ライフサイエンスコーパス: be determined with

1 zirconia (110) surface in contact with water was determined with ~0.5 A resolution by high-resolution

2 notype, phenotype, or both for each subgroup was determined with 10-fold cross-validated areas under

3 on cognitive tests (ADAS_cog, MMSE, and FAQ) was determined with 2 different correlation methods.

4 genes present in one copy per haplotype) can be determined with 250 bp reads.

5 er 80 putatively annotated molecular species are determined with 40 mum spatial resolution.

6 These findings demonstrate that ketones can be determined with a differential mobility spectrometry

7 The elastic ratio kappa /kappa can be determined with a few percent statistical accuracy.

8 cognitive and affective deficits remains to be determined with a large cohort of participants.

9 However, its level can be determined with a simple UV spectrophotometric measur

10 oint for use in drug intervention trials can be determined with a single urine collection for albumin

11 stablished to be traceable to the SI and can be determined with a small associated measurement uncert

12 adaptation upon an intervention that cannot be determined with a static fasting measurement.

13 The NMR structure of SrtA has been determined with a backbone coordinate precision of

14 are numerous examples where the line centre is determined with a precision of less than 10(-6) of th

15 od was monitored and the Au(0) concentration was determined with a deviation of less than 5%.

16 gmented epithelium (RPE) viability threshold was determined with a fluorescence assay.

17 Also, xanthine oxidase activity was determined with a linear measurement range of 0.01-1

18 y, the viscosity of several pressure sensors was determined with a material testing machine and range

19 Airway resistance was determined with a mechanical ventilator.

20 The gingival transcriptome was determined with a microarray analysis and focused on

21 ermore, the abnormal functional connectivity was determined with a network-based statistic (NBS) appr

22 GDF-15 was determined with a pre-commercial electrochemilumines

23 RhoA activation was determined with a Rhotekin binding assay.

24 Malignancy was determined with a sensitivity of 100% and specificit

25 ACh was determined with a sensitivity of 392.4 mA M(-)(1) cm

26 t predictors, risk for IMA type II endoleaks was determined with a sensitivity of 78% (39 of 50) and

27 FADS haplotype status was determined with a single nucleotide polymorphism (rs

28 The activation status of monocytes was determined with a single-chain antibody, MAN-1, whic

29 Particle pH was determined with a thermodynamic model using measured

30 l age in diagnosing asthma at 6 years of age was determined with a validation set.

31 , and baseline plasma levels of 102 proteins were determined with a bead-based immunoassay.

32 eir independent associations with LRM, which were determined with a Cox proportional hazards model.

33 analysis, whereas serum cytokines/chemokines were determined with a cytometric bead array.

34 Sorption coefficients (K(oc)) were determined with a dynamic HPLC-based column method

35 crucial importance for the specific binding were determined with a label-free nuclear magnetic reson

36 fraction, a marker of interstitial fibrosis, were determined with a model for transcytolemmal water e

37 Group 5 allergen levels were determined with a Phl p 5-specific ELISA in 2 fract

38 Sensitivity and specificity were determined with a receiver operator characteristic

39 TRX1 and TRX80 plasma levels were determined with a specific ELISA.

40 611 on keratinocytes preincubated with HNP-1 were determined with a standard antibiotic test.

41 on and its contribution to export production were determined with a suite of geochemical and biologic

42 small-scale wood combustion of various fuels were determined with a system consisting of an aerosol p

43 1) and T2* of healthy human brain and muscle were determined with a three-dimensional density-adapted

44 s (CA) 2+3, CA4+dentate gyrus, and subiculum were determined with a user-independent segmentation met

45 ATG-exposure measures were determined with a validated pharmacokinetics model.

46 ility of oil bodies from pumpkin (Cucurbita) were determined with a view to patterning oil body size

47 ol, and recently, additional structures have been determined with agonist bound.

48 The binding epitope was determined with alanine scanning.

49 The activity of hNit2/omega-amidase was determined with alpha-ketoglutaramate and succinamat

50 tion of the actinides in the GTS groundwater was determined with AMS over 6 orders of magnitude from

51 nstant K of the isotope exchange reaction to be determined with an external reproducibility of better

52 content of the serum samples and GCF eluates was determined with an agar diffusion bioassay.

