ライフサイエンスコーパス: sensory region

1 itrary and complex acoustic patterns, within sensory regions.

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

3 h retinotopic activity in lower level visual sensory regions.

4 >80% persisting over a 3 week period in all sensory regions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 Sensory regions of neocortex are organized as arrays of

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

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

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

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

34 Sensory regions of the brain integrate environmental cue

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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