ライフサイエンスコーパス: medial entorhinal cortex

1 y arise from other brain structures than the medial entorhinal cortex.

2 ve properties of stellate cells (SCs) in the medial entorhinal cortex.

3 innervation by the LEC rather than from the medial entorhinal cortex.

4 x, motor cortex, and the spatially selective medial entorhinal cortex.

5 spacings along the dorsal-to-ventral axis of medial entorhinal cortex.

6 iability of layer III pyramidal cells of the medial entorhinal cortex.

7 periodicity along the dorsal-ventral axis of medial entorhinal cortex.

8 l excitability in layer II stellate cells of medial entorhinal cortex.

9 during persistent gamma oscillations in the medial entorhinal cortex.

10 pal structures bordered by the subiculum and medial entorhinal cortex.

11 can transmit a visually matched HD signal to medial entorhinal cortex.

12 alize the spatial information carried by the medial entorhinal cortex.

13 parasubiculum, and the superficial layer of medial entorhinal cortex.

14 network activity from the hippocampus to the medial entorhinal cortex.

15 s considerably compared with the neighboring medial entorhinal cortex.

16 elated with noradrenergic innervation in the medial entorhinal cortex.

17 extends more caudally in the BF than to the medial entorhinal cortex.

18 g and theta-nested gamma oscillations in the medial entorhinal cortex.

19 silateral hippocampus, and the contralateral medial entorhinal cortex.

20 ular layer (MML) that receive input from the medial entorhinal cortex, 3) the commissural/association

21 postSUB, Prh, lateral entorhinal cortex, and medial entorhinal cortex: all of these areas are critica

22 Neurons in the medial entorhinal cortex alter their firing properties i

23 ate between effective communication with the medial entorhinal cortex and CA3, which have different r

24 ine levels and locus coeruleus fibres in the medial entorhinal cortex and dentate gyrus, with no fran

25 imaging to examine ketamine's impacts on the medial entorhinal cortex and hippocampus, which contain

26 g in size along the dorsoventral axes of the medial entorhinal cortex and hippocampus.

27 ove computational processes onto lateral and medial entorhinal cortex and hippocampus.

28 splay loss of layer III pyramidal neurons in medial entorhinal cortex and hyperexcitability and hyper

29 ation in computations carried out within the medial entorhinal cortex and imply that tuning of neural

30 nase II selectively in superficial layers of medial entorhinal cortex and its upstream regions.

31 uctural development of superficial-layers of medial entorhinal cortex and parasubiculum in rats.

32 rea providing one of the major inputs to the medial entorhinal cortex and part of a network involved

33 m upstream regions (cornu ammonis area 3 and medial entorhinal cortex) and generates itself a faster

34 verexpresses both P301L tau (uniquely in the medial entorhinal cortex) and mutant APP/PS1 (in a wides

35 ural basis of grid cell activity, we compare medial entorhinal cortex architecture in layer 2 across

36 Grid cells in medial entorhinal cortex are an attractive model system

37 Deep layers of the medial entorhinal cortex are considered to relay signals

38 amics of stellate neurons in layer II of the medial entorhinal cortex are important for neural encodi

39 ggesting that cells receiving input from the medial entorhinal cortex are more sensitive to spatial c

40 re propose that separate circuits within the medial entorhinal cortex are specialized for performing

41 place cells in hippocampus and grid cells in medial entorhinal cortex are temporally organized by con

42 Grid cells in medial entorhinal cortex are thought to act as a neural

43 emory function may involve grid cells in the medial entorhinal cortex, but the mechanism of generatin

44 compared to other brain regions, such as the medial entorhinal cortex, CA1, and CA3.

45 e demonstrate that the superficial layers of medial entorhinal cortex can also generate high frequenc

46 hat neurons in the superficial layers of the medial entorhinal cortex can be classified based on thei

47 he spatial firing patterns of neurons in the medial entorhinal cortex can be predicted by electrophys

48 wn that an intrinsic fast gamma mechanism in medial entorhinal cortex can be recruited by optogenetic

49 ecent studies have suggested that the caudal medial entorhinal cortex (cMEC) is specialized for path

50 In mammals, grid cells in the medial entorhinal cortex construct a neural spatial map

51 iring patterns of neurons in the dorsocaudal medial entorhinal cortex (dcMEC) and hippocampal CA1 neu

52 Finally, a medial entorhinal cortex-dependent task revealed that al

53 ated that their grid cell system, within the medial entorhinal cortex, did not map the local environm

54 cording studies in the dorsocaudal region of medial entorhinal cortex (dMEC) of the rat reveal cells

55 cells and neurons of the deep layers of the medial entorhinal cortex (dMEC) while rats learned a nov

56 t never by stimuli applied to deep layers of medial entorhinal cortex (dMEC).

