ライフサイエンスコーパス: temporal expression

1 oughout the corneal stroma with differential temporal expression.

2 ulated by HIV according to their patterns of temporal expression.

3 ysregulation of embryonic myosin heavy chain temporal expression.

4 e HCMV translation products and follow their temporal expression.

5 We find, for all major patterns of temporal expression, a substantive amount of gene expres

6 in several parameters, including spatial and temporal expression, allosteric regulation, and heat sta

7 s to be close correlation of the spatial and temporal expression among Maml1, Notch1 and Hes1 in the

8 as shown for three candidates by spatial and temporal expression analyses in five grape cultivars.

9 Temporal expression analyses revealed that CDX4 was expr

10 Spatial and temporal expression analyses revealed that PPARgamma imp

11 Temporal expression analysis of conserved and novel miRN

12 Temporal expression analysis of PTM5 in staged vascular

13 ed by Kar4, on average, are delayed in their temporal expression and exhibit a more stringent dose re

14 rier function assays to delineate the spatio-temporal expression and function of matriptase in mouse

15 Since beta subunits vary both in their temporal expression and localisation within neurones, be

16 ter model, we reproduced the observed spatio-temporal expression and localization patterns of these p

17 of PMP22 at cell junctions, we examined the temporal expression and protein localization during deve

18 e present study were to determine the spatio-temporal expression and putative E regulation of EBP1 in

19 enes differed from one another in both their temporal expression and response to IFN-gamma.

20 Furthermore, the temporal expression and selective inhibition of FGF rece

21 ures of plaque vulnerability, although their temporal expression and their respective value in predic

22 , we extend previous approaches to perform a Temporal Expression-based Analysis of Metabolism (TEAM).

23 ndent sample set demonstrated characteristic temporal expression changes for each gene.

24 e used to examine the cell specificities and temporal expression characteristics of selected promoter

25 ssion efficiency, cell type specificity, and temporal expression characteristics.

26 ression in known JH target tissues, in which temporal expression corresponds with periods of hormone

27 0 genes - and particular wiring that elicits temporal expression coupled to organelle morphogenesis.

28 ar targeting of MtPT4 is mediated by precise temporal expression coupled with a transient reorientati

29 ce of biomolecular interaction networks from temporal expression data is presented.

30 ets of neural precursors generating distinct temporal expression domains within the plane of the neur

31 Results provide information on the temporal expression during caryopsis development for a s

32 ry elements necessary for proper spatial and temporal expression during development in transgenic mic

33 signaling factors that varied in spatial and temporal expression during development of the mouse ENS.

34 n of p75 to certain types of neurons and its temporal expression during development prompted speculat

35 of the TKDPs, coupled with their restricted temporal expression during development, likely reflects

36 Differential temporal expression during the developmental cycle was s

37 ental timing in C. elegans, and their proper temporal expression ensures cell lineage patterns are co

38 s, but sequences determining its spatial and temporal expression have not been identified.

39 xible tool to determine genes having similar temporal expression, hence possibly related biological f

40 Proper spatial and temporal expression in the anterior endoderm prechordal

41 hese data may account for the differences in temporal expression IN VIVO: we have previously reported

42 are controlled by several genes whose spatio-temporal expression is tightly regulated.

43 Spatial and temporal expression levels of the potential VvGT genes w

44 genomic regulatory code, for the spatial and temporal expression of a key developmental control gene.

45 RNA secondary structure and the temporal expression of adenosine deaminase acting on RNA

46 The aim of this study was to investigate the temporal expression of angiogenic biomarkers during woun

47 ption factors, thus coordinating the spatial-temporal expression of AP-1-regulated genes.

48 a mechanism involving restricted spatial and temporal expression of Arp2/3 complex and N-WASP, whose

49 Previously, we identified temporal expression of beta-catenin during liver develop

50 chosen as a model to define the spatial and temporal expression of BHMT during development.

