ライフサイエンスコーパス: be downregulated in

1 Here we show that miR-148a is downregulated in 15 out of 16 samples (94%) of cancer

2 Moreover, miR-26 was downregulated in 2 obese mouse models compared with

3 ression of an ERBB3-binding protein 1 (EBP1) is downregulated in 8-day old hamster ovaries concurrent

4 rotein levels of Notch receptors and ligands are downregulated in a time- and learning-specific manne

5 t nuclear receptor binding protein 1 (NRBP1) is downregulated in a range of human tumours, where low

6 We show that Sin3A is downregulated in a variety of human tumors and that S

7 D21A transcript, protein and activity levels were downregulated in a largely ERFVII-dependent manner.

8 We show that RARRES2 expression is downregulated in ACC as compared with normal and beni

9 tabolic pathways, and OXPHOS proteins in SAT are downregulated in acquired obesity, and are associate

10 We have shown that TIMP3 is downregulated in adipogenesis, and by inflammatory si

11 of which Neurod1, Enpp1, Slc27a2, and Plcxd1 are downregulated in adult mutant mice.

12 nd EGFR signaling, induced in early SCC CSC, were downregulated in advanced SCC.

13 asthmatic patients (P < .05), whereas PGES2 was downregulated in AEC-HLF cocultures (2.2-fold, P < .

14 KL is downregulated in airways from COPD patients.

15 ocaine- and amphetamine-regulated transcript was downregulated), in alignment with leptin suppression

16 factor 1 (WIF1), a secreted Wnt antagonist, is downregulated in all human primary cervical tumors an

17 miR-30c is downregulated in AML, especially in normal karyotype

18 CXXC5 mRNA was downregulated in AML with MLL rearrangements, t(8;21

19 After DNA damage, cyclin F is downregulated in an ATR-dependent manner to allow acc

20 d with the cell cycle and cell proliferation were downregulated in aneuploid cells.

21 TIE2 expression was downregulated in angiogenic ECs, which abundantly ex

22 IRS1 mRNA and protein levels were downregulated in aortae of hypertensive rats.

23 ferator-activated receptor gamma (PPARgamma) is downregulated in APCs isolated from the lungs of emph

24 Here we found that ACE2 was downregulated in apelin-deficient mice.

25 viously unknown, primate-specific miRNA that is downregulated in ASD and that regulates the epidermal

26 lated, whereas genes linked to proliferation are downregulated in ASN absence.

27 ant and malignant skin neoplasia, E-cadherin is downregulated in association with reduced XPC and DDB

28 Several genes that oppose T cell activation were downregulated in asthma, suggesting enhanced activa

29 d that the expression of miR-145/143 cluster was downregulated in astrocytic tumors compared to norma

30 ses in expression of the miRNA miR30a, which is downregulated in ATC compared with differentiated thy

31 We found that miR-26 was downregulated in atrial samples from AF animals and

32 We found that Ets1 is downregulated in B cells by BCR or TLR signaling thro

33 PAX6 was downregulated in beta cells of diabetic db/db mice a

34 termined that a regulator of Dnmts, miR-29b, is downregulated in bone marrow of dKI AML mice.

35 pha7 nAChR-dependent calcium signal cascades are downregulated in both 15q13.3 deletion and duplicati

36 al structures, including multiple mRNAs that are downregulated in both inhibitory GABAergic and excit

37 In addition, NDY1-regulated miRNAs are downregulated in both normal and cancer mammary stem

38 Compared with normal human skin, SIRT1 is downregulated in both AD and non-AD lesions.

39 We found that Ctgf expression is downregulated in both Wnt1-Cre; Tgfbr2(fl/fl) and Osr

40 Additionally, PTCH1 expression was downregulated in both clusters suggesting involvemen

41 of the prosurvival Bcl-2 family member Mcl-1 was downregulated in both mir-125a-overexpressing IEC-6

42 Renal levels of PPARalpha were downregulated in both type 1 and type 2 diabetes mo

43 hat the highly conserved brain miRNA miR-219 is downregulated in brain tissue taken at autopsy from p

