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1 ections were found with diverse areas of the precentral and parietal cortex, including S1.
2                               In the insula, precentral and postcentral gyri NTDE signals were greate
3 ands produced increases in blood flow in the precentral and postcentral gyri of the right hemisphere.
4 elative growth rates in the formation of the precentral and postcentral gyri, right superior temporal
5 uage-related areas, including bilateral STG, precentral and postcentral gyri, supplementary motor are
6 dept foot motor skill who activated both the precentral and postcentral gyri.
7  associated with ALS in brain regions of the precentral and postcentral gyrus, the paracentral lobule
8 ncreased connectivity in a network including precentral and sensory-motor areas, whereas after 30 min
9  in medial temporal cortex, but reduction in precentral and sensory-motor areas.
10 amaged left hemisphere language areas, right precentral and superior temporal gyrus, as well as left
11 ortical motor (ProM) areas is connected with precentral areas 3, 1, and 2 as well as with the rostral
12 , posterior frontal (BA 6), parietal (BA 7), precentral (BA 4), postcentral (BA 3), occipital (BA 18)
13  and rostral subdivisions of gigantocellular precentral cortex (areas 4c, 4i, and 4r) in macaque monk
14 luding medial agranular cortex (AGm), medial precentral cortex (PrCm), and frontal orienting field (F
15  PI by reducing hyper-responses to SS in the precentral cortex and insula.
16 ve data showing that microstimulation of the precentral cortex evokes complex movements, and conclude
17          The increased response to SS in the precentral cortex was associated with longer wake time a
18 h the left inferior frontal/anterior insula, precentral cortex, and mesial frontal cortex.
19 he brainstem, centrum semiovale, frontal and precentral cortex, and significantly reduced NA/Cho in t
20       PI showed hyper-responses to SS in the precentral cortex, prefrontal cortex, and default mode n
21  cortex [frontal eye field (FEF), PreCC/IFS (precentral cortex/inferior frontal sulcus)] and parietal
22 tomical and functional lesions spread beyond precentral cortices and corticospinal tracts, to include
23 e infralimbic, dorsal peduncular, and medial precentral cortices have dense intrinsic projections, bu
24 rietal, calcarine, postcentral, central, and precentral cortices), and to obtain an unbiased estimate
25 arahippocampus, insula, and the parietal and precentral cortices.
26 reater activation in the superior medial and precentral frontal cortices.
27 involved the bilateral superior-temporal and precentral gyri immediately following question onset; at
28 al thinning in the left inferior frontal and precentral gyri in subjects who remain well.
29 rtex of both cerebral hemispheres except for precentral gyri in the second one.
30 ric functional connectivity of the bilateral precentral gyri positively correlated with fractional an
31 he healthy comparison group in the bilateral precentral gyri, anterior cingulate cortex, and middle a
32 lobule, and also cingulate, paracentral, and precentral gyri, compared with the non-hallucinators.
33 nterior cingulate cortex, the left and right precentral gyri, the left and right anterior temporal co
34 rontotemporal regions, cingulate and lateral precentral gyri.
35 ncy BOLD fluctuations between left and right precentral gyri.
36 ontal, middle temporal, middle occipital and precentral gyri.
37 ent conditions namely in the left hemisphere precentral gyrus (BA 4), the left hemisphere superior pa
38 precentral gyrus (BA 9) on the left, and the precentral gyrus (BA 6) and cerebellum bilaterally.
39 tex (Brodmann area [BA] 22) bilaterally, the precentral gyrus (BA 9) on the left, and the precentral
40 nvolvement of the brainstem and the inferior precentral gyrus (IPCG).
41 c masks of the superior frontal gyrus (SFG), precentral gyrus (PcG), middle frontal gyrus (MFG), orbi
42 , are represented as motor primitives in the precentral gyrus (PrG).
43  posterior inferior frontal gyrus (PIFG) and precentral gyrus (PrG); the impairment was immediately r
44 oca's region) and the ventral portion of the precentral gyrus (speech motor cortex) resulted in the m
45 herapy in the right prefrontal cortex (right precentral gyrus [Brodmann's area 9], inferior frontal g
46          The fraction of pixels in the right precentral gyrus above a confidence level of 95% for cor
47  smaller fraction of the pixels in the right precentral gyrus above the confidence level.
