ライフサイエンスコーパス: expression level

1 27a targets the METTL7A 3'UTR to repress its expression level.

2 on can impact the entire distribution of the expression level.

3 , while YY1 overexpression increased ATP6V1A expression level.

4 lleles per cell were induced, a sign of high expression level.

5 d1 complexes are strongly influenced by Hrd1 expression levels.

6 ce chaperonin dependence and improve protein expression levels.

7 DKK1 and upregulation of keratin 17 protein expression levels.

8 tochastic bimodality despite increasing mean expression levels.

9 , and pseudogenes) was associated with islet expression levels.

10 readings from the Space Shuttle, and protein expression levels.

11 near these genes that likely influence their expression levels.

12 d block cellular gene expression at very low expression levels.

13 protein binding to their promoters and alter expression levels.

14 pressed open chromatin, glycolysis and Glut1 expression levels.

15 s to upregulate surface CD83, CD86, and CCR7 expression levels.

16 respect to improved experimentally observed expression levels.

17 ng expression fluctuations (noise) from mean expression levels.

18 studies that looks for haplotypic effects on expression levels.

19 ters and terminators, and variable transgene expression levels.

20 and muscle and correlated to GLUT1 and GLUT5 expression levels.

21 ing CD32A (FCGRIIA) protein and CD32B/C mRNA expression levels.

22 ns (TADs) and then model the dynamics of TAD expression levels.

23 explained by sexual dimorphisms in receptor expression levels.

24 ticularly for target cells with reduced EGFR expression levels.

25 ailor K(+) channel functional properties and expression levels.

26 OBPs and CSPs showed very high expression levels.

27 ort and the long 3'UTR produced similar mRNA expression levels.

28 n quantitative trait locus modulating CHRNA4 expression levels.

29 gh changes both in protein sequence and gene expression levels.

30 hest methylation levels correlate with lower expression levels.

31 inding exceeds scavenging at higher receptor expression levels.

32 Here we describe genetic effects on gene expression levels across 44 human tissues.

33 oject aims to characterize variation in gene expression levels across individuals and diverse tissues

34 ber of expression contexts rather than lower expression levels across the entire ancestral expression

35 (IAPs) family member, exhibited a decreased expression level after DHM treatment, which may be attri

36 ice as well as the known links between TIEG1 expression levels/allelic variations and patients with o

37 d with that detected through the use of gene expression levels alone.

38 ic polyTE insertion genotypes to B cell gene expression levels among 445 individuals from 5 human pop

39 UTR) has been shown to influence HLA class I expression level and associate with disease outcomes.

40 immunosuppressive role in immune cells, its expression level and role in endothelial cells (ECs) are

41 ulin) and demonstrate a relationship between expression level and the subsequent quality of PALM imag

42 the operon-encoded BioH might differ in its expression level and/or activity from the freestanding B

43 BAX expression levels and cytosolic conformation regulate se

44 an inverse relationship between TNFAIP3/A20 expression levels and IL-17A production.

45 e-wide method capable of capturing both gene expression levels and isoform diversity at the single-ce

46 We demonstrate that the expression levels and length of truncated ORF1 proteins

47 d ILC2 activation, resulting in higher IL-13 expression levels and M2 macrophage expansion in adipose

48 han protein-coding transcripts and had lower expression levels and more sample specific expression.

49 These adjustments involve fine-tuning of expression levels and mutual interactions among electron

50 ar and cytoplasmic functions, have different expression levels and nuclear-cytoplasmic partitioning.

51 ealing substantial cell-to-cell variation in expression levels and propagation of this variation betw

52 tion of the antigen binding region, receptor expression levels and signal capacity have all linked BC

53 orithm that was based on polymorphism-driven expression levels and specificities, we predicted and te

54 me altering genomic variants can impact gene expression levels and the structure of protein products,

55 d showed the lowest metastasis-specific gene expression levels and TP53 mutation rates.

