ライフサイエンスコーパス: experiment(|s) (with|using)

1 A chemotaxis experiment with 1 muM progesterone was performed that si

2 Across 21 experiments using 106 litters, median (95% CI) hemispher

3 An online experiment with 1153 participants further replicated the

4 observations from a laboratory-in-the-field experiment with 128 users of forest commons in Bolivia a

5 Isotope labeling experiments with (15)N-labeled P.A. confirm that the nit

6 Control experiments with (18)O-labeled water and TEMPO provided

7 ended sediment as the inocula in a secondary experiment with 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3

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

9 in triplicate for ex vivo diagnostic biopsy experiments with 25 gauge (25 G) needle, 27 gauge (27 G)

10 interspecific competition using a greenhouse experiment with 35 natural accessions of Arabidopsis tha

11 -harvest losses were investigated in a field experiment with 5 replications per scenario.

12 Pulse-chase experiments with 5-EU allowed us to determine RNA stabil

13 A field experiment with 65 spring genotypes and 9 winter genotyp

14 We conducted a phylogenetic comparative experiment with 74 grass species, conceptualising morpho

15 Here, we simulated an mDC experiment using a custom computational algorithm for vi

16 ved in epigenetic regulation of lung cancer, experiment using a DNA methyltransferase inhibitor (5-az

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

18 ar the M point is confirmed through a detwin experiment using a piezo device.

19 ombine, in a wild primate, an open diffusion experiment with a modeling approach: Network-Based Diffu

20 ineral-associated C in a 4 year manipulation experiment with a semi-arid grassland on China's Loess P

21 In vivo experiments using a B16F10 mouse melanoma model demonstr

22 illustrate the utility of camera trap-based experiments using a case study, we propose a study desig

23 Mutagenesis experiments using a conditional knockout constructed in

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

25 We first formalize associative learning experiments using a low number of tunable design variabl

26 o perform dynamic nuclear polarization (DNP) experiments using a single-chip-integrated microsystem h

27 Incineration experiments using a tubular furnace and subsequent ICP-M

28 structed pressures were also calculated from experiments with a catheter balloon embedded in a plasti

29 Results from experiments with a continuous reactor hosting a strain o

30 Our preliminary experiments with a liquid jet at a bending magnet X-ray

31 Here, by combining lineage-tracing experiments with a model of severe glandular injury in t

32 Finally, experiments with a panel of patient-derived Vif isolates

33 Experiments with a quartz crystal microbalance also prov

34 Experiments with a T. dentrificans mutant strain defecti

35 We combine historical and new experiments with (a) a constant injection rate; (b) a co

36 Experiments with acidic stretch-derived peptides demonst

37 y time- and work-efficient biotransformation experiments with activated sludge and mixtures of chemic

38 al and metatranscriptomic data obtained from experiments with activated sludge grown at different sol

39 m electrodes, which was still present in our experiments with active looking.

40 trated performing NMR enantiodifferentiation experiments using alpha,alpha'-bis(trifluoromethyl)-9,10

41 In final experiment using an appetitive object discrimination tas

42 ogenous modulation was confirmed in a second experiment using an EEG-based closed-loop system.

43 an increase in grain yield of 11.3% in field experiments using an agronomically appropriate plant den

44 resistance, we conducted long-term exposure experiments using an Escherichia coli K-12 model strain.

45 Additional experiments using an in vitro model of the blood-brain b

46 Indeed, recent experiments with an actomysin motility assay suggest tha

47 te sample evolution in IR pump - X-ray probe experiments with an unprecedented time resolution.

48 Experiments with animals from both sexes revealed that d

49 Experiments with anti-Thy1.1.

50 ries also uncover complexities: Results from experiments with Arabidopsis leaves in conventional cont

51 g, X-ray crystallography, and gel filtration experiments with asparagine, aspartate, and valine as PK

52 n summary, any inference from photobleaching experiments with B > 0.1 is likely to be unreliable, but

53 Previous co-culture experiments using bacteria and mutants of temperate phag

54 Experiments with BAFF-deficient B6.Baff(-/-) Bcl2(Tg) mi

55 Experiments with bird predators suggest these signal com

56 xpression of CD31 and CD11b, and mechanistic experiments using blocking antibodies confirmed a functi

57 of frameshift peptides in T cell stimulation experiments using blood mononuclear cells isolated from

