ライフサイエンスコーパス: by measuring

1 The risk of atherosclerosis was evaluated by measuring (1) presence of subclinical atherosclerosis

2 By measuring (1)H-(15)N dipolar-coupling as well as (15)

3 host response was evaluated on ICU admission by measuring 19 plasma biomarkers reflecting organ syste

4 ation of 500-800 nonredundant protein groups by measuring 20 ng, or <0.2% of the total protein conten

5 inhaled corticosteroids (ICSs) is often done by measuring 24-hour urine free cortisol (UFC) excretion

6 SI was assessed by measuring 29 cytokines and the redox state of circula

7 ics of enzyme-bound substrates and cofactors by measuring (31)P relaxation rates over a large magneti

8 ge pump injection, the detector is evaluated by measuring a few common chemicals in DI water at multi

9 emonstrate the sensitivity of this technique by measuring a homologous alcohol series across the 0.1-

10 By measuring a variable interfibrillar stiffness (EIF),

11 the acetate microbiosensor was demonstrated by measuring acetate concentration depth profiles within

12 anoeuvres increasing sympathetic outflow and by measuring activity-dependent slowing at 2 Hz stimulat

13 Here, by measuring aerosols in Sao Paulo, the authors find tha

14 obtained in humans (both males and females) by measuring afterimage durations over the entire range

15 is of natural variation in visual senescence by measuring age-dependent decline in phototaxis using D

16 Treatment outcome was assessed by measuring aided speech intelligibility in a time-reve

17 t can rapidly quantify PT/INR within seconds by measuring alterations in the viscoelastic properties

18 By measuring and comparing olfactory bulb outputs to inp

19 By measuring and integrating the current needed to trans

20 owth rates of cell populations were assessed by measuring areas of the same individual colonies versu

21 erimentally interrogate these two hypotheses by measuring arm kinematics while varying movement direc

22 Arterial inflammation was assessed by measuring arterial (18)F-FDG uptake and calculating t

23 Eight lean subjects were studied by measuring arteriovenous concentrations of metabolites

24 We validate this platform by measuring Bell inequality violations and performing q

25 trocytes during epileptogenesis, as assessed by measuring biochemical and histological markers.

26 nterpretation skill through medical training by measuring both diagnostic accuracy and eye movements

27 By measuring both frontostriatal white matter (WM) integ

28 By measuring both the elemental and biochemical composit

29 By measuring both the perturbation of the (95)Mo/(96)Mo

30 nglia during both acute and latent infection by measuring both viral and host transcriptomes on days

31 nitrite was evaluated on protein oxidation (by measuring carbonyl groups), protein nitrosation (by m

32 Apoptosis was determined by measuring Caspase-3 or by TUNEL assay.

33 The response to treatment was assessed by measuring cB-12 and neurophysiologic variables at bas

34 ne the immunological capacity of the ligand, by measuring cell proliferation, maturation markers and

35 city of LbL-assembled nanofilms was assessed by measuring cell viability.

36 s of PGPC-treated endothelial cells observed by measuring cellular elastic moduli using atomic force

37 ABL was calculated by measuring cemento-enamel junction and alveolar crest

38 Vascular reactivity was established by measuring changes in blood-oxygen-level-dependent (BO

39 V-Makona pathogenesis in cynomolgus macaques by measuring changes in immune cell frequencies, plasma

40 ies in 2014, producing long sequencing reads by measuring changes in ionic flow when single-stranded

41 Furthermore, by measuring changes of cytoplasmic calcium concentratio

42 th, with sub-millimetre transverse aperture, by measuring changes of the kinetic state of relativisti

43 gment compatibility was further investigated by measuring chimeric polymerase activity and growth of

44 , these BJT sensors are further investigated by measuring chloride levels in artificial human sweat f

45 Their activities were evaluated by measuring chlorophyll content of dark-grown transform

46 n porous silica has been explored previously by measuring chromatographic elution profiles, but such

47 Proteasomal degradation was quantified by measuring chymotrypsin-like activity of the 26S prote

48 o be gut motility, and tested this mechanism by measuring colonization in hosts with enteric nervous

49 ssing mechanisms are routinely characterized by measuring contrast response functions (CRFs).

