ライフサイエンスコーパス: decreased expression

1 nover were overrepresented in the genes with decreased expression.

2 l categories with significantly increased or decreased expression.

3 oters of stem cell genes, resulting in their decreased expression.

4 ctivation of resting T cells resulted in its decreased expression.

5 These changes were associated with decreased expression and activation of the class III his

6 Decreased expression and activity of CaV1.2 calcium chan

7 zoxazolamine-induced paralysis, secondary to decreased expression and activity of Cyp3a11 and Cyp2b10

8 3'-UTR, causing mRNA degradation as well as decreased expression and activity of MITF.

9 Either intravenous or gastric loading led to decreased expression and activity of renal Pi transporte

10 Because decreased expression and function of bone morphogenetic

11 ) replication of RSVand Sendai virus, due to decreased expression and secretion of type I and III int

12 pression is abnormal in psoriatic skin, with decreased expression correlating with recruitment of T-c

13 We also found evidence for decreased expression divergence of the homoeologous gene

14 Of the miRs that showed decreased expression following DES treatment, miR-18b an

15 -C alleles that carry a C2 epitope, there is decreased expression frequency of the cognate receptor,

16 Moreover, many repressed genes also show decreased expression in 35S:CRF6 overexpressing plants.

17 seq to identify a subset of transcripts with decreased expression in both nuclear and cytoplasmic fra

18 Persistent AF activity was associated with decreased expression in genes and gene sets related to i

19 Interestingly, there was also a trend for decreased expression in mild Alzheimer's disease hippoca

20 2 disease risk variants were associated with decreased expression in peripheral and mucosal tissues a

21 P = 0.0076), resulting mainly from slightly decreased expression in the ND and increased expression

22 ays p.i., approximately 28% of miRNAs showed decreased expression in the VEH/SIV group compared to no

23 to the syncytiotrophoblast layer, and showed decreased expression later in gestation.

24 apoptosis (IAPs) family member, exhibited a decreased expression level after DHM treatment, which ma

25 Immunohistochemistry revealed significantly decreased expression level of ADAM12 protein in the KBD

26 Decreased expression level of phosphorylated AKT suggest

27 ermore, association between inflammation and decreased expression levels of MAGI3, PTEN, and TJP1 in

28 erologous CD8 T-cell proliferations, display decreased expression levels of PD-1 as well as PD-L1, an

29 -like morphology and marker expression, with decreased expression levels of PEC markers.

30 classic M1 proinflammatory macrophages) and decreased expression levels of proinflammatory and profi

31 Furthermore, we demonstrate that decreased expression levels of SDCCAG3 correlate with de

32 This decreased expression may contribute to increased oxidati

33 ted genes, and we confirm experimentally the decreased expression of 19 microRNAs with 11 correspondi

34 or of beta-1,3-glucan synthesis, for 21 days decreased expression of a broad panel of inflammatory ma

35 VSG internalization results in decreased expression of a tsetse microRNA (mir-275) and

36 Moreover, IGF1R-deficient macrophages had decreased expression of ABCA1 and ABCG1 and reduced lipi

37 1ham2 RNA interference transgenic lines with decreased expression of acetyltransferases from the MYST

38 ession of a phosphatase, CD45 and reciprocal decreased expression of activated LCK.

39 High-risk SMM patients showed at baseline decreased expression of activation-(CD25/CD28/CD54), typ

40 dition, western blot analyses show obviously decreased expression of active caspase-3 in methazolamid

41 The effects of increased or decreased expression of ACYL-COENZYME A:DIACYLGLYCEROL A

42 of Sir2, Su(var)3-9, and Dicer-2, as well as decreased expression of Adar, mitigated age-related incr

43 ailure of negative selection, facilitated by decreased expression of Aire rather than impaired regula

44 wth on formate increased fhl1 expression but decreased expression of all other hydrogenases.

