ライフサイエンスコーパス: experiment

1 ngi from the longest-running plant diversity experiment.

2 lfonamide moiety improved the agreement with experiment.

3 our results in a complementary common garden experiment.

4 yclization based on the results of a control experiment.

5 ma structure similar to that observed in the experiment.

6 4 in nucleus were detected with Western blot experiment.

7 paradigm and implement it in a reaching task experiment.

8 A systematically improves the agreement with experiment.

9 ining the tip-sample distance during an SICM experiment.

10 ises that must be made when designing an SRM experiment.

11 ological processes that are perturbed by the experiment.

12 result was confirmed by confocal microscopy experiments.

13 lain the findings of the reported behavioral experiments.

14 ited states and rationally design validating experiments.

15 ation derived from chemical cross-linking/MS experiments.

16 as only based on bioinformatic analyses, not experiments.

17 g the full exploitation of many metabolomics experiments.

18 ptual biases revealed through the behavioral experiments.

19 merous applications in the design of new NMR experiments.

20 ng to a significant loss of information from experiments.

21 lipids in data acquired by LC-MS and shotgun experiments.

22 rrect for them, in both live- and fixed-cell experiments.

23 nable the interpretation and optimization of experiments.

24 ural changes in boutons in long-term imaging experiments.

25 qualitative and quantitative IgE inhibition experiments.

26 graphy-MS (GC-MS) data relative to labelling experiments.

27 que properties using analytical modeling and experiments.

28 dies, now bridging to the wild through field experiments.

29 from data obtained with repeated independent experiments.

30 to illustrate conformations found by the NMR experiments.

31 iseases are often inferred from transmission experiments.

32 ron spectroscopy and atomic force microscopy experiments.

33 presents a considerable complexity in these experiments.

34 iquid and the thermal hysteresis observed in experiments.

35 rea and by hydrogen-deuterium exchange (HDX) experiments.

36 stry, RT-PCR, northern blot and western blot experiments.

37 flavonoids combining sensitive NMR and HPLC experiments.

38 tify significant changes in activity between experiments.

39 Here, we report the results of those experiments.

40 ac materials in a readily accessible way for experiments.

41 o free-air CO2 enrichment (FACE) and chamber experiments.

42 g the same width used for an anticipated DDA experiment (+/-0.5 Da).

43 In Experiment 1, memory for shared properties improved and

44 In Experiment 1, participants made forced-choice judgments

45 Proportions were spaced linearly in Experiments 1 and 2 and logarithmically in Experiment 3.

46 In Experiments 1 and 2, participants viewed pairs of images

47 In experiments 1 and 2, we trained older CD-1 mice to lever

48 In Experiment 2, memory for shared properties improved acro

49 Experiment 2a examined the effects of PL inactivation on

50 n Experiments 1 and 2 and logarithmically in Experiment 3.

51 ine its resistance phenotype and in a second experiment, a subset was chosen to compare fitness (fecu

52 biome was confirmed in fecal transplantation experiments: adult maternally separated rats were subjec

53 g/larvae/day over 6 days) and, in a separate experiment, adults (lower dose of 0.066 microg/adult bee

54 n this study, we report a new shock recovery experiment aimed at synthesizing decagonal quasicrystals

55 sanctuaries for the virus can inform future experiments aimed at further clarifying this issue.

56 owfall events occurred during a 3-year field experiment, allowing us to examine their effects on the

57 These experiments also highlight the applicability of RT-QuIC

58 The kinetics experiments also shed light on the effects of chloride c

59 we performed a bromodeoxyuridine pulse-chase experiment and found that a subset of ependymal layer ce

60 tio Pheq:Phaxo is 79(15):21(15) and 71:29 by experiment and theory (M06-2X calculations), respectivel

61 combining single-molecule force-spectroscopy experiments and coarse-grained simulation.

62 ature than has previously been documented in experiments and comparable to or stronger than the effec

63 The results of detailed experiments and finite element modeling of metal micro-d

64 Further in vitro cell culture experiments and gene expression analysis revealed a majo

65 ternal friction observed in the two types of experiments and in the simulations.

66 Collision induced dissociation experiments and Kendrick mass defect analyses corroborat

67 Moreover, experiments and modeling show that the select-field ampl

68 tions for certain classes of high-throughput experiments and the analysis of noisy datasets.