50 ta and brachiocephalic artery was quantified by measuring contrast-to-noise ratios (CNRs) versus musc

51 e performance of this novel sensor is tested by measuring creatinine in real urine samples (N=50) and

52 The degree of crowding was determined by measuring crowding zone (the distance between a targe

53 esponse was assessed in a subset of subjects by measuring cytokine expression from monocytes cultured

54 confirmed the accuracy of subset enrichment by measuring cytokine production.

55 to mites at age 6 and 18 months was assessed by measuring Der p 1 weight/weight concentration in hous

56 ndent changes in diaphragm function in vivo, by measuring diaphragm movement amplitude.

57 Further, by measuring directly the reversibility of slow protocol

58 using relative k-tuple composition, followed by measuring dissimilarity between contigs using [Formul

59 etrieval of DNA adducts from archived tissue by measuring DNA adducts derived from four other classes

60 A higher specificity was achieved by measuring E2 without derivatization, compared to meth

61 et of metrics to directly compare strategies by measuring effectiveness of risk reduction as a functi

62 circuits underlie behavior is routinely done by measuring electrical activity from single neurons in

63 vement across the membrane-the gating charge-by measuring electrical capacitor properties of membrane

64 sensory epithelia and the spiral ganglion - by measuring electrophysiological properties and gene ex

65 Efficacy was assessed by measuring engraftment of gene-modified hematopoietic

66 lity for analysis of ENM in complex matrices by measuring ENM agglomeration and sedimentation in muni

67 By measuring entire classes of chemicals in archived bio

68 and proinflammatory responses were assessed by measuring expression of cell surface markers (adhesio

69 e metabolic responses to diets were assessed by measuring fasting serum concentrations of glucose, in

70 ified in the diaphragm and tibialis anterior by measuring fiber diameter.

71 s were analyzed for atrophy and regeneration by measuring fiber size and by performing immunostaining

72 Vascular status was assessed by measuring flow-mediated vasodilation (FMD), brachial

73 ergy transfer in vivo is primarily monitored by measuring fluorescence signals from the small fractio

74 We addressed this question by measuring fMRI responses in 11 subjects with amusia a

75 alamic glucose detection was studied in vivo by measuring food intake and insulin secretion in respon

76 es were studied with electron microscopy and by measuring force development of the sarcomeres.

77 Quadriceps fatigue was assessed by measuring force in response to femoral nerve stimulat

78 in development with diffusion tensor imaging by measuring fractional anisotropy and the apparent diff

79 namic monitoring of belatacept was performed by measuring free CD86 on monocytes.

80 life of anhydrous cow milk fat was evaluated by measuring Free Fatty Acids, peroxide value, Thiobarbi

81 The practical performance was determined by measuring FRET efficiency and photostability of tande

82 We addressed this hypothesis by measuring GABA, glutamate, glutamine, and the sum of

83 We characterized this interstitial space by measuring gap sizes, angles formed between adjacent c

84 This is done usually by measuring gene expression at different stages of the

85 variation across individuals and cell types by measuring gene expression levels, chromatin accessibi

86 By measuring genome-wide transcript and protein expressi

87 he activity of recombinant Gcd1 in vitro and by measuring gluconate levels in strains lacking enzymes

88 mphocyte activation test (LAT) was conducted by measuring granulysin and interferon-gamma to confirm

89 The LAT by measuring granulysin showed a sensitivity of 59.3% an

90 Abeta levels and (4) mitochondrial function by measuring H2O2, lipid peroxidation, cytochrome c oxid

91 hylmercury from fish consumption is assessed by measuring hair mercury concentration, whereas exposur

92 atitis C virus (HCV) infection is determined by measuring HCV RNA at specific time points throughout

93 y stimulus-evoked responses in behaving rats by measuring hemodynamic responses in the primary visual

94 R, used for quantification of this reservoir by measuring HIV DNA, requires external calibration; a c

95 ER stress was monitored by measuring HSPA5, CHOP and spliced XBP1 gene expressio

96 We validated our method by measuring HX of CBP, the intrinsically disordered nuc

97 Glucose has been quantified by measuring hydrogen peroxide (H2O2) reduction by chron

98 spliced XBP1 gene expression, and type I IFN by measuring IFNB1 (IFN-beta) and CXCL10 expression in h

