ライフサイエンスコーパス: mRNA expression

1 rs and may act as gatekeepers of monoallelic mRNA expression.

2 calcium ionophore exhibited increased Duox-1 mRNA expression.

3 the latter of which exhibited increased Erk5 mRNA expression.

4 ced p21 protein levels without affecting p21 mRNA expression.

5 , with the risk allele associated with lower mRNA expression.

6 lated and one down-regulated) had consistent mRNA expression.

7 adily reconcilable with regional patterns of mRNA expression.

8 licing is an important mechanism to regulate mRNA expression.

9 ce, followed by a delayed reduction in GluA2 mRNA expression.

10 s the degree of PABP-mediated enhancement of mRNA expression.

11 1 at the Atgl promoter and up-regulated Atgl mRNA expression.

12 overexpression of PPARdelta increased LPCAT3 mRNA expression.

13 (EROD) activity, porphyrin accumulation, and mRNA expression.

14 3'UTR of SMARCD1 and down-regulated SMARCD1 mRNA expression.

15 nanoclusters can downregulate TET1 and TET2 mRNA expression.

16 lative to wild-type SRY at similar levels of mRNA expression.

17 signature and IL-1 receptor-like 1 (IL1RL1) mRNA expression.

18 rt by transcriptional downregulation of Fbn2 mRNA expression.

19 educed surface expression without decreasing mRNA expression.

20 which rather associated with reduced PIK3CA mRNA expression.

21 ial cells were correlated with regional TSPO mRNA expression.

22 e observed genetic effects by affecting VASP mRNA expression.

23 0, and chemokine (C-C motif) ligand 2 (CCL2) mRNA expression.

24 own inhibited hepcidin (HAMP) messenger RNA (mRNA) expression.

25 ome staining and fibrotic marker protein and mRNA expression 14 days after AKI revealed that wild-typ

26 lation of steroid receptors with genome-wide mRNA expression across different regions in the mouse br

27 e, we performed a systematic analysis of ARE-mRNA expression across multiple cancer types.

28 ted of mucus and had elevated levels of MUC2 mRNA expression after G. duodenalis exposure.

29 dampened cyclooxygenase-2 and interleukin-8 mRNA expression after lipopolysaccharide induction in Ca

30 Western blot and mRNA expression analyses in mice yielded consistent data

31 ochemical staining of tissue microarrays and mRNA expression analyses revealed a positive association

32 Protein and mRNA expression analyses revealed that kidney proximal t

33 mRNA expression analysis of proteins involved in establi

34 Global mRNA expression analysis revealed that SMCR8 regulates t

35 Using a RhoGTPase mRNA expression analysis we identified RhoC as the highe

36 est and most widespread correlations between mRNA expression and biometry parameters including axial

37 equired for BP-mediated stimulation of c-Myc mRNA expression and cell proliferation.

38 t mice, as marked by decreased Arg1 and Il10 mRNA expression and decreased interleukin (IL)-4, IL10 a

39 We analyzed genome-wide mRNA expression and DNA methylation in cervical and ante

40 t, cellular non-cleavable HuR controls COX-2 mRNA expression and enzymatic activity.

41 ociation between placental ANGPT2 and CXCL14 mRNA expression and fetal, maternal and delivery-specifi

42 IL12A mRNA expression and IL-12 and IL-35 protein levels were

43 ardless of diet, decreased fetal liver Pparg mRNA expression and increased placental androgen recepto

44 (Tg) rats followed by assessment of IL-1beta mRNA expression and inflammasome activation (ASC oligome

45 e of a functional TOLLIP variant on monocyte mRNA expression and M. tuberculosis-induced monocyte imm

46 also linked to TERT upregulation, with TERT mRNA expression and outcome using a well-characterized c

47 es TNF-induced interleukin 6 (IL-6) and IL-8 mRNA expression and protein secretion from A549 lung epi

48 We found reduced mRNA expression and reduced protein levels of fission ge

49 tified individual and shared defects in PLP1 mRNA expression and splicing, oligodendrocyte progenitor

50 vel methodology that combines four datasets: mRNA expression and the associated regulatory factors of

51 In vivo, both IL-10 mRNA expression and the number of IL-10(+) CD45(+) cells

52 Specifically, MDM2 upregulated the mRNA expression and translation of another component of

53 in association with downregulation of PTPRT mRNA expression and upregulation of pSTAT3 expression.