56 E. ulmoides exhibits high expression levels and/or gene number expansion for multi

57 upon both KRAS mutational status and protein expression level, and acquired resistance is often assoc

58 tagonist of M3R, depending on the cell type, expression level, and signaling pathway downstream of th

59 hat across clones MAE status correlates with expression level, and that in human tissue data sets, MA

60 ols agonist efficacy by setting RGS2 protein expression levels, and affecting the rate at which cells

61 t alterations in DNA copy numbers (CN), gene expression levels, and DNA methylation profiles.

62 able genetic factors influence SERPING1 gene expression levels, and that these associations are obser

63 at reducing average tumor size, beta-catenin expression levels, and the number of aberrant crypt foci

64 ggesting that pathogenic variants acting via expression level are less likely to involve MAE genes.

65 Genetic variants affecting gene-expression levels are a major source of phenotypic varia

66 nflammatory bowel disease (IBD), and whether expression levels are associated with clinical outcomes.

67 gene expression, and eGenes are genes whose expression levels are associated with genetic variants.

68 ges suggest that alpha-1-antitrypsin protein expression levels are controlled at the posttranscriptio

69 Indeed, high Blimp1 expression levels are detected in invasive p130Cas/ErbB2

70 cer histopathology, but estimations of Ki-67 expression levels are inconsistent and understanding of

71 ke and luminal human breast tumours, and its expression levels are tightly coupled with those of glyp

72 Homer1 expression levels are upregulated in balloon-injured vs.

73 t mutated CATAC elements, imparted increased expression levels as well as rhythmic regulation.

74 an be used to characterize variation in gene expression levels at high resolution.

75 500 and Glyma.13G194400 with relatively high expression levels at seed development stage compared wit

76 ory regions is likely to also influence gene expression levels at these loci.

77 t-effective PET discovery process, involving expression level (Bmax) and biodistribution determinatio

78 However, at normal expression levels, Btn2p and Cur1p eliminate most newly

79 with various statins strongly increased LDLR expression levels but did not improve VSV attachment or

80 e shown that neurons are sensitive to TDP-43 expression levels, but the specific defects caused by TD

81 nuclear factor (NF)-kappa B-p65 and cytokine expression levels by quantitative polymerase chain react

82 individuals and cell types by measuring gene expression levels, chromatin accessibility, and DNA meth

83 We also demonstrate that Dmxl2 expression levels control the pruning of GnRH dendrites,

84 ade human gliomas, shows that high Caspase-8 expression levels correlate with a worse prognosis.

85 es compared with normal thyroid and that its expression levels correlate with T regulatory (Treg) lym

86 Consistent with these findings, fibulin-3 expression level correlated with the invasive ability of

87 In mice, subcutaneous AT Tshb expression levels correlated directly with circulating c

88 Importantly, NKG2D ligand expression levels correlated with enhanced susceptibilit

89 g GFI1 level in leukemic cells with low GFI1 expression level could be a therapeutic approach.

90 In bone marrow MSCs, FOXP1 expression levels declined with age in an inverse manner

91 rescue mice maintain endogenous CB1 receptor expression level, detailed anatomical studies are necess

92 Moreover, the TrkC-miR2 expression level discriminated grades of tumor malignanc

93 es, we tracked duplicate retention patterns, expression-level divergence, and subcellular markers of

94 id F1 hybrids and suggest that high-parental expression-level dominance plays an important role in he

95 re starting population, suggesting that GATA expression levels drive a phenotypically relevant source

96 ated with an increase in IFN-stimulated gene expression levels during HEV replication.

97 runtime of the IsoEM and IsoDE packages for expression level estimation and differential expression.

98 ns of MITEs have no detectable effect on the expression level for host genes across accessions.

99 Messenger RNA expression levels for 198 mitochondrially localized ener

100 to confer risk of T2D via the regulation of expression levels for a large number (266) of cis-regula

101 ion outliers, or individuals showing extreme expression levels for a particular gene, across 44 human

102 There are few datasets describing baseline expression levels for total cell-free circulating RNA fr

103 e statistical testing of differences in mean expression levels has been extensively studied, testing

104 Although MAGEA1's expression levels have been evaluated as one of the canc

105 Their expression levels have been reported to be elevated in s

106 eculate that the observed maximum in the lac expression level helps to save cellular resources by lim

107 The expression levels hpf and hflX are coregulated by genera

108 rly-onset bipolar disorder and a higher gene expression level in human prefrontal cortex.

