ライフサイエンスコーパス: level of expression

1 age to have a lower CpG content and a higher level of expression.

2 ion of Ago3 and Ago4 that may prevent a high level of expression.

3 to two groups having a high or 10-fold lower level of expression.

4 rol on cotyledon specific expression and the level of expression.

5 bgenome, and with little regard for a gene's level of expression.

6 o exploit receptors with relatively moderate levels of expression.

7 of library type and across the full range of levels of expression.

8 ences of APOBEC3 protein function at natural levels of expression.

9 tomes and known miRNAs due to non-detectable levels of expression.

10 uced into tobacco chloroplasts to yield high levels of expression.

11 cted insertion strategy to ensure equivalent levels of expression.

12 owth medium manipulation allows intermediate levels of expression.

13 cost, particularly in genes with the highest levels of expression.

14 ng and maintaining the stability of decigram levels of expression.

15 B cells in the periphery exhibit increasing levels of expression.

16 d escape groupings differ primarily by their levels of expression.

17 ous murine tau, consistent with its elevated levels of expression.

18 nescence versus proliferation depends on its levels of expression.

19 /delta-alpha-gamma/delta receptors at higher levels of expression.

20 activity at the promoter, mRNA, and protein levels of expression.

21 ulated by its oligomerization status and its levels of expression.

22 promoter and intronic regions lead to a low level of expression, a 2.2-kb deletion causes a truncate

23 prostate cancer, but evidence for increased levels of expression accompanying cancer progression has

24 investigate whether an alteration in Nedd4-2 levels of expression affects general nervous system func

25 ed SIMPLEx (solubilization of IMPs with high levels of expression), allows the direct expression of s

26 L/G410L) resulted in a substantially reduced level of expression, altered glycosylation, degradation

27 ble fraction of the transcriptome differs in level of expression among individuals.

28 ewly generated stable cells revealed varying levels of expression among the PREX2 isoforms, which was

29 owever, regulation of these complexes at the level of expression and activity remains poorly understo

30 CD86 was low in resting B cells, whereas the level of expression and association increased primarily

31 Here, we investigated the level of expression and behavioral function of 5-HT(2A)

32 ein reporters by measuring both the absolute level of expression and fold-change in expression using

33 t function in the lens because of its higher level of expression and observed ezrin-specific cross-li

34 ariation system, it is still unclear why the level of expression and the rate at which tprK diversifi

35 would in turn depend on their cell-specific level of expression and/or activation from signals in th

36 s followed by alteration of the patterns and levels of expression and adaptive changes in the coding

37 intersectional genetic tools to achieve high levels of expression and cell-type specificity, providin

38 y of the cytoplasmic domain, to increase its levels of expression and duration on the surface of CD8(

39 ulated by p53 in terms of genes affected and levels of expression and has implications for the appear

40 The relatively high levels of expression and of supramolecular aggregation i

41 uced cytokine response, we identified higher levels of expression and phosphorylation of the transcri

42 gions, consistent with these genes' opposing levels of expression and roles in modulating anxiety beh

43 verlap with existing annotations, had a high level of expression, and showed a high level of uniquene

44 of the HIRA histone chaperone, despite high levels of expression, and in this background, mobilizati

45 tral regions of the retina express Pax2, and levels of expression are decreased with increasing dista

46 ta, and VEGF, and found that the pattern and levels of expression are dependent on both brain region

47 Higher levels of expression are likely to account for the oblig

48 The abcc6a showed a relatively high level of expression at 5 days post-fertilization (d.p.f.

49 al alleles of these genes and measured their level of expression at different life stages in response

50 ng evidence of association with differential levels of expression at GSDML, IKZF3, and MED24, as well

51 to tune transcriptional networks to targeted levels of expression at will.