99 acterized the aphid immune response to fungi by measuring immune cell concentration and gene expressi

100 Sensing was achieved by measuring impedance changes associated with cortisol

101 mPT onset was assessed by measuring in situ mitochondrial volume using the 'thi

102 nd MAPK-pathway dependencies were quantified by measuring in vitro cell growth responses to combinati

103 Here, we investigated this issue by measuring, in human subjects (three males), the suppr

104 By measuring internal concentrations of azoxystrobin and

105 Cellular response was determined by measuring intracellular ATP, extracellular metabolite

106 discrete free energies and define activation by measuring intrinsic affinities for ligand of each sta

107 By measuring its phase-resetting responses to temperatur

108 Autophagy activity was determined by measuring LC3 II and P62.

109 microscopic detection of autophagosomes and by measuring LC3B protein lipidation and autophagy-relat

110 processes that cause neurodegeneration in AD by measuring levels of metabolites and metals in brain r

111 Sucrose preference was tested by measuring liking ratings of 3 desserts of varying suc

112 elastography-which estimates liver fibrosis by measuring liver stiffness-and serum biomarkers of fib

113 By measuring longitudinal changes in individuals' body m

114 Here, we addressed this question by measuring low-intensity deviant responses from single

115 Here we address this issue by measuring magnetic susceptibility in the two most stu

116 itivity of these QCM-P devices was evaluated by measuring mass changes for both deposited gold film a

117 By measuring mate choice in F2 hybrid females, we allowe

118 approach has been conceptually demonstrated by measuring material-specific temperatures within a tur

119 episodic memory reveals the benefit afforded by measuring memory on a continuous scale, allowing func

120 ticks and B. mayonii-infected nymphal ticks by measuring metabolism every 24 hours over the course o

121 s to better understand the source of methane by measuring methane plumes at 1- to 3-m spatial resolut

122 nsation assay and on mitochondrial viability by measuring mitochondrial potential and size.

123 hanges in biological systems can be captured by measuring molecular expression from different levels

124 ergot alkaloids to virulence of N. fumigata by measuring mortality in the model insect Galleria mell

125 tudied mitochondrial and synaptic activities by measuring mRNA and the protein levels of mitochondria

126 e possibility of predicting the risk for AMR by measuring mRNA transcripts of AMR-associated genes in

127 , and the value of the ETC as a drug target, by measuring Mtb's respiration using extracellular flux

128 PK/pharmacodynamic (PD) model was developed by measuring mucosal tissue concentrations of tenofovir,

129 By measuring N-methyl-d-aspartic acid receptor (NMDAR)-d

130 an inorganic perovskite (IP) single crystal by measuring nanoindentation creep and stress relaxation

131 neuron's activity is typically accomplished by measuring neural responses to repeated presentations

132 substitutions conferred a fitness advantage by measuring neutralizing antibody titer against reporte

133 uring carbonyl groups), protein nitrosation (by measuring nitrosamines), and proteolysis.

134 Beta cell proliferation was assessed by measuring nucleotide analog 5-ethynyl-2'-deoxyuridine

135 By measuring of fluorescence resonance energy transfer (

136 Consolidation was assessed by measuring performance on the same task 24 h later.

137 HIV-1 transcription was quantified by measuring plasma HIV-1 RNA during MGN1703 administrat

138 This method was applied in Hong Kong by measuring PM2.5 and CO concentrations along a route c

139 e effectiveness of this compensation process by measuring postural behaviour in adult survivors of ch

140 ent activation energy (Ea ), were determined by measuring potential rates of denitrification and anam

141 e through side-channel attacks (for example, by measuring power consumption, timing or electromagneti

142 r EW_dmGWAS and standard gene-based analysis by measuring precision and recall of each method on sepa

143 We assessed inflammatory (im)balance by measuring pro-inflammatory interleukin-6 and anti-inf

144 We have confirmed some of the mRNA data by measuring protein, and significant down-regulation of

145 havioral differences on an ocean-basin scale by measuring puffins' among-colony differences in migrat

146 Assessment of aortic stiffness was evaluated by measuring pulse wave velocity, aortic strain, and dis

147 PNPO activity was quantified by measuring pyridoxal 5'-phosphate (PLP) concentrations

148 ose an elegant approach to detect symmetries by measuring quantum currents.

