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

1 tion regions, including putamen, insula, and lateral prefrontal cortex.

2 s signals, including visual cortex and right lateral prefrontal cortex.

3 anterior cingulate cortex, and the anterior lateral prefrontal cortex.

4 on in working memory mediated by the ventral lateral prefrontal cortex.

5 apparent distal from the stimulation site in lateral prefrontal cortex.

6 more consistent activation of the medial and lateral prefrontal cortex.

7 a single session even after ablation of the lateral prefrontal cortex.

8 proving its functional interactions with the lateral prefrontal cortex.

9 ities may be partially segregated within the lateral prefrontal cortex.

10 tex, insula, rostral anterior cingulate, and lateral prefrontal cortex.

11 isual cortex and less activation in the left lateral prefrontal cortex.

12 al prefrontal cortex, and bilaterally in the lateral prefrontal cortex.

13 vioral conflict) depended on activity in the lateral prefrontal cortex.

14 tivation of prefrontal area 46 of the dorsal lateral prefrontal cortex.

15 ain, caudate, cingulate, and most regions of lateral prefrontal cortex.

16 t parahippocampal gyrus, and some regions of lateral prefrontal cortex.

17 ory cortex, and increases in connectivity to lateral prefrontal cortex.

18 , mirroring the broader organization seen in lateral prefrontal cortex.

19 rting working memory function in the primate lateral prefrontal cortex.

20 y recording neural activity bilaterally from lateral prefrontal cortex.

21 ory occurs, this conflict is resolved by the lateral prefrontal cortex.

22 s of broad spiking excitatory neurons in the lateral prefrontal cortex.

23 art of area 12 [12o]), cingulate cortex, and lateral prefrontal cortex.

24 ivity via control mechanisms mediated by the lateral prefrontal cortex.

25 rizations, by behavioral significance in the lateral prefrontal cortex.

26 ree additional networks are proposed for the lateral prefrontal cortex: 1) a ventrolateral network (V

27 oad resulted in diminished activation of the lateral prefrontal cortex, a key region of the cognitive

28 Anterior cingulate and lateral prefrontal cortex (ACC/PFC) are believed to coor

29 ory control mechanism supported by the right lateral prefrontal cortex achieves these functions.

30 associated with reduced subsequent anterior-lateral prefrontal cortex activity that reflects correct

31 with a specific activity pattern in anterior lateral prefrontal cortex (alPFC(47)).

32 at we might have done), whereas the anterior lateral prefrontal cortex (alPFC) compares simulations o

33 proaches suggest that one area, the anterior lateral prefrontal cortex (alPFC), is highly specialized

34 Furthermore, expectation-related activity in lateral prefrontal cortex also correlated with the magni

35 Neural activity in lateral prefrontal cortex and a multivariate pattern of

36 ical regions including the striatum, insula, lateral prefrontal cortex and anterior cingulate in resp

37 nnections between anterior cingulate cortex, lateral prefrontal cortex and anterior striatum.

38 strongest in the anterior part of the right lateral prefrontal cortex and bilateral supplementary mo

39 The later increase of right ventral lateral prefrontal cortex and caudate for reversal of st

40 However the lateral prefrontal cortex and caudate nucleus showed a n

41 greater coding of model-based signatures in lateral prefrontal cortex and diminished coding of model

42 profile between the caudate nucleus and the lateral prefrontal cortex and dissociative experiences.

43 neously recorded from multiple electrodes in lateral prefrontal cortex and dorsal striatum, two inter

44 Additionally, activity in the lateral prefrontal cortex and functional connectivity be

45 tivity relative to controls, particularly in lateral prefrontal cortex and lateral temporal lobe regi

46 nts, connectivity was enhanced with the left lateral prefrontal cortex and lower with the right poste

47 onnectivity in two networks involving 1) the lateral prefrontal cortex and medial caudate nucleus and

48 g reward anticipation (P < 0.001) and in the lateral prefrontal cortex and midbrain at the time of re

49 y mainly converged at the ventral and dorsal lateral prefrontal cortex and orbitofrontal cortex.