53 Circulating ZAG was determined with an ELISA kit.

54 agents on hyaluronan and collagen synthesis was determined with an enzyme-linked immunosorbent assay

55 with cotton threads, and corneal sensitivity was determined with an esthesiometer.

56 r the absence of the two error contributions was determined with an F-test between the ordinary least

57 The total arsenic concentration was determined with an ICP-MS method.

58 The antioxidant capacity was determined with an ORAC assay, and total phenolic co

59 tional head movement, frequency, and B0 shim were determined with an integrated volumetric navigator.

60 spiro-fermenting, and fermenting yeast cells were determined with an integrative biophysical approach

61 pulmonary function and imaging measurements were determined with analysis of variance (ANOVA), Holm-

62 Significant differences between groups were determined with analysis of variance.

63 The MID in the RTSS was determined with anchor-based methods (using the GRCS

64 Metabolic effect sizes were determined with and without accounting for regional

65 Plasma levodopa levels were determined with and without nalbuphine, and postmor

66 l stage, risk assessment, and treatment plan were determined with and without the contribution of BMB

67 ctures of AH from Granulibacter bethesdensis were determined, with and without the substrate analogue

68 rlying layers of the uranium oxide materials were determined with angstrom-level resolution.

69 l composition, and calcium's content in milk were determined with AOAC methods.

70 dhesion, migration/invasion, and EMT markers were determined with APT or a mutant control aptamer (Mu

71 Examination indication was determined with associated ICD-9 diagnostic code; 95

72 ld), and for old field stars whose ages have been determined with asteroseismology.

73 A disease-free state was determined with at least 6 months of follow-up.

74 inkage in the absence of soluble Abeta(1-40) are determined with atomic force microscopy (AFM).

75 Nodule volume was determined with automated volumetric analysis.

76 Air-exchange rates (AER) were determined with average (95% CI) AER of 12 (10-14)

77 The step size between consecutive iterations is determined with backtracking line search.

78 trains were genotyped, and their time origin was determined with Bayesian phylogenetic methods.

79 ce bearing Colo205 xenografts: tissue uptake was determined with biodistribution studies, and small-a

80 mation that the identity of the major isomer is determined with catechothiolate systems.

81 tageous as the mode of inheritance could not be determined with certainty in many instances.

82 onclusions regarding this progression cannot be determined with certainty.

83 inical effects of these abnormalities cannot be determined with certainty; none of the subjects had a

84 0.0001) and viscosity (r = 0.78, P < 0.0001) were determined with collagen fraction, but not with cel

85 Tumor growth was determined with colony formation in vitro or in vivo

86 Tissue fibrosis was determined with colorimetric analysis of trichrome-s

87 bility and proliferation of epithelial cells were determined with commercial kits after incubating th

88 ry, and intraabdominal adipose tissue (IAAT) was determined with computed tomography.

89 on cultures of live rat hippocampal neurons was determined with confocal microscopy.

90 are listed for liver transplantation should be determined with consideration of median wait times, a

91 ence of hearing impairment in these neonates was determined, with corresponding 95% confidence interv

92 redictors of LAE over 5.8 years of follow-up were determined with Cox multivariable analysis.

93 Subsequent care was determined with CT angiography findings: Patients wi

94 G class are too large for their structure to be determined with current NMR methodologies.

95 by flow cytometry, and bronchial contraction was determined with cytokine-treated human lung sections

96 by cinchona alkaloid-derived primary amines is determined with density functional calculations.

97 l-Cysteine and l-Cystine were determined with detection limit of 0.125% (w/w) in

98 ygen evolving complex in photosystem II have been determined with DFT methods for large models.

99 between tauMODIS versus tauAERONET at 550 nm is determined with different spatial and temporal size w

100 geneous rate constant (k0) for CO2 reduction were determined with different quaternary ammonium elect

101 nding strength (logKapp) of herbal infusions were determined with Differential Pulse Anodic Stripping

102 ected in the associated endothermic energies were determined with differential scanning calorimetry.

