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1  on the same neural populations that process visual input.
2 entation of head direction in the absence of visual input.
3 reated and then matched against the incoming visual input.
4 epresentations even in the absence of actual visual input.
5 rmed a maturational transition regardless of visual input.
6  and how these signals are combined with the visual input.
7 ophthalmic subjects, who have never received visual input.
8 s were indeed decorrelated compared with the visual input.
9 n to increasing the physical contrast of the visual input.
10 e reared in the dark to remove all patterned visual input.
11  in a visual system with drastically reduced visual input.
12 ions are flexible and rapidly reorganized by visual input.
13 ictable from neuronal responses generated by visual input.
14 ts are mutually inhibitory and depend on the visual input.
15 women), increasingly so with the addition of visual input.
16 e-to-face, providing concurrent auditory and visual input.
17 s that generalize from specific instances of visual input.
18 ires the brain to perform computation on the visual input.
19 o the more reliable position provided by the visual input.
20 layers to respond with different kinetics to visual input.
21 tinothalamic and thalamocortical transfer of visual input.
22 urred in a top-down manner, independently of visual input.
23  congruent stimulation were dominated by the visual input.
24 ffect our conscious perception of concurrent visual input.
25 situs could be attributed to the presence of visual input.
26 tion of mushroom bodies in ants, focusing on visual input.
27  does not depend upon normal organization of visual input.
28 f saccades or static presentation of natural visual input.
29 uring intrinsically generated disruptions to visual input.
30  recognize them from both dynamic and static visual input.
31 t that we make causes an abrupt shift of the visual input.
32 ps on the retina, causing a discontinuity in visual input.
33 nkeys can be individually changed by altered visual input.
34 crimination task with high- and low-contrast visual input.
35  information and modulating attention toward visual input.
36 te to rapid extraction of the content of the visual input.
37 na to detect the orientation of edges in the visual input.
38 al responses is not fixed but depends on the visual input.
39  on previous perception rather than previous visual input.
40 acts the neural representations of identical visual input.
41 viding two potential pathways for processing visual inputs.
42 es on feedforward and lateral integration of visual inputs.
43 error correction in predicting task-relevant visual inputs.
44 ion depended on the spatial frequency of the visual inputs.
45 involved in the conceptual identification of visual inputs.
46 uning of branches in regions with mismatched visual inputs.
47 eurons that extract salient information from visual inputs.
48 olving attentional modulation of subcortical visual inputs.
49 ginal gyrus in mediating competition between visual inputs.
50  constrains the perceptual interpretation of visual inputs.
51 ory inputs, whereas the caudal half receives visual inputs.
52 ivity in the tectum or by exposure to random visual inputs.
53 ut their effects on the neural processing of visual inputs.
54  color, orientation, and motion direction of visual inputs.
55  not whilst walking, the switch initiated by visual inputs.
56 m diverse modalities including olfactory and visual inputs.
57 occurrence was modulated by ongoing sensory (visual) input.
58 rom initial retinotopic (i.e., eye-centered) visual input?
59 to our understanding of how the SC processes visual inputs, a critical step in comprehending visually
60              The fact that she could process visual input accurately for the purposes of guiding acti
61 of the firing process that, given the recent visual input, accurately predicts the timing of individu
62 g visual response properties and integrating visual inputs across their receptive fields (RFs).
63 nder affecting spatial performance, and (ii) visual input affects veering.
64 (V1), where neurons are thought to integrate visual inputs along contours defined by an association f
65 P) nucleus, which receives both auditory and visual inputs, also projects to Dm and is the only dorsa
66              This growth is modulated by the visual input and accelerates considerably when the eye d
67              Eye blinks cause disruptions to visual input and are accompanied by rotations of the eye
68 del has been proposed that includes impaired visual input and central visual processing, impaired bra
69                           Despite reports of visual input and cognitive tasks modulating the VOR thro
70 he brain is capable of integrating "natural" visual input and direct cortical-somatosensory stimulati
71 yer (SGS) of the superior colliculus receive visual input and excite intermediate layer (SGI) neurons
72        To evaluate potential sources of this visual input and how they enter into the circuitry of th
73  eye field (FEF), an area that receives both visual input and information about imminent saccades.
74 ight hand, thereby creating conditions where visual input and motor output involve the same or opposi
75                            Mediating between visual input and motor output, the posterior parietal co
76 ng between grid cells exist independently of visual input and of spatially periodic firing.