50 cutive function network on epicentres in the lateral prefrontal cortex and perhaps the posterior pari

51 ces between two delayed rewards, whereas the lateral prefrontal cortex and posterior parietal cortex

52 In contrast, regions of the lateral prefrontal cortex and posterior parietal cortex

53 rging evidence from both studies showed that lateral prefrontal cortex and posterior parietal cortex

54 ity fully mediating the relationship between lateral prefrontal cortex and reported craving.

55 was linked with higher activity in the left lateral prefrontal cortex and right parietal cortex, sug

56 ion, higher activation increases in inferior lateral prefrontal cortex and superior posterior parieta

57 ed to theta frequency neural oscillations in lateral prefrontal cortex and suppressing irrelevant inf

58 egative activations, which were localized to lateral prefrontal cortex and temporo-occipital cortex.

59 ed by sustained gamma activity in the dorsal lateral prefrontal cortex and the anterior cingulate cor

60 rcuit spanning the hippocampus, the anterior lateral prefrontal cortex and the anterior cingulate cor

61 The SMA/PMA, dorso-lateral prefrontal cortex and the cerebellum are concern

62 so modulated functional connectivity between lateral prefrontal cortex and the profit-sensitive regio

63 e evidence implicates the involvement of the lateral prefrontal cortex and theta oscillations in dete

64 ditionally draws on parametric modulation of lateral prefrontal cortex and unfavorable impression cha

65 the activity of neurons was recorded in the lateral prefrontal cortex and ventral intraparietal sulc

66 ional connectivity to higher centres (dorsal lateral prefrontal cortex) and the basal ganglia (in par

67 egions: the medial frontal cortex, the right lateral prefrontal cortex, and a posterior region surrou

68 bilateral activation in the visual cortices, lateral prefrontal cortex, and amygdala in response to t

69 sitive connectivity to the dorsal cingulate, lateral prefrontal cortex, and insula and negative conne

70 In addition, different regions of the left lateral prefrontal cortex, and perhaps anterior temporal

71 tations, e.g. the inability of the posterior lateral prefrontal cortex, and possibly the superior med

72 ons in the anterior cingulate cortex, dorsal lateral prefrontal cortex, and right inferior parietal l

73 at includes inferior parietal cortex, dorsal lateral prefrontal cortex, and the dorsal striatum, has

74 , including the visual cortex, right ventral lateral prefrontal cortex, and the dorsal striatum.

75 mpus, basal ganglia, anterior temporal lobe, lateral prefrontal cortex, and visual cortex, as well as

76 a frequency at which they synchronize across lateral prefrontal cortex, anterior cingulate cortex and

77 Dense connections with dorsal and lateral prefrontal cortex/anterior cingulate cortex cogn

78 e that the dorsal and ventral regions of the lateral prefrontal cortex are innately specialized for t

79 ntron 11 at the Tau gene in AD female dorsal lateral prefrontal cortex as compared to healthy control

80 tivariate fMRI pattern analysis revealed the lateral prefrontal cortex as the only region that encode

81 h increased volume and thickness of the left lateral prefrontal cortex as well as increased thickness

82 ence, to identify regions of the left dorsal lateral prefrontal cortex associated with the anticipati

83 Endogenous preparation seems to involve lateral prefrontal cortex (BA 46/45) and posterior parie

84 ards, providing causal evidence for a neural lateral-prefrontal cortex-based self-control mechanism i

85 sk structure was represented within left mid-lateral prefrontal cortex, bilateral precuneus, and infe

86 We recorded neural activity in the lateral prefrontal cortex, bilaterally, as two male nonh

87 al cues recruited the anterior cingulate and lateral prefrontal cortex, brain areas associated with d

88 nd MDD non-suicides (MDD, N=9) in the dorsal lateral prefrontal cortex (Brodmann Area 9) of sudden de

89 Thus, whereas damage to the lateral prefrontal cortex (Brodmann's area 9) in monkeys

90 Increased striatal-dorsal lateral prefrontal cortex connectivity strength was posi

91 ciated with increased dorsal striatal-dorsal lateral prefrontal cortex connectivity uniquely in CUs.

92 The aggregate value and risk responses in lateral prefrontal cortex contrasted with pure value sig

93 an IPS with strong functional connections to lateral prefrontal cortex demonstrate activity selective

94 cts, are thought to initiate from the dorsal lateral prefrontal cortex (DLPFC) and then trigger the b

95 The dorsal-lateral prefrontal cortex (dlPFC) integrates information

96 e largest eQTL reference panel for the dorso-lateral prefrontal cortex (DLPFC) to create a set of gen

97 regions, the frontal pole (FP) and the dorso-lateral prefrontal cortex (DLPFC), respectively, involve

98 area (MSTd), parietal area 7a, and the dorso-lateral prefrontal cortex (dlPFC).

