ライフサイエンスコーパス: be assayed

1 nd crowns, and quantitative Axin2 expression is assayed.

2 lation in order that the correct populations are assayed.

3 y, and migration of eosinophils on periostin was assayed.

4 of this pathway in human autoimmune uveitis was assayed.

5 tic acid) to inhibit TMAO-demethylase enzyme was assayed.

6 act, potassium sorbate and their combination was assayed.

7 tion factors encoded in the human genome has been assayed.

8 n peripheral blood mononuclear cells (PBMCs) were assayed.

9 and Foxp3 methylation in MLN CD4(+) T cells were assayed.

10 metabolism, and markers of thyroid function were assayed.

11 m different plant parts of Allium fistulosum were assayed.

12 ell as circulating measures of inflammation, were assayed.

13 sodium erythorbate, and the quality indexes were assayed.

14 responses of phytoplankton functional groups were assayed.

15 /PSA, SAX/PSA, Envi-Carb-II /SAX/PSA and C18 were assayed.

16 regulatory networks and biological functions were assayed.

17 H) and pancreatic lipase inhibitory capacity were assayed.

18 ing mixes, extracts, and molecular allergens were assayed.

19 observed when combined antioxidant compounds were assayed.

20 John's Wort, sage, marjoram and thyme were assayed.

21 eurotrophic factors, and vascular parameters were assayed.

22 e and phenylethanolamine-N-methyltransferase were assayed.

23 eramidase protein and enzyme activity levels were assayed.

24 outgrowth assays from resting CD4(+) T cells were assayed.

25 tting, Angolan outpatient samples (n = 1267) were assayed.

26 vective drying (CDP) and ohmic heating (OHP) were assayed.

27 nd the type of sorbent or extraction solvent were assayed.

28 ctin, d-dimer, FVIII, and C-reactive protein were assayed.

29 hydrolysates and fractions <10kDa and <3kDa were assayed.

30 W264.7 cells co-cultured with MC3T3-E1 cells were assayed.

31 Roux limb glucose consumption was assayed after surgery by positron emission and compu

32 ctivity of this new class of macrocycles has been assayed and analyzed.

33 estinal bioavailability of PFSP anthocyanins was assayed and compared with the bioavailability of Red

34 erminal modifications of the native ProTx II was assayed and resulted in the identification of protox

35 Manual and in situ derivatization was assayed and the chromatographic response was higher

36 Localization of DSCAM was assayed and the protein was localized near to cone s

37 Further metabolism of the tested compounds was assayed and their transport modulated in an attempt

38 ad, IgG, and initial neutralization response were assayed and correlated with clinical and VAS inform

39 ast Kent Goldings (EKG) and Tettnanger (TET) were assayed and robust statistical approaches were appl

40 ay configurations, competitive and sandwich, were assayed and their performance for IgE determination

41 ks after finishing therapy, plasma Ab levels were assayed, and bone marrow was harvested.

42 Channel activity was assayed as ionic currents under patch clamp and as o

43 mycotoxin concentration in the raw materials were assayed as factors.

44 5 candidate 12-HETER1 promoter cis elements were assayed as luciferase reporter fusions in Chinese h

45 apause by a photoperiodic (short-day) signal were assayed as they traversed the diapause developmenta

46 okines by peripheral blood mononuclear cells was assayed, as were regulatory T-cell numbers and funct

47 he pathophysiology of THAP1 mutations should be assayed at multiple ages and neuronal types and suppo

48 cal advances have enabled DNA methylation to be assayed at single-cell resolution.

49 Oviductal gene expression was assayed at the RNA (quantitative RT-PCR) and protein

50 Serum CRP levels were assayed at a central laboratory, and single-nucleot

51 ples from 27 pulmonary tuberculosis patients were assayed at diagnosis and during treatment.

52 as bentonite (B) and potassium caseinate (C) were assayed at different concentrations.

