the ventral object pathway mediating facial expression and identity perception, discrimination and recognition (Ungerleider and Bell 2011); the motion pa…”
BackgroundAcuña, C., Pardo‐Vázquez, J. L., & Leborán, V. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9194-y · Cited by 19
“ventral and dorsal streams carry complementary information about the characteristics of the stimuli and their spatial properties, respectively (Boussaoud et al. 1990; Desimone and Ungerleider 1986; Maunsell and van Essen 1983; Pandya and Yeterian 1990; Ungerleider and Mishkin 1982; Webster et al. 1994).”
BackgroundEvidence for distinct brain networks in the control of rule-based motor behavior
Granek, J. A., & Sergio, L. E. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00233.2014 · Cited by 19
“, 2008), k) (Maunsell and van Essen, 1983), l) (Boussaoud et al., 1990; Maunsell and van Essen, 1983), m) (Maunsell and van Essen, 1983), n) (Colby et al.”
Development of social systems neuroscience using macaques
Isoda, M., Noritake, A., & Ninomiya, T. (2018) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.94.020 · Cited by 19
Churchland, A. K., Huang, X., & Lisberger, S. G. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00941.2005 · Cited by 19
Crossed Corticostriatal Projections in the Macaque Brain
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Benetti, S., Ferrari, A., & Pavani, F. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1108354 · Cited by 22
Planning and control in action
Glover, S. (2004) · Behavioral and Brain Sciences · doi:10.1017/s0140525x04520022 · Cited by 18
Responses of neurons in area VIP to self-induced and external visual motion
Gabel, S., Misslisch, H., Gielen, C. C. A. M., & Duysens, J. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1268-5 · Cited by 18
Troubled reaching after right occipito-temporal damage
Rizzo, M., Rotella, D. L., & Darling, W. G. (1992) · Neuropsychologia · doi:10.1016/0028-3932(92)90041-j · Cited by 18
Neuronal Representations Supporting Three-Dimensional Vision in Nonhuman Primates
Rosenberg, A., Thompson, L. W., Doudlah, R. C., & Chang, T. (2023) · Annual Review of Vision Science · doi:10.1146/annurev-vision-111022-123857 · Cited by 16
Grasping and Perceiving Objects
Jacob, P. (2005) · Cambridge University Press eBooks · doi:10.1017/cbo9780511610608.008 · Cited by 17
Real-Time Biologically Inspired Action Recognition from Key Poses Using a Neuromorphic Architecture
Layher, G., Brosch, T., & Heiko Neumann, B. (2017) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2017.00013 · Cited by 17
“STS has been suggested to be a point of convergence of the separate dorsal “where” and the ventral “what” pathways (Boussaoud et al., 1990; Felleman and Van Essen, 1991), containing cells which integrate form and motion information of biological objects (Oram and Perrett, 1996) and selectively respond to, e.”
Background14C-Deoxyglucose mapping of the monkey brain during reaching to visual targets
Savaki, H. E., & Dalezios, Y. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00080-x · Cited by 17
Bakola, S., Gregoriou, G. G., Moschovakis, A. K., Raos, V., & Savaki, H. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4224-06.2007 · Cited by 17
“Key words: saccades; temporal cortex; motion complex; MT; MST; FST; V4; V5; TPO; TEO”
BackgroundInfluentialConnectivity of the Cingulate Sulcus Visual Area (CSv) in Macaque Monkeys
Castro, V. D., Smith, A. T., Beer, A., Leguen, C., Vayssière, N., Héjja‐Brichard, Y., Audurier, P., Cottereau, B. R., & Durand, J. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa301 · Cited by 17
Organization of parietoprefrontal and temporoprefrontal networks in the macaque
Giarrocco, F., & Averbeck, B. B. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00092.2021 · Cited by 18
Viewing a forelimb induces widespread cortical activations
Raos, V., Kilintari, M., & Savaki, H. E. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.12.010 · Cited by 17
“…visual area (V5/MT) which is situated in the posterior (lower) bank (Maunsell and Van Essen, 1983a; Zeki, 1974), the medial superior temporal area (MST) in the anterior (upper) bank, and the fundus of the superior temporal area (FST) (Boussaoud et al., 1990; Desimone and Ungerleider, 1986).”
