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1 ased the eEPSCs amplitude 30% throughout the light-dark cycle.
2 physiological processes to the environmental light-dark cycle.
3 tide-deficient mice under the influence of a light-dark cycle.
4 tarch content were determined throughout the light-dark cycle.
5 of exercise driven at various phases of the light-dark cycle.
6 g of activity while under the influence of a light-dark cycle.
7 ynchronizes behavior and metabolism with the light-dark cycle.
8 cess that must be appropriately timed to the light-dark cycle.
9 s sacrificed at 3-h intervals throughout the light-dark cycle.
10 s of animals are powerfully entrained by the light-dark cycle.
11 adian clock period with that of the external light-dark cycle.
12 ion of the endogenous clock to a new shifted light-dark cycle.
13 ontinuous dark, continuous light, or a 12-hr light-dark cycle.
14 od-entrainable rhythms when pitted against a light-dark cycle.
15 ent sleep is altered exposure to the natural light-dark cycle.
16 control gene expression as a function of the light-dark cycle.
17 ted into host flies entrained to an opposite light-dark cycle.
18 turnover by both environmental light and the light-dark cycle.
19 ocalization changes significantly during the light-dark cycle.
20 tion of sleep and wakefulness across a 12:12 light-dark cycle.
21 ostella transcriptomes over 48 hours under a light-dark cycle.
22 electric lighting in addition to the natural light-dark cycle.
23 of activity and rest with the environmental light-dark cycle.
24 hich it performs better than a standard 24-h light-dark cycle.
25 aks during the "active" or dark phase of the light/dark cycle.
26 ical terminal shell, is paced by the diurnal light/dark cycle.
27 ters that measured CBT rhythms under a 12:12 light/dark cycle.
28 both identifiable anatomical nuclei and with light/dark cycle.
29 mice were monitored continuously in a 12:12 light/dark cycle.
30 t were rhythmically expressed over a 24-hour light/dark cycle.
31 t may be regulated in the course of a normal light/dark cycle.
32 imulation at selected times over the 12:12 h light/dark cycle.
33 primarily synchronized to local time by the light/dark cycle.
34 inate their activities with the natural 24-h light/dark cycle.
35 constant light as they do under an ordinary light/dark cycle.
36 xample of the costs of living in a disrupted light/dark cycle.
37 with stage of the estrous cycle and with the light/dark cycle.
38 onship with the external world thanks to the light/dark cycle.
39 ights-on and lights-off transitions during a light/dark cycle.
40 le photoreceptors to link timekeeping to the light/dark cycle.
41 f the circadian timing system to the natural light/dark cycle.
42 be synchronized between SCN cells and to the light/dark cycle.
43 hanges do not result from food intake or the light/dark cycle.
44 mechanical stimuli oscillates throughout the light/dark cycle.
45 n gerbils at selected times during a 12:12 h light:dark cycle.
46 prague-Dawley rats, maintained under a 12:12 light:dark cycle.
47 se in nighttime sleep, when animals are in a light:dark cycle.
48 e normal entrainment of circadian rhythms to light dark cycles.
49 nize the body's circadian rhythms from local light-dark cycles.
50 ies evolved in tropical regions under stable light-dark cycles.
51 behavioral rhythms when flies are exposed to light-dark cycles.
52 ions) in constant darkness as well as 12:12h light-dark cycles.
53 n the entrainment of the molecular clocks to light-dark cycles.
54 ression patterns were revealed under diurnal light-dark cycles.
55 ves, and oscillations entrained to simulated light-dark cycles.
56 vivo and in vitro, which entrain to 24-hour light-dark cycles.
57 eetiolation, but daily at dawn under diurnal light-dark cycles.
58 does not mediate entrainment of the clock to light-dark cycles.
59 ances of daily rhythms in rodents exposed to light-dark cycles.
60 mplitude depends on both feeding-fasting and light-dark cycles.
61 d non-rhythmic patterns of expression during light-dark cycles.
62 lular localization of a subset is subject to light-dark cycles.
63 glucose levels during starvation and through light/dark cycles.
64 nd maintains nutrient homeostasis throughout light/dark cycles.
65 tivity under standard (high light intensity) light/dark cycles.
66 y predict particular phases of the day under light/dark cycles.
67 or sustained rhythms in the absence of daily light/dark cycles.
68 s different during long-day versus short-day light/dark cycles.
69 enous circadian rhythmicity to environmental light/dark cycles.
70 and to noise and that entrained to simulated light/dark cycles.
71 ene expression and attenuated entrainment to light/dark cycles.
72 synthesis, and transcription during diurnal light/dark cycles.
73 th and development with the prevailing daily light/dark cycles.
74 tion and dehydration repeatable over several light/dark cycles.
75 ning PDF expression mediates activity during light/dark cycles.