48 d increases in ECN connectivity in the right precentral gyrus and decreases in DMN connectivity in th
49 elated positively with RSFC between the left precentral gyrus and other motor regions, and between Br
50 , and dorsal cortical areas (checking); left precentral gyrus and right orbitofrontal cortex (hoardin
51 n cortical areas were identified between the precentral gyrus and the anterior bank of the intraparie
52 anxiety with cortical thickness in bilateral precentral gyrus and the dorsolateral prefrontal cortex.
53 ing in the precentral sulcus, connecting the precentral gyrus and the SMA; (2) U-fibres running in th
54 ulate cortex (P < .001) and a cluster in the precentral gyrus bilaterally (P = .004).
55 11)C-CNS 5161 uptake in caudate, putamen and precentral gyrus compared to the patients without dyskin
56 RI), that a region of the medial wall of the precentral gyrus consistently activates during both volu
57 ate, right superior temporal gyrus and right precentral gyrus during psychography compared to their n
58 al gyrus with high correlation with the left precentral gyrus for the finger-tapping state versus the
59                                       In the precentral gyrus from amyotrophic lateral sclerosis samp
60 ignificantly compared to the activity in the precentral gyrus from control samples (22.7 +/- 0.5 nmol
61 atched on reading abilities, with only right precentral gyrus GMV surviving this second analysis.
62  primary motor cortical region in the caudal precentral gyrus is not connected with the posterior par
63        These findings suggest that the right precentral gyrus merges oculomotor and somatomotor space
64          Neurons in a restricted zone in the precentral gyrus of macaque monkeys respond to tactile,
65                 We examined samples from the precentral gyrus of the cerebral cortex, a region affect
66 ap study identified the superior part of the precentral gyrus of the insula (in the anterior insula)
67  that included a discrete region of the left precentral gyrus of the insula, a cortical area beneath
68 sula, anterior insula or superior tip of the precentral gyrus of the insula.
69 talase were not significantly altered in the precentral gyrus or cerebellar cortex in the patient sam
70 This sound-related somatotopic activation in precentral gyrus shows that, during speech perception, s
71 ally, however, distinct motor regions in the precentral gyrus sparked by articulatory movements of th
72 ildren had a stronger activation in the left precentral gyrus than did adults in response to unhealth
73 kening relative to HR-well subjects and left precentral gyrus thickening relative to HR-well and HC i
74 mproving behaviour, while hypertrophy in the precentral gyrus was associated with declining behaviour
75 e level of 95% for correlation with the left precentral gyrus was calculated for each subject.
76                                 Bilaterally, precentral gyrus was most frequently activated (82%) fol
77                              Activity in the precentral gyrus was related to affective empathy.
78 d pixels to a region of interest in the left precentral gyrus were calculated.
79               Increases in blood flow in the precentral gyrus were correlated with increases in react
80 with low-ED cues in the insula, declive, and precentral gyrus were negatively related to appetitive t
81                    Greater FA in the SCR and precentral gyrus white matter were associated with bette
82          A plot of the fraction of the right precentral gyrus with high correlation with the left pre
83 egions (e.g., in the caudate, cingulate, and precentral gyrus) and decreased activation in the insula
84 et regions (cLBP study, thalamus; ALS study, precentral gyrus) was normalized with the SUV from candi
85 previously, such as parafascicular thalamus, precentral gyrus, and dentate nucleus of the cerebellum.
86 ons, not seen in normals, in fusiform gyrus, precentral gyrus, and intra-parietal sulcus.
87 gulate cortex with supplementary motor area, precentral gyrus, and postcentral gyrus.
88 r activation in the cuneus, parietal lobule, precentral gyrus, and superior temporal gyrus.
89 aged the superior frontal and parietal gyri, precentral gyrus, and the caudate.
