ライフサイエンスコーパス: expression profile

1 transduction while still retaining a CM gene expression profile.

2 t with their restricted and highly regulated expression profile.

3 entify gene clusters that share a comparable expression profile.

4 splaying a highly distinct stress-responsive expression profile.

5 mone receptor (TRalpha 3) has a differential expression profile.

6 ssion, and treatment with RFP14 opposes this expression profile.

7 LC differentiation marked by a low cytokine expression profile.

8 describing the experimentally observed gene-expression profile.

9 ficit treatment than other genotype-specific expression profiles.

10 lap between hepatic Cyp51(-/-) and Rorc(-/-) expression profiles.

11 s, we present two network models to generate expression profiles.

12 MR imaging phenotypes to be linked with gene expression profiles.

13 olysialyltransferases are based on different expression profiles.

14 NA-seq data to compare Oncopig and human STS expression profiles.

15 ificantly alter cellular phenotypes and gene expression profiles.

16 to obtain detailed and accurate HERV-K HML-2 expression profiles.

17 s and characterized by tissue/organ specific expression profiles.

18 TP2B1 displayed anthracycline-dependent gene expression profiles.

19 cue reference transcriptome and compare gene expression profiles.

20 ipotent progenitors do not exhibit different expression profiles.

21 e and non-edge components from the generated expression profiles.

22 nd ovarian tumor samples based on their gene expression profiles.

23 alecto) consists of conserved and unique ISG expression profiles.

24 enome-wide DNA methylation patterns and gene expression profiles.

25 s, resulting in dramatic alterations in gene expression profiles.

26 rse in their physiology, structure, and gene expression profiles.

27 logical pathways and exhibit highly variable expression profiles.

28 s targeting inhibitory SMADs to analyze gene expression profiles.

29 ir resistance- and virulence-associated gene expression profiles.

30 ogether with a new dataset of 265 ccRCC gene expression profiles.

31 nostics and to follow up alterations in gene expression profiles.

32 d stage could be improved by intragraft gene expression profiling.

33 type was determined by Lymph2Cx digital gene expression profiling.

34 n in UCB were available from genomewide gene expression profiling.

35 ne of the most repressed genes using genomic expression profiling.

36 Based on the expression profiles, 19 genes were further analysed by q

37 ions) and by applying genome-wide blood gene expression profiling (582 admissions).

38 We therefore devised integrated tDNA expression profiling, a method that combines RNAPIII map

39 ncRNA genes with high-confidence 5' ends and expression profiles across 1,829 samples from the major

40 Here we study genomic and expression profiles across 127 multisector or longitudin

41 that promoters and enhancers, based on their expression profiles after stimulus, belong to different

42 We identified 4 host gene expression profiles, among which catabolic remodeling, a

43 By using gene expression profile analysis and functional clustering, P

44 We performed gene expression profile analysis by RNA sequencing of subsets

45 We performed gene expression profiling analysis of 542 human acute myeloid

46 Unsupervised gene expression profiling analysis, including principal compo

47 Tumor type was classified by gene expression profile and American Joint Committee on Cance

48 orted that caused a muted innate immune gene expression profile and decreased immune cell infiltratio

49 C-derived microglia have the phenotype, gene expression profile and functional properties of brain-is

50 provides interactive tools for exploring the expression profiles and coexpression network.

51 iption factors which control the global gene expression profiles and consequently the cell functionin

52 nograft tumours were reflected in their gene-expression profiles and epigenomes.

53 icly available leukemic stem cell (LSC) gene expression profiles and gene expression data generated f

54 OC metastatic units with respect to cadherin expression profiles and invasive behavior; however, the

55 l characteristics determined, and their gene expression profiles and markers of differentiation ident

56 Gene-expression profiles and mutant analyses suggest that met

57 ic females profoundly influenced aortic gene expression profiles and promoted AAA severity.

58 PANDA uses gene expression profiles and published relationships among ge

59 ll clones showed multiple chemokine receptor expression profiles and secretion of diverse effector mo

60 Using a combination of tissue protein expression profiling and bioinformatics, we discovered t

61 Expression profiling and functional studies in vitro and

62 Expression profiling and in vitro mechanistic studies sh

63 th a combination of global and targeted gene-expression profiling and the expression of key pluripote

64 promoters of various strengths and temporal expression profiles, and 10 protein-localization, degrad

65 rats segregated on the basis of their miRNA expression profiles, and a similar finding was observed

66 ts accumulate BES1, have altered global gene expression profiles, and have compromised stress respons

67 o subpopulations based on their protein-mRNA expression profiles, and that different subpopulations h

68 more broadly to their developmental antennal expression profiles, and to the transcription factor com

69 To this end, we performed a comparative expression profiling approach using light- and dark-grow

70 By using a genome-wide gene expression profiling approach, we identified RAB20 and T

71 nd occipital regions, while interhemispheric expression profiles are associated with frontotemporal r

72 lar mechanisms that shape and regulate their expression profiles are largely unknown.