69 tivity, which was shown by pathway inhibitor experiments and Western blot analysis to be mediated via

70 odulatory structure over the duration of the experiment, and thereby discover trial-to-trial variabil

71 onstruction of adaptive laboratory evolution experiments, and identification of stress tolerance and

72 ed nights, continuous light, sucrose feeding experiments, and photosynthesis inhibition to tease apar

73 these domains are determined from titration experiments, and proton-exchange rates are measured at p

74 rradiance value (500 W m(-2)) during all the experiments, and the main photoproducts formed were char

75 g, psychophysics, and traditional behavioral experiments, and we also summarize the current studies o

76 Computational experiments are scriptable and should be easy to reprodu

77 Current experiments are taking the first steps toward noise-resi

78 In vitro experiments are widely used to forecast reef-building co

79 tant implications for the design of lifespan experiments as autotoxins can influence the regulation o

80 etwork, which is corroborated by mutagenesis experiments as well as detailed atomistic simulations.

81 Extensive benchmarking experiments based on both five-fold cross-validation and

82 sproves that quasi-equilibrium exists in our experiments between protons in the near-membrane layers

83 This proposal is at odds with 40 years of experiments, but involves the key assumption that gA mon

84 equilibrium dialysis device to fit their own experiments by choosing membranes of various material an

85 Thus, collision experiments can be used to prepare small NP ensembles on

86 In our first experiment, chicks begged significantly longer in respon

87 Experiments combined with ellipsoid packing models revea

88 Furthermore, incubation experiments conducted with naturally methane-enriched wa

89 Pharmacological experiments confirmed that the effects depended on choli

90 Genetic and biochemical experiments consistently demonstrated that the increased

91 ions and a 50-member climate change ensemble experiment, consisting of historical hindcasts (1850-200

92 As laser cooling experiments continue to bring massive mechanical systems

93 Together, these experiments define synaptic dysfunction at NMJs experien

94 Competition experiments demonstrate that additions of allylmagnesium

95 Biochemical and electrophysiological experiments demonstrate that high shear stress-induced m

96 Electrophysiological experiments demonstrate that KCTD12/KCTD16 hetero-oligom

97 Additional experiments demonstrate that optogenetic activation of D

98 Current-clamp experiments demonstrate that serotonergic afferents are

99 Our benchtop experiments demonstrate that the CFF process is able to

100 Seeding experiments demonstrate that the output variation may be

101 ynomolgus platelet activation in vitro These experiments demonstrate that the SEFL modifications succ

102 Furthermore, in vivo experiments demonstrate that the transcription of severa

103 Receptor pull-down experiments demonstrate that VEGF165b inhibition versus

104 DNA photocleavage experiments demonstrate that, upon photoactivation, the

105 Our laboratory experiments demonstrated substantial thermal effects.

106 Column experiments demonstrated that a low concentration (10 mg

107 Our previous preclinical in vivo experiments demonstrated that only certain HCV-NS5B prod

108 mature peptide and site-directed mutagenesis experiments demonstrated that the first two cysteines ar

109 using an event-related functional MRI (fMRI) experiment design.

110 Experiments done on the altricial rat and precocial guin

111 in a recent publication, was varied between experiments; edaphic and mean atmospheric conditions wer

112 As shown through stopped-flow kinetic experiments, electron transfer capable cytb 5 - cyt c co

113 A competition experiment established that the reaction involves format

114 on of omics data and RNA immunoprecipitation experiments established DGCR8 as a direct interactor of

115 t the stage for non-invasive high-throughput experiments evaluating sleep and breathing patterns on m

116 Recent experiments exploring this phenomenon proved that light-

117 ted mixture in air for two weeks in separate experiments followed by a comprehensive behavioral and c

118 p researchers to better design spin trapping experiments for food matrices.

119 Yet, despite the importance of such experiments for translational medicine, there have been

120 on of solid-state NMR and circular dichroism experiments found the latter orientation to be dominant.

121 cribed how we intended to replicate selected experiments from the paper "Inhibition of BET recruitmen

122 cribed how we intended to replicate selected experiments from the paper "The common feature of leukem

123 Transcription perturbation experiments further indicate that R-loop induction corre

124 Neuropharmacological experiments further reveal that vCA1 GLP-1R activation r

125 In a laboratory experiment, groups whose members could make moral judgme

126 Transgenic- and cell line-based experiments have identified 5'-flanking conserved sequen

127 h previous shock compression simulations and experiments have provided conflicting information about

128 Recent experiments have shown a heterogeneous promoter activity

129 r) interfaces, both computer simulations and experiments have shown that chaotropic ions actually exh

130 clinical trials in cancer patients, and our experiments highlight concerns on the homeostasis and re

131 Our experiments highlight the contingent nature of predator-

132 A recent crystal structure and in vitro experiments highlighted potential residues mediating the

133 Affinity chromatography experiments identified the primary target of the compoun

134 Two experiments illustrate potential applications of the Hal

135 rates the paradigm of uniting simulation and experiment in a statistical model to study the structure

136 a long-term leaf litter addition and removal experiment in a tropical forest in Panama.

