ライフサイエンスコーパス: mRNA level

1 one of the highest amplitude rhythms at the mRNA level.

2 the exclusive co-expression of Sox2 and T at mRNA level.

3 lated RAB25 is inversely correlated with its mRNA level.

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

5 an regulate the expression of MOR-1Bs at the mRNA level.

6 as well as region-specific expression at the mRNA level.

7 the two processes that buffers steady-state mRNA levels.

8 rly, depletion of PTENP1 did not impact PTEN mRNA levels.

9 to assess the effects of those mutations on mRNA levels.

10 is integral to cell cycle control of histone mRNA levels.

11 nt reduced enzyme activity without affecting mRNA levels.

12 ptor alpha (ERalpha), increases uterine Igf1 mRNA levels.

13 ence of a significant decrease in HIF-1alpha mRNA levels.

14 veral proteins, although BpuR did not impact mRNA levels.

15 s in the absence of corresponding changes in mRNA levels.

16 a apoM concentrations correlate with AT APOM mRNA levels.

17 d ~75% reduction in LPS induced pro-IL-1beta mRNA levels.

18 number and size, without any change in Tex14 mRNA levels.

19 ed with dopamine/metabolite ratios and gnrh2 mRNA levels.

20 manner, without affecting the corresponding mRNA levels.

21 these mice correlated inversely with Tnfsf11 mRNA levels.

22 levels do not always correlate directly with mRNA levels.

23 des the MDM4 locus, and showed elevated MDM4 mRNA levels.

24 normal tissues confirmed tissue-specific RD3 mRNA levels.

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

26 NaCT expression is associated with decreased mRNA levels.

27 e translation rate of PGRN without affecting mRNA levels.

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

29 Chop (-/-) mice also showed reduced SERPINA1 mRNA levels.

30 correlation coefficient between protein and mRNA levels.

31 cDNA indicated that ATF4 up-regulates LAMP3 mRNA levels.

32 with multiple mechanisms acting to regulate mRNA levels.

33 no obvious effects on their putative target mRNA levels.

34 ime quantitative PCR measured CSF2 and CSF2R mRNA levels.

35 dose-dependent effect of the vector on RPE65 mRNA levels.

36 f1 is required for the regulation of histone mRNA levels.

37 to the somatic cells and reduces the cognate mRNA levels.

38 at RP translation rates were proportional to mRNA levels.

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

40 Effects on target mRNA levels accumulate as the mRNA population approaches

41 heir expression was highly correlated at the mRNA level across multiple publicly available CRPC datas

42 to account for tumor proportion nor variable mRNA levels across cell types.

43 Hypothalamic urotensin I mRNA levels also increased in spring and were higher in

44 tion to the amygdala similarly increases the mRNA level and protein expression of BDNF and IGF-1 in M

45 We examined APOM mRNA level and secretion in AT from 485 individuals enro

46 lation between INPP4B expression and both AR mRNA levels and AR transcriptional output.

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

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

49 ow that Spn1 is globally required for normal mRNA levels and for normal splicing of ribosomal protein

50 ll the carrier mothers displayed normal RLIM mRNA levels and had highly skewed X chromosome inactivat

51 resulted in a decrease or increase in Kr-h1 mRNA levels and its promoter activity, respectively.

52 In humans, adipose tissue KDM5C mRNA levels and KDM5C genetic variants were associated w

53 ing of the inverse relationship between pho8 mRNA levels and Pho8 activity, we examined the effects o

54 PvDBP gene amplification leads to increased mRNA levels and protects P. vivax in vitro against invas

55 both tumor necrosis factor alpha (TNF-alpha) mRNA levels and protein levels in comparison to the 20-m

56 expression without a change in TOP2alpha/170 mRNA levels and resulted in enhancement of etoposide-ind

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

58 Within 3 h of DD exposure, Lhcf2 mRNA levels and transcription were strongly suppressed a

59 ct of MAF1 on global translation via reduced mRNA levels and translation efficiencies for several rib

60 late physiologic gene expression by altering mRNA levels and tuning protein translation.

61 ignaling mutant had little effect on the dev mRNA level, and dev mRNA was not less stable in the C-si

62 oblast growth factor (FGF) 19/15 protein and mRNA levels, and 7alpha-hydroxy-4-cholesten-3-one.