73 Corticostriatal gene expression profiles are predominately associated with mo

74 that these epigenetic modifications and gene expression profiles are reversible after skeletal muscle

75 not ILC2 or ILC3 cells, were enriched in the expression profiles associated with CD4, CD8, and B cell

76 opment, we characterised the glomerular gene expression profile at an early stage of disease progress

77 Correlation analysis of gene expression profiles at the tipping point indicates trans

78 ores and facilitates search of RNA-Seq based expression profiles available from the modENCODE consort

79 ECs to this process by comparing their gene expression profile before (P5) and after (P30) the criti

80 Differences in genetic expression profile between these three cell types sugges

81 We performed inter-species comparative gene expression profiling between AD patient brains and the A

82 tic injuries evoke surprisingly similar gene expression profiles, but there is limited information on

83 We evaluated temporal cerebellar expression profiles by RNA sequencing of ATXN2Q127 mice

84 aturation, as assessed by surface phenotype, expression profiling by gene array, and functional abili

85 Expression profiling by RNA-sequencing revealed 77 genes

86 Combining the mutation status with the gene expression profiles can efficiently identify the cancer-

87 High throughput mRNA expression profiling can be used to characterize the res

88 e is sufficient to induce metabolic and gene expression profiles characteristic of colorectal cancer

89 sualization modules that include time course expression profiles, clustering, gene ontology enrichmen

90 ildren displayed a distinctive monocyte gene expression profile compared to lean controls.

91 compares them with large data sets of normal expression profiles compiled from public sources, in reg

92 factors likely regulating the pathway, their expression profiles could not explain the differences ob

93 art disease by integrating gene and microRNA expression profiling data from hearts of T. cruzi infect

94 dbDEMC 2.0 documents 209 expression profiling data sets across 36 cancer types an

95 The first is gene expression profiling data usually do not contain time co

96 Hierarchical clustering based on gene expression profiles delineated brain regions into struct

97 er for gamma-H2AX foci decay ratios and gene expression profiles derived from ex vivo-irradiated pati

98 The temporal expression profiles displayed by taste organoids may als

99 des the first insight into A. baumannii gene expression profiles during a life-threatening mammalian

100 cquire unique structural properties and gene expression profiles during animal development.

101 death-1, CTLA4, and TIM-3 displayed discrete expression profiles during drug-induced T cell activatio

102 ing proteins play a key role in shaping gene expression profiles during stress, however, little is kn

103 HCC mimicked this gene expression profile, even in cases that were morphologica

104 GADD45B was also repressed in mRNA expression profiling experiments when KSHV miRNAs were i

105 HSP70-1 was identified via expression profiling following IL-5 stimulation.

106 A-seq) datasets from NCBI-SRA and calculated expression profiles for different tissues and cell-lines

107 grating single-cell transcriptomes with bulk expression profiles for hundreds of tumors, we refined H

108 show that thick ILs share S. pennellii-like expression profiles for putative regulators of cell shap

109 ertheless, there is a limited description of expression profiles for these transcripts in human subje

110 subcortical regions studied by ENIGMA, gene expression profiles for three pathways were significantl

111 nesis mechanisms and the genesis of specific expression profiles for tRNA-derived ncRNAs.

112 Expression profiling for immune-related genes was perfor

113 Ell Regularized Inference using TIme-stamped Expression profileS) for the inference of GRNs from sing

114 mRNA and miRNA expression profile frequently performed the best, follow

115 Differences in expression profiles from baseline to week 12 of the huma

116 nerated and compared with a database of gene expression profiles from cells treated with other bioact

117 Our method integrates novel gene expression profiles from each major non-malignant cell t

118 modeling, in vitro experimentation, and gene expression profiles from patient cohorts displaying tumo

119 loped using in silico generated mixture gene expression profiles from single stressor data were able

120 We have generated lncRNA expression profiles from the CD34+ haematopoietic stem a

121 We separated gene expression profiles from tumor, stromal, and immune cell

122 signature that is conserved within the gene expression profiles from whole kidney biopsies of patien

123 ore, integrative analyses (microRNA and gene expression profiling from the same biopsy sample) identi

124 is robust to platform/batch effects in gene expression profiles generated by multiple platforms.

