ライフサイエンスコーパス: lateral nucleus

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

2 e placed into different locations within the lateral nucleus.

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

4 and lateral central nucleus and the ventral lateral nucleus.

5 rated in the dorsolateral subdivision of the lateral nucleus.

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

7 predominant in the massively expanded human lateral nucleus.

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

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

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

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

12 t convey fearful auditory information to the lateral nucleus.

13 s expressed in GABAergic interneurons of the lateral nucleus.

14 nuclei and provide little innervation to the lateral nucleus.

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

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

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

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

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

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

21 that in mice on regular diet, neurons in the lateral nucleus accumbens (NAcLat) projecting to the ven

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

23 motes aversion and reduces DA release in the lateral nucleus accumbens.

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

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

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

27 2 and Te3 target different subregions of the lateral nucleus and that Te2, but not Te3, projects to t

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

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

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

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

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

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

34 nuclei, including the parabrachial internal lateral nucleus, and the posterior triangular and medial

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

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

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

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

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

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

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

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

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

44 oportionate atrophy of the right mediodorsal lateral nucleus in HRE carriers and showed that C9orf72

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

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

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

48 Lateral nucleus (LA) lesions blocked acquisition of both

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

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

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

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

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

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

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

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

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

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

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

60 Rs) facilitates neuronal excitability in rat lateral nucleus of central amygdala (CeL).

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

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

63 The central lateral nucleus of the amygdala (CeLC) is a key region f

64 tion of aversive learning via actions in the lateral nucleus of the amygdala (LA) [1, 2].

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

89 For example, a cell cluster in the ventral lateral nucleus of the amygdala (vLa) is enriched in hum

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

116 he medial prefrontal cortex - but not to the lateral nucleus of the central amygdala (CEAl) - were fo

117 onal roles of catecholamines innervating the lateral nucleus of the cerebellum (LCN).

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

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

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

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

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

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

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

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

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

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

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

129 , medullary reticular formation, and central lateral nucleus of the thalamus, and found that these co

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

131 fastigial neurons projecting to the central lateral nucleus of the thalamus-but not fastigial neuron

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

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

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

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

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

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

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

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

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

141 l nucleus of the ventral telencephalon [Vs], lateral nucleus of the ventral telencephalon [Vl], ventr

142 the MDD group, volumes of the amygdala right lateral nucleus (p = 0.05, r(2) = 0.24), left cortical n

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

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

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

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

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

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

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

150 n of fastigial neurons targeting the central lateral nucleus robustly inhibited seizures.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 1 (NMDAR1) in rat and cat ventral posterior lateral nucleus (VPL) and in the associated sector of th

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

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

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

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

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

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

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

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

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