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1 motor performance, aversive conditioning and spatial navigation.
2 h a role in processing natural scenes during spatial navigation.
3 ppocampus of higher mammals are critical for spatial navigation.
4 lay behavioral abnormality in locomotion and spatial navigation.
5 ance to the goal or their conjunction during spatial navigation.
6 MEC) is specialized for path integration and spatial navigation.
7 findings, depressed patients showed impaired spatial navigation.
8 tex (EC) as key neural structures underlying spatial navigation.
9 olved in multisensory heading perception for spatial navigation.
10 e hippocampus, including episodic memory and spatial navigation.
11 s requiring Hip-mPFC interactions, including spatial navigation.
12 ts with hippocampal lesions were impaired in spatial navigation.
13 ests that these cell types are important for spatial navigation.
14 ed, but little is known about other kinds of spatial navigation.
15 e and platform-crossing scores indicative of spatial navigation.
16 tional insight into the neural mechanisms of spatial navigation.
17 key cellular mechanism for ensuring reliable spatial navigation.
18 entral complex, a brain region implicated in spatial navigation.
19 ghts into how cognitive maps are used during spatial navigation.
20 s markedly similar to those activated during spatial navigation.
21 mental simulation and future thinking beyond spatial navigation.
22  neural substrate for path integration-based spatial navigation.
23 o elucidate the neural mechanisms supporting spatial navigation.
24 rely upon integrated sensory information for spatial navigation.
25 ong-term potentiation as well as deficits in spatial navigation.
26 al system encodes a map of space that guides spatial navigation.
27 ns coding for head-direction are crucial for spatial navigation.
28 s a metric capable of supporting large-scale spatial navigation.
29 ex are thought to act as a neural metric for spatial navigation.
30 cipate in circuits involved in cognition and spatial navigation.
31 ortex, is essential for memory formation and spatial navigation.
32 ssibly supporting cognitive processes beyond spatial navigation.
33 omotor function, verbal episodic memory, and spatial navigation.
34 of hippocampal neurons to support memory and spatial navigation.
35 nimal's direction of heading are crucial for spatial navigation.
36 olling autonomous adaptive robots capable of spatial navigation.
37  hippocampus was related to the emergence of spatial navigation.
38        The hippocampus, a region crucial for spatial navigation [6-12] and episodic memory [13-18], h
39 e hippocampus has a well-documented role for spatial navigation across species, but its role for spat
40  same neurons that represent location during spatial navigation also code elements of verbal recall.
41 hypothesize that mechanisms that evolved for spatial navigation also support tracking of elapsed time
42 sentations, evolved for encoding distance in spatial navigation, also support episodic recall and the
43 tion, constitutes a fundamental mechanism of spatial navigation and a keystone for the development of
44 y improved motor coordination and normalized spatial navigation and anxiety of Gpr88(-/-) mice.
45 idence that different brain systems underlie spatial navigation and contextual learning has implicati
46  one task, HPC and DSL selectively supported spatial navigation and cue response, respectively.
47 rity of the hippocampus is critical for both spatial navigation and episodic memory, but how its neur
48                        Across the domains of spatial navigation and episodic memory, the hippocampus
49 an introduction to the mechanisms underlying spatial navigation and how they relate to general proces
50                     Furthermore, deficits in spatial navigation and long-term memory, major cognitive
51 cal field potential-plays a critical role in spatial navigation and memory by coordinating the activi
52                                              Spatial navigation and memory depend on the neural codin
53 ntorhinal cortex (MEC) is a major center for spatial navigation and memory.
54 ially selective neurons that are crucial for spatial navigation and memory.
55 nal cortex and part of a network involved in spatial navigation and memory.
56 ial entorhinal cortex (MEC) is important for spatial navigation and memory.
57 ical periods for alcohol-induced deficits in spatial navigation and passive avoidance learning were i
58 e OPA is causally involved in boundary-based spatial navigation and suggest that the OPA is the perce
59 a dorsal component generally associated with spatial navigation, and a ventral component primarily as
60  in support of movement planning, execution, spatial navigation, and autonomic responses to gravito-i
61 asized the importance of parietal cortex for spatial navigation, and efforts to identify the electrop
62 of cognitive abilities, including reasoning, spatial navigation, and memory.
