ライフサイエンスコーパス: diurnal rhythm

1 factors, including hormones, bile acids, and diurnal rhythm.

2 omeric localization appears dependent on the diurnal rhythm.

3 s) both for leaf developmental gradients and diurnal rhythm.

4 the crater that appear and disappear with a diurnal rhythm.

5 sed in the stem, and 10 STs responded to the diurnal rhythm.

6 vity to high-fat diet-induced disruptions of diurnal rhythm.

7 ation and maltose metabolism showed a strong diurnal rhythm.

8 euroendocrine dopaminergic neurons exhibit a diurnal rhythm.

9 tration of 5-HT in the hemolymph expressed a diurnal rhythm.

10 or severe stressors also disturbs sleep and diurnal rhythms.

11 glial-mediated lipid metabolism in sleep and diurnal rhythms.

12 nance of PNNs, but not in the maintenance of diurnal rhythms.

13 t and intact synchrony between circadian and diurnal rhythms.

14 ated to the estimated plastochron length and diurnal rhythms.

15 ive to circulating factors with circadian or diurnal rhythms.

16 Telemetry showed disturbances in diurnal rhythms a few days before death and, later, elec

17 ile de Bree and Mouritis et al. describe how diurnal rhythms affect the degree of BCG-induced innate

18 te the recovery and realignment of sleep and diurnal rhythms after circadian disruption.

19 N were less adverse with persistence of some diurnal rhythms, albeit with significant waveform altera

20 onducted and showed age-related reduction of diurnal rhythm amplitude selectively in the hippocampal

21 aging was associated with a blunting of the diurnal rhythm and a significant linear increase in cort

22 n conclusion, RORalpha is a key regulator of diurnal rhythm and fasting induction of CYP8B1, which re

23 first evidence that hGH synthesis follows a diurnal rhythm and of dynamic associations of the circad

24 tion displayed a sensitive regulation by the diurnal rhythm and phase-shift.

25 g without caloric reduction, sustains robust diurnal rhythms and can alleviate metabolic diseases.

26 Synchrony between environmental diurnal rhythms and intracellular circadian rhythms is e

27 s source of energy and information to detect diurnal rhythms and seasonal changes.

28 nd that all cell types have transcripts with diurnal rhythms and that top rhythmic transcripts are la

29 studies: increased average levels, a blunted diurnal rhythm, and enhanced response to stressors.

30 Additionally, it was more sensitive under a diurnal rhythm, and had more complex gene networks than

31 ely 43% of the astrocyte transcriptome has a diurnal rhythm, and key metabolic pathways were enriched

32 o hours for hormone secretion, ultradian and diurnal rhythms, and weeks for changes in endocrine glan

33 Diurnal rhythms are commonly found in behavioral respons

34 It is hypothesized that these diurnal rhythms are entrained by the cyclic production o

35 metabolism, and electrophysiology, all have diurnal rhythms, as does the neurohumoral control of car

36 e temperature (at 12 h) and the activity and diurnal rhythm (at day 4) of the 25G-treated CLP group r

37 Imposing a food intake diurnal rhythm by time-restricted feeding (TRF; food was

38 nes is regulated developmentally and follows diurnal rhythms controlled by a circadian clock.

39 Diurnal rhythm disruption immediately after MI impaired

40 Short-term diurnal rhythm disruption immediately after MI impairs r

41 less sensitive to pathological disruption of diurnal rhythms during obesity than metabolic tissues an

42 Rats used for cyclic light and diurnal rhythm experiments were removed from their light

43 recently shown that CART peptides exhibit a diurnal rhythm in blood that is affected by food intake

44 In a validation study, the presence of a diurnal rhythm in BNP and NT-proBNP concentrations was e

45 PINA expression exhibits a dramatic diurnal rhythm in both pineal gland and retina with 100-

46 that NPAS2 knockdown in the NAc disrupts its diurnal rhythm in expression.

47 Herein, we demonstrate the existence of a diurnal rhythm in GLP-1 secretory responses to an oral g

48 clock, and glucose tolerance demonstrates a diurnal rhythm in healthy humans with better glucose tol

49 In mice, there is a diurnal rhythm in hepatic AADA mRNA concentration, with

50 lating ZAG levels exhibited a characteristic diurnal rhythm in humans, with a major nocturnal rise oc

51 Numerous studies have demonstrated a diurnal rhythm in indices of pulmonary function in both

52 There was a diurnal rhythm in IOP in the marmosets: IOP was higher d

53 There was a loss of a diurnal rhythm in micturition patterns and a large incre

54 rats, thereby suggesting the existence of a diurnal rhythm in MPOA cGMP/NO efflux which may particip

55 not elicit changes in p-ERK, nor was there a diurnal rhythm in p-ERK levels, nor could rapid changes

56 protein abundance of cry2 and phyA showed a diurnal rhythm in plants grown in short-day but not in p

57 o a behavioral stressor without altering the diurnal rhythm in plasma corticosterone.

