ライフサイエンスコーパス: thalamic nucleus

1 ar nuclei, as well as in the paraventricular thalamic nucleus.

2 lateral hind limb motor cortex and reticular thalamic nucleus.

3 T and CbMT and with neurons in the reticular thalamic nucleus.

4 hypothalamic area and to the paraventricular thalamic nucleus.

5 ons to the VLO via the pEn and the submedial thalamic nucleus.

6 e labeled after injections in the paratenial thalamic nucleus.

7 , while the RM2 labeled the mediodorsal (MD) thalamic nucleus.

8 of the cotransporter were found in somata of thalamic nucleus.

9 he magnocellular division of the mediodorsal thalamic nucleus.

10 part from GABAergic neurons of the reticular thalamic nucleus.

11 parvicellular part of the ventral posterior thalamic nucleus.

12 l features were found in the paraventricular thalamic nucleus.

13 arise from PV-IR neurons in the mediodorsal thalamic nucleus.

14 us pallidus interna or ventralis intermedius thalamic nucleus.

15 halami and avoided the adjoining mediodorsal thalamic nucleus.

16 nterior to bregma projected to the gustatory thalamic nucleus.

17 development of mouse ventral posterior (VP) thalamic nucleus.

18 , basolateral amygdala, and anterior ventral thalamic nucleus.

19 he ventral thalamus and the dorsal posterior thalamic nucleus.

20 a portion of the right ventral posteromedial thalamic nucleus.

21 al cortex, ventral striatum, and mediodorsal thalamic nucleus.

22 limbic structures, and with the mediodorsal thalamic nucleus.

23 eus were found to project to the mediodorsal thalamic nucleus.

24 rom the anterior nucleus to the intercalated thalamic nucleus.

25 entral thalamic nucleus and the anteromedial thalamic nucleus.

26 to the dLGN as well as in the subgeniculate thalamic nucleus.

27 ions from the medial half of the mediodorsal thalamic nucleus.

28 ing area of the ventroposterior medial (VPM) thalamic nucleus.

29 , within the area of the ventroposteromedial thalamic nucleus.

30 , septum, globus pallidus, and the reticular thalamic nucleus.

31 of the cingulate cortex and paraventricular thalamic nucleus.

32 he dorsolateral pons and the paraventricular thalamic nucleus.

33 [(3)H]Ro 15-1788 binding in the mediodorsal thalamic nucleus (15%), compared to non-punished control

34 barrel field and cell bodies of the ventral thalamic nucleus; 4) olfactory-associated structures and

35 tricular hypothalamus (34%), paraventricular thalamic nucleus (64%), and cerebral cortex (63%).

36 GAD67 is strongly expressed in the anterior thalamic nucleus (A).

37 at contain the afferents to the anterodorsal thalamic nucleus (AD) from the lateral mammillary body a

38 the postsubiculum (PoS) and anterior dorsal thalamic nucleus (AD) of the rat that discharge as a fun

39 ed vision, we recorded from the anterodorsal thalamic nucleus (ADN) and its postsynaptic target in th

40 ead direction cell circuit, the anterodorsal thalamic nucleus (ADN) and the dorsal tegmental nucleus

41 direction (HD) cells in the rat anterodorsal thalamic nucleus (ADN) fire relative to the animal's dir

42 ucleus (magnocellular part), lateroposterior thalamic nucleus, all six pretectal nuclei, superficial

43 lamo-amygdala projections varies within each thalamic nucleus along the rostro-caudal axis.

44 al norBNI injection in the ventral posterior thalamic nucleus (an adjacent brain region) did not bloc

45 t the mammillo-thalamic tract (MTT)/anterior thalamic nucleus (AN) complex would be critical for reco

46 Two-photon calcium imaging reveals that a thalamic nucleus and a downstream structure, the habenul

47 ending auditory information from the central thalamic nucleus and as a major afferent to the vocal pa

48 (glc) responses in the ventral posteromedial thalamic nucleus and barrel cortex but not in the spinal

49 la, the cerebral cortex, and the mediodorsal thalamic nucleus and decreased alpha2 mRNA levels in the

50 medial geniculate body (MGB), the reticular thalamic nucleus and dorsal nucleus of the lateral lemni

51 creased beta2 mRNA levels in ventroposterior thalamic nucleus and gamma2 mRNA levels in the CA2 area

52 dorsal thalamus (MDT) is the major olfactory thalamic nucleus and links the olfactory archicortex wit

53 us, dentate gyrus, medial habenular nucleus, thalamic nucleus and pontine nucleus.

54 reased c-fos activity in the anterior medial thalamic nucleus and the anterior cingulate cortex.

55 structures project to both the anteroventral thalamic nucleus and the anteromedial thalamic nucleus.