109 onclusion, the relatively low endogenous Spl expression level in insulin-secreting cells contributes

110 However, it is unclear how their expression level in neurons is regulated.

111 689879) contributed to increased ileal MAGI3 expression level in non-IBD controls.

112 the epigenetic effect of the changes in gene expression level in the F1 hybrids showed that the major

113 nterfering RNA (siRNA) clusters had a higher expression level in the F1 hybrids than in the parents,

114 rs3217869 risk genotype and decreased CCND2 expression levels in a collection of 119 prostate cancer

115 Augmenting P2Y14 R expression levels in aged/diseased hCPCs antagonizes sen

116 q) is a powerful approach for measuring gene expression levels in cells and tissues, but it relies on

117 s differentially recruited to fine-tune gene expression levels in each cardiac chamber.

118 llular vesicle (EV)-associated RNAs with low expression levels in early-stage cancer remains a challe

119 Restoring P2Y14 R expression levels in functionally compromised hCPCs via

120 Human gene expression levels in humanized mouse livers were analyze

121 scular endothelial cells (MECs) and that LPP expression levels in intratumoral MECs correlated with s

122 ACTB mRNA expression levels in lymphoblastic lines and fibroblasts

123 This increase in TRU1 expression levels in modern maize is supported by compar

124 In vivo studies indicated that TRAF1 expression levels in mouse skin are induced by short-ter

125 titative PCR (qRT-PCR) we demonstrate snoRNA expression levels in murine ageing and OA joints and ser

126 ed liver metastasis formation in vivo Talin1 expression levels in patient CTC's correlated with progn

127 rom plasma, and both DNA genotyping and mRNA expression levels in peripheral blood mononuclear cells

128 8)F-FES uptake correlate well with AR and ER expression levels in representative biopsies.

129 iated with programmed death ligand 1 (PD-L1) expression levels in several cancers, but PD-L1 expressi

130 iation of gene expression and maintenance of expression levels in spatial and temporal manner.

131 Low Nr3c2 expression levels in the CeA were significantly associat

132 y, we trained a classifier based on the gene expression levels in the non-infected cells, and demonst

133 rough the hole and its relation to the lamin expression levels in the nuclear envelope.

134 MCs from mouse mutants differing in Munc13-4 expression levels in their MCs revealed that as levels o

135 ion seems essential for reaching high enzyme expression levels in these tissues.

136 estigation of microarray-based gene and exon expression levels in whole blood in a cohort of 5257 ind

137 We assessed global RNA expression levels in whole blood samples from 150 partic

138 eatly increased our ability to identify gene expression levels, including at specific developmental s

139 ients with Alzheimer's disease (AD), and its expression levels influence the onset of the AD-like phe

140 Census algorithm to convert relative RNA-seq expression levels into relative transcript counts withou

141 mediate MIIP-S303 dephosphorylation and its expression level inversely correlates with metastatic ca

142 hly expressed in lung cancer tissues and its expression level is critical for lung cancer cell prolif

143 COUP-TFII protein expression level is high in undifferentiated progenitors

144 whereby in natural hosts, in which the CCR5 expression level is low, the use of CXCR6 or other corec

145 We demonstrate that expression levels largely determine whether MDGAs act se

146 k allele is associated with increased SLC4A7 expression level, NBCn1 availability and function as ref

147 At low expression levels, neither reference nor variant APOL1s

148 with all three models recapitulated the Fshb expression levels obtained in pituitary gonadotrope cell

149 tage IV or recurrent NSCLC and a PD-L1 tumor-expression level of 1% or more to receive nivolumab (adm

150 tion about metabolic fluxes depending on the expression level of a critical enzyme.

151 e to predict TF combinations controlling the expression level of a given gene.

152 ation of two gene variables depending on the expression level of a third variable (LA scouting gene).