63 acetate, increase differentiation-associated mRNA levels, and that EtOH decreases pluripotency-relate

64 stabilized MSec protein levels, but not its mRNA levels, and the chaperone activity of ERp29 was req

65 ltrated leukocyte frequency, Cd11b and Cd11c mRNA levels, and the frequencies of mature dendritic cel

66 s under greater evolutionary constraint than mRNA levels, and translation efficiency represents a pri

67 ts of the effects of miRNAs on tail lengths, mRNA levels, and translational efficiencies.

68 at GC content influences cell state-specific mRNA levels, and we reveal how translational mechanisms

69 translation inhibitors when measuring TE or mRNA levels, and will hopefully aid in future experiment

70 late-stage serous ovarian cancer, high Rgnef mRNA levels are associated with decreased progression-fr

71 Moreover, TMEM203 mRNA levels are associated with disease activity, as ass

72 s to investigate whether altered cathepsin Z mRNA levels are associated with osteoporosis in clinical

73 Hepatic SULT1E1 mRNA levels are constitutively up-regulated in type 1 di

74 mRNA levels are determined by the balance between mRNA s

75 Unlike STING, TMEM203 mRNA levels are elevated in T cells from patients with s

76 Mechanistically, we demonstrate that HB-EGF mRNA levels are increased in beta-cells in response to g

77 We show that Gadd45b mRNA levels are increased in susceptible but not resilie

78 ts and primary HGSOC tumors, ZC3H18 and E2F4 mRNA levels are positively correlated with BRCA1 mRNA le

79 Low FBXL7 mRNA levels are predictive of poor survival in patients

80 WERING1 (PEP1) represses flowering until its mRNA levels are reduced during vernalization.

81 ifferentiation and scaling growth, and their mRNA levels are regulated by insulin receptor signaling.

82 o be reduced in the brain at the protein and mRNA levels, arguing that apolipoprotein E4 genotype lea

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

84 rong increase in Reln gene expression at the mRNA level, as well as a slight upregulation at the prot

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

86 GnRHR mRNA levels at e10.5 and e12.5 were comparable to pituit

87 The difference in protein and mRNA levels between cases and controls was extracted and

88 At the mRNA level, both of prestin's exons 17 and 18 were entir

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

90 levels was independent of changes in TIMP-3 mRNA levels, but correlated with shedding of LRP1.

91 -UTR-mediated translational silencing at the mRNA level by hnRNP E1.

92 h muscle actin staining by 56% and periostin mRNA levels by 60% compared with control.

93 antisense oligonucleotides (ASOs) can reduce mRNA levels by acting through the no-go decay pathway.

94 rough the maintenance of cellular 14-3-3zeta mRNA levels by the RBP nucleolin.

95 ed thyroglobulin and sodium/iodide symporter mRNA levels, cell migration, and proliferation in HTori3

96 damage/frequency of TUNEL+ cells, increased mRNA levels coding for TNFalpha/CXCL1/CXCL2/CXCL10, high

97 Smokers had lower lung CYP2A mRNA levels compared with nonsmokers.

98 In patients, RNF4 protein and mRNA levels correlate with poor prognosis and with resis

99 from the TCGA (n = 499), where highest AZGP1 mRNA levels correlated to improved overall survival (p =

100 wed that in epimastigotes, TcHTE protein and mRNA levels decrease in response to increments in heme c

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

102 The mRNA level depends on the 5'-untranslated region of the

103 portions simultaneously, while accommodating mRNA level differences across cell types.

104 cancer patients with low intratumor ferritin mRNA levels display longer 3- and 5-year overall surviva

105 se activity and promotes host shutoff at the mRNA level during productive lytic infection.

106 -5p directly attenuates spliced XBP1 (XBP1s) mRNA levels during ER stress and thus regulates the proa

107 analysis of the mechanisms governing edited mRNA levels during T. brucei development and the first t

108 fficiency are minimal compared to effects on mRNA levels, even for newly transcribed target mRNAs.

109 XRN1, exhibited suppressed protein, but not mRNA, levels, explaining the build-up of aberrant RNAs t

110 Independent from mRNA-level fluctuations, this newer paradigm modernizes

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

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

113 mRNA levels for lysosomal-associated membrane protein 3

114 lidated that YY1 is expressed at protein and mRNA levels for MCF10A and 184A1, respectively.