45 ic N-methyl-D-aspartate (NMDA) receptors and decreased expression of alpha-amino-3-hydroxy-5-methylis

46 reased expression of mesenchymal markers and decreased expression of an epithelial marker.

47 aginal cell DNA which may be associated with decreased expression of an estrogen-responsive gene.

48 d with OA derived extracellular vesicles had decreased expression of anabolic genes and elevated expr

49 lpha-Klotho in association with enhanced BP, decreased expression of angiotensin converting enzyme 2,

50 Extracts decreased expression of anti-apoptotic proteins (survivi

51 organ, leads to elevated cactus mRNA levels, decreased expression of antimicrobial peptides, and vuln

52 sufficient for infection in cell lines with decreased expression of antiviral IFN genes at baseline.

53 The decreased expression of any component of this ternary co

54 Because of decreased expression of argininosuccinate synthetase and

55 lung DCs (LDC), lung CD64(+) macrophages had decreased expression of B cell activation genes and indu

56 This was associated with decreased expression of Bcl-xL and increased acetylated

57 eatment increased expression of miR-200a and decreased expression of beta-catenin in HSC.

58 that the relA knockout strains demonstrated decreased expression of beta-hemolysin/cytolysin, an imp

59 ading glioblastoma 2 (GLI2), followed by the decreased expression of both smoothened and GLI2.

60 ation of mTOR by leucine or deletion of TSC1 decreased expression of brown adipocyte-related genes UC

61 These effects were paralleled by decreased expression of c-Myc and stemness-related genes

62 ORC1-mediated 4EBP1 phosphorylation leads to decreased expression of c-MYC and subsequent upregulatio

63 While downregulation of SALL4 leads to a decreased expression of c-Myc at both protein and mRNA l

64 Decreased expression of C9orf72 is seen in expansion car

65 other cytokines associated with AD and with decreased expression of cathelicidin.

66 ations have immature CD56(dim) NK cells with decreased expression of CD16, perforin, CD57, and impair

67 monocyte-derived macrophages, SSRI treatment decreased expression of CD4 (p < .0001) and CXCR4 (p = .

68 In PBMCs, SSRI treatment decreased expression of CD4 (p = .009), CCR5 (p = .008),

69 The strains exhibit decreased expression of CDKN2A (both p16(INK4a) and p19(

70 Patients with AA had decreased expression of chloride intracellular channel 4

71 hepatic total cholesterol concentration and decreased expression of cholesterol metabolism related g

72 the data is indicated by the observation of decreased expression of claudin-1 and nuclear beta-caten

73 This protection was associated with decreased expression of cleaved (activated) caspases 9 a

74 the phosphorylation of ERK, together with a decreased expression of cleaved caspase-3 in mice treate

75 y loss of interdigitating foot processes and decreased expression of components of the slit diaphragm

76 The results identify that in old males decreased expression of CRABP2 leads to cell proliferati

77 Reduced function of pTregs correlated with decreased expression of CTLA-4, interleukin-10, and tran

78 tion of G2/M progression was associated with decreased expression of cyclin A, cyclin B, cyclin E, cd

79 ates with activation of p53 and p21(Cip) and decreased expression of cyclin B1.

80 of cyclin-dependent kinase inhibitor p21 and decreased expression of cyclin B1.

81 /G1-phase cell cycle arrest, as indicated by decreased expression of cyclins and CDKs and increased e

82 We show that decreased expression of cystatin B in patient fibroblast

83 This was likely due to decreased expression of cytokine and chemokine genes in

84 th the degeneration of DA axon terminals and decreased expression of DA neuron-enriched genes tyrosin

85 Decreased expression of DGAT1 led to an increased percen

86 Infection with NiggV but not NiggA led to decreased expression of Dicer and Ago 2, suggesting that

87 Down-regulation of vaspin in KCs resulted in decreased expression of differentiation-associated genes

88 Taken together, our studies demonstrate that decreased expression of DMT1 in intestinal mucosa leads

89 erations in DNA methylation were apparent in decreased expression of DNA methyltransferase 3a and met