58 Experiments with BMMCs and RBL-2H3 MCs demonstrated that

59 We benchmark the experiment with bootstrapping heuristic methods scaling

60 Two-season greenhouse pot experiments with Brassica rapa L. were performed with an

61 Experiments with cancer cells showed that expression of

62 activity, as monitored by in vitro cleavage experiments using casein or E-cadherin as substrates and

63 pidemiological analysis with neurobiological experiments using cell and animal models based on a hypo

64 ponses characteristic of UPS inhibition, and experiments using cellular reporter proteins have shown

65 e consisted of 128 measurements taken from 4 experiments with CH(4) measurements taken in respiration

66 Experiments using chelators and imaging both indicated t

67 Experiments using chemical, molecular and cell biology m

68 Immunofluorescence experiments with CHIKV replicase with manipulated proces

69 ere, to evaluate this prediction, we conduct experiments with Chinese and Sumerian laws that are mill

70 However, across two field experiments with Chinese factory workers and American un

71 alyzed ex vivo and in vitro using trans-well experiments with cholangiocytes.

72 nalyzed ex vivo and in vitro using transwell experiments with cholangiocytes.

73 te quantitation-based quantitative proteomic experiments with clpC1- and clpP2-depleted Mtb cells sug

74 In free-flight experiments with CO(2), adding a dark contrasting visual

75 ttentional modulation phenomenon in separate experiments with colorless words (word-only) and words w

76 in living HEK293 cells, competition binding experiments using commercially available SMO ligands (SA

77 n vitro reconstitution assay and egg extract experiments with computational modeling to show that dif

78 Here, we combine in vitro reconstitution experiments with computational modeling to study a minim

79 Combining human psychophysical experiments with computational modeling we show that the

80 odel nanopesticides by combining soil column experiments with computational modelling.

81 Experiments with CRISPR-Cas9-edited sorghum further indi

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

83 Finally, titration experiments with cyclic voltammetry provided varying and

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

85 d bioaccumulation (including dietary uptake) experiments with Daphnia magna using five different CP t

86 Twenty-three experiments with data on 16,241 individuals (mean propor

87 In two experiments using deep neural networks, we examined the

88 Plant inoculation experiments with deletion mutants in the individual gene

89 ilities for integrating field and laboratory experiments with detailed genetic sequencing.

90 Additional experiments with diazo group transfer to lithium hydrazi

91 Results from flow-through adsorption experiments with dibromoacetic acid (DBAA) as a model HA

92 ext for the interpretation and comparison of experiments using different fragments and tissues to rep

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

94 In two greenhouse experiments with different growth conditions, we monitor

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

96 In this study we perform numerical experiments with different uplift altitudes using the Na

97 Through experiments with dilute RBC suspensions, we find an off-

98 ity compared to that observed in the control experiments with direct current.

99 Parallel experiments with direct intracranial virus infection gen

100 Experiments using distinct inhibitors of the accommodati

101 ge-fractionated HEK293T cell lysate in XL-MS experiments using disuccinimidyl sulfoxide (DSSO) cross-

102 We performed a validation experiment with domestic dogs, monitoring them by video

103 In experiments using dominant negative mutants, cdc42 activ

104 UV/vis titration experiments with eight anions in acetonitrile revealed h

105 We conducted two experiments using electrical stimulation in rhesus monke

106 g, which is crucial for high time resolution experiments with elevated illumination intensity.

107 Across five field experiments with employees of a large organization (n =

108 ogeneous ambient iron-particles and in vitro experiments with engineered versus ambient, incidental i

109 The method was validated by spike-recovery experiments with equilibrated soil-water-AFFF and analyt

110 NMR time-course experiments with excess formaldehyde in solution show fo

111 rom carefully randomized and well-controlled experiments with explicitly stated outcomes as the princ

112 Experiments using exposure to specific components of sol

113 Our pull-down experiments with extracts of synchronized cells show tha

114 Subsequent experiments using fall armyworm evaluating the influence

115 Here, through multiple (13)C-metabolomics experiments with Fe-replete and Fe-limited cells, we unc

116 We present results of parallel experiments using ferrihydrite (2.0 g L(-1)) and Fe(2+)(

117 During previous experiments with ficolin-2 and ficolin-3, we have observ

118 and utility of the procedures in simulation experiments using fluorescent beads and then apply them

119 tracentrifugation techniques and DNA binding experiments with fluorescently labeled DNA oligonucleoti

120 hibits disaggregation of luciferase in vitro Experiments with fluorescently tagged HSP-17 under the c

121 We perform computational experiments using four well-known feature ranking method

122 After experiments with four common bacteria (i.e. E.

123 e way to performing attosecond time-resolved experiments with free-electron lasers.