77 llmarks of processing for different types of visual input and provide a promising path forward to inv
78 mic took place during a period of unchanging visual input and showed characteristics of both serial a
79 ern of activity in his hippocampus even when visual input and task were held constant.
80 sentations fully depend on the match between visual input and top-down attentional set: only objects
81 ders: They serve to represent many different visual inputs and convey a neural image of the scene dow
82 vity in low-light conditions to detect small visual inputs and decreases its sensitivity in bright-li
83  neural network, which received eye-centered visual inputs and head-centered vestibular inputs, repro
84 aptic modification can be induced by natural visual inputs and may be part of the underlying mechanis
85 ion in XMAC results from invasion by ectopic visual inputs and not from deafferentation.
86  cells carry about the future state of their visual inputs and show that nearly every cell in the ret
87 ecall of imprinting memory received indirect visual inputs and was determined by environmental stimul
88 pattern completion, firing in the absence of visual input, and nonlinear responses to environmental m
89  the subject as blink-induced alterations of visual input are blanked out without jeopardizing the pe
90  visual cortex, the first cells that receive visual input are simple cells in layer 4.
91  action when abrupt external triggers in the visual input are unavailable.
92 activity in the visual cortex during natural visual input are unknown.
93                   It has been suggested that visual inputs are fed to the navigational network in cor
94                                              Visual inputs arise from both the retina and visual cort
95 osterior suprasylvian field, whose principal visual input arises from cortical areas that appear to b
96 ral neuronal targets rather than confounding visual input, as they persisted unabated in carriers of
97 eract with the world while being deprived of visual input at a specified orientation.
98 opment, possibly as a consequence of altered visual input at the time of dendritic arbor refinement.
99 features do not result from exclusive use of visual inputs because we found much shorter delays and a
100 nderstanding someone is easier when there is visual input, because visual cues like mouth and tongue
101 for resolving the ambiguities often posed by visual inputs, because motor commands contain additional
102                  Blinks profoundly interrupt visual input but are rarely noticed, perhaps because of
103  which size-distance scaling is not based on visual inputs but on extraretinal cues.
104 ead movements are not directly controlled by visual input, but by internal estimation mechanisms simi
105 presentation can operate temporarily without visual input, but is updated from the vestibular system
106 b neurones have access to and can respond to visual input, but such signals are unlikely to be direct
107 mechanical or optical effects of blinking on visual input by combining pupil-independent retinal stim
108 ght compromise attempts to rescue or restore visual input by various interventional approaches.
109 h as the adaptation to a sustained change in visual inputs by prism goggles in humans, are not known.
110 the signals generated by neural responses to visual input can be either enhanced by increasing or sup
111 in our path or the sudden shift of a target, visual input can rapidly alter foot trajectory.
112 pears to be indirect, there is evidence that visual input can reach the motor cortex at relatively sh
113        Thus, for each cortical complex cell, visual inputs can be decomposed into two distinct types
114 tion judgment task, we found that, even when visual input changed randomly over time, perceived orien
115 oral modulation can change its sign when the visual input changes, a phenomenon that we call response
116 c range, even as the pattern and strength of visual inputs changes over development, suggesting that
117                                              Visual input consisting of natural scenes scanned by var
118                                         In a visual input containing many bars, one of them saliently
119                   New transformations of the visual input continue to be found: at least half of the
120  that dendritic spikes that are triggered by visual input contribute to a fundamental cortical comput
121                                   Absence of visual input did not weaken correlations, but other sour
122 refore, our data suggest that the absence of visual input does not prevent the emergence of functiona
123                                           Is visual input during critical periods of development cruc
124   These developmental changes require normal visual input during development and are disrupted by NMD
125                                     Abnormal visual input during development has dramatic effects on
126                                   Unbalanced visual input during development induces persistent alter
127 d input in normal snakes, partial absence of visual input during development may alter central organi
128  the lateral cerebellum (D zones) respond to visual inputs during visually guided tracking and it has
129                           Abnormal binocular visual input early in life contributes to poor outcomes
130  of behavioral studies in which VWM-matching visual input elicits a stronger behavioral and perceptua
131 Here, we demonstrate for the first time that visual input elicits an enhanced neural response when it
132 s with respect to the arrival of a subset of visual inputs evoked by local light stimulation on the r
133 are mostly intrinsically generated, and that visual input exerts but a modulatory influence.
