ライフサイエンスコーパス: experiment

1 collision-activated dissociation (CAD; MS(2) experiments).

2 ible between individual organoids/iPSC lines/experiments).

3 sked by acclimation effects in the long-term experiment.

4 at least a month before participating in the experiment.

5 80% of the proteins identified in the entire experiment.

6 magnitude less than the equivalent step-scan experiment.

7 tify gene regulatory properties suggested by experiment.

8 data revealing adaptive mutations during the experiment.

9 6 genes that responded to the climate change experiment.

10 equence in a 1000-generation yeast evolution experiment.

11 ir cognate antigen specificities in a single experiment.

12 proposed mechanism, as does a TEMPO trapping experiment.

13 e based on the measured imperfections of the experiment.

14 dence ratings only in the second half of the experiment.

15 fraction is observed following the retention experiment.

16 f nine different HAAs in a similar reduction experiment.

17 is confirmed by dynamic ternary breakthrough experiments.

18 proton detection under the conditions of our experiments.

19 ison with high-resolution force spectroscopy experiments.

20 minimal phototoxicity required in live-cell experiments.

21 the iridescent treatment fared best in both experiments.

22 is mechanism has not been directly tested in experiments.

23 cations, including both in vitro and in vivo experiments.

24 ticles via the analysis of Taylor dispersion experiments.

25 tribution applied to single molecule pulling experiments.

26 esting the surface site specificity of these experiments.

27 alanine-scanning mutagenesis (CASM) to guide experiments.

28 the corresponding bulk FCD loss agrees with experiments.

29 persaturation reproduced key features of the experiments.

30 nal flow, which we observe in agreement with experiments.

31 de highly credible candidates for biological experiments.

32 gn and interpretation of visual neuroscience experiments.

33 ed through quantum chemical calculations and experiments.

34 opy, end group analysis, and chain extension experiments.

35 ing trapped ion mobility spectrometry (TIMS) experiments.

36 , such as that from microarray or sequencing experiments.

37 s such as the design of guide RNA for CRISPR experiments.

38 the design and interpretation of preference experiments.

39 bserved during in situ infrared spectroscopy experiments.

40 interactions shared by chromatin interaction experiments.

41 cal, chicks performed randomly, as expected (Experiment 1).

42 In Experiment 1, manually-obtained cell counts were compare

43 In Experiment 1, we tested a range of different triangle ty

44 re positively correlated across individuals (Experiments 1 and 3).

45 ce also varied between flight cage and field experiments (-10 to 37% in the same cultivar and year),

46 Across two experiments, of which experiment 2 was a preregistered replication, 160 toddle

47 peted, only the self-advantage was detected (Experiment 2).

48 In Experiment 2, we manipulated distance while keeping angl

49 Similarly, in Experiment 3, no long-lasting differences in these measu

50 d upside-down, disrupting global processing (Experiment 4).

51 e regardless of the number or origin of seed experiments; (4) exploit a high-dimensional, complex par

52 the former 4 tasks in just over 100 hundred experiments (~8 experimental hours) - a factor of 5x fas

53 M (Standard Reference Material) and recovery experiments after spiking in food samples (Tea, coffee,

54 glut2) gene, coupled with immunofluorescence experiments against tyrosine hydroxylase (TH) or dopamin

55 ted (1)H-(17)O heteronuclear correlation NMR experiments allow for a rapid identification and differe

56 Our high-treatment experiment also identified crucial interactions between

57 Pull-down experiments also confirm the physical interactions of Sc

58 Our experiments also highlight the fact that assessments of

59 These experiments also suggest water is proximal to the select

60 s work demonstrates the utilisation of multi-experiment analysis to identify constitutive QTLs and ca

61 ntly, we emphasize critical aspects of a TIS experiment and highlight the extension and applicability

62 The combined experiment and simulation results show that when Li atom

63 We analyze data from both preclinical mouse experiments and a clinical trial of FMT to validate our

64 rate that the information provided by HDX-MS experiments and by the model of exchange are sufficient

65 icrobiomes from parents and during cohousing experiments and evaluated susceptibility to oral inflamm

66 We performed co-immunoprecipitation experiments and found a lower amount of KChIP3 bound to

67 es mechanistic insights that help in further experiments and modeling.

68 Here, we combine single-molecule FRET experiments and molecular dynamics studies to elucidate

69 ientific domains that involve time-intensive experiments and multi-dimensional design spaces.