103 and the neuronal SNARE complex, one of which was determined with diffraction data from an X-ray free-

104 the posterior limbs of the internal capsules was determined with diffusion-weighted magnetic resonanc

105 FDG) and apoptosis ((99m)Tc-rhAnnexin V-128) were determined with digital autoradiography.

106 amine (cinchona amine) organocatalyst, have been determined with dispersion-corrected density functi

107 Formation of R-loops was determined with DNA: RNA hybrid-specific S9.6 antibo

108 Percentage body fat was determined with dual-energy X-ray absorptiometry, an

109 Total hip and spine areal BMD were determined with dual-energy x-ray absorptiometry (D

110 of ECV biogenesis and signaling have yet to be determined, with ECV detection being a challenge and

111 Hybridization between probe and target was determined with electrochemical impedance spectrosco

112 Finally, a structure of ORC was determined with endogenous DNA bound in the core rev

113 Concentration of CXCL13 was determined with enzyme-linked immunosorbent assay in

114 The results indicated that the ratio can be determined with excellent reproducibility in multiple

115 or Hg and MeHg, high bioaccessibility values were determined with exception of grilled meagre, displa

116 s of a class B N-hydroxylating monooxygenase were determined with FAD in oxidized (1.9 A resolution)

117 histone H2AX (gammaH2AX) foci per lymphocyte was determined with fluorescence microscopy.

118 imals, intratumoral doxorubicin accumulation was determined with fluorimetry and correlated with the

119 rations of gaseous ozone and nitrogen oxides were determined with Fourier-transform infrared spectros

120 The rate coefficients were determined with FT-ICR mass spectrometry under sing

121 ng elastic modulus, and beta stiffness index were determined with general linear models.

122 ment (the home and the work/study addresses) were determined with geographic information system (GIS)

123 ollicles, and absence of a dominant follicle were determined, with girls who were highly suspected of

124 meters, [Lac](blood) during CWR exercise can be determined with good accuracy.

125 ngle-point SUPREX because peptide masses can be determined with greater precision than intact protein

126 Salivary nitrite concentration was determined with Griess reagent.

127 The limits of detection (LOD) are determined, with high precision, to 6.33 and 9.22 ng

128 Glycopeptide composition and structure can be determined with high mass-accuracy mass spectrometry,

129 brium method allowed oxidation potentials to be determined with high precision (</= +/-6 mV).

130 -protein complex for which the structure has been determined with high resolution and since then this

131 tion tensor is diagonal, and matrix elements were determined with high accuracy.

132 ein (CRP), interleukin-6, and lipid profiles were determined with high-sensitivity assays in serum.

133 An additional 505 surveillance intervals were determined with histology input.

134 Final diagnosis was determined with histopathologic verification (n = 25

135 New blood vessel formation was determined with human umbilical vein endothelial cel

136 ntrations and active levels of MMP2 and MMP3 were determined with immunoassay ELISA and activity assa

137 cAMP levels were determined with immunoassays or fluorescent resonan

138 July 2012 for ImmunoCAP(R)) and tropomyosin was determined with ImmunoCAP(R) (CAP-FEIA, Phadia) .

139 ween phosphorylation of STAT3 and PD-1/PD-L1 were determined with immunostaining of human and mouse H

140 on cultures of live rat hippocampal neurons were determined with immunostaining, Western blot, and e

141 t compositions in these ternary systems have been determined with increasing electric field applied a

142 Sixty-three different elements were determined with inductively coupled-plasma mass spe

143 The labeling efficiency was determined with instant thin-layer chromatography an

144 Repeatability was determined with intraclass correlation coefficients,

145 The three-dimensional structure of CDA was determined with isoguanine in the active site.

146 Muscle strength at the knee and ankle was determined with isokinetic dynamometry.

147 component of the reaction, as well as kobs , is determined with just a few experiments using a simple

148 5-year, all-cause mortality for each tertile was determined with Kaplan-Meier curves and compared by

149 uskal-Wallis tests, and the prognostic value was determined with Kaplan-Meier curves.

