ライフサイエンスコーパス: putamen

1 P(ND) was 9% in D2-rich regions (caudate and putamen).

2 basal ganglia (P < 0.01 for both caudate and putamen).

3 l striatum) and with ex-smokers (caudate and putamen).

4 , caudate; 67 +/- 11%, thalamus; 52 +/- 11%, putamen).

5 howed reduced compensatory activation in the putamen.

6 through compensatory hyperactivation of the putamen.

7 ssing within the right caudate and posterior putamen.

8 0.25 in the temporal cortex and 1.92 in the putamen.

9 tal regions: caudate, nucleus accumbens, and putamen.

10 ol analysis of connectivity within the motor putamen.

11 positive effect on DAT binding in the right putamen.

12 n regions with the highest expression in the putamen.

13 in the right hippocampus to .84 in the left putamen.

14 ediated the lower connectivity in the dorsal putamen.

15 l premotor regions and the thalamus upon the putamen.

16 nd extensive outgrowth into the transplanted putamen.

17 d-forward connections from the cortex to the putamen.

18 cingulate zone in the medial wall and in the putamen.

19 tion of the coupling of TPJ with FEF and the putamen.

20 ared with the nonstimulated condition in the putamen.

21 ective of predictability, was reduced in the putamen.

22 entary motor area (preSMA) and the bilateral putamen.

23 of Meynert, and efferent projections to the putamen.

24 faster in a discrete subregion of the dorsal putamen.

25 ral region, cerebellum, thalamus, insula and putamen.

26 of altered mean volume of caudate nucleus or putamen.

27 in inclusion bearing oligodendrocytes in the putamen.

28 e related to lesions in and around the right putamen.

29 insight into the genetic architecture of the putamen.

30 ding total gray matter, cerebral cortex, and putamen.

31 motor area fibers (M1/LPMCv) curved over the putamen.

32 within the left and right lentiform nucleus/putamen.

33 lia structures, preferentially affecting the putamen.

34 lum in control subjects but different in the putamen.

35 ar decrease in striatal binding ratio in the putamen.

36 a less vulnerable structure compared to the putamen.

37 tex, lingual gyrus, posterior cingulate, and putamen.

38 and increased ReHo in right caudate and left putamen.

39 e reward-related activity in the right-sided putamen (0.20 [0.93]; F35,3 = 5.64; P = .003).

40 eds, -0.79 [0.18] vs -0.08 [0.65]; P = .04), putamen (-0.55 [0.35] vs 0.50 [0.33]; P = .001), thalamu

41 ntia nigra (2.0 x 10(11) vector genomes) and putamen (1.0 x 10(12) vector genomes) or sham surgery.

42 e caudate (2.54 +/- 0.79 vs. 3.68 +/- 0.56), putamen (1.39 +/- 1.04 vs. 4.41 +/- 0.54), ventral stria

43 D and SBRHR were found in the caudate (0.6), putamen (1.7 and 1.4), ventral striatum (0.7), and SN (0

44 reases of [(18)F]DOPA uptake in the anterior putamen, [(11)C]raclopride binding in the posterior stri

45 and D2/3 occupancies of 43% (caudate), 25% (putamen), 43% (thalamus).

46 -81%), followed by the ipsilateral posterior putamen (-67%).

47 opposite to the symptomatic side) posterior putamen (-81%), followed by the ipsilateral posterior pu

48 low-calorie food images increased insula and putamen activation and reduced OFC activation compared w

49 algorithms identified robust differences in putamen activation patterns.

50 re lenient threshold also revealed increased putamen activation.

51 ht striatum (caudate) volume, left striatum (putamen) activation during cue reactivity, and lower fun

52 potentiated caudate, nucleus accumbens, and putamen activations and increased caudate-amygdala and c

53 functional connectivity between amygdala and putamen after stress, this increase in connectivity was

54 p=0.0002; all other age ranges, p<0.0001; in putamen: all age ranges, p<0.0001).

