ライフサイエンスコーパス: be down-regulated

1 ransferase that methylates 1,7-paraxanthine, is down-regulated.

2 curs after anaphase onset when CDK1 activity is down-regulated.

3 reas epithelial markers, such as E-cadherin, are down-regulated.

4 undant even though their corresponding mRNAs are down-regulated.

5 tion-reduction and steroid metabolic process are down-regulated.

6 rs of oil-added ducks, while the C12:0 ratio was down-regulated.

7 expression of pri-miRNA161 and pri-miRNA173 was down-regulated.

8 lf5/cyclin D1 axis was up-regulated and Klf4 was down-regulated.

9 ctural genes involved in eugenol production, was down-regulated.

10 rylation of one cluster of modified residues was down-regulated.

11 Mmp2 were up-regulated whereas p21 (Cdkn1a) was down-regulated.

12 ith U373MG glioblastoma cells in which Rap1A was down-regulated.

13 ucer, adenosine-5'-phosphosulfate reductase, was down-regulated.

14 se was up-regulated, whereas pyruvate kinase was down-regulated.

15 ressed collaterals including miRNA-352 which was down-regulated.

16 e of six mitochondrion-related nuclear genes was down-regulated.

17 e) and 107 (microwaved sample) protein spots were down regulated.

18 phA3 cytokine/tyrosine-kinase (TK) receptors were down regulated.

19 rticipate in the Alzheimer's disease pathway were down-regulated.

20 were elevated, while neuroinflammatory genes were down-regulated.

21 ry and field, while creb and pka transcripts were down-regulated.

22 7(-/-) mice, whereas DNA damage repair genes were down-regulated.

23 ion-channel transport and cardiac conduction were down-regulated.

24 , while the other sulfite network components were down-regulated.

25 ially expressed: 71 were up-regulated and 45 were down-regulated.

26 , cell cycle and reproduction (cdc20, ccnb1) were down-regulated.

27 in kinase phosphatase-1 messenger RNA levels were down-regulated.

28 t levels of IRF5 mRNA and protein expression were down-regulated.

29 sed proteins a V-ATPase and a 14-3-3 protein were down-regulated.

30 over, both alpha- and gamma-ENaC transcripts were down-regulated.

31 key iron transporters (AfuA, FhuC, and FhuD) being down-regulated.

32 C3 expression was down-regulated 2-fold in retinas of omega-3 LCPUFA-f

33 ceptor beta and insulin receptor substrate 1 were down-regulated 2-fold by Kcne2 deletion, characteri

34 der anaerobic conditions, both Id1 and c-Myc are down-regulated (50-70%), and overexpression of oxyge

35 a), and its metabolic and angiogenic targets are down-regulated (50-85%) in skeletal muscles of mdx m

36 lin protein/78-kDa glucose-regulated protein was down-regulated, activating transcription factor 6, a

37 contractions in the guinea pig ileum, which are down-regulated after chronic, but not acute, exposur

38 ly of transcription factors, Sox4 and Sox11, are down-regulated after the epoch of hair cell developm

39 ter VSG while genes in inflammatory pathways are down-regulated after VSG.

40 However, the mechanisms by which p63 is down-regulated after acute OE injury remain unknown.

41 125a-5p is highly expressed in VSMCs, but it is down-regulated after vascular injury in vivo.

42 n of Rho-associated protein kinase 2 (ROCK2) was down-regulated after EM2 treatment.

43 imary human hepatocytes, SIRT1 messenger RNA was down-regulated after GCA treatment, potentially thro

44 p-STAT3 and downstream signals were down-regulated after sorafenib and SC-1 treatment i

45 Particularly photosynthesis-related genes are down-regulated and genes belonging to the functional

46 mples revealed that both ts-3676 and ts-4521 are down-regulated and mutated in patient tumor samples.

