ライフサイエンスコーパス: control experiment

1 that caused by the hot binding buffer (blank control experiment).

2 r this cyclization based on the results of a control experiment.

3 nt to physical deformation compared with the control experiment.

4 e pH than the P-PONbs themselves, a critical control experiment.

5 three-component reaction is supported by the control experiment.

6 /- 1.0 per thousand), were also similar to a control experiment.

7 h of mild cold exposure served as a positive control experiment.

8 equires additional data from an SssI-treated Control experiment.

9 found through lengthy systematically planned control experiments.

10 s using TfOH formed in situ was ruled out by control experiments.

11 ocess, as evident by spectroscopic study and control experiments.

12 to the PCT analyte which was evident through control experiments.

13 anecarboxamides is proposed based on several control experiments.

14 The results have been made conclusive with control experiments.

15 e' by determining classical disturbance with control experiments.

16 acin to suppress FFA compared with 11 saline control experiments.

17 eighboring brain areas, is presented through control experiments.

18 immunosensor was confirmed with two types of control experiments.

19 er thiophenol 7 and phenol 8 is supported by control experiments.

20 1)H NMR, kinetic isotope effect studies, and control experiments.

21 n was substantiated by positive and negative control experiments.

22 action is proposed by performing a series of control experiments.

23 tions without the need to perform additional control experiments.

24 ical process is likely, supported by several control experiments.

25 5 mum) and heavier particles than those from control experiments.

26 emove the need for costly and time-consuming control experiments.

27 to a lesser extent when Aq1 is used than in control experiments.

28 Randomized controlled experiment.

29 lic pathways affected in a single, carefully controlled experiment.

30 been supported by the results from a set of controlled experiments.

31 eme events has been limited due to a lack of controlled experiments.

32 phytes) can modify plant disease severity in controlled experiments.

33 our knowledge comes from non-crop plants in controlled experiments.

34 ated through a series of deuterium-labelling-controlled experiments.

35 of acute SKP-SC transplantation versus media control (Experiment 1) and versus nerve-derived SC or de

36 CS over the left occipital cortex, while, in control Experiment 2, participants received sham and act

37 As a control experiment, a monogold complex was synthesized.

38 On the basis of control experiments, a plausible reaction mechanism for

39 the methylation levels not considered in the controlled experiment, a feature that is paramount in th

40 oise exposure experiments, as only carefully controlled experiments allow to establish cause-and-effe

41 A double-blind, placebo-controlled experiment allowing individuals to lie privat

42 , with no opsin expression) and food-seeking control experiments also failed to produce the same effe

43 nreversible flux decline was observed in all control experiments and a cross-flow rinse with the feed

44 i, the complexity of natural movies, and the control experiments and analyses all suggest that a more

45 Control experiments and computational studies revealed t

46 Control experiments and computational studies support a

47 Control experiments and density functional theory (DFT)

48 Control experiments and density functional theory calcul

49 ocess is carefully investigated with various control experiments and density functional theory simula

50 A few control experiments and deuterium labeling studies were

51 cis-trans isomerization was supported by the control experiments and deuterium labeling studies.

52 chanistic approach was well supported by the control experiments and deuterium-labeling studies and b

53 xazole formation is proposed on the basis of control experiments and DFT calculations.

54 nalytical protocols, validated by systematic control experiments and high-resolution SEM imaging, sho

55 Predominance of arsenite in control experiments and no evidence of surface-bound thi

56 Both control experiments and photophysical studies supported

57 eactions involving carbon-centered radicals, control experiments and spectroscopic studies suggest th

58 ition, we validate our CIU protocols through control experiments and systematic statistical evaluatio

59 detected that alternans was Ca(2+) driven in control experiments and voltage driven in the presence o

60 Controlled experiments and mechanistic investigations wi

61 on of the observed trends requires long-term controlled experiments and multi-model ensembles to redu

62 However, using carefully controlled experiments and multivariate analyses, we dem

63 ectron transfer pathway was established by a control experiment, and a butylated hydroxytoluene-trapp

64 ith all six-carbon-substituted arene motifs, control experiments, and gram-scale synthesis make the s

65 Control experiments are in support of a homogeneous mole

66 ical role in determining expansion speed but controlled experiments are lacking.

