ライフサイエンスコーパス: microarray analyses

1 ed from the 3 groups of Ts cells and used in microarray analyses.

2 amplification of cDNA ends (RACE), and tiled microarray analyses.

3 , compared with non-tumor tissues, in tissue microarray analyses.

4 human blood basophils in whole-transcriptome microarray analyses.

5 inhibitory genes, as revealed by genome-wide microarray analyses.

6 r PARG in MCF-7 cells followed by expression microarray analyses.

7 h early OA and normal controls in 2 separate microarray analyses.

8 e bone microarchitecture and extract RNA for microarray analyses.

9 nisms, C/EBPalpha targets were identified by microarray analyses.

10 ease-associated mutations were identified by microarray analyses.

11 er, real-time reverse transcription-PCR, and microarray analyses.

12 d on expression of neuronal markers and cRNA microarray analyses.

13 ia to profile gene expression patterns using microarray analyses.

14 rum sensing are prominently displayed in our microarray analyses.

15 gene transcription profiles were studied by microarray analyses.

16 ve expression in reciprocal hybrids based on microarray analyses.

17 for 1, 4, 24, 48, and 72 h using large scale microarray analyses.

18 RNAs containing AREs were assessed by custom microarray analyses.

19 gene expression changes were compared using microarray analyses.

20 ed by helminth-specific immune responses and microarray analyses.

21 analyzed and also used in complementary DNA microarray analyses.

22 s were assessed by using whole transcriptome microarray analyses.

23 nd then subjected to miRNA and messenger RNA microarray analyses.

24 Microarray analyses also revealed the ectopic expression

25 odel of heterotopic heart transplantation by microarray analyses and a unique profile was detected in

26 Microarray analyses and confirmatory PCR and Western ana

27 CD8+ T cells in vitro were determined by DNA microarray analyses and confirmed by RT-PCR analyses and

28 Studies were also performed using microarray analyses and confirmed the biofilm-specific u

29 glycans bound by CHIKV, we conducted glycan microarray analyses and discovered that CHIKV preferenti

30 Microarray analyses and double-immunohistochemistry demo

31 antibody co-immunoprecipitation, followed by microarray analyses and downstream bioinformatics, 'RIP-

32 -regulated transcriptome via gene expression microarray analyses and ER ChIP-Seq, and to examine resp

33 with type 2 diabetes and control subjects by microarray analyses and found significant differences in

34 Here we performed microarray analyses and identified the basic helix-loop-

35 We conducted microarray analyses and in situ hybridization to discove

36 ng whole-exome sequencing and/or chromosomal microarray analyses and/or direct Sanger sequencing.

37 ent of larger sample collections, chromosome microarray analyses, and high-throughput sequencing.

38 prostate cancer relevant gene signatures in microarray analyses, and inhibited growth of ERG-positiv

39 he power of distributed computing to perform microarray analyses, and provides seamless access to res

40 global transcription patterns determined by microarray analyses, and the implications of the D39 gen

41 l subjects was interpreted to be "normal" by microarray analyses, and their rearrangements would not

42 lax treatment with death pathway inhibition, microarray analyses, and/or electron microscopy indicate

43 obulin reactivity data obtained from protein microarray analyses; and (ii) known protective antigens

44 Microarray analyses at key points during weight gain upo

45 s of BAHD genes by "in silico" northern- and microarray-analyses based on public databases, and by RT

46 cDNA microarray analyses bolstered by expression studies, flo

47 ated genes are not identified in traditional microarray analyses, but may theoretically be closely fu

48 le describes methods to improve the power of microarray analyses by defining internal standards to ch

49 Microarray analyses by several laboratories, including o

50 Protease- and protease inhibitor-specific microarray analyses (CLIP-CHIP) of laser-dissected leuko

51 Microarray analyses compared gene expression profiles of

52 Microarray analyses comparing resting latently infected

53 Microarray analyses comparing these cytologically and de

54 Microarray analyses confirm the reduction in IL-2 produc

55 Quantitative real-time PCR and microarray analyses confirmed PEDF down-regulation at th

56 Microarray analyses confirmed that IL-4 upregulated T(H)

57 Microarray analyses confirmed the differential expressio

58 Microarray analyses defined a set of defense-associated

59 Microarray analyses demonstrate statistically significan

60 Mutagenesis and microarray analyses demonstrate that VqmA activates vqmR

61 Microarray analyses demonstrate that Zbtb32(-/-) seconda

62 Synovial microarray analyses demonstrated decreased IgG reactivit

63 Microarray analyses demonstrated that MIM is the only me

64 and following temperature-shift, comparative microarray analyses demonstrated unequivocally that RpoS