55 tional connectivity of the midbrain with the putamen, amygdala, and hippocampus (P < .05, whole brain

56 did not show activation in the left ventral putamen and amygdala when anticipating rewards or in the

57 r, dopamine synthesis capacity in the dorsal putamen and caudate head was positively correlated with

58 ctivation of the right middle frontal gyrus, putamen and caudate in response to errors.

59 -CIT uptake ratios were 0.97 and 0.76 in the putamen and caudate nucleus, respectively.

60 s of the primate dorsal striatum, within the putamen and caudate nucleus, signal the uncertainty of o

61 etic variants influencing the volumes of the putamen and caudate nucleus.

62 significantly elevated GPC+PC levels in ACC, putamen and caudate of RC BD-I patients compared to heal

63 increased for multiple system atrophy in the putamen and caudate, and increased for progressive supra

64 mia alone in the thalamus, internal capsule, putamen and caudate, and there was reduced cleaved caspa

65 y eliminates the DA terminals in the caudate-putamen and causes cell bodies in the midbrain to degene

66 Drinking activations in the putamen and cerebellum also correlated with the unpleasa

67 ATL hyperconnectivity with the right ventral putamen and claustrum and the temporoparietal junction.

68 wed that the SURs of the bilateral posterior putamen and contralateral anterior putamen had a sensiti

69 phia, accompanied by recruitment of anterior putamen and dorsolateral prefrontal cortex.

70 ), dentate and caudate nucleus, red nucleus, putamen and globus pallidus by T2* MRI at baseline and a

71 ugar, sugar caused greater activation in the putamen and gustatory regions than did fat, increasing s

72 ers from controls in the caudate nucleus and putamen and higher D1-receptor density in the nucleus ac

73 of potential rewards; reduced activation in putamen and insula during the anticipation of potential

74 rease in rsFC between the DLPFC and the left putamen and insula.

75 Increased GBC was found in the right putamen and left cerebellar cortex.

76 ala, and decreased metabolism in the caudate/putamen and medial geniculate nucleus.

77 Optogenetic stimulation in the caudate-putamen and neocortex of "histaminergic" axonal projecti

78 effective connectivity between the posterior putamen and other areas of the motor circuit during tapp

79 vailable imaging revealed that right ventral putamen and pallidum atrophy correlated with higher rewa

80 Putamen and pallidum volume augmentations were positivel

81 ted by greater connectivity between the left putamen and paracingulate gyrus during reward anticipati

82 ed compensatory hyperactivation of bilateral putamen and posterior insula, and machine learning algor

83 idated the compensatory relationship between putamen and premotor cortex by showing, in the control s

84 linear increase in connectivity between the putamen and primary motor cortex after levodopa intake d

85 nt, patients had elevated fALFF in bilateral putamen and right caudate, and increased ReHo in right c

86 ion of embryonic dopaminergic neurons in the putamen and subsequently exhibited major motor improveme

87 AAV2-neurturin delivery to the putamen and substantia nigra bilaterally in PD was not s

88 Sections of the post-commissural putamen and substantia nigra pars compacta were processe

89 and efficacy of AAV2-neurturin delivered to putamen and substantia nigra.

90 pharmacokinetic-occupancy curves in caudate, putamen and thalamus.

91 and the salience network, including insula, putamen and thalamus.

92 s, amygdala, caudate, hippocampus, pallidum, putamen and thalamus.

93 reduced functional connectivity between the putamen and the dorsolateral prefrontal cortex in OCD pa

94 h connectivity between sensorimotor areas of putamen and the reward-related ventromedial prefrontal c

95 poral gyrus, the middle cingulate gyrus, the putamen and the superior parietal lobules.

96 e transporter availability in ADHD (caudate, putamen and ventral striatum: +24%, p<0.01); whereas the

97 and D2/3 occupancies of 61% (caudate), 49% (putamen) and 69% (thalamus).

