ライフサイエンスコーパス: expression analyses

1 (HGS) ovarian cancer using gene and protein expression analyses.

2 with HPLC, complemented by gene and protein expression analyses.

3 nd an outcome of interest in high throughput expression analyses.

4 is not detected by traditional differential expression analyses.

5 y examining 3' UTR and CDS sequences in gene expression analyses.

6 about the quality of many published gene co-expression analyses.

7 scope based on both gene sequence and tissue expression analyses.

8 d increased myeloid bias in single-cell gene expression analyses.

9 on, in vitro gel retardation assays and gene expression analyses.

10 termined by histological appearance and gene expression analyses.

11 tensively studied using unbiased genome-wide expression analyses.

12 than 580 million RNA-Seq reads to facilitate expression analyses.

13 those identified by traditional differential expression analyses.

14 ting were used for messenger RNA and protein expression analyses.

15 elopment/function, we performed whole-genome expression analyses.

16 females in a murine model via histologic and expression analyses.

17 ese may be distinguished by comparative gene expression analyses.

18 to multiple genes and isoforms, complicating expression analyses.

19 T cells (CTL) using flow cytometry and gene expression analyses.

20 e mechanistic insight using gene and protein expression analyses.

21 g biochemical, immunohistochemical, and gene expression analyses.

22 expression quantitative trait loci and gene expression analyses.

23 lla replication within macrophages with gene expression analyses.

24 these cells through immunostaining and gene expression analyses.

25 l framework in order to perform differential expression analyses.

26 e-wide transcription factor binding and gene expression analyses.

27 ng meta-analysis and employ pathway and gene expression analyses.

28 munophenotyped using mass cytometry and gene expression analyses.

29 n in CSB neurons using unbiased RNA-seq gene expression analyses.

30 alidate findings from global RNA- or protein-expression analyses.

31 Comparative embryonic gene expression analyses across tetrapod species suggest ASHC

32 Systematic expression analyses across tissues and developmental sta

33 Cytokine expression analyses after exposure to S. sciuri W620 sho

34 ance estimation is an important step in gene expression analyses aimed at identifying differentially

35 Gene expression analyses allowed us to classify genotypes bas

36 Genome-wide expression analyses and binding experiments indicate tha

37 mRNA expression analyses and dual-luciferase promoter assays

38 sequencing followed by unbiased genome-wide expression analyses and found that a population of uncou

39 To identify mechanisms, we carried out gene expression analyses and found that several genes, includ

40 f ICM using differential whole transcriptome expression analyses and functional in vitro cardiomyocyt

41 By performing gene expression analyses and functional studies via RNA inter

42 ocesses for isolation of intact microRNA for expression analyses and genomic DNA (gDNA) for CpG methy

43 rformed integrated genome-wide chromatin and expression analyses and identified Ikaros target genes i

44 Gene expression analyses and immunostaining revealed microgli

45 s or focal laser uncaging, coupled with gene expression analyses and Notch invalidations, to address

46 underlying isolated MR, we performed LV gene expression analyses and overlaid regulated genes into in

47 Gene expression analyses and promoter-GUS fusion assays docum

48 ormed comprehensive comparative digital gene expression analyses and revealed novel transcription sta

49 , 3D bone imaging, electron microscopy, gene expression analyses and safety assessments.

50 Based on gene expression analyses and transplantation studies, we foun

51 Expression analyses and unbiased gene expression profili

52 Global gene expression analyses and validation revealed that IL-15 r

53 These data were combined with gene expression analyses, and candidate enhancers were identi

54 rates comparative genomics data, global gene expression analyses, and intrinsic properties of transcr

55 -directed mutagenesis, mouse and human brain expression analyses, and patch clamp techniques were per

56 henotypic characterizations of veg2 mutants, expression analyses, and the use of protein-protein inte

57 ants and perform allele-specific binding and expression analyses at seven top candidate loci: 9p21.3,

58 cells (ESCs) and to conduct multiplexed gene expression analyses at the single-cell level by using 48

59 More specifically, the combined use of co-expression analyses based on self-organizing maps with s

60 nges in leukocyte and neutrophil genome-wide expression analyses between healthy and injured mice (p

61 Prior gene expression analyses, both large and small, have been dic

62 ated CTC from the HVB were subjected to gene expression analyses by quantitative polymerase chain rea

63 atin immunoprecipitation sequencing and gene expression analyses carried out by us revealed that BACH

