ライフサイエンスコーパス: high-pass

1 analysis predicts that sensory processing is high pass.

2 e region-of-interest extraction, followed by high-pass and Sobel filtering for emphasis of low-level

3 tical model to design the high transmission (high pass) and high reflection (low pass) unit cell.

4 Furthermore, a model incorporating the high-pass controller matches animal behavior, whereas th

5 ements of the gating charge should produce a high-pass current noise described by an inverse Lorentzi

6 High-pass digital filtering was also applied to remove t

7 mentally test and model the performance of a High-Pass Electrical Mobility Filter (HP-EMF) that can b

8 arpening increases contrast by combining the high pass filter output with the base image.

9 ncy activity, either by adding an additional high-pass filter (phenomenological) or by incorporating

10 The cell nuclei were segmented using a high-pass filter algorithm, which allowed quantification

11 atory events can be visualized by applying a high-pass filter and increasing the time and amplitude s

12 These movements were passed through a high-pass filter and multiplied by a gain factor before

13 ctical experiments on the four-op-amp biquad high-pass filter circuit show that this model outperform

14 band-pass filter circuit, four-op-amp biquad high-pass filter circuit, and Tow-Thomas filter circuit

15 EEG systems necessarily include a high-pass filter early in the measurement chain to remov

16 ork would function as a spatial and temporal high-pass filter for excitatory inputs.

17 According to computational modeling, the high-pass filter implemented by K(V)1 channels matches t

18 s led to the hypothesis that nAChRs act as a high-pass filter in the dopaminergic microcircuit.

19 ransducer adaptation accounts for a variable high-pass filter observed in the acoustic tuning curve.

20 tion of closely related odors, by imposing a high-pass filter on transmitter release from ePN termina

21 tatory hippocampal synapses, STP serves as a high-pass filter optimized for the transmission of infor

22 ctance, thereby primarily accounting for its high-pass filter properties.

23 Synchrony thus allows the CbN to high-pass filter Purkinje inputs, facilitating sensory-e

24 lz absorbers turning the swim bladder into a high-pass filter responsible for the absence of low freq

25 inhibition is more accurately described as a high-pass filter than as a simple inhibition, and that t

26 KCa3.1 channels thus contribute to a high-pass filter that allows Purkinje cells to respond p

27 ions, but feedforward inhibition generates a high-pass filter that only transmits the initial activat

28 The interlayer transition zone acts as a high-pass filter that preferentially reflects low-freque

29 network of passive components that acts as a high-pass filter to distort and attenuate the signal tha

30 cluded that a single glomerulus may act as a high-pass filter to enhance stimulus contrast through me

31 nclude that a single glomerulus may act as a high-pass filter to enhance the contrast between differe

32 The ANF spike generator adds a high-pass filter via its depolarization-rate threshold t

33 This high-pass filter, built in to the mammalian amplifier, a

34 dynamic spike threshold that functions as a high-pass filter, enhancing spike timing in response to

35 ion balance in a manner that would support a high-pass filter, including glial glutamate transporters

36 tation/inhibition balance that can support a high-pass filter, shifting from unfavourable to favourab

37 es due to synaptic facilitation, producing a high-pass filter.

38 re transient, an effect similar to that of a high-pass filter.

39 th decreasing frequency, characteristic of a high-pass filter.

40 This current functions as a high-pass filter.

41 ntral phase advance mechanisms behave like a high-pass filter.

42 arization because K(V)1 channels implement a high-pass filter.

43 he olfactory bulb are proposed to mediate a 'high-pass' filter at a single glomerulus that selectivel

44 are proposed to mediate an intraglomerular 'high-pass' filter through inhibition targeted onto a glo

45 d that cerebral autoregulation behaves as a 'high-pass' filter, recommended frequency bands have been

46 High-pass filtered data show strong correlations with dy

47 t show that the low frequency component of a high-pass filtered signal can be restored by deconvoluti

48 norm minus one [ENMO], Euclidian norm of the high-pass filtered signals [HFEN], and HFEN plus Euclide

49 iltered telephone speech (300-3,400 Hz, BP), high-pass filtered speech (f > 300 Hz, HP, i.e., distort

50 These observations demonstrate strong high pass filtering and modest bandpass filtering capabi

51 In addition, we demonstrate that high-pass filtering (200 Hz) of cyclic voltammograms rec

52 data, we showed that, with the exceptions of high-pass filtering and bad channel interpolation, autom

53 ough the network contributed to the observed high-pass filtering but not to the low-pass filtering.

54 Also, high-pass filtering discriminated against ascorbic acid,

55 benefit of this method is to avoid error of high-pass filtering methods which systematically under-r

56 cells to test a number of predictions of the high-pass filtering model.

57 High-pass filtering of dendritic plateaus by axonal K(+)

58 fMRI maps are retrieved through low-pass and high-pass filtering of frequency-demodulated signals.

59 es previously reported but poorly understood high-pass filtering seen in electrosensory afferents and

60 w-frequency signals, whereas I(M) implements high-pass filtering that improves spike-time coding of h

61 Instead, it is countered by high-pass filtering that is intrinsic to the mammal's el

62 pipeline performed significantly better than high-pass filtering the data.

63 mental effects were found to be mitigated by high-pass filtering to select photoacoustic signal compo

64 The model performs high-pass filtering with frequency-dependent time consta

65 (trough-to-peak approximately 350 mus after high-pass filtering), suggesting that these cells have t

66 of basilar membrane displacement modified by high-pass filtering, indicating that only relatively min

67 ns optimally encoded natural stimuli through high-pass filtering, thereby implementing temporal white

68 is, gain adaptation, spectral whitening, and high-pass filtering-predicted trajectories show poor fit

69 owever, these neurons showed low-, band-, or high-pass filtering.

70 luctuations, and be sharpened by presynaptic high-pass filtering.

71 NM cells act as high-pass filters by responding only to discrete synapti

72 s exhibiting such NMDAR-BK coupling serve as high-pass filters for incoming synaptic inputs, precludi

73 between processes that give rise to low- and high-pass filters generate the observed resonance.

74 ganglion cells, where they serve as low- and high-pass filters, respectively, of EPSPs.

75 ration impaired the ability to distinguish a high-pass harmonic sound from noise.

76 The design of optimal FIR low pass (LP), high pass (HP), and band stop (BS) filters is achieved b

77 male and male human observers viewed low- or high-passed images of round or elongated animals and too

78 Vanishing optotypes (VOs) are pseudo high-pass letters whose mean luminance matches the backg

79 that a low-pass behavior is controlled by a high-pass neural filter nevertheless matches previously

80 g: low-pass neurons tuned to long intervals, high-pass neurons tuned to short intervals, and bandpass

81 ECG and myopotential, it is possible to use high-pass or band-pass filtering to specifically isolate

82 l of calyx afferents and contribute to their high-pass properties.

83 nded because of too few eligible patients or high pass rates with little variation.

84 equency-doubling technology perimetry (FDT), high-pass resolution perimetry (HPRP), and standard auto

85 those neurons exhibiting either low-pass or high-pass response functions.

86 ray of animals, these data suggest that such high-pass sensory filters may be a general mechanism use

87 Outside the fovea, high-pass VOs display significant differences in their d

88 locity microbubble echoes are removed during high pass wall filtering.