90 This phenomenon could be attributed to the decreased expression of DNA-protein kinase catalytic sub

91 Decreased expression of EGFR and RELA was validated by b

92 Mitochondrial changes, including decreased expression of electron transport chain subunit

93 We also showed a decreased expression of ELOVL5 in patients' blood at 40

94 The patient had decreased expression of endothelium-bound thrombomodulin

95 videnced by increased rates of apoptosis and decreased expression of Eomes and Bcl2 early during the

96 EAC cells incubated with trastuzumab decreased expression of epithelial markers (CD24, CD29,

97 on of proteolysis in endothelial cells, with decreased expression of extracellular matrix remodeling-

98 s downregulated in HCC patient specimens and decreased expression of FBP1 associated with poor progno

99 monstrated by reduced collagen abundance and decreased expression of fibronectin-1, collagen I, alpha

100 chors mGluR5 to the cell surface, as well as decreased expression of FKBP5, implicating aberrant gluc

101 Overall, decreased expression of FOXP1 protein was associated wit

102 ranscription factor CUX1, thereby leading to decreased expression of FTO and retinitis pigmentosa GTP

103 expressions of mitochondrial fission genes, decreased expression of fusion genes and synaptic genes

104 educing sensory glutamate release results in decreased expression of GABA-synthesizing enzymes GAD65

105 rsisted at 3 years but were characterized by decreased expression of genes associated with chronic im

106 correlation between loss of HF formation and decreased expression of genes associated with proliferat

107 Inactivation of MLL1 leads to decreased expression of genes bound by NHA9 and MLL1 and

108 ulation of ploidy changes is associated with decreased expression of genes controlling chromosome seg

109 olved in lipogenesis mediated by SREBP1c and decreased expression of genes involved in fatty acid bet

110 es6Delta, and ino80Delta mutants demonstrate decreased expression of genes involved in glycolysis and

111 nscriptional regulators TCF4 and NEUROD6 and decreased expression of genes involved in long-term pote

112 This deficit can be explained by decreased expression of genes involved in mature neuron

113 ssation of leaf and stem growth at anthesis, decreased expression of genes involved in stem cell wall

114 ssion of PU.1 in CD4(+) T cells and observed decreased expression of genes involved with the function

115 ed and control plants revealed significantly decreased expression of genes related to photosynthesis,

116 cathepsin S inhibitor or siRNA significantly decreased expression of growth differentiation factor-15

117 otective against asthma) was correlated with decreased expression of GSDMB in BEC and BAL (P = 1.3 x

118 Overexpression of AGL15 results in decreased expression of HAE as well as a delayed absciss

119 paired SynT differentiation and specifically decreased expression of hCYP19A1, GCM1, and Fzd5, which

120 higher fasting insulinemia, concomitant with decreased expression of hepatic gluconeogenic genes.

121 Ex12 mice showed decreased expression of hepcidin and increased expressio

122 osis, and the antiangiogenic factor GAX, and decreased expression of HIF-1alpha and proangiogenic fac

123 A GluR1 subunits and the neuronal GluT3, but decreased expression of hippocampal brain-derived neurot

124 Here we show that decreased expression of histones or a defect in nucleoso

125 eased protein expression of MUC16, SIRPA and decreased expression of HLA-DRB1 was further demonstrate

126 s, reduced colony-forming activity in vitro, decreased expression of Hox genes in the hematopoietic s

127 man immature DCs coinfected with HIV/Mtb had decreased expression of human leukocyte antigen antigen

128 This observation was associated with decreased expression of hypoxia-inducible factor 1alpha.

129 are uniformly anti-inflammatory despite the decreased expression of IL-10.

