ライフサイエンスコーパス: by measuring

1 prove deep-water is retained by the seamount by measuring 2.4x higher bacterial concentrations in the

2 The instrumental accuracy was assessed by measuring a series of methane gases with a range of d

3 By measuring a time series of interfacial positions and

4 t up to a concentration of 1 muM (determined by measuring A7r5 cell line D-myo-inositol-1-phosphate a

5 he VOC sensing performance was characterized by measuring acetone and ethanol vapors at their charact

6 Here, by measuring activation of the MAPK pathway downstream o

7 valuation of synthetic zeolites (Zeolite1-6) by measuring AEC and resistance to attrition and compres

8 e mouse models and assessed for renal injury by measuring albuminuria and examining kidney histology.

9 sign function to noncoding genetic variants, by measuring allelic effects on gene expression in the c

10 to Al(OH)(3) was tested in two mouse models by measuring allergic manifestations upon peanut challen

11 analysed by Near Infrared Spectroscopy, and by measuring alveographic parameters.

12 ty of periodontal destruction was determined by measuring alveolar bone loss under a stereomicroscope

13 sessed using a murine model of periodontitis by measuring alveolar bone resorption and gingival IL-17

14 e, we confirm the formation of the Au-C bond by measuring an analogous series of molecules prepared e

15 By measuring and analyzing the scattering mean free path

16 ection from immune-enhanced disease, whether by measuring antibodies, T cells or intrinsic host respo

17 e demonstrate the broad utility of the assay by measuring antibody functionality of sera from small a

18 tools to investigate influenza antigenicity by measuring antibody-antigen binding are an active area

19 By measuring any controlled-release pellets, particles,

20 derived from induced pluripotent stem cells-by measuring apolipoprotein B production and secretion,

21 intervention effects on parasite infections by measuring Ascaris lumbricoides, Trichuris trichiura,

22 We demonstrate device utility by measuring ATP release from flowing red blood cells us

23 acterized the EEG phenotypes of Fmr1-KO rats by measuring basal EEG power and auditory steady state r

24 macina helicina to ocean temperatures and pH by measuring biomarkers of oxidative stress, antioxidant

25 Colitis intensity was investigated by measuring body weight changes, stool consistency/blee

26 ing of local redox processes on a 6 mum spot by measuring both differential reflectivity (SEED-R) and

27 By measuring both glycolytic and mitochondrial activity

28 By measuring both OCl(-) and pH voltammetrically, over t

29 We first characterise the sound fields by measuring both phase and amplitude maps, and then sho

30 t probe, and SR calcium content was assessed by measuring caffeine-stimulated release.

31 Coronary calcification was quantified by measuring calcium score, mass, and volume.

32 This prediction was experimentally verified by measuring cAMP levels in cells under different condit

33 itative analysis of cooperative interactions by measuring Cbf1p binding at synthetic promoters with m

34 ls was analyzed in CRS without NP and CRSwNP by measuring cell and activation markers via immunohisto

35 ndard-of-care chemotherapeutics was assessed by measuring cell viability after drug exposure.

36 immortalized gingival keratinocytes (TIGKs) by measuring cell viability, cell lysis and apoptosis.

37 speech-in-noise deficits are better assessed by measuring central (grouping) processes alongside audi

38 ntrols and J20-hAPP mice at 6 months of age, by measuring cerebral haemodynamics and neural activity

39 ach is sensitive to biological perturbations by measuring changes in DNA synthesis after limb denerva

40 s influenced by facial and vocal information by measuring changes in oxygenated hemoglobin (HbO) usin

41 By measuring changes in RNA structure following eIF4A in

42 ored the reactogenicity of 4CMenB components by measuring changes in temperature, cytokines, and gene

43 Ultrasound assessment of FMD was performed by measuring changes in the diameter of the brachial art

44 ally characterize the quality of the profile by measuring changes in the signal with respect to ampli

45 By measuring changes in torque upon unwinding of the dou

46 We demonstrate the utility of this approach by measuring chromatin accessibility across 136,463 rest

47 By measuring chromosome doubling force (the force requir

48 ften infer hepatic de novo lipogenesis (DNL) by measuring circulating fatty acid (FA) markers; howeve

49 ent, islet function can be monitored in vivo by measuring circulating glucose and human insulin; howe

50 etry (DOF) assesses deep tissue RBC dynamics by measuring coherent fluctuations of multiply scattered

51 se wine during fermentation was investigated by measuring color, polyphenol content and thiol aromas.