76 lays a diurnal pattern in plants grown under light/dark cycles.
77 gated its physiology and transcriptome under light/dark cycles.
78 nderlies Suc-induced hypocotyl elongation in light/dark cycles.
79 to daily environmental changes, most notably light/dark cycles.
80 onstant darkness and also in the presence of light:dark cycles.
81 esses and synchronize these to environmental light:dark cycles.
82 gation is accentuated in these mutants under light:dark cycles.
83 crodissection (LCM) and RNA-seq over a 24 hr light / dark cycle.
84 d to the phasing of cellular events with the light : dark cycle.
85 ock-regulated transcripts was observed under light- dark cycles.
86 oots and roots in constant conditions and in light : dark cycles.
87 s in the evening would entrain subjects to a light:dark cycle 1 h longer than their own circadian per
88 nd behavior, however, evolved in the natural light-dark cycle [1], and electrical lighting is thought
89 roduced an electrical current in response to light/dark cycles (12 h/12 h) over 12 months of operatio
90 llus gallus) were raised in either a 12-hour light-dark cycle (12L/12D) or in CL, with or without opa
91 3 days of free-running through an ultradian light-dark cycle (2.5 h wake in dim light, 1.5 h sleep i
92 ol flies, 72 genes showed diurnal rhythms in light-dark cycles; 22 of these also oscillated in free-r
94 fails to abolish PER and TIM oscillation in light-dark cycles, although it does impair rhythmic beha
96 rily evident when LG was assessed across the light-dark cycle and ABN was not associated with these m
97 expression data from different stages of the light-dark cycle and across a wide variety of tissues sh
98 m and livers were collected during a 24-hour light-dark cycle and analyzed by RNA-seq, metabolomic, a
99 entrained to the 24-h day by exposure to the light-dark cycle and feedback from the sleep-wake cycle.
100 in all tissues exhibit normal FAA both in a light-dark cycle and in constant darkness, regardless of
101 ck adapts to seasonal changes in the natural light-dark cycle and is timed later in the modern enviro
102 tical areas differentially varies across the light-dark cycle and likely is responsible, in part, for
103 growth, chicks were maintained on a 12-hour light-dark cycle and were monocularly form-vision depriv
104 the antenna during and after entrainment to light-dark cycles and after photic input is eliminated b
105 esponds preferentially to temperature versus light-dark cycles and entrains to the release from strat
106 on of PER1, PER2, and ghrelin is rhythmic in light-dark cycles and in constant darkness with ad libit
107 r localization of PERIOD and TIMELESS during light-dark cycles and in constant darkness, as well as p
108 ythms are observed in wild-type flies during light-dark cycles and in constant darkness, but are abol
109 uration of morning activity is lengthened in light-dark cycles and light pulses evoke longer lasting
110 ient mice are similar to Vip(-/-) mice under light-dark cycles and only somewhat worse in constant co
112 abbage (Brassica oleracea) is entrainable by light-dark cycles and results in enhanced herbivore resi
113 We entrained Siberian hamsters to various light-dark cycles and then tracked their activity into c
114 when the rabbits were maintained on a normal light/dark cycle and after they were maintained on a lig
116 ese mice showed normal entrainment to a 12 h light/dark cycle and free run in constant darkness with
117 ormal biological variations obeying the 24-h light/dark cycle and have been shown to play a critical
118 that melanopsin mRNA levels were rhythmic in light/dark cycle and in constant darkness in congenic co
119 ions of 5-HT during the light portion of the light/dark cycle and lowest concentrations during the da
125 tandard laboratory conditions of rectangular light/dark cycles and constant warm temperature, Drosoph
128 o dim light at night (dLAN) disrupts natural light/dark cycles and impairs endogenous circadian rhyth
133 e mice show normal entrainment to both 12 hr light/dark cycles and to a 1 hr skeletal photoperiod.
134 paA null; crm1 mutants are able to grow in a light:dark cycle and have no detectable oscillations of
136 re mainly restricted to the photophase under light:dark cycles and subsequently became arrhythmic or
138 ization of activity rhythms to phase-shifted light:dark cycles and that elevation of DA tone through
139 ing their habitat of origin (high food and a light:dark cycle), and suffered from almost complete rep
140 CN regardless of diet or time within the 24h light-dark cycle, and are therefore suitable to be used
141 ierarchy, synchronizing to the environmental light-dark cycle, and coordinates the phases of peripher
142 maximally in the light portion of the daily light-dark cycle, and parietal lobe seizures occurred no
143 model self-synchronizes, entrains to ambient light-dark cycles, and desynchronizes in constant bright
144 sal from torpor in SCNx animals held under a light/dark cycle, and their absence in constant light, s
145 hole plants given drought treatments, during light/dark cycles, and during dehydration of detached le
146 any significant pupil reflex, to entrain to light/dark cycles, and to show any masking response to l
147 thm of hypocotyl elongation was entrained by light-dark cycles applied to the imbibed seed and its pe
148 nous period close to or equal to the natural light-dark cycle are considered evolutionarily adaptive
149 hat were differentially regulated during the light/dark cycle are identified, many of which were asso
150 to a natural winter 9 hr 20 min:14 hr 40 min light-dark cycle as compared to the modern electrical li
151 to environmental changes, specifically daily light-dark cycles, as well as rhythmic food intake.