130 Inasmuch as the decreased expression of IL-32, which is involved in dend

131 Vaccination decreased expression of IL-6 and MCP-1 and reduced macro

132 filtration of leukocytes and macrophages and decreased expression of IL-6 were revealed in the muscle

133 ence of nuclear translocation of RelA with a decreased expression of IL-6, IL-12p40, and IL-17A.

134 mice is not due to defects in homeostasis or decreased expression of IL-7Ralpha, as transgenic expres

135 ortant for iNKT17 differentiation, including decreased expression of IL-7Ralpha, BATF and c-Maf and i

136 Instead, mTORC1 inhibition led to decreased expression of immunoglobulin-binding protein (

137 We consistently observed decreased expression of inflammation-related genes NLRP3

138 n species, attenuated elastin breakdown, and decreased expression of inflammatory cytokines and macro

139 Enforced Akt/mTORC1 signaling also decreased expression of inhibitory receptors TIM3 and PD

140 ormality; however, VHR-knockout cells showed decreased expression of integrins and FAK but stronger F

141 UTX-deficient T cells showed decreased expression of interleukin-6 receptor-alpha and

142 r suppressor protein p53 and correlates with decreased expression of its target gene TXNL1.

143 in Fx-/- mice fed standard chow, leading to decreased expression of its target Hes1.

144 d a profound loss of tissue differentiation, decreased expression of keratin 4 (KRT4) and cornulin (C

145 levels of ERK, RSK, ELK1 and DR5 along with decreased expression of Ki67.

146 was induced in the KMT6(kd) strain, in which decreased expression of KMT6 is accompanied by reduced H

147 oupled with increased NF-kappaB activity and decreased expression of LC3, a hallmark of the autophagi

148 expression of fibrosis genes and remarkably decreased expression of let-7a and increased expression

149 There was decreased expression of let-7a in BDL and Mdr2(-/-) chol

150 L, and lipolysis; 45% worsening of IMGU; and decreased expression of lipid metabolism genes.

151 ithelial V-like antigen (eva) expression and decreased expression of lipolytic enzymes (hormone-sensi

152 ls, increased lymphatic vessel leakiness and decreased expression of lymphatic specific markers compa

153 ctivation and increased granulocytes; and 4) decreased expression of lymphocyte related genes and lym

154 These cells also had decreased expression of major histocompatibility complex

155 ers and bone resorption activity, as well as decreased expression of many inflammatory markers.

156 ale changes in gene expression, resulting in decreased expression of many nearby genes.

157 This was quantified with decreased expression of markers along the specification

158 Significantly decreased expression of mature Let-7a and the miR-200 fa

159 gakaryocytic differentiation, as revealed by decreased expression of megakaryocytic differentiation m

160 h may be post-transcriptionally modulated by decreased expression of microRNA-155 in Treg-DC.

161 (Ly294002) of PI3K/AKT pathway significantly decreased expression of miR-21 and CSC markers and upreg

162 with lean individuals, overweight humans had decreased expression of miR-26a in the liver.

163 Decreased expression of mismatch repair (MMR) gene MSH2

164 ransition showed metabolic shifts, including decreased expression of mitochondrial electron transport

165 thymoma viral oncogene homolog signaling and decreased expression of mitogen-inducible gene 6 (MIG6),

166 sd10 and Acaa2, and blunted VLDL export with decreased expression of Mttp and its product microsomal

167 Ash1l deficiency also decreased expression of multiple Hox genes in hematopoie

168 unding the cuticle of the abdomen results in decreased expression of multiple HSR genes in proximal a

169 tients with recessive RYR1 mutations exhibit decreased expression of muscle-specific microRNAs, incre

170 ockdown resulted in increased E-cadherin and decreased expression of N-cadherin and snail transcripti

171 Mutations in the NF1 gene result in decreased expression of neurofibromin, a negative regula

172 iology associated with neuroinflammation and decreased expression of neuronal activity marker, which

173 ated to increased levels of intact AnxA1 and decreased expression of NF-kappaB and Mcl-1.

