ライフサイエンスコーパス: pattern of expression

1 n mRNA-binding protein that has an oncofetal pattern of expression.

2 hbouring genes to control the spatiotemporal pattern of expression.

3 f the expressed genes) displayed a circadian pattern of expression.

4 e Pnt-GFP and Yan adopt a mutually exclusive pattern of expression.

5 st-located aspartyl protease that alters its pattern of expression.

6 cluding some ion channels, shows a circadian pattern of expression.

7 patially restricted and temporally regulated pattern of expression.

8 omas, formed a third cluster with a discrete pattern of expression.

9 ivergence for genes with a conserved uniform pattern of expression.

10 tion was used to determine the miRNA spatial pattern of expression.

11 displays a minor ampullate gland-restricted pattern of expression.

12 ng its function is to precisely localize its pattern of expression.

13 o identify genes with a cartilage-restricted pattern of expression.

14 e to their sequence homology and overlapping pattern of expression.

15 llular and molecular basis for its transient pattern of expression.

16 skeletal development show a slowly accruing pattern of expression.

17 gene displays an aciniform gland-restricted pattern of expression.

18 os did not restore Bmp2 and Bmp4 to a normal pattern of expression.

19 fin enhancer associated with this apomorphic pattern of expression.

20 unctional YFP:FEA4 fusion recapitulated this pattern of expression.

21 art, 117 of which exhibit a cardiac-enriched pattern of expression.

22 mbination to confer a high amplitude diurnal pattern of expression.

23 ed from leaves and inflorescences showed two patterns of expression.

24 in all proteomes exhibited drought regulated patterns of expression.

25 ltiple signals to give rise to many distinct patterns of expression.

26 n alternate RNA isoforms and tissue-specific patterns of expression.

27 ve a role in TAG accumulation based on their patterns of expression.

28 T promoters also show highly tissue-specific patterns of expression.

29 ed at least in part by genes with sex-biased patterns of expression.

30 focusing on areas that show species-specific patterns of expression.

31 of the third chromosome and show overlapping patterns of expression.

32 ological basis underlying these differential patterns of expression.

33 rget genes that exhibit cell type-restricted patterns of expression.

34 erved and unknown genes, as well as distinct patterns of expression.

35 profiles are correlated with tissue-specific patterns of expression.

36 enylpropanoid pathway have similar circadian patterns of expression.

37 ans-acting factors that determine particular patterns of expression.

38 ost zebrafish miRNAs exhibit tissue specific patterns of expression.

39 buted, whereas CCP2 and 3 exhibit restricted patterns of expression.

40 s is driven by hub genes with human-specific patterns of expression.

41 9 to mutate enhancers that control different patterns of expression.

42 drive novel cell-type- and temporal-specific patterns of expression.

43 -DPB1 alleles are classified by high and low patterns of expression.

44 ell wall synthesis showed different temporal patterns of expression.

45 of these 3 family members exhibits different patterns of expression.

46 he timing of opa activity impacts the proper patterning of expression.

47 hat exhibit unique but partially overlapping patterns of expression [3].

48 The remaining genes with divergent patterns of expression (55%) were regulated by a combina

49 c-Fos expression in rats presented similar patterns of expression according to the function of the

50 ific gene to find other genes with a similar pattern of expression across the different tissues.

51 tal disorder in reading that exhibits varied patterns of expression across children.

52 ionally diverse GPCR isoforms with different patterns of expression across different tissues.

53 Genes with similar functions and coordinated patterns of expression across environments are clustered

54 enes were cold inducible, but showed varying patterns of expression across the growing season.