52 ate the intracranial effects of microgravity by measuring combined changes in intracranial volumetric

53 raditionally, biomagnification is quantified by measuring contaminant concentrations in animal tissue

54 Tissue properties can be evaluated by measuring contractile function, responsiveness to ele

55 e and demonstrate equivalent CPL measurement by measuring CPL spectra of two reference europium(III)

56 Immunological tolerance was studied by measuring Cyp c 1-specific antibodies and cellular re

57 protein changes with immunoblotting and t-SP by measuring dendritic spine morphology and alpha-amino-

58 cerebellar slices and assessed Cb1R activity by measuring depolarization-induced suppression of excit

59 which we call the "partial masking factor," by measuring detection thresholds in backgrounds of cont

60 e we confirm the mantle source of this water by measuring deuterium-to-hydrogen ratios in these melt

61 ll micro- and nano-morphology of live tissue by measuring differences in the sub-micron spatial mass

62 ctoparasite, Varroa destructor, was examined by measuring differentially expressed genes (DEGs) in br

63 defined by Welfare Loss (WL) was calculated by measuring disability-adjusted-life-years lost to brea

64 We assessed performance by measuring discrimination, calibration, and net benefi

65 By measuring DNA mobility in living cells, we show that

66 d for delivery of 400 IU/mL insulin solution by measuring droplet size distribution, plume geometry,

67 Monitoring the change of bacterial viability by measuring electrochemical Faradaic current is a promi

68 -induced damage in wild-type and sfr8 plants by measuring electrolyte leakage from freeze-thawed leaf

69 titative, and high-throughput phenotypic AST by measuring electrons transferred from the interiors of

70 nsequences of observed mutations were tested by measuring enzyme activity and by cell and animal mode

71 e of the SiPM as a highly sensitive detector by measuring enzyme activity in single cells.

72 Morphometric analysis was performed by measuring epithelial height in proportion to thicknes

73 he generality of this method is demonstrated by measuring exciton transport for both luminescent and

74 unctional inhibition of miR-145 was assessed by measuring expression of the target genes ITGbeta8 (in

75 e to identify extracellular matrix expansion by measuring extracellular volume fraction (ECV).

76 f white matter alterations could be achieved by measuring fiber density (FD) - a novel non-tensor-der

77 We quantified the enhancement by measuring fight patterns characteristic of female and

78 The aptasensor performance was validated by measuring fish samples spiked with known concentratio

79 he process of recording bulk neural activity by measuring fluorescence changes in activity sensitive

80 nctional impact of these genetic alterations by measuring gemcitabine metabolites, reactive oxygen sp

81 This new system was tested by measuring glucose-stimulated insulin secretion from s

82 in vitro by AnnexinV-FITC/7-AAD staining and by measuring GM-CSF-induced mediator release in culture

83 Candidate genes were identified by measuring growth as a readout of reporter activity.

84 We meet this goal by measuring H/D and (12) C/(13) C kinetic isotope effec

85 gnitive resources on audiovisual integration by measuring high-density electroencephalography (EEG) i

86 HIV-1 reservoirs were determined by measuring HIV-1 DNA in peripheral blood mononuclear c

87 By measuring hydration status during hibernation, we sho

88 ionary mechanisms underlying these responses by measuring indirect genetic effects (IGEs) that occur

89 By measuring individual differences in temporal discount

90 bly transfected with the human P2X1 receptor by measuring inhibition of the ATP-induced calcium influ

91 ore the potential benefits of this probiotic by measuring inhibition of the periodontal pathogens Por

92 By measuring interictal spikes in patients with a range

93 to increased cereal fiber intake was tested by measuring intestinal serotonin of mice fed for 9 wk o

94 ate the biological application of an MC3-ISM by measuring intracellular a(Cl), and the response to an

95 1A receptor compared to the wild type allele by measuring its ligand binding affinity, CCL2 scavengin

96 oprene exposure in the general US population by measuring its urinary metabolite, N-acetyl-S-(4-hydro

