ライフサイエンスコーパス: microarray

1 genotyped 34,174 samples using a whole-exome microarray.

2 ollowed for six-months against a Ct-proteome microarray.

3 ing epitopes were identified by oligopeptide microarray.

4 and a hepatocellular carcinoma (HCC) tissue microarray.

5 pression in purified B cells was measured by microarray.

6 ulting compounds were used to construct a HS microarray.

7 earts at postnatal day (P) 1, P7 and P28 via microarray.

8 immunofluorescence in the PD-L1 index tissue microarray.

9 was subjected to transcriptome profiling by microarray.

10 on of lncRNAs and mRNAs was determined using microarray.

11 , or comparatively at the genome level using microarrays.

12 n assessments of the allograft tissue, using microarrays.

13 munostaining for CYP27A1 in annotated tissue microarrays.

14 mical microscopy (SECM) imaging of molecular microarrays.

15 is able to identify viable Legionella on DNA microarrays.

16 using Ras-functionalized supported membrane microarrays.

17 ene-expression changes using gene expression microarrays.

18 cross multiple regions in GBM patient tissue microarrays.

19 - and IgG4 -specific fluorescence on silicon microarrays.

20 riation by genotyping, with the Ovine SNP50K microarray, 394 individuals from five populations of fat

21 of 18 [27.8%]; P = .02) than for chromosomal microarray (8 of 101 [7.9%]).

22 er (ACC) were first screened by Taqman Human Microarray A-cards.

23 Net was generated from 57 rice anther tissue microarrays across all developmental stages.

24 cular tools for glycoscience, such as glycan microarrays, affinity resins, and reference standards.

25 then examined using whole-genome expression microarrays (Affymetrix).

26 Microarray analyses and confirmatory PCR and Western ana

27 We conducted microarray analyses of DF-1 and CEFs, under both normal

28 Microarray analyses revealed G-protein-coupled receptor

29 Despite this reduction, microarray analyses suggested the existence of a residua

30 Using microarray analyses these subjects showed a reduction in

31 Using cell-based knockdown approaches and microarray analyses we found that (1) MYT1L is required

32 Whole-transcript microarray analysis (770,317 probes, interrogating 28,85

33 Microarray analysis and comparison with human DKD showed

34 Microarray analysis and real-time PCR were used to exami

35 However, on microarray analysis C-82 treatment strongly up-regulated

36 In addition, the results of the microarray analysis corroborated previous findings conce

37 PBMC microarray analysis detected 117 genes that were differe

38 Although microarray analysis has identified localized determinant

39 Microarray analysis identified reduced reticulon-1 mRNA

40 Microarray analysis identified six miRNAs differentially

41 s in this study highlights the importance of microarray analysis in adults with unexplained childhood

42 An RNA microarray analysis of B16F10-Nex2 melanoma cells with S

43 Transcriptomic profiles were generated by microarray analysis of blood from 610 patients with asth

44 Consequently, gene expression microarray analysis of CD4(+) T cells following P. yoeli

45 Differential cell counts, microarray analysis of cell pellets, and SOMAscan analys

46 By microarray analysis of DeltapflB, differential regulatio

47 ha on molecular pathways during nephritis by microarray analysis of glomerular extract gene expressio

48 Time-course microarray analysis of glomeruli during nephrotoxic seru

49 Microarray analysis of heart tissue RNA revealed that th

50 -IRIS, we performed longitudinal whole-blood microarray analysis of HIV-infected patients with TBM an

51 Microarray analysis of IL-17 family cytokines was perfor

52 Microarray analysis of IRE1alpha- and XBP1-depleted cell

53 Microarray analysis of miR-183 family cluster overexpres

54 By performing a microarray analysis of mouse prostate tissue to screen d

55 We first performed a microarray analysis of mPFC gene expression changes indu

56 Microarray analysis of mRNA from Ctcf CKO mouse hippocam

57 Microarray analysis of receptor activator of NF-kappaB l

58 enes involved in this process we performed a microarray analysis of RPE cells pre- and post-FR treatm

59 mechanisms through which ES affects repair, microarray analysis of wound biopsy samples was performe

60 re measured using reverse transcriptase PCR, microarray analysis or high-throughput sequencing.

