ライフサイエンスコーパス: running

1 ticular cartilage volume after 75 minutes of running.

2 ed across moving behaviors, including during running.

3 dynia and increases the motivation for wheel running.

4 area), at rest and post maximal incremental running.

5 knee kinematic patterns in both walking and running.

6 continually integrating tactile stimuli with running.

7 r aerobic power (p = 0.458; d = 0.04) during running.

8 lly available sports bras during walking and running.

9 the soleus, or any other leg muscle, during running.

10 ion of avocado prior to submaximal treadmill running.

11 nal testing showed improvements in treadmill running.

12 Free-running 216 GHz "Vernier" solitons sample and divide the

13 es significantly decreased immediately after running 3 (65 +/- 3 ms to 62 +/- 3 ms; p = 0.04) and 10

14 efore, immediately after, and 24 hours after running 3 and 10 miles.

15 ned more higher frequency components at fast running (50% signal power in frequencies below ~ 14 Hz)

16 A free-running 5D flow MRI framework consistently captured card

17 When running a lab we do not think about calamities, since th

18 mments describe the joy of teaching methods, running a lab, and being a solo female.

19 -hydroxybenzoate, and triphenyl phosphate-by running a matrix spike of the reference standards and us

20 , including commands for converting formats, running a reasoner, creating import modules, running rep

21 douts per patient and avoid ETL crashes when running a tranSMART loading routine.

22 Unlike the wild-type control, the beam running ability of ssTnT-KO mice had a blunted response

23 make contacts with the enzyme in the valley running across both Cat and Hpx domains.

24 ze the time evolution of RRI correlations in running across various training and racing events under

25 mice show a gene-dose dependent reduction in running activity also seen in another hypophosphatemic m

26 ise after injury resulted in greater overall running activity and greater reversal of allodynia.

27 owed a profound reduction in voluntary wheel running activity at both 6 and 12 months of age.

28 muscle mass after weaning and reduced wheel-running activity but normal forced treadmill performance

29 3 mutants also have trouble regulating wheel-running activity in constant darkness.

30 ifferences in cortical Abeta42 levels, wheel-running activity, and circadian free-running period (tau

31 loosely cross-linked bundles of microtubules running all along axons, with only minor roles played by

32 ace between them and a continuous DNA duplex running along a central channel.

33 One week of running also induces switching from ACh to GABA expressi

34 nalysis are carried out on a microcontroller running an efficient algorithm based on the sliding Disc

35 Cytoscape app to enable a user interface for running analyses and visualizing results.

36 ct of EBF and age at weaning on gross motor, running and climbing scores was strongest among children

37 ore than three times the standard during hot-running and idling operations in the real world.

38 c grafts and were therefore amenable to both running and interrupted 7-0 Vicryl sutures without chees

39 ns and horses) and happenings and acts (like running and jumping) that are much more easily identifie

40 at rely on dorsomobility of the spine during running and leaping, but our results are independent of

41 was yet further increased during escape-like running and most particularly at gallop.

42 Moreover, we find that voluntary wheel running and muscle-specific peroxisome proliferator-acti

43 t circadian regulation of stomata under free running and Pseudomonas syringae challenge conditions as

44 ive evolution has been the subject of a long-running and recently renewed debate, but little work has

45 comparison of co-activation patterns between running and rest epochs and analysis of the recurrence o

46 Standing, straight running, and curved running were simulated starting from

47 nables an efficient push-off when walking or running, and was critical for the evolution of bipedalis

48 lower critical speed (CS)) during treadmill running; and ii) local K(ATP) channel inhibition (5 mg k

49 mice exhibited an adaptive decrease in total running, appropriate food anticipatory activity, and inc

50 te that the kinematics of walking and aerial running are conserved when moving on the treadmill and i

51 ral polarized supracellular F-actin network, running around the egg chamber on the basal side of foll

52 prediction of curved running using straight running as tracking data revealed the necessity of avoid

53 but treated mice were less active in a wheel running assay.

