ライフサイエンスコーパス: expression profile

1 h-TIP5 expression, and a TIP5-regulated gene expression profile.

2 s of a set of microRNAs, starting from their expression profile.

3 e-associated secretory phenotype (SASP) gene expression profile.

4 as well as a dysregulated hepatic lipid gene expression profile.

5 KRAS in cell lines that differ in their tRNA expression profile.

6 nedione (A4), each steroid exhibited its own expression profile.

7 ogenitor populations and the epithelial gene expression profile.

8 of heterogeneous tissues based on their gene expression profiles.

9 y biomarker genes for lung cancer using gene expression profiles.

10 , for which we obtained wild-type and mutant expression profiles.

11 tle is known about their characteristic gene expression profiles.

12 nt a minority of patients studied using gene expression profiles.

13 the human brain and show cell type-specific expression profiles.

14 -of-the-art GRNs correspond to measured gene-expression profiles.

15 , this suggests an evolutionary shift in the expression profiles.

16 on ChIP-seq data sets with thousands of gene expression profiles.

17 ction neurons defined by their distinct gene-expression profiles.

18 nctive tissue or cell subtypes based on bulk expression profiles.

19 including body images and whole-genome gene expression profiles.

20 al samples and estimate tissue/cell-specific expression profiles.

21 es, anatomical localization, as well as mRNA expression profiles.

22 ng to catalog DA neurons based on their gene expression profiles.

23 sponders and nonresponders had distinct gene expression profiles.

24 ed central miRNAs and specified common miRNA expression profiles.

25 l effector molecule through single-cell gene expression profiling.

26 use brain striatal cells, and performed gene expression profiling.

27 CD40L (sCD40L) on T24 bladder carcinoma gene expression profiling.

28 ene sequencing, copy-number arrays, and gene expression profiling.

29 dies have begun to provide compendia of cell expression profiles(1-9), it has been difficult to syste

30 n patients with melanoma showed via targeted expression profiling(17) that B cell signatures were enr

31 By integrating miRNA and mRNA expression profiles, a total of 870 genes were predicted

32 spectral patterns specific to the ECM3 gene expression profile, achieving a high spectral classifica

33 8% of protein-coding genes have similar gene expression profiles across all pipelines.

34 Next, we compared the gene expression profiles across the three time points (1-, 7-

35 examined social status-dependent brain gene expression profiles across vertebrates, yet social statu

36 positively selected GC B cells led to a gene expression profile alike that of MBCs and increased MBC

37 is is revealing increasing diversity in gene expression profiles among brain cells.

38 Gene expression profiles among Indian children with confirmed

39 We explored changes in gene expression profiles among patients with SCD hospitalized

40 ormed chromatin immunoprecipitation and gene expression profiling analyses to identify genes regulate

41 However, microRNA (miRNA) expression profiling analysis revealed that EV fractions

42 The gene expression profiling analysis showed that PRLT2/89-33 ha

43 -like process characterised by a unique gene expression profile and 3D genome folding signature, medi

44 Here, we studied the expression profile and functional role of LAT1 in bladde

45 Pathway analysis of the gene expression profile and in vitro functional studies revea

46 seq (snRNA-seq) data to generate a reference expression profile and learn gene-specific bulk expressi

47 We define the gene expression profiles and anatomical locations of 58 cell

48 lly indistinguishable and share similar gene expression profiles and biallelic TSC2 mutations, suppor

49 ntified based on unbiased clustering of gene expression profiles and canonical markers.