137 els on infants' persistence, we conducted an experiment in which 15-month-olds were assigned to one o

138 lise the wildtype protein in co-transfection experiments in a human RPE cell line.

139 Experiments in cultured cells, brain slices, and in livi

140 rguably explain a range of poorly understood experiments in gated graphene structures at low doping.T

141 We combined mathematical modelling with experiments in heart cells from guinea pigs to determine

142 In vitro experiments in human blood suggested that cavitation may

143 and the underlying neural processing of TFS, experiments in humans and animals were conducted to demo

144 Experiments in knockout mice revealed a major role for T

145 h17 immune responses in vivo in immunization experiments in mice and conferred protection in a murine

146 tions, we carried out a series of behavioral experiments in sighted and congenitally blind subjects.

147 as carried out using a series of competition experiments in the liver.

148 controlled electrochemical charge injection experiments in the nonsolvent electrolyte reveal decompo

149 n a 40 times lower rate constant compared to experiments in which no buffer was added.

150 Here we describe experiments in which we studied binocular interactions i

151 Cell-surface labeling experiments indicate that the dominant form of TMPRSS13

152 ate spectral reconstruction, rendering these experiments ineffective for high-throughput applications

153 Here, by performing the reverse experiment, injecting mouse PSCs into Pdx-1-deficient ra

154 , and this publication includes building and experiment instructions to set the stage for disseminati

155 Experiments involved two exposure groups (high and low)

156 overcome this barrier, we studied a natural experiment involving genetically inherited traits, and f

157 Excellent agreement between theory and experiment is achieved for the entire applied frequency

158 ltrafast electron diffraction and microscopy experiments is currently limited by the available experi

159 elay in vivo and shorter AP latency in slice experiments, is consistent with increased synaptic effic

160 Taken together, these experiments lay a foundation for the incorporation of em

161 ts provide an empirical baseline for tagging experiments, life histories extrapolated from otolith mi

162 In the small-animal PET experiments, LNCaP tumors were clearly visualized.

163 In some experiments, Mefv(-/-) mice were given injections of rec

164 cross an initial study and two preregistered experiments (N = 262), infants in the Effort condition m

165 RNA sequencing (RNA-seq) experiments now span hundreds to thousands of samples.

166 creased sensitivity to transient species for experiments obeying the modulated excitation paradigm an

167 compensatory FANCA somatic mutation from an "experiment of nature" in monozygotic twins both prevente

168 was validated by a combination of simulation experiments of Ras overexpression and catalase knockout

169 parameter for ligand donation, derived from experiments on a high-valent chromium species, is now av

170 ar basis of TAD formation, we performed Hi-C experiments on cells depleted for the Forkhead transcrip

171 As shown in control experiments on in vitro alphaB- and gammaD-crystallin, 2

172 m(3) in all cases), consistent with previous experiments on methylglyoxal.

173 Classic experiments on social groups dealing with truth statemen

174 lie social information use, using a suite of experiments on social insects as case studies.

175 However, behavioural experiments on subjects with only rod function reveals t

176 in silico functional analyses and wet bench experiments, our findings highlight new biological pathw

177 In 3 experiments participants were exposed to a standard CC p

178 The control experiments performed by resonance elastic light scatter

179 w-pressure, ambient-temperature ion mobility experiments performed in a radio frequency-confining dri

180 These experiments-performed under biologically relevant condit

181 ricosus) submitted to a 5 week acidification experiment (pHT of 8.1, 7.7, and 7.4).

182 from ion mobility-mass spectrometry (IM-MS) experiments provide a promising orthogonal dimension of

183 Sedimentation-velocity experiments provided insight into the isomerization proc

184 A field experiment provides causal evidence that working adults

185 re examined by transwell assay and depletion experiments, respectively.