54 at 1.5 meters per second by 9.3% and that of running at 2.5 meters per second by 4.0% compared with l

55 Female mice underwent forced wheel running at 37.5 degrees C/40% relative humidity until sy

56 images, recorded from 10 humans walking and running at a range of speeds (0.7-5.0 m s(-1)), to quant

57 nse to impact forces elicited by walking and running at a range of speeds.

58 , consuming CHO before, during and after HIT running attenuates bone resorption, effects that are ind

59 A spot and 3-minute running average of CO(Cheetah) was used.

60 expression causing abnormal circadian wheel-running behavior.

61 heral clocks remain phase-locked to the free-running behavioral rhythm.

62 that the trackways reflect both walking and running behaviors.

63 tching provides the basis by which sustained running benefits motor skill learning, presenting a targ

64 By collecting, analyzing, and running bioassays involving mite-infested and control br

65 ry behavior under light/dark cycles and free-running bioluminescence rhythms with periods of ~21-31 h

66 push-off against the ground when walking or running bipedally.

67 either of these downstream effectors reduced running capacity in mice.

68 By running computer simulations, we show that regulating th

69 hm under constant light and temperature free-running conditions.

70 s show 24 h rhythms in expression under free-running conditions; (iv) Serpentine receptor 10 (SR10) h

71 n all persist in entrained larvae under free-running constant conditions, indicating circadian drive.

72 We thereby avoid the cost of running control experiments while simultaneously increas

73 This running controller derived from natural variability echo

74 particularly animals, sodium is essential to running costly Na-K ATPases.

75 This work resolves a long-running debate about Y-chromosomal out-of-Africa/back-to

76 Here we show that voluntary running decreases hematopoietic activity in mice.

77 n swimming, in contrast to that in flying or running, decreases with increasing body size, consistent

78 synchronized to detection events from a free-running detector covering the 900 to 1700 nm range.

79 lantar flexor muscle-tendon mechanics during running differs between rearfoot and forefoot striking.

80 acity, displaying an approximate doubling of running distance compared with WT mice.

81 Glycine increased voluntary running distance in mdx mice by 90% (P < 0.05) after 2 w

82 er birth the body weight and the spontaneous running distance of the mutant mice were 20% and 50% low

83 e IL-13 signaling was sufficient to increase running distance, glucose tolerance, and mitochondrial a

84 All exercise groups increased their running distances during ELE.

85 s greatly from passive entrapment in webs to running down prey items on foot.

86 energy expenditure during running (improves running economy).

87 calf muscle biomechanics but may not improve running economy.

88 patterns correlate with enhanced or reduced running efficiency.

89 spiratory physiology, perceived exertion and running endurance during exercise, and changed satiety p

90 training-mediated mitochondrial biogenesis, running endurance, and beneficial glycemic effects were

91 We find that one week of voluntary wheel running enhances the acquisition of motor skills in norm

92 Running Ensemble on a subset of data after removing the

93 As the largest and longest-running epidemiologic society in North America, SER has

94 As an application and running example, password generation schemas are humanly

95 the mechanistic origin of hyperpnoea during running exercise.

96 ysis, but also by the computational costs of running exhaustive computations on large and high-dimens

97 The iSeq100 instrument is capable of running existing TB WGS and targeted NGS library prepara

98 The most frequent problems are running experiments with too high precursor concentratio

99 earned in one twenty-four hour experiment by running five bioreactors in parallel.

100 In this prospective study, a free-running five-dimensional (5D) flow sequence was implemen

101 female C57bl/6J mice underwent forced wheel running for 1.5-3 h in a 37.5 degrees C/40% relative hum

102 62 transfections generated stable cell lines running for 28 weeks with and without selection, with in

103 rom neurons in the dorsal CA1 region of rats running for palatable tastes delivered via intra-oral ca

104 e implications of additional direct pathways running from cortex to basal ganglia and between basal g

105 nostril representation is an oblique sulcus running from lateral (surface) to medial (inside).

