ライフサイエンスコーパス: mRNA expression

1 ced SREBP2 nuclear translocation, and Srebf2 mRNA expression.

2 and mucus metaplasia, while decreasing IL-17 mRNA expression.

3 edly alters results as exemplified with IFNG mRNA expression.

4 survival differences based on HIF1A CNV and mRNA expression.

5 othesis will be addressed by the analyses of mRNA expression.

6 pha in both normoxia and hypoxia by reducing mRNA expression.

7 3) and increased (P = 0.037) placental IGF-2 mRNA expression.

8 was accompanied by diminished TET1 and TET2 mRNA expression.

9 with adipose tissue Hif1alpha as well as IL6 mRNA expression.

10 also challenged with heat shock to quantify mRNA expression.

11 from mouse brains and assessed differential mRNA expression.

12 by an overwhelming predominance of low ERCC1 mRNA expression.

13 psy at screening for the analysis of FGFR1-3 mRNA expression.

14 ssive roles of HDAC1 and Sp1 in GM2-synthase mRNA expression.

15 ed 5-HT-sensitive behaviors and neurotrophic mRNA expression.

16 K1, glucose transporter 1 (GLUT1), and GLUT3 mRNA expression.

17 SLE patient serum promoted IL-6 and IL-1beta mRNA expression.

18 n individual CpG sites correlated with FCGRT mRNA expression.

19 ignificantly increased NOX5, mPGES1 and iNOS mRNA expression.

20 and its amplification leads to increased FAK mRNA expression.

21 not modulate IL-1beta-induced TGFB1 or BMP2 mRNA expression.

22 binding to the IL-5 gene and decreased IL-5 mRNA expression.

23 ritis disease activity and with synovial TNF mRNA expression.

24 vity in the DLPFC, as well as decreased PFK1 mRNA expression.

25 d the decrease in ID1 protein but not in ID1 mRNA expression.

26 corresponding with observed changes in c-Fos mRNA expression.

27 estingly, high glucose had no effect on G6PD mRNA expression.

28 eta-induced TGFB1 and partially reduced BMP2 mRNA expression.

29 increased cartilage oligomeric protein, COMP mRNA expression.

30 d timing of developmentally regulated edited mRNA expression.

31 i67, PAX8 and Myc and decreased PTEN and RB1 mRNA expression.

32 ith the EJC and TREX complexes in supporting mRNA expression.

33 not lead to global dysregulation of cellular mRNA expression.

34 DNAm levels at 39 DMPs were correlated with mRNA expression.

35 QTLs associated with protein levels, but not mRNA expression.

36 coding RNA that epigenetically controls HAS2 mRNA expression.

37 colysis in T cells and decreased their Glut1 mRNA expression.

38 NA (8.8%) and greater exercise-induced c-Myc mRNA expression (25%; Week 2, all P < 0.05).

39 mirror movements would exhibit decreased DCC mRNA expression, a functional ipsilateral corticospinal

40 ALT) based on presence of C-circles and TERT mRNA expression (above or below median TERT expression).

41 from induction of inflammatory lung cytokine mRNA expression after RSV challenge.

42 mRNA expression analysis and differential proteomics on

43 Here, we describe the identification and mRNA expression analysis of duck IL-23p19 (duIL-23p19) i

44 ntricular endomyocardial biopsies (n=12) for mRNA expression analysis, and compared baseline transcri

45 gnificant upregulation of CX3CR1 and TMEM119 mRNA expression and a downregulation of CD163 mRNA expre

46 that JAM2 variants lead to reduction of JAM2 mRNA expression and absence of JAM2 protein in patient's

47 IAP also inhibited LPS-induced IL-1beta mRNA expression and activation of NF-kappaB.

48 ings demonstrate that assaying TMM with TERT mRNA expression and C-circles provides precise stratific

49 RNA expression and a downregulation of CD163 mRNA expression and CD14 protein expression across the f

50 FAAs correlated significantly with PPARalpha mRNA expression and CYP4A protein expression in kidney,

51 of high-fat fed mice displayed lower Atg16l1 mRNA expression and IRS1 protein content, and adipose ti

