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

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

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

5 kers were significantly repressed during the dark phase.

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

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

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

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

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

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

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

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

14 nificant mean IOP elevations only during the dark phase.

15 y represses inflammatory pathways during the dark phase.

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

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

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

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

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

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

22 light phase and suppression during the late dark phase.

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

24 gradually and peaked in the late subjective dark phase.

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

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

27 ined approximately constant in the light and dark phases.

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

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

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

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

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

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

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

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

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

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

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

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

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

41 163 mul (n = 8) during a 20 min trial in the dark phase, but markedly less during the light phase (42

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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