| Q45911173 | 50 Years of Stereoblindness: Reconciliation of a Continuum of Disparity Detectors With Blindness for Disparity in Near or Far Depth. |
| Q35092679 | 7 tesla FMRI reveals systematic functional organization for binocular disparity in dorsal visual cortex |
| Q35881538 | A Modality-Specific Feedforward Component of Choice-Related Activity in MT. |
| Q38852525 | A Model of Binocular Motion Integration in MT Neurons. |
| Q37083863 | A causal role for V5/MT neurons coding motion-disparity conjunctions in resolving perceptual ambiguity. |
| Q28649556 | A common framework for the analysis of complex motion? Standstill and capture illusions |
| Q35069756 | A functional link between MT neurons and depth perception based on motion parallax |
| Q34637921 | A leaky-integrator model as a control mechanism underlying flexible decision making during task switching |
| Q48716221 | A logarithmic, scale-invariant representation of speed in macaque middle temporal area accounts for speed discrimination performance. |
| Q36740514 | A map for horizontal disparity in monkey V2 |
| Q51983048 | A model that integrates eye velocity commands to keep track of smooth eye displacements. |
| Q94593592 | A motion-in-depth model based on inter-ocular velocity to estimate direction in depth |
| Q36940391 | A neural basis for the spatial suppression of visual motion perception |
| Q30482241 | A neural representation of depth from motion parallax in macaque visual cortex |
| Q30612372 | A novel role for visual perspective cues in the neural computation of depth |
| Q41207420 | A simple approach to ignoring irrelevant variables by population decoding based on multisensory neurons |
| Q47327570 | A unifying motif for spatial and directional surround suppression. |
| Q48250866 | Acute alcohol exposure impairs neural representation of visual motion speed in the visual cortex area posteromedial lateral suprasylvian cortex of cats |
| Q52038200 | Adaptation in macaque MT reduces perceived speed and improves speed discrimination. |
| Q48749892 | Adaptive estimation of three-dimensional structure in the human brain |
| Q37323031 | Aging affects the neural representation of speed in Macaque area MT. |
| Q27303019 | Anisotropy in spatial summation properties of human Ocular-Following Response (OFR) |
| Q34537023 | Area MT encodes three-dimensional motion |
| Q30414208 | Area V5-a microcosm of the visual brain |
| Q64104890 | Areal differences in depth cue integration between monkey and human |
| Q92403019 | Autonomous Development of Active Binocular and Motion Vision Through Active Efficient Coding |
| Q48607888 | Behavioral receptive field for ocular following in humans: dynamics of spatial summation and center-surround interactions |
| Q41870639 | Biased associative representations in parietal cortex |
| Q38651493 | Binocular Mechanisms of 3D Motion Processing |
| Q34621930 | Binocular depth perception and the cerebral cortex. |
| Q35679285 | Binocular disparity tuning and visual-vestibular congruency of multisensory neurons in macaque parietal cortex |
| Q81213910 | Binocular energy responses to natural images |
| Q28742139 | Binocular vision |
| Q48510473 | Breaking camouflage: responses of neurons in the middle temporal area to stimuli defined by coherent motion |
| Q48350548 | Change in choice-related response modulation in area MT during learning of a depth-discrimination task is consistent with task learning. |
| Q37119670 | Clustering of self-motion selectivity and visual response properties in macaque area MSTd |
| Q35126779 | Coding of stereoscopic depth information in visual areas V3 and V3A. |
| Q88812353 | Cognition as a Window into Neuronal Population Space |
| Q33981356 | Combining feature selection and integration--a neural model for MT motion selectivity |
| Q47366257 | Computation of Object Size in Visual Cortical Area V4 as a Neural Basis for Size Constancy. |
| Q48340847 | Conjunctions between motion and disparity are encoded with the same spatial resolution as disparity alone |
| Q47867072 | Contrast dependence of suppressive influences in cortical area MT of alert macaque. |
| Q49052271 | Contrast sensitivity of MT receptive field centers and surrounds |
| Q48714860 | Contrast-dependent OFF-dominance in cat primary visual cortex facilitates discrimination of stimuli with natural contrast statistics. |
| Q79947507 | Contribution of area MT to stereoscopic depth perception: choice-related response modulations reflect task strategy |
| Q48324412 | Contribution of middle temporal area to coarse depth discrimination: comparison of neuronal and psychophysical sensitivity. |
| Q30501246 | Contributions of indirect pathways to visual response properties in macaque middle temporal area MT |
| Q48666263 | Decoding conjunctions of direction-of-motion and binocular disparity from human visual cortex |
| Q90002962 | Dichoptic vision in the absence of attention: neither fusion nor rivalry |
