ライフサイエンスコーパス: caudate-putamen

1 n (the core of the nucleus accumbens and the caudate putamen).

2 s dorsal to the VP (e.g., nucleus accumbens, caudate putamen).

3 and lower levels in the corpus callosum and caudate putamen.

4 r are colocalized in the cerebral cortex and caudate putamen.

5 +)-NeuN(+)-betaIII-tubulin(+) neurons to the caudate putamen.

6 the cingulate cortex, nucleus accumbens, and caudate putamen.

7 ing levels of both ligands were found in the caudate putamen.

8 n the occipital cortex, parietal cortex, and caudate putamen.

9 3/J mice SSTR-3 mRNA was not detected in the caudate putamen.

10 levation of SSTR-1 and -3 mRNAs in the mouse caudate putamen.

11 us, and cortex but not to the hippocampus or caudate putamen.

12 Aergic DARPP-32+ medium spiny neurons in the caudate-putamen.

13 dala or the nucleus accumbens but not to the caudate-putamen.

14 increases in ubiquitin levels were unique to caudate-putamen.

15 at maintains extensive axonal projections to caudate-putamen.

16 ine uptake in both the nucleus accumbens and caudate-putamen.

17 mpus and cortex and smallest in thalamus and caudate-putamen.

18 allidal neurons which lie in the dorsomedial caudate-putamen.

19 of labelled varicosities in the dorsolateral caudate-putamen.

20 somedial accumbens along its border with the caudate-putamen.

21 rgent projections to multiple regions of the caudate-putamen.

22 f which project to the nucleus accumbens and caudate-putamen.

23 of RNA extracted from rat frontal cortex and caudate-putamen.

24 the cortex and thalamus but disagree in the caudate-putamen.

25 opamine-innervated, neuronal subtypes in the caudate-putamen.

26 Neuropeptide Y was elevated in the caudate-putamen.

27 otor cortices (18%, P<0.01) and dorsolateral caudate putamen (17%, P<0.01), but not in the ventrolate

28 s, all three drugs increased accumulation in caudate putamen 3-5 times, and indomethacin and probenec

29 naive rats, quinpirole decreased LCGU in the caudate/putamen (84% of control), lateral habenula (80%

30 pallidum (82% of control) as well as in the caudate/putamen (86% of control), lateral habenula (77%

31 the exception of cingulate cortex and caudal caudate-putamen, a significantly greater response was ob

32 [(18)F](R)-FIPCT uptake in the caudate/putamen achieved transient equilibrium at 75 min

33 ine in the nucleus accumbens relative to the caudate-putamen after systemic cocaine administration.

34 in several other brain areas, including the caudate-putamen, amygdala, and brainstem regions such as

35 Brain areas analyzed were caudate, putamen, amygdaloid complex, hippocampal format

36 S decreased 5-HT release in the dorsolateral caudate-putamen, an area implicated in the etiology of H

37 llosum, habenulae, septum, fornix, thalamus, caudate putamen and a few in fasciculus retroflexus and

38 l septum, from the posterior thalamus to the caudate putamen and cerebral cortex, and from the parabr

39 and D(4) receptors in nucleus accumbens and caudate putamen and D(2) receptors in medial prefrontal

40 C38, a marker for GABAergic neurons, in the caudate putamen and lateral shell of the accumbens.

41 nstrated that individual neurons in both the caudate putamen and lateral shell of the nucleus accumbe

42 ate presynaptic dopaminergic function in the caudate putamen and nucleus accumbens of adult male rats

43 cocaine administration, were measured in the caudate putamen and nucleus accumbens of C57BL/6J and 12

44 zation of the CXCL12 receptor, CXCR4, in the caudate putamen and nucleus accumbens of the adult rat b

45 The ability of terminals in the caudate putamen and nucleus accumbens to release and reg

46 sphorylation in the two striatal structures (caudate putamen and nucleus accumbens).

47 ra and ventral tegmental area project to the caudate putamen and nucleus accumbens, where they modula

48 ra and ventral tegmental area project to the caudate putamen and nucleus accumbens/olfactory tubercle

49 1r immunoreactivity (gfD1r-IR), found in rat caudate putamen and rat retina were virtually identical

50 Persistent injury to the caudate putamen and thalamus at P1 was significantly cor

51 the anterior portion of cerebral cortex, the caudate putamen and thalamus compared with vehicle.