98 h the DAT-rich striatum (caudate nucleus and putamen) and the SERT-rich extrastriatal brain regions (

99 n the caudate body, 17% higher in the dorsal putamen, and 17% higher in the ventral striatum in patho

100 l cortex, thalamus, ventral striatum, dorsal putamen, and anterior cingulate cortex in OCD.

101 l cortex, thalamus, ventral striatum, dorsal putamen, and anterior cingulate cortex.

102 al symptoms and MRI involvement of thalamus, putamen, and brainstem resembling Leigh syndrome.

103 ical regions, including the corpus callosum, putamen, and cerebellum.

104 s well the supplementary motor area, insula, putamen, and cerebellum.

105 Substantia nigra, putamen, and cortical p11 protein levels were assessed i

106 were detected in the dorsal caudate nucleus, putamen, and globus pallidus but the observed variation

107 and decreases in subregions of the caudate, putamen, and hippocampus in 22q-dup relative to 22q-del

108 arly between the left IFG and left pallidum, putamen, and insular cortex, is associated with reduced

109 nnectivity between the VTA and the habenula, putamen, and medial prefrontal cortex, whereas the SN ex

110 or frontal lobe, cingulate cortex, fusiform, putamen, and medial temporal lobe.

111 increased SERT binding in amygdala, caudate, putamen, and median raphe nucleus.

112 nts and obese subjects (in insula, amygdala, putamen, and orbitofrontal cortex).

113 cluding the amygdala, hippocampus, thalamus, putamen, and pallidum), as well as insular cortex, is as

114 ecruitment of the prefrontal cortex, insula, putamen, and thalamus, which collectively forged the for

115 three regions of interest (the caudate, the putamen, and the medial orbitofrontal cortex) were teste

116 er variability of temporal cortex, thalamus, putamen, and third ventricle volumes, consistent with bi

117 larly in the thalamus, caudate, pallidum and putamen, and this was most apparent in secondary progres

118 ilability compared with nonsmokers (caudate, putamen, and ventral striatum) and with ex-smokers (caud

119 transporter type 2 density for the caudate, putamen,and substantia nigra were 21.50%, 58.20%, and 21

120 y load-dependent activation in the bilateral putamen, anterior-dorsal insula, supplementary motor are

121 ese results suggest that the hippocampus and putamen are involved in binding together holistic event

122 teral deactivation of claustrum, insula, and putamen, areas activated during itch processing.

123 e anterior and posterior insular cortex, the putamen, as well as subcortical white matter connections

124 associated with greater iron content in the putamen at baseline, neither age nor metabolic risk infl

125 m study shows that whole brain, cortical and putamen atrophy occurs throughout the 10-year follow-up

126 us type 2 (AAV2)-neurturin injected into the putamen bilaterally failed to meet its primary endpoint,

127 deficit (65% or less of age-expected lowest putamen binding ratio) at baseline, 14 (67%) converted t

128 In the posterior putamen, binding ratios were significantly lower in MSA-

129 er T1R (P = 0.01) in the globus pallidus and putamen but were not associated with whole-blood mangane

130 CYP46A1 protein levels were decreased in the putamen, but not cerebral cortex samples, of post-mortem

131 was significantly reduced in PD caudate and putamen by 53 and 55%, respectively; (3) the VMAT2 trans

132 ft-derived dopaminergic reinnervation of the putamen can be maintained for a quarter of a century des

133 ld correlation (MFC) in the globus pallidus, putamen, caudate nucleus, and thalamus for 22 patients w

134 p by challenge effects were most profound in putamen, caudate, midbrain, thalamus, and cerebellum.

135 ed for progressive supranuclear palsy in the putamen, caudate, thalamus, and vermis, and decreased in

136 nt was negatively associated with rsFC DLPFC-putamen changes across all subjects.

137 gnificantly increased activation in the left putamen compared with TD patients and healthy controls.