152 cetic acid continuously over several days of light-dark cycles at relatively high quantum yields, dem
153 conditions, early runner mice entrained to a light/dark cycle at an advanced phase, approximately 3 h
154 (approximately 1.5 lux in the angle of gaze) light-dark cycle] at three approximately 24-h periods: 2
155 ow that they retain a memory of the previous light-dark cycle before returning to their own free-runn
156 lator is therefore likely to be entrained to light/dark cycles both through transcriptional and post-
157 phasing is seen in seedlings entrained by a light-dark cycle but not in seedlings entrained by a tem
158 hronizing rest-activity rhythms with delayed light-dark cycles but is important for proper phasing, w
160 gifer tarandus) is acutely responsive to the light/dark cycle but not to circadian phase, and also th
161 hamsters exhibited normal entrainment to the light-dark cycle, but MSG treatretain-->ment counteracte
162 active phase (the light period of the human light-dark cycle, but the mouse dark period) and the res
164 trol rhodopsin availability during the daily light-dark cycle by novel mechanisms not discerned from
166 ioral and physiological processes with daily light-dark cycles by driving rhythmic transcription of t
167 cadian rhythms are entrained to the external light/dark cycle by photic signaling to the suprachiasma
168 ythms in hamsters are entrained to the daily light:dark cycle by photic information arriving from the
169 E (CRY) synchronizes these feedback loops to light:dark cycles by binding to and degrading TIMELESS (
171 etabolism during diurnal growth, even though light-dark cycles can drive metabolic rhythms independen
172 constant conditions, and plants entrained in light/dark cycles coincident with the entrainment of the
174 in a summer 14 hr 39 min:9 hr 21 min natural light-dark cycle compared to a typical weekend in the mo
175 null in ipRGCs reentrain faster to a delayed light/dark cycle compared with mice expressing virally e
178 P levels appear critical for survival under light:dark cycles, conditions in which RpaB phosphorylat
180 ing to the morning in continuous dark and in light-dark cycles, consistent with the specification of
181 ly entraining hamsters to T cycles (non-24-h light/dark cycles) consisting of a single 1-h light puls
183 erance compared with mice in a standard (LD) light/dark cycle, despite equivalent levels of caloric i
185 that Suc-induced hypocotyl elongation under light/dark cycles does not involve another proposed suga
186 A sensitivity of the circadian clock to light/dark cycles ensures that biological rhythms mainta
187 These rhythms are entrained by the daily light/dark cycle, ensuring that the internal clock time
188 to a natural summer 14 hr 40 min:9 hr 20 min light-dark cycle entrains the human circadian clock to s
191 regulated upon exposure to light during 11hr light/dark cycle experiments under identical conditions.
192 hythms of all cells were coupled to external light-dark cycles far more strongly than the cellular cl
193 (a)) of 6.5 degrees C were housed in a 12 hr light/dark cycle for 19 months followed by 11 months in
194 ol turtles were maintained in a regular 12-h light/dark cycle from hatching until 4 weeks of age, whe
196 tween rest/activity cycles and environmental light/dark cycles have been degraded or even broken.
197 either -15 D lenses or diffusers in a normal light/dark cycle; (ii) wearing either +15 D lenses, -15
199 expression of 10 classic HKG across the 24h light-dark cycle in the SCN of mouse offspring exposed t
202 e state in dry seeds but rapidly entrains to light/dark cycles in ambient temperatures upon imbibitio
203 from standard intensity light:dark cycles to light:dark cycles in which the intensity of the light ph
204 ion (SF) without hypoxia for 5 days (12-hour light/dark cycle) in two inbred mouse strains with low (
205 g conditions (permanent darkness vs. 12:12 h light:dark cycle) in a 2 x 2 factorial design, allowing
207 ved and remains synchronized to the external light-dark cycle, indicating that there is an additional
208 ved and remains synchronized to the external light-dark cycle, indicating that there is an additional
209 expression is quickly perturbed by shifts in light-dark cycles, indicating that this molecular rhythm
210 re of how a physiologically relevant diurnal light-dark cycle influences the metabolism in a photosyn
212 lian master circadian pacemaker to the daily light/dark cycle is mediated exclusively through retinal
213 ntrainment of the circadian pacemaker to the light:dark cycle is necessary for rhythmic physiological
214 ctivity rhythms with respect to the external light:dark cycle is reversed in diurnal and nocturnal sp
