ライフサイエンスコーパス: dorsolateral prefrontal cortex

1 pe was linked to smaller volumes in the left dorsolateral prefrontal cortex.

2 nterior cingulate cortex and to left IFG and dorsolateral prefrontal cortex.

3 hibitory control signal originating from the dorsolateral prefrontal cortex.

4 re associated with reduced activation of the dorsolateral prefrontal cortex.

5 regions within the intraparietal sulcus and dorsolateral prefrontal cortex.

6 anied by recruitment of anterior putamen and dorsolateral prefrontal cortex.

7 d to increased dynamic RSFC between MPFC and dorsolateral prefrontal cortex.

8 ct current stimulation (tDCS) over the right dorsolateral prefrontal cortex.

9 ckness in bilateral precentral gyrus and the dorsolateral prefrontal cortex.

10 perigenual anterior cingulate cortex and the dorsolateral prefrontal cortex.

11 emporo-parieto-occipital junction (TPOJ) and dorsolateral prefrontal cortex.

12 e and decreases during implementation in the dorsolateral prefrontal cortex.

13 al striatum, but a negative association with dorsolateral prefrontal cortex.

14 om a meta-analysis of gene expression in the dorsolateral prefrontal cortex.

15 rate of cortical thinning in the medial and dorsolateral prefrontal cortex.

16 dala to the subgenual anterior cingulate and dorsolateral prefrontal cortex.

17 , precuneus, lateral occipital, temporal and dorsolateral prefrontal cortex.

18 were generated using frozen tissue from the dorsolateral prefrontal cortex.

19 nterior cingulate, medial frontal gyrus, and dorsolateral prefrontal cortex.

20 red, in up to 40 daily sessions, to the left dorsolateral prefrontal cortex.

21 found between perception and GABA levels in dorsolateral prefrontal cortex.

22 ent conventional open-label rTMS to the left dorsolateral prefrontal cortex.

23 ctivity of the right Crus I/II with the left dorsolateral prefrontal cortex.

24 load observed in healthy individuals in left dorsolateral prefrontal cortex.

25 IC sources in or near medial prefrontal and dorsolateral prefrontal cortex.

26 d bilaterally sequentially to left and right dorsolateral prefrontal cortex 750 pulses/side at 20 Hz

27 atum, and (iv) reduced brain activity in the dorsolateral prefrontal cortex (a correlate of willpower

28 tDCS was applied to the dorsolateral prefrontal cortex, a frequent target for mo

29 reduced functional connectivity between the dorsolateral prefrontal cortex, a region thought to play

30 f high-calorie foods significantly increased dorsolateral prefrontal cortex activation and suppressed

31 Within the PS group, dorsolateral prefrontal cortex activation correlated wit

32 Dorsolateral prefrontal cortex activation during inhibit

33 Posttreatment dorsolateral prefrontal cortex activation was reduced in

34 d that trauma-exposed youth failed to dampen dorsolateral prefrontal cortex activity and engage amygd

35 family income at age 9 and ventrolateral and dorsolateral prefrontal cortex activity at age 24.

36 f emotion type and associated with increased dorsolateral prefrontal cortex activity compared with th

37 n activity in Brodmann area 10 and the right dorsolateral prefrontal cortex activity when regulating

38 lied 5 days per week for 3 weeks to the left dorsolateral prefrontal cortex (added to the ongoing tre

39 gions, anterior and posterior cingulate, and dorsolateral prefrontal cortex all contributed reliably

40 le patients trait anger positively modulated dorsolateral prefrontal cortex-amygdala coupling.

41 odulatory effects of trait anger on amygdala-dorsolateral prefrontal cortex and amygdala-lateral orbi

42 igh-level cognitive control functions (i.e., dorsolateral prefrontal cortex and anterior cingulate co

43 o-occurring with structural abnormalities in dorsolateral prefrontal cortex and anterior cingulate co

44 ests the striatal afferent connection to the dorsolateral prefrontal cortex and basal ganglia circuit

45 lgesia was associated with activation of the dorsolateral prefrontal cortex and deactivation of senso

46 patients showed significantly increased left dorsolateral prefrontal cortex and decreased left hippoc

47 e show that BICC1 mRNA is upregulated in the dorsolateral prefrontal cortex and dentate gyrus of huma

48 several task-relevant regions, including the dorsolateral prefrontal cortex and DMN regions, was posi