51 The temporal expression of biglycan and decorin on the apica

52 The temporal expression of cap5 and hla and the regulatory g

53 phorylation event is required for the normal temporal expression of cell-cycle-regulated genes such a

54 Temporal expression of chlamydial genes during the intra

55 The spatio-temporal expression of CTLA-2beta mRNA precisely overlap

56 hritic inflammation, we demonstrate that the temporal expression of cytokines during the incubation p

57 elopmental events by controlling spatial and temporal expression of developmental patterning genes vi

58 ved cells that may contribute to the spatial-temporal expression of DSPP during tooth development.

59 The spatial-temporal expression of DSPP is largely restricted during

60 n this study, we determined the cellular and temporal expression of EAAT1-3 in the developing human c

61 The spatial and temporal expression of EGFP, under the control of the Xe

62 that a risk allele that perturbs the spatial/temporal expression of EN2 could significantly alter nor

63 , Smith, and colleagues demonstrate that the temporal expression of Epo is critical for determining w

64 The spatial and temporal expression of Fgf3 and Fgf8 in pharyngeal endod

65 vation in order to ensure proper spatial and temporal expression of forespore-specific genes.

66 Enhancer binding proteins (EBPs) control the temporal expression of fruiting body development-associa

67 ng the sequences that direct the spatial and temporal expression of genes and defining their function

68 To test this hypothesis, the temporal expression of genes and proteins associated wit

69 ogy require detailed knowledge of the spatio-temporal expression of genes and proteins.

70 ian clock, which is critical for the correct temporal expression of genes and their products, is cont

71 tory mechanism that controls the spatial and temporal expression of genes during development.

72 Mapping the temporal expression of genes during human brain developm

73 nt role for Pkc1p in controlling the correct temporal expression of genes in the cell cycle.

74 modules (CRMs) act sequentially to regulate temporal expression of genes, but how the switch from on

75 atory sequences that control the spatial and temporal expression of genes.

76 In Caenorhabditis elegans, the spatial and temporal expression of germline genes is controlled post

77 croarray data revealed a differential spatio-temporal expression of GGPPS genes.

78 The transcriptional basis of the spatial-temporal expression of guidance cues and their cognate r

79 ranscriptional repressor and controls normal temporal expression of haploid cell genes during spermio

80 tent with emerging evidence that the precise temporal expression of Hox genes is crucial for the esta

81 the EE results in a significant delay in the temporal expression of Hoxc8.

82 tation for virus production, but the correct temporal expression of IE2 86 and IE2 40 together has th

83 The temporal expression of IL-12Rbeta2 on OX40-stimulated CD

84 Temporal expression of IL-17 and IL-23 in submandibular

85 We examined the temporal expression of IL-1beta, IL-4, IL-6, IL-10, IL-1

86 our study demonstrate for the first time the temporal expression of inflammatory genes during LPS-ind

87 eloping retinal neurons is important for the temporal expression of intrinsic fate determinants but n

88 ll functioning depends on the precise spatio-temporal expression of its genetic material.

89 The temporal expression of JADE1S correlated with the acetyl

90 ting that the ecdysone pathway regulates the temporal expression of let-7 in Drosophila.

91 The temporal expression of LGBP and proPO genes in healthy a

92 translational regulation in fine-tuning the temporal expression of localized RNA, and this may provi

93 Temporal expression of MMP-9 inversely correlated with M

94 ) soluble factors alone regulate spatial and temporal expression of morphogenetic molecules and proce

95 n of bvgAS transcription is required for the temporal expression of multiple phenotypic phases that o

96 criptional events to control the spatial and temporal expression of muscle-specific genes.