138 d that neural signals in the hippocampus and putamen contained information about all of these event a

139 In CA, MP-induced metabolic increases in putamen correlated negatively with addiction severity.

140 Greater increase of fALFF in the left putamen correlated with less improvement in positive sym

141 terfering particles (DIPs), into the caudate-putamen (CP) and scored for an innate immune response an

142 ncluded the nucleus accumbens (NAS), caudate-putamen (CP), hippocampus, and medial thalamus.

143 ng basis for differences between the caudate putamen (CPu) and nucleus accumbens (NAc).

144 us accumbens (NAc), hippocampus, and caudate putamen (CPu) in morphine-induced conditioned place pref

145 of NBQX (0, 0.3 mug/0.3 mul) in the caudate putamen (CPu) on CS responding in the non-alcohol contex

146 ), caudate (d=-0.11), hippocampus (d=-0.11), putamen (d=-0.14), and intracranial volume (d=-0.10) wer

147 3 vs -0.07), hippocampus (d=-0.12 vs -0.06), putamen (d=-0.18 vs -0.08), and intracranial volume (d=-

148 eech production, but some patients with left putamen damage can produce speech remarkably well.

149 ud and picture naming in a patient with left putamen damage.

150 Putamen dopamine terminal loss at disease onset most lik

151 tex, ventral striatum, parietal lobe, dorsal putamen, dorsal caudate, amygdala, and hippocampus.

152 athways that compensate for loss of the left putamen during speech production.

153 r the caudate (F(2,90) = 8.2, p = 0.001) and putamen (F(2,90) = 6.6, p = 0.002), but not the ventral

154 ric change in the hippocampus, amygdala, and putamen from early to mid-adolescence was associated wit

155 pallidus, cingulate cortex, insula, caudate, putamen, frontal cortex, temporal cortex, and thalamus.

156 Importantly, the putamen functional connectivity within the consolidated

157 amen tCho/Cr and apnea hypopnea index; right putamen GABA/Cr and baseline SaO2; left putamen PE/Cr an

158 individuals, showed that KCTD17 is part of a putamen gene network, which is significantly enriched fo

159 hemisphere reward circuit regions including putamen, globus pallidus, insula and thalamus.

160 ircuits-head of the caudate nucleus (hCaud), putamen, globus pallidus, thalamus-and four cortical reg

161 Bilaterally increased thalamic mI/Cr, putamen Glx/Cr, and Glu/Cr, and bilaterally decreased th

162 revealed that reduction of FP-CIT uptake in putamen greater than 25% discriminated patients with DAT

163 follows: cingulate cortex > insula > caudate/putamen > frontal cortex > temporal cortex > thalamus, c

164 posterior putamen and contralateral anterior putamen had a sensitivity of 100% and specificity of 100

165 A region of the brain called the putamen has a central role in our ability to keep a beat

166 A region of the brain called the putamen has a central role in procedural memory consolid

167 bitofrontal cortex, insula, globus pallidus, putamen, hippocampus, and amygdala) and homeostatic (hyp

168 gdala, raphe nuclei region, caudate nucleus, putamen, hippocampus, and anterior cingulate cortex of p

169 T uptakes in the whole striatum, caudate and putamen in manifest and premanifest HDGECs compared with

170 related with BPND in the caudate nucleus and putamen in nonsmokers and female smokers but not in male

171 relief events, indicating a pivotal role of putamen in regulation of behaviour and habit formation i

172 cingulate gyrus post-cocaine and in the left putamen in the abstinence/saline condition.

173 fied localized regions around the insula and putamen in the neonatal Jacobian map that were positivel

174 ubjects, that lower connectivity through the putamen increased connectivity through premotor cortex.

175 ally in striatal regions in proximity to the putamen (increased fractional anisotropy, P = .01, false

176 20 million cells by stereotactic ipsilateral putamen injection.

177 a right hemisphere cluster encompassing the putamen, insula, and inferior frontal gyrus.