47 ferentiation genes (KRT1, KRT10, DSC1, DSG1) being down-regulated and late differentiation genes (SPR

48 In this study we determined that autophagy is down-regulated and inversely correlated with miR-224

49 We found that, like ts-3676, ts-4521 is down-regulated and mutated in CLL.

50 thylarginine dimethylaminohydrolase activity is down-regulated and PRMT1 protein expression is up-reg

51 cence the canonical miRNA biogenesis pathway is down-regulated and specific miRNAs are generated by a

52 osis occurs under conditions where cyclin D1 is down-regulated and the cell cycle arrested in G2 phas

53 tion, CD86 expressed by transitional B-cells was down regulated and T-cell proliferation was reduced.

54 (mCaROCK1), we found that irisin production was down-regulated and the mice developed obesity and in

55 due to the fact that both p70S6K and Smurf1 were down-regulated and negatively correlated with TRIB2

56 in human breast tumors, PTTG1 protein levels were down-regulated and the reduction was significantly

57 In mom1-3 ovules, both SUF4 and EC1 genes are down-regulated, and EC1 genes show higher levels of

58 In diabetes, IRS-1 is down-regulated, and cells become resistant to insulin

59 which is mainly stabilized by Cx43 in vivo, was down-regulated, and its characteristic staining rema

60 ant Htt neurons, fission genes Drp1 and Fis1 were down-regulated, and fusion genes Mfn1, Mfn2 and Opa

61 il-treated mutant Htt neurons, fission genes were down-regulated, and fusion genes were up-regulated,

62 known KCNE3 partners KCNC4 and KCNH2 (mERG) were down-regulated, and KCNK4 (TRAAK) was up-regulated

63 mature: 99% of them during early maturation were down-regulated, and preferentially associated with

64 Many fatty acids were down-regulated, and the levels of the polyamines, s

65 1 accumulated, W1-COE and its paralog W2-COE were down-regulated, and the phenotype was nonglaucous a

66 Expression of LmxGT1 is down-regulated approximately 20-fold by increasing ce

67 (HS), critical to establish CCL21 gradients, was down-regulated around lymphatics by anti-VEGFR-3 and

68 ARID5B expression is down-regulated at the double-negative 2-4 stages in n

69 uding the S6 ribosomal protein (S6rp), which is down-regulated at the onset of myelination, and N-myc

70 and describe a novel mechanism by which CYLD is down-regulated at the transcriptional level in MOLF/E

71 Its expression was down-regulated at the BTB in stage VIII-IX tubules,

72 ative regulation of axon extension processes were down-regulated at 3 h.

73 receptor expressions studied in mouse aortas were down-regulated at 6 and 18 hours in endotoxemic mic

74 low-density lipoprotein-5 (bone mass marker) were down-regulated at M12 in OVX-Diet rats.

75 CtrA activity is down-regulated both by dephosphorylation and by prote

76 ally by GABA release: Axonal GABAA receptors are down-regulated but dendritic receptors are up-regula

77 report here that Krt17 expression initially is down-regulated but later is strongly up-regulated by

78 levels and inhibitors of apoptosis proteins were down-regulated, but force production remained norma

79 , as well as other copper-deficiency markers are down-regulated by copper.

80 g to gene ontology analysis of proteins that are down-regulated by miR-7.

81 t levels of Cu/Zn superoxide dismutase (CSD) are down-regulated by miR398.

82 Photosynthetic light harvesting can be down-regulated by nonphotochemical quenching (NPQ).

83 In this study, we showed that MIF expression is down-regulated by 0.75 +/- 0.10-fold of the control i

84 2 in an autocrine manner, and PGE2 secretion is down-regulated by cell-to-cell contact, attenuating i

85 In most Brachypodium accessions BdODDSOC2 is down-regulated by cold, and in one of the winter acce

86 onsumer of methyl donors, and this synthesis is down-regulated by dietary/supplemental creatine.

87 hyaluronic acid-CD44 independent manner that is down-regulated by inhibitors of the JAK/STAT pathway

88 nd CCNJ, a protein controlling cell mitosis, is down-regulated by miR-98 via targeting 3'-untranslate

89 Importantly, SL synthesis is down-regulated by mutations in genes of the Nod LCO s

90 by which protein synthesis in starved cells is down-regulated by phosphorylation of the universally

91 agment 1, have actin-activated MgATPase that is down-regulated by phosphorylation.