215 A previously observed in animals housed in a light:dark cycle is the result of the activity of retina
218 DNA microarray analysis of An. gambiae under light/dark cycle (LD) and constant dark (DD) conditions.
219 ythmicity resulting from exposure of mice to light/dark cycle (LD) and constant darkness (DD) conditi
220 der standard growth conditions, on a 12:12-h light-dark cycle, Lingulodinium polyedrum Fe-SOD exhibit
221 ation of c-Fos expression across the 24-hour light-dark cycle may also be different in these subdivis
222 al estimate of time that anticipates diurnal light/dark cycles, may synchronize physiological behavio
225 of their internal clocks in relation to the light-dark cycle more similar to earlier chronotypes.
228 K Strain) were raised either under a 12-hour light-dark cycle of normal light or under constant light
230 eared in seasonal photoperiods consisting of light/dark cycles of 8:16, 16:8, and 12:12 h, respective
233 rats were exposed to either a standard 12:12 light-dark cycle or a chronic shift-lag paradigm consist
239 nts sense and adapt to darkness in the daily light-dark cycle, or how they adapt to unpredictable env
240 lso advanced under temperature cycles, but a light/dark cycle partially corrects the defects in miR-1
242 Under normal conditions of an alternating light/dark cycle, proliferating cell nuclear antigen (PC
243 luding entrainment of the circadian clock to light-dark cycles, pupillary light responsiveness, and l
246 nas of Opn4(-/-);rd1/rd1 mice synchronize to light/dark cycles regardless of the phase of the master
248 ce are phase advanced and fragmented under a light/dark cycle, reminiscent of the disturbed sleep pat
250 city in the SCN remained phase-locked to the light-dark cycle, restricted feeding rapidly entrained t
252 l cortex of wild-type mice kept in a 24-hour light-dark cycle revealed that Per1, Per2, and Cry1 mRNA
253 iptome in synchronized cells grown on a 24-h light-dark cycle reveals the choreography of gene expres
254 while the mice were maintained in a standard light/dark cycle, SCN neurons remained intact, and neuro
255 Chlorella sorokiniana cells grown with a 7:5 light-dark cycle showed that the NADH:NR activity, as we
256 sensitive to seasonal changes in the natural light-dark cycle, showing an expansion of the biological
257 se plants exhibit some circadian function in light/dark cycles, showing that the Arabidopsis circadia
258 Chlamydomonas cell cycle is synchronized by light-dark cycles, so in principle, these transcriptiona
262 uroendocrine responses to HFS throughout the light-dark cycle suggests uncoupling of hypothalamic res
264 RCs accurately predict entrainment to non-24 light-dark cycles (T-cycles) and constant light (LL).
265 Many causes have been suggested, including light-dark cycles, temperature/weather, and infectious a
267 the amount of benzoic acid during the daily light/dark cycle that were retained in continuous darkne
269 repeated light exposures using a 3.5 h/3.5 h light/dark cycle, the circadian and homeostatic drives o
272 When seedlings were maintained on a 24-h light/dark cycle, there was a stromal Ca(2+) burst after
273 gans and melatonin levels fluctuate over the light:dark cycle; there are also conflicting data on the
276 re analyzed in grass rats transferred from a light/dark cycle to constant darkness and aroused in ear
278 ression is phased by the circadian clock and light/dark cycles to the beginning of the day, the time
279 ype mice transferred from standard intensity light:dark cycles to light:dark cycles in which the inte
281 adian rhythm follows a simple scaling law in light-dark cycles, tracking midday across conditions wit
283 eus (SCN) are entrained to the environmental light/dark cycle via intrinsically photosensitive retina
285 ing of wheel-running rhythms relative to the light/dark cycle was used as a measure of the timing of
287 By conducting experiments with out-of-phase light:dark cycles, we confirm that indeed, it is the fun
292 nths) Per1-luc transgenic rats, entrained to light-dark cycles, were killed, and tissues were removed
293 arouse during the day in the presence of the light/dark cycle, whereas entry into and arousal from to
295 ic nucleus (SCN) is entrained by the ambient light/dark cycle, which differentially acts to cause the
296 he entrainment of the circadian clock by the light-dark cycle, while in mammals they perform an impor
297 uprachiasmatic nucleus (SCN) is reset by the light-dark cycle, while timed food intake is a potent sy
298 icted feeding (RF) [mice housed under a 12-h light-dark cycle with lights on between zeitgeber time (
299 tumor xenografts to demonstrate how altering light/dark cycles with dim LEN (dLEN) speed the developm
300 uccessfully entrained to a new, 6 h advanced light-dark cycle within an average of 4.5 +/- 0.1 days.
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