BackgroundInfluentialVertical meridian representation on the prelunate gyrus in area V4 of macaque
Youakim, M., Bender, D. B., & Baizer, J. S. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00608-6 · Cited by 16
Vakalopoulos, C. (2005) · Medical Hypotheses · doi:10.1016/j.mehy.2005.05.016 · Cited by 16
“This is exemplified by the reciprocal relationship of cortical areas such as the dorsal medial superior temporal (MSTd) and 7a and the ambiguity inherent in the projections from MT to V4 [2,32] MSTd projects to area 7a as a columnar pattern (C).”
BackgroundMultiple Cortical Representations of Optic Flow Processing
Raffi, M., & Siegel, R. M. (2004) · Springer eBooks · doi:10.1007/978-1-4020-2092-6_1 · Cited by 16
Visual Processing in the Primate Brain
Pasternak, T., Bisley, J. W., & Calkins, D. J. (2003) · Wiley eBooks · doi:10.1002/0471264385.wei0306 · Cited by 16
A neural network model of spiral–planar motion tuning in MSTd
Beardsley, S. A., Ward, R. L., & Vaina, L. M. (2003) · Vision Research · doi:10.1016/s0042-6989(02)00608-9 · Cited by 15
The Hand Sees Visual Periphery Better Than the Eye: Motor-Dependent Visual Motion Analyses
Gomi, H., Abekawa, N., & Shimojo, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4741-12.2013 · Cited by 14
“In addition, the dorsal part of MST has connections to the area 7b (Andersen et al., 1990; Boussaoud et al., 1990), which could send signals to the primary motor cortex via the ventral part of the premotor area (Shipp et al., 1998).”
BackgroundOptic flow selectivity in the macaque parieto-occipital sulcus
Pitzalis, S., Hadj‐Bouziane, F., Bò, G. D., Guedj, C., Strappini, F., Meunier, M., Farnè, A., Fattori, P., & Galletti, C. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02293-w · Cited by 15
“Interestingly, in macaque, MST neurons present response properties similar to those of V6 neurons, in that both have large receptive fields, responsive to direction and speed of moving visual stimuli and both receive strong direct inputs from V1 (Boussaoud et al. 1990; Sousa et al. 1991; Palmer and Rosa 2006; Galletti…”
BackgroundÓScalaidhe, S. P., Rodman, H. R., Albright, T. D., & Gross, C. G. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(96)00131-3 · Cited by 15
Bertini, G., Buffalo, E. A., Weerd, P. D., Desimone, R., & Ungerleider, L. G. (2004) · Neuroreport · doi:10.1097/01.wnr.0000134847.86625.15 · Cited by 15
“Alternatively, or in addition, there is evidence for cortico-cortical routes to TE through dorsal stream areas [21], areas in the superior temporal sulcus [22,23], and through the parahippocampal region [24].”
BackgroundFunctional imaging of the intraparietal cortex during saccades to visual and memorized targets
Bakola, S., Gregoriou, G. G., Moschovakis, A. K., & Savaki, H. E. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.02.030 · Cited by 15
“…linked with cortical areas processing visual information such as the dorsal and ventral visual streams (Andersen et al., 1990; Blatt et al., 1990; Boussaoud et al., 1990; Stanton et al., 1995; Ungerleider and Desimone, 1986) as well as with saccade centers such as the superior colliculi and the…”
Which image is in awareness during binocular rivalry? Reading perceptual status from eye movements
Hayashi, R., & Tanifuji, M. (2012) · Journal of Vision · doi:10.1167/12.3.5 · Cited by 14
“…reported; Distler, Boussaoud, Desimone, & Ungerleider, 1993), an indirect connection via V4 (Maunsell & van Essen, 1983; Ungerleider & Desimone, 1986), an ascending relay through STP (Baizer et al., 1991; Boussaoud et al., 1990), and top-down modulation onto the common lower visual areas (V1/V2).”