58 Reward response may follow the diurnal rhythm in self-reported positive affect, peaking

59 onstrating that CART peptides also exhibit a diurnal rhythm in several brain regions, notably the nuc

60 Results suggest a diurnal rhythm in synaptic transmission specific to the

61 A diurnal rhythm in the dark-adapted ERG responses was obs

62 There exists a misalignment of the NP-BP diurnal rhythm in the obese, which may contribute to the

63 ng sodium depletion, and as a consequence of diurnal rhythm in the suprachiasmatic nucleus.

64 tion of estrogen deprivation-induced loss of diurnal rhythm in TST.

65 ults show that cAMP concentrations exhibit a diurnal rhythm in young rats, and that this rhythm is to

66 To determine whether the diurnal rhythms in axial length and choroidal thickness

67 Canonical circadian genes had diurnal rhythms in both sexes with similar amplitude and

68 east cancer patients often exhibit disrupted diurnal rhythms in circulating glucocorticoids (GCs), su

69 ndent hormone module is critical to maintain diurnal rhythms in circulating lipids.

70 program in Chlamydomonas reinhardtii, or how diurnal rhythms in gene expression and metabolism shape

71 Diurnal rhythms in gene expression have been detected in

72 Here we identify diurnal rhythms in gene expression in the human dorsolat

73 epithelial structure and function that drive diurnal rhythms in gut microbiota.

74 step in understanding the normal function of diurnal rhythms in humans and model organisms in these r

75 how that the intestinal microbiota generates diurnal rhythms in innate immunity that synchronize with

76 Diurnal rhythms in IOP, axial length, and choroidal thic

77 In control flies, 72 genes showed diurnal rhythms in light-dark cycles; 22 of these also o

78 ibitum access to the running wheel to assess diurnal rhythms in locomotor activity.

79 a critical role for BMAL1 in controlling the diurnal rhythms in Ly6C(hi) monocyte numbers.

80 Ablation of Klf4 expression abolished diurnal rhythms in phagocytic activity, recapitulating t

81 Calorie restriction reprograms diurnal rhythms in protein translation to regulate metab

82 2-h later in females than males, suggesting diurnal rhythms in reward may be delayed in females.

83 used a "time-of-death" approach to identify diurnal rhythms in RNA transcripts in human cortical reg

84 used a "time-of-death" approach to identify diurnal rhythms in RNA transcripts in these three human

85 Groups of rats with strong diurnal rhythms in sleep-wake organization were killed a

86 ice exhibit blunted GC rhythms and a loss of diurnal rhythms in the activity of paraventricular hypot

87 in many brain regions, and included loss of diurnal rhythms in the hippocampal CA2 and CA3 subfields

88 helping to understand the normal function of diurnal rhythms in these regions and how disruption coul

89 However, diurnal rhythms in transcript expression have not been i

90 echanism might be used for the regulation of diurnal rhythms in translation and/or RNA processing in

91 g (20-wk)-induced obesity in mice, abolished diurnal rhythms in whole body metabolic flexibility, and

92 The influences of diurnal rhythms involving a variety of ocular parameters

93 to achieve the normal nadir in the cortisol diurnal rhythm, loss of sensitivity of ACTH-secreting tu

94 nces in anxiety and spatial learning/memory, diurnal rhythm may interact with other factors to influe

95 The dramatic diurnal rhythm of 3OST2 is regulated by central clock-co

96 s project preferentially to LC and express a diurnal rhythm of activation that correlates with LC neu

97 r clock in atherosclerotic lesions induces a diurnal rhythm of apoptosis regulated by circadian Mir21

98 Our results demonstrate that there is a diurnal rhythm of beta-endorphinergic neuronal activity

99 of 10 mmHg (P < 0.0001), reversed the normal diurnal rhythm of blood glucose (P < 0.03), doubled cort

100 stoperative day 4 am through day 7, a robust diurnal rhythm of corticosterone (p < .001) with a modes

101 ticosterone to the amygdala had no effect on diurnal rhythm of corticosterone secretion.

102 ed rapidly when compared with changes in the diurnal rhythm of cortisol, suggesting that leptin level

103 The short-day-specific diurnal rhythm of cry2 is determined primarily by blue l

104 riation and to investigate the presence of a diurnal rhythm of cTnT.

105 ms of a subset of liver genes and alters the diurnal rhythm of de novo lipogenesis.

106 with both intermittent fasting and adjusted diurnal rhythm of feeding improving health and function,

107 sults in obesity in mice with a shift in the diurnal rhythm of food intake, a result that is not seen

108 are consistent with the possibility that the diurnal rhythm of GA levels plays a role in floral initi

109 ow the central circadian clock regulates the diurnal rhythm of hepatic insulin sensitivity, with impl

110 These findings suggest that the diurnal rhythm of histamine release entrains striatal fu

111 se of the skin circadian clock, reverses the diurnal rhythm of IMQ-induced ISG expression in the skin

112 ucleus (SCN) (SCN(GABA) neurons) control the diurnal rhythm of insulin-mediated suppression of hepati

113 of cyanobacteria are inherently tied to the diurnal rhythm of light availability.

