ライフサイエンスコーパス: increased expression

1 ) with 557 showing decreased and 329 showing increased expression.

2 Here, we show that increased expression and activation of the tyrosine kina

3 ino acid change Arg363His is associated with increased expression and nuclear mobility, as well as lo

4 nsequently, CD81 depletion results in SAMHD1 increased expression, decreasing the availability of deo

5 se CaMK2N2 expression, but we show that such increased expression does not affect LTM after retrieval

6 ne fusion in Arabidopsis thaliana The intron increased expression from all transcribed positions but

7 ic extinction-induced, but not fear-induced, increased expression in both extinction-rescued S1 mice

8 current CCND1 3'UTR mutation associated with increased expression in endometrial cancer.

9 rapeutic target in advanced cancers based on increased expression in primary human cancers, facilitat

10 y expressed, and enriched in genes that show increased expression in response to biotic and abiotic s

11 Increased expression in response to low Zn levels was ob

12 gions is accompanied by local amplification, increased expression in some cases, interruption of gene

13 anoma and in melanoma patients and that this increased expression is dependent on an IL-1R-MyD88 path

14 pe, but not mutated CATAC elements, imparted increased expression levels as well as rhythmic regulati

15 Consistently, clinical HLRCC tissues showed increased expression levels of both FOXM1 and its prolif

16 elevated PAK4 expression is coincident with increased expression levels of c-Met and the p85alpha su

17 Both groups demonstrated increased expression levels of fibroblast growth factor-

18 Additionally, rhIFN-gamma increased expression levels of pattern recognition recep

19 within dimeric/oligomeric complexes and that increased expression levels of the receptor favored a gr

20 RNAs and extended 3' ends have significantly increased expression levels over their nonstructured cou

21 In NK cells, CD16a stimulation induced increased expression of 276 transcripts (FC > 2x, false

22 xplained by immunohistochemical data showing increased expression of 5-HT2CR in non-GABAergic BLA cel

23 ne expression, as the mybs1 mutant displayed increased expression of a hexokinase gene (HXK1), chloro

24 Cells expressing the iTango system exhibit increased expression of a marker gene in the presence of

25 omyocytes from Gas2l3-deficient mice exhibit increased expression of a p53-transcriptional program in

26 The loss of macroH2A1 increased expression of a panel of stemness-associated g

27 KDM5i treatment alone increased expression of a small number of genes, whereas

28 e expression profiling analysis demonstrates increased expression of a specific set of transcription

29 Transcriptomics analyses showed increased expression of A20 (tumor necrosis factor alpha

30 deaminases gene cluster APOBEC3 resulting in increased expression of A3A, which is shown to be of cli

31 resistin, fed-state and fasting insulin and increased expression of adipogenic transcription factors

32 emonstrated that this compound significantly increased expression of Ah-responsive genes such as Cyp1

33 sceptibility to IPF was also associated with increased expression of AKAP13 mRNA in lung tissue from

34 nd adipose tissue, which was associated with increased expression of aldehyde dehydrogenase family 1

35 FAK activation is associated with increased expression of alpha-smooth muscle actin (alpha

36 ire a profibrotic phenotype characterized by increased expression of alpha-smooth muscle actin and co

37 g hepatotropic viral infection and displayed increased expression of alternative Mvarphi activation m

38 2 suppressed expression of CYP24A1, but also increased expression of an exon 10-skipped CYP24A1 splic

39 steroids improved sarcolemmal repair through increased expression of annexins A1 and A6, which mediat

40 ismatch repair subtypes were associated with increased expression of antitumor immunity, including ac

41 HNF-1beta mutant kidneys showed increased expression of aquaporin-2 mRNA but mislocalize

42 iosynthetic pathways is partially due to the increased expression of AR splice variants.