97 The distinct spatial and temporal expression of nocturnin and PARN suggests that

98 is-acting sequences control the regional and temporal expression of NR2A, implicating distinct regula

99 novo infection, pTyr(705)-STAT3 promoted the temporal expression of ORF59, a viral replication protei

100 The temporal expression of PAI-1 was examined by real-time P

101 reviously, and here we find that the complex temporal expression of pb in the labium is like that of

102 The spatial and temporal expression of plant and fungal N metabolism gen

103 Temporal expression of positive and negative angiogenic

104 bioinformatics to determine the spatial and temporal expression of proteins in cells, tissues and wh

105 ic process, we set to determine the distinct temporal expression of proteins regulating the formation

106 We found that MKs regulate the temporal expression of Pyk2 and its subcellular localiza

107 erse transcription-PCR was used to study the temporal expression of qsrP, acfA, and ribB during the e

108 In this study, we examined the spatio-temporal expression of recently discovered ERalpha36 (ES

109 In M0 MDM, the temporal expression of representative genes from Salmone

110 on of molecular clock proteins influence the temporal expression of SCN neuronal state or intercellul

111 The surprisingly restricted spatial and temporal expression of SDR1 suggests the dynamic mobiliz

112 These results suggest that proper spatio-temporal expression of Sema3c, regulated positively by F

113 However, the specific spatial and temporal expression of semaphorin 6B (Sema6B) in chick c

114 hermore, we characterized the structures and temporal expression of seven novel spliced early transcr

115 Gene cluster analysis showed differences in temporal expression of SfAV-1a genes, enabling their ass

116 a determinacy factor, regulates the spatial-temporal expression of SGL1 during leaf morphogenesis an

117 Varying the temporal expression of Slc26a4 revealed that E16.5 to P2

118 Temporal expression of Snai1 mirrored that of vimentin a

119 Spatial and temporal expression of specific basic-helix-loop-helix (

120 oenvironments established by the spatial and temporal expression of specific signaling molecules are

121 ient to recapitulate the correct spatial and temporal expression of SpPks.

122 Based on these results, we propose that the temporal expression of T3S genes in Chlamydia is control

123 oding RNA molecules that control spatial and temporal expression of targeted genes through post-trans

124 authors describe studies on the spatial and temporal expression of the CFH gene and localization of

125 ess to these growth factors is determined by temporal expression of the cytokine-specific IL-2 recept

126 with iron, H2O2 and hemin treatment, and the temporal expression of the genes is very similar.

127 novel system that allows tightly controlled temporal expression of the IE2 proteins and provides com

128 Here, we study the temporal expression of the inhibitory receptor programme

129 plays an important role in co-ordinating the temporal expression of the LEE by controlling grlRA expr

130 We propose that Mce1R facilitates balanced temporal expression of the mce1 products required for or

131 We analyzed the evolution and temporal expression of the microRNA complement and seque

132 is study was to characterize the spatial and temporal expression of the mouse Ctrp5 gene, determine t

133 is study was to characterize the spatial and temporal expression of the mouse Mfrp gene, determine ti

134 t this early priming is required for correct temporal expression of the myeloid master regulator PU.1

135 The temporal expression of the phoPR promoters was investiga

136 ied a cardiovascular progenitor based on the temporal expression of the primitive streak (PS) marker

137 We also used these data to define the temporal expression of the spore proteome, and in doing

138 similarly to endogenous Sry, the spatial and temporal expression of the Sry-EGFP transgene was invest

139 predictably, or depend on changes in spatial-temporal expression of the targeted gene.

140 onserved in eudicots directs the spatial and temporal expression of the transcription factor DUO1 to

141 olanaceous species depends on sequential and temporal expression of the WUSCHEL-RELATED HOMEOBOX (WOX

142 lencers, function to control the spatial and temporal expression of their target genes.

143 In order to address the temporal expression of these important genes in vivo, th

144 Understanding the temporal expression of these molecules could afford bett

145 The temporal expression of these patterns over 72 hrs was si

146 tion of ahrC transcription revealed that the temporal expression of this locus observed in wild-type

147 dback control of the gyrase promoter and the temporal expression of three topoisomerases.

