ライフサイエンスコーパス: reverberation

1 flect persistence of an active memory (i.e., reverberation).

2 well as indirectly via reflections known as reverberation.

3 ed by statistical regularities of real-world reverberation.

4 ) depth and distance-dependent loss of AM in reverberation.

5 an, additive white and pink (1/f) noise, and reverberation.

6 eld potentials, indicative of local synaptic reverberation.

7 processing pathway for sound localization in reverberation.

8 ism for improving directional sensitivity in reverberation.

9 tion is severely degraded in the presence of reverberation.

10 vironment, constrained by a prior on natural reverberation.

11 y transmission with bicuculline enhanced the reverberation.

12 acellular stores also modulated the level of reverberation.

13 release by strontium substantially enhanced reverberation.

14 l role in the emergent phenomenon of network reverberation.

15 in recurrently connected networks as active reverberation.

16 are complicated by post-shock annealing and reverberations.

17 of the activity patterns through hundreds of reverberations.

18 usly, and that the existence of long-lasting reverberation after a novel experience requires addition

19 sis to explain these observations is seismic reverberation after impact events.

20 Increased reverberation also reduced SRM in all listening conditio

21 to the vowel /i/ in four different levels of reverberation and analyzed based on their spectro-tempor

22 s are often decorrelated between the ears by reverberation and background noise, degrading the fideli

23 gs are interpreted in the context of network reverberations and self-sustained activity in neural sys

24 al location in two room conditions (low/high reverberation) and identified target speech in the prese

25 ction between hearing loss, hearing aid use, reverberation, and performance in auditory selective att

26 evolutionary dynamics of HGT and its genetic reverberations, and recommend careful examination of bac

27 e effective than single pulses in triggering reverberation, apparently by eliciting higher levels of

28 he actual cellular processes underlying such reverberation are not well understood.

29 e in IED secondary afterdischarges and their reverberation between CA3a and CA3c, and (3) shift in th

30 e signals, but their abilities degraded when reverberation characteristics deviated from those of rea

31 However, in quiet and across nearly all reverberation conditions, musicians showed more robust r

32 Such wave-mediated reverberation could contribute to short-term memory and

33 Thus, oscillatory reverberations create something out of nothing: A third

34 ience-dependent effect, is more resistant to reverberation degradation which may explain their enhanc

35 Although reverberation degraded both rate and temporal coding of

36 We find that reverberation degrades the directional sensitivity of si

37 sensory processing such as an intracortical reverberation during the processing of visual stimuli.

38 Reverberation encountered in everyday environments can s

39 discriminated only if the monaural sound in reverberation had AM.

40 For both groups, reverberation had little effect on the neural encoding o

41 ntal and modeling work has begun to test the reverberation hypothesis at the cellular level.

42 an psychophysical pitch-discrimination task, reverberation impaired the ability to distinguish a high

43 een hypothesized to be sustained by synaptic reverberation in a recurrent circuit.

44 es are available, directional sensitivity in reverberation is comparable throughout the tonotopic axi

45 erious problem; stability can be achieved if reverberation is largely mediated by NMDA receptors at r

46 ation can be achieved robustly if excitatory reverberation is primarily mediated by NMDA receptors; o

47 t iron L emission has enabled us to detect a reverberation lag of about 30 s between the direct X-ray

48 ing conditions including each combination of reverberation level (T60=0, 270, and 540 ms), number of

49 ole mass measurements based on emission line reverberation mapping can be calibrated against other dy

50 a corresponding correction to emission line reverberation masses of black holes if they are calibrat

51 Further, reverberation of past evoked states in spontaneous spiki

52 arly afterglow emission can be understood as reverberation of the energy input measured by prompt emi

53 pontaneous spiking activity shows detectable reverberation of the movie-evoked responses.

54 er, long-lasting (up to approximately 48 h) "reverberation" of neural activity patterns induced by a

55 des resilience to the degradative effects of reverberation on subcortical representations of pitch an

56 We investigated the effects of reverberation on the directional sensitivity of single n

57 To assess the effect of reverberation on the neural coding of amplitude envelope

58 g of amplitude envelope relatively robust in reverberation: one general mechanism operating for all s

59 tions (e.g., interaural decorrelation due to reverberation), or, in humans, bilateral clinical device

60 Reverberation profoundly distorts the sound from a sourc

61 er cent of its current age, so GRB afterglow reverberations provide clues about the environments arou

62 s degradation increases with both increasing reverberation strength and channel bandwidth.

63 e maintain better directional sensitivity in reverberation than high-CF cells sensitive to ITDs in th

64 Measurements of the early afterglow reverberations therefore probe the structure of the envi

65 ulation method allowing precise control over reverberation times and sound-source locations.

66 The observed reverberation timescale is comparable to the light-cross

67 we did not observe significant long-lasting reverberation using either the template matching or the

68 The reverberation was likely to arise from recurrent excitat

69 ng asynchronous release by EGTA-AM abolished reverberation, whereas elevating asynchronous release by

70 Models of persistent activity often invoke reverberations within local cortical circuits, but long-