97 The infection was monitored by measuring joint swelling, Borrelia culture, polymeras

98 By measuring key metabolites and environmental pH, we de

99 The platform sensitivity was determined by measuring known concentrations of hsa-miR-21-5p spike

100 (ERT) in Fabry disease is typically assessed by measuring left ventricular mass index using echocardi

101 We observe this phenomenon by measuring lifetimes spanning four orders of magnitude

102 ferentiate cancerous and non-cancerous cells by measuring lipid and protein peak intensity within the

103 Liver fibrosis was estimated by measuring liver stiffness using transient elastograph

104 Microvascular dysfunction was quantified by measuring maximum arteriolar (aMax) and venular dilat

105 y and semiquantitatively in diseased vessels by measuring maximum tissue-to-background ratio.

106 is a partial V2 receptor agonist (determined by measuring MDCK cell line cAMP accumulation), producin

107 al dysfunction from HMW-Abeta(1-42) exposure by measuring membrane integrity, reactive oxygen species

108 Here, by measuring membrane potential dynamics of Bacillus sub

109 By measuring membrane tension during early differentiati

110 We also assessed maternal mercury exposure by measuring mercury concentrations in both blood and eg

111 nced autophagy in renal tubules, as assessed by measuring microtubule-associated protein 1A/1B-light

112 of exclusively breastfed Indonesian infants by measuring milk volume and micronutrient concentration

113 Here, we analyzed ASD primary fibroblasts by measuring mitochondrial bioenergetics, ultrastructura

114 ors or vehicle on mPTP opening were assessed by measuring mitochondrial swelling and calcium retentio

115 By measuring muscle growth over 12-h periods in live pre

116 tained with the proposed method was verified by measuring NIST SRM 3149 standard over different days

117 In conclusion, by measuring noninvasive cardio-respiratory parameters,

118 By measuring nuclear bomb test-derived 14C in genomic DN

119 rotection in Cuba and the Florida Keys, USA, by measuring nutrient concentrations, microbial abundanc

120 metabolic stress, and mitochondrial function by measuring O(2) consumption rates (OCR) and the membra

121 By measuring odorant-dependent sniffing, we gain a sensi

122 Here, we do just that by measuring OPA responses to first-person perspective m

123 Mitochondrial function was assessed by measuring oxygen consumption rates in permeabilized m

124 s study, we characterize the R(ee) landscape by measuring P(R(ee)) for low molecular weight (MW: 0.22

125 the toads' acoustic responses were analyzed by measuring parameters important for reproductive succe

126 effects of host age on C. cunea mass rearing by measuring parasitism, development and adult fertility

127 kpoint inhibition in cancer can be predicted by measuring PDL1 expression of tumor cells.

128 man spectroscopy for use in PAT applications by measuring pharmaceutical blends of varying active ing

129 nonhydrolizable P) fractions were quantified by measuring phosphate, phosphate after phosphatase addi

130 Both methods have been validated by measuring pK(a) values of compounds, for which values

131 irus (HIV) infection and is usually assessed by measuring plasma levels of bacterial lipopolysacchari

132 latelets and leukocytes in mice and men, and by measuring plasma serotonin levels and leukocyte activ

133 ypothesis of functional compartmentalization by measuring pressures in a beetle and recording abdomin

134 Oxidative stress was analyzed by measuring protein thiol oxidation and antioxidant mRN

135 nstruct the evolving microenvironment of CAC by measuring proteomic changes and extracellular matrix

136 By measuring pupillary dilatation in response to these s

137 chanism for plasticity in craniofacial shape by measuring rates of bone deposition within functionall

138 ic shock patients, to study immune responses by measuring rates of cytokine secretion from single T c

139 minutes without phosphodiesterase inhibitors by measuring real-time cAMP dynamics using the cAMP diff

140 le and position changes in one-shot learning by measuring recognition accuracy of Korean letters pres

141 method to quantify anthocyanin color change by measuring red chromatic shift by digital analysis.

142 binding and downstream signaling, monitored by measuring reduction in cellular cAMP levels.