149 tion for membrane-bound peptides or proteins by measuring RDCs using magic-angle spinning (MAS) in co

150 mulus that engages the reticulospinal tract, by measuring reaction times from electromyographic activ

151 train of Microcystis aeruginosa were studied by measuring reactive oxygen species (ROS) generation an

152 inations was performed within less than 2min by measuring real-time evolution of both correlation and

153 ng in sensory systems is typically addressed by measuring receptive fields in a fixed, sensor-based c

154 strains during human infection were assessed by measuring release of interleukin 8 from AGS cells (to

155 of phthalates on placental function in vitro by measuring relevant candidate genes and proteins.

156 By measuring responses of MSTd neurons in two male rhesu

157 ly the necessity of TPs for the anion effect by measuring responses to NaCl and Na-gluconate (small a

158 mechanisms underlying increased relatedness by measuring root aerenchyma volume (RAV), a trait which

159 nosing pertussis; the diagnosis is confirmed by measuring serum anti-pertussis toxin (anti-PT) or ant

160 , and, second, tumor growth can be estimated by measuring serum prostate-specific antigen (PSA, a PCa

161 By measuring slow activation and deactivation at steady

162 d tillage management effects were quantified by measuring soil nitrous oxide (N2 O) and methane (CH4

163 Here we investigated the origin of tuning by measuring sound-induced 2-D vibrations within the mou

164 harge plasma in our system was characterized by measuring spatially resolved gas temperatures (378-14

165 ry, we demonstrate this multiplexed approach by measuring specific affinity of two well-characterized

166 The single mismatch was detected by measuring strand displacement-induced resistance (and

167 In this study, by measuring subnanometer vibrations directly from the r

168 riations in ion transport in polymer devices by measuring subnanometre volumetric expansion due to io

169 We further complement our transport assays by measuring substrate binding to detergent-purified SbM

170 with CMV pp65 or IE-1 peptide pools and then by measuring T-cell expression of CD107a, IFN-gamma, tum

171 nsions of CMV-specific T cells were detected by measuring T-cell surface levels of 4-1BB (CD137), bin

172 By measuring telomerase activity at the single-cell leve

173 xposure to natural, depleted, and enriched U by measuring the (235)U/(238)U, (234)U/(238)U, and (236)

174 The equation was validated by measuring the 4 parameters by echocardiography in 100

175 r benchmark networks and compare the results by measuring the ability of each index to characterize n

176 ue added for improving clinical CAD practice by measuring the absolute level of rest and maximal myoc

177 This model was evaluated by measuring the absorbance and fluorescence response of

178 aughter product in the material was followed by measuring the accumulated (230)Th daughter product re

179 It can be assessed by measuring the acetazolamide-induced change in regiona

180 taphylococcus aureus detection was developed by measuring the activity of secreted nuclease from the

181 e examined passive GM electrotonic structure by measuring the amplitudes and apparent reversal potent

182 By measuring the angular distribution of dissociation fr

183 Performance was assessed by measuring the area under the receiver operating chara

184 gen consumption with (11)C-acetate (PET) and by measuring the arterial input function using (99m)TcO4

185 al intervals between consecutive trials, and by measuring the behavioral impact and ERP responses fro

186 A T cell mounts an immune response by measuring the binding strength of its T cell receptor

187 By measuring the biochemical affinity of target enhancer

188 By measuring the biodistribution of 30 nanoparticles to

189 Here, we directly test five major models by measuring the biophysical properties of fluorescently

190 By measuring the brain's electromagnetic activity, we sh

191 We have demonstrated the use of CalQuo (2) by measuring the calcium response in genetically modifie

192 oxidant activity of the films was determined by measuring the capacity to scavenge 2,2 diphenyl-1-pic

193 ls having pore diameters from 300 to 1000 nm by measuring the capillary-driven liquid rise.

194 The PSMA is detected and quantified by measuring the change in differential pulse voltammetr

195 la typhimurium cells, and detection was done by measuring the change in impedimetric response of deve

196 We analysed this complex physiological trait by measuring the changes in primary metabolism that occu

197 By measuring the chemical forces above the different spe

198 In this study, we resolve the discrepancy by measuring the chromophore exchange rate of the bound

199 Here, by measuring the closed- and open-state reactivity of MT

200 The oligonucleotide targets were detected by measuring the color change of AgNPs, giving detection

201 characterize a patient's level of hemolysis by measuring the color of blood plasma.