57 ate that the systematic modulation along the medial entorhinal cortex dorsoventral axis of grid popul

58 ring of grid and non-grid cells in the mouse medial entorhinal cortex during a location memory task.

59 mbles of grid cells in superficial layers of medial entorhinal cortex during active exploratory behav

60 f spatial location and movement speed in the medial entorhinal cortex during the 'active' theta state

61 findings provoke reconsideration of how the medial entorhinal cortex dynamically represents space an

62 Neurons in the medial entorhinal cortex encode location through spatial

63 Neurons in the medial entorhinal cortex exhibit a grid-like spatial pat

64 Grid cells in the rodent medial entorhinal cortex exhibit remarkably regular spat

65 eural activity in pre- and parasubiculum, or medial entorhinal cortex, from P11 onward, 3-4 days befo

66 lls in the hippocampus and grid cells in the medial entorhinal cortex have different codes for space.

67 which receives spatial information from the medial entorhinal cortex; however, the source of the 'wh

68 ll firing fields recorded in layer II of the medial entorhinal cortex in behaving animals.

69 n neurons of presubiculum, parasubiculum and medial entorhinal cortex in horizontal slices from rat b

70 n-selective dissociation between lateral and medial entorhinal cortex in humans, and between perirhin

71 rid-cell responses recorded from layer II of medial entorhinal cortex in rats have been observed to r

72 recorded extracellularly in layer II of the medial entorhinal cortex in rats.

73 s in layer II stellate-like cells of the rat medial entorhinal cortex in vitro.

74 es from the dentate gyrus/hilus (DGH) to the medial entorhinal cortex, instead of a re-entrant loop.

75 Layer 3 of the medial entorhinal cortex is a major gateway from the neo

76 The medial entorhinal cortex is part of a neural system for

77 ddressed structure-function relationships in medial entorhinal cortex layer 3 by combining anatomical

78 ubset of local GABAergic interneurons and by medial entorhinal cortex layer 3 neurons.

79 Conversely, the direct CA1 to medial entorhinal cortex layer 5 circuit is essential sp

80 and the circuit, CA1 to dorsal subiculum to medial entorhinal cortex layer 5, play a crucial role se

81 The spatial receptive fields of neurons in medial entorhinal cortex layer II (MECII) and in the hip

82 The function of medial entorhinal cortex layer II (MECII) excitatory neu

83 Medial entorhinal cortex layer II contains pyramidal isl

84 Stellate cells (SC) in the medial entorhinal cortex manifest intrinsic membrane pot

85 The firing patterns of grid cells in medial entorhinal cortex (mEC) and associated brain area

86 e presubiculum provides a major input to the medial entorhinal cortex (MEC) and contains cells that e

87 ided into functionally distinct regions, the medial entorhinal cortex (MEC) and the lateral entorhina

88 The superficial layers of the medial entorhinal cortex (MEC) are a major input to the

89 rmance and the activity of grid cells of the medial entorhinal cortex (MEC) are affected in these mic

90 Stellate cells in the medial entorhinal cortex (MEC) are considered to constit

91 Grid cells in medial entorhinal cortex (MEC) are crucial components of

92 Stellate cells in layer II of medial entorhinal cortex (mEC) are endowed with a large

93 tably the way that grid cell inputs from the medial entorhinal cortex (MEC) are processed to form pla

94 Here we show that ripple bursts in CA1 and medial entorhinal cortex (MEC) are temporally associated

95 Grid cells in medial entorhinal cortex (MEC) can be modeled using osci

96 The superficial layers of the medial entorhinal cortex (MEC) contain spatially selecti

97 The medial entorhinal cortex (MEC) contains specialized neur

98 single-unit activity in the hippocampus and medial entorhinal cortex (MEC) correlate with elapsed ti

99 The medial entorhinal cortex (MEC) creates a neural represen

100 of undegraded substrate, but neurons in the medial entorhinal cortex (MEC) display accumulation of s

101 Neural circuits in the medial entorhinal cortex (MEC) encode an animal's positi

102 Grid cells in the medial entorhinal cortex (MEC) encode position using a d

103 enetic stimulation of BLA projections to the medial entorhinal cortex (mEC) enhances the consolidatio

104 By chemogenetically silencing medial entorhinal cortex (MEC) excitatory activity durin

105 Grid cells within the medial entorhinal cortex (MEC) exhibit a regular hexagon

106 Grid cells in the medial entorhinal cortex (MEC) exhibit remarkable spatia

107 Grid cell modules in the medial entorhinal cortex (MEC) express activity patterns

108 rid, border, and head-direction cells in the medial entorhinal cortex (MEC) forming key components of

109 The network of grid cells in the medial entorhinal cortex (MEC) forms a fixed reference f

110 possibly reflecting altered hippocampal and medial entorhinal cortex (MEC) function.