61 1) to 10(5)GUmicroL(-1) were analyzed on the microarray analysis platform MCR 3.

62 Microarray analysis revealed a significantly modified pr

63 Microarray analysis revealed enhancements in IL-6- and I

64 Tissue microarray analysis revealed that >98% of ovarian cancer

65 Microarray analysis revealed that 214 mRNAs were upregul

66 Microarray analysis revealed that OsKO2, which encodes e

67 mRNA profiling by microarray analysis revealed that the expression of PTPR

68 Microarray analysis showed enrichment of DNA replication

69 MiRNA microarray analysis showed OA specific exosomal miRNA of

70 Liver microarray analysis showed that high mIndy expression wa

71 Tissue microarray analysis showed that the disease-free surviva

72 Microarray analysis suggested downregulated macrophage m

73 In this study, we observed by microarray analysis that several type I IFN-associated g

74 We conducted an miRNA microarray analysis using RNA from a parental cell line,

75 Microarray analysis was performed and gene expression ch

76 Microarray analysis was performed on blood samples from

77 The microarray analysis was performed on infected Arabidopsi

78 20 most differentially expressed genes after microarray analysis were identified across all condition

79 nificant differences at transcript levels by microarray analysis were identified for macrosclerid cel

80 lecular profiling, including DNA methylation microarray analysis, and did unsupervised class discover

81 and during akinete differentiation using DNA microarray analysis, and found to include multiple genes

82 Microarray analysis, quantitative RT-PCR, and immunoblot

83 miRNA microarray analysis, reverse transcription polymerase ch

84 In this study we analyzed, using microarray analysis, the bacterial modulation of miRNAs

85 Based on microarray analysis, we have identified a role for micro

86 microglial exosomes were collected for miRNA microarray analysis, which showed that the expression le

87 ose tissue biopsy samples were collected for microarray analysis.

88 d with H pylori P12 wt or P12Deltacgt, using microarray analysis.

89 re collected to measure gene expression with microarray analysis.

90 Gene expression was determined using microarray analysis.

91 genes, monitored by both flow cytometry and microarray analysis.

92 orted tonsillar ILC3s were assessed by using microarray analysis.

93 activation, combining polysome profiling and microarray analysis.

94 les per group was employed in transcriptomic microarray analysis.

95 7 and screened for possible effects by mRNA microarray analysis.

96 ults to those from four previously published microarray and BeadChip analyses of the same cell popula

97 Furthermore, microarray and chromatin immunoprecipitation sequencing

98 ponents were analyzed in sera using allergen microarray and compared between 5 French regions accordi

99 d significance was evaluated by using tissue microarray and immunohistochemistry.

100 , we performed a correlative gene-expression microarray and in vivo imaging analysis, and identified

101 Tissue microarray and microfluidics staining methods have emerg

102 provides a wealth of data but utilization of microarray and next generation sequencing (NGS) data for

103 allows visitors to access already processed microarray and NGS data from non-human primate models of

104 Further analysis by microarray and qPCR indicated that the expression of FT

105 Microarray and qRT-PCR analysis of human hair follicles

106 nd gene expression profiles were compared by microarray and quantitative PCR analyses.

107 Microarray and quantitative polymerase chain reaction (q

108 with no history of periodontitis (H), using microarray and quantitative reverse transcription polyme

109 roxic lung injury using the omics platforms: microarray and Reverse Phase Proteomic Array.

110 concentrations of ammonium were analyzed by microarray and reverse transcription quantitative PCR, a

111 ation of GWAS and eQTL data from the TwinsUK microarray and RNA-Seq cohort in lymphoblastoid cell lin

112 Extension of the experiment to microarray and RNA-seq data from tendon identified gende

113 ent underlying biology of gene expression in microarray and RNA-Seq data.