92 Here we report that Atgl is down-regulated by the basal transcription factor Sp1

93 This pathway is down-regulated by virus- and host-encoded enzymes tha

94 CD2AP.Cbl-3/c complex, suggesting that Ret9 was down-regulated by a fundamentally different mechanis

95 loop in prostate cancer: miR-190a expression was down-regulated by AR activation; YB-1 functions are

96 The expression of spl was down-regulated by cytokines in INS1E cells and rat i

97 methylation showed that LOC146880 expression was down-regulated by DNA methylation in its promoter.

98 owed that leaf hydraulic conductance (Kleaf) was down-regulated by exogenous ABA, with strong variati

99 on proteins corneodesmosin and desmoglein-1, was down-regulated by histamine.

100 and ACAN expression in OA chondrocytes that was down-regulated by IL-1beta.

101 mitochondrial permeability transition pore, was down-regulated by miR-7 through targeting 3'-untrans

102 Oskn2:beta-glucuronidase reporter expression was down-regulated by OsGRF3 and OsGRF10 in vivo, sugges

103 se experiments revealed that vascular IGF-1R was down-regulated by platelet miR-223.

104 f miR-17/92 cluster and miR-374b/421 cluster was down-regulated by THC.

105 In contrast, the expression of TRIM59 was down-regulated by TLR3 and TLR4 ligands in both huma

106 (TNF-alpha, IL-6, IL-12, TGF-beta, and VEGF) were down regulated by DMDD.

107 red by flux through pyruvate dehydrogenase), were down-regulated by beta-lapachone treatment.

108 Seventy four genes were up-regulated and 9 were down-regulated by both ligands.

109 g, and regulation of immune system processes were down-regulated by caffeine at 3 h.

110 nearly all of the mitochondria-related genes were down-regulated by EE.

111 he beta-catenin signaling target connexin-43 were down-regulated by FH535, and functional blockade of

112 xtent by PKA-CQR and of the transcripts that were down-regulated by FSH, 76% were also down-regulated

113 mponents of the circadian central oscillator were down-regulated by NF and LPS, suggesting that a roo

114 ive role during early stages of the process, were down-regulated by NF and LPS.

115 tified a large number of cellular genes that were down-regulated by TAZ.

116 As these potentiated interactions were down-regulated by two pharmacotherapies, this effec

117 When PLCbeta1 or TRAX is down-regulated, differentiation does not occur.

118 l to identify multiple neuronal tissues that are down-regulated due to pathogen infection in C. elega

119 xposure or beta3-adrenergic stimulation, and is down-regulated during brown adipocyte differentiation

120 p protein EZH2 (enhancer of zeste homolog 2) is down-regulated during osteoblastic differentiation of

121 The expression of bta-miR-23a was down-regulated during differentiation of PDGFRalpha(

122 Expression of the precursors of the miR393 was down-regulated during mycorrhization in three differ

123 synthase, biosynthesis, and Hym hydrogenase were down-regulated during C2H2 inhibition, consistent w

124 Several PEG-responsive proteins were down-regulated, especially photosynthetic proteins.

125 roapoptotic tumor suppressor gene DPPIV/CD26 was down-regulated, followed by an increase in extracell

126 Additionally, activity in the network was down-regulated for acceptability, but not blame, jud

127 ant morphological changes and one week later were down-regulated gradually, while those in Modules 2

128 As were up regulated (>2 fold) and 35 miRNAs were down regulated (>2fold) compared to controls.

129 mMRP-5 (all orthologs of HRGs in C. elegans) are down-regulated in heme-treated B. malayi, as compare

130 Finally, we demonstrate that Rheb levels are down-regulated in the AD brain, which is consistent

131 are up-regulated and downstream SRF targets are down-regulated in the hearts of MCKCUG-BP1 mice, whi

132 and "ts-53," respectively), ts-46, and ts-47 are down-regulated in these malignancies.