50 y, cocaine exposure persistently alters gene expression profiles and electrophysiological properties

51 PDZK1IP1 (p = 0.0206) with RA-specific gene expression profiles and elevated expression of the ST6GA

52 (genotype DH1) and compared tissue-specific expression profiles and in vitro products of their recom

53 most effectors show conserved spatiotemporal expression profiles and likely function, some H. sacchar

54 By combining gene expression profiles and MRI-defined hypoxia levels in ca

55 These cells exhibit altered gene expression profiles and serve as a barrier, preventing n

56 las of full-thickness skin, determining gene expression profiles and spatial locations that define 56

57 genes in the lipoxygenase pathway, and both expression profiles and VOCs discriminated amongst culti

58 Here, using single-cell gene expression profiling and anatomical circuit analyses of

59 Gene expression profiling and flow cytometry were used to cha

60 ester revealed their unique phenotypes, gene expression profiles, and differing capacities to increas

61 ct proliferation rates, lineage biases, gene expression profiles, and gene dependencies.

62 rs acquire the somatic genomic changes, gene expression profiles, and immune microenvironment that ch

63 on residual HIV burden, transcriptional gene expression profiles, and immune responses in HIV-infecte

64 ) and subjected them to DNA sequencing, gene expression profiling, and high-throughput drug screening

65 y epidemiological, cell biological, and gene expression profiling approaches, we report here multiple

66 nd preselect CD8(+) T cells with a cytotoxic expression profile are lacking.

67 le, multi-tissue gene expression data, where expression profiles are obtained from multiple tissues o

68 a detailed description of chemosensory gene-expression profiles as they relate to sensory tissue (an

69 molecularly characterize LELC-B through RNA expression profiling as well as immunohistochemistry (IH

70 also associated with an altered immune gene expression profile, as well as with monocyte activation

71 ytes displayed an enhanced inflammatory gene expression profile associated with high glycemic burden.

72 e patient-derived stromal cells exhibit gene expression profiles associated with early osteoblastic d

73 We retrieved detailed gene expression profiles associated with known, but rare, sta

74 ifferent types of tissues have distinct gene expression profiles associated with specific function or

75 In the current paper, we assessed the miRNA expression profile at different age time points and brai

76 , assessment of T cell infiltration and gene expression profile at the DTH biopsy site corresponds to

77 genous regulatory RNAs which alters the gene expression profiles at a particular time and type of tis

78 The gene expression profile, before folding begins in the maturin

79 genetic and epigenetic variation as well as expression profiles between the Gransden and Reute ecoty

80 This is the first analysis of gene expression profiles beyond Vitis to mealybug-transmitted

81 rkers for neurological damage based on their expression profiles both across the body and within the

82 Through an integrated analysis of expression profiling, Brd2/Brd4 cistrome data, and chang

83 Here, we applied an immune-based gene expression profile by NanoString platform to identify wh

84 ulates the cell differentiation-related gene expression profile by suppressing Wnt pathway activity a

85 the regulatory matrix between miRNA and mRNA expression profiles by solving multiple linear programmi

86 Furthermore, gene expression profiling by next-generation sequencing alone

87 Gene expression profiling by RNA-Seq and qRT-PCR revealed exp

88 Here, we present prokaryotic expression profiling by tagging RNA in situ and sequenci

89 We analyzed Notch regulation by examining expression profiles (by quantitative reverse transcripti

90 n of core reactions, such as thresholding of expression profiles, can significantly change model cont

91 The altered gene expression profile caused by reducing histone sumoylatio

92 ent work meticulously studies the functional expression profile changes of VGSCs during the processes

93 transcripts revealed PE-fed larvae retain an expression profile consistent with normal intestinal fun

94 Significant downregulation of gene expression profiles consistent with local innate immune

95 orphism information with the QTL mapping and expression profiling data led to identification of 396 d

96 reduction is often used to visualize complex expression profiling data.

97 Analysis of MM patient gene expression profiling database showed that ENO1 expressio

98 nd, on the basis of clustering of their gene-expression profiles, defined 16 immune-cell states.

99 lysis revealed distinct disease-related gene expression profiles depending on anatomical location, wi

100 After day 1, gene expression profiles differed depending upon the source o

101 We aimed to identify gene expression profile differences in innate immunity pathwa

102 x locus and examining their gene content and expression profiles during flower development in wild an

103 c gradient of two negatively correlated gene-expression profiles, each containing hundreds of genes.

