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  anterior midcingulate cortex, and the right premotor areas).
2 a, the pre-supplementary motor area, and the premotor area.
3 e metabolite's effect on the SCC-FC with the premotor area.
4 rk, exerting Granger causality on the dorsal premotor area.
5 a single electrode located over the motor or premotor area.
6 h includes neurons that project to the vocal premotor area.
7 d, resembled the pattern for macaque ventral premotor area.
8 al connectivity of M1 with somatosensory and premotor areas.
9 l primary sensorimotor cortex and the mesial premotor areas.
10 nal (premovement) activation over the mesial premotor areas.
11 inct classes of neurons in primary motor and premotor areas.
12 he expansion of descending output from these premotor areas.
13  nuclei (CbN) transmit cerebellar signals to premotor areas.
14 ting posterior temporal and inferior frontal/premotor areas.
15 ) within a selective network of parietal and premotor areas.
16 of synchronized Purkinje cells to downstream premotor areas.
17 r layers convey the processed information to premotor areas.
18 ivity in rostral prefrontal cortex (PFC) and premotor areas.
19 n activity in right PMd and connected medial premotor areas.
20 al regions coordinated with sensorimotor and premotor areas.
21  effective connectivity among prefrontal and premotor areas.
22 ceived similar proportions of afferents from premotor areas 6M and 6DC, and from the prefrontal corte
23                                              Premotor areas acted as relay from parietal to medial pr
24  play a driving role in the network, whereas premotor areas acted as relays from parietal to medial p
25 nal left prefrontal, parietal, and bilateral premotor areas, again independently from stimulus modali
26            Yet, inactivation of a downstream premotor area (ALM), but not orbitofrontal cortex, confi
27 t, naming tools selectively activated a left premotor area also activated by imagined hand movements,
28 orrelated with connectivity between the left premotor area and left supplementary motor area, for bot
29 mary motor cortex, supplementary motor area, premotor area and superior parietal lobule, based on the
30    This activity is likely to originate from premotor areas and could be modulated by auditory feedba
31 y face, but also forelimb representations of premotor areas and M1 as well as prefrontal cortex, FEF,
32           Accordingly, integrating LFPs from premotor areas and M1 could enhance the performance and
33  nuclei, nucleus raphe magnus, pontine blink premotor area, and superior salivatory nucleus.
34 tor cortex areas - the primary motor cortex, premotor area, and supplementary motor area, respectivel
35 re speech areas, including Broca's area, the premotor area, and the supplementary motor area.
36  cortex [LMCx; sensorimotor (SM) and lateral premotor areas] and the medial motor cortex [MMCx; suppl
37                                        These premotor areas are components of complex anatomical netw
38  in monkeys gave rise to the hypothesis that premotor areas are inherently involved not only when obs
39 We thus establish that superior temporal and premotor areas are not only involved in biological motio
40 al VLPFC and anterior insula, rostral to the premotor area, are activated during inhibition of both m
41 k to their respective subpallial sensory and premotor areas, as found by previous studies.
42 ound underactivity of the cortical motor and premotor areas associated with articulation and speech p
43                              The ipsilateral premotor area (Brodmann area 6), bilateral posterior par
44 ily exhibits effector-specific LFP activity, premotor areas compute more effector-independent aspects
45 t premotor area (P < 0.05), as well as other premotor area connections.
46                                Both of these premotor areas contain a distinct digit representation,
47 f task performance may involve activation of premotor areas contralateral to the site of rTMS, simila
48  second one originating in lateral motor and premotor areas controlling voluntary facial movements.
49                                           In premotor areas, differences related to hand use were onl
50 l network (primary somatosensory and frontal premotor area) during the loss of consciousness (LOC) in
51 s in medial frontal cortex, but not a nearby premotor area, encode the relative value of available op
52                                              Premotor area F5 acted as a hub that shared the visual c
53                          The macaque ventral premotor area F5 hosts two types of visuomotor grasping
54      Here, we tested the activity of ventral premotor area F5 mirror neurons (MNs) while monkeys obse
55 , we compared the response of monkey ventral premotor area F5 neurons tested during pragmatic (PT) or
56        Here, we show that MNs of the ventral premotor area F5 of macaque monkeys are particularly sen
57 , the anterior intraparietal area (AIP), and premotor areas F5 and F6, while monkeys performed a Go/N
58  intraparietal (AIP) and the rostral ventral premotor area (F5) in the macaque, which are both part o
59 s not require HVC (high vocal center), a key premotor area for singing in adult birds, but does requi
60                               Prefrontal and premotor areas form dense projection fields surrounded b
61 unk and face representations, as well as the premotor areas, had dense callosal connections.
62             Here, we present evidence that a premotor area has a potential role in storing previous t
63 g of area HVC in the Bengalese finch brain-a premotor area homologous to the mammalian premotor corte
64 ea 6Va in the marmoset is similar to ventral premotor areas identified in other simian primates, and
65 is known to also evoke activity in motor and premotor areas in frontal cortex.
66    What is the role of ipsilateral motor and premotor areas in motor learning?
67 rders indicates increased neural activity in premotor areas in patients with hypokinetic catatonia.
68 dings suggest the involvement of the frontal premotor areas in strategic planning such as rule follow
69 lts strongly suggest that the output of song premotor areas in the forebrain is continuously monitore
70     We found that, in both monkeys, multiple premotor areas in the frontal lobe along with the primar
71 direct and prominent as that from any of the premotor areas in the frontal lobe.
72 egion leads to consider an important role of premotor areas in the reward circuitry supporting action
73 n, compared with observation of emotions, in premotor areas including the inferior frontal cortex, as
74 , whereas VA projections target more rostral premotor areas (including cingulate and presupplementary
75 in the robust nucleus of arcopallium (RA), a premotor area intermediate between HVC and the motor neu
76 immediate reduction of connectivity with the premotor area is paralleled by an enhancement in the con
77 how the activation of one cortical area (the premotor area) is transmitted to the rest of the brain.