133 In contrast, the ASncmtRNAs are down-regulated in tumor cells regardless of tissue o

134 miR-214, and LHX6 expression was detected to be down-regulated in erlotinib-resistant HCC827 cells.

135 an upstream autophagy inducer, was found to be down-regulated in GBM.

136 analyzed miR-133b expression and found it to be down-regulated in HCC patient samples and induced in

137 We found expression of TFF2 to be down-regulated in human PDAC by hypermethylation of i

138 tein claudin 1 (Cldn-1) has been reported to be down-regulated in nonlesional skin of atopic dermatit

139 Importantly, we show that iso3, known to be down-regulated in several cancers, competes with RBBP

140 ArgBP2 is known to be down-regulated in some aggressively metastatic cancer

141 the mitotic kinases, Aurora A and Plk1, that is down regulated in human seminoma.

142 ZPR1 is down regulated in SMA patients.

143 p120ctn is down-regulated in 60% of ESCC tumors, whereas EGFR is

144 Cyclin D3 is down-regulated in a dose-dependent manner in beta cel

145 We show here that TrkC expression is down-regulated in a large fraction of human colorecta

146 oplasmic tRNAs tK(UUU), tQ(UUG) and tE(UUC), is down-regulated in a proteasomal dependent fashion.

147 trahydrofolate reductase (MTHFR) gene, which is down-regulated in bm2 mutant plants.

148 and qPCR indicated that the expression of FT is down-regulated in both OsbHLH068-overexpressing Arabi

149 Finally, we show that CDKN3 protein is down-regulated in brain tumors.

150 Here, we show that SOD2 itself is down-regulated in breast cancer cell lines.

151 expressed on normal breast epithelial cells is down-regulated in breast cancer.

152 mediated by the DNA methylase, DNMT3A, which is down-regulated in cells lacking p38alpha, but once re

153 Here we show that miR-148a is down-regulated in cells with acquired TRAIL-resistanc

154 g ducts of mice and rats, and its expression is down-regulated in Dahl salt-sensitive rats fed a high

155 anscript; miR-198 expression in healthy skin is down-regulated in favor of FSTL1 upon wounding, which

156 We have shown that peach PpeS6PDH gene is down-regulated in flower buds after dormancy release,

157 contrast to other cancers, PICK1 expression is down-regulated in grade IV astrocytic tumor cell line

158 hetic enzyme cystathionine-gamma-lyase (CSE) is down-regulated in growth-restricted placentas.

159 We report that miR-1271 expression is down-regulated in HCC tumor samples and inversely cor

160 metabolism of many carcinogens and drugs and is down-regulated in HCC.

161 inducer of hepatocytic differentiation that is down-regulated in HCC.

162 RNA (miR)-122, a bona fide tumor suppressor, is down-regulated in hepatocellular cancer (HCC).

163 rce this result, we also show that Tif1gamma is down-regulated in HSCs during aging in 20-mo-old wild

164 We also found that expression of miRNA-200b is down-regulated in human breast cancer during lymph no

165 Moreover, NCoR is down-regulated in human hepatocarcinomas and in the m

166 glandin E2 (PGE2), through its receptor EP4, is down-regulated in human systemic inflammatory disease

167 Notably, SAT1 expression is down-regulated in human tumors, and CRISPR-cas9-media

168 Muscular secreted frizzled-related protein 2 is down-regulated in ICU-acquired weakness patients and

169 We previously showed that aPKC is down-regulated in intestinal epithelia under inflamma

170 We found that miRNA-122 (miR-122) is down-regulated in liver biopsy specimens of patients

171 Consistently, hCDC14A is down-regulated in many tumor tissues and reduced hCDC

172 xpressed in many cancers, including RCC, and is down-regulated in metastatic versus primary ccRCC.

173 e 2 of the gibberellin biosynthesis pathway, is down-regulated in OsbZIP48(OE) and up-regulated in Os

174 We found that pulmonary PPARgamma is down-regulated in patients with IPF.

175 olved in gametogenesis in Chlamydomonas pCRY is down-regulated in pregametes and gametes, and in the

176 arbonate secretor in the human biliary tree, is down-regulated in primary biliary cholangitis.