63 potentially linked with cognitive functions, spatial navigation, and the homeostatic control of abnor
64 nt hippocampus exhibit spatial tuning during spatial navigation, and they are reactivated in specific
65 vo, exhibit spatial tuning during head-fixed spatial navigation, and undergo robust remapping of thei
66 or which most data are available to date, to spatial navigation are causally linked to disinhibition
67 at support the late postnatal development of spatial navigation are currently unknown.
68  present evidence for a neural code of human spatial navigation based on cells that respond at specif
69 l neurons and hippocampal place cells during spatial navigation behavior has yet to be elucidated.
70 ort how whole-brain networks are involved in spatial navigation behaviors and how normal aging alters
71 the rat hippocampus appeared not only during spatial navigation but also in the absence of changing e
72 l-entorhinal circuit is involved not only in spatial navigation, but also in a variety of memory-guid
73 ckade on tasks of verbal episodic memory and spatial navigation, but effects on attentional/psychomot
74 f evidence implicates the role of the RSC in spatial navigation, but it is unclear whether this struc
75 centration changes have been detected during spatial navigation, but little is known about the condit
76 pus is critical for some forms of memory and spatial navigation, but previous research has mostly neg
77 y prominent roles in computational models of spatial navigation, but their exact function remains unk
78   Theta oscillations facilitate encoding and spatial navigation, but to date, it has been difficult t
79 correlated with behaviors such as memory and spatial navigation, but we do not understand its specifi
80 of episodic memory in humans is the study of spatial navigation by path integration in rodents.
81                                              Spatial navigation can serve as a model system in cognit
82 ture integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness.
83 ain region frequently linked to processes of spatial navigation, contains neurons that discharge as a
84                    The authors aimed to link spatial navigation deficits previously documented in dep
85 nt spatial learning, whereas experience with spatial navigation delayed both concurrent and subsequen
86                                              Spatial navigation depends on dissociable memory systems
87 of behaviors via this system is required for spatial navigation during chemotaxis.
88  in vertebrates, the primacy of olfaction in spatial navigation, even in visual specialists, and prop
89 e-trial level, making a theta-phase code for spatial navigation feasible.
90 y perception, motor sequence generation, and spatial navigation, forging a direct link between cellul
91                     No previous study of bee spatial navigation has been able to follow animals' move
92 ever, the role of theta oscillators in human spatial navigation has not been explored.
93       Sensory perception, working memory and spatial navigation have been hypothesized to use phase c
94 ode for location and facing direction during spatial navigation have been investigated extensively; h
95 he neural mechanisms underlying ground-level spatial navigation have been investigated, but little is
96                          We show that during spatial navigation, hippocampal CA1 place cells maintain
97 Our aim was to determine whether allocentric spatial navigation impairment would be proportional to r
98 ndividual hippocampal CA1 place cells during spatial navigation in a virtual reality environment, mim
99 l cortices exhibit theta oscillations during spatial navigation in animals and humans, and in the for
100      Learning based on hippocampal-dependent spatial navigation in female rats was assessed at identi
101 o identify the electrophysiological signs of spatial navigation in humans have been stymied by the di
102 ency of 4-8 Hz) have long been implicated in spatial navigation in rodents; however, the role of thet
103 ntation (DTD) have a life-long impairment in spatial navigation in the absence of brain damage, neuro
104 ative understanding of the cellular basis of spatial navigation in the entorhinal cortex.
105                                              Spatial navigation in the real-world is a complex task t
106              High-level cortical systems for spatial navigation, including entorhinal grid cells, cri
107                           Sex differences in spatial navigation indicate that women may focus on posi
108                                              Spatial navigation is a complex process requiring integr
109                                              Spatial navigation is a complex process, but one that is
110                                              Spatial navigation is a fundamental part of daily life.
111                                  In rodents, spatial navigation is a major mode of goal-directed beha
112                                              Spatial navigation is a multisensory process involving i
113                                              Spatial navigation is an essential human skill that is i
114  and females differ in their use of cues for spatial navigation is an important question.