49 l activity in classic 'control' regions (eg, dorsolateral prefrontal cortex and dorsal anterior cingu

50 ges in the interhemispheric effects from the dorsolateral prefrontal cortex and dorsal premotor corte

51 al-directed action, such as ventromedial and dorsolateral prefrontal cortex and dorsomedial striatum,

52 Functional interactions between the dorsolateral prefrontal cortex and hippocampus during wo

53 her microglial activation is elevated in the dorsolateral prefrontal cortex and hippocampus of untrea

54 )], that span the lateral prefrontal cortex (dorsolateral prefrontal cortex and inferior frontal gyru

55 Samples of dorsolateral prefrontal cortex and inferior parietal lob

56 lateral prefrontal cortex, particularly the dorsolateral prefrontal cortex and its connections, were

57 vortioxetine reduced activation in the right dorsolateral prefrontal cortex and left hippocampus duri

58 er volumes relative to controls in the right dorsolateral prefrontal cortex and left hippocampus, alo

59 ability to regulate the interaction between dorsolateral prefrontal cortex and M1.

60 y, as well as interactions between the right dorsolateral prefrontal cortex and medial and lateral pa

61 ask performance in ASD, whereas that between dorsolateral prefrontal cortex and parietal cortex (Brod

62 rior cingulate) and decision-making regions (dorsolateral prefrontal cortex and parietal cortex).

63 ve cognitive control requiring processing by dorsolateral prefrontal cortex and parietal cortex.

64 Abnormal emotion (dorsolateral prefrontal cortex and right inferior fronta

65 terior cingulate, orbitofrontal cortex, left dorsolateral prefrontal cortex and right inferior fronta

66 of structure (decreased grey matter in right dorsolateral prefrontal cortex and right inferior tempor

67 ed functional connectivity between the right dorsolateral prefrontal cortex and right superior occipi

68 de network; 2) hypoconnectivity between left dorsolateral prefrontal cortex and subgenual anterior ci

69 d the most consistent underactivation in the dorsolateral prefrontal cortex and temporal pole, while

70 ddiction-relevant brain regions, such as the dorsolateral prefrontal cortex and the angular and cingu

71 al cortical inhibition [LICI]) from the left dorsolateral prefrontal cortex and the left motor cortex

72 control and addiction-related processes (eg, dorsolateral prefrontal cortex and ventral striatum).

73 nferior and superior frontal gyri, including dorsolateral prefrontal cortex and ventrolateral prefron

74 gulation despite increased activation of the dorsolateral prefrontal cortex and ventrolateral prefron

75 specifically ventromedial prefrontal cortex, dorsolateral prefrontal cortex, and anterior cingulate c

76 the sgACC and the default mode network, left dorsolateral prefrontal cortex, and insula, and reduced

77 ostral and dorsal anterior cingulate cortex, dorsolateral prefrontal cortex, and lateral orbitofronta

78 tal seed regions and the anterior cingulate, dorsolateral prefrontal cortex, and limbic regions such

79 -subcortical circuitry engaging anterior and dorsolateral prefrontal cortex, and midbrain.

80 nique projections from orbitofrontal cortex, dorsolateral prefrontal cortex, and parietal regions.

81 mical connections from orbitofrontal cortex, dorsolateral prefrontal cortex, and posterior parietal c

82 learning-related activation in the striatum, dorsolateral prefrontal cortex, and the MTL during the e

83 la induced by single TMS pulses to the right dorsolateral prefrontal cortex; and 4) greater ventromed

84 in a network of regions including bilateral dorsolateral prefrontal cortex, anterior cingulate and a

85 riatum --> insula --> medial frontal cortex, dorsolateral prefrontal cortex, anterior cingulate corte

86 nction within the frontal lobe involving the dorsolateral prefrontal cortex, anterior cingulate corte

87 ties and volumes of pyramidal neurons of the dorsolateral prefrontal cortex, anterior cingulate corte

88 rts, we tested whether GMV and NAA/Cr in the dorsolateral prefrontal cortex are associated with fatig

89 to quantify GAD67 and Zif268 mRNA levels in dorsolateral prefrontal cortex area 9 from 62 matched pa

90 tural brain marker-volume of left hemisphere dorsolateral prefrontal cortex-associated with the magni

91 were assessed in four frontostriatal tracts (dorsolateral prefrontal cortex-associative striatum, dor

92 integrated information is used by the right dorsolateral prefrontal cortex at the time of the decisi

93 udies should evaluate regions other than the dorsolateral prefrontal cortex, at other time points, an

94 EF and DB were associated with the rostral dorsolateral prefrontal cortex bilaterally.

95 ex while recalling resulted in activation in dorsolateral prefrontal cortex bilaterally.

