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2 ng oscillatory desynchronization between the frontopolar and -parietal cortex leads to more inaccurat
4 s showed significant activation in the right frontopolar and right inferior prefrontal cortices, alth
6 gions with the ventral prefrontal cortex and frontopolar and sensory cortices; and decreased connecti
8 agues shed new light on the roles of lateral frontopolar and ventromedial prefrontal cortices in task
10 ctive monitoring (posterior dorsolateral and frontopolar), and phonological maintenance/rehearsal (po
11 tic regions were localized in left inferior, frontopolar, and dorsolateral prefrontal cortex in contr
12 lt mode-like network, one orbitofrontal, one frontopolar, and one network resembling the human salien
13 cortex but increased activity in precuneus, frontopolar, and premotor cortex, compared to those of c
14 implicate orbitofrontal, medial prefrontal, frontopolar, and ventrolateral cortical networks in the
15 has a key role in working memory tasks, and frontopolar area 10 is recruited in complex multitask op
16 w highlights the importance of targeting the frontopolar area and tailoring the treatment according t
19 hic maturational coupling was found within a frontopolar-centered prefrontal system involved in compl
21 oarchitectonically defined regions including frontopolar cortex (area 10), Broca's area (area 45), fr
22 oup showed greater gray matter volume in the frontopolar cortex (BA9/10) compared with those in the l
24 nnectivity (CFC) increased in domain-general frontopolar cortex (for both word and face matching) but
27 ncentives suggests causal involvement of the frontopolar cortex (FPC) in effort-based decision-making
32 cement-learning model and fMRI, we show that frontopolar cortex (FPC) tracks the relative advantage i
33 eory regarding the most anterior sector, the frontopolar cortex (FPC), is that it is involved in expl
34 most anterior part of the prefrontal cortex [frontopolar cortex (FPC)], and is believed to sit atop a
35 nding initial choices and another in lateral frontopolar cortex (lFPC), which was only engaged by dem
38 k change and area under the curve) of medial frontopolar cortex (mFPC), lateral prefrontal cortex (lP
42 magnetic resonance imaging to show that the frontopolar cortex and intraparietal sulcus are preferen
43 wledge about the anatomy and connectivity of frontopolar cortex and provides an integrative summary o
45 ntal cortex, accumulating data highlight the frontopolar cortex as a promising therapeutic target for
46 answer the question: what, if anything, does frontopolar cortex contribute to goal-directed cognition
48 how that the inferior lateral prefrontal and frontopolar cortex encode both reliability signals and t
49 ards as individual utility while the lateral frontopolar cortex encodes group utility (i.e., pending
50 y participants demonstrated that the lateral frontopolar cortex exerts downstream influence on the ve
51 on is enhanced by psychotherapy and that the frontopolar cortex exerts downstream influence on ventro
52 we observed quadratic confidence effects in frontopolar cortex for detection but not discrimination.
56 , OFC, vmPFC, anterior cingulate cortex, and frontopolar cortex was associated with threat exposure.
57 in cognitive control (anterior cingulate and frontopolar cortex) brain regions following oxytocin adm
58 nction of one of its largest subregions (the frontopolar cortex) remain enigmatic and underspecified.
59 n prefrontal and parietal regions, including frontopolar cortex, and parallel encoding of these compu
60 in the lateral prefrontal cortex (PFC), the frontopolar cortex, and temporal regions in subjects wit
61 n) of (18)F-FEAnGA was most increased in the frontopolar cortex, frontal cortex, bulbus olfactorius,
62 al lobule and premotor cortex, and also left frontopolar cortex, significantly discriminated intended
63 al magnetic stimulation to inhibit the right frontopolar cortex, we were able to selectively inhibit
64 nodes of the default mode network, including frontopolar cortex-a region thought to modulate LPFC con
69 ciety for Neuroscience minisymposium Primate Frontopolar Cortex: From Circuits to Complex Behaviors w
70 ized neural modules within the human lateral frontopolar cortices (LFPCs) support "relational integra
72 sleep had increased sleep spindle density in frontopolar electrodes, suggesting the involvement of di
73 cingulate (ACC), anterior insular (AI), and frontopolar (FP) cortices of small odontocetes, includin
74 ibited heightened alpha power at the midline frontopolar (Fpz) and beta power at the midline occipita
76 otivation, and mentalizing network involving frontopolar-medial-prefrontal and temporo-parietal circu
78 ients in the dorsolateral prefrontal cortex, frontopolar prefrontal cortex, left orbitofrontal cortex
79 tosensory (areas 3b/3a/1/2), motor (area 4), frontopolar (prefrontal area 10), and visual (areas 17/1
81 rATL (active and sham condition) or the left frontopolar region while participants attempted to solve
82 bition, as well as in anterior cingulate and frontopolar regions implicated in other executive functi
83 the left anterior cingulate gyrus, bilateral frontopolar regions, bilateral ventrolateral prefrontal
84 lateral (starting at the central sulcus and frontopolar regions, sweeping toward the mid and superio
85 mental rotation and showed linear trends at frontopolar sites from 200 to 700 ms and centrofrontal s
86 l connectivity and the electric field at the frontopolar stimulation site (r = 0.42, p corrected = 0.