134 perception of visual motion and provides the visual inputs for behaviors such as smooth pursuit eye m
135 gest a temporal constraint on the pattern of visual inputs for effective induction of stable synaptic
136 d by associative learning with olfactory and visual inputs for some neurons, and these neurons encode
137 ide a quantitative account of how elementary visual inputs form the ganglion cell receptive field.
138 cipital lesion that selectively disconnected visual input from a region of the brain that housed "opt
139 This may reflect a gradual transformation of visual input from an initial retinotopic representation
140 binocular stimulus designed to correlate the visual input from both eyes.
141 d mice to show that most SCN neurons receive visual input from just one eye.
142 e used immersive virtual reality to decouple visual input from motion-related interoception by manipu
143 a laminated structure, where each layer gets visual input from only one eye [1, 2].
144 wo types of bipolar interneurons that convey visual input from photoreceptors to a circuit that compu
145 of the Drosophila adult brain that processes visual input from the compound eye.
146  the region of cortex that normally receives visual input from the damaged area of the retina.
147                                  The massive visual input from the eye to the brain requires selectiv
148  systematically biased (i.e., pulled) toward visual input from the recent past.
149 TEMENT The superior colliculus (SC) receives visual input from the retina in its superficial layers (
150 nt sized, two-dimensional Gaussian sample of visual input from the retinotopic map laid out across th
151 t, primarily in alterations in the principal visual input from the thalamus, but the significant chan
152 al size in the dorsal stream and required no visual input from the ventral stream.
153 ypothesis, the VWFA develops at the nexus of visual inputs from retinotopic cortices and linguistic i
154 s (SC) is a midbrain nucleus that integrates visual inputs from the retina and primary visual cortex
155 ior colliculus (SC) are the major targets of visual inputs from the retina.
156 variously named caudal nucleus, which relays visual inputs from the SC to temporal visual cortex, is
157 sponses in auditory cortex are influenced by visual inputs from the superior temporal sulcus (STS), a
158                               Differences in visual inputs from the two eyes have been studied extens
159    Synaptic circuits in the retina transform visual input gathered by photoreceptors into messages th
160                                         When visual input has conflicting interpretations, conscious
161 e preserved ability to accurately respond to visual inputs has been demonstrated, a phenomenon referr
162 ty to extract probabilistic information from visual inputs has been reported in human adults and infa
163 , or the firing may depend upon the apparent visual input image stream.
164 ction of the approximately 15,000 elementary visual inputs impinging retinotopically onto the LGMD's
165  temporal correlation of spatially separated visual inputs implemented across neighboring retinotopic
166 M enhances the neural response to concurrent visual input in a content-specific way.
167 es in the spatial processing of eye-specific visual input in binocular primary visual cortex.
168  is the principal telencephalic recipient of visual input in humans and monkeys.
169 s and parts of the mushroom bodies receiving visual input in males, winged females, and workers of ca
170 ar projections to the Xenopus tectum require visual input in order to establish matching topographic
171 logical results underscore the importance of visual input in resolving perceptual ambiguity in a nois
172  to understand the series of operations from visual input in the retina to behavior by observing and
173                                 By degrading visual input in various ways, we are able to quantify th
174 topographically and establish alignment with visual inputs in the SC using a gradient-matching mechan
175                       (1) Without changes in visual input (including fixational eye movements), stati
176  stimulus onset (-200 to 0 ms), attention to visual input increased ongoing alpha power in IT relativ
177 o perform visual discriminations on the same visual input inspired a novel interpretation of the func
178 hus, the LGN employs at least three modes of visual input integration, each exhibiting different degr
179 ulation is grouped with synchronous attended visual input into a multisensory object, resulting in th
180  remarkable ability to integrate fragmentary visual input into a perceptually organized collection of
181 yet nonconscious ability to transform unseen visual input into motor output can be retained, a condit
182                                     Rewiring visual input into the auditory cortex at birth, however,
183 me, reflecting the brain's transformation of visual inputs into coherent category representations.
184 ided eye and arm movements transform generic visual inputs into effector-specific motor commands.
185 perceive a stable visual scene, although our visual input is constantly changing.
186 ort the hypothesis that correlated binocular visual input is essential for the maintenance of normal
187 ence is recreated after only a subset of the visual input is provided.
188                                              Visual input is relayed to V1 through segregated transie
189                                              Visual input is remarkably diverse.
190 r auditory input in mice and determined that visual input is required for accurate approach, allowing
191 ken together, these results demonstrate that visual input is required to sustain grid cell periodicit
192 ; a large set of poorly known codings of the visual input is transmitted to the brain.