44 ZBTB4 is downregulated in breast cancer and modulates p53 resp

45 B4 (zinc-finger and BTB domain containing 4) is downregulated in breast cancer patients, and that its

46 ential cellular functions, Pfn1's expression is downregulated in breast cancer, the significance of w

47 CALML3 expression is downregulated in breast cancers and transformed cell

48 Here we report that miR-873 is downregulated in breast tumor compared with normal ti

49 identified one Wnt target gene, Pitx2, that was downregulated in Brg1 mutant endothelial cells but w

50 e led to the misconception that these miRNAs are downregulated in cancer.

51 MicroRNA-26 was downregulated in canine AF atria; experimental micro

52 , a protein expressed in cardiomyocytes that was downregulated in cardiac hypertrophy and human heart

53 at PPM1F messenger RNA levels in human blood were downregulated in cases with symptoms of comorbid PT

54 ways and functions of the measured cytokines were downregulated in cases, except cell death pathways,

55 h the adult prostate or CD133-PrEC, and RBM3 is downregulated in cells cultured in soft agar or expos

56 In addition, IRAK1 expression is downregulated in cells transfected with miR-K9 and du

57 e expression of 10 DNA damage response genes was downregulated in cells treated with etoposide and si

58 erently expressed, 2 were upregulated and 14 were downregulated in children with active CMA compared

59 lum calcium-ATPase type 2a, Kv1.4, and Kv4.3 were downregulated in CKD rats.

60 nds, growth arrest-specific 6 and Protein S, were downregulated in classically activated cells.

61 Clinically, SCP1 and SCP3 are downregulated in clear cell renal cell carcinoma (cc

62 were enriched in cancer-related pathways and were downregulated in clinical metastatic versus localiz

63 viously, we could show that miR-138 and -424 are downregulated in CLL cells.

64 er regulator class II transactivator (CIITA) are downregulated in CML compared with non-CML stem/prog

65 In contrast, SPARC was downregulated in CN-AML patients harboring mutations

66 1), a crucial player in pyruvate metabolism, is downregulated in colon adenocarcinomas.

67 Finally, we show that PEA15 expression is downregulated in colon, breast, and lung cancer sampl

68 The expression of miR-502 was downregulated in colon cancer patient specimens comp

69 MiR-873 has been revealed to be downregulated in colorectal cancer and glioblastoma.

70 n the colon and are consistently reported as being downregulated in colorectal and other cancers.

71 evels of lipoprotein ApoA1 expression, which is downregulated in Crohn's disease patients and causall

72 v3310 gene product SapM, previously shown to be downregulated in D-Mtb.

73 During the L1/L2 transition, OIG-1 is downregulated in DD neurons by the transcription fact

74 in the nuclei of follicle cell epithelia and is downregulated in delaminating epithelia as expression

75 anistic target of rapamycin (mTOR) signaling is downregulated in dGBA knock-out flies, with a concomi

76 hanistic target of rapamycin (mTOR) activity is downregulated in dGBA-deficient flies and rapamycin a

77 ependent on adequate GLP1R expression, which is downregulated in diabetes.

78 cell survival through inhibition of FOXO3a, was downregulated in diabetic CD34(pos)-PCs and inversel

79 Accordingly, miR-200s are downregulated in Dicer-KO CDs, its direct target gen

80 Nr3c1, and confirmed our prediction that Fos is downregulated in diminuendo homozygotes.

81 ls multiple tumour suppressive functions and is downregulated in diverse types of human cancers throu

82 Moreover, the FGF10 pathway is downregulated in Dlx5(-/-) mice, and activation of FG

83 example, ERO1LB, DOCK10, IGSF11, and PRR14L were downregulated in donors with hyperglycemia and corr

84 Here we show that RLIM levels are downregulated in embryonic cells undergoing rXCI.

85 d in Klf5 knockout (KO) embryos at E3.0, and was downregulated in embryos overexpressing Klf5 Further

86 Previously, we found that LZTFL1 is downregulated in epithelial tumors, including lung ca

87 Consequently, miR-200c was downregulated in ERG-positive PCa, and miR-200c targ

88 1 expression, and consequently IdoA content, was downregulated in ESCC cells.