70 Here, we report both experiments and simulations on the dynamic network self-

71 Combined experiments and simulations show the excitation of guide

72 Zhabotinsky micro-oscillators are studied in experiments and simulations.

73 Previous biophysical experiments and structural modeling have suggested that

74 In vitro DNA-binding experiments and structural prediction show that CTM prov

75 ation was observed at the end of the 12-week experiment, and phosphate was found to drive Zn speciati

76 with SNP-Lasso and Q + K-LMM in a simulation experiment, and showed that the new method is more power

77 ta from two followup studies (one lab, three experiments, and 1.2e4 observations).

78 otein's IgE reactivity was analyzed in ELISA experiments, and cross-reactivity with allergens of othe

79 six-carbon-substituted arene motifs, control experiments, and gram-scale synthesis make the synthetic

80 s supported by equilibrium dialysis, STD-NMR experiments, and inhibition analysis of GD3-binding towa

81 rotein)-an observation supported by previous experiments-and that the transition state ensemble was c

82 ptic plasticity rules inferred from in vitro experiments are correct in physiological conditions.

83 moss transplant and leaf litter manipulation experiment at three sites with paired paper birch (Betul

84 cal and genetic spatial data from functional experiments based on genetic, surgical and pharmacologic

85 growth rates of plant populations, including experiments beyond range boundaries, density-dependent p

86 We mimic parameter uncertainty in in vitro experiments by incorporating model error that shifts the

87 However, such experiments can be time-consuming and costly, which has

88 ing many design parameters in time-consuming experiments causes bottlenecks in a broad range of scien

89 orate phosphate into biomolecules, prebiotic experiments commonly use molar phosphate concentrations

90 Ex situ bioreactor experiments confirm that responses occur within five hou

91 Exclosure experiments confirmed that exposed reefs were less contr

92 In vitro single-molecule experiments confirmed that yeast condensins extrude loop

93 Colocalization experiments confirmed that, upon FAC treatment, TfR1 was

94 d these questions in a series of genome-wide experiments coupled to a novel bioinformatic analysis ap

95 ed isoprene SOA and aqueous-phase laboratory experiments coupled to the S(IV)-autooxidation chemistry

96 Together, these experiments demonstrate that ACh can modulate population

97 Here, in vitro experiments demonstrate that TAN1 directly binds microtu

98 Bacterial community transplantation experiments demonstrated a causal role of a properly ass

99 pull down and chromatin immunoprecipitation experiments demonstrated that beta-catenin is part of a

100 Silencing and chromatin immunoprecipitation experiments demonstrated that cAMP response elements bin

101 Finally, pulldown experiments demonstrated that miR-125b physically intera

102 +/- 20 W/kg at 80 Hz) in cyclical work loop experiments designed to simulate the in vivo dynamics of

103 Other experiments dissect the nature of that regulation of act

104 rs was systematically evaluated by design of experiments (DOEs) using three different FDA-approved hu

105 strating that its effect on decay depends on experiment duration and sampling frequency.

106 In each experiment, eight different decoder algorithms were comp

107 otoelectron spectroscopy, hydrogen evolution experiments, electrospray ionization mass spectrometry,

108 Initial validation experiments employed mycobacteria DNA, either extracted

109 mic range combined in a 21T MALDI FT-ICR MSI experiment enable researchers to visualize molecular str

110 in-8 expression, confirming the cell culture experiments' findings.

111 High-throughput sequencing experiments followed by differential expression analysis

112 n order to evaluate the different classes of experiment for studies of IDRs or IDPs in both dilute an

113 d tangles, in agreement with simulations and experiments for commonly used climbing and sailing bends

114 adjudicate between theories, we must design experiments for which the theories make distinct predict

115 These data include experiments from the literature, simulated assays, and p

116 nown features of motor learning in lab-based experiments generalize to a real-world task.

117 ation of the LFP has occurred mostly through experiment, giving rise to a variety of semiempirical mo

118 Hundreds of field experiments have demonstrated ecological release in livi

119 For example, in the last 15 years, experiments have progressed from measuring single intera

120 However, recent in vivo tracking experiments have revealed the presence of SSCs not only

121 ctroscopic measurements(7-10), and transport experiments have shown changes in the Landau level degen

122 To date, however, few experiments have successfully demonstrated plasma-driven

123 assays, and acute in vivo myeloid-depletion experiments identify activation of IGF1R as a critical c

124 Together, our experiments identify AHR signalling in enteric neurons a

125 Column experiments imaged with high-resolution X-ray computed t

126 activity in the kidney endothelium, in vitro experiments implicated a humoral factor in the anti-infl

127 We use a spatially replicated, multiyear experiment in four agricultural settings to test if enha

128 In an exploratory experiment in mice, a VHH-PTH peptide conjugate showed b

129 We implemented an experiment in which seedlings of 12 European/North Afric

130 ve parasitoid on its host using a laboratory experiment in which we independently varied daylength an

131 We manipulated consciousness in two experiments in a group of healthy males and measured bra

132 ace of UO(2) at the time scale of laboratory experiments in a solution saturated with respect to amor

133 Electron balances from laboratory experiments in batch and column reactors showed that 3.6

134 ed hand pollination treatments in controlled experiments in flight cages and in the field.