52 depicts rhythmic control imposed upon basic mRNA expression and poly(A) regulation processes, includ

53 elopment revealed dynamic regulation of Il7r mRNA expression and rapid upregulation of IL7Ralpha surf

54 iple cancer phenotypes by altering miRNA and mRNA expression and stability, as well as through effect

55 uction in hypothalamic Pomc, Cartpt and Prlh mRNA expression and to defects in the reproductive syste

56 tions and how this relates to variability in mRNA expression and to disease loci.

57 labsorption-dependent induction of cecal Cck mRNA expression and, in mouse GLUTag and human NCI-H716

58 posure during neurogenesis on messenger RNA (mRNA) expression and DNA methylation (DNAm) profiles.

59 TFP causes loss of radiation-induced Nanog mRNA expression, and activation of GSK3 with consecutive

60 an increase in monocarboxylate transporter 1 mRNA expression, and decreases in HXK1, PFK1, glucose tr

61 ated IL-6 promoter activation and endogenous mRNA expression are significantly abrogated by DNAJB3 bo

62 Furthermore, using 4 genome-wide mRNA expression arrays of HUVECs during normoxia and aft

63 We demonstrate a reduction in NARS1 mRNA expression as well as in NARS1 enzyme levels and ac

64 We confirmed our findings with mRNA expression assays of Rhbdf2 in extreme-phenotype mi

65 ed both Toll-like receptor 3 (TLR3) and TLR4 mRNA expression at 6 hpi and 12 hpi.

66 ction of the CART-mRNA complexes resulted in mRNA expression at the site of administration, transfect

67 with this, a strong positive correlation of mRNA expression between DZIP3 and Cyclin D1 in different

68 O cell line, mMOR-1G has no effect on mMOR-1 mRNA expression but greatly increases mMOR-1 protein exp

69 e presence of Nm modification increases Pxdn mRNA expression but inhibits its translation, regulating

70 aR) and methyl CpG-binding protein 2 (MeCP2) mRNA expression, but did not alter spine density in adul

71 s further demonstrate that BBR induces TRIB1 mRNA expression by a transcriptional mechanism via ERK s

72 2856 significantly blunts sGC alpha and beta mRNA expression by more than 90%.

73 native lengthening of telomeres (ALT)], TERT mRNA expression by RNA-sequencing, whole-genome/exome se

74 -time PCR demonstrated the reduction of AQP5 mRNA expression by the transfection of miR-1226-3p and a

75 scriptional changes by developing a baseline mRNA expression catalogue of wild-type mice during early

76 These studies ignored the role of mRNA expression changes in driving tumorigenic mechanism

77 tric, immunohistochemical and messenger RNA (mRNA) expression changes in coeliac disease patients cha

78 e copy loss of HIF1A or high levels of HIF2A mRNA expression correlate with altered immune microenvir

79 with diabetes revealed that decreased DUSP4 mRNA expression correlated with reduced estimated glomer

80 Selection by FGFR mRNA expression could be a useful additional biomarker t

81 Here, we generated single-cell mRNA expression data from wild-type, DNMT3A, DNMT3A/3B a

82 Here, we leveraged mRNA expression data generated from nearly 12,000 human

83 matical modeling to integrate time series of mRNA expression data with sleep-wake history, which esta

84 known pseudogenes, were different, such that mRNA expression declined in the mature OSNs relative to

85 Both ID1 protein and mRNA expression decreased during myoblast differentiatio

86 es which, together with differences in their mRNA expression, determines their nett extracellular lev

87 Silencing of SUB1 mRNA expression did not affect parasite viability, excys

88 to provide an integrative analysis of miRNA/mRNA expression during human oral wound healing; the res

89 We examined the mRNA expression for selected autonomic markers in sample

90 oxidative enzyme, NOX2, was increased, while mRNA expression for the antioxidative enzymes, SOD1, GPx