178 oup-by-age interactions were observed in the putamen, insula, and orbitofrontal cortex (indicating re

179 sification, we show that the hippocampus and putamen integrate event attributes across all of these l

180 The left putamen is known to be important for speech production,

181 um (DLS), corresponding roughly to the human putamen, led to tic-like stereotypies after either acute

182 related hypoactivation was found in the left putamen, left inferior frontal gyrus (pars opercularis),

183 s in new patients who had damage to the left putamen, left premotor cortex, or both.

184 increased grey matter in right insula, right putamen, left temporal pole, and bilateral thalamus) and

185 ontal, insula, middle and superior temporal, putamen, lingual, cuneus, and cerebellum).

186 For the caudate and putamen, LL showed higher DRD2 availability than HH; HL

187 umber of WM differences in the region of the putamen located between the inferior fronto-occipital fa

188 It is provisionally concluded that the putamen may be particularly important in endogenous prim

189 positive emotions in the nucleus accumbens, putamen, medial prefrontal and midbrain in healthy volun

190 d with methadone exhibited increased caudate/putamen metabolism, whereas buprenorphine produced incre

191 range, showed increases in activation in the putamen, mid-insula, Rolandic operculum, and precuneus t

192 of signal and noise correlation of pairs of putamen MSNs were strongly shifted toward positive corre

193 nucleus (n = 4), whole thalamus (n = 3), and putamen (n = 2).

194 ft putamen PE/Cr and baseline SaO2; and left putamen NAA/Cr and SaO2 nadir (all p < 0.05).

195 e, and occipital lobe as well as caudate and putamen nuclei, after adjusting for age (P < 0.05).

196 he brain regions studied (thalamus, caudate, putamen, nucleus accumbens, globus pallidus, and substan

197 brain regions (cortex, hippocampus, caudate-putamen, nucleus accumbens, thalamus, and hypothalamus)

198 anterior cingulate cortex (ACC), caudate and putamen of 16 RC BD-I, 34 non-RC BD-I and 44 healthy con

199 d dopamine turnover in the bilateral ventral putamen of consuming smokers.

200 riptome by RNA sequencing in the caudate and putamen of nine TS and nine matched normal control subje

201 e 312 in neurons and oligodendrocytes in the putamen of patients with multiple system atrophy.

202 3 T to explore the metabolic profile in the putamen of patients with Parkinson disease.

203 ProSavin after bilateral injection into the putamen of patients with Parkinson's disease.

204 ative biomarkers of Parkinson disease in the putamen of patients.

205 n prefrontal cortical layers and the caudate-putamen of rhesus monkeys, trained in a spatial-versus-o

206 y, we found higher CBF in the right pallidum/putamen of the cannabis users compared with nonusers.

207 ients, with no changes being detected in the putamen or globus pallidus.

208 t did not significantly decrease BPND in the putamen or the substantia nigra or in any region when me

209 ability over the first year, and lower right putamen (OR=0.06, p=0.01) and mean total striatal (OR=0.

210 ow-up, most substantially in the caudate and putamen (P < .001 for both).

211 a sexual cue-reactivity paradigm in the left putamen (P < .001).

212 rontal gyri, superior temporal gyri, and the putamen (p < .001).

213 11)C-IMA107 BPND in the caudate (P < 0.001), putamen (P < 0.001) and globus pallidus (P = 0.025) in p

214 atic time-of-day effect focusing on the left putamen (p < 0.001).

215 was linked to smaller caudate (P < .001) and putamen (P = .01) volumes (both corrected for total brai

216 es were observed in the caudate (p = 0.1) or putamen (p = 0.8) following methylphenidate injection.

217 and psychostimulant-medicated ADHD patients (putamen, P = .006; caudate nucleus, P = .010; thalamus,

218 xes of brain iron than did control subjects (putamen, P = .012; caudate nucleus, P = .008; thalamus,

219 orter binding (all age ranges in caudate and putamen, p<0.0001) and (18)F-FDOPA uptake (in caudate: a

220 after long-term treatment (caudate: p<0.007; putamen: p<0.005).