135 This was confirmed by competition experiments in isogenic TP53-WT and TP53-null (TP53(-/-)

136 Octa) that were used in in vivo immunization experiments in mice.

137 ing a variety of genetic tools and epistasis experiments in P. putida, we uncovered an 'upstream' cas

138 Aroma recombination experiments in pea protein samples confirmed the sensory

139 Anion transport experiments in POPC-based large unilamellar vesicles sho

140 lobal data fitting was achieved by including experiments in the forward and reverse directions to cor

141 Experiments in the presence of an osmoticant agent sugge

142 Moreover, Med19 loss of function experiments in vivo or in cellulo indicate that it is re

143 is question, we conducted two functional MRI experiments in which we dissociated the periods related

144 We apply each method to a mesocosm experiment, in which we aim to predict species richness

145 Time-resolved experiments indicate that the critical process for photo

146 Benchmarking experiments indicate that the ensemble neural network re

147 Biochemical experiments indicated that cytoplasmic Cx43 had a half-l

148 The results of our experiments indicated that Grubbs-type catalysts possess

149 o copurified with iron, and NMR spectroscopy experiments indicated that YecA binds iron via its MBD.

150 ction between Med19 and Med1 by GST pulldown experiments indicating privileged contacts between these

151 The experiment introduced unjustified payment inequality bas

152 Remarkably, controlled experiments involving isolated atmospheric ions and neat

153 ng selective reverse INEPT FESTA (SRI-FESTA) experiment is described, based on the use of a modulated

154 accessible to inspection, modification, and experiment, is adaptable as an educational tool, and pro

155 s ago in Vonnegut's pioneering cloud seeding experiments, it remains unclear what makes a material a

156 heory and cognitive research and designed an experiment leveraging construal level theory (CLT).

157 body postures between the two species during experiments may reflect aspect of signal integration.

158 s re-usable configurations to be defined for experiment metadata and local data collection, and handl

159 rom 16 055 datasets using 12 high-throughput experiment methods (e.g. H3K4me1/H3K27ac, DNase-seq/ATAC

160 The NMR experiments monitor processes in both electrodes individ

161 We further caution that behavioural experiments need to consider the possibility of context

162 In a separate experiment, non-breeders were placed alone in a novel aq

163 the model were validated in continuous wash experiments of chopped iceberg lettuce, and predicted th

164 to describe both the growth dynamics in our experiments of firefly luciferase-expressing Hep3B tumor

165 icore ring fibers provide a new platform for experiments of quantum effects in low-loss optical fiber

166 Across two experiments, of which experiment 2 was a preregistered r

167 osecond time-resolved X-ray pump/X-ray probe experiment on protein nanocrystals.

168 es for combating these challenges during IMS experiments on a hybrid QhFT-ICR MS.

169 a common mechanism for phenomena observed in experiments on both atrial and ventricular cardiac cells

170 Motivated by recent experiments on magnetically frustrated heavy fermion met

171 nally, we compare quantitatively our data to experiments on membrane-catalyzed amyloid aggregation of

172 Analogue experiments on phyllosilicates formed under low temperat

173 Experiments on three benchmark datasets suggest that the

174 Recent experiments on twisted bilayer graphene have shown a hig

175 e and repair on 3D genome folding using Hi-C experiments on wild type cells and ataxia telangiectasia

176 od for surveying cell populations from large experiments or clinical samples with the depth and resol

177 conduct ecologically relevant global change experiments over the long times commensurate with the pa

178 ove the growth rate of CNT in the BO-planner experiments over the seed experiments up to a factor 8;

179 In one experiment, participants were provided with a pre-specif

180 In all histological experiments, PC2 immunoreactivity in neighboring alpha-c

181 In laboratory and numerical experiments, physical quantities are known with a finite

182 formulae for the empirical curves that these experiments produce, called access period response curve

183 Results: Initial photoradiosynthesis experiments produced (89)Zr-DFO-azepin-onartuzumab in le

184 These experiments provide evidence that global ocean change ca

185 advances in chromosome conformation capture experiments provide partial information on the chromatin

186 s in pure rovibronic states are desirable in experiments ranging from cold chemistry to searches for