104 de biopsy; the tissue morphology and antigen expression profile enable classification into one of the

105 However, expression profiles, especially when collected in large

106 Metabolomic and gene expression profiling established STAT1 deletion in adipo

107 Gene expression profiling experiments have shown induction of

108 mples covering more than 50 cancer types and expression profiles for 12,442 distinct compounds.

109 We identify likely gene expression profiles for muscle, nervous system, tegument

110 Gene expression profiles for several thousand genes are forma

111 whole-genome bisulfite sequencing, and gene expression profiles from cells entering replicative sene

112 xpression signature to compound-induced gene expression profiles from large drug libraries, researche

113 d analysis of a large public dataset of gene expression profiles from newly diagnosed de novo DLBCL p

114 Comparing expression profiles from sensitive and resistant cell li

115 of human chlamydia-infection data with bulk expression profiles from six cell types and prior marker

116 ery pipeline was developed to integrate gene expression profiles from The Cancer Genome Atlas and ess

117 ng our recently developed tool deTS and gene expression profiles from two reference tissue panels: th

118 alysis to a compendium of 108 RNA-sequencing expression profiles from two S. aureus clinical strains

119 By integrating gene expression profiling, genetics and comprehensive phenoty

120 d tumor thickness on prognostication by gene expression profiling (GEP) class.

121 Increasing number of gene expression profiles has enabled the use of complex model

122 Cancer classification based on gene expression profiles has provided insight on the causes o

123 As two-arm studies with gene expression profiling have been rarer than similar one-ar

124 Information-rich assays, such as gene-expression profiling, have generally not permitted effic

125 ma was defined by one of the following: gene expression profiling high risk (GEP(hi)), t(14;16), t(14

126 first trimester dNK; and 3) protein and gene expression profiles identified multiple differences betw

127 ese genetic subtypes also have distinct gene expression profiles, immune microenvironments, and outco

128 s and obese mice elicits a fasting-like gene expression profile, improves glucose metabolism, de-repr

129 PN induced a unique gene expression profile in mDCs, including the gene that enco

130 ) components in chRCC that differed from the expression profile in renal oncocytoma.

131 yperinflation, and the nasal epithelial gene-expression profile in severe COPD.

132 This unique age-related gene expression profile in the red sea urchin nervous system

133 Gene expression profiles in 10-mum pixels conformed into the

134 Here, we examined gene expression profiles in a total of 150 RNA samples from t

135 changes in immune cell infiltrates and gene expression profiles in both the gut lamina propria and t

136 anoString technology and investigated miRNAs expression profiles in first week postpartum HM exosomes

137 ll responses and the promotion of T(h)1 gene expression profiles in GC T(fh) cells.

138 use bioinformatics to determine OPRM1 brain expression profiles in higher primates and to look for r

139 Gene expression profiles in homologous tissues have been obse

140 PKbeta1 and AMPKbeta2 lead to different gene expression profiles in human induced pluripotent stem ce

141 mining large-scale phenotype-associated gene expression profiles in hundreds of mouse clonal cell lin

142 Dynamic gene expression profiles in innate cells, such as myeloid-der

143 linical or hematological variables, and gene expression profiles in PBLs associated to activation (CD

144 n female germ cells, we analyzed global gene expression profiles in perinatal ovaries from wildtype,

145 e two isoforms differ substantially in their expression profiles in plant organs and in response to e

146 The PYP/XES expression profiles in sweet orange and in other Citrus

147 iol and tamoxifen elicited differential gene expression profiles in the carotid artery.

148 ear elements (SINEs) show cell type-specific expression profiles in the mouse hippocampus.

