コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 mpus is implicated in associative memory and spatial navigation.
2 s a metric capable of supporting large-scale spatial navigation.
3 ex are thought to act as a neural metric for spatial navigation.
4 cipate in circuits involved in cognition and spatial navigation.
5 ortex, is essential for memory formation and spatial navigation.
6 omotor function, verbal episodic memory, and spatial navigation.
7 nimal's direction of heading are crucial for spatial navigation.
8 olling autonomous adaptive robots capable of spatial navigation.
9 hippocampus was related to the emergence of spatial navigation.
10 motor performance, aversive conditioning and spatial navigation.
11 h a role in processing natural scenes during spatial navigation.
12 ppocampus of higher mammals are critical for spatial navigation.
13 lay behavioral abnormality in locomotion and spatial navigation.
14 MEC) is specialized for path integration and spatial navigation.
15 ed of movement, implicating these signals in spatial navigation.
16 findings, depressed patients showed impaired spatial navigation.
17 tex (EC) as key neural structures underlying spatial navigation.
18 olved in multisensory heading perception for spatial navigation.
19 e hippocampus, including episodic memory and spatial navigation.
20 ts with hippocampal lesions were impaired in spatial navigation.
21 ests that these cell types are important for spatial navigation.
22 ed, but little is known about other kinds of spatial navigation.
23 e and platform-crossing scores indicative of spatial navigation.
24 dinate neuronal firing to support memory and spatial navigation.
25 ell populations and associated with accurate spatial navigation.
26 re in memory using coding schemes typical of spatial navigation.
27 dy theoretical models of the brain's role in spatial navigation.
28 e their cognitive abilities in the domain of spatial navigation.
29 alternating between remote visual search and spatial navigation.
30 ned reward locations in dCA1 and iCA1 during spatial navigation.
31 odes make an essential contribution to socio-spatial navigation.
32 interrogate the dynamics of behavior during spatial navigation.
33 ring SWR-associated memory consolidation and spatial navigation.
34 sleep, and context- and experience-dependent spatial navigation.
35 t lead to generic deficits in orientation or spatial navigation.
36 be a potential link of sensory decisions to spatial navigation.
37 -place associations and guide olfactory-cued spatial navigation.
38 le in cognitive functions such as memory and spatial navigation.
39 nvolved in learning and memory as well as in spatial navigation.
40 Both regions are involved in spatial navigation.
41 the hippocampal formation and is involved in spatial navigation.
42 itive functions, such as episodic memory and spatial navigation.
43 ion (HD) and provide an internal compass for spatial navigation.
44 ion is thought to be critical for memory and spatial navigation.
45 ta oscillations-that contribute to facets of spatial navigation.
46 onal activity and related functions, such as spatial navigation.
47 al system encodes a map of space that guides spatial navigation.
48 ssibly supporting cognitive processes beyond spatial navigation.
49 of hippocampal neurons to support memory and spatial navigation.
50 ance to the goal or their conjunction during spatial navigation.
51 s requiring Hip-mPFC interactions, including spatial navigation.
52 tional insight into the neural mechanisms of spatial navigation.
53 key cellular mechanism for ensuring reliable spatial navigation.
54 entral complex, a brain region implicated in spatial navigation.
55 ghts into how cognitive maps are used during spatial navigation.
56 s markedly similar to those activated during spatial navigation.
57 mental simulation and future thinking beyond spatial navigation.
58 neural substrate for path integration-based spatial navigation.
59 o elucidate the neural mechanisms supporting spatial navigation.
60 rely upon integrated sensory information for spatial navigation.
61 ong-term potentiation as well as deficits in spatial navigation.
62 ns coding for head-direction are crucial for spatial navigation.
64 g that of grid cells, which is well known in spatial navigation(8,9), to integrate dimensions in this
65 ms of this study were to (a) investigate the spatial navigation abilities of AD patients in VR enviro
66 ed in a video game(16) to measure non-verbal spatial navigation ability in 397,162 people from 38 cou
69 e hippocampus has a well-documented role for spatial navigation across species, but its role for spat
70 same neurons that represent location during spatial navigation also code elements of verbal recall.
