ライフサイエンスコーパス: opercular

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 ce performance benefit from elevated cingulo-opercular activity, but not to the same extent as younge

5 periments), in addition to bilateral frontal-opercular and anterior cingulate activations.

6 ators and verify that nasotemporal inputs to opercular and calcarine V1 are unequal, with a consisten

7 l regions, and tonic components, centered on opercular and insular areas, and involving human parieta

8 tory, default mode, fronto-parietal, cingulo-opercular and salience systems-engage dynamically in coh

9 eractivity in the ventral premotor, Rolandic opercular and sensorimotor cortex bilaterally and Heschl

10 reased ventral attention but reduced cingulo-opercular and subcortical system segregation with increa

11 nction: increased functioning of the cingulo-opercular and ventral attention networks as well as decr

12 between frontoparietal, subcortical, cingulo-opercular, and default-mode networks.

13 lution to produce the efficient gill-pumping opercular apparatus of teleosts.

14 2 as well as with the rostral portion of the opercular area which resembles the second somatosensory

15 ata indicate that damage in the right insulo-opercular areas contributes to PSH.

16 the medial bank of the intraparietal sulcus, opercular areas PGop/PFop, and the retroinsular area, fr

17 The connections of the frontoparietal opercular areas were studied in rhesus monkeys by using

18 aged voxels in right hemispheric insular and opercular areas.

19 the development of muscles attaching to the opercular bone (gill cover), but not other adjacent musc

20 d around the frontoparietal (FP) and cingulo-opercular (CO) cortex.

21 ism to affect neural activity in the cingulo-opercular (CO) network involved in core cognitive contro

22 luding the default mode (DM) and the cingulo-opercular (CO) networks.

23 ctivate executive regions within the cingulo-opercular control network, including the frontal pole, c

24 , language, fronto-parietal control, cingulo-opercular control, and default mode.

25 ngulate, frontal pole, medial temporal lobe, opercular cortex and right orbitofrontal cortex.

26 ortex (OMPFC) and the temporal, insular, and opercular cortex have been analyzed with anterograde and

27 key regions in the human ventral frontal and opercular cortex have functional counterparts in the mon

28 The rostral opercular cortex including the gustatory and proisocorti

29 ator method for the calcarine cortex and the opercular cortex separately.

30 o generate a commonly activated right fronto-opercular cortex volume of interest (VOI).

31 In right anterior insular/opercular cortex, neural activity predicted subjects' ac

32 No ocular dominance columns were visible in opercular cortex, where the central visual field is repr

33 lar, lateral frontal, posterior temporal and opercular cortex.

34 the lateral frontoparietal (FP) and cingulo-opercular cortex.

35 The cingulo-opercular effect increased for participants with the bes

36 was used to test the hypothesis that cingulo-opercular engagement provides performance benefit for ol

37 tion with sustained Shh expression within an opercular epithelial fold, whereas Shh is only transient

38 the kinematics of lower jaw depression--the opercular four-bar linkage apparatus--among Lake Malawi

39 its strong connections with both ventral and opercular frontal regions, one feature of the influence

40 oventral nerve innervates the mandibular and opercular lines.

41 ion of a frontal midline node of the cingulo-opercular MDC affected learning rates specifically durin

42 lular vesicles to the plasma membrane in the opercular membrane within the first hour in seawater, wh

43 SGK1 in gill and its functional analog, the opercular membrane, after seawater transfer precedes the

44 et(+) cells become restricted to the forming opercular muscles and a loss of Ret signalling results i

45 have a normal skeleton with small or missing opercular muscles and tightly closed mouths.

46 in forming opercular muscles, but not in non-opercular muscles derived from the same muscle anlagen.

47 ogenic gene expression is reduced in forming opercular muscles, but not in non-opercular muscles deri

48 mesenchymal cells in and around the forming opercular muscles.

49 frontoparietal network (FPN), the cingulate-opercular network (CON), and the ventral and dorsal atte

50 wed decreased FC between DMN and the cingulo-opercular network (CON), as well as the thalamus.

51 local efficiency of the whole brain, cingulo-opercular network (CON), frontoparietal network, and aud

52 These results indicate that elevated cingulo-opercular network activity is not simply a reflection of

53 at increased magnitude and extent of cingulo-opercular network activity was significantly associated

54 n demands increased the coherence of cingulo-opercular network activity.

55 ted by enhanced coupling between the cingulo-opercular network and the dorsal attention network.

56 apid, adaptive online control, and a cingulo-opercular network apparently important for set-maintenan

57 icits elevated activity throughout a cingulo-opercular network that is hypothesized to monitor and mo

58 ozygotes show higher activity in the cingulo-opercular network underlying alertness maintenance and h

59 nterior cingulate forms part of the cingular-opercular network, which has a broad role in cognition a

60 een the default mode network and the cingulo-opercular network.

61 s, the default mode network, and the cingulo-opercular network.

62 network, frontoparietal network, and cingulo-opercular network.

63 ive attention systems, including the cingulo-opercular network.

64 etween the nucleus accumbens and the cingulo-opercular network.

65 pital gyri, left precentral gyrus, bilateral opercular part of the inferior frontal gyrus, left hippo

66 her the left anterior supramarginal gyrus or opercular part of the left inferior frontal gyrus has be

67 The mid opercular region (areas 1 and 2) is connected with pre-

68 The caudal opercular region is connected with the dorsal portion of

69 The rostral parietal opercular region is connected with the postcentral porti

70 e found in the left inferior frontal cortex (opercular region) and the rostral-most region of the rig

71 y, included the left anterior insula/frontal opercular region.

72 nonverbal information, whereas left frontal opercular regions appear to be involved specifically in

73 fied with functional neuroimaging: a cingulo-opercular salience network (SN) and a frontoparietal exe

74 tal central executive network (CEN), cingulo-opercular salience network (SN), and the medial prefront

75 omical and functional integrity of a cingulo-opercular "salience" network.

76 y, this increased integration of the cingulo-opercular/salience network significantly moderated the r

77 rk integration, predominantly of the cingulo-opercular/salience network, increased with age.

78 onmentally driven control (salience, cingulo-opercular) systems.

79 asymmetries tended to be slightly smaller in opercular V1 and greater in calcarine V1.

80 d nonverbal immediate memory correlated with opercular volume.

81 tion, significantly greater total cortex and opercular volumes.