89 pidermal expression of complement components was downregulated in ex vivo injured skin lacking the st

90 ciated with calcium channel trafficking that is downregulated in failing hearts.

91 colleagues demonstrate that AIRE expression is downregulated in females as the result of estrogen-me

92 d ECM proteins are targets for miR-29, which was downregulated in fibroblasts grown on IPF-derived EC

93 The expression of AaGPx3 was downregulated in fungal strains carrying defective N

94 ether, these data suggest that, although BLM is downregulated in G1 phase in order to promote NHEJ-me

95 These results demonstrate that miR-145 is downregulated in glial tumors and its low expression

96 lity for small molecular tracers, and Cyp1b1 was downregulated in glioma vessels in which BBB functio

97 r (G-CSF) receptor-triggered granulopoiesis, is downregulated in granulocytic progenitors of severe c

98 and Lamc2 as novel NNE-expressed genes that are downregulated in Grhl2 mutants.

99 I is an imprinted tumor-suppressor gene that is downregulated in >60% of ovarian cancers, and its los

100 ere, we demonstrated that expression of FBP1 was downregulated in HCC patient specimens and decreased

101 The expressions of miR-200c and miR-141 were downregulated in HCC-BDTT (4.5- and 4.8-fold decrea

102 P2Y14 R is downregulated in hCPCs derived from HF patients with

103 P2Y14 R was downregulated in hCPCs derived from patients with a

104 expression of several of the same genes that were downregulated in HCT116 cells, including the MYC on

105 e mRNA levels of key striatal genes known to be downregulated in HD.

106 ived neurotrophic factor (BDNF), a gene that is downregulated in HD, in the presence of mutant Htt.

107 the most striking change was for TLR5, which was downregulated in healthy smokers (1.4-fold, p < 10(-

108 Ten genes important in cardiac metabolism were downregulated in heart failure, with SLC27A4 and KC

109 PEPCK and G6Pase transcript levels are downregulated in hepatocytes from GCN5L1 liver speci

110 roduct, damaged DNA-binding protein (DDB)-2, is downregulated in high-grade colon cancers, and it pla

111 s robustly regulated by BDNF/TrkB signaling, is downregulated in hippocampus (male/female) and upregu

112 how that expression of the MHC class I genes is downregulated in HPV-positive keratinocytes in an E7-

113 oded in the same miR cluster (miR-23b/-27b), are downregulated in human metastatic prostate cancer co

114 m (CNS)-specific PGC-1alpha (CNS-PGC-1alpha) are downregulated in human PD brain, in A30P alpha-syn t

115 domain-containing 1 (PDZK1) was revealed to be downregulated in human clear cell renal cell carcinom

116 LIFR is downregulated in human breast carcinomas and inversel

117 Here we show that RSPO2 expression is downregulated in human colorectal cancers (CRCs) due

118 iovascular profile comparable to apelin, and is downregulated in human disease and rodent PAH models,

119 The novel JMC protein SPEG is downregulated in human failing hearts.

120 tent with tumor suppression, CCN1 expression is downregulated in human HCC.

121 Importantly, FOXA1 is downregulated in human NEPC tumors compared to primar

122 NOV is downregulated in human prostate cancer wherein AR and

123 Further, this pathway was downregulated in human Alzheimer's Disease (AD) brai

124 eceptor 1-related protein y/CD46) expression was downregulated in human and murine OB; and C3a, a mar

125 We showed that expression of RORalpha was downregulated in human breast cancer tissue and cell

126 Furthermore, SIN3B was downregulated in human prostate adenocarcinoma corre

127 the transcriptional level and, like JunB, it was downregulated in human squamous cell carcinoma cells

128 SIRT2 protein expression levels were downregulated in hypertrophic hearts from mice.

129 We demonstrated that the level of PRDX3 was downregulated in ICP placentas as well as bile acids

130 tion indicated that mRNA for L-NFL and NF132 was downregulated in identified reticulospinal neurons b

131 nes, chemokines, and anti-microbial peptides were downregulated in Ikkepsilon-deficient tissues, subs

132 ceptor associated with synaptic development, was downregulated in IL after fear extinction.