53 The products were assayed at increasingly low concentration, with the

54 a-smooth muscle actin-positive blood vessels were assayed at postoperative day 7 by colony formation

55 suppressed, chronically infected individuals were assayed at two time points separated by a 4- to 6-m

56 Serotype-specific immunoglobulin G was assayed before and 4 weeks postvaccination to calcul

57 ress-related and decline-related changes can be assayed, but usually through means that are highly di

58 Furthermore, it can be assayed by DTI, potentially offering a quick, noninva

59 ials as molecular dosing containers has also been assayed by the diffusion and photorelease of p-benz

60 chain, the polyphosphate chain concentration is assayed by coupling the enzymes exopolyphosphatase (p

61 A buffer placed in brief contact in the skin was assayed by (1)H NMR spectroscopy.

62 Ascorbate was assayed by 2,6-dichlorophenolindophenol titration, a

63 Sb migration was assayed by HG-AFS for total determination and HPLC-I

64 Sodium was assayed by ICP-MS, including rigorous quality contro

65 Ki-67 expression was assayed by immunohistochemistry.

66 Cell death was assayed by LDH and MTT methods.

67 HPV16 E6 DNA was assayed by polymerase chain reaction (PCR) and in si

68 ified for each maternal-infant pair, and MMc was assayed by quantitative polymerase chain reaction.

69 CR) and in situ hybridization; HPV16 E6 mRNA was assayed by reverse transcriptase PCR.

70 Oxidative stress was assayed by single cell imaging of dihydroethidium.

71 e antioxidant capacity of the herbs extracts was assayed by spectrophotometric methods by using three

72 lications of the Au@MnO@SiO2 Janus particles were assayed by a cell viability analysis by coincubatin

73 Soluble Abeta oligomers were assayed by a single antibody sandwich enzyme-linked

74 Whole blood samples were assayed by Affymetrix GeneChip Human Genome U133 Pl

75 Combinations of domain-coated beads were assayed by Bio-Plex technology as a high-throughput

76 Centromere size and location were assayed by chromatin immunoprecipitation for the hi

77 iadin antibodies of both IgG and IgA classes were assayed by ELISA in 44 non-celiac gluten sensitivit

78 Pre- and postinfection sera were assayed by enzyme-linked immunosorbent assay with N

79 Dynamics were assayed by fluorescence anisotropy of the fluoresce

80 Various types and lengths of mismatches were assayed by fluorimetry, and in many instances, our

81 Extracts were assayed by GC-FID, GC-MS, and LC-MS for the identif

82 and 16 pesticides whereas Cd, As, Pb and Hg were assayed by ICP-MS.

83 IRT3 and cleaved caspase-9 (CC-9) expression were assayed by immunoblotting with or without SIRT3 enf

84 Analyses of DC were assayed by liquid chromatography - tandem mass spec

85 Plasma specimens were assayed by liquid chromatography tandem mass spectr

86 Cytokines were assayed by means of ELISA.

87 esistant (HOMA-IR > 7, n = 9) obese subjects were assayed by microarray (Illumina HumanHT-12).

88 in vivo- and in vitro-cultured pollen tubes were assayed by microarray analyses, revealing over 500

89 dlings when apyrase expression is suppressed were assayed by microarray and quantitative real-time-PC

90 Isolates were assayed by polymerase chain reaction for genes enco

91 ton samples (63-200 and > 200 mum fractions) were assayed by polymerase chain reaction for the preval

92 Saos-2 osteoblasts on new and treated disks were assayed by propidium iodide/DNA stain assay and con

93 Channel mRNAs were assayed by quantitative polymerase chain reaction.

94 nges in the expression of Stat5 target genes were assayed by quantitative real-time PCR assay.

95 genes in the TGF-beta signaling pathway and were assayed by quantitative RT-PCR for their associatio

96 Saliva swabs were assayed by real-time polymerase chain reaction for

97 TGF-beta inhibitor, and CTGF protein levels were assayed by Western blot analysis.

98 Three different temperature regimes were assayed (controlled, semi-controlled and non-contro

99 n groups of macromolecule-bound antioxidants were assayed: dietary fiber (DF), protein and lipid-boun

100 pulations, though small brain regions cannot be assayed due to low mitochondrial yield.

101 n an open-ended approach wherein an endpoint is assayed during or after the biological event of inter

102 Three measures of t-SP were assayed during reinstatement: dendritic spine morph

103 Barcoded proteins are assayed en masse in aqueous solution and subsequentl

104 trations of insulin, peptide YY, and ghrelin were assayed every 30 minutes.

105 It was assayed ex vivo in resected lung tissues collected f

106 s only a few close relatives of sponges have been assayed for sterols.

