ライフサイエンスコーパス: caudate nucleus

1 the prediction of forthcoming demand in the caudate nucleus.

2 mplicated in the pathophysiology of OCD, the caudate nucleus.

3 the cortical regions with connections to the caudate nucleus.

4 us, putamen, pallidum, nucleus accumbens, or caudate nucleus.

5 temporal gyrus, insula, fusiform gyrus, and caudate nucleus.

6 s influencing the volumes of the putamen and caudate nucleus.

7 dorsal striatum, including activation in the caudate nucleus.

8 g frontal and parietal cortex, thalamus, and caudate nucleus.

9 lus, the thalamic reticular nucleus, and the caudate nucleus.

10 luding the hippocampus, the thalamus and the caudate nucleus.

11 upregulation of dopamine (DA) release in the caudate nucleus.

12 gyrii, as well as the anterior cingulate and caudate nucleus.

13 lications to the whole striatum, putamen, or caudate nucleus.

14 ted in reversal learning, such as the medial caudate nucleus.

15 me in insular cortex and increased volume of caudate nucleus.

16 cortices, with mild involvement also of the caudate nucleus.

17 alterations in 3D chromatin structure in the caudate nucleus.

18 right lentiform nucleus and extended to the caudate nucleus.

19 atients, mainly in the nucleus accumbens and caudate nucleus.

20 thway might elicit neuritic outgrowth to the caudate nucleus.

21 allele in the left anterior insula and right caudate nucleus.

22 odulating neural signals in the amygdala and caudate nucleus.

23 eral nucleus of the amygdala and tail of the caudate nucleus.

24 ergic modulation of neuronal activity in the caudate nucleus.

25 arison subjects in metabolic activity in the caudate nucleus.

26 the prefrontal and parietal cortices and the caudate nucleus.

27 es reached only marginal significance in the caudate nucleus.

28 en, smaller in anterior putamen, smallest in caudate nucleus.

29 teral and dorsomedial prefrontal cortex, and caudate nucleus.

30 did not differ across species in the medial caudate nucleus.

31 lt mode and multiple control networks in the caudate nucleus.

32 rom -0.13 in the dorsal raphe to 0.88 in the caudate nucleus.

33 ervation selectively localized to the medial caudate nucleus.

34 s, and decreased in the hippocampus, but not caudate nucleus.

35 11-labeled [11C]PMP acetylcholinesterase and caudate nucleus [11C]DTBZ monoaminergic positron-emissio

36 There was mild hypometabolism in the caudate nucleus (-8.4% vs. control, F((2,22)) = 3.2, P <

37 usion within and outside MCA territory, e.g. caudate nucleus (9+/-6 ml per 100 g per min at 60 min vs

38 extent of signal reduction in the bilateral caudate, nucleus accumbens and midbrain correlating with

39 o sucrose in dopamine-related brain regions (caudate, nucleus accumbens) were large in older adults.

40 involved in reward processing, including the caudate, nucleus accumbens, amygdala, anterior insula, a

41 ls, also exhibited significantly potentiated caudate, nucleus accumbens, and putamen activations and

42 was investigated in three striatal regions: caudate, nucleus accumbens, and putamen.

43 not smoke, particularly in the left ventral caudate/nucleus accumbens and left ventral putamen (rang

44 An overall decrease in ventral caudate/nucleus accumbens binding potential in those who

45 error regression within the caudate, ventral caudate/nucleus accumbens, and anterior and posterior in

46 tchoice changes in preference are tracked in caudate nucleus activity.

47 f synchronously generated S cells within the caudate nucleus adjoining the ganglionic eminence, poten

48 We found that spike activity in the caudate nucleus after each trial corresponded to an inte

49 The medial caudate nucleus also shows hyperactivity in humans lacki

50 1) the lateral prefrontal cortex and medial caudate nucleus and 2) the supplementary motor area, sup

51 an increase in tonic dopamine levels in the caudate nucleus and a corresponding reduction in D2/D3 r

52 s with schizophrenia would display preserved caudate nucleus and abnormal prefrontal cortex activatio

53 two bilateral convergence zones (one in the caudate nucleus and another in the putamen) that consist

54 ural representation of aversive value in the caudate nucleus and anterior cingulate cortex.