187 Our high-pressure experiments reveal continuous strengthening in samples w

188 paramagnetic resonance, and NMR spectroscopy experiments reveal that a disorder-to-order transition o

189 Specifically, the experiments reveal that both PrP(106-126) and hIAPP indu

190 Strikingly, our experiments reveal that islets from T2D patients contain

191 Recent experiments reveal that micro-structured tungsten can ex

192 water as the feed with low surface tension, experiments reveal that the number of polyelectrolyte la

193 Our in vitro experiments reveal that this feature stems mainly from t

194 Analysis of a 96-plex perturbation experiment revealed changes in cell population structure

195 Finally, a rescue experiment revealed that YY1-regulated BMP6 expression i

196 Our experiments revealed PLD3 as the principal acid 5' exonu

197 Field experiments revealed strong broad- and narrow-sense trai

198 entiviral shRNA knockdown and reconstitution experiments revealed that both a functional ECT2 BRCT do

199 analysis with qPCR, flow cytometry and ELISA experiments revealed that GM-CSF blockage in monocytes s

200 Our experiments revealed that this haloarchaeon can hydrolyz

201 Desorption and regeneration experiments revealed that TLSB could be desorbed with HC

202 e-resolved emission and transient absorption experiments revealed that upon excitation, our multichro

203 Our experiments show how selection can enhance evolvability

204 NMR studies and mutation experiments show that both acidic and basic residues can

205 ne can accept up to three methyl groups, and experiments show that protein-protein binding free energ

206 Despite the segregation reward, our experiments show that spatial integration can be achieve

207 on transfer, and hydrogen-deuterium exchange experiments show that the variant exists in a major nati

208 Extensive experiments showed that DeepCDR outperformed state-of-th

209 In vitro experiments showed that human embryonic stem cell-derive

210 Dye loading experiments showed that mechanical stimulation increased

211 Complementary MD simulations and FRET experiments showed that open-to-closed transitions in th

212 the surfactant were also measured, and NOESY experiments showed that phenols were located in the hydr

213 Immunostaining experiments showed that vinculin, talin, integrin alpha(

214 Subsequent shipboard light exposure experiments showed ultrastructural changes in the photop

215 ared (13)CO-detect versus (1)H(alpha)-detect experiments, showing that significant sensitivity gains

216 A direct-waveguide experiment shows that the propagation length of surface

217 ed using a wide variety of set-ups(2-4), but experiments so far have yielded seemingly contradictory

218 in conformation and readouts from functional experiments, such as genome editing and reporter assays.

219 Chemical perturbation experiments suggest that mechanically evoked responses r

220 Transient experiments suggested that the difference is related to

221 Moreover, in utero transplantation experiments suggested that the rostrocaudal dispersion o

222 At pH 3.5 in batch experiments, sulfidogenesis started within 4 days, reach

223 diagnosed with systemic sclerosis and to an experiment that examined multiple lots of a human 51-cyt

224 In addition, we performed a ChIP-Seq experiment that identified ANT binding sites in developi

225 interpret and identifies the mechanisms and experiments that best characterize the system.

226 y, we conducted three computational decoding experiments that investigated decoding accuracy: (1) bas

227 to complement this traditional approach with experiments that probe proteins in a T-dependent fashion

228 We corroborated by western blotting experiments that PTPN14 and CAV1 co-inmunoprecipitated i

229 vided are the results of several mechanistic experiments that suggest the process features an MHAT-in

230 By time-of-flight (TOF) neutron diffraction experiments, the influence of segregation-induced micros

231 target in a follow-up single-cell sequencing experiment, thereby decreasing cost.

232 We performed lineage tracing experiments to determine the fates of peribiliary mesenc

233 he software's capabilities, we undertook ITC experiments to determine the respective CMCs of n-octyl

234 e of existing data and the design of further experiments to elucidate signalling mechanisms within th

235 We have used multi-year field experiments to examine the physiological and life-histor

236 cing now allows comparisons between multiple experiments to identify commonalities in stress response

237 NA-seq has increased the scope of sequencing experiments to include more complex designs, such as des

238 utomatically incorporates feedback from past experiments to inform future decisions and can be genera

239 imulations were used in tandem with in vitro experiments to investigate changes in depolymerization b

240 This is one of the first whole-ecosystem experiments to involve replicated metagenomic assessment

241 h as mass cytometry are enabling time series experiments to monitor the temporal evolution of cell st

242 , quasi-classical dynamics calculations, and experiments to study in detail the mechanism of carbon-c

243 (strain MIT9215) through a series of growth experiments under iron- and cobalt-limiting conditions.