125 ted tomographic (CT) image features and gene expression profiles generated by RNA sequencing for pati

126 Gene expression profile (GEP) testing segregates uveal melano

127 nted an automatically generated RN with gene expression profiles (GEP) from a cohort of multiple myel

128 Here, we analyzed gene expression profiles (GEPs) using RNA from baseline tumor

129 pt set overlapped with muscle unloading gene expression profiles (>/=1.5-fold change; P < 0.05).

130 This inference is supported by gene expression profiles highlighting mitochondrial dysfuncti

131 atin immunoprecipitation sequencing and gene expression profiling identified candidate ATOH1 targets

132 Whole genome mRNA expression profiling identified nicotinamide N-methyltra

133 bolomic analysis and transcriptome-wide mRNA expression profiling identified reduced levels of severa

134 Global gene expression profiling identified the transcription factor

135 Here, we dissected the monocyte gene expression profile in childhood obesity using an Illumin

136 (hCD2) reporter mice revealed a similar gene expression profile in CT-induced intestinal Th17 cells a

137 t genetic branches, thus creating a cohesive expression profile in each CLL sample despite the presen

138 The gene expression profile in monocytes isolated from ZIKV- and

139 gy manifested as a dramatically altered gene expression profile in Npm1(cA);Flt3(ITD) , but not Npm1(

140 onsible for Lyme disease, modulates its gene expression profile in response to the environments encou

141 By analyzing micro-RNA expression profiles in a set of patient-derived prostate

142 quantified densities of IC subsets, and gene expression profiles in anal SCCs from HIV-positive vs HI

143 p sequencing analysis, we investigated miRNA expression profiles in central and limbal regions of nor

144 and functional features, together with gene expression profiles in immunocompetent adults experienci

145 We analyzed lncRNA expression profiles in mouse hearts at postnatal day (P)

146 ng data set to analyze male and female miRNA expression profiles in mouse, opossum, and chicken.

147 trimethylated lysine 9 in histone), and gene-expression profiles in naive, effector memory (EM), and

148 In this study, we investigated host gene expression profiles in nasopharyngeal (NP) swabs and who

149 tch guideline suggests use of validated gene-expression profiles in patients with estrogen receptor (

150 The expression profiles in response to TH treatment were tis

151 imilation in this bacterium, changes in gene expression profiles in response to variations in the ava

152 ression patterns in human brains and laminar-expression profiles in the developing neocortex, highlig

153 Comparison of the gene expression profiles in the egg, nymph and adult stages r

154 isruptions were associated with altered gene expression profiles in the male fetal brain and suggeste

155 x-specific outcomes, we assessed genome-wide expression profiles in the placenta and fetal brain.

156 Here the authors analyze gene expression profiles in the prostate and show that stroma

157 Applying this antibody for protein expression profiling in 44 normal and 21 malignant human

158 Gene expression profiling in Apc-mutant and Ctnnb1-mutant mou

159 senchymal cells, in conjunction with in situ expression profiling in bone cells, we identified bone l

160 We performed genome-wide gene expression profiling in peripheral blood leukocytes of a

161 On protease gene expression profiling in whole lung tissue, cathepsin K g

162 Purpose Gene-expression profiles increasingly are used in addition to

163 Gene expression profiles indicate multiple states of microgli

164 Gene expression profiles indicated that, in GCB DLBCL cancer

165 Gene expression profiling indicated substantial down-regulati

166 Gene expression profiling indicates that mouse tumors resembl

167 Our global gene expression profiling indicates that the non-SMAD JAK1/ST

168 We introduce GEPIA (Gene Expression Profiling Interactive Analysis), a web-based

169 cost, high-throughput reduced representation expression profiling method that we term L1000.

170 ing quantitative histology (n = 61) and gene expression profiling (n = 48).

171 wild-type plants as relative control for the expression profiles obtained from light-grown pap7-1 mut

172 We present the first comprehensive expression profile of all known 27 human TRP genes in me

173 e, we present a time-course comparative gene expression profile of Caturra (susceptible) and Hibrido

174 for >1 month exhibited stable alterations in expression profile of epigenetic writers/erasers and chr

175 control individuals to investigate the gene expression profile of IGF1 and IGF1R on different develo

176 The gene expression profile of luminal-type breast cancer patient

177 hese data indicate that the specialized gene expression profile of mature microglia requires continuo

178 The comparative gene expression profile of MDR E. coli 381 and the reference

179 le-cell RNA sequencing to determine the gene expression profile of MECs across four developmental sta

180 ogrammed cells which retained a typical gene expression profile of mesendodermal cells and were unabl

181 information is available concerning the gene expression profile of metacyclic forms.

