ライフサイエンスコーパス: phase delay

1 ) or exhibit slowed membrane repolarization (phase delay).

2 ions of chemotherapy agents that impose an S-phase delay.

3 les arrest with damaged chromosomes and an S phase delay.

4 f Xe-Wee1 is required for the Mos-mediated M-phase delay.

5 metamaterial bricks-each encoding a specific phase delay.

6 t Xe-Wee1 is required for the Mos-mediated M-phase delay.

7 ignalling elements that contribute solely to phase delay.

8 caffeine could be mediated via override of S-phase delay.

9 e Arabidopsis gene EID1 is responsible for a phase delay.

10 protein in centrosome reduplication during S-phase delay.

11 inein distribution is not dependent on the S-phase delay.

12 rmined through an error function of THz wave phase-delay.

13 thereby minimizing imaging distortions from phase delays.

14 ls and impaired sensitivity in light induced phase delays.

15 n (P<0.05) in the magnitude of light-induced phase delays.

16 mpletely blocked the effect of CHA on photic phase delays.

17 iotic divisions in response to pre-meiotic S-phase delays.

18 es both daytime phase advances and nighttime phase delays.

19 ircadian periods were associated with larger phase delays.

20 s by 55%, but had no effect on light-induced phase delays.

21 , but not the magnitude of 8-OH-DPAT-induced phase-delays.

22 the baclofen-induced phase-advances than the phase-delays.

23 essure, while activity of Bar(Crh/Vglut2) is phase delayed.

24 resulted in a phase advance (3 x 21 h) and a phase delay (3 x 27 h) compared with during a 24-h cycle

25 se at ZT11, 1 h before lights off, induced a phase delay (62.1 +/- 21.1 min; P = 0.0003).

26 Accounting for phase delays across voxels further improved detection, d

27 e linear regression of light exposure during phase delay/advance portions of the phase response curve

28 d 48 h; diagnostic CT at 24 h using a triple-phase delay after administration of contrast; and diagno

29 Phase delays after a light pulse given during the mid-su

30 larger phase shifts, but were more likely to phase-delay after the 9-hour advance (to phase shift in

31 data, including trajectory measurements and phase delay analyses, to estimate these parameters under

32 Adjustable zero-phase delay and equiphase control are demonstrated in si

33 1st at ZT 7 and a 2nd at ZT 12, i.e., a 6 h phase delay and hence twice the delay obtained after a s

34 ctivity rhythm in a dose-dependent manner at phase delay and phase advance time points.

35 rest-activity rhythms that are significantly phase delayed and more poorly entrained to the 24-hour d

36 wever, significantly inhibited light-induced phase delays and advances in a manner similar to that pr

37 Both phase delays and advances induced by NMDA were blocked b

38 Phase delays and advances were observed during early and

39 Histamine injections resulted in light-like phase delays and advances, indicating that the neurotran

40 In this study, we focused on phase delays and assayed TIM degradation within individu

41 stigate this possibility, we compared photic phase delays and Fos-like immunoreactivity in mice which

42 caffeine treatment potentiated light-induced phase delays and phase advances in response to a 30 min

43 K252a blocked or strongly inhibited both the phase-delaying and -advancing effects of light during th

44 tive night, resulting in augmentation of the phase-delaying and -advancing effects of light.

45 e ability of the NK1 antagonist to block the phase-delaying and/or the phase-advancing effects of lig

46 cone modulation sensitivities, M- and L-cone phase delays, and flicker spectral sensitivities under t

47 gradation within s-LNvs is not necessary for phase delays, and similar assays in other genotypes indi

48 cone modulation sensitivities, M- and L-cone phase delays, and spectral sensitivities as a function o

49 The S phase delay appears to be due to the stalling and collap

50 trough Bmal1 expression induced significant phase delays (applied at peak: 27.2 +/- 10.2 min; P = 0.

51 r to posterior direction with intersegmental phase delays appropriate for crawling.

52 lower decay of dusk components, and a slight phase delay at the next dawn, possibly due to abrogated

53 e SCN of Syrian hamsters induced significant phase delays at circadian time (CT) 13.5 and phase advan

54 tinct time-dependent interactions, enhancing phase delays at early night but abolishing phase advance

55 The phase delay between a point heat source and a set of det

56 On a finer timescale, the phase delay between intracellular and extracellular ripp

57 cell recordings, systematically altering the phase delay between two groups of periodic simulated inp

58 tion (early blockade) or the immune effector phase (delayed blockade).

