ライフサイエンスコーパス: lateral nucleus

1 al thalamus, including the ventral-posterior lateral nucleus.

2 and lateral central nucleus and the ventral lateral nucleus.

3 rated in the dorsolateral subdivision of the lateral nucleus.

4 llular division of the basal nucleus and the lateral nucleus.

5 ly, the posterior interposed nucleus and the lateral nucleus.

6 tatory signals were enhanced in the PAM(+/-) lateral nucleus.

7 in the autistic amygdala overall and in its lateral nucleus.

8 the medial nucleus and two divisions of the lateral nucleus.

9 t convey fearful auditory information to the lateral nucleus.

10 s expressed in GABAergic interneurons of the lateral nucleus.

11 nuclei and provide little innervation to the lateral nucleus.

12 l, paracentral, oval paracentral, or central lateral nucleus.

13 the location of the tracer injection in the lateral nucleus.

14 e placed into different locations within the lateral nucleus.

15 o five reliably defined subdivisions: 1) the lateral nucleus, 2) the basal nucleus, 3) the accessory

16 into five reliably defined subdivisions: (1) lateral nucleus, (2) basal nucleus, (3) accessory basal

17 ns (x 10(6)) for each region was as follows: lateral nucleus 4.00, basal nucleus 3.24, accessory basa

18 In the lateral nucleus 50% of somatostatin, 30% of parvalbumin

19 in the pathway from external capsule to the lateral nucleus, a pathway that mediates information fro

20 reinforcing circuit from anterior cortex to lateral nucleus accumbens via VTA-DA neurons.

21 lume is increased 62% between species in the lateral nucleus and 48% in the central nucleus.

22 mmissural projection arises primarily in the lateral nucleus and exhibits a fine topography in that a

23 co-distributed in the ICM distributed in the lateral nucleus and lateral capsular division of the cen

24 2 and Te3 target different subregions of the lateral nucleus and that Te2, but not Te3, projects to t

25 targeted the ventromedial subdivision of the lateral nucleus and the adjacent part of the anterior ba

26 o the anterior division (VLa) of the ventral lateral nucleus and the parvocellular part of the ventra

27 ncipal neurons per case were selected in the lateral nucleus and traced using Neurolucida software in

28 The dorsal cortex, lateral nucleus, and NCO showed increases of 42.3, 49.0,

29 to the lateral central nucleus, dorsolateral lateral nucleus, and posterior basolateral nucleus.

30 r (the ventral anterior nucleus, the ventral lateral nucleus, and the oral ventroposterolateral nucle

31 cleus (BMAp) sends a dense projection to the lateral nucleus, and to restricted parts of the central

32 r collicular targets were the dorsal cortex, lateral nucleus, caudal cortex, and intercollicular tegm

33 nd intralaminar nuclei including the central lateral nucleus (CL) and the centre median nucleus (CM).

34 laterodorsal thalamic nucleus (LD), central lateral nucleus (CL), and posterior thalamic nucleus (Po

35 ; with moderate projections from VP, central lateral nucleus (CL), lateral posterior nucleus (LP), an

36 Additionally, the human lateral nucleus contained 59% more neurons than predicte

37 In humans, the lateral nucleus contained the highest number of neurons

38 Spine density is lower on macaque lateral nucleus dendrites compared with rat (-22%) but e

39 of the mammalian medial nucleus, but not the lateral nucleus homologue.

40 feedback interneurons effectively divide the lateral nucleus in transverse processing modules that pr

41 our findings suggest that an emphasis on the lateral nucleus is the main characteristic of amygdala s

42 The lateral nucleus (LA) is the input station of the amygdal

43 Lateral nucleus (LA) lesions blocked acquisition of both

44 tubule formation, as highly expressed in the lateral nucleus (LA) of the amygdala as well as in the t

45 phorylated in the amygdala, specifically the lateral nucleus (LA), at 60 min, but not 15, 30, or 180

46 showed the highest alpha1 expression in the lateral nucleus (La), whereas alpha3 was prominent in in

47 itory projections enter the amygdala via the lateral nucleus (LA).

48 r nucleus and the caudal part of the central lateral nucleus labeled fibers and boutons mainly in the

49 teral parafascicular nucleus and the central lateral nucleus labeled mainly the middle association te

50 The amygdala, including the lateral nucleus (LAT) of the basolateral amygdala comple

51 Novel forms of presynaptic plasticity in the lateral nucleus may also contribute to fear memory forma

52 ity-dependent reconsolidation process in the lateral nucleus of amygdala (LA) [1-5].

53 ation of neurons ( approximately 10%) in the lateral nucleus of amygdala (LA) were recruited at the t

54 eling was restricted to small patches in the lateral nucleus of amygdala, intercalated cell masses (I

55 Spines are equally long in the lateral nucleus of rat and macaque, but spines are longe

56 irhinal cortex (PR) and immediately adjacent lateral nucleus of the amygdala (ALa).