52 However, EM-induced FOSir was absent in the caudate putamen and the accumbens nucleus, both areas of

53 three subdivisions of the basal ganglia, the caudate, putamen and globus pallidus in brown capuchin m

54 ume and diffusivity changes in the thalamus, caudate, putamen and hippocampus and examined diffusion

55 patients had higher (11)C-CNS 5161 uptake in caudate, putamen and precentral gyrus compared to the pa

56 describe pharmacokinetic-occupancy curves in caudate, putamen and thalamus.

57 l dopamine transporter availability in ADHD (caudate, putamen and ventral striatum: +24%, p<0.01); wh

58 ry processes mediated by the hippocampus and caudate-putamen and (ii) bias the brain toward the use o

59 s rapidly eliminates the DA terminals in the caudate-putamen and causes cell bodies in the midbrain t

60 increase in mitochondrial DNA damage in the caudate-putamen and cerebellum.

61 II maximally inhibited 50% of binding in the caudate-putamen and had no effect on 125I-epibatidine bi

62 Neurotoxic injury of the caudate-putamen and lateral globus pallidus unilaterally

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

64 Therefore, we characterized the caudate-putamen and nucleus accumbens extracellular acet

65 Extracellular DA in the caudate-putamen and nucleus accumbens, evoked by electri

66 rizations along the dorsolateral edge of the caudate-putamen and sparsely-packed arborizations more m

67 disease (PD) including the cerebral cortex, caudate-putamen and substantia nigra pars compacta.

68 ay and dopaminergic neuronal degeneration in caudate-putamen and substantia nigra.

69 teral projections mainly to both the ventral caudate-putamen and the amygdala, but not to the dorsal

70 ue levels of DA were higher in the MPOA, the caudate-putamen and the bed nucleus of stria terminalis

71 nt throughout the cerebral cortex, thalamus, caudate-putamen and the hippocampus.

72 rs (10-30 microg of MPEP) in the dorsomedial caudate-putamen and the similar cytological expression p

73 PPI - dorsolateral (dlCPu) and medial (mCPu) caudate/putamen and core (NACc) and medial shell (NACms)

74 he amygdala, and decreased metabolism in the caudate/putamen and medial geniculate nucleus.

75 ograde tracers, placed into the dorsolateral caudate/putamen and the nucleus accumbens, were used to

76 of the midbrain project to the dorsolateral caudate/putamen and to the ventromedially located nucleu

77 ns (cerebellum, cortex, substantia nigra and caudate-putamen) and skin fibroblasts from HD patients.

78 all spontaneously active neurons in dorsal (caudate-putamen) and ventral (accumbens, core) striatum;

79 NA expression levels in cortex, hippocampus, caudate putamen, and amygdala decreased during the secon

80 at brains were mostly located in the cortex, caudate putamen, and amygdala with an extremely low dens

81 ajor axonal pathways and in the hippocampus, caudate putamen, and cerebellum.

82 rs in the rostral nucleus accumbens, rostral caudate putamen, and layer I of the rostral cingulate co

83 ve neurons were consistently observed in the caudate putamen, and moderately or weakly labeled neuron

84 er types avoided the nucleus accumbens core, caudate putamen, and the globus pallidus.

85 n the olfactory tubercle, nucleus accumbens, caudate putamen, and the layer VI of the neocortex compa

86 as also increased in the olfactory tubercle, caudate putamen, and the nucleus accumbens of mu-opioid

87 mages showed an increased local field in the caudate, putamen, and globus pallidus of patients relati

88 Three basal ganglia structures (caudate, putamen, and globus pallidus) and one compariso

89 ologic features of the basal ganglia nuclei (caudate, putamen, and globus pallidus) in children with

90 The average sizes of the caudate, putamen, and globus pallidus, but not of the th

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

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

93 ed behavioral approach tendencies by biasing caudate, putamen, and nucleus accumbens but not amygdala

94 acial cues in reward-related regions such as caudate, putamen, and nucleus accumbens but not the amyg

95 nding in the hippocampus, prefrontal cortex, caudate, putamen, and substantia nigra.

