戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1           We hypothesized that this abnormal opercular activity might be the neural substrate of the
2  tested the prediction that elevated cingulo-opercular activity provides word-recognition benefit on
3                             Elevated cingulo-opercular activity was associated with an increased like
4 here remains no direct measurement of insulo-opercular activity when humans anticipate taste.
5 ce performance benefit from elevated cingulo-opercular activity, but not to the same extent as younge
6 periments), in addition to bilateral frontal-opercular and anterior cingulate activations.
7 ators and verify that nasotemporal inputs to opercular and calcarine V1 are unequal, with a consisten
8  network incorporating default-mode, cingulo-opercular and central executive regions exhibits hypocon
9 Significant parcels/regions included cingulo-opercular and default mode network regions, specifically
10 ogether, these findings suggest that cingulo-opercular and default mode regions typically implicated
11 dle and superior) and regions of the cingulo-opercular and default networks in individuals with OCD.
12 rietal and somatomotor networks with cingulo-opercular and dorsal attention networks.
13 s involved in cognitive control: the cingulo-opercular and fronto-parietal networks.
14 l regions, and tonic components, centered on opercular and insular areas, and involving human parieta
15 tory, default mode, fronto-parietal, cingulo-opercular and salience systems-engage dynamically in coh
16 eractivity in the ventral premotor, Rolandic opercular and sensorimotor cortex bilaterally and Heschl
17 ical brain regions, particularly for cingulo-opercular and sensorimotor networks.
18 licate the significance of targeting cingulo-opercular and somato-cognitive action network connectivi
19 nt diet-specific differences between insular-opercular and somatomotor networks at 2 months of age, d
20 reased ventral attention but reduced cingulo-opercular and subcortical system segregation with increa
21 nction: increased functioning of the cingulo-opercular and ventral attention networks as well as decr
22 between frontoparietal, subcortical, cingulo-opercular, and default-mode networks.
23 repeat trials across frontoparietal, cingulo-opercular, and temporo-occipital regions.
24 premature aging of the default mode, cingulo-opercular, and visual networks was linked to reduced hom
25 ing for age in the dorsal attention, cingulo-opercular, and visual systems at birth is associated wit
26 lution to produce the efficient gill-pumping opercular apparatus of teleosts.
27 2 as well as with the rostral portion of the opercular area which resembles the second somatosensory
28 ata indicate that damage in the right insulo-opercular areas contributes to PSH.
29 the medial bank of the intraparietal sulcus, opercular areas PGop/PFop, and the retroinsular area, fr
30        The connections of the frontoparietal opercular areas were studied in rhesus monkeys by using
31 aged voxels in right hemispheric insular and opercular areas.
32  the development of muscles attaching to the opercular bone (gill cover), but not other adjacent musc
33  This movement can expand the spiracular and opercular cavities during feeding and respiration, which
34 d around the frontoparietal (FP) and cingulo-opercular (CO) cortex.
35 ism to affect neural activity in the cingulo-opercular (CO) network involved in core cognitive contro
36 luding the default mode (DM) and the cingulo-opercular (CO) networks.
37 ystems, the frontoparietal (FPN) and cingulo-opercular (CON) networks, have distinct but complementar
38 ociated with an atypical increase in cingulo-opercular connectivity with increasing age from childhoo
39 were systematic, with convergence of cingulo-opercular control and somatomotor networks in the ventra
40 ctivate executive regions within the cingulo-opercular control network, including the frontal pole, c
41 , language, fronto-parietal control, cingulo-opercular control, and default mode.
42 ngulate, frontal pole, medial temporal lobe, opercular cortex and right orbitofrontal cortex.
43 as significantly different in the developing opercular cortex compared to the insula.
44 ortex (OMPFC) and the temporal, insular, and opercular cortex have been analyzed with anterograde and
45 key regions in the human ventral frontal and opercular cortex have functional counterparts in the mon
46                                  The rostral opercular cortex including the gustatory and proisocorti
47 ator method for the calcarine cortex and the opercular cortex separately.