96 t the executive control circuitry, including dorsolateral prefrontal cortex (cluster-corrected P < .0

97 had increased activity in the contralateral dorsolateral prefrontal cortex compared with patients wi

98 y between the posterior cingulate cortex and dorsolateral prefrontal cortex, compared with HC subject

99 We found that neuronal activity in the dorsolateral prefrontal cortex conveyed the necessary in

100 in gray matter volume in the hippocampus and dorsolateral prefrontal cortex correlate with our abilit

101 onnectivity of the right caudate to the left dorsolateral prefrontal cortex could reflect change in n

102 tary motor area, inferior parietal lobe, and dorsolateral prefrontal cortex despite similar overall p

103 f 561 immune genes and 20 immune pathways in dorsolateral prefrontal cortex (DLPFC) (144 schizophreni

104 ed with the unmedicated patient group in the dorsolateral prefrontal cortex (DLPFC) (MR, 0.26 mm; P =

105 zophrenia, is often associated with aberrant dorsolateral prefrontal cortex (dlPFC) activation.

106 multimodal executive system anchored on the dorsolateral prefrontal cortex (DLPFC) and a salience sy

107 onnectivity seeded from the right IFG to the dorsolateral prefrontal cortex (DLPFC) and anterior cing

108 n distributed neural circuitry including the dorsolateral prefrontal cortex (DLPFC) and appear to ari

109 We applied anodal tDCS over the left dorsolateral prefrontal cortex (DLPFC) and cathodal tDCS

110 onal spike activities of single units in the dorsolateral prefrontal cortex (dlPFC) and the anterior

111 othesis that interactions between regions of dorsolateral prefrontal cortex (dlPFC) and ventromedial

112 ne density on layer 3 pyramidal cells in the dorsolateral prefrontal cortex (DLPFC) appears to contri

113 and functional alterations of neurons in the dorsolateral prefrontal cortex (dlPFC) are thought to co

114 lation indicated the involvement of the left dorsolateral prefrontal cortex (DLPFC) as well as left M

115 r mechanisms, on the recruitment of the left dorsolateral prefrontal cortex (DLPFC) as well as on the

116 er a temporary neural disruption of the left Dorsolateral Prefrontal Cortex (DLPFC) can improve impli

117 rTMS) of Brodmann Area (BA) nine of the left dorsolateral prefrontal cortex (DLPFC) can produce analg

118 n working memory that reflect dysfunction of dorsolateral prefrontal cortex (DLPFC) circuitry.

119 It has been suggested that the dorsolateral prefrontal cortex (DLPFC) contributes in th

120 We found that lesions of the human dorsolateral prefrontal cortex (DLPFC) decreased the eff

121 Neurons in the dorsolateral prefrontal cortex (DLPFC) encode a diverse

122 odes children's own preferences and the left dorsolateral prefrontal cortex (dlPFC) encodes the proje

123 , dorsal anterior cingulate (ACC), and right dorsolateral prefrontal cortex (DLPFC) evident only in S

124 ment of working memory that relies on normal dorsolateral prefrontal cortex (DLPFC) function.

125 amygdala activation and reduced amygdala and dorsolateral prefrontal cortex (dlPFC) functional coupli

126 Neurons in the primate dorsolateral prefrontal cortex (dlPFC) generate persiste

127 od-oxygen-level-dependent (BOLD) signal, and dorsolateral prefrontal cortex (DLPFC) glutamate+glutami

128 l direct current stimulation (tDCS) over the dorsolateral prefrontal cortex (DLPFC) has been effectiv

129 Although the dorsolateral prefrontal cortex (DLPFC) has long been con

130 Here we show that the dorsolateral prefrontal cortex (DLPFC) implements a flex

131 ajority of glutamatergic genes tested in the dorsolateral prefrontal cortex (DLPFC) in MDD (F21,59=2.