96 pical neuroleptic was associated with higher caudate, putamen, and thalamus volumes, whereas a higher

97 and N-acetylaspartate in the left and right caudate, putamen, and thalamus were scaled into concentr

98 e metabolic rates bilaterally in the ventral caudate, putamen, and thalamus.

99 Caudate, putamen, and total brain volumes were quantifie

100 l D2R availability compared with nonsmokers (caudate, putamen, and ventral striatum) and with ex-smok

101 easured in the subdivisions of the striatum (caudate, putamen, and ventral striatum) in addition to t

102 rsomedial and ventrolateral quadrants of the caudate-putamen, and in the rostrobasal cell cluster, ro

103 as seen in the piriform cortex, hippocampus, caudate/putamen, and cerebellar cortex.

104 the cerebral cortex, hippocampus, thalamus, caudate/putamen, and olfactory bulb, with lower levels i

105 levels for gb2 were virtually absent in the caudate/putamen, and significantly lower in the medial b

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

107 suggests that lateral sensorimotor areas of caudate putamen are important for responding based on ex

108 post-synaptic areas (frontal cortex, septum, caudate putamen), as well as significantly higher plasma

109 signals in both health and disease from the caudate-putamen, as well as possibly from other subcorti

110 sal ganglia, cortex above the diencephalon], caudate-putamen, basal forebrain, hypothalamus, hippocam

111 no effect on ethanol-induced Fos-IR changes (caudate putamen, bed nucleus of the stria terminalis, an

112 amphetamine, MK-801 did not increase FLI in caudate-putamen, bed nucleus of the stria terminalis, or

113 cells that were placed unilaterally into the caudate-putamen brain region of a patient suffering from

114 ts' cerebellum, cortex, substantia nigra and caudate-putamen brain regions.

115 ntration in the nucleus accumbens (NAcc) and caudate putamen but not the medial prefrontal cortex or

116 associated with a selective decrease in the caudate-putamen but not nucleus accumbens extracellular

117 ctive decrease in the dopamine response, the caudate-putamen but not nucleus accumbens extracellular

118 mine binge decreased acetylcholine levels in caudate-putamen, but had no effect on levels in nucleus

119 e show that inactivation of the dorsolateral caudate-putamen, but not other structures previously imp

120 gia after restoration of DA signaling in the caudate putamen by viral gene therapy.

121 sted in retinae of goldfish and rat, and rat caudate putamen, by using immunoblots and light microsco

122 inding sites compared to normotensive WKY in caudate putamen, CA3 region of the hippocampus, cingulat

123 ochemical manipulation of the hippocampus or caudate-putamen can bias an animal toward the use of a s

124 In the caudate putamen (CauP), a locus with low specific bindin

125 rtex, olfactory tubercle, nucleus accumbens, caudate-putamen, claustrum, dorsal endopiriform nucleus,

126 In the dorsal portion of the caudate putamen, core and shell of the nucleus accumbens

127 lateral ventricle, in zones adjacent to the caudate putamen, corpus callosum, and lateral septal nuc

128 to a lesser extent, in the hippocampus (HP), caudate putamen (CP) and frontal cortex (FC).

129 olfactory bulb (MOB), cerebral cortex (CTX), caudate putamen (CP), hippocampus (HP), thalamus (TH), a

130 brain areas including the hippocampus (HI), caudate putamen (CP), the hypothalamic paraventricular n

131 ctive interfering particles (DIPs), into the caudate-putamen (CP) and scored for an innate immune res

132 ithin the SN, while loss of RN in the SN and caudate-putamen (CP) was slower and required > or =100 n

133 sponse included the nucleus accumbens (NAS), caudate-putamen (CP), hippocampus, and medial thalamus.

134 measured in the nucleus accumbens (NAc) and caudate putamen (CPu) after 3-day 'binge' pattern cocain

135 underlying basis for differences between the caudate putamen (CPu) and nucleus accumbens (NAc).