48 orally-specific activity in the human insulo-opercular cortex that underlies anticipatory evaluation
49 o generate a commonly activated right fronto-opercular cortex volume of interest (VOI).
50                    In right anterior insular/opercular cortex, neural activity predicted subjects' ac
51  No ocular dominance columns were visible in opercular cortex, where the central visual field is repr
52 lar, lateral frontal, posterior temporal and opercular cortex.
53  the lateral frontoparietal (FP) and cingulo-opercular cortex.
54                                  The cingulo-opercular effect increased for participants with the bes
55 was used to test the hypothesis that cingulo-opercular engagement provides performance benefit for ol
56 tion with sustained Shh expression within an opercular epithelial fold, whereas Shh is only transient
57  the kinematics of lower jaw depression--the opercular four-bar linkage apparatus--among Lake Malawi
58 its strong connections with both ventral and opercular frontal regions, one feature of the influence
59 epilepsy (n = 9) or insular and only deepest opercular involvement (n = 3) at seizure onset.
60 oventral nerve innervates the mandibular and opercular lines.
61 ion of a frontal midline node of the cingulo-opercular MDC affected learning rates specifically durin
62 lular vesicles to the plasma membrane in the opercular membrane within the first hour in seawater, wh
63  SGK1 in gill and its functional analog, the opercular membrane, after seawater transfer precedes the
64 tional division of an auditory and a cingulo-opercular module and the emergence of a conjoined audito
65 et(+) cells become restricted to the forming opercular muscles and a loss of Ret signalling results i
66 have a normal skeleton with small or missing opercular muscles and tightly closed mouths.
67 in forming opercular muscles, but not in non-opercular muscles derived from the same muscle anlagen.
68 ogenic gene expression is reduced in forming opercular muscles, but not in non-opercular muscles deri
69  mesenchymal cells in and around the forming opercular muscles.
70 ty in specific directions within the cingulo-opercular network (average effect size, d = 0.72).
71  functional connectivity between the cingulo-opercular network (CO) and medial prefrontal cortex (mPF
72 s/mediums.SIGNIFICANCE STATEMENT The cingulo-opercular network (CON) and frontoparietal network (FPN)
73 the frontoparietal network (FPN) and cingulo-opercular network (CON) are engaged during control, but
74 the frontoparietal network (FPN) and cingulo-opercular network (CON) exhibits reductions earliest dur
75 ecame more strongly connected to the cingulo-opercular network (CON), an executive control network th
76  frontoparietal network (FPN), the cingulate-opercular network (CON), and the ventral and dorsal atte
77 wed decreased FC between DMN and the cingulo-opercular network (CON), as well as the thalamus.
78 ity to each other, as well as to the cingulo-opercular network (CON), critical for action(5) and phys
79    Three major cortical networks-the cingulo-opercular network (CON), default mode network (DMN), and
80 local efficiency of the whole brain, cingulo-opercular network (CON), frontoparietal network, and aud
81 the frontoparietal network (FPN) and cingulo-opercular network (CON).
82 rontoparietal network (FPN), and the cingulo-opercular network (CON).
83  dorsal attention network (DAN), and cingulo-opercular network (CON)], (ii) higher within-network con
84 r activation state (state 1), a high cingulo-opercular network activation state (state 2), and a high
85 These results indicate that elevated cingulo-opercular network activity is not simply a reflection of
86 at increased magnitude and extent of cingulo-opercular network activity was significantly associated
87 n demands increased the coherence of cingulo-opercular network activity.
88 ted by enhanced coupling between the cingulo-opercular network and the dorsal attention network.
