ライフサイエンスコーパス: lateral intraparietal area

1 al (frontal eye fields) and parietal cortex (lateral intraparietal area).

2 neurons was comparable with that seen in the lateral intraparietal area, a cortical area that is a pa

3 atterns of activity were not observed in the lateral intraparietal area, an area linked to the fronto

4 nse modulates the activity of neurons in the lateral intraparietal area, an area of primate cortex th

5 mologs of macaque parietal areas such as the lateral intraparietal area and parietal reach region.

6 l areas, including the frontal eye field and lateral intraparietal area, and one of their direct, sub

7 x, motion-selective dorsal stream areas, the lateral intraparietal area, and the frontal eye fields.

8 For both tasks, firing rates in the lateral intraparietal area appeared to reflect the accum

9 Much evidence implicates the lateral intraparietal area as a candidate priority map i

10 an oscillation in neural firing rate in the lateral intraparietal area consistent with such a role.

11 ation and electrical microstimulation in the lateral intraparietal area during a visuospatial discrim

12 Neurons in area 7a and the lateral intraparietal area fire before and during visual

13 The lateral intraparietal area, for example, responds prefer

14 It will describe evidence that the lateral intraparietal area, frontal eye field and superi

15 Neurons in the lateral intraparietal area, frontal eye field, and super

16 This region may correspond to the lateral intraparietal area in macaque monkeys.

17 Injections into a portion of the lateral intraparietal area labeled second-order neurons

18 vity of posterior parietal cortex (including lateral intraparietal area LIP) neurons while monkeys le

19 Although the lateral intraparietal area (LIP) and frontal eye field (

20 recorded simultaneously from neurons in the lateral intraparietal area (LIP) and SC while monkeys ma

21 us of the superior temporal sulcus (FST) and lateral intraparietal area (LIP) and the animals correct

22 ed oculomotor response tasks, neurons in the lateral intraparietal area (LIP) and the frontal eye fie

23 cent hypothesis suggests that neurons in the lateral intraparietal area (LIP) and the parietal reach

24 t 150 ms after a saccade, gain fields in the lateral intraparietal area (LIP) are unreliable.

25 was shown that single neurons in the macaque lateral intraparietal area (LIP) can predict the amount

26 g, recent evidence shows that neurons in the lateral intraparietal area (LIP) carry both spatial and

27 The lateral intraparietal area (LIP) contains spatially sele

28 In contrast, the selectivity of cells in the lateral intraparietal area (LIP) did not directly depend

29 For example, neurons in the lateral intraparietal area (LIP) encode both the locatio

30 Neurons in the lateral intraparietal area (LIP) encoded these attention

31 studies have shown that some neurons in the lateral intraparietal area (LIP) exhibit anticipatory re

32 e found that single neurons in the macaque's lateral intraparietal area (LIP) exhibit gradual firing

33 eaches than saccades, whereas signals in the lateral intraparietal area (LIP) gave better predictions

34 The lateral intraparietal area (LIP) has been implicated as

35 The macaque lateral intraparietal area (LIP) has been implicated in

36 nt years a distributed network including the lateral intraparietal area (LIP) has been implicated in

37 ort to elucidate these circuits, the primate lateral intraparietal area (LIP) has been interpreted as

38 decades, neurophysiological responses in the lateral intraparietal area (LIP) have received extensive

39 rsolateral prefrontal cortex (dlPFC) and the lateral intraparietal area (LIP) in monkeys using a memo

40 The lateral intraparietal area (LIP) in the macaque contains

41 ovelty affects visual salience in the monkey lateral intraparietal area (LIP) in ways that are indepe

42 We tested the hypothesis that the lateral intraparietal area (LIP) integrates disparate ta

43 The lateral intraparietal area (LIP) is a subdivision of the

44 The lateral intraparietal area (LIP) is essential for this p

45 We previously found that neurons in the lateral intraparietal area (LIP) of Macaca mulatta refle

46 neurons in the frontal eye fields (FEFs) and lateral intraparietal area (LIP) of macaques are prefere

47 It has been suggested that the lateral intraparietal area (LIP) of macaques plays a fun

48 corded the activity of single neurons in the lateral intraparietal area (LIP) of rhesus macaques to d

49 lected in the firing rates of neurons in the lateral intraparietal area (LIP) of rhesus monkeys perfo

50 an initial study of neural responses in the lateral intraparietal area (LIP) of the cerebral cortex

51 rk has suggested that neural activity in the lateral intraparietal area (LIP) of the monkey brain ref

52 The activity of neurons in the lateral intraparietal area (LIP) of the monkey predicts

53 neurons in the middle temporal area (MT) and lateral intraparietal area (LIP) of two macaque monkeys.