111 Principal neurons in rodent medial entorhinal cortex (MEC) generate high-frequency b

112 Medial entorhinal cortex (MEC) grid cells exhibit firing

113 Both hippocampal place fields and medial entorhinal cortex (MEC) grid fields increase in s

114 The medial entorhinal cortex (mEC) has been identified as a

115 The grid cell network in the medial entorhinal cortex (MEC) has been subject to thoro

116 Principal cells in layer V of the medial entorhinal cortex (MEC) have a nodal position in

117 We tested these ideas by recording medial entorhinal cortex (MEC) head-direction cells whil

118 The medial entorhinal cortex (MEC) hosts many of the brain's

119 firing rate coding properties of neurons in medial entorhinal cortex (MEC) in a mouse model of tauop

120 lls, and conjunctive correlates found in the Medial Entorhinal Cortex (MEC) indicate the presence of

121 his may be achieved by how grid cells in the medial entorhinal cortex (MEC) input to place cells.

122 By contrast, in response to medial entorhinal cortex (MEC) inputs, abGCs directly ex

123 mination of UP states in slices from the rat medial entorhinal cortex (mEC) involves GABA(B) receptor

124 The medial entorhinal cortex (MEC) is a major center for spa

125 , neural activity in the hippocampus and the medial entorhinal cortex (MEC) is correlated to navigati

126 The medial entorhinal cortex (MEC) is hypothesized to functi

127 The medial entorhinal cortex (MEC) is important for spatial

128 The interplay between hippocampus and medial entorhinal cortex (mEC) is of key importance for

129 The medial entorhinal cortex (MEC) is part of the brain's ne

130 ABSTRACT: The medial entorhinal cortex (mEC) is strongly involved in s

131 The medial entorhinal cortex (mEC) is strongly involved in s

132 on a two-dimensional surface, neurons in the medial entorhinal cortex (MEC) known as grid cells are a

133 Silencing the medial entorhinal cortex (mEC) largely abolished extrace

134 In animals with medial entorhinal cortex (MEC) lesions, the temporal org

135 studies suggest that intrinsic properties of medial entorhinal cortex (MEC) neurons contribute to the

136 We demonstrate that medial entorhinal cortex (mEC) neurons from the mouse mo

137 or cellular-resolution functional imaging of medial entorhinal cortex (MEC) neurons in mice navigatin

138 Medial entorhinal cortex (MEC) neurons severely lost the

139 hing is known about Kv2 channel functions in medial entorhinal cortex (mEC) neurons, which are involv

140 ms recorded in the superficial layers of the medial entorhinal cortex (MEC) of freely moving rats.

141 Neurons within the superficial layers of the medial entorhinal cortex (MEC) often discharge in border

142 The medial entorhinal cortex (mEC) plays a key role in spati

143 Neurons of the medial entorhinal cortex (MEC) provide spatial represent

144 The medial entorhinal cortex (MEC) receives moderate input f

145 Grid cells in the medial entorhinal cortex (MEC) respond when an animal oc

146 that the lateral entorhinal cortex (LEC) and medial entorhinal cortex (MEC) send parallel independent

147 n along the transverse axis of CA1, with the medial entorhinal cortex (MEC) sending denser projection

148 of the cells recorded in layer II of rodent medial entorhinal cortex (MEC) show a triangular grid pa

149 nuous in time, and it has been proposed that medial entorhinal cortex (mEC) supports memory retention

150 tributions of the dentate gyrus (DG) and the medial entorhinal cortex (MEC) to phase precession.

151 o question the influence of VIP cells in the medial entorhinal cortex (MEC), a region key for navigat

152 k, we consider the question of cell types in medial entorhinal cortex (MEC), a region likely to be in

153 al neurons from slice preparations of rodent medial entorhinal cortex (MEC), but their functional rol

154 a dedicated subpopulation of neurons in the medial entorhinal cortex (MEC), is correlated with runni

155 The medial entorhinal cortex (MEC), presubiculum (PrS), and

156 As animals navigate, neurons in medial entorhinal cortex (MEC), termed grid cells, disch

157 s of the lateral entorhinal cortex (LEC) and medial entorhinal cortex (MEC), the two primary cortical

158 nation of the boundary between neocortex and medial entorhinal cortex (MEC), two abutting cortical re

159 pocampus, but less is known about changes in medial entorhinal cortex (MEC), which is the primary spa

160 ectively process object information; and the medial entorhinal cortex (MEC), which selectively proces

161 mutation on layer II stellate neurons of the medial entorhinal cortex (mEC), which transmit excitator

162 The medial entorhinal cortex (MEC)-hippocampal network plays

163 correct errors in path integration in mouse medial entorhinal cortex (MEC).

