ライフサイエンスコーパス: mRNA level

1 in level with no corresponding change on the mRNA level.

2 ated expression of glycolytic enzymes at the mRNA level.

3 2 translation without an effect on the Cdc42 mRNA level.

4 200b, miR-200c, or miR-217 enhanced mortalin mRNA level.

5 uster that was not readily identified at the mRNA level.

6 lated RAB25 is inversely correlated with its mRNA level.

7 on to indicate promoter activities at single-mRNA level.

8 proteasomes, but it does not affect the Mig6 mRNA level.

9 glucose content by increasing PEPCK and G6P mRNA level.

10 60% of the tumors exhibiting a reduced Grb14 mRNA level.

11 ion can be traced at the genomic DNA and the mRNA level.

12 py number was positively correlated with its mRNA level.

13 rchitecture and insufficient variation of TF mRNA level.

14 normal tissues confirmed tissue-specific RD3 mRNA levels.

15 10 mRNA, with no concomitant change in ARAP1 mRNA levels.

16 kinase ERK2 over what would be predicted by mRNA levels.

17 actors may be at play, including higher KRAS mRNA levels.

18 ked decrease in steady-state OGA protein and mRNA levels.

19 pletion of NDP52 or MVI reduces steady-state mRNA levels.

20 a time and dose-dependent decrease in TRIB3 mRNA levels.

21 g that the aptamer did not globally suppress mRNA levels.

22 serves as a monitor to control ILP7 and ILP8 mRNA levels.

23 S-derived cardiomyocytes at both protein and mRNA levels.

24 rite, despite several-fold elevation of Fmr1 mRNA levels.

25 levels were positively correlated with MMP7 mRNA levels.

26 ron defects, the movement defects, and Gap43 mRNA levels.

27 e translation rate of PGRN without affecting mRNA levels.

28 that this has a measurable global impact on mRNA levels.

29 correlate with the increase in steady-state mRNA levels.

30 n them than gene levels, mutations, and even mRNA levels.

31 T cells that corresponded to increased IL-2 mRNA levels.

32 signal variations not related to the actual mRNA levels.

33 red cPLA2 activity along with COX2 and 5-LOX mRNA levels.

34 14 significantly reduced ATP5G1 steady-state mRNA levels.

35 y impulsive (HI) rats expressed lower zif268 mRNA levels.

36 ked the ability of HISs to increase hepcidin mRNA levels.

37 a roots, and quantified YFP fluorescence and mRNA levels.

38 a from lean volunteers had no effect on IL32 mRNA levels.

39 urface expression of NaV1.5 without changing mRNA levels.

40 correlation coefficient between protein and mRNA levels.

41 e as well as by quantitative measurements of mRNA levels.

42 significantly lowered GLUT2 and increased PK mRNA levels.

43 y with AR expression at both the protein and mRNA levels.

44 ctivity (1.5- to 2.7-fold) as well as PGC-1a mRNA levels (1.5- to 5-fold) in rat soleus muscle and wh

45 evel upregulated glycolysis by increasing GK mRNA level; 2.70% dietary arginine level upregulated glu

46 site-directed RNA editing to repair, at the mRNA level, a disease-causing guanosine to adenosine (G

47 w muscle fibers had been investigated at the mRNA levels, a comprehensive analysis at proteomic and m

48 ed H3K9me1, supporting that changes in Prdm2 mRNA levels affected its activity.

49 While AGO1-miR-1 down-regulated the mRNA level, AGO2-let-7 delayed the timing of translation

50 evious observations that compensation at the mRNA level also varies among Drosophila cell lines and y

51 creased CELF1 expression downregulating Cx43 mRNA level and a pathogenic role for elevated CELF1 leve

52 CELF1 in the infarcted heart preserved Cx43 mRNA level and ameliorated the cardiac phenotypes of the

53 otactin levels are tightly controlled at the mRNA level and at the protein level through endocytosis

54 One, TRmD, depends on the mRNA level and defines the amplification exponent.

55 correlated with reductions in hepatic Srebp2 mRNA level and mature Srebp2 protein abundance.

