ライフサイエンスコーパス: premotor area

1 rk, exerting Granger causality on the dorsal premotor area.

2 a single electrode located over the motor or premotor area.

3 h includes neurons that project to the vocal premotor area.

4 d, resembled the pattern for macaque ventral premotor area.

5 al regions coordinated with sensorimotor and premotor areas.

6 nal (premovement) activation over the mesial premotor areas.

7 ting posterior temporal and inferior frontal/premotor areas.

8 al connectivity of M1 with somatosensory and premotor areas.

9 ) within a selective network of parietal and premotor areas.

10 of synchronized Purkinje cells to downstream premotor areas.

11 r layers convey the processed information to premotor areas.

12 ivity in rostral prefrontal cortex (PFC) and premotor areas.

13 n activity in right PMd and connected medial premotor areas.

14 nuclei (CbN) transmit cerebellar signals to premotor areas.

15 effective connectivity among prefrontal and premotor areas.

16 l primary sensorimotor cortex and the mesial premotor areas.

17 ceived similar proportions of afferents from premotor areas 6M and 6DC, and from the prefrontal corte

18 Premotor areas acted as relay from parietal to medial pr

19 play a driving role in the network, whereas premotor areas acted as relays from parietal to medial p

20 nal left prefrontal, parietal, and bilateral premotor areas, again independently from stimulus modali

21 t, naming tools selectively activated a left premotor area also activated by imagined hand movements,

22 orrelated with connectivity between the left premotor area and left supplementary motor area, for bot

23 mary motor cortex, supplementary motor area, premotor area and superior parietal lobule, based on the

24 This activity is likely to originate from premotor areas and could be modulated by auditory feedba

25 y face, but also forelimb representations of premotor areas and M1 as well as prefrontal cortex, FEF,

26 nuclei, nucleus raphe magnus, pontine blink premotor area, and superior salivatory nucleus.

27 re speech areas, including Broca's area, the premotor area, and the supplementary motor area.

28 cortex [LMCx; sensorimotor (SM) and lateral premotor areas] and the medial motor cortex [MMCx; suppl

29 These premotor areas are components of complex anatomical netw

30 in monkeys gave rise to the hypothesis that premotor areas are inherently involved not only when obs

31 We thus establish that superior temporal and premotor areas are not only involved in biological motio

32 al VLPFC and anterior insula, rostral to the premotor area, are activated during inhibition of both m

33 ound underactivity of the cortical motor and premotor areas associated with articulation and speech p

34 The ipsilateral premotor area (Brodmann area 6), bilateral posterior par

35 t premotor area (P < 0.05), as well as other premotor area connections.

36 Both of these premotor areas contain a distinct digit representation,

37 f task performance may involve activation of premotor areas contralateral to the site of rTMS, simila

38 l network (primary somatosensory and frontal premotor area) during the loss of consciousness (LOC) in

39 Premotor area F5 acted as a hub that shared the visual c

40 The macaque ventral premotor area F5 hosts two types of visuomotor grasping

41 Here, we tested the activity of ventral premotor area F5 mirror neurons (MNs) while monkeys obse

42 Here, we show that MNs of the ventral premotor area F5 of macaque monkeys are particularly sen

43 intraparietal (AIP) and the rostral ventral premotor area (F5) in the macaque, which are both part o

44 s not require HVC (high vocal center), a key premotor area for singing in adult birds, but does requi

45 Prefrontal and premotor areas form dense projection fields surrounded b

46 unk and face representations, as well as the premotor areas, had dense callosal connections.

47 g of area HVC in the Bengalese finch brain-a premotor area homologous to the mammalian premotor corte

48 ea 6Va in the marmoset is similar to ventral premotor areas identified in other simian primates, and

49 is known to also evoke activity in motor and premotor areas in frontal cortex.

50 What is the role of ipsilateral motor and premotor areas in motor learning?

51 dings suggest the involvement of the frontal premotor areas in strategic planning such as rule follow

52 lts strongly suggest that the output of song premotor areas in the forebrain is continuously monitore

53 direct and prominent as that from any of the premotor areas in the frontal lobe.

54 n, compared with observation of emotions, in premotor areas including the inferior frontal cortex, as

55 , whereas VA projections target more rostral premotor areas (including cingulate and presupplementary

56 in the robust nucleus of arcopallium (RA), a premotor area intermediate between HVC and the motor neu

57 how the activation of one cortical area (the premotor area) is transmitted to the rest of the brain.

