コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 but can also control the end of a locomotor bout.
2 MSN networks to signal the end of a movement bout.
3 ascular protection from subsequent ischaemic bouts.
4 ected, and initiation of subsequent foraging bouts.
5 and lower pH than controls for all exercise bouts.
6 lt mosquitoes through a sequence of activity bouts.
7 0b limits the duration of individual feeding bouts.
8 hing, indicating that dive types occurred in bouts.
9 E in neurons that regulate Drosophila flight bouts.
10 feedforward control of subsequent locomotor bouts.
11 controls the orientation of successive swim-bouts.
12 pation changed across consecutive locomotion bouts.
13 p primarily by modulating the length of wake bouts.
14 ood search and for undertaking longer flight bouts.
15 (1-9.59 minutes) and "long" (>/=10 minutes) bouts.
16 ng activity changes strongly during whisking bouts.
17 ity over several injury-induced regeneration bouts.
18 s only phase locked to visually evoked gamma bouts.
19 ortionally in response to subsequent feeding bouts.
20 er enhanced by two additional daily exercise bouts.
21 nvolved in the orientation-selection of swim bouts.
22 required for fast, straight, forward walking bouts.
23 intense activities into succeeding cataplexy bouts.
24 ning transitions between individual grooming bouts.
25 healthful alternative to prolonged sedentary bouts.
26 .001), vigorous physical activity minutes in bouts (4.1; 95% CI, 2.7-5.6; P < .001), and total accele
27 4-4.35) minutes for MVPA undertaken in short bouts, 4.16 (95% CI:3.11-5.20) minutes for long bouts, a
28 eline in time in MVPA weekly in >/=10-minute bouts, accelerometer counts, and counts/minute at 3 mont
29 files were assessed throughout each exercise bout and in response to brachial artery FMD, measured pr
30 pha, occurs in response to a single exercise bout and is further enhanced by two additional daily exe
32 s gave less grooming at the beginning of the bout and were more likely to abandon a grooming bout, wh
33 opaminergic neurons exhibit shortened flight bouts and a disinterest in seeking food, accompanied by
35 tions of sitting time with physical activity bouts and beneficial metabolic outcomes, even in individ
36 tral nervous system usually characterized by bouts and remissions and typically followed by a seconda
37 ed associations between individuals' walking bouts and walking risk, measured as mean exposure to the
39 ts, 4.16 (95% CI:3.11-5.20) minutes for long bouts, and 7.55 (95% CI:5.86-9.24) minutes for all MVPA
40 nonstationary, typically occurring in short bouts, and the peak frequency of this rhythm is modulate
41 drowsiness, rather than RIS-dependent sleep bouts, appears to be important for increasing survival a
42 ield potential oscillation occurred in short bouts (approximately .4 s)-rather than continuously-and
43 and its accrual in prolonged, uninterrupted bouts are associated with all-cause mortality, suggestin
44 mental variables, if earlier, longer calling bouts are energetically costly, and therefore limited by
46 ed simulation models called MBITES (Mosquito Bout-based and Individual-based Transmission Ecology Sim
49 specific autoantibodies can initiate disease bouts by cooperating with the autoreactive T cells in he
50 day and 3 step intensity measures (extended bout cadence, peak 30-minute cadence, and peak 1-minute
54 cient in the mitochondrial Glu transporter A BOUT DE SOUFFLE (BOU) and identified 27 differentially e
56 pamine transmission throughout the footshock bout did not predict performance but rather was modulate
57 ]; P for trend < 0.001) and longer sedentary bout duration (HR, 1.03 [CI, 0.67 to 1.60]; HR, 1.22 [CI
58 (high sedentary time [>/=12.5 h/d] and high bout duration [>/=10 min/bout]) had the greatest risk fo
59 High total sedentary time or high sedentary bout duration alone were not associated with differences
62 ted in higher sleep amounts and longer sleep bout duration during the night, while overexpression had
63 se infusions markedly increased mean feeding bout duration for both food types and produced a modest
64 total feeding duration, and average feeding bout duration for the palatable-food condition only but
65 ed as the reciprocal of the average activity bout duration in minutes, with higher fragmentation indi
66 iation of total sedentary time and sedentary bout duration showed that participants in the upper quar
68 vigorous physical activity, longer sedentary bout duration was dose-dependently associated with incre
70 -response associations of sedentary time and bout duration with CVD were linear (P-nonlinear >0.05, e
71 high total sedentary time and high sedentary bout duration) had the highest levels of homeostatic mod
72 e; 7.7, 9.6, and 12.4 min/bout for sedentary bout duration) in models that included moderate to vigor
73 s in time spent in NREM sleep and NREM sleep bout duration, verifying the presence of increased sleep
76 ified as having high sedentary time and long bout durations had significantly higher risk for CVD (HR
81 es of the weight that they support as mating bouts, during which males ride on top of females, start
86 uences govern the selection of discrete swim-bout events that subserve the fish navigation in the pre
87 Each session included two 30 min exercise bouts followed by 20 and 40 min of recovery, respectivel
88 4, 24, 48, and 72 h after the first exercise bout for determination of amino-terminal propeptide of c
89 total sedentary time; 7.7, 9.6, and 12.4 min/bout for sedentary bout duration) in models that include
92 ics of locomotion over a hundred of thousand bouts from hundreds of mutant and control sibling larvae
93 e report that a heavy-load strength training bout greatly alters the structure of the membrane networ
96 a second MLR stimulation stops the locomotor bout if it is of lower intensity than the initial stimul
97 nd objectively measured MVPA in >/=10-minute bouts in 60-75 year olds at 3 and 12 months, with no eff
98 einstatement increased the number of rearing bouts in an open field, possibly suggesting an increase
101 tocol 2, participants performed two exercise bouts in which muscle fibre recruitment was manipulated
102 al PFC (dmPFC) prior to an active bout, or a bout initiated by the focal mouse, but not during a pass
105 advantage of this structure by categorizing bouts into discrete types and representing their behavio
106 onged sedentary bouts with shorter sedentary bouts is associated with reductions in all-cause mortali
107 ragers (being neither larger nor making more bouts); larger bees with more antennal olfactory sensill
109 o components were positively correlated with bout length (posterior cingulate cortex, inferior occipi
110 and significant genetic correlations between bout length and two gray matter covariation components.
