ライフサイエンスコーパス: thalamus

1 ancies of 43% (caudate), 25% (putamen), 43% (thalamus).

2 hippocampus), Ch4 (cortical lobes), and Ch5 (thalamus).

3 ies of 61% (caudate), 49% (putamen) and 69% (thalamus).

4 oss-modal integration in the primary sensory thalamus.

5 E-180 only in the parietotemporal cortex and thalamus.

6 citatory synaptic inputs from the cortex and thalamus.

7 imary sensorimotor and parietal cortices and thalamus.

8 le a similar trend was observed in the right thalamus.

9 er the intrinsic spindling mechanisms of the thalamus.

10 ventral striatum, hypothalamus and anterior thalamus.

11 adenosine receptor signaling in the auditory thalamus.

12 iated with structural neuroplasticity in the thalamus.

13 by reduced perfusion to posterior insula and thalamus.

14 ex via the lateral geniculate nucleus of the thalamus.

15 bition are driven with equal strength by the thalamus.

16 roups of neurons in cortex, hippocampus, and thalamus.

17 e ventralis intermedius (Vim) nucleus of the thalamus.

18 ral connectivity between the hippocampus and thalamus.

19 by viral manipulation of mmu-miR-15b in the thalamus.

20 ls that detect blue light and project to the thalamus.

21 tal lobe, supramarginal gyrus, striatum, and thalamus.

22 the lateral geniculate nucleus (LGN) of the thalamus.

23 ss the mouse lateral posterior and posterior thalamus.

24 nsory and motor neurons in the brainstem and thalamus.

25 thalamic system in the primate ventral motor thalamus.

26 gulate cortex, amygdala, and medial pulvinar thalamus.

27 tal lobe, supramarginal gyrus, striatum, and thalamus.

28 caudate, hippocampus, pallidum, putamen and thalamus.

29 and the paralaminar portions of the auditory thalamus.

30 ections to the nucleus ovoidalis (Ov) in the thalamus.

31 tic-occupancy curves in caudate, putamen and thalamus.

32 imulation of the centromedian nucleus of the thalamus.

33 six cortical regions, including PFC, and the thalamus.

34 rs, such as the ventral striatum and midline thalamus.

35 allidus to EP targets within epithalamus and thalamus.

36 terpolaris cells that further project to the thalamus.

37 ions, such as the lateral habenula (LHb) and thalamus.

38 results in exuberant growth into the dorsal thalamus.

39 llidus (0.23% increase, P = .009), posterior thalamus (0.26% increase, P < .001), substantia nigra (0

40 (22%), cerebellum(17.39%), brainstem(9%) and thalamus(4%).

41 Among neurons retrogradely labeled from the thalamus, 43%, 8%, and 22% were Fos-positive following i

42 occupancies (65 +/- 8%, caudate; 67 +/- 11%, thalamus; 52 +/- 11%, putamen).

43 We show that the paraventricular thalamus, a nucleus of the dorsal midline thalamus, is i

44 l radial glial progenitors in the developing thalamus actively divide and produce a cohort of neurona

45 es, posterior parietal cortex, striatum, and thalamus after overdrinking, relative to thirst.

46 middle cerebellar peduncle (MCP), pons, and thalamus after repeated administration of the liver-spec

47 The SUV from target regions (cLBP study, thalamus; ALS study, precentral gyrus) was normalized wi

48 ns, the clock receives input from the visual thalamus, although the role of this geniculohypothalamic

49 12 volumes of interest (VOIs): the bilateral thalamus, amygdala, hippocampus, dorsal striatum and ven

50 f the dopamine receptor Drd2 in the auditory thalamus, an abnormal sensitivity of thalamocortical pro

51 ecrease the gain and tuning precision in the thalamus and all layers of the cortical column, dependin

52 superior colliculus, pulvinar nucleus of the thalamus and amygdala) for the same stimuli seen freely

53 ub nodes and an abnormal integration of left thalamus and basal ganglia.

54 ns to insular cortex via the paraventricular thalamus and basolateral amygdala.

55 ed a reduction in glucose uptake in the left thalamus and bilateral inferior parietal lobe.

56 s, not only to the striatum, but also to the thalamus and brainstem.

57 ARAS structures included limbic structures, thalamus and certain neocortical areas, which is consist

58 Although interactions between the thalamus and cortex are critical for cognitive function,

59 We propose that structural damages in the thalamus and cortex are mostly responsible for clinical

60 hips between delta and higher frequencies in thalamus and cortex generate frequency mismatches in int

61 However, the mechanisms whereby the thalamus and cortex interact in generating these sleep p

62 barreloids and barrels in the contralateral thalamus and cortex represent each whisker.

