ライフサイエンスコーパス: sensory region

1 orm the neurons that innervate all inner ear sensory regions.

2 itrary and complex acoustic patterns, within sensory regions.

3 nificantly more non-neurons than the primary sensory regions.

4 to implement top-down attentional control of sensory regions.

5 h retinotopic activity in lower level visual sensory regions.

6 >80% persisting over a 3 week period in all sensory regions.

7 plementary to that of BMP4 in the vestibular sensory regions.

8 performance are the ones connecting primary sensory regions.

9 encephalized brains through marked growth in sensory regions.

10 enes in sensory dysfunction already in early sensory regions.

11 les and more stable neural patterns, even in sensory regions.

12 ssociation cortex to broadly involve primary sensory regions.

13 However, an alternative view suggests sensory regions also integrate inputs with current task

14 isual stimuli have been demonstrated both in sensory regions and in higher cortical areas.

15 s acquisition begins in the parieto-temporal sensory regions and is subsequently consolidated and str

16 dicted mean reward emerges early in parietal/sensory regions and later in frontal cortex.

17 he integration of functional connectivity in sensory regions and the disintegration in associative re

18 enitors throughout the epithelium of all six sensory regions, and later on during sensory cell differ

19 ical hierarchy, with short states in primary sensory regions, and long states in lateral and medial p

20 he view that DMN activity and the associated sensory regions are actively involved in maintaining mem

21 Primary sensory regions are believed to instantiate stable neura

22 ls of neural disentanglement, in which early sensory regions build an overcomplete representation of

23 ted decrease in the recruitment of posterior sensory regions coupled with an increased recruitment of

24 Neural populations from various sensory regions demonstrate dynamic range adaptation in

25 providing contextual temporal information to sensory regions, driving perceptual and behavioral selec

26 Within sensory regions, fluctuations of high-frequency (64-200

27 Cognitive, striatal, and sensory regions graded their responses to changes in pre

28 t to feedforward pathways, motor feedback to sensory regions has received much less attention.

29 in the alpha to beta range in task-relevant sensory regions have been suggested to play an important

30 Traditionally, sensory regions have been viewed as separate from such c

31 n an anterior temporal lobe hub and upstream sensory regions in humans.

32 coordinates from parietal control regions to sensory regions in humans.

33 puts from ipsilateral SHELL with inputs from sensory regions in surrounding nidopallium, suggesting t

34 performance, further challenging the role of sensory regions in VSTM storage.

35 We conclude that these early sensory regions, in addition to their primary sensory fu

36 abundant input from affective, arousal, and sensory regions including the basolateral amygdala (BLA)

37 tion areas, but was also seen in the primary sensory region investigated.

38 ause non-primary sensory input to a cortical sensory region is often weak or modulatory.

39 that during active exploration the relevant sensory region is primed for enhanced sensory discrimina

40 Feedback from movement to sensory regions is hypothesized to play critical roles i

41 Information processing in early sensory regions is modulated by a diverse range of inhib

42 tails adjustment of evidence accumulation in sensory regions (Kloosterman et al., 2019), but the pres

43 mbalance in higher-order feedback to primary sensory regions, leading to an increased focus on local

44 parietal regions and both dorsal and ventral sensory regions [LIP, IPSa, ventral IPS, lateral occipit

45 This raised the question of how sensory regions maintain memory representations during t

46 st that poor learning of sound statistics in sensory regions may underlie the poor representations of

47 was increased effective connectivity between sensory regions (motion-sensitive medial temporal area M

48 namic range adaptation is neither limited to sensory regions nor to rescaling of monotonic stimulus i

49 amodal patterns included activity in primary sensory regions not directly relevant to the task (e.g.,

50 -to-basal gradient of SOX2 expression in the sensory region of the cochlea, reflecting the pattern of

51 The sensory region of the mammalian hearing organ contains t

52 racer microinjected into the caudal visceral sensory region of the NST, and also by immunocytochemica

53 al properties of the mammalian brain is that sensory regions of cortex are formed of multiple, functi

54 remodeling rates are similar across primary sensory regions of different modalities, but may differ

55 Sensory regions of neocortex are organized as arrays of

56 In sensory regions of primate neocortex, the calcium-bindin

57 lateral axonal projections in both motor and sensory regions of spinal cord.

