ライフサイエンスコーパス: antiphase

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

2 d choroidal thickness tended to fluctuate in antiphase.

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

4 d with gratings pulsed spatially in phase or antiphase.

5 osed of two circadian oscillators cycling in antiphase.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 polar couplings, generates strongly enhanced antiphase NMR signals.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

72 d by polarization orientation and structural antiphase relationships.

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

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

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

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

77 In contrast, antiphase stimulation in the same individuals desynchron

78 Antiphase summation is typically thought to produce an e

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

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

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

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

83 Bursting approaches antiphase to cAMP waves, with accelerating transcription

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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