ライフサイエンスコーパス: global gene expression

1 pact of CovS on CovR phosphorylation and GAS global gene expression.

2 in genes, with minimal off-target changes in global gene expression.

3 rnative to microarray-based methods to study global gene expression.

4 of human genomes and their association with global gene expression.

5 d the effects of single copy mutant K-Ras on global gene expression.

6 imilar effects to overexpressing HP1alpha in global gene expression.

7 romatin and effects of Gbeta(2) depletion on global gene expression.

8 oral program integrating DNA replication and global gene expression.

9 its expression in NIH 3T3 cells and analyzed global gene expression.

10 of diverse transcription factors that drive global gene expression.

11 es, thereby acting as a positive modifier of global gene expression.

12 SC lots from each center were compared using global gene expression.

13 logy to characterize the temporal changes in global gene expression after contusive SCI in mice.

14 neural crest-derived cells (CNCCs) to define global gene expression along the dorsoventral axis of th

15 called RNA-seq has been widely used to study global gene expression, alternative exon usage, new exon

16 Quantitative and global gene expression analyses (microarray and RNAseq)

17 Unbiased global gene expression analyses demonstrate that MECP2 f

18 Global gene expression analyses following Setd8 knockdow

19 Global gene expression analyses reveal that trisomy 12 p

20 Furthermore, global gene expression analyses show that GW9662 treatme

21 Global gene expression analyses suggested that Rb mainta

22 Global gene expression analyses were conducted using spl

23 s that integrates comparative genomics data, global gene expression analyses, and intrinsic propertie

24 terol metabolism were assessed together with global gene-expression analyses in peripheral blood mono

25 RNA-sequencing (RNA-seq) allows global gene expression analysis at the individual transc

26 Global gene expression analysis identified a molecular s

27 Global gene expression analysis identified ablated Tiam2

28 Global gene expression analysis identified that PELP1-cy

29 Global gene expression analysis in AD-HIES patient skin

30 Global gene expression analysis indicated that 47% of an

31 A global gene expression analysis of AS versus empty vecto

32 Here, we performed global gene expression analysis of human dermal papilla

33 Global gene expression analysis of infected hNPCs reveal

34 Global gene expression analysis of KDM3A-depleted cells

35 Global gene expression analysis of knockout hearts befor

36 Global gene expression analysis of mesenchymal stem cell

37 A global gene expression analysis of S100A12-activated mon

38 cale experimental approach that involved the global gene expression analysis of strains D23580 and 4/

39 sequencing, X-chromosome inactivation study, global gene expression analysis on Epstein-Barr virus (E

40 Global gene expression analysis on liver identified Tpcn

41 While global gene expression analysis profiles the average exp

42 This global gene expression analysis provides new insights in

43 Global gene expression analysis revealed changes in gene

44 Global gene expression analysis revealed marked differen

45 Global gene expression analysis revealed that genes upre

46 Global gene expression analysis revealed that infection-

47 Consistent with methylome alterations, global gene expression analysis reveals that the vast ma

48 x5 and other B-lineage-associated genes, and global gene expression analysis suggested that the reduc

49 ation assays, surface antigen profiling, and global gene expression analysis to identify the lines ex

50 h infection assays, genome resequencing, and global gene expression analysis to study the effect of t

51 To test for MR function in skeletal muscle, global gene expression analysis was conducted on human m

52 Global gene expression analysis was performed on HMEC li

53 Global gene expression analysis, data intersection, path

54 Global gene-expression analysis has shown remarkable dif

55 Global gene-expression analysis of the transgenic plants

56 Global gene-expression analysis showed that the steroid

57 xpression was defined by Hic-5 depletion and global gene-expression analysis.

58 early muscle marker genes are reprogrammed, global gene expression and accessibility changes are sti

59 By integrating global gene expression and computational analyses, we di

60 Based on comparisons of global gene expression and DNA methylation between the w

61 Using global gene expression and DNA methylation profiling, we

62 nduced DNA methylation, we analyzed parallel global gene expression and DNA methylation using normal

63 igate this effect, we have characterized the global gene expression and epigenetic profiles of multip

64 ts that overexpressing these proteins had on global gene expression and freezing tolerance.