174 ear factor-kappaB (NF-kappaB) activation and decreased expression of NF-kappaB target genes matrix me

175 at the diagnosis of malignancy, including a decreased expression of NKp46 and decreased numbers of N

176 In male mice, decreased expression of NRXN3 mRNA was observed in CA1 a

177 umor progression was more closely related to decreased expression of nuclear CDC25B than to changes i

178 We found that constitutive NIK expression decreased expression of numerous Treg signature genes an

179 of FEN1 and SUR4, increased ceramide levels, decreased expression of nutrient transporters, and induc

180 Furthermore, Cav3.2 inhibition decreased expression of oncogenes (PDGFA, PDGFB, and TGF

181 harmacologic inhibition of DOT1L resulted in decreased expression of oncogenic canyon-associated gene

182 ed optic nerve pathological states, we found decreased expression of one major metalloproteinase prot

183 rs and intramembranous bone formation and by decreased expression of osteoclastic markers and bone re

184 versely, adenovirus Dkk1-treated mice showed decreased expression of osteogenic markers, coupled with

185 rotizing enterocolitis patients also exhibit decreased expression of oxidative phosphorylation genes.

186 ased expression of ZFP871 is responsible for decreased expression of p53 in the PCBP4-deficient MEFs

187 ELENA1 knockdown plants show decreased expression of PATHOGENESIS-RELATED GENE1 (PR1)

188 ns This increase in survival correlated with decreased expression of pattern recognition receptors on

189 RNAi-mediated silencing of NR4A1 decreased expression of PAX3-FOXO1A and its downstream e

190 The decreased expression of PCSK9 and conversely increased L

191 against melanoma in a syngeneic model, with decreased expression of PD-L1 and of matrix metallo-prot

192 esenchymal stem/stromal cells, likely due to decreased expression of PDGF-AA and BMP2.

193 mural cells, an effect that associated with decreased expression of PDGFRbeta and p57kip2, a cyclin-

194 arget of the Hippo pathway, which results in decreased expression of phosphatase and tensin homologue

195 M6/TRM61 mRNA and tRNAi(Met) expression with decreased expression of PKCalpha mRNA was detected in hi

196 d pathology impaired histone acetylation and decreased expression of plasticity genes, while aging al

197 dominal aortic aneurysms and correlated with decreased expression of predicted miR-181b targets, tiss

198 dominal aortic aneurysms and correlated with decreased expression of predicted miR-181b targets, tiss

199 t under glucose deprivation (GD) conditions, decreased expression of presenilin 1 (PS1) results in de

200 BS microbiota had reduced DSS colitis with a decreased expression of pro-inflammatory cytokines from

201 induces NEFM, RET, and VACHT and results in decreased expression of proapototic (BMF, BIM), adrenerg

202 3) A tendency for decreased expression of progesterone receptor co-activat

203 pression of IL-10, IL-17, and granzyme B and decreased expression of programmed death 1 on these cell

204 D8(+) T cells with an effector phenotype and decreased expression of programmed death receptor-1 (PD-

205 Higher expression of p27 and decreased expression of proliferating cellular nuclear a

206 This enhanced adhesion was associated with decreased expression of protein kinase A regulatory subu

207 and DNA replication and damage repair, and a decreased expression of proteins responsible for core ex

208 Decreased expression of PTEN and/or PTENP1 resulted in d

209 Overall decreased expression of PTEN was observed in intimal SMC

210 blocks primitive hematopoiesis, as shown by decreased expression of pu.1, mpo, and l-plastin; and di

211 ocalization and decrease in visual pigments, decreased expression of retinoic acid-responsive genes a

212 induction of interferon-stimulated genes and decreased expression of ribosomal proteins and translati

213 tient specimens revealed correlation between decreased expression of RKIP and increased expression of

214 Decreased expression of RKIP has been described in sever

215 We identified decreased expression of RNASET2 as a component of TL1A-m

216 We found decreased expression of Rpt1, Rpt3, and Rpt6, subunits o

217 ngevity pathways exhibit small nucleoli, and decreased expression of rRNA, ribosomal proteins, and th