149 life, and measured DNA methylation and gene expression profiles in upper airway mucosal cells and as

150 We performed gene expression profiling in 265 left atrial samples from pat

151 Expression profiling in human pre-implantation embryos a

152 Protein expression profiling in islets confirms perturbation in

153 muscle loss, we conducted a large-scale gene expression profiling in quadriceps muscle of arctic grou

154 Unbiased mRNA expression profiling in the medial PFC (mPFC) of materna

155 As advances in single-cell gene expression profiling increase the accuracy and the cover

156 DD and BNF, and the distinct tissue-specific expression profiles indicate different functional specia

157 Moreover, gene expression profiling indicated a broad negative impact o

158 Further, expression profiling indicated significant differences i

159 Surface phenotype and NanoString gene expression profiling indicated the closest steady-state

160 Gene-expression profiling indicates that Trp53DeltaIECAktE17K

161 Importantly, the cytokine expression profile induced by 40 Hz flicker was differen

162 ation RNA sequencing to investigate the gene expression profiles intrinsic to this disease.

163 l repertoire of cardiac cells and their gene expression profiles is a fundamental first step in this

164 Gene expression profiling is emerging as a tool for tuberculo

165 We hypothesized that variants with similar expression profiles may be the product of biological noi

166 tionship between clinical responses and gene expression profiles may shed light on the mechanisms und

167 pplication of our method to time series gene expression profiles measured in peripheral blood from a

168 Minority Gene Expression Profiling (MGEP) refers to a scenario where t

169 Our data combined the analysis of gene expression profiling microarrays and gene methylation pr

170 pitulates the histological features and gene expression profile observed in human patients.

171 In this study, we examined the gene expression profile of a CRE Escherichia coli clinical is

172 ature but the result of normalizing the gene-expression profile of actively proliferating aneuploid c

173 ng demonstrated distinct changes in the gene-expression profile of circulating platelets of COVID-19

174 nic stem cells and successfully captured the expression profile of endogenous retroviruses in single

175 profiling across this phenotypic series, the expression profile of every gene can be correlated with

176 This report presents the miRNA expression profile of experimental human oral wounds and

177 nduced EMT in cancer cells and modulated the expression profile of genes implicated in EMT and metast

178 hesized that isolating and studying the gene expression profile of invasive tumor cell subpopulations

179 ovel human OFC signature genes and probe the expression profile of known coloboma genes, along with a

180 anslational relevance of these findings, the expression profile of MDK-depleted tumors was enriched i

181 The single-cell expression profile of mES and drug treated cells reveal

182 gene expression of MMP9 and CD44, alter the expression profile of nine miRNAs, and increased the try

183 The aim of this study was evaluated the mRNA expression profile of pediatric Acute Lymphoblastic Leuk

184 However, a rescue in the expression profile of pluripotency factors was not obtai

185 We describe the expression profile of proteins that regulate gene expres

186 nd in vitro suppression assays, and the gene expression profile of rapamycin-conditioned Treg cells b

187 Global gene expression profile of stem cells reveals significant inf

188 To clarify the expression profile of the e1m promoter-driven GPR56 in p

189 divisions of the airways and the stable gene expression profile of these regions better defines condi

190 In this study, we evaluated the gene expression profile of two contrasting Eucalyptus grandis

191 Using the gene expression profiles of 1,038 lung tissue samples, we per

192 We obtained expression profiles of 17,757 genes from 8,758 cells fro

193 We established the bulk gene expression profiles of 78 ICCs.

194 ule microbial hormones drastically alter the expression profiles of antibiotics and other drugs in ac

195 Strikingly, differential gene expression profiles of both whole muscle and, to a lesse

196 Using the expression profiles of brain region-specific GCN edges,

197 forms and provides a new tool for screening expression profiles of cell culture clones, monitoring p

198 Meanwhile, large-scale gene expression profiles of cellular responses to chemical co

199 Finally, paternal diet modified the expression profiles of central epigenetic regulators of

200 Computational analysis of gene expression profiles of DNA glycosylases in gastric speci

201 th this hypothesis, we found that brain gene expression profiles of DWV-A infected bees resembled tho

202 Another 16 VOCs correlated strongly with expression profiles of eleven key genes in the lipoxygen

203 nding preferences that correlate with glycan expression profiles of host cells targeted by each bacte

204 anges to the higher-order chromatin and gene expression profiles of human cells.