136 Membranes of rat caudate putamen (CPu) and thalamus or CHO-HA-rMOR cells

137 ucleus (MnPO), periventricular nucleus (Pe), caudate putamen (CPU) and the ependymal lining of the ve

138 stem in the cortex, nucleus accumbens (NAc), caudate putamen (CPu) and the region containing the subs

139 as restoration of dopamine production to the caudate putamen (CPu) does not fully restore the hyperlo

140 ), nucleus accumbens (NAc), hippocampus, and caudate putamen (CPu) in morphine-induced conditioned pl

141 and sends a glutamatergic projection to the caudate putamen (CPu) in rat.

142 oration of dopamine synthesis to the central caudate putamen (CPu) of DD mice rescues feeding and sur

143 abel dopaminergic axons and terminals in the caudate putamen (CPu) of rats 7 days prior to a neurotox

144 e effect of NBQX (0, 0.3 mug/0.3 mul) in the caudate putamen (CPu) on CS responding in the non-alcoho

145 In the hippocampus (HIP) and caudate putamen (CPu), pERK and FosB/DeltaFosB levels we

146 early genes (IEGs) c-Fos and JunB in the rat caudate putamen (CPu).

147 ny corresponding drug-induced changes in the caudate-putamen (CPu) after L-DOPA administration.

148 5 from the globus pallidus (GP), 98 from the caudate-putamen (CPu) and 23 from the central nucleus of

149 RTI-121-labeled dopamine transporters in the caudate-putamen (CPu) and cortex as well as depletion of

150 tyrosine hydroxylase immunoreactivity in the caudate-putamen (CPu) and decreases in CPu tissue dopami

151 possible mechanisms by which neurons in the caudate-putamen (CPu) and globus pallidus (GP) participa

152 and MKP-1 phosphorylation (p-MKP-1), in the caudate-putamen (CPu) and nucleus accumbens (NAc) of Fis

153 MOR activation was first detected in the caudate-putamen (CPU) at e12.5, and by e15.5, activity h

154 t, is induced in nucleus accumbens (NAc) and caudate-putamen (CPu) by repeated exposure to drugs of a

155 n blot, were found to be elevated in NAc and caudate-putamen (CPu) of FR relative to AL rats.

156 protein were induced in the hippocampus and caudate-putamen (CPu), accompanied by increased caspase-

157 ession in the nucleus accumbens core (NAcC), caudate-putamen (CPu), and subthalamic nucleus.

158 ine-induced c-Fos and JunB expression in the caudate-putamen (CPu), the mu receptor antagonist, beta-

159 Jun-B, in the dorsomedial portion of the rat caudate-putamen (CPu).

160 al pathways (substantia nigra, SN and dorsal caudate-putamen, CPu).

161 ctural MRI to measure concurrent declines in caudate/putamen D2 neuroreceptor binding and tissue volu

162 ride positron emission tomography to measure caudate/putamen D2 receptor binding.

163 in regional metabolism and network activity, caudate/putamen DAT binding, and Unified Parkinson's Dis

164 erminalis, septal nuclei, nucleus accumbens, caudate putamen, diagonal band, amygdala, hypothalamus,

165 behaviors characteristic of DA injections in caudate-putamen did not occur.

166 , we examined the effects of a) dorsolateral caudate putamen (dlCPu) lesions on cocaine self-administ

167 c to dorsomedial and ventromedial regions of caudate-putamen (dmCPu, vmCPu).

168 ml g(-1)), followed by ventricular regions (caudate putamen, ependyma, hippocampus, 0.05-0.14 ml g(-

169 with ERalpha in the MeA (MeA-ERalpha) or the caudate-putamen (ERalpha control) or luciferase (MeA-sit

170 pear to diffuse readily or accumulate in the caudate-putamen even though there was some penetration a

171 tly upregulated in the lateral region of the caudate-putamen exclusively in postweanling mice after c

172 measurements in the test experiment for the caudate putamen, frontal cortex, cerebral cortex, hippoc

173 ptors was measured in the nucleus accumbens, caudate putamen, frontal cortex, olfactory tubercle and

174 e globus pallidus, cingulate cortex, insula, caudate, putamen, frontal cortex, temporal cortex, and t

175 revealed increased transcript levels in the caudate-putamen, frontal cortex, and spinal cord of this