55 tant SNpc tier neurons displayed coordinated patterns of expression across the human brain, their pro

56 We examined the pattern of expression among three major breast cancer su

57 syncytin 1/2, and GCM1 each displayed unique patterns of expression among different trophoblast popul

58 yme degrading H(2)O(2), shows an oscillating pattern of expression and activity, antiphasic to zCry1a

59 However, the pattern of expression and allelic variation at these loc

60 atumoral heterogeneity, which extends to the pattern of expression and amplification of receptor tyro

61 and those that display a TH lineage-specific pattern of expression and are intragenic or adjacent to

62 We characterized their pattern of expression and defined their role in muscle h

63 Our results show that the pattern of expression and polarization of all TLRs in pr

64 In this study, we found a different pattern of expression and regulation between IDO1 and ID

65 brane-associated isoforms, each with its own pattern of expression and regulation.

66 Interestingly, 4R tau exhibited a distinct pattern of expression and subcellular localization, sugg

67 ress AMPA receptors, but their developmental pattern of expression and targeting mechanisms are unkno

68 These roles are consistent with their pattern of expression and with the regional influence of

69 stions, we investigated temporal and spatial patterns of expression and assembly of photoreceptor pre

70 Here, we investigated the patterns of expression and clustering of soluble and EV-

71 ining 640 genes displayed unique and complex patterns of expression and could thus not be grouped int

72 In this study, we examine the patterns of expression and evolution in takeout and the

73 N/P ratios, elucidating nutrient-responsive patterns of expression and facilitating a quantitative c

74 s that exhibit distinct temporal and spatial patterns of expression and functional properties.

75 but the precise developmental and positional patterns of expression and gene networks are almost enti

76 at capture strain and pathogenicity-specific patterns of expression and helped identify important reg

77 from these Astragalus species to investigate patterns of expression and interactions with sulfate and

78 Here, we review current understanding on patterns of expression and modes of regulation of sensor

79 n factors revealed remarkable constraints on patterns of expression and phosphorylation within transc

80 e mutations are mostly masked by overlapping patterns of expression and redundant function as well as

81 ng RNA species that show complex overlapping patterns of expression and regulation.

82 ific chromatin accessibility to sex-specific patterns of expression and regulatory variation.

83 On the basis of its position, pattern of expression, and function in neuroblastoma cel

84 RECA2 and RECA3 have similar patterns of expression, and mutants of either display th

85 mong groups of genes with varying functions, patterns of expression, and phylogenetic histories.

86 suboptimization produce specific, but weak, patterns of expression, and we suggest that clusters of

87 ated gene networks, where timing and dynamic patterns of expression are critical, may be particularly

88 es and time points, proteome and genome-wide patterns of expression are more readily discernible.

89 determined region and that distinct regional patterns of expression are observed between isoforms, re

90 natively spliced genes with varying temporal patterns of expression are revealed, including TGIF1, in

91 identified miRNAs whose spatial and temporal patterns of expression are suggestive of functional role

92 nder Spo0A control did not exhibit a bimodal pattern of expression as expected for a bistable switch.

93 ls in vitro and their frequently overlapping patterns of expression at inflammatory sites in vivo.

94 instead enabling the return of more complex patterns of expression behaviour.

95 The shared pattern of expression between MS15 and MS180 conditions

96 t, and analyses demonstrate highly conserved patterns of expression between adult zebrafish, humans,

97 f land plants and can result from changes in patterns of expression, binding site divergence, and/or

98 ily allow appreciation of 3-dimensional (3D) patterns of expression, but this can be accomplished by

99 cale expression survey, we show that complex patterns of expression by many genes underlie embryonic

100 TAT signaling pathway and induce overlapping patterns of expression, called 'interferon signatures',

101 get genes and the factors that control their patterns of expression--can show remarkable evolutionary

102 timates are useful to study the evolutionary pattern of expression conservation.