143 ience during the interruptions was monitored by measuring refraction while marmosets were seated at t

144 del for physiological research was validated by measuring release, metabolism and transport of purine

145 By measuring respiratory and inert gas levels in the pro

146 We do this by measuring responses to standardised hand pollination

147 on the determination of the retention factor by measuring separation efficiency of individual protein

148 Immunogenicity was assessed by measuring serotype-specific opsonophagocytic activity

149 of PCV13 followed by PPSV23 in IBD patients by measuring serotype-specific pneumococcal immunoglobul

150 Sensitization was identified by measuring sIgE levels.

151 rbon dot-facilitated delivery were validated by measuring significant reductions in the target gene t

152 ivo optical vibrometry we tested this theory by measuring sound-evoked motility in the 13-25 kHz regi

153 these connections has also been demonstrated by measuring spike transmission probabilities in pyramid

154 of biological magnetoreception to be tested by measuring spin decoherence directly in the time domai

155 on and its control can be tracked indirectly by measuring stable RNAs, it is only by directly measuri

156 characterize this variability in importance by measuring sub-regional intolerance, i.e., the depleti

157 We tested this hypothesis by measuring substantial macroscopic CDI, in physiologic

158 ived Ags, which can be quantified indirectly by measuring surface expression levels of CD5.

159 myocardial function, which is not indicated by measuring systolic functional parameters using with a

160 By measuring TFP dynamics, we found that the retraction

161 The approach is evaluated by measuring the (13)C polarization of ethyl acetate-1-(

162 hat the Bragg peak position can be estimated by measuring the acoustic wave amplitudes from the marke

163 change-gel OECT to record biological signals by measuring the action potentials of a Venus flytrap is

164 of active microneedles is evaluated in vitro by measuring the amount of IgG antibody (as a model drug

165 he identification of bioactive intermediates by measuring the antibiotic activity and acute toxicity,

166 By measuring the antinociceptive and respiratory depress

167 hase 2 clinical trial dataset (MLN02, n=146) by measuring the area under the curve of the receiver op

168 c fluid flow in graphene at room temperature by measuring the associated stray magnetic field.

169 Furthermore, by measuring the association of PTEN with MAGI proteins

170 ated with histone modifications in real-time by measuring the balance between histone-modifying enzym

171 g simulated data, and benchmark the pipeline by measuring the binding properties of the well-studied,

172 g autosomal ancient DNA (aDNA) contamination by measuring the breakdown of linkage disequilibrium in

173 anges in areas near to the skin-like sensors by measuring the capacitances between the array of elect

174 reductant, and energy provision was assessed by measuring the carbon flow through the metabolic netwo

175 dical examinations (2007-2009 and 2012-2013) by measuring the carotid-femoral pulse wave velocity (cf

176 MSO and K(2)CrO(4) was dynamically monitored by measuring the cell detachment rate during more than 3

177 of LPS molecules was monitored in real-time by measuring the change in refractive index (RI) in the

178 of A. minutum cells present in water samples by measuring the charge-transfer resistance changes of t

179 structure of the MA lattice was interrogated by measuring the cleavage of the murine leukemia virus (

180 By measuring the codon frequencies at the ribosome activ

181 The products are detected in situ by measuring the conductance and molecular junction elon

182 s, and functional information can be deduced by measuring the coronary flow reserve.

183 We do so by measuring the correlated diffusion of extracellularly

184 The HTI is experimentally characterized by measuring the critical behaviors of the wave function

185 By measuring the current at the end of each potential st

186 CAV progression was assessed by measuring the Delta change in plaque volume (PV) and

187 charge and magnetic properties of the system by measuring the dependence of its optical response on a

188 estigate peptide-lipid membrane interactions by measuring the detachment (last-rupture) force distrib

189 , the performance of the HSIFC was confirmed by measuring the different CSRs for the different types

190 By measuring the diffusion of 400 nm streptavidin-coated

191 ly detect the ionic strength of the solution by measuring the diffusion width of the ions and the pH

192 ow-affinity (nonspecific background) binding by measuring the duration of individual binding events a

193 ave killing" temporal pattern, was validated by measuring the dynamics of p53 accumulation, cell fate

194 Biologic confounders were minimized by measuring the ECV fraction and excluding patients wit

195 the effect of satiety gut hormone modulation by measuring the effect of the somatostatin analog octre

196 variant data on a major clinical MBL, VIM-2, by measuring the effect of thousands of VIM-2 mutants on