59 We show these mice exhibit phase delayed body temperature and locomotor activity wi

60 udy of the duration-response relationship to phase-delaying bright light.

61 eas cantharidin and calyculin A caused large phase delays but no persistent effect on period.

62 nocking down Cdk5 in the SCN of mice affects phase delays but not phase advances.

63 The conferred rhythms in NIH/3T3 cells were phase delayed by 4-12 hr relative to SCN2.2 circadian pa

64 Patients with SAD were phase delayed by 50 minutes for the entire period (P = .

65 WAY162720 (10 mg/kg) inhibited light-induced phase delays by nearly 75%, but had no effect on light-i

66 re maintained on a light/dark cycle that was phase-delayed by 9 hr.

67 -14 while a GABA(B) antagonist increased the phase delays caused by light.

68 Furthermore, light pulses known to induce phase delays caused significant elevation in mTim mRNA.

69 and Dbp mRNAs in liver exhibit a significant phase delay compared with control.

70 s did not significantly affect light-induced phase delays compared to mice treated with gold-thiogluc

71 2D materials can offer only a small optical phase delay - consequence of the atomic thickness.

72 ogenous application of little SAAS induces a phase delay consistent with light-mediated cues regulati

73 locked to cortical ripples during NREM, with phase delays consistent with ripple generation through p

74 Moreover, EIS phase delay correlated with anatomic markers of plaque b

75 SMRTER by RNAi is sufficient to cause a G(2) phase delay, demonstrating that regulation of SMRTER pro

76 adian misalignment, either phase advanced or phase delayed, did not result in any changes in appetite

77 ascertain whether rest-activity rhythms were phase delayed, diminished in amplitude, or more poorly e

78 Further, phase delay discriminated severe stenosis (>=70%) with a

79 t the same frequency and amplitude, but with phase delays distributed across the array.

80 A frequent observation is a sleep onset phase delay during winter.

81 effect on the magnitude of muscimol-induced phase delays during the daytime.

82 ycin led to a significant attenuation of the phase-delaying effect of early-night light.

83 ection of a GABA(B) agonist also reduced the phase-delaying effects of light at CT 13.5-14 while a GA

84 ate that humans are highly responsive to the phase-delaying effects of light during the early biologi

85 are consistent for a role of oxytocin in the phase-delaying effects of light on circadian activity rh

86 A frequency-dependent phase delay enables spectral shaping for filtering, rout

87 ayed maturation of heterochromatin during G1-phase delays establishment of a silent chromatin state.

88 Larger phase delays, facilitated by longer circadian periods, r

89 ll cycle, namely, G1 arrest with MD and an S phase delay followed by a G2/M arrest with HP.

90 ting cells in mitosis, while Vpr causes a G2 phase delay followed by endoreplication and reversion of

91 Phase delays following photic stimulation were reduced i

92 e light input is redundant to CRY; 3-h light phase delays (Friday) followed by 3-h light phase advanc

93 shed for aMT6 onset and acrophase with large phase delays from 7:00 pm to 10:00 pm and large phase ad

94 gs in the glaucoma group, habitual IOP curve phase delay, habitual IOP variation, diurnal-to-nocturna

95 and, at microwave frequencies, the inertial phase delay has been buried under electron scattering.

96 ype C is associated with a prolonged viremic phase, delayed hepatitis B e antigen (HBeAg) seroconvers

97 wth, cold sensitivity, and a pronounced G2/M phase delay, implicating overlapping roles for Rad23 and

98 2 receptor agonist, blocked the NMDA-induced phase delay in a similar manner as NPY.

99 The 12-hr cold pulse caused a 4-hr phase delay in both rhythms, whereas the 20-hr cold puls

100 eas the 20-hr cold pulse resulted in a 12-hr phase delay in both rhythms.

101 with a shorter period, larger amplitude, and phase delay in females as compared to males.

102 we found that far-red enrichment generated a phase delay in GI expression and enhanced CO expression

103 the discrete nanorings, we measured negative phase delay in our composite 'chess metamaterial'.

104 that these effects are all attributable to a phase delay in the core molecular clockwork.