55 hese unassigned voxels were localised to the caudate nucleus and anterior putamen, overlapping with e

56 ividuals exhibit abnormal development of the caudate nucleus and associative cortical areas, suggesti

57 tivity between the right DLPFC and the right caudate nucleus and bilateral (para)cingulate gyrus incr

58 volumetric differences in the frontal lobes, caudate nucleus and cerebellum, and hyperactivity was re

59 ed away from the injection tract towards the caudate nucleus and corpus callosum.

60 The caudate nucleus and cortical regions with connections to

61 tients with PD showed less activation in the caudate nucleus and greater activation in a region of pr

62 ectivity differences by placing seeds in the caudate nucleus and Heschl's Gyrus (HG) of both hemisphe

63 Furthermore, increased activity in bilateral caudate nucleus and hippocampus for the cued relative to

64 Functional connectivity between the caudate nucleus and hippocampus was also increased after

65 ned period, volume reduction occurred in the caudate nucleus and hippocampus, but iron content increa

66 tal cortex bilaterally, the head of the left caudate nucleus and in bilateral putamen.

67 entified within the peri-infarct zone in the caudate nucleus and in ipsilateral cingulate cortex (pos

68 occipital-parietal lobes, but a larger right caudate nucleus and lateral ventricles.

69 tigate the contributions of the hippocampus, caudate nucleus and midbrain dopaminergic system to diff

70 ly with activity in the body and tail of the caudate nucleus and negatively with activity in the hipp

71 or, middle and posterior cingulate cortices, caudate nucleus and nucleus accumbens (corrected P = 0.0

72 iatal D(2)/D(3) receptor availability in the caudate nucleus and nucleus accumbens that reached stati

73 ate cortices (anterior, mid- and posterior), caudate nucleus and nucleus accumbens.

74 opamine D2-type receptor (D2R) levels in the caudate nucleus and performance in a discrimination reve

75 l activity in the inferior frontal gyrus and caudate nucleus and performance of a go/nogo task in par

76 (p<0.05; corrected) abnormalities within the caudate nucleus and planum temporale.

77 es striatal-frontal connectivity between the caudate nucleus and prefrontal cortex during motor timin

78 While diffuse plaques, including those in caudate nucleus and presubiculum, were less prominently

79 ping (P < .05), and group differences in the caudate nucleus and pulvinar thalamus, compared with con

80 , AcH3 and AcH4 expression from cells in the caudate nucleus and Purkinje cells of the cerebellum in

81 n methamphetamine users from controls in the caudate nucleus and putamen and higher D1-receptor densi

82 Caudate nucleus and putamen DAT function was clearly low

83 D was positively correlated with BPND in the caudate nucleus and putamen in nonsmokers and female smo

84 The caudate nucleus and putamen underwent severe neuronal lo

85 The neuropil of both the caudate nucleus and putamen was invaded with reactive as

86 r DAT nor D2/D3 receptor availability in the caudate nucleus and putamen was predictive of social ran

87 based methods in both the DAT-rich striatum (caudate nucleus and putamen) and the SERT-rich extrastri

88 ce of multipolar ChAT-ir interneurons in the caudate nucleus and putamen, whereas monkeys have a more

89 ported a cognition-action separation between caudate nucleus and putamen-a striatal sub-division uniq

90 utamen, and long finger-like branches in the caudate nucleus and putamen.

91 The left caudate nucleus and right cerebellum were more active in

92 d to D(2)/D(3) receptor availability in left caudate nucleus and right lateral putamen/claustrum (p <

93 nt differences were seen in the hippocampus, caudate nucleus and thalamus of the preterm rabbits.