43 Intriguingly, increased expression of Arf in tumor stromal cells, as i

44 nses in liver and spleen, as associated with increased expression of arginase I and the cytokines IL1

45 increased immunosuppression as evidenced by increased expression of arginase-1 in CD11b(+)Gr1(+) cel

46 ng apoE inducible mouse models, we show that increased expression of astrocytic apoE4, but not apoE3,

47 Meanwhile, the increased expression of ATF4 and HO-1 mRNAs were observe

48 sion of HuR, Bcl2, cyclin E, and Bcl-XL with increased expression of Bax and p27 in CMLD-2-treated NS

49 We found that increased expression of Bcl-6 in CD4(+) Th cell populati

50 expression of IL-7Ralpha, BATF and c-Maf and increased expression of Bcl11b and Lef1.

51 t 8 weeks, we observed two distinct waves of increased expression of beta cell functional and prodiff

52 inactive Cas9 (dCas9) in MVM-infected cells increased expression of both cyclin B1 protein and RNA,

53 fter repeated cocaine exposure, resulting in increased expression of both genes in D2-type medium spi

54 , Wnt3a and NP12 stabilized beta-catenin and increased expression of both Nanog and VEGFR2.

55 activation of Elk-1 transcription factor and increased expression of c-Fos gene.

56 MUC1 induces increased expression of c-myc in EVs that induces prolif

57 e damage during ischemia was associated with increased expression of C3/C3 fragments primarily in the

58 In particular, an increased expression of Cad-11 can be detected on the pl

59 Constitutive activation of RhoA led to increased expression of CCL2, IL6, TNF-alpha, and CXCL10

60 an essential autophagy gene, FIP200, in NSCs increased expression of Ccl5 and Cxcl10 in a p53-indepen

61 Also, patients' DCs present an increased expression of CD62L and a tendency to overexpr

62 immune cells, especially CD8(+) T cells, and increased expression of cell proliferation markers.

63 reduced expression of pluripotency factors, increased expression of cell-lineage-affiliated developm

64 Using this model, we show increased expression of cellular prion protein (PrP(C))

65 racterized by infiltration with neutrophils, increased expression of chemokine (C-X-C motif) ligand (

66 For duplications, we found that increased expression of CHRNA7 mRNA is associated with h

67 adaptation by S. aureus to obesity/T2D with increased expression of clfA that is associated with the

68 We found that low SES was related to increased expression of conserved transcriptional respon

69 l CD4(+) T cells from patients with ALF have increased expression of CTLA4 compared to individuals wi

70 palmar epidermis demonstrated significantly increased expression of CTSB, as well as stronger staini

71 We could demonstrate mechanistically increased expression of Cxcl10 by hepatocytes, and conse

72 t the loss of Twist1 in IPF lung fibroblasts increased expression of CXCL12 downstream of increased e

73 ced pulmonary fibrosis, which is mediated by increased expression of CXCL12.

74 and induced cell cycle arrest accompanied by increased expression of cyclin-dependent kinase inhibito

75 The increased expression of cyp1a (2.49 +/- 0.28-fold), udpg

76 riments of immunohistochemistry (IHC) showed increased expression of cytoplasmic HMGB1 in dengue-extr

77 ed ADSC differentiation, characterized by an increased expression of cytoplasmic lipids and perilipin

78 This respiratory burst was associated with increased expression of cytosolic components of the NADP

79 essing plants after elf18 treatment confirms increased expression of defense-related genes compared w

80 evious findings in schizophrenia to identify increased expression of developmentally and genetically

81 mesenchymal to epithelial transition (MET), increased expression of differentiation markers and pres

82 4166 induced phosphorylation of NFkappaB and increased expression of dual specificity phosphatase 6 (

83 Both CSE and CS treatment induced increased expression of Duox-1, and silencing of Doux-1

84 phenotypic inversion of EMT, correlated with increased expression of E-cadherin and beta-catenin, and

85 Loss of atypical E2Fs resulted in increased expression of E2F target genes, including E2f1

86 We therefore speculated whether increased expression of EBI2 would lead to an expanded B

87 Increased expression of EGFR in myeloid cells from the c

88 nal reprogramming is shown to be mediated by increased expression of eIF4E and its increased availabi

