ライフサイエンスコーパス: be downregulated in

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

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

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

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

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

6 ter, was identified, my lab observed that it was downregulated in adipocytes but not in skeletal musc

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

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

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

10 et ITPR1 (confirmed by luciferase assay) and was downregulated in AF atrial cardiomyocytes; microRNA-

11 egulator of G protein-coupled receptors that is downregulated in aggressive human prostate tumors.

12 KL is downregulated in airways from COPD patients.

13 nuclear mitotic apparatus protein 1 (NuMA1) is downregulated in AIS-deficient neonatal mouse brains

14 FXR was downregulated in all hepatocyte cell lines and prima

15 these families revealed that Zo-1 and Cldn18 were downregulated in all phenotypes, while increased Cl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

33 We found that TFEB is downregulated in both human and mouse aortic aneurysm

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

35 This miR was downregulated in both ED groups (ie, ED and RGED).

36 s, we identified lncRNA 1810058I24Rik, which was downregulated in both human and murine myeloid cells

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

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

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

40 miR-127 is downregulated in breast cancer, where it has been sho

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

42 Mucin 1-CT expression was downregulated in bronchial epithelial cells and peri

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

44 Notably, USP11 is downregulated in cancer patients, and correlates with

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

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

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

48 Some proapoptotic genes were downregulated in caspase-3-proficient cells.

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

50 that approximately two-thirds of transcripts were downregulated in cells expressing any of these vira

51 The expression of IL-17RD is downregulated in certain solid tumors, which has led

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

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

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

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

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

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

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

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

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

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

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

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

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

65 eport that protein kinase C (PKC)lambda/iota is downregulated in de novo and during therapy-induced N

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

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

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

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

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

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

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

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

74 Wnt signaling is downregulated in embryonal rhabdomyosarcoma (ERMS) an

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

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

77 K effector phospho-myosin light chain (pMLC) were downregulated in endothelial cells by severe hypoxi

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

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

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

81 In vitro, hsa_circ_0001445 was downregulated in extracellular vesicles secreted by

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

83 l death, inflammation, and tuft cell markers were downregulated in fat-1 mice in response to EtOH, wh

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

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

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

87 Th17 cell differentiation was downregulated in galectin-9-deficient T cells, and t

88 sis demonstrates that several of these genes are downregulated in GBM, potentially through epigenetic

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

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

91 S, 3 h), both pheromone and opioid signaling were downregulated in gpa-3 mutants.

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

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

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

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

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

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

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

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

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

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

102 is showed that most of the identified miRNAs were downregulated in heat-treated groups.

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

104 nteracting proteins, GSK3alpha and GSK3beta, were downregulated in Het mice, whereas the levels of PD

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

106 miR-186 was downregulated in high-risk neuroblastoma patients, a

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

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

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

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

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

112 e found that enteric NCC express LAMR, which is downregulated in human and murine HSCR.

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

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

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

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

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

118 t with this phenotype, WWP2 expression level is downregulated in human OA cartilage.

119 NOV is downregulated in human prostate cancer wherein AR and

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

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

122 MiR-30e-3p was downregulated in human and rat HCCs, and its downreg

123 In addition, expression of miR-1185-1 was downregulated in human colorectal cancer tissues, wh

124 ion of hormone-sensitive lipase (HSL), which was downregulated in human PDAC.

125 Furthermore, SIN3B was downregulated in human prostate adenocarcinoma corre

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

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

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

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

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

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

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

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

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

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

136 accumulating evidence indicates that Geminin is downregulated in late S-phase due to an unknown mecha

137 As expected, CIITA was downregulated in LCLs.

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

139 ling that all but one of the piRNAs examined are downregulated in leprosy skin lesions.

140 acearum": the apoptosis-inducing factor AIF3 was downregulated in LsoA-infected psyllids, while the i

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

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

143 concomitant with NAMPT upregulation, miR410 is downregulated in lungs of mice exposed to hypoxia-ind

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

145 om P. chabaudi chabaudi AS-infected mice and is downregulated in Malat1(-/-) Th1 and Th2 cells.

146 cision induced Emr1 and Irf8 gene expression was downregulated in males, but not in females, followin

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

148 We show that edited CYb mRNA is downregulated in mammalian bloodstream forms (BSF) at

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

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

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

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

155 BAP1 was downregulated in metastatic adenocarcinoma breast ce

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

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

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

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

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

161 9 (miR-29) negatively regulates fibrosis and is downregulated in multiple fibrotic organs and tissues

162 hypertrophy-promoting protein that we showed is downregulated in multiple mouse models of cancer cach

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

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

165 One protein in particular, COPBI, was downregulated in mutant FUS-expressing cells under s

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

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

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

169 The tumor-suppressive miR-186 that is downregulated in neuroblastoma and in TGFbeta-treated

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

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

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

173 CLDN1 and CLMP expression were downregulated in nonresponding hairdressers and pat

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

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

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

177 We recently showed that DNAJB3 co-chaperone is downregulated in obese and diabetic patients and that

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

179 ant in eye development and phototransduction were downregulated in oil-exposed larvae, with an increa

180 MicroRNA-509 was reported to be downregulated in OS.

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

182 While CHIP is downregulated in ovarian carcinoma, induced expressio

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

184 indicated that the expression of miR-522-3p was downregulated in paclitaxel-resistant cells.