105 hose of controls (p = 0.0032) and a one-hour phase delay in the timing of maximum cortisol levels (p

106 Phase delay in this mutant on DD1 was exacerbated in the

107 Cortisol rhythms were significantly phase delayed in the ADHD group.

108 inistered intracerebroventricularly, induced phase delays in behavioral circadian rhythms and SCN act

109 nistered in the early night, they both evoke phase delays in behavioral rhythms.

110 n the SCN and severely dampens light-induced phase delays in behavioral rhythms.

111 In developing larvae, extended M-phase delays in late-dividing cell lineages were associa

112 Analogous mitotic defects cause M phase delays in mitotic germline proliferation.

113 f wild-type mice, whereas it produced 50-min phase delays in the circadian behavior of Clock/+ mice.

114 plied during the mid-subjective night induce phase delays in the circadian rhythm of locomotor activi

115 pplied in the early subjective night induced phase delays in the time of peak firing, whereas doses i

116 creased nocturnal activity and a significant phase-delay in their rhythms of core-body temperature an

117 escence rhythm during the subjective day and phase-delays in the late subjective night.

118 s manifest in both field potential and, with phase delay, in excitatory synaptic inputs to fast spiki

119 Additionally, we show that phase-delayed inhibition creates a synchrony filter that

120 where stimuli are encoded through synchrony, phase-delayed inhibition enables the creation of a decod

121 iring a more elaborate network architecture, phase-delayed inhibition has been observed in multiple s

122 We show that phase-delayed inhibition is capable of creating a synchr

123 approach to investigate the efficacy of the phase-delayed inhibition motif in detecting synchronized

124 neuron with a high spike threshold, or (2) a phase-delayed inhibition network motif.

125 ous input spikes (absolute synchrony), while phase-delayed inhibition requires a fixed fraction of in

126 a high spike threshold or by a decoder using phase-delayed inhibition.

127 EIS with phase delay integrates key atherosclerosis features that

128 The phase delay is also reproduced in the cognate SSTR1 rece

129 histones H3 and H4, suggesting that the G(2) phase delay is due not to global changes in genome integ

130 For 16-kHz tones, the phase delay is up to 6pi radians over the observed cochl

131 adian misalignment, either phase advanced or phase delayed, is a concomitant disturbance of the gluco

132 ore antidepressant than evening light, which phase-delayed it.

133 :D cycle (L:D), constant dark (DD), or a 6-h phase-delayed L:D cycle (pdL:D) were treated with Estrad

134 early gene c-Fos in the SCN in response to a phase-delaying light pulse.

135 his study suggests caution when interpreting phase delay measurements as continuously propagating wav

136 Phase-delayed misalignment increased rapid eye movement

137 circumvents prior limitations caused by the phase-delay mismatch in conventional systems and relaxes

138 They superimpose waves with a mutual phase delay, modifying light intensity.

139 The late S-phase delay, noted at 8 h following irradiation, and a r

140 Phase delays occurred when the light stimulus was centre

141 rhythms and that sundowning is related to a phase delay of body temperature caused by Alzheimer's di

142 tivated outward conductance in OFF-UBCs, the phase delay of ON UBCs is caused by a late rebound curre

143 of CH-275, an SSTR1 agonist, normalizes the phase delay of the circadian clock in SST-deficient mice

144 ugh ryanodine receptors in the light-induced phase delay of the circadian clock restricted to the ear

145 heir circadian clocks shifted after a 9 hour phase delay of the light/dark, sleep/wake and meal sched

146 blished to describe the relationship between phase delay of the received THz wave and the plane stres

147 h a time-varying voltage and quantifying the phase delay of the resulting current.

148 We show that 2 wk of DLE induces a phase delay of ~2 to 3 h in mice, comparable to that rep

149 tribute to light-induced phase advancing and phase delaying of the clock.

150 Maximum phase delays of 2.2 +/- 0.3 hr were obtained at CT 14, a

151 Average phase delays of 26.4 ms for the EEG --> EMG direction an

152 t pulses of 30, 100, 300 or 1000 lux induced phase delays of circadian activity rhythms of similar ma

153 deprivation in the early rest period induces phase delays of circadian locomotor activity rhythm.

154 lses administered in the early night induced phase delays of circadian rhythms which were attenuated

155 Furthermore, pupil reflex, light-induced phase delays of the circadian clock and period lengtheni

156 specific to phase advances as light-induced phase delays of the circadian pacemaker achieved early i

157 Light exposure in the early night induces phase delays of the circadian rhythm in melatonin in hum

158 The phase delays of the coherent alpha oscillations match th

159 orrelations, with time delays that match the phase delays of the coherent oscillations.