63 garding prior sensory experience between the thalamus and cortex to promote cortical plasticity.

64 staining was lower in both TG groups in the thalamus and cortex.

65 inputs creates bilateral whisker maps in the thalamus and cortex.

66 alateral whisker representations in the same thalamus and cortex.SIGNIFICANCE STATEMENT The whisker s

67 kin-Huxley network model of a hyperpolarized thalamus and corticothalamic inputs.

68 Globus pallidus-thalamus and dentate nucleus-pons SI ratios were calcula

69 ied to estimate the hidden properties of the thalamus and explore the mechanism of the Parkinsonian s

70 ons, dorsal root ganglia (DRG), spinal cord, thalamus and forebrain.

71 ed persistently lower axial diffusion in the thalamus and internal capsule across groups (P = .02).

72 ource of cholinergic innervation for sensory thalamus and is a critical part of an ascending arousal

73 e loss in the territory of the somatosensory thalamus and is accompanied by disruptions thalamic meta

74 reased neuronal loss and astrogliosis in the thalamus and less thalamic fiber loss by diffusion tenso

75 with regionally significant declines in the thalamus and nucleus ruber.

76 Anatomical connectivity between the thalamus and PFC was reduced in schizophrenia.

77 retains intact optic projections to the SCN, thalamus and pretectum and a functional GHT.

78 Descending projections from the thalamus and related structures to the midbrain are evol

79 es of some of this output are relayed to the thalamus and tectum.

80 gionally-specific alterations in the lateral thalamus and thalamocortical pathways in extremely prete

81 we demonstrate mistuning sensitivity in the thalamus and that feedback from the primary auditory cor

82 anscripts, but not the HOXA5 protein, in the thalamus and the cortex, from postnatal stages to adult

83 brain structure at the interface between the thalamus and the cortex.

84 mation of bilateral whisker maps in both the thalamus and the cortex.

85 abnormal functional connectivity between the thalamus and the dorsolateral and anterior prefrontal co

86 Activation of the thalamus and the inferior frontal gyrus (pars triangular

87 c drug propofol are synchronized between the thalamus and the medial prefrontal cortex.

88 voked synaptic potentials between the visual thalamus and visual cortex in an intact animal.

89 t putamen, left temporal pole, and bilateral thalamus) and function (increased brain activity in left

90 ed to the visual information conveyed to the thalamus, and (2) how alert versus nonalert awake brain

91 superior colliculus, pulvinar nucleus of the thalamus, and amygdala, enables rapid and automatic face

92 Our results suggest that the PCC, thalamus, and basal ganglia are key components of a LC-n

93 We propose a framework in which the LC, PCC, thalamus, and basal ganglia comprise a functional arousa

94 e LC to only a subset of these regions (PCC, thalamus, and caudate nucleus) covaried with the level o

95 rimary somatosensory areas in the brainstem, thalamus, and cortex in one sea lion pup and the externa

96 DN/MCP, DN-to-pons, GP-to thalamus, and GP-to-cerebrospinal fluid ratios were meas

97 nt SERT pathology in raphe nuclei, striatum, thalamus, and hypothalamus and associations with aging,

98 ocampus, caudate-putamen, nucleus accumbens, thalamus, and hypothalamus) of BAC aldh1l1-translational

99 la, caudate, hippocampus, pallidum, putamen, thalamus, and lateral ventricle).

100 e (thickness) of the right amygdala and left thalamus, and localized increases and decreases in subre

101 from the midline and posterior intralaminar thalamus, and moderate projections from the posterior be

102 red in the globus pallidus, dentate nucleus, thalamus, and pons.

103 ration occurring at the level of the sensory thalamus, and provide evidence for dynamic regulation of

104 ralateral ventroposteromedial nucleus of the thalamus, and subsequently to the cortex.

105 emicircularis, the medial hindbrain, and the thalamus, and the flow of information among these region

106 ections from the dorsal column nuclei to the thalamus, and thence to somatosensory wulst.

107 egatively impacts nAChR efficacy in auditory thalamus, and this is probably the result of a loss of n

108 vity in infralimbic cortex and medial dorsal thalamus, and to an increase in the spatiotemporal dynam

109 supranuclear palsy in the putamen, caudate, thalamus, and vermis, and decreased in the superior cere

110 ch the projections from the brainstem to the thalamus are disrupted.