58 Neurons in dorsal sensory regions of the bat SC responded selectively to e

59 It is generally held that non-primary sensory regions of the brain have a strong impact on fro

60 Sensory regions of the brain integrate environmental cue

61 Does perceptual awareness arise within the sensory regions of the brain or within higher-level regi

62 Prior expectations shape neural responses in sensory regions of the brain, consistent with a Bayesian

63 CPG15 is expressed in sensory regions of the brain, including the visual, audi

64 by synergising cryo-EM with MS, we identify sensory regions of the CSN that mediate its stepwise act

65 its expression is soon restricted to the non-sensory regions of the developing ear.

66 permanent loss of critical cell types in the sensory regions of the inner ear, including hair cells,

67 omatosensory) regions of the nidopallium and sensory regions of the intercollicular nucleus of the mi

68 ub-nuclei but extends only slightly into the sensory regions of the lateral tier.

69 LTP was also reduced in the motor and sensory regions of the neocortex.

70 sensory development in dorsal or lateral non-sensory regions of the otic vesicle.

71 ene expression domain initially includes the sensory regions of the semicircular canals, known as the

72 nd to second- and third-order neurons within sensory regions of the spinal cord on days 5 and 6 p.i.

73 ior knowledge before activity in lower-level sensory regions of the superior temporal gyrus.

74 In the V3 (oral sensory) region of the ganglion, thermoreceptive neurons

75 cortex, located at the junction of multiple sensory regions, projects to several cortical and subcor

76 accompanied by reduced basal connectivity of sensory regions, reduced activation of somatosensory cor

77 ical reinstatement was found in higher-order sensory regions, reflecting reactivation of complex obje

78 ex increases its effective connectivity with sensory regions representing the evidence, is modulated

79 as to its entrainment of ambient rhythms in sensory regions, sensory inflow tends to be rhythmic; th

80 Functional connectivity within the primary sensory regions showed the highest discrimination capabi

81 ibitory receptor transcript levels in caudal sensory regions suggest that abnormalities early in the

82 sults show executive processing in typically sensory regions, suggesting that the development and ult

83 primary sensory neurons and in second-order sensory regions than it is in motor areas of the brain.

84 part of the insula may be an integrated oral sensory region that plays a key role in flavor perceptio

85 separation by (1) resolving interference in sensory regions that project to the hippocampus, thus re

86 ated with a reactivation of some of the same sensory regions that were activated during perception of

87 ee different techniques to investigate how a sensory region, the insula cortex (IC), connects with th

88 es in neuro-biological aging between the two sensory regions, the observed between-modality differenc

89 dynamic circuit between the PPC and earlier sensory regions then enables observers to attend prefere

90 s in the stimulus, respectively) may involve sensory regions to a similar extent.

91 f the S2 cortex as a critical hub connecting sensory regions to higher-order cortical and subcortical

92 eals a nested hierarchy from short events in sensory regions to long events in high-order areas (incl

93 ng processes that engage lateral frontal and sensory regions to successfully encode event features, a

94 ell networks in the stria vascularis and the sensory region toward the maturation of the mammalian co

95 he mouse cochlea, and is not specific to all sensory regions until late otic vesicle stages.

96 Neural priming in early sensory regions was unaffected by left-frontal TMS--a fi

97 eractions that occur in hierarchically early sensory regions where convergent inputs from the auditor

98 tion enters the cortex via modality-specific sensory regions, whereas actions are produced by modalit

99 es on a feedforward flow of information from sensory regions, which is modulated by a feedback drive.

100 This phenomenon differentiates primary sensory regions with high congruence of sex effects and

101 the centrencephalic, paralimbic and unimodal sensory regions, with the specific exclusion of areas wh

102 monstrate that Notch can only induce ectopic sensory regions within a certain time window of developm