133 NA) expression profile identified genes that were downregulated in ILT3-induced human CD8(+) T suppre

134 We found that HPSE mRNA is downregulated in in vitro-expanded T cells, which may

135 showed that tight junction protein occludin was downregulated in induced cells.

136 In humans, ESRP1 is downregulated in inflamed biopsies from inflammatory

137 in contrast to RGCs, neither c-myc nor mTOR was downregulated in injured peripheral sensory neurons.

138 xpression levels of the chIL-17RA transcript were downregulated in intestinal tissues from chickens i

139 processes, e.g., p21, Brca1, and E-cadherin, were downregulated in K5.CtBP1 skin.

140 ther small GTPases, including Rab3 and Rab7, was downregulated in kidneys from Ctns-/- mice and in hu

141 As expected, CIITA was downregulated in LCLs.

142 beta-ketoacyl CoA synthase gene (PotriKCS1) was downregulated in leaves from non-alkene-producing ac

143 of the stearoyl-CoA desaturase 1 (Scd1) gene is downregulated in LSCs and that Scd1 plays a tumor-sup

144 ruppel-like family of transcription factors, is downregulated in lung cancer cell lines that have bee

145 In this study, we confirmed that GPC5 was downregulated in lung adenocarcinoma tissues compare

146 In this study, we found that miR-27a is downregulated in macrophages following stimulation th

147 gland-specific genes and mitochondrial genes were downregulated in males with resistant Y chromosomes

148 es a polycomb group protein that is known to be downregulated in many types of human cancers, althoug

149 apoptosis activators and tumor suppressors, being downregulated in many human cancers, although thei

150 r of cancer cell invasion and its expression is downregulated in many advanced, poorly differentiated

151 Subunits alpha4 and delta were downregulated in maternal LS, likely reflecting a r

152 dency for dexamethasone-upregulated genes to be downregulated in MCN patients.

153 d that basic fibroblast growth factor (bFGF) was downregulated in MDA-MB-231-injected tibiae from the

154 ated receptor gamma (PPARG/Pparg) expression was downregulated in mDCs of smokers with emphysema and

155 order (MDD) have noted that the cAMP cascade is downregulated in MDD and upregulated by antidepressan

156 ly, a previous report showed that CtBP1 mRNA was downregulated in melanoma.

157 oded by the same miR cluster (miR-23b/-27b), are downregulated in metastatic, castration-resistant tu

158 BAP1 was downregulated in metastatic adenocarcinoma breast ce

159 wer in AS(-/-) mice than in AS(+/+) mice and was downregulated in mice of both genotypes in response

160 ing and TGFbeta-regulated genes encoding ECM are downregulated in Mkl2(-/-) ES cells and the vasculat

161 ied a putative STAT3 target gene, NR4A3 that was downregulated in MKN28 GC daughter cells overexpress

162 A conserved RNA-binding protein that is downregulated in most animals as they develop from em

163 stem cells of 11 adults with ASD that MOCOS is downregulated in most of them when compared with 11 a

164 Of interest, miR-29 was downregulated in most HCV-infected patients.

165 at ten-eleven translocation protein 1 (TET1) was downregulated in mouse nucleus accumbens (NAc), a ke

166 GAP is a critical tumor suppressor gene that is downregulated in multiple aggressive cancers, such as

167 We find that LINC-PINT is downregulated in multiple types of cancer and acts as

168 omponents of the myostatin signaling pathway is downregulated in muscle wasting or atrophying disease

169 ion at baseline in fresolimumab nonimprovers were downregulated in mycophenolate mofetil improvers, s

170 y stages of oligodendrocyte development, but are downregulated in myelinating oligodendrocytes.