54 Neurons in the lateral intraparietal area (LIP) play a role in these fu

55 The lateral intraparietal area (LIP) plays a crucial role in

56 dies suggest that neural activity in macaque lateral intraparietal area (LIP) provides a useful windo

57 For example, neurons in the lateral intraparietal area (LIP) reflect learned associa

58 Neurons in the lateral intraparietal area (LIP) reflected concurrent ac

59 Firing rates of neurons in the lateral intraparietal area (LIP) reflected the accumulat

60 ommunicated by eye movements, neurons in the lateral intraparietal area (LIP) represent the accumulat

61 studies indicate that neural activity in the lateral intraparietal area (LIP) represents the gradual

62 Many neurons in the lateral intraparietal area (LIP) responded more strongly

63 We examine lateral intraparietal area (LIP) responses during a visu

64 Recordings in the lateral intraparietal area (LIP) reveal that parietal co

65 ulation appears substantially earlier in the lateral intraparietal area (LIP) than in an anatomically

66 nstrate that the responses of neurons in the lateral intraparietal area (LIP) to a task-irrelevant di

67 We investigated neural responses in the lateral intraparietal area (LIP) to transient, distracti

68 ts to define retinotopic maps in the macaque lateral intraparietal area (LIP) using histological, ele

69 ffects of electrical microstimulation in the lateral intraparietal area (LIP) while monkeys performed

70 nd correlated the activity of neurons in the lateral intraparietal area (LIP) with the monkey's atten

71 Here, we show that neurons in the primate lateral intraparietal area (LIP), a cortical area previo

72 ctivity from populations of neurons from the lateral intraparietal area (LIP), a cortical node in the

73 To answer this, we focus on the lateral intraparietal area (LIP), an area that has been

74 300 ms after cue in frontal eye field (FEF), lateral intraparietal area (LIP), and cuneus support ear

75 rding from macaque frontal eye fields (FEF), lateral intraparietal area (LIP), and pulvinar.

76 any parietal neurons, such as in the macaque lateral intraparietal area (LIP), are strongly influence

77 e analyzed single-neuron recordings from the lateral intraparietal area (LIP), during a perceptual de

78 Neurons in one of its subdivisions, the lateral intraparietal area (LIP), have visual responses

79 ea four (V4), inferior temporal cortex (IT), lateral intraparietal area (LIP), prefrontal cortex (PFC

80 sion, we recorded from single neurons in the lateral intraparietal area (LIP), which has been implica

81 e movements may be guided by activity in the lateral intraparietal area (LIP), which is thought to re

82 versible pharmacological inactivation of the lateral intraparietal area (LIP), which plays a role in

83 ormation that is used to solve the task, and lateral intraparietal area (LIP), which represents the t

84 direct neural correlate of decisions in the lateral intraparietal area (LIP).

85 ust neuronal category representations in the lateral intraparietal area (LIP).

86 about the internal circuitry of the primate lateral intraparietal area (LIP).

87 he lateral bank of the intraparietal sulcus [lateral intraparietal area (LIP)] specifically biased ch

88 vity in the posterior parietal cortex [human lateral intraparietal area (LIP)], the anterior cingulat

89 jections centered in the neighboring ventral lateral intraparietal area (LIPv) revealed inputs mainly

90 We demonstrate that decision-related lateral intraparietal area neurons typically undergo gra

91 dlPFC), the frontal eye field (FEF), and the lateral intraparietal area of macaque monkeys during a v

92 , we recorded from individual neurons in the lateral intraparietal area of monkeys performing a task

93 putative marmoset frontal eye field-and the lateral intraparietal area of two male marmosets and rec

94 Neuronal responses in the monkey lateral intraparietal area revealed that bound changes a

95 icity for effector choice, with cells in the lateral intraparietal area selective for saccades and ce

96 Neurons in the lateral intraparietal area showed anticipatory activity

97 provided a better statistical description of lateral intraparietal area spike trains than diffusion-t

98 al visual areas of behaving rhesus macaques (lateral intraparietal area, ventral intraparietal area,

99 We studied the activity of neurons in monkey lateral intraparietal area while monkeys performed a vis

100 We recorded the activity of neurons in the lateral intraparietal area while monkeys performed an in