99 out high channel count recordings in dorsal-lateral prefrontal cortex (dlPFC; 768 electrodes) while

100 task-irrelevant information)], that span the lateral prefrontal cortex (dorsolateral prefrontal corte

101 , medial frontal gyrus, and bilateral dorsal lateral prefrontal cortex during emotion downregulation

102 terior insula/frontal operculum and anterior lateral prefrontal cortex during error processing but sh

103 ned neural activations within the medial and lateral prefrontal cortex during game play as a function

104 of COMT genotype in the ventral striatum and lateral prefrontal cortex during reward anticipation (P

105 genes was found in the ventral striatum and lateral prefrontal cortex during reward anticipation and

106 cluster in the posterior portion of the left lateral prefrontal cortex emerged as the largest locatio

107 Lateral prefrontal cortex encoded profit gained from har

108 match/non-match judgments is present in the lateral prefrontal cortex even when subjects are not req

109 The lateral prefrontal cortex facilitates calculated, reason

110 absence of synchrony over medial-frontal and lateral-prefrontal cortex following errors.

111 uditory cortex, superior temporal gyrus, and lateral prefrontal cortex for deviation by frequency, in

112 temporal dynamics of activation within right lateral prefrontal cortex, from a transient to predomina

113 For instance, individual variation in lateral prefrontal cortex function (and that of associat

114 Lateral prefrontal cortex had a more general role in det

115 The lateral prefrontal cortex has been classically defined a

116 While the lateral prefrontal cortex has been proposed to serve thi

117 ecific components of this process within the lateral prefrontal cortex has yet to be clarified.

118 d with increased activity in hippocampus and lateral prefrontal cortex; however, the latter structure

119 how perturbations to the human (both sexes) lateral prefrontal cortex impact the storage and control

120 f the respective roles of the left and right lateral prefrontal cortex in active thought.

121 ng using multi-electrode recordings from the lateral prefrontal cortex in non-human primates performi

122 uch previous work has focused on the role of lateral prefrontal cortex in such decisions, the contrib

123 resent, they point to a general role for the lateral prefrontal cortex in the control of attention an

124 results provide support for the role of the lateral prefrontal cortex in understanding others' emoti

125 ns of the medial frontal cortex (in rats) or lateral prefrontal cortex (in nonhuman primates) impair

126 re of an SPE in the intraparietal sulcus and lateral prefrontal cortex, in addition to the previously

127 behavioural and EEG study, we focused on the lateral prefrontal cortex including dorsal and ventral p

128 ingulate cortices and less activation in the lateral prefrontal cortex, inferior parietal lobule, and

129 of effective connectivity, we show that the lateral prefrontal cortex influences the strength of com

130 and increased stress-induced activity in the lateral prefrontal cortex, insula, striatum, right amygd

131 A portion of the left lateral prefrontal cortex is a unique location where del

132 y systems, while a more dorsal area in right lateral prefrontal cortex is activated when actions must

133 The lateral prefrontal cortex is involved in the integration

134 The functional organization of lateral prefrontal cortex is not well understood, and th

135 In this hypothesis, the lateral prefrontal cortex is primarily involved in maint

136 hether orbital prefrontal cortex (O-PFC) and lateral prefrontal cortex (L-PFC) are necessary for eval

137 alyses of the cognitive control functions of lateral prefrontal cortex (lateral PFC) and anterior cin

138 the role of dorsal premotor cortex (PMd) and lateral prefrontal cortex (LPF) of healthy subjects in t

139 orrelate with the activity level in the left lateral prefrontal cortex (LPFC) [10, 13], a causal link

140 of these mOFC value representations via the lateral prefrontal cortex (lPFC) [3, 6].