| Q39140476 | Disambiguating Necker cube rotation using a location cue: what types of spatial location signal can the visual system learn? |
| Q42073560 | Disambiguation of Necker cube rotation by monocular and binocular depth cues: relative effectiveness for establishing long-term bias |
| Q36989213 | Disparity channels in early vision |
| Q91966970 | Disparity level identification using the voxel-wise Gabor model of fMRI data |
| Q44540546 | Disparity-based coding of three-dimensional surface orientation by macaque middle temporal neurons. |
| Q34159826 | Disparity-tuned population responses from human visual cortex |
| Q48821982 | Disparity-tuning characteristics of neuronal responses to dynamic random-dot stereograms in macaque visual area V4. |
| Q47445836 | Dissociation of Self-Motion and Object Motion by Linear Population Decoding That Approximates Marginalization |
| Q30496735 | Does the middle temporal area carry vestibular signals related to self-motion? |
| Q52017584 | Dynamics of the influence of segmentation cues on orientation perception. |
| Q35911887 | Early computational processing in binocular vision and depth perception. |
| Q36661424 | Effect of vertical disparities on depth representation in macaque monkeys: MT physiology and behavior |
| Q36984196 | Estimating distance during self-motion: a role for visual-vestibular interactions |
| Q35138393 | Feature attention for binocular disparity in primate area MT depends on tuning strength |
| Q30485980 | Fine discrimination training alters the causal contribution of macaque area MT to depth perception |
| Q36594007 | Frontal eye field neurons assess visual stability across saccades. |
| Q35547921 | Functional architecture for disparity in macaque inferior temporal cortex and its relationship to the architecture for faces, color, scenes, and visual field. |
| Q100738338 | Functional links between sensory representations, choice activity, and sensorimotor associations in parietal cortex |
| Q37422603 | Global motion perception in 2-year-old children: a method for psychophysical assessment and relationships with clinical measures of visual function |
| Q36103938 | Global motion perception is independent from contrast sensitivity for coherent motion direction discrimination and visual acuity in 4.5-year-old children. |
| Q91689385 | Going with the Flow: The Neural Mechanisms Underlying Illusions of Complex-Flow Motion |
| Q37056967 | Higher order visual processing in macaque extrastriate cortex |
| Q36799874 | Increasing the accuracy of electromagnetic inverses using functional area source correlation constraints. |
| Q36649487 | Integrating motion and depth via parallel pathways. |
| Q40756165 | Integration of Multiple Spatial Frequency Channels in Disparity-Sensitive Neurons in the Primary Visual Cortex. |
| Q46132199 | Interactions between speed and contrast tuning in the middle temporal area: implications for the neural code for speed. |
| Q37130936 | Joint representation of depth from motion parallax and binocular disparity cues in macaque area MT. |
| Q37441459 | Joint tuning for direction of motion and binocular disparity in macaque MT is largely separable |
| Q30480120 | Linking neural representation to function in stereoscopic depth perception: roles of the middle temporal area in coarse versus fine disparity discrimination |
| Q42543756 | MT neurons combine visual motion with a smooth eye movement signal to code depth-sign from motion parallax |
| Q44557646 | Macaque middle temporal neurons signal depth in the absence of motion. |
| Q35598714 | Mapping the macaque superior temporal sulcus: functional delineation of vergence and version eye-movement-related activity |
| Q37012603 | Mechanisms underlying the transformation of disparity signals from V1 to V2 in the macaque |
| Q98282896 | Modelling binocular disparity processing from statistics in natural scenes |
| Q36984032 | Multimodal coding of three-dimensional rotation and translation in area MSTd: comparison of visual and vestibular selectivity |
| Q38027547 | Multiplexing in the primate motion pathway |
| Q48858407 | Multivoxel pattern selectivity for perceptually relevant binocular disparities in the human brain |
| Q27323558 | Neural architectures for stereo vision. |
| Q48345613 | Neural correlates of disparity-defined shape discrimination in the human brain |
| Q48693272 | Neural correlates of fine depth discrimination in monkey inferior temporal cortex. |
| Q39239051 | Neural mechanisms of oculomotor abnormalities in the infantile strabismus syndrome |
| Q37346339 | Neural mechanisms of speed perception: transparent motion |
| Q34537011 | Neural representation of motion-in-depth in area MT |
| Q48787396 | Neurons in dorsal visual area V5/MT signal relative disparity. |
| Q45868488 | Nonhuman Primate Studies to Advance Vision Science and Prevent Blindness |