56 MEP50 suppresses hINV mRNA level and promoter activity.

57 tex (mPFC)-DNA methyltransferase 3a (Dnmt3a) mRNA levels and a subsequent decrease in mPFC-global DNA

58 in resistance, including inhibition of IRS-1 mRNA levels and activation of gluconeogenesis-related ge

59 nthesis regulated at the transcriptional and mRNA levels and by proteasomal degradation.

60 ificant effects on pro-inflammatory cytokine mRNA levels and cytokine protein secretion activities.

61 arked by significantly reduced Nos2 and Il1b mRNA levels and decreased interferon (IFN)-gamma, tumor

62 ions in endogenous shha and shha target gene mRNA levels and developmental defects associated with nu

63 al of DXO from cells increases NAD(+)-capped mRNA levels and enables detection of NAD(+)-capped intro

64 with H. rubrisubalbicans increased the ACCO mRNA levels and ethylene production.

65 essed the effect of the nonsense mutation on mRNA levels and evaluated the NMJ transmission in VAMP1(

66 duction in DNA methyltransferase 3a (Dnmt3a) mRNA levels and global DNA methylation in the medial pre

67 Relative to bHRs, bLRs had lower FGF2 mRNA levels and increased association of a repressive ma

68 ed: (1) plasma and brain levels of SS31, (2) mRNA levels and levels of mitochondrial dynamics, biogen

69 imulation with leukotriene D4 increased iNOS mRNA levels and NO production in cultured BAL macrophage

70 tissues of Tg26 mice also displayed enhanced mRNA levels and protein expressions of inflammasome mark

71 Sepsis caused reduced mRNA levels and reductions in protein concentrations in

72 rved a significant correlation between MMP13 mRNA levels and RUNX2 gene expression in human OA chondr

73 BCL2 i-motif promoter DNA structures lowered mRNA levels and subsequently enhanced sensitivity to a s

74 receptor/transporter protein densities with mRNA levels and uncovered unique associations between pr

75 ed cells was associated with increased c-Jun mRNA levels and was blocked by inactivation of the JNK1/

76 tely ( approximately 0.50) with PD1 and CD8A mRNA levels and weakly ( approximately 0.35) with CD4 an

77 epatic cells and liver tissue reduced LPCAT3 mRNA levels, and exogenous overexpression of PPARdelta i

78 ewer Insulin+ cells, decreased Ins1 and Ins2 mRNA levels, and increased Pdx1 and Hes1 mRNA levels wit

79 mRNAs, increased eIF4E-bound PTC-containing mRNA levels, and subsequent eIF4E-dependent translation.

80 uploidy can be moderately compensated at the mRNA level - aneuploid gene expression is shifted toward

81 ing (6 weeks) increased soleus muscle PGC-1a mRNA levels ( approximately 25%) and the mitochondrial e

82 FIL3 (E4BP4), ZEB2, PRDM1 (BLIMP1), and RORA mRNA levels are higher in CD56(dim) cells.

83 PID1 tumor mRNA levels are highly correlated with longer survival i

84 TGF-beta1 mRNA levels are increased in mouse models of iron overlo

85 estabilize cell-cell contacts and (ii) CdGAP mRNA levels are inversely correlated with E-cadherin pro

86 in medulloblastoma, and in cases where FBW7 mRNA levels are low, SOX9 protein is significantly eleva

87 We show that HOPX mRNA levels are reduced in OSCC and NPC cell lines and t

88 primary NSCLCs demonstrated that low TRIM14 mRNA levels are significantly associated with poorer pro

89 nscriptional mechanisms as the corresponding mRNA levels are unaffected.

90 ng six chemokine 3'-UTRs increased chemokine mRNA levels as expected.

91 At baseline, IL-1alpha, IL-6 and IL-8 mRNA levels as well as TLR-4 protein expression were sig

92 BDNF mRNA levels, assessed by quantitative PCR and in situ hy

93 nhibition resulted in the reduction of AR-V7 mRNA levels but did not affect total AR transcript level

94 1-[(18)F]FDAM does not correlate with GLUT5 mRNA levels but is linked to GLUT5 protein levels.