107 lf of the nucleic acid extracted from plasma is assayed for HIV-1 RNA.

108 lood was sampled postoperatively, and plasma was assayed for 25-OHD by liquid chromatography-tandem m

109 removed to generate a 14-member library that was assayed for agonist activity at the mouse MC1R, MC3R

110 and the resulting sodium pertechnetate 99mTc was assayed for chemical, radiochemical, and radionuclid

111 (64)Cu-L19K-FDNB was assayed for covalent binding to VEGF in vitro.

112 ene expression profiles, and cell-free fluid was assayed for cytokines.

113 d from 75 type 2 diabetes regions, each gene was assayed for effects on multiple disease-relevant phe

114 Urine was assayed for glycocalyx breakdown products (glycosami

115 After imaging, the cartilage was assayed for its water, glycosaminoglycan, and collag

116 PfRH5-specific IgG was assayed for parasite growth-inhibitory activity.

117 Plasma was assayed for residual viremia (HIV-1 RNA) by qPCR.

118 The cell culture medium was assayed for the presence of the fluorescent signal u

119 All excised nodal packets (n = 36) were assayed for (99m)Tc activity, which established a l

120 105 asymptomatic healthy control individuals were assayed for 13 proteins relevant to cardiovascular

121 nts with surveillance or indication biopsies were assayed for 133 unique metabolites by quantitative

122 y treatment and before recurrence (n = 336), were assayed for 25(OH)D.

123 collected at 26 weeks' gestation or earlier were assayed for 25(OH)D.

124 Plasma obtained upon admission and over time were assayed for 26 inflammatory mediators and analyzed

125 ion With Initial Glargine Intervention trial were assayed for 284 biomarkers to identify those that c

126 Patient samples (13) were assayed for 3 biomarker proteins with results well

127 Blood samples were assayed for 3-O-methylglucose to estimate glucose a

128 d and complemented and the resulting strains were assayed for acid survival.

129 Pigs (n = 255) were assayed for aggressiveness (tendency to attack in r

130 t and delivery plasma samples from 681 women were assayed for antibodies against recombinant antigens

131 llege students living in a non-outbreak area were assayed for antibodies and memory B cells (MBCs) to

132 The resulting compounds were assayed for antimicrobial activity against the ESKA

133 concentrates coming from aqueous treatments were assayed for antioxidant activity using the followin

134 of SPDEF were expressed in CRC cells; cells were assayed for beta-catenin activity and studied in im

135 sex, cryopreserved baseline plasma specimens were assayed for biomarkers of inflammation, including h

136 Cdx2-eGFP cells from end-gestation placenta were assayed for cardiac differentiation in vitro and in

137 intervention and at 4-month follow-up, which were assayed for circulating IL-6, a biomarker of system

138 eriodontitis (CP) and 25 healthy individuals were assayed for cluster of differentiation14(+) (CD14(+

139 These assemblies were assayed for contiguity, internal consistency, and a

140 ents and children provided hair samples that were assayed for cortisol.

141 Plasma and CSF collected pre-ART were assayed for cytokines and chemokines using a 17-ple

142 The cage hosts were assayed for dipeptide binding using competition ESI

143 Positive samples were assayed for encapsidated EBV DNA, which is potentia

144 agnosed with prostate cancer, among whom 884 were assayed for ERG (426 ERG-positive).

145 (n = 44) from low-income-households in Dhaka were assayed for fecal indicator bacteria (enterococci,

146 control subjects (n = 16 pairs, 32 samples) were assayed for genome-wide messenger RNA (mRNA) expres

147 onamides differing in tails combination that were assayed for hCAs I, II, IV, and XII inhibition.

148 Paired semen and blood samples were assayed for HCV RNA levels.

149 Sera were assayed for IgE and gamma-tocotrienol levels.

150 Patient sera from days 1, 3 and 7 were assayed for IL-1beta and IL-10 by ELISA and compare

151 Patient sera from days 1, 3, and 7 were assayed for IL-1beta and IL-10 by enzyme-linked imm

152 trol subjects and patients with mastocytosis were assayed for IL-6, tryptase, and sIL-6R.

153 enantiomers and racemate of each metabolite were assayed for inhibition of the heat-shock response,

154 The plasma samples were assayed for insulin, glucose-dependent insulinotrop

155 after lipopolysaccharide-induced lung injury were assayed for leptin.