171 proteins involved in fatty acid utilization were downregulated in myocardial samples from the failin

172 dditionally, we found that IQGAP1 expression was downregulated in myofibroblasts associated with huma

173 xpressed in haemogenic endothelium cells and is downregulated in nascent blood precursors.

174 Since the newly identified pathways are downregulated in neurodegenerative diseases, includi

175 d ST8sia6) that mediate alpha2,8 sialylation are downregulated in NKAP-defcient RTEs.

176 reast cancer metastasis suppressor 1 (BRMS1) is downregulated in non-small cell lung cancer (NSCLC),

177 MUC1-CT-GRalpha complex was downregulated in NP-CR tissue.

178 cGK (cGMP-dependent protein kinase) activity was downregulated in Npr2(+/-) valves, and CNP triggered

179 TIA1 is reported to be downregulated in obese patients, although it is not k

180 sive role for human adipose tissue function, being downregulated in obesity and increased during diff

181 ation and restricted cell motility (SHROOM2) was downregulated in OE21 but upregulated in OE33 cells.

182 sion, Dpp signaling is extinguished, and Nos is downregulated in one daughter cell, causing it to swi

183 Here we demonstrated that miR-26a is downregulated in osteosarcoma CSCs when derived by ei

184 While CHIP is downregulated in ovarian carcinoma, induced expressio

185 -200a-429, miR-200c-141, and miR-183-96-182, were downregulated in p21-deficient cells.

186 miR-424 and miR-503 were downregulated in PAH, exerted antiproliferative eff

187 However, miR-424 is downregulated in patient metastases versus matched pr

188 e found that the expression level of miR-19b is downregulated in patients with idiopathic rapid eye m

189 d by the histone demethylase JARID1B, MANTIS was downregulated in patients with idiopathic pulmonary

190 Expression of PPAR-gamma was downregulated in patients with preeclampsia compared

191 vation cohort, one of these miRNAs, miR-150, was downregulated in patients with remodeling (DeltaEDV>

192 LP, in vitro mineralization, and osteonectin were downregulated in PDL cells.

193 Here we show that miR-125a is downregulated in peripheral CD4(+) T cells of human a

194 cer of actin-depolymerizing factor activity, is downregulated in platelet messenger RNA (mRNA) from s

195 FSGS patients and PAN-treated rats, miR-30s were downregulated in podocytes.

196 regulator of pulmonary differentiation that is downregulated in poorly differentiated lung adenocarc

197 Finally, we show that Gomafu is downregulated in post-mortem cortical gray matter fro

198 Accordingly, BDNF was downregulated in post-dependent rats on microarray a

199 on levels of the majority of imprinted genes are downregulated in primary tumors compared to normal c

200 Further analyses showed that CASP7 is downregulated in primary prostate tumors and metastat

201 which belongs to the largest RTK Eph family, was downregulated in primary B cells post-EBV infection

202 abundantly expressed in healthy corneas and is downregulated in proinflammatory conditions.

203 PPARD was downregulated in prostate cancer specimens.

204 rget of rapamycin complex 1 (mTORC1) pathway was downregulated in proximal tubular cell lines derived

205 N-termini of several proteases were downregulated in prt6, including RD21A.

206 f the same genes were independently found to be downregulated in Q175 KI mice compared to WT (5.2e-7

207 d that miR-205 promotes radiosensitivity and is downregulated in radioresistant subpopulations of bre

208 19a-3p, broadly conserved among vertebrates, was downregulated in RAW264.7 macrophage cells of the M2

209 GRHL2 was downregulated in recurrent mouse tumors that had evo

210 nt with these data, Gtl2-Dio3-encoded miRNAs are downregulated in regenerating Mef2a knockout muscle,

211 Sirt6 is downregulated in renal biopsies from patients with po

212 NC1 is specifically expressed in kidney, and is downregulated in renal cell carcinoma; also, its low

213 EM2, FRAS1 was absent and the other proteins were downregulated in rescued kidneys, consistent with a

214 ine pigment epithelium-derived factor (PEDF) is downregulated in resected human brain metastases of b

215 se in patients with breast cancer, and Par-4 is downregulated in residual tumor cells that survive ne

216 sistant neuroblastoma cells, wherein miR-137 is downregulated in resistant cells.

