ライフサイエンスコーパス: global gene expression

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

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

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

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

5 imilar effects to overexpressing HP1alpha in global gene expression.

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

7 oral program integrating DNA replication and global gene expression.

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

9 of diverse transcription factors that drive global gene expression.

10 ts had dramatically divergent effects on GAS global gene expression.

11 ve control over cellular processes including global gene expression.

12 cription initiation can profoundly influence global gene expression.

13 ights into how clocks drive daily rhythms in global gene expression.

14 chromosome and genetic background affecting global gene expression.

15 ells (RGCs) differ in survival signaling and global gene expression.

16 As (miRNAs) are noncoding RNAs that regulate global gene expression.

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

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

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

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

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

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

23 Global gene expression analyses and validation revealed

24 Unbiased global gene expression analyses demonstrate that MECP2 f

25 Global gene expression analyses following Setd8 knockdow

26 Global gene expression analyses reveal that trisomy 12 p

27 Furthermore, global gene expression analyses show that GW9662 treatme

28 Global gene expression analyses suggested that Rb mainta

29 Global gene expression analyses were conducted using spl

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

31 Global gene expression analyses, validated by mRNA and p

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

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

34 Global gene expression analysis demonstrated that exogen

35 Global gene expression analysis identified a molecular s

36 Global gene expression analysis identified ablated Tiam2

37 Global gene expression analysis identified that PELP1-cy

38 Global gene expression analysis indicated that 47% of an

39 Global gene expression analysis indicated that the BMP-d

40 Global gene expression analysis indicated that transcrip

41 A global gene expression analysis of AS versus empty vecto

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

43 Global gene expression analysis of infected hNPCs reveal

44 Global gene expression analysis of KDM3A-depleted cells

45 Global gene expression analysis of knockout hearts befor

46 Global gene expression analysis of mesenchymal stem cell

47 A global gene expression analysis of S100A12-activated mon

48 Global gene expression analysis of teratomas formed by B

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

50 Global gene expression analysis on liver identified Tpcn

51 This global gene expression analysis provides new insights in

52 Global gene expression analysis revealed changes in gene

53 Global gene expression analysis revealed marked differen

54 Global gene expression analysis revealed that genes upre

55 Global gene expression analysis revealed that infection-

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

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

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

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

60 Global gene expression analysis was performed on HMEC li

61 Global gene expression analysis, data intersection, path

62 dent investigators that evaluate methods for global gene expression analysis.

63 Global gene-expression analysis of the transgenic plants

64 Global gene-expression analysis showed that the steroid

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

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

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

68 Using global gene expression and DNA methylation profiling, we

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

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

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

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

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

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

75 as modulated with siRNAs, and the effects on global gene expression and growth of human and murine HC

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

77 system in Pseudomonas aeruginosa influences global gene expression and mediates pathogenesis.

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

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

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

81 Global gene expression and secretome analysis reveals th

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

83 een the two proteins was also established in global gene expression and transcriptional reporter stud

84 lR), another LacI/GalR family member, in GAS global gene expression and virulence.

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

86 Global gene-expression and methylome analyses of TKO EBs

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

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

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

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

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

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

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

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

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

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

97 ment was demonstrated by a strong overlap in global gene expression between B cells isolated from ant

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

99 ds provide substantial amount information on global gene expression but do not always reflect the act

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

101 t the first PKC isozyme-specific analysis of global gene expression by microarray using RNAi depletio

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

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

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

105 Global gene expression can be quantified from the number

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

107 Global gene expression changes associated with upregulat

108 Further analysis of global gene expression changes during reprogramming reve

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

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

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

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

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

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

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

116 lear-resident histone acetylation nor marked global gene expression changes.

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

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

119 Global gene expression comparisons between Bintje and up

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

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

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

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

124 Using global gene expression data from the mouse brain, plant

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

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

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

128 Both targeted and global gene expression differences in the transcriptome

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

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

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

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

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

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

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

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

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

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

139 This facilitated studies of global gene expression in a way that avoided many of the

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

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

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

143 tudies and the future potential of measuring global gene expression in epithelial cells that are in t

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

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

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

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

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

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

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

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

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

153 at thiol peroxidases are major regulators of global gene expression in response to H(2)O(2).

154 Using a detailed systems-level analysis of global gene expression in rice, we reveal the SHN regula

155 The pattern of global gene expression in Salmonella enterica serovar Ty

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

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

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

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

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

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

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

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

164 his work represents the first examination of global gene expression involving triacylglycerol and fat

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

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

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

168 Global gene expression measurements are increasingly obt

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

170 Retrospective study of global gene expression (microarray) profiles of LSC-enri

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

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

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

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

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

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

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

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

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

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

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

182 1 x g, microgravity has been shown to alter global gene expression patterns and protein levels in cu

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

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

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

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

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

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

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

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

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

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

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

194 rtium will produce comprehensive datasets of global gene expression patterns, regulatory elements and

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

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

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

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

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

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

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

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

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

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

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

206 This study presents global gene expression profiles associated with GA immun

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

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

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

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

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

212 Analysis of global gene expression profiles in nondiseased primary p

213 tures associated with lethality, we compared global gene expression profiles in spleen samples from m

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

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

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

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

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

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

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

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

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

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

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

225 Clustering of maize tissues based on global gene expression profiles resulted in formation of

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

227 Global gene expression profiles were determined and comp

228 E1 was present in the nucleus, and analyzing global gene expression profiles with or without inductio

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

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

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

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

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

234 Both global gene expression profiling and quantitative revers

235 Moreover, global gene expression profiling did not distinguish lar

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

237 Global gene expression profiling identified the transcri

238 Global gene expression profiling identifies clear featur

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

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

241 Global gene expression profiling in skin and peripheral

242 Our global gene expression profiling indicates that the non-

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

244 Further, global gene expression profiling of CSCs revealed an act

245 Global gene expression profiling of EML1 cells at differ

246 Global gene expression profiling of HPAIV-infected endot

247 Global gene expression profiling of infected mouse lungs

248 Global gene expression profiling of MCF7 cells revealed

249 Global gene expression profiling of motor neurons isolat

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

251 Recently, global gene expression profiling of patient samples led

252 Global gene expression profiling of post-ischemic kidney

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

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

255 Global gene expression profiling revealed that more than

256 Global gene expression profiling revealed that the expre

257 Single-cell global gene expression profiling showed that undifferent

258 Global gene expression profiling suggested that Smchd1 n

259 We used global gene expression profiling to evaluate changes in

260 Global gene expression profiling was performed for 4 nor

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

262 unohistochemical evaluation and subjected to global gene expression profiling.

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

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

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

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

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

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

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

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

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

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

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

274 Global gene expression studies demonstrated that, while

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

276 Global gene expression studies suggest that RD26 can act

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

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

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

280 Here, we use a global gene expression survey to more comprehensively id

281 Because of their importance to global gene expression, the binding of these NAPs to the

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

283 erichia coli is an O(2) sensor that modifies global gene expression to adapt the cell to anaerobic gr

284 We examined changes in global gene expression to define pathways regulated by d

285 Global gene expression (transcriptome) profiling reveale

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

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

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

289 Global gene expression was assayed using human microarra

290 Global gene expression was compared between PDGF-stimula

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

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

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

294 Bacteria comprehensively reorganize their global gene expression when faced with starvation.

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