64 ing chromatin immunoprecipitation assays and expression analyses, CD47 expression was found to be reg

65 ditional loss-of-function models, genomewide expression analyses, chromatin immunoprecipitation, and

66 ed transcriptomics and phylogenetic and gene expression analyses clearly identified specific gene mem

67 spite the recent advance of single-cell gene expression analyses, co-measurement of both genomic and

68 Using single-cell gene expression analyses combined with different reporters fo

69 rst global DNA promoter methylation and gene expression analyses comparing human cancers to their rep

70 Genomic, mRNA, and protein expression analyses confirmed that the new cell systems

71 Expression analyses confirmed that ZIM2as is expressed i

72 Expression analyses confirmed the brain-specific distrib

73 Notably, mRNA and protein expression analyses confirmed the renal expression of th

74 Transient, conditional, and ectopic expression analyses consistently supported a role for Ga

75 ith loneliness in this sample, although gene expression analyses controlled for AD diagnosis).

76 Gene expression analyses could distinguish tumors of differen

77 Gene expression analyses coupled with chromatin immunoprecipi

78 Coexpression, microarray, and real-time expression analyses demonstrate a correlation between Cg

79 from chromatin immunoprecipitation and gene expression analyses demonstrate that ATHB7 and ATHB12 ac

80 Unbiased global gene expression analyses demonstrate that MECP2 functions as

81 Gene expression analyses demonstrate that Postn-Cre ablates H

82 Expression analyses demonstrate that Sema6A and PlexA4 p

83 Organ weights and gene expression analyses demonstrated that adipose tissue is

84 hIP) combined with sequencing (ChIP-seq) and expression analyses demonstrated that IRF2-occupied gene

85 Our findings are further reinforced by gene expression analyses demonstrating the upregulation of EM

86 s an important data preparation step in gene expression analyses, designed to remove various systemat

87 Notably, the expression analyses detected the transcription of a RNAS

88 ait locus (eQTL) mapping and allele-specific expression analyses, discovering substantial evidence fo

89 Expression analyses distinguished tumors generated from

90 ion, including localization studies, dynamic expression analyses, epigenetic modification monitoring,

91 Furthermore, gene expression analyses established the ability of DKK2 to d

92 n conjunction with quantitative RT-PCR-based expression analyses, established a combination of transc

93 Gene expression analyses focused on a set of target genes put

94 Global gene expression analyses following Setd8 knockdown demonstrat

95 Furthermore, gene expression analyses found that the TGFbeta/TNFalpha-deri

96 ant B-cell precursors, and according to gene expression analyses from 207 children with minimal resid

97 Reporter gene assays and SnRK1 target gene expression analyses further demonstrate that PP2C inhibi

98 Epigenetic and RNA-expression analyses further discriminated the offspring'

99 Gene expression analyses further identified six genes (TSPAN2

100 The use of transgenic mice and gene expression analyses has revealed novel pathways involved

101 Expression analyses have been used to find such markers,

102 Gene expression analyses highlighted the association between

103 icial hibernation, hormonal treatments, gene expression analyses, hormone measurements, and vitelloge

104 In addition, our gene expression analyses identified a subgroup of tumours ass

105 oupled with transcriptional profiling and co-expression analyses identified a suite of proteins that

106 Gene expression analyses identified dysregulation of miRNA-44

107 Gene expression analyses identified Pdk1-dependent changes in

108 Genome-wide expression analyses identified that the majority of STAT

109 Finally, homoeolog-specific gene expression analyses identify TaAGL33 and its splice vari

110 ow able to go past the traditional gene-wise expression analyses in a variety of ways, analysing expr

111 We used ChIP and differential gene-expression analyses in Arabidopsis seedlings overexpress

112 for three candidates by spatial and temporal expression analyses in five grape cultivars.

113 Genome-wide gene expression analyses in liver cells performed in this stu

114 Furthermore, we performed eQTL and co-expression analyses in lung tissue.

115 Comparative expression analyses in MEP, MkP, and ErP populations rev

116 Western blot and mRNA expression analyses in mice yielded consistent data.

117 Gene expression analyses in neuroblastoma cell lines suggest

118 nsmission electron microscopy (TEM) and gene expression analyses in order to assess diverse cellular

119 lism were assessed together with global gene-expression analyses in peripheral blood mononuclear cell

120 Genome-wide differential gene expression analyses in the cerebral cortex and cerebellu

121 lyses of the mutated genes in zebrafish, and expression analyses in zebrafish, mouse, and human.