193 ck of predictive information to the earliest visual input level (e.g., [6]), in line with predictive
194  with their visual selectivity only when the visual input matched that expected from the fly's moveme
195                        Active suppression of visual input may account for this perceptual continuity,
196 lopment of the visual system, the pattern of visual inputs may have an instructive role in refining d
197                                      Reduced visual inputs may weaken the vestibulo-ocular reflex, an
198 isions, not explained by this feature of the visual input, may be attributed to a combination of dete
199 visual scenes to guide behavior and thought, visual input needs to be organized into discrete units t
200 m body Kenyon cells that are postsynaptic to visual input neurons appear to integrate visual as well
201 ing of the attended speaker, whereas without visual input no significant attentional modulation was o
202                            In the absence of visual input, occipital ("visual") brain regions respond
203            We investigated whether congruent visual input of an attended speaker enhances cortical se
204  perceptual process capable of analyzing the visual input of the entire retinal image and pinpointing
205  can be modified rapidly and specifically by visual inputs of defined spatiotemporal patterns, in a m
206                                          How visual inputs of specific spatiotemporal patterns shape
207                                              Visual input often arrives in a noisy and discontinuous
208               We found that the influence of visual input on the neural tracking of the audio speech
209                               The pattern of visual inputs onto a tectal neuron was tracked over time
210  entrains to task structure independently of visual input or of standard neural predictors of haemody
211 on arises automatically from early bottom-up visual inputs or whether it depends on late top-down con
212 t item in WM enhanced processing of matching visual input, other "accessory" items in memory suppress
213 (V1) is especially susceptible to changes in visual input over a well-defined critical period, during
214                   How does the brain compare visual inputs over space and time to extract motion?
215  field: the anatomical focus of neglect; the visual input pathways implicated; impairments of spatial
216 primary vestibular, secondary vestibular and visual input pathways.
217 nput per se, nor by simultaneous tactile and visual input per se, nor by a shift in attention toward
218       The effect is not evoked by tactile or visual input per se, nor by simultaneous tactile and vis
219 ever, it is not clear what role the photopic visual input plays in this process and whether mouse myo
220                                              Visual inputs provide two to three layers of processes i
221                                              Visual input provides important landmarks for navigating
222 ference frame depend on the structure of the visual input, rather than just on retinal landmarks?
223  a substrate rather than a mere correlate of visual input regulation.
224                 In response to this abnormal visual input, retinal neural networks cause an excessive
225 datory insect larvae using a small number of visual inputs seem to distinguish complex image targets.
226 irectional tuning develops before vision and visual input serves primarily to anchor firing direction
227 perception, we combined spectral analysis of visual input signals, neural modeling, and gaze-continge
228 inar and cellular labeling is independent of visual input, since immunostaining is similar in 5-week
229           We conclude that in the absence of visual input, spoken language colonizes the visual syste
230  undergoes activity-dependent refinement and visual inputs strengthen, tectal neurons adapt their int
231 oustic /ba/ and hear /fa/ (illusion-fa), the visual input strengthens the weighting of the phone /f/
232 when a channel is strongly stimulated by the visual input, such that sensory noise is negligible, the
233 is within-saccade correction did not rely on visual input, suggesting that the brain monitored the oc
234 affect the behavioral response to concurrent visual input, suggesting that visual representations ori
235 ken, the TeO is organized in 15 layers where visual input targets the superficial layers while audito
236 ld enhance the neural response to concurrent visual input that matches the content of VWM.
237 ments of human observers from the changes in visual input that they normally cause.
238 sk if this optimization biases perception of visual inputs that are perceptually bistable.
239 mitantly with the parallel processing of the visual input, the activity initiated retinotopically and
240 we hypothesized that, even in the absence of visual input, the brain optimizes both auditory-only spe
241 hese findings suggest that in the absence of visual input, the eyes revert to a "default" growth stat
242                            In the absence of visual input, the selective modulation of this language-
243                   Although small relative to visual inputs, the projection from the fAES is of partic
244 gmentation theoretically involves passage of visual input through two layers of spatial linear filter
245 the primate retina and may therefore provide visual input to both the lateral geniculate nucleus and
246 F neurons in layers 2/3 of V1, which provide visual input to higher cortical areas, may explain why h
247                                              Visual input to layer 4 cortical cells between electrica
248 characterizing a fast automatic component of visual input to oculomotor competition.