71 hypothesize that mechanisms that evolved for spatial navigation also support tracking of elapsed time
72 sentations, evolved for encoding distance in spatial navigation, also support episodic recall and the
73 tion, constitutes a fundamental mechanism of spatial navigation and a keystone for the development of
75 light on the neural mechanisms that underlie spatial navigation and awareness of others in real-world
76 idence that different brain systems underlie spatial navigation and contextual learning has implicati
80 campus, a brain region that is important for spatial navigation and episodic memory, benefits from a
81 rity of the hippocampus is critical for both spatial navigation and episodic memory, but how its neur
85 w studies apply them to characterizing human spatial navigation and even fewer systematically compare
87 subjected to 6 months of EE showed improved spatial navigation and had significantly fewer plaques i
88 l circuits involved in visual perception and spatial navigation and highlight the major remaining kno
89 an introduction to the mechanisms underlying spatial navigation and how they relate to general proces
92 ngle-neuron and macroscopic brain signals of spatial navigation and may provide a mechanistic basis f
94 cal field potential-plays a critical role in spatial navigation and memory by coordinating the activi
95 gions best known for their cognitive role in spatial navigation and memory corresponds to precise phy
100 cognitive maps in the hippocampus underlying spatial navigation and memory, by identifying hippocampa
110 ical periods for alcohol-induced deficits in spatial navigation and passive avoidance learning were i
111 erentially involved in memory consolidation, spatial navigation and pattern separation, complex funct
112 he same environment of hippocampal-dependent spatial navigation and striatal-dependent approach of a
113 e OPA is causally involved in boundary-based spatial navigation and suggest that the OPA is the perce
114 nal turn-by-turn navigation promotes passive spatial navigation and ultimately, poor spatial learning
116 a dorsal component generally associated with spatial navigation, and a ventral component primarily as
117 itive functions, including scene perception, spatial navigation, and autobiographical memory retrieva
118 in support of movement planning, execution, spatial navigation, and autonomic responses to gravito-i
119 asized the importance of parietal cortex for spatial navigation, and efforts to identify the electrop
121 or learning, memory, pattern separation, and spatial navigation, and its dysfunction is associated wi
122 enance of attention, behavioral flexibility, spatial navigation, and learning and memory, those cogni
123 mpus (HPC) is essential for tasks of memory, spatial navigation, and learning, calcium imaging of lar
126 potentially linked with cognitive functions, spatial navigation, and the homeostatic control of abnor
127 nt hippocampus exhibit spatial tuning during spatial navigation, and they are reactivated in specific
128 vo, exhibit spatial tuning during head-fixed spatial navigation, and undergo robust remapping of thei
131 or which most data are available to date, to spatial navigation are causally linked to disinhibition
134 me brain regions and neural codes supporting spatial navigation are recruited when humans use languag
135 present evidence for a neural code of human spatial navigation based on cells that respond at specif
136 e direct influence of place cell activity on spatial navigation behavior has not yet been demonstrate
137 l neurons and hippocampal place cells during spatial navigation behavior has yet to be elucidated.
138 ort how whole-brain networks are involved in spatial navigation behaviors and how normal aging alters
142 the rat hippocampus appeared not only during spatial navigation but also in the absence of changing e
143 l-entorhinal circuit is involved not only in spatial navigation, but also in a variety of memory-guid
144 ckade on tasks of verbal episodic memory and spatial navigation, but effects on attentional/psychomot
145 f evidence implicates the role of the RSC in spatial navigation, but it is unclear whether this struc
146 centration changes have been detected during spatial navigation, but little is known about the condit
148 pus is critical for some forms of memory and spatial navigation, but previous research has mostly neg
149 y prominent roles in computational models of spatial navigation, but their exact function remains unk
150 Theta oscillations facilitate encoding and spatial navigation, but to date, it has been difficult t
151 structures are critical for both memory and spatial navigation, but we do not fully understand the n
152 correlated with behaviors such as memory and spatial navigation, but we do not understand its specifi
158 activity in PMd-cck projections to thalamic spatial navigation circuits is necessary for context-spe
159 ture integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness.
160 mporal sequences that are thought to mediate spatial navigation, cognitive processing, and motor acti
161 ain region frequently linked to processes of spatial navigation, contains neurons that discharge as a
162 in an adapted T-maze guided by 2-dimensional spatial navigation cues and relearn the location when sp
163 tructures and neuronal networks that mediate spatial navigation, decision-making, sociality, and crea
165 nt spatial learning, whereas experience with spatial navigation delayed both concurrent and subsequen
167 Learning and memory deficits, including spatial navigation difficulties, are common in autism sp
169 he representation of the environment, reduce spatial navigation efficiency, distort distance estimati
170 its roles in conscious memory consolidation, spatial navigation, emotion, and motivated behaviors.