65 tions of miR-301a to GALNT13 corroborated by microarray analyses demonstrating an inverse correlation

66 cDNA microarray analyses disclosed the targets affected by Ga

67 isomeric oligosaccharides and demonstrate by microarray analyses distinct binding activities of antib

68 In glycan microarray analyses, each CRD of Gal-8 showed different

69 From the microarray analyses emerged a lower expression of lipoge

70 Based on microarray analyses, endogenous gene expression is not s

71 d after 7 to 14 days of therapy was used for microarray analyses exploring EGFR pathway activity and

72 ranscriptomics was performed by whole genome microarray analyses followed by functional pathway analy

73 By contrast, using three microarray analyses followed by quantitative RT-PCR conf

74 elayed-early genes (DEGs, at 120 minutes) by microarray analyses, followed by quantitative real-time

75 as isolated from snap-frozen IEN lesions for microarray analyses, followed by quantitative reverse tr

76 Microarray analyses found that strains defective in PlcH

77 Microarray analyses have detected differential gene expr

78 Microarray analyses have led to the postulated existence

79 Microarray analyses have revealed that WNT5a acts to dow

80 Quantitative microarray analyses have shown increased expression of i

81 Microarray analyses have shown that ribavirin increases

82 Studies of the host response, including microarray analyses, have relied on the close relationsh

83 l analysis of primary library expression and microarray analyses, here we have shown that nuclear fac

84 The microarray analyses highlighted that BA strongly affecte

85 DNA microarray analyses identified 92 and 77 genes with alte

86 Genome-wide microarray analyses identified differentially expressed

87 Microarray analyses identified distinct gene level alter

88 Microarray analyses identified genes of the early and la

89 In addition, microarray analyses identified many G2/M genes as being

90 Gene microarray analyses identified potential molecular mecha

91 Whole-genome microarray analyses identified sod2, encoding the antiox

92 Moreover, microarray analyses implicated NICD-induced p63 down-reg

93 Data from gene expression microarray analyses imply that XBP1(S) acts through regu

94 istology was used to validate the results of microarray analyses in a larger cohort of long-term surv

95 ssion level changes in previous ChIP-seq and microarray analyses in Isl1-deficient cell lines, we fou

96 ute to excessive drinking, here we performed microarray analyses in laser microdissected rat ACC afte

97 consequences of loss of sacsin, we performed microarray analyses in sacsin knockdown cells and ARSACS

98 using AGO2 immunoprecipitation (AGO2-IP) and microarray analyses in two breast cancer cell lines, MCF

99 Tissue microarray analyses in two independent clinic cohorts al

100 Our structural and glycan microarray analyses, in the context of other high-resolu

101 DNA microarray analyses indicate that a limited number of ge

102 expression studies combined with genome-wide microarray analyses indicate that LecRK-VI.2 positively

103 Recent microarray analyses indicate that the BBA05 gene is diff

104 Expression microarray analyses indicated that CSF1, but not IL34, i

105 Microarray analyses indicated that Foxl1(+) cells expres

106 Microarray analyses indicated that insertion/deletion mu

107 Finally, microarray analyses indicated that underexpression of Pc

108 Comparison with parallel microarray analyses indicates a significantly greater se

109 te RNA coimmunoprecipitation with downstream microarray analyses indicates that GRN mRNA is directly

110 Well powered microarray analyses (N = 49 arrays), immunohistochemistr

111 We performed tissue microarray analyses of 205 human PDAC samples to measure

112 Microarray analyses of 80 LMSs and 24 leiomyomas showed

113 re we present single-nucleotide polymorphism microarray analyses of a single CLL patient over 29 year

114 Microarray analyses of apc mutants and Rdh5 morphants re

115 Similarly, microarray analyses of benign nevi and primary melanomas

116 Microarray analyses of brain gene expression in three se

117 We used whole-genome microarray analyses of CD138-enriched plasma cells from

118 Tissue microarray analyses of clinical lung and bladder tissues

119 Microarray analyses of COL and the isogenic bshA mutant

120 Microarray analyses of control- and vitamin D(3)-treated

121 the behavioral phenotype was examined using microarray analyses of dentate gyrus and nucleus accumbe

