ライフサイエンスコーパス: antiphase

1 nt in the two brain regions (in phase versus antiphase).

2 osed of two circadian oscillators cycling in antiphase.

3 d 9 Hz) when summed spatially in phase or in antiphase.

4 as in-phase, and the second condition was in antiphase.

5 e keeps both PDF-dependent clock circuits in antiphase.

6 d choroidal thickness tended to fluctuate in antiphase.

7 ing the two negative feedback loops to be in antiphase.

8 d with gratings pulsed spatially in phase or antiphase.

9 sition HR exists at which in-phase shifts to antiphase above which CO decreases when HR further incre

10 a-band oscillations were again approximately antiphase across participants for correct versus incorre

11 m consists of two clusters that oscillate in antiphase and can each occupy multiple fixed spatial dom

12 als with x = 1/4 and 1/3 exhibit complicated antiphase and chiral domain structures related to orderi

13 systems, leading to novel dynamics including antiphase and cryptic cycles.

14 ut an increase in cost for swimmers flapping antiphase, and (2) in inline arrangements, flow coupling

15 neurons, compared with the model, prohibited antiphase behavior.

16 Antiphase behaviour of monsoon systems in alternate hemi

17 sensible heating mechanism both in-phase and antiphase behaviours of northern and southern hemisphere

18 ith a period of approximately 80 min, was in antiphase between the SCN and other brain areas, and ano

19 millennial-scale climate evolution should be antiphased between the northern and southern hemispheres

20 ting a variety of phase relations, including antiphase, between excitation and inhibition in response

21 However, no antiphase boundaries (APBs) are observed for films grown

22 Particularly, antiphase boundaries (APBs) as planar defects have been

23 due to NiO addition induce the formation of antiphase boundaries (APBs) that are enriched in Yb and

24 he ferroelectric domain walls and structural antiphase boundaries are mutually locked and this strong

25 o the localization of phonons and magnons by antiphase boundaries coupled to magnetic domains.

26 From the exploration of antiphase boundaries in bilayer-perovskites, here we dis

27 n and control of quantum many-body states at antiphase boundaries in kagome lattice superconductors a

28 fit dislocations, threading dislocations and antiphase boundaries in lattice- and polarity-mismatched

29 lectron microscopy reveals the prevalence of antiphase boundaries in nanoparticles that have signific

30 Strong antiferromagnetic interactions across antiphase boundaries support multiple magnetic domains e

31 twinning and intergrowth defects as well as antiphase boundaries were detected.

32 ic structure shows defect ordering along the antiphase boundaries, giving a larger T(N) and a higher

33 In addition, antiphase boundaries, originating at step terraces of Sr

34 We also discover a zipper-like nature of antiphase boundaries, which are the reversible creation/

35 7 nm in size, which impinge on each other at antiphase boundaries.

36 Antiphase boundary (APB) and twin boundary (TB) separati

37 lation concerning the role of the ubiquitous antiphase boundary (APB) defects in magnetite, however,

38 MgAl2 O4 substrate show the presence of the antiphase boundary defects.

39 as well as to twinning, stacking faults and antiphase boundary defects.

40 by spinal "half-center" networks coupled in antiphase by reciprocal inhibition.

41 ect-detection two-dimensional IPAP (in-phase antiphase) CACO NMR spectroscopy to monitor the ionizati

42 arates into two components, 12 h apart, with antiphase circadian oscillations in the left and right S

43 nchronous between left and right GPi with an antiphase clustering of phase differences.

44 accurate measurement of relaxation rates for antiphase coherence and two-spin order led us to conside

45 er exchange dominates the 15N relaxation for antiphase coherence with respect to 1H through scalar re

46 ived contrast was veridical for in-phase and antiphase conditions, and monocular presentation, but in

47 es to coupling when the SCN network is in an antiphase configuration, but opposes synchrony under ste

48 GABAA signaling to couple the network in an antiphase configuration, but promotes synchrony under st

49 Remarkably, daily antiphase cycles of sodium and potassium currents also d

50 ormation of multiple twinning interfaces and antiphase defects, which are effective scatterers of hea

51 non-destructively characterise and quantify antiphase domains (APDs) in GaP thin films grown on diff

52 tion-direction states is degenerate with two antiphase domains, and these eight structural variants f

53 in the left and right clock nuclei cycle in antiphase during 'splitting.'