124 xus (MORN) domain; previous yeast two-hybrid experiments with full-length and MORN-truncated ARC3 sho

125 Experiments with functionalized and bare AuNS illustrate

126 Genetic loss and overexpression experiments using genetically encoded reporters and defi

127 i)xG(s) effects when interpreting results of experiments using genetically modified animals, since th

128 synchrotron X-ray diffraction and scattering experiments with geochemical modeling to contribute to f

129 Hierarchical sensitivity experiments using global climate models quantify the rel

130 Experiments with Glp1r reporter mice and a validated GLP

131 In contrast, comparable experiments with Gt desorbed predominantly (57)Fe(II), s

132 oess, kaolin) on DMT in a controlled feeding experiment with guinea pigs.

133 d roughness values exceed those from feeding experiments with guinea pigs who received plants with di

134 tation of past literature and future in vivo experiments using head-fixed animals.

135 Experiments with helix-breaking proline substitutions in

136 In experiments with heterologously expressed protein, the e

137 EC model was calibrated with data from batch experiments with heterotrophic denitrifying communities,

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

139 In experiments with higher initial variability, a greater c

140 in automated microfluidic Brownian dynamics experiments using holographic optical tweezers and achie

141 In this experiment with human subjects of both sexes, we tested

142 Finally, experiments using human cord blood and airway epithelial

143 ng retina signaling pathways, and conducting experiments with human detectors and optical states with

144 Experiments with human gastric organoids grown as monola

145 Furthermore, in vitro experiments with human keratinocytes and synovial fibrob

146 Psychophysical experiments with human subjects characterize the visual

147 This paper conducts price formation experiments with human subjects located in large complex

148 Experiments with hybrid viruses are illuminating how SAR

149 ntly altered by L sigmodontis infection, and experiments with IL-10(-/-) mice demonstrated that IL-10

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

151 A full optoPlate-96 experiment with immunofluorescence analysis can be perfo

152 Here we perform controlled experiments with increasing carrier proteome amounts and

153 ast years, there has been a great advance in experiments using isolated myofibrils and sarcomeres tha

154 However, in pairwise preference experiments with J+ CMV- and J- CMV-infected plants, aph

155 A-seq transcriptome profiling of tomato, and experiments with jasmonic and salycilic acid deficient t

156 In addition, our functional rescue experiment using Jpx-deletion mutant cells shows that hu

157 Additionally, in vivo experiments with Jun(f)(/f)JunB(f/f)K5cre-ER(T) mice wer

158 ement with data from a 96 h in vivo exposure experiment with juvenile rainbow trout.

159 here their atypical behavior in competitive experiments with labeled ghrelin (GHR), namely, the stro

160 dy, we conducted two separate functional MRI experiments with language learners (male and female), on

161 Food choice experiments with leaves from wild-type and SOT1 knockdow

162 Domain-swapping experiments with LGR4 and LGR5 revealed that the seven-t

163 both output ports, as confirmed in numerous experiments with light or even matter.

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

165 se different mechanisms with a decomposition experiment using litter from four abundant species (Achn

166 solated from the murine stomach in coculture experiments with live bacteria mimicking the infected st

167 e validate these computational results using experiments with live guenons, showing that facial trait

168 Field-based experiments with longer-term exposure of both CO(2) and

169 Our findings were confirmed by numerical experiments using low- and high-resolution versions of t

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

171 Experiments with Lp at pH 7.0 were conducted in carbonat

172 Immunoprecipitation experiments with lysates of HSV-infected neurons showed

173 (coined OPEX) to identify informative omics experiments using machine learning models for both exper

174 Combining uncaging experiments with mathematical modeling, we were able to

175 Experiments with MC-deficient Kit(W-sh/W-sh) mice system

176 To date, most native MS experiments with membrane proteins are based on detergen

177 been demonstrated only in proof-of-principle experiments with microwave clocks of limited stability.

178 Experiments with MIN6 cells cultured at different densit

179 anTraX can handle large-scale experiments with minimal human involvement, allowing res

180 d at those VIPs, even in competitive binding experiments with minute virus of mice using dual-label S

181 Experiments with mixtures of nucleotides suggest that th

182 and provide new hypotheses for neuroscience experiments using model systems.

