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1 h and throat tightness after severe coughing bouts).
2 that were "missed" by the first stimulation bout.
3 he beginning and signaling the end of a lick bout.
4 ance between the first and the last foraging bout.
5 hing, indicating that dive types occurred in bouts.
6 ng activity changes strongly during whisking bouts.
7 E in neurons that regulate Drosophila flight bouts.
8 ity over several injury-induced regeneration bouts.
9 s only phase locked to visually evoked gamma bouts.
10 ortionally in response to subsequent feeding bouts.
11 er enhanced by two additional daily exercise bouts.
12 P > 0.05) at the end of both 700 W exercise bouts.
13 evy walks in nearly one-half of all foraging bouts.
14 ut the structure and function of these sleep bouts.
15 sensitized NCX to self-activation by 0 Na(+) bouts.
16 hermy - wherein they exploit episodic torpor bouts.
17 e by increasing the number of waking and REM bouts.
18 emperature and EEG recordings of sleep stage bouts.
19 feedforward control of subsequent locomotor bouts.
20 controls the orientation of successive swim-bouts.
21 0b limits the duration of individual feeding bouts.
22 pation changed across consecutive locomotion bouts.
23 p primarily by modulating the length of wake bouts.
24 (1-9.59 minutes) and "long" (>/=10 minutes) bouts.
28 .001), vigorous physical activity minutes in bouts (4.1; 95% CI, 2.7-5.6; P < .001), and total accele
29 4-4.35) minutes for MVPA undertaken in short bouts, 4.16 (95% CI:3.11-5.20) minutes for long bouts, a
30 an-like problems over several dozen foraging bouts; 5) the instability of visitation schedules in som
31 eline in time in MVPA weekly in >/=10-minute bouts, accelerometer counts, and counts/minute at 3 mont
32 t Ca(2+) via L-type Ca(2+) channels, 0 Na(+) bouts activated Ca(2+) influx efficaciously, indicating
34 files were assessed throughout each exercise bout and in response to brachial artery FMD, measured pr
35 pha, occurs in response to a single exercise bout and is further enhanced by two additional daily exe
36 s gave less grooming at the beginning of the bout and were more likely to abandon a grooming bout, wh
37 tions of sitting time with physical activity bouts and beneficial metabolic outcomes, even in individ
38 tral nervous system usually characterized by bouts and remissions and typically followed by a seconda
39 ed associations between individuals' walking bouts and walking risk, measured as mean exposure to the
41 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
42 e show reduced NREM sleep time, shorter NREM bouts, and decreased power in the low delta range during
43 nonstationary, typically occurring in short bouts, and the peak frequency of this rhythm is modulate
45 and its accrual in prolonged, uninterrupted bouts are associated with all-cause mortality, suggestin
48 ity physical activity (MVPA) in >/=10-minute bouts, as advised in World Health Organization guideline
49 rs, 2 days, and 27 days following an initial bout (B1) of lengthening contractions (LCs) and 2 days f
51 ted from an increased frequency of REM sleep bouts but not their duration, indicating an effect on me
53 hastened sleep onset, reduced length of wake bouts by 50%, increased total time in non-REM and REM sl
55 specific autoantibodies can initiate disease bouts by cooperating with the autoreactive T cells in he
58 on alone) even 24 h beyond a single exercise bout, casting doubt on the importance of nutrient timing
59 n life span or in the number of reproductive bouts compared with Daphnia from lakes with landlocked a
65 ]; P for trend < 0.001) and longer sedentary bout duration (HR, 1.03 [CI, 0.67 to 1.60]; HR, 1.22 [CI
66 (high sedentary time [>/=12.5 h/d] and high bout duration [>/=10 min/bout]) had the greatest risk fo
67 High total sedentary time or high sedentary bout duration alone were not associated with differences
68 ty indicates that the amplitudes of activity bout duration and bout number are augmented in TASK-3 mu
72 ted in higher sleep amounts and longer sleep bout duration during the night, while overexpression had
73 se infusions markedly increased mean feeding bout duration for both food types and produced a modest
74 total feeding duration, and average feeding bout duration for the palatable-food condition only but
75 iation of total sedentary time and sedentary bout duration showed that participants in the upper quar
76 vigorous physical activity, longer sedentary bout duration was dose-dependently associated with incre
78 high total sedentary time and high sedentary bout duration) had the highest levels of homeostatic mod
79 e; 7.7, 9.6, and 12.4 min/bout for sedentary bout duration) in models that included moderate to vigor
80 n-rapid eye movement (NREM) sleep time, NREM bout duration, and EEG delta power during NREM sleep, an
81 s in time spent in NREM sleep and NREM sleep bout duration, verifying the presence of increased sleep
82 pressed motor activity and increased feeding bout duration-a profile opposite to that seen with DAMGO
87 lly established after a bee made 26 foraging bouts, during which time only about 20 of the 120 possib
92 fer from wild types in the number of licking bouts, even though these bouts were shorter in length, s