52 tional repression, resulting in differential levels of expression based on Irr affinity for target pr

53 gh genetic background may also influence the level of expression bias and tissue specificity for some

54 al regulatory region, but it promotes higher levels of expression by targeting the poly (A) tails of

55 proliferative state and that modulating its level of expression can cause entry or exit from senesce

56 question is whether these comparatively low levels of expression can successfully satisfy the string

57 and bidirectional deviations from its normal level of expression cause chromosome missegregation, ane

58 e synergistically elevated compared with the levels of expression caused by the corresponding single-

59 lle biogenesis, and calcium regulation whose levels of expression change concomitant with decreased c

60 strong, leaf-preferred promoter that enables levels of expression comparable to Zm-Ubi1 in this organ

61 abundant macronuclear chromosomes have lower levels of expression compared to less abundant chromosom

62 nalysis of the TM902CB strain reveals higher levels of expression, compared with the 3D7 (atovaquone-

63 Search criteria included high levels of expression, conservation in all parasite strai

64 This lower level of expression correlated with hyperacetylation of

65 ed from mouse, dog and human tissues and its level of expression correlates with their myogenic compe

66 spondence between the measured and predicted levels of expression, demonstrating the transferability

67 Results suggest that not only are the levels of expression different for each type of bone for

68 Here we characterized the levels of expression, distribution, and association of a

69 otency TFs plays a large role in setting the levels of expression driven by CREs in ES cells.

70 We conclude that, at normal levels of expression during bacterial infection, NleB1/N

71 whereas the TA isoforms showed generally low levels of expression, except in a few tumors.

72 repressed the IRAK-M promoter, allowing low levels of expression; following LPS stimulation, the IRA

73 rection of expression level dominance (total level of expression for both homoeologs) and homoeolog e

74 score, hence indicating an overall increased level of expression for the selected inflammatory-relate

75 Quantitative PCR showed low levels of expression for both synemin mRNAs, which peake

76 The levels of expression for five genes (apl-1, dyn-1, act-5

77 ost genes often approximate the patterns and levels of expression for gar genes, consistent with subf

78 ese results provide indications, at the gene level of expression, for the role of IC lateralization i

79 ectable in human leukocytes compared to fair levels of expression found in other human tissues.

80 et effects while still providing therapeutic levels of expression from integration.

81 Under physiologic levels of expression, HER2 heterodimerizes with other me

82 as restricted to the epithelium with highest level of expression in ductal and centroacinar cells.

83 stance, as well as its distinguishingly high level of expression in many types of cancer, survivin ha

84 ute myeloid leukemia (AML) and, based on the level of expression in mononuclear cells (MNCs), we divi

85 Here, we report that RasGRP3 showed a high level of expression in multiple human melanoma cell line

86 ted cells at e18.5 and in adult with highest level of expression in somatotrope cells.

87 tissues but appeared to exhibit the greatest level of expression in the foot.

88 apeutic target in cancer because of its high level of expression in tumors.

89 The baseline level of expression in vivo and degree to which expressi

90 Of these, two genes showed higher levels of expression in 'Red Delicious' than in 'Golden

91 ngle-copy lacS in the chromosome or at lower levels of expression in a plasmid.

92 ound in A2497-infected cells compared to the levels of expression in A2497P(-)-infected cells.

93 Ps, PPKs and mechanoreceptors had consistent levels of expression in all libraries.

94 d spinal cord is required uniformly for high levels of expression in all Neurog1 domains, even those

95 n lipid-rich areas with significantly higher levels of expression in atheromatous than in fibrous pla

96 We also found 15 miRNAs with high levels of expression in both neurons and glia, and many

97 drive SOP gene expression: RhoD mediates low levels of expression in both thoracic and abdominal SOP

98 nd CABIN1 interact at ectopic and endogenous levels of expression in cells, and we isolate the quater

99 , PTPLB-RSRC1, and SP3-PTK2) that had strong levels of expression in corresponding NPC tissues.

100 second change occurred that resulted in high levels of expression in D. melanogaster.

101 These profiles govern the levels of expression in each clone.

102 essed primarily in beta cells, showed higher levels of expression in islets from normal compared with

103 opment of the murine mammary gland with high levels of expression in mammary stem-cell enriched cultu

104 ed in these cells, whereas they exhibit high levels of expression in mature DCs.