89 ology, including mitochondrial architecture, increased expression of electron transport chain protein

90 OTCH1 signalling in tumour xenografts led to increased expression of endothelial FABP4 that decreased

91 In addition, HDAC11KO T cells had increased expression of Eomesodermin (Eomes) and TBX21 (

92 ariants; both mouse and human tumors exhibit increased expression of epigenetic reprogramming factors

93 signal regulated kinase proteins and with an increased expression of epithelial-to-mesenchymal transi

94 In Hjv(-/-) mice, increased expression of exogenous MT2 in the liver signi

95 Aortic tissue from Micu2(-/-) mice had increased expression of extracellular matrix remodeling

96 3H in tumorigenesis have been interested and increased expression of FAM83H and MYC in hepatocellular

97 f mice with the ADRB3 agonist CL316,243 (CL) increased expression of fatty acid synthase (FASN) and m

98 therapeutic agent for HCC cases that exhibit increased expression of FGF19.

99 of TSP1 activation of TGFbeta, reversed the increased expression of fibrotic molecules.

100 and monocytes/macrophages in capillaries and increased expression of five biologically relevant genes

101 1 showed increased suppressive function, and increased expression of Foxp3 and TGF-beta.

102 In the setting of viral hepatitis, increased expression of Gal-9 drives the expansion of re

103 We observed increased expression of GATA3 by lamina propria T cells

104 conate levels in loz1Delta cells result from increased expression of gcd1 By analyzing the activity o

105 We observed increased expression of genes associated with inflammato

106 volved in mature neuron function, along with increased expression of genes atypical of the olfactory

107 In contrast, obeticholic acid increased expression of genes encoding enzymes involved

108 uscle mass in PINTA745-MCAO mice involved an increased expression of genes encoding myofibrillar prot

109 upregulated in the outer retina and there is increased expression of genes involved in glucose metabo

110 Initial responses to P limitation showed increased expression of genes involved in P uptake and a

111 the inoculum suspension concomitant with an increased expression of genes involved in stress respons

112 r osteogenic differentiation, perhaps due to increased expression of genes involved in the control of

113 MCH increased expression of genes regulating hypoxia signall

114 MCH increased expression of genes regulating sodium (SCNN1-B

115 iptomes from orange morphs had significantly increased expression of genes related to immune response

116 s, while single-cell RNA-seq analyses showed increased expression of genes related to reactive oxygen

117 CP was characterized by the increased expression of genes related to responses to ex

118 ses indicated that IPF lung fibroblasts have increased expression of genes that are targets of mEV-en

119 luding higher CCL17 and IL-10 production and increased expression of genes with important immune func

120 rcinoma (PDAC) and generally correlates with increased expression of HER2, the underlying mechanism r

121 To determine the effects of increased expression of human aldosterone synthase (hAS)

122 ing metagenomic sequencing related SAMHD1 to increased expression of human endogenous retrovirus K (H

123 We observed increased expression of IFN-beta, IFN-lambda1/IL-29, OAS

124 RNASET2 knockdown in T cells increased expression of IFNG and intercellular adhesion

125 De novo DSA ABMR was characterized by increased expression of IFNgamma-inducible, natural kill

126 erbated pathology of skin inflammation, with increased expression of IL-17-induced keratinocyte-deriv

127 that STAT1-deficient mice had significantly increased expression of IL-33 and IL-23, cytokines that

128 We confirmed the increased expression of IL-36alpha in the renal tubular

129 posure of HTEpC cells to both CSE and IL-17A increased expression of IL-6 and IL-8 in a concentration

130 adhesion, and transendothelial migration via increased expression of IL-6 and monocyte chemoattractan

131 odel (mEER) caused systemic inflammation and increased expression of Il1b in the brain while inducing

132 rast, CD4 T cells of nonresponders exhibited increased expression of IL2 and STAT5 genes, which are k

133 atients with IBD, and mice with colitis, had increased expression of IL28 compared with controls; lev

