ライフサイエンスコーパス: light period

1 ce, declining to near zero by the end of the light period.

2 ts together with pH inside corals during the light period.

3 levels, leaves were harvested throughout the light period.

4 dark, followed by high expression into early light period.

5 ter-soluble glucans increased rapidly in the light period.

6 survival and phototrophic growth during the light period.

7 amino acids that accumulated in the previous light period.

8 educing integrated photosynthesis during the light period.

9 at is also sensitive to the extension of the light period.

10 dark period and total sleep and NREM during light period.

11 hout the 12-h dark period and following 12-h light period.

12 ore dark onset but not when given before the light period.

13 d then accumulates during the following 12-h light period.

14 ached its lowest levels in the middle of the light period.

15 a period of prolonged darkness prior to the light period.

16 th the daily peak occurring during the early light period.

17 measurements were made in the middle of the light period.

18 tly by initiation and degradation during the light period.

19 est during the dark period and lowest in the light period.

20 rowth rates during the night than during the light period.

21 nhardtii, peaking once each day in the early light period.

22 core body temperatures were lower during the light period.

23 ates during the night following the extended light period.

24 d decreased growth for the first part of the light period.

25 ns in both SWS and REMS in both the dark and light periods.

26 e fructans in chicory roots, grown under two lighting periods: 12 h (T-12 h) and 24 h continuous ligh

27 At the beginning of the light period, (13)C was incorporated into nucleic diphos

28 ith the highest levels detected in the early light period (2-6 h) and the late dark period (4-6 h).

29 allowed to sleep during the first 4 h of the light period (4S(+)) but not during the following 20 h (

30 during the dark period in comparison to the light period and a 'W-shaped' pattern of activity during

31 001) showing a trough towards the end of the light period and a peak in the mid-dark period.

32 ions were strictly controlled with a 16-hour light period and an 8-hour dark period.

33 immunoreactive (c-Fos-ir) neurons during the light period and early dark period in photostimulated vs

34 period, decreased at later times during the light period and eventually reached a level where they w

35 educed respiratory exchange ratio during the light period and lower energy expenditure.

36 Recordings from the 10-h light period and the 12-h dark period were examined sepa

37 The mean results for the 12-hour light period and the 12-hour dark period were compared.

38 tufA transcription also peaked early in the light period and, moreover, that this transcriptional os

39 protein D1, accumulated primarily during the light period, and net transcription reached a peak betwe

40 reduced light levels or to low CO(2) for one light period, and returned to growth conditions.

41 ear the beginning and towards the end of the light period, and this pattern was inversely related to

42 neutral lipids) was observed throughout the light period, and water-soluble glucans increased rapidl

43 nation and its steady state level during the light period are downregulated by phototropin, whereas t

44 its processing via Rubisco in the subsequent light period - are now reasonably well understood in ter

45 s spent less time in SWS and REMS during the light period but more time in SWS and REMS in the dark p

46 phase (the human dark period, but the mouse light period), but also synchronizes the ubiquitous peri

47 tion of a high-fat diet during the inactive (light) period by increasing futile creatine cycling in m

48 Extension of the light period causes photoperiod stress in Arabidopsis th

49 ce spent more time awake at the onset of the light period due to altered ISF lactate dynamics.

50 ription of nifHDK was initiated prior to the light period, followed by psbA and finally psaA.

51 to a level observed during NREM sleep in the light period in controls suggesting that the sleep-wake

52 r significantly decreased REM during the 8-h light period in mice receiving SAL and in mice receiving

53 tic activation of BF Npas1(+) neurons in the light period increased the amount of wakefulness and the

54 At the ending of each light period, IOP was measured under illumination.

55 ikinase (PPDK) catalyze two key steps during light-period malate decarboxylation that underpin second

56 During the light period, malate decarboxylation concentrates CO(2)

57 dark period (mean, 17.10 mm Hg) than in the light period (mean 11.84 mm Hg).

58 during the dark period and lower during the light period (mean change, 3.6 mm Hg; P < 0.005).

59 the physiology of photosynthesis during the light periods, notably stimulating cyclic electron flow

60 romoted NREMS and suppressed REMS during the light period of the day.

61 starch excess phenotype in leaves during the light period of the growth cycle due to an apparent incr

62 diurnal alternance of the active phase (the light period of the human light-dark cycle, but the mous

63 onsequence of metabolism at the start of the light period, of the high levels of malto-oligosaccharid

64 injecting carbachol at the beginning of the light period or beginning of the dark period, we sought

65 y tested in plants perturbed by a night-time light period or by mutations in starch degradation pathw

66 ygen 5-6% at 60 cycles h(-1) for 12 h during light period) or intermittent air (IA; control) and (2)

67 se shifts of the sleep-wake cycle in a short light period (photoperiod) paradigm.

68 gametes into seawater following an inductive light period (potentiation), and gamete expulsion from p

69 COD) loading rate to the removal rate in the light period prevented substrate availability during the

70 hat CO activation of FT occurs only when the light period reaches a certain length and preventing pre

71 FS also significantly decreased light period REM whereas mFS did not.

72 23 (16.6%) of the 139 neurones tested in the light period responded.

73 ral nucleus of the amygdala (CNA) during the light period significantly reduced REM, shortened sleep

74 Light period stomatal closure was also perturbed, and th

75 and approximately 4 times more active during light periods than old rats.

76 is to maintain rods at saturation during the light period, then in retinal regions where light intens

77 p, NREM and REM; however, mNE also increased light period total sleep and NREM, but not REM.

78 When the duration of the daily light period was manipulated experimentally, melatonin-o

79 and non-responsive neurones in the dark and light periods was highly significant (P < 0.01, Fisher's

80 (3) species can synthesize malate during the light period, we argue that the switch to night-time mal

81 uctuating light conditions, in which the low light periods were repeatedly interrupted with high ligh

82 In contrast, during the light period, when these mice are normally inactive and

83 wake time (decreased total sleep) during the light period, which corresponds to human night time.

84 a new mechanism for sensing the duration of light period, which is important for seasonal changes in

85 d is performed during the rodents' inactive (light) period, which could potentially undermine the con