91 Moreover, mRNA expression for the prooxidative enzyme, NOX2, was i

92 At that time, average cytoplasmic mRNA expression from alpha and beta genes decreased, rel

93 cer analyses of APE2 genomic alterations and mRNA expression from cancer patients using available dat

94 nclusions: This study of sputum microRNA and mRNA expression from patients with asthma demonstrates t

95 high or low CD31 expression groups utilizing mRNA expression from RNA-sequence data in The Cancer Gen

96 Qualitative analysis of mRNA expression identified also fusion transcripts invol

97 -8) and increased anti-inflammatory cytokine mRNA expression (IL-10 and IL-13).

98 Il25, Il33, Il4, Il5, Il13, muc5ac, and gob5 mRNA expression, ILC2 expansion, mucus metaplasia, and a

99 ions, rather than promoters, correlated with mRNA expression, implying that changes in expression res

100 utes to the establishment of 12-h rhythms of mRNA expression in a manner dependent on Spliced Form of

101 mRNA expression in BALF cells was quantified by using Ta

102 Quantitative analysis of mRNA expression in blood samples revealed selective over

103 e, and delivery of the plasmid DNA, and NPC1 mRNA expression in brain, spleen, and liver were confirm

104 Analysis of PREX1 mRNA expression in breast cancer cDNA arrays and a METAB

105 nal exhaled nitric oxide, CCL26 and SERPINB2 mRNA expression in bronchial tissues also reduced.

106 eletal muscle regeneration, suppressed Fbxl2 mRNA expression in C2C12 myoblasts and triggered signifi

107 IL-17 each suppressed Il25, Il33, and muc5ac mRNA expression in cultured airway epithelial cells.

108 Quantitative PCR analysis confirmed SH3TC2 mRNA expression in different peripheral nervous system t

109 ll as increased VEGFR1 and interleukin-1beta mRNA expression in females, and reduced brain derived ne

110 d p53 transcriptional-defects promote MYO18B mRNA expression in HCCs.

111 This variant was linked with PCSK6 mRNA expression in healthy aortas and plaques but also w

112 at mass, and increased adipose tissue leptin mRNA expression in HFD-treated recipient mice.

113 4 was associated with EAA and with increased mRNA expression in hippocampus (p = 0.0015).

114 The effects of genetic variation in FOLH1 on mRNA expression in human brain and NAAG levels using 7-T

115 Finally, we observed a low level of H19 mRNA expression in human HCC tissues from patients with

116 We show NK1R mRNA expression in human spinal cord, underscoring the t

117 Tissue Expression portal indicated that PIGR mRNA expression in kidney correlates to the expression o

118 Correlation of miR-182 with mRNA expression in laser-capture microdissected benign p

119 eukin-17 (IL-17) producing T cells and IL-17 mRNA expression in lesions representing severe periodont

120 (+) mice from severe HILI and decreased Mmp9 mRNA expression in Ly-6C(lo) and Ly-6C(hi) interstitial

121 esult in the transcriptional deregulation of mRNA expression in melanoma cells and assess how these c

122 th addiction in humans, and increased htr1aa mRNA expression in mutant larvae.

123 In vivo, the normal amplitude of Period mRNA expression in outer ear skin is dependent on both t

124 serum IgG1 and IgE levels, more IL-4, IL-13 mRNA expression in OVA-sensitized skin, and lower Th1 im

125 yed higher discrepancies between protein and mRNA expression in paired primary/metastatic melanoma or

126 associated with the increased level of SLA-1 mRNA expression in porcine cells compared to that of the

127 ecticide-challenged mosquitoes, or increased mRNA expression in pyrethroid-resistant Ae. aegypti, by

128 RBP4 mRNA expression in SAT correlated with the expression of

129 butyrate-mediated activation of GM2-synthase mRNA expression in SK-RC-45 cells was accompanied by Sp1

130 In parallel, we observed increased GIP-R mRNA expression in subcutaneous abdominal adipocytes fro

131 quence but is associated with increased FAN1 mRNA expression in the cerebral cortex.