244 in the BO-planner experiments over the seed experiments up to a factor 8; (2) rapidly improve its pr

245 ral and neural data from a task-set learning experiment using a network model.

246 In pulse chase experiments using a deconvolved, confocal line scanning

247 n of cultured human and mouse macrophages in experiments using recombinant TSP4 variants and in cells

248 the presence of RDX was evaluated in abiotic experiments using substoichiometric, stoichiometric, and

249 ulation of plant immunity is corroborated by experiments using the specific NKCC inhibitor bumetanide

250 form the loops of typical sizes seen in Hi-C experiments using these low-effective-diffusion constant

251 In two field experiments using wild birds and humans, we measured bot

252 In three experiments using word stimuli, domain-relevant and atyp

253 Numerous experiments utilizing powerful pulsed lasers with peak-i

254 c activity can be mapped from the same SECCM experiment via local voltammetry, which demonstrates the

255 In the deletion experiments we excised ~ 15 kilobases of DNA that contai

256 Via three experiments we show that similar results are achieved ac

257 In a proof-of-principle experiment, we demonstrate high-fidelity operation that

258 to PTPN14 and using a PTPN14 knockout rescue experiment, we demonstrate that the degradation of PTPN1

259 s part of NASA's Arctic-Boreal Vulnerability Experiment, we sampled 79 stands (47 burned, 32 unburned

260 2013-2016 extraordinary drought as a natural experiment, we studied four co-occurring woodland tree s

261 cular, via a synergy between NMR and kinetic experiments, we demonstrate the presence of a misfolded

262 In the experiments, we detect instability and localize its sour

263 rgy transfer-based biosensors in patch clamp experiments, we discovered a robust voltage dependence o

264 escence spectroscopy, and cell fractionation experiments, we found that depending on the alternative

265 Using immunofluorescence and tracing experiments, we found that fibers positive for dopamine

266 andomized genomes and evolutionary selection experiments, we found that tropism could be redirected t

267 Along with these in vivo experiments, we further analyze Abeta42 toxicity and its

268 By using in vivo imaging and transfusion experiments, we further confirmed that senescent erythro

269 ng and calibrating an active vertex model to experiments, we have simulated numerically a confluent c

270 emporal analysis from multimodal single-cell experiments, we introduce an extension of the RNA veloci

271 Across two experiments, we modeled performance on a probabilistic d

272 e Forster resonance energy transfer (smFRET) experiments, we studied how frameshift-inducing stem-loo

273 Experiments were conducted in isolated human cardiomyocy

274 The adsorption experiments were conducted with an initial Hg(0) concent

275 ltiple timescales observed in the pump-probe experiments were connected to local structural fluctuati

276 The electrochemical experiments were in accordance with Raman spectra and su

277 Although experiments were performed under permissive conditions,

278 Experiments were performed with a mIRage IR microscope w

279 ng intact plants, and guard cell patch-clamp experiments were performed.

280 ovements for such native top-down sequencing experiments were possible by leveraging IM separation, w

281 effects observed in four out of five of our experiments were statistically equivalent to zero (P < 0

282 he "external lock-in effect" in barium block experiments, whereby the binding of external K(+) impede

283 as studied by performing deuterium-labelling experiments, which indicated that the gamma-C(sp(3) )-H

284 resonance imaging and electromyography (EMG) experiment with viewing of emotional and neutral faces a

285 Nevertheless, acute toxicity experiments with (212)Pb-anti-mCD38 established a toxic

286 Here, we use a combination of genetic rescue experiments with CSLD-CESA chimeric proteins, in vitro b

287 Gain-of-function and loss-of-function experiments with CYR61 in vivo point to it being a key c

288 makes it much easier to perform correlation experiments with different biomarkers independently.

289 rast response functions were measured in two experiments with different tasks to control for attentio

290 Parallel experiments with direct intracranial virus infection gen

291 is method predicts the results of unobserved experiments with high accuracy, while making no assumpti

292 tro Likewise, in in vivo human GBM xenograft experiments with immunodeficient mice, mAb treatment inh

293 Cosedimentation experiments with liposomes revealed that the Aster-B GRA

294 estigations into these processes and enables experiments with lower, relevant particle concentrations

295 Results from experiments with murine xenografts and 2D and 3D co-cult

296 duce distinct signal waveforms and performed experiments with suspended human cancer cells to charact

297 Biochemical experiments with synaptosomes from Slc38a1 knock-down mi

298 We performed behavioral and brain-based experiments, with the latter employing electroencephalog

299 ramount for properly designing and executing experiments within the central nervous system.

300 ing unknown mixtures of analytes in a single experiment, without separation or pre-treatment before d