65 MicroRNAs (miRNAs) are regulators of global gene expression and function in a broad range of

66 We used global gene expression and genome-wide binding analyses

67 nd loss-of-function approaches combined with global gene expression and genome-wide transcription fac

68 e findings indicate that lincRNA-p21 affects global gene expression and influences the p53 tumor supp

69 in longevity across mammals at the level of global gene expression and metabolite levels and reveals

70 te the validity of this concern, we compared global gene expression and methylation profiles between

71 Here, we integrated global gene expression and proteomic analyses and identi

72 Global gene expression and secretome analysis reveals th

73 ounteract the effects of ATF3 or CSL loss on global gene expression and suppress CAF tumor-promoting

74 hereas filaggrin haploinsufficiency affected global gene expression and was characterized by a type 1

75 Global gene-expression and methylome analyses of TKO EBs

76 (PEV), and the link among rDNA copy number, global gene expression, and chromatin regulation.

77 ing system to control SpeB production, alter global gene expression, and enhance virulence.

78 Although average telomere length, global gene expression, and microbiome changes returned

79 f the role of the Y chromosome in modulating global gene expression, and suggest a link with modifica

80 Using an unbiased global gene expression approach in conditional p120-cate

81 s, there are also fundamental differences in global gene expression as pathogenic filamentous fungi u

82 sis was employed to determine alterations in global gene expression associated with miR-10a in embryo

83 In the present study, we investigated the global gene expression associated with stomach carcinoge

84 Global gene expression at 8 and 24 h was analyzed by dee

85 Our previous map of global gene expression, based on ~400K single nucleotide

86 vaccine and performed a timed assessment of global gene expression before and after vaccination.

87 A comparison of global gene expression between severe and mild disease c

88 red the relationship between sexual mode and global gene expression by comparing two selfing species,

89 te a statistical model for the regulation of global gene expression by multiple regulatory programs a

90 RNAi and further determination of changes in global gene expression by RNAseq, and composition of pri

91 can alleviate shRNA-mediated perturbation of global gene expression by specifically de-repressing off

92 Global gene expression can be quantified from the number

93 ssess a highly homogeneous morphology, size, global gene expression, cellular composition, and struct

94 all relationship between cell commitment and global gene expression changes are still unclear.

95 Global gene expression changes associated with upregulat

96 Further analysis of global gene expression changes during reprogramming reve

97 about the effects of caffeine stimulation on global gene expression changes in neurons.

98 We analyzed global gene expression changes in seedlings grown in med

99 is study provides clinical trial evidence of global gene expression changes occurring in the human co

100 n this work, we describe the biochemical and global gene expression changes of epimastigotes under hy

101 sion of endogenous Oct4, Nanog and Klf4, and global gene expression changes that enriched for transcr

102 We determined global gene expression changes using Illumina HiSeq-base

103 process and identification of the associated global gene expression changes.

104 itro differentiation conditions and measured global gene-expression changes using gene expression mic

105 n entire developmental pathway, we generated global gene expression, chromatin accessibility, histone

106 Global gene expression comparisons between Bintje and up

107 ecent hypothesis-driven studies that utilize global gene expression data for elucidating the molecula

108 Analyses of global gene expression data from adipose tissue, skeleta

109 Analysis of global gene expression data from HOXA5-depleted MCF10A b

110 ociated with the hippocampus, I analyzed the global gene expression data from post-mortem hippocampal

111 parameters in cervical cancer combined with global gene expression data to reveal their underlying m

112 ys and Affymetrix HTA 2.0 arrays to generate global gene expression data with doxycycline induction.

113 l practices can lead to misinterpretation of global gene expression data.

114 Both targeted and global gene expression differences in the transcriptome

115 Biological pathways were compared using global gene expression differences.

116 Global gene-expression differences in ectopic T1 vs. T2/

117 Depletion of NusA altered global gene expression directly and indirectly via readt

118 al. (2014) uncover extensive oscillations in global gene expression during C. elegans development, in

119 ription factor participates in reprogramming global gene expression during Cu insufficiency in order

120 We have profiled global gene expression during optic fissure morphogenesi

121 s to monitor their environment and reprogram global gene expression during specific stages of infecti

122 er significantly from primary mDA neurons in global gene expression, especially in genes related to n

123 omparable to adult articular chondrocytes in global gene expression, extracellular matrix production,

124 rray analysis of a SS cell line, we surveyed global gene expression following combined PKCbeta-GSK3 t

125 We assayed peripheral blood leucocyte global gene expression for a prospective discovery cohor

126 d metal ions and induce distinct patterns of global gene expression from established LRAs.

