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

1 ons including the amygdala, hypothalamus and dorsolateral prefrontal cortex.

2 ferent periods of a delayed-response task in dorsolateral prefrontal cortex.

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

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

5 hibitory control signal originating from the dorsolateral prefrontal cortex.

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

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

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

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

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

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

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

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

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

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

16 regions within the intraparietal sulcus and dorsolateral prefrontal cortex.

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

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

19 with stronger connectivity between sgACC and dorsolateral prefrontal cortex.

20 ns in the anterior hippocampus, amygdala and dorsolateral prefrontal cortex.

21 ilin receptor is reduced in the amygdala and dorsolateral prefrontal cortex.

22 re significantly preferentially expressed in dorsolateral prefrontal cortex.

23 coding of reward magnitude by neurons in the dorsolateral prefrontal cortex.

24 ortex, dorsal anterior cingulate cortex, and dorsolateral prefrontal cortex.

25 ional 10-Hz rTMS or iTBS rTMS applied to the dorsolateral prefrontal cortex, 5 days/week over 4-6 wee

26 ace pupillary changes, infants recruited the dorsolateral prefrontal cortex, a brain region linked to

27 Dorsolateral prefrontal cortex activation during inhibit

28 Posttreatment dorsolateral prefrontal cortex activation was reduced in

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

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

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

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

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

34 ce, a scarcity mindset decreased activity in dorsolateral prefrontal cortex, an area well known for i

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

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

37 mmonMind Consortium, comprising two regions: dorsolateral prefrontal cortex and anterior cingulate co

38 uted to saccadic action selection, including dorsolateral prefrontal cortex and anterior cingulate co

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

40 stribution of the NT5C2 protein in the human dorsolateral prefrontal cortex and cortical human neural

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

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

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

44 le total uncertainty is represented in right dorsolateral prefrontal cortex and drives random explora

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

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

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

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

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

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

51 changes were predicted from activity in left dorsolateral prefrontal cortex and precuneus while makin

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

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

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

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

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

57 or parietal cortex, less deactivation of the dorsolateral prefrontal cortex and thalamus, and increas

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

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

60 r of self-gathered information activated the dorsolateral prefrontal cortex and the midbrain, whereas

61 ed functional connectivity between the right dorsolateral prefrontal cortex and the parietal cortex i

62 ion, changes in the connectivity between the dorsolateral prefrontal cortex and the posterior default

63 etically predicted proteins derived from the dorsolateral prefrontal cortex and these outcomes.

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

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

66 gulate cortex), frontoparietal network (left dorsolateral prefrontal cortex), and salience network (r

67 ivity in behaving monkeys from the amygdala, dorsolateral prefrontal cortex, and auditory cortex.

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

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

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

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

72 nt brain regions (anterior cingulate cortex, dorsolateral prefrontal cortex, and primary visual corte

73 l cortex, the dorsal anterior cingulate, the dorsolateral prefrontal cortex, and the lateral orbitofr

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

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

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

77 d, whereas connectivity with regions such as dorsolateral prefrontal cortex (associated with emotion

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

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

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

81 te stimulation was associated with increased dorsolateral prefrontal cortex beta power following feed

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

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

84 n the anterior cingulate cortex and later in dorsolateral prefrontal cortex, caudate and ventral stri

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

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

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

88 Interestingly, activity in the dorsolateral prefrontal cortex correlated with gait impa

89 Both caudate and dorsolateral prefrontal cortex demonstrated a beta power

90 e predicted expression or splicing levels in dorsolateral prefrontal cortex (DLFPC) and peripheral mo

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

92 Smaller right dorsolateral prefrontal cortex (DLPFC) (i.e., middle and

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

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

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

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

97 sis showed greater connectivity between left dorsolateral prefrontal cortex (dlPFC) and left inferior

98 ted with the age of onset of SCZ in both the dorsolateral prefrontal cortex (DLPFC) and orbitofrontal

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

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

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

102 cusing on the bilateral thalami and the left dorsolateral prefrontal cortex (DLPFC) as our regions of

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

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

105 posterior superior temporal sulcus (pSTS) or dorsolateral prefrontal cortex (DLPFC) before having par