182 T gene mutation slightly influenced the gene expression profile of MTC.

183 Genome-wide expression profile of neonatal Nkx2.5+ cardiomyoblasts s

184 which was distinctly different from the gene expression profile of pathogenic Th17 cells.

185 pathologic phenotype in relation to the mRNA expression profile of proinflammatory cytokines.

186 The expression profile of SCZ risk genes across cortical reg

187 acrine-acting factors were identified in the expression profile of the cervical tumor microenvironmen

188 This finding prompted us to compare the gene expression profile of the ES cell- and adult progenitor-

189 ial population dictates the microRNA (miRNA) expression profile of the host, which, in turn, through

190 relevant ratios, as well as an improved gene expression profile of the malignant cells.

191 The expression profiles of 26 genes involved e.g. in the imm

192 The expression profiles of 39 candidate transcripts encoding

193 ingle-cell snapshot expression data based on expression profiles of 48 genes in 2,167 blood stem and

194 populations, which allows us to compare the expression profiles of a receptor protein in natural kil

195 ected the survival, body condition, and gene expression profiles of a subsequent fish generation.

196 associated with compensatory changes in the expression profiles of CCL2, CCL7, and CCL12.

197 structed co-expression networks based on the expression profiles of conserved human lncRNAs and prote

198 time PCR (qRT-PCR) we have measured the gene expression profiles of each of the Ras isoforms in a pan

199 Analyzing sample-paired miRNA and gene expression profiles of GBM, our data showed that this al

200 ere were no distinct differences in the gene expression profiles of hereditary and sporadic MTCs.

201 We then analyzed gene expression profiles of human breast cancer patients and

202 ersonalizing treatment regimes based on gene expression profiles of individual tumors will facilitate

203 nibus (GEO) public datasets, we screened the expression profiles of inflammasome sensors NLRP3, NLRC4

204 n 9 human liver cell lines and compared with expression profiles of its potential targets associated

205 es, with no significant correlation with the expression profiles of key genes in the pathway, suggest

206 riptome reconstruction, we establish dynamic expression profiles of lncRNAs at different stages of ol

207 In our study, genome-wide expression profiles of more than 200 renal biopsies from

208 understand the mechanisms, we examined gene expression profiles of multi-tissues from outbred mice f

209 ne responses; and (2) RNA sequencing-derived expression profiles of nasal cells, before and after HDM

210 tive of this study was to define global gene expression profiles of NDCs at key stages of embryonic d

211 We focused on the expression profiles of olfactory receptor genes and tran

212 more than 2.0-fold change when compared the expression profiles of P1 to P7, P1 to P28, and P7 to P2

213 We collected publicly available expression profiles of patient-derived normal pancreatic

214 Furthermore, comparison of gene expression profiles of PDAC cells retaining or lacking K

215 in the chemokine receptor and beta1 integrin expression profiles of progenitors between the first and

216 Here we present gene expression profiles of purified microglia isolated at au

217 of Zc3h13 or Pten mutations altered the gene expression profiles of Rb1 mutants, rendering them more

218 this study provides a rich resource of gene expression profiles of term intravillous and extravillou

219 pite serial homology of all silk glands, the expression profiles of the glue-forming aggregate glands

220 We focused on the expression profiles of the key genes related to the oil

221 We hypothesized that the gene expression profiles of these differentiated cells could

222 genome and analyzed the genomic content and expression profiles of these genes.

223 th the DNA methylation status as well as the expression profiles of these IFN-associated genes were c

224 electrophoresis (2D-DIGE) to compare protein expression profiles of transparent and opaque variants o

225 Our aim was to determine the nasal protein expression profiles of WRA caused by different kind of e

226 Proteomics data were integrated with gene expression profiling of 121 carotid endarterectomies and

227 Expression profiling of 182 cases of lung adenocarcinoma

228 dy, we used whole-genome sequencing and gene expression profiling of 215 human induced pluripotent st

229 By performing gene expression profiling of 4,383 lncRNAs in 82 liver sample

230 Gene expression profiling of 534 single ICM cells identified

231 Gene expression profiling of 84 oxidative stress and 249 infl

232 A systematic expression profiling of AmAChE1 over a year-long cycle o

233 Global gene expression profiling of Ccn6(fl/fl) mammary carcinomas a

234 counterparts, here we deploy human-specific expression profiling of CRC PDXs to assess cancer-cell i

235 Here, we conducted gene expression profiling of human neuroepithelial stem cell-

236 pplication of the CLEAR score to independent expression profiling of intratumoral ccRCC regions demon

237 Microarray gene expression profiling of IVIg-generated pTreg revealed up

238 at MD Anderson Cancer Center underwent gene expression profiling of leukemic cells.