153 ic structure and function by restraining the expression level of active zone (AZ) and synaptic vesicl

154 Furthermore, the expression level of c-Jun was significantly higher in TN

155 umber, inherent potency of sgRNA guides, and expression level of Cas9 and sgRNA, in determining CRISP

156 typical feature of astrocytes is their high expression level of connexin43 (Cx43), a protein forming

157 II C-terminal domain (CTD) and affecting the expression level of CTD phosphatase-like 3 (CPL3), AtCPS

158 ecreased transcriptome-wide variation in the expression level of highly constrained genes.

159 hydrogel was capable of down regulating the expression level of IL-1beta in LPS induced macrophage c

160 Simultaneously, high expression level of IL-6R mRNA correlates with better su

161 A microarray analysis, which showed that the expression level of miR-124-3p increased most apparently

162 e of inflammation is sufficient to alter the expression level of proteins relevant to the pathogenesi

163 -transcribing parasites are dependent on the expression level of PTEF, and the alleviation of upstrea

164 f various stresses, as a result of the lower expression level of RESPIRATORY BURST OXIDASE HOMOLOG D

165 ntranslated region intron that determine the expression level of the gene.

166 ern blot analysis indicated that the protein expression level of the mutant form of MIP was remarkabl

167 L-6, and IL-8) across stimuli, a higher gene expression level of TLR2 (P = .02) and TLR9 (P = .02), a

168 mical observations, a 2-fold increase in the expression level of wild-type PFN1, but not the ALS-link

169 Expression levels of 17 genes characterizing type 1, typ

170 NPs) from the custom-made PsychArray and the expression levels of 190 multiplex immunoassay profiled

171 We analyzed expression levels of 20 genes and sequenced exon regions

172 evealed that DC3000 significantly alters the expression levels of 71% effector targets and their down

173 suitable for computational inference of the expression levels of 81% of non-measured transcripts.

174 When the sample size is small or the expression levels of a gene are highly dispersed, the NB

175 Here we discover a pattern in the expression levels of a sparse subset of genes among cell

176 The expression levels of Adipoq and fatty acid synthesis-rel

177 ly associated with changes in methylation or expression levels of adjacent genes.

178 inimization process, which causes the scaled expression levels of all transcript isoforms to follow t

179 The accessions were selected based on the expression levels of ANNEXIN1, a drought-related marker.

180 his study was to determine whether the early expression levels of any of these 16 genes are predictiv

181 ng reverse-phase protein arrays, we measured expression levels of approximately 230 key cancer-relate

182 As protein expression levels of AROM, estrogen and androgen recepto

183 tly, clinical HLRCC tissues showed increased expression levels of both FOXM1 and its proliferation-as

184 PAK4 expression is coincident with increased expression levels of c-Met and the p85alpha subunit of P

185 Na(+) levels were not increased, and expression levels of Ca(2+)- or Na(+)-handling proteins

186 Transcriptional expression levels of candidate genes were measured in pe

187 ion, we verified miR-449b could regulate the expression levels of CDK6, c-MYC, HDAC1 and BCL-2.

188 replication is a requirement for the highest expression levels of certain genes.

189 Interestingly, the expression levels of CIITA and MHC-II significantly incr

190 Based on protein expression levels of common endothelial markers using fl

191 , nor did we observe that ZnO NPs reduce the expression levels of CT mRNA and protein.

192 C) imaging is limited mainly by insufficient expression levels of facilitative glucose transporter (G

193 Both groups demonstrated increased expression levels of fibroblast growth factor-2, transfo

194 with increased collagen accumulation, higher expression levels of fibronectin-1, collagen I, alpha-sm

195 are correlated with protein amounts and mRNA expression levels of five major human sulfotransferase (

196 a molecular signature measuring the relative expression levels of four host messenger RNAs, was devel

197 Expression levels of four novel GAD1 transcripts (8A, 8B

198 rong and significant correlation between the expression levels of FOXM1 and AURKA.

199 The expression levels of FXR1 (fragile X mental retardation

200 In comparing expression levels of genes between the mouse tumor and n

201 Compared with wild-type, the expression levels of genes encoding several transporters

202 e PHD inhibitors significantly increased the expression levels of genes involved in gluconeogenesis i

203 ry proteins controlling the context-specific expression levels of genes.