183 Experiments with model compounds showed that fulvic acid

184 Biochemical experiments with model nucleosomes demonstrate sufficien

185 We show how investigations combining experiment with molecular simulation are revealing funda

186 We combine our SAXS and SANS experiments with molecular dynamics simulations and prev

187 Surprisingly, experiments using monosynaptic rabies virus showed that

188 In fluorescent microscopy experiments using mouse fibroblasts deficient in PARP-1,

189 n addition, we review insights obtained from experiments with murine models of allergic airway and sk

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

191 evels affect the ESR, we performed epistasis experiments with mutations in rpd3 and msn2/4 combined w

192 We designed experiments with natural and synthetic stimuli to measur

193 Previous experiments using network-targeted noninvasive brain sti

194 Here, we present additional experiments with neuronal NOS (nNOS) and inducible NOS (

195 ution rates were similar to those of abiotic experiments with nitrite (from 1.15 x 10(-14) to 4.94 x

196 ing supercritical fluid chromatography (SFC) experiments with NMR.

197 Control experiments with non-crosslinkable ligands, as well as t

198 ther than the actuator drug, particularly in experiments using nonhuman primates.

199 more, ddPCR experiments on serum samples and experiments with nuclease indicated the contribution of

200 r 5A and 5B displayed sensitivity to HM, and experiments with nullisomic-tetrasomic (NT) lines furthe

201 omprehensive series of isotope fractionation experiments with numerous Fe(II)-bearing minerals as wel

202 med a balanced parallel and crossover design experiment with omnivorous common bulbuls Pycnonotus bar

203 tified 6935 and 5474 proteins in TMT 10-plex experiments with one microgram of lysate protein and 200

204 Z3 domain (CRIPT), and results from previous experiments using only the isolated PDZ domain are consi

205 In vitro experiments using osteoarthritis-like conditions affecte

206 In patch-clamp experiments with outside-out patches, THIK-1 currents we

207 to the ~20% enhancement seen in parallel FCS experiments using p-nitrophenyl phosphate (pNPP) as subs

208 Experiments with pairs of freely-swimming fish reveal th

209 owground C dynamics, we conducted a girdling experiment with plots distributed across 1 km(2) of tree

210 Experiments using pressured preparation time further sup

211 l activation, perform a 96-plex perturbation experiment with primary human mammary epithelial cells a

212 Using microfluidic experiments with Pseudomonas aeruginosa and Escherichia

213 bserved in Xenopus egg extracts and in vitro experiments with purified components is a consequence of

214 Experiments with purified enzymes indicated that viperin

215 binding assays and surface plasmon resonance experiments with purified proteins, we demonstrate that

216 eNOS is a direct interaction as supported in experiments with purified proteins.

217 A new paradigm of "mixed catalyst-substrate" experiments with pyrimidine and pyridine systems allows

218 compared to alternative TIMS-q-FT-ICR MS/MS experiments with quadrupole isolation at nominal mass (~

219 Experiments with radiographers of varied levels of exper

220 Controlled biodiversity-ecosystem function experiments with random biodiversity loss scenarios have

221 Our experiments with real readsets demonstrate that Apollo i

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

223 This observation was supported by experiments with recombinant bacterial enzymes, along wi

224 Biochemical experiments with recombinant mouse enzymes demonstrated

225 dation products and was confirmed by spiking experiments using respective compounds.

226 Experiments with resting cells prepared from T. kivui cu

227 nd connecting results from isolated in vitro experiments with results from in vivo and whole-organism

228 Experiments with selectively receptor-blinded viruses in

229 Feeding experiments with sheep have shown negligible effects of

230 Combined with binding experiments with site-directed ETS1 mutants, the molecul

231 We combined batch experiments with size-exclusion and reversed phase liqui

232 ion types, based on a common garden dry-down experiment with species originating across a rainfall gr

233 Experiments using specific antagonists suggest that occl

234 We examine this issue in experiments with starlings (Sturnus vulgaris) and show t

235 ining time-resolved two-photon photoemission experiments with state-of-the-art numerical calculations

236 el established that, in stochastic collision experiments with steady-state oxidation at disk UMEs in

237 cryptic colouration and survival in a field experiment with stick insects.

238 using a set of behavioural and neuroimaging experiments with stimuli that strongly trigger curiosity

239 TCM transformation experiments using strain CF revealed pronounced normal c

240 Here, we present Comparison of Hi-C Experiments using Structural Similarity (CHESS), an algo

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

242 tants were determined in competition kinetic experiments using sulfite as a competitor.