114 Transcriptomic approaches (microarray and RNA-seq) have been a tremendous advance f

115 Here we show by microarray and RNAi that guanine nucleotide-binding prot

116 Recently, the high-throughput microarray and sequencing technologies have promoted the

117 d the production of a low-cost polymer based microarray and tested its analytical performance for int

118 Using Biolog phenotype microarrays and comparative metabolite profiling we demo

119 mance using 16S rRNA gene-based phylogenetic microarrays and flow cytometry.

120 Here, using human lung cancer tissue microarrays and fresh frozen tissues, we found that the

121 lysis of data collected from 57 carbohydrate microarrays and identified molecular markers reflecting

122 (TD) children were compared by using lectin microarrays and lectin-magnetic particle conjugate-assis

123 ication of high throughput platforms such as microarrays and mass-spectrometry has indicated multiple

124 ents, immunohistochemical staining of tissue microarrays and mRNA expression analyses revealed a posi

125 ghly complex molecular technologies, such as microarrays and next-generation sequencing, have identif

126 Microarrays and other surface-based nucleic acid detecti

127 d gene expression changes using high-density microarrays and pathway analyses (Gene Ontology, Kyoto E

128 Using custom microarrays and proteomics to characterize expression re

129 Microarrays and RNA sequencing are widely used to profil

130 Samples were genotyped via microarray, and SNPs that could not be genotyped were im

131 sing reverse transcription-quantitative PCR, microarrays, and flow cytometry, or indirectly, by the p

132 ation sequencing (ChIP-seq), protein-binding microarrays, and transcriptomic approaches.

133 ulfated proteins in yeast and human proteome microarrays, and we expect such approaches to contribute

134 We developed a high-throughput quantitative microarray antibody capture assay for anti-HDV immunoglo

135 The quantitative microarray antibody capture assay's unique performance c

136 as hybridized onto Nanostring human v2 miRNA microarray array and expression data were analyzed on nS

137 RNA-Seq has supplanted microarrays as the preferred method of transcriptome-wid

138 The platforms included (i) cellulose-coated microarray assay, (ii) enzyme-linked immunosorbent assay

139 continuous titer measurement from a protein microarray assay.

140 plications to performing such analyses using microarray based approaches are discussed.

141 edial-lateral axes of the chick tectum using microarray based transcriptional profiling and identifie

142 A comprehensive DNA microarray-based assay was performed on all isolates to

143 We conducted an eQTL investigation of microarray-based gene and exon expression levels in whol

144 Using microarray-based gene expression profiling, we show that

145 Microarray-based genome-wide profiling indicated up-regu

146 jor CM proteins were measured with a peptide microarray-based immunoassay.

147 Microarray-based initial studies on the mechanism of act

148 Genome-wide microarray-based transcription analysis identified overe

149 Microarray-based transcriptomic analysis on iN cells fro

150 and bioluminescence) are downregulated, and microarray-based transcriptomics demonstrating that indo

151 Many methods exist for assessing CNAs using microarrays, but considerable technical issues limit cur

152 n-vaccinated mice and show that high-quality microarrays can be performed from RNA isolated from CD15

153 carbapenemase genes using a Check-MDR CT101 microarray (Check-Points, Wageningen, the Netherlands) a

154 a distinct location of the surface of a DNA microarray chip through specific hybridization with comp

155 Here we generated a set of genomic microarray chips covering about 8000 bp flanking the pre

156 Glycan microarrays containing a series of synthetic glycans res

157 Here, we created high-density carbohydrate microarrays containing chemically extracted cell wall po

158 s examined by immunohistochemistry on tissue microarrays, containing EAC, high grade dysplasia (HGD),

159 acent pancreatic tissue in 3 separate tissue microarrays covering 38 patients.