176 from blood was increased in cerebral cortex, caudate putamen, globus pallidus, entopeduncular nucleus

177 throughout basal ganglia (nucleus accumbens, caudate-putamen, globus pallidus, substantia nigra) in t

178 reactivity included the cerebral cortex, the caudate-putamen, globus pallidus, the hippocampal format

179 binding in the cerebral cortex, cerebellum, caudate/putamen, globus pallidus, substantia nigra, and

180 phA4 protein revealed discrete expression in caudate/putamen, globus pallidus, substantia nigra, cere

181 nked as follows: cingulate cortex > insula > caudate/putamen > frontal cortex > temporal cortex > tha

182 overlying diencephalon, the olfactory bulbs, caudate-putamen, hippocampus, tectum, and lower brainste

183 ne and amphetamine in the prefrontal cortex, caudate-putamen, hypothalamus, or cerebellum.

184 cantly increased mean dopamine levels in the caudate putamen in the C57BL/6J mice (with a 3-h mean of

185 icant deficits throughout all aspects of the caudate-putamen in animals exposed to METH.

186 performance, and that lesions of the lateral caudate putamen increased choice response time for the S

187 f Parkinson's disease, density of binding in caudate-putamen increased at KA, but not NMDA or AMPA re

188 ion of apomorphine into the NAcc but not the caudate putamen induced partner preferences in the absen

189 Caudate putamen infarction never occurred without cardia

190 rculum in response to food intake and in the caudate, putamen, insula, thalamus, and orbitofrontal co

191 Medial (mCPu), lateral, and complete (CPu) caudate-putamen lesions affected speed and accuracy of s

192 e prominent differences in areas such as the caudate, putamen, locus coeruleus, medial habenula, and

193 Affected structures included the caudate putamen, medial geniculate nucleus, lateral geni

194 cal forebrain in Lhx8 mutants, including the caudate-putamen, medial septal nucleus, nucleus of the d

195 s treated with methadone exhibited increased caudate/putamen metabolism, whereas buprenorphine produc

196 t expression included thalamic relay nuclei, caudate-putamen, molecular layer of the dentate gyrus, a

197 ression of 5-HT(2A) receptors in the cortex, caudate putamen, NAc and hippocampus of rat brain.

198 al, two somatomotor, one cerebellar, and one caudate-putamen network), and four "higher-order" associ

199 glutamatergic projections within the cortex, caudate putamen nucleus (CPN), hippocampal formation, an

200 y terminate in patch-like regions within the caudate putamen nucleus (CPN).

201 in the striatal circuitry originating in the caudate putamen nucleus (CPN).

202 These include the caudate-putamen nucleus (CPN) and the globus pallidus, w

203 The dorsolateral caudate-putamen nucleus (CPN) and the nucleus accumbens

204 nt, delta-opioid receptors (DORs) in the rat caudate-putamen nucleus (CPN) appear later than mu-opioi

205 The patch compartments of the caudate-putamen nucleus (CPN) are enriched in mu-opioid

206 Prefrontal corticostriatal afferents to the caudate-putamen nucleus (CPN) have been implicated in mo

207 tion of delta-opioid receptors (DORs) in the caudate-putamen nucleus (CPN) produces regionally distin

208 and against cardiac and brain RyR in the rat caudate-putamen nucleus (CPN), one of the few regions ex

209 ed, respectively, by 32%, 35% and 30% in the caudate putamen, nucleus accumbens and ventral pallidum

210 esions in four sites: the medial and lateral caudate putamen, nucleus accumbens, and olfactory tuberc

211 aminergic nerve terminal-rich brain regions (caudate putamen, nucleus accumbens, and ventral pallidum

212 rontal cortex, temporal cortex, hippocampus, caudate, putamen, nucleus accumbens, amygdala, thalamus,

213 any of the brain regions studied (thalamus, caudate, putamen, nucleus accumbens, globus pallidus, an

214 e decreased at postnatal day 21 (P21) in the caudate-putamen, nucleus accumbens and frontal cortex bu

215 -2Rbeta induced marked increases in c-Fos in caudate-putamen, nucleus accumbens and prefrontal cortex

