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

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

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

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

4 proving its functional interactions with the lateral prefrontal cortex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 Lateral prefrontal cortex encoded profit gained from har

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

68 The lateral prefrontal cortex facilitates calculated, reason

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 The lateral prefrontal cortex (LPFC) and anterior cingulate

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

155 The lateral prefrontal cortex plays an important role in wor

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 The lateral prefrontal cortex was implicated in both attenti

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

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

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

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

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

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

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

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

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

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

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

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

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

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