57 erm potentiation (LTP) can be induced in the lateral nucleus of the amygdala (LA) after stimulation o

58 Thereafter, single-unit activity in the lateral nucleus of the amygdala (LA) and freezing behavi

59 alized to dendritic shafts and spines in the lateral nucleus of the amygdala (LA) and is postsynaptic

60 that Arc/Arg3.1 protein is regulated in the lateral nucleus of the amygdala (LA) by retrieval of an

61 tion from the posterior thalamus reaches the lateral nucleus of the amygdala (LA) by way of two pathw

62 that transmit auditory CS information to the lateral nucleus of the amygdala (LA) increases auditory-

63 The lateral nucleus of the amygdala (LA) is a crucial part o

64 The lateral nucleus of the amygdala (LA) is a crucial site o

65 The lateral nucleus of the amygdala (LA) is an essential com

66 inputs converging on a single neuron in the lateral nucleus of the amygdala (LA) is only modified wh

67 suggests that synaptic plasticity within the lateral nucleus of the amygdala (LA) may be responsible

68 on in the medial geniculate nucleus (MGN) to lateral nucleus of the amygdala (LA) pathway, a key segm

69 The lateral nucleus of the amygdala (LA) receives excitatory

70 , NGFI-A, Zif 268, Krox 24) increases in the lateral nucleus of the amygdala (LA) shortly following c

71 Auditory information can reach the lateral nucleus of the amygdala (LA) through a monosynap

72 Synaptic plasticity in the lateral nucleus of the amygdala (LA) underlies this form

73 neutral and aversive stimuli converge in the lateral nucleus of the amygdala (LA), in which alteratio

74 converge on post-synaptic neurons within the lateral nucleus of the amygdala (LA).

75 areas of auditory cortex that project to the lateral nucleus of the amygdala (LA).

76 ducing stimulation of thalamic inputs to the lateral nucleus of the amygdala (LA).

77 anoate (AP7), into either central nucleus or lateral nucleus of the amygdala (LAMG) significantly red

78 cortical and thalamic auditory inputs to the lateral nucleus of the amygdala (LAn) mediate encoding o

79 The lateral nucleus of the amygdala (LAT) is necessary for t

80 stimuli enhances activity of neurons in the lateral nucleus of the amygdala (LAT), which is thought

81 cal layers 5, 6, hippocampal layers CA(2,3), lateral nucleus of the amygdala and in the dorsal raphe

82 zinc-containing neurons, is enriched in the lateral nucleus of the amygdala and in the temporal area

83 Perineuronal nets were reduced in the lateral nucleus of the amygdala and lateral entorhinal c

84 RM also projected to the lateral nucleus of the amygdala and tail of the caudate

85 known about the behavioral importance of the lateral nucleus of the amygdala for the storage of impli

86 e report that synapses in projections to the lateral nucleus of the amygdala implicated in auditory f

87 n contrast, FAE increased 5-HTT sites in the lateral nucleus of the amygdala in the adult animal, sug

88 ptor glycine site agonist at synapses in the lateral nucleus of the amygdala may depend on the level

89 This suggests that NGFI-A mRNA in the lateral nucleus of the amygdala may play a role in conte

90 lack of TRPC4 potentiation in neurons in the lateral nucleus of the amygdala through two Galphaq/11 p

91 el of emotional learning, is conveyed to the lateral nucleus of the amygdala via two routes: directly

92 rast to c-fos, NGFI-A mRNA expression in the lateral nucleus of the amygdala was greater in the delay

93 potentiation (LTP) in auditory inputs to the lateral nucleus of the amygdala was recently linked to t

94 H-BP containing cells in the basolateral and lateral nucleus of the amygdala were lower in 24-month-o

95 included bidirectional connections with the lateral nucleus of the amygdala, afferent inputs from th

96 out the auditory conditioned stimulus to the lateral nucleus of the amygdala, but not in other condit

97 ting depression of CS-evoked activity in the lateral nucleus of the amygdala, consistent with fear re

98 cluding in the NTS, AP, lateral PBN, central lateral nucleus of the amygdala, dorsal lateral bed nucl

99 trema, lateral parabrachial nucleus, central lateral nucleus of the amygdala, dorsal lateral bed nucl

100 ogical recording techniques to show that the lateral nucleus of the amygdala, long thought to be crit

101 Blocking HDAC3 activity in the lateral nucleus of the amygdala, on the other hand, enha

102 ptide, as being highly expressed both in the lateral nucleus of the amygdala, the nucleus where assoc

103 on important for some forms of learning, the lateral nucleus of the amygdala, using in vivo intracell

104 al excitability in projection neurons in the lateral nucleus of the amygdala.

105 ment-binding proteins (CREB) in cells of the lateral nucleus of the amygdala.

106 (including the dorsal, ventral, central, and lateral nucleus of the area ventralis [Vd, Vv, Vc, and V

107 rior hypothalamus, external amygdala, dorsal lateral nucleus of the hypothalamus, dorsal lateral nucl

108 central and lateral nuclei of the amygdala, lateral nucleus of the hypothalamus, olfactory tubercle,

109 arcuate nucleus and restricted areas of the lateral nucleus of the hypothalamus.

