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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
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
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
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
34 rging evidence from both studies showed that lateral prefrontal cortex and posterior parietal cortex
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
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
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
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
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
67 match/non-match judgments is present in the lateral prefrontal cortex even when subjects are not req
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
75 d with increased activity in hippocampus and lateral prefrontal cortex; however, the latter structure
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
86 y systems, while a more dorsal area in right lateral prefrontal cortex is activated when actions must
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
95 ical brain states.SIGNIFICANCE STATEMENT 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
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
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
107 omical connectivity between the thalamus and lateral prefrontal cortex (LPFC) in schizophrenia and to
110 ste-processing areas, as well as a region of lateral prefrontal cortex (LPFC) lining the principal su
116 n over medial frontal cortex (MFC) and right lateral prefrontal cortex (lPFC) synchronized theta ( ap
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
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
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
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
142 d output gating demands demonstrated greater lateral prefrontal cortex (PFC) recruitment and frontost
144 electrophysiology from the human medial and lateral prefrontal cortex (PFC) to better understand the
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
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,
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
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
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
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
174 functional connectivity between striatum and lateral prefrontal cortex was associated with increased
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
181 the ventral anterior cingulate cortex on the lateral prefrontal cortex was significantly reduced in y
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
186 memory tasks involve the same regions of the lateral prefrontal cortex when all factors unrelated to
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
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