56 the SGN/V mainly projected to the posterior thalamic nucleus and the lateral hypothalamus (lateral t

57 ensembles of HD neurons in the antero-dorsal thalamic nucleus and the post-subiculum of mice by compa

58 dial caudate bilaterally, the right pulvinar thalamic nucleus and the right orbitofrontal cortex.

59 Each sector is connected to more than one thalamic nucleus and to more than one cortical area, and

60 Expression also was low in the reticular thalamic nucleus and zona incerta.

61 as the hippocampal formation, anterioventral thalamic nucleus, and basolateral amygdala.

62 ns, such as striatal medium spiny, reticular thalamic nucleus, and cerebellar Purkinje neurons.

63 trigeminal nuclei, the ventral posteromedial thalamic nucleus, and the barrel region of the somatosen

64 ted with atrophy in the left medial pulvinar thalamic nucleus, and this region further showed diminis

65 ; parasubthalamic nucleus; ventral posterior thalamic nucleus; area postrema; and nucleus of the soli

66 body, suprageniculate nucleus, and reticular thalamic nucleus, as well as of the inferior colliculi,

67 posteromedial nucleus (POm), a paralemniscal thalamic nucleus associated with broad receptive fields

68 logical evidence for a role for the anterior thalamic nucleus (ATN) in human memory formation.

69 The anterior thalamic nucleus (ATN) is thought to play an important r

70 intermingled with inputs to the mediodorsal thalamic nucleus, but again there was little or no colla

71 sion in the habenula and the paraventricular thalamic nucleus, but the response at these sites did no

72 peptide receptors in the ventroposteromedial thalamic nucleus by specifically co-staining for the cal

73 icant input in a specific area, that a given thalamic nucleus can influence areas as far as 20 mm apa

74 In addition, single cells in one dorsal thalamic nucleus can receive convergent inhibitory input

75 e connected tract and a measure of connected thalamic nucleus cell density.

76 timulation of the centrolateral intralaminar thalamic nucleus (CL) resulted in the specific activatio

77 ectifier K(+) channels in the central medial thalamic nucleus (CMT) are important targets for volatil

78 ings indicate that the Pf is an intralaminar thalamic nucleus critical for behavioral flexibility, in

79 e amount of the ventroposterior medial (VPM) thalamic nucleus devoted to representation of ipsilatera

80 We found that single units in the thalamic nucleus DLM of urethane-anesthetized adult male

81 ded directly from pallidal axon terminals in thalamic nucleus DLM, and found that all terminals exhib

82 rget, the medial portion of the dorsolateral thalamic nucleus (DLM).

83 , and the medial portion of the dorsolateral thalamic nucleus (DLM).

84 to the posterior portion of the dorsomedial thalamic nucleus (DMP).

85 from nTTD to the contralateral somatosensory thalamic nucleus dorsalis intermedius ventralis anterior

86 ain stimulation of the ventralis intermedius thalamic nucleus for essential tremor underwent function

87 ostnatal day (P) 0, in the ventral posterior thalamic nucleus from P2, and in the posteromedial barre

88 ohippocampal nucleus, fimbria, anteroventral thalamic nucleus, frontal and parietal cortex.

89 orebrain, including the PVN, paraventricular thalamic nucleus, habenula, medial amygdala, ventrolater

90 he magnocellular division of the mediodorsal thalamic nucleus has an important and general role in me

91 at the anticipatory property of anterodorsal thalamic nucleus HD cells was still present in lesioned

92 um that project upon the nucleus rotundus, a thalamic nucleus homologous to the mammalian caudal/infe

93 s, and, most prominently the paraventricular thalamic nucleus), hypothalamus (medial preoptic area, p

94 ut the role of the magnocellular mediodorsal thalamic nucleus in memory processing, indicating that i

95 e volume and neuronal number of the pulvinar thalamic nucleus in schizophrenia patients were measured

96 s, with the exception of the paraventricular thalamic nucleus, in which responsiveness was maintained

97 the primary motor cortex or the centromedian thalamic nucleus indicate that both corticostriatal and

98 amus (MDT) is a higher-order corticocortical thalamic nucleus involved in cognition and memory.

99 The paraventricular thalamic nucleus is innervated almost exclusively by the

100 The anterior thalamic nucleus is laterally bordered by a distinct GAD

101 s show that delta frequency stimulation of a thalamic nucleus is sufficient to produce deficits in WM

102 These findings suggest that every auditory thalamic nucleus is under some degree of descending cont

103 uclei investigated included LP, laterodorsal thalamic nucleus (LD), central lateral nucleus (CL), and

104 ines into OT and nucleus ovoidalis (OV), the thalamic nucleus leading to AAr.