94 Caudate nucleus and thalamus volumes were unaffected by

95 left prefrontal cortex, anterior cingulate, caudate nucleus and thalamus, and recruited more areas,

96 rmed) centrality values in OCD for volume of caudate nucleus and thalamus, and surface area of parace

97 We found both, caudate nucleus and the hippocampus to be activated by p

98 between the connectivity profile between the caudate nucleus and the lateral prefrontal cortex and di

99 Higher grey-matter volumes in the caudate nucleus and the left cerebellum at age 14 years

100 significant linear effects of the ARs in the caudate nucleus and the orbitofrontal cortex for all of

101 in the anterior cingulate gyrus, head of the caudate nucleus and the posterolateral orbitofrontal cor

102 intrastriatal cell bodies were found in the caudate nucleus and the precommissural putamen, consider

103 ergic input from the substantia nigra to the caudate nucleus and the putamen.

104 Abnormalities were also found in the caudate nucleus and the putamen.

105 osis, mediated by aberrant activation of the caudate nucleus and the temporo-parietal junction.

106 i bilaterally (L>R), anterior cingulate, and caudate nucleus and the temporo-parietal-occipital junct

107 l connectivity of orbito-frontal cortex with caudate nucleus and to structural changes within limbic

108 tington's disease, HD), the relevance of the caudate nucleus and VCSL on cortical visual processing i

109 la (P = .007), and rostral head of the right caudate nucleus and ventral putamen and globus pallidus

110 -level-dependent response differences in the caudate nucleus and ventral striatum during reward antic

111 Here, we show that neurons in the primate caudate nucleus and ventral striatum modulate their acti

112 d by prior-enhanced connectivity between the caudate nucleus and ventrolateral prefrontal cortex, whi

113 Presupplementary motor area, caudate nucleus, and anterior insula activation was asso

114 gered endogenous opioid release in thalamus, caudate nucleus, and anterior insula.

115 ght lateral geniculate nucleus [LGN]), right caudate nucleus, and bilateral prefrontal regions.

116 icant decreases in the mediodorsal thalamus, caudate nucleus, and cerebellum as well as increases in

117 binding sites in the hippocampus, thalamus, caudate nucleus, and cerebellum but not in the corpus ca

118 eceptors, such as the hippocampus, thalamus, caudate nucleus, and cerebellum.

119 parison of transcriptomes from frontal pole, caudate nucleus, and hippocampus of multiple adult human

120 insula, cuneus, fusiform gyrus, thalamus and caudate nucleus, and increased GM predominantly in tempo

121 ppocampi, temporal and parietal lobes, right caudate nucleus, and insulae in patients with MCI to AD

122 e anterior cingulate cortex, the head of the caudate nucleus, and medial temporal lobe structures.

123 subiculum, hippocampus, hypothalamus, medial caudate nucleus, and nucleus accumbens as well as the ma

124 r dopamine release in the nucleus accumbens, caudate nucleus, and putamen among Ser23 carriers, after

125 onoamine levels in the orbitofrontal cortex, caudate nucleus, and putamen could explain variance in b

126 refrontal cortex (vmPFC), nucleus accumbens, caudate nucleus, and putamen.

127 tified for ADHD and volumes of the amygdala, caudate nucleus, and putamen.

128 nucleus accumbens, the rostral ventromedial caudate nucleus, and rostral ventromedial putamen.

129 gulate cortex (PCC), superior frontal gyrus, caudate nucleus, and substantia nigra.

130 ation (MFC) in the globus pallidus, putamen, caudate nucleus, and thalamus for 22 patients with ADHD

131 recruitment of the superior temporal gyrus, caudate nucleus, and thalamus.