127 We investigated alterations to global gene expression (GE) in nontransformed human smal

128 This analysis reveals that the magnitude of global gene expression heterogeneity is regulated in res

129 ovo steroidogenic immune cells, defining the global gene expression identity of these steroid-produci

130 ole of poly(ADP-ribose) polymerase (PARP) on global gene expression in a lymphoblastoid B cell line.

131 RNA-Seq has provided valuable insights into global gene expression in a wide variety of organisms.

132 nal regulators with the ability to influence global gene expression in addition to modulating gene ex

133 We then profiled global gene expression in blood from individual mice usi

134 engers, carboxy-PTIO and DMSO, on changes in global gene expression in cultured normal human fibrobla

135 We analyzed the global gene expression in epithelium collected intraoper

136 te-limiting steps have been shown to control global gene expression in eukaryotes: preinitiation comp

137 rk highlights the hierarchical patterning of global gene expression in floral development, and suppor

138 of VP35 and VP24 with the IRADs disabled on global gene expression in human DC.

139 n in CF following TLR signaling, we profiled global gene expression in immortalized human CF and non-

140 Global gene expression in mouse HBCs reveals broad upreg

141 ecific neuronal genes, while dispensable for global gene expression in murine ES cells.

142 ct of genome-wide cardiac DNA methylation on global gene expression in myocardial samples from end-st

143 s complex are critical for the regulation of global gene expression in ocular cells, making LOXL1-AS1

144 lie skin specific manifestation, we analyzed global gene expression in peripheral blood of a small co

145 d sequencing for the time-course analysis of global gene expression in practically any organism.

146 In the present study, we compared global gene expression in primitive, fetal definitive, a

147 his study provides a detailed description of global gene expression in seven successive developmental

148 n, ISGF3-independent signaling in regulating global gene expression in STAT1-, STAT2-, or IRF9-defici

149 echanism by which satellite repeats regulate global gene expression in trans via piRNA-mediated gene

150 y defects in ribosome synthesis by analyzing global gene expression in various cellular models of DBA

151 dy, we utilized RNA-Seq technology to assess global gene expression in white lupin cluster roots, nor

152 In comparing global gene expression in wild-type, TLR9-, or STAT3-def

153 and in vivo and caused widespread changes in global gene expression, including up-regulation of myoge

154 bisphenol A (BPA) has been reported to alter global gene expression, induce epigenetic modifications,

155 e to the difficulty in embryo isolation, the global gene expression involved in plant embryogenesis,

156 We presently describe that global gene expression is similar in cytokine-treated an

157 these resources for exploring the balance of global gene expression levels between excitatory AMPA re

158 ch is accompanied by a substantial change in global gene expression levels.

159 We aimed to assess whether global gene expression measured in whole blood of health

160 a major contributing factor to the change of global gene expression, metabolic pathways and activatio

161 ma by an unbiased, detailed interrogation of global gene expression.Methods: BAL cell expression was

162 To investigate the causes, we compared the global gene expression of aged and young bone marrow-der

163 the histopathology, genome architecture, and global gene expression of donor tumors.

164 To directly compare global gene expression of hPSC-PCs with developing mouse

165 hroughput-sequencing approach to compare the global gene expression of Rice black-streaked dwarf viru

166 bacterial factors in H. pylori pathogenesis, global gene expression of six H. pylori isolates was ana

167 can obviously have a strong influence on the global gene expression of the bacterium that produces it

168 llect incipient PCT cells and analyzed their global gene expression on Affymetrix Mouse Genome 430A m

169 o bind to individual genes can customize the global gene expression output of cells.

170 rient limitation, we examined transitions in global gene expression over short time scales, induced b

171 introgression lines, as well as a divergent global gene expression pattern between the low-PEV and h

172 To address this gap, we compared the global gene expression pattern of primary human hepatocy

173 HC), to determine whether they show the same global gene-expression pattern and high ESR1 mRNA expres

174 e workflow identifies four subtypes based on global gene expression patterns and ontologies.

