ライフサイエンスコーパス: thalamic nucleus

1 al outcome using SF-36 scores (right central thalamic nucleus).

2 of the cingulate cortex and paraventricular thalamic nucleus.

3 he dorsolateral pons and the paraventricular thalamic nucleus.

4 ional subnetworks in a primary somatosensory thalamic nucleus.

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

6 lateral hind limb motor cortex and reticular thalamic nucleus.

7 hypothalamic area and to the paraventricular thalamic nucleus.

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

9 e labeled after injections in the paratenial thalamic nucleus.

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

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

12 he magnocellular division of the mediodorsal thalamic nucleus.

13 parvicellular part of the ventral posterior thalamic nucleus.

14 l features were found in the paraventricular thalamic nucleus.

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

16 us pallidus interna or ventralis intermedius thalamic nucleus.

17 halami and avoided the adjoining mediodorsal thalamic nucleus.

18 nterior to bregma projected to the gustatory thalamic nucleus.

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

20 , basolateral amygdala, and anterior ventral thalamic nucleus.

21 he ventral thalamus and the dorsal posterior thalamic nucleus.

22 a portion of the right ventral posteromedial thalamic nucleus.

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

24 limbic structures, and with the mediodorsal thalamic nucleus.

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

26 ll type that connects the SC to the pulvinar thalamic nucleus.

27 dial prefrontal cortex (mPFC), and reticular thalamic nucleus.

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

29 part from GABAergic neurons of the reticular thalamic nucleus.

30 rom the anterior nucleus to the intercalated thalamic nucleus.

31 entral thalamic nucleus and the anteromedial thalamic nucleus.

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

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

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

35 , within the area of the ventroposteromedial thalamic nucleus.

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

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

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

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

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

41 of the TRN-synapse with the posterior medial thalamic nucleus, a higher-order structure that carries

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

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

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

45 head, however, HD cells in rat anterodorsal thalamic nucleus (ADN) and other brain areas fire alread

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

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

48 eal that neurons located in the anterodorsal thalamic nucleus (ADN) specifically project onto MEC int

49 Ventral posteromedial thalamic nucleus afferents in GC make synapses with exci

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

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

52 wnstream regions, including the anteromedial thalamic nucleus (AM), reinforced behavior and activated

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

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

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

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

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

58 g chemo and optogenetic suppression of motor thalamic nucleus and corpus callosotomy.

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

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

61 ynaptic excitatory connections from anterior thalamic nucleus and from retrosplenial cortex converge

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

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

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

65 ysiological signals in the centromedian (CM) thalamic nucleus and primary motor (M1) cortex that diff

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

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

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

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

70 amocortical loop that links the anterodorsal thalamic nucleus and the postsubiculum (dorsal presubicu

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

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

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

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

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

76 obus pallidus internus, ventral intermediate thalamic nucleus, and dentate nucleus, and observed abno

77 rom PV-positive neurons in the medial dorsal thalamic nucleus, and from SOM-positive neurons in the v

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

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

80 (PL) cortex to the anterior paraventricular thalamic nucleus (aPVT) maintain high-frequency activity

81 the anterior portion of the paraventricular thalamic nucleus (aPVT) which express corticotrophin-rel

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

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

84 ain, such as parabrachial nucleus and medial thalamic nucleus, as well as sensory-discriminative pain

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

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

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

88 synapses of Po versus ventral posteromedial thalamic nucleus axons in the whisker sensory cortex.

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

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

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

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

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

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

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

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

97 Although the central medial thalamic nucleus (CMT) is connected to many nodes in thi

98 in the foraging network, the central medial thalamic nucleus (CMT), has received little attention so

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

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

101 enetic inhibition of the right ventrolateral thalamic nucleus did not alter inter-hemispheric seizure

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

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

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

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

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

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

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

109 (2020) find evidence that central lateral thalamic nucleus electrical stimulation reactivates the

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

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

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

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

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

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

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

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

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

119 Similarly, the secondary visual thalamic nucleus in mice (the lateral posterior nucleus,

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

121 ial thalamic nucleus (POm), the higher-order thalamic nucleus in the rodent somatosensory system, is

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

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

124 The mediodorsal thalamus is a higher-order thalamic nucleus involved in a variety of chemosensory-d

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

126 The paraventricular thalamic nucleus is innervated almost exclusively by the

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

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

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

130 The pulvinar, the largest thalamic nucleus, is a highly interconnected structure s

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

132 The laterodorsal thalamic nucleus (LD), with strong connections to visual

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

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

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

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

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

138 the pulvinar in mice, the lateral posterior thalamic nucleus (LP).

139 conveys this information to the mediodorsal thalamic nucleus, magnocellular part (MDmc).

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

141 cells.SIGNIFICANCE STATEMENT The mediodorsal thalamic nucleus (MD) and basolateral amygdala (BLA) sen

142 eives converging inputs from the mediodorsal thalamic nucleus (MD) and basolateral amygdala (BLA).

