ライフサイエンスコーパス: be down-regulated

1 Similar changes are seen when C3PO is down-regulated.

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

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

4 which cell division, growth, and metabolism are down-regulated.

5 ated, while genome-wide cancer-related genes are down-regulated.

6 e alignment defects in these cells when they are down-regulated.

7 sion of proteins responsible for lipogenesis was down regulated.

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

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

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

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

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

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

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

15 mportant neuronal marker during development, was down-regulated.

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

17 genes (DEGs) vs. fresh-frozen, 98% of which were down-regulated.

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

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

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

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

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

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

24 7(-/-) mice, whereas DNA damage repair genes were down-regulated.

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

26 DEGs, of which 118 were up-regulated and 68 were down-regulated.

27 (IL6), and arginine decarboxylase 2 (ADC2)) were down-regulated.

28 ment such as suberin and lignin biosynthesis were down-regulated.

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

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

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

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

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

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

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

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

37 125a-5p is highly expressed in VSMCs, but it is down-regulated after vascular injury in vivo.

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

39 only MMP gene family member whose expression was down-regulated after FXR activation.

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

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

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

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

44 sets of 56 and 22 protein-coding genes that are down-regulated and up-regulated in pin1Delta cells,

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

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

47 We also found that AURKA is down-regulated and primary cilia formation is enhance

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

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

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

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

52 d 1735 differentially expressed genes (DEGs) were down-regulated and 1369 were up-regulated in cold-s

53 SD induction, auxin genes IAA, ARF and SAURs were down-regulated and circadian genes including PIF3 a

54 C(4)-related genes were down-regulated and subsequently fully expressed upo

55 of the durian pulp revealed that 15 proteins were down-regulated and three other proteins were up-reg

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

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

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

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

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

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

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

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

64 1 accumulated, W1-COE and its paralog W2-COE were down-regulated, and the phenotype was nonglaucous a

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

66 We further demonstrate that MAOA is down-regulated as a result of IL-6/IL-6R/STAT3 signal

67 estingly, UBR5, and to a lesser degree UBR4, were down-regulated as cellular demand for antibody expr

68 ome formation genes (needed for translation) were down-regulated as compared with unrestricted DO.

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

70 tion that occurs when cortical contractility is down-regulated at the junctions between those neighbo

71 IP3 as a relapse biomarker, whose expression was down regulated at a relapse compared to remission in

72 CP1 and starch synthase IIIa (SSIIIa), which was down-regulated at the protein level in the CS8 line.

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

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

75 at least 2-fold in CLL, while 701 fragments were down-regulated at least 2-fold.

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

77 st all differentially expressed escape genes are down-regulated but most differentially expressed ina

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

79 controls, and determined that such fragments are down-regulated by 5-fold in CLLs vs. normal controls

80 Tms from diverse substrates whose activities are down-regulated by acylation but are required for bio

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

82 ptome analysis showed that most of the genes are down-regulated by ethylene in shoots, and a DNA bind

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

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

85 AS2 expression and HA accumulation by AoSMCs are down-regulated by the metabolic sensor SIRT1.

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

87 ontexts, we found that the gene GDPGP1/mcp-1 is down-regulated by a variety of stresses.

88 erior part of the default-mode network (DMN) is down-regulated by both normal ageing and Alzheimer's

89 2 in an autocrine manner, and PGE2 secretion is down-regulated by cell-to-cell contact, attenuating i

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

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

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

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

94 in culture showed that LINC00346 expression is down-regulated by p53.

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

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

97 suppressor, and we establish herein that it is down-regulated by the miR-23b cluster, which is cruci

98 al knockdown experiments, we found that BCL2 is down-regulated by TNF inhibition.

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

100 hereas the ammonia-transporting RhBG protein was down-regulated by about 50%.

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

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

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

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

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

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

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

108 unaffected by inhibition of mTOR, unless RHA was down-regulated by siRNA.

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

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

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

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

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

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

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

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

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

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

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

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

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

122 ifies a class of lipids, acyl-carnitines, as being down-regulated during Wolbachia infection.

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

124 cells at the BBB, then demonstrated that DHH is down-regulated during experimental autoimmune encepha

125 PRMT5 is down-regulated during infection and the prmt5 mutant

126 O-GlcNAc signaling is down-regulated during macrophage proinflammatory acti

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

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

129 In BRAF-mutant melanoma, Dnmt1 was down-regulated during response to B-Raf and MEK inhi

130 eral genes related to antimicrobial function were down-regulated during ACS compared to VOC.

131 d that genes related to erythroid maturation were down-regulated during acute infections, whereas imm

132 verall a significant number of small GTPases were down-regulated during adipogenesis.