122 res of the identified exons/transcripts, and expression analyses including previously published RNA-S

123 Complementation and expression analyses indicate that ccdA2 encodes the prim

124 Morphological, histological, and in situ RNA expression analyses indicate that Cul4 acts at axil and

125 Expression analyses indicate that HCT1 mRNA accumulates

126 Gene expression analyses indicate that NHFs and MWFs separate

127 Genome-wide expression analyses indicate that TAZ/YAP, TEADs, and TG

128 Inhibition assays and gene expression analyses indicate that the uptake and transpo

129 e (FC) of 2.0 as a threshold value, the gene expression analyses indicated that 19 genes were differe

130 Gene expression analyses indicated that Brg1 regulates a sign

131 Expression analyses indicated that cell cycle factors mp

132 Expression analyses indicated that Fam20a is expressed i

133 Genome-wide gene expression analyses indicated that GATA3 regulated a sim

134 Gene expression analyses indicated that granulocytes are the

135 Our phenotypic and gene expression analyses indicated that PUB4 promotes express

136 Expression analyses indicated that TAG1 and TAGL1 act to

137 Gene expression analyses indicated that the addition of CS -

138 Lineage tracing and marker expression analyses indicated that the new beta-cells we

139 Recent ChIP-seq and RNA expression analyses indicated that WhiA and WhiB regulat

140 logy through large-scale genetic and protein expression analyses, little is known about the underlyin

141 Genetic mapping and gene expression analyses localized the sld mutation within th

142 We used a combination of microarray expression analyses of a diverse set of tissues and func

143 We performed phylogenetic and expression analyses of a leaf developmental regulator (C

144 In gene expression analyses of adipose tissue, expression of the

145 ng epithelial cells, and deep-sequencing and expression analyses of airway epithelial cells revealed

146 we present structural, biochemical, and gene expression analyses of another putative Mtb secreted dis

147 Co-expression analyses of AtPIP2;1 with endomembrane marker

148 Time-series gene expression analyses of bulk cells have difficulty distin

149 e in CaM-mediated signaling pathways by gene expression analyses of CaM KMT and phenotypic characteri

150 d in most part on experiments utilizing gene expression analyses of cell lines and tumor tissue.

151 Expression analyses of cell-wall synthetic genes and wal

152 Second, global expression analyses of copt2-1 versus wild-type Arabidop

153 Expression analyses of cytokines in peritoneal tissue an

154 Expression analyses of early corneas suggest an involvem

155 Single-cell gene expression analyses of FACS-sorted macrophages revealed

156 Expression analyses of genes associated with the abscisi

157 Immunohistochemical and gene expression analyses of giant cell arteritis-affected tem

158 lthough this hypothesis is well supported by expression analyses of individual X-linked genes and by

159 We performed functional and expression analyses of isolated liver cells.

160 Further, biochemical and gene expression analyses of key enzymes from these pathways p

161 In-depth expression analyses of lncRNAs with genomic loci adjacen

162 oice for gene discovery through differential expression analyses of microarray and high-throughput PC

163 Expression analyses of miR-383 in PCa clinical tissues e

164 mbocytopenia (ITP), we performed genome-wide expression analyses of mRNA and microRNA in T cells from

165 th of Myc-dependent tumors in mice, and gene expression analyses of Myc-high human breast cancers sug

166 Gene expression analyses of NAC-treated NPC1ASO mice suggeste

167 Gene expression analyses of non-myocyte cells isolated from H

168 Gene and protein expression analyses of Opa1 and Fis1 were performed on c

169 Integrated ChIP-seq and gene expression analyses of patient-derived cell lines reveal

170 sor of secondary metabolism is shown by gene expression analyses of polyketide synthases and the dete

171 Gene expression analyses of publically-available data (n = 23

172 However, expression analyses of Robo2 at this stage raised the po

173 Gene expression analyses of seed-specific tryptophan-dependen

174 ith human total and enriched blood leukocyte expression analyses of severe trauma patients at 0.5, 1,

175 Moreover, in differential expression analyses of simulated and real datasets, BPSC

176 Integrated in situ and real-time expression analyses of stage-specific markers highlighte

177 Expression analyses of the 44 genes encoded in this geno

178 hnology, we perform whole transcriptome gene expression analyses of the larval genital imaginal disc

179 ological and immunocytochemical analyses and expression analyses of the marker genes demonstrated tha

