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1 perties is the spatially selective firing of hippocampal 'place cells'.
2  be precisely connected to the properties of hippocampal place cells.
3 te reorganization of the firing locations of hippocampal place cells.
4 ough replay of sequential neural activity in hippocampal place cells.
5 gdala can produce stress-like alterations on hippocampal place cells.
6 ts underlying the spatial firing patterns of hippocampal place cells.
7 hanges in firing rates, but not locations of hippocampal place cells.
8 onsible for the phase-distance invariance of hippocampal place cells.
9  previously identified such responses within hippocampal place cells [1], the activity of which is th
10   Although these spatial functions depend on hippocampal place cells(2,3), the relationship between p
11 tail the possible head-directional tuning of hippocampal place cells across species.
12  memory task, providing causal evidence that hippocampal place cells actively support spatial navigat
13 s during observation also predict subsequent hippocampal place cell activities during sharp-wave ripp
14    Visual cues exert a powerful control over hippocampal place cell activities that encode external s
15      The V1 location-specific activity leads hippocampal place cell activity both spatially and tempo
16                                              Hippocampal place cell activity in subsequent SIA episod
17                    We therefore examined rat hippocampal place cell activity in the context of spatia
18                                              Hippocampal place cell activity spans spatial and non-sp
19 thesis, we inactivated the mPFC and recorded hippocampal place cell activity while animals were perfo
20 es to an environment result in plasticity of hippocampal place cell activity, while in the absence of
21                                              Hippocampal place-cell activity associated with theta os
22                                              Hippocampal place-cell activity associated with theta os
23                                    Models of hippocampal place cells and entorhinal grid cells based
24           In healthy brains, spatially tuned hippocampal place cells and entorhinal grid cells exhibi
25              In these experiments, we record hippocampal place cells and local field potential from t
26 predictions about the expected properties of hippocampal place cells and other cells of the proposed
27 atial cues, consistent with prior studies of hippocampal place cells and providing a rich representat
28              Although ADN HD cells (and also hippocampal place cells and theta cells) were identified
29                                              Hippocampal place cells and time cells seem well suited
30 ent study examines the effects of ethanol on hippocampal place-cell and interneuron activity in freel
31 body of literature on the characteristics of hippocampal "place cells" and their relevance for our un
32 ucidate the links among synaptic plasticity, hippocampal place cells, and spatial memory, place cells
33 c conditional plasticity for actively firing hippocampal place cells, and that the BLA mediates this
34                                              Hippocampal place cells are a model system of how the br
35                                              Hippocampal place cells are activated sequentially as an
36                 The unitary firing fields of hippocampal place cells are commonly assumed to be gener
37                               In particular, hippocampal place cells are hypothesized to encode the S
38                                              Hippocampal place cells are important for spatial learni
39                                              Hippocampal place cells are influenced by both self-moti
40                                              Hippocampal place cells are key to episodic memories.
41                                              Hippocampal place cells are known for their spatially se
42                                              Hippocampal place cells are neurons thought to be import
43                                              Hippocampal place cells are one such representation, fir
44                                              Hippocampal place cells are spatially tuned neurons that
45    Even during completely novel experiences, hippocampal "place cells" are rapidly configured such th
46 ignaling of fear influences the stability of hippocampal place cells as a function of threat distance
47 s process, here we interrogated ensembles of hippocampal place cells as rats explored 15 novel linear
48  potential relationships between engrams and hippocampal place cells, as well as the molecular, cellu
49                                              Hippocampal place cells can show similar firing patterns
50 t al. discover that neuronal firing rates of hippocampal place cells code for periodically repeating
51 e data also support the hypothesis that aged hippocampal place cells, compared with young, may more o
52                                              Hippocampal place cells contribute to mammalian spatial
53         In particular, the modality by which hippocampal place cells contribute to spatial memory is
54                                              Hippocampal place cells convey spatial information throu
55 preplay analyses to previously published rat hippocampal place cell data.