111 rhomboid (Rh) nuclei of the ventral midline thalamus are reciprocally connected with the hippocampus

112 gy of PD and support interventions targeting thalamus as a potential therapeutic strategy.

113 es in the right occipito-parietal cortex and thalamus, as well as in the left insula and adjacent tem

114 Specifically, metabolic increases in the thalamus, as well as metabolic decreases in insular cort

115 Furthermore, this refocus on the limbic thalamus, as well as the rest of Papez circuit, would ha

116 P < 0.05 for all regions except striatum and thalamus at 1 h after injection).

117 dex of the 95th percentile within the entire thalamus at 1 year was independently associated with poo

118 cephalon, preoptic region, hypothalamus, and thalamus at all stages investigated.

119 The paraventricular thalamus balances the competing behavioral demands of da

120 compare SI and SI ratios (DN to pons, GP to thalamus) between case patients and control patients.

121 n observed in infarcts initially sparing the thalamus but interrupting thalamo-cortical or cortico-th

122 own diverse connectivity patterns across the thalamus, but whether this diversity translates to thala

123 uron excitation by GT release in ventrobasal thalamus, CA1 hippocampus, and somatosensory cortex.

124 To understand whether the isolated thalamus can generate multiple distinct oscillations, we

125 s and triggered endogenous opioid release in thalamus, caudate nucleus, and anterior insula.

126 osum, anterior commissure, internal capsule, thalamus, caudoputamen, and cortex).

127 Photoinhibition of the thalamus caused a short-latency and near-complete collap

128 ptations in infralimbic cortex-medial dorsal thalamus circuitry observed after stress reflect a compe

129 ure of these oscillations in both cortex and thalamus closely parallel those observed in the human el

130 in a delay in RGC axons reaching the dorsal thalamus compared with that seen in wild-type littermate

131 ed the reduction to areas of the mediodorsal thalamus connected to lateral PFC.

132 The thalamus connects the cortex with other brain regions an

133 putamen > frontal cortex > temporal cortex > thalamus, consistent with the reported KOR distribution

134 We discovered that the thalamus contributed proportionately only half as many s

135 dies across rodents and primates showing how thalamus contributes to attentional control.

136 Moreover, the pulvinar nucleus of the thalamus covaried with both of these spatially specific,

137 st, we now show that feedback from cortex to thalamus critically regulates refinement of the retinoge

138 mpus (Cohen's d=-0.232; P=3.50 x 10(-7)) and thalamus (d=-0.148; P=4.27 x 10(-3)) and enlarged latera

139 The SI in the globus pallidus, thalamus, dentate nucleus, and pons was measured at unen

140 p to be a critical regulator of nonlaminated thalamus development and organization.

141 We review recent studies of mouse thalamus, discussing how they revealed general principle

142 and dorsal lateral geniculate nucleus of the thalamus (dLGN) are morphologically and physiologically

143 We recorded spikes from the ALM and thalamus during tactile discrimination with a delayed di

144 level is the main determinant of whether the thalamus exhibits trough-max PAC, which is associated wi

145 esponse in the right IFG (F1,78 = 14.87) and thalamus (F1,78 = 14.97) (P < .05), and weaker corticoth

146 d with increases in cerebellar FCD in NM and thalamus FCD in HD.

147 These findings suggest: the thalamus generates a novel rhythm under GABAA potentiati

148 ced in very specific brain areas such as the thalamus, globus pallidus and orbitofrontal regions of t

149 gulate, amygdala) and sub-cortical (putamen, thalamus, globus pallidus, cerebellum) regions.

150 orical information relay, indicates that the thalamus has a much broader role in cognition than previ

151 However, the thalamus has extensive connections with the entire cereb

152 The most common receptive field in rodent thalamus, however, is center-surround with push-pull.

153 l cortex, and greater GM volume in posterior thalamus, hypothalamus and midbrain.

154 d the SERT-rich extrastriatal brain regions (thalamus, hypothalamus, and pons).

155 axis, especially from cortex/hippocampus to thalamus/hypothalamus posteriorly.

156 ially posteriorly from cortex/hippocampus to thalamus/hypothalamus.

157 cohol significantly increased FCD within the thalamus, impaired cognitive and motor functions, and af

158 uts from sensorimotor cortex or intralaminar thalamus in brain slices from control and dopamine-deple

159 uctural connectivity between hippocampus and thalamus in comparison to brains from animals with no ne

160 receptor 7 mRNA expression increases in the thalamus in FFI.