103 ty and growth, we suggest that these altered patterns of expression contribute to the greater growth

104 Although temporal patterns of expression control plant traits of agricultu

105 onstrate that under normoxic conditions Flk1 patterns of expression correlate well with our previous

106 n vivo SIV/macaque model of HAD and that the pattern of expression correlates with recurrence of vira

107 The temporal and spatial pattern of expression demonstrates that neuronal caspase

108 ost abundantly expressed of the Nrgs and its patterns of expression differ both temporally and spatia

109 By separately analyzing the robustness and pattern of expression differences across these cell popu

110 The pattern of expression differs in CD4(+) and CD8(+) T cel

111 sexual selection vs. drift in shaping broad patterns of expression, divergence, and polymorphism rem

112 eletal muscle, yet little is known about its pattern of expression during embryonic and postnatal dev

113 This complementary pattern of expression during subsequent cell migration i

114 X1, LAX1 and LAX2) show specific and dynamic patterns of expression during early leaf development in

115 nrf2a and nrf2b displayed distinct patterns of expression during embryonic development; nrf

116 groups exhibiting rhythmic and non-rhythmic patterns of expression during light-dark cycles.

117 found that these mRNA species have different patterns of expression during myogenesis.

118 es reveal complex and dynamic spatiotemporal patterns of expression during this period.

119 ation clusters demonstrate a similar overall pattern of expression for in vitro and ex vivo PCs.

120 cripts in infected larvae revealed a typical pattern of expression for ISGs in the liver, gut, and bl

121 pe of these subsets revealed an "a la carte" pattern of expression for the various NK receptors, func

122 ons were then used to determine the temporal patterns of expression for 145 transcriptional regulator

123 ymbiotic interaction, revealing differential patterns of expression for 2,030 genes and pointing to t

124 Patterns of expression for A. thaliana show that GlsA/ZF

125 The results were compared to the observed patterns of expression for CB1 mRNA, protein, and agonis

126 chain reaction (RT-PCR) has shown equivalent patterns of expression for MAST1 and 2 in multiple tissu

127 ants indicates changes in the spatiotemporal patterns of expression for p27(kip1), Atoh1 and hair cel

128 f our findings by showing remarkably similar patterns of expression for PCPH and PKC delta, thus stro

129 In the rodent neocortex there are distinct patterns of expression for the Kv3.1b and Kv3.2 channel

130 t showed a linearly increasing or decreasing pattern of expression from the preneoplastic ganglia to

131 RLR displayed a differential but overlapping pattern of expression; GHR had high expression in liver

132 We show that genes with a conserved uniform pattern of expression have significantly higher levels o

133 Bimodal patterns of expression have recently been shown to be us

134 ssed genes, their respective allele-specific patterns of expression have the potential to affect brai

135 ich there are sufficient ESTs show different patterns of expression, i.e., with cv Chinese Spring exp

136 were characterized by a typical and expected pattern of expression; i.e., levels of OR mRNA peaking i

137 Because DLX5 has a restricted pattern of expression in adult tissues, it may serve as

138 factors, ERG exhibits a highly EC-restricted pattern of expression in cultured primary cells and seve

139 nge was often true of genes with a wild-type pattern of expression in ganglion cells, bipolar cells,

140 y, its molecular abundance in cells, and its pattern of expression in primary cancer cells.

141 mice and zebra finches revealed a conserved pattern of expression in the "limbic system." We suggest

142 ion of the data set revealed an up-regulated pattern of expression in the ACEC of genes involved in g

143 sion of nPTB results in a mutually exclusive pattern of expression in the brain, where the loss of PT

144 most tissues, but we observed an unexpected pattern of expression in the brain.

145 show that tagged HmLAR2-EGFP has a punctate pattern of expression in the growth cones of the CC, par

146 GCTM-5 epitope shows a much more restricted pattern of expression in the normal adult pancreas relat

147 GPCR101 mRNA expression showed a similar pattern of expression in the rostral ventromedial parvoc

148 actor receptor superfamily with a widespread pattern of expression in tissues such as the brain, live

149 We propose that the pattern of expression in vitro does not reflect gene exp

150 DRs by identifying genes that show different patterns of expression in a number of clinical entities.

151 , exhibit distinct but partially overlapping patterns of expression in adult mammalian neurons: Syb1

152 lus (IC), but have not examined the cellular patterns of expression in detail.

153 hat AtPME3 and AtPMEI7 genes had overlapping patterns of expression in etiolated hypocotyls.

