ライフサイエンスコーパス: low-amplitude

1 not oscillate or possibly oscillated with a low amplitude.

2 nerated from micro seismicity have extremely low amplitude.

3 of pp4 results in short period rhythms with low amplitude.

4 ation were observed to have long periods but low amplitudes.

5 pecially problematic in detecting peaks with low amplitudes.

6 One-megahertz low-amplitude (0.18 MPa) continuous wave ultrasound dire

7 activation (82+/-18 versus 37+/-11 ms); (3) low-amplitude (0.47+/-0.16 versus 3.74+/-1.60 mV) and fr

8 It has been found that low-amplitude (+/-1 V) square wave excitation can prolon

9 ltammetry, while a high-frequency (100 kHz), low-amplitude (10 mV rms) sine wave was added to the vol

10 n stiffness by up to 90% when subjected to a low-amplitude (5%), repetitive (dynamic) compression.

11 At each step, a low-amplitude (6 cm H2O) sinusoidal signal was alternate

12 regular initiation, aberrant conduction, and low amplitude activity could contribute to the pathogene

13 tiated in dendritic layers associated with a low amplitude "afterdischarge termination oscillation" (

14 f the beta-barrel as a collective rocking of low amplitude and of hundreds of nanoseconds time scale.

15 ereas others expressed a diurnal rhythm with low amplitude and significant activity during the day.

16 However, when capillaries are not present, low amplitudes and high set points produce images with p

17 ght, but the WS2 appeared inverted except at low amplitudes and high set points.

18 frq protein and mRNA are low, resulting in a low-amplitude and long-period oscillation of the clock.

19 higher frequencies, short inspiratory times, low amplitudes, and low mean airway pressures for healin

20 GB3, all three observables reflect the same low-amplitude anisotropic motions arising from fluctuati

21 orate the bilayers, followed by a prolonged, low-amplitude ( approximately 65 mV) voltage clamp to mo

22 ck-responsive element sufficient to confer a low-amplitude (approximately 2-fold) circadian oscillati

23 The region of low amplitude between the aorta and left ventricle, whic

24 /-35 ms), giving rise to broad and sometimes low-amplitude bifurcated T waves and an increased transm

25 olypeptide isolated from SDS-PAGE displays a low-amplitude broad spectrum with a peak at 553 nm, simi

26 n amplitude of 3 N to simulate exercise; (2) low amplitude, broad frequency vibration with frequency

27 A low-amplitude, broad-duration (40-50 ms) central peak of

28 ructed into a rhythmogenic process producing low amplitude burstlets and preinspiratory activity that

29 We characterized the disrupted locus of the low amplitude but still rhythmic mutant (M16) as the rpo

30 the post-wave Ca2+ increase, and during the low-amplitude Ca2+ responses evoked by threshold histami

31 Directly imposing high- or low-amplitude Ca2+ signals with an extracellular gradien

32 ast, phorbol 12-myristate 13-acetate induced low amplitude calcium oscillations, slower translocation

33 low binding capacity that transduced only a low amplitude calcium signal, suggesting the involvement

34 ptors that had normal binding but transduced low amplitude calcium signals, while other mutations in

35 ons demonstrate that only bats emitting such low-amplitude calls hear moth echoes before their calls

36 Low amplitude circadian oscillations in the molecular ci

37 admission, mechanical ventilation and absent/low amplitude compound muscle action potentials.

38 ross different catalogs and is of remarkably low amplitude, consistent with an effective Omega approx

39 Yet, low-amplitude currents at similar frequencies have been

40 se to photoperiod is observed, and this very low amplitude cycling of some phytochrome proteins is ou

41 ation of extrasynaptic NMDARs, produced only low-amplitude cytoplasmic Ca(2+) spikes and modest, nond

42 each precordial lead as the total number of low-amplitude deflections that deviated from their respe

43 ion potentials, but we found no evidence for low-amplitude dendritic spikes that have been reported f

44 The first stage consists of a sustained, low-amplitude depolarization (plateau activity) lasting

45 tate, whereas Gprk2 mutants produce constant low-amplitude EAG responses.

46 imb tonic rigidity and posttonic clonus; (6) low-amplitude EEG during postictal depression.

47 ized high-frequency stimulation (LHFS) using low-amplitude electric pulses instituted within a formed

48 of which were immediately followed by brief, low-amplitude electrical stimulation to the amygdala.

49 Both frontal and parietal TMS elicited a low-amplitude electroencephalographic (EEG) slow wave co

50 (r=0.64, P<0.0001), many isthmuses had very low-amplitude electrograms, and EUS could not be identif

51 cally blind from birth with nonrecordable or low-amplitude ERGs.