54 llular respiration and PGC-1alpha and NDUFS1 mRNA expression and was blocked by inhibitors of Gbetaga

55 IL-1beta, TNF-alpha, and IL-6 messenger RNA (mRNA) expression and positive staining for IL-6.

56 It analyzes both continuous (e.g. mRNA expression) and binary omics data (e.g. discretized

57 of VIP on p38 and ERK phosphorylation, c-Fos mRNA expression, and GnRH release.

58 ology, interferon regulatory factor 4 (IRF4) mRNA expression, and nuclear factor of activated T cells

59 However, PDE10A mRNA expression appears comparable among NT, hWT, and hM

60 n factors SREBP1 and 2, whose activation and mRNA expression are stimulated by mTORC1 signaling.

61 We studied IL-32 mRNA expression as well as expression of other proinflam

62 High EGFL7 mRNA expression associates with lower complete remission

63 steroidogenic melanocortin 2 receptor (MC2R) mRNA expression between high- (HR) and low-responsive (L

64 ly to a rapid increase in cutaneous cytokine mRNA expression but also an increase in serum cytokine l

65 ry (U-IRI) led to sustained low-level Chi3l1 mRNA expression by renal cells and promoted macrophage p

66 approach for quantification of differential mRNA expression by targeted resequencing of complementar

67 We show that miRNA and mRNA expression can be a highly heritable molecular trai

68 mRNA expression clustering refined prior clustering anal

69 Blood PHLDA3 mRNA expression correlated with drug exposure ( R(2) = 0

70 ide DREAM complex binding data, p53-depedent mRNA expression data and a genome-wide definition of phy

71 de of transcriptional activity inferred from mRNA expression data and protein reporter data in the co

72 transcription factors when benchmarked with mRNA expression data and transgenic reporter assays.

73 By analyzing The Cancer Genome Atlas mRNA expression data for HGS ovarian cancer patient samp

74 Using Braincloud mRNA expression data, we identified a robust and specifi

75 age of publicly available cell type specific mRNA expression databases in order to identify potential

76 enotypes, multivariate analyses on published mRNA expression datasets of over 600 primary NSCLCs demo

77 on AMPA glutamate receptor 2 (GluR2) subunit mRNA expression decreased after SH, and, albeit increase

78 GATA-3, IL-5 and eotaxin mRNA expression decreased significantly after EPIT (P <

79 We found that whereas NUMBL mRNA expression decreases upon stimulation of wild type

80 nses consist of two types: one subtype loses mRNA expression during activation, whereas the other mai

81 ssed various neuron-specific proteins, their mRNA expression during neuronal differentiation recapitu

82 Moreover, increased blood cytokines mRNA expression (especially of IL-1beta) identifies pati

83 In naive Th cells, Ets-2 mRNA expression, Ets-2 protein levels, and Ets-2 binding

84 allele (AA) showed significantly lower CD28 mRNA expression ex-vivo than either GG or AG (p < 0.001)

85 LUT1 50:1), the opposite was found for GLUT5 mRNA expression (GLUT5 1:6).

86 r partner and cholesterol-7alpha-hydroxylase mRNA expression, implicates bile salt hydrolase activity

87 LG-5, ALG-1 and ALG-2, as well as changes in mRNA expression in alg-5, alg-1 and alg-2 mutants.

88 to investigate the prognostic values of S100 mRNA expression in breast cancer.

89 we observed a significant increase in RBM28 mRNA expression in breeds with lean phenotypes.