115 All treatments upregulated mRNA levels for osteoprotegerin (OPG) in comparison to P

116 However, PEDV administration increased mRNA levels for phosphoenolpyruvate carboxykinase 1, arg

117 RNA sequencing showed high mRNA levels for the delta-subunit in the LSO.

118 Here, we measure E. coli single cell mRNA levels for two stress responses that depend on bact

119 levels are positively correlated with BRCA1 mRNA levels, further supporting ZC3H18 role in regulatin

120 more, stage I patients with lower NF-kappaB2 mRNA levels had better 5-year survival in univariate and

121 GWAS variants that cannot be detected at the mRNA level, highlighting the utility of dissecting pQTL

122 s, we found an increase of angiogenin at the mRNA level in response to hypoxia.

123 strength of stabilizing selection acting on mRNA levels in a species is strongly associated with tha

124 anscription factor for APOE and mediates its mRNA levels in an age-dependent manner.

125 Both PrP(C) protein and mRNA levels in astrocytes were comparable with those in

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

127 ype potassium (K(A) ) channels, decreased at mRNA levels in bladder afferent and double-labelled neur

128 ectly investigate this question, we profiled mRNA levels in both neuroretina and retinal pigment epit

129 lysome-associated (translationally enhanced) mRNA levels in both subsets.

130 chizophrenia quantifying synaptic protein or mRNA levels in brain tissue.

131 ype for AS, was associated with higher FADS2 mRNA levels in calcified valve tissue, whereas FADS1 mRN

132 Several candidate therapies reduce Pmp22 mRNA levels in CMT1A rodent models, but development of b

133 aptic plasticity requires a tight control of mRNA levels in dendrites.

134 We detected increased Trpm3 mRNA levels in dorsal root ganglion neurons innervating

135 1,25(OH)2D3 increased CYP27B1 mRNA levels in HCEC, but had no effect on CYP27B1 protei

136 mRNA levels in HIV-specific CD8(+) T-cells exhibited del

137 ts for RT-qPCR experiments, when quantifying mRNA levels in human NV and EM CD8(+) T cells.

138 deacetylase inhibitors (HDACi) increase FXN mRNA levels in induced pluripotent stem cell (iPSC)-deri

139 close to ducts, and increased Sox9 and Ngn3 mRNA levels in islets, but lineage-tracing experiments r

140 Low HLA-I APM mRNA levels in melanoma metastases before immune checkpo

141 ld increase in primiR-199a1 and primiR-199a2 mRNA levels in mouse islets cultured in 10 mm glucose co

142 d that lncRNA-CCL2 positively regulated CCL2 mRNA levels in multiple primary ECs and EC cell lines.

143 1, where it increases nascent RNA but lowers mRNA levels in O(3)-exposed human airway epithelial cell

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

145 epression and subsequent differences in TAF1 mRNA levels in patients may be potentiated in the brain

146 ivation, numerous studies have measured TERT mRNA levels in populations of cells or in tissues.

147 no prior experience with TMT; and (ii) CB(2) mRNA levels in rat prefrontal cortex were elevated 7 day

148 wer hippocampal alpha5-GABA(A)Rs protein and mRNA levels in schizophrenia.

149 ung CYP2A13, CYP2A6, and CYP2A7 (and CYP1A2) mRNA levels in smokers and nonsmokers were assessed in G

150 brillary acidic protein, as well as TNFalpha mRNA levels in the brain, indicating reduced neuroinflam

151 In addition we measured the changes of mRNA levels in the CA for the 13 enzymes of the JH biosy

152 Airway inflammation, mRNA levels in the lungs, and airway hyperresponsiveness

153 ta2 nicotinic acetylcholine receptor subunit mRNA levels in the nucleus accumbens and medial prefront

154 is Area and Severity Index score, and NFKBIZ mRNA levels in the skin decreased during anti-IL-17A tre

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

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

157 mice demonstrated a marked reduction in Cfl2 mRNA levels in various tissues including skeletal muscle

158 s; (3) the relationship between K(+) channel mRNA levels in ventricles and peripheral blood mononucle

159 s) and demonstrated a ~90% reduction of IRF8 mRNA levels in vitro (PV < 0.0001), alongside a notable

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

161 ull-length (exon 7 including) SMN2 (SMN2-FL) mRNA level increases were highest in lumbar and thoracic

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

163 effects were independent of changes in IGF2R mRNA levels, indicating likely posttranslational mechani

164 s well as IFN-alpha, IFN-beta, and TNF-alpha mRNA levels induced by Sendai virus infection.