186 Together, these experiments reveal a novel type of plasticity at CA1 hip

187 Chromatin immunoprecipitation experiments reveal increased binding of the repressor fa

188 HR-MAS (1)H NMR and neutron scattering experiments reveal that this macroscopic response of the

189 Our experiments reveal the extensive integration of signals

190 cific profiling and genetic loss-of-function experiments revealed a critical role for FOXO transcript

191 Characterization experiments revealed blue-emissive, well-dispersed GQDs

192 Field experiments revealed that in protected salt marshes expe

193 Adoptive transfer experiments revealed that intrahepatically differentiate

194 Biochemical as well as functional experiments revealed that Spt6 could compete for binding

195 Moreover, fate-mapping experiments revealed that the timing of SOX2 expression

196 Isothermal titration calorimetry experiments revealed tight binding to McpX(PR) with diss

197 scattering and multi-angle light scattering experiments, revealed that ObgE is a monomer in solution

198 This simple experiment reveals a surprisingly complex pathway by whi

199 erefore, we propose that more multifactorial experiments should be considered in studying Earth syste

200 Genetic experiments show that ectopic dATM is sufficient to prom

201 sites from probe capture data, the verified experiments show that more than 90% viral integration se

202 Finally, gain-of-function experiments show that Pth4 can alter calcium/phosphorus

203 Experiments show that spike-triggered stimulation perfor

204 ovo Rosetta modeling and competitive binding experiments show that the acidic tip of the E. coli Hfq

205 enetic studies and transcriptional profiling experiments show that this single protein is implicated

206 Dialysis experiments show that, for a 15 kDa polyelectrolyte, a 5

207 The experiments showed excellent performance for nonplanar s

208 Control experiments showed no labeling of TG2 knock-out mice.

209 Response surface experiments showed that a 10g/l liquid to solid ratio, 5

210 These experiments showed that alpha-cellular and beta-cellular

211 against in all populations, our competition experiments showed that antibiotics significantly increa

212 Tandem MS/MS experiments showed that DMSO could modify the dissociati

213 Consistent with this result, co-IP experiments showed that GpsB complexes with EzrA, StkP,

214 First, our field experiments showed that the mean number of species obser

215 Cohousing experiments showed that the microenvironment also played

216 These experiments showed that TMAO red-shifts the OH stretch o

217 Further experiments showed that ZxAKT1-silenced plants exhibited

218 We present a theoretical model and a set of experiments showing how soft electrodes can be successfu

219 This experiment shows that children who see movie characters

220 not random: models that overestimated at one experiment simulated greater yield enhancements at the o

221 ble of performing an unprecedented in silico experiment-simulating an entire mammal red blood cell li

222 Based on epistasis experiments, SMG-1 does not appear to act in any of the

223 ases were observed to form on warming in the experiment: Sn, Cs2Se3, Cs4Se16, Cs2Se5, Cs2Sn2Se6, Cs4P

224 At the end of the experiment some metabolites will have incorporated the l

225 In the experiment, subjects repeatedly play a strategic game th

226 ss, designing high-throughput reporter assay experiments such as massively parallel reporter assays (

227 Dark-rearing experiments suggest that visual experience determines wh

228 Further experiments suggested that NS1-mediated inhibition of th

229 microbial electrochemical cell, and isotopic experiments supported AOM-EET to the anode.

230 Gene silencing experiments targeting alpha1D reduced the migration and

231 Here we report an experiment that realizes a multiplexed DLCZ-type quantum

232 With a computational experiment that simulates an intervention similar to mas

233 we show using functional GFP reconstitution experiments that Kenyon cells and dopamine neurons from

234 In these experiments, the cortical LFP is measured by multielectr

235 Throughout the experiments, the strength of the ensemble-encoded CS-US

236 membrane proteins in a static quenching FRET experiment: the model of Veatch and Stryer, derived in 1

237 minantly exploited P sources in the seedling experiment: the N2 fixer with high N2 fixation and root

238 We conduct a field experiment to assess the influence of warming and altere

239 dense phenotypic information enables such an experiment to be applied to human subjects in the form o

240 e, we have undertaken crosslinking and other experiments to address more fully the question of FliG n

241 We used theory and experiments to address this question in the pathogenic b

242 should be taken into account when designing experiments to assess degradation of Mg-based implants.