216 eus of the hypothalamus, olfactory tubercle, caudate-putamen, nucleus accumbens and substantia nigra

217 having a striatal composition, including the caudate-putamen, nucleus accumbens, and olfactory tuberc

218 Fourteen striatal subterritories in caudate-putamen, nucleus accumbens, and olfactory tuberc

219 rog), both groups displayed increased FLI in caudate-putamen, nucleus accumbens, bed nucleus of the s

220 cortical brain regions (cortex, hippocampus, caudate-putamen, nucleus accumbens, thalamus, and hypoth

221 A4 mRNA levels were prominent in the DA-rich caudate/putamen, nucleus accumbens and globus pallidus,

222 hetamine-induced monoamine reductions in the caudate-putamen occur rapidly, peak at 75-80% below cont

223 cytes in the cortex, septum, hippocampus and caudate putamen of Id4(-/-) adult brains were decreased,

224 her protein levels were also observed in the caudate putamen of iP rats compared with iNP rats.

225 ex area 1 and rostral subventricular zone of caudate putamen of isoflurane-preconditioned rats than r

226 e five somatostatin receptors (SSTRs) in the caudate putamen of male C57BL/6J and 129P3/J mice.

227 of DeltaFosB also occurs exclusively in the caudate putamen of periadolescent mice after amphetamine

228 erations in the NMDA channel activity in the caudate-putamen of adult rats, and may be responsible fo

229 male rats, maximal [3H]MK-801 binding in the caudate-putamen of female ISO rats was lower than female

230 ubiquitin levels particularly as seen in the caudate-putamen of HD patients.

231 Maximal [3H]MK-801 binding in the caudate-putamen of male ISO rats was 58% higher compared

232 hetamine (40 mg/kg s.c.) was investigated in caudate-putamen of male Sprague-Dawley rats.

233 firing in prefrontal cortical layers and the caudate-putamen of rhesus monkeys, trained in a spatial-

234 inase (RSK), and c-Fos protein levels in the caudate/putamen of Fischer rats.

235 ccumulated upon neurons in the neocortex and caudate/putamen of infected mice and interacted with nat

236 (17%, P<0.01), but not in the ventrolateral caudate putamen or any subfield of the hippocampus.

237 implanted with a CMA guide cannula into the caudate putamen or nucleus accumbens.

238 overy, dialysis probes were lowered into the caudate putamen or the nucleus accumbens and mice were p

239 nificant differences on P0, P7 or P14 in the caudate-putamen or frontal cortex, suggesting that cell

240 N-positive or NeuN-negative cells in the P21 caudate-putamen or frontal cortex.

241 responsivity does not involve changes in the caudate-putamen or nucleus accumbens extracellular dopam

242 ume changes in dorsal or ventral hippocampi, caudate-putamen, or thalamus were not detectible.

243 structures analyzed (P<0.05) except for the caudate putamen (P=0.09) and the globus pallidus (P=0.12

244 .002) in protocol 1 and specifically, in the caudate/putamen (P<0.01) in both protocols.

245 as intracranial volume, but larger bilateral caudate, putamen, pallidum and lateral ventricle volumes

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

247 bels to each voxel, including left and right caudate, putamen, pallidum, thalamus, lateral ventricles

248 luding the cingulate cortex, frontal cortex, caudate-putamen, paraventricular nucleus of the hypothal

249 l formation, temporal pole), striatum (i.e., caudate, putamen), precuneus, and cerebellum.

250 ated with decreased uptake of (3)H-NE in the caudate putamen (R=0.436, p=0.033) and locus coeruleus (

251 In the caudate-putamen, reduced ADC was often associated with i

252 iring in the localized prefrontal layers and caudate-putamen region exhibited similar location prefer

253 njection of Cre recombinase into the central caudate putamen restores feeding and normalizes locomoti

254 Restoration of DA production within the caudate putamen restores feeding on regular chow and nes

255 to express Cre recombinase into the central caudate putamen restores normal Th gene expression to th

256 placing [3H]WIN 35 428 binding at DAT in rat caudate putamen revealed that the 4'-azido-3'-iodophenyl

257 8 binding at the dopamine transporter in rat caudate-putamen revealed that aromatic substitutions on

258 je cells, with high levels also in thalamus, caudate putamen, septal nucleus, nucleus accumbens, amyg

259 Reductions in caudate-putamen serotonin began earlier and were ultimat

260 showed increases in CBF and MUA, whereas the caudate-putamen showed decreased CBF with increased MUA.

