ライフサイエンスコーパス: be determined with

1 tein diffusivity, protein hydrodynamic radii were determined with +/-0.25 A resolution.

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

3 The ratio of ED to DLP was determined with 16-section CT scanners from four ven

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

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

6 nments for the isotope-enriched Cys residues were determined with 2D versions of standard triple-reso

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

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

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

13 Currently, drug action is determined with a fluorimetric/colorimetric assay bas

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

15 Adhesion to collagen type I was determined with a binding assay.

16 GCF volume was determined with a calibrated gingival fluid meter.

17 spase-3 activation after glutamate treatment was determined with a carboxyfluorescein caspase-3 detec

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

19 Calcium absorption was determined with a dual stable isotope method using 4

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

21 Airway resistance was determined with a mechanical ventilator.

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

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

24 RhoA activation was determined with a Rhotekin binding assay.

25 Prior LOC eating was determined with a semistructured clinical interview.

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

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

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

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

30 The number of epithelial cell layers was determined with a stereological method of point coun

31 Particle pH was determined with a thermodynamic model using measured

32 in telomerase-immortalized, human RPE cells was determined with a UBE2E3-specific antibody.

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

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

35 Concentration and biological activity were determined with a chemical assay and zone of inhibi

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

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

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

39 s, and changes in corneal light transmission were determined with a fiber-optic spectrophotometer.

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

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

42 m dot labels of the secondary aptamer, which were determined with a novel solid-contact Cd2+-selectiv

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

44 Sensitivity and specificity were determined with a receiver operator characteristic

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

46 611 on keratinocytes preincubated with HNP-1 were determined with a standard antibiotic test.

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

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

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

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

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

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

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

54 The binding epitope was determined with alanine scanning.

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

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

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

58 Circulating ZAG was determined with an ELISA kit.

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

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

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

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

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

64 l glucose uptake (MGUp) rate and utilization were determined with an input function derived by the hy

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

81 Nodule volume was determined with automated volumetric analysis.

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

83 s independently associated with colonization were determined with backward stepwise logistic modeling

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

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

86 , and the X-ray structure of the protein has been determined with bound MgADP to 1.6 A resolution.

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

88 conformation of the Tg(6) CH(3) group cannot be determined with certainty from the NMR data.

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

90 onclusions regarding this progression cannot be determined with certainty.

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

92 Association of p27 with ubiquitin E3 ligase was determined with coimmunoprecipitation followed by im

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

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

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

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

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

98 l effect of the antimicrobial rBALF peptides was determined with corresponding deletion mutants.

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

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

101 he three-dimensional structure of LmACR2 has been determined with crystallographic methods and refine

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

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

104 Cortical BW concentration was determined with custom-designed MR imaging sequences

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

120 ucture and growth direction of the nanowires were determined with electron diffraction.

121 st show how the optimal resolution range can be determined with English books which have been transfo

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

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

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

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

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

127 These temperatures were determined with fluorescence lifetime imaging (FLIM

128 um mobilization, and nitric oxide generation were determined with fluorescence viability markers, imm

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

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

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

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

133 l is proportional to the lifetime, which can be determined with good reproducibility (typically <100

134 ed temporal shifts and signal propagation to be determined with good spatial and temporal resolution.

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

136 Salivary nitrite concentration was determined with Griess reagent.

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

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

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

140 nonlabile nuclei of a given biomolecule can be determined with high resolution, which becomes partic

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

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

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

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

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

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

147 cAMP levels were determined with immunoassays or fluorescent resonan

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

149 to the apical or basal surface of RPE cells was determined with immunocytochemistry.

150 Rp1h protein location was determined with immunofluorescence microscopy.

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

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

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

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

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

156 Repeatability was determined with intraclass correlation coefficients,

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

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

159 5-year, all-cause mortality for each tertile was determined with Kaplan-Meier curves and compared by

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

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

162 Binding parameters were determined with kinetic modeling analysis.

163 Myocardial fibrosis was determined with late gadolinium enhancement (replace

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

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

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

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

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

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

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

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

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

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

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

175 he AAS and age to predict estimated VO(2max) was determined with multiple regression analysis.

176 Serum cytokine concentrations were determined with multiplex assays.

177 betaPV IgG seroresponses were determined with multiplex serology.

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

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

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

181 The surface pit pattern was determined with NBI or FICE in all patients.

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

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

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

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

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

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

188 Qualitative identification of cations can be determined with over 96% of accuracy in a concentrati

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

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

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

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

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

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

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

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

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

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

199 that the VZV particle-to-PFU ratio has never been determined with precision.

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

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

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

203 ect of BSP on MMP-2 modulation by inhibitors was determined with purified components and in cell cult

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

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

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

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

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

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

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

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

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

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

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

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

216 istic curve (AUC) for each evaluation method was determined, with retrospective selection of suggeste

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

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

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

220 amounts of each MyHC isoform in each sample were determined with scanning densitometry.

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

222 Analytical performance was determined with six environmentally relevant model c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

241 tic regression, and genome-wide significance was determined with the False Discovery Rate-Beta Unifor

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

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

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

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

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

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

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

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

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

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

252 og/mL) on cell attachment to collagen type I was determined with the use of fluid-phase cell attachme

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

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

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

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

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

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

259 d the substrate profiles for the two enzymes were determined with the aid of combinatorial dipeptide

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 exes for three template-primer DNA sequences were determined, with the Y-family Sulfolobus solfataric

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

285 HPV status was determined with three validated commercial tests to

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

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

288 Apoptosis was determined with TUNEL assay.

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

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

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

297 uantification of FAK and Src phosphorylation was determined with Western blot analysis of whole cell

298 ZBED4 subcellular localization was determined with Western blot analysis.

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