177 HBI1 expression is down-regulated in response to different PAMPs.

178 deacetylase and activator of fat oxidation, is down-regulated in response to high fat feeding, the r

179 hich surface expression of the Vbeta5(+) TCR is down-regulated in response to Mtv-8 and recombination

180 Because IRS-1 is down-regulated in states of insulin resistance that o

181 We found that Gbx2 expression is down-regulated in Tbx1(+/-) embryos and is restored t

182 We report that hsa-miR-31-5p (miR-31) is down-regulated in TFH; we showed that BCL6 suppresses

183 hannel tetramerization domain containing 12, is down-regulated in the CSC-like cells of CRC.

184 the most widely characterized family member, is down-regulated in the depressed brain and plays a pro

185 in 3 (Ucn3), a marker for mature beta cells, is down-regulated in the early stages of T2D in mice and

186 transforming growth factor-beta1 expression is down-regulated in the Lamc3(-/-) retina, and SMAD sig

187 es with a QTL for rice blast resistance, and is down-regulated in the ospal4 mutant line; this may ex

188 an endothelial-specific, proangiogenic miR, is down-regulated in the peripheral muscles of patients

189 rticoid regulated kinase 1 (SGK1) expression is down-regulated in the postmortem PFC of PTSD subjects

190 Interestingly, secondary to this bmp4 is down-regulated in the Xenopus eyes.

191 ession of several key slit diaphragm protein was down regulated in pGR KO mice.

192 Clinically, PTPRF was down-regulated in 42% HCC (37/89), 67% gastric cance

193 Salt-inducible HSFA6b expression was down-regulated in ABA-insensitive and -deficient mut

194 Notably, when Alk4 was down-regulated in adult wild-type mice, muscle mass

195 We found that expression of miR-3189-3p was down-regulated in astrocytoma and glioblastoma clini

196 e 3 (Sec14l3) - a putative target of Creb1 - was down-regulated in both asthma models and in NHBE cel

197 F, Has2 and Ccl5 were up-regulated and Ccl11 was down-regulated in CAF in co-culture.

198 Moreover, TFAM expression was down-regulated in comparison to the control (p < 0.0

199 ferator-activated receptor-gamma (PPARgamma) was down-regulated in control animals after AMI and up-r

200 of the transcription factor EB (TFEB), which was down-regulated in cystinosis.

201 In vivo, expression of Fam65b was down-regulated in developing zebrafish to determine

202 Consistently, hepatic Sort1 was down-regulated in diabetic mice, which was partially

203 Kbtbd2 was down-regulated in diet-induced obese insulin-resista

204 The expression of miR-101 was down-regulated in fibrotic lungs from patients with

205 In clinical samples, miR-125b-5p was down-regulated in gallbladder cancer whereas Bcl2 wa

206 BER genes NEIL3 was down-regulated in IFN-treated patients.

207 defense priming in systemic plant immunity, was down-regulated in leaves by joint stress and conferr

208 IRF5 in HCV-induced HCC, as IRF5 expression was down-regulated in livers from HCV-positive versus HC

209 We found that PPARgamma was down-regulated in lung tissue and epithelial cells o

210 SHP2 was down-regulated in lungs and lung fibroblasts obtaine

211 Also, ANGPTL7 was down-regulated in metastatic liver colonies of color

212 miR-126 was down-regulated in metastatic versus primary tumors a

213 nuclear factor 4A-driven gene network, which was down-regulated in mouse hepatocyte nuclear factor 4A

214 The functionally essential sGC beta1-subunit was down-regulated in patients with COPD and in CS-expos

215 SMARCD1 was down-regulated in patients with non-small cell lung

216 NEDD4 was down-regulated in persons taking statins, and simvas

217 A fifth miRNA, mir-6722, was down-regulated in persons with AD and mild cognitive

218 We found that Ctgf mRNA was down-regulated in primary sternal chondrocytes from

219 primary methyltransferase acting on H3K9me2, was down-regulated in response to (*)NO, and changes in

220 In human HSCs, BAMBI expression was down-regulated in response to LPS and TNF-alpha.

221 ntified a serine protein kinase, SRPK3, that was down-regulated in RMS cells and found that expressio

222 he chemokine CCL5 was up-regulated and CCL11 was down-regulated in SF in co-culture.