132 Although prior work has implicated the dorsolateral prefrontal cortex (DLPFC) in norm-based jud

133 rated reduced dendritic spine density in the dorsolateral prefrontal cortex (DLPFC) in schizophrenia.

134 anscranial magnetic stimulation (TMS) of the dorsolateral prefrontal cortex (DLPFC) is an established

135 Conflict monitoring theory assumes that the dorsolateral prefrontal cortex (DLPFC) is causally invol

136 We found that damage to the dorsolateral prefrontal cortex (dlPFC) led to a more pos

137 We hypothesized that dorsolateral prefrontal cortex (dlPFC) lesions, due to t

138 curring de novo, in brain-expressed genes of dorsolateral prefrontal cortex (DLPFC) neurons.

139 levels, have frequently been reported in the dorsolateral prefrontal cortex (DLPFC) of schizophrenia

140 mation relevant for credit assignment in the dorsolateral prefrontal cortex (dlPFC) of two male rhesu

141 ial magnetic stimulation (rTMS) of the right dorsolateral prefrontal cortex (DLPFC) on working memory

142 The extent of dorsolateral prefrontal cortex (DLPFC) plasticity in Alz

143 The dorsolateral prefrontal cortex (DLPFC) plays a pivotal r

144 The dorsolateral prefrontal cortex (DLPFC) plays a pivotal r

145 The dorsolateral prefrontal cortex (DLPFC) plays an importan

146 t the volume of the rostral part of the left dorsolateral prefrontal cortex (DLPFC) predicted an indi

147 othalamus, midbrain, right insula, and right dorsolateral prefrontal cortex (DLPFC) regions supported

148 Dorsolateral prefrontal cortex (DLPFC) retrieval activat

149 om nonhuman primate studies, posits that the dorsolateral prefrontal cortex (dlPFC) stores and mainta

150 The primate dorsolateral prefrontal cortex (dlPFC) subserves top-dow

151 activity of neural circuitry in the primate dorsolateral prefrontal cortex (DLPFC) supports a range

152 as closely associated with feedback from the dorsolateral prefrontal cortex (DLPFC) to V1.

153 ical inhibition (LICI) was measured from the dorsolateral prefrontal cortex (DLPFC) using combined tr

154 The dorsolateral prefrontal cortex (DLPFC) was chosen as con

155 s in the anterior cingulate cortex and right dorsolateral prefrontal cortex (DLPFC) were compared via

156 We hypothesized that the hippocampus and dorsolateral prefrontal cortex (dlPFC) would play a key

157 le high-frequency rTMS session over the left dorsolateral prefrontal cortex (DLPFC) would reduce cue

158 direct current stimulation (tDCS) over left dorsolateral prefrontal cortex (dlPFC) yielded a close m

159 ree latent brain factors (amygdala, pACC and dorsolateral prefrontal cortex (DLPFC)) to test the effe

160 anscranial direct current stimulation of the dorsolateral prefrontal cortex (dlPFC), a critical neura

161 sociated with reduced activation in the left dorsolateral prefrontal cortex (DLPFC), a region of the

162 P down-regulates the BOLD signal in the left dorsolateral prefrontal cortex (dlPFC), a risk-integrati

163 have implicated orbitofrontal cortex (OFC), dorsolateral prefrontal cortex (DLPFC), and anterior cin

164 ilateral superior parietal lobule, bilateral dorsolateral prefrontal cortex (DLPFC), and bilateral mi

165 igation-guided rTMS was applied to the right dorsolateral prefrontal cortex (DLPFC), and fMRI and fun

166 monstrated greater fMRI response in caudate, dorsolateral prefrontal cortex (dlPFC), and intraparieta

167 sorders generally involve dysfunction of the dorsolateral prefrontal cortex (dlPFC), but there are fe

168 e frontal lobes [anode electrode at the left dorsolateral prefrontal cortex (DLPFC), cathode electrod

169 ed with decreased gamma activity in the left dorsolateral prefrontal cortex (dlPFC), decreased theta

170 st in anterior cingulate cortex (ACC) before dorsolateral prefrontal cortex (dlPFC), followed by medi

171 c input and implicated in schizophrenia (the dorsolateral prefrontal cortex (DLPFC), hippocampus and

172 from a priori regions of interest: bilateral dorsolateral prefrontal cortex (DLPFC), medial frontal/c

173 ween the bilateral hippocampus and the right dorsolateral prefrontal cortex (DLPFC), mirroring clinic

174 e found that threat affected activity in the dorsolateral prefrontal cortex (dlPFC), rather than the

175 In the post-mortem dorsolateral prefrontal cortex (DLPFC), we found strikin

176 ells in layer 3 (L3) and layer 5 (L5) of the dorsolateral prefrontal cortex (DLPFC), we sought to det

177 ons in several cortical areas, including the Dorsolateral Prefrontal Cortex (DLPFC).

