ライフサイエンスコーパス: caudate nucleus

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

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

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

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

5 teral and dorsomedial prefrontal cortex, and caudate nucleus.

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

7 right lentiform nucleus and extended to the caudate nucleus.

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

9 thway might elicit neuritic outgrowth to the caudate nucleus.

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

11 odulating neural signals in the amygdala and caudate nucleus.

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

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

14 ergic modulation of neuronal activity in the caudate nucleus.

15 arison subjects in metabolic activity in the caudate nucleus.

16 the prefrontal and parietal cortices and the caudate nucleus.

17 es reached only marginal significance in the caudate nucleus.

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

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

20 and in volumes of the right frontal lobe and caudate nucleus.

21 ffective connection from ventral midbrain to caudate nucleus.

22 d uptake are similar for the putamen and the caudate nucleus.

23 jects with single-voxel (1)H-MRS of the left caudate nucleus.

24 medication, however, affects the size of the caudate nucleus.

25 zophrenia suggest high choline levels in the caudate nucleus.

26 ippocampus, mammillary bodies, thalamus, and caudate nucleus.

27 ervation selectively localized to the medial caudate nucleus.

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

29 the prediction of forthcoming demand in the caudate nucleus.

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

31 the cortical regions with connections to the caudate nucleus.

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

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

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

35 dorsal striatum, including activation in the caudate nucleus.

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

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

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

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

40 11-labeled [11C]PMP acetylcholinesterase and caudate nucleus [11C]DTBZ monoaminergic positron-emissio

41 36%), left posterior putamen (18%), and left caudate nucleus (12%) of the patients than in the compar

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

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

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

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

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

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

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

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

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

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

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

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

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

55 The medial caudate nucleus also shows hyperactivity in humans lacki

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

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

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

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

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

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

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

63 lored in the major functional domains of the caudate nucleus and compared with the putamen, using fas

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

65 The caudate nucleus and cortical regions with connections to

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

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

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

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

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

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

72 m contiguous slices were used to measure the caudate nucleus and lateral ventricles in 15 right-hande

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

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

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

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

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

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

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

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

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

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

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

84 ificantly increased, up to 130% in the right caudate nucleus and putamen and up to 116% in both the r

85 The caudate nucleus and putamen exhibited the highest uptake

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

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

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

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

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 e experiments indicate a causal role for the caudate nucleus and thalamus in automatic inhibitory mot

94 Caudate nucleus and thalamus volumes were unaffected by

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 putamen, internal capsule, external capsule, caudate nucleus, and globus pallidus.

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

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

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

118 f gray matter (cortex, thalamus, head of the caudate nucleus, and lentiform nucleus).

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

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

121 amine into synaptosomes from frontal cortex, caudate nucleus, and nucleus accumbens from wild-type, N

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

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

124 ncreased in the ipsilateral globus pallidus, caudate nucleus, and putamen.

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

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

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

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

129 sts between the caudal two-thirds of Pf, the caudate nucleus, and the SNr.

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

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

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

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

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

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

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

137 measurable effects after injections into the caudate nucleus, basolateral amygdala, hippocampus, vent

138 er an ideal group for the measurement of the caudate nucleus because they may be genetically related

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

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

141 n between prefrontal cortex and ventromedial caudate nucleus (CAUD) activity] suggest that the post-a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 nctional and effective connectivity of human caudate nucleus following sulpiride treatment, which is

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

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

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

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

177 cerebral white matter, hippocampus-amygdala, caudate nucleus, globus pallidus plus putamen, and dienc

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

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

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

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

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

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

184 , was markedly elevated in the neocortex and caudate nucleus in HD patients.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

202 The caudate nucleus is a part of the visual corticostriatal

203 The caudate nucleus is commonly active when learning relatio

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

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

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

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

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

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

210 The caudate nucleus may be involved in the repetitive moveme

211 components of these circuits, such as in the caudate nucleus, may result in neurobehavioral syndromes

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

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

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

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

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

217 g lasting memory, including the hippocampus, caudate nucleus, nucleus basalis and cortex.

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

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

220 tracranial administration of MV-CEA into the caudate nucleus of Ifnar(ko) CD46 Ge did not result in c

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

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

223 indwelling cannula implanted into the right caudate nucleus of normal rats or i.t. in rats bearing e

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

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

226 e of Neuron, demonstrate that neurons in the caudate nucleus of the basal ganglia signal which dimens

227 and white matter for the 4 major lobes, and caudate nucleus of the brain were compared in patients a

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

229 d human lymphoblastoid B-cell lines into the caudate nucleus of the nude rat resulted in lethal CNS t

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

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

239 pretreatment glucose metabolism in the right caudate nucleus (partial r=-0.53), improvement of major

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

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

242 Thus, the caudate nucleus provides interpretive monitoring of ongo

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

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

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

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

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

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

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

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

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

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

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

254 significant metabolic decreases in the right caudate nucleus, right ventrolateral prefrontal cortex (

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

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

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

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

259 ty in the ventral prefrontal cortex, ventral caudate nucleus, thalamus, and hippocampus.

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

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

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

263 Here we identify neurons in the monkey caudate nucleus that create a spatially selective respon

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

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

266 radient of increasing Ki values from head of caudate nucleus to rostral putamen to caudal putamen.

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

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

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

270 9 for the respective target regions putamen, caudate nucleus, ventral striatum, and substantia nigra,

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

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

273 nd significant, inverse correlations between caudate nucleus volume and the severity of perseveration

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

275 are consistent with the findings of reduced caudate nucleus volume reported in studies of neurolepti

276 Caudate nucleus volume was unrelated to BDNF levels or s

277 ute (13.1%, 13.2%) and relative (9.1%, 9.2%) caudate nucleus volumes in never-medicated subjects with

278 Reduced caudate nucleus volumes may be a good candidate marker f

279 Caudate nucleus volumes were initially abnormal for pati

280 Caudate nucleus volumes were significantly (P =.008) sma

281 The caudate nucleus was also segmented and examined in relat

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

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

284 Functional connectivity of caudate nucleus was modulated specifically by dopaminerg

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 The volume of the caudate nucleus was significantly correlated with the pe

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

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

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 he association of intrinsic pathology in the caudate nucleus with abnormalities in working memory in

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