205 The gene expression profiles of invading microtumors were analyze

206 functional association network based on the expression profiles of isoforms derived from multiple RN

207 infection may result from distinct regional expression profiles of key bile acid receptors that regu

208 of other Glbs in nodules, the spatiotemporal expression profiles of Lbs and Glbs at the mRNA and prot

209 While we have previously characterized the expression profiles of major SV cell types in the adult

210 dim(tdT) and bright(tdT) cells had different expression profiles of matrix-associated genes (Svep1, I

211 e applied our computational framework to the expression profiles of miRNA/mRNA of INS-1, at different

212 Our data indicate that dampening gene expression profiles of monocyte and neutrophil activatio

213 between miRNAs and mRNAs from their matched expression profiles of more than 9000 primary tumors.

214 rtant to understand the normal developmental expression profiles of NRGs and ErbBs in specific neuron

215 anslation programs contribute to shaping the expression profiles of oncogenes.

216 While we find that expression profiles of orthologous genes in different sp

217 miRDB now hosts the expression profiles of over 1000 cell lines and presents

218 Voluminous gene expression profiles of patients with cancer have been ac

219 Global gene expression profiles of PBMCs from 43 drug-naive patients

220 istribution of dopaminergic function and the expression profiles of polygenic risk for schizophrenia.

221 Here, we tested the hypothesis that gene expression profiles of protein-coding genes expressed in

222 We applied DESMOND on expression profiles of samples from two large breast can

223 stic IMputation to reduce dropout effects in Expression profiles of single-cell sequencing), on synth

224 eases, total Bdnf mRNA levels, with distinct expression profiles of specific exons, in the hippocampu

225 filing (MGEP) refers to a scenario where the expression profiles of specific genes of interest are co

226 The expression profiles of these candidates, including ACT,

227 The expression profiles of these MADS-box genes were analyze

228 ubTCMR showed heterogeneous and intermediate expression profiles of transcripts that were upregulated

229 or validation purposes and to elucidate gene expression profiles of tumor-interacting monocytes and m

230 The gene expression profiles of two different types of studies, n

231 effective in estimating cell proportions and expression profiles of unknown cell types based on simul

232 hows extensive remodeling, with differential expression profiles of ~1100 transcripts and ~2200 prote

233 covery phase, we performed genome-wide miRNA expression profiling of 124 fresh, paired colorectal tum

234 Cytokine expression profiling of BIA-ALCL cell lines and clinical

235 We hypothesized that gene expression profiling of human melanomas using a new RNA

236 We conducted a comparative expression profiling of immune response genes in periphe

237 PE-seq2 for fluorescence, morphological, and expression profiling of individual primary cells from a

238 In summary, expression profiling of PreC CatD -positive layer III ne

239 l polarized signaling in the aorta with gene expression profiling of sorted cell populations and sing

240 Here, gene expression profiling of the bone marrow along disease pr

241 Gene expression profiling of the isolated cell protrusions su

242 MicroRNA expression profiling of the lung tissue was performed us

243 Global gene expression profiling of the lungs of infected dogs revea

244 Notably, cell types with divergent gene-expression profiles often shared very similar properties

245 Gene expression profiling on the cerebral vessels isolated fr

246 unctional relationships in data such as gene expression profiles or somatic mutation catalogs from tu

247 and the accompanying drastic changes in gene expression profiles play fundamental roles in multistep

248 and adipocyte estrogen/testosterone receptor expression profiles provide preliminary insights into th

249 1, neutrophils were characterized by a gene expression profile proximal to bone marrow neutrophils (

250 A specific gene expression profile, referred to as ECM3 (Extracellular M

251 ealed substantially altered gene and protein expression profiles, respectively.