132 rmore, we tested the effects of KIF3B mutant mRNA expression in the developing zebrafish retina.

133 ization showed a near complete loss of Foxn1 mRNA expression in the embryonic thymic bud.

134 SNCA mice had 1,000-fold higher human SNCA mRNA expression in the gut, and twofold higher gut expre

135 Moreover, we found the intensity of mRNA expression in the liver correlated with the pKa of

136 IL-33 induced its own mRNA and ST2L mRNA expression in the lung.

137 dization and quantitative PCR to assess CFTR mRNA expression in the lungs, immunohistochemistry to lo

138 e, including lower serum IgG2a and IFN-gamma mRNA expression in the skin.

139 e promoter mutations associated with reduced mRNA expression in TP53, TLE4, and TCF4.

140 G2k5d formulated DLNPs successfully mediated mRNA expression in tumors and simultaneously illuminated

141 stigated the profiling of cardiac lncRNA and mRNA expression in type 2 diabetic db/db mice with and w

142 CVH animals showed a downregulation of SERT mRNA expression in urothelium, suggesting increased 5-HT

143 ologic FAK catalytic inhibition reduces Sost mRNA expression in vitro and in vivo.

144 e evaluated for their ability to inhibit Ttr mRNA expression in vitro.

145 We found that Ct-1 mRNA expression in white adipose tissue directly involve

146 erum metabolites and skeletal muscle general mRNA expressions in aging mice toward the profiles obser

147 ectin-1 receptor messenger ribonucleic acid (mRNA) expression in the macrophages.

148 BDNF mRNA expression increased in the medial prefrontal corte

149 We found that the combination of both mRNA expression information and biomedical knowledge gre

150 enome Atlas also revealed that increased CFH mRNA expression is associated with improved survival in

151 Here, we show that low SASH1 mRNA expression is associated with poor survival in aden

152 vailability confirmed that hypothalamic pomc mRNA expression is dependent on longer-term photoperiod

153 Transcriptional regulation of mRNA expression is necessary to maintain cell identity a

154 We show that APE2 mRNA expression is positively correlated with PCNA, APE1

155 atic analyses revealed that diminished SAR1B mRNA expression is significantly associated with higher

156 the 35 genes using qRT-PCR and the trend of mRNA expression is similar to that of RNA-seq data .

157 ations suggest genetic variants can decrease mRNA expression levels by increasing usage of intronic P

158 o functions as a tumor suppressor, and ABHD5 mRNA expression levels correlate with patient survival f

159 rats exhibited increased striatal Rgs4 with mRNA expression levels enriched in SP MSNs.

160 ere, we demonstrate that higher GM2-synthase mRNA expression levels in various cancer cells and in hu

161 n mouse GLUTag and human NCI-H716 cells, Cck mRNA expression levels increased in response to propiona

162 ion Omnibus (GEO) datasets, we then examined mRNA expression levels of 71 genes encoding enzymes regu

163 Pg infection reduced mRNA expression levels of endothelial NOS (eNOS), Nrf2,

164 Cytolytic score (CYT), calculated from mRNA expression levels of granzyme and perforin, positiv

165 The mRNA expression levels of IL-6, IL-1 beta, and iNOS were

166 The mRNA expression levels of MYBPC3 were significantly redu

167 t rs165940 significantly correlates with the mRNA expression levels of PDE4D in the cerebellum (p-val

168 bserved, including alternative splicing, and mRNA expression levels of proto-oncogenes and tumor supp

169 The mRNA expression levels of ST6GAL-I and SOX9 in human gas

170 The mRNA expression levels of those genes encoding the ident

171 ential and in some cases opposite effects on mRNA expression levels.

172 RNAs) and messenger RNAs (mRNAs) to regulate mRNA-expression levels through interactions with both 5'

173 We analyzed pro-TRH-mRNA expression, mapped TRH-immunoreactive elements in t

174 Here, we integrate genome-wide measures of mRNA expression, miRNA expression, DNA methylation, and

175 yzed The Cancer Genome Atlas (TCGA) data for mRNA expression, mutations, and copy number variation (C

176 rrelate with clinical features of asthma and mRNA expression networks.