105 Axons from thalamic nucleus LP were observed to form a dense band d

106 In the rat, the lateral posterior thalamic nucleus (LP) has reciprocal connections with ar

107 The lateral posterior thalamic nucleus (LP) may also play a role in directed a

108 n of the MGN (MGd) and the lateral posterior thalamic nucleus (LP).

109 , loss of neurons from the ventral posterior thalamic nucleus may also reflect loss of response to af

110 thalamus (MT), specifically the mediodorsal thalamic nucleus (MD) and the nucleus submedius (Sm), to

111 The mediodorsal thalamic nucleus (MD) is the principal relay nucleus for

112 The effects of lesions of the medial dorsal thalamic nucleus (MD) on blocking and latent inhibition

113 The mediodorsal thalamic nucleus (MD) receives convergent inputs from su

114 eus accumbens is directed to the mediodorsal thalamic nucleus (MD) via its projections to the ventral

115 reciprocal connections with the mediodorsal thalamic nucleus (MD), the nature of information transfe

116 Damage to the magnocellular mediodorsal thalamic nucleus (MDmc) in the human brain is associated

117 h a pathway to the magnocellular mediodorsal thalamic nucleus (MDmc), which may convey signals about

118 ed by lesions of nucleus uvaeformis (Uva), a thalamic nucleus necessary for song production.

119 dal neurons of layer II/III FC, ventromedial thalamic nucleus neurons, and striatal medium spiny and

120 ons, and striatal medium spiny and reticular thalamic nucleus neurons.

121 ance statement: Cells in the anterior dorsal thalamic nucleus normally fire in relation to the animal

122 The volumes of Rt (a thalamic nucleus not involved in song) and the telenceph

123 BAergic inhibitory currents in the reticular thalamic nucleus (nRT) in brain slices.

124 of thalamocortical (TC) cells via reticular thalamic nucleus (nRT) neurons, especially during oscill

125 Neurons of the inhibitory reticular thalamic nucleus (nRT) receive excitatory inputs from co

126 clei from the anterior pole of the reticular thalamic nucleus (NRT) were studied after injections of

127 Rhythmic bursting in the reticular thalamic nucleus (nRt), arising from interplay between C

128 ple unit activity of area 29b, and in the AV thalamic nucleus, occurring in synchrony with the field

129 or cingulate cortical area 29b and in the AV thalamic nucleus occurs independently of hippocampal the

130 the protomap hypothesis that neurons of each thalamic nucleus originate sequentially from separate li

131 mesencephalicus lateralis pars dorsalis, the thalamic nucleus ovoidalis, field L, the shelf of the hi

132 s subcortical connections of paraventricular thalamic nucleus (Pa) following small anterograde and re

133 Ventral anterior thalamic nucleus pars densicellularis (VAdc) as delineat

134 demonstrated previously that parafascicular thalamic nucleus (PF)-controlled neurons in the posterio

135 central lateral nucleus (CL), and posterior thalamic nucleus (Po).

136 culosum, nucleus of Meynert, paraventricular thalamic nucleus, posterior hypothalamic nucleus, periaq

137 he posterior division of the paraventricular thalamic nucleus (pPVTh) exhibits increased numbers of F

138 iencephalic complex of the central posterior thalamic nucleus/prepacemaker nucleus (CP/PPn), which al

139 The principal results were that 1) every thalamic nucleus projected to more than 1 field (range,

140 , also projects to Dm and is the only dorsal thalamic nucleus projecting to the pallium.

141 The paraventricular thalamic nucleus (PVT) is a component of the midline tha

142 Paraventricular thalamic nucleus (PVT) neurons receive hindbrain and hyp

143 The paracentral thalamic nucleus received an input only from the interna

144 cortex, we hypothesized that the pulvinar, a thalamic nucleus, regulates cortical synchrony.

145 d CRF peptide content in the paraventricular thalamic nucleus relative to ddY controls.

146 he cortex was suppressed while the reticular thalamic nucleus remained uniformly active.

147 GABAA receptor-mediated neurotransmission in thalamic nucleus reticularis (nRT) and ventrobasalis com

148 ia GABAergic synapses, excite neurons in the thalamic nucleus reticularis, and both excite and inhibi

149 lowing CTb injections in the paraventricular thalamic nucleus, retrogradely labeled cells were found

150 jections of Fluoro-Gold into the mediodorsal thalamic nucleus, retrogradely labeled neurons were dete

151 ed by ADX in the lateral amygdala, reticular thalamic nucleus, retrosplenial cortex or primary somato

152 We illuminated channelrhodopsin-2 in the thalamic nucleus reuniens (RE) at delta frequency and me

153 as immunologically detected in the reticular thalamic nucleus (RT), the medial longitudinal fasciculu

154 in the CA1 of the hippocampus, the reticular thalamic nucleus (RTN) and the primary fissure of the ce

155 y expressed in dendritic spines in reticular thalamic nucleus (RTN) neurons, but the functional impac

156 ret as the previously unidentified reticular thalamic nucleus (RTN) of teleosts.