105 dentified 29 heritable transcripts for which levels of expression in peripheral blood correlate stron

106 y-expressed in neural progenitors, with high levels of expression in proliferating type I neuroblasts

107 Many genes exhibit altered levels of expression in response to abiotic stress, whic

108 R1 gene was universally expressed, with high levels of expression in specific tissues/organs includin

109 The CAPN1 gene shows high levels of expression in the brain and nervous system and

110 throughout embryonic development, with high levels of expression in the developing brain, retina, op

111 dization detection of CB1 mRNA revealed high levels of expression in the medial septum (MS) and the d

112 d in the optic neuroepithelium, with highest levels of expression in the nasal optic stalk.

113 only one condition, likely due to differing levels of expression in the two conditions.

114 t the nSMase2 protein stability and thus its level of expression is also post-translationally regulat

115 timulation of in vitro angiogenesis, and its level of expression is reduced in neovessels in vivo.

116 the disease, involve HVE-genes for which the level of expression is undistinguishable among healthy i

117 with varying cell context and time-dependent levels of expression, it can give rise to a wide range o

118 genes (L and H) and have bred mice with four levels of expression: L/L, approximately 20%; L/+, appro

119 compare inhibited gene expression to native levels of expression, lack of the need to alter the M. t

120 of a synthetic 5'UTR optimized for a higher level of expression may be challenging.

121 nging proteins to study because of their low level of expression, multidomain structure, and complex

122 f the microbial life cycle, with the highest levels of expression noted in feeding ticks and with swi

123 Macrophages from LAP patients had a lower level of expression of 12-lipoxygenase ( approximately 3

124 efects in ribosome synthesis by changing the level of expression of a limited subset of genes involve

125 fter prolonged silencing, a reduction in the level of expression of adipogenic genes.

126 The high level of expression of AGXT2L1 in human brain, as well a

127 ermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the coun

128 rto not been possible to tune up or down the level of expression of any endogenous gene.

129 on vs. the bone marrow could dictate a lower level of expression of aquaporin-1 on the mature red cel

130 A comparison of the level of expression of B7 molecules by APC and CD4 T cel

131 e cells that also includes negativity or low level of expression of CD127.

132 MLDS-induced diabetes was influenced by the level of expression of CD39.

133 ubtypes based on several criteria, including level of expression of certain markers.

134 sity of a population by adjusting the global level of expression of CheR and CheB while keeping their

135 We compared the level of expression of CIC target genes on Hs683-IDH1(R1

136 urationally synchronized, as assessed by the level of expression of costimulatory surface molecules.

137 These findings demonstrate that a high level of expression of DA L can cause the death of myeli

138 calisation of DeltaD varies according to the level of expression of DeltaC: in the anterior PSM, wher

139 Variations in the level of expression of distinct miRNAs have been observe

140 The high level of expression of efflux transporters (e.g., P-glyc

141 ed inflammasome activity associated with low level of expression of endogenous inflammasome inhibitor

142 We used the 8F1 antibody to measure the level of expression of ERCC1 protein by means of immunoh

143 gh several ongoing trials are evaluating the level of expression of ERCC1, no consensus has been reac

144 NR-coactivator binding resulted in a reduced level of expression of five different NR target genes in

145 naive WT mice had a >20-fold increase in the level of expression of found in inflammatory zone 1 (FIZ

146 Friedreich's ataxia is caused by a decreased level of expression of frataxin, a putative iron chapero

147 R/K140E), and Gck(K140E/K140E)) and with the level of expression of GCK in liver.

148 ESCd display a high level of expression of genes implicated in migration and

149 However, our data do suggest that a higher level of expression of genes that protect against oxidat

150 This results in a precise control of the level of expression of growth factors in the embryo.

151 s reveals a positive correlation between the level of expression of heparanase and RANKL.

152 ing the transitional phase of infection, the level of expression of IFN-lambda mRNA was higher in fol

153 The level of expression of integrins alphav and beta3 and th

154 The level of expression of ion channels has been demonstrate

155 ic plants, and reveals the importance of the level of expression of key genes in the origin and evolu

156 unctional effects, in that it influenced the level of expression of MAP2K7 mRNA in human PFC.

