ライフサイエンスコーパス: dark phase

1 sessed across the light-dark cycle or in the dark phase).

2 housing conditions, social status, and light/dark phases).

3 with peak expression level during the early dark phase.

4 eding at a fixed clock time, in the original dark phase.

5 light phase and mania-like behaviors in the dark phase.

6 y, and are observed predominantly during the dark phase.

7 S duration and bouts were largest during the dark phase.

8 harvested from male mice during the light or dark phase.

9 activity in the three species shifted to the dark phase.

10 LB/c mice near the beginning of the light or dark phase.

11 kers were significantly repressed during the dark phase.

12 SLD mice and with reduced potency during the dark phase.

13 y represses inflammatory pathways during the dark phase.

14 the light phase differs from activity in the dark phase.

15 ce of cell division in the first half of the dark phase.

16 d rapid eye movement sleep (REMS) during the dark phase.

17 t the E(2) suppression of T(SKIN) during the dark phase.

18 when working to avoid shock in the light or dark phase.

19 arousal during SIH and SF compared with the dark phase.

20 tration of BDNF protein is higher during the dark phase.

21 phase of the circadian cycle than during the dark phase.

22 timulated to feed by fasting or onset of the dark phase.

23 zation was observed during the middle of the dark phase.

24 ted, and cellular TWCA1 decreased during the dark phase.

25 ' pattern of activity during the 12 h of the dark phase.

26 nificant mean IOP elevations only during the dark phase.

27 and the peak appeared in the late subjective dark phase.

28 n in the middle light phase and in the early dark phase.

29 t before the beginning of the normal 12-hour dark phase.

30 when it was injected at the beginning of the dark phase.

31 light phase, and decreased in the subjective dark phase.

32 light phase and suppression during the late dark phase.

33 gradually and peaked in the late subjective dark phase.

34 an pattern and peaks at the beginning of the dark phase.

35 f REM sleep propensity was slower during the dark phase.

36 ived injections at the onset of the light or dark phase.

37 ts did not correlate with performance in the dark-phase.

38 ed synaptic throughput between the light and dark phases.

39 matin remodeling complexes between light and dark phases.

40 iod, with region-specific peaks during light-dark phases.

41 ard lighting to measure IOP during light and dark phases.

42 ined approximately constant in the light and dark phases.

43 white fluorescent light during each 12-hour dark phase (0-345 microW/cm2) resulted in a dose-depende

44 e protein Fos, were higher at the end of the dark phase (2300 h) compared to values obtained at the e

45 ed significantly higher pressures during the dark phase (27.9 +/- 1.7 mm Hg) than during the light ph

46 nificantly improved sleepiness (sleep in the dark phase: 34% +/- 4% vs. 26% +/- 3%; P < 0.01), cognit

47 day (CT 10) to C3H/HeN mice kept in constant dark phase advanced circadian rhythms of wheel running a

48 y intake is restricted to 8 h/day during the dark phase) alone or combined with aerobic exercise (AE)

49 e with DA levels at their highest during the dark phase and lowest during the light phase.

50 e sharply at the beginning of the subjective dark phase and peaked shortly thereafter.

51 d sharply at the beginning of the subjective dark phase and peaked shortly.

52 ls fluctuated with peaks occuring during the dark phase and the nadirs occuring during the light phas

53 became circadian arrhythmic after DPS, both dark-phase and light-phase URs were abolished.

54 Wakefulness time was also reduced during the dark phase, and this effect was concentrated at the phot

55 y relative to adult mice near the end of the dark phase, and with time-dependent changes in basal for

56 in AIMD mice increased during both light and dark phases, and this was accompanied by frequent transi

57 ration was enhanced in the first half of the dark phase but depressed in the second.

58 ity (FAA) and attenuated activity during the dark phase but FAA was not associated with increases in

59 ng behavior, and body temperature during the dark phase but maintained normal circadian rhythmicity.

60 163 mul (n = 8) during a 20 min trial in the dark phase, but markedly less during the light phase (42

61 Increased sleep during the dark phase, caused by HFD in wild type animals, was alle

62 t on 5-HT release in the SCN during the late dark phase compared with mid light phase, indicating tha

63 above chance, they had lower accuracy in the dark-phase compared to controls (p = 0.036).

64 cardiac Per1 abundance increased during the dark phase, concurrent with the rise in heart rate and p

65 three-choice task with both light-phase and dark-phase conditions.

66 re similar whether given during the light or dark phase, despite the large diurnal variations in base

67 Exercise at ZT17, middle of the dark phase, did not alter the muscle clock phase.

68 pe muscle, while this response was lost with dark-phase dosing.