204 The expression levels of GHRH and its receptor (GHRH-R) meas

205 Expression levels of glial intermediate filaments (GFAP,

206 ncing of SALL4 in cancer cells decreased the expression levels of Glut1 and inhibited glycolysis in c

207 Furthermore, in combination, the expression levels of hsa-miR-146a-5p and hsa-miR-30a-5p

208 solated from the paraffin material, and gene expression levels of IL-32 alpha, beta, and gamma isofor

209 Higher expression levels of IL-33 in cadherin-11-deficient mice

210 of LPS together with iC3b or fibrinogen, the expression levels of IL-6 and TNF-alpha in integrin alph

211 Higher expression levels of IL1R1, IL1RAP, and IL4R were associ

212 IMBD inhibited gp120-induced RNA and protein expression levels of IL6 and IL8, but not that of CCL5 i

213 f vigorous increase in number and changes in expression levels of inflammation-related genes, monitor

214 us showed impaired growth and induced higher expression levels of innate immune genes in infected cel

215 se five EC-associated cytokines could change expression levels of intrinsic resistance factors, or mo

216 ls modulated epithelial permeability and the expression levels of junctional proteins.

217 olymerase chain reaction was used to measure expression levels of key ion transport proteins.

218 In this study, we showed that the expression levels of LDHA mRNA and protein were signific

219 or kappaB (NF-kappaB) directly regulates the expression levels of lipid desaturases, and inhibition o

220 lular TNFalpha immunoreactivity, and reduced expression levels of macrophage factors that are associa

221 eq shows quantitative capability to estimate expression levels of mature tRNAs, and has high reproduc

222 biomarker analyses correlated efficacy with expression levels of MET ligand hepatocyte growth factor

223 chment Analysis (GSEA) demonstrated that low expression levels of miR-30a had the tendency to associa

224 Two SNVs are associated with expression levels of nearby genes, and SNVs at 3 loci ar

225 Protein expression levels of NF-kappaB, AP1, p-STAT3, p-AKT, p-I

226 In vivo, kidney expression levels of NFkappaB2 p100 and p52 increased ra

227 Messenger RNA expression levels of nuclear factor kappa-light-chain-en

228 Messenger RNA expression levels of p38 mitogen activated protein kinas

229 Additionally, rhIFN-gamma increased expression levels of pattern recognition receptors, such

230 1 proinflammatory macrophages) and decreased expression levels of proinflammatory and profibrotic mar

231 The mRNA and protein expression levels of proinflammatory cytokines IL6, IL8

232 Cell viability was evaluated, and expression levels of Runx2, Alp, Ocn, Rankl, and Opg wer

233 on data sets allowed to observe that high co-expression levels of SCD1, beta-catenin, YAP/TAZ and dow

234 transcription polymerase chain reaction, the expression levels of secretin, and VIP were measured.

235 nscriptomics data to KEGG pathways, we found expression levels of secretory phospholipase A2 (sPLA2),

236 sed an increase in endogenous RCS and higher expression levels of senescence marker genes, leading to

237 can act as antisense transcripts to repress expression levels of sense genes from the opposite stran

238 /monocyte clade, as supported by higher mRNA expression levels of several dendritic cell-associated g

239 sion of the SHH pathway, as shown by altered expression levels of several target genes.

240 ecretions, we analyzed by means of qPCR, the expression levels of six of the CYP450 genes most abunda

241 The mRNA expression levels of some genes related to neurotransmis

242 The expression levels of some markers for AML subtypes and c

243 We show that the expression levels of SOX5, SOX6, and SOX21 (SOX5/6/21) t

244 els contains a series of X-Y plots depicting expression levels of subsystems of that panel, e.g. subs

245 The expression levels of tau and TDP-43 were inverse in the

246 Interestingly, the relative expression levels of Tau isoforms containing either 3 (3

247 associated with reduced inflammation, lower expression levels of TGF-beta and proteases associated w

248 mbient temperatures correlated with relative expression levels of the BARLEY MADS-box genes VERNALIZA