218 ells (definitive hematopoiesis), as shown by decreased expression of runx1 and c-myb However, adtrp1

219 in differentiating neural cells we observed decreased expression of schizophrenia-associated gene Fe

220 Decreased expression of SDH-A and COX-I demonstrated tha

221 ts and APTX-depleted Hela cells is caused by decreased expression of SDHA and genes encoding CoQ bios

222 ts with OA undergoing total knee replacement decreased expression of senescent and inflammatory marke

223 sponses to GA and brassinosteroid and showed decreased expression of several common target genes of D

224 Ductal cells exhibit aberrant polarity and decreased expression of several cystic disease genes, so

225 ion, deletion of this region in HEK293 cells decreased expression of several of the same genes that w

226 in number and density of synaptic vesicles, decreased expression of several presynaptic proteins, an

227 on showed DDR1 silencing was associated with decreased expression of several ribosomal proteins and e

228 Decreased expression of Sipa1l3 in zebrafish and mouse c

229 Decreased expression of SLC25A46 results in increased st

230 blocked the activation of primary HSCs, with decreased expression of smoothened, GLI2 and ILK compare

231 The altered lipid content was attributed to decreased expression of sn-1,2 diacylglycerol acyltransf

232 ted substantial activation of p53 and STAT3, decreased expression of SOCS7, and increase in profibrot

233 t was also demonstrated that c-Myc knockdown decreased expression of Sp TFs and STAT3 These results d

234 BITC also decreased expression of specificity proteins (Sp) Sp1, S

235 s-of-function mutations in STAG2, as well as decreased expression of STAG2 or STAG3 proteins in sever

236 wnstream effector, STAT3, which leads to the decreased expression of STAT3 target genes that are asso

237 K9.361 injection also decreased expression of stimulatory Fcgamma receptors, e

238 terferon-gamma, and fractalkine as well as a decreased expression of synaptophysin, a neuronal activi

239 AF susceptibility was associated with decreased expression of targets of several transcription

240 rence affected viral splicing and, like 1C8, decreased expression of Tat, Gag and Env.

241 with a shRNA against TCP80 not only exhibit decreased expression of TCP80 and RHA but also display d

242 eads to increased mature let-7, which causes decreased expression of TGF-betaRI, TGF-betaRIII, and SM

243 Decreased expression of TGFB pathway signaling ligands w

244 We show that decreased expression of the androgen receptor (AR) in lu

245 sverse aortic constriction, corresponding to decreased expression of the angiogenic factor VEGF.

246 ed inflammation under high-SS conditions and decreased expression of the antiinflammatory factor KLF-

247 l BA, colonocytes from WD-fed mice exhibited decreased expression of the BA transporters FABP6, OSTbe

248 A2AAR-KO mice had decreased expression of the beta-cell-specific markers p

249 rliest signaling alterations in CRC, and the decreased expression of the bile acid apical transporter

250 mponent protein expression, they demonstrate decreased expression of the calcium-dependent protein ki

251 ystem (UPS) was detected which resulted in a decreased expression of the deubiquitinating enzyme USP1

252 ity associated with infection sites, and had decreased expression of the early auxin responsive gene

253 pressive Tregs in the injured myocardium and decreased expression of the gene encoding IFN-gamma, a k

254 t of rapamycin complex 1 (mTORC1) signaling, decreased expression of the glucose transporter Glut1 an

255 specification of hemangioblasts, as shown by decreased expression of the hemangioblast markers, etsrp

256 n mice is cell intrinsic and associated with decreased expression of the high affinity IL-2 receptor

257 lation of histone H3, which coincided with a decreased expression of the histone deacetylase HDAC2.