156 Both maternal and cord serum samples were assayed for levels of IgG1 and IgG3 specific for MS

157 ay for Campylobacter Stool and blood samples were assayed for markers of intestinal permeability and

158 PBMC from uveitis patients were assayed for MC5r expression on monocytes and A2Ar o

159 DILI patients (n = 98, n = 28, and n = 143) were assayed for microRNA-122 (miR-122), glutamate dehyd

160 livary samples from 118 predialysis patients were assayed for MMP-8 by immunofluorometric assay.

161 Feces and diet were assayed for Mn, fat, and gross energy (GE).

162 isolated with laser-capture microdissection, were assayed for mtDNA deletions, copy number, and prese

163 mutated auxin responsive elements (AuxREs), were assayed for nematode-dependent gene expression.

164 Both were assayed for OM using immunohistochemistry (IHC) for

165 Plasma samples were assayed for P-tau (using an antibody that specifica

166 Metabolites that signficantly increased were assayed for PMN priming activity in vitro.

167 cus at baseline and 4 weekly visits after MC were assayed for pro-inflammatory cytokines and HIV RNA.

168 nally, single viable epithelial cells (which were assayed for PTP activity immediately after collecti

169 Tissue samples from participants were assayed for PTX3 levels using enzyme-linked immunos

170 A set of these pleiotropic mutants were assayed for reduced toxicity in Drosophila melanoga

171 s of differentially abundant phloem proteins were assayed for SAR competence.

172 throughput genetics, 5560 minigene molecules were assayed for splicing in human HEK293 cells.

173 r STAT3-mutant patients and healthy controls were assayed for survival, apoptosis, proliferation, and

174 cipants the peripheral blood and nasal cells were assayed for T-cell activation and transcriptomic pr

175 ts displaying yellowing and inedible fruits, were assayed for the presence of phytoplasma DNA.

176 CCT5 complexes were assayed for their ability to suppress aggregation o

177 synthesized molecules, as a racemic mixture, were assayed for their EcDXR inhibitory potency.

178 asmodium falciparum DHODH, all the compounds were assayed for their effect on P. falciparum growth.

179 The two most effective compounds were assayed for their effect on several apoptosis marke

180 nse against this toxin, the two CPB variants were assayed for their trypsin sensitivity.

181 The samples were assayed for total antioxidant capacity and SOD acti

182 obtained during 7-12 years of effective ART were assayed for total HIV-1 DNA and 2-long terminal rep

183 nts with surveillance or indication biopsies were assayed for urinary CXCL10 using enzyme-linked immu

184 rospectively observed patients with melanoma were assayed for vitamin D and CRP.

185 de that occurred in Long Island, NY, in 2009 were assayed for XUV and PTA3 expression and compared wi

186 Interleukin-6 abundance could be assayed from concentrations as low as 50 pM (an order

187 RTL was assayed from blood or saliva samples.

188 Over 500 million CD4+ T cells were assayed from both participants in a humanized mouse

189 osterone, and cotinine (nicotine metabolite) were assayed from third trimester maternal sera.

190 mentalized in water-in-oil emulsion droplets are assayed, has emerged as a powerful format for direct

191 Peptides are assayed in a 96-well dot blot apparatus using membra

192 re flavor components of foods and spirits or are assayed in indirect methods for detecting the presen

193 When several genes are assayed in parallel these effects can be estimated a

194 icates of 15 samples (i.e., 120 analyses) to be assayed in <120 min.

195 The biosensor cells can be assayed in a high throughput, noninvasive manner, wit

196 d the transcriptomes of hundreds of cells to be assayed in an unbiased manner, opening up the possibi

197 g these molecules as adulteration markers to be assayed in combined IEF-immunoblotting procedures; th

198 Up to 2,000 cells can be assayed in one experiment at a rate of 6 s per cell.

199 e, any specific histone modification has not been assayed in more than a few individuals in the human

200 atio) overcomes this limitation but has only been assayed in small cohorts.