249 tational model we predicted that biasing the visual input to orthogonal orientation in the two eyes s
250 plicating the need for rapid transmission of visual input to perceive motion.
251 dy investigated how neural representation of visual input to PFC neurons is regulated by dopamine.
252 ividuals to process conceptual, auditory and visual input to regain relatively fine voluntary control
253 ect representation and isolating subcortical visual input to the amygdala.
254 urrent knowledge about the precise timing of visual input to the cortex relies largely on spike timin
255 the amacrine cell interacted both with other visual input to the ganglion cell and with transmission
256 e the first detailed characterization of the visual input to the human retina during normal head-free
257  analogs, where the relative contribution of visual input to the multimodal sensory input of the EC i
258     This is in contrast to honey bees, where visual input to the mushroom bodies is more prominent an
259 d real-world scenes involves the matching of visual input to the observer's attentional set--an inter
260 ntly observed that the power spectrum of the visual input to the retina during ocular drift is largel
261 ntroduced by fixational eye movements in the visual input to the retina, which emphasize the high spa
262                                  KEY POINTS: Visual input to the suprachiasmatic nucleus circadian cl
263                      These data suggest that visual inputs to auditory cortex can enhance spatial pro
264 he receptive field arrangement of ON and OFF visual inputs to cortex.
265 rate retina are instrumental in transforming visual inputs to extract contrast, motion, and color inf
266 y present in areas that are known to provide visual inputs to MSTd.
267 senstein-Reichardt correlator (HRC), relates visual inputs to neural activity and behavioral response
268 th computational goals of the transform from visual inputs to neural responses, or the roles of the n
269  study the mechanisms of the transforms from visual inputs to neural responses.
270 ex interactions of excitatory and inhibitory visual inputs to neurons in the turtle's accessory optic
271 petition between incompatible or interfering visual inputs to reach awareness is resolved before thos
272 overexpression overrides the requirement for visual inputs to stimulate laminar refinement and dendri
273 he form, organization, and dimensionality of visual inputs to the brain and will serve as a platform
274                                  We describe visual inputs to the calyces of the mushroom bodies of t
275 sgranular region is the primary recipient of visual inputs to the rat retrosplenial cortex.
276  higher visual areas convey distinctly tuned visual inputs to V1 that serve to boost V1 neurons' resp
277  sensory inputs, including somatosensory and visual inputs, to produce a representation of the body.
278 rior commissures depriving one hemisphere of visual input (Tract and Split), two animals with transec
279 is unclear in these previous studies whether visual input truly enhances detection of tactile stimuli
280 f auditory cortex activity by the discrepant visual input underlies the ventriloquist illusion.
281  one or both eyes that blocked all patterned visual input until the cataractous lenses were removed a
282 state-dependent manner, i.e. its response to visual inputs varies with the motor context, a mechanism
283  postulated that the amygdala first receives visual input via a rapid subcortical route that conveys
284 put via the ventrolateral toral nucleus, and visual input via the optic tectum, and it projects to bo
285 revious work assumed that the elimination of visual input was sufficient to enhance plasticity in the
286 oustic /fa/ and hear /ba/ (illusion-ba), the visual input weakens the weighting of the phone /f/ repr
287  activations to matched and mismatched audio-visual inputs were contrasted with the combined response
288 he M component is predominantly dependent on visual input, whereas the A component requires the inter
289 or movement vector planning relies mostly on visual input, whereas the estimate used to compute the j
290 l role of LIPS is the same regardless of the visual input, whereas the functional role of LpMTG diffe
291 n are shaped by the statistical structure of visual input, which leads to more selective coding of fe
292 ed is usually rationalized by its match with visual input, which typically includes stationary or slo
293  interactions between competing auditory and visual inputs while varying spatial proximity, which aff
294 l cortex permits rapid categorization of the visual input, while the frontal cortex is part of a capa
295 and critically depends on the integration of visual input with motor output, likely impacts both moto
296  suggests that abnormal integration of audio-visual input with sensorimotor network activity is an im
297 on results from the integration of bottom-up visual input with top-down expectations.
298  This may reflect the demands of integrating visual inputs with the output response for the control d
299 ncephalon plays a major role in responses to visual input, yet regulation of neuronal differentiation
300 hape the V1 population response to different visual inputs, yet it is poorly understood.

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