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1 temporal cortex; non-fluent variant, frontal operculum).
2 k of the lateral sulcus, continuing onto the operculum.
3 l performance were found in the left frontal operculum.
4 y non-discriminatory activity in the frontal operculum.
5 tal cortices, and the contralateral parietal operculum.
6 s) possess a single hyoid arch ray-supported operculum.
7 ere observed in the left anterior insula and operculum.
8 n activity localized to the lateral parietal operculum.
9 ifference in the anterior insula and frontal operculum.
10 mary taste cortex consists of the insula and operculum.
11 ior temporal sulcus WM and the left parietal operculum.
12 s including the planum temporale and frontal operculum.
13 ng yogurt elicited higher CBF in the frontal operculum 30 and 120 min after a meal.
14 idiosyncratic scleritome, which comprises an operculum, a conical shell and, in some taxa, a pair of
15 and pain network including bilateral insula, operculum, ACC, and left S1/M1.
16 ork, namely the left anterior insula/frontal operculum (AI/FO) and the visual word form area (VWFA).
17 /msFC) and bilateral anterior insula/frontal operculum (aI/fO) showed reliable start-cue and sustaine
18 , frontal/parietal medial, and right frontal operculum, an alcohol exposure effect.
19 lateral dACC and the right dorsal AI/frontal operculum and a lower parasympathetic tone, without sign
20 form cortex, whereas response in the frontal operculum and anterior insula (fO/aI) increased with olf
21 rea as well as right anterior insula/frontal operculum and anterior lateral prefrontal cortex during
22 omes, these were centred on the left frontal operculum and caudate nucleus in non-fluent primary prog
23 ulcus, intraparietal sulcus, insula, frontal operculum and cerebellar vermis.
24 ation between two seed regions (left frontal operculum and hippocampus) and pain network including bi
25 ted to reduced perfusion in the left frontal operculum and insula, whereas fear symptoms were associa
26 g reveals associations in the right Rolandic Operculum and Insula, with these regions linked to lower
27 ially to the drink, whereas the right insula/operculum and left orbitofrontal cortex respond to FO+ a
28 unched function leads to an expansion of the operculum and loss of the collar at its boundary.
29 e morphological traits such as the chitinous operculum and periostracum of fossil snails due to their
30 e not only the shell, but also the chitinous operculum and periostracum, soft body, and excrements.
31 n regions located in the left insula/frontal operculum and posterior cingulate cortex, which were ass
32 e in gray matter volume in the right frontal operculum and right superior temporal lobe.
33 s learning recruited the left insula/frontal operculum and the left superior parietal lobe, among oth
34 the anterior centripetal FC that produce the operculum and the posterior columnar FC that produce the
35 d more posteriorly, in and near the parietal operculum and ventral postcentral gyrus.
36 al (e.g., dorso/ventrolateral, right frontal operculum) and frontal medial cortices, as well as tempo
37 rior frontal cortex, anterior insula/frontal operculum, and anterior prefrontal cortex.
38  processing, including the cingulate cortex, operculum, and frontal lobe, as well as in the temporal
39  greater activation in the caudate, parietal operculum, and frontal operculum in response to food int
40 n were the paracingulate gyrus, left frontal operculum, and medial fronto-polar cortex.
41 nnections were found with PMd, SMA, anterior operculum, and posterior operculum/inferior parietal are
42 ivation in the putamen, mid-insula, Rolandic operculum, and precuneus to a cue signaling impending mi
43 th activity in the bilateral insula, frontal operculum, and secondary somatosensory cortex.
44 um, Heschl gyrus, precentral gyrus, rolandic operculum, and superior and inferior occipital lobes.
45 dial frontal cortex, anterior insula/frontal operculum, and thalamus, activity remained near baseline
46 ula extending into the putamen, the Rolandic operculum, and thalamus, which produced large activation
47 ncrease was present in the amygdala, frontal operculum-anterior insular cortex, ventromedial prefront
48 er in intrinsic activity of the left frontal operculum/anterior insula from the left frontoparietal n
49 in dorsal anterior cingulate cortex, frontal operculum/anterior insula, and especially lateral anteri
50  inconsistently across cases in the anterior operculum (AO), posterior operculum/inferior parietal co
51          The anterior insula and the frontal operculum are regarded as the primary taste cortex.
52 lastic trait used to characterise body size, operculum area.
53 eral temporoparietal junction, right frontal operculum, bilateral dorsal premotor cortex, right super
54 nd occipitotemporal cortex, the left frontal operculum, bilateral regions within the cerebellum, prim
55 he middle frontal gyrus bilaterally, frontal operculum bilaterally and in the cerebellar vermis.
56                    Modulation of the frontal operculum by the yogurt containing the olive oil extract
57 hird and fourth ventricles, corpus callosum, operculum, cerebellum, and brain stem.
58                                     Parietal operculum, corona radiata, and internal capsule differen
59 he left hemisphere (e.g., temporal gyrus and operculum cortex).
60  greater independence of the jaws, hyoid and operculum during evolution and exhibit more varied morph
61 geny, our data suggest that the holocephalan operculum evolved in concert with gill arch appendage re
62 c responses were observed in anterior insula/operculum extending into the orbitofrontal cortex (OFC).
63  activity organizes a sharp boundary for the operculum fate.
64 izations including centripetal migration and operculum formation.