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

166 Baseline mRNA levels may provide a prognostic indicator for respo

167 adverse events, reductions in induced ALAS1 mRNA levels, nearly normalized levels of the neurotoxic

168 rward loop) and miR-1010 to reduce nAcRbeta2 mRNA levels (negative feedback loop).

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

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

171 ain Reaction (qPCR), we measured protein and mRNA levels of a panel of microglial markers across four

172 A three-fold increase was noted in mRNA levels of ACVR1C/ALK7, a type I receptor of the TGF

173 0.4% and 2.0% ripasudil-treated groups, and mRNA levels of angiogenic and pro-inflammatory factors i

174 pithelization, immune cell infiltration, and mRNA levels of angiogenic and pro-inflammatory factors i

175 RNA sequencing analysis revealed that the mRNA levels of antABC encoding enzymes for the synthesis

176 both the circulating levels and the hepatic mRNA levels of BMP9 have been recently associated with v

177 in a reduced number of conidia and decreased mRNA levels of brlA, the key asexual developmental activ

178 AMs from old mice expressed higher mRNA levels of CCL2, IFN-beta, IL-10, IL-12p40, TNF-alph

179 CD11b(+) AMs from old mice expressed higher mRNA levels of CCL2, IL-1beta, and IL-6, whereas CD11c(+

180 High mRNA levels of CCL7, -8, -17, -20 and -25 predicted a de

181 chain reaction was performed to evaluate the mRNA levels of CD147 and MMP-2 in HGFs and U937 cells.

182 The mRNA levels of cytoprotective enzymes (NQO1, HO-1, AKR1C

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

184 was observed despite no change in protein or mRNA levels of electron transport chain complexes.

185 ptible mice but is consistent with increased mRNA levels of enkephalinases in the NAc of susceptible

186 h as filaggrin, occludin, and claudin-1, and mRNA levels of filaggrin, loricrin, and involucrin.

187 Our results demonstrated that overall mRNA levels of GATA6 were significantly decreased in the

188 mRNA levels of glucocorticoid receptor alpha and cortico

189 The mRNA levels of glutamine synthetase (GLUL), beta-catenin

190 We examined mRNA levels of Gremlin 1 in key target tissues for insul

191 owed a significant (P <0.05) decrease, while mRNA levels of GSK-3beta were elevated.

192 e transcriptome and observed that it affects mRNA levels of hundreds of genes that are significantly

193 Here, the relationship between mRNA levels of HvCslF6, HvCslF9, HvGlbI (1,3;1,4)-beta-g

194 e immunosuppression remarkably decreased the mRNA levels of ifn-g, il-6, tgf-b, il-4, and tnf-a in th

195 ained Cxcl1 and Ccl2 mRNAs but a decrease in mRNA levels of IFNalpha/beta pathway genes as well as Il

196 Immunoreactivity and mRNA levels of IGF-1, TGF-beta1, and beta3-adrenoceptor

197 ereas CD11c(+) CD11b(-) AMs expressed higher mRNA levels of immune-regulatory cytokines IFN-beta and

198 ely recapitulated the effects of HDAC3/6i on mRNA levels of inflammatory mediators in P. gingivalis-i

199 oliferating beta-cells, and expressed higher mRNA levels of insulin, Glut2, Pdx1, MafA and Nkx6.1, bu

200 d asexual sporulation coupled with increased mRNA levels of key developmental activators.

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

202 ted by increased ear thickness and increased mRNA levels of key proinflammatory cytokines.

203 ovirus LOXL2 -treated implants showed higher mRNA levels of LOXL2, ACAN, and other anabolic genes com

204 The mRNA levels of LXRA and LDLR were increased, in addition

205 e combination regimen markedly decreased the mRNA levels of MCP1 and CRP and both mRNA and protein le

206 The mRNA levels of mouse PL genes were robustly decreased in

207 M2 immunoreactivity and M3 mRNA levels of muscarinic receptor were increased at day

208 ess, mature oligodendrocyte cell numbers and mRNA levels of myelination-related genes.