178 ial direct current stimulation (tDCS) of the dorsolateral prefrontal cortex (DLPFC).

179 cognitive function reliant on area 46 of the dorsolateral prefrontal cortex (dlPFC).

180 linked to a decrease in the activity of the dorsolateral prefrontal cortex (dlPFC).

181 pines on deep layer 3 pyramidal cells in the dorsolateral prefrontal cortex (DLPFC).

182 this response could also be evoked from the dorsolateral prefrontal cortex (dlPFC).

183 by dorsomedial prefrontal cortex (DMPFC) and dorsolateral prefrontal cortex (DLPFC).

184 that flexibility is mainly subserved by the dorsolateral prefrontal cortex (DLPFC).

185 of neurons within Brodmann's Area 46 of the dorsolateral prefrontal cortex (dlPFC).

186 s3749034 and with the expression of GAD25 in dorsolateral prefrontal cortex (DLPFC).

187 a (SZ) is associated with dysfunction of the dorsolateral prefrontal cortex (DLPFC).

188 ts involve dysfunction of the newly evolved, dorsolateral prefrontal cortex (dlPFC).

189 in-positive (PV) interneurons in the primate dorsolateral prefrontal cortex (DLPFC).

190 es is associated with neural activity in the dorsolateral prefrontal cortex (dlPFC).

191 100 kb of the lead SNP are expressed in the dorsolateral prefrontal cortex (DLPFC): UNC5C, ENC1, and

192 to examine the expression of 58 genes in the dorsolateral prefrontal cortex (DLPFC, comprised of Brod

193 nd insula but increased BOLD activity in the dorsolateral prefrontal cortex (dlPFC; local maxima corr

194 ons important in top-down executive control (dorsolateral prefrontal cortex [dlPFC]), here we test wh

195 Seed-based (bilateral dorsolateral prefrontal cortex, DLPFC) rsFC analysis was

196 When pain was controllable, the dorsolateral prefrontal cortex downregulated pain-evoked

197 We stimulated over the left dorsolateral prefrontal cortex during a declarative memo

198 ce that NRXN1 expression is highest in human dorsolateral prefrontal cortex during critical developme

199 e observed both reduced 1) activation of the dorsolateral prefrontal cortex during encoding and 2) de

200 ignificant differences localized to the left dorsolateral prefrontal cortex during response selection

201 Notably, [oxy-Hb] change in the left dorsolateral prefrontal cortex during SAT showed a posit

202 tDCS was administered over the right dorsolateral prefrontal cortex during the retrieval-prac

203 long with blunted responses of the bilateral dorsolateral prefrontal cortex, during the processing of

204 evance of the findings and the proposal that dorsolateral prefrontal cortex dysfunction represents a

205 In the postnatal dorsolateral prefrontal cortex, expression levels were n

206 e efficacy of 10-Hz rTMS applied to the left dorsolateral prefrontal cortex for the treatment of pred

207 The optimal target in the dorsolateral prefrontal cortex for treating depression w

208 ain transcriptome in high-quality postmortem dorsolateral prefrontal cortex from 11 individuals diagn

209 olymerase chain reaction in human postmortem dorsolateral prefrontal cortex from 286 nonpsychiatric c

210 olymerase chain reaction in human postmortem dorsolateral prefrontal cortex from 286 nonpsychiatric c

211 encing of poly-A RNA derived from postmortem dorsolateral prefrontal cortex from people with BD, alon

212 n basket cell (PVBC) inputs in area 9 of the dorsolateral prefrontal cortex from schizophrenia and ma

213 or calretinin-positive (CR+) neurons in the dorsolateral prefrontal cortex from schizophrenia subjec

214 agnetic stimulation (rTMS) targeted over the dorsolateral prefrontal cortex has been shown to modulat

215 nual anterior cingulate cortex [sgACC], left dorsolateral prefrontal cortex, hippocampus, and basolat

216 Mean diffusivity (MD) was computed for dorsolateral prefrontal cortex, hippocampus, parahippoca

217 In the right dorsolateral prefrontal cortex IC cluster, the beta band

218 of the causal influence of the insula on the dorsolateral prefrontal cortex in cocaine users.