161 e added modulation of DLPFC circuitry by the thalamus in human may contribute to species-specific, hi

162 tivity of the left amygdala to the posterior thalamus in male but not female patients.

163 connectivity increases in visual cortex and thalamus in NM, but in HD, increases in precuneus FCD we

164 is useful and essential in the study of the thalamus in Parkinsonian state.

165 poses a broader and more central role of the thalamus in the genesis of multiple distinct thalamo-cor

166 ishes a critical role for the ventral medial thalamus in the propagation of this exaggerated beta ran

167 predictions about the role of the cortex and thalamus in these oscillations.

168 ingle-unit activity from the anterior dorsal thalamus in transgenic mice that lack functional horizon

169 These results signify a greater role for the thalamus in visual processing and provide a functional p

170 gmental area/pontine reticular formation and thalamus, in addition to the LC, also covaried with the

171 lamus (PVT), a nucleus of the dorsal midline thalamus, in this interaction.

172 parietal, and frontal cortex as well as the thalamus, including both the lateral geniculate nucleus

173 rget six nuclei in the anterior midbrain and thalamus, including the posterior thalamus, the zona inc

174 connected bidirectionally with parts of the thalamus, including the ventral medial and ventral anter

175 hus, silencing calcium waves in the auditory thalamus induces Rorbeta upregulation in a neighbouring

176 teral geniculate nucleus (LGN) of the dorsal thalamus, influencing stimulus size tuning, response gai

177 d in pain, reward, and emotional processing (thalamus, insula, orbitofrontal cortex, hippocampus, and

178 he subdivision of the posterior group of the thalamus into four subnuclei (anterior, lateral, medial,

179 identified that iron accumulates within the thalamus ipsilateral to infarct after a delay with a foc

180 try index was used to compare R2* within the thalamus ipsilateral versus contralateral to infarct and

181 Our results show that the thalamus is a circuit hub in motor preparation and sugge

182 eriences trough-max or peak-max PAC, and the thalamus is a critical component of propofol-induced cor

183 converging evidence suggests that the human thalamus is a critical hub region that could integrate d

184 results demonstrate that the avian auditory thalamus is a structurally and functionally heterogeneou

185 The thalamus is a structure critical for information process

186 her vertebrates, nor is it known whether the thalamus is also involved or how it influences masking.

187 Moreover, the thalamus is engaged by tasks requiring multiple cognitiv

188 The thalamus is globally connected with distributed cortical

189 These findings support the idea that the thalamus is involved in integrating information across c

190 aging experiments, we further found that the thalamus is involved in multiple cognitive functions.

191 as been extensively studied, the role of the thalamus is just beginning to be elucidated.

192 nctional networks.SIGNIFICANCE STATEMENT The thalamus is traditionally viewed as a passive relay stat

193 ar thalamus, a nucleus of the dorsal midline thalamus, is integral to this behavioral competition.

194 leus reuniens (Re), a nucleus of the midline thalamus, is part of a cognitive network including the h

195 6%; P = .003 and right: +9.5%; P = .02), and thalamus (left: +11.6%; P = .002 and right: +11.1%; P =

196 he development of receptive fields in visual thalamus (LGN) and cortex (VC).

197 y connects the visual cortex with the visual thalamus (LGN) in the feedback direction and enables the

198 connectivity between the PFC and mediodorsal thalamus may be 1) reduced in schizophrenia and 2) relat

199 Changes to the thalamus may be a critical part of how propofol accompli

200 peak or trough of this SWO; this implies the thalamus may be the source of propofol-induced PAC.

201 istent with the rodent literature, the human thalamus may integrate visual and body-based, orientatio

202 Furthermore, results suggest that the thalamus may play a key role underlying the association

203 The mediodorsal thalamus (MD) shares reciprocal connectivity with the pr

204 s main thalamic counterpart, the mediodorsal thalamus (MD).

205 The mediodorsal thalamus (MDT) is the major olfactory thalamic nucleus a

206 uits shape signal processing in the auditory thalamus (medial geniculate body, MGB) is poorly underst

207 nAChRs) within the circuitry of the auditory thalamus (medial geniculate body, MGB).

208 Single units were recorded from auditory thalamus [medial geniculate body (MGB)] of young awake,

209 nset group with localised volume loss in the thalamus, medial temporal lobe and temporal neocortex.