209 tions, moderately lowered ROS, but increased mRNA levels of p27 and PARP1; all compatible with enhanc

210 le-specific alternative splicing, increasing mRNA levels of P2RX7L and another isoform, P2RX7E, which

211 ytes to elevated [Ca(2+) ] levels, affecting mRNA levels of PDGF-BB, RICTOR, and MIR17HG as mediators

212 RNA-sequencing data, we identified elevated mRNA levels of periostin in the hearts of TAC-operated m

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

214 W2580 treatment also significantly decreased mRNA levels of pro-inflammatory factors, without alterat

215 termine via qRT-PCR potential changes in the mRNA levels of pro-inflammatory genes.

216 Conversely, mRNA levels of pro-inflammatory markers (IL-6, IL-1beta,

217 ) overweight young adults had higher urinary mRNA levels of renin, angiotensinogen, IL-18 and CTGF.

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

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

220 We first analyzed the mRNA levels of selected molecular markers in response to

221 quantitative PCR (qPCR) results in eWAT, the mRNA levels of several adipokines, including Retn (encod

222 tingly, loss of CDK8 robustly normalized the mRNA levels of Skn7-dependent genes in the fcp1 mutant b

223 ne promoters but paradoxically increased the mRNA levels of Skn7-dependent oxidative stress-induced g

224 Rik-203 knockdown reduced mRNA levels of Sox1 and Nestin, the markers of neural pr

225 d staining, liver hydroxyproline content and mRNA levels of TGF- beta and collagen in the liver.

226 T cells, CD11b(+)Ly6C(hi) myeloid cells, and mRNA levels of Th1 inflammatory cytokines are elevated i

227 Herein, we examined mRNA levels of the 15 mouse Cyp2c and 7 mouse Cyp2j isof

228 ction (qRT-PCR) was performed to measure the mRNA levels of the alpha (alpha) and beta (beta) isoform

229 on targets of BMP signaling, we measured the mRNA levels of the BDNF receptor TrkB and of P/Q-type Ca

230 Upon differentiation, mRNA levels of the MBP gene, encoding myelin basic prote

231 mediated phosphorylation of prolidase since mRNA levels of the protein were not altered upon cocaine

232 downregulated FcepsilonRI at the protein and mRNA levels of the receptor's alpha-chain, analyzed by f

233 tent with this interpretation, MA had higher mRNA levels of the reinnervation-promoting cytokine fibr

234 ypoxia, with Bmp9(-/-) mice exhibiting lower mRNA levels of the vasoconstrictor peptide ET-1 (endothe

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

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

237 Notch2 ASOs decreased the induction of mRNA levels of TNF superfamily member 11 (Tnfsf11, encod

238 criptional effects underscored the increased mRNA levels of TRX2 and TSA1 observed in the fcp1 mutant

239 genes involved in inflammation, whereas the mRNA levels of UCP2 and PPARD were decreased in peripher

240 s show that the expression of PyST increases mRNA levels of UNC5B by approximately 3-fold in osteosar

241 elial cells (ECs), which exhibited increased mRNA levels of VEGFR1, Delta-like (DLL) 3, and Notch2 bu

242 the effects of inhibiting tRF-GG on histone mRNA levels, on activity of a histone 3' UTR reporter, a

243 After normalizing total RP mRNA levels per sample, we find highly consistent tissue

244 Analysis of mRNA levels, promoter-GUS activity, and protoplast trans

245 olds, Faecalibacterium correlated with IL-10 mRNA levels (r(s) = 0.49(,) P(adj) = 0.02) with the same

246 e myeloid leukemia patients indicate that cf-mRNA levels reflect the transcriptional activity of bone

247 In addition, NKKC1 mRNA levels remained stable, indicating that ALD modulat

248 ydrofolate reductase (DHFR, salvage pathway) mRNA levels showed a significant (P <0.05) decrease, whi

249 Interestingly, inducible NOS mRNA levels showed a significant (P <0.05) increase at 1

250 Cathepsin Z mRNA level strongly correlated with low bone mineral den

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

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

253 TRP channels are expressed in the IVD on the mRNA level, thereby revealing novel therapeutic candidat

254 C-specific ICAM 3 nonintegrin at protein and mRNA levels, thereby affecting C-type lectin receptor-in

255 ulate MDR proteins by managing corresponding mRNA levels through post-transcriptional regulation base

256 uced nonsense-mediated decay, others reduced mRNA levels through the no-go decay pathway, since deple

257 in on Klotho protein levels without altering mRNA levels, thus mainly abrogating the increased protei

258 y down-regulating its expression both at the mRNA level via viral RNA endonuclease PA-X and at the po

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

260 mice, whereas about 12-fold decrease in Wnt6 mRNA level was found in MeCP2K412R sumo-mutant mice.

