scholarly article | Q13442814 |
P2093 | author name string | R J Snowden | |
R A Andersen | |||
R G Erickson | |||
S Treue | |||
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2768-2785 | |
P577 | publication date | 1991-09-01 | |
P1433 | published in | Journal of Neuroscience | Q1709864 |
P1476 | title | The response of area MT and V1 neurons to transparent motion | |
P478 | volume | 11 |
Q64113194 | A Normalization Circuit Underlying Coding of Spatial Attention in Primate Lateral Prefrontal Cortex |
Q52071981 | A bayesian model for the measurement of visual velocity. |
Q49016838 | A biologically plausible model of early visual motion processing. I: theory and implementation |
Q44670673 | A comparison of monkey and human motion processing mechanisms |
Q48460382 | A model of neuronal responses in visual area MT. |
Q34671860 | A motion area in human visual cortex |
Q34330115 | A multiplicative model for spatial interaction in the human visual cortex |
Q48566052 | A network model of motion processing in area MT of primates |
Q48436501 | A neural model of border-ownership from kinetic occlusion |
Q48689742 | A physiological model for motion-stereo integration and a unified explanation of Pulfrich-like phenomena |
Q52418100 | A psychophysically motivated model for two-dimensional motion perception |
Q30513864 | A three-dimensional spatiotemporal receptive field model explains responses of area MT neurons to naturalistic movies |
Q47327570 | A unifying motif for spatial and directional surround suppression. |
Q80196143 | Adaptation changes the direction tuning of macaque MT neurons |
Q104456979 | Adaptation to geometrically skewed moving images: An asymmetrical effect on the double-drift illusion |
Q73733272 | Adaptation to temporal modulation can enhance differential speed sensitivity |
Q35581106 | Aging, perceptual learning, and changes in efficiency of motion processing |
Q81152184 | An extension of the transparent-motion detection limit using speed-tuned global-motion systems |
Q51908426 | An integrated microcircuit model of attentional processing in the neocortex. |
Q80055933 | An oblique effect for transparent-motion detection caused by variation in global-motion direction-tuning bandwidths |
Q34537023 | Area MT encodes three-dimensional motion |
Q38042613 | Asynchrony in visual consciousness and the possible involvement of attention |
Q53085024 | Attention does more than modulate suppressive interactions: attending to multiple items. |
Q71984190 | Attentional modulation of adaptation to two-component transparent motion |
Q48943991 | Attentional modulation of visual motion processing in cortical areas MT and MST. |
Q34489627 | Atypical integration of motion signals in Autism Spectrum Conditions |
Q43068479 | Bifurcation analysis applied to a model of motion integration with a multistable stimulus |
Q79252791 | Both monocular and binocular signals contribute to motion rivalry |
Q89700478 | But Still It Moves: Static Image Statistics Underlie How We See Motion |
Q48180491 | Can spatial and temporal motion integration compensate for deficits in local motion mechanisms? |
Q46832494 | Center-surround antagonism based on disparity in primate area MT. |
Q60041040 | Challenging the distribution shift: Statically-induced direction illusion implicates differential processing of object-relative and non-object-relative motion |
Q48161836 | Characteristics of visual evoked potentials generated by motion coherence onset |
Q41893956 | Characterizing the effects of multidirectional motion adaptation. |
Q48663367 | Combining spatial and feature-based attention within the receptive field of MT neurons |
Q38539790 | Common circuit design in fly and mammalian motion vision |
Q52022895 | Computational model for neural representation of multiple disparities. |
Q33566247 | Computational models of cortical visual processing |
Q51633564 | Computing relative motion with complex cells. |
Q48340847 | Conjunctions between motion and disparity are encoded with the same spatial resolution as disparity alone |
Q35639023 | Construction and evaluation of an integrated dynamical model of visual motion perception |
Q50657988 | Contour inflections are adaptable features. |
Q52610136 | Criterion-free measurement of motion transparency perception at different speeds. |
Q43984214 | Deficits of motion transparency perception in adult developmental dyslexics with normal unidirectional motion sensitivity |
Q51648060 | Dendritic computation of direction selectivity and gain control in visual interneurons. |