160 Cytogenetics 2.7 M Microarrays/CytoScan HD arrays allowed mapping of homozy

161 munohistochemistry (IHC) staining and public microarray data analysis showing that DACH1 was higher i

162 t feature selection approaches developed for microarray data cannot handle multivariate temporal data

163 Expression microarray data from the kidney cortex and medulla, live

164 The HS microarray data guided the selection of compounds that c

165 ounding effects of ITH using gene expression microarray data obtained from multiple tumour regions of

166 involved in SA-induced folate accumulation, microarray data of responsive genes in Arabidopsis were

167 We used microarray data on whole blood from two independent case

168 Integration analysis of mRNA-miRNA microarray data revealed a potential role of 51 dysregul

169 Analysis of ovarian cancer gene microarray data showed that higher expression of Nectin-

170 and an R function which uses DNA methylation microarray data to infer tumor subtypes with the conside

171 nomes pathway enrichment cluster analyses of microarray data using wild-type and c-Jun-deleted macrop

172 n the present study, the whole transcriptome microarray data were generated from peripheral blood mon

173 ds developed for bulk RNA sequencing or even microarray data, and the suitability of these methods fo

174 ressed miRNAs in human cancers obtained from microarray data.

175 f false positives and false negatives in the microarray data.

176 uency) copy-number variants (CNVs) using SNP microarray data.

177 were also compared with a publicly available microarray dataset from a study of American college stud

178 study were also validated in an independent microarray dataset generated from MS hippocampus.

179 e set enrichment and pathway analysis of the microarray dataset showed enrichment in axon guidance an

180 e applied the general mixture model to three microarray datasets for lung cancer studies.

181 The microarray datasets from nine rice male sterile mutants,

182 d EBI ArrayExpress for human gene expression microarray datasets.

183 been done in maize (Zea mays), mostly using microarray datasets.

184 on of two cores of breast tumour tissue in a microarray, done in a central laboratory by technicians

185 veloped two species-specific gene expression microarrays, each targeting over 12 000 transcripts, inc

186 vidually addressable electrochemical droplet microarray (eDMA).

187 ginally designed to work with human or mouse microarray expression data for 21 cell or tissue (C/T) t

188 ed and subsequently used to develop a glycan microarray for high-throughput, fluorescence-based scree

189 The working range of the silicon microarray for total hen's egg-specific IgE was comparab

190 hemistry and in situ hybridization on tissue microarrays for 958 tumors.

191 The results demonstrate the utility of microarrays for high-resolution mapping of antibody resp

192 Last, the application of spheroid microarrays for spheroid-based drug screens was demonstr

193 for multiplexed NIR-fluorescence enhancement microarrays, for early cancer diagnosis and therapeutic

194 chemical markers (n = 727 women) and Agilent microarrays, for MammaPrint risk scoring (n = 652 women)

195 A polymer microarray formed from commercially available monomers t

196 blood mononuclear cells were quantified via microarray gene chips.

197 Microarray gene expression analysis indicated downregula

198 Importantly, the bioinformatics analysis of microarray gene expression data derived from a set of hi

199 Paired microarray gene expression data derived from peripheral

200 n an assay on the NanoString platform, using microarray gene expression data of matched fresh frozen

201 tein interaction (PPI) network, we simulated microarray gene expression data under case and control c

202 Microarray gene expression profiling of IVIg-generated p

203 We performed microarray gene expression profiling on a large sample o

204 onal eQTL analysis in 4,896 peripheral blood microarray gene expression samples.