180 performed microarray-based comparative gene expression analyses of the pollen mother cell stage in s

181 along with systems-based comparative and co-expression analyses of these transcriptome maps identifi

182 Gene expression analyses of transgenic corn plants confirmed

183 this study, we performed phenotypic and gene-expression analyses of treatment-naive and engineered to

184 Metabolomic and gene expression analyses of urine and tissue samples from mic

185 Gene expression analyses on abdominal tissue were used to ide

186 proper cis-regulatory element activity, and expression analyses on both Hand2 conditionally null and

187 Gene expression analyses on both mRNA and microRNAs show a mo

188 Gene expression analyses on brains from these mice show chang

189 Whole-transcriptome gene expression analyses on WNT-dependent KDR(+)CD235a(-) def

190 Stable transgene expression analyses, on multiple independent lines per c

191 i2a-Sxi1alpha heterodimer using whole genome expression analyses paired with in silico and in vitro b

192 The co-expression analyses performed by using RNA-Seq data supp

193 Expression analyses performed on a panel of several diff

194 antitative muscle morphology, gene and miRNA expression analyses, proteasome activity, motor activity

195 Gene expression analyses (quantitative PCR, RNA sequencing) s

196 d of age) was detected in the hydrolysis and expression analyses, respectively.

197 Gene expression analyses reveal a failure to extinguish genes

198 Expression analyses reveal an up-regulation of CAII and

199 Transcriptome co-expression analyses reveal significantly correlated expr

200 Subsequent gene-expression analyses reveal that complex antibiotic-induc

201 Global gene expression analyses reveal that trisomy 12 profoundly af

202 Gene expression analyses revealed a more regulatory profile f

203 ical staining of tissue microarrays and mRNA expression analyses revealed a positive association betw

204 Gene expression analyses revealed both a pronounced upregulat

205 Gene expression analyses revealed CD68 and the redox-related

206 Further mRNA expression analyses revealed differential expression of

207 Expression analyses revealed increased levels of IL-36al

208 Gene-expression analyses revealed reciprocal changes of genes

209 Gene expression analyses revealed significant overlap of TNFa

210 Moreover, gene-expression analyses revealed that anti-RSPO treatment in

211 Expression analyses revealed that Bdnf (brain-derived ne

212 Genome wide expression analyses revealed that BDNF and NT4 mutant mi

213 Comprehensive gene expression analyses revealed that BM-CD31(+) cells expre

214 Temporal expression analyses revealed that CDX4 was expressed exc

215 Instead, genome-wide and gene-specific expression analyses revealed that Cpdm mesenchymal cells

216 In patients with non-small cell lung cancer, expression analyses revealed that high TLR7 expression w

217 Our genome-wide gene expression analyses revealed that human melanoma cell li

218 Protein and mRNA expression analyses revealed that kidney proximal tubule

219 Gene expression analyses revealed that MKs are the source of

220 Expression analyses revealed that native TP0326 is expre

221 Spatial and temporal expression analyses revealed that PPARgamma impacts gene

222 Gene expression analyses revealed that Sox9 was expressed exc

223 Comparative expression analyses revealed that the core ExoR regulon

224 Gene expression analyses revealed that UPL3 expression is neg

225 Expression analyses revealed the abundance of Pten trans

226 sland methylation and genome-wide microarray expression analyses revealed the persistence of hypergly

227 Using genome-wide expression analyses (RNA sequencing) in pericarps and si

228 Gene expression analyses show strong correlation between the

229 Mechanistically, genome-wide expression analyses show that anti-RANKL therapy promote

230 Expression analyses show that AtNIP7;1 is selectively ex

231 Furthermore, global gene expression analyses show that GW9662 treatment suppresse

232 Gene expression analyses show that Jarid2 and E(z) (Enhancer

233 Chromatin-binding and eRNA expression analyses show that LED associates with and ac

234 Sequence and expression analyses show that SRGAP2C is the most likely

235 Liver histology and gene expression analyses showed increased inflammation and li

236 Expression analyses showed that GhCesA2-A(T) and GhCesA2

237 Genome-wide expression analyses showed that IBH1 and IBL1 act interd

238 Gene expression analyses showed that regulation of the cell m

239 Gene expression analyses showed that upon loss of Notch2, the

240 Expression analyses showed up-regulation of WNT3A, GSK3B

241 Genome-wide expression analyses similarly reveal distinct roles for

242 re verified using bisulfite-mapping and gene-expression analyses, subsequently tested in a second tis