90 ly, we observed upregulation of endoglin/ID1 mRNA expression in chronic HCV patient liver biopsy samp

91 f this isoform represses the canonical NDC80 mRNA expression in cis, thereby inhibiting Ndc80 protein

92 gand binding and changes in RNA structure to mRNA expression in cis.

93 Quantitative RT-PCR was used to investigate mRNA expression in colonic tissue and dorsal root gangli

94 ever, in line with previous reports of ASIC3 mRNA expression in dorsal root ganglia neurons, we found

95 c association between rs31746 and PCDH-beta8 mRNA expression in frontal cortex tissue (P<1 x 10(-5)).

96 of P2Y2R increased TF promoter activity and mRNA expression in HCAEC.

97 Consistently, vitamin D regulated TRAIL mRNA expression in HME-1 cells.

98 We have systematically compared the GPCR mRNA expression in human and mouse islets to determine t

99 sue and a correlation between CDC6 and CHEK1 mRNA expression in human cancers.

100 , which was associated with decreased TOLLIP mRNA expression in infant monocytes.

101 age disequilibrium and associated with PRPF6 mRNA expression in lymphoblastoid cells from 373 Europea

102 these potassium channels when compared with mRNA expression in METH-addicted rats.

103 all molecules that were able to enhance PAX2 mRNA expression in MOE cells.

104 ) and Xanthine/Xanthine Oxidase induced TRAP mRNA expression in mouse macrophages, but only RANKL als

105 atal toxicity was associated with high Il36r mRNA expression in neonatal liver, resulting in increase

106 cancer cells, and analyse their protein and mRNA expression in normal and cancer tissues.

107 al clinical and biological function of IL-6R mRNA expression in ovarian cancer.

108 t caused an increase in alkaline phosphatase mRNA expression in PDL-CD105(+) cells after 7 days of os

109 We find that their mRNA expression in primary human bronchial cells is stim

110 EC incubation with OxPAPC also induced EP4 mRNA expression in pulmonary ECs and lung tissue.

111 sequence markedly reduces the levels of gfp mRNA expression in S. cerevisiae cells, with a concomita

112 he hippocampus and in NLGN1, NRXN2 and NRXN3 mRNA expression in S1 cortex were detected in FMR1-KO mi

113 cTnT mRNA expression in skeletal muscle was not detectable in

114 G shore of the CNTFRalpha gene regulated its mRNA expression in TCGA datasets.

115 Decreased TET2 mRNA expression in TCGA PCa tumours is strongly associat

116 By profiling mRNA expression in the bone marrow mesenchymal progenito

117 mplex involved in regulating proinflammatory mRNA expression in the heart.

118 ifferences in NLGN3, NRXN1, NRXN2, and NRXN3 mRNA expression in the hippocampus and in NLGN1, NRXN2 a

119 ssociation between protein concentration and mRNA expression in the human brain by comparing the 5-HT

120 creased Il13 and Il17a and increased Tgfbeta mRNA expression in the jejunum; numbers of CD103(+) dend

121 Cry deficiency correlates with reduced Igf-1 mRNA expression in the liver and skeletal muscles.

122 vels of PDYN 3'UTR in vitro and had elevated mRNA expression in the medial nucleus accumbens shell (N

123 ry and elevation in Col1a1, FnEDA, and TIMP1 mRNA expression in the obstructed kidney.

124 nished expression of SK2/SK3 channel subunit mRNA expression in the supraoptic nucleus of HF rats.

125 In addition, the relative mRNA expression in the three germ layers and the trophob

126 TREM-2 mRNA expression in the whole lung was significantly high

127 olygyrus bakeri infection downmodulated CLEC mRNA expression in these cells.

128 abase analysis revealed upregulation of CDC6 mRNA expression in tumour compared to normal tissue and

129 trategy elicits an up to 20-fold increase in mRNA expression in vitro and an approximately fourfold i

130 ng that IRPs exert a positive effect on Pfn2 mRNA expression in vivo.