95 not affect the upregulation of COX-2 at the mRNA level, but it reduced the half-life of COX-2 protei

96 We show that BBS4 and cilia regulate FSTL1 mRNA levels, but BBS4 also modulates FSTL1 secretion.

97 t, protein levels do not scale linearly with mRNA levels, but instead scale with the abundance of mRN

98 ST1 have stop codons that are created on the mRNA level by a novel polyadenylation mechanism found on

99 ed genes were tested for DNA methylation and mRNA levels by using bisulfite pyrosequencing and quanti

100 ources of variability, and found that scaled mRNA levels can account for most of the mean-level-varia

101 At the protein and mRNA levels, cells surviving H2O2 treatment show a reduc

102 he last third of embryonic development, UCN3 mRNA levels changed differentially in the various brain

103 ical epithelial surface and also had reduced mRNA levels compared to biglycan.

104 mice showed a 50% decrease in vaginal Prr5l mRNA levels compared to controls.

105 essed significantly higher intragraft CYP3A5 mRNA levels compared to steroid-refractory patients (n =

106 d not result in significant changes to IL-23 mRNA levels, confirming that the aptamer did not globall

107 r RING1 and YY1 binding protein (RYBP) whose mRNA levels correlate with improved insulin sensitivity

108 Since wun2 mRNA levels correlate with the levels of other maternal

109 beta effects on JunD protein levels, but not mRNA levels, correlated with its effects on cell prolife

110 sed in gonadotrope-precursor cells, but Tet1 mRNA levels decrease markedly with completion of cell di

111 phila immune organ, leads to elevated cactus mRNA levels, decreased expression of antimicrobial pepti

112 sly-miR160 legitimate site of SlARF16A, its mRNA levels did not change in response to sly-miR160 dow

113 ed quantitative (q)PCR to test whether GPR30 mRNA levels differ in males in breeding vs. nonbreeding

114 Striking increases in GAL and GALR3 mRNA levels, especially in the noradrenergic locus coeru

115 inflammasome sensors was dysregulated at the mRNA level except for the NLRP12.

116 some isotypic inclusion was observed at the mRNA level, expression in the BCR was examined.

117 We analyzed the mRNA levels for 36,778 transcript expression traits (pro

118 f the CCR4-Not deadenylase complex, restored mRNA levels for a class of downregulated, H3K36me3-rich

119 This correlated with LSO mRNA levels for glycinergic and glutamatergic ionotropic

120 aggravated arthritis severity and increased mRNA levels for key cytokines and chemokines such as IL-

121 In contrast, the mRNA levels for p53 did not increase, indicating that it

122 Iron depletion reduced mRNA levels for the majority of the affected proteins, i

123 Consistent with this, mRNA levels for the SK3 subunit of SK channels are signi

124 Here we report that increased mRNA levels for the SK3 subunit of SK-type K(+) channels

125 DNMT3L overexpression also increased mRNA levels for TP53 and APP, effectors of TSPYL5 Furthe

126 Despite similar expression at the mRNA level from the wild-type and chimeric MLL alleles,

127 wed that LPS treatment significantly altered mRNA levels from 2563 genes.

128 this information is usually lost when global mRNA levels from tissues are measured using reverse tran

129 n prostate tumor tissues, and verified their mRNA level in a panel of prostate cancer cell lines.

130 We studied DNM2 mRNA level in adults with B- and T-cell ALL.

131 ht correlate with Sin1 protein level but not mRNA level in colorectal cancer patients.

132 Their interactions regulate mRNA level in specific subcellular regions and determine

133 Exogenous EGF increased S100A4 mRNA levels in 231BR-EGFP cells (1.40+/-0.02-fold, P<0.0

134 Moreover, CT-1 mRNA levels in adipose tissue showed significant circadi

135 Diptericin (Dipt), but did not increase Dipt mRNA levels in air.

136 with its specific agonists increased LPCAT3 mRNA levels in all three hepatic cell lines.