219 nal connectivity between the putamen and the dorsolateral prefrontal cortex in OCD patients, as well

220 ted inverted-U response was observed in left dorsolateral prefrontal cortex in patients and was assoc

221 e 226 genes, 9 differed in expression in the dorsolateral prefrontal cortex in patients with BP: CACN

222 tribute to lower levels of GAD67 mRNA in the dorsolateral prefrontal cortex in schizophrenia.

223 of ErbB4 transcripts is dysregulated in the dorsolateral prefrontal cortex in schizophrenia.

224 ed prefrontal regions (orbitofrontal cortex, dorsolateral prefrontal cortex, inferior frontal gyrus,

225 involved in language control, including the dorsolateral prefrontal cortex, inferior parietal lobule

226 inputs (lower-order), with less weighting of dorsolateral prefrontal cortex inputs (higher-order).

227 The dorsolateral prefrontal cortex is downregulated, diminis

228 europsychology studies have established that dorsolateral prefrontal cortex is essential in spatial w

229 ing the intraparietal sulcus, precuneus, and dorsolateral prefrontal cortex is involved in selecting

230 mory activation in PMDD, specifically in the dorsolateral prefrontal cortex, is related to PMDD sever

231 e (Glx), were measured by 1H MRS in the left dorsolateral prefrontal cortex (l-DLPFC) and bilateral h

232 Left dorsolateral prefrontal cortex (L-DLPFC) tDCS induced an

233 prefrontal cortex (Brodmann area 10) and the dorsolateral prefrontal cortex (lateral Brodmann 9) whil

234 interneurons were laser microdissected from dorsolateral prefrontal cortex layers 2 and 4, respectiv

235 tal evidence that increasing activity in the dorsolateral prefrontal cortex leads to greater evidence

236 in the alcohol-dependent group included the dorsolateral prefrontal cortex, medial prefrontal cortex

237 default (posterior cingulate) and executive (dorsolateral prefrontal cortex) networks.

238 ng the cognitive deficits and dysfunction of dorsolateral prefrontal cortex observed in this disorder

239 lation and histone acetylation data from the dorsolateral prefrontal cortex of 411 older adults who h

240 lternating current stimulation over the left dorsolateral prefrontal cortex of human participants [n

241 67), a key enzyme for GABA synthesis, in the dorsolateral prefrontal cortex of individuals with schiz

242 ed, and DNA methylation was increased in the dorsolateral prefrontal cortex of male suicide subjects,

243 n by recording single-unit activity from the dorsolateral prefrontal cortex of monkeys that were perf

244 predictor of both GMV and NAA/Cr in the left dorsolateral prefrontal cortex of patients with CFS.

245 associated with neuronal alterations in the dorsolateral prefrontal cortex of patients with CFS.

246 The CommonMind Consortium sequenced RNA from dorsolateral prefrontal cortex of people with schizophre

247 idal cell volumes in layers III and V in the dorsolateral prefrontal cortex of post-stroke and vascul

248 rom the contribution of interactions between dorsolateral prefrontal cortex of the FPN and precuneus

249 onotonically decreased BOLD signal change in dorsolateral prefrontal cortex on Day 1 as a function of

250 anial direct current stimulation of the left dorsolateral prefrontal cortex or a sham stimulation con

251 as indexed by [(18)F]FEPPA VT, in either the dorsolateral prefrontal cortex or the hippocampus.

252 positive valence tasks; and hyperactivity in dorsolateral prefrontal cortex (P < .001) and superior t

253 atment increased activation in both the left dorsolateral prefrontal cortex (PFC) and supplementary m

254 ntal state and harm information, whereas the dorsolateral prefrontal cortex plays a crucial, final-st

255 lly defined network includes portions of the dorsolateral prefrontal cortex, posteromedial prefrontal

256 The changes in dorsolateral prefrontal cortex pyramidal cells were not

257 ctive regional pyramidal cell atrophy in the dorsolateral prefrontal cortex-rather than neuronal dens

258 tion of activation in the striatum and right dorsolateral prefrontal cortex (rDLPFC; ie, the degree t