160 Period2 accompanied both phase advances and phase delays of the RPE-choroid clock, thus suggesting t

161 tamate- and optic chiasm stimulation-induced phase delays of the SCN circadian neuronal activity rhyt

162 Unlike light, which can phase delay or advance the central pacemaker, stressors

163 inhibiting Cdc2 activation and causing a G2 phase delay or arrest.

164 n the morning or afternoon/evening to induce phase delays or phase advances, respectively, without ca

165 N infusion of BDNF did not potentiate either phase-delaying or phase-advancing effects of light on th

166 001); increased absolute range of conduction phase delay (P<0.001 and P<0.001); increased conduction

167 sc) increased the magnitude of light-induced phase delays (P<0.01) and c-fos mRNA expression in the p

168 to cell-cycle alterations associated with S-phase delay, perturbed DNA replication, and activation o

169 Coincident with hydroxyurea-induced S-phase delay, Pol eta-deficient cells undergo more replic

170 The phase delay portion peaks about 11 h after the dim light

171 Neither GABA(B) drug altered the phase delays produced by microinjection of a peptide coc

172 s critical, however, because constitutive or phase-delayed promoters failed to sustain coherent rhyth

173 nt regions within a myocyte alternate out of phase, delayed propagating Ca(2+) waves develop at their

174 ts daily cycling expression but with a novel phase, delayed relative to those of the better-character

175 consistent with ITD being remodeled toward a phase delay representation along the forebrain pathway.

176 ITDs in low-frequency channels, resembling a phase delay representation.

177 fter light exposure, however, the behavioral phase-delay response and the expression of light-induced

178 ectations, we found that half of the maximal phase-delaying response achieved in response to a single

179 iological tissues by assessing impedance and phase delay responses to alternating current at multiple

180 nduced Fos expression in the SCN, behavioral phase-delay responses to 15-min light pulses in constant

181 nist eliminated NPY blockade of NMDA-induced phase delays, suggesting that the Y5 receptor is capable

182 s had longer free-running periods and larger phase delays than African-Americans.

183 es of the phosphatase inhibitors resulted in phase delays that were greatest near subjective dawn.

184 By contrast, phase-delays that can be induced by lights pulses given

185 geber time (ZT) 10 on the first day in vitro phase delayed the rhythm of firing rate expressed by SCN

186 duration was over 5 times more effective at phase delaying the circadian pacemaker (1.07+/-0.36 h) a

187 ashes were at least 2-fold more effective in phase delaying the circadian system as compared with exp

188 nstrate that evening exposure to an LE-eBook phase-delays the circadian clock, acutely suppresses mel

189 cycle and could show both phase advances and phase delays, the latter dominated.

190 We import phase-delay time plots from chaotic systems theory as a

191 adjacent mid-Atlantic spreading center using phase-delay times of seismic surface waves, which show a

192 icrowave ground together enable the inertial phase delay to be resolved from the electron scattering.

193 rface to provide azimuthally-dependent local phase delay to the radiated wavefront, we shrink the thi

194 ircuit to output voltage pulses with various phase delays to demonstrate improved pumping efficiency

195 The NMDA-induced phase delay was blocked by coapplication of NPY (0.02-20

196 ment with caffeine, and a complete loss of S-phase delay was observed after UV irradiation.

197 he inhibitory effect of CHA on light-induced phase delays was dose dependent over a range of 0.1 to 5

198 tenance of posterior-directed intersegmental phase delays, we induced fictive crawling in isolated wh

199 und signal-corrected values of impedance and phase delay were determined.

200 Appropriate phase delays were also absent in DA-treated chains of ga

201 Attenuated phase delays were also seen in animals bearing a point m

202 Although appropriate intersegmental phase delays were always absent, when one ganglion was t

203 Phase delays were not blocked by a combination of NMDA [

204 Phase delays were not caused by activation of ionotropic

205 As previously observed, light-induced phase delays were significantly attenuated in fed mice p

206 ng expiration evoked either phase advance or phase delay, whereas in anaesthetized mice with high f (

207 ng expiration evoked either phase advance or phase delay, whereas in anaesthetized mice with high f (

208 /MAPK, and in the early night, light-induced phase delays, which are mediated predominantly by NMDA r