210 18F-AV-1451 uptake in the putamen, pallidum, thalamus, midbrain, and in the dentate nucleus of the ce

211 = 13), substantia nigra (n = 13), posterior thalamus (n = 12), red nucleus (n = 10), colliculi (n =

212 ncle (n = 7), caudate nucleus (n = 4), whole thalamus (n = 3), and putamen (n = 2).

213 bservation that loss of a single gene in the thalamus of an adult wild-type animal is sufficient to c

214 RNA that targets Drd2 and is enriched in the thalamus of both humans and mice.

215 miR-15b, Wnt4 expression was elevated in the thalamus of F1 mice due to the inheritance of DNA methyl

216 ods on data from the cortex, hippocampus and thalamus of rat, mouse, macaque and marmoset, demonstrat

217 e report that neurons in the primary sensory thalamus of the mouse vibrissal system (the ventral post

218 trated abnormal connectivity with the visual thalamus only in epilepsy patients with photosensitivity

219 ive neurons innervating the cheek project to thalamus or LPb.

220 iode (LED)-based illumination, either of the thalamus or the peripheral tissues, induced JF-NP-26-med

221 -progressive lesions to the basal ganglia or thalamus, or both, and is characterised by abnormal post

222 (P = 0.0014), hippocampus (P = 0.0005), and thalamus (P < 0.0001).

223 (P = .004), dentate nucleus (P = .023), and thalamus (P = .002) showed a significant correlation wit

224 (P = .002), dentate nucleus (P = .046), and thalamus (P = .026) and T2 of the whole brain (P = .004)

225 ectively), in the Ch5 terminal region of the thalamus (P = 0.0003), and in the striatum (P = 0.0042).

226 y lower (18)F-FDG uptake than WT mice in the thalamus (P = 0.0004) and hippocampus (P = 0.0332).

227 in volume size in the pallidum (p=0.95) and thalamus (p=0.39) between people with ADHD and controls.

228 dren and adults for the pallidum (p=0.79) or thalamus (p=0.89).

229 sing between the prefrontal cortex (PFC) and thalamus, particularly the mediodorsal nucleus.

230 eq analysis was conducted in the cerebellum, thalamus-pituitary and liver of tilapia treated with equ

231 sive (FDR < 0.05) in the tilapia cerebellum, thalamus-pituitary and liver, respectively.

232 The mediodorsal thalamus plays a critical role in cognition through its

233 The thalamus plays a critical role in the genesis of thalamo

234 (BC) and the posterior medial nucleus of the thalamus (POm).

235 ding the reticular formation, basal ganglia, thalamus, posterior cingulate cortex (PCC), precuneus, a

236 n neuronal birth in the hypothalamus, dorsal thalamus, posterior tuberculum, and the preoptic region,

237 the posterior paraventricular nucleus of the thalamus (pPVT) participates in cocaine-seeking behavior

238 th vertebrates indicates that the vertebrate thalamus, pretectum, and midbrain domains jointly corres

239 toinhibition of delay activity in the ALM or thalamus produced contralesional neglect.

240 namic findings, which included the posterior thalamus (pulvinar) and the medio-dorsal thalamic nuclei

241 ntly greater variability of temporal cortex, thalamus, putamen, and third ventricle volumes, consiste

242 frontal cortex, posterior cingulate cortex, thalamus, putamen, pallidum, caudate, hippocampus, and b

243 their axonal projections to paraventricular thalamus (PVT) excitatory neurons immediately (in 2 to 3

244 itment of the paraventricular nucleus of the thalamus (PVT) for the retrieval and maintenance of fear

245 e for the rat paraventricular nucleus of the thalamus (PVT), a nucleus of the dorsal midline thalamus

246 The paraventricular nucleus of thalamus (PVT), which projects to the NAc monosynaptical

247 pars orbitalis (r = -0.40, p = 0.009), left thalamus (r = -0.41, p = 0.009), and right thalamus (r =

248 t thalamus (r = -0.41, p = 0.009), and right thalamus (r = -0.51, p = -0.002) were shown, through gra

249 significant correlation was found for GP-to-thalamus ratios and number of gadoxetic acid administrat

250 GP-to-thalamus ratios differed significantly between the study

251 The thalamus receives sensory input from different circuits

252 mice, disrupting adenosine signaling in the thalamus rejuvenates plasticity in the auditory cortex a

253 showed localized inward deformations of the thalamus relative to healthy controls (HC, n=22), and ab

254 ticothalamic projection in the ventral motor thalamus remains poorly understood.