Q55649810 | Determinants of asynchronous processing in vision. |
Q48405804 | Differential ambiguity reduces grouping of metastable objects |
Q73727377 | Differential effect of attention to translation and expansion on motion aftereffects (MAE) |
Q44466550 | Differential processing: towards a unified model of direction and speed perception |
Q48384022 | Directional tuning of motion-sensitive cells in the anterior superior temporal polysensory area of the macaque |
Q34533925 | Discerning nonrigid 3D shapes from motion cues |
Q34499364 | Disrupted gamma-band neural oscillations during coherent motion perception in heavy cannabis users |
Q48961054 | Distinct cortical responses to 2D figures defined by motion contrast |
Q48378122 | Distracter suppression dominates attentional modulation of responses to multiple stimuli inside the receptive fields of middle temporal neurons. |
Q36380923 | Distributed and Dynamic Neural Encoding of Multiple Motion Directions of Transparently Moving Stimuli in Cortical Area MT. |
Q46636611 | Diverse suppressive influences in area MT and selectivity to complex motion features. |
Q55402873 | Dynamic Visual Cues for Differentiating Mirror and Glass. |
Q92186855 | Dynamic nonlinearities enable direction opponency in Drosophila elementary motion detectors |
Q36174515 | Dynamics of macaque MT cell responses to grating triplets |
Q46910923 | Encoding of three-dimensional structure-from-motion by primate area MT neurons |
Q40956373 | Enhancement and suppression in the visual field under perceptual load |
Q40470118 | Evidence and Counterevidence in Motion Perception. |
Q84982399 | Evidence for a subtractive component in motion adaptation |
Q48418013 | Exogenously cued attention triggers competitive selection of surfaces |
Q42047814 | Exploring the mechanisms underlying surface-based stimulus selection |
Q48213435 | Eye movements elicited by transparent stimuli |
Q38241534 | Feature integration and object representations along the dorsal stream visual hierarchy |
Q34044067 | Global motion perception deficits in autism are reflected as early as primary visual cortex |
Q77793002 | Global motion processing is not tuned for binocular disparity |
Q77797763 | Global-motion detection with transparent-motion signals |
Q48490419 | Greater plasticity in lower-level than higher-level visual motion processing in a passive perceptual learning task |
Q52232533 | Heading detection using motion templates and eye velocity gain fields. |
Q35902413 | Hierarchy of direction-tuned motion adaptation in human visual cortex |
Q48249784 | Human V5 demonstrated by magnetoencephalography using random dot kinematograms of different coherence levels |
Q36787100 | Human ocular following initiated by competing image motions: evidence for a winner-take-all mechanism |
Q34980122 | Human primary visual cortex (V1) is selective for second-order spatial frequency |
Q34440789 | Influence of correspondence noise and spatial scaling on the upper limit for spatial displacement in fully-coherent random-dot kinematogram stimuli |
Q52091153 | Integration of Contour and Terminator Signals in Visual Area MT of Alert Macaque. |
Q45948011 | Integration of motion and stereopsis in middle temporal cortical area of macaques. |
Q37354022 | Inter-ocular contrast normalization in human visual cortex |
Q36287160 | Interacting competitive selection in attention and binocular rivalry |
Q41935624 | Intermittent ambiguous stimuli: implicit memory causes periodic perceptual alternations |
Q81235217 | Local and global limitations on direction integration assessed using equivalent noise analysis |
Q42736503 | Low-level mechanisms do not explain paradoxical motion percepts |
Q42368334 | Low-level mediation of directionally specific motion aftereffects: Motion perception is not necessary |
Q45284025 | MLA-sensitive cholinergic receptors involved in the detection of complex moving stimuli in retina |
Q73689756 | Magnetic response of human extrastriate cortex in the detection of coherent and incoherent motion |
Q48254837 | Microstimulation of visual cortex affects the speed of perceptual decisions |
Q39251837 | Monkey and humans exhibit similar motion-processing mechanisms |
Q34842375 | Motion area V5/MT+ response to global motion in the absence of V1 resembles early visual cortex |
Q73733281 | Motion contrast: a new metric for direction discrimination |
Q52241653 | Motion detection on flashed, stationary pedestal gratings: evidence for an opponent-motion mechanism. |