110 bed the origins of neocortical inputs to the lateral nucleus of the macaque monkey amygdala based on

111 identify cortical areas that project to the lateral nucleus of the macaque monkey amygdaloid complex

112 trees are increased by 250% in length in the lateral nucleus of the monkey compared with the rat (6,0

113 ed neurons were concentrated in the external lateral nucleus of the parabrachial complex (elPB) but w

114 lic reticular nucleus), respiratory control (lateral nucleus of the solitary tract), locomotor or exp

115 or system, posterior division of the ventral lateral nucleus of the thalamus (VL), the mediodorsal nu

116 eus of the brainstem and the ventroposterior lateral nucleus of the thalamus is comparable to that pr

117 cerebellum and basal ganglia via the ventral lateral nucleus of the thalamus supports its role in pro

118 lateral nucleus of the hypothalamus, dorsal lateral nucleus of the thalamus, dorsal ventricular ridg

119 Neurons of the lateral nucleus of the trapezoid body (LNTB), the most p

120 cs, help to define three subdivisions of the lateral nucleus of the trapezoid body (LNTB).

121 hlear nuclei, dorsal periolivary nuclei, and lateral nucleus of the trapezoid body and the contralate

122 by glycine and GABA immunoreactivity in the lateral nucleus of the trapezoid body may be generalizab

123 istribution of axosomatic innervation in the lateral nucleus of the trapezoid body were revealed in w

124 class and form one of three subnuclei of the lateral nucleus of the trapezoid body, called the poster

125 immunoreactive nuclei, and one of these, the lateral nucleus of the trapezoid body, contains cell bod

126 The other two subnuclei of the lateral nucleus of the trapezoid body, its main and hilu

127 dentify other organizational features of the lateral nucleus of the trapezoid body.

128 erritory included VApc, VLo, and the ventral lateral nucleus pars caudalis (VLc), with the density of

129 leus pars principalis (VApc) and the ventral lateral nucleus pars oralis (VLo) following the GPi inje

130 the central portion of the ventral posterior lateral nucleus pars oralis (VPLo) and nucleus X (X) fol

131 ed in (1) the rostral portion of the ventral lateral nucleus, pars caudalis, (2) the caudal portion o

132 dalis, (2) the caudal portion of the ventral lateral nucleus, pars caudalis, (3) the mediodorsal nucl

133 Targets included the lateral nucleus, peri-supraoptic nucleus, and subparaven

134 hAT)-immunopositive cells in the retrodorsal lateral nucleus (RDLN) of the spinal cord were studied i

135 f the fact that glutamatergic neurons of the lateral nucleus send a primarily unidirectional projecti

136 Certain amygdala nuclei, such as the lateral nucleus, show relatively greater phylogenetic ex

137 lthough the intense neuropil staining in the lateral nucleus suggests that distal dendrites of pyrami

138 tic synapses was significantly higher in the lateral nucleus than in the BL nucleus (33% vs. 18%).

139 projections originated predominately in the lateral nucleus, the intermediate and parvicellular divi

140 to the amygdala terminated primarily in the lateral nucleus, the magnocellular and parvicellular div

141 ), and dorsal (VLd) divisions of the ventral lateral nucleus; the pallidum largely projected to the a

142 + neurons differed in the two nuclei: in the lateral nucleus, they were almost exclusively innervated

143 d that a specific amygdala circuit, from the lateral nucleus to the medial nucleus (LA-MeA), is requi

144 However, it is unclear how the lateral nucleus transforms these inputs, because its int

145 ate nucleus of the cerebellum to the ventral lateral nucleus (VL) of the thalamus in Macaca mulatta.

146 everal thalamic nuclei including the ventral lateral nucleus (VL), anterior pulvinar (PA), VPl, and t

147 s report focuses on STT input to the ventral lateral nucleus (VL), where prior anterograde tracing st

148 rs magnocellularis, VAmc) and in the ventral lateral nucleus (VL).

149 1 (NMDAR1) in rat and cat ventral posterior lateral nucleus (VPL) and in the associated sector of th

150 ocuses on STT input to the ventral posterior lateral nucleus (VPL) and the subjacent ventral posterio

151 e examined the role of the ventral posterior lateral nucleus (VPL) as a possible substrate for large-

152 Field potentials in the ventral posterior lateral nucleus (VPL) in thalamic brain slices from lesi

153 and thalamic inputs from the ventroposterior lateral nucleus (VPL).

154 contacts with proximal dendrites (33% in the lateral nucleus vs. 46% in the BL nucleus).

155 , thalamic afferent synapses in the PAM(+/-) lateral nucleus were deficient in long-term potentiation

156 Neurons projecting to the lateral nucleus were distributed in all layers of the do

157 egion of the insula project primarily to the lateral nucleus, with little or no innervation of other

158 f fibers and terminals in the dorsal part of lateral nucleus, with moderate labeling of fibers in the