141 The anatomical organization of the lateral prefrontal cortex (LPFC) afferents to the anteri

142 iking during periods of uncertainty in both, lateral prefrontal cortex (LPFC) and anterior cingulate

143 ical brain states.SIGNIFICANCE STATEMENT The lateral prefrontal cortex (LPFC) and anterior cingulate

144 The lateral prefrontal cortex (LPFC) and anterior cingulate

145 We recorded single-neuron activity from the lateral prefrontal cortex (LPFC) and prearcuate cortex (

146 curve) of medial frontopolar cortex (mFPC), lateral prefrontal cortex (lPFC) and primary somatosenso

147 l areas in the rhesus monkey, the high-order lateral prefrontal cortex (LPFC) and the primary visual

148 The hippocampus (HPC) and the lateral prefrontal cortex (LPFC) are two cortical areas

149 Here, we targeted the activity of the lateral prefrontal cortex (LPFC) as a common substrate f

150 mPFC) is thought to work in conjunction with lateral prefrontal cortex (lPFC) as a part of an action-

151 dentified that patterns of activation in the lateral prefrontal cortex (LPFC) as well as in face-sele

152 Medial prefrontal cortex (MPFC) and lateral prefrontal cortex (LPFC) both contribute to goal

153 s showed significant activations in the left lateral prefrontal cortex (LPFC) compared to baseline re

154 We show that during such comparisons, the lateral prefrontal cortex (LPFC) contains accurate repre

155 study recorded neural signals in the macaque lateral prefrontal cortex (LPFC) during a retro-cueing t

156 Neurons in the primate lateral prefrontal cortex (LPFC) encode working memory (

157 The primate lateral prefrontal cortex (LPFC) encodes visual stimulus

158 Neurons in the lateral prefrontal cortex (LPFC) have been shown to enco

159 The lateral prefrontal cortex (LPFC) in nonhuman primates, s

160 omical connectivity between the thalamus and lateral prefrontal cortex (LPFC) in schizophrenia and to

161 wo functional MRI experiments that implicate lateral prefrontal cortex (LPFC) in this function.

162 We investigated the role of the lateral prefrontal cortex (lPFC) in this relationship, u

163 The role of the lateral prefrontal cortex (lPFC) in working memory (WM)

164 l maps with the field.SIGNIFICANCE STATEMENT Lateral prefrontal cortex (LPFC) is critical for functio

165 The lateral prefrontal cortex (LPFC) is disproportionately e

166 The lateral prefrontal cortex (LPFC) is essential for higher

167 Although the lateral prefrontal cortex (LPFC) is known to mediate top

168 functions largely specific to humans such as lateral prefrontal cortex (LPFC) is of major interest in

169 ls of behavioral and emotion regulation, the lateral prefrontal cortex (LPFC) is postulated to mainta

170 ste-processing areas, as well as a region of lateral prefrontal cortex (LPFC) lining the principal su

171 rmed by analyzing the neural activity in the lateral prefrontal cortex (LPFC) of behaving monkeys.

172 The lateral prefrontal cortex (LPFC) of humans enables flexi

173 The lateral prefrontal cortex (lPFC) of primates is hypothes

174 The lateral prefrontal cortex (LPFC) of primates plays an im

175 Monkey experiments have suggested that lateral prefrontal cortex (LPFC) participates in learnin

176 Neurons in primate lateral prefrontal cortex (LPFC) play a critical role in

177 The lateral prefrontal cortex (LPFC) plays a central role in

178 Neuronal activity in the lateral prefrontal cortex (LPFC) reflects the structure

179 A lateral prefrontal cortex (LPFC) region's activity was f

180 he posterior fundus of area 46 in the monkey lateral prefrontal cortex (LPFC) responds to rule change

181 The lateral prefrontal cortex (LPFC) serves as a critical hu

182 n over medial frontal cortex (MFC) and right lateral prefrontal cortex (lPFC) synchronized theta ( ap

183 The contribution of the lateral prefrontal cortex (LPFC) to working memory is th

184 e depth of three small, shallow sulci in the lateral prefrontal cortex (LPFC) was linked to reasoning

185 sruption of function of left, but not right, lateral prefrontal cortex (LPFC) with low-frequency repe

186 ation of the selected action was stronger in lateral prefrontal cortex (lPFC), and occurred earlier i

187 Modeling and neural recordings from lateral prefrontal cortex (LPFC), anterior cingulate cor

188 Higher-level cognition depends on the lateral prefrontal cortex (LPFC), but its functional org

189 rally, include the nucleus accumbens (NAcc), lateral prefrontal cortex (LPFC), insula, subgenual ante

190 s LFPs in executive brain areas, such as the lateral prefrontal cortex (LPFC), thought to be involved

191 rain regions, such as the dorsal part of the lateral prefrontal cortex (lPFC), to increase the level

192 ortex (ACC), orbitofrontal cortex (OFC), and lateral prefrontal cortex (LPFC), which are associated w

193 mined information timing and flow across the lateral prefrontal cortex (LPFC), while monkeys carried

194 ion of the anterior cingulate (ACC) and left lateral prefrontal cortex (LPFC).