BackgroundZhao, B., Zhang, Y., & Chen, A. (2021) · The Journal of Physiology · doi:10.1113/jp281913 · Cited by 14
“On the other hand, the STP area is a large structure, extending from the parietal lobe to the temporal pole, and it is usually divided into at least two functionally distinct sub-regions: the anterior portion (STPa) and the posterior portion (STPp) of the superior temporal polysensory area (Boussaoud et al. 1990; Fell…”
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The Perception of Depicted Motion
Dobrez, L. (2013) · Arts · doi:10.3390/arts2040383 · Cited by 16
“1990, Goodale 1993 [38–41]).”
BackgroundRole of Population Receptive Field Size in Complex Visual Dysfunctions
de Best, P. B., Raz, N., Guy, N., Ben‐Hur, T., Dumoulin, S. O., Pertzov, Y., & Levin, N. (2019) · JAMA Neurology · doi:10.1001/jamaneurol.2019.2447 · Cited by 14
Neurobiological models of normal and abnormal visual development
Atkinson, J., & Braddick, O. (2005) · Psychology Press eBooks · doi:10.4324/9780203989395-12 · Cited by 15
Stepniewska, I., & Kaas, J. H. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25489 · Cited by 12
“These areas in the MT surround are thought to highly reflect the dominant M cell inputs to MT from V1 due to interconnections with MT. Collectively MTc, MST, and FST project into the parietal components of the dorsal stream (Boussaoud et al., 1990).”
BackgroundKüçük, E., Foxwell, M. J., KAISER, D. H., & Pitcher, D. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02139 · Cited by 16
“…functions performed in a particular brain area can be deduced (at least partially) by the anatomical connectivity of that area (Pitcher et al., 2020; Kravitz et al., 2013; Kravitz et al., 2011; Boussaoud, Ungerleider, & Desimone, 1990; Desimone & Ungerleider, 1986; Ungerleider & Desimone, 1986).”
The brain computes dynamic facial movements for emotion categorization using a third pathway
Yan, Y., Zhan, J., Garrod, O., Chen, C., Ince, R. A. A., Jack, R. E., & Schyns, P. G. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2423560122 · Cited by 13
“The rapid differentiation of emotions at this early stage suggests an efficient processing of diagnostic AUs (e.g. Lip Corner Puller, AU12 in happy), facilitating early differentiation through the lateral pathway.”
InfluentialMiyakawa, N., Banno, T., Abe, H., Tani, T., Suzuki, W., & Ichinohe, N. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00017 · Cited by 14
“In macaque monkeys, FST has been described as a region that receive strong direct input from a motion-selective area, MT (Boussaoud et al., 1990; Felleman and Van Essen, 1991; Kravitz et al., 2013), and is reported by Mysore et al. (2010) that some neuron here are selective to ‘‘3D…”
BackgroundMethodResultLaminar mechanisms of saccadic suppression in primate visual cortex
Denagamage, S., Morton, M. P., Hudson, N. V., Reynolds, J. H., Jadi, M. P., & Nandy, A. S. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112720 · Cited by 16
The responsiveness of biological motion processing areas to selective attention towards goals
Herrington, J. D., Nymberg, C., Faja, S., Price, E. T., & Schultz, R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.077 · Cited by 13
“A more specific account focuses on the putative role of STS as a convergence zone between visual and motor representations of human movement (Boussaoud et al., 1990; Felleman and Van Essen, 1991; Milner, 2006; Oram and Perrett, 1996).”