131 cope in situ hybridization, we detected CB2R mRNA expression in VTA DA neurons in wildtype and DAT-Cn

132 Moreover, DUSP5 mRNA expression increased during obesity development con

133 Consistent with in vivo findings, DUSP5 mRNA expression increased in adipocytes in response to T

134 Netrin-4, but not netrin-1 mRNA expression, increased in response to relative hypox

135 g factor 3 receptor and toll-like receptor 7 mRNA expression increases in the thalamus in FFI.

136 developed for mRNA delivery, the inefficient mRNA expression inside cells remains a major challenge.

137 HBEGF mRNA expression is decreased in human neuroblastoma tumo

138 Elevated myosin heavy chain 7 mRNA expression is detected in left ventricles.

139 Importantly, we show MMP13 mRNA expression is mirrored by nascent hnRNA transcripti

140 Furthermore, FOF2 mRNA expression is regulated by autonomous pathway gene

141 ochrome P450 family 24 subfamily A member 1) mRNA expression is up-regulated by 25(OH)D3 at 250-500 n

142 ows significant association with a decreased mRNA expression level of IL-37 (n = 168, P = 3.78 x 10(-

143 ons was observed between SULT activities and mRNA expression levels (r(2) </= 0.48 except one).

144 y neurons (MSNs) of C57BL/6J mice, analysing mRNA expression levels and immunoreactivity of GlyR subu

145 Despite its greater diversity, HLA-B mRNA expression levels determined in 178 European Americ

146 omoter regions with estimated differences in mRNA expression levels for the classical class I loci.

147 ACTB mRNA expression levels in lymphoblastic lines and fibrob

148 red from plasma, and both DNA genotyping and mRNA expression levels in peripheral blood mononuclear c

149 It was previously reported that mRNA expression levels in the prefrontal cortex at old a

150 ties are correlated with protein amounts and mRNA expression levels of five major human sulfotransfer

151 activated T cells, TEX and DEX up-regulated mRNA expression levels of multiple genes.

152 Mice exposed to ppDIO did not show altered mRNA expression levels of orexin and melanin-concentrati

153 phage/monocyte clade, as supported by higher mRNA expression levels of several dendritic cell-associa

154 The mRNA expression levels of some genes related to neurotra

155 Furthermore, high mRNA expression levels of Stat3 or Jab1 in colon cancer,

156 The mRNA expression levels of the anti-inflammatory cytokine

157 Here we presented the changes in mRNA expression levels of three genes (MMP2, TIMP2, and

158 First, we identified that peripheral mRNA expression levels of two complement genes (C5, SERP

159 TERT mRNA expression levels were significantly higher in tumo

160 the magnitude of enhancer transcription, TF mRNA expression levels, TF motif P-values, and enrichmen

161 he short and the long 3'UTR produced similar mRNA expression levels.

162 changing CD32A (FCGRIIA) protein and CD32B/C mRNA expression levels.

163 ms; however, selection on protein/peptide or mRNA expression markers has not yet been proven useful.

164 PBMC FcepsilonRIalpha mRNA expression measured on study entry significantly im

165 Col1a1 (seal) mRNA expression occurred at greatly reduced levels compa

166 mmediately decreased basal transcription and mRNA expression of 18 genes, which predominately encode

167 We show that PHA-4 directly activates mRNA expression of a broad cohort of epithelial genes, i

168 CN-105 was also associated with reduction in mRNA expression of a subset of inflammatory and immune-r

169 mRNA expression of activin and TGF-beta pathway members

170 In the present study, mRNA expression of all 6 LPA receptor genes was detected

171 rtoli cell by suppressing AMH production and mRNA expression of AMH, SOX9, DHH, and COL2A1.