221 ranial volume, but larger bilateral caudate, putamen, pallidum and lateral ventricle volumes.

222 surface-based shape metrics of the caudate, putamen, pallidum, and nucleus accumbens in 53 depressed

223 ortex, posterior cingulate cortex, thalamus, putamen, pallidum, caudate, hippocampus, and brain stem.

224 volumes, but not to volumes of the thalamus, putamen, pallidum, nucleus accumbens, or caudate nucleus

225 elevant for ADHD, including the hippocampus, putamen, pallidum, thalamus, midbrain with pons (compris

226 ontrols, increased 18F-AV-1451 uptake in the putamen, pallidum, thalamus, midbrain, and in the dentat

227 a developmental shift in bilateral posterior putamen/pallidum clusters from preferential connectivity

228 that are partially mediated by thalamic and putamen pathology.

229 ight putamen GABA/Cr and baseline SaO2; left putamen PE/Cr and baseline SaO2; and left putamen NAA/Cr

230 egative correlations were found between left putamen PE/Cr and SaO2 nadir.

231 The SURs of bilateral caudate, anterior putamen, posterior putamen, substantia nigra, and nucleu

232 lementary motor cortex with the sensorimotor putamen predicted more severe tics.

233 ventromedial prefrontal cortex, supported by putamen, provides an expected value-related input to the

234 BPND in the caudate (r = -0.54; P = 0.011), putamen (r = -0.48; P = 0.022), and globus pallidus (r =

235 BPND in the caudate (r = -0.65; P = 0.005), putamen (r = -0.51; P = 0.025), and globus pallidus (r =

236 ND in the caudate (r = -0.73; P = 0.031) and putamen (r = -0.74; P = 0.031).

237 triatal binding ratios (SBRs) and caudate-to-putamen ratios (CPRs).

238 hesus macaque, AAV delivery of miHDS1 to the putamen reduced HTT expression with no adverse effects o

239 the localized prefrontal layers and caudate-putamen region exhibited similar location preferences on

240 pha-synuclein positive in the left and right putamen, respectively.

241 e displaced PE2I from DAT in the caudate and putamen, resulting in 62+/-4% cocaine occupancy.

242 dorsal anterior cingulate cortex, bilateral putamen, right caudate, and thalamus, whereas metacognit

243 ed with a lower reduction in GMV in the left putamen (SDM estimate = -0.911; P < .001).

244 how that functional connectivity between the putamen (seed) and other subcortical structures was lowe

245 Dopaminergic markers in the dorsal putamen showed a modest loss at 1 year after diagnosis i

246 The right putamen showed increased mI/Cr and decreased tCho/Cr, an

247 and 822 upregulated genes in the caudate and putamen (striatum) of TS individuals.

248 lateral caudate, anterior putamen, posterior putamen, substantia nigra, and nucleus accumbens were si

249 8) F-flortaucipir uptake in globus pallidus, putamen, subthalamic nucleus, midbrain, and dentate nucl

250 -by-diagnosis interaction in the caudate and putamen supports the relevance of different brain develo

251 and baseline oxygen saturation (SaO2); right putamen tCho/Cr and apnea hypopnea index; right putamen

252 u/Cr, and bilaterally decreased thalamic and putamen tCho/Cr and GABA/Cr occurred in OSAS vs healthy

253 udate nucleus, globus pallidus, hippocampus, putamen, thalamus, and brainstem) were derived from stru

254 l orbitofrontal gyri, right anterior insula, putamen, thalamus, and caudate, and midbrain and pons.

255 in the raphe nuclei region, caudate nucleus, putamen, thalamus, and insula cortex (P < .05 corrected)

256 s, amygdala, caudate, hippocampus, pallidum, putamen, thalamus, and lateral ventricle).

257 ate, frontal cortex, hypothalamus, pallidum, putamen, thalamus, and ventral striatum) showed signific

258 sula, cingulate, amygdala) and sub-cortical (putamen, thalamus, globus pallidus, cerebellum) regions.