106 clude, therefore, that Delta-DFT facilitates running gas-phase MD simulations with quantum chemical a

107 ) for the study of animal demography include running goodness-of-fit tests on a general starting mode

108 ith data from two of the largest and longest-running grassland biodiversity experiments (the Jena Exp

109 Long-running gravity currents are flows that are submerged be

110 Walking and running have fundamentally different biomechanics, which

111 calcium imaging of CA1 sequence dynamics in running head-fixed mice and network modeling, we show th

112 Wheel running improved serum biochemistry with decreased creat

113 RP treatment, in contrast to voluntary wheel running, improved myocardial phenotype and function.

114 es athlete aerobic energy expenditure during running (improves running economy).

115 and June 28, 2018, with the PLA intervention running in 32 villages from June, 2016, to December, 201

116 December, 2017, and the mHealth intervention running in 32 villages from Oct 21, 2016, to Dec 24, 201

117 see a person walking on a train or an animal running in a herd, we recognize the individual's movemen

118 truggling to get her research project up and running in a new country, a mother gets inspiration from

119 ex-wide activity patterns is restructured by running in an area-specific manner, resulting in a shift

120 t motion and the deviation from the HMP when running in different footwear conditions.

121 during controlled limb loading, walking, and running in healthy humans.

122 Importantly, long-term (4 months) voluntary running in KIKO mice starting at a young age (2 months)

123 We show that chronic voluntary wheel running in mice increases stress resilience and increase

124 Voluntary wheel running in mice scaled the GABAergic input to abDGCs by

125 , on energy expenditure, and voluntary wheel running in mice.

126 server node (or in 11 min on 31 server nodes running in parallel).

127 e is 600 Mpixel per sec with six microscopes running in parallel.

128 t and training by studying the synergies for running in preschoolers and diverse adults from sedentar

129 O(2) max and critical speed during treadmill running in rats due, in part, to impaired convective and

130 peed-duration relationship) during treadmill running in rats, before and after systemic K(ATP) channe

131 argeted gas chromatography-mass spectrometry running in selective ion monitoring mode-based method.

132 guished from the flexor tendons of the hands running in the carpal tunnel.

133 is not clear how a neuronal dynamical system running in the fixed human anatomical connectome can giv

134 Here, we examined respiratory changes during running in the resourceful mouse model.

135 ured in whole-cell recordings from male mice running in virtual corridors (Domnisoru et al., 2013).

136 delity is greatly increased during treadmill running (in M1 neurons) and visual stimulation (in V1 ne

137 ted whether physical activity (chronic wheel running) increases stress resilience and galanin express

138 nd abolished activity (e.g., voluntary wheel running)-induced anxiolytic effect and adult DG neurogen

139 asymptomatic male runners by characterizing running-induced changes in knee cartilage composition.

140 nes are not supported by the world's longest running insect population database: annual moth biomass

141 Running is thought to be an efficient gait due, in part,

142 For long-running jobs or large memory needs we provide detailed g

143 [OR] 3.08 [95% CI 2.52-3.77]), and sponsors running large numbers of trials were significantly more

144 loride, sodium, potassium and bicarbonate by running linear mixed models adjusting for covariates and

145 pipeline requires ~3 h on a desktop computer running Linux or Mac OS with R support.

146 IT licence and can be deployed on any server running Linux or Mac OS.

147 thin the mPFC-AcbSh pathway had no effect on running, locomotor activity, or feeding under ad libitum

148 attempted measurements indicated evaporative running loss emissions from a 9-year-old fleet.

149 trument noise indicates possible evaporative running loss emissions with the probability increasing w

150 of the HC/CO(2) correlation is defined as a running loss index (RLI) for each measurement.