205 Microarrays have allowed the interrogation of thousands

206 Single molecule microarrays have been used in quantitative proteomics, i

207 suicide and depression using oligonucleotide microarrays have often failed to distinguish these two p

208 tive reverse transcription-PCR (qRT-PCR) and microarrays have shown a significant transient upregulat

209 r IgE reactivity to a comprehensive panel of microarrayed HDM allergen molecules and to S. aureus and

210 ablished using the shotgun human milk glycan microarray (HM-SGM-v2) showed fair-to-poor correlation,

211 uctures has been demonstrated by fluorescent microarray immunoassay and LSPR measurements, recording

212 l (electron microscopy), biochemical (GC-MS, Microarray immunoassay, Rock-Eval) and spectroscopic (ED

213 DFIC interaction, we performed a genome-wide microarray in intact and MDFIC-deficient A549 cells that

214 ication of the phase III randomized MINDACT (Microarray in Node-Negative and 1 to 3 Positive Lymph No

215 NADSYN1 and TCF7) that were concealed using microarrays, including four non-coding RNAs.

216 A comparative microarray investigation of the EPiR response reveals a

217 This suggests that the copoly(DMA-NAS-MAPS) microarray is a low-cost, self-producible alternative to

218 Our plasmonic microarray is composed of gold nanohole sensor arrays th

219 In human prostate tumor tissue microarrays, loss of PTEN correlates with increased PTK6

220 Microarray mapping and RNase H cleavage identified acces

221 O specificities of lectins established using microarrays may not accurately reflect their true HMO-bi

222 ic data while new data types include protein microarray, metabolic pathways, compounds, quantitative

223 The microarray method and reaction system were optimized.

224 Microarray methods provided new information in 47% of th

225 Using GEM microarray model, we found ARF dysregulates Hippo and Wn

226 We explored a tissue microarray of 1,432 primary breast tumors from patients

227 Analyzing a tissue microarray of 608 breast carcinoma patient specimens, we

228 We constructed a tissue microarray of 999 colon cancer specimens from patients w

229 The microarray of antibody droplets can be prespotted on a s

230 genes indicative of AMI were nominated from microarray of enriched CEC samples, and then verified fo

231 vation, we performed large-scale comparative microarrays of murine bone marrow-derived mast cells and

232 Microarrays of proximal tubular cells and podocytes with

233 Using microarrays of synthetic oligosaccharides, the LM26 epit

234 PennCNV-Affy software to analyze Affymetrix microarrays of the first 152,728 genotyped individuals.

235 rwent whole-genome sequencing and expression microarray on bulk biospecimens.

236 recombinant HDV delta antigen is printed by microarray on slides coated with a noncontinuous, nanost

237 Applying genome-wide miRNA microarrays on the phenotypically distinct smooth muscle

238 e to the expression data generated by either microarray or RNA-seq platforms.

239 used simulation data as well as experimental microarray or sequencing data to illustrate the usefulne

240 erimental methods, including protein binding microarrays (PBM) and high-throughput SELEX (HT-SELEX),

241 motifs from methods such as protein-binding microarrays (PBMs) and systematic evolution of ligands b

242 Using a high-resolution microarray platform and established methods to assess co

243 ofile in childhood obesity using an Illumina microarray platform on sorted monocytes of 35 obese chil

244 or living cell screenings using the droplet microarray platform with the sequential electrochemical

245 of publicly deposited data across a range of microarray platforms and RNA-Seq data.

246 the accuracy and information obtained by two microarray platforms applied on a well-characterized ped

247 U133 Plus 2.0 are the two most commonly used microarray platforms for human samples; the HG-U133 Plus

248 The microarray platforms studied here demonstrated acceptabl

249 lations between RNA sequencing (RNA-seq) and microarray platforms, but have not studied their concord

250 The main read-out methods of most microarray platforms, however, are based on optical tech

251 We assessed the microRNA (miRNA) microarray profile of tissues derived from Lebanese pati

252 Microarray profiles in CCA samples (n = 104) showed decr

253 AF onset) TG mice were investigated by mRNA microarray profiling in comparison with age-matched wild

254 s differentially expressed, using NanoString microArray profiling, were validated with qPCR.