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

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

108 t-induced mGluR5 signaling in the postmortem dorsolateral prefrontal cortex (DLPFC) derived from 17 p

109 o for group differences in activation of the dorsolateral prefrontal cortex (DLPFC) during WM perform

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

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

112 For example, dendritic spines in the primate dorsolateral prefrontal cortex (dlPFC) express the molec

113 ceive either active or sham rTMS to the left dorsolateral prefrontal cortex (dlPFC) for 20 consecutiv

114 n expression and/or phosphorylation state in dorsolateral prefrontal cortex (DLPFC) from 22 pairs of

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

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

117 ndrial functional pathways were obtained for dorsolateral prefrontal cortex (DLPFC) gray matter and l

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

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

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

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

122 tively), and the role of the hippocampus and dorsolateral prefrontal cortex (dlPFC) in mediating such

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

124 tudies in adults highlighted the role of the dorsolateral prefrontal cortex (DLPFC) in regulating agg

125 Dorsolateral prefrontal cortex (dlPFC) is associated wit

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

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

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

129 Dorsolateral prefrontal cortex (DLPFC) maintains goal re

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

131 tic and total tissue fractions obtained from dorsolateral prefrontal cortex (dlPFC) of 15 MDD and 15

132 states of UPR sensor pathway proteins in the dorsolateral prefrontal cortex (DLPFC) of 22 matched pai

133 s no systematic overview of glutamate in the dorsolateral prefrontal cortex (DLPFC) of patients with

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

135 e analyzed expression levels of these TFs in dorsolateral prefrontal cortex (DLPFC) of SCZ patients.

136 We examined bioenergetic pathways in the dorsolateral prefrontal cortex (DLPFC) of subjects with

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

138 n activity in a high-level, executive area - dorsolateral prefrontal cortex (dlPFC) of unrestrained m

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

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

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

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

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

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

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

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

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

148 Here we find cells in the dorsolateral prefrontal cortex (dlPFC) that reflect vari

149 ermined that HDAC2 mRNA levels were lower in dorsolateral prefrontal cortex (DLPFC) tissue from donor

150 tion, and 3) precision targeting of the left dorsolateral prefrontal cortex (DLPFC) to subgenual ante

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

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

153 en quantify spatial gene expression in human dorsolateral prefrontal cortex (DLPFC) using spectral im

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

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

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

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

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

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

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

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

162 ional connectivity (FC) between amygdala and dorsolateral prefrontal cortex (DLPFC), and had increase

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

164 ed activity in primary auditory cortex (AC), dorsolateral prefrontal cortex (dlPFC), and the basolate

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

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

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

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

169 xon-exon junctions in multiple brain regions-dorsolateral prefrontal cortex (DLPFC), hippocampus, and

170 this study, we tested the involvement of the dorsolateral prefrontal cortex (dlPFC), in anxiety expre

171 rnal rhythms in gene expression in the human dorsolateral prefrontal cortex (dlPFC), in schizophrenia

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

173 l lobe circuits, with a central role for the dorsolateral prefrontal cortex (DLPFC), relatively intac

174 clude the striatum of the basal ganglia, the dorsolateral prefrontal cortex (DLPFC), the dorsal anter

175 recorded extracellular spiking activity from dorsolateral prefrontal cortex (dlPFC), the frontal eye

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

177 ,000 circRNAs species were identified in the dorsolateral prefrontal cortex (DLPFC), we observed lowe

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

179 Working memory relies on the dorsolateral prefrontal cortex (dlPFC), where microcircu

180 to directly measure evoked activity from the dorsolateral prefrontal cortex (DLPFC), which is of cons

181 eas the mesocortical DA system-including the dorsolateral prefrontal cortex (dlPFC)-is critical for s

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

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

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

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

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

187 t stimulation (HD-tDCS) to the left or right dorsolateral prefrontal cortex (DLPFC).

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

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

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

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

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

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

194 dorsal anterior cingulate cortex (dACC) and dorsolateral prefrontal cortex (dlPFC).

195 d after a session of 10 Hz rTMS to the right dorsolateral prefrontal cortex (dlPFC).