90 ior temporal and middle occipital gyri, left precentral gyrus, bilateral opercular part of the inferi
91 ead rotation was observed bilaterally in the precentral gyrus, both medial and lateral to the hand ar
92 ared with passive movements, although in the precentral gyrus, hand, elbow, and shoulder movements sh
93 l area 6VR, in the most anterior part of the precentral gyrus, has strong connections with the rostra
94 electrically excitable cortex located on the precentral gyrus, including cortex sometimes considered
95 significantly less gray matter volume in the precentral gyrus, middle and superior frontal gyri, fron
96 nia patients exhibited decreased ReHo in the precentral gyrus, middle occipital gyrus, and posterior
97 elated to hand velocity in the contralateral precentral gyrus, postcentral gyrus, and inferior pariet
98 s, frontal inferior operculum, Heschl gyrus, precentral gyrus, rolandic operculum, and superior and i
99 rality in the medial superior frontal gyrus, precentral gyrus, Rolandic operculum, superior parietal
100 ngulate, gyrus rectus, orbitofrontal cortex, precentral gyrus, superior frontal cortex, middle fronta
101 he left pars opercularis, extending into the precentral gyrus, was activated to a greater extent by d
102 hout special foot skill mainly activated the precentral gyrus, which differed from those with more ad
103 tations of rules from both levels except for precentral gyrus, which represented only low-level rule
104  reductions in the left inferior frontal and precentral gyrus, which were greater in HR-well subjects
105 f an association between hand preference and precentral gyrus-morphology in chimpanzees (Pan troglody
106 pounds (Cho) ratios were calculated from the precentral gyrus.
107  in dorsolateral prefrontal cortex and right precentral gyrus.
108 n the left ventromedial PFC (vmPFC) and left precentral gyrus.
109 al insula, bilateral dorsal caudate and left precentral gyrus.
110 ) were in the anterior temporal lobe and the precentral gyrus.
111 ercularis, and the junction with the ventral precentral gyrus.
112 rtex in and near the Sylvian fissure and the precentral gyrus.
113 e and expressive aphasia; and (iv) bilateral precentral/left posterior superior-frontal regions and s
114 ingulate cortex has extensive projections to precentral medial cortex and caudally directed projectio
115 ing in rhesus monkey to define subregions in precentral motor cortex (M1), injected isotope tracers i
116  with significant increases in activation in precentral (P<.001) and postcentral gyri (P = .03) and t
117  ventrolateral prefrontal cortex, as well as precentral/postcentral gyri during processing of threate
118 me loss than the other pathologies, although precentral/postcentral gyri volume was reduced in compar
119 al interference trials was only found in the precentral/postcentral gyrus.
120 s showed higher BOLD activation to SS in the precentral, prefrontal, fusiform, and posterior cingulat
121  neural stimulation studies (suppressing the precentral region and/or enhancing the anterior temporal
122 lso showed greater activation in a bilateral precentral region.
123 ntrast to the LOTC, the early recruitment of precentral regions does not contain the detailed informa
124                                 By contrast, precentral regions, though recruited early, have access
125 ly in the medial and superior prefrontal and precentral regions.
126 n representations substantially earlier than precentral regions.
127 lpha-band oscillations (9-13 Hz) recorded at precentral sites strongly predicted scaling exponents of
128    Here, we recorded neurons from the medial precentral subregion of mouse prefrontal cortex to exami
129 lcal pattern, namely, the interposition of a precentral sulcal segment between the central sulcus and
130 perior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), anatomically interdigitated wi
131 perior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), interleaved with two bilateral
132 01) and was more frequently connected to the precentral sulcus (P < .001) in patients with FCD2 than
133 d that neural activity persists in the human precentral sulcus (PCS) during WM delays.
134 arietal sulcus (IPS0-IPS3) and two along the precentral sulcus (PCS) that contained reliable retinoto
135  decreased right-lateralized activity in the precentral sulcus (PrCS) and posterior parietal cortex (
136 at are biased for visual attention, superior precentral sulcus (sPCS) and inferior precentral sulcus
137  regions in lateral frontal cortex, superior precentral sulcus (sPCS) and inferior precentral sulcus
138 ently shown that the superior element of the precentral sulcus (sPCS), near the caudal end of the sup
139 ory attention, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal su
140 ntion regions, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal su
141 he lateral parietal cortex, and the superior precentral sulcus (thought to contain the human homolog
142 l sulcus and the junction of the left medial precentral sulcus and superior frontal sulcus.
143 ided bias in the bifurcation of the inferior precentral sulcus, an anatomical feature that occurs muc
144 reconstructions: (1) U-fibres running in the precentral sulcus, connecting the precentral gyrus and t
145 uction in the cerebral cortex, including the precentral, superior and middle temporal, and lingual gy
146 d points, the middle temporal (T = 4.25) and precentral (T = 6.47) gyri, and one right ILF end point,
147 ntrum semiovale, and from frontal, parietal, precentral, temporal and occipital cortices.
148 ed with increasing left inferior frontal and precentral thickness.
149 variance, 0.05), calcarine (variance, 0.05), precentral (variance, 0.06), parietal (variance, 0.08),

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