197 ess the rheological properties of the system by measuring the effective shear viscosity, finding that

198 n the budding yeast Saccharomyces cerevisiae by measuring the effects of thousands of point mutations

199 f imprinted peptide templates were optimized by measuring the electrochemical responses to target pep

200 ied to detect carcinoembryonic antigen (CEA) by measuring the end-product of immunoassay performed on

201 We tested this hypothesis by measuring the excretion rates of nitrogen and phospho

202 lar amino acid uptake and protein synthesis, by measuring the expression and phosphorylation of AKT,

203 duced proinflammatory response was evaluated by measuring the expression levels of key cytokines and/

204 dicting evofosfamide sensitivity in patients by measuring the expression of canonical bioreductive en

205 ormance in soils cannot be directly assessed by measuring the expression of functional genes.

206 inflammation was assessed histologically and by measuring the expression of inflammatory markers in t

207 re and after the development of compulsivity by measuring the extent to which bilateral aDLS infusion

208 savoy cabbage, curly kale and green pepper, by measuring the ferritin response in a simulated digest

209 ogen preparations were thoroughly determined by measuring the fibrin-stabilizing factor; fibronectin;

210 ion of the oxidized linseed oil was assessed by measuring the flow properties of the exposed oil usin

211 The reaction was monitored by measuring the fluorescence intensity at lambda(660nm)

212 This theory is validated by measuring the force dependence of protein L unfolding

213 By measuring the force necessary to flatten curls, we ca

214 We addressed this question by measuring the free energy change for a number of back

215 By measuring the frequency shift induced by the change i

216 We do so by measuring the genetic basis of cryptic colouration an

217 sion length is obtained in the various HOIPs by measuring the giant magnetoresistance (GMR) response

218 By measuring the half-lives of two PARP1-mRNA targets we

219 Cardiotoxicity was also assessed by measuring the heart rate, stroke volume, and cardiac

220 Here, we overcome this problem by measuring the heterogeneity of synthetic analogues of

221 de novo synthesis in peripheral blood cells by measuring the incorporation of stable isotope-labeled

222 Cost-effectiveness was determined by measuring the incremental cost-effectiveness ratio (I

223 By measuring the inelastic scattering of light, Raman sp

224 tection with <5 s response time was achieved by measuring the intensity attenuation of the waveguide

225 By measuring the intensity dependence of the external op

226 cancer cells was observed for the compounds by measuring the intracellular accumulation of gold usin

227 metabolic crosstalk were extensively studied by measuring the kinetics of bacterial growth, cell morp

228 ol that quantifies in vivo muscle energetics by measuring the kinetics of PCr recovery after exertion

229 By measuring the kinetics of spread at early time points

230 nical strain at wearing sites to lung volume by measuring the local circumference changes of the ches

231 -lived metastable electronic state in an HCI by measuring the mass difference between the ground and

232 In principle, AIF might be obtained by measuring the molar activity (A(m); ratio of radioact

233 By measuring the multiscale distribution of the antibody

234 e ferromagnetic nanolayer which are detected by measuring the net magnetization precession.

235 led significant effects in allergic rhinitis by measuring the number of AR medications and demonstrat

236 VF) dynamics for every heart was carried out by measuring the number of filaments formed after wave b

237 We examined the RA status of subjects by measuring the number of tender and swollen joints, an

238 mine how visibility interacts with reporting by measuring the P3b event-related potential, one of the

239 degradation of these compounds was evaluated by measuring the PCDD/F concentration reduction in soil

240 The optical rotation angle is determined by measuring the phase difference between two harmonical

241 At present, TNF is mainly detected by measuring the precursor or the mature cytokine of bul

242 ce of the waveguide sensor was characterized by measuring the Raman spectra of the benzene derivative

243 By measuring the rates of thermally activated vortex mot

244 By measuring the rates of transcriptional initiation and

245 tection in the proposed detector is achieved by measuring the ratio of the absorbed power in two clos

246 Following this approach, by measuring the ratio of the resistance change in the t

247 Spatial spread can be estimated by measuring the receptive field (RF) and multiplying by

248 lysate into the porous matrix was monitored by measuring the red shift in the reflectivity.