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

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

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

136 Kv4.2 channel expression is down-regulated following hippocampal seizures and in

137 HDAC4 and HDAC5 were down-regulated following SPS, and these changes wer

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

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

140 This pathway is down-regulated homeostatically when fasting causes in

141 Many cell wall related genes are down regulated in mus-3 mul-1.

142 us genes involved in gemcitabine sensitivity are down regulated in the resistant line upon CM03 treat

143 ed from distinct genes of pre-tRNA(His), and are down-regulated in CLL 3- to 5-fold vs. normal B cell

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

145 regulate oxidative stress in the lean state are down-regulated in obesity as a consequence of inflam

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

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

148 Other glossy genes tended to be down-regulated in glossy mutants; by contrast stress-

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

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

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

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

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

154 ZPR1 is down regulated in SMA patients.

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

156 per pilosebaceous unit of normal human skin, is down-regulated in acne.

157 Interestingly, we find that Gish expression is down-regulated in aging guts and that increasing Gish

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

175 is a widely distributed nuclear lncRNA that is down-regulated in NAFLD.

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

177 which encodes a stathmin family protein and is down-regulated in PD brains, as a key regulator funct

178 trophoblast and that ETC protein expression is down-regulated in placentas of infants with intrauter

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

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

181 We show that MAOA is down-regulated in primary NPC tissues and its down-re

182 tive regulator of adipocyte differentiation, is down-regulated in RCC and shows a differential expres

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

184 Moreover, miR-26a is down-regulated in serum exosomes and islets of obese

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

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

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

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

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

190 some studies have demonstrated that miR-27b is down-regulated in the oral specimens of patients suff

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

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

193 D(+)-dependent deacetylase Sirtuin 1 (SIRT1) is down-regulated in triple-negative breast cancer.

194 r partial hepatectomy, we found that DN-DBC1 is down-regulated in vivo during regeneration.

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

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

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

198 MICA expression was down-regulated in advanced fibrosis stages.

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

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

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

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

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

204 Further, SMAD/TGF-beta1 signaling was down-regulated in CSF plasmablasts/plasma cells.

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

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

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

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

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

210 ysaccharides and related regulatory systems, was down-regulated in host-like media when compared to M

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

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

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

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

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

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

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

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

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

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

221 -glucose co-transporter 2 (Sglt2) expression was down-regulated in RPTs of both male and female KO mi

222 The Cancer Genome Atlas and found that MBNL1 was down-regulated in several common cancers.

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

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

225 ch was highly expressed in CCA human tumors, was down-regulated in SOX17-transduced CCA cells.

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

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

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

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

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

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

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

233 EHD2 expression itself was down-regulated in the visceral fat of two obese mous

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

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

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 ement (ABRE) element within their promoters, were down-regulated in AtVIP2 overexpressor lines.

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

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

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

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

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 that play a pivotal role in memory function, were down-regulated in head trauma-related disorders.

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

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

248 -1271, miR-145, miR-99b, miR-191 and miR-10b were down-regulated in low RFI pigs.

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

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

251 arkers (Lgr5, Olfm4, Smoc2, Msi1, and Ascl2) were down-regulated in organoids incubated with etomoxir

252 t-tagged miR in cells where PLCbeta1 or C3PO were down-regulated in PC12 cells and find substantial d

253 Over 90% (n = 1767) of these genes were down-regulated in PDX models and enriched in stroma

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

255 2-mediated oxidative stress response pathway were down-regulated in PMNs of diseased patients.

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

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

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

259 0.75, respectively; P < 0.05); both pathways were down-regulated in the greatest-ADG compared with le

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

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

262 In contrast, inflammation-related genes were down-regulated in the RV and while oxidative phosph

263 cS), and enzymes of chlorophyll biosynthesis were down-regulated in the yellow leaf tissue.

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

265 %) of S-palmitoylation sites on 254 proteins were down-regulated in Zdhhc13-deficient mice, represent

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

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

268 found reduced in human cancers, but how PTEN is down-regulated is not fully understood.

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

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

271 was upregulated and Bcl-2 and Bcl-xL levels were down-regulated on treatment with PRF/BCP.

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

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

274 cohorts demonstrate that MPI gene expression is down-regulated proportionate to fibrosis in chronic l

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

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

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

278 n which the transcriptional activity of FlrA is down-regulated through a negative feedback loop.

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

280 ved in iodine efflux during oxidative stress are down-regulated under increasing pCO(2) , suggesting

281 DH kinase 1, highly expressed under hypoxia, is down-regulated under normoxic conditions, leading to

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

283 ynthesis, as well as photosynthetic activity were down-regulated under the same conditions.

284 lk between AnxA8 and Wnt signalling, as both are down-regulated upon fenretinide (FR)-mediated RPE tr

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

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

287 , whereas negative regulators of the pathway were down-regulated upon NANOG expression.

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

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

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

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

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

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

294 2 days earlier than normal MT channels, and being down-regulated with the emergence of the normal ch

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

296 lycemic wild type mice, renal Bmf expression was down-regulated with up-regulation of hnRNP F.

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

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

299 expression of many fewer genes, 77% of which were down-regulated with no significant enrichment of KE

300 astly, a putative target of RORbeta, Thsd7a, is down-regulated without RORbeta, and Thsd7a knock-out