56 may be to help localize the firing fields of hippocampal place cells during formation and use of the
57 l interaction of visual cortical neurons and hippocampal place cells during spatial navigation behavi
58 ional imaging, we found large populations of hippocampal place cells during virtual navigation, globa
59 l navigation capacity involves the replay of hippocampal place-cells during awake states, generating
60                                              Hippocampal place cells encode an animal's current posit
61                                              Hippocampal place cells encode an animal's past, current
62                    This suggests that dorsal hippocampal place cells encode space independently of it
63                                              Hippocampal place cells encode spatial information in ra
64                                              Hippocampal place cells encode the animal's location.
65                                              Hippocampal place cells encode the animal's spatial posi
66 a rhythms temporally coordinate sequences of hippocampal place cell ensembles during active behaviors
67                                              Hippocampal place cell ensembles form a cognitive map of
68 lidation [14, 15], since the reactivation of hippocampal place cell ensembles occurs during ripples [
69 smission probabilities on the ability of the hippocampal place cell ensembles to produce a cognitive
70  Recent progress has identified sequences of hippocampal place cells, evolving at multiple timescales
71 uring navigation to a goal, a portion of the hippocampal place cells exhibit directional preferences,
72                                              Hippocampal place cells exhibit spatially selective acti
73          Lastly, reductions in the number of hippocampal place cells exhibiting significant theta rhy
74                      During periods of rest, hippocampal place cells feature bursts of activity calle
75 eriment, CNQX disrupted the stability of rat hippocampal place cell fields in a familiar environment.
76                                              Hippocampal place cells fire at different rates when a r
77                                              Hippocampal place cells fire at discrete locations as su
78                                              Hippocampal place cells fire at specific locations in th
79 el activity patterns produced when groups of hippocampal place cells fire in sequences that reflect a
80                                              Hippocampal place cells fire selectively when a rat occu
81                                              Hippocampal "place cells" fire selectively when an anima
82     Therefore, we tested the hypothesis that hippocampal place cell firing is impaired after PAE by p
83 information is encoded by location-dependent hippocampal place cell firing rates and sub-second, rhyt
84 ght to critically depend on the integrity of hippocampal place cell firing.
85 track, in a correlated fashion with those of hippocampal place cells firing at overlapping locations.
86 l neurons that are functionally coupled with hippocampal place cells for spatial processing during na
87                                              Hippocampal place cells form a map of the environment of
88                                              Hippocampal place cells form a spatial 'map' which is mo
89 nd frequent awake replay of sequences of rat hippocampal place cells from a previous experience.
90     The representation of distinct spaces by hippocampal place cells has been linked to changes in th
91 he origin of the spatial receptive fields of hippocampal place cells has not been established.
92                                              Hippocampal place cells have been proposed to have a rol
93     Consistent with this idea, the firing of hippocampal "place cells" have been shown to represent n
94 patial firing pattern owing to feedback from hippocampal place cells (i.e. a hexagonal pattern of rem
95 during naturalistic spike trains recorded in hippocampal place cells in exploring rodents.
96            Recording from large ensembles of hippocampal place cells in freely behaving rats, we obse
97                                              Hippocampal place cells in freely moving rodents display
98                       Experiments that track hippocampal place cells in mice navigating the same real
99 aset that contains the spike activity of rat hippocampal place cells in the CA1, CA2, and CA3 subregi
100                                              Hippocampal place cells, in turn, encode place using sen
101          A number of computational models of hippocampal place cells incorporate attractor neural net
102                      Here we show that, like hippocampal place cells, many neurons in the primary vis
103 ressive improvement in spatial coding in new hippocampal place cell maps depends on the existence of
104                                We argue that hippocampal place-cell maps are metric in all three dime
105 onstrated in a computational model, that the hippocampal place cells may ultimately be interested in
106  An important issue is understanding how the hippocampal place-cell network represents specific prope
107 e map of space, thought to be implemented by hippocampal place cells: neurons that exhibit location-s
108 lcium imaging and electrophysiology to track hippocampal place cells over 2 weeks of online spatial r
109 ere represented by the temporal relations of hippocampal place cell pairs within cycles of theta osci
110 pocampal manipulations, and the discharge of hippocampal place cell populations judiciously alternate
111             Medial entorhinal grid cells and hippocampal place cells provide neural correlates of spa
112      During both sleep and awake immobility, hippocampal place cells reactivate time-compressed versi
113 irment, the location-dependent firing of CA1 hippocampal place cells remained mostly intact.