196 emory, an executive function mediated by the dorsolateral prefrontal cortex (dlPFC).

197 frontal lobe with decreased activity in the dorsolateral prefrontal cortex (DLPFC).

198 articular, it did impact the FC between left dorsolateral prefrontal cortex (DLPFC)/inferior frontal

199 100 kb of the lead SNP are expressed in the dorsolateral prefrontal cortex (DLPFC): UNC5C, ENC1, and

200 ere, we found that, in common marmosets, the dorsolateral prefrontal cortex (dlPFC; peak at A8aD) has

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

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

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

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

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

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

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

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

209 When applied to subcutaneous adipose and dorsolateral prefrontal cortex expression datasets with

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

211 Although working memory tasks often engage dorsolateral prefrontal cortex, few studies have investi

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

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

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

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

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

217 RNA-seq datamining (hippocampus, dorsolateral prefrontal cortex, fusiform gyrus and super

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

219 Moreover, in 6 out of 11 tissues (aorta, dorsolateral prefrontal cortex, hippocampus, pancreas, s

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

221 We performed proteomic sequencing of dorsolateral prefrontal cortex in 438 older individuals

222 DoC patients with the anode placed over left-dorsolateral prefrontal cortex in a prospective open-lab

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

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

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

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

227 oncentration of lactate in postmortem brain (dorsolateral prefrontal cortex) in subjects with schizop

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

229 tal-striatal activation, specifically in the dorsolateral prefrontal cortex, inferior frontal gyrus,

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

231 eakdown between the cerebellum and the right dorsolateral prefrontal cortex is associated with negati

232 The dorsolateral prefrontal cortex is downregulated, diminis

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

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

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

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

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

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

239 y associated with MD values in the bilateral dorsolateral prefrontal cortex, left orbitofrontal corte

240 ng (MRI)-guided coil positioning to the left dorsolateral prefrontal cortex method was also compared.

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

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

243 associated with increased FOLH1 mRNA in the dorsolateral prefrontal cortex of brains from unaffected

244 18 and TNF, is increased in the amygdala and dorsolateral prefrontal cortex of children with ASD as c

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

246 riptomics to examine ~80,000 nuclei from the dorsolateral prefrontal cortex of male individuals with

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

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

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

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

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

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

253 tial cues and choice-related activity before dorsolateral prefrontal cortex or the amygdala.

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

255 renia risk and expression at 89 genes in the dorsolateral prefrontal cortex (P <= 9.43 x 10-6), inclu

256 We found increased lactate in the dorsolateral prefrontal cortex (p = 0.043, n = 16/group)

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

258 fied a specific network including medial and dorsolateral prefrontal cortex (PFC) in default mode net

259 nnectivity between the hippocampus and right dorsolateral prefrontal cortex (PFC), which in turn was

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

261 Here, we investigated whether neurons in dorsolateral prefrontal cortex process risk derived from

262 l executive" (FPN) network anchored in right dorsolateral prefrontal cortex (rDLPFC) and posterior pa

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

264 isual networks after stimulation of the left dorsolateral prefrontal cortex resulted in faster task p

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

266 tients with major depression undergoing left dorsolateral prefrontal cortex rTMS and to determine ass

267 ze 10,559 high-quality circRNAs in 589 human dorsolateral prefrontal cortex samples.

268 ross-validate in hundreds of non-overlapping dorsolateral prefrontal cortex samples.

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

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

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

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

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

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

275 insula, left inferior parietal lobule, left dorsolateral prefrontal cortex/superior frontal gyrus, a

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

277 esponse inhibition, connectivity between the dorsolateral prefrontal cortex/supramarginal gyrus and s

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

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

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

281 In dorsolateral prefrontal cortex, this difference increase

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

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

284 A breakdown of connectivity in a specific dorsolateral prefrontal cortex-to-cerebellum network dir

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

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

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

288 Seeds in the amygdala and dorsolateral prefrontal cortex were explored.

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 rontal gyrus, the frontal eye field, and the dorsolateral prefrontal cortex, which are implicated in

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

298 tivity profiles of the medial prefrontal and dorsolateral prefrontal cortex while GAD was specificall

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