243 in the late 1930s as a way to use laboratory experiments to better understand uncontrollable fear and

244 ees of four provenances at two common garden experiments to characterize provenance-specific variatio

245 me impacts honeybee health, and we performed experiments to determine whether antibiotic exposure inc

246 ne NMR spectroscopy and electrophysiological experiments to explore the functional properties of muta

247 We used cross-species expression experiments to show that Alx1 proteins from distantly re

248 copy, and open-circuit potential versus time experiments to understand the galvanic replacement proce

249 In a proof-of-principle experiment, treatment of these two subtypes with targete

250 Using a training set of 24 experiments, two real-time indicators based on correlati

251 Sedimentation experiments typically take approximately 3 h of preparat

252 Four experiments used pointing or left/right 2-alternative fo

253 20 equiv NH3 per Os center in a single batch experiment using Cp*2Co and [H2NPh2][OTf] as reductant a

254 velopmental ontogeny, we conducted a mapping experiment using Euphrates poplar (Populus euphratica),

255 was estimated from energy-transfer quenching experiments using a series of organic triplet donors (E(

256 ChIP-sequencing experiments using an anti-O-GlcNAc antibody revealed sig

257 curve in small-angle X-ray scattering (SAXS) experiments using isolated GluA2 ligand-binding domain (

258 In patch-clamp experiments using native cerebral arterial myocytes, mem

259 amine reactants are employed in competition experiments using polar solvents, such as DMF, no "mixed

260 pable of influencing interpretations of many experiments using targeted genome manipulations such as

261 sm spectroscopy and dynamic light scattering experiments verified that individual BSA monomers in bul

262 A dynamic (99m)Tc tracer experiment was performed to investigate the capabilities

263 In laser ablation experiments we found that cap cells retracted by approxi

264 The experiments we review span a range of methodological tec

265 Using live-imaging and perturbation experiments we show that leaf orientation, morphology an

266 dreds to thousands of samples within a given experiment, we have developed a data streaming platform,

267 In two psychophysics and neuroimaging experiments, we characterized the response properties, t

268 From the results of the kinetics experiments, we determined that the reversion of the qua

269 grade viral tracing and c-Fos immunostaining experiments, we found that a proportion of vCA1 neurons

270 Based on neutron total scattering experiments, we have determined that the local structure

271 tion-based predictions and FRET sensor-based experiments, we investigated the conformational dynamics

272 In animal experiments, we observed significantly lower pH and high

273 By using a combination of theory and experiments, we show that epithelial surface cells not o

274 in vitro sperm manipulation and competition experiments, we show that rapid changes in sperm velocit

275 Using these experiments, we then demonstrate that, in the pentamer,

276 In these experiments, we used backward conditioning and contingen

277 Experiments were carried out in piglets first sensitized

278 Anatomical and electrophysiological experiments were conducted to examine the neural connect

279 d on the observations in humans, mechanistic experiments were designed in a mouse model of resuscitat

280 immunohistochemistry, and ex vivo HGF ELISA experiments were performed on murine xenografts of U87MG

281 m-UV (VUV) photoionization mass spectrometry experiments were performed to understand the ion-molecul

282 Control experiments were performed with untreated plants and the

283 es, phylogenetic analyses, and pathogenicity experiments were performed.

284 ained by a transcranial magnetic stimulation experiment, where subjects whose frontal control was tem

285 rate CLIP-Seq, knockdown and over expression experiments, which are inherently noisy and suffer from

286 chastic simulation that exactly mimics these experiments, while imposing the 1:1 constraint.

287 of 8% after 24 h of operation in biofouling experiments, while that of the control membranes had a g

288 ncounter when designing and analysing animal experiments will improve the reliability of in vivo rese

289 Here we conduct a microcosm experiment with laboratory protist community subjected t

290 QC data and experiments with 14 synthetic reference peptides indicat

291 two times higher than that for typical bulk experiments with a commercial rotating ring disk electro

292 Perturbation experiments with a miR-218-5p mimic or inhibitor demonst

293 or amine-containing micropollutants in batch experiments with activated sludge that has so far gone u

294 Optical pulse-chase experiments with Dendra2-tagged aSyn versions indicated

295 Crossflow rejection experiments with dilute feed composition indicate that b

296 Experiments with inhibitors of protein kinase G (PKG), p

297 ay rule" for embryo research stipulates that experiments with intact human embryos must not allow the

298 Data mining of RNA-Seq experiments with mouse models of intestinal HIF-2alpha o

299 2PPM experiments with non-mutated fluorescently labeled Galph

300 In two evolution experiments with the facultatively sexual rotifer Brachi