151 rtainty intervals (UIs) for our estimates by running low and high scenarios using the lower and upper

152 In addition, the phase of free-running luminescence rhythms can be modulated pharmacolo

153 ormations at the lumbo-sacral border in fast-running mammals, while slower, ambulatory mammals more r

154 ), and then augmenting each sublist with the running maximum interval end.

155 noise in Model 3 and were similar for a 1-y running mean exposure.

156 bserved a positive association between a 3-y running mean of PM2.5 and an overall incident MI with an

157 we observed a strong association with a 3-y running mean of PM2.5, with an HR = 1.69 (95% CI: 1.33,

158 g means of these pollutants, as well as 23-y running means of NO2 and NOx, with both overall and fata

159 o examine the association between 1- and 3-y running means of these pollutants, as well as 23-y runni

160 sources like sensorimotor noise perturb the running motion incessantly, making each step variable.

161 m strategy beats all classical strategies by running multiple equivalent tests in a quantum superposi

162 mography (SD-OCT) revealed a thin, dark band running nasotemporally just dorsal to the pecten, which

163 TN for each dwelling and derived 1-y and 5-y running nighttime averages.

164 ecursor structure unambiguously dictated the running of the "zipping program," resulting in the rolli

165 ansmits data via Bluetooth to an Android app running on a tablet.

166 From humans driving on the highway, to ants running on a trail, the main challenge faced by all coll

167 were seated for 60 min at rest, followed by running on a treadmill at a submaximal level and then re

168 his end, we imaged the dorsal cortex of mice running on a treadmill populated with tactile cues.

169 m imaging of head-fixed male and female mice running on a treadmill, we find that only a minority of

170 rmed a spatial task in a virtual corridor by running on a wheel and licking at a reward location.

171 brought down the time taken of the software running on an NVIDIA Volta 100 (V100) Graphic Processing

172 speed in place cell data recorded from rats running on linear tracks.

173 ch enables this limitation to be overcome by running on more powerful hardware.

174 er switching blocks the beneficial effect of running on motor skill learning.

175 specify and execute BLAST searches by either running on the same host as the webserver, with a self-c

176 ascular anatomy, with large conduit arteries running on the surface of the organ providing tissue per

177 Analyzing whole-cell data from mice running on virtual tracks, we show that DAPs do occur du

178 e well documented for sets of traits such as running or swimming but only a limited number of studies

179 Along with free-running oscillator circuits, we measure repression respo

180 at ground contact in walking (p = 0.005) and running (p = 0.037).

181 In parallel, the late running paradigm was associated with reduced muscle fibr

182 m, the S4 helix breaks into two helices, one running parallel to the membrane surface, analogous to t

183 rs using both rearfoot and forefoot striking running patterns, to characterize plantar flexor muscle-

184 a high computation cost because it requires running PCA separately for each study sample on the augm

185 n of PEMFs and exercise for 6 weeks enhanced running performance and upregulated muscular and adipose

186 In an attempt to improve their distance-running performance, many athletes race with carbon fibe

187 , wheel-running activity, and circadian free-running period (tauDD).

188 mmalian circadian system, shortened the free-running period in mice.

189 maintaining the length of the circadian free-running period of locomotor activity and normal sleep pa

190 ions to establish a remarkably constant free-running period over a wide range of temperatures.

191 re the three properties of entrainment, free-running period, and temperature compensation (TC).

192 nized columns of reciprocal axonal processes running perpendicular to the layers, an arrangement high

193 ing, using an alternate activation wavefront running perpendicular to the VT isthmus may increase sen

194 ponse, real-time measurement capability, low running power, and the feasibility to miniaturize to a p

195 cost system state preparations and expensive running procedures and measurement apparatuses in gate-m

196 y interval (HIT) (8 x 5 min at 85% VO2peak ) running protocol (interspersed by 3.5 h) under dietary c

197 o build a high-fidelity processor capable of running quantum algorithms in an exponentially large com

198 y or physically active (10-12 weeks of wheel running) rats.