223 ibitor, secreted frizzled-related protein 2, was down-regulated in skeletal muscle of ICU-acquired we

224 miR-188-5p expression was down-regulated in the brain tissues from AD patients

225 The BMP pathway was down-regulated in the colons of human progastrin mic

226 Further, c-Fos was down-regulated in the hippocampus, together with a r

227 ation found that BMP/Smad4 signaling pathway was down-regulated in the K14-cre;Bmp2(f/f);Bmp4(f/f)ame

228 Megalin mRNA was down-regulated in the KO embryonic spinal cord (SC)

229 The expression of miRNA-193b-3p was down-regulated in the mouse spleen and liver and in

230 We found that miR-663 was down-regulated in the mtDNA-depleted Rho(0) line.

231 xpression of multiple enamel matrix proteins was down-regulated in the mutant ameloblasts, the cleava

232 e expression of synapsin genes SYN1 and SYN2 was down-regulated in vivo and in vitro by alphaSyn olig

233 t time that NCX1 mRNA and protein expression was down-regulated in Wilms tumor and RCC.

234 ression status, and the majority of the rest were down-regulated in abiotic stresses and up-regulated

235 mma (PPAR-gamma) and downstream target genes were down-regulated in adipose tissue from participants

236 iogenesis, including c-MYC, c-MYB, and VEGF, were down-regulated in association with a decline in hyp

237 ding 443 that were up-regulated and 373 that were down-regulated in ATH tissues.

238 cbl1 shoots, while a different set of genes were down-regulated in cbl1 but not in WT roots.

239 ral drug metabolism and BA transporter genes were down-regulated in Cic-L(-/-) liver, and that BA was

240 teractions and NK cell-mediated cytotoxicity were down-regulated in cKO decidua compared with control

241 In Salix, Rubisco activase transcripts were down-regulated in contaminated trees across all 10

242 posterior localization of Osk in the oocyte, were down-regulated in enok mutants.

243 In addition, Camta1, Camta2, and Nkx2-2 were down-regulated in GK rat islets, and knockdown of C

244 itrite levels and apelin and NOS3 expression were down-regulated in HAPE-p (P < 0.001).

245 Interestingly, 16 of these 18 genes were down-regulated in high-grade glioma.

246 up-regulated genes in JGM-treated BPH, which were down-regulated in JGM-treated WBPH.

247 -1271, miR-145, miR-99b, miR-191 and miR-10b were down-regulated in low RFI pigs.

248 TGFbeta pathway, including pSMAD2 and pERK, were down-regulated in LTBP4 mutant human dermal fibrobl

249 in A, and Growth factor-independent 1 (Gfi1) were down-regulated in Mtgr1(-/-) whole intestines and M

250 ies in PGK mutants showed that PGK1 and PGK3 were down-regulated in pgk3.2 and pgk1.1, respectively.

251 2-mediated oxidative stress response pathway were down-regulated in PMNs of diseased patients.

252 CBFs and CBF regulon genes were down-regulated in rdm4 but not nrpe1 (the largest s

253 many glycosylation sites on surface proteins were down-regulated in statin-treated cells compared to

254 s were up-regulated whereas 36% of LPE genes were down-regulated in the absence of this receptor.

255 Interestingly, these mitochondrial proteins were down-regulated in the CTX model thereby linking oxi

256 ins were differentially up-regulated and 400 were down-regulated in the fast muscle compared with slo

257 0.75, respectively; P < 0.05); both pathways were down-regulated in the greatest-ADG compared with le

258 script as well as protein levels, while they were down-regulated in the GSH-depleted phytoalexin defi

259 etylase sirtuin 1, a ChREBP-negative target, were down-regulated in the liver of alcohol-fed mice, th

260 f the beta cell transcriptional network that were down-regulated in the Nkx2.2(KO) mice, were maintai

261 n and its interaction partner, NHERF2, which were down-regulated in the streptozotocin group.