261 inimal effects of syntaxin-3 cKO, syntaxin-3 mRNA level was very low in hippocampal and cortex pyrami

262 No significant difference in CHM mRNA levels was seen between two patients' fibroblasts a

263 evelopmental timing of altered mitochondrial mRNA levels, we also reveal transcript-specific developm

264 mRNA levels were also evaluated in 69 patients using qua

265 KLRA*02 mRNA levels were also generally higher than KLRA*01 Coll

266 7 was enriched as a regulator of genes whose mRNA levels were altered in fcp1 and cdk8Delta mutants a

267 MMP1 protein and mRNA levels were analyzed by immunosorbent assay, Wester

268 KLF5 mRNA levels were assessed in isolated cardiomyocytes fro

269 d immunosorbent assay (ELISA) or V-Plex, and mRNA levels were assessed via reverse transcriptase quan

270 In addition, higher Bcl3 mRNA levels were associated with inferior OS in stages I

271 Thy1 protein and mRNA levels were decreased dramatically during adipogene

272 In this report, MAP3K8 mRNA levels were found decreased in the lungs of IPF pat

273 Oas1a and Oas1b mRNA levels were higher in infected RNase L(-/-) mice, i

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

275 7a1) activity and sterol 12alpha-hydroxylase mRNA levels were induced, while ileum FXR target genes w

276 We previously determined that HDAC2 mRNA levels were lower in dorsolateral prefrontal cortex

277 Sirtuin 1 (SIRT) mRNA levels were lower in PLAC when compared to DM+RSV,

278 and susceptible brains, but Oas1a and Oas1b mRNA levels were lower in RNase L(+/+) mice of both type

279 Moreover, HGF mRNA levels were measured by quantitative reverse transc

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

281 Since dystrophin mRNA levels were not different in tKO, this finding sugg

282 the disease-relevant organ, the brain, Gys1 mRNA levels were reduced by 85% and GYS1 protein deplete

283 RNA foci and DMPK 3'UTR mRNA levels were reduced in both the heart and skeletal

284 gene expression analysis revealed that Trib1 mRNA levels were significantly elevated by BBR treatment

285 Branchial PRLR mRNA levels were significantly elevated by stage 5 of me

286 Also, we found that mRNA levels were significantly higher in qRT-PCR evaluat

287 Compared with control dams, Angptl4 mRNA levels were significantly lower in iBAT, gonadal wh

288 Brain OPN mRNA levels were similar in both nursed groups, but the

289 ssed in NSCLC (P < 0.001 for all), only RelB mRNA levels were strongly increased in cancerous specime

290 Ribosomal protein S6K (S6K) messenger RNA (mRNA) levels were increased and AMPKalpha and mRNAs enco

291 ly modified with 2'-O-methoxyethyl decreased mRNA levels when targeted to coding regions of mRNAs in

292 specific, with males expressing reduced DBH mRNA levels whereas females were unchanged.

293 ely estimate tumor fractions and cell types' mRNA levels, which are currently unavailable in other me

294 Inducible expression of Bcl6 increased MLL mRNA levels, which was reversed by genetic deletion and

295 and a notable reduction in Grin2b and Gria2 mRNA levels, which was strongly inversely associated wit

296 4(+) T cells during AKI was confirmed at the mRNA level with quantitative real-time PCR and at the pr

297 is because mice show autoregulation of Thap1 mRNA levels with upregulation at the non-affected locus.

298 in or leptin receptors decreases, total Bdnf mRNA levels, with distinct expression profiles of specif

299 Here, we observed enriched Amt (AeAmt1) mRNA levels within reproductive organs of the arboviral

300 rylated Stat3 to determine if changes at the mRNA level would be reflected at the protein level.