185 is therapeutically promising, yet how BMPR2 is downregulated in PAH is unclear.

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

187 Finally, DGCR8 was downregulated in pathologically and naturally aged h

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

189 urthermore, both FLG and HRNR protein levels are downregulated in patients with atopic dermatitis.

190 Given that PPP1R3A is downregulated in patients with AF, this regulatory su

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

192 Finally, microRNA 218-5p, which is downregulated in patients with IPF, suppressed 15-PGD

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

194 show that the AGEs clearance receptor AGER1 was downregulated in patients with NASH and diabetes and

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

196 nverted 1 (MAGI1), and MAGI2 mRNA expression was downregulated in patients with severe ACD.

197 (FLG1), FLG2, and loricrin (LOR) expression were downregulated in patients with ACD.

198 levels of circRNAs DNAJC6, TMEM56 and MBOAT2 were downregulated in patients with HCM.

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

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

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

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

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

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

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

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

207 PPARD was downregulated in prostate cancer specimens.

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

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

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

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

212 19a-3p, broadly conserved among vertebrates, was downregulated in RAW264.7 macrophage cells of the M2

213 Sirt6 is downregulated in renal biopsies from patients with po

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

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

216 Aurora kinase was upregulated and pCDK1 was downregulated in resistant tumors from both xenograf

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

218 Finally, ALDH12 expression in maize and moss is downregulated in response to salt and drought stresse

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

220 expression of tissue factor (gene name, F3) were downregulated in response to GSTO1 KO.

221 A number of cytochrome P450 genes were downregulated in response to infection.

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 gulating presomitic mesoderm differentiation are downregulated in Sall4 mutants.

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

226 Finally, we show that microRNA-126 was downregulated in senescent endothelial cells and mic

227 own as a brake on immune cell activation and is downregulated in several gammaherpesvirus-driven mali

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

229 vere asthma, and the MUC1-CT/GRalpha complex was downregulated in severe asthma cells.

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

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

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

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

234 ch was highly expressed in CCA human tumors, was downregulated in SOX17-transduced CCA cells.

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

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

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

238 , we found immune and inflammatory processes were downregulated in subgroup 2, a configuration previo

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

240 sociated with the AKT-mTOR signaling cascade are downregulated in SZ DLPFC.

241 during CD229 CAR T cell production, as CD229 is downregulated in T cells during activation.

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

243 In contrast, miR-30b-5p was downregulated in T2DKD (0.82-fold, p = 0.006) and in

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

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

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

247 is expressed in the pharyngeal endoderm and is downregulated in Tbx1 mutant mice.

248 ndings, expression of SGMS1 in tumor tissues was downregulated in TCGA cohort only.

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

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

251 Zeb2 levels are downregulated in the embryonic rodent midbrain durin

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

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

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

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

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

257 ETV1 is downregulated in the LA during cardiac pressure overl

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

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

260 s a major regulator of cardiac functions and is downregulated in the majority of heart failure cases.

261 ll group of subjects we also show that GPR56 is downregulated in the PFC of individuals with depressi

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

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

264 stochemistry and Western blotting, PPARalpha was downregulated in the corneas of humans with diabetes

265 AIM2 was downregulated in the CP group compared with the H, G

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

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

268 ed that the expression of Bmp4 and DeltaNp63 was downregulated in the mutant corneas, which was assoc

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

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

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

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

273 xpression of several cambial regulator genes was downregulated in the stems of the transgenic trees i

274 POP1 and POP2 were downregulated in the CP and AgP, and AgP and G grou

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

276 TRIM20, TRIM16, and CARD18 were downregulated in the G, CP, and AgP groups compared

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

278 a-hydroxylase), and vitamin D receptor (VDR) were downregulated in the livers of mice fed an HFD (GSH

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

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

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

282 mitochondrial function and protein synthesis were downregulated in the sensory epithelium of P0 cochl

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

284 MUC1 expression was downregulated in these patients.

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

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

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

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

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

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

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

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

295 protein kinase that modulates EGFR turnover, is downregulated in vemurafenib-resistant melanoma cells

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

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

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

299 markers for odontoblast differentiation that are downregulated in Wls(Shh-Cre) teeth, act as direct d

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