249 port a new development of K(d) determination by measuring the reduction in donor fluorescence due to

250 We determine the diffusion constant by measuring the relaxation of an imposed density modula

251 he hydrolytic capacity of BglA was evaluated by measuring the released volatiles in the gas phase wit

252 tin and compared their metastatic potentials by measuring the rupture force of cancer cells represent

253 By measuring the SBA concentration of 15 commercially av

254 effect of five salts on phenol partitioning by measuring the Setschenow coefficients (K(S)).

255 eteronuclear couplings, as demonstrated here by measuring the sign and magnitude for proton-fluorine

256 in vitro kinetics of Abeta(1-42) aggregation by measuring the size distributions of aggregates during

257 By measuring the spraying current, the average specific

258 By measuring the statistical burden of variations (i.e.,

259 e of the emitted THG signal is also analyzed by measuring the Stokes parameters with different polari

260 valuated the divergent dimerization behavior by measuring the strength of each radical association by

261 The corrosion process was monitored by measuring the surface pH, corrosion product compositi

262 compensate for morphophysiological variation by measuring the system dynamics of individual knifefish

263 Pre-corneal tear film stability was assessed by measuring the tear break-up time (TBUT) and the tear

264 By measuring the tested materials with a liquid metal in

265 Temperature changes can be monitored by measuring the thermal emission with thermal imaging.

266 trogen receptor modulator effect as assessed by measuring the tibia weight and calcium content.

267 DX-MS) enables the study of protein dynamics by measuring the time-resolved deuterium incorporation i

268 HV) reactivation have been studied primarily by measuring the total or average activity of an infecte

269 By measuring the transcriptional dynamics of several Kru

270 Here, by measuring the translocation activity of individual Sc

271 ehaviour in an optical-lattice Hubbard model by measuring the transport lifetime for a mass current e

272 ogical state of the resulting superconductor by measuring the tunnelling conductance at the edge of t

273 on sources relative to traffic is determined by measuring the urban enhancement of individual compoun

274 imultaneously detects temperature and strain by measuring the variables at only two measurement frequ

275 topoietic cell lines with that of FeLV-A 61E by measuring the viral RNA copy numbers.

276 hite matter volume as well as local atrophy (by measuring the volume of thalamus, corpus callosum, su

277 the system, and verify their critical nature by measuring their dependence on the system size.

278 rticle solutions are routinely characterized by measuring their extinction spectrum (with UV-vis spec

279 s allow label-free detection of biomolecules by measuring their intrinsic charges.

280 e the organization of transmembrane proteins by measuring their mobilities within a cell's plasma mem

281 s of the nine developed samples are obtained by measuring their permittivity spectra using an open-en

282 t activities of clovamide and these extracts by measuring their superoxide radical scavenging capabil

283 of BP control and related clinical processes by measuring theory-derived pragmatic BP control metrics

284 nert gases, sulphur hexafluoride and ethane, by measuring these gases in the proximal pulmonary arter

285 By measuring this irreversibility in several biological

286 We tested this hypothesis by measuring time intervals for gliding runs and pauses

287 We demonstrate this technique by measuring tractions generated by both single human ne

288 Myocardial damage was studied by measuring troponin release in both groups.

289 Renal function was further quantified by measuring tubular extraction rate (TER) using (99m)Tc

290 e properties of these complexes were studied by measuring turbidity, particle size distribution, zeta

291 ctive effort also compromises bone strength, by measuring using computed tomography thoracic vertebra

292 ude of bias in predicting disease risk posed by measuring vaccination rates at coarse spatial scales.

293 onography to evaluate vitreous structure and by measuring visual acuity and contrast sensitivity func

294 ard patients' vital signs, supporting nurses by measuring vital signs frequently and accurately.

295 We developed and validated such approach by measuring voluntary oral consumption of THC-containin

296 of three commercial fortifiers were assessed by measuring well-recognized indexes of heat load.

297 We tested this hypothesis by measuring whether neural representations of people co

298 Here, we aimed to address this question by measuring, with optical tweezers, the real-time repli

299 experimentally proved the CANCAN-ES paradigm by measuring YO-PRO-1 dye uptake in CHO-K1 cells which w

300 We demonstrate the utility of PrimalSeq by measuring Zika and West Nile virus diversity from var