52 Detection of low-amplitude events is critical to survival; for exampl

53 can be excited for fields ranging between a low amplitude excitation threshold and a high amplitude

54 When low-amplitude excitatory postsynaptic potentials (EPSPs)

55 ve largely been distinguished into two types-low amplitude fast oscillations (LAF), or high amplitude

56 oteins exhibited a minor contribution from a low-amplitude fast decay, consistent with local motion o

57 here vole dynamics shifted from a high- to a low-amplitude fluctuation regime in the mid-1990s.

58 LA AFL circuits had either flat or low-amplitude forces in the inferior leads.

59 The termination of low-amplitude fractionated activity in the PVs preceded

60 in constant darkness, the dKO mice exhibited low-amplitude, fragmented rhythms and attenuated light r

61 The focal ERG showed signals of borderline low amplitude from the fovea with the multifocal ERG, th

62 As a practical matter, low-amplitude, genome-wide oscillations, a ubiquitous bu

63 oad with rest periods and may be promoted by low-amplitude high-frequency stimuli.

64 lectroencephalogram (EEG) recordings display low-amplitude, high-frequency fluctuations.

65 topic exchange mechanism involving localized low-amplitude, high-frequency motions that do not requir

66 putational studies suggested that additional low-amplitude, high-frequency oscillations were also pos

67 eflex effects on inspiratory motor output of low-amplitude, high-frequency pressure oscillations (HFP

68 system to an ecologically relevant range of low-amplitude, high-frequency stimuli.

69 egular and fast spiking units) by presenting low-amplitude, high-frequency vibrissa stimulation.

70 Low-amplitude hyperpolarizing potentials were recorded i

71 Low-amplitude ICMS at different PM locations thus evokes

72 nocturnal switch in myometrial activity from low amplitude, infrequent contractures to high amplitude

73 rat resulted in robust apneusis (lengthened low amplitude inspiration due to loss of post-inspirator

74 Age was mainly correlated with the low-amplitude introduction and build-up phases, dominanc

75 in all four phases, but most strongly in the low-amplitude introduction and high-amplitude climax pha

76 it and impaired contralateral pursuit, (2) a low-amplitude ipsilesional right-beating nystagmus witho

77 scillations of KaiC phosphorylation, whereas low-amplitude KaiC phosphorylation rhythms persist in th

78 (reflecting activity of the caller) with the low-amplitude let-down phase.

79 owing Gaboxadol exposure is characterized by low-amplitude LFPs, during which dFB-induced effects are

80 the MOD-1 receptor in AIY neurons to promote low-amplitude locomotor behavior characteristic of well

81 Depletion of TRAP150 caused low-amplitude, long-period rhythms, identifying it as a

82 enuinely in a straight conformation or was a low-amplitude, long-wavelength helix.

83 As the CaM C lobe sites are populated by low amplitude/low frequency (global) Ca2+ signals, but o

84 During the SII acquisition, a low-amplitude mechanical vibration is applied to the hea

85 such as fixational drift, smooth pursuit and low-amplitude mechanical vibrations of the eyes.

86 cluding depolarization block and depolarized low amplitude membrane oscillations (DLAMOs), have been

87 no membrane activity or display depolarised low-amplitude membrane oscillations, to neurones that we

88 scale, whereas those in Switch II experience low-amplitude motion on the nanosecond time scale and ch

89 trometry, were used to locate differences in low-amplitude motion when SH2 was bound to the peptide.

90 xperimental investigation of these harmonic, low-amplitude motions, however, has proven challenging.

91 Low amplitude muscle vibration (0.5 ms; 80 Hz; duration

92 one short period (22 h) mutant (M2) and two low amplitude mutants, one of which showed apparent arhy

93 Among low-amplitude mutants, one mutant, tnp6, had an insertio

94 ectrocochleography (ECochG) showed prolonged low amplitude negative potentials without auditory nerve

95 ed chloride current (ICl(Ca)) and sustained, low amplitude non-selective cation current (ICat).

96 s, trpv1(-/-) mice had a higher frequency of low-amplitude, non-voiding bladder contractions.

97 ictable component of the QRS and manifest as low-amplitude notches and slurs.

98 weak currents are remarkable considering the low amplitude of the electric fields acting on the brain

99 The low amplitude of water signatures could be explained by

100 , and the existing sic-1 mutant both exhibit low-amplitude or arrhythmic expression of core circadian

101 mutations of these sites show short period, low amplitude, or arrhythmic conidiation rhythms in cons

102 hase with cycles in Per1 and Per2; there was low-amplitude oscillation of Cry1 and Cry2.