157 ulations of macrophages that differ in their level of expression of MHC class II (MHC II).

158 ice with rHEP-MIP1alpha resulted in a higher level of expression of MIP-1alpha at the site of inocula

159 In this study, we identified a high level of expression of miR-155 in a human lung adenocarc

160 significant inverse correlation between the level of expression of miR200-b and VEGFR-2.

161 A low level of expression of mJHBP in Ae. aegypti larvae sugge

162 iption and alternative splicing uncouple the level of expression of MYH7b and miR-499 when their coex

163 rticular PTMs correlated with changes in the level of expression of numerous oncogenes, consistent wi

164 The association of outcome with the level of expression of patients' and donors' HLA-C allot

165 -1 Tat protein significantly upregulated the level of expression of PD-L1.

166 cardiac fibroblasts in culture affected the level of expression of Pdlim3, Itga6, and Gpr158.

167 nts after SIV infection and suggest that the level of expression of restriction factors may contribut

168 hesus macaque model of AIDS, we examined the level of expression of rhesus enteric alpha-defensins (R

169 KIR(-)CD56(+) T cells have >25-fold higher level of expression of RORC than the KIR(+) counterpart

170 k-down grains associated with changes in the level of expression of several C1A peptidases were also

171 ector functions due to the regulation of the level of expression of target Ags and responses by stimu

172 involved and significant differences in the level of expression of the affected gene and exons in th

173 Here, we show that the level of expression of the betaDG subunit as well as the

174 There was a lower level of expression of the Gal antigen and of SLA class

175 ence of lactate exhibited an increase in the level of expression of the main myelin regulator gene Kr

176 severe in 1 patient, and correlated with the level of expression of the mHAg-encoding genes in lung t

177 -was detected colorimetrically, and the high level of expression of the omega-domain of beta-gal in t

178 by induction of the partner protomer and the level of expression of the partner required to generate

179 % of the total, and was not dependent on the level of expression of the retinal pigment epithelium is

180 rsible, and the severity correlated with the level of expression of the risk allele.

181 This study suggests that the level of expression of the Saa3 gene could be utilized f

182 Although the level of expression of the sadC gene does not seem to be

183 negates this synergy and limits the overall level of expression of the Yki/Sd-dE2F1 target genes.

184 ng function that act as eQTLs and change the level of expression of their target genes in lung tissue

185 The level of expression of these cell-cycle regulatory genes

186 mixed glial cells, consistent with the high level of expression of TRIL in these cells.

187 d vimentin-null cell lines, we show that the level of expression of vimentin IFs (VIFs) correlates wi

188 orrelation between those organs size and the level of expression of VviANT1 the grapevine homolog of

189 ding male meiotic X inactivation, increasing level of expression of X-linked genes in male testes, an

190 carrier-mediated intestinal thiamin uptake, level of expressions of thiamin transporters (thiamin tr

191 Levels of expression of 14-3-3 epsilon protein were foun

192 Conversely, the levels of expression of 3 myogenic regulatory factors-mu

193 emonstrate that ADT-2 is required for normal levels of expression of a DBL-1-responsive transcription

194 The infected cells have high levels of expression of a large cluster of viral miRNAs,

195 Clinically, high levels of expression of alpha-catulin and ILK were assoc

196 The levels of expression of alternatively spliced variants o

197 Moreover, we report that the levels of expression of annexin A2 in human glioma sampl

198 Recent reports of reduced levels of expression of both Aldh1a1 mRNA and protein in

199 Lower levels of expression of both genes in blood were associa

200 The association of rs2155219 with higher levels of expression of C11orf30, which may be involved

201 ence of tortuous vascular networks with high levels of expression of CD31, vascular endothelial cadhe

202 in inflamed muscle is characterized by high levels of expression of CD68, CCL-2, TNF-alpha, and IL-6

203 sion of most of its genes but preserves high levels of expression of certain key genes, such as those

204 we have examined in detail the patterns and levels of expression of chemokine, cytokine, and chemoki