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

123 Microarray analyses of differentially expressed genes in

124 Using RNA immunoprecipitation and microarray analyses of endfeet, we discover FMRP-bound t

125 s of virulence gene expression is limited to microarray analyses of expression at selected time point

126 Microarray analyses of gene expression in rrp6Delta stra

127 Microarray analyses of genes expressed at these lower le

128 nal gene expression profiles is essential if microarray analyses of genetic profiles are to produce r

129 In microarray analyses of HeLa cells, a set of 19 genes rel

130 Microarray analyses of human platelet RNA demonstrated t

131 A3 and NR4A1, was altered by insulin in cDNA microarray analyses of human skeletal muscle, we studied

132 We have performed a series of microarray analyses of hyperpigmented compared with less

133 protein sequence phylogeny with whole-genome microarray analyses of induced cell cultures and develop

134 proteases involved, we performed genome-wide microarray analyses of invasive human melanomas and beni

135 Microarray analyses of isolated lymphatic endothelium fr

136 Microarray analyses of leukocytes in the infected Mavs(-

137 Microarray analyses of livers from db/db mice lacking MK

138 Microarray analyses of mature rodent microRNAs and quant

139 Microarray analyses of MCF-7 cells transfected with cont

140 Microarray analyses of MDA-MB-453 cells show that wherea

141 To address this issue, we performed microarray analyses of miRNA expression in the four prin

142 Microarray analyses of mouse hypothalamus cells expressi

143 Microarray analyses of mRNA isolated from primary normal

144 Microarray analyses of mRNA transcript expression identi

145 Microarray analyses of mRNAs over-expressed in strains l

146 Microarray analyses of nasal epithelial cells from acute

147 pression in p53 knockout cells, we conducted microarray analyses of p53(+/+) and p53(-/-) immortalize

148 Thus, microarray analyses of patient peripheral blood leukocyt

149 Microarray analyses of peripheral blood leukocytes have

150 We performed microarray analyses of peripheral blood mononuclear cell

151 schizophrenia and comparison subjects and by microarray analyses of pooled samples of individually di

152 Microarray analyses of primary PCA cells derived from th

153 of this disease in the kidney, we performed microarray analyses of renal biopsy samples from patient

154 Microarray analyses of rop6(DN) plants revealed that maj

155 ified previously as an altered transcript in microarray analyses of samples from human AD cases.

156 We compared the results of karyotype and microarray analyses of samples obtained after delivery.

157 ts unique to the Atoh1-derived lineage using microarray analyses of specific bHLH-sorted populations

158 Microarray analyses of spinal cord from two different se

159 Our microarray analyses of strain Newman also revealed that

160 By microarray analyses of strain Newman, we found that ClpC

161 In addition, tissue microarray analyses of TGCTs revealed that expression of

162 Microarray analyses of the effect of doxycycline on gene

163 On the basis of miRNA microarray analyses of the hippocampal total RNA isolate

164 We performed microarray analyses of the IkappaBalpha- and RelA-defici

165 Time-series microarray analyses of the mouse tissue identified the f

166 EMs based on in vitro drug sensitivities and microarray analyses of the NCI-60 cancer cell line panel

167 Laser microdissection-microarray analyses of the rgd2-R mutant shoot apical me

168 Microarray analyses of transcriptional profiles showed m

169 Using miRNA and gene expression microarray analyses of uterine tissues, we identified a

170 Microarray analyses of whole blood RNA revealed zinc-res

171 Microarray analyses on cells grown aerobically and anaer

172 favorable prognosis, we performed expression microarray analyses on FOXA1-positive and ER-positive (M

173 performed quantitative mass spectrometry and microarray analyses on protein and RNA isolated from the

174 We performed time course DNA microarray analyses on the mouse dentate gyrus to determ

175 We perform genome-wide microarray analyses, on parental, mybE- and dimB- cells,

176 The detailed structural and glycan microarray analyses presented here highlight the idea th

177 Microarray analyses previously revealed age-dependent ch

178 ong HemEPCs, HemECs, and cbEPCs, revealed by microarray analyses, provided further indication of an E

179 Here we used microarray analyses, real-time reverse transcription PCR

180 Microarray analyses, real-time RT-PCR, and in situ hybri

181 opy number by whole-exome sequencing and SNP microarray analyses, respectively.