201 Solubilization has been assayed in the 4-50 degrees C range, and the result

202 tion in copy number (CNV) of specific HvCBFs was assayed in a panel of 41 barley genotypes using RT-q

203 is (Arabidopsis thaliana) stem wax secretion was assayed in a series of vesicle-trafficking mutants,

204 Mitochondrial H2O2 production was assayed in arterioles using mito peroxy yellow 1.

205 Concurrent serum cystatin C was assayed in banked serum samples.

206 For comparison of performance, CA19-9 was assayed in blinded independent sets of samples colle

207 Binding specificity was assayed in CD-1 and sEH knock-out mice and Papio anu

208 thylation at approximately 470,000 CpG sites was assayed in CD4(+) T cells using the Illumina Infiniu

209 Collagen content was assayed in cell culture supernatant.

210 BPA was assayed in first-trimester urine samples from 385 pa

211 Expression of MEIS1 was assayed in left ventricular cardiac tissue and prima

212 influence of PBO on Shh pathway transduction was assayed in mouse and human cell lines.

213 In vitro, caspase activity was assayed in Per1/2-specific small interfering RNA-tra

214 Diagnostic performance was assayed in simple broth-enriched blood samples and s

215 acylation on the prion-like seeding of SOD1 was assayed in spinal cord extracts of transgenic mice e

216 Under optimal conditions, method validation was assayed in the aqueous solutions.

217 rase activity with locomotor activity, which was assayed in the same flies with video recording.

218 Transport function of the mutants was assayed in transient transfectants by measurement of

219 sinophil-lineage-committed progenitors (EoP) were assayed in 21 severe eosinophilic asthmatics, 19 mi

220 anganese, molybdenum, nickel, lead and zinc) were assayed in a cohort of 949 individuals using mass s

221 transmitter mothers, and 47 infected infants were assayed in an HIV-1-inducible green fluorescent pro

222 Whole bacteria (Escherichia coli O157:H7) were assayed in buffer as well as 5% diluted human whole

223 ated rejection (AMR) + and 15 who were AMR-, were assayed in C1q-binding assays (C1q Screen; One Lamb

224 spot mutations in ESR1 and PIK3CA from ctDNA were assayed in clinical trial samples from ER+ metastat

225 Isolated proteins were assayed in ELISA and ELISA inhibition, basophil act

226 Factor XIII-A transcripts were assayed in human umbilical blood haemopoietic cell

227 e N3, N-Acetyl-L-Cysteine and Pluronic F-68) were assayed in order to improve production yields in a

228 Plasma BMP9 and BMP10 levels and activity were assayed in patients with PAH with GDF2 variants and

229 rotein, cytokines and chemokines, and leptin were assayed in plasma and corresponding biological proc

230 Biomarkers were assayed in plasma samples obtained from 341 subject

231 ycolytic flux and mitochondrial respiration, were assayed in real time for a panel of wild-type (wt)

232 Enantiomers of 2-methylbutyl acetate were assayed in red and white commercial wines from vari

233 Fifteen anionophores were assayed in single cells by monitoring anion transpo

234 health and self-renewal of the crypts which were assayed in situ by confocal fluorescence microscopy

235 SP and IL-1beta levels were assayed in the culture medium by ELISA.

236 Levels of MYOM3 fragments were assayed in therapeutic model systems: (1) restorati

237 Smooth-muscle cells from mouse tracheas were assayed in vitro for signaling pathways.

238 al trial patients with matched clinical data were assayed in vitro to determine murine macrophage upt

239 A selection of derivatives were assayed in vitro to indirectly evaluate their effec

240 and replication capacities of these mutants were assayed in vitro.

241 B-lymphocyte survival and Ig production were assayed in vitro.

242 d hits in the screen (first step) then could be assayed individually for inhibition of binding of liv

243 The biomarker panel was assayed on 590 urine specimens: 183 control samples,

244 Phosphoglucomutase 1 enzyme activity was assayed on cell extracts.

245 ian cancer, fresh frozen tumor DNA (n = 485) was assayed on Illumina Infinium HumanMethylation450 Bea

246 Cytosine-phosphate-guanine (CpG) methylation was assayed on the HumanMethylation450k microarray, and

247 CpG methylation in isolated B lymphocytes was assayed on the Illumina HumanMethylation450 BeadChip

248 Cell proliferation was assayed over time, and migration was evaluated by Li

249 The method allows for more samples to be assayed per unit time, it uses less solvent than othe

250 Three different approaches were assayed: pre-incubation of bacteria and compounds b

251 idence for inference and therefore could not be assayed precisely by TREDPARSE.