239 Global gene expression profiling of post-ischemic kidneys showed tha

240 e transcriptome sequencing, we compared gene expression profiling of pre- and post-treatment bone mar

241 Additionally, expression profiling of renal tissues from stone formers

242 Expression profiling of Setd1b(Gdf9) cKO MII oocytes rev

243 Gene expression profiling of SYNCRIP-depleted cells demonstra

244 Expression profiling of these genes during the course of

245 Gene expression profiling of TNBC has identified molecular su

246 erials and Methods We performed digital gene expression profiling on a cohort of 245 formalin-fixed,

247 We performed microarray gene expression profiling on a large sample of resected lung

248 antifying biological processes by using gene expression profiles over a sample population, which invo

249 xeno-free protocol produces cells with gene expression profiles, oxygen consumption rates, nitric ox

250 The relative ssts/D2 expression profile, particularly sst5 and/or sst5TMD4 le

251 evelopment of an inexpensive and direct gene expression-profiling platform.

252 e genotypes and tumor specific mutations and expression profiles related to DXME genes.

253 at they possess fundamentally different gene expression profiles related to factors that regulate pos

254 stering of participants based on global gene expression profiles revealed that participants with sign

255 d drove experimental metastasis in vivo Gene expression profiling revealed a strong association betwe

256 Gene expression profiling revealed a subset of Forkhead box (

257 Gene expression profiling revealed comparable levels of IFNG

258 Gene expression profiling revealed primary and metastatic cel

259 Our in-depth gene expression profiling revealed that 84% of genes are expr

260 Molecular stratification based on gene expression profiling revealed that breast cancers could

261 Global gene expression profiling revealed that the expression of BR

262 Genetic dissection and expression profiling revealed that this role is specific

263 Integrated tDNA expression profiling reveals domain-level and loop-based

264 Gene expression profiling reveals molecular similarities of m

265 ecific and cell type-specific reference gene expression profiles (RGEPs) from tumour-derived single-c

266 We performed gene expression profile, RNA sequence, whole-exome and genome

267 Western blot analysis and gene expression profiling showed that ECs treated with M1 mac

268 e found that some heat-treated fish had gene expression profiles similar to untreated controls of the

269 Here, we provide comprehensive HERV-K HML-2 expression profiles specific for productively HIV-1-infe

270 Gene expression profile status was class 1 in 247 tumors (70%

271 Brain gene expression profiling studies of suicide and depression u

272 Expression analyses and unbiased gene expression profiling studies offer a molecular explanati

273 d when p16 is inactivated by looking at gene expression profiling studies.

274 Recent fate-mapping studies and gene-expression profiles suggest that commonly used protocols

275 This refined expression profiling technique distinguished genes truly

276 y the reported technique for successful gene expression profile testing and prognostic classification

277 stant to Gyrodactylus and had different gene expression profiles than lake sticklebacks.

278 validated by RT-qPCR, often showed opposite expression profiles than the related miRNAs.

279 n aquatic environments, where it displays an expression profile that is distinct from that during inf

280 e, we show that ATF4 controls a hepatic gene expression profile that overlaps with GCN2 but is not re

281 totoxic activity, produce IL-22, and have an expression profile that overlaps with those of natural k

282 -like ALL, is a high-risk subset with a gene expression profile that shares significant overlap with

283 a suggest that TMEs possess distinct protein expression profiles that are biologically and therapeuti

284 is applied to explore gene modules for gene expression profiles through weighted correlation network

285 e functional alterations in cancers based on expression profiles to explore cancer malignant process

286 microscopy, quantitative pathology, and gene expression profiling to analyze TLS formation in human l

287 Therefore, we have used cellular expression profiling tools to define the distinct miRNA

288 The Ph-like gene expression profile was identified in 341 of 1389 patient

289 In this study, microRNA expression profile was investigated in Treg cells isolat

290 ment analysis of our recently published gene expression profiles was performed.

291 miRNome expression profiling was performed in a mouse model of p

292 Because of its more restricted tissue expression profile, we have therefore turned to PAR4 as

293 Using global gene expression profiling, we show that KDM3A positively regu

294 Using microarray-based gene expression profiling, we show that Ly6C(hi) iMOs isolate

295 Global gene and miRNA expression profiles were also determined using paired RN

296 Intestines were collected from mice and gene expression profiles were compared by microarray and quan

297 Host immune response gene expression profiles were generated by quantitative polym

298 was similar to that of controls and cytokine expression profiles were only marginally altered.

299 n tumor development, each resulted in a gene expression profile with significant overlap.

300 As datamining associates PRP expression profiles with hypoxia or oxidative stress and