Q48449630 | Motion evoked brain potentials parallel the consistency of coherent motion perception in humans |
Q34577654 | Motion integration by neurons in macaque MT is local, not global |
Q41683717 | Motion opponency in visual cortex |
Q36945126 | Motion processing, directional selectivity, and conscious visual perception in the human brain |
Q77190152 | Motion rivalry impairs motion repulsion |
Q61714302 | Motion transparency promotes synchronous perceptual binding |
Q30478144 | Moving from spatially segregated to transparent motion: A modelling approach |
Q34657720 | Multiple uses of visual motion. The case for stability in sensory cortex |
Q91674839 | Neural Correlates of Sensory Abnormalities Across Developmental Disabilities |
Q36289057 | Neural computations governing spatiotemporal pooling of visual motion signals in humans |
Q41747538 | Neural correlates of contrast detection at threshold |
Q46599345 | Neural correlates of implied motion |
Q28214957 | Neural correlates of structure-from-motion perception in macaque V1 and MT |
Q49034896 | Neural dynamics of motion integration and segmentation within and across apertures |
Q37346339 | Neural mechanisms of speed perception: transparent motion |
Q41518932 | Neural mechanisms of visual motion perception in primates |
Q34537011 | Neural representation of motion-in-depth in area MT |
Q71684267 | Neural responses to velocity gradients in macaque cortical area MT |
Q48223838 | Neuronal adaptation to visual motion in area MT of the macaque |
Q39023468 | Neurons in Primate Visual Cortex Alternate between Responses to Multiple Stimuli in Their Receptive Field |
Q48787396 | Neurons in dorsal visual area V5/MT signal relative disparity. |
Q41238363 | Neurophysiology: neural fingerprints of visual attention |
Q34063197 | Normalization of neuronal responses in cortical area MT across signal strengths and motion directions |
Q79878628 | Object-based cross-feature attentional modulation from color to motion |
Q36826062 | Ocular following responses of monkeys to the competing motions of two sinusoidal gratings |
Q49111031 | Ocular responses to motion parallax stimuli: the role of perceptual and attentional factors |
Q39791954 | On event-based optical flow detection |
Q46793390 | Opponent backgrounds reduce discrimination sensitivity to competing motions: effects of different vertical motions on horizontal motion perception |
Q81395836 | Opponent-motion mechanisms are self-normalizing |
Q35945792 | Optogenetic Activation of Normalization in Alert Macaque Visual Cortex |
Q34430405 | Orientation selectivity of motion-boundary responses in human visual cortex |
Q45154498 | Orthogonal motion after-effect illusion predicted by a model of cortical motion processing |
Q91781374 | Pattern Motion Processing by MT Neurons |
Q44976239 | Perception of three-dimensional structure from motion |
Q64938790 | Perceptual Transparency From Cast Shadow. |
Q35546938 | Perceptual and neural consequences of rapid motion adaptation. |
Q41850877 | Perceptual asynchrony for motion |
Q48545039 | Perceptual costs for motion transparency evaluated by two performance measures |
Q34551406 | Perceptual learning of motion direction discrimination with suppressed and unsuppressed MT in humans: an fMRI study |
Q50735340 | Perceptual separation of transparent motion components: the interaction of motion, luminance and shape cues. |
Q37419929 | Phenomenology and neurophysiological correlations: two approaches to perception research |
Q92489691 | Population receptive field estimates for motion-defined stimuli |
Q42946339 | Predicting human perceptual decisions by decoding neuronal information profiles. |
Q82793327 | Predicting the motion after-effect from sensitivity loss |
Q72113360 | Preservation of Pointing Accuracy Toward Moving Targets After Extensive Visual Cortical Ablations in Cats |
Q42836450 | Psychophysical and rTMS Evidence for the Presence of Motion Opponency in Human V5. |
Q82791401 | Pushing the limits of transparent-motion detection with binocular disparity |
Q41179686 | Reconciling coherent oscillation with modulation of irregular spiking activity in selective attention: gamma-range synchronization between sensory and executive cortical areas |
Q37078564 | Reduction in direction discrimination with age and slow speed is due to both increased internal noise and reduced sampling efficiency |
Q48659142 | Representation of motion boundaries in retinotopic human visual cortical areas |
Q81168915 | Responses to direction and transparent motion stimuli in area FST of the macaque |