199 least in mice and in the presently examined running regimes, without phasic constraints from limb mo

200 running a reasoner, creating import modules, running reports, and various other tasks.

201 ements with directional changes, e.g. curved running, requires detailed three dimensional models whic

202 off 7.4 and 5.7 kilograms during walking and running, respectively, and are in a range that has shown

203 Voluntary wheel running resulted in multiple beneficial systemic effects

204 31 and PDF may act on DN1ps to regulate free-running rhythmicity in a hierarchical manner.

205 complements PDF function in regulating free-running rhythmicity using male flies.

206 ut not DH31R, in DN1ps mainly regulates free-running rhythmicity.

207 s during a prolonged post-mitotic period and running scales both SST and PV synaptic afferents.

208 Averted hospitalizations are measured by running scenarios obtained by selectively relaxing the i

209 r, cost, and sample quantity associated with running separate potentiometric or conductometric titrat

210 the first to demonstrate the feasibility of running separate voxel-wise structural equation models t

211 information is accessible about the previous running sequences of the gate-model QNN.

212 bioinspired material architecture for use in running shoe midsoles.

213 footwear that increases HMP deviation during running show higher reductions of knee joint articular c

214 In these mice, voluntary wheel running significantly improved myocardial phenotype and

215 Does the brain achieve this understanding by running simulations in a mental physics engine, which re

216 the new method, termed synchro-excited free-running single photon counting (SEFR-SPC), excitation pu

217 The running-specific prosthetic (RSP) configuration used by

218 owed that the auditory brainstem response to running speech is modulated by selective attention, evid

219 c locations and velocity signals that encode running speed and head direction.

220 vity depended not only on vision but also on running speed and pupil size, regardless of retinal illu

221 puts change neural dynamics as a function of running speed and time.

222 oes not affect modulation of firing rates by running speed at each time scale tested.

223 We use the PTP model to assess the effect of running speed in place cell data recorded from rats runn

224 consider firing rate to be linearly tuned by running speed in real-time.

225 Several physiological indices of running speed in the entorhinal cortex showed reduced ga

226 Conversely, neural representation of running speed information was significantly disturbed, w

227 , we show that modulation of firing rates by running speed is independent of MSDB inputs.

228 leaping, but our results are independent of running speed per se.

229 corresponding to the visual stimulus, mouse running speed, and experimentally measured neuronal corr

230 nt correlation between synaptic activity and running speed, demonstrating the importance of correctin

231 hich in wild-type mice are tightly linked to running speed, was invariant in rTg4510 mice during loco

232 In contrast, visual inputs do not alter the running speed-dependent gain in neuronal firing rates.

233 entorhinal cortex (MEC), is correlated with running speed.

234 ison to predictions based on the stimulus or running speed.

235 sible to reduce metabolic rates of different running speeds and uphill walking, further demonstrating

236 introducing a preconditioning step prior to running square wave voltammetry on the electrochemical f

237 e tracking database allows users to view job running status in real time and visualize >100 quality m

238 ehensive visualizations such as heatmaps and running sum curves with background distributions.

239 s that employ enrichment scores created from running sums of univariate phenotype-attribute correlati

240 al wall was closed using a slowly absorbable running suture in a mass closure technique with "large b

241 ns rats in response-based and cue-based maze-running tasks, we demonstrate that phasic dorsolateral s

242 BASF and the Heidelberg University have been running the Catalysis Research Laboratory together in He

243 th lactic and citric acids than acetic acid, running the experiments at the same pH of 3.8-4.0 units.

244 d LPS adsorption further up to ~100% just by running the LPS-containing water through the membrane un

245 time on a cluster of eight GPUs compared to running the method on a single GPU.

246 Code for processing the data and running the models is provided as a series of R packages

247 Notably, running the reaction in this manner renders it effective

248 device at the testing site, the strips after running the test can be transported and read at a centra

249 nals are stable for at least 10 months after running the test.