261 However, the caudate-putamen showed fMRI, CBV, and CBF decreases desp

262 However, AMPH injections into dorsal control caudate putamen sites produced a modest, dose-dependent

263 r with primary neuronal pathology within the caudate-putamen (striatum).

264 os expression in the ventral tegmental area, caudate putamen, substantia nigra pars reticulata, entor

265 d nuclear (beta-polymerase) targets from the caudate-putamen, substantia nigra and cerebellum regions

266 d ventricles and periventricular structures (caudate, putamen, thalamus, hippocampus).

267 re numerous in the ventral and ventrolateral caudate-putamen than in the dorsal caudate-putamen, wher

268 N in the ventrolateral thalamic nucleus, the caudate putamen, the accumbens nucleus, the medial septu

269 The dopamine (DA) inputs to the caudate putamen, the nucleus accumbens, and the amygdala

270 ere injected into discrete subregions of the caudate-putamen, the nucleus accumbens, or the amygdala.

271 medial and caudodorsal subterritories of the caudate-putamen, the rostrobasal cell cluster and latera

272 the bed nuclei of the stria terminalis; the caudate-putamen; the globus pallidus; the lateral septum

273 ) release in the nucleus accumbens (NAc) and caudate-putamen through an indirect mechanism that invol

274 for displacement of [(3)H]WIN 35 428 in rat caudate putamen tissue.

275 he displacement of [(3)H]WIN 35 428 from rat caudate putamen tissue.

276 ine uptake inhibition (IC(50) values) in rat caudate putamen tissue.

277 mined by inhibition of [3H]WIN 35,428 in rat caudate putamen tissue.

278 2.1]heptane derivatives were measured in rat caudate-putamen tissue and found to be 100-3000-fold les

279 ,428 (2b) and inhibit dopamine uptake in rat caudate-putamen tissue.

280 gene expression in the nucleus accumbens and caudate-putamen, two structures known to be involved in

281 binding than patients without fatigue in the caudate, putamen, ventral striatum and thalamus.

282 Regions of interest for the caudate, putamen, ventral striatum, SN, and cerebellum w

283 Regions of interest for the caudate, putamen, ventral striatum, substantia nigra (SN

284 croprobes were used, the average BPND in the caudate putamen was 0.94, and no significant changes in

285 sity of Ang II receptor binding sites in the caudate putamen was 407+/-26 fmol/g, in the nucleus accu

286 owever the tissue content of dopamine in the caudate putamen was decreased, representing a diminution

287 Only the caudate/putamen was examined in protocol 2.

288 l levels of dopamine in the dialysate of the caudate putamen were 4.2+/-0.2 nM in C57BL/6J mice and 5

289 Extracellular concentrations of NE in the caudate putamen were significantly decreased in response

290 te NMDA, AMPA and KA receptor binding in rat caudate-putamen were examined by quantitative in vitro r

291 ssue contents of dopamine within the NAc and caudate-putamen were not significantly different in ko c

292 ality in saline controls and the dorsomedial caudate-putamen, where Fos was correlated with respondin

293 rolateral caudate-putamen than in the dorsal caudate-putamen, where labeled neurons were restricted t

294 amine uptake (IC50 range = 10-371 nM) in rat caudate putamen, whereas ligands with a nonbasic nitroge

295 ormally contribute to the medial part of the caudate-putamen, whereas late-born striatal cholinergic

296 ncrease in DNA damage in mitochondria of the caudate-putamen while there was no significant DNA damag

297 croglial activation and apoptosis, including caudate/putamen, white matter, and, in juvenile-onset ca

298 binding from the dopamine transporter in rat caudate putamen with K(i) values ranging from 13.9 to 47

299 1.0 nmol) activated both ERK 1/2 and CREB in caudate-putamen with no difference between feeding group

300 ice were inoculated stereotaxically into the caudate/putamen with 3 x 10(5) PFU of the gamma(1)34.5-