132 dial pain system (medial thalamus, amygdala, caudate nucleus, anterior cingulate gyrus, insular corte

133 (11)C-DTBZ binding was measured in the caudate nucleus, anterior putamen, and posterior putamen

134 les of the serotonin and dopamine within the caudate nucleus are poorly understood, this study compar

135 The results revealed the caudate nucleus as the key brain structure involved in s

136 er, model-based fMRI analyses identified the caudate nucleus as the key structure involved in selecti

137 rward planning are expressed in the anterior caudate nucleus as values of individual branching steps

138 y stimuli led to increased activation of the caudate nucleus associated with reward processing, angry

139 Higher iron content in the caudate nucleus at baseline predicted lesser improvement

140 between the right orbito-frontal cortex with caudate nucleus bilaterally.

141 tral (head) and caudal (tail) regions of the caudate nucleus, both of which target the superior colli

142 d (1.0 mg/kg, i.v.) dopamine overflow in the caudate nucleus but not in the nucleus accumbens.

143 ates include the frontal eye field (FEF) and caudate nucleus, but their distinct roles are not unders

144 nglia circuit through the tail of the monkey caudate nucleus (CDt) guides such object-directed saccad

145 We now report that the tail of the caudate nucleus (CDt) may serve to control a visuomotor

146 imental, has been applied to the cerebellum, caudate nucleus, centromedian thalamus, anterior thalamu

147 Four brain regions were analyzed: caudate nucleus, cerebellum, prefrontal association cort

148 etabolism in the frontal and temporal lobes, caudate nucleus, cingulate gyrus, and mediodorsal nucleu

149 5 vs. 1.285 x 10(-3) mm(2)/s, p = 0.031) and caudate nucleus (CN) (1.319 vs. 1.394 x 10(-3) mm(2)/s,

150 of 3 separate striatal areas (putamen (PT), caudate nucleus (CN) and accumbens nucleus (NAC)) from p

151 he striatum, which includes a differentiated caudate nucleus (CN) and the putamen in rabbits.

152 n neurons of the prefrontal cortex (PFC) and caudate nucleus (CN) have not been studied in awake, fre

153 ese experiments was to determine whether the caudate nucleus (CN) plays a role in retrieval of previo

154 ccumbens (NAc), prefrontal cortex (PFC), and caudate nucleus (CN) under general anesthesia.

155 the prefrontal cortex (PFC), the head of the caudate nucleus (CN), and the ventral anterior nucleus (

156 gulate cortex (PCC), upper precuneus (UPCU), caudate nucleus (CN), cingulate motor area (CMA), supple

157 neuronal dysmaturation response to HI in the caudate nucleus (CN), which contributes to motor and cog

158 hippocampus, thalamus, globus pallidus, and caudate nucleus compared with 26 control males (effect s

159 s pallidus, pulvinar thalamus, thalamus, and caudate nucleus, compared with control subjects with R2*

160 found that distinct circuits of the primate caudate nucleus control behavior selectively in the flex

161 Patients' reduced activation within the caudate nucleus correlated negatively with paranoia scor

162 sed connectivity between the DN and the left caudate nucleus could play a role in balance impairment

163 subset of these regions (PCC, thalamus, and caudate nucleus) covaried with the level of arousal.

164 ted from previous studies, activation of the caudate nucleus differentiated between positive and nega

165 lassifier based on the specialization of the caudate nucleus distinguished patients from controls wit

166 n the right ventral tegmental area and right caudate nucleus, dopamine-rich areas associated with mam

167 d both independent cognitive predictions for caudate nucleus dopaminergic (F = 7.25; P = .008) and co

168 ts with neocortical cholinergic deficits had caudate nucleus dopaminergic deficits.

169 </= -2) global cognitive impairment scores, caudate nucleus dopaminergic denervation was relatively

170 pically occurs in the context of significant caudate nucleus dopaminergic denervation.

171 ed changes in neuronal activity occur in the caudate nucleus during trace EBC.