217 egulator of receptor tyrosine kinases (RTK), is downregulated in resistant derivatives of breast canc

218 medulloblastoma-specific GLI1 binding sites are downregulated in response to JQ1 treatment, supporti

219 cyclin-D1, and less mRNA from Hath-1, which is downregulated in response to Wnt.

220 ways, MAPK pathway, as well as redox enzymes were downregulated in response to disruption of glutamin

221 a microRNA predicted to target MDM4 (miR191) was downregulated in retinoblastoma relative to human fe

222 data sets showed that wild-type switch genes are downregulated in ripening-deficient mutants.

223 ich inhibit serotonin synthesis and release, are downregulated in SAD, and serotonin transporter avai

224 cl (Fanconi anemia, complementation group L) is downregulated in SALL4B Tg leukemic and pre-leukemic

225 Last, p21-activated kinases (PAKs) were downregulated in SAP102 KD neurons.

226 s and bioinformatics analysis show that Ate1 is downregulated in several types of human cancer sample

227 responsive genes, which promote cell growth, were downregulated in shoot apices that accumulated incr

228 involved in cellular redox homeostasis which is downregulated in skeletal muscle differentiation.

229 We find that the SPAR-encoding lncRNA is downregulated in skeletal muscle upon acute injury, a

230 we show that expression of Baf60c and Deptor was downregulated in skeletal muscle in obesity, accompa

231 c basis for previous observations that SRPK1 is downregulated in some cancer contexts and upregulated

232 sis of cultured valve interstitial cells and is downregulated in stenotic aortic valves.

233 -beta and guanylate-binding proteins (GBPs), are downregulated in STING knockout (KO) macrophages inf

234 A, a key enzyme in cAMP and cGMP catabolism, is downregulated in striatal projections to entopeduncul

235 Notably, Pla2g1b was downregulated in susceptible mice and inhibited by I

236 volved in the development of hemopathies and is downregulated in T-lymphomas, such as anaplastic larg

237 Interestingly, miR-873 was observed to be downregulated in tamoxifen-resistant MCF-7/TamR cells

238 roduction and subsequent T cell recruitment, is downregulated in TAMs through Mer tyrosine kinase-dep

239 hat the microRNA (miRNA) cluster miR-132/212 is downregulated in tauopathies such as AD.

240 orthologue (14-3-3 protein zeta/YWHAZ) that was downregulated in temporary ponds in both species.

241 actin cytoskeleton (including Rock1, Rock2) were downregulated in TFAP2C-depleted embryos.

242 Zeb2 levels are downregulated in the embryonic rodent midbrain durin

243 egulators, including cyclin D1 and survivin, are downregulated in the germinative zone of the MAPK1-d

244 tly repress transcription of many genes that are downregulated in the mammal.

245 itories in the mouse, as E-cadherin needs to be downregulated in the primitive streak and in the epib

246 in-mitochondria), was uniquely identified as being downregulated in the DeltaHog1 background during g

247 itis, an animal model of multiple sclerosis, is downregulated in the brain at onset and peak of disea

248 levated in the egg apparatus at maturity but is downregulated in the central cell.

249 xcellent study revealing that MPL expression is downregulated in the context of the mutant protein, J

250 Our results show that beta-actin is downregulated in the corneal stroma of patients with

251 s an endogenous neuroprotective peptide that is downregulated in the diabetic eye.

252 We also observed that CDK2 is downregulated in the glomeruli of obese Zucker rats b

253 ecific polyadenylation protein CFIm25, which is downregulated in the human seminomas.

254 Furthermore, GPR35 expression is downregulated in the lungs of Cxcl17(-/-) mice, which

255 Elafin is downregulated in the majority of breast cancer cell l

256 Plexin-B2 expression is downregulated in the olfactory bulb as interneurons i

257 transmembrane ligand for the NOTCH receptor, is downregulated in the PTEN-null fibroblasts leading to

258 molecule shown to inhibit Calcium signaling, was downregulated in the absence of DKK3.