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

144 The mediodorsal thalamic nucleus (MD) is reciprocally connected with the

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

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

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

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

149 The connectivity of the mediodorsal thalamic nucleus (MD) with extrahippocampal regions and

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

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

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

153 barrels, whereas the higher-order posterior thalamic nucleus (medial part, POm) most densely innerva

154 ventral posterior medial (VPM) somatosensory thalamic nucleus most densely innervates layer 4 (L4) ba

155 The medial pulvinar thalamic nucleus (MPu) is an evolutionary novelty of the

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

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

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

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

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

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

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

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

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

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

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

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

168 One hub, the reticular thalamic nucleus (of the ventral thalamus), was found in

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

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

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

172 These data indicate that subparafascicular thalamic nucleus-parathyroid hormone 2 neurons integrate

173 d nucleus, ventral posterior division of the thalamic nucleus, paraventricular hypothalamic nucleus,

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

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

176 onal pathway from the posterior intralaminar thalamic nucleus (PIL) to the medial preoptic area (MPOA

177 fection, we investigated the mouse Posterior thalamic nucleus (Po) cell axons that simultaneously inn

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

179 ents from the higher-order, posterior medial thalamic nucleus (POm) gate synaptic plasticity in layer

180 lation recorded from S1 and posterior medial thalamic nucleus (POm) of cortico-thalamo-cortical (CTC)

181 The posteromedial thalamic nucleus (POm), the higher-order thalamic nucleu

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

183 that lesioning the posterior paraventricular thalamic nucleus (pPVT) impairs habituation.

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

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

186 ion of the inferior pulvinar (unilateral), a thalamic nucleus previously demonstrated to be involved

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

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

189 The paraventricular thalamic nucleus (PVT) integrates subcortical signals re

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

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

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

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

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

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

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

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

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

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

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

201 The thalamic nucleus reuniens (NR) is necessary to extinguis

202 Recent data support the role of the thalamic nucleus reuniens (RE) and its projections to th

203 ify L-type calcium channel (LTCC)-expressing thalamic nucleus reuniens (RE) as a critical component r

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

205 uit screen in mice, we identified a group of thalamic nucleus reuniens (RE) neurons activated during

206 lasticity of excitatory projections from the thalamic nucleus reuniens (Re) onto LS GABAergic neurons

207 ations and mediated by connectivity with the thalamic nucleus reuniens (RE).

208 prefrontal cortex, the hippocampus, and the thalamic nucleus reuniens constitute a typical example o

209 equivalent stimulation of afferents from the thalamic nucleus reuniens.

210 Recordings collected from the CM thalamic nucleus revealed a low-frequency power (3-10 Hz

211 e the specific contribution of the reticular thalamic nucleus (RT), a key modulator of thalamocortica

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

213 stem, namely, GABAergic neurons of reticular thalamic nucleus (RTN) and TC neurons in different senso

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

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

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

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

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

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

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

221 apses from the higher-order posterior medial thalamic nucleus showed rapid morphologic changes in bot

222 m the right medial mediodorsal magnocellular thalamic nucleus showed reduced FC in PD hallucinators a

223 The right medial mediodorsal thalamic nucleus shows both connectivity and volume loss

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

225 ith ascending projections into the submedius thalamic nucleus (SubM) and ventrolateral orbital cortex

226 or mice, the primate RE is a matrix-dominant thalamic nucleus, suggesting signal traffic to the upper

227 erm dynamics of TRN inhibition in the spared thalamic nucleus support cross-modal plasticity in the a

228 , than those between Po and ventro-posterior thalamic nucleus synapses in S1.

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

230 Cortical L6 and reticular thalamic nucleus terminals are evenly distributed across

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

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

233 he medial subregion of the pulvinar (mPLV)-a thalamic nucleus that has undergone significant evolutio

234 a topographically and functionally organized thalamic nucleus that is largely dedicated to visual pro

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

236 we identify neurons in the subparafascicular thalamic nucleus that nonlinearly integrate medial preop

237 However, one midline thalamic nucleus that projects to key nodes in the forag

238 r nucleus of the thalamus (PVT) is a midline thalamic nucleus that shapes motivated behaviors via its

239 Nucleus reuniens (NRe) is a midline thalamic nucleus that sits at the nexus of this circuit,

240 osensory cortex, and secondary somatosensory thalamic nucleus (the posterior medial nucleus, POm).

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

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

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

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

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

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

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

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

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

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

251 This higher order thalamic nucleus therefore conveys diverse contextual si

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

253 Synapses from the posterior medial thalamic nucleus to edge TRN cells evoke slower, less de

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

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

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

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

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

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

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

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

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

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

264 lap with the ventrolateral posterior ventral thalamic nucleus (VLpv) correlated with tremor relief fr

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

266 nitiation.(1-4) In rodents, the ventromedial thalamic nucleus (VM) is one of the critical nodes that

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

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

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

270 cellular region of the ventral posteromedial thalamic nucleus (VPMpc), dramatically reduces GC taste

271 Each thalamic nucleus was distinguished by expression of a co

272 The reticular thalamic nucleus was found to be primarily responsible f

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

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

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

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

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

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

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

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

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