137 RT-qPCR showed reduced Spr1 mRNA levels in all transformants analysed, and these cor

138 lied transcriptomics analysis to compare SGs mRNA levels in Anopheles stephensi fed on non-infected a

139 plication initiation, we analyzed changes in mRNA levels in Bacillus subtilis cells with and without

140 antly lower MERS-CoV titers and MERS-CoV and mRNA levels in challenged mice than those in unvaccinate

141 reaction revealed the downregulation of SPEG mRNA levels in failing human hearts.

142 sed Vegfa expression but did not affect Sox9 mRNA levels in gonadal explants.

143 We observed global dysregulation of mRNA levels in H3K36R animals that correlates with the i

144 1,25(OH)2D3 increased CYP27B1 mRNA levels in HCEC, but had no effect on CYP27B1 protei

145 a administration resulted in increased HMGCR mRNA levels in human adipocytes.

146 nd serum levels by 50%, despite normal Fgf23 mRNA levels in long bones.

147 d via mortality and down-regulation of Diap1 mRNA levels in M. domestica larvae injected with D. radi

148 dexamethasone (DEX) decreased TGF-beta group mRNA levels in normal mice.

149 ative correlation was observed between RUNX2 mRNA levels in OA chondrocytes and the percentage methyl

150 (r=0.24, P=0.03) between serum VEGF and IL-6 mRNA levels in patients with schizophrenia.

151 oposide, or bleomycin suppress Rag1 and Rag2 mRNA levels in primary pre-B cells, pro-B cells, and pro

152 ated with the time at which HSV-1 genome and mRNA levels in primary skin lesions started to decline i

153 We measured steady-state mRNA levels in Scots pine transition zone and sapwood us

154 Quantitative measurement of mRNA levels in single cells is necessary to understand p

155 significantly upregulated ACC, FAS and G6PDH mRNA levels in the fat synthesis pathway and resulted in

156 These findings suggest that low D2 mRNA levels in the nucleus accumbens core, likely mediat

157 In Study 2, we measured Nr3c2 mRNA levels in the PFC and CeA of dependent and nondepen

158 Our results show that MKP-2 mRNA levels in the spinal cord and lymphoid organs of EA

159 cytes, despite the strong decrease in Themis mRNA levels in these subsets.

160 There were no differences, however, in iNOS mRNA levels in total BAL cells in uncontrolled as compar

161 correlation between c-MYC activity and SPOP mRNA levels in two independent PC patient cohorts.

162 natal exposure to genistein on gene specific mRNA levels in vaginal tissue.

163 amma haploinsufficiency normalized PPARgamma mRNA levels in VDR(-/-) keratinocytes and restored anage

164 ks significantly (1.8-fold) up-regulated Pxr mRNA levels in WT mice.

165 was recently detected at the messenger RNA (mRNA) level in human periodontitis.

166 oles of each individual S100, especially the mRNA level, in breast cancer patients remain elusive.

167 1beta, and cluster of differentiation (cd)68 mRNA levels increased after exercise only in ATF3-KO mic

168 of tumor necrosis factor-alpha and amyloid A mRNA levels increased in the epidermis, but not in the l

169 d cytokine (IL1beta, IL6, IL12 and TNFalpha) mRNA levels indicating that these critical pathways were

170 t diet-induced obese (DIO) rats, the apoA-IV mRNA level is significantly reduced and that the estroge

171 regulation during SAR induction, we examined mRNA levels, microRNA (miRNA) expression, and their regu

172 We quantified the mRNA level of 17 DC-specific transcription factors and o

173 Endurance training increased the basal mRNA level of hexokinase-2, hormone sensitive lipase, gl

174 -7 increases fusion events by increasing the mRNA level of one of the cell-recognition molecules, CED

175 The mRNA level of preproenkephalin in the rostral ventrolate

176 Remarkably, a coordinated increase in the mRNA level of Rfrp in the dorso/ventromedial hypothalamu

177 dcd4 knockdown increased the protein but not mRNA level of stress-activated-protein kinase interactin

