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

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

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

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

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

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

6 elated with noradrenergic innervation in the medial entorhinal cortex.

7 during persistent gamma oscillations in the medial entorhinal cortex.

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

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

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

11 silateral hippocampus, and the contralateral medial entorhinal cortex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

40 Neurons in the medial entorhinal cortex encode location through spatial

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 Medial entorhinal cortex layer II contains pyramidal isl

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

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

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

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

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

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

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

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

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

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

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

70 The medial entorhinal cortex (MEC) contains specialized neur

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

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

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

74 Medial entorhinal cortex (MEC) grid cells exhibit firing

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 Conversely, medial entorhinal cortex represents relevant locations a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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