154 Robust methods for identifying patterns of expression in genome-wide data are important

155 es in tumor development and show deregulated patterns of expression in HCC.

156 und to exhibit distinct temporal and spatial patterns of expression in hepatocytes, cholangiocytes, a

157 a/delta) are nuclear receptors with distinct patterns of expression in many cell types both within an

158 g cortisol deactivation, exhibited different patterns of expression in normal (squamous epithelium an

159 ith taste stimuli and with identifying their patterns of expression in taste cells sheds light on cod

160 44 planarian bHLH homologs, determined their patterns of expression in the animal and assessed their

161 tructure of Pax6, the roles it plays and its patterns of expression in the brain have been highly con

162 G1 and SynDIG4 have distinct yet overlapping patterns of expression in the central nervous system, wi

163 hat Six1 and Six2 exhibit partly overlapping patterns of expression in the developing mouse embryonic

164 iple environmental parameters to account for patterns of expression in the field of co-expressed gene

165 genes, and include genes with human-specific patterns of expression in the frontal pole.

166 The altered patterns of expression in the hybrids indicate decreases

167 and 3 subfamilies of HERV-K, with a specific pattern of expression including intact open reading fram

168 s being expressed in erythroblasts and their patterns of expression indicated they are likely to be i

169 The pattern of expression indicates that 5-HT has a developm

170 The pattern of expression influenced by the microbiome is co

171 This pattern of expression is atypical and the reverse of wha

172 We show that this dynamic pattern of expression is controlled by both short- and l

173 Importantly, a similar pattern of expression is found in post-mortem spinal cor

174 Typically, this pattern of expression is regulated by differentially met

175 A similar pattern of expression is seen as cultured myoblasts diff

176 ed as a molecular component of the BBB whose pattern of expression is specifically altered during MS

177 erentiation and cell re-programming and this pattern of expression is specifically de-regulated in iP

178 Because this pattern of expression is suggestive of a role in innate

179 g neuronal molecular markers with restricted patterns of expression is a crucial step in dissecting t

180 nction, knowledge about their spatiotemporal patterns of expression is essential.

181 Correlation pattern of expression levels could be a novel measurer f

182 This biphasic pattern of expression may reflect a dual function of SNP

183 gulated in HL cell lines, recapitulating the pattern of expression observed following EBV infection o

184 Overall, the patterns of expression observed have suggested that the

185 n polymorphism (SSCP) platform to detect the pattern of expression of 20 homoeologous sets of single-

186 This pattern of expression of 5-HT(2A) and mGlu2 receptors wa

187 A strong correlation between the pattern of expression of a biomarker and sensitivity to

188 ], and further analysis revealed a circadian pattern of expression of all four Id genes in multiple t

189 The circadian pattern of expression of an array of metabolic genes in

190 vocal motor nucleus congruent with the known pattern of expression of aromatase-containing glial cell

191 of this study is to determine the level and pattern of expression of beta2-ARs in human valve inters

192 s modes of secondary growth reflect a mosaic pattern of expression of different developmental-regulat

193 U-homeodomain proteins) to control a similar pattern of expression of different target genes in a mec

194 There were significant differences in the pattern of expression of E(2)-induced genes c-myc, c-fos

195 Both the intensity and pattern of expression of each marker were significantly

196 The unique pattern of expression of each receptor suggests that the

197 We interrogated the pattern of expression of esophagus-specific signature ge

198 hos1 causes a shift in the regular long-day pattern of expression of flowering locus T (FT) transcri

199 provide the first evidence of a differential pattern of expression of ISG54 and ISG56 genes by IFN-al

200 the Apc(1638N/+) mice, there was a perturbed pattern of expression of lineage-specific markers along

201 The pattern of expression of metalloproteases (MPs) was anal

202 and species-dependent, we postulate that the pattern of expression of neuronal melatonin receptor typ

203 We have asked if the pattern of expression of nonphosphorylated neurofilament

204 and maintenance, this study investigated the pattern of expression of p53, its family members, and it

205 A complex pattern of expression of p73 isoforms makes it difficult

206 din dehydrogenase-driven degradation and the pattern of expression of PGE(2) receptors.