177 Based on the differential mRNA expression observed upon EXO-NGS analysis, we indep

178 We also examine the mRNA expression of 13 other DNA repair and DDR genes fro

179 temperatures decreased (P = 0.026) placental mRNA expression of a glucose transporter (GLUT-3) and in

180 dase (SA-beta-gal) activation, and increased mRNA expression of a subset of transcripts encoding fact

181 mRNA expression of ACE2 was measured by quantitative RT-

182 The levels of mRNA expression of adenosine receptors, CD39 and CD73 of

183 othelial cell markers (e.g. CD31) as well as mRNA expression of angiogenic factors (e.g., Vegfa, Flt1

184 In tibial bone, the mRNA expression of bone formation related genes such as

185 and zen2-specific enhancers to regulate the mRNA expression of both genes.

186 unction with real-time PCR revealed a higher mRNA expression of Bruton's tyrosine kinase (BTK) gene i

187 The protein and mRNA expression of CD147 in HGFs were enhanced after tra

188 Moreover, mRNA expression of closely related and islet beta-cell-e

189 n the CTSB locus were identified to decrease mRNA expression of CTSB.

190 bjects with obesity had significantly higher mRNA expression of CysC in white adipose tissue.

191 Similarly, protein and mRNA expression of cytokines were higher in CD4(+) T cel

192 LPS activated mRNA expression of different pro-inflammatory cytokines

193 erinatal exposure, we investigated miRNA and mRNA expression of dopaminergic (DA) neurons of the VTA

194 y due to epigenetic imprinting and sustained mRNA expression of effector genes.

195 While the mRNA expression of EMT transcription factors SNAI1 and S

196 atus of 0-1 were evaluated prospectively for mRNA expression of ERCC1 level and then randomly assigne

197 y, tissue hydroxyproline content, and tissue mRNA expression of fibrosis-associated genes (Ccl11, Il1

198 inhibited PBMCs proliferation and increased mRNA expression of forkhead box P3 (FOXP3), a transcript

199 In CBA/CaJ mice, ovariectomy decreases mRNA expression of Gsta4, and the levels of GSTA4 protei

200 Importantly, mRNA expression of heme oxygenase 1 (HO-1), a potential

201 mRNA expression of HIF1-alpha and Tbeta-4 along with hem

202 lization that was accompanied with increased mRNA expression of histamine H(1) and cysteinyl leukotri

203 broiler chickens under heat stress (HS) and mRNA expression of host cytokines that might affect the

204 mRNA expression of HSCs activation markers and FXR engag

205 21.9 mum), cellular apoptosis, and elevated mRNA expression of hypertrophy-related and profibrotic m

206 ated, as measured by significantly decreased mRNA expression of IRF7, IFNB1, and ISG15 on stimulation

207 se bone marrow-derived macrophages increased mRNA expression of M1 markers.

208 effector and exhaustion programs, including mRNA expression of members of the NR4A family of nuclear

209 ty purification and qPCR was used to compare mRNA expression of nrg1,2,3,4 and erbB1,2,3,4 in PV and

210 ld assess the prognostic value of their PBMC mRNA expression of OXTR, AVPR1A, and IGF1.