259 tures compared with the Fgmcm1 mutant, which was downregulated in the expression of genes involved in

260 oreover, CD55 was upregulated, whereas RANKL was downregulated in the gingival tissue of the 10 mug/k

261 We found that Hand2 expression was downregulated in the hindlimb field and that Shh exp

262 After seroconversion, perforin expression was downregulated in the lamina propria, but not in the

263 lectin, critical for T-cell entry into skin, was downregulated in the majority (52%) of MCCs (n=56),

264 Sonic hedgehog (Shh) signal transduction was downregulated in the mutant forebrain, consistent wi

265 sion of genes for several thylakoid proteins was downregulated in the mutants, but the relative level

266 During ischemic stroke, Bif-1 expression was downregulated in the penumbra of wild-type mice.

267 arginine-specific proteinase, respectively, was downregulated in the pgn_1932 mutant.

268 The expression of the beta-actin gene was downregulated in the stroma of the six KC corneas bu

269 inants of H. ducreyi adherence to HFF cells, were downregulated in the csrA mutant.

270 hich 46 genes were upregulated and 200 genes were downregulated in the fibrotic cell lines compared t

271 microarray analysis revealed that 152 genes were downregulated in the hippocampal dentate gyrus regi

272 Consistently, these three molecules were downregulated in the induced pluripotent stem cell-

273 ole in regulating free fatty acid metabolism were downregulated in the livers, but not in the adipose

274 inal mucus showed that 60% of the genes that were downregulated in the luxO mutant were involved in a

275 ceptor (PPAR)-gamma coactivator (PGC)-1beta, were downregulated in the M-ERRalpha(-/-) muscles at the

276 Both CCNE2 and CDC6 were downregulated in the microarray data.

277 Geh lipase) and low-molecular-weight toxins were downregulated in the mutant.

278 t, the ETEC colonization factors CS1 and CS3 were downregulated in the presence of bile, consistent w

279 enes known to be involved in spermatogenesis were downregulated in the testes of knock-out mice, as w

280 gulated and miR-122, miR-296-5p and miR-503# were downregulated in the uninvolved colonic mucosa of A

281 MUC1 expression was downregulated in these patients.

282 Cxcl3 is downregulated in Tis21-null GCPs of EGL and lesions;

283 carried out by glucose transporter 3 (GLUT3) was downregulated in TKI-sensitive LAD cells.

284 s, p-mTOR (p=0.03) and PI3K-alpha (P = 0.04) were downregulated in treatment responsive residual tumo

285 Both miRs were downregulated in tumor necrosis factor (TNF)-alpha-

286 ure products of MIR-491 (miR-491-5p and -3p) are downregulated in tumors compared with the normal bra

287 In addition, miR-339-5p expression is downregulated in tumors harboring wild-type TP53, sug

288 Niche-associated genes CD144 and ABCB5 were downregulated in tumors derived from CD133 knockdow

289 rmal fibroblasts following skin wounding but was downregulated in tumour stroma.

290 ugh earlier reports showed that BR signaling is downregulated in twd1, how TWD1 is integrated in BR s

291 ough expression of CRTH2 on blood leukocytes is downregulated in UC, CRTH2 is present in colon tissue

292 inal epithelium and that SERPINA1 and Elafin were downregulated in vaginal tissues from women with PO

293 important in maintaining podocyte function, is downregulated in various glomerular diseases.

294 Sef is downregulated in various human carcinomas, in a manne

295 changes in mitochondrial membrane potential, is downregulated in vascular smooth muscle cells in cult

296 n2 and ODDSOC2, repressors of flowering that are downregulated in vernalized plants.

297 ) modulates S1P-dependent responses; and (3) is downregulated in vitro and in vivo by tumor necrosis

298 the TCR strength for optimal Foxp3 induction is downregulated in vitro.

299 persisted in Mmp10(-/-) BMDM long after they were downregulated in wild-type cells.

300 Camp gene expression was downregulated in young BBdp rat islets before the on