172 mRNA expression of APOBEC3 family of genes (A3A, A3B, A3

173 IL-1beta upregulated mRNA expression of AT1R, IL-1beta, IL-6, IL-8, tumor nec

174 spleen, and substantial decreases in splenic mRNA expression of both inflammasome components (Nlrp3,

175 Interestingly, we have observed that the mRNA expression of CB1 and CB2 receptors was decreased i

176 like 1 (Fstl1), and significant decreases in mRNA expression of chordin, kielin/chordin-like protein,

177 both in aortic sinus and spleen with higher mRNA expression of CTLA4 (3 fold), Foxp3 (1.4 folds) and

178 he induction of oxidative stress and altered mRNA expression of dopamine receptors, tyrosine hydroxyl

179 njugated form, TDCA, significantly inhibited mRNA expression of fatty acid transport protein 5 in the

180 ohol exposure (2.5 g/kg, i.p.) increased the mRNA expression of Fgf2 in the dorsal hippocampus, nucle

181 excessive glutamate transmission upregulated mRNA expression of Fgfrs and their ligands Fgfs Deleting

182 creased renal tubular lesions from day 2 and mRNA expression of fibrosis-related genes from day 4 com

183 er enzymes related to lipogenesis and higher mRNA expression of Fitm1.

184 mRNA expression of GATA3 and Tbet was analyzed in sorted

185 DHT exposure also reduced the mRNA expression of genes involved in metabolic pathways

186 We report significant increases in mRNA expression of gremlin 1, noggin, follistatin, and f

187 psy was taken after 2-3 years, the cutaneous mRNA expression of GSTT2, CTSA, PPARG, CDA, ENPP1 and NR

188 s that associated with increased hypoxia and mRNA expression of Hif1alpha and Vegf and increased ktra

189 T-oligo also inhibited mRNA expression of human telomerase reverse transcriptas

190 ha levels were measured in supernatants, and mRNA expression of IFN-alpha pathway genes was determine

191 Surprisingly, WM enhanced the mRNA expression of IFN-I and TNF-alpha, and TNF-alpha pr

192 nchial epithelial cells with IL-17A enhanced mRNA expression of IL-17RA and increased release of IL-8

193 on of effector cells with IL-2 downregulated mRNA expression of inhibitory NKR-P1A NK cell receptor,

194 Overexpression of c-Jun reduced protein and mRNA expression of ITPR2 in Huh7 cells, whereas knockdow

195 ST6Gal-I KD also alters mRNA expression of key gemcitabine metabolic genes, RRM1

196 th higher lactate dehydrogenase activity and mRNA expression of Ldha, Mct1, and Mct4 as well as with

197 Elevated mRNA expression of liver IL-6, IL-17A, IL-17F, TGF-beta1

198 In parallel, mRNA expression of myosin heavy chain 7 and natriuretic

199 how increased osteoclast differentiation and mRNA expression of osteoclast marker genes.

200 with decreased alpha-smooth muscle actin and mRNA expression of other HSC activation markers.

201 mbers, this was not accompanied by increased mRNA expression of other Th2 cytokines (IL-4 or IL-13).

202 s for nasal symptoms, self-reported NHR, and mRNA expression of PGP9.5; TRPV1; transient receptor pot

203 d ss-oxidation was associated with decreased mRNA expression of Pparalpha and its targets Cpt1, Aox,

204 pendent reporter gene (SRE-LUC) activity and mRNA expression of pro-proliferative and pro-migratory M

205 oscopy, immunohistochemistry, and intrarenal mRNA expression of proinflammatory and profibrotic media

206 Furthermore, P4 treatment showed decreased mRNA expression of proinflammatory cytokines, and partia

207 Our results indicated that high mRNA expression of S100A8, S100A9, S100A11 and S100P wer

208 Finally, mRNA expression of several ESC/E(Z) complex genes were i

209 wn-like structures in VAT along with reduced mRNA expression of some macrophage markers and chemokine

210 ams had lower liver triglyceride content and mRNA expression of Srebf1c.