58 blood flow in a network comprising the left premotor area, left anterior cingulate, and right ventra

59 rtical projections to layer I of the frontal/premotor area M2 of the rat neocortex, we have used fluo

60 pikes/s), unlike large cells that project to premotor areas (maximal rate, approximately 400 spikes/s

61 (WGA-HRP) in dorsal (PMD) and ventral (PMV) premotor areas of owl monkeys.

62 How do the motor and premotor areas of the brain assemble motor sequences so

63 patients, including components generated by premotor areas of the cortex as well as the primary moto

64 de new insights into the organization of the premotor areas of the frontal lobe.

65 ictal activities spread to frontal (lateral premotor area, orbitofrontal cortex, supplementary motor

66 neurons (PNs) (HVC(RA)) that innervate song premotor areas, other PNs (HVC(X)) that innervate a basa

67 the left primary motor cortex and the right premotor area (P < 0.05), as well as other premotor area

68 n the bilateral anterior lobe of cerebellum, premotor area, parietal cortex, left prefrontal cortex,

69 ents had greater activity in the cerebellum, premotor area, parietal cortex, precuneus and prefrontal

70 , supplementary motor areas (SMA), the right premotor area (PMA), superolateral sensorimotor areas, t

71 n, we examined neural activity in the dorsal premotor area (PMd) and the effects of its local inactiv

72 , we studied neuronal activity in the dorsal premotor area (PMd) and the medial intraparietal area (a

73 ere we simultaneously record from the dorsal premotor area (PMd) in frontal cortex and the parietal r

74 in the primary motor cortex (M1), the dorsal premotor area (PMd), and the ventral premotor area (PMv)

75 y-, and rule-related activity) in the dorsal premotor area (PMd), the cingulate motor areas (CMA), an

76 ers into the primary motor area (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supple

77 acers into primary motor cortex (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supple

78 icited movements from the dorsal and ventral premotor areas (PMD, PMV), the caudal and rostral divisi

79 The ventral premotor area (PMv) is a major source of input to the pr

80 dorsal premotor area (PMd), and the ventral premotor area (PMv) of cebus monkeys.

81 ea (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and

82 ex (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and

83 (PMDc) and rostral (PMDr) divisions, ventral premotor area (PMV), supplementary motor area (SMA), pre

84 ns of a conventional tracer into the ventral premotor area (PMv).

85 e primary sensorimotor cortex and the mesial premotor areas, probably including the supplementary mot

86 eater decrease of rCBF in lateral and medial premotor areas, putamen, and thalamus, including the sti

87 rea 8C is more akin to that characterizing a premotor area, rather than a prefrontal area.

88 TYP showed reduced activation in sensory and premotor areas relative to younger ones.

89 tio-temporal sequence combination, bilateral premotor areas represented spatial and temporal features

90 motor cortex, supplementary motor cortex and premotor areas responded to higher stimulation currents

91 activation in supplementary motor area, left premotor area, right thalamus, bilateral inferior fronta

92 s area and left-hemisphere supplementary and premotor areas; storage of spatial information activates

93 sory relays and sits immediately upstream of premotor areas, suggesting that it may be involved in th

94 erior occipital gyri, fusiform gyri, ventral premotor area, superior parietal lobule, cerebellum and

95 In a premotor area that is responsible for holding the eyes s

96 that they projected to multiple sensory and premotor areas: the optic tectum, the nucleus of the med

97 lays were those of motor, somatosensory, and premotor areas; the longer ones were those of temporal,

98 The projections from other premotor areas to M1, the PMd, and the PMv are more mode

99 y level of motor control, from telencephalic premotor areas to superfast syringeal muscles.

100 We found that the densest inputs from the premotor areas to the digit representation in M1 origina

101 Disruption of activity in premotor areas using transcranial magnetic stimulation p

102 plementary motor area (SMA) and dorsolateral premotor areas was observed.

103 gyrus, superior parietal lobule, and dorsal premotor area) was relevant for monitoring the online co

104 gyrus, inferior parietal lobule, and ventral premotor area) was specifically involved in processing k

105 Additional groups of the sympathetic premotor areas were labeled by 6 days post-injection, in

106 Conversely, the ventral premotor areas were preferentially connected with the la

107 or areas (primary, supplementary, and caudal premotor areas), whereas VA projections target more rost

108 an increase in activity in medial and right premotor areas without affecting task performance.