Wimmer, K., Spinelli, P., & Pasternak, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0843-16.2016 · Cited by 13
“…dominance was only detectable in increased response strength and shorter latencies, consistent with their direct origins in motion processing areas MT or MST within the same hemisphere (Barbas, 1988; Boussaoud et al., 1990; Schall et al., 1995; Petrides and Pandya, 2006; Ninomiya et al., 2012).”
BackgroundHorn, A. K. E., & Adamczyk, C. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10009-4 · Cited by 13
What causes scale errors in children?
Glover, S. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.08.002 · Cited by 13
Biological motion influences the visuomotor transformation for smooth pursuit eye movements
Coppe, S., de Xivry, J. O., Missal, M., & Lefèvre, P. (2010) · Vision Research · doi:10.1016/j.visres.2010.08.009 · Cited by 13
Steering Transforms the Cortical Representation of Self-Movement from Direction to Destination
Jacob, M., & Duffy, C. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2368-15.2015 · Cited by 13
“Nevertheless, the selective adaptation of MSTd neuronal receptive field segments might reflect adaptation of input from adjacent MT (Boussaoud et al., 1990; VanWezel and Britten, 2002; Kohn and Movshon, 2004; Glasser et al., 2011).”
BackgroundThe Analysis of Motion Signals and the Nature of Processing in the Primate Visual System
Orban, G. A. (1992) · Springer eBooks · doi:10.1007/978-3-642-77840-7_2 · Cited by 13
Sulpizio, V., Strappini, F., Fattori, P., Galati, G., Galletti, C., Pecchinenda, A., & Pitzalis, S. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02549-z · Cited by 12
Visuo-vestibular heading perception: a model system to study multi-sensory decision making
Zeng, Z., Zhang, C., & Gu, Y. (2023) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2022.0334 · Cited by 13
“Microstimulation in VIP also fails to bias monkeys ’ heading perception based on optic flow [114], yet a significant effect is observed when smooth pursuit eye movements are required during heading judgement [117].”
BackgroundInfluentialLinguistic and spatial information for action
Bartolo, A., Weisbecker, A., & Coello, Y. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.06.011 · Cited by 12
A computational model for the neurobiological substrates of visual attention
de Carvalho, L. A. V., & Roitman, V. L. (1995) · International Journal of Bio-Medical Computing · doi:10.1016/0020-7101(94)01032-v · Cited by 12
13 Neurophysiology of Action Recognition
Grossman, E. D. (2008) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195188370.003.0015 · Cited by 11
Hierarchical computation of 3D motion across macaque areas MT and FST
Thompson, L. W., Kim, B., Rokers, B., & Rosenberg, A. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113524 · Cited by 10
“15,17,20,21,27,39,47,48 Taking this together with the pre-sent findings and evidence of connections to visual areas in the ventral pathway, 38,49,50 it is conceivable that FST contributes to the binding of object identity and 3D motion, enabling the tracking of specific objects through space.”
BackgroundMultisensory coding of self-motion and its contribution to navigation
Mao, D., & Gu, Y. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00970-x · Cited by 12
Dynamic reconfiguration of macaque brain networks during natural vision
Ortiz-Rios, M., Balezeau, F., Haag, M., Schmid, M. C., & Kaiser, M. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118615 · Cited by 11
When the Brain Meets the Eye: Tracking Object Motion
Masson, G. S., Montagnini, A., & Ilg, U. J. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0781-3_8 · Cited by 12
“Interestingly, all three of these areas provide outputs to subcortical nuclei of the neural circuit for pursuit ( Boussaoud et al. 1990 ).”