171 in vertebrates, the primacy of olfaction in spatial navigation, even in visual specialists, and prop
173 y perception, motor sequence generation, and spatial navigation, forging a direct link between cellul
174 entangle the circuitry underlying memory and spatial navigation functions of the parasubiculum.SIGNIF
180 nal, and head direction (HD) networks during spatial navigation have been clearly documented, while t
183 ode for location and facing direction during spatial navigation have been investigated extensively; h
184 he neural mechanisms underlying ground-level spatial navigation have been investigated, but little is
185 sponses of grid cells in contexts other than spatial navigation have presented a challenge to existin
187 Our aim was to determine whether allocentric spatial navigation impairment would be proportional to r
190 ndividual hippocampal CA1 place cells during spatial navigation in a virtual reality environment, mim
191 l cortices exhibit theta oscillations during spatial navigation in animals and humans, and in the for
192 Learning based on hippocampal-dependent spatial navigation in female rats was assessed at identi
193 o identify the electrophysiological signs of spatial navigation in humans have been stymied by the di
195 ency of 4-8 Hz) have long been implicated in spatial navigation in rodents; however, the role of thet
197 ntation (DTD) have a life-long impairment in spatial navigation in the absence of brain damage, neuro
213 understanding of the neuronal mechanisms of spatial navigation is derived from chronic recordings in
223 ion traditionally associated with memory and spatial navigation, is also involved in metabolic regula
225 navigation, we can engage users in their own spatial navigation, leading to a better spatial understa
226 couraged to take an active role in their own spatial navigation, leading to more accurate cognitive m
231 ese animals that presumably mediate accurate spatial navigation, little has been done to determine th
232 c risk factors (e.g., APOE, age, and sex) on spatial navigation make it difficult to identify persons
233 Among these individuals, deterioration in spatial navigation, manifested by poor hippocampus-depen
234 1 activity, interferes in the development of spatial navigation memory, and may play a role in normal
235 l and lateral entorhinal cortex (MEC/LEC) in spatial navigation, memory and related disease, their hu
239 ientific studies have typically investigated spatial navigation on a horizontal 2D plane, leaving muc
240 Rats were trained on a plus maze in either a spatial navigation or a cue-response task (sequential tr
243 y encoding by designing an interactive human spatial navigation paradigm combined with multimodal neu
245 riables may be independently associated with spatial navigation performance, and as to whether gender
246 rimination with two behavioral assays: (i) a spatial navigation radial arm maze task and (ii) a spati
247 MTL) is known to support episodic memory and spatial navigation, raising the possibility that its tru
248 wide range of behaviors, including feeding, spatial navigation, reproduction, and auditory processin
255 ution calcium imaging to potentially include spatial navigation, social behavior, feeding and reward.
256 d offers an explanation for similar flexible spatial navigation strategies in arthropods and vertebra
259 ks in the plus maze: a hippocampus-dependent spatial navigation task and a hippocampus-independent cu
260 ined exposure group took longer to learn the spatial navigation task compared with all other groups.
261 terneurons as mice performed a goal-directed spatial navigation task in new visual virtual reality (V
262 rat hippocampal CA1 cells were examined in a spatial navigation task in which two cylindrical landmar
263 ggest that temporal order memory tested in a spatial navigation task may provide a selective behavior
264 ction were quantified while rats performed a spatial navigation task requiring rapid memory formation
265 This intervention enhanced performance on a spatial navigation task that requires the encoding and r
266 RSC theta oscillation (4-8 Hz) in an active spatial navigation task where participants actively ambu
267 ed with an enhanced incidence of errors in a spatial navigation task, but it did not affect spatial c
268 l magnetic resonance imaging in a continuous spatial navigation task, in which frequent changes to th
270 is treatment restored the ability to learn a spatial navigation task, which is associated with hippoc
274 hysiology and display behavioral deficits in spatial navigation tasks consonant with a deficit in the
276 uman single-neuron recordings during virtual spatial navigation tasks to identify neurons providing a
278 When the clustering model is applied to spatial navigation tasks, so-called place and grid cell-
284 igation of the brain areas involved in human spatial navigation, the traditional focus has been on vi
285 onses in brain regions typically involved in spatial navigation: the medial prefrontal cortex and the
286 ore infusion, all groups demonstrated normal spatial navigation (training on days 1 and 2), whereas 3
287 ntrahippocampal ANI infusions on allocentric spatial navigation using the Morris water maze, a task w
288 ocial behavior using a sociability task, for spatial navigation using the Morris watermaze, for fear
290 h age, cognitive performance, as measured by spatial navigation, was found to have an inverted u-shap
291 or postural control, gaze stabilization, and spatial navigation, we propose that detecting the direct
292 ecording human single-neuron activity during spatial navigation, we show that spatially tuned neurons
294 o draw parallels between interval timing and spatial navigation, where direct analogies can be made b
296 nhance the ability to integrate objects into spatial navigation, which would be an advantage for migr
297 tics of theta oscillations during ambulatory spatial navigation, while highlighting some fundamental
298 otential of behavioral and neural markers of spatial navigation, with a particular emphasis on neurod
299 a novel perspective on neural mechanisms of spatial navigation within richer sensory environments, a