ライフサイエンスコーパス: diurnal cycle

1 me corresponding to dusk in the absence of a diurnal cycle).

2 speed is greater during the dark period of a diurnal cycle.

3 that pace rhythms of gene expression to the diurnal cycle.

4 a light-dependent way to adjust vision on a diurnal cycle.

5 electron donor, with lifetimes exceeding the diurnal cycle.

6 prediction of growth properties over a full diurnal cycle.

7 r in guard cells of intact leaves during the diurnal cycle.

8 outheastern United States, with the expected diurnal cycle.

9 bidopsis leaves at different points during a diurnal cycle.

10 es and malate (Mal) synthesis imposed over a diurnal cycle.

11 re through the awake and sleep phases of the diurnal cycle.

12 he active than during the rest period of the diurnal cycle.

13 ctic steady state changes with time during a diurnal cycle.

14 s, yet temperatures fluctuate throughout the diurnal cycle.

15 nt at the end of the illumination phase of a diurnal cycle.

16 ally expressed at distinct phases during the diurnal cycle.

17 cantly reduces mating success throughout the diurnal cycle.

18 that are later mobilized as part of a robust diurnal cycle.

19 ecessary for cycling of sxe1 mRNA during the diurnal cycle.

20 to analyze the transcriptome throughout the diurnal cycle.

21 bolism do not change appreciably through the diurnal cycle.

22 ch content than the wild-type throughout the diurnal cycle.

23 vents whose photosensitivity varies during a diurnal cycle.

24 rhythmic transcription during a circadian or diurnal cycle.

25 variance in the exometabolome across the two diurnal cycles.

26 iod = 4.1 h), both showed co-expression with diurnal cycles.

27 to 4 hours after onset of the nocturnal and diurnal cycles.

28 tatistics of C. reinhardtii are modulated by diurnal cycles.

29 iolated growth, but may also function during diurnal cycles.

30 d and functions that define the seasonal and diurnal cycles.

31 uclear hormone receptors display interlinked diurnal cycling.

32 PMSR2 at the end of the night in a short-day diurnal cycle alleviates this potential burden on metabo

33 ersus form 2) appeared to change during this diurnal cycle, along with changes in the PSII monomer/di

34 Polysome loading was investigated during the diurnal cycle, an extended night, and low CO2 in Arabido

35 ce results in deregulated autophagy over the diurnal cycle and altered gene expression causing abnorm

36 t on the Gross Primary Productivity seasonal-diurnal cycle and contributed to approximately 7% higher

37 ine metabolism during the light phase of the diurnal cycle and evaluated the presence of diurnal and

38 trainment of leaf daytime respiration to the diurnal cycle and that time of day should be accounted f

39 these changes were consistent throughout the diurnal cycle and were sustained at 24 weeks.

40 spectrometry, in total leaf extracts over a diurnal cycle and when exposed to conditions that promot

41 This indicated that natural diurnal cycles and meal consumption do not appear to sig

42 uct-to-parent reversion mechanism results in diurnal cycling and substantial regeneration of TBA meta

43 d that LD abundance was modulated during the diurnal cycle, and characterization of LDAP misexpressio

44 s may differ functionally with regard to the diurnal cycle, and that these differences may be reflect

45 Changes in leaf starch content over the diurnal cycle are largely brought about by changes in th

46 tal SWCRE bias, but such errors in the cloud diurnal cycle are masked by other compensating errors, i

47 For this and other microalgal species, diurnal cycles are well known to control the metabolism,

48 erns in wood cell wall biosynthesis, suggest diurnal cycle as a possible cue in the regulation of car

49 n ([O2]) in all replicates exhibited regular diurnal cycles associated with daytime photosynthesis an

50 Samples were collected every 6 h across two diurnal cycles at 5 replicate sampling sites with high s

51 s are not solely controlled by cues from the diurnal cycle but that strain-specific intracellular met

52 Stratocumulus are strongly modulated by the diurnal cycle, but many previous observational studies h

53 sted during the light or dark portion of the diurnal cycle, but the process was significantly acceler

54 al processes that vary across the day-night (diurnal) cycle, but if and how the circadian clock regul

55 um to monitor the CO(2) levels caused by the diurnal cycles caused by the metabolism of the aquatic p

56 ression and photodamage are dynamic over the diurnal cycle, Chlamydomonas populations acclimated to l

57 The mechanism by which diurnal cycles control the transitory biosynthesis and d

58 ral chemoreception in a vigilance-state- and diurnal-cycle-dependent manner and indicate a role for o

59 the CO(2) response in a vigilance-state- and diurnal-cycle-dependent manner.

60 spheric Hg(0)g exchange resulting in typical diurnal cycles due to photochemcial reduction at the sur

61 immune clearance of the brain throughout the diurnal cycle, even in hypo- or hyper-glycemia.

62 iency is differentially regulated during the diurnal cycle for genes with 5'-Terminal Oligo Pyrimidin

63 were analyzed at various time points in the diurnal cycle in homozygous rds/rds retinas which lack p

64 xogenous fatty acid in adipose tissue over a diurnal cycle in lean (n = 9) and abdominally obese men

65 clouds and an improved representation of the diurnal cycle in model-observation comparisons, especial

66 rays to measure mRNA accumulation during the diurnal cycle in the livers of (1) wild-type mice, (2) a

67 hesis under -N and + N conditions during the diurnal cycle in wild type and a psbA4 deletion strain o

68 versibly modulated by the photoreceptor over diurnal cycles in Arabidopsis seedlings.