65 nsular, cerebellum, basal ganglia, thalamus, operculum, frontoparietal cortices, and sensory cortices
66 steichthyan-like compact pharynx with a bony operculum helping constrain the origin of an elongate el
67 cluded the caudate, cuneus, frontal inferior operculum, Heschl gyrus, precentral gyrus, rolandic oper
68 l gyrus together with the bilateral parietal operculum (i.e. the anatomical site of the secondary som
69 ocated mostly in the anterior insula/frontal operculum in both healthy controls (8 out of 12) and LTL
70 sociated activity within the medial parietal operculum in response to feedforward visual or somatosen
71 the caudate, parietal operculum, and frontal operculum in response to food intake and in the caudate,
72 ngulate cortex, anterior insula, and frontal operculum in response to poorer speech intelligibility a
73 ivation in the bilateral insula and Rolandic operculum; increasing fat content did not elicit greater
74 ior frontal gyrus, middle frontal gyrus, and operculum, indicating a similar neural network underlies
75  PMd, SMA, anterior operculum, and posterior operculum/inferior parietal area.
76 es in the anterior operculum (AO), posterior operculum/inferior parietal cortex (PO/IP), and posterio
77 sylvian division supplied the frontoparietal operculum, insula and superior temporal gyrus.
78                     Activity in the parietal operculum, insula, and inferior and superior frontal gyr
79  sensation and vision, in the frontoparietal operculum, insula, ventral bank/fundus of the superior t
80 ppocampus, parahippocampal gyrus and frontal operculum/insular cortex of the right hemisphere and, to
81 s to the superomedial aspect of the temporal operculum, just posteriorly to Heschl's gyrus.
82 es found in the Heschl's gyrus, the parietal operculum, left Broca's area and the left arcuate fascic
83  effect with involvement of Heschl, Rolandic operculum, limbic lobe, subcortical gray nuclei followed
84 of the supratemporal plane with the parietal operculum, located mainly in the posterior half of the p
85 ter volumes, namely in the bilateral frontal operculum, medial frontal gyrus, bilateral hippocampal c
86 or temporal gyrus; left frontal and parietal operculum, medial frontal gyrus, orbital prefrontal cort
87  the supplementary motor area (SMA), frontal operculum, middle frontal gyri, and inferior parietal lo
88 recruitment of the hippocampus, SMA, frontal operculum, middle frontal gyrus, and inferior parietal l
89 n in the follicle cells that will create the operculum of the eggshell.
90 somatic sensory-related areas in the frontal operculum (OPf) and dysgranular insular area (Id).
91 tions, including areas of the insula/frontal operculum, orbitofrontal cortex and striatum.
92                                 The parietal operculum, particularly the cytoarchitectonic area OP1 o
93 We previously demonstrated that the parietal operculum (parts OP1/OP4) is activated with CMR exercise
94  supplementary motor area (SMA) and parietal operculum (PO) predominantly activated before tic onset
95 in bilateral orbitofrontal cortex, thalamus, operculum, posterior and anterior (subgenual) cingulate
96 inal gyri, superior temporal cortex, central operculum/posterior insula, and supplementary motor area
97 lobe, intraparietal sulcus, insula, parietal operculum, precuneus, and parietal medial areas.
98 s (visual processing and attention), frontal operculum (primary gustatory cortex) when anticipating p
99 ulcus (RTPJ/pSTS), planum temporale/parietal operculum (PT/PO), and posterior lateral orbitofrontal c
100 g planum temporale (PT) and parieto-temporal operculum (PTO).
101 activity, localized primarily to the frontal operculum rather than the insula.
102 functional connectivity between the parietal operculum (related to speed) and postcentral gyrus (rela
103                 In contrast, the left insula/operculum responds preferentially to the drink, whereas
104 e may reduce striatal, insular, and Rolandic operculum responsivity to food cues, which might decreas
105 e may reduce striatal, insular, and Rolandic operculum responsivity.
106 udomedial orbitofrontal cortex (OFC), insula/operculum, striatum and midbrain] or whether they ate ch
107 te and nurse cell complex which patterns the operculum structure of the mature eggshell.
108 ispositioning of the oocyte, and a shortened operculum, suggesting that Cct1 plays multiple roles dur
109 or frontal gyrus, precentral gyrus, Rolandic operculum, superior parietal gyrus, angular gyrus, and m
110 as well as the right anterior insula/frontal operculum, supramarginal gyrus, and medial orbitofrontal
111 oduced differential activation in the insula/operculum, thalamus, hippocampus, amygdala, and caudolat
112  region of the right anterior insula/frontal operculum than healthy controls (P = 0.02).
113 n were significantly weaker in the patient's operculum than in normal controls.
114 ater BOLD response to sounds in the parietal operculum, the location of secondary somatosensory corte
115 luster comprising the contralateral parietal operculum together with the anterior and posterior insul
116 tion, the activation of the right insula and operculum tracked online ratings of the aversiveness for
117                        One area, the frontal operculum, was distinguished by selectively interacting
118           In frontal motor areas and frontal operculum, where most labeled cells were located, almost
119 nsation did not evoke a BOLD response in the operculum, while sounds that produced strong somatosensa
120 These were found in the insula and overlying operculum, with regions in the anterior and middle insul
121 , y, z = 7, 59, 12; F = 8.53), right frontal operculum (x, y, z = 23, 23, 12; F = 8.25), and right an

 
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