243 We used a common garden experiment with sun and shade treatments to test for var

244 The experiments with SUR1-KO beta-cells point to a direct ef

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

246 Biochemical experiments with synaptosomes from Slc38a1 knock-down mi

247 ths and weaknesses, we performed a series of experiments with synthetic data and compared its perform

248 We conduct four experiments with tasks involving multiple alternatives a

249 Next, in vitro experiments using Tcf21-expressing murine podocyte cell

250 otope effects of strain CF were identical to experiments with TCM and Vitamin B(12) (epsilon(13)C(Vit

251 In a greenhouse inoculation experiment using the black cottonwood (Populus trichocar

252 n reaction time was predicted after a single experiment using the monitoring kit showing how efficien

253 The combination of these experiments using the 2D-LC-CRMS strategy enables the se

254 stinguishable images in our phenotype rescue experiments using the endothelial tube formations assay,

255 wed by high-throughput sequencing (ChIP-seq) experiments using the human HepG2 cell line for 208 chro

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

257 PLIN2 expression via PPARgamma, we performed experiments using the widely used PPARgamma antagonist 2

258 s provide important outcomes-related data in experiments with the animal models that are essential fo

259 Together, these results, obtained from experiments with the chromatin regulator SIN3 and the me

260 Binding experiments with the complement components C3b and C5b-9

261 illingness to work, as observed in classical experiments with the D2-antagonist haloperidol.

262 These claims were based on experiments with the motile ciliate Stentor coeruleus.

263 During four different evolution experiments with the opportunist betaproteobacterium Bur

264 The results of comparative experiments with the TCN, LSTM, and EEMD-LSTM methods sh

265 The experiments with the viscoelastic media led to contradic

266 ntrations in Delhi using several sensitivity experiments with the Weather Research and Forecasting mo

267 ne optical spectroscopy and light-scattering experiments with theoretical modeling to show the revers

268 Here, we combined optomechanical experiments with theory and simulations to analyze knott

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

270 Combining our experiments with thin film active chiral fluid theory we

271 In a proof-of-concept experiment using this technology in an agricultural soil

272 ral resolution of X-ray transient absorption experiments with this beamline is measured to be 11 fs f

273 ing molecule, which was confirmed by in vivo experiments with this initial anchoring molecule in rats

274 combines data across scales from 33 mesocosm experiments with those from 14 river basins and 22 cross

275 Similar experiments using three HULIS samples with distinctly di

276 In several interlocking discrimination experiments with three male observers, we confirm this l

277 The present study used zebrafish exposure experiments with three model compounds with distinct thy

278 The most frequent problems are running experiments with too high precursor concentrations, too

279 Recent experiments with triethylammonium (TEAH(+)) donating the

280 Experiments with truncated mutant C/EBPbeta demonstrated

281 Experiments using TUNEL, BrdU, progenitor labeling, and

282 Here we report a series of experiments with twig-mimicking larvae of the American p

283 We used a long-term (10 month) in situ experiment with two phylogenetically diverse scleractini

284 were used in a factorial, repeated measures experiment with two treatments and two periods.

285 AA-nano-ZVI) particles were tested in column experiments using two solution chemistries and silica co

286 ests and in situ electron microscopy cutting experiments with two micromechanical testing setups.

287 Isotopic labeling experiments using U(13)C-glucose showed that loss of MPC

288 t was functionally analyzed by voltage-clamp experiments using various heterologous cell expression s

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

290 ly computer-simulated, thus allowing virtual experiments with virtual reference standards.

291 re quantified in PET teabags after migration experiments with water and food simulants C (20% v/v eth

292 iral modes in the bulk, we conduct transport experiments using wedge-shaped Cd(3)As(2) nanostructures

293 we report results from in vitro and in vivo experiments with WhiD from Streptomyces venezuelae (SvWh

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

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

296 Co-inoculation experiments with Wt and Deltaexlx-gh5 rescued the moveme

297 ofluidic cell for an in operando synchrotron experiment using X-ray attenuation.

298 Ins2 (Akita)/KO mice and, likewise, in vitro experiments with XBP1 siRNA.

299 reduce sample waste by more than 95% for SFX experiments with XFELs performed with liquid jets and ca

300 We conducted a mesocosm experiment with zooplankton communities and their fish p