249 Here we show that the expression levels of the disulfide-bond A oxidoreductase

250 frequencies of responding cells but not the expression levels of the early activation marker molecul

251 Identical to clinical CRPC, the expression levels of the full-length AR (twofold, P < 0.

252 This effect is accompanied by higher expression levels of the gibberellic acid (GA) catabolic

253 The expression levels of the immature-like neutrophil signat

254 PINA1 mRNAs encode exactly the same protein, expression levels of the individual mRNAs vary substanti

255 We then assessed the expression levels of the remaining candidates in exosome

256 In addition to IL-27, gene expression levels of the specific IL-27 receptor (IL27RA

257 Expression levels of the top identified gene were measur

258 The strong correlation between the expression levels of these known marker genes and the ex

259 First, we identified that peripheral mRNA expression levels of two complement genes (C5, SERPING1)

260 ted HHV-8 infection of iDDC, as shown by low expression levels of viral proteins and DNA.

261 telomerase repeat addition processivity and expression level on telomere elongation and length maint

262 subset and organs targeted, but not antigen expression level or VHH affinity.

263 s as one of a handful of genes whose altered expression levels or allelic variations are associated w

264 xtended 3' ends have significantly increased expression levels over their nonstructured counterparts.

265 stigate variability in an individual's exRNA expression levels over time.

266 lline and dexamethasone in maintaining HDAC2 expression levels, preventing hearing loss in LPS-expose

267 as observed between SULT activities and mRNA expression levels (r(2) </= 0.48 except one).

268 nd direct protein-protein interaction, their expression levels rely on the presence of each other, an

269 eatic cancer cell lines with high and low TF expression levels, respectively.

270 Very low expression levels, resulting in infrequent DUX4 + myonuc

271 ave the same target motif but have different expression levels, revealing this important feature for

272 In primary human PDAC, YAP expression levels strongly correlate with an MDSC gene s

273 finity required drastically reduced receptor expression levels, suggesting that scavenging pathways c

274 y an increase in connexin 43 and connexin 40 expression levels, suggesting their role in the developm

275 The absence of cytotoxicity at physiologic expression levels suggests variant-dependent intracellul

276 magnitude of enhancer transcription, TF mRNA expression levels, TF motif P-values, and enrichment of

277 genin is only detected in female gonads with expression levels that are rather variable among female

278 CD8 T-cell function is modulated by antigen expression levels, the percentage of HCV-infected cells,

279 ate of change in expression and the absolute expression level to identify TRN connections.

280 membrane integration efficiency and protein expression levels to predict protein sequence modificati

281 w in tumors expressing TCRalphabeta, but its expression level was high and clonality was detected in

282 A significant increase in IL18 expression levels was observed in HIV-associated anal SC

283 To analyze telomerase at its low endogenous expression level, we genetically engineered human plurip

284 ation efficiency and experimentally observed expression levels were cumulative and largely independen

285 SIRT2 protein expression levels were downregulated in hypertrophic hea

286 n samples from a single patient, upregulated expression levels were found for most proinflammatory in

287 Menin and miR-24 expression levels were measured in the following intrahe

288 mples were sensitive to venetoclax, and BCL2 expression levels were negatively correlated (r = -0.52;

289 nical specimens, we also showed that miR-152 expression levels were negatively correlated with beta-c

290 Gene expression levels were opposite to methylation status, a

291 rtantly, elevated CXCR7 and depressed CXCL12 expression levels were prominent features of clinical br

292 alpha5beta1 and alpha6beta4 integrin expression levels were quantified on 20 different cell l

293 Here, we found that miR-218 expression levels were significantly downregulated in lu

294 TERT mRNA expression levels were significantly higher in tumors ha

295 iting catalytic polypeptide 3A (A3A) and A3G expression levels were significantly upregulated in huma

296 Gene expression levels were strongly associated with cell dif

297 and one of its SPL target genes have inverse expression levels, which is tightly correlated with grea

298 s system can be used to control in vivo gene expression levels with low background, large dynamic ran

299 lls to IL-1 stimuli and changes the cytokine expression levels within infected cell populations.

300 At least six miRNAs show cycling expression levels within the pigment dispersing factor (