202 modulation of TFEB expression in HeLa cells by measuring the cytosolic Ca(2+) response after capacit

203 method that estimates evolutionary distances by measuring the decay of exact substring matches as a f

204 estimated the extent of caveolar deformation by measuring the density of caveolin-1 projected onto a

205 ed the mechanism of strand photodissociation by measuring the dependence of its rate on light intensi

206 appropriateness for a home-monitoring device by measuring the device's retest variability at 2 months

207 odified with hexadecyl groups (C16) followed by measuring the diffuse reflectance spectra on the surf

208 nt systems were straightforwardly determined by measuring the diffusion coefficient of an appropriate

209 By measuring the dimensions of a collection of labeled a

210 hin a large network of European laboratories by measuring the elastic properties of gels and living c

211 Extracellular volume quantifies MF by measuring the extracellular compartment depicted by t

212 hilst keeping the physical stimulus constant by measuring the eye movement behaviour of a single grou

213 ox state in the auditory cortex was assessed by measuring the FAD+/NADH ratio using fluorescence imag

214 deduced the behaviour of fossil vertebrates by measuring the floccular fossae (FF).

215 s allows the target molecules to be detected by measuring the fluorescence intensity of each droplet.

216 ion of serum proteins, are directly examined by measuring the forces arising as an Atomic Force Micro

217 e we quantify the total CO2 input rate, both by measuring the global length of subduction zones in pl

218 We confirmed these predictions by measuring the growth dynamics of Escherichia coli uti

219 ntial for O2 reduction to H2O2 was estimated by measuring the H(+)/H2 open-circuit potential under th

220 We tested the efficiency of our method by measuring the HX-MS signal intensities of myoglobin p

221 e in second iron-sulfur cluster coordination by measuring the in vitro production of CO, CN(-), and (

222 ctivity was demonstrated in rodent PD models by measuring the induction of FXR target genes in variou

223 tribution of the atomic gases in the lattice by measuring the inelastic loss of doublons.

224 This hypothesis has been tested previously by measuring the information transfer between brain area

225 real-time heptane detection is accomplished by measuring the intensity attenuation at lambda = 3.0-3

226 have been isolated using laser tweezers and, by measuring the intensity modulation of elastic back-sc

227 etection of clenbuterol in milk was achieved by measuring the intensity of colour change that was pro

228 al and fractional iron absorption), assessed by measuring the isotopic label abundance in erythrocyte

229 on NLRP3 inflammasome activity was evaluated by measuring the level of interleukin-1beta and -18 in t

230 n trimming and curing, trimming was followed by measuring the loss of GFP-labeled Sup35 foci from bot

231 ions, in a sensitive and quantitative manner by measuring the luminescence output in a discontinuous

232 We test this hypothesis by measuring the mental search strategy in rats through

233 Our approach was verified by measuring the moduli of polyacrylamide gels of known

234 g in vitro GID was evaluated by SDS-PAGE and by measuring the nitrogen content of ultrafiltration (3k

235 changes in use for vitreoretinal procedures by measuring the number of allowed services using data f

236 By measuring the number of makeable designs as we acquir

237 e particles via an adhesion mechanism, i.e., by measuring the number of particles that adhered to the

238 probes the mechanical properties of material by measuring the optical frequency shift induced by phot

239 By measuring the overall atomic loss from colliding clou

240 This blockage was quantified by measuring the oxidation current of the electroactive

241 s amperometric determination of both species by measuring the oxidation current of the mediator in ea

242 By measuring the particle size and the particle number d

243 Lipid oxidation was tracked by measuring the peroxide value, acidity, conjugated die

244 We validate the theory by measuring the pH response of an extended gate ISFET p

245 We demonstrate the method by measuring the polarisation state of the electromagnet

246 By measuring the polarized emission of individual quantu

247 dard of truth (i.e., diagnosis at follow-up) by measuring the positive percentage of agreement (equiv

248 ting experiments quantify the ion atmosphere by measuring the preferential ion interaction coefficien

249 to Phl p 12 in profilin-sensitized patients, by measuring the prevalence, strength and cross-reactivi