207 neurulating embryos, and changes the normal pattern of expression of ten different genetic regulator

208 of the present study was to investigate the pattern of expression of the clock genes in the retina o

209 In addition, we uncover an aberrant pattern of expression of the gene encoding the chemokine

210 s corroborated by a mosaic, glomerulus-based pattern of expression of the HCN2 (hyperpolarization-act

211 The pattern of expression of the immediate early gene produc

212 dual colon cancer neoplasms, we examined the pattern of expression of the ligands, epidermal growth f

213 planation for the intermediate-late temporal pattern of expression of the p30tof, p13, and p12/8 mRNA

214 These data indicate that the pattern of expression of these neural-enriched IG20-SVs

215 s targets and compare these effects with the pattern of expression of these targets in human NASH.

216 iments in rat brain demonstrated a conserved pattern of expression of this ion channel between rodent

217 Oscillations in patterns of expression of a large fraction of yeast gene

218 echanisms of HCV immune evasion, we analyzed patterns of expression of a major inhibitory receptor on

219 The patterns of expression of a set of conserved development

220 and in primary DLBCLs, there were reciprocal patterns of expression of BCL6 and the SYK tyrosine phos

221 uced by general anesthetics, we examined the patterns of expression of c-Fos protein in the brain and

222 titative RT-PCR to assay for spatio-temporal patterns of expression of different anthocyanin pathway

223 We found that, during learning, the cellular patterns of expression of early response genes (ERGs) ar

224 multiple modifications in the developmental patterns of expression of genes known to influence learn

225 In addition, single-cell patterns of expression of interferons (IFN) and IFN-stim

226 dependently of other cells, by using spatial patterns of expression of marker genes(5,6)-which often

227 These findings were consistent with patterns of expression of miR-214, ALCAM, and miR-148b i

228 Precise patterns of expression of miRNAs suggest their specific

229 The striking reciprocal patterns of expression of MT1-MMP and MT2-MMP indicate t

230 ired to direct the proper timing and correct patterns of expression of quorum-sensing-regulated targe

231 rent neurons to stimulation as well as their patterns of expression of receptors and neuropeptide tra

232 been using immunohistochemistry to study the patterns of expression of several different proteins to

233 These findings suggest that temporal patterns of expression of specific components of LSD1 co

234 in interactions that may result from altered patterns of expression of such variants.

235 , resulting in distinct temporal and spatial patterns of expression of the ATX1 and ATX2 genes.

236 aluating whether mutations result in altered patterns of expression of the immediate early gene c-fos

237 Furthermore, the different patterns of expression of these presynaptic genes sugges

238 The sequences and patterns of expression of these splice variants are high

239 developing mouse intestine shows reciprocal patterns of expression of TLR4 and TLR9, the receptor fo

240 This study examined in detail the patterns of expression of var in a well-characterized sa

241 pment of multiple cancers that have distinct patterns of expression of viral proteins and microRNAs (

242 rmined and compared the spatial and temporal patterns of expression of Wnt3a, Msgn1 and Tbx6 at a tim

243 ed, however, exhibit a unique spatiotemporal pattern of expression, particularly during cortical deve

244 ed by increased expression at later times, a pattern of expression previously reported for several ge

245 Consistent with this pattern of expression, ptc-3(RNAi) reveals an additional

246 eling has predicted that this highly focused pattern of expression requires auxin to sequentially ind

247 The analysis of parent-of-origin patterns of expression resulted in the identification of

248 Broad age-related patterns of expression revealed by these data recapitula

249 tional RNA-binding protein with an oncofetal pattern of expression shown to be implicated in the deve

250 This pattern of expression significantly differed from that o

251 l of these genes have a dorsal-ventral (D-V) pattern of expression similar to that of short- or mediu

252 Corresponding to their patterns of expression, siRNA-mediated knockdown of Galp

253 one orthologous genes that considered global patterns of expression specificity, strong gene markers,

254 Their unique patterns of expression, structure, and binding partners

255 sition of enzyme coding loci on the map, and patterns of expression suggest multiple linked loci.