175 g of the Earth, has been shown to influence global gene expression patterns and protein levels in cu

176 1 x g, microgravity has been shown to alter global gene expression patterns and protein levels in cu

177 end, we examined differentiation potential, global gene expression patterns and Sp1 target regions i

178 In this study we showed that global gene expression patterns are very similar between

179 For many years, the relationship among global gene expression patterns associated with determin

180 Here, we examine global gene expression patterns in corals and their intr

181 studies on injured epidermis, we showed that global gene expression patterns in highly occluded versu

182 We compared global gene expression patterns in livers from wildtype,

183 In this study, we compared global gene expression patterns in progeny of damaged an

184 merged as a powerful methodology to quantify global gene expression patterns in various contexts from

185 Here we compared the global gene expression patterns of CTBs from PAS cases t

186 Analysis of global gene expression patterns of soybean CIPK family r

187 signaling induces large scale changes in the global gene expression patterns of vascular tumors, incl

188 at H2B monoubiquitination does not influence global gene expression patterns, but instead ensures sel

189 d phytohormones, specialized metabolites and global gene expression patterns, in combination with het

190 vides a general method for understanding how global gene-expression patterns are choreographed.

191 sess shifts in cyanobacterial abundances and global gene-expression patterns in response to natural a

192 In the present study, global gene expression prior to and after the onset of l

193 iOPCs exhibit a bipolar morphology and global gene expression profile consistent with bona fide

194 In both cases, a common global gene expression profile is observed, but downstre

195 For evaluating the global gene expression profile of cells carrying p.T120A

196 Herein, a global gene expression profile of Mycobacterium leprae-i

197 Global gene expression profile of stem cells reveals sig

198 propensity, cellular proliferative rate, and global gene expression profile when compared with unalte

199 ith an efficiency of up to 70% in 28 d and a global gene-expression profile comparable to primary hum

200 We also derived a fusion-type-associated global gene-expression profile.

201 the transcription factors which control the global gene expression profiles and consequently the cel

202 ld not be used to predict outcome but rather global gene expression profiles and epigenetic status of

203 activated preferentially by NGF, we compared global gene expression profiles between cells treated wi

204 systems biology network analysis approach to global gene expression profiles derived from common in v

205 We investigated global gene expression profiles from HCC arising in diff

206 Here, we compared pathology and global gene expression profiles in lung tissue from BALB

207 ontribute to its pathogenesis, we determined global gene expression profiles in muscles of rats aged

208 Analysis of global gene expression profiles in nondiseased primary p

209 expressed in female germ cells, we analyzed global gene expression profiles in perinatal ovaries fro

210 We employ network analysis of global gene expression profiles in tumors derived from a

211 is study, we analyzed the effects of IL-4 on global gene expression profiles of Ag-induced memory CD8

212 This study aimed to investigate global gene expression profiles of BK viremia and nephro

213 the first in-depth comparison of DOX-induced global gene expression profiles of hearts and PBMCs.

214 We examined the global gene expression profiles of human CD8(+) TN and T

215 In light of this, we compared global gene expression profiles of impaired epitope-spec

216 ow that there are significant differences in global gene expression profiles of isolated osteosarcoma

217 The differences between the respective global gene expression profiles of macrophages, derived

218 The objective of this study was to define global gene expression profiles of NDCs at key stages of

219 Therefore, in this study, global gene expression profiles of ovary and brain of fe

220 Global gene expression profiles of PBMCs from 43 drug-na

221 Remarkably, global gene expression profiles of PS34CD45(-) cells cor

222 RNA sequencing to generate comprehensive and global gene expression profiles of this gland at differe

223 archical clustering of participants based on global gene expression profiles revealed that participan

224 Global gene expression profiles showed similarities betw

225 Global gene expression profiles were determined and comp

226 n dsk2 mutants accumulate BES1, have altered global gene expression profiles, and have compromised st

227 stem cells, including cell surface markers, global gene expression profiles, and in vivo pluripotenc

228 We assessed iHep maturity by global gene expression profiles, hepatic polarity, secre

229 similar cytotoxic function, cell death, and global gene expression profiles, these cells had greater

230 On the basis of global gene expression profiling and chromatin immunopre

231 Both global gene expression profiling and quantitative revers

232 Moreover, global gene expression profiling did not distinguish lar

233 This study represents the first use of global gene expression profiling from healthy human brai

234 Global gene expression profiling identified the transcri

235 Global gene expression profiling identifies clear featur

236 d each of 100 TFs with shRNA and carried out global gene expression profiling in mouse embryonic stem

