ライフサイエンスコーパス: acrophase

1 CT-1 deficiency caused a phase shift of the acrophase.

2 whereas sunrise had greatest power for T(b) acrophase.

3 non-linear parameters MESOR, amplitude, and acrophase.

4 ar circadian parameters MESOR, amplitude and acrophase.

5 traclass correlation coefficients of the CLS acrophase (0.6 [95% CI, 0.0 to 0.9]; P = .03), CLS bathy

6 atistically significant cosine + linear fit (acrophase 03:24 +/- 20 h:min, amplitude 0.05 +/- 0.01 ng

7 The average circadian amplitude between acrophase and nadir was 75.6% in lean, 51.7%, in obese a

8 he magnitude and direction of linear change, acrophase and slope estimates also differed between grou

9 The 24-hour IOP curve acrophases and amplitudes for OHTNs were closer to those

10 ding signal, maximum signal, minimum signal, acrophase, and bathyphase (P > .15).

11 Insulin sensitivity reached its maximum (acrophase) around noon, being 54% higher than during mid

12 Comparisons of acrophase, bathyphase, amplitude, and the midline estima

13 Comparison of acrophase, bathyphase, amplitude, midline estimating sta

14 over time with mean T(b) increasing and T(b) acrophase becoming earlier as the season progressed.

15 anscripts showed a similar temporal order of acrophases but with a 7.6 hours phase shift.

16 anscripts showed a similar temporal order of acrophases but with a ~7.6 hours phase shift.

17 There was no sex difference in acrophase, but females had a significantly smaller ampli

18 ther chronobiological parameters (amplitude, acrophase, circadian quotient, and goodness-of-fit coeff

19 ical group exhibited an absence of nocturnal acrophase compared to the medically treated group.

20 coma group exhibited an absence of nocturnal acrophase (difference: P = .011).

21 during the 24-h free access period, with the acrophase in activity being significantly earlier in EAP

22 ight, while the timing of activity onset and acrophase is delayed in aged mice compared to younger mi

23 red to urinary 6-sulphatoxymelatonin (aMT6s) acrophase measured on the diurnal schedule and last cons

24 6s) were measured from evening onset, cosine acrophase, morning offset and duration of excretion.

25 We also found that the acrophase of molecular circadian clock component REV-ERB

26 rity of sundowning was associated with later acrophase of temperature, less correlation of circadian

27 of HRV endpoints did not change but the 12-h acrophase of TF-HRV did (P < 0.0001), perhaps consolidat

28 of body temperature and activity and in the acrophase of the circadian rhythm for temperature.

29 ine cosine curve was used for melatonin, and acrophase of the cosine curve for aMT6s.

30 On nights, working during the circadian acrophase of the urinary melatonin rhythm led to poorer

31 e shifts were measured for the cosine-fitted acrophase of urinary 6-sulphatoxymelatonin (aMT6s), as w

32 During the second mission, 24-h acrophases of HRV endpoints did not change but the 12-h

33 That is, the timing of the peak (acrophase) of multiple circadian rhythms (leaf movement,

34 Significant PRCs were found for aMT6s acrophase, onset and duration, with peak phase advances

35 re significant changes in mean T(b) and T(b) acrophase over time with mean T(b) increasing and T(b) a

36 (4) /PER3 (4) subjects advanced their aMT6s acrophase (p < 0.05), and showed a trend of advanced sle

37 of sCTX showed a cosine rhythm in all males (acrophase (peak) time (mean +/- SEM) 02:48 +/- 14 h:min,

38 The amplitudes of the aMT6s onset and acrophase PRCs are comparable to expectations for bright

39 rticipants with a later daily activity peak (acrophase) reported poorer sexual function (beta = -0.31

40 tivity rhythms (RARs): normalized amplitude, acrophase representing the peak activity time, interdail

41 om nonheart failure brain-dead donors showed acrophase shifts, or weak or complete loss of circadian

42 circadian indicators (MESOR, amplitude, and acrophase) showed significant differences between sexes,

43 ine temperature curve, and later temperature acrophase than did the healthy subjects.

44 lity of motor activity, and a later activity acrophase (time of peak) than did the healthy individual

45 deviated from 24 hours (P = .007) and daily acrophase (time of the peak of the fit circadian rhythm)

46 Melatonin amplitude and acrophase timing were generally preserved in awake patie

47 t shift schedules, the model predicted aMT6s acrophase to within +/- 1 hour in 42% and +/- 2 hours in

48 ing shift workers, the model predicted aMT6s acrophase to within +/- 1 hour in 66% and +/- 2 hours in

49 TAP acrophase was able to assess eveningness.

50 ose free from dementia, each hour of delayed acrophase was associated with delirium risk (HR = 1.13,

51 sion, fragmentation, and potentially delayed acrophase were associated with delirium risk.

52 thma, and its amplitude, percent rhythm, and acrophase were comparable to those of peak expiratory fl

53 The model predicted aMT6s acrophase with an absolute mean error of 0.69 h on the d

54 e curves were established for aMT6 onset and acrophase with large phase delays from 7:00 pm to 10:00