93 ovide evidence that the "frequency-modulated bout" (FMB), a social call emitted only by male bats (ex
94 Each session included two 30 min exercise bouts followed by 20 and 40 min of recovery, respectivel
95 4, 24, 48, and 72 h after the first exercise bout for determination of amino-terminal propeptide of c
96 total sedentary time; 7.7, 9.6, and 12.4 min/bout for sedentary bout duration) in models that include
99 e report that a heavy-load strength training bout greatly alters the structure of the membrane networ
102 nd objectively measured MVPA in >/=10-minute bouts in 60-75 year olds at 3 and 12 months, with no eff
103 einstatement increased the number of rearing bouts in an open field, possibly suggesting an increase
106 ragers (being neither larger nor making more bouts); larger bees with more antennal olfactory sensill
109 that this increased both song rate and song bout length in low singers, suggesting that high densiti
114 g sedentary time in prolonged, uninterrupted bouts may be deleteriously associated with biomarkers of
115 as midge allergen-challenge-induced scratch bouts, midge allergen-induced IL-13 and IL-4 production
116 and the charity group an additional 32 MVPA bout min per week (12-51; p=0.0013) compared with contro
117 he Fitbit group logged an additional 37 MVPA bout min per week (19-56; p=0.0001) and the charity grou
118 and the charity group an additional 21 MVPA bout min per week (2-39; p=0.0310); the difference betwe
119 A decrease in physical activity of -23 MVPA bout min per week (95% CI -42 to -4; p=0.0184) was seen
120 the cash group logged an additional 29 MVPA bout min per week (95% CI 10-47; p=0.0024) and the chari
123 entive was most effective at increasing MVPA bout min per week at 6 months, but this effect was not s
125 effective at stemming the reduction in MVPA bout min per week seen in the control group, but we iden
126 oderate-to-vigorous physical activity (MVPA) bout min per week, was measured via a sealed acceleromet
127 support (95% CI 365-989); additional MVPA in bouts (min/wk) were 33 for postal (95% CI 17-49) and 35
130 the amplitudes of activity bout duration and bout number are augmented in TASK-3 mutants well beyond
131 Dopamine (0.5-100 muM) reduced fictive swim bout occurrence and caused both spontaneous and evoked e
132 rom mdx and wildtype mice performed a single bout of 100 electrically stimulated eccentric contractio
133 l parity) vicariously experienced the defeat bout of a male conspecific, by a male CD1 aggressor, for
134 The effort exerted and vigor to initiate a bout of active lever presses were signaled by dopamine t
136 red mutations should be expected in a single bout of adaptation, relative to the number of unlinked m
140 t occur in mouse skeletal muscle 1 h after a bout of electrically evoked maximal-intensity contractio
141 ic factors in response to (1) a single acute bout of exercise and (2) chronic exercise training resul
148 reas higher-frequency activity (even a short bout of gamma frequency oscillations) converts the corti
153 ears, BMI 22.2 +/- 1.6) received a 15 minute bout of local cryotherapy, delivered via ice cup massage
159 dy aimed to determine the effect of a single bout of resistance exercise at different intensities on
160 ell as immediately, 1 and 3 h after an acute bout of resistance exercise in a fed (FED; 20 g Protein/
164 , via release from immobilization or intense bout of training, significantly reduced mental movement
168 curred during contractile fatigue testing (3 bouts of 25 100 Hz tetanic contractions; duty cycle = 0.
169 sis rates while completing 9 sessions of 4-8 bouts of 30 s duration on a cycle ergometer separated by
172 med highly demanding HIIT consisting of 30-s bouts of all-out cycling with 4-min rest in between bout
176 evoked a hyperlocomotor response (with rapid bouts of bottom swimming and frequent 'bouncing' motions
177 lopment in the murine prostate, and previous bouts of CD8-driven prostatitis may promote invasion in
178 pidemic clonality," demonstrating occasional bouts of clonal propagation in an otherwise recombining
182 affected children had experienced recurrent bouts of diarrhea in early childhood, which is a common
185 the success of acanthomorphs, as exceptional bouts of diversification have occurred across a wide arr
189 ransient increases of stressors during acute bouts of exercise or exercise training stimulate enhance
192 responses, but the quiescent periods between bouts of exploratory behaviors have not been well studie
194 his pattern did not reverse when considering bouts of fictive locomotion that were flexor vs. extenso
196 rians, and bilaterians underwent independent bouts of gene expansion in channel families involved in
200 g from sensory neurons can trigger recurrent bouts of herpes stromal keratitis (HSK), an inflammatory
202 play occurs within sharp wave-ripples: short bouts of high-frequency activity in area CA1 caused by e
206 een deeper and lighter sleep within extended bouts of inactivity, with deeper sleep intensities after
208 Seven healthy males completed four 6 min bouts of LI and four 6 min bouts of HI single-legged kne
209 o sucrose solution, PENK KOs exhibited fewer bouts of licking than wild types, even though the length
213 an experimental model of focal asynchronous bouts of muscle regeneration in wild-type (WT) mice.