150 Interobserver agreement was determined with kappa statistics, and the Student t

151 Binding parameters were determined with kinetic modeling analysis.

152 Myocardial fibrosis was determined with late gadolinium enhancement (replace

153 Concentration of MMP-9 in saliva samples was determined, with linearity in the range of 10-200ng/

154 The predictive value of the models was determined with logistic regression.

155 The radius of a spherical protein shell can be determined with <10 nm error by fitting an equation t

156 de indicates that helix orientation can also be determined with <4.2 degrees accuracy.

157 RIEs) for a large group of compound families were determined with LTP-Orbitrap-MS and compared to tho

158 moter haplotypes' transcriptional activities were determined with luciferase reporter assays.

159 y and strength (mean fluorescence intensity) was determined with Luminex.

160 ickness across a fovea-centered 4-mm segment was determined with MATLAB.

161 imulations, in which the photoproduct ratios were determined with maximum errors of 3%.

162 Serious adverse event rates could not be determined with meta-analysis.

163 Wear depth and volume loss were determined with micro-computed tomography.

164 Factors related to laminar depth were determined with mixed-effects modeling.

165 The sensitivity and specificity of each test was determined, with molecular genotype serving as the g

166 Pre-treatment and post-treatment tumor sizes were determined with MRI.

167 Serum cytokine concentrations were determined with multiplex assays.

168 betaPV IgG seroresponses were determined with multiplex serology.

169 ween the PVI and cardiovascular risk factors was determined with multivariable analysis.

170 The NA affinity and velocity values were determined with NA enzymatic studies.

171 n both fresh and aged Cu-SSZ-13 and Cu-ZSM-5 are determined with nanometer resolution using atom prob

172 y produced cytokines on osteoclast formation were determined with neutralizing antibodies.

173 Pb(2+) concentrations at the well were determined with numerical reactive transport simula

174 chain reaction, and statistical significance was determined with one-way analysis of variance (Kruska

175 Differences between age groups were determined with one-way analysis of variance and Tu

176 e, postoperative complications, and survival was determined with (ordinal) logistic, linear, and Cox

177 nally resolved emission rates of POPs, which were determined with our combined measurement and modeli

178 que G protein-coupled receptors (GPCRs) have been determined, with over 370 structures in total bound

179 the incidence of postoperative complications was determined, with particular emphasis on superficial

180 xtent of heat treatment in LWE samples could be determined with PCA of the CE measurements.

181 HLA-A*11:01 ligand sequences were determined with PEAKS software and confirmed by com

182 al that have not been previously identified, were determined with peptide specificity.

183 ibial volumetric BMD and cortical dimensions were determined with peripheral quantitative computed to

184 e the B[a]P contamination of the sample, can be determined with picomolar sensitivity.

185 The Abeta status was determined with Pittsburgh Compound B-positron emiss

186 SAP progression was determined with point-wise linear regression analysi

187 nit cell parameters of the obtained crystals were determined with powder X-ray diffraction.

188 an, the relative position of the emitter can be determined with precision better than 5 nm in a proce

189 Total antimony was determined with previous sample treatment using 0.1%

190 y for liver transplantation for each patient was determined with prior and revised transplantation al

191 entia; 63 men, 31 women; mean age, 40 years) were determined with proton (hydrogen 1 [(1)H]) MR spect

192 Cerebral metabolites were determined with proton decoupling in a parieto-occi

193 on energies in the range of 96 +/- 19 kJ/mol are determined, with Pt leading to the lowest energy bar

194 essenger RNA (mRNA) for biglycan and decorin was determined with quantitative real-time polymerase ch

195 m the multicenter cohort) Expression of ompA was determined with quantitative reverse-transcription p

196 actions reported by Tius and co-workers have been determined with quantum chemical calculations.

197 Breakthrough reaction rates were determined with random-effects modeling and meta-re

198 The diagnostic accuracy of each phase was determined with receiver operating characteristic (R

199 The discrimination performance of all models was determined with receiver operating characteristics (

200 eed values for fibrosis grades F0 through F3 were determined with receiver operating characteristic (

201 Optimal cut-off values were determined with receiver operating characteristic c

202 ncentrations of ash, potassium and magnesium were determined with reference methods and LIBS.