172 ry input structure of the basal ganglia, the caudate nucleus, encode three aspects of decision making

173 However, neurons in the caudate nucleus encoded the difference in the temporally

174 ntially expressed mRNAs were detected in the caudate nucleus, followed by motor cortex, then cerebell

175 timulations of the hippocampus, amygdala, or caudate nucleus, followed by sacrifice and immunohistoch

176 s overlooked specialization of the posterior caudate nucleus for executive functions, often considere

177 otonergic degeneration in human ventromedial caudate nucleus from individuals with an APOE epsilon4 a

178 teromers was next demonstrated in postmortem caudate nucleus from schizophrenic subjects, even though

179 egions (amygdala, anterior cingulate cortex, caudate nucleus, frontal cortex, hippocampus, insula, th

180 In contrast, caudate nucleus gene expression is highly conserved.

181 rtical regions (nucleus accumbens, amygdala, caudate nucleus, globus pallidus, hippocampus, putamen,

182 the nucleus accumbens, amygdala, brainstem, caudate nucleus, globus pallidus, putamen and thalamus,

183 ned brain areas with low FA values including caudate nucleus, globus pallidus, putamen, superior temp

184 and cortical regions with connections to the caudate nucleus had markedly abnormal hemispheric specia

185 fronto-striato-thalamic circuits-head of the caudate nucleus (hCaud), putamen, globus pallidus, thala

186 The basal ganglia, especially the caudate nucleus 'head' (CDh) of the striatum, receive in

187 volumes of the nucleus accumbens, amygdala, caudate nucleus, hippocampus, and putamen are smaller in

188 multidimensional discrimination task in the caudate nucleus, hippocampus, anterior and posterior cin

189 Similar results were seen in mouse caudate nucleus homozygous for APOE epsilon4 via targete

190 he DRD1 transcript in DLPFC, hippocampus and caudate nucleus in a large cohort of subjects (~700), in

191 a2+ signaling and degeneration of MSN in the caudate nucleus in HD.

192 ebellum (granule cell layer), as well as the caudate nucleus in humans and chimpanzees.

193 crease in dopamine innervation of the medial caudate nucleus in humans is a species-typical character

194 metry revealed atrophy of the cerebellum and caudate nucleus in manifesting patients (P = 0.04 and 0.

195 We recorded neuronal activity in the caudate nucleus in monkeys during categorization behavio

196 al ganglia, we recorded from the FEF and the caudate nucleus in monkeys performing an asymmetrically

197 re centred on the left frontal operculum and caudate nucleus in non-fluent primary progressive aphasi

198 e medial nucleus accumbens shell (NAcSh) and caudate nucleus in postmortem human brains.

199 ese results underscore the importance of the caudate nucleus in relation to cognitive fatigue.

200 ontrols, and was significantly higher in the caudate nucleus in secondary progressive MS (12.9/s vs 1

201 icantly lower bilaterally in the head of the caudate nucleus in the group with diabetes and depressio

202 eral and inferolateral prefrontal cortex and caudate nucleus in the Tourette group relative to compar

203 n interaction between cortical areas and the caudate nucleus, in which the caudate body supports both

204 at electrical microstimulation in the monkey caudate nucleus influences both choice and saccade respo

205 ties with a predilection for the head of the caudate nucleus, insula, and cortical spread to the limb

206 ing in functional connectivity involving the caudate nucleus, insula, medial prefrontal cortex and ot

207 tex, and midcingulate cortex, as well as the caudate nucleus involved in the reward system.

208 nd was associated with a reduced dentate and caudate nucleus iron content compared to placebo.

209 The caudate nucleus is a part of the visual corticostriatal

210 The caudate nucleus is commonly active when learning relatio

211 The anterior caudate nucleus is essential for goal-directed behavior

212 The caudate nucleus is known to have a role in behavioral mo

213 has demonstrated that neural activity in the caudate nucleus is modulated by task-relevant action val

214 No significant changes were detected in the caudate nucleus (lateral or medial) or in the cingulate,

215 te matter, cortex, cerebellum, thalamus, and caudate nucleus, many of which could compromise the cont

216 that focal biophysical abnormalities in the caudate nucleus may be central to the pathophysiology of

217 The caudate nucleus may be involved in the repetitive moveme

218 Rats were then given hippocampus, medial caudate nucleus (MCN), or cortical control lesions.

219 urves showed high accumulation in the insula/caudate nucleus, moderate uptake in the thalamus, and th

220 = 10), superior cerebellar peduncle (n = 7), caudate nucleus (n = 4), whole thalamus (n = 3), and put

221 low in the nucleus accumbens (n = 4) and the caudate nucleus (n = 5) using in vivo microdialysis.