252 on with tetramethylammonium hydroxide (TMAH) was assayed prior to inductively coupled plasma mass spe

253 tome-wide m(6)A patterns in Arabidopsis have been assayed recently.

254 n two distinct chromatin features like these are assayed separately in populations of cells, it is im

255 tform in which many mutant mouse embryos can be assayed simultaneously, recovering robust morphologic

256 from 268 FFPE tumor samples, miR expression was assayed (simultaneously) using the nCounter human mi

257 t experiment, only limited number of samples were assayed, thus the classical 'large p, small n' prob

258 Three of the most used hydrolases were assayed to catalyze the process, and beta-glucosida

259 ion, gene expression, and protein expression were assayed to explore the effects of these inhibitors

260 chicken skin, porcine limb, and bovine liver were assayed to investigate the effect of anatomical het

261 holipid secretion and taurocholate transport were assayed to investigate the effect of selected drugs

262 This approach allows TREs to be assayed together with gene expression levels and othe

263 ertilized, fertilized and fertilized + DMPP) were assayed under two contrasting soil water content le

264 ssays by our device, a total of 1030 samples are assayed using three immunoassay methods to detect si

265 al model for toxicity and animal disease can be assayed using an electrochemical approach.

266 -translational regulatory mechanism that can be assayed using high-throughput mass spectrometry (MS).

267 pt levels from all nine csp genes have never been assayed using the same technique or in the same cel

268 Intracellular reactive species content was assayed using 2',7'-dichlorofluorescein diacetate dy

269 Salivary total alpha-synuclein was assayed using a highly sensitive Luminex assay and o

270 Spatial learning/memory was assayed using an automated radial 8-arm maze (RAM),

271 Function was assayed using dual cell two-electrode voltage clamp

272 Global gene expression was assayed using human microarray chips.

273 Oviductal telomere length was assayed using Southern blotting.

274 development for treatment of cancer patients was assayed using the MDM2-binding CueO enzyme.

275 anic acids in the examined pumpkin cultivars was assayed using the method of high performance liquid

276 ermined using HPLC, and antioxidant activity was assayed using the TEAC system based on the 2,2'-azin

277 umbilical vein endothelial cell permeability were assayed using a Transwell system.

278 IL-6 levels were assayed using an enzyme linked immunosorbent assay

279 The samples were assayed using commercially available ELISAs.

280 Glucose transport and consumption were assayed using ex vivo jejunal loops.

281 ygen species levels and mitochondrial stress were assayed using fluorogenic probes, microscopy, and f

282 baseline and after 12 months of peanut SLIT were assayed using ImmunoCAP for IgE and IgG4 against wh

283 , Wales, and Northern Ireland during 2014-15 were assayed using MATS and compared with 2007-08 data.

284 lume plasma samples (>20 ml) from 7 patients were assayed using Mega-iSCA, and HIV-1 RNA was quantifi

285 ve patch-test sites from non-atopic patients were assayed using quantitative PCR and immunohistochemi

286 g (20-24 years) and old (54-70 years) donors were assayed using ribonucleic acid sequencing (RNA-seq)

287 to ozone or short-fragment HA (sHA), and AHR was assayed via flexiVent.

288 rns were determined and functional diversity was assayed via measurements of potential enzyme activit

289 DNA from brain and blood tissue was assayed via the Illumina Infinium Methylation 450 K

290 Cytokine levels were assayed via multiplex enzyme-linked immunosorbent a

291 ues were mutated to alanine, and kcat and Km were assayed whenever kinase and/or cyclase activity was

292 ze them together, particularly when datasets are assayed with different technologies, because biologi

293 Survival of mammalian cells was assayed with good result.

294 ThDP was assayed with great sensitivity (3831mAM(-1)cm(-2)) o

295 rtichoke (Cynara scolymus L.) flower extract was assayed with the aim of replacing animal rennet in t

296 Primary tumors were assayed with a validated gene expression assay that

297 vors of B. tabaci infected by I. fumosorosea were assayed with I. fumosorosea.

298 All compounds were assayed with nNOS, their IC50, KI, and kinact value

299 the second year of antiretroviral treatment were assayed with three FDA-approved platforms: UltraSen

300 Splenocytes from VACV-WR-infected mice were assayed without prior expansion against the soluble