259 iatal and midbrain) and prefrontal cortical (dorsolateral prefrontal cortex) regions during reward an

260 RNA sequencing data of human dorsolateral prefrontal cortex revealed relatively high

261 zation in the 6-12 Hz range within the right dorsolateral prefrontal cortex, right frontal eye-fields

262 l anterior cingulate cortex (dACC), and left dorsolateral prefrontal cortex seeds and by relative hyp

263 nd fewer normalized streamlines in the right dorsolateral prefrontal cortex-sensorimotor striatum and

264 hermore, normalized streamlines in the right dorsolateral prefrontal cortex-sensorimotor striatum neg

265 rmalized streamlines in the right-hemisphere dorsolateral prefrontal cortex-sensorimotor striatum pre

266 eral prefrontal cortex-associative striatum, dorsolateral prefrontal cortex-sensorimotor striatum, ve

267 ted into ventrolateral prefrontal cortex and dorsolateral prefrontal cortex subregions.

268 between these systems by disruption of right dorsolateral prefrontal cortex, such that participants m

269 ns in contralateral ventral premotor cortex, dorsolateral prefrontal cortex, supramarginal gyrus, and

270 anterior cingulate (t = 2.27; P = .04), and dorsolateral prefrontal cortex (t = 2.44; P = .03) were

271 ontrols, among three brain regions including dorsolateral prefrontal cortex, temporal cortex and cere

272 , hypometabolism and/or hypoperfusion in the dorsolateral prefrontal cortex, the anterior and middle

273 PD had reduced activation in the ipsilateral dorsolateral prefrontal cortex, the globus pallidus inte

274 t PD had reduced activity in the ipsilateral dorsolateral prefrontal cortex, the globus pallidus inte

275 work of areas, including the dorsomedial and dorsolateral prefrontal cortex, the intraparietal sulcus

276 evels at individual CpG sites generated from dorsolateral prefrontal cortex tissue using a bead assay

277 riven by reduced effective connectivity from dorsolateral prefrontal cortex to anterior prefrontal co

278 rain activation, driven in part by increased dorsolateral prefrontal cortex to midbrain connectivity.

279 sorders in the microarray-based "BrainCloud" dorsolateral prefrontal cortex transcriptome.

280 ramidal neuron dendrites in Brodmann area 46 dorsolateral prefrontal cortex using the Golgi-Cox techn

281 ate cortex (dACC), and the ventrolateral and dorsolateral prefrontal cortex (VLPFC, DLPFC).

282 anticipatory and outcome-locked activity in dorsolateral prefrontal cortex was greater for safe than

283 Response to high-probability rewards in dorsolateral prefrontal cortex was inversely associated

284 onnectivity of the right caudate to the left dorsolateral prefrontal cortex was negatively associated

285 ced change in connectivity from right IFG to dorsolateral prefrontal cortex was proportional to the c

286 covariates, cortical thickness of the right dorsolateral prefrontal cortex was significantly thinner

287 Application of active 10-Hz rTMS to the left dorsolateral prefrontal cortex was well tolerated but wa

288 In further morphometric analysis of the dorsolateral prefrontal cortex, we showed that neither d

289 inhibition (ie, N100 and LICI) from the left dorsolateral prefrontal cortex were selected.

290 s across the two tasks were localized to the dorsolateral prefrontal cortex, where responses were inc

291 e associated with hypoactivation of the left dorsolateral prefrontal cortex, whereas behavioral sympt

292 fortful DM) leading to activation across the dorsolateral prefrontal cortex, whereas experts are expe

293 fortful DM) leading to activation across the dorsolateral prefrontal cortex, whereas experts are expe

294 the primary visual cortex and highest in the dorsolateral prefrontal cortex, whereas the GABA measure

295 novices showed significant activation of the dorsolateral prefrontal cortex, whereas this activation

296 novices showed significant activation of the dorsolateral prefrontal cortex, whereas this activation

297 The antisaccade task requires the dorsolateral prefrontal cortex, which is part of the pre

298 Suppressing imagination engaged the right dorsolateral prefrontal cortex, which modulated activati

299 s resulted in significant activation in left dorsolateral prefrontal cortex while recalling resulted

300 (BMI) had lower activation in the bilateral dorsolateral prefrontal cortex while viewing unhealthy c