182 scription-PCR, real-time PCR, and Affymetrix microarray analyses) resulted in the identification of f

183 However, microarray analyses reveal a group of genes for which ER

184 Microarray analyses reveal a unique but overlapping gene

185 Microarray analyses reveal that 300 genes are regulated

186 ure isolation of RNA from larval neurons and microarray analyses reveal that balboa is also highly en

187 Microarray analyses reveal that Slx/Slxl1 deficiency aff

188 Microarray analyses reveal that this respecification is

189 Seventeen comparative microarray analyses revealed 15 genes that were differen

190 Microarray analyses revealed 416 up- and 961 down-regula

191 Microarray analyses revealed 45 specific HS genes modifi

192 Microarray analyses revealed a cluster of 142 DCA- and I

193 Protein microarray analyses revealed a number of proteins with s

194 ic effect in female Wwox(hep-/-) mice, where microarray analyses revealed an increase in plasma trigl

195 Microarray analyses revealed differential regulation of

196 Microarray analyses revealed G-protein-coupled receptor

197 Moreover, microarray analyses revealed no compensatory changes in

198 Notably, microarray analyses revealed severe defects in signaling

199 Microarray analyses revealed similar profiles of induced

200 Furthermore, microarray analyses revealed that 125 and 19 genes were

201 MicroRNA microarray analyses revealed that 25 and 20 microRNAs we

202 Microarray analyses revealed that 40 and 186 genes had >

203 Microarray analyses revealed that a variety of antioxida

204 Microarray analyses revealed that Attim17-1 displayed al

205 Microarray analyses revealed that CBX6 governs a complex

206 Microarray analyses revealed that cdGMP stimulated the t

207 However, genome-wide microarray analyses revealed that each additional antige

208 Fluorescence-activated cell sorting and cDNA-microarray analyses revealed that each subclone was comp

209 Microarray analyses revealed that expression of several

210 Microarray analyses revealed that mds3 Delta/Delta cells

211 Microarray analyses revealed that mithramycin targeted m

212 Microarray analyses revealed that RA-treated CYP26A1(-/-

213 Expression microarray analyses revealed that RBP2 promoted expressi

214 Gene expression microarray analyses revealed that RSK1 orchestrated a pr

215 Microarray analyses revealed that Rsp represses 75 genes

216 Quantitative proteomics and microarray analyses revealed that the AbcR sRNAs predomi

217 Allelic exchange replacement and microarray analyses revealed that the Rrp1 regulon consi

218 Microarray analyses revealed that TRAF6-deficient CD8 T

219 Genome-wide microarray analyses revealed that unliganded PR-B induce

220 Furthermore, microarray analyses revealed that, compared to wild-type

221 Microarray analyses revealed transcriptomic differences

222 Focused microarray analyses revealed upregulation of IL-18 and I

223 In this study, we report lymphatic tissue microarray analyses, revealing for the first time stage-

224 vitro-cultured pollen tubes were assayed by microarray analyses, revealing over 500 transcripts spec

225 The results of glycoproteomic and microarray analyses show that FUT8 globally modifies sur

226 function of Rv2302 is still unknown, recent microarray analyses show that Rv2302 is upregulated in r

227 Microarray analyses show that SOCS3 modulates a distinct

228 Subsequent microarray analyses showed changes to gene signatures in

229 IAM accelerated chromosomal instability, and microarray analyses showed reduced NIAM mRNA expression

230 Carbohydrate microarray analyses showed that 222G variants bind a bro

231 Our previous microarray analyses showed that inhibition of Arabidopsi

232 Signaling/microarray analyses showed that P15-1 blocks RHAMM-regul

233 Furthermore, microarray analyses showed that Wilms tumor 1 (WT1) gene

234 Microarray analyses showed upregulation of 14q32 microRN

235 Moreover, luciferase reporter and microarray analyses suggested that B23 attenuated GCN5-m

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

237 Here, we describe novel probe-level microarray analyses that reveal connections between mRNA

238 Here, we show by glycan microarray analyses that the two mutations responsible f

239 Using Affymetrix microarray analyses, the global transcriptome was measur

240 Using microarray analyses these subjects showed a reduction in

241 We used microarray analyses to address the integration of the GA

242 Applying microarray analyses to an E. coli strain with impaired R

243 d immunohistochemical and whole human genome microarray analyses to characterize human skin in situ t