BackgroundClustering of heading selectivity and perception-related activity in the ventral intraparietal area
Shao, M., DeAngelis, G. C., Angelaki, D. E., & Chen, A. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00556.2017 · Cited by 11
Wang, Q., Liao, C., Stepniewska, I., Gabi, M., & Kaas, J. H. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25123 · Cited by 11
The temporal pattern of motion in depth perception derived from ERPs in humans
Lamberty, K., Gobbelé, R., Schoth, F., Büchner, H., & Waberski, T. D. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.04.101 · Cited by 11
Differential activity to shapes under shape-from-motion condition in macaque middle temporal area
Handa, T., Katai, S., Kuno, R., Unno, S., Inoue, M., & Mikami, A. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.06.029 · Cited by 11
Optic Flow and Autonomous Navigation
Campani, M., Giachetti, A., & Torre, V. (1995) · Perception · doi:10.1068/p240253 · Cited by 12
Functional Organization of Human Visual Cortical Areas
Gulyás, B. Z. (1997) · Cerebral cortex · doi:10.1007/978-1-4757-9625-4_16 · Cited by 11
Insights from the Evolving Model of Two Cortical Visual Pathways
Baker, C. I., & Kravitz, D. J. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02192 · Cited by 11
Ritchie, J. B., Montesinos, S., & Carter, M. J. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02191 · Cited by 11
Vakalopoulos, C. (2006) · Medical Hypotheses · doi:10.1016/j.mehy.2006.08.013 · Cited by 11
Neuronal correlates of motion‐defined shape perception in primate dorsal and ventral streams
Handa, T., & Mikami, A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14121 · Cited by 10
“The uSTS in the dorsal pathway has reciprocal connections with the medial superior temporal area, which is another motion- sensitive area (Boussaoud et al., 1990), and connections with the ITC (including lSTS) (Saleem, Suzuki, Tanaka, & Hashikawa, 2000).”
BackgroundInfluentialChapter 3 Building blocks for time-to-contact estimation by the brain
Lappe, M. (2004) · Advances in psychology · doi:10.1016/s0166-4115(04)80005-0 · Cited by 10
“The properties of MT neurons are well suited for establishing a cortical representation of motion in the visual field, solving computational problems in the estimation of visual motion such as the aperture problem (Movshon et al., 1985; Pack and Born, 2001). temporal sulcus (Boussaoud et al., 1990).”
BackgroundStephen, J. M., Ranken, D. M., & Aine, C. J. (2006) · Brain Topography · doi:10.1007/s10548-006-0004-z · Cited by 10
“Ungerleider and colleagues have also established a connection between dorsal and ventral streams and peripheral and foveal stimulation, respectively (Ungerleider and Desimone 1986; Boussaoud et al. 1990, 1991; Baizer et al. 1991).”
BackgroundVisual responses in the temporal cortex to moving objects with invariant contours
Tanaka, Y. Z., Koyama, T., & Mikami, A. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1058-0 · Cited by 10
“Although the connectivity is not very dense, there is also evidence suggesting that the area in which we recorded may receive direct inputs from the MST (Boussaoud et al. 1990; Seltzer and Pandya 1994; Cusick et al. 1995; Cusick 1997).”
BackgroundFlat map areal topography in Macaca mulatta based on combined MRI and histology
Sultan, F. R., Hamodeh, S., Murayama, Y., Saleem, K. S., & Logothetis, N. K. (2010) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2010.03.023 · Cited by 9
“[24], Hof and Morrison [25], Cusick et al.”
Background“Congruent” and “Opposite” Neurons: Sisters for Multisensory Integration and Segregation
Zhang, W., Wang, H., Wong, K. Y. M., & Wu, S. (2016) · Rare & Special e-Zone (The Hong Kong University of Science and Technology) · Cited by 9
Sex differences in the brains of capuchin monkeys ( Sapajus [Cebus] apella )
Hecht, E. E., Reilly, O. T., Benítez, M. E., Phillips, K. A., & Brosnan, S. F. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24950 · Cited by 9
Motion perception and its disorders
Barton, J. J. S. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-821377-3.00013-1 · Cited by 9
Barbas, H. (2006) · Cambridge University Press eBooks · doi:10.1017/cbo9780511545917.004 · Cited by 9
Boyd, J. D., & Matsubara, J. A. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-05714-1.00031-5 · Cited by 10
Attention, intention and salience in the posterior parietal cortex
Taylor, K. E., & Stein, J. F. (1999) · Neurocomputing · doi:10.1016/s0925-2312(98)00135-0 · Cited by 9
“It is interconnected with a wide range of cortical and subcortical areas [21], including visual [1,9], auditory [12], limbic [7] and frontal areas [11].”