178 mRNA levels of ACC oxidase and ethylene levels also incr

179 n of DISC1 increased protein levels, but not mRNA levels of beta-site APP-Cleaving Enzyme 1 (BACE1),

180 ches off bile acid synthesis by reducing the mRNA levels of bile acid synthesis genes, including chol

181 macrophage infiltration and reduced hepatic mRNA levels of both pro-inflammatory and pro-fibrotic ge

182 Islets size, number, and mRNA levels of catalase and superoxide dismutase were in

183 mRNA levels of CGA, CGB, PPARG, CYP19A1, CYP11A1, PTGS2,

184 Quantitative PCR showed that the mRNA levels of chemokine C-C motif ligand (ccl)8 and che

185 Alterations in mRNA levels of D2R and CRF1 were also assessed.

186 Our results show that mRNA levels of DNA methyltransferase were increased in d

187 ntegrative omics analyses, and discover that mRNA levels of DTL, DCAF4, 12 and 13 are consistently el

188 Cellular localization of FAM13A protein and mRNA levels of FAM13A in COPD lungs were assessed using

189 epatic lipogenesis as reflected by increased mRNA levels of fatty acid synthase (Fas) and acetyl-CoA

190 inic acid administration at postnatal day 6, mRNA levels of Fgf9, Fgf10, Fgfr2c, and Fgfr3b in S1 cor

191 miR-25 (primary, precursor, and mature) and mRNA levels of genes indicated in the in vivo study show

192 muscle and adipose tissues of mice, reducing mRNA levels of genes involved in triglyceride synthesis.

193 This was associated with reduced mRNA levels of Glut2 and islet beta-cell transcription f

194 .5 months, MENX-affected rats show decreased mRNA levels of hypothalamic GHS-R1a, neuropeptide Y (NPY

195 -gamma pathway, as demonstrated by increased mRNA levels of Ifng and higher levels of phospho-signal

196 The mRNA levels of IgG4 and IgE, genes specific for Th2 cell

197 In conclusion, our results showed that mRNA levels of IL-6R in ovarian cancer was positively as

198 The mRNA levels of IL17A were found significantly lower in s

199 Bronchoalveolar lavage cell mRNA levels of iNOS or iNOS expression in central and al

200 PNtg-DHT mice displayed increased pancreatic mRNA levels of insulin receptors, Pdx1 and Igf1R, sugges

201 s known to increase NCC abundance, and renal mRNA levels of its precursor angiotensinogen are increas

202 In addition, HepG2(SOCS3) express higher mRNA levels of key enzymes involved in the de novo lipog

203 not the level of clonality, correlated with mRNA levels of key inflammatory mediators (e.g., IL-13,

204 ctivation to asparaginase, yet surprisingly, mRNA levels of key ISR gene targets such as Atf5 and Tri

205 learning and consolidation, we observed that mRNA levels of key proteoglycan components of PNNs were

206 h circulating triacylglycerol levels and the mRNA levels of lipogenic genes in the liver and skeletal

207 ve and treatment studies, evidenced by lower mRNA levels of macrophage marker genes including F4/80,

208 antitative trait loci analysis revealed that mRNA levels of many target genes are genotype dependent.

209 Protein and mRNA levels of NDPK-C were upregulated in end-stage huma

210 YAC128 mouse brain presented higher mRNA levels of PDK1-3 and PDH phosphorylation and decrea

211 LC-DG and PB significantly reduced the mRNA levels of pro-inflammatory cytokines and TLR-4 whil

212 itation of Sirius Red staining and increased mRNA levels of profibrotic genes, including connective t

213 of the phosphorylation state of JNK1 and the mRNA levels of proinflammatory cytokines.

214 we aimed to investigate the effects of RT on mRNA levels of regulatory components related to intramyo

215 at IL-34-Mphis possess significantly greater mRNA levels of select restriction factor genes than CSF-

216 Biopsies were analysed for mRNA levels of selected genes, and GLUT4 and Akt protein

217 Likewise, the mRNA levels of spr-5 were also significantly decreased i

218 /2, increased pY-STAT3 levels, and increased mRNA levels of STAT3 target genes up to 79% of control.