148 The temporal expression of tissue-specific PCs varied in wil

149 Thus, in angiogenesis, the temporal expression of TNF is critical: it delays angiog

150 ng the high intraocular pressure METHOD: The temporal expression of TNF-alpha was ascertained with im

151 redox functions and may control spatial and temporal expression of TR1 transcripts.

152 combinatorial rules that control the phased temporal expression of transcription factors, histones,

153 uses heat-induction to precisely control the temporal expression of transgenes, we labeled two popula

154 The observed changes correlated with the temporal expression of TSP2 in the ischemic muscle of wi

155 We propose that the dynamic spatial and temporal expression of Tubb2b reflects specific function

156 forward regulatory motif, which controls the temporal expression of u-shaped.

157 like (upd-like) cause changes in spatial and temporal expression of upd-like in the developing wing a

158 Using this system, we were able to control temporal expression of vGPCR and to monitor its expressi

159 tween amino acids 271 and 275, modulates the temporal expression of viral genes.

160 in accelerated virus growth and accelerated temporal expression of viral proteins.

161 The proper temporal expression of virulence genes during infection

162 embryonic life is dependent on molecules the temporal expression of which is tightly regulated.

163 (Trp53) gene, we examined the impact of the temporal expression of wild type p53 in preventing stem

164 generation, we adopted a method to alter the temporal expression of WldS protein in neurons by chemic

165 The specific cellular and temporal expressions of HO-2 and HO-1 were characterized

166 We found that each HDAC has a distinct temporal expression pattern and regulates transcription

167 The ZRS drives the early spatio-temporal expression pattern in the limb of tetrapods.

168 transcripts, as well as the miR156-dependent temporal expression pattern of a 35S::GUS-SPL3 transgene

169 the lacZ expression completely agrees with a temporal expression pattern of Crx during retinal develo

170 The temporal expression pattern of cyp-5 was further determi

171 The spatial and temporal expression pattern of dlf1 indicates a threshol

172 reporter that recapitulates the spatial and temporal expression pattern of endogenous Tctex-1.

173 the normal postnatal brain, the spatial and temporal expression pattern of FGFR3 parallels the appea

174 we have determined the detailed spatial and temporal expression pattern of FOXP2 mRNA in the develop

175 d in tube-forming endothelial cells reveal a temporal expression pattern of genes primarily associate

176 Therefore, our results reveal a temporal expression pattern of miR-17-92 by antigen-spec

177 d out a detailed analysis of the spatial and temporal expression pattern of the gene Fgf10, by compar

178 To address the spatial and temporal expression pattern of the two homologs, C-termi

179 ndicate that RNAi does not contribute to the temporal expression pattern of this gene.

180 We found that the spatio-temporal expression pattern of VEGF in the ectoderm corr

181 talloproteinase 7 (MMP7) as an enzyme with a temporal expression pattern that corresponded with carti

182 genes that must be expressed, as well as the temporal expression pattern, for the development of func

183 We clustered the genes by temporal expression pattern, identified transcription fa

184 ollagen type I genes showed a similar spatio-temporal expression pattern, indicating their co-regulat

185 When grouped by temporal expression pattern, these TFs explain much of t

186 in DNA supercoiling that correlates with the temporal expression pattern.

187 ption factor (lin-29) primarily controls the temporal expression pattern.

188 ative cluster analysis grouped into distinct temporal expression patterns >900 known human genes that

189 or co-expression network based comparison of temporal expression patterns (NACEP).

190 in callosal fibers based on both spatial and temporal expression patterns and analysis of gene-target

191 0A4 in normal mammary gland, its spatial and temporal expression patterns and possible function in br

192 Spatial and temporal expression patterns appear to have been evoluti

193 identified two PG-specific P450 genes whose temporal expression patterns are correlated with changes

194 Interestingly, these spatial and temporal expression patterns coincide with the expressio

195 Temporal expression patterns demonstrated that the super

196 Each ligand displays differential temporal expression patterns during embryogenesis and sp

197 eplichores largely corresponds both to their temporal expression patterns during growth and to an inf

198 Transcript abundance levels and temporal expression patterns for double-strand break rep

199 the current study, we found distinct spatial-temporal expression patterns for the mRNA of TIMP family

200 The spatial and temporal expression patterns in C. elegans embryos of 10

201 lso show that genetic manipulations of their temporal expression patterns in mice alter the timing of

202 rtcl genes display highly correlated spatio-temporal expression patterns in roots, despite the signi

203 s pathway of melanin, were cloned, and their temporal expression patterns in the integument were comp

204 lopmental enhancers with desired spatial and temporal expression patterns in the zebrafish brain.