222 dopaminergic compartment of the putamen and caudate nucleus not only in manifest SCA17 patients (P =

223 Robust and differential activation of the caudate nucleus occurred only when a perception of conti

224 neurons, were increased significantly in the caudate nucleus of CR monkeys, suggesting a role for gli

225 on of the BG by muscimol injections into the caudate nucleus of monkeys and assessing behavior of Par

226 s in the lateral prefrontal cortex (PFC) and caudate nucleus of monkeys as they performed a trial-and

227 striatal (123)I-FP-CIT binding ratios in the caudate nucleus of PSP patients than in that of both PD

228 striatal (123)I-FP-CIT binding ratios in the caudate nucleus of PSP patients than in that of both PD

229 specific bottom-up cues, and they place the caudate nucleus of the dorsal striatum at the center of

230 omatic L1 insertions, in the hippocampus and caudate nucleus of three individuals.

231 300 single neurons from cerebral cortex and caudate nucleus of three normal individuals, recovering

232 ution of visual corticostriatal loop and the caudate nucleus on generating selective response within

233 paminergic depletions of the marmoset medial caudate nucleus on serial discrimination reversal learni

234 re was no evidence of altered variability of caudate nucleus or frontal lobe volumes.

235 re was no evidence of altered mean volume of caudate nucleus or putamen.

236 left, but the opposite pattern in the right, caudate nucleus (P < .001).

237 performance correlated with lower CBF in the caudate nucleus (P = .01), thalamus (P = .04), frontal c

238 han did control subjects (putamen, P = .012; caudate nucleus, P = .008; thalamus, P = .012) and psych

239 -medicated ADHD patients (putamen, P = .006; caudate nucleus, P = .010; thalamus, P = .021).

240 rtex, and right inferior parietal lobule and caudate nucleus, perhaps reflecting conflict experienced

241 These results imply that the caudate nucleus plays causal roles in coordinating decis

242 ajor input station of the basal ganglia, the caudate nucleus, plays a causal role in integrating unce

243 te cortex and between the right amygdala and caudate nucleus predicted the magnitude of reduction in

244 Thus, the caudate nucleus provides interpretive monitoring of ongo

245 Volumes of the caudate nucleus, putamen, and globus pallidus and gray a

246 Differences were detected in the dorsal caudate nucleus, putamen, and globus pallidus but the ob

247 wer necrotic lesions in the cerebral cortex, caudate nucleus, putamen, and in hippocampal sectors CA1

248 Binding potential for caudate nucleus, putamen, and substantia nigra was evalu

249 the following areas: level of basal ganglia (caudate nucleus, putamen, corpus callosum, posterior lim

250 l subcortical gray matter volumes (thalamus, caudate nucleus, putamen, globus pallidus, hippocampus,

251 served in the amygdala, raphe nuclei region, caudate nucleus, putamen, hippocampus, and anterior cing

252 two groups did not differ in volumes of the caudate nucleus, putamen, or frontal white matter region

253 inding potential in the raphe nuclei region, caudate nucleus, putamen, thalamus, and insula cortex (P

254 al, occipital, parietal, and temporal lobes; caudate nucleus; putamen; and thalamus.

255 elated regions (nucleus accumbens, r = 0.29; caudate nucleus, r = 0.27) to unhealthy FF commercials p

256 Caudate nucleus recordings (n = 4) revealed multi-scale

257 d in the substantia nigra (SNc), dentate and caudate nucleus, red nucleus, putamen and globus pallidu

258 n and/or 6-hydroxydopamine (6-OHDA) into the caudate nucleus, respectively, modeling the lesions seen

259 ratios were 0.97 and 0.76 in the putamen and caudate nucleus, respectively.