69 ocotyl cell elongation to peak at dawn under diurnal cycles in Arabidopsis thaliana.

70 in chromatin accessibility that accompanies diurnal cycles in ventricular myocytes.

71 either constant darkness or 12 h light/dark diurnal cycles, including several noncoding RNAs (ncRNAs

72 cription of the volatilization dynamics on a diurnal cycle (increasing efficiency factor from 0.85 to

73 the regulation of photosynthesis during the diurnal cycle is hypothesized to be linked with nitrogen

74 Thus, Pol III transcription during the diurnal cycle is regulated both in response to nutrients

75 for glucose (liver) and lipid metabolism has diurnal cycles (nadir a.m.) opposite that of control sub

76 are U snoRNA host genes (Uhgs), a family of diurnal cycling noncoding RNAs that encode the precursor

77 ase (night) and the light phase (day) of the diurnal cycle, nor did they change between early and lat

78 We conclude that the diurnal cycle of anion channel gene transcription, rathe

79 ry nitrite maximum and the plausibility of a diurnal cycle of archaeal ammonia oxidation activity in

80 trial radiation is strongly modulated by the diurnal cycle of clouds (DCC).

81 es have broadened the scope for studying the diurnal cycle of ecosystem functions.

82 ostationary observation data in refining the diurnal cycle of inventoried NO(x) emissions, thereby mo

83 Analysis of the diurnal cycle of mean hourly precipitation suggests that

84 a comparative transcriptome analysis of the diurnal cycle of nine members of Archaeplastida, and we

85 pattern is the reverse of the physiological diurnal cycle of people without diabetes who are more in

86 e that methane production is associated with diurnal cycle of sunlight, indicating that this producti

87 ed from an emergent relationship between the diurnal cycle of the relative humidity profile and E.

88 sp70 mRNA levels in the light paralleled the diurnal cycle of total cell protein synthesis.

89 In low prey-addition treatments, the regular diurnal cycles of [O2] were disrupted, but a regime shif

90 notion that ecological features such as the diurnal cycles of light and day, sunlight exposure, seas

91 ng point at ~45 h as [O2] was decoupled from diurnal cycles of photosynthesis and respiration.

92 We report measurements of characteristic diurnal cycles of precursor gases and particles.

93 llations in peripheral tissues are driven by diurnal cycles of rest-activity and food intake or are a

94 grown in greenhouse conditions under natural diurnal cycles of solar irradiation, the ratio of phosph

95 Changes in diurnal cycles of temperature and vapor-pressure deficit

96 ted is indicated by correlations between the diurnal cycles of the OVOC measurements and solar radiat

97 ogy of virtually all living organisms to the diurnal cycles of their environments.

98 To investigate whether the diurnal cycling of the transcript levels is only a respo

99 icate that SBEIIa is required for the proper diurnal cycling of transitory starch within the leaf and

100 eep during both dark and light phases of the diurnal cycle only in SHRs.

101 However, the impact of diurnal cycles or daily meals on circulating analytes ar

102 ocioeconomic status, the underlying cortisol diurnal cycle, or subjective experience during the stres

103 Diurnal cycles provide a tractable system to study the r

104 to later initiation of the rest phase of the diurnal cycle seen in controls in late adolescence.

105 Moreover, exceptional diurnal cycling stability is observed in the ST-OSCs bas

106 t, where sea breeze convection dominates the diurnal cycle, storm frequency has doubled in deforested

107 synchronization of biological processes with diurnal cycles such as activity and rest.

108 nd that these emissions exhibit a pronounced diurnal cycle that closely follows photosynthetically ac

109 probably connected to the interplay between diurnal cycles that drive photosynthetic cell growth and

110 During the diurnal cycle, the amount of leaf starch is higher in dp

111 both the daytime and night-time phase of the diurnal cycle, the latter of which remains uncertain in

112 (NO), and PM(2.5) increments showed distinct diurnal cycles; the NO(2) increment peaks at ~9 ppb duri

113 zes physical and metabolic activity with the diurnal cycle through a transcriptional-posttranslationa

114 Estradiol and the diurnal cycle thus interact to induce shifts in both GAB

115 in wakefulness during the dark period of the diurnal cycle to a level observed during NREM sleep in t

116 ld measurements with AquaDust through a full diurnal cycle to confirm the robustness of the technique

117 photosystem organization changes during the diurnal cycle to favor either noncyclic electron flow, w

118 both cultivars demonstrates a high-amplitude diurnal cycle under these conditions; however, ACC oxida

119 operties of PSII were studied throughout the diurnal cycle using O2-flash-yield and pulse-amplitude-m

120 However, when the dark period in a normal diurnal cycle was cut short artificially by transferring

121 th exhibit comparable variation on a natural diurnal cycle, while PHYB1 also exhibits variation but w

122 tilization from bare soil exhibits usually a diurnal cycle with a potentially large decrease when the

123 HO2 was observed to have a diurnal cycle with morning concentrations suppressed by

124 th (222)Rn and CO2 concentrations followed a diurnal cycle with night time concentrations higher than

125 bit abnormal fuel utilization throughout the diurnal cycle, with increased glucose oxidation near the