Q36337549 | Responses to second-order texture modulations undergo surround suppression |
Q42099276 | Selective attention through phase relationship of excitatory and inhibitory input synchrony in a model cortical neuron |
Q34017929 | Sensory competition in the face processing areas of the human brain |
Q41173152 | Sensory integration deficits support a dimensional view of psychosis and are not limited to schizophrenia. |
Q47677908 | Sensory perception in autism |
Q37629762 | Similar adaptation effects in primary visual cortex and area MT of the macaque monkey under matched stimulus conditions |
Q41292350 | Similar contrast sensitivity functions measured using psychophysics and optokinetic nystagmus. |
Q34445749 | Slow eye movements |
Q47328774 | Smoothness of stimulus motion can affect vection strength. |
Q73948546 | Spatial frequency tuning for 3-D corrugations from motion parallax |
Q47848582 | Spatial proximity modulates the strength of motion opponent suppression elicited by locally paired dot displays. |
Q43757179 | Spatial scale of motion segmentation from speed cues. |
Q41671954 | Spatial summation in the receptive fields of MT neurons. |
Q36953686 | Spatial summation properties of the human ocular following response (OFR): evidence for nonlinearities due to local and global inhibitory interactions |
Q21129146 | Spatial warping by oriented line detectors can counteract neural delays |
Q52076789 | Speed and direction of locally-paired dot patterns. |
Q73733269 | Speed tuning of motion segmentation and discrimination |
Q26866226 | Spikes, BOLD, attention, and awareness: a comparison of electrophysiological and fMRI signals in V1 |
Q74595271 | Stereoscopic segregation of transparent surfaces and the effect of motion contrast |
Q53030552 | Stimulus-contrast-induced biases in activation order reveal interaction between V1/V2 and human MT+. |
Q34158691 | Stimulus-dependent modulation of suppressive influences in MT |
Q52006356 | Subjective appearance of ambiguous structure-from-motion can be driven by objective switches of a separate less ambiguous context. |
Q48547579 | Subtractive and divisive adaptation in the human visual system |
Q49385841 | Synchronous and asynchronous perceptual bindings of colour and motion following identical stimulations. |
Q36312174 | Task-dependent influences of attention on the activation of human primary visual cortex |
Q42435576 | Temporal dynamics of decision-making during motion perception in the visual cortex |
Q57043184 | The Hierarchical nature of perceiving direction of motion in depth from optic flow |
Q48957332 | The analysis of complex motion patterns by form/cue invariant MSTd neurons |
Q87886439 | The coupling of vision with locomotion in cortical blindness |
Q64115324 | The direction after-effect is a global motion phenomenon |
Q100422628 | The effect of action on perceptual feature binding |
Q74783579 | The effect of complex motion pattern on speed perception |
Q60213718 | The effects of ageing on reaction times to motion onset |
Q79185149 | The efficiency of speed discrimination for coherent and transparent motion |
Q35151464 | The influence of spatiotemporal structure of noisy stimuli in decision making |
Q37382989 | The normalization model of attention |
Q48564720 | The response of neurons in areas V1 and MT of the alert rhesus monkey to moving random dot patterns |
Q35560292 | The responses of V1 cortical neurons to flashed presentations of orthogonal single lines and edges |
Q52172162 | The role of terminators and occlusion cues in motion integration and segmentation: a neural network model. |
Q36151640 | The vergence eye movements induced by radial optic flow: some fundamental properties of the underlying local-motion detectors |
Q33359314 | Top-down and bottom-up mechanisms in biasing competition in the human brain |
Q52361080 | V1 responses to transparent and nontransparent motions. |
Q36571276 | Velocity computation in the primate visual system. |
Q73986550 | Velocity decomposition and surface decomposition--reciprocal interactions between motion and form processing |
Q36077550 | Visual attention: the past 25 years |
Q84184833 | Visual motion gradient sensitivity shows scale invariant spatial frequency and speed tuning properties |
Q48879994 | Visual motion integration by neurons in the middle temporal area of a New World monkey, the marmoset |
Q37982694 | Visual pathways serving motion detection in the mammalian brain |
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