111 nce revealed a significant rearing effect on bout length, with human-reared chimpanzees engaging in l
114 te stochastic model of rodent feeding at the bout level in order to perform quantitative behavioural
115 g sedentary time in prolonged, uninterrupted bouts may be deleteriously associated with biomarkers of
116 as midge allergen-challenge-induced scratch bouts, midge allergen-induced IL-13 and IL-4 production
117 and the charity group an additional 32 MVPA bout min per week (12-51; p=0.0013) compared with contro
118 he Fitbit group logged an additional 37 MVPA bout min per week (19-56; p=0.0001) and the charity grou
119 and the charity group an additional 21 MVPA bout min per week (2-39; p=0.0310); the difference betwe
120 A decrease in physical activity of -23 MVPA bout min per week (95% CI -42 to -4; p=0.0184) was seen
121 the cash group logged an additional 29 MVPA bout min per week (95% CI 10-47; p=0.0024) and the chari
124 entive was most effective at increasing MVPA bout min per week at 6 months, but this effect was not s
126 effective at stemming the reduction in MVPA bout min per week seen in the control group, but we iden
127 oderate-to-vigorous physical activity (MVPA) bout min per week, was measured via a sealed acceleromet
128 support (95% CI 365-989); additional MVPA in bouts (min/wk) were 33 for postal (95% CI 17-49) and 35
130 Dopamine (0.5-100 muM) reduced fictive swim bout occurrence and caused both spontaneous and evoked e
131 rein one mouse witnesses the physical defeat bout of a conspecific from the safety of an adjacent com
132 l parity) vicariously experienced the defeat bout of a male conspecific, by a male CD1 aggressor, for
133 The effort exerted and vigor to initiate a bout of active lever presses were signaled by dopamine t
136 r FUT2 SNP rs601338, the risk ratios for >=1 bout of diarrhea during ages 6-12 months and ages 12-24
137 t occur in mouse skeletal muscle 1 h after a bout of electrically evoked maximal-intensity contractio
138 is study, we assessed the effect of a single bout of endurance exercise on the skeletal muscle clock
139 ze MyoPS rates during recovery from a single bout of endurance exercise.This trial was registered at
147 flammatory environment is produced with each bout of exercise, and long-term anti-inflammatory effect
153 reas higher-frequency activity (even a short bout of gamma frequency oscillations) converts the corti
154 Seven untrained men performed a standardized bout of high-intensity interval exercise trial following
158 ears, BMI 22.2 +/- 1.6) received a 15 minute bout of local cryotherapy, delivered via ice cup massage
162 investigated the lasting effects of a single bout of neonatal inflammation on adult respiratory contr
164 stus lateralis biopsies before and after one bout of RE, after 12 weeks of EET (cycling), and after a
166 dy aimed to determine the effect of a single bout of resistance exercise at different intensities on
167 ell as immediately, 1 and 3 h after an acute bout of resistance exercise in a fed (FED; 20 g Protein/
171 eurons that were activated during a previous bout of torpor is sufficient to initiate the key feature
172 , via release from immobilization or intense bout of training, significantly reduced mental movement
173 rpose herein was to assess the effect of one bout of treadmill exercise on skeletal muscle clock phas
174 .5 g leucine) mycoprotein (MYCO) following a bout of unilateral resistance-type exercise (contralater
177 prolonged sitting interrupted with 2-minute bouts of (ii) light- or (iii) moderate-intensity treadmi
179 thatclpP1 has undergone remarkably frequent bouts of accelerated sequence evolution and architectura
181 istance translocation arises when successive bouts of active transport were linked by periods of free
182 s freed from synaptic clusters undergo ~1 um bouts of active transport, initiated by nearby elongatio
187 pidemic clonality," demonstrating occasional bouts of clonal propagation in an otherwise recombining
188 lean mice, caloric restriction (CR) induces bouts of compulsive binge feeding separated by prolonged
190 On day 2, subjects performed three 6-min bouts of cycling at ventilatory threshold, in a single-b
196 ransient increases of stressors during acute bouts of exercise or exercise training stimulate enhance
199 rians, and bilaterians underwent independent bouts of gene expansion in channel families involved in
202 play occurs within sharp wave-ripples: short bouts of high-frequency activity in area CA1 caused by e
203 hin ~200 ms, but animals routinely engage in bouts of high-frequency sniffing spanning several second
206 mic preconditioning (RIPC), induced by brief bouts of ischaemia followed by reperfusion, confers vasc
207 adaptations that protect against subsequent bouts of ischaemia; however, the effect of RIPC repeated
208 o sucrose solution, PENK KOs exhibited fewer bouts of licking than wild types, even though the length
209 peaks in vivo: these peaks coincide with the bouts of locomotor activity and result from independent
212 imize endurance performance during prolonged bouts of moderate- to high-intensity exercise as well as
213 human-reared chimpanzees engaging in longer bouts of mutual gaze compared to mother-reared and wild-
218 artate (LOLA) in patients with cirrhosis and bouts of overt hepatic encephalopathy (OHE) are missing.