252 Gene expression profiling results identified p53 pathway as a

253 Immunophenotypic and gene expression profiles revealed a unique spectrum of memory

254 Expression profiling revealed significant differential e

255 Gene expression profiling revealed that epithelial-mesenchyma

256 Time-resolved whole genome expression profiling revealed that RNLs and "classical"

257 lution and others with substantially altered expression profiles, revealing extensive plasticity of c

258 Gene expression profiling reveals VGLL1 as a member of a uniq

259 Gene expression profiling showed a similar differentiation ab

260 In these cases, gene expression profiling showed diminished expression of gen

261 ding drug-gene phenotype similarity and gene expression profile similarity that capture information o

262 These datasets delineate gene expression profiles spanning key differentiation events

263 the GSC model in light of recent single-cell expression profiling studies.

264 response to VEGF, including VEGFR2, and gene expression profiles, such as that of neuronal pentraxin

265 irculating CD103(+) cells also shared a gene expression profile that is closer to that of gut CD4 T c

266 modification profile promotes a unique gene expression profile that supports enhanced tumor developm

267 immune cell subsets expressing distinct mRNA expression profiles that are, in part, dictated by the s

268 ion publicly-available human microarray gene-expression profiles, these profiles were measured using

269 Genes showing a similar expression profile to Arg1 were enriched for STAT6 trans

270 the bimodal behavior of RNA-sequencing gene expression profiles to identify altered gene sets in het

271 ation on samples' tissue of origin with gene expression profiles to improve prediction performance.

272 tumors undergoing prognostic biopsy for gene expression profiling to assess the relationship between

273 onse to stress and use circuit-specific gene expression profiling to uncover novel downstream targets

274 The gene expression profiles under the thermoneutral and heat str

275 d through traditional means, the large-scale expression profiles underlying each cell type remain unk

276 ext-generation sequencing technologies, gene expression profiling using RNA-seq has increased the sco

277 Ttpa expression profile was not altered by the VitE status de

278 The HBV-induced gene expression profile was similar to that induced by toll-l

279 f NCI-60 compound screening results and gene expression profiles was performed.

280 Comparative gene expression profiling was performed between 2 murine mode

281 Coupling pMEI genotypes with gene expression profiles, we identify pMEI-associated express

282 ferent assumptions based on the shape of the expression profile were used to identify genes that coul

283 Gene expression profiles were also determined after disease-m

284 The gene expression profiles were determined by microarray analys

285 atment-induced changes in lesional skin gene expression profiles were evaluated using Affymetrix arra

286 ffered in the ways in which their brain gene expression profiles were influenced by parental experien

287 Distinct Spn and host gene-expression profiles were observed during colonization an

288 Marked changes in TCC protein expression profiles were observed when clozapine treatme

289 Genome-wide gene expression profiles were obtained and biomarker identifi

290 Moreover, these anatomically distinct gene expression profiles were recapitulated within individual

291 rformed, and histochemical analysis and gene expression profiling were performed on fat and muscle bi

292 previously proposed blood biomarkers exhibit expression profiles which could limit their diagnostic e

293 ent a novel approach integrating lncRNA-mRNA expression profiles with clinical characteristics to ide

294 data integration techniques, combining gene expression profiles with computationally generated metab

295 al understanding by associating SN cell type expression profiles with specific disease risk.

296 nd highlight the potential of combining gene expression profiling with clinical data to predict treat

297 or tissue microarray (TMA) cores and by gene expression profiling with EdgeSeq Immuno-Oncology Assay

298 By combining genome-wide expression profiling with pharmacological STAT6 inhibiti

299 -seq2) for combining single-cell imaging and expression profiling, with substantial improvements in t

300 howed that Fkbp8-/- embryos have an abnormal expression profile within tissues harvested at posterior