216 different OFF regimens: 5 short (2 h daily) bouts of OFF followed by morphological analysis of prima
221 artate (LOLA) in patients with cirrhosis and bouts of overt hepatic encephalopathy (OHE) are missing.
222 on of HIV replication during and after acute bouts of P. falciparum malaria may be due, at least in p
224 nsolidated skills are modified over multiple bouts of practice and in response to newfound challenges
225 us work has also shown that intense seasonal bouts of predation by anadromous alewife has selected fo
229 between host-imposed quiescence and sporadic bouts of replication to complete its life cycle, however
237 ce are polyphasic, exhibiting multiple sleep bouts of sleep several minutes long within a 24-h period
241 ibitum-maintained rats were exposed to daily bouts of sweetened-fat intake, predator stress, or intra
243 onic phase that is characterized by rhythmic bouts of synchronized network activity called afterdisch
244 Cell stress is implicated in triggering bouts of systemic inflammation in patients with autoinfl
245 against this overall pattern of shortening, bouts of telomere length increase occur in some individu
248 ge," such that features acquired in distinct bouts of training are combined in an animal's mind, so t
249 sustained elevations in IL-6 due to repeated bouts of unaccustomed activities or prolonged exercise w
250 aining (HIT), referring to alternating short bouts of very intense anaerobic exercise with recovery p
251 nd intercalation (ie, intermittent recurrent bouts of viremia with homologous virus interspersed with
254 Strong gamma activity patterned in short bouts (one to three cycles), occurred when PVs and PYRs
260 plying Na(+)-free (0 Na(+)) solution for 5 s bouts, repeated each 10 s, which should evoke [Ca(2+)]i
262 y step-counts and time in MVPA (in >/=10-min bouts), respectively, measured objectively by accelerome
263 hirty minutes following the last stimulation bout, samples of diaphragm muscle were obtained from the
265 chondrial oxidative capacity are observed in bouts separated by 4 d, whereas a chronic profibrotic st
266 re, an increased proportion of the REM sleep bouts stemmed from periods of low REM sleep drive quanti
267 protective allele showed less post-exercise bout strength loss, less soreness, and lower creatine ki
268 d with repeated stress, and some changes (PS bouts, SWS time, body temperature, locomotor activity) p
269 ong ending, as well as an abrupt increase in bout syntactic complexity, peaking in the last quintile
273 tion by other animals) had longer incubation bouts than those that are readily visible or who activel
275 In this latter bat, we documented 5 torpor bouts that lasted >/=16 days and a flightless period tha
277 ts precede and accompany spontaneous running bouts, that selective chemogenetic silencing of natural
278 s such as the duration and speed of swimming bouts, the tail-beat frequency, and the choice of gait.
279 pared the temporal structure of vocalization bouts, the types of vocalizations, the patterns of sylla
280 t forelimb loading was completed in a single bout to induce the formation of woven bone (WBF loading)
283 the median length of one parent's incubation bout varied from 1-19 h, whereas period length-the time
285 Lip-smacking at the beginning of grooming bouts was significantly more often followed by longer an
286 g than wild types, even though the length of bouts was similar to that of wild types, a pattern that
288 wing the last of the four daily induced wake bouts, we examined the brains and observed a chimeric pa
290 F(24) and median (interquartile range) cough bouts were high (14.9 +/- 0.4 coughs/h and 85 [39-195] b
291 at both the prevalence and duration of theta bouts were increased relative to the sighted participant
294 e number of licking bouts, even though these bouts were shorter in length, suggesting that they exper
295 step-counts and weekly MVPA in >/=10-minute bouts were significantly higher in the intervention than
297 t and were more likely to abandon a grooming bout, while bouts were less likely to be reciprocated.
298 than 100 s) can be considered reorientation bouts, while shorter pauses (of less than 6 s) appear to
299 feeding assay that measures individual meal-bouts with high temporal resolution at nanoliter scale.
300 dicated a shorter duration of preseizure REM bouts, with a maximum transition to seizure at approxima
301 e in rodents, however, theta occurs in short bouts, with average durations of approximately 400 ms, w
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