ライフサイエンスコーパス: pattern of expression

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

2 patially restricted and temporally regulated pattern of expression.

3 fin enhancer associated with this apomorphic pattern of expression.

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

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

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

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

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

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

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

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

12 skeletal development show a slowly accruing pattern of expression.

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

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

15 c enhancer was identified that controls this pattern of expression.

16 larly for genes exhibiting a tissue-specific pattern of expression.

17 (MMP-20, enamelysin) has a highly restricted pattern of expression.

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

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

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

21 hbouring genes to control the spatiotemporal pattern of expression.

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

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

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

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

26 -DPB1 alleles are classified by high and low 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 ell wall synthesis showed different temporal patterns of expression.

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

41 carried out up to 48 h to determine spatial patterns of expression.

42 characterized to reveal spatial and temporal patterns of expression.

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

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

45 9 to mutate enhancers that control different patterns of expression.

46 in all proteomes exhibited drought regulated patterns of expression.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 ar localization, evolutionary relationships, patterns of expression and the phenotypes of correspondi

79 These genes exhibited highly tissue-specific patterns of expression and were enriched for distinct pa

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

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

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

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

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

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

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

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

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

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

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

91 The shared pattern of expression between MS15 and MS180 conditions

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

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

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

95 the normal epidermal tissue architecture and pattern of expression by a mechanism(s) that does not co

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

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

98 ting that relative levels as well as spatial patterns of expression contribute to functional differen

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

100 Although temporal patterns of expression control plant traits of agricultu

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

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

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

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

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

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

107 This complementary pattern of expression during subsequent cell migration i

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

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

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

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

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

113 The pattern of expression for all of these receptors was sim

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

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

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

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

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

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

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

121 sis of the overall cytokine profile revealed patterns of expression for growth-regulated oncogene, MC

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

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

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

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

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

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

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

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

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

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

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

133 The spatial pattern of expression in developing seeds was characteri

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

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

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

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

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

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

140 (VYS) endoderm and shows a highly restricted pattern of expression in the embryo proper at later stag

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

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

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

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

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

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

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

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

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

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

151 ns possibly are responsible for differential patterns of expression in maize and sorghum floral and v

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

153 t they had distinct but somewhat overlapping patterns of expression in mature plants.

154 that NHERF-2 and mGluR5 exhibit overlapping patterns of expression in mouse brain, being found most

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

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

157 44 planarian bHLH homologs, determined their patterns of expression in the animal and assessed their

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

159 e 4 HCN subunits have unique but overlapping patterns of expression in the CNS.

160 ns, the catenins, have unique spatiotemporal patterns of expression in the developing olfactory syste

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

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

163 The altered patterns of expression in the hybrids indicate decreases

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

165 ng data set uncovers several NR clades whose patterns of expression indicate their ability to coordin

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

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

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

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

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

171 d zebrafish embryos and an apparently normal pattern of expression is maintained in Shh-/- mouse embr

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

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

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

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

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

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

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

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

180 ted collinear expression of 5' HoxD genes, a pattern of expression long considered a developmental ha

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

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

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

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

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

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

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

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

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

190 Here, we describe the pattern of expression of BMP receptors, including Bmpr-I

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 The pattern of expression of sodium channels differs in diff

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

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

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

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

210 The pattern of expression of the immediate early gene produc

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

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

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

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

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

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

217 The patterns of expression of a set of conserved development

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

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

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

221 The patterns of expression of gel-forming mucins in epitheli

222 period of embryogenesis sculpts not only the patterns of expression of genes involved in sex determin

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

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

225 Precise patterns of expression of miRNAs suggest their specific

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

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

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

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

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

231 behaviour in these cells is linked to their patterns of expression of specific sodium channel isofor

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

233 Varying patterns of expression of the exon 1 isoforms were obser

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

235 Herein, the temporal and spatial patterns of expression of the mouse ZIP1, 3, 4, and 5 ge

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

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

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

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

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

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

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

243 g the genes with the greatest variability in patterns of expression, predicted promoter sequences wer

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

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

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

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

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

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

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

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

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

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

254 The observed patterns of expression suggest that complex regulation o

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

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

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

258 This pattern of expression suggests maternal inheritance of J

259 The cellular pattern of expression suggests that neuroD regulates asp

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

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

262 hylaminopurine during S limitation yielded a pattern of expression that was largely similar to that s

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

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

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

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

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

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

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

270 s, but also highlighted distinctly different patterns of expression that were greater than difference

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

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

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

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

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

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

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

278 ounts for genetic relatedness and identifies patterns of expression variation that are affected by na

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

280 , some of which co-expressed nNOS, but their pattern of expression was not altered by these manipulat

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

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

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

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

285 of maternal dietary zinc deficiency on these patterns of expression were examined.

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

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

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

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

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

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

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

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

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

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

296 beta2 nAChR (alpha4beta2) displayed distinct patterns of expression, with alpha7 targeted preferentia

297 ed genes revealed activation domain-specific patterns of expression, with each cluster also showing d

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

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

300 Clustering of genes based on their temporal patterns of expression yielded just three super clusters