195 , lateral intraparietal (LIP), and posterior lateral prefrontal cortex (LPFC-p) displays attentional

196 changes in effective connectivity among the lateral-prefrontal cortex (lPFC), anterior-cingulate cor

197 ndings to those in the rhesus monkey (V1 and lateral prefrontal cortex [LPFC]).

198 ernative notion that specific regions of the lateral prefrontal cortex make identical executive funct

199 Feature representations in parietal and lateral prefrontal cortex may in turn be utilized to pro

200 e to impairments in self-control; and 3) the lateral prefrontal cortex modulates trait motivation and

201 Age-related increases in value-based lateral prefrontal cortex modulation mediated the relati

202 ntations.SIGNIFICANCE STATEMENT We show that lateral prefrontal cortex neurons encode working memory

203 d with CUD by using RNA sequencing of dorsal-lateral prefrontal cortex neurons.

204 e, we recorded single-neuron activity in the lateral prefrontal cortex of macaque monkeys before and

205 re we recorded single-neuron activity in the lateral prefrontal cortex of macaque monkeys before and

206 both by collecting neural activity in dorsal-lateral prefrontal cortex of macaques using eight microe

207 d the activity of hundreds of neurons in the lateral prefrontal cortex of male macaque monkeys during

208 -making, we recorded single neurons from the lateral prefrontal cortex of monkeys before and after th

209 Here, we show that the lateral prefrontal cortex of non-human primates contains

210 prominent grey matter loss was found in the lateral prefrontal cortex, orbitofrontal cortex, amygdal

211 Because of its importance in WM, the lateral prefrontal cortex, particularly the dorsolateral

212 with greater anterior insula and attenuated lateral prefrontal cortex (PFC) activation during emotio

213 We examined the activity of neurons in the lateral prefrontal cortex (PFC) and caudate nucleus of m

214 locybin increased activity in the medial and lateral prefrontal cortex (PFC) and left caudate, and de

215 h previous work has suggested a role for the lateral prefrontal cortex (PFC) and medial temporal lobe

216 ty simultaneously from multiple sites in the lateral prefrontal cortex (PFC) and the hippocampus (HPC

217 Although research implicates lateral prefrontal cortex (PFC) in executive control and

218 The lateral prefrontal cortex (PFC) in humans and other prim

219 Lateral prefrontal cortex (PFC) is regarded as the hub o

220 We recorded lateral prefrontal cortex (PFC) neural activity while mo

221 the ventral intraparietal area (VIP) and the lateral prefrontal cortex (PFC) of rhesus monkeys.

222 al intracerebral infusions to inactivate the lateral prefrontal cortex (PFC) of the New World marmose

223 d output gating demands demonstrated greater lateral prefrontal cortex (PFC) recruitment and frontost

224 When pain is controllable, the lateral prefrontal cortex (PFC) seems to inhibit pain pr

225 electrophysiology from the human medial and lateral prefrontal cortex (PFC) to better understand the

226 Regions within lateral prefrontal cortex (PFC) were examined that, in a

227 f 8,333 voxels and 21,512 voxels in the left lateral prefrontal cortex (PFC) were predictive of impai

228 The lateral prefrontal cortex (PFC), a hub of higher-level c

229 anial magnetic stimulation (rTMS) over right lateral prefrontal cortex (PFC), a region involved in th

230 fluence cognition-related neural activity in lateral prefrontal cortex (PFC), as evidence for an inte

231 Within lateral prefrontal cortex (PFC), both additive (inferior

232 ly medial temporal lobe (MTL) structures and lateral prefrontal cortex (PFC), have been identified in

233 responses were significantly reduced in the lateral prefrontal cortex (PFC), the frontopolar cortex,

234 that correlates with neural activity in the lateral prefrontal cortex (PFC).