205 The significantly higher levels of expression of cKIT, monocyte chemoattractant p

206 This cooperation gave rise to higher levels of expression of critical mutually dependent cyto

207 C. difficile prsW mutant exhibited decreased levels of expression of CsfT and CsfU but not of CsfV.

208 Lack or low levels of expression of CX3CL1-CX3CR1 by tumor cells ide

209 D8(+) memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surv

210 e arrest was accompanied by markedly reduced levels of expression of E2F3, an E2F family member, and

211 (Arabidopsis thaliana) lines with modulated levels of expression of each individual gene involved in

212 ethyl-N-nitrosourea (ENU), regardless of the levels of expression of Egr1 and Tp53.

213 This is consistent with higher levels of expression of eomesodermin in transferred and

214 These cell lines present different levels of expression of epithelial-to-mesenchymal transi

215 Asyn-knockout primary neuronal cultures, the levels of expression of ER signaling pathways, known to

216 ested, RCC and STS cells exhibited increased levels of expression of fibronectin and an activated for

217 The levels of expression of FoxO1A, FoxO3A, and FoxO4 appear

218 Additionally, increased levels of expression of genes associated with airway rem

219 Programmed death-1 (PD-1) receptor and high levels of expression of genes associated with major hist

220 Levels of expression of genes associated with stress, in

221 ventral brainstem astrocytes display higher levels of expression of genes encoding proteins associat

222 rains of C. elegans nematodes with different levels of expression of green fluorescent protein (GFP)

223 in cell culture was inversely related to the levels of expression of GRP78 and that both proteins int

224 The levels of expression of heme-oxidized IRP2 ubiquitin lig

225 This is consistent with the lower levels of expression of IFN-gammaR2 in lymphoid than in

226 vertant viruses, the mutants induce moderate levels of expression of interferon-stimulated genes (ISG

227 ian virus-derived NS segments provoked lower levels of expression of interferon-stimulated genes in c

228 with RRV VP4 and UK NSP1 genes induced high levels of expression of IRF3-dependent p54 in biliary ti

229 Statistically significant increases in the levels of expression of many of these genes were found i

230 sed disease severity correlates with reduced levels of expression of markers implicated in NCC pathol

231 Finally, the levels of expression of memory, costimulatory, and inhib

232 High levels of expression of miR-19 family members were found

233 littermate controls, had 2- to 6-fold higher levels of expression of mRNAs for immediate early genes

234 Levels of expression of multiple DNA damage repair pathw

235 nscriptome exhibited altered expression; the levels of expression of multiple virulence genes were al

236 The correct levels of expression of Myf5 and MyoD result from activa

237 qRT-PCR analysis also showed lowered levels of expression of nociceptor-specific pre-mRNA tra

238 specific and correlates with relatively high levels of expression of OAS genes, which are necessary b

239 on of p53 by ATM/ATR kinase led to increased levels of expression of p21, an inhibitor of G1-S-phase

240 CD31(+) cells had higher levels of expression of proangiogenic genes on microarra

241 ell as static cultures of AGM, exhibit lower levels of expression of prostaglandin synthases and redu

242 n applied this method to quantitate absolute levels of expression of protein kinase C (PKC) isoforms

243 Quantitative PCR showed high levels of expression of purinergic P2Y1 receptors and SK

244 etabolism is brought about by changes in the levels of expression of relatively few genes, but this i

245 These SNPs can result in altered levels of expression of some miRNAs from the BART varian

246 While changes in the levels of expression of some of the pluripotency markers

247 This is accompanied by lower levels of expression of SREBP-1c and SREBP-2 and genes o

248 s that can alter the coding potential and/or levels of expression of subsets of mRNAs in the mammalia

249 une responses by quantitative PCR showed low levels of expression of Th1 (IFN-gamma, IL-2, IL-12) and

250 diator component Med15/Gal11 to drive normal levels of expression of the ATP-binding cassette transpo

251 On the other hand, elevated levels of expression of the chimera cause the accumulati

252 eromers, individual clones were assessed for levels of expression of the constitutively expressed pro

253 (+) T cells in HIV controllers showed higher levels of expression of the cytolytic proteins granzymes

254 in Tlr6-/- mice also corresponded with lower levels of expression of the pathogen-recognition recepto

255 drial apoptotic machinery by fine-tuning the levels of expression of the proapoptotic protein BIM.