89 apid, adaptive online control, and a cingulo-opercular network apparently important for set-maintenan
90                       Regions of the cingulo-opercular network best match the optimal connectivity pr
91                                   The insulo-opercular network functions critically not only in encod
92 task-related connectivity within the cingulo-opercular network may mediate the cognitive benefits ass
93 nctioning and development within the cingulo-opercular network may warrant further investigation as a
94  previously identified and named the cingulo-opercular network on the basis of its anatomy.
95       Finally, activity throughout a cingulo-opercular network supported the transfer and implementat
96 icits elevated activity throughout a cingulo-opercular network that is hypothesized to monitor and mo
97 ozygotes show higher activity in the cingulo-opercular network underlying alertness maintenance and h
98 esting-state connectivity within the cingulo-opercular network was associated with a significant inte
99 ystem (the fronto-parietal network , cingulo-opercular network, and default mode network), has strong
100  in OCD (the frontoparietal network, cingulo-opercular network, and default mode network).
101 nterior cingulate forms part of the cingular-opercular network, which has a broad role in cognition a
102 etween the nucleus accumbens and the cingulo-opercular network.
103 een the default mode network and the cingulo-opercular network.
104 s, the default mode network, and the cingulo-opercular network.
105 network, frontoparietal network, and cingulo-opercular network.
106 ive attention systems, including the cingulo-opercular network.
107 nial-temporal, dorsal attention, and cingulo-opercular networks as collectively predictive of cogniti
108  and regions of the default-mode and cingulo-opercular networks, exerted a diverse set of effects on
109 centrated among the default mode and cingulo-opercular networks.
110 atively correlated with salience and cingulo-opercular networks.
111 res have been unable to separate insular and opercular onset.
112 .417 [95% CI = -0.731, -0.104]), and cingulo-opercular (p = 0.009, parameter estimate = -0.883 [95% C
113 nsula, right precentral gyrus, and the right opercular part of inferior frontal gyrus (posterior vent
114 pital gyri, left precentral gyrus, bilateral opercular part of the inferior frontal gyrus, left hippo
115 her the left anterior supramarginal gyrus or opercular part of the left inferior frontal gyrus has be
116 al resting-state networks, i.e., the cingulo-opercular (r = 0.62; p < 0.001) and somato-cognitive act
117                                      The mid opercular region (areas 1 and 2) is connected with pre-
118                                   The caudal opercular region is connected with the dorsal portion of
119                         The rostral parietal opercular region is connected with the postcentral porti
120 e found in the left inferior frontal cortex (opercular region) and the rostral-most region of the rig
121  indicative of reorganization of the frontal opercular region.
122 y, included the left anterior insula/frontal opercular region.
123  nonverbal information, whereas left frontal opercular regions appear to be involved specifically in
124 regions, in particular PFt, and the parietal opercular regions in decision processing and demonstrate
125 fied with functional neuroimaging: a cingulo-opercular salience network (SN) and a frontoparietal exe
126 tal central executive network (CEN), cingulo-opercular salience network (SN), and the medial prefront
127  core cognitive control systems: (i) cingulo-opercular "salience" network (SN) anchored in the right
128 omical and functional integrity of a cingulo-opercular "salience" network.
129 ilar association with atrophy of the cingulo-opercular, salience or language networks, or with global
130 tive control networks, including the cingulo-opercular, salience, and dorsal attention networks.
131 y, this increased integration of the cingulo-opercular/salience network significantly moderated the r
132 rk integration, predominantly of the cingulo-opercular/salience network, increased with age.
133              Many previous studies of insulo-opercular seizures have been unable to separate insular
134 ments such as the jaws, pectoral girdle, and opercular series, and the posteroanterior pattern of squ
135 onal connectivity within and between cingulo-opercular, striato-thalamic, and default mode networks w
136 onmentally driven control (salience, cingulo-opercular) systems.
137 asymmetries tended to be slightly smaller in opercular V1 and greater in calcarine V1.
138 d nonverbal immediate memory correlated with opercular volume.
139 tion, significantly greater total cortex and opercular volumes.

 
Page Top