134 In a regression model, increased expression of IL5 and IL17A mRNAs distinguishe

135 These changes were accompanied by increased expression of immune genes in adipose tissue a

136 In vivo, mAAQ was associated with increased expression of immune modulators PD-L1 (program

137 ol feeding decreased miR181b-3p in liver and increased expression of importin alpha5 in nonparenchyma

138 Treatment of BMDCs with oxLDL ICs increased expression of inflammasome-related genes Il1a,

139 ated genes in these cells was examined, with increased expression of inflammatory (NLR family pyrin d

140 atment of control HEEs with arachidonic acid increased expression of inflammatory cytokines, 12-hydro

141 al pneumonia, Miwi2-deficient mice exhibited increased expression of inflammatory mediators and incre

142 trate an exhausted phenotype associated with increased expression of inhibitory receptors, decreased

143 smoke accelerated development of colitis and increased expression of interferon gamma in the small in

144 Increased expression of Interleukin (IL)-33 has been det

145 Downregulated miRNAs were associated with increased expression of interleukin 8 (IL-8), CXCL2, IL-

146 stretch to RAW 264.7 macrophages resulted in increased expression of interleukin receptor 1 messenger

147 nsion of Th17-type CD4 T cells was seen with increased expression of interleukin-17 and interleukin-2

148 pr of liver X receptor-alpha (LXRalpha) with increased expression of its lipogenic targets Srebp1c, C

149 We further demonstrate increased expression of KATII and KMO, but not IDO, in v

150 We found increased expression of KIBRA and phosphorylated YAP pro

151 This current is likely due to the increased expression of Kir2.1 channels.

152 In UN-KC-6141 cells, PI3K and MEK signaling increased expression of KLF5; a high level of KLF5 incre

153 of keratin 4 (KRT4) and cornulin (CRNN), and increased expression of KRT5 and KRT14.

154 t brains following neonatal infection showed increased expression of kynurenine amino transferase II

155 t LCE3B/C-del was associated with a markedly increased expression of LCE3A, a gene directly adjacent

156 ANX - A1 (-/-) mice exhibited significantly increased expression of LV pro-inflammatory and pro-fibr

157 reases in tumor-infiltrating lymphocytes and increased expression of lymphocyte-homing signals in the

158 The chemical exposure also increased expression of major inflammatory cytokines, in

159 l nonrepressed 2 serine/threonine kinase and increased expression of mammalian target of rapamycin, s

160 ndent deposition of hyaluronic acid (HA) and increased expression of markers for alternative activati

161 cells in skin and digit joints as well as by increased expression of matrix metalloproteases and bone

162 ng cells obtained after H1152 treatment show increased expression of mature beta cell markers and imp

163 Increased expression of MCM8 in prostate cancer is assoc

164 Increased expression of mcr-1 results in decreased growt

165 at have lost epithelial characteristics with increased expression of mesenchymal genes, have decrease

166 occurring in PLNs of T1D patients, involving increased expression of miR-125a-5p on Treg cells which

167 mia-reperfusion injury (IRI) associated with increased expression of miR-146a in both allografts and

168 The increased expression of miR-323-3p and noncoding RNA nc8

169 An increased expression of miR-323-3p in PBMCs from patient

170 lacking A2AR develop an 'OA phenotype' with increased expression of Mmp13 and Col10a1.

171 The OX lines also displayed increased expression of Mn transporters and were more se

172 s increased protease activity coincided with increased expression of mRNA for kallikreins (KLKs), wit

173 We validated increased expression of multiple miRNAs, including miR12

174 RNA-sequencing analysis showed an increased expression of MYBL1 in tumor cells with OGT kn

175 n, enhanced its transcriptional activity and increased expression of MYC-regulated genes.

176 aH222P/H222P mice, which was associated with increased expression of myocardial connexin 43.