103 mutant flies manifest high trough values and low amplitude oscillations.

104 l deletion, displays increased stability and low-amplitude oscillations, consistent with previous rep

105 s: an initial postmitotic pulse, followed by low-amplitude oscillations.

106 (nRT) play a critical role in generation of low-amplitude oscillatory bursting involving mutually in

107 ese results demonstrate that high-frequency, low-amplitude oscillatory pressure waves in the UA, simi

108 The 2:1 ventricular conduction and low-amplitude P waves challenged the diagnosis of 4 of 2

109 nt decreasing-velocity or linear drift and a low-amplitude periodic oscillation.

110 ations between small earthquakes and ongoing low-amplitude periodic stresses indicate increased fault

111 A low-amplitude phase, detected in concurrence with the ma

112 During eupnoeic activity, low-amplitude post-inspiratory (post-I) discharge was on

113 he core of the reentry registered no or very low amplitude potentials.

114 >/=114 ms; root mean square 40 <20 muV, and low-amplitude potentials 40 >38 ms) were defined as havi

115 se include internal electric field-dependent low-amplitude protein motions and the reorganization of

116 sional electroanatomic voltage maps revealed low-amplitude regions in the inferior or posterior left

117 ) for high amplitudes, but failed to predict low amplitude responses.

118 Low-amplitude responses were influenced by both starting

119 anifested within the inter-spike interval as low amplitude rhythmic oscillations in the 4-12 Hz frequ

120 cadian rhythms, others have irregular and/or low-amplitude rhythms.

121 pecies adapted to high mean temperatures and low-amplitude seasonal fluctuations; an increase in seas

122 strategic imposition of a high-frequency and low-amplitude shear perturbation orthogonal to the prima

123 was obtained and analyzed for fQRS duration, low amplitude signal duration<40 mV (LAS40), and root-me

124 h the cochlea also uses resonance to amplify low-amplitude signals and to generate a spatial map of f

125 of this molecular network; amplification of low-amplitude signals by hair bundles seems to be univer

126 ECGI noninvasively imaged the low-amplitude signals of AF in a wide range of patients

127 ithin scar characterized by fractionated and low-amplitude signals usually occurring late during sinu

128 Increasing intervals of low-amplitude small herbivore population fluctuations ar

129 aveform from sharp, high-amplitude to broad, low-amplitude spikes.

130 sway dependence was most apparent when using low amplitude stiffness-measuring perturbations, and the

131 his study, the first to our knowledge to use low-amplitude stimulation of LDT in freely moving cats,

132 Five hours of chronic low-amplitude stimulation of the LDT induced a highly si

133 ally, we demonstrate that the application of low-amplitude stimuli can entrain bundle motility either

134 es two types of energy waves: high-frequency low-amplitude stress waves and long-duration low-frequen

135 sphorylation of ERK1/2, while high-, but not low-, amplitude stretch caused phosphorylation of JNKs.

136 These results indicate that low-amplitude, subthreshold current pulses are sufficien

137 that preceded particle uptake followed by a low amplitude sustained calcium increase.

138 Prolonged low-amplitude synaptic currents in biopsied anconeus mus

139 rome (CMS) associated with rapidly decaying, low-amplitude synaptic currents, and trace its cause to

140 Among control animals, some low-amplitude T(b) rhythms during torpor were driven by

141 inger as in (a) whilst performing self paced low amplitude tapping of the (i) index finger, (ii) thum

142 e circadian mechanism in Neurospora, we used low-amplitude temperature cycles to compare WT and frq-n

143 ased on the ecology of nematodes, we applied low-amplitude temperature cycles to synchronize populati

144 required for behavioural synchronization to low-amplitude temperature cycles.

145 e by performing frequent relocation jumps of low amplitude that seem unrelated to localized hydrodyna

146 heir IN was converted to waveforms with very low amplitudes that yielded higher NAFX values and allow

147 0 Hz), rather than the low-frequency (2 Hz), low-amplitude, tonic GABAergic drive common to wild-type

148 seismic instruments often record coincident low-amplitude tremor in a narrow (1-5 cycles per second)

149 g) as compared with wild-type mice that have low amplitude (Type 1) phase resetting.

150 The anomaly, which consists of low-amplitude variance in obliquity (a node) and a minim

151 tested by applying short (1.5 s) periods of low amplitude vibration to single intrinsic hand muscles

152 We applied low-amplitude vibration to the abductor pollicis brevis

153 onfined, high-restitution grains, subject to low-amplitude vibration, can serve as experimentally-acc