259 dala, caudate, hippocampus, globus pallidus, putamen, thalamus, lateral ventricles.

260 ne in the caudate nucleus and another in the putamen) that consisted of voxels with unique projection

261 In the putamen, the observed kinetics (positive [Formula: see t

262 n in the bilateral insula extending into the putamen, the Rolandic operculum, and thalamus, which pro

263 e in the nucleus accumbens (NAc) and caudate-putamen through an indirect mechanism that involves stri

264 Functional decoding mapped the left putamen to cognitive aspects of music perception/reprodu

265 an immediate hypersensitivity of preSMA and putamen to levodopa, which heralds the failure of neural

266 Functional connectivity from the putamen to other fronto-striatal regions was also greate

267 impaired axonal transport of neurturin from putamen to substantia nigra.

268 f striato-cortical feedback connections from putamen to the pre-supplementary motor area (Pcorrected

269 midbrain tracer uptake was shifted from the putamen to widespread corticolimbic areas.

270 Decreased FP-CIT putamen uptake greater than 25% predicts synucleinopathy

271 preterm brain, regions around the insula and putamen using neonatal deformation-based morphometry, an

272 ance images showed an absent or disappearing putamen, variable cerebellar atrophy and highly variable

273 Regions of interest for the caudate, putamen, ventral striatum, SN, and cerebellum were drawn

274 Regions of interest for the caudate, putamen, ventral striatum, substantia nigra (SN), and ce

275 (95% CI 2.26-4.16), a reduction of one SD in putamen volume (imaging domain) increased risk by 3.32 t

276 Increases in left putamen volume (P<0.03) occurred with ECT.

277 001), cortical (-3.4% vs -1.8%, p=0.009) and putamen volume changes (-10.6% vs -3.8%, p=0.003) compar

278 Variants influencing putamen volume clustered near developmental genes that r

279 men volume than bipolar I patients, and left putamen volume correlated positively with left ventral s

280 s approach to the GWAS summary statistics of putamen volume in the ENIGMA cohort, a total of 15 indep

281 the hippocampus and attenuated reduction in putamen volume over time were associated with the onset

282 Second, reduced bilateral putamen volume prospectively predicted anhedonia severit

283 r II patients had significantly greater left putamen volume than bipolar I patients, and left putamen

284 anticipation) was positively associated with putamen volume.

285 severity, but only among youth with smaller putamen volume.

286 ta = 1.07; 95% CI, 0.50 to 1.64) and smaller putamen volumes (beta = -1.16; 95% CI, -1.86 to -0.46) w

287 rations in total gray matter and caudate and putamen volumes in unaffected siblings suggest that thes

288 for thalamus, lateral ventricle, caudate and putamen volumes, and rightward asymmetry for amygdala an

289 s were used, the average BPND in the caudate putamen was 0.94, and no significant changes in the test

290 However, only the putamen was significantly different, and it correlated w

291 vity (e.g., thalamus, amygdala, hippocampus, putamen) was associated positively with maternal mental

292 l junction on the frontal eye fields and the putamen were modulated by (Bayes-optimal) updates.

293 ienting responses in right FEF, TPJ, and the putamen were significantly modulated by precision-depend

294 mentary motor area, primary motor cortex and putamen when patients suppressed a motor response.

295 the left hippocampus, amygdala, and ventral putamen when receiving unexpected rewards (control condi

296 The strongest effects were found for the putamen, where a novel intergenic locus with replicable

297 T-ir interneurons in the caudate nucleus and putamen, whereas monkeys have a more heterogeneous repre

298 activation and apoptosis, including caudate/putamen, white matter, and, in juvenile-onset cases, als

299 also includes subcortical regions, like the putamen with connections to the insular cortex.

300 3) in the cerebellum to 3.71 mL/cm(3) in the putamen, with a BPND of 0.25 in the temporal cortex and