243 Electroretinography and gene expression analyses suggest a nonautonomous, RPE-depende

244 Genetic and expression analyses suggest that Baf1 is required to rea

245 Gene expression analyses suggest that double deletion not onl

246 Those findings, coupled with single-cell expression analyses, suggest that a continuum of progeni

247 Gene expression analyses suggested a variety of biological pr

248 Gene expression analyses suggested that differential expressi

249 both survivin and sfrp2 through promoter and expression analyses suggested that increased resistance

250 Histomorphometric and gene expression analyses suggested that neurofibromin, by inh

251 Global gene expression analyses suggested that Rb maintains the "sta

252 esults of geNorm, NormFinder, and BestKeeper expression analyses support the use of actin and ribosom

253 diffuse intrinsic pontine gliomas, and gene expression analyses supported an important role for dere

254 ations and counterintuitively, temporal gene expression analyses supported up-regulated osteoclastoge

255 strated through 3'-UTR luciferase assays and expression analyses that Connexin43 (Cx43) is a novel di

256 We previously performed global expression analyses that identified a set of approximate

257 38 expression was consistent with prior gene expression analyses that identified the alpha soluble NS

258 sequence also facilitated high resolution co-expression analyses that revealed three distinct cluster

259 Together with expression analyses, these results indicate that sub-fun

260 In conjunction with the aforementioned gene expression analyses, these results strongly suggest that

261 Expression analyses through mRNA in situ hybridization a

262 le mapping with population genomics and gene expression analyses to identify a gene, cortex, that reg

263 hes including metabonomic profiling and gene expression analyses to identify probable candidate genes

264 or enriched in HCs, extending previous gene expression analyses to reveal novel HC proteins and isof

265 We used mutational and gene expression analyses to validate both candidate genes and

266 h massively parallel DNA sequencing and gene expression analyses uncovered genes, including HOX genes

267 Further gene expression analyses uncovered that intercellular purine

268 omplements but is distinct from differential expression analyses, under the general goal of understan

269 In silico and in vivo expression analyses unraveled differential accumulation

270 Extensive gene expression analyses using a complete set of promoter-bet

271 Global gene expression analyses, validated by mRNA and protein deter

272 atrial pairs were subjected to whole-genome expression analyses via next-generation sequencing of sm

273 his pealeii Through lineage tracing and gene expression analyses, we demonstrate that cells expressin

274 aining and quantitative and comparative gene expression analyses, we determined that Prox1 upregulati

275 From transcript expression analyses, we found that HKL1 and HXK1 have di

276 Using mass cytometry and gene expression analyses, we identified 2 populations of hepa

277 Using sequencing and gene expression analyses, we identified a subgroup of HCA cha

278 combined in silico prediction and microarray expression analyses, we identified and validated the sph

279 By integrating ChIP-seq and expression analyses, we identify target genes that requi

280 Using dual-luciferase assay and over-expression analyses, we reveal for the first time that B

281 Using various expression analyses, we revealed a high co-overexpressio

282 ranscriptome and genome sequencing, and gene expression analyses, we show that a single gene, doubles

283 Immunohistochemical and gene expression analyses were also completed on xenograft tum

284 Global gene expression analyses were conducted using splicing-sensit

285 This included IL2RA, where allele-specific expression analyses were consistent with its interaction

286 Biochemical and ectopic expression analyses were consistent with peripheral asso

287 BAC cloning and expression analyses were employed to characterize these

288 Gene expression analyses were performed by RT-PCR.

289 First, whole-genome cellular and viral gene expression analyses were performed in lymph nodes of MCF

290 Expression analyses were performed on 37 PCas and 36 unm

291 Immunostaining and gene expression analyses were performed to establish the expr

292 Expression analyses were performed with tumors harvested

293 Functional and genome-wide expression analyses were performed.

294 Gene expression analyses were subsequently performed for iden

295 ole immunohistochemistry, and bacterial gene expression analyses were used to assess whether tubercul

296 In vivo mexB and armR expression analyses were used to corroborate in vitro Na

297 s combined with nutrient, jasmonate and gene expression analyses were used to test: whether RWW adult

298 Here we combined single-cell gene-expression analyses with 'machine-learning' approaches t

299 Combining detailed expression analyses with gain- and loss-of-function stud

300 The comprehensive expression analyses with simple clicking through GEPIA g