220 atients demonstrate shorter, more fragmented bouts of physical activity throughout the day and lower
221 and altered tissue expression preceded major bouts of positive selection in the African ape lineage,
222 nsolidated skills are modified over multiple bouts of practice and in response to newfound challenges
227 between host-imposed quiescence and sporadic bouts of replication to complete its life cycle, however
234 ific assemblies of multimodal neurons during bouts of sensory driven co-activity, leaving a trace of
236 cipants (5 females) completed a total of six bouts of single-leg knee-extension exercise (60% peak wo
237 ce are polyphasic, exhibiting multiple sleep bouts of sleep several minutes long within a 24-h period
241 Cell stress is implicated in triggering bouts of systemic inflammation in patients with autoinfl
242 against this overall pattern of shortening, bouts of telomere length increase occur in some individu
245 ge," such that features acquired in distinct bouts of training are combined in an animal's mind, so t
247 sustained elevations in IL-6 due to repeated bouts of unaccustomed activities or prolonged exercise w
248 aining (HIT), referring to alternating short bouts of very intense anaerobic exercise with recovery p
250 Strong gamma activity patterned in short bouts (one to three cycles), occurred when PVs and PYRs
251 sical activity (either in total or in 10-min bouts or more), daily sedentary time, body-mass index, o
252 dorsal-medial PFC (dmPFC) prior to an active bout, or a bout initiated by the focal mouse, but not du
256 t not for replacement with shorter sedentary bouts (per 30 minutes, HR = 1.00; 95% CI: 0.96, 1.03).
257 t that songbirds crossed deserts with flight bouts performed at various altitudes according to specie
260 y step-counts and time in MVPA (in >/=10-min bouts), respectively, measured objectively by accelerome
264 d with repeated stress, and some changes (PS bouts, SWS time, body temperature, locomotor activity) p
266 ong ending, as well as an abrupt increase in bout syntactic complexity, peaking in the last quintile
270 tion by other animals) had longer incubation bouts than those that are readily visible or who activel
272 In this latter bat, we documented 5 torpor bouts that lasted >/=16 days and a flightless period tha
274 ts precede and accompany spontaneous running bouts, that selective chemogenetic silencing of natural
275 ssociation for replacing prolonged sedentary-bout time with LIPA and MVPA but not for replacement wit
278 e, to ensure quick recovery between exercise bouts, to optimize adaptations to exercise training, and
279 ly, marked renewal processes-to evaluate how bout types and interbout intervals are selected by the f
281 ve movements and vocalizations that occur in bouts, typically many times in a single day, and are oft
282 the median length of one parent's incubation bout varied from 1-19 h, whereas period length-the time
284 Lip-smacking at the beginning of grooming bouts was significantly more often followed by longer an
285 g than wild types, even though the length of bouts was similar to that of wild types, a pattern that
287 wing the last of the four daily induced wake bouts, we examined the brains and observed a chimeric pa
289 ivated by stressors in vivo, whereas feeding bouts were associated with reduced activity of these neu
290 at both the prevalence and duration of theta bouts were increased relative to the sighted participant
293 step-counts and weekly MVPA in >/=10-minute bouts were significantly higher in the intervention than
296 t and were more likely to abandon a grooming bout, while bouts were less likely to be reciprocated.
297 feeding assay that measures individual meal-bouts with high temporal resolution at nanoliter scale.
298 or MVPA) or 2) replacing prolonged sedentary bouts with shorter sedentary bouts is associated with re
299 e in rodents, however, theta occurs in short bouts, with average durations of approximately 400 ms, w
300 variables, (b) subsurface foraging occurs in bouts, with distinct periods of searching and capture te