78  blood flow in a network comprising the left premotor area, left anterior cingulate, and right ventra
79    Population activity in visual area AM and premotor area M2 during the delay period was dominated b
80 rtical projections to layer I of the frontal/premotor area M2 of the rat neocortex, we have used fluo
81                                     Cortical premotor area, M2 cortex in rodents, is the most affecte
82 pikes/s), unlike large cells that project to premotor areas (maximal rate, approximately 400 spikes/s
83  (WGA-HRP) in dorsal (PMD) and ventral (PMV) premotor areas of owl monkeys.
84                         How do the motor and premotor areas of the brain assemble motor sequences so
85  patients, including components generated by premotor areas of the cortex as well as the primary moto
86 de new insights into the organization of the premotor areas of the frontal lobe.
87  sequences of feeding through projections to premotor areas of the jaw.
88  ictal activities spread to frontal (lateral premotor area, orbitofrontal cortex, supplementary motor
89  neurons (PNs) (HVC(RA)) that innervate song premotor areas, other PNs (HVC(X)) that innervate a basa
90  the left primary motor cortex and the right premotor area (P < 0.05), as well as other premotor area
91 n the bilateral anterior lobe of cerebellum, premotor area, parietal cortex, left prefrontal cortex,
92 ents had greater activity in the cerebellum, premotor area, parietal cortex, precuneus and prefrontal
93  from interneurons within the peritrigeminal premotor area (Peri5).
94 , supplementary motor areas (SMA), the right premotor area (PMA), superolateral sensorimotor areas, t
95                   Primary motor cortex (M1), premotor area (PMA), supplementary motor area, as well a
96 n, we examined neural activity in the dorsal premotor area (PMd) and the effects of its local inactiv
97 , we studied neuronal activity in the dorsal premotor area (PMd) and the medial intraparietal area (a
98 ere we simultaneously record from the dorsal premotor area (PMd) in frontal cortex and the parietal r
99 in the primary motor cortex (M1), the dorsal premotor area (PMd), and the ventral premotor area (PMv)
100 y-, and rule-related activity) in the dorsal premotor area (PMd), the cingulate motor areas (CMA), an
101 ers into the primary motor area (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supple
102 acers into primary motor cortex (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supple
103 icited movements from the dorsal and ventral premotor areas (PMD, PMV), the caudal and rostral divisi
104                                  The ventral premotor area (PMv) is a major source of input to the pr
105  dorsal premotor area (PMd), and the ventral premotor area (PMv) of cebus monkeys.
106 ea (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and
107 ex (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and
108 (PMDc) and rostral (PMDr) divisions, ventral premotor area (PMV), supplementary motor area (SMA), pre
109 ns of a conventional tracer into the ventral premotor area (PMv).
110 e primary sensorimotor cortex and the mesial premotor areas, probably including the supplementary mot
111 eater decrease of rCBF in lateral and medial premotor areas, putamen, and thalamus, including the sti
112 rea 8C is more akin to that characterizing a premotor area, rather than a prefrontal area.
113 TYP showed reduced activation in sensory and premotor areas relative to younger ones.
114 tio-temporal sequence combination, bilateral premotor areas represented spatial and temporal features
115 motor cortex, supplementary motor cortex and premotor areas responded to higher stimulation currents
116 activation in supplementary motor area, left premotor area, right thalamus, bilateral inferior fronta
117 s area and left-hemisphere supplementary and premotor areas; storage of spatial information activates
118 sory relays and sits immediately upstream of premotor areas, suggesting that it may be involved in th
119 erior occipital gyri, fusiform gyri, ventral premotor area, superior parietal lobule, cerebellum and
120 esponses in the owl's forebrain and midbrain premotor area that are consistent with coding schemes pr
121                                     HVC is a premotor area that integrates auditory feedback and is n
122                                         In a premotor area that is responsible for holding the eyes s
123 irds, whereas HVC (used as a proper name), a premotor areas that gates auditory input into the vocal
124  that they projected to multiple sensory and premotor areas: the optic tectum, the nucleus of the med
125 lays were those of motor, somatosensory, and premotor areas; the longer ones were those of temporal,
126  shape includes, in addition to parietal and premotor areas, three clearly distinct regions in infero
127                   The projections from other premotor areas to M1, the PMd, and the PMv are more mode
128 y level of motor control, from telencephalic premotor areas to superfast syringeal muscles.
129    We found that the densest inputs from the premotor areas to the digit representation in M1 origina
130                    Disruption of activity in premotor areas using transcranial magnetic stimulation p
131  the various layers of the primary motor and premotor areas varies depending on the target striatal z
132                                   Two of the premotor areas, ventral area 6 (area 6V) and the supplem
133 etween ipsilesional primary motor cortex and premotor areas was linked to interhemispheric rerouting
134 plementary motor area (SMA) and dorsolateral premotor areas was observed.
135 onal primary motor cortex and contralesional premotor areas was related to intrahemispheric rerouting
136  gyrus, superior parietal lobule, and dorsal premotor area) was relevant for monitoring the online co
137 gyrus, inferior parietal lobule, and ventral premotor area) was specifically involved in processing k
138         Additional groups of the sympathetic premotor areas were labeled by 6 days post-injection, in
139                      Conversely, the ventral premotor areas were preferentially connected with the la
140 or areas (primary, supplementary, and caudal premotor areas), whereas VA projections target more rost
141 evealed the engagement of right parietal and premotor areas, which have been linked to language selec
142  an increase in activity in medial and right premotor areas without affecting task performance.

 
Page Top