219 blunted the denervation-induced decrease in mRNA levels of TGF-beta group, while dexamethasone (DEX)

220 on and TGF-beta gene expression, we measured mRNA levels of TGF-beta in denervation mouse bone and fo

221 n denervation mouse bone and found decreased mRNA levels of TGF-beta1, TGF-beta2 and TGF-beta3.

222 In proximal tubular cells, mRNA levels of the amino acid transporter gene SLC38A2 w

223 at DNA methylation inversely correlated with mRNA levels of the candidate genes.

224 from persons with recurrent HSV-2, while the mRNA levels of the CCR10 ligand CCL27 were equivalent in

225 CSDS also altered mRNA levels of the circadian rhythm-related gene mPer2 w

226 Both sexes show a 50% reduction of mRNA levels of the genes located within the 16p11.2 regi

227 show that the gonadal steroid DHP modulates mRNA levels of the putative receptor for PGF2alpha (Ptgf

228 red with that of the wild type, however, the mRNA levels of the wild-type and mutant cells were compa

229 led significant inverse associations between mRNA levels of these genes and neutrophil influx.

230 naddicted rats were accompanied by increased mRNA levels of these potassium channels when compared wi

231 Moreover, the mRNA levels of three ABA biosynthesis genes, ABA1, NCED9

232 modulator involved in anxiety behaviors, the mRNA levels of tryptophan hydroxylase (TPH) 1, TPH2 (bot

233 The mRNA levels of VEGF and VEGFR-2 were quantified by qRT-P

234 ytoplasmic accumulation, and increase in the mRNA levels of YAP/TEAD-regulated genes (Ctgf and Areg).

235 Protein levels, but not mRNAs levels, of EtOH-metabolizing enzymes, including al

236 hough multiple isoforms are expressed at the mRNA level, only a single polypeptide that co-migrates w

237 Increases in mRNA level or stability of pro-inflammatory cytokines/ch

238 esponse to Notch signaling, independently of mRNA levels or codon usage.

239 hich was associated with increased VAT Glut4 mRNA levels (P < 0.05).

240 Biglycan protein and mRNA levels peaked as the palatal shelves adhered.

241 on of NF-kappaB and an increased Gata3/T-bet mRNA level ratio, consistent with a type 2 helper T-cell

242 nregulated by the loss of PRMT5, while their mRNA levels remain unchanged, which is counterintuitive

243 NA interference, which act at the genome and mRNA level, respectively.

244 nd induce Plk1 knockdown on both protein and mRNA levels resulting in G2/M-arrest and apoptosis.

245 Moreover, HFD-regulated H3K27Ac and mRNA levels returned to similar levels as control mice.

246 However, the analysis of Themis mRNA levels revealed that Themis gene expression is rapi

247 driver of clinical symptoms, placental Flt1 mRNA levels strongly correlate with maternal blood press

248 fferentiation without concomitant changes in mRNA levels, suggesting that BET proteins are regulated

249 ciated with corresponding shifts in tryptase mRNA levels, suggesting that copper affects tryptase gen

250 d overexpression increases their cytoplasmic mRNA levels, suggesting that enhanced mRNA export by SRS

251 d MPO protein, but normal MPO messenger RNA (mRNA) levels supporting a posttranscriptional defect in

252 In all brain parts, UCN3 mRNA levels tended to increase toward hatching, except f

253 (n = 67) had significantly lower claudin-18 mRNA levels than did those from healthy controls (n = 42

254 hat, to compensate for reduction in mortalin mRNA level, the cells increased the rate of synthesis of

255 xpression has been well characterized at the mRNA level, the localization of receptor protein, and, b

256 onally regulating riboswitches also regulate mRNA levels through an indirect control mechanism ensuri

257 TABRIC TNBC dataset (n = 217), we found CDK7 mRNA levels to be correlated with patient prognosis.

258 nscripts, we also compared changes in mature mRNA levels to levels of transiently expressed pre-mRNA.