203 tors, including hospital quality of MI care, were determined with regression modeling.

204 omise, the optimal source of MSCs has yet to be determined with respect to major histocompatibility c

205 Phenolic profile of 13 grapevine varieties was determined, with respect to three different parts of

206 of protein complexes in all other fractions were determined with respect to their amounts in flowers

207 CXR severity, sensitivity, and specificity were determined with respect to time after onset of symp

208 icity and adhesion behavior of the thin film was determined with respected to the indentation deforma

209 Functional expression of TRP channels was determined with reverse transcription polymerase cha

210 The expression of Opa3 was determined with RT-PCR, quantitative PCR, and Wester

211 HHV-6 DNA, variant type, and viral loads were determined with samples (cord blood, peripheral blo

212 noglycoside acetyltransferase (3)-IIIb (AAC) are determined with several experimental methods.

213 The (234)U- and (236)U-inclusive ratios were determined with similar accuracy in enriched sample

214 Analytical performance was determined with six environmentally relevant model c

215 onomer and soluble aggregates of bevacizumab were determined with size-exclusion high-performance liq

216 , mechanistic target of rapamycin, and 70S6K was determined with specific antibodies.

217 Peripapillary RNFL thickness was determined with spectral-domain optical coherence to

218 Motif similarities were determined with STAMP, classifying the 407 sequence

219 The levels of corneal fibrosis were determined with stereomicroscopy, slit lamp biomicr

220 lecular extension of thousands of DNA probes is determined with sub-micron precision using a robust a

221 y functions, the absolute vertical positions were determined with sub-10-nm localization precision.

222 X) in aqueous droplets of phenethylamine has been determined with submillisecond temporal resolution

223 hod allows kinetic isotope effects (KIEs) to be determined with substantially less material or shorte

224 X-ray structures of HPP were determined with sulfate, L-histidinol phosphate, an

225 ifferences in gene expression between groups were determined with t-statistics using the limma packag

226 In separate experiments, dose responses were determined with TG containing only docosahexaenoic

227 The CYP activities are determined with the help of prefluorescent, enzyme-s

228 Fifteen elements are determined with the system (Ba, Cs, Li, Rb, Cr, Sr,

229 enabling double bond positions of MUBCFA to be determined with the analogous alpha and omega diagnos

230 centrations of the isomers in solutions have been determined with the standard deviation of 3.1%, whe

231 n a red wine (Raimat, Catalonia, Spain) have been determined, with the Donnan Membrane Technique (DMT

232 w test in plasma and dried blood spots (DBS) was determined with the 2nd International HIV-1 RNA WHO

233 The flexural strength of the aluminas was determined with the 4-point bending test.

234 l cost per quality-adjusted life-year (QALY) was determined with the addition of alirocumab versus pl

235 The X-ray structure of the GluCl-Fab complex was determined with the allosteric agonist ivermectin an

236 and extent of heterogeneity between studies was determined with the Cochran Q and I(2) tests.

237 per kilogram of body weight) administration was determined with the following equation: V(L)[(L(20)/

238 The functional outcome at 12 months was determined with the Glasgow Outcome Scale-Extended (

239 M value was determined with the HEC method at PET imaging.

240 beta-Cell function was determined with the hyperglycemic clamp and morphome

241 Extent of heterogeneity between studies was determined with the I(2) test.

242 Survival was determined with the Kaplan-Meier method, and the sur

243 ive manner and the selectivity of the system was determined with the selectivity coefficients of appr

244 Statistical significance was determined with the Student t test, the paired t tes

245 Total water intake was determined with the use of a 24-h dietary recall and

246 y of older adults, the diagnosis of dementia was determined with the use of a detailed in-home cognit

247 xisting sensitivity to peanut extract, which was determined with the use of a skin-prick test--one co

248 Urine osmolality was determined with the use of freezing-point depression

249 t, whereas the adipose tissue content of ALA was determined with the use of gas chromatography in all