115                                              Spatial navigation is believed to be guided in part by r
116                                   Given that spatial navigation is considered to be a model of how th
117  understanding of the neuronal mechanisms of spatial navigation is derived from chronic recordings in
118                       A central component of spatial navigation is determining where one can and cann
119                    Although it is clear that spatial navigation is impaired during aging, the network
120                                              Spatial navigation is often used as a behavioral task in
121                             In many species, spatial navigation is supported by a network of place ce
122                         A central element of spatial navigation is the ability to recognize the landm
123                           A key component of spatial navigation is the ability to use visual informat
124                                   Successful spatial navigation is thought to employ a combination of
125                              We investigated spatial navigation learning and hippocampal interneurons
126 reased anxiety-like behavior and deficits in spatial navigation learning.
127 ese animals that presumably mediate accurate spatial navigation, little has been done to determine th
128    Among these individuals, deterioration in spatial navigation, manifested by poor hippocampus-depen
129 1 activity, interferes in the development of spatial navigation memory, and may play a role in normal
130 l and lateral entorhinal cortex (MEC/LEC) in spatial navigation, memory and related disease, their hu
131 orhinal cortex (mEC) is strongly involved in spatial navigation, memory, dementia and epilepsy.
132 orhinal cortex (mEC) is strongly involved in spatial navigation, memory, dementia and epilepsy.
133                                       During spatial navigation, neural activity in the hippocampus a
134 ientific studies have typically investigated spatial navigation on a horizontal 2D plane, leaving muc
135 Rats were trained on a plus maze in either a spatial navigation or a cue-response task (sequential tr
136            Offspring were tested in either a spatial navigation or an avoidance task as juveniles or
137 y encoding by designing an interactive human spatial navigation paradigm combined with multimodal neu
138 ds on retention are not due to disruption of spatial navigation per se.
139 rimination with two behavioral assays: (i) a spatial navigation radial arm maze task and (ii) a spati
140  wide range of behaviors, including feeding, spatial navigation, reproduction, and auditory processin
141                     Both episodic memory and spatial navigation require temporal encoding of the rela
142                                    Efficient spatial navigation requires not only accurate spatial kn
143            We also contrasted the respective spatial navigation scores of the real-space human Morris
144           Goal-directed behaviour outside of spatial navigation similarly requires a representation o
145 ie the cessation of exploratory activity and spatial navigation skills during hibernation.
146 ution calcium imaging to potentially include spatial navigation, social behavior, feeding and reward.
147 d offers an explanation for similar flexible spatial navigation strategies in arthropods and vertebra
148 rons called grid cells that form part of the spatial navigation system.
149 ks in the plus maze: a hippocampus-dependent spatial navigation task and a hippocampus-independent cu
150 ined exposure group took longer to learn the spatial navigation task compared with all other groups.
151 rat hippocampal CA1 cells were examined in a spatial navigation task in which two cylindrical landmar
152 ggest that temporal order memory tested in a spatial navigation task may provide a selective behavior
153  This intervention enhanced performance on a spatial navigation task that requires the encoding and r
154 l magnetic resonance imaging in a continuous spatial navigation task, in which frequent changes to th
155 is treatment restored the ability to learn a spatial navigation task, which is associated with hippoc
156 ing the specificity of memory deficit in the spatial navigation task.
157 hysiology and display behavioral deficits in spatial navigation tasks consonant with a deficit in the
158 iminated the typical male advantage found in spatial navigation tasks.
159 ect, gait impairment, motor coordination and spatial navigation tests.
160                                       During spatial navigation, the head orientation of an animal is
161 ore infusion, all groups demonstrated normal spatial navigation (training on days 1 and 2), whereas 3
162 ntrahippocampal ANI infusions on allocentric spatial navigation using the Morris water maze, a task w
163 ocial behavior using a sociability task, for spatial navigation using the Morris watermaze, for fear
164                                  Allocentric spatial navigation was tested in the real-space version
165 or postural control, gaze stabilization, and spatial navigation, we propose that detecting the direct
166 dance, path integration, discrimination, and spatial navigation were assessed.
167             The hippocampus is essential for spatial navigation, which may involve sequential learnin
168 tics of theta oscillations during ambulatory spatial navigation, while highlighting some fundamental
169 otential of behavioral and neural markers of spatial navigation, with a particular emphasis on neurod
170                                       During spatial navigation, women typically navigate an environm

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