114 that contextual fear conditioning results in hippocampal place cell remapping and long-term stabiliza
115                                              Hippocampal place cells replay spatial paths during immo
116                                              Hippocampal place-cell replay has been proposed as a fun
117                                              Hippocampal place cells represent location, but their ro
118                                              Hippocampal place cells represent the cellular substrate
119                             For example, the hippocampal place cell representation of location was pr
120 mpaired the retrieval of a previously stored hippocampal place cell representation regardless of age.
121                           Here, we show that hippocampal place cell representations are intact in the
122  to two differently shaped environments, the hippocampal-place-cell representations of those environm
123 trials and are correlated with activities of hippocampal place cells representing the same trajectori
124                 The activity of ensembles of hippocampal place cells represents a hallmark of an anim
125 e) were previously shown to exhibit impaired hippocampal place cell selectivity.
126                              Reactivation of hippocampal place cell sequences during behavioral immob
127                                    Replay of hippocampal place cell sequences has been proposed as a
128                                              Hippocampal place cell sequences have been hypothesized
129 We investigated whether such coordination of hippocampal place cell sequences is disrupted during err
130                                              Hippocampal place cells show position-specific activity
131        In contrast, the activity patterns of hippocampal place cells span distinct low-dimensional ma
132 oded by "theta sequences," ordered series of hippocampal place cell spikes that reflect the order of
133 In a recent study, Heiser et al. showed that hippocampal place cell stability and spatial encoding we
134                                    We review hippocampal place cell studies that examine how spatial
135                                              Hippocampal place cells support reward-related spatial m
136                                              Hippocampal 'place cells' systematically shift their pha
137                                              Hippocampal place cells take part in sequenced patterns
138                                Additionally, hippocampal place cells tend to develop a secondary plac
139                      Common examples include hippocampal place cells that fire at preferred locations
140     Replay is the sequential reactivation of hippocampal place cells that represent previously experi
141 ry depends on the reactivation ('replay') of hippocampal place cells that were active during recent b
142  show, using physiological evidence from rat hippocampal place cells, that the path-integration gain
143 h rate and place representations are used by hippocampal place cells to encode behavioral episodes, r
144  a conjunctive code that potentially enables hippocampal place cells to jointly represent spatial and
145                   Aversive stimuli can cause hippocampal place cells to remap their firing fields, bu
146 ptors and compared the changes in downstream hippocampal place cells to those of neurons in MEC.
147 complements the positional signal carried by hippocampal place cells; together, the directional and p
148                                              Hippocampal place cells underlie spatial navigation and
149                              In-flight, most hippocampal place cells were socially modulated and repr
150 e more similar to canonical, sparsely firing hippocampal place cells, whereas neurons in the distal s
151 elative to an environment's geometry, unlike hippocampal place cells, which activate at particular ra
152 GNIFICANCE STATEMENT We investigated whether hippocampal place cells, which compute a self-localizati
153 prevent the storage of stable "rate maps" by hippocampal place cells, which in turn may contribute to
154  which the brain represents space is through hippocampal place cells, which indicate when an animal i
155 the neural basis of this theory, we examined hippocampal place cells, which represent spatial informa
156                                We focused on hippocampal "place cells," which primarily represent the
157  of memories, we recorded large ensembles of hippocampal place cells while male rats ran repeated spa
158 tation of environmental location provided by hippocampal place cells while mice navigated a virtual r
159 ession is a well known phenomenon in which a hippocampal place cell will fire action potentials at su
160  a preconfigured network of taste-responsive hippocampal place cells with large fields, whose spatial
161 irectly the neurophysiological correlates of hippocampal place cells with navigational planning and a
162 kg ethanol potently suppressed the firing of hippocampal place-cells without altering place-field loc
163 ion information to entorhinal grid cells and hippocampal place cells, yaw plane optic flow signals li

 
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