| Q46023844 | Optic Flow Signals in Extrastriate Area MST: Comparison of Perceptual and Neuronal Sensitivity |
| Q47384387 | Optimal size for perceiving motion decreases with contrast |
| Q48474195 | Orientation specificity of contrast adaptation in mouse primary visual cortex |
| Q30502073 | Parallel input channels to mouse primary visual cortex |
| Q37298792 | Parietal reach region encodes reach depth using retinal disparity and vergence angle signals |
| Q24800325 | Perceptual "read-out" of conjoined direction and disparity maps in extrastriate area MT |
| Q37202354 | Perceptual integration for qualitatively different 3-D cues in the human brain |
| Q34502636 | Population anisotropy in area MT explains a perceptual difference between near and far disparity motion segmentation. |
| Q41828291 | Population coding in sparsely connected networks of noisy neurons |
| Q42475102 | Presetting Basal Ganglia for Volitional Actions |
| Q36747545 | Proactive control of sequential saccades in the human supplementary eye field |
| Q51644287 | Pursuing motion illusions: a realistic oculomotor framework for Bayesian inference. |
| Q48828407 | Quantitative characterization of disparity tuning in ventral pathway area V4. |
| Q37078564 | Reduction in direction discrimination with age and slow speed is due to both increased internal noise and reduced sampling efficiency |
| Q47316151 | Reduction in receptive field size of macaque MT neurons in the presence of visual noise |
| Q51614821 | Rejection of false matches for binocular correspondence in macaque visual cortical area V4. |
| Q35902451 | Representation of 3-D surface orientation by velocity and disparity gradient cues in area MT. |
| Q51968013 | Representation of shapes, edges, and surfaces across multiple cues in the human visual cortex. |
| Q48165583 | Representation of stereoscopic depth based on relative disparity in macaque area V4. |
| Q30412784 | Responses of neurons in the marmoset primary auditory cortex to interaural level differences: comparison of pure tones and vocalizations. |
| Q81168915 | Responses to direction and transparent motion stimuli in area FST of the macaque |
| Q49016489 | Responses to random dot motion reveal prevalence of pattern-motion selectivity in area MT. |
| Q48109124 | Saccade reaction times are influenced by caudate microstimulation following and prior to visual stimulus appearance |
| Q48302999 | Saccade suppression by electrical microstimulation in monkey caudate nucleus. |
| Q33873908 | Sample skewness as a statistical measurement of neuronal tuning sharpness |
| Q46346489 | Sensitivity of neurons in the middle temporal area of marmoset monkeys to random dot motion. |
| Q48302642 | Simple reaction times to cyclopean stimuli reveal that the binocular system is tuned to react faster to near than to far objects |
| Q45907642 | Spatial characteristics of motion-sensitive mechanisms change with age and stimulus spatial frequency. |
| Q30480126 | Spatial reference frames of visual, vestibular, and multimodal heading signals in the dorsal subdivision of the medial superior temporal area |
| Q48369033 | Spatial summation, end inhibition and side inhibition in the middle temporal visual area (MT). |
| Q42959275 | Spatiotemporal specificity of contrast adaptation in mouse primary visual cortex |
| Q48236922 | Stereopsis activates V3A and caudal intraparietal areas in macaques and humans |
| Q27342650 | Stereopsis is adaptive for the natural environment |
| Q41976796 | Stereoscopic Segmentation Cues Improve Visual Timing Performance in Spatiotemporally Cluttered Environments |
| Q33294713 | Stimulus motion propels traveling waves in binocular rivalry |
| Q41480541 | Subspace mapping of the three-dimensional spectral receptive field of macaque MT neurons. |
| Q26795622 | Suppressive mechanisms in visual motion processing: From perception to intelligence |
| Q51932085 | Temporal dynamics of 2D and 3D shape representation in macaque visual area V4. |
| Q37866699 | The Pulfrich effect in the clinic. |
| Q50506762 | The effect of monocular depth cues on the detection of moving objects by moving observers. |
| Q80725406 | The effect of overall stimulus velocity on motion parallax |
| Q34618245 | The integration of disparity, shading and motion parallax cues for depth perception in humans and monkeys |
| Q36991186 | The neural basis of depth perception from motion parallax |
| Q48270181 | The role of cortical area V5/MT+ in speed-tuned directional anisotropies in global motion perception. |
| Q48211915 | The spatial profile of macaque MT neurons is consistent with Gaussian sampling of logarithmically coordinated visual representation |
| Q34474348 | The stroboscopic Pulfrich effect is not evidence for the joint encoding of motion and depth |
| Q48516689 | Visual impairment by surrounding noise is due to interactions among stimuli in the higher-order visual cortex |