235 compared them to previous recordings in the lateral prefrontal cortex (PFC).

236 bsent in patients with lesions restricted to lateral prefrontal cortex (PFC).

237 By contrast, reward signals in lateral prefrontal cortex (PFl) are consistent with a ro

238 ue of whether distinct anatomical sectors of lateral prefrontal cortex play different functional role

239 netic resonance imaging study shows that the lateral prefrontal cortex plays a key role in inferring

240 These results suggest that the lateral prefrontal cortex plays a key role in inferring

241 The lateral prefrontal cortex plays an important role in wor

242 uroimaging has implicated the left posterior lateral prefrontal cortex (pLPFC) as a key neural substr

243 rrespond to controlled processes and include lateral prefrontal cortex, posterior parietal cortex, me

244 Here we show that neurons in lateral prefrontal cortex reflect the early stages of th

245 Neural activity in the lateral prefrontal cortex reflected the category of visu

246 erior frontal gyrus, or via damage to dorsal lateral prefrontal cortex regions, resulting in deterior

247 r insula and orbitofrontal cortex, bilateral lateral prefrontal cortex (right middle frontal gyrus an

248 al rostral anterior cingulate cortex (rACC), lateral prefrontal cortex, right anterior insula, supram

249 Thus the lateral prefrontal cortex seemed to interact with the an

250 In contrast, an area in lateral prefrontal cortex, selectively activated during

251 d an extended scene-selective network in the lateral prefrontal cortex, separate clusters responsive

252 ant activations were seen in the right dorso-lateral prefrontal cortex, supplementary motor areas (SM

253 mulation coil over a subject-specific dorsal lateral prefrontal cortex target, and 50 repetitive tran

254 etwork activity by stimulating a site in the lateral prefrontal cortex that is strongly connected to

255 cortical regions, nodes of which include the lateral prefrontal cortex, the so-called lateral occipit

256 ion goal representations were present in mid-lateral prefrontal cortex, they were not modulated by em

257 ld in working memory where it can be used by lateral prefrontal cortex to plan and organize behavior

258 Event-related potentials over lateral prefrontal cortex, typically observed for instru

259 interactions between visual area V4 and the lateral prefrontal cortex using simultaneous local field

260 relates with cerebral blood flow in the left lateral prefrontal cortex, ventral striatum, superior te

261 of emotional responses activates the ventral lateral prefrontal cortex (vlPFC) and dampens amygdala a

262 tween caudal auditory cortex and both ventro-lateral prefrontal cortex (VLPFC, including area 44) and

263 rior default mode network (W=3.79), case #2: lateral prefrontal cortex (W=2.79) and salience network

264 Tight coupling between the insula and lateral prefrontal cortex was also observed during decis

265 functional connectivity between striatum and lateral prefrontal cortex was associated with increased

266 The right lateral prefrontal cortex was engaged by RI, DD, and WM

267 The lateral prefrontal cortex was implicated in both attenti

268 ance imaging was higher, but activity in the lateral prefrontal cortex was lower, than with suprathre

269 ompanied by a double dissociation: the right lateral prefrontal cortex was more activated when switch

270 Activation in the right lateral prefrontal cortex was now more ventral than in s

271 Activation within the lateral prefrontal cortex was predicted by ambiguity pre

272 the ventral anterior cingulate cortex on the lateral prefrontal cortex was significantly reduced in y

273 We hypothesize that intact regions of lateral prefrontal cortex were able to detect response c

274 gement, and money-induced activations in the lateral prefrontal cortex were associated with parallel

275 alysis of fMRI data showed that striatum and lateral prefrontal cortex were sensitive to RPE, as show

276 Many neurons in the lateral prefrontal cortex were tuned for quantity irresp

277 memory tasks involve the same regions of the lateral prefrontal cortex when all factors unrelated to

278 Greater activation of the lateral prefrontal cortex when off medication predicted

279 lationship between reward dependence and the lateral prefrontal cortex, where regional gray-matter vo

280 cingulate) and executive functioning areas (lateral prefrontal cortex), whereas a repeated-measures

281 es regarding food PS may be processed in the lateral prefrontal cortex, which is a region that is imp