205 Methods for capturing these spatial and/or temporal expression patterns include in situ hybridizati

206 scription factors, whose defined spatial and temporal expression patterns may also be influenced by a

207 Temporal expression patterns of AhR target genes were al

208 expression reveals constitutive spatial and temporal expression patterns of all gene family members

209 role of miR398 in specifying the spatial and temporal expression patterns of CSD1 and CSD2 mRNAs.

210 anscription-PCR to determine the spatial and temporal expression patterns of each AtKT/KUP gene acros

211 The spatial and temporal expression patterns of FGFs and FGFRs and the a

212 s in the heme active site structures and the temporal expression patterns of HbO and HbN suggest that

213 Temporal expression patterns of hypoxia-inducible factor

214 f this study was to elucidate how changes in temporal expression patterns of individual components of

215 lia have come via monitoring the spatial and temporal expression patterns of individual transcription

216 The spatial and temporal expression patterns of Notch signaling genes in

217 ntial for generating the complex spatial and temporal expression patterns of Notch target genes durin

218 Temporal expression patterns of other lncRNA-messenger R

219 o illuminate its properties, the spatial and temporal expression patterns of PKHD1 were determined in

220 nt and function, we examined the spatial and temporal expression patterns of SRC-1 and characterized

221 rs regulating various aspects of the spatial-temporal expression patterns of TCF7L2, including expres

222 Temporal expression patterns of the Bordetella pertussis

223 ervous system, we determined the spatial and temporal expression patterns of the gene products of AHI

224 The spatial and temporal expression patterns of the genes provide inform

225 and verified genes by qPCR revealed that the temporal expression patterns of these genes are consiste

226 The spatial and temporal expression patterns of these two genes show ext

227 ential to accurately measure the spatial and temporal expression patterns of transcription factors an

228 er analysis of these genes revealed distinct temporal expression patterns of transcriptional activati

229 models for the prediction of precise spatio-temporal expression patterns on the one side, and crude,

230 Spatial and temporal expression patterns show startling similarity b

231 d to be essential for permitting spatial and temporal expression patterns that approximate normal end

232 g the mycorrhiza-induced genes, two distinct temporal expression patterns were evident.

233 ng analysis, 13 miRNA clusters with distinct temporal expression patterns were identified.

234 However, the temporal expression patterns were strongly dependent on

235 has an unusual developmental cycle marked by temporal expression patterns whose mechanisms of regulat

236 se gene and betaVPE) that shared spatial and temporal expression patterns with seed storage proteins.

237 ins having a common function exhibit similar temporal expression patterns, and genes specifying funct

238 By determining spatial-temporal expression patterns, reporter constructs provid

239 CesA gene family has adapted differentially temporal expression patterns, suggesting an integrated r

240 to be accompanied by a change in spatial and temporal expression patterns, suggesting that duplicated

241 ression level information in addition to the temporal expression patterns, we can uncover sequence-le

242 genes clustered into four anatomical and six temporal expression patterns.

243 te specificity, kinetic characteristics, and temporal expression patterns.

244 egulated clusters based on the similarity of temporal expression patterns.

245 s that exhibit diverse structural layout and temporal expression patterns.

246 f storage components showed several distinct temporal expression patterns.

247 nt and identified new genes with interesting temporal expression patterns.

248 athways differing in biological function and temporal expression patterns.