255 PRG-2 electroporation in the PRG-2(-/-) thalamus restored the aberrant cortical innervation.

256 0.05 after Bonferroni correction in the left thalamus, right amygdala, right hippocampus, left ventra

257 tal cortex (RSC-->PPC-->M2) and anteromedial thalamus (RSC-->AM-->M2).

258 gration (fusiform, somatosensory cortex, and thalamus), salience detection (anterior insula), and lea

259 ontrast, subcortical regions, especially the thalamus, show higher variability in schizophrenia patie

260 ll species (mice, rats, monkeys, and humans) thalamus showed highest [(18) F]Nifene binding with refe

261 work (dorsal anterior cingulate, insula, and thalamus) showed early learning task-related hyperconnec

262 F]Nifene binding in all brain regions, with thalamus showing >15% than males.

263 T1-weighted images was seen in the posterior thalamus, substantia nigra, red nucleus, cerebellar pedu

264 tion in mammals from nTTD to the ventrobasal thalamus, suggesting that the ascending trigeminal pathw

265 refrontal cortex (PFC), that the mediodorsal thalamus sustains these representations without relaying

266 tensities (SIs) in the globus pallidus (GP), thalamus (T), dentate nucleus (DN), and pons (P) were me

267 pretectum is reciprocally connected with the thalamus, tectum, octavolateral area, and habenula.

268 and long-range glutamatergic inputs from the thalamus that form Type I synapses.

269 rograde tracers were injected into the taste thalamus (the medial parvicellular portion of the ventra

270 dbrain and thalamus, including the posterior thalamus, the zona incerta, and the anterior pretectum.

271 teral geniculate nucleus (LGN) of the dorsal thalamus, these changes have pronounced effects on the s

272 osensory information is thought to arrive in thalamus through two glutamatergic routes called the lem

273 delivering stimulation to the ventrolateral thalamus, timed according to the patient's tremor rhythm

274 r BCHE (butyrylcholinesterase), expressed in thalamus tissue.

275 es excitatory inputs from the cortex and the thalamus to control diverse functions.

276 reflects unidirectional flow of signals from thalamus to cortex.

277 gs of local neural populations in cortex and thalamus to detect neurophysiologically defined slow cal

278 tive function, the exact contribution of the thalamus to these interactions remains unclear.

279 ter structural integrity between L-DLPFC and thalamus, two key components of the neuromodulatory netw

280 in the dorsal caudate, orbitofrontal cortex, thalamus, ventral striatum, dorsal putamen, and anterior

281 in the dorsal caudate, orbitofrontal cortex, thalamus, ventral striatum, dorsal putamen, and anterior

282 tween change in cognition and change in left thalamus volume differed between groups, with a signific

283 ortex, the major target of the somatosensory thalamus (VPM), respond to touch, but have low spike rat

284 Spatial distribution within the thalamus was analysed on an average R2* map from the ent

285 Test-retest reproducibility in the thalamus was more than 90% in both mice and rats.

286 Using all 253 subjects, the thalamus was parceled into functional regions of interes

287 eurons in the paraventricular nucleus of the thalamus was primarily contacted by medial hypothalamic

288 tegmental area, striatum, hypothalamus, and thalamus), we describe how activity of specific cell typ

289 The basal ganglia and/or thalamus were also commonly involved with calcifications

290 e dentate nuclei, pons, globus pallidus, and thalamus were harvested and analyzed with inductively co

291 tients with an infarct initially sparing the thalamus were prospectively evaluated clinically and wit

292 In addition, spontaneous LFOs in the thalamus were selectively associated with the headache a

293 ex, parietotemporal cortex, hippocampus, and thalamus whereas the increase in (18)F-GE-180 binding wi

294 a2 subunit-containing GABAA receptors in the thalamus, which can contribute to tonic inhibition under

295 nation of inhibitory synapses in the ventral thalamus, which lead to hyperexcitability in the thalamo

296 This is imparted by the thalamus, which relays information from the periphery to

297 n by the subcortical pulvinar nucleus of the thalamus while also disentangling the mechanisms underly

298 l cortices, default mode network regions and thalamus, while HD had higher FCD in cerebellum.

299 reased connectivity between the striatum and thalamus with the ventral attention network, and greater

300 on while the Mediodorsal nucleus (MD) of the thalamus would support familiarity and indirectly also b