157 The reticular thalamic nucleus (RTN) plays a pivotal role in that it r

158 nto different regions of the MD or reticular thalamic nucleus (RTN) produced retrograde transynaptic

159 ecipient LPN constitutes a third category of thalamic nucleus ("second-order") that integrates conver

160 vision of the MGB (MGm), the suprageniculate thalamic nucleus (SG) and brachium of the IC (bic), and

161 The parvocellular subparafascicular thalamic nucleus (SPFp) is located in the posterior thal

162 tral anterior thalamic nucleus/ventrolateral thalamic nucleus), targeted neurons in L2/3 through L5B,

163 The posterior thalamic nucleus, tertiary gustatory nucleus proper, and

164 r the projection from the MD (a higher-order thalamic nucleus that does not receive direct input from

165 ortical neurons in a basal ganglia-recipient thalamic nucleus that is necessary for vocal variability

166 re magnocellular division of the mediodorsal thalamic nucleus, the animals were impaired both in scen

167 containing cells are found in the reticular thalamic nucleus, the basal forebrain, the vestibular co

168 MUA outside of the SCN in the ventrolateral thalamic nucleus, the caudate putamen, the accumbens nuc

169 Furthermore, we identified a GAD67-positive thalamic nucleus, the intercalated nucleus (IC), which i

170 lateral septal nucleus, the paraventricular thalamic nucleus, the medial preoptic area, the ventrome

171 Neuronal number in the mediodorsal thalamic nucleus, the principal source of thalamic proje

172 Broca, the medial septal nucleus, reticular thalamic nucleus, the striatum and globus pallidus, the

173 in the medial preoptic area, paraventricular thalamic nucleus, the subparaventricular zone, and the h

174 Acting on this vital relay is another thalamic nucleus, the thalamic reticular nucleus (TRN).

175 fields were observed in the paraventricular thalamic nucleus; the lateral hypothalamic area; and the

176 This higher order thalamic nucleus therefore conveys diverse contextual si

177 imarily comprised the dorsomedial nucleus, a thalamic nucleus thought to be an important component of

178 ses of neurons in the ventral posterolateral thalamic nucleus to noxious colorectal distention are dr

179 on (from the medial part of the dorsolateral thalamic nucleus to the lateral magnocellular nucleus of

180 is of fewer projections from the mediodorsal thalamic nucleus to the prefrontal cortex in schizophren

181 a projection from nTTD to the contralateral thalamic nucleus uvaeformis, a multi-sensory nucleus con

182 cellular subdivision of the ventral anterior thalamic nucleus (VAdc) of Macaca mulatta was analyzed w

183 of sensory processing in the rat ventrobasal thalamic nucleus (VB) has been extensively studied in vi

184 ng of (18)F-nifrolidine to the anteroventral thalamic nucleus, ventral posteriomedial thalamus, dorso

185 c regions, including VA/VL (ventral anterior thalamic nucleus/ventrolateral thalamic nucleus), target

186 alimbic cortex, hippocampus, paraventricular thalamic nucleus, ventromedial hypothalamic nucleus, dor

187 Projections from thalamic nucleus VL are present in the dense dorsolatera

188 the posteroventral part of the ventrolateral thalamic nucleus (VLpv), the main source of thalamic inp

189 ntation of a finger in the ventral posterior thalamic nucleus (VPL) of macaque monkeys.

190 hypothalamus (LH), or medial ventroposterior thalamic nucleus (VPM) 7 days before injection of an inf

191 es to record from the ventroposterior medial thalamic nucleus (VPM) and primary somatosensory cortex

192 Each thalamic nucleus was distinguished by expression of a co

193 and in the associated anterior ventral (AV) thalamic nucleus, was monitored while rabbits underwent

194 show significant differences (in any dorsal thalamic nucleus) when compared with their wildtype litt

195 ected at low levels in the lateral posterior thalamic nucleus which received input from areas associa

196 thermoregulatory center'), and the reticular thalamic nucleus, which is known to inhibit the somatomo

197 The parafascicular thalamic nucleus, which plays the role in the pathogenes

198 lamic nuclei, except for the central lateral thalamic nucleus, which received no parabrachial afferen

199 relay in this circuit is the paraventricular thalamic nucleus, which receives convergent input from o

200 orded HD cell activity from the anterodorsal thalamic nucleus while the animal was locomoting in an u

201 nucleus of stria terminalis, paraventricular thalamic nucleus, zona incerta, and medial subparaventri