67 power of this novel methodology by analyzing controlled experiments as well as genuine population gen

68 g this effect, but it has not been tested in controlled experiments at atomic resolution.

69 However, controlled experiments at the cellular scale are challen

70 In a controlled experiment, Bd infection significantly altere

71 We demonstrate why use of specific control experiments can prevent assumptions that VEGF-A1

72 cross the endolysosomal membrane), including control experiments, can be completed within 1 h.

73 reaction is predicted by conducting various control experiments, competitive reactions, furoindole f

74 Through numerous control experiments, conductance noise analysis and tran

75 Control experiments conducted with one affinity tag only

76 XPS analysis and rigorous control experiments confirm covalent attachment of the d

77 Control experiments confirm that the same reaction does

78 Control experiments confirm the crucial role of the anio

79 Control experiments confirmed that the diminished respon

80 Control experiments confirmed that this washout was due

81 Additional control experiments confirmed the absence of morphine an

82 Control experiments confirming adsorption of proteins on

83 reaction path were unraveled by a series of control experiments coupled with density functional theo

84 A series of control experiments demonstrate that a synergistic inter

85 Further, control experiments demonstrate the crucial role that Te

86 Control experiments demonstrate the directing effect of

87 Control experiments demonstrated that these mutant Rrn3

88 Control experiments demonstrated the heterogeneous natur

89 Control experiments demonstrated the molecular recogniti

90 A control experiment designed to assess iGluSnFR's dynamic

91 the reaction and from a standardized set of control experiments designed to identify and then elimin

92 In the preliminary mechanistic studies, control experiments, deuterium labeling experiments, and

93 Control experiments, deuterium labeling, and kinetic stu

94 tion mechanism has been investigated through control experiments, deuterium labeling, radical clock,

95 Control experiments, DFT calculations, and DOSY NMR stud

96 DSC control experiments do not show the second domain, sugge

97 Deuterium labelling studies and control experiments enable a potential mechanism to be e

98 Several control experiments establish that the reaction proceeds

99 The positive control experiments established retention of the carbony

100 Control experiments established that Kv2.2 was not expre

101 This method was validated by series of control experiments, establishing that protoplast isolat

102 zes both components in the cerebellum, while control experiments exclude potential sources elsewhere.

103 Furthermore, additional sets of control experiments favor the involvement of unimolecula

104 ransformation, sorption control, and abiotic control experiments for 15 MPs with cationic-neutral spe

105 Control experiments further validate and rule out other

106 We demonstrate, through controlled experiments guided by simulations, how acoust

107 The control experiments have also demonstrated that the bioa

108 Mechanistic studies and control experiments have elucidated the role of these ad

109 Control experiments have unraveled the key intermediates

110 More than 500 controlled experiments have collectively suggested that

111 llutants in tissues of animals, few, if any, controlled experiments have examined whether ingested pl

112 Controlled experiments have shown that global changes de

113 Control experiments illustrate the need for the transann

114 edox-inactive diphenyl tetrazine ligand as a control experiment illustrates that the redox activity a

115 e of excess PPh3 yields OPPh3 in 173% yield; control experiments implicate 6, NO2(*), and free NO3(-)

116 (1)H NMR studies, coupled with control experiments, implied that catalytic chloride-bou

117 A control experiment in which participants observed choice

118 In a control experiment in which we used a standard size-weig

119 ring the preceding FeS inhibition period and control experiments in the absence of FeS.