250 Mucosal transcriptome in rectal biopsies was determined with the use of microarrays.HPDs did not

251 Ex vivo thrombus formation was determined with the use of the Badimon chamber.

252 The risk of renal outcomes was determined with the use of time-to-event analyses wi

253 a slight predominance of the axial conformer was determined, with the ratio 1-ax:1-eq = 54(9):46(9) (

254 Chemical profiles (phenolic compounds) were determined with the aid of HPLC-DAD/MS.

255 rn, mean vascular density, and mitotic index were determined with the aid of immunohistochemical stai

256 centrations of nine fortified vitamin juices were determined with the aim to study the FA degradation

257 mpacts/benefits resulting from biodiesel use were determined with the Air Quality Benefits Assessment

258 In this study, structures of 2B4 were determined with the antiplatelet drugs clopidogrel

259 y and reproducibility of manual segmentation were determined with the Dice similarity coefficient and

260 The anthocyanins were determined with the differential pH method and the

261 ulimic, hyperphagic, and other types of EDs) were determined with the Expali algorithm (n = 48,824).

262 SIgE, sIgG, sIgG4 were determined with the FEIA method (Pharmacia CAP Syst

263 ssible progression" and "likely progression" were determined with the GPA.

264 ts, i.e., cluster formulas, for these phases were determined with the guide of the Friedel oscillatio

265 Sighting, motor, and sensory dominance were determined with the hole-in-the-card test, converge

266 llergen 2 population threshold distributions were determined with the individual minimal eliciting do

267 hat characteristics of interaction sets that were determined with the same experimental methods were

268 MICs generated by both methods were determined with the same inoculum suspension.

269 onation parameters and propulsion properties were determined with the software package EXPLO5 V6.02.

270 ntralateral limb) between the two modalities were determined with the two-tailed paired t test.

271 luxes of leucine, before and after the meal, were determined with the use of a [1-(13)C]leucine intra

272 Polymorphisms were determined with the use of a TaqMan assay.

273 Final diagnoses were determined with the use of algorithms and a set of

274 se to a 2 degrees C rise in body temperature were determined with the use of Caco-2 and HT29 intestin

275 vered from duodenal aspirate from each child were determined with the use of culture-independent meth

276 and beta-carotene in labeled doses and serum were determined with the use of HPLC, gas chromatography

277 al oxygen uptake ([Formula: see text]O2 max) were determined with the use of indirect calorimetry in

278 -specific protein intake and health outcomes were determined with the use of models that adjusted for

279 CFU cutoffs that best predict VISA and hVISA were determined with the use of receiver operating chara

280 er the curve (AUCi) method, and serum lipids were determined with the use of standard assays.The cons

281 Drug susceptibilities were determined with the Vitek 2 system.

282 y and accuracy of the quantitation using MRM were determined, with the detection limit in the femtomo

283 SVOC concentrations and OC and EC fractions were determined with thermal extraction-gas chromatograp

284 HPV status was determined with three validated commercial tests to

285 Airway smooth muscle function was determined with tissue myography, intracellular calc

286 l phagocytosis and intraphagosomal processes were determined with triple-labeled Escherichia coli, co

287 Apoptosis was determined with TUNEL assay.

288 ood choices and prepregnancy body mass index were determined with two tandem mass spectrometric metho

289 and sous-vide (SV) thermally processed beef were determined with UHPLC-ESI/MS.

290 Central corneal thickness was determined with ultrasonic pachymeters of the same m

291 l types or between disease/normal tissues to be determined with unprecedented breadth.

292 n flow rate through individual nanotubes can be determined with unprecedented sensitivity and without

293 racheal, thyroidal, and vascular structures, were determined with US, and tracheal measurements were

294 Seleno-methylselenocysteine was determined with values ranging from 1.03-2.03+/-0.2

295 ncentrations photoproduced from DOM isolates were determined with varying concentrations of chloride

296 imination thresholds for oral point pressure were determined with Von Frey Hairs.

297 Morphological differences were determined with voxel-based morphometry, in SPM8.

298 and middle gyrus of temporal neocortex (CX) were determined with western blots and compared between

299 nd 0.05% deltamethrin WHO-impregnated papers was determined with wild-caught sand flies.

300 Crystal structures were determined with wild-type and K103N HIV-1 reverse t