211 Similarly, at 24 h postsurgery the mRNA expression of structural proteins (GFAP and AQP4) w

212 mRNA expression of Th1/Th2/Th17-associated cell markers

213 This was associated with increased mRNA expression of Th2 and Th17 cytokines.

214 3 activation, thereby resulting in decreased mRNA expression of the apoptosis-related gene, Bax, and

215 The mRNA expression of the beta variant of the glucocorticoi

216 Increased mRNA expression of the cardiac stress marker natriuretic

217 The mRNA expression of the histamine receptors was measured

218 Gene-set analysis revealed an increase in mRNA expression of the mediators of autophagy (eg, CDKN2

219 tolerability, pharmacokinetics (PK), and by mRNA expression of the p53 target gene pleckstrin homolo

220 luorescein isothiocyanate-dextran 4 kDa, and mRNA expression of tight junctions.

221 ring macrophages, manifested by elevation in mRNA expression of Tnfalpha and Il1beta, increased intra

222 mRNA expression of Treg/Th1/Th2/Th17-associated cell mar

223 essing TIL function, we compared genome-wide mRNA expression of tumor-specific CD8(+) T cells from th

224 10995 G-allele was associated with increased mRNA expression of VASP (vasodilator-stimulated phosphop

225 ption factor YY1 and ATP6V1A, and found that mRNA expression of YY1 had significant correlation with

226 rs12445022 is associated with mRNA expression of ZCCHC14 in arterial tissues (p = 9.4

227 The mRNA expressions of a battery of genes related to biotra

228 Here, we systematically analyzed mRNA expressions of representative TRIM molecules in hum

229 ansaminase elevations, hepatic inflammation (mRNA expressions of TNFalpha, MCP1, IL1beta, MIP2 and E-

230 ase phenotypes, as well as on messenger RNA (mRNA) expression of nearby genes, and on DNA methylation

231 Messenger RNA (mRNA) expression of proinflammatory innate and T-cell-de

232 Messenger RNA (mRNA) expression of vascular endothelial growth factor (

233 Because RGS2 mRNA expression often is strikingly and transiently up-r

234 effects of immune genes genetic variants and mRNA expression on depression's risk, severity, and resp

235 dentified significant changes in patterns of mRNA expression over cancer development but the function

236 table adaptive immune response as defined by mRNA expression pattern is reproducible and sufficient t

237 pported this model and revealed differential mRNA expression patterns in these tissues.

238 Finally, we analyze mRNA expression patterns in Xenopus embryos for each TAC

239 ain reaction array to analyze messenger RNA (mRNA) expression patterns in rectal mucosal samples from

240 In addition, its mRNA expression predicted poor outcome across breast can

241 n lung cancer has identified hub genes whose mRNA expression predicts cancer progress and patient res

242 Identification of genes whose basal mRNA expression predicts the sensitivity of tumor cells

243 histopathologic phenotype in relation to the mRNA expression profile of proinflammatory cytokines.

244 The mRNA expression profile was significantly different betw

245 Analysis of mRNA expression profiles in breast tumors demonstrates t

246 echanisms of estrus expression in gilts, the mRNA expression profiles of follicular tissue from Large

247 d into subpopulations based on their protein-mRNA expression profiles, and that different subpopulati

248 gnized infections and reveals antiviral host mRNA expression profiles.

249 High throughput mRNA expression profiling can be used to characterize th

250 GADD45B was also repressed in mRNA expression profiling experiments when KSHV miRNAs w

251 Whole genome mRNA expression profiling identified nicotinamide N-meth

252 metabolomic analysis and transcriptome-wide mRNA expression profiling identified reduced levels of s

253 related with all 3 probes extracted for TSPO mRNA expression (r = 0.80, r = 0.79, and r = 0.90), but

254 elated with higher BCL2:BCL2L1 and BCL2:MCL1 mRNA expression ratios.