262 le control and 9 genes involved in apoptosis were down-regulated in the treatment tumor tissues versu

263 sis and fatty acid biosynthesis; these genes were down-regulated in wild-type or WRI1-overexpressing

264 %) of S-palmitoylation sites on 254 proteins were down-regulated in Zdhhc13-deficient mice, represent

265 Genes involved in various metabolic pathways were down regulated, including genes involved in cell gr

266 Ninety genes were up-regulated and 18 genes were down-regulated, including genes with potential regu

267 and parathyroid hormone-like peptide (Pthlh) were down-regulated, indicating compromised Hh signaling

268 ts, but in aggressive osteosarcomas, miR-874 is down-regulated, leading to elevated CCNE1 expression

269 Interestingly, the majority of these genes are down-regulated, linking malignant transformation to

270 artery occlusion (MCAO) model of stroke, LSR was down-regulated, linking loss of LSR and pathological

271 l stages of development to define genes that are down-regulated or up-regulated by the lec1 mutation.

272 -miR-585-3p, hsa-miR-508-3p and hsa-miR-626) were down-regulated (P < 0.05; fold regulation </=-2) in

273 erogeneous nuclear ribonucleoproteins A2/B1, are down-regulated post-transcriptionally only in Tg-Ran

274 posterior end of the IM, but its expression is down-regulated prior to UB outgrowth at E10.5.

275 e nuclear factor of activated T cells (NFAT) was down-regulated progressively in accordance to the si

276 ive immunity-related signaling pathways, and were down-regulated relative to control subjects.

277 nd RORgammat are up-regulated, whereas FoxP3 is down-regulated, resulting in enhanced Th1 and Th17 ex

278 d expression of Bcl-2 and IAP family members were down-regulated, resulting in high levels of caspase

279 Results show pro-inflammatory cytokines were down-regulated significantly post antibiotic treatm

280 lved in flavonoid biosynthesis were found to be down-regulated specifically in the salinity tolerant

281 gnals such as CC chemokine receptor 7 (CCR7) are down-regulated, T cell intrinsic S1PR1 is the master

282 ge-sharing hypothesis, most young duplicates are down-regulated to match expression levels of single-

283 EPO) expression 1246-fold, whereas renal EPO was down-regulated to 6.7% of normal levels.

284 and the two predicted target genes of miR395 were down-regulated under the same conditions.

285 These target mRNAs are down-regulated upon WT1 depletion in cell culture an

286 14-3-3 protein beta/alpha/YWHAB (14-3-3beta) is down-regulated upon miR-152 overexpression, although

287 normal human keratinocytes YIPF4 expression was down-regulated upon differentiation and this reducti

288 and the downstream targets MMP7 and survivin were down-regulated upon BMVC or BMVC4 treatments.

289 n), and the basement membrane (Collagen IV), were down-regulated upon SRF depletion.

290 k, and Pi3K/Akt/mTor signaling pathway genes were down-regulated upon vitamin D supplementation.

291 production from an equivalent number of MSCs was down-regulated via gap junctional intercellular comm

292 Further, CXCR3-B-induced apoptosis was down-regulated when we overexpressed HO-1.

293 the infecting virus was specialist but they were down-regulated when infecting with generalist.

294 , ferritin OsFER2 and ferredoxin OsFd1 mRNAs are down-regulated whereas the transcriptional iron regu

295 Complexes I, III, and IV were down-regulated, whereas complexes II and V were up-

296 keletal organization, and cell proliferation were down-regulated, whereas stress-related proteins wer

297 2 days earlier than normal MT channels, and being down-regulated with the emergence of the normal ch

298 ing energy deficit, muscle protein synthesis is down-regulated with concomitant increases in ubiquiti

299 zed in HCC cells and anti-apoptotic proteins were down regulated with apoptosis in ~27% of the tumor

300 Both CPSI and CFHR2 were down-regulated with decreased plasma levels (p < 0.