244 t cell functions, we carried out comparative microarray analyses to characterize the global transcrip

245 We used microarray analyses to demonstrate that Geminin overexpr

246 We used microarray analyses to determine changes in steady-state

247 Some centers are using DNA microarray analyses to determine the effects of botanica

248 Our aim was to utilize whole-genome microarray analyses to determine the true extent of gene

249 d the meaning of these changes, we conducted microarray analyses to examine the following: (i) the on

250 We used microarray analyses to explore the presence of known vir

251 We conducted gene expression microarray analyses to identify distinct and commonly dy

252 laria (ECM) and high-density oligonucleotide microarray analyses to identify host molecules that are

253 We used microarray analyses to identify male-biased, asexual fem

254 Using microarray analyses to identify mouse genes enriched in

255 the Idd9 genotype and its phenotype, we used microarray analyses to investigate the gene expression p

256 In this study, we performed time series microarray analyses to investigate transcriptome dynamic

257 unoprecipitation (CLIP) with subsequent ChIP microarray analyses to profile miR responses and their d

258 e quantitative polymerase chain reaction and microarray analyses to show that it represses the transc

259 ombinatorial approach, including mRNAseq and microarray analyses, to identify targets co-regulated by

260 Current microarray analyses typically focus on identifying diffe

261 Microarray analyses unexpectedly demonstrated that SpxR

262 s in global gene expression were observed in microarray analyses upon loss of Ada3.

263 Whole-genome microarray analyses using a single-nucleotide polymorphi

264 We conducted spotted microarray analyses using arrays harboring 8308 human ge

265 okines in HSCs and progenitors, we performed microarray analyses using Lineage(-) Sca-1(+) c-Kit(+) (

266 erformed oligonucleotide-based transcriptome microarray analyses using RNA isolated from mutant fly s

267 Microarray analyses using the Affymetrix soybean GeneChi

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

269 oduce superior results in the sandwich ELISA microarray analyses we performed.

270 Here, using microarray analyses, we demonstrate that increased expre

271 Using both protein immunohistochemistry and microarray analyses, we demonstrate that MERTK expressio

272 Using microarray analyses, we find that myosin-X (Myo10) is a

273 Integrating ChIP-Seq and microarray analyses, we identified 645 basal and 654 ind

274 Using microarray analyses, we identified ABCG1, encoding an AB

275 ng the down-regulated genes revealed by cDNA microarray analyses, we identified Aurora-A, a centrosom

276 Employing 2 independent, genome-wide microarray analyses, we identified CD200 as a highly dyn

277 Combination of in silico prediction and microarray analyses, we identified that miR-4487 and miR

278 uencing, in vivo functional studies and gene microarray analyses, we investigated the role of WWOX in

279 Through microarray analyses, we previously identified in potato

280 By microarray analyses, we showed that younger women (<55 y

281 unds in athymic mice, and biopsy samples for microarray analyses were collected at multiple in vitro

282 Gene expression microarray analyses were conducted on blood samples from

283 Affymetrix MicroArray analyses were conducted on human NP cells and

284 Microarray analyses were conducted to evaluate the paraq

285 of hydrogen limitation and growth rate, and microarray analyses were conducted.

286 Comparative microarray analyses were performed against publicly avai

287 Microarray analyses were performed to analyze the mechan

288 Biochemical and microarray analyses were performed to identify different

289 Microarray analyses were performed to identify genes exp

290 Microarray analyses were performed to profile genome-wid

291 Microarray analyses were performed, and confirmatory rea

292 under these conditions, and gene expression microarray analyses were performed.

293 ed with copper under multiple conditions and microarray analyses were previously performed to better

294 In this study, microarray analyses were used to examine a set of potent

295 ed and an integrated series of bioinformatic microarray analyses were used to identify altered genes

296 Microarray analyses were used to identify impacted recep

297 Microarray analyses were used to: identify and functiona

298 Here, we combined extensive statistical microarray analyses with behavioral testing to comprehen

299 as aeruginosa was characterized by phenotype microarray analyses with single and double mutants and t

300 Microarray analyses with ST-2 bone stroma cells demonstr