255 signment approaches to simulate results from microarray/qRT-PCR platforms and a local probabilistic m

256 al approaches, such as bisulfite sequencing, microarrays, quantitative real-time PCR, colorimetry, Ra

257 ts of transcriptional profiling using custom microarrays representing 1,042 genes in the drosophilid

258 ntitative polymerase chain reaction and mRNA microarray, respectively, on lung tissue of 30 patients

259 qRT-PCR analysis confirmed the microarray results, that KIR2DL4, IL6 and SELE were high

260 , and we replicated previous human and mouse microarray results.

261 all transcriptome-wide PE analyses to date (microarray, RNA-Seq and PAS-Seq) are NRIP1 (RIP140), a t

262 and immunoprecipitation, mass spectrometry, microarray, several knockdown approaches, CRISPR-Cas9, a

263 these genetic connections, splicing-specific microarrays show that H2A.Z and the Swr1 ATPase are requ

264 f the antibody solutions nor a sophisticated microarray spotter is needed.

265 Several large scale tissue microarray studies have revealed that the expression of

266 graphy-mass spectrometry (HPLC-MS) assay and microarray study were conducted on transcriptome changes

267 iation studies are typically performed using microarray technologies that only assay a very small fra

268 ng, quantitative real time PCR (qRT-PCR) and microarray technology besides novel techniques based on

269 ssinus were tested by means of ImmunoCAP and microarray technology, respectively, in sera collected a

270 Microarray testing offers opportunities for improved sIg

271 in clinical diagnostics using cytogenetic or microarray testing.

272 ed target genes of Arabidopsis Thaliana from microarray time series data obtained under multiple biot

273 hodological approach that combines Phenotype MicroArray(TM) and SSR genotyping appeared useful to ass

274 ery different metabolic profile by Phenotype MicroArray(TM).

275 In this study, the application of tissue microarray (TMA) analysis to a sample of femoral bone sp

276 early stage NSCLC from digitized H&E tissue microarray (TMA) slides.

277 imaging have demonstrated that large tissue microarrays (TMA) can be imaged in a matter of minutes.

278 two independent clinical cohorts from tissue microarrays (TMA: n = 208 patients) and whole sections (

279 ican American (AA) and 144 White TNBC tissue microarrays (TMAs) pooled from four hospitals.

280 ed the ability of the polymer coated silicon microarray to be comparably sensitive to the ImmunoCAP I

281 this study, we used a variola virus proteome microarray to characterize and differentiate antibody re

282 We have used this microarray to interrogate the C-terminal tails of a smal

283 evaluation, and high-resolution whole genome microarray to investigate for a genetic causal link to i

284 In light of these findings, we used a microarray to investigate the expression patterns of oth

285 eQTL integration have predominantly employed microarrays to quantify gene-expression.

286 ne expression was compared quantitatively by microarrays using RNA extracted from all three condition

287 The mimotope microarray was applied to the analysis of fumonisin B1 i

288 son, a flow-based chemiluminescence (CL) DNA microarray was developed that is able to quantify viable

289 A 6 x 6 recessed Au nanoring-ring electrodes microarray was fabricated over a glass substrate using f

290 m, whereas for total cow's milk, the silicon microarray was less sensitive.

291 Comparative ImmunoCAP ISAC microarray was performed in patients with food allergy o

292 In this cross-sectional study, genome-wide microarray was used to evaluate a cohort of 143 adults w

293 Using a circRNA microarray, we identified 226 differentially expressed c

294 on pipelines and an exome-tiling chromosomal microarray were also applied to identify intragenic CNVs

295 The results of the mRNA microarray were confirmed in isolated CD4+T cells and in

296 Carbohydrate microarrays were generated to enable the detailed epitop

297 Microarrays were used to compare the skin and tuber-fles

298 n sequencing, autozygosity mapping, and apex microarray, were tried to reach a diagnosis; all partici

299 wo key contemporary techniques in the field: microarrays, which quantify a set of predetermined seque

300 Probing a custom-designed proteome microarray with sera from 35 healthy US adults revealed