ライフサイエンスコーパス: light cycle

1 the dark cycle), and 2200L (continued in the light cycle).

2 rhythms to acute light pulses and shifts in light cycle.

3 hours during the middle of the daily 12 hour light cycle.

4 hours during the middle of the daily 12-hour light cycle.

5 less of when the rats were tested during the light cycle.

6 s that were tested at different times in the light cycle.

7 did sedentary rats when tested early in the light cycle.

8 ng periods when feeding is restricted to the light cycle.

9 esponding with the dark portion of the prior light cycle.

10 transient pulse of expression 4 hr into the light cycle.

11 n areas and their response to changes in the light cycle.

12 re regulated by changes in the environmental light cycle.

13 ctivity and its adjustment to changes in the light cycle.

14 y of stimuli, most notably the environmental light cycle.

15 o vary according to the phase of the natural light cycle.

16 brain that are coupled to the environmental light cycle.

17 r entraining endogenous rhythms to the daily light cycle.

18 onation events that control the speed of the light cycle.

19 ng large, abrupt shifts in the environmental light cycle.

20 ltant stored energy is used to drive the PYP light cycle.

21 amination of pH effects on the wild-type PYP light cycle.

22 low protein (PYP) undergoes a self-contained light cycle.

23 during the high light phases of fluctuating light cycles.

24 y the clock and thus synchronized with daily light cycles.

25 reset by in vitro exposure to phase-shifted light cycles.

26 ess, even in the presence of (phase-shifted) light cycles.

27 sure to resonant or nonresonant 24-h or 20-h lighting cycles.

28 little consideration given to environmental lighting cycles.

29 light was turned on), 1000 (3 hours into the light cycle), 1000D (continued in the dark cycle), 1900

30 s obtained when testing occurred late in the light cycle, an effect driven by a difference in the amo

31 sessment across the light-dark phases of the light cycle and across multiple postpartum days.

32 ression also peak in at the beginning of the light cycle and are controlled by the circadian clock.

33 levels were shifted to the beginning of the light cycle and coincided with the nadir of leptin.

34 a, granule cell migration accelerates during light cycles and decelerates during dark cycles.

35 ce deficient in Magel2 expression entrain to light cycles and express normal running-wheel rhythms, b

36 like growth factor 1 (IGF-1) are high during light cycles and low during dark cycles.

37 Light cycles and sprouting influenced the potential anti

38 Synchronization between the environmental lighting cycle and the biological clock in the suprachia

39 n the liver independently of the SCN and the light cycle, and they suggest the need to reexamine the

40 The rhythms were entrained by light cycles applied in vitro and were free-running in c

41 ith pH demonstrate that both phases in PYP's light cycle are actively controlled by the protein compo

42 germination and under diurnal and circadian light cycles are also characterized.

43 Light cycles are the most important external cue for the

44 Daily light cycles are well known environmental cues for setti

45 trations in leaves are altered by daily dark/light cycles, as well as the continuing rise in atmosphe

46 l rhythm experiments were removed from their light cycles at different times (24-hour clock): 0700 (b

47 mutants flowered very early during long-day light cycles, but not during short days.

48 tivation in synchronized cells grown in dark/light cycles compared with induction under low CO2.

49 lar cycle, individuals respond to artificial light cycles created by social and work schedules.

50 Light-cycle disruption elevated intestinal T(H)17 cell f

51 In these animals, the aberrant light cycle does not impair mood and learning, despite t

52 xposure to summer- and winter-like circadian light cycles during development and adulthood.

53 Therefore, seasonal light cycles experienced during retinal development and

54 cromol/kg s.c., 4 injections during the 12-h light cycle for 4 days) decreases DNMT1 mRNA and protein

55 twice daily, at the beginning and end of the light cycle, for 1 week.

56 ony of biological rhythms from environmental light cycles has dramatic consequences for human health.

57 rs decelerates granule cell migration during light cycles (high IGF-1 levels) but does not alter migr

58 levels) but does not alter migration during light cycles (high IGF-1 levels).

59 xamined the behavioural consequences of this light cycle in animals that lack intrinsically photosens

60 anti-xlProminin-1 antibodies varied with the light cycle in this frog.

61 IP during the day before a shift in either a light cycle in vivo or a temperature cycle in vitro.

62 olecular circadian clock can be entrained by lighting cycles in vitro, but that rods, cones, and mela

63 na are locally synchronized by environmental light cycles independent of the suprachiasmatic nuclei (

64 starch accumulation at the beginning of the light cycle, inhibited photosynthesis, and affected intr

65 d metabolic functions with the environmental light cycle is essential for health, and dysfunction of

66 gested that the synchrony of temperature and light cycles is important in promoting floral initiation

67 Both mutations cause interesting changes in light cycle kinetics.

68 Animals exposed to the aberrant light cycle maintain daily corticosterone rhythms, but t

69 Utilizing continuous sound recordings, light cycle manipulations, hormone implants, and in situ

70 sential in determining whether environmental lighting cycles need to be considered in hospital nurser

71 TR) transcription oscillates during dark and light cycles not only in the suprachiasmatic nucleus (SC

72 We trapped a key early intermediate in the light cycle of PYP at temperatures below -100 degrees C,

73 f the bleached signaling intermediate in the light cycle of PYP was determined by millisecond time-re

74 it increased frequency of feeding during the light cycle of the day and develop an obese phenotype un

75 es was either phase advanced relative to the light cycle or absent.

76 hen ad libitum feeding was restricted to the light cycle, peak corticosterone levels were shifted to

77 ugh the phase of SCN rhythms relative to the light cycle remains unchanged.

78 Mice exposed to short, winter-like, light cycles showed enduring deficits in photopic retina

79 Red cabbage sprouts produced under light cycles showed the highest antioxidant activity (57

80 res learning in mice exposed to the aberrant light cycle, suggesting that the mood deficit precedes t

81 Here we show, using an aberrant light cycle that neither changes the amount and architec

82 to advances and delays of the environmental light cycle, the circadian rhythm of light emission from

83 For rats reared in a reversed light cycle, the light-induced loss of rhodopsin was als

84 After a 6 hr advance or delay in the light cycle, the pineal, paraventricular nucleus of the

85 petioles of cassava leaves at the end of the light cycle to inhibit starch remobilization during the

86 rvals during an approximately 40-minute dark-light cycle using spectral domain optical coherence tomo

87 Reentrainment to an advancing light cycle was also accelerated in RKIP(-/-) mice.

88 The 24-hour light cycle was initiated between 1 and 4 weeks of age a

89 When the lighting cycle was advanced by 6 hours, the time of noct

90 a light-sensing protein interact to create a light cycle, we performed time-resolved spectroscopy on

91 ider how they are entrained by environmental light cycles, where they operate within the fly and how