256 endothelial cells resulted in a decrease in levels of expression of the proinflammatory cytokines in

257 sors, OE) and lower (RNA interference, RNAi) levels of expression of the regulatory psbS gene and ana

258 s in the mouse neocortex depends on the high levels of expression of the transcription factor CTIP1;

259 concentration, internal fluctuations in the levels of expression of the transcription factors are co

260 bohydrates or peptides in media restored the levels of expression of the virulence genes in the CvfA(

261 The levels of expression of these ECF sigma factors increase

262 ise spatio-temporal patterns and appropriate levels of expression of these two signaling molecules in

263 labelling of bladder wall identified higher levels of expression of TREK-1 in detrusor smooth muscle

264 High levels of expression of wild-type Flt3 characterize many

265 The overall levels of expression of X-linked genes were indistinguis

266 In this study, we showed that high levels of expression of ZNF217 mRNA are associated with

267 killer (NK) cells and T cells exhibit a low level of expression on only a subset of cells.

268 umerous tumor tissues and correlation of the level of expression on tumor cells with adverse clinical

269 tical TECs subsets defined by different Ly51 levels of expression on the ontogeny.

270 orders are not gene deletions but changes in levels of expression or activity of a gene product; cons

271 Tumor grade did not influence the levels of expression or secretion.

272 they are interchangeable for measuring mean levels of expression over four orders of magnitude.

273 The predictive subnetworks vary in levels of expression over time but exhibit increased sim

274 ronment for genes with very high maximal net levels of expression, owing to transcriptional traffic j

275 ation one different production factor at two levels of expression: pig genotype (local breed vs. indu

276 role of POR in HAP activation at endogenous levels of expression, POR knock-outs were generated in H

277 overexpressed in breast carcinomas, and the level of expression positively correlated with expressio

278 e-specific manner, we show that altering its levels of expression produces changes in mitochondrial s

279 these receptors are regulated largely at the level of expression, protease-mediated ectodomain sheddi

280 n may in part be genetically determined, and level of expression regulates IFN-alpha signaling, which

281 that SNX27 is synaptically enriched and its level of expression regulates targeting of AMPARs to the

282 n of the gene bodies and restoration of high levels of expression requires remethylation by DNMT3B.

283 essing cone proteins in rods or changing the level of expression seem to show that many of the molecu

284 r all conditions, no changes occurred in the level of expression, sequence, or nuclear export of PHO1

285 ean-showed significantly lower Ka and higher levels of expression than their homoeologs in chromosoma

286 uning strategy and achieved an unprecedented level of expression that enables imaging of fluorescent-

287 and uncovers a distinct class of genes with levels of expression that have been constrained early in

288 We present LOX (Level Of eXpression) that estimates the Level Of gene eX

289 wed that the P(UBQ10) promoter gives similar levels of expression to that driven by the native SYP121

290 ns is more than compensated by its increased level of expression under inflammation.

291 ver, it has also been shown that an elevated level of expression (upregulation) of P16 is involved in

292 ed to identify genes exhibiting high and low levels of expression variation across tissues or genotyp

293 one deacetylase 1 mutation tend to show high levels of expression variation within and between specie

294 Levels of expression varied from one to 62 HIV RNA molec

295 y expressed in all tissues examined and high level of expression was found in transition stage embryo

296 ly increased; for H19 and Igf2 the increased level of expression was independent of the CTCF-binding

297 and controls, a stronger and more persistent level of expression was observed in the group with diabe

298 s maintained in RORgamma(-/-) mice, the peak level of expression was significantly reduced in several

299 Highest levels of expression were noted in the crypt fraction.

300 Syntaxin4/SNAP23 in vitro, a combination of levels of expression (which vary by >30-fold), subcellul