249 Twist2 are themselves controlled by spatial-temporal expression, phosphoregulation, dimer choice and

250 ocedure to identify genes that have a common temporal expression profile across two or more experimen

251 his study, we have characterized the spatial-temporal expression profile of a recently identified rec

252 surprising since it does not follow from the temporal expression profile of CtrA and, in turn, simula

253 The temporal expression profile of lncRNAs revealed two nove

254 ecture, and explain the rising, then falling temporal expression profile of the alx1 gene in terms of

255 tasets, we generated a gene network based on temporal expression profile similarities.

256 This temporal expression profile, along with its fibronectin-

257 n transcription, resulting in an oscillatory temporal expression profile.

258 for development: beginning from their spatio-temporal expression profiles and extending to their down

259 Its spatial-temporal expression profiles are also different from tho

260 The differences in temporal expression profiles are consistent with cultiva

261 The temporal expression profiles displayed by taste organoid

262 These HD proteins exhibit distinct temporal expression profiles during osteoblast different

263 leg muscle identified positively correlated temporal expression profiles for some gene classes, and

264 ing wild-type germline development to define temporal expression profiles for these genes.

265 The temporal expression profiles indicate that 5% of the gen

266 constructed DNA microarrays and analysed the temporal expression profiles of 1817 among the 2129 uniq

267 d transcript counting method we characterise temporal expression profiles of 23,642 genes.

268 However, the temporal expression profiles of alphaSMA and collagen I

269 Affymetrix HuGene FL oligonucleotide arrays, temporal expression profiles of ARGs in widely used horm

270 Furthermore, the temporal expression profiles of four regulatory genes in

271 MS) and immunohistochemistry to evaluate the temporal expression profiles of gangliosides during the

272 Moreover, our quantitative studies of the temporal expression profiles of Mm-antiNos1 RNA in the m

273 Here, we compare temporal expression profiles of one-to-one orthologs in

274 characterization of a database that contains temporal expression profiles of sequences found in 35,28

275 ting of muscular dystrophy, we characterized temporal expression profiles of the diaphragm in dystrop

276 We determined the temporal expression profiles of the IR-responsive genes

277 inct clusters of genes that have overlapping temporal expression profiles suggesting they have a key

278 smids, 37 promoters of various strengths and temporal expression profiles, and 10 protein-localizatio

279 nservation of let-7-C microRNA sequences and temporal expression profiles, these findings indicate th

280 re grouped into six clusters according their temporal expression profiles.

281 g15 and cpg15-2 diverge in their spatial and temporal expression profiles.

282 different fli1+ cell types display distinct temporal expression profiles.

283 sified into four clusters based on different temporal expression profiles.

284 odeling process and were clustered into four temporal expression profiles; transiently up- or downreg

285 Temporal expression profiling was utilized to define tra

286 ownstream targets of MyoD were identified by temporal expression, promoter data base mining, and gel

287 However, neither Hinfp function nor its temporal expression relative to histone H4 genes during

288 Experiments manipulating its temporal expression showed that Pla allows Y. pestis to

289 Further, analysis of its temporal expression showed that the construct is express

290 Temporal expression studies of TaIAR3 indicate that the

291 Spatial and temporal expression studies using GFP and LacZ promoter

292 olutionary conservation and the cellular and temporal expression suggest that Trib may be required fo

293 protein expression indicated tissue-specific temporal expression that was associated with the early s

294 n combined with specific methods of cell and temporal expression, the extension of this approach to h

295 noid biosynthesis beyond correct spatial and temporal expression, their predicted subcellular localiz

296 ionality reduction, and identifies canonical temporal expression trajectories (e.g., degradation, gro

297 Based on their spatial and temporal expression, transcription factors of the Forkhe

298 defining biologically relevant pathways and temporal expression trends were identified by using a se

299 g with selection of targets with spatial and temporal expression well aligned to interventional requi

300 in this regulatory hierarchy requires early temporal expression, which is characteristic of low-thre