ライフサイエンスコーパス: level of expression

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

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

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

4 on the localization of METTL5 but alter its level of expression.

5 ontrol of gene activation or increase in the level of expression.

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

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

8 affects cellular metabolism dependent on the level of expression.

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

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

11 reads generated from known genes at varying levels of expression.

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

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

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

15 owth medium manipulation allows intermediate levels of expression.

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

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

18 d cellular injury and restored SMPDL3b basal levels of expression.

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

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

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

22 irions proportionally to their intracellular levels of expression.

23 o exploit receptors with relatively moderate levels of expression.

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

25 cted insertion strategy to ensure equivalent levels of expression.

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

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

28 We observed little change in levels of expression across these ages.

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

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

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

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

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

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

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

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

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

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

39 idization assays were used for assessing the levels of expression and cell-type localization of PPARg

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

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

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

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

44 (0.04%), and transcripts that display lower levels of expression and stochastic noise(7-9) and highe

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

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

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

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

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 ely; and transiently altering their relative levels of expression can modulate stem-cell competence i

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

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

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

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 in human endometriotic lesion tissue, the level of expression correlates with survival status of t

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

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

68 an input-output function describing how the level of expression depends upon the parameters of the r

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

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

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

72 a dominant murine CD4(+) T cell antigen, its level of expression during the bacterial developmental c

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

74 uring late T-cell development with very high levels of expression during thymocyte selection, followe

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

76 cells, EIF4E-regulated proteins with reduced levels of expression following ribavirin treatment inclu

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

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

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

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

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

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

83 picardial subpopulations are defined by high levels of expression for the transcription factors BNC1

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

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

86 In most cases, the level of expression from maternal and paternal alleles w

87 without NPM1 mutations and also assessed the level of expression from the wild-type and mutant allele

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

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

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

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

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

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

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

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

96 pared to the initial evaluation, overall the level of expression in these gene categories remained st

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

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

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

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

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

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

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

104 Microarray found that compared with their levels of expression in control tissue, the levels of ex

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

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

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

108 AMHD1 phosphorylation, CDK1, exhibited lower levels of expression in female-derived macrophages in al

109 grin alpha3 and CD26 respectively, with high levels of expression in human pancreatic and other cance

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

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

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

113 low-risk haplotype generated 12%-20% higher levels of expression in PANC-1 and CFPAC-1 cells compare

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

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

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

117 In particular, TRP channels showing high levels of expression in sensory neurons such as TRPV1, T

118 the behavior of 337 genes whose much higher levels of expression in symbiotic than aposymbiotic anem

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

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

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

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

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

124 of a human B cell-specific lncRNA with high levels of expression in three types of B cell cancer and

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

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

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

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

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

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

131 ) T cells, and we observed that its relative level of expression modulates differentiation as well as

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

133 r pair is also uniquely able to maintain low levels of expression noise across a wide range of temper

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

135 on, we compared the phenotype, function, and level of expression of a comprehensive panel of 579 immu

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

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

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

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

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

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

142 The level of expression of CD137L, however, did not modulate

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

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

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

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

147 iptional profiling of strains with a reduced level of expression of core degradosome ribonucleases pr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 The level of expression of ion channels has been demonstrate

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

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

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

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

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

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

171 ated by CRISPR-Cas9 technology displayed low level of expression of mutant CCN6 protein and inhibited

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

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

174 -1 Tat protein significantly upregulated the level of expression of PD-L1.

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

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

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

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

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

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

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

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

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

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

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

186 % of the total, and was not dependent on the level of expression of the retinal pigment epithelium is

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

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

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

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

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

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

193 However, EHV-1 reduced the cellular level of expression of tyrosine kinase 2 (TYK2) at 12 hp

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

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

196 levels of expression in control tissue, the levels of expression of 126, 241, and 545 genes were mor

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

198 mass cytometry to simultaneously measure the levels of expression of 24 surface markers on peripheral

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

200 We were able to quantify the relative levels of expression of 55 and 49 small GTPases accompan

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

202 While we observed similar levels of expression of alpha(1) receptor-encoding mRNA

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

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

205 Keap1(f/f) pups was accompanied by increased levels of expression of antioxidant genes and GSH as ass

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

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

208 ealed that lymphoid tissues have the highest levels of expression of both genes, and custom antibodie

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

225 Levels of expression of genes associated with stress, in

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

227 -responsive cells were characterized by high levels of expression of glucocorticoid receptor (GR) enc

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

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

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

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

232 correlates with the failure to activate high levels of expression of interferon-inducible genes in gl

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

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

235 In addition, levels of expression of many genes encoding mediators of

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

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

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

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

240 Levels of expression of multiple DNA damage repair pathw

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

242 The levels of expression of nuclear-encoded, TIM23-transport

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

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

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

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

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

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

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

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

251 hereas psoriasis was characterized by higher levels of expression of T(H)17-related (IL-17A/F and IL-

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

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

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

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

256 Finally, significantly lower levels of expression of the NPR2 protein were detected i

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

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

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

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

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

262 The levels of expression of these ECF sigma factors increase

263 anding the factors affecting the pattern and levels of expression of these genes is important for dee

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

265 man IAV (either H1N1 or H3N2) induced higher levels of expression of type I (IFN-alpha and IFN-beta)

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

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

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 ital tract in response to infection, and low levels of expression persisted after the infection clear

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

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

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

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

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

281 We have evaluated the overall levels of expression, protein activity, as well as the b

282 detected in all leukemic MCL samples and its level of expression rapidly increased upon BCR stimulati

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

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

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

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

287 This high level of expression seems to correlate with poor metasta

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

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

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

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

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

293 The results were compared with levels of expression (using RNA-seq) and DNA methylation

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

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

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

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

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

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

300 se functional impacts of Kv2.1 depend on its level of expression, which varies with sex.