164 mic oscillations and grid cell firing in the medial entorhinal cortex (MEC).

165 s in the medial temporal lobe, including the medial entorhinal cortex (MEC).

166 lized cells, and projects to layer II of the medial entorhinal cortex (MEC).

167 ode of the navigation circuitry of mice, the medial entorhinal cortex (MEC).

168 f experimentally recorded PV+ neurons in the medial entorhinal cortex (mEC).

169 theta' waves and interacts strongly with the medial entorhinal cortex (MEC).

170 Layer3 pyramidal neurons projected to the medial entorhinal cortex (MEC).

171 C) and path integration information from the medial entorhinal cortex (MEC).

172 , mainly targeting superficial layers of the medial entorhinal cortex (MEC).

173 uts to the projection neurons of layer II of medial entorhinal cortex (MEC-LII) in mice.

174 en by a direct pathway from layer III of the medial entorhinal cortex (MECIII) to the hippocampal CA1

175 m appears as a linear structure flanking the medial entorhinal cortex mediodorsally.

176 To investigate how the medial entorhinal cortex might contribute to temporal lo

177 se regions include the medial prefrontal and medial entorhinal cortex (mPFC and MEC), which are of br

178 We show that dendrites of medial entorhinal cortex neurons are highly excitable an

179 Chronic recordings in the medial entorhinal cortex of behaving rats have found gri

180 l firing and local field potentials from the medial entorhinal cortex of freely foraging mice, while

181 Grid cells recorded in the medial entorhinal cortex of freely moving rats exhibit f

182 regions/layers in the dorsal hippocampus and medial entorhinal cortex of rats during exploration.

183 cells and interneurons were performed in the medial entorhinal cortex of the in vitro isolated guinea

184 he effect of large-scale inactivation of the medial entorhinal cortex on temporal, as well as spatial

185 the locus coeruleus prior to accrual in the medial entorhinal cortex or hippocampus, and tau patholo

186 acellular stimulation of the subiculum, deep medial entorhinal cortex or superficial pre- or parasubi

187 ccessfully reproduces response fields in the medial entorhinal cortex, particularly object vector cel

188 ion, or 'remapping', signal might be through medial entorhinal cortex, perhaps via the grid cells.

189 and limited to the superficial layers of the medial entorhinal cortex, pre- and parasubiculum.

190 During spatial navigation, grid cells in the medial entorhinal cortex process speed and direction of

191 k has established that stellate cells of the medial entorhinal cortex produce prominent intrinsic sub

192 Although neurons in the medial entorhinal cortex provide a maplike representatio

193 Within the medial entorhinal cortex, representation of location by

194 Conversely, medial entorhinal cortex represents relevant locations a

195 of various functional maps in regions of the medial entorhinal cortex resides in conductance gradient

196 In contrast, inactivation of the medial entorhinal cortex resulted in a pervasive reorgan

197 eletions of Teneurin-3 and Teneurin-4 in the medial entorhinal cortex revealed that they are required

198 Firing fields of grid cells in medial entorhinal cortex show compression or expansion a

199 ocations along the dorsal to ventral axis of medial entorhinal cortex show differences in the frequen

200 Neurons from layer II of the medial entorhinal cortex show subthreshold membrane pote

201 Representation of head direction in medial entorhinal cortex shows a gradient of precision,

202 applied to the activity of grid cells in the Medial Entorhinal Cortex suggests that this activity lie

203 presence of two speed signals in the rodent medial entorhinal cortex that are differentially affecte

204 s proximal CA1 is innervated by cells in the medial entorhinal cortex that are responsive to space.

205 Both bats and rats exhibit grid cells in medial entorhinal cortex that fire as they visit a regul

206 th optogenetic activation of layer II of the medial entorhinal cortex that theta frequency drive to t

207 that for stellate neurons in layer II of the medial entorhinal cortex, the waveform of postsynaptic p

208 We analyze a recent large-scale recording of medial entorhinal cortex to characterize the presence an

209 pyramidal neurons from acute slices of mouse medial entorhinal cortex, we find that subthreshold inpu

210 ses formed by afferents from the lateral and medial entorhinal cortex were compared, and differences

211 lum is a major input structure of layer 2 of medial entorhinal cortex, where most grid cells are foun

212 tal portions of the subiculum project to the medial entorhinal cortex, whereas proximal portions proj

213 din-positive pyramidal neurons in layer 2 of medial entorhinal cortex, which might be relevant for gr

214 enhanced excitatory synaptic inputs from the medial entorhinal cortex, which we find itself also medi

215 s are spatially modulated neurons within the medial entorhinal cortex whose firing fields are arrange