259 s of Secisbp2 resulted in greatly diminished mRNA levels, translational activity and Sec incorporatio

260 ed COL1A2 protein expression, leaving COL1A2 mRNA levels unchanged.

261 ulated their transcription rates to increase mRNA levels under fast growth.

262 the CRD comprises <10% of LARP4 codons, the mRNA levels vary >20 fold with synonymous CRD substituti

263 mors than in non-TNBC tumors, and high c-Jun mRNA level was associated with shorter disease-free surv

264 MYC mRNA level was reduced upon p62 deletion by siRNA and in

265 TNF-alpha and IL-1beta mRNA levels was dependent on the reference gene used and

266 landscape better reflects cell identity than mRNA levels, we enable 'enhancer cytometry' for enumerat

267 type III domain-containing protein 5 (FNDC5) mRNA levels were absent or reduced in the dentate gyrus

268 Hypothalamic agrp mRNA levels were also higher in gravid compared to brood

269 IL-17C mRNA levels were also significantly greater among cagA-p

270 Protein expression and mRNA levels were analyzed by Western blotting, flow cyto

271 TLR)2, TLR4, and nuclear factor (NF)-kappa B mRNA levels were analyzed using real-time quantitative p

272 nterleukin (IL)-1alpha, IL-6, IL-8 and IL-10 mRNA levels were assessed by real-time PCR and Toll like

273 wth factor 19 (FGF19) on hepatic transporter mRNA levels were assessed in rat hepatoma cells and in m

274 Relative colonic TNF-alpha and IL-1beta mRNA levels were calculated.

275 Acylation was increased, and OGA protein and mRNA levels were decreased in ovarian tumor cell lines n

276 Both p11 protein and mRNA levels were decreased in PD patients.

277 HIP1R mRNA levels were decreased in seminal vesicle tissue fro

278 CYP1A2, CYP3A4 and CYP2E1 mRNA levels were decreased, while miRNAs were increased

279 Eosinophil FOXP3 and galectin-10 mRNA levels were determined by qPCR.

280 BaP-induced Cyp1a1 and Cyp1b1 mRNA levels were higher 4 hours after dosing at noon tha

281 PIK3CA mRNA levels were increased in metastases compared to the

282 embryonic fibroblasts (MEFs); moreover, ECD mRNA levels were increased, suggesting impaired ECD tran

283 SERPINB3 and SERPINB4 mRNA levels were knocked down in cultured CD27(-)CD4(+)

284 ession were significantly higher while IL-10 mRNA levels were lower in PI-IBS D than in HC in both il

285 ver was analyzed by immunohistochemistry and mRNA levels were measured by quantitative reverse transc

286 Claudin-18.1 mRNA levels were measured in airway epithelial brushings

287 normal prostates and prostate tumors, IL-17 mRNA levels were positively correlated with MMP7 mRNA le

288 IL-34 mRNA levels were quantified by real-time quantitative PC

289 CXCR3 ligand mRNA levels were selectively increased in skin biopsy sp

290 Whole-blood GUCY1A3 mRNA levels were significantly lower in individuals homo

291 Pfn2 mRNA levels were significantly reduced in duodenal sampl

292 Irs1 mRNA levels were similar between all four groups of offs

293 e microarray screening, we found that Cx3cr1 mRNA levels were substantially higher in microglia deriv

294 However, GRP78 mRNA levels were unchanged, suggesting a posttranscripti

295 APOBEC3A, -B, -C, -D/E, and-G mRNA levels were up-regulated in IFN-treated patients.

296 ons as a transcription factor, increased KDR mRNA levels, whereas the WT1(+KTS) isoform, which acts p

297 cient COX1 mRNA translation without altering mRNA levels, which results in a decrease in the steady-s

298 ession analysis showed coexpression of APOL1 mRNA levels with a group of intrarenal transcripts that

299 ns2 mRNA levels, and increased Pdx1 and Hes1 mRNA levels with a high number of DBA+ cells.

300 found to be differentially expressed at the mRNA level, with a significant upregulation of SLC30A1,