114 ransferase is the enzyme responsible for the diurnal rhythm of melatonin production in the pineal gla

115 The diurnal rhythm of metabolic gene expression driven by th

116 eptors, is involved in the regulation of the diurnal rhythm of ocular growth.

117 es were drawn at 07:00 and 19:00 h to assess diurnal rhythm of plasma corticosterone.

118 We conclude that the diurnal rhythm of plasma leptin in young males is entrai

119 y the physiologic factor(s) that entrain the diurnal rhythm of plasma leptin, leptin levels were meas

120 Moreover, our results demonstrate that the diurnal rhythm of PS demarcation of POS tips is not intr

121 ed-measures imaging procedure to explore the diurnal rhythm of reward activation.

122 fasting and feeding had little effect on the diurnal rhythm of RORalpha mRNA expression, but fasting

123 f transport conduits, and (2) a shift in the diurnal rhythm of sugar metabolism and export in needle

124 The normal, meal-related fluctuations and diurnal rhythm of the ghrelin level were absent after ga

125 hybridizations showed strong induction and a diurnal rhythm of transcript abundance with a maximum ea

126 -ERBbeta in adult mouse hepatocytes disrupts diurnal rhythms of a subset of liver genes and alters th

127 Mice lacking PGC-1alpha show abnormal diurnal rhythms of activity, body temperature and metabo

128 des cue-independent anticipatory signals for diurnal rhythms of baseline glucose levels and glucose t

129 egnancy, all four experimental groups showed diurnal rhythms of beta-endorphinergic neurons.

130 We also describe strong diurnal rhythms of cellular fluorescence in wild-type ce

131 Following infection, we measured diurnal rhythms of clock gene expression in the lung, lo

132 The SCN clock regulates physiological diurnal rhythms of endogenous glucose production (EGP) a

133 The presence of diurnal rhythms of entry into and arousal from torpor in

134 weight and adiposity but also phase-advances diurnal rhythms of feeding and metabolism into the light

135 Oscillating diurnal rhythms of gene transcription, metabolic activit

136 neural and secreted factors in physiological diurnal rhythms of glucose metabolism and their patholog

137 At the genome-wide level, diurnal rhythms of H3K4me3 and another histone mark H3K9

138 o be the rate-limiting factor in driving the diurnal rhythms of overall protein synthesis.

139 these tissues and they demonstrated distinct diurnal rhythms of protein expression in the retina-RPE-

140 t is a robust entrainment cue that regulates diurnal rhythms of the gut microbiome.

141 Concurrent diurnal rhythms of these secretions could potentiate the

142 To better understand the effects of diurnal rhythm on mouse behaviors, we compared the resul

143 heat and cold signal transduction, sleep and diurnal rhythm regulation, effects of immunophilin ligan

144 lic and autonomic dysregulation with blunted diurnal rhythms, specific sleep pattern pathologies and

145 preclinical findings suggest that disrupted diurnal rhythms such as found in modern intensive care u

146 The level of O2 transcript follows a diurnal rhythm that appears controlled by the circadian

147 yed rectifier (FDR) potassium currents has a diurnal rhythm that peaks during the day.

148 and NT-proBNP, but not MR-proANP, exhibit a diurnal rhythm that results in even higher diagnostic ac

149 Intermeal ghrelin levels displayed a diurnal rhythm that was exactly in phase with that of le

150 ic nucleus, cardiac physiology fluctuates in diurnal rhythms that can be partly or entirely circadian

151 rize features of the microbiota that undergo diurnal rhythms, their development, their impact on the

152 1C) expression, and its own expression has a diurnal rhythm, thereby explaining the rhythmic nature o

153 M sleep and core body temperature (ClockLab) diurnal rhythms to the altered light/dark cycle.

154 coding for cytokines showed tissue-specific diurnal rhythms under LD and were lost with exposure to

155 This was not true for diurnal rhythms under pentobarbital and avertin, but bot

156 tion for a cytokine offers the basis for the diurnal rhythms underlying a dynamic symbiotic conversat

157 The cortisol diurnal rhythm was preserved in all groups of patients.

158 er adults, day-to-day variations in cortisol diurnal rhythms were predicted from both prior-day and s

159 vels, gut microflora, time of year, and even diurnal rhythm, which had a direct impact on innate immu

160 Systemic insulin sensitivity shows a diurnal rhythm with a peak upon waking(1,2).

161 ine day, plasma leptin demonstrated a strong diurnal rhythm with an amplitude of 21%, zenith at 2400

162 in the hypothalamus which exhibit a distinct diurnal rhythm with high activity during wakefulness, an

163 sCRP) has previously been reported to have a diurnal rhythm with higher levels upon awakening and low

164 were arrhythmic, whereas others expressed a diurnal rhythm with low amplitude and significant activi

165 l gland, ptc1 expression exhibits a dramatic diurnal rhythm with peak expression at midnight.