69 Mean IOP for light and dark phases during the experimental period were compared

70 Dark-phase effects were remarkably consistent regardless

71 nation cycle that included defined light and dark phases (either 12-hour light:12-hour dark or 8.5-ho

72 ether, restricting food intake to the active dark phase enhanced adaptation to shifts in the light-da

73 On the other hand, dark phase feeding accelerated adaptation of core body t

74 h shifts) combined with ad libitum feeding, dark phase feeding or feeding at a fixed clock time, in

75 ent did not distinguish between daylight and dark phase; however, it reorganized with change in photo

76 ll WAF fractions were neuroactive, eliciting dark-phase hypoactivity and fraction-specific hyperactiv

77 xamine whether sleep/wake state and/or light/dark phase impact DA terminal neurotransmission in male

78 ilability from 8 h to 12 h during the active dark phase in db/db mice prompted isocaloric feeding and

79 Noticeably, these metabolites peaked in the dark phase in non-tumor bearing mice, which corresponds

80 a time-of-day-dependent manner (lower in the dark phase) in the blood and brains of surgical control

81 athetic nerves, which are more active in the dark phase, in this circadian rhythm?

82 roduced optic nerve lesions, both light- and dark-phase IOP determinations are necessary for accurate

83 For fellow eyes, mean light- and dark-phase IOP was 21 +/- 1 and 31 +/- 1 mm Hg, respecti

84 he increase of basal pupil size in the early dark phase is not related to the nocturnal increase of b

85 d were most common at around the light phase:dark phase (L:D) and D:L transition points of the circad

86 ifference was found in 24-h food intake, and dark-phase meal frequency or meal size between F344.Cck1

87 ine did not change significantly between the dark phase (night) and the light phase (day) of the diur

88 etabolic profile in the light as well as the dark phase of a diel cycle.

89 sleep duration was only increased during the Dark Phase of the circadian day.

90 e offspring and peaks during the "active" or dark phase of the light/dark cycle.

91 mine secreted by the pineal gland during the dark phase of the photoperiod.

92 re hyperactive during both the light and the dark phases of the 24-hr cycle.

93 and awake IOP measured in both the light and dark phases of the circadian cycle for 34 days.

94 , High) requires assessment across the light-dark phases of the light cycle and across multiple postp

95 restriction to the rats during their active (dark) phase of the day, which selectively decreased the

96 er the SAT was practiced during the light or dark phase or in constant-light conditions.

97 C neurons was investigated during either the dark phase or the light phase, following different compo

98 (WT) mice when working for reward during the dark phase or when working to avoid shock in the light o

99 positive correlation with performance in the dark-phase; performance on additional cognitive tests di

100 As a result, the dark phase persists up to densities high enough for a da

101 competitive antagonist luzindole before the dark phase preceding constant light exposure were substa

102 en in the SCN where they peaked early in the dark phase, providing further evidence that the differen

103 maximum difference in IOP between light and dark phases ranged from 6.4 mm Hg to 16.6 mm Hg.

104 Dark phase restricted feeding partially restored whole b

105 d effect of promoting insulin release in the dark phase, resulting in mania-like behaviors and hippoc

106 (DLS) striatum in Npas2 mutant females after dark phase self-administration.

107 (DLS) striatum in Npas2 mutant females after dark phase self-administration.

108 us humor and the vitreous humor in the early dark phase showed no difference between the two eyes.

109 erior chamber depth were larger in the early dark phase than in the middle light phase.

110 ne is more likely to increase IOP during the dark phase than the light.

111 biased selection strategy (p < 0.01) in the dark-phase than light-phase.

112 During light and dark phases the RHT inputs to 55% and 33% of recorded ne

113 ed twice, near both the start and end of the dark phase; this twin-peaking group is significantly enr

114 se induced plant signals released during the dark phase to choose sites for oviposition adds a new di

115 m, NOR and TST are best performed during the dark phase to observe actual baseline outcomes for SHR a

116 ion adducts were found between the light and dark phases under non-stress conditions.

117 traocular pressure (IOP) at 2 hours into the dark phase was determined for both eyes.

118 roglia are most ramified at the onset of the dark phase, we do not find diurnal differences in PNN in

119 istently larger pupil size in the subjective dark phase were observed.

120 with a smaller stereotypic effect during the dark phase when compared to administration during the li

121 ng the light phase and lowest during the mid-dark phase, when plasma melatonin levels were lowest and

122 notably, it increased sleep duration in the dark phase-when mice are normally more likely to be awak

123 urrent density of 17.5 mA x m(-2) during the dark phase, whereas a much lower current of approximatel

124 REM sleep duration during both the Light and Dark Phase, whereas NREM sleep duration was only increas

125 htly increased wakefulness in both light and dark phases, whereas inhibition of BF cholinergic neuron

126 are enriched in transcripts that peak in the dark phase, while metabolic processes are primarily enri

127 idate, however, varied between the light and dark phase, with a smaller stereotypic effect during the