120 Control experiments in the presence of competing boronic

121 In control experiments in which the surface was inoculated

122 Controlled experiment in a natural environment of parent

123 In a subsequent controlled experiment in flat-panel photobioreactors, Ch

124 cts of toe springs on foot biomechanics in a controlled experiment in which participants walked in sp

125 n coal was quantitatively determined through controlled experiments in a continuously fed drop-tube f

126 utilizing up to nine different filaments by controlled experiments in a test chamber.

127 oxidized organic compounds (OVOCs) requires controlled experiments in enclosures, but enclosures hav

128 standardised hand pollination treatments in controlled experiments in flight cages and in the field.

129 We tested this hypothesis in two randomized controlled experiments in online courses (n = 17,963).

130 A control experiment, in which outcomes but no cues were p

131 The results were supported by various control experiments including with electron-deficient ar

132 NMR, X-ray diffraction, and catalytic control experiments indicate that in this case an FI lig

133 Control experiments indicate that light promotes the rea

134 Control experiments indicated that earplugging did not d

135 In two control experiments, infants failed to learn the very sa

136 Here, we report controlled experiments injecting a fluid into a miscible

137 Many types of control experiments (internal, positive, negative, and f

138 Control experiments involving infusion of natural insuli

139 further evaluate its efficacy with real-time control experiments involving upper-limb amputees.

140 Remarkably, controlled experiments involving isolated atmospheric io

141 monia detection methods and the execution of control experiments is given as they are crucial to the

142 Control experiments isolate the individual dynamics, whi

143 al residual systematic bias through negative control experiments, lending credibility to our effect e

144 In a control experiment, looming bias disappeared when spectr

145 logenetic effects on species interactions in controlled experiments may depend on the lability of few

146 ction sustainability is explained with a few controlled experiments, mechanistic studies, and applica

147 In control experiments mimicking the systemic but not the c

148 In a control experiment (n = 20), we further explore the infl

149 In a randomized and sham-controlled experiment, neuronavigation-guided rTMS was a

150 As a control experiment, nifedipine, a L-type voltage sensiti

151 /CdS/Au heterostructures with the results of control experiments on CdSe/CdS nanorods exposed to gold

152 As shown in control experiments on in vitro alphaB- and gammaD-cryst

153 In this study, we performed a controlled experiment on 10 polydomous wood ant (Formica

154 (a) the time-dependent behavior observed in controlled experiments on humans, (b) the findings of a

155 In control experiments, only low-level, non-specific uptake

156 cations across the globe, including a 39-day controlled experiment over the Pacific Ocean.

157 In a behavioral control experiment, pain threshold-a proxy of endogenous

158 The control experiments performed by resonance elastic light

159 Through the control experiments performed by using some other nucleo

160 Control experiments performed with the reverse peptide (

161 elaborated on a mechanism proposal based on control experiments performed.

162 ed using finite element (FE) simulations and controlled experiments performed on phantoms with known

163 In control experiments, perfusion solution was supplemented

164 scopic analysis of gold pi-ACP complexes and control experiments point to the sp hybridization of the

165 Although lack of a controlled experiment presents numerous challenges, impl

166 Carefully designed control experiments provide a gold standard for benchmar

167 Through controlled experiments, quantified by a hydrodynamic mod

168 In part this is because a control experiment regarding the putatively critical rol

169 the FP-tagged proteins, making the design of control experiments relatively straightforward.

170 Control experiments reveal that among all common aryl el

171 Control experiments reveal that the cyclization, followe

172 Control experiments reveal that the size of the Ag domai

173 A control experiment revealed that identical TMS pulses at

174 ctivity of deuterium-labeled substrates, and control experiments revealed that nucleophilic attack to

175 exes at 30% RH by a factor of 10 relative to control experiments (RH < 1%, or no FeCl3 under humid co

176 stereochemical analysis together with these control experiments, rigorous multinuclear NMR analysis,

177 Control experiments rule out possible confounds related

178 Control experiments ruled out explanations based on poor

179 Control experiments ruled out that this inhibition is du

180 Control experiments, sans the BBD diazonium radical init

181 Control experiments serve to confirm that the response s

182 Results of a control experiment show that attention-induced suppressi

183 Control experiments show that such enhancement of ORR by

184 pecific and can reach deep brain structures; control experiments show that they cannot be explained b