250 We tested this a priori hypothesis by measuring the proximity-dependent modulation of the h

251 We investigate the band structures by measuring the quasimomentum of the Bose-Einstein cond

252 tructure of murine CD4 T cell memory subsets by measuring the rates of influx of new cells and using

253 n hybrid perovskite with its single crystals by measuring the ratio of the re-emitted photons to the

254 A calibration curve was created by measuring the reaction rate of various samples with d

255 al grouping of two-dimensional image-regions by measuring the reaction times of human participants an

256 he STAT1 transcription factor was determined by measuring the relative affinity to hundreds of varian

257 By measuring the response of the circadian rhythm to dar

258 Opioid tolerance was assessed by measuring the response to a challenge dose of morphin

259 e is used to determine the bounded BPA level by measuring the sample/electrode interfacial capacitanc

260 ar to the substrate surface, were determined by measuring the Seebeck coefficient, electrical conduct

261 tion levels can be quantitatively determined by measuring the signal amplification during FRET.

262 systematically investigated time-domain MRX by measuring the signal dependence on the applied field,

263 demonstrate the application of the technique by measuring the silicate and borate depth profiles in t

264 istance complements computed partial charges by measuring the size of orbital lobes that best overlap

265 Blockade Ab relative avidity was evaluated by measuring the slope of blockade Ab neutralization cur

266 By measuring the spin waves over the full Brillouin zone

267 The power of this assay is demonstrated by measuring the state of hyperphosphorylation from tau

268 We validated our system and analysis by measuring the stiffness of cross-linked dextran micro

269 ell-suppressive function was also quantified by measuring the suppression of autologous effector T-ce

270 We validated the method by measuring the surface tension of water in oil microdr

271 Objective imaging parameters were assessed by measuring the SUV and coefficient of variation in dif

272 The evolution of this process was assessed by measuring the time (t) dependence of the particle ana

273 We tested this prediction by measuring the time course of EPSCs in ON-type SBACs i

274 By measuring the time evolution of surface reflectivity

275 By measuring the tissue pH and comparing with the values

276 with diffuse intrinsic pontine glioma (DIPG) by measuring the tumor uptake of (89)Zr-labeled bevacizu

277 eptive fields in mouse primary visual cortex by measuring the tuning of pyramidal neurons in the join

278 oped preparation and imaging techniques, and by measuring the turgor pressures in the leaves of a tal

279 noparticle delivery to multiple target cells by measuring the uptake of biotinylated nanoparticles by

280 ation in stored grain samples was determined by measuring the uric acid content of their aqueous extr

281 cilia motion can experimentally be assessed by measuring the velocity of micro-beads traveling throu

282 Validation of the technique is carried out by measuring the xylem vulnerability of 13 conifers and

283 idal stability of these NPs was investigated by measuring their aggregation kinetics in different aqu

284 erial viruses were experimentally determined by measuring their flux across large pore membranes and

285 ed intra-individual variability of microRNAs by measuring their levels in the CSF from healthy indivi

286 de extract and its fractions were determined by measuring their protein precipitating capacity (PPC)

287 in a small multiplicative error in few steps by measuring their rates of encounter with other agents.

288 ding pockets on protein surfaces are grouped by measuring their structural similarities.

289 with two metals, Al and Cu, was investigated by measuring thermal conductance using the time-domain t

290 utility of this polyprotein was demonstrated by measuring three diverse target proteins: an alpha-hel

291 abrogated LPS-induced tolerance, as defined by measuring TNF-alpha levels in the culture supernatant

292 By measuring transcriptional output in embryonic stem ce

293 perties of in vitro BRB models were assessed by measuring transendothelial electrical resistance, per

294 ransporters reconstituted in proteoliposomes by measuring transporter equilibrium potentials.

295 fectively activated both receptors, assessed by measuring two different cell signalling pathways whic

296 frequency accuracy of the system is verified by measuring two metamaterial samples and a lactose film

297 Sodium intake, which is usually assessed by measuring urinary sodium excretion, has been inconsis

298 including defining a novel type of phenotype by measuring variability as a specific parameter.

299 ision was studied in unexperienced observers by measuring visual evoked potentials from 64-channels.

300 al diagnostic applications were demonstrated by measuring Zika antigen in a simulated human serum.