54 human primate fetal liver in an intact phase-antiphase fashion and that Npas2, a paralog of the Clock

55 model also predicted the existence of stable antiphase firing at frequencies below approximately 30 H

56 roximately 30 Hz, but no evidence for stable antiphase firing was found using the experimentally dete

57 itatory coupling, inhibitory coupling led to antiphase for no delay, very short delays and delays clo

58 s consumer-resource cycles become longer and antiphase (half-period lag, so consumer maxima coincide

59 simulations, support the conclusion that an antiphased hemispheric temperature response to ocean cir

60 The current study provides a rare report of antiphase homotopic synchrony in human GPi, potentially

61 gher Rabi frequency, and the lifetime of the antiphase HP o-H(2) resonance is extended by several-fol

62 n dual oscillators whose outputs are held in antiphase i.e., ~12.4 hr apart.

63 er right anterior sensors were approximately antiphase in a prestimulus time window, and thus success

64 ales, suggesting that hydrologic cycles were antiphased in the northerly versus southerly subtropics.

65 Our findings also demonstrate antiphasing in climate response between low and midlatit

66 The clear hemispheric antiphasing indicates that the sphere of influence of th

67 circuit generates both spatially opponent, "antiphase" inhibition ("push-pull"), and spatially match

68 onnectivity within the auditory cortices and antiphase (interhemispheric phase lag 180 ) TACS modulat

69 ted to these conditions, and when exposed to antiphase light and temperature cycles (cold photoperiod

70 We show that antiphase light-temperature cycles (negative day-night t

71 nked (1)H-(1)H pairs can be used to generate antiphase magnetization between noncoupled spins.

72 In contrast, antiphase modulation increases decision accuracy, confid

73 bitory neural populations contribute more to antiphase modulation.

74 and reveal a novel regulatory module of two antiphase negative feedback loops that allows for the fi

75 polar couplings, generates strongly enhanced antiphase NMR signals.

76 l manifestation of this effect wherein large antiphase o-H(2) signals are observed, with (1) H enhanc

77 an interhemispheric pattern of precipitation antiphasing occurred on multicentury timescales in respo

78 for these reorganizations may have been the antiphasing of polar insolation associated with orbital

79 in the left and right halves oscillating in antiphase, on a timescale of 20 s, and coupled to equall

80 Given this complex cell inhibition, antiphase or "push-pull" inhibition from tuned simple in

81 different dynamics, including phase-shifted, antiphase or synchronized oscillations, as well as stabl

82 k in which each side of the SCN exhibits two antiphase oscillating subregions, here termed "core-like

83 " and "shell-like," in addition to the known antiphase oscillation between the right and left SCN.

84 amic bipolar plasmon is characterized by the antiphase oscillation of massless electrons and holes in

85 y 12 hr) locomotor activity bouts reflect an antiphase oscillation of the left and right sides of the

86 We observe the antiphase oscillation of the two-qubit 01 and 10 states,

87 of so-called 'localized clusters'--periodic antiphase oscillations in one part of the medium, while

88 of subsequent inputs over time and (ii) slow antiphase oscillations in the impact of external sensory

89 ) for Xenopus tadpole swimming that involves antiphase oscillations of activity between the left and

90 nuum of mechanisms in circuits that generate antiphase oscillations, with 'release' and 'escape' mech

91 this conflict by switching from in-phase to antiphase oscillations.

92 to the North Atlantic, in agreement with the antiphase pattern of precipitation variability across th

93 ated to bilayers by ZipA, which propagate as antiphase patterns with respect to those of Min as revea

94 This antiphasing persisted throughout the last 25 glacial cyc

95 eous build-up of in-phase ('zero-state') and antiphase ('pi-state') 'superfluid' states in a solid-st

96 ed changes in the proportion of in-phase and antiphase populations of SCN oscillators and suggests no

97 ch as the 8.2 ka event, Anjohibe exhibits an antiphase precipitation signal to the Northern Hemispher

98 cally antagonistic functions, but that their antiphase regulation allows them to coordinately regulat

99 -modulated changes of the wave's cadence, an antiphase relationship between orderliness and accelerat

100 sphere monsoon reconstruction illustrates an antiphase relationship to Northern Hemisphere monsoon in

101 nsgaard-Oeschger interstadials-a first order antiphase relationship with northern hemisphere summer m

102 intracellular Ca(2+) levels fluctuate in an antiphase relationship with rhythmic ATP accumulation in

103 a coherence was modified toward a consistent antiphase relationship, and these changes occurred in pr

104 ture variations in West Greenland display an antiphased relationship to temperature changes in Irelan

105 ling ferroelectric, magnetic, and structural antiphase relationships were found in multiferroic h-YMn

106 d by polarization orientation and structural antiphase relationships.