211 mRNA expression of PAX9, MSX1, AXIN2, and RUNX2 (known t

212 igh doses (0.5 and/or 1 mM) of 3-MPA reduced mRNA expression of Pck2 and genes associated with serine

213 nding proteins to demonstrate that increased mRNA expression of profilin1 (Pfn1), Arp3, cofilin1, Ena

214 Ductular reaction, LF, as well as the mRNA expression of proinflammatory genes increased in no

215 In addition, mRNA expression of proinflammatory mediators was increas

216 ssion by 75% and significantly decreased the mRNA expression of psoriasis markers, including Defb4, I

217 on when cultured on bone slices, and altered mRNA expression of related chemokine receptors and ligan

218 ein expression of tight junctions and induce mRNA expression of several genes involved in the formati

219 induced behavior corresponded with increased mRNA expression of several inflammatory genes, including

220 mRNA expression of T helper type 17/T helper type 22-rel

221 The mRNA expression of TGF-beta (EMT-inducer) showed no sign

222 C-1 selective blocking antibody or silencing mRNA expression of the channel by RNA interference, inhi

223 s on existing microarray data, we found that mRNA expression of the CSF1R ligand, CSF-1, is increased

224 ate that, in astrocytes, ER stress regulates mRNA expression of the IL-6 family of cytokines that is,

225 ed from CCR3-deficient mice showed increased mRNA expression of the osteoclast activator-related gene

226 showed that PALS-22 and PALS-25 regulate the mRNA expression of the predicted ubiquitin ligase compon

227 thermore, HDAC inhibitor treatment increased mRNA expression of the sialyltransferases GM3 synthase (

228 with round spermatid arrest, we find reduced mRNA expression of transition protein (Tnp1 and Tnp2) an

229 slocation of Nrf2, which in turn upregulated mRNA expression of uridine phosphorylase 1 (UPP1).

230 Relative mRNA expression of VEGF in the cornea was quantified by

231 erglycemia were prevented by KB-R7943, while mRNA expression of venular NCX isoforms was unaltered.

232 The mRNA expressions of bone sialoprotein (BSP), collagen ty

233 normal, together with the down regulation of mRNA expressions of Collagen I and transforming growth f

234 Desipramine administration downregulated mRNA expressions of IL-1beta, iNOS, COX-2, and TIMP-1 wh

235 Gingival mRNA expressions of interleukin (IL)-1beta, inducible ni

236 We analyzed the mRNA expressions of signature luminal and basal genes in

237 5, 2017, 866 patients were screened for FGFR mRNA expression, of whom 126 patients were treated (23 F

238 erhans cells, and leukocytes) had increasing mRNA expression over the course of 72 h, irrespective of

239 uster genes on the basis of their changes in mRNA expression over time, using bulk RNA-seq or microar

240 ive subtype (p = 0.03), and increased MKI-67 mRNA expression (p < 0.01) in both cohorts.

241 K-293 significantly increased Q0(bolton)-AAT mRNA expression (p = 0.03) and Q0(bolton)-AAT truncated

242 (P = 0(.)04), 1.7-fold increase in TGFbeta1 mRNA expression (P = 0.03), and 114% greater T-cell infi

243 the MTX infusion time (P = 1.5 x 10-3), FPGS mRNA expression (P = 2.1 x 10-3), and MTX systemic clear

244 ed and treated with VEGF A and FGF 2 and the mRNA expression pattern of EGR family members were docum

245 The aim of this study was evaluated the mRNA expression profile of pediatric Acute Lymphoblastic

246 rface marker was identified by comparing the mRNA expression profile of wild-type CD4(+) NKT cells wi

247 ated the regulatory matrix between miRNA and mRNA expression profiles by solving multiple linear prog

248 rous immune cell subsets expressing distinct mRNA expression profiles that are, in part, dictated by

249 present a novel approach integrating lncRNA-mRNA expression profiles with clinical characteristics t

250 By integrating miRNA and mRNA expression profiles, a total of 870 genes were pred

251 tEnrichr are created from the Gene Ontology, mRNA expression profiles, GeneRIF, pathway databases, pr

252 perties, anatomical localization, as well as mRNA expression profiles.

253 Unbiased mRNA expression profiling in the medial PFC (mPFC) of ma

254 n regions, both of which are associated with mRNA expression QTLs.

255 Skeletal muscle Dicer mRNA expression remained significantly decreased by 80%

256 IntMTQ, which benefits from the mRNA expressions reported by the other platforms, provid

257 demonstrate the improvements detected in G4, mRNA expression results were similar.