260 ori region of interest analysis of the right caudate nucleus, right temporo-parietal junction and med

261 have revealed that the head and tail of the caudate nucleus selectively and differentially process f

262 However the lateral prefrontal cortex and caudate nucleus showed a non-linear U-shape relationship

263 mate dorsal striatum, within the putamen and caudate nucleus, signal the uncertainty of object-reward

264 tly, mitochondrial PCR array profiling in HD caudate nucleus specimens showed increased mRNA expressi

265 volumes of four deep grey matter structures (caudate nucleus, thalamus, subthalamic nucleus and lenti

266 amo-cortical network comprising the putamen, caudate nucleus, thalamus, supplementary motor area, pre

267 m disorders had greater volumes of the right caudate nucleus than comparison subjects as well as a re

268 ofrontal cortex, anterior temporal lobe, and caudate nucleus than PCA, and PCA showed more asymmetric

269 best classification of ischemic core for the caudate nucleus, the lentiform nucleus, and the insula (

270 the striosomes than the matrix in the monkey caudate nucleus, the opposite was found in the mouse str

271 Activity was also present in the caudate nucleus, the thalamus, and the cerebellum.

272 For the caudate nucleus, there was a significant game x group in

273 1907 ranged from 3.7 +/- 1.5 mL/cm(3) in the caudate nucleus to 14.5 +/- 5.3 mL/cm(3) in the occipita

274 ns known to track expected value such as the caudate nucleus, together with anterior cingulate cortic

275 itry that includes the prefrontal cortex and caudate nucleus, two regions that show prominent changes

276 s were found for the target regions putamen, caudate nucleus, ventral striatum, and substantia nigra

277 9 for the respective target regions putamen, caudate nucleus, ventral striatum, and substantia nigra,

278 Volumes of interest for the putamen, caudate nucleus, ventral striatum, substantia nigra, tha

279 The 2T model VT values for the putamen, caudate nucleus, ventral striatum, substantia nigra, tha

280 Clozapine treatment led to reductions in caudate nucleus volume in three separate studies.

281 Caudate nucleus volume was unrelated to BDNF levels or s

282 The caudate nucleus was also segmented and examined in relat

283 alysis established that activity in the left caudate nucleus was associated with increased activity i

284 nal capsule adjacent to the head of the left caudate nucleus was found in PD-ICB, but not surviving c

285 The caudate nucleus was reduced only after symptomatic onset

286 ents, the decreased connectivity in the left caudate nucleus was related with worse balance performan

287 our study, the MTR in the head of the right caudate nucleus was significantly lower in the MDD group

288 al ventromedial prefrontal regions and right caudate nucleus (washing); putamen/globus pallidus, thal

289 peduncle and pontine tegmentum alongside the caudate nucleus were implicated as critical structures.

290 FA in the SN and CBF in the caudate nucleus were inversely correlated with motor dys

291 putamen in both genders and the putamen and caudate nucleus were significantly smaller in older than

292 opaminergic system, the hippocampus, and the caudate nucleus were to different degrees significantly

293 The effect was specific to caudate nucleus, where growth rate was doubled.

294 d via a neural representation of risk in the caudate nucleus, whereas the representations of other de

295 uent trial in both prefrontal cortex and the caudate nucleus which is correlated with behavioral adju

296 We recorded neural activity in the anterior caudate nucleus while monkeys made saccades to multiple

297 corded from phasically active neurons in the caudate nucleus while monkeys performed a probabilistica

298 in dopamine transmission in the left medial caudate nucleus while simultaneously producing significa

299 In the caudate nucleus with increased BMI we saw the upregulati

300 iosome and matrix compartments of the monkey caudate nucleus, with the exception of a small amount of