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1                         Greater increases in frontopolar activation were associated with improvement
2 ng oscillatory desynchronization between the frontopolar and -parietal cortex leads to more inaccurat
3                                      Thinner frontopolar and language cortex correlated with immune s
4 s showed significant activation in the right frontopolar and right inferior prefrontal cortices, alth
5                                              Frontopolar and temporal increases observed in our study
6 agues shed new light on the roles of lateral frontopolar and ventromedial prefrontal cortices in task
7 subjects, and between cortical regions BA10 (frontopolar) and BA20 (inferior temporal).
8 ctive monitoring (posterior dorsolateral and frontopolar), and phonological maintenance/rehearsal (po
9 tic regions were localized in left inferior, frontopolar, and dorsolateral prefrontal cortex in contr
10 lt mode-like network, one orbitofrontal, one frontopolar, and one network resembling the human salien
11  cortex but increased activity in precuneus, frontopolar, and premotor cortex, compared to those of c
12  has a key role in working memory tasks, and frontopolar area 10 is recruited in complex multitask op
13 etwork linking aMCC to the frontoinsular and frontopolar as well as some subcortical regions.
14           Convergent evidence indicates that frontopolar Brodmann area 10, and more generally the ant
15 hic maturational coupling was found within a frontopolar-centered prefrontal system involved in compl
16                                   Given that frontopolar connectivity with ventromedial regions durin
17 oarchitectonically defined regions including frontopolar cortex (area 10), Broca's area (area 45), fr
18 oup showed greater gray matter volume in the frontopolar cortex (BA9/10) compared with those in the l
19 nnectivity (CFC) increased in domain-general frontopolar cortex (for both word and face matching) but
20                                      Lateral frontopolar cortex (FPC) may also adjudicate response co
21       Here, we investigate the role that the frontopolar cortex (FPC) plays in motivating cognitive a
22 cement-learning model and fMRI, we show that frontopolar cortex (FPC) tracks the relative advantage i
23 eory regarding the most anterior sector, the frontopolar cortex (FPC), is that it is involved in expl
24 most anterior part of the prefrontal cortex [frontopolar cortex (FPC)], and is believed to sit atop a
25 nding initial choices and another in lateral frontopolar cortex (lFPC), which was only engaged by dem
26 frontal gyrus, precommitment engaged lateral frontopolar cortex (LFPC).
27              Psychotherapy increased lateral frontopolar cortex activity and connectivity with the ve
28                                          The frontopolar cortex also displayed a greater variety of t
29  magnetic resonance imaging to show that the frontopolar cortex and intraparietal sulcus are preferen
30                     In particular, the human frontopolar cortex and the frontoinsular cortex had a si
31 ranial direct current stimulation over right frontopolar cortex during a reward-learning task.
32 how that the inferior lateral prefrontal and frontopolar cortex encode both reliability signals and t
33 y participants demonstrated that the lateral frontopolar cortex exerts downstream influence on the ve
34 on is enhanced by psychotherapy and that the frontopolar cortex exerts downstream influence on ventro
35        This suggests a causal role for right frontopolar cortex in directed, but not random, explorat
36                          We hypothesize that frontopolar cortex mediates abstract relational integrat
37 , OFC, vmPFC, anterior cingulate cortex, and frontopolar cortex was associated with threat exposure.
38 in cognitive control (anterior cingulate and frontopolar cortex) brain regions following oxytocin adm
39  in the lateral prefrontal cortex (PFC), the frontopolar cortex, and temporal regions in subjects wit
40 n) of (18)F-FEAnGA was most increased in the frontopolar cortex, frontal cortex, bulbus olfactorius,
41 al lobule and premotor cortex, and also left frontopolar cortex, significantly discriminated intended
42 al magnetic stimulation to inhibit the right frontopolar cortex, we were able to selectively inhibit
43  dorsal anterior cingulate gyrus, and medial frontopolar cortex.
44 ncluded the orbitofrontal, ventromedial, and frontopolar cortex.
45 ncluding white matter association tracts and frontopolar cortex.
46 ized neural modules within the human lateral frontopolar cortices (LFPCs) support "relational integra
47 connectivity of the dorsolateral frontal and frontopolar cortices.
48  cingulate (ACC), anterior insular (AI), and frontopolar (FP) cortices of small odontocetes, includin
49                                   Changes in frontopolar function during deliberate regulation of neg
50 otivation, and mentalizing network involving frontopolar-medial-prefrontal and temporo-parietal circu
51                                          The frontopolar N350 has been implicated in processes that c
52 tosensory (areas 3b/3a/1/2), motor (area 4), frontopolar (prefrontal area 10), and visual (areas 17/1
53 bition, as well as in anterior cingulate and frontopolar regions implicated in other executive functi
54 the left anterior cingulate gyrus, bilateral frontopolar regions, bilateral ventrolateral prefrontal
55  lateral (starting at the central sulcus and frontopolar regions, sweeping toward the mid and superio
56  mental rotation and showed linear trends at frontopolar sites from 200 to 700 ms and centrofrontal s

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