258 derlies Cas9-mediated regulation of FTN_1103 mRNA expression; see accompanying Amendment.

259 beta-catenin mRNA expression showed a strong positive correlation wit

260 ssification, the following was observed: (i) mRNA expression showed distinct clustering of MSF, (ii)

261 widespread natural variation in human NMNAT2 mRNA expression so it is important to establish whether

262 Additionally, male mice had greater CD36 mRNA expression than females in the striatum, hippocampu

263 protein abundance, but had similar or higher mRNA expression than other breeds.

264 n primary striatal neurons increases Gadd45b mRNA expression through a dopamine receptor type 1 (DRD1

265 or cancer phenotypes beyond that provided by mRNA expression through resolving intratumoral heterogen

266 e mNLS variant reduced TNF-alpha or IFN-beta mRNA expression to a similar extent as did WT SAMHD1, su

267 al systems in which lncRNA interference with mRNA expression underlies a regulated biological respons

268 We measured microRNA and mRNA expression using quantitative RT-PCR.

269 tion between CNOT3 and CDKN1A (encoding p21) mRNA expression using the combined datasets of normal lu

270 SPP1 mRNA expression was analysed using qPCR (n = 100) and OP

271 was determined by Western blot analysis, and mRNA expression was analyzed by microarray.

272 PPP1R1B mRNA expression was assessed in the METABRIC cohort (n =

273 eous melanoma data set showed that high GILT mRNA expression was associated with improved overall sur

274 in all biomarker groups, although high CCNE1 mRNA expression was associated with relative resistance

275 iomarker, coenzyme A synthase (COASY), whose mRNA expression was consistently elevated in radioresist

276 early B cell development in humans and IL33 mRNA expression was decreased in B cell chronic lymphocy

277 anylate kinase inverted 1 (MAGI1), and MAGI2 mRNA expression was downregulated in patients with sever

278 PTCH1 mRNA expression was measured in bronchial epithelial cel

279 Furthermore, CPT1A mRNA expression was negatively associated with CHO intak

280 Pulmonary ACE2 mRNA expression was not different between subjects with

281 antly attenuated, whereas IL-33-induced ST2L mRNA expression was preserved, although no autoamplifica

282 myofibroblast response as measured by Acta2 mRNA expression was reduced by inhibition of HA synthesi

283 Following tamoxifen treatment, Dicer mRNA expression was significantly decreased by 87%.

284 SIRT6 protein, but not mRNA, expression was markedly reduced in VSMCs in human

285 assess cellular phenotypes, mRNA uptake and mRNA expression, we found that, unlike other cell types,

286 stension of satellites (SADS) and p16(Ink4a) mRNA expression were identified in alveolar bone osteocy

287 Protein abundance and mRNA expression were measured by Western blot and quanti

288 Age-related increases in CD36 mRNA expression were observed in the male hippocampus an

289 However, increases in NADPH oxidase 1 (Nox1) mRNA expression were observed in the treatment group com

290 Furthermore, 9 mRNAs expression were significantly and independently co

291 ntiated from IL-10RB-/- iPSCs lacked IL-10RB mRNA expression, were unable to phosphorylate STAT3, and

292 s found to be highly sensitive for increased mRNA expression when macrophages were polarized with IL-

293 f positive and negative regulators of MYO18B mRNA expression which reflects the survival of HCC patie

294 cription start site correlated with high HLF mRNA expression, which was itself associated with poor s

295 results from reduced HIV-1 protein, but not mRNA, expression, which in turn correlates with reduced

296 ed proteins were tested with associations of mRNA expression with histological severity of muscle fro

297 iRNAs (DEmiRs) in all tissues and correlated mRNA expression with known and predicted target mRNAs.

298 CSCs, as well as association of high plectin mRNA expression with poor patient survival in lung adeno

299 or IRF4 (increased IL-10 secretion and Arg1 mRNA expression), with IRF4 levels being lower in GM-CSF

300 along with a concomitant decrease of grin2A mRNA expression within PV interneurons.