250 d, and the efforts and resources invested in running the trial are not rewarded.

251 provide such information, but setting up and running these simulations is not straightforward and req

252 able mice exhibited a pronounced increase in running throughout the light cycle, which dramatically p

253 maintained high performance and competitive running time across all datasets.

254 studied their performance, in terms of both running time and accuracy, on simulated as well as on bi

255 there remains large room for improvements in running time and accuracy.

256 The running time and space requirement of all procedures is

257 With a running time below 5 min, our method is applicable to la

258 osed divide-and-conquer framework, has O(n5) running time for datasets with n species.

259 tially with the number of sub-chains; such a running time scaling is impractical for many application

260 n these so-called Factorial HMMs has a naive running time that scales as the square of the number of

261 only once, there is a significant saving in running time when compared with VQSR (4 versus 50 min ap

262 return a tree and it has dramatically faster running time within the same divide-and-conquer framewor

263 er experience with significant reductions in running time, ~3.5 min for the analysis of all five majo

264 Here we present the longest running time-series of DMS-water (DMS(W)) concentrations

265 The approximate algorithm has running-time O(nd) for an n-individual pedigree on which

266 ater in older, male participants with slower running times (p < 0.05 for all).

267 We analyze the asymptotic worst-case running times and provide experimental results that demo

268 ate its performance in terms of accuracy and running times on two gold standard datasets: the UK Biob

269 It notably exhibits sub-linear running times with sample size, provides highly accurate

270 We do so by running transects of salt and sugar baits and inferring

271 er at breast height at the world's only long-running tropical forest drought experiment.

272 rates for 176 trees from the world's longest running tropical forest drought experiment.

273 ifying the exercise intensity (%VO(2max)) of running under different treadmill grades and speeds.

274 Finally, %VO(2max) of running under different treadmill speeds and grades was

275 the leaky-wave open-ended feeding slot-lines running underneath the patches.

276 water flow are mitigated within 24 hours of running up to 10 miles.

277 The prediction of curved running using straight running as tracking data revealed

278 ss, and height configurations affect maximum running velocity (v(max)) and the underlying biomechanic

279 tudy examined how exercise (12-min treadmill running versus walking) mediated amygdala reactivity to

280 esponse performance, deliberation movements, running vigor, and outcome insensitivity) are quite clos

281 less of animal state (anesthetized vs awake, running vs stationary), SC depth (most superficial lamin

282 sedentary, SED) or presence (voluntary wheel running, VWR) of aerobic exercise.

283 rtical impact forces with faster walking and running was consistent with changes in both magnitude an

284 In female mice, voluntary wheel running was decreased (P < .05) in the HET vs WT animals

285 ts performing rotarod exercise and treadmill running, was improved in the presence of CK-2066260.

286 etagenomic library constructed from domestic running water samples.

287 gressively-drying mineral matrix that has no running water; ecosystem constraints were then considere

288 We conclude that intense recreational use of running waters transiently increases the anthropogenic D

289 62.2, n = 1833) for small, medium, and large running waters was validated and used for risk mapping a

290 .g. rotarod, treadmill, grip test, and wheel running), we observed that mTORC1 activity was significa

291 In everyday tasks such as walking and running, we often exploit the work performed by external

292 Standing, straight running, and curved running were simulated starting from a random initial gu

293 Mice freely accessed a running wheel during three postnatal periods: the 4(th)

294 d that three weeks of ad libitum access to a running wheel in their home cage increased galanin mRNA

295 Whereas running wheel withdrawal quickly reverses leptin levels,

296 rees C or when housed at 28 degrees C with a running wheel.

297 When subjected to downhill treadmill running, wild-type and mdx mice expressing recombinant d

298 musculoskeletal model to be specialized for running with directional changes.

299 Consistently, neurons encoding running-with-touch are more abundant in L2/3 and they en

300 e tested the hypothesis that voluntary wheel running would improve musculoskeletal health in a CKD ra