185 Control experiments showed no labeling of TG2 knock-out

186 Control experiments showed that 1 is not cytotoxic in th

187 Control experiments showed that space-constrained coding

188 Control experiments showed that such deactivations in bo

189 Control experiments showed that the optimal combination

190 Control experiments showed the effect was specific to th

191 Psychophysical control experiments showed this result was not explained

192 of drug to the nearby VTA was falsified by a control experiment showing that bilateral infusions of b

193 effect of stimulation 1 hr postreactivation (control experiment), showing that memory strengthening i

194 atasets with the considerations of data from control experiment, signal to noise ratios, biological v

195 reaction have been demonstrated with several control experiments, spectroscopic analysis, and quantum

196 enrolled 98 in a randomized pretest-posttest controlled experiment starting August 15, 2010, that eva

197 (EPR) studies, isotopic labeling, and other control experiments suggest a radical-based mechanism.

198 Control experiments suggest that an older report of "MbO

199 Comparisons with control experiments suggest that the remarkable activity

200 Control experiments suggested that the CuCl alone does n

201 Humans have shown similar responses in controlled experiments, suggesting shared mechanisms acr

202 The control experiments support the proposed mechanistic pat

203 orescence quenching, cyclic voltammetry, and control experiments support the proposed radical-carbani

204 Several control experiments support the role of hemiaminal/imine

205 Different control experiments support the validity of the energy a

206 In this paper, we perform a controlled experiment, taking into account data backfill

207 We carefully replicate our results in a control experiment that furthermore show that the releva

208 guration has been established by a necessary control experiment that rules out the possibility of a d

209 ns of the food limitation hypothesis using a controlled experiment that provided supplementary insect

210 Here, we report controlled experiments that can induce either beading or

211 Here we show by isotope-controlled experiments that unsaturated C3,5,7,9-monocar

212 ologies similar to those obtained in ex situ control experiments the reaction rates are much higher,

213 In stress-controlled experiments, the system simply breaks when pu

214 nd real-time quantitative PCR along with key control experiments to quantify the methylation fraction

215 entation and labeling chemistries; selecting control experiments to unambiguously demonstrate FRET an

216 The authors report on the first controlled experiment to examine the memory-enhancing ef

217 ite the small sample size, this is the first controlled experiment to investigate pangolin foraging b

218 urce represents a new method which enables a controlled experiment to mimic the effects of sunlight u

219 Experiments were performed (a) in a controlled experiment to prove the concept and to confir

220 Our platform enables highly-controlled experiments to be performed which provide ins

221 Here, we used controlled experiments to identify physiological thresho

222 This study presents laboratory-controlled experiments to investigate the mechanisms gov

223 heir emergence, and expand the evidence from controlled experiments to real-world social networks.

224 cally investigating the products obtained in controlled experiments, to demonstrate the formation of

225 Control experiments used equimolar NaCl loads.

226 Control experiments using a mixture of two DNA molecules

227 Control experiments using an IgG protein revealed that o

228 unction of protein concentration, along with control experiments using carefully chosen protein analo

229 ptical properties, which was rationalized by control experiments using compounds bearing pyrenemethyl

230 LEMS experiments, the intensity ratios from control experiments using conventional ESI-MS deviated f

231 Control experiments using enantioenriched 3-hydroxy-2-ox

232 both cholesterol and beta2AR, as shown with control experiments using ergosterol and a control membr

233 Control experiments using maleic acid (cis-butenedioic a

234 and match both results in literature and in control experiments using microscale thermophoresis.

235 Control experiments using other therapeutic antibodies (

236 Control experiments using two 39E DNAzyme mutants reveal

237 's expectations of generosity in a series of controlled experiments using the dictator game.