BackgroundWithin- and between-hemifield generalization of repetition suppression in inferior temporal cortex
Fabbrini, F., & Vogels, R. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00361.2020 · Cited by 8
An investigation of the white matter microstructure in motion detection using diffusion MRI
Csete, G., Szabó, N., Rokszin, A., Tóth, E. M., Braunitzer, G., Benedek, G., Vécsei, L., & Kincses, Z. T. (2014) · Brain Research · doi:10.1016/j.brainres.2014.05.006 · Cited by 8
“, 2000), and was suggested to make up a complex: V5/MT+ (Boussaoud et al., 1990; Morrone et al., 2000).”
BackgroundNavigational path integration by cortical neurons: origins in higher-order direction selectivity
Page, W. K., Sato, N., Froehler, M. T., Vaughn, W. J., & Duffy, C. J. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00197.2014 · Cited by 8
“In these respects, MSTd subfields show properties like those of neurons in the adjacent middle temporal area (MT) (Felleman and Kaas 1984; Livingstone et al. 2001) that projects to MST (Boussaoud et al. 1990).”
BackgroundAlexander, B., Laycock, R., Crewther, D. P., & Crewther, S. G. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00638 · Cited by 8
“, 2004) and parietal cortex (e.g., Blatt et al., 1990; Boussaoud et al., 1990; Hardy and Lynch, 1992; Clower et al., 2001; Rushworth et al., 2006; Leh et al., 2008) that bypass V1 have also been described.”
BackgroundDemonstrations of Spatiotemporal Integration and what they Tell us about the Visual System
Schiller, P. H., & Carvey, C. E. (2006) · Perception · doi:10.1068/p5564 · Cited by 8
“It is also known that cortical areas, such as MT and MST, that play a significant role in motion perception, receive a more pronounced input from the parasol system and a much less extensive input from the midget system (Lee et al 1979; Boussaoud et al 1990; Schiller and Lee 1994).”
BackgroundReceptive field organization of disparity‐sensitive cells in Macaque medial superior temporal cortex
González, F., Perez, R., Justo, M. S., & Bermúdez, M. A. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01626.x · Cited by 8
“MST projects to the posterior parietal cortex (Neal et al., 1988, 1990; Boussaoud et al., 1990) and therefore it could be considered a potential candidate for providing the parietal cortex with visual information about the location of objects in space.”
Background
Metadata
- Authors
- Boussaoud, D., Ungerleider, L. G., & Desimone, R.
- Affiliations
- National Institute of Mental Health (US)
- National Institutes of Health (US)
- Corresponding author
- Ungerleider, Leslie G.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1990-06-15
- Volume
- 296
- Issue
- 3
- Pages
- 462-495
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1989600183
- Cited by
- 634
- References
- 108
- Citations by year
- 2026: 5 · 2025: 14 · 2024: 8 · 2023: 11 · 2022: 10 · 2021: 19 · 2020: 14 · 2019: 12 · 2018: 13 · 2017: 20 · 2016: 15 · 2015: 15 · 2014: 11 · 2013: 13 · 2012: 14
- FWCI
- 11.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Keywords
- medial superior temporal area, motion analysis, cortical connectivity, extrastriate cortex, superior temporal sulcus, parietal cortex, frontal eye field, area MT, area V4, V2, cortical hierarchy, directionally selective neurons, macaque visual system
- MeSH terms
- Animals, Fluorescent Dyes, Macaca, Macaca fascicularis, Motion Perception, Visual Cortex, Visual Pathways
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