256 licle cells, although the timing and spatial patterns of expression suggest that amplification is not

257 The observed patterns of expression suggest that complex regulation o

258 Collectively, these patterns of expression suggest that TCF7L2 has distinct

259 This pattern of expression suggested that BT2 mRNA could be l

260 Ns, IFN lambda 1 (IFNL1) showed a widespread pattern of expression, suggesting a different cell-to-ce

261 host and pathogen gene pairs with correlated patterns of expression, suggesting interaction.

262 This pattern of expression suggests maternal inheritance of J

263 Nonetheless, the pattern of expression suggests that atypical ORs may be

264 The cellular pattern of expression suggests that neuroD regulates asp

265 ispensable for cDC development, its specific pattern of expression supports the notion that cDCs cons

266 i-inflammatory IL-2C treatment and uncover a pattern of expression that reveals potentially beneficia

267 cantly in their species of origin and in the pattern of expression that they induce, have the capacit

268 expressed miRNA showed a cell type-specific pattern of expression that was linked to the epigenetic

269 We analyze the global patterns of expression that are regulated by KaiA versus

270 e found microRNAs and mRNAs with overlapping patterns of expression that correlated with alcohol cons

271 adds a further facet to the already diverse patterns of expression that have been observed for HSS i

272 -associated miRNAs (dystromiRs) show dynamic patterns of expression that mirror the progression of mu

273 It identified both specific and ubiquitous patterns of expression that strongly correlate with adja

274 ies failed to identify genes with consistent patterns of expression that were below the selected sign

275 expression between the two species and also patterns of expression that will likely impact on immuno

276 porters are closely related and have similar patterns of expression, they have distinct activities in

277 s directly, and by affecting the fibronectin pattern of expression through its regulation of Shh.

278 alamic tanycytes, and showed a complementary pattern of expression to markers of hypothalamic ependym

279 activation, was >12-fold and had a parallel pattern of expression to PPARGC1A.

280 The Gsx genes in Xenopus show similar patterns of expression to their mammalian homologues dur

281 his formalism to identify genes with spatial patterns of expression using fluorescence in-situ hybrid

282 enotypic diversity and the interpretation of patterns of expression variation in disease.

283 pair via a set of receptors (5HT(1-7)) whose pattern of expression varies among cell lineages.

284 The same pattern of expression was seen on the tk and gC genes on

285 GLUT isoforms generally have a non-redundant pattern of expression, we used Vglut3 knockout mice to a

286 Both intensity and pattern of expression were scored for each marker.

287 Collectively, the observed patterns of expression were consistent with the Warburg

288 vidual OR expression was diverse; levels and patterns of expression were unique for each OR.

289 In the inflamed EAE spinal cord however, the patterns of expressions were reversed, that is, a signif

290 ulation of Zic4 expression, as well as novel patterns of expression which may represent unique proces

291 ntally regulated, and changes in this normal pattern of expression, which occur in several brain diso

292 asses 189 kb of genomic DNA, shows a complex pattern of expression with both spatial and temporal reg

293 Tbx22 exhibits a similar pattern of expression with that of Mn1 along the anterop

294 imilar with one another, and forms recurrent patterns of expression with prognostic relevance.

295 Interestingly, RME1 displays a biphasic pattern of expression, with a first phase independent of

296 dopted a new promoter that drives an altered pattern of expression, with highest levels in neural tis

297 d immunohistochemistry revealed a widespread pattern of expression, with labeled cells and/or process

298 stingly, Aire has a highly tissue-restricted pattern of expression, with only mTECs and peripheral ex

299 AP1/FUL) genes show distinct but overlapping patterns of expression within rice (Oryza sativa) and wi

300 eral mature miRNAs exhibit a tissue-specific pattern of expression without an apparent tissue-specifi