237 A major goal of global gene expression profiling in plant seeds has been

238 Global gene expression profiling in skin and peripheral

239 Our global gene expression profiling indicates that the non-

240 Global gene expression profiling of Ccn6(fl/fl) mammary

241 Global gene expression profiling of EML1 cells at differ

242 Global gene expression profiling of HPAIV-infected endot

243 Global gene expression profiling of human and mouse isle

244 Global gene expression profiling of infected mouse lungs

245 Global gene expression profiling of MCF7 cells revealed

246 In this study, we performed global gene expression profiling of mouse tumor-infiltra

247 Recently, global gene expression profiling of patient samples led

248 Global gene expression profiling of post-ischemic kidney

249 ection against type 1 diabetes, we performed global gene expression profiling of splenocytes using hi

250 Global gene expression profiling of the lungs of infecte

251 n in breast cancer cells in combination with global gene expression profiling revealed p53 (TP53) sig

252 Global gene expression profiling revealed that more than

253 Global gene expression profiling revealed that the expre

254 Single-cell global gene expression profiling showed that undifferent

255 Global gene expression profiling suggested that Smchd1 n

256 We used global gene expression profiling to evaluate changes in

257 Global gene expression profiling was performed for 4 nor

258 cal melanoma samples, normal melanocytes and global gene expression profiling we have investigated th

259 Furthermore, molecular studies, including global gene expression profiling, have provided evidence

260 Using global gene expression profiling, we show that KDM3A pos

261 In the present study, we performed global gene-expression profiling and ChIP coupled with d

262 etween transcription factor (TF) binding and global gene expression programs as multipotent cells dif

263 w that as cells enter G0, their survival and global gene expression programs become increasingly depe

264 ta sets to elucidate the regulatory logic of global gene expression programs in mouse embryonic stem

265 ns of computational normalization to compare global gene expression programs in steady-state and dyna

266 cle provide the structural framework for the global gene expression programs of the individual chromo

267 ng sites; all of which play immense roles in global gene expression regulation.

268 wt EBOV induced a weak global gene expression response, including markers of DC

269 sing a time-course transcriptomics approach, global gene expression responses of each cultivar were a

270 Here, we report on global gene expression responses to VOR and examine the

271 whereas single-cell RNA-seq, which measures global gene expression, separates cells from their nativ

272 nhibition of known MSI-targets, and a shared global gene expression signature similar to shRNA deplet

273 l- and vitamin D(3)-treated PrP/SCs revealed global gene expression signatures consistent with induct

274 Comparison of global gene expression signatures showed that transcript

275 ediated synthesis of eIF4G imposes increased global gene expression stochasticity and reduced viabili

276 Global gene expression studies demonstrated that, while

277 sent a novel approach to this issue by using global gene expression studies in conjunction with a sys

278 Global gene expression studies suggest that RD26 can act

279 Using ontological analysis of global gene expression studies, we demonstrate that many

280 ll-type proportion or pathway activity, from global gene expression studies.

281 We performed a comparative global gene expression study using data from morphologic

282 In a global gene expression study, we found higher expression

283 and hypermutator phenotypes, in addition to global gene expression subtypes.

284 ide arrays are now routinely used to profile global gene expression, there is still a lack of tools f

285 a host, Pseudomonas aeruginosa orchestrates global gene expression to adapt to the host environment

286 Global gene expression (transcriptome) profiling reveale

287 estigate chromatin accessibility changes and global gene expression under extended darkness and contr

288 First, we look at how fungi change their global gene expression upon recognition of the host envi

289 Here we study post-SCI mRNA editing and global gene expression using massively parallel sequenci

290 Global gene expression was assayed using human microarra

291 Global gene expression was compared between PDGF-stimula

292 med cell lines on cellular functionality and global gene expression, we report that TFIIB is dispensa

293 in global histone acetylation and changes in global gene expression were observed in microarray analy

294 Here, changes in global gene expression were studied in root, male and fe

295 ase in cell viability and alterations in the global gene expression with a broad range of biochemical

296 GapR also affects global gene expression with a chromosomal bias from orig

297 We studied non-heart-beating donor rats for global gene expression with Affymetrix microarrays, hepa

298 roglioma display a high degree of overlap in global gene expression with no clear distinctions betwee

299 on or improvement has significantly affected global gene expression, with many genes targeted by sele

300 e sequences calls for quantitative models of global gene expression, yet predicting gene expression p