107 (Hz-->Nz)], two-spin order [RNH(2HzNz)], and antiphase [RNH(2HzNx,y)] rates were determined for 52 of

108 Here we show that the antiphasing seen in the tropical records is also present

109 o present lip movements and speech sounds in antiphase specifically with respect to the theta oscilla

110 These in-phase and antiphase states reflect the band structure of the one-d

111 e flagellar orientation reveals in-phase and antiphase states, consistent with dynamical theories.

112 In contrast, antiphase stimulation in the same individuals desynchron

113 Antiphase summation is typically thought to produce an e

114 rturning Circulation (AMOC), resulting in an antiphase temperature response between the hemispheres (

115 The buildup rate of such antiphase terms is highly sensitive to local geometry, i

116 While polar ice cores attest to an antiphased thermal pattern at millennial timescales, rec

117 i were presented at maximum strength, but in antiphase, they had no influence over vision for low tem

118 f these genes was Grem2, which oscillated in antiphase to BMP signaling.

119 Bursting approaches antiphase to cAMP waves, with accelerating transcription

120 nduced by light, and its level oscillates in antiphase to frq sense RNA.

121 ically fired only 1-2 spikes per ripplet, in antiphase to FS spikes, and received synchronous sequenc

122 phases of these rhythms are approximately in antiphase to one another, similar to those of eyes in a

123 f microglial synaptic phagocytosis which was antiphase to REV-ERBalpha expression.

124 tisense frequency (frq) transcripts cycle in antiphase to sense frq transcripts in the dark, and are

125 ion of prototypic GABAergic GPe neurons fire antiphase to subthalamic nucleus (STN) neurons, often ex

126 rates in the afternoon, substance P acts in antiphase to suppress dopamine signaling and "pull down"

127 ression, demonstrating an early morning peak antiphase to that of the Mir21 strands.

128 undergo daily rhythms in abundance that are antiphase to the cycling observed for the RNA products f

129 ect exposure to low-intensity light, even in antiphase to the illumination of shoots.

130 Thus, Hro-hes transcription cycles in antiphase to the nuclear localization of HRO-HES protein

131 le in PER and TIM immunoreactivity almost in antiphase to the other DNLs and to the LNs.

132 ach light pulse to discharge rhythmically in antiphase to the pGABA neurons.

133 f ApC/EBP protein with peak levels at night, antiphase to the rhythm in LTS.

134 llate at the same frequency as and precisely antiphase to the wings; they detect body rotations durin

135 ycles in the RNA levels of dclock (dClk) are antiphase to those of period (per).

136 ts of E cells exhibit molecular oscillations antiphase to those of wild-type flies, single cry mutant

137 with TRN spikes, whereas late cells fired in antiphase to TRN activity and also had higher firing rat

138 -promoting evening cells, maintaining stable antiphase via the largest PDFME entrained by extraocular

139 Clock expression, in parallel with Bmal1, in antiphase with cycles in Per1 and Per2; there was low-am

140 (CoM) oscillates about its average speed in antiphase with head drag.

141 o licking, but their activity was usually in antiphase with that of SNR neurons, suggesting inhibitor

142 ting HSCs and their progenitors fluctuate in antiphase with the expression of the chemokine CXCL12 in

143 The BMAL1 rhythm was in approximate antiphase with the other clock genes.

144 levels were rhythmic and maximal in precise antiphase with the peak in cytosolic Ca(2+).

145 st moments for target detection (in phase or antiphase with the preceding rhythm) depended on whether

146 ow regions of cortex that seem to respond in antiphase with the primary stimulus.

147 l H3K4me2 oscillation, H3K4me2 oscillates in antiphase with transcription but in phase with H2A.Z. In

148 onounced shifts in monsoon rainfall that are antiphased with precipitation records for East Asia and