238 Here, we perform a control experiment, using an aerosol time-of-flight mass

239 ts of five relevant double-blind, randomized controlled experiments, using a total of 4,556 undecided

240 Here we show through controlled experiments, using real and simulated observa

241 Control experiments validate our method's performance an

242 Control experiments verified that these evoked twitches

243 Quenching and control experiments verified that TMPD(*+) was formed fr

244 A control experiment was performed with a crystalline film

245 A controlled experiment was conducted from 2010 to 2014 to

246 Oxidation in controlled experiments was compared in standard double d

247 In combination with a series of control experiments we speculate that the SPO ligand dem

248 Based upon these observations and those from control experiments, we conclude that the blockage is pr

249 Through control experiments, we find that the catalyst's chemica

250 Based on control experiments, we hypothesize that binding to the

251 der diffraction measurements, and additional control experiments, we propose that these peak red shif

252 In a controlled experiment, we show that this effect is not d

253 Based on results from controlled experiments, we propose a possible reaction m

254 A number of control experiments were also conducted to verify whethe

255 Several control experiments were carried out to get insight into

256 A series of control experiments were carried out, which revealed tha

257 Control experiments were conducted by reacting Au144(SCH

258 Several control experiments were performed and provided strong e

259 Control experiments were performed in 9 animals.

260 Control experiments were performed to confirm the involv

261 Control experiments were performed to investigate the ca

262 Control experiments were performed with untreated plants

263 t the sorption coefficients derived from our control experiments were small and showed no notable pH-

264 Control experiments were systematically performed in cul

265 A series of designed and controlled experiments were also performed in order to s

266 A number of controlled experiments were conducted to postulate the r

267 mportant practical details of how to conduct controlled experiments when using them.

268 In contrast, a control experiment where participants practiced opposing

269 A control experiment where the methyl ester derivative of

270 We present data from a controlled experiment where the initial template concent

271 tio of protein LFQ intensities in sample and control experiments, where free AEBSA added to the contr

272 We thereby avoid the cost of running control experiments while simultaneously increasing the

273 erties by performing a resonant coherent THz control experiment with few 10 fs resolution.

274 The selectivity for S(8) formation in a control experiment with the conventional 1-bioreactor li

275 Storm evolution in the control experiment with wet antecedent soils most resemb

276 Control experiments with (18)O-labeled water and TEMPO p

277 external calibration procedures and regular control experiments with a sedimentation coefficient sta

278 Control experiments with absent magnetic exposure showed

279 Control experiments with AgNO3 indicated metallic Ag par

280 hese configurations was further confirmed by control experiments with asymmetrically designed buckmin

281 selectivity compared to that observed in the control experiments with direct current.

282 Control experiments with empty wild-type virus and a sal

283 Further control experiments with glucose microbiosensors did not

284 No response to analyte was detected in control experiments with nanoparticles imprinted with an

285 Control experiments with non-crosslinkable ligands, as w

286 Control experiments with preformed Rh(II)-Rh(III) comple

287 n of PSA in pH 7.4 1x PBS solutions, whereas control experiments with proteins that do not bind to th

288 Control experiments with stiffer, gel-phase 1,2-dipalmit

289 on constant, but no response was observed in control experiments with target analogues.

290 A double-blind, randomized, placebo-controlled experiment with eighth graders (total n = 536

291 by the technical difficulties in performing controlled experiments with currently available neuroima

292 etermined from carefully randomized and well-controlled experiments with explicitly stated outcomes a

293 Here we perform controlled experiments with increasing carrier proteome

294 the integration of real-time environmentally controlled experiments with wide-field low photo-toxic i

295 A third control experiment, with participants rating names, demo

296 les and current collector was confirmed in a control experiment without biofilm.

297 ing highly diluted labeled proteins and also control experiments without biospecific analytes.

298 15-20% additional phosphorylation sites than control experiments without FAIMS.

299 ned to be 3 orders of magnitude greater than control experiments without sonication at ambient temper

300 spective identifications, as compared to the control experiment (without FAIMS).