255 and integrating allelic expression, overall mRNA expression, regulatory motif perturbation, and chro

256 ed to the development of methods to quantify mRNA expression, relatively little effort has been spent

257 r, these Dicer-resistant genes constitute an mRNA expression signature that is present in numerous hu

258 on/off effects on GR-binding and subsequent mRNA expression: some genes were highly dependent on the

259 These regional parameters and messenger RNA (mRNA) expression specific to endothelial cells were corr

260 reased collagen deposition, collagen 1 and 3 mRNA expression, TGF-beta production, and activation of

261 g the function of p53 to directly induce p21 mRNA expression, this process indirectly requires p53, p

262 inverse gains of methylation with decreasing mRNA expression throughout pregnancy, supporting a role

263 We have produced an mRNA expression time course of zebrafish development acr

264 tional activity profile of a gene from given mRNA expression time series or protein reporter time ser

265 hromatin accessibility, DNA methylation, and mRNA expression to induce a default neuronal state.

266 served that SIRT1 repressed LEF1 protein and mRNA expression, ultimately reducing LEF1 transcriptiona

267 In characterizing mRNA expression using principal component analysis, S100

268 follicles from patients with IPF, and AKAP13 mRNA expression was 1.42-times higher in lung tissue fro

269 METHODS AND S100A8 and S100A9 mRNA expression was 13.0-fold (P=0.012) and 5.1-fold (P=

270 In EMT6 tumors, GLUT5 mRNA expression was 20,000-fold lower compared with GLUT

271 RAMP1 mRNA expression was also detected in the posterior hypot

272 Left ventricular NOD2 mRNA expression was also induced in CVB3-induced myocard

273 Phrenic motoneuron NMDA NR1 subunit mRNA expression was approximately fourfold greater in AA

274 This pattern of increased ESC/E(Z) mRNA expression was confirmed in a larger cohort by qRT-

275 Specific mRNA expression was evaluated by classical and quantitat

276 METHODS AND Endomyocardial biopsy NOD2 mRNA expression was higher in CVB3-positive patients com

277 Programmed cell death-1 mRNA expression was increased in tissue homogenates from

278 In a different set of postmortem brains, p11 mRNA expression was measured in dopaminergic cells from

279 mERbeta2 mRNA expression was measured in mouse tissues.

280 Furthermore, GLUT4 mRNA expression was mediated by glucose-dependent activa

281 Significant up-regulation of C3 and CFB mRNA expression was noted in chemically induced mouse cS

282 When analyzed longitudinally, an early IL-10 mRNA expression was observed.

283 Colonic FPRL1 mRNA expression was positively correlated with the histo

284 SFRP1 mRNA expression was reduced by both RS (P = 0.005) and p

285 h resected PDAC, we show that increasing uPA mRNA expression was significantly associated with poorer

286 9) and at time of AR (n = 88), tissue CYP3A5 mRNA expression was significantly higher in CYP3A5*1 all

287 Whereas IL-5 mRNA expression was significantly increased in freshly i

288 Of note, IL-5 mRNA expression was significantly increased in purified

289 Gingival IL-10 mRNA expression was significantly increased, whereas exp

290 Using RNA interference, Ov-tsp-2 and tsp-3 mRNA expression was significantly suppressed for up to 2

291 ed P2X currents and proinflammatory cytokine mRNA expression were blocked by the Cx43 blockers Gap26

292 ased maximum DAMGO response, MOR protein and mRNA expression were decreased in female compared with m

293 thelial growth factor-A, VEGF-C, and VEGF-R2 mRNA expression were increased in VECs when cocultured w

294 FcepsilonRIalpha protein levels and mRNA expression were measured in unstimulated cells by u

295 Oxytocin receptor and connexin-43 mRNA expression were reduced in the myometrium from 8-mo

296 al electrical resistance, paracellular flux, mRNA expression, Western blotting, and immunofluorescenc

297 tely 20% upregulation of COL2A1 and aggrecan mRNA expression), which reversed the effect of IL-1beta.

298 of TFPI-2 contributed to inhibition of MMP-2 mRNA expression, which could be reversed after the nucle

299 ) have shown a negative correlation of IDO-1 mRNA expression with outcomes.

300 fication; it allows facile quantification of mRNA expression with subcellular resolution on a standar