258 ed CAR T cells (CTL019), in association with decreased expression of the immunosuppressive molecule p

259 There is decreased expression of the intracellular signaling path

260 s and microglial accumulation accompanied by decreased expression of the LPC receptor G2A, whereas MS

261 horylated SMAD2/3 (p-SMAD2/3) and NFATC2 and decreased expression of the major matrix-related genes S

262 The increase in PP2A activity is caused by decreased expression of the MID1 ubiquitin ligase that m

263 normal human diploid fibroblasts results in decreased expression of the mTOR inhibitor DDIT4 (REDD1)

264 city to use glycolysis, a function linked to decreased expression of the NAD(+)-dependent protein dea

265 Decreased expression of the neuronal marker MAP2 and syn

266 LR12 decreased expression of the NLRP3, pro-caspase-1 and pro

267 Attenuated TEWL correlated with decreased expression of the pro-inflammatory marker S100

268 xpression of the anti-oxidant marker CAT and decreased expression of the pro-oxidant marker NOX-4.

269 ic cells with dinaciclib resulted in rapidly decreased expression of the prosurvival protein Mcl-1, a

270 Furthermore, DOCA treatment led to decreased expression of the slit diaphragm-associated pr

271 ng in cystinosis was found to associate with decreased expression of the small GTPase Rab11 and the R

272 miscarriage is associated with significantly decreased expression of the T-cell co-receptor CD8 and t

273 onsequence of ATMIN repression in hypoxia is decreased expression of the target gene, DYNLL1.

274 AF susceptibility was associated with decreased expression of the targets of CREB/ATF family,

275 , reduced inflammation and eosinophilia, and decreased expression of the Th2 cytokine IL-13 and the l

276 30% decrease in transepithelial resistance, decreased expression of the tight junction scaffold prot

277 Mutant kidneys also had decreased expression of the UT-A urea transporter and co

278 ersely, overexpression of HDAC11 resulted in decreased expression of these genes.

279 ne (CHS), whereas the mybs2 mutant exhibited decreased expression of these genes.

280 impaired TEC maturation and function such as decreased expression of thymotropic chemokines, decrease

281 METH administration decreased expression of tight junction (TJ) proteins and

282 ession of matrix metalloproteases as well as decreased expression of tissue inhibitor of metalloprote

283 in mtDNA, and impaired neuritogenesis with a decreased expression of transthyretin, which is known to

284 tective against asthma) were correlated with decreased expression of TSLP in BAL (P = 7.9 x 10(-11) a

285 d activation of microglia and astrocytes and decreased expression of tyrosine hydroxylase in periglom

286 Clinically, decreased expression of USP49 in patients with pancreati

287 revealed a decreased copy number of UT2 and decreased expression of UT2 in genomic and transcriptomi

288 pression of E-cadherin and beta-catenin, and decreased expression of vimentin and snail, which is par

289 ction, GYY4137 treatment was associated with decreased expression of viral proteins and mRNA, suggest

290 expression of the AtlA murein hydrolase and decreased expression of wall-teichoic acids.

291 In the Tet1-deficient crypt, decreased expression of Wnt target genes such as Axin2 a

292 r medullary collecting duct 3 (mIMCD3) cells decreased expression of Wnt11, Krt23, and Slo4c1 DUSP8 o

293 we show that disruption of HNF4alpha caused decreased expression of XBP1 and reduced cellular ER net

294 del of uninephrectomy, RCH is accompanied by decreased expression of ZO-2 and nuclear expression of Y

295 y, volume fraction, and bone formation rate; decreased expressions of osterix, collagen I, and osteoc

296 ite branches and total neurite length, and a decreased expression on RhoA and neurodegenerative prote

297 , for a subset of genes showing increased or decreased expression, the respective gain or loss of H3K

298 , when FOXP1 protein expression was nuclear, decreased expression was also associated with favorable

299 Interestingly, genes with increased or decreased expression were clustered in cellular polysacc

300 xcitatory and inhibitory synaptic genes show decreased expression with age and are positively correla