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

6 ignalling elements that contribute solely to phase delay.

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

8 metamaterial bricks-each encoding a specific phase delay.

9 protein in centrosome reduplication during S-phase delay.

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

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

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

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

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

15 es both daytime phase advances and nighttime phase delays.

16 ircadian periods were associated with larger phase delays.

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

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

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

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

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

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

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

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

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

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

27 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

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

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

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

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

32 Phase delays and advances were observed during early and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 -14 while a GABA(B) antagonist increased the phase delays caused by light.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

72 Phase delays following photic stimulation were reduced i

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

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

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

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

77 2 receptor agonist, blocked the NMDA-induced phase delay in a similar manner as NPY.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Phase-delayed misalignment increased rapid eye movement

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

113 Phase delays occurred when the light stimulus was centre

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

168 Phase delays were not caused by activation of ionotropic

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

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