177 and immunofluorescence results indicating an increased expression of Nav1.7 associated with spontaneo

178 We demonstrate that ES contributes to increased expression of neural differentiation biomarker

179 lly examined CM gene expression and observed increased expression of neuronal markers Dcx, Map2, and

180 Increased expression of neurotensin receptor 1 (NTR1) ha

181 , with FOXJ2 phosphorylation associated with increased expression of newly identified NEK6 transcript

182 ed with control (P <0.001) and significantly increased expression of NF-kappaB mRNA in neutrophils (P

183 We now report that increased expression of NKG2D ligands after virus infect

184 Our results demonstrate distinctive, increased expression of NLRP3, caspase-1, and IL-1beta i

185 d that cutaneous leishmaniasis patients have increased expression of NLRP3, leading to high levels of

186 clinically relevant doses of FTY720 to mice increased expression of NPC1 and -2 in brain and liver a

187 FTY720 greatly increased expression of NPC1 and -2 in human NPC1 mutant

188 Real-time RT-PCR also showed dramatically increased expression of osteogenesis marker genes only i

189 Interestingly, increased expression of osteogenic differentiation-relat

190 combination treatment remarkably (P < 0.05) increased expression of p-Akt and anti-apoptotic protein

191 ited AKT phosphorylation, activated PTEN and increased expression of p-eIF2a.

192 te-derived DCs (MDDCs) is associated with an increased expression of p21cip1/waf, a cell cycle regula

193 reatment marrow samples revealed a trend for increased expression of PD-L1 in responding patients and

194 cluster and miR-125a-5p are downregulated by increased expression of PDGFR-alpha or PDGFR-beta in NSC

195 ne causes FOXO1 localization in the nucleus, increased expression of pERK1/2, and drug resistance.

196 JUNV infection leads to increased expression of PKR as well as its redistributio

197 ased phosphorylation of STAT3 on Ser727, and increased expression of PML, a STAT3 transcriptional tar

198 aloside IV treatment, as demonstrated by the increased expression of PPARalpha and SERCA2a.

199 istent with in vitro findings, significantly increased expression of proapoptotic and proinflammatory

200 d TGF-beta1-induced enhanced ROS production, increased expression of profibrotic and proinflammatory

201 This was associated with an increased expression of profibrotic genes and transformi

202 e-treated SPL-overexpressing cells exhibited increased expression of prohibitin 2 (Phb2), involved in

203 tes incubated with L. infantum significantly increased expression of proinflammatory genes for IL-6,

204 nd IL-17C+KO primary keratinocytes confirmed increased expression of proinflammatory molecules, sugge

205 Hippo-deficient cardiomyocytes have increased expression of proliferative genes and stress r

206 he lung myeloid compartment characterized by increased expression of prometastatic genes, including i

207 ith differences in structural remodeling and increased expression of proteins involved in cardiac fun

208 tes, activation of FXR with obeticholic acid increased expression of proteins that regulate amino aci

209 Immunohistochemical staining showed increased expression of pSMAD158 and VEGF in the MCC and

210 l as UC mucosa, and between inflammation and increased expression of PTPN22 in colonic IBD mucosa, wa

211 We found that lal(-/-) ECs displayed increased expression of Rab7, a late endosome/lysosome-a

212 Smurf2-deficient osteoblasts display increased expression of RANKL, the central osteoclastoge

213 We found increased expression of RTN1A and ER stress markers in t

214 l analysis, we found that IPF MPCs displayed increased expression of S100 calcium-binding A4 (S100A4)

215 We found increased expression of S100A12 in the epidermis of huma

216 on in the Wnt pathway, and qPCR confirmed an increased expression of secreted frizzled-related protei

217 Thus, increased expression of sEH is a key determinant in the

218 ATP injection increased expression of several markers for regenerative

219 id content were enhanced in roots along with increased expression of several nitrate assimilatory gen

220 MEAN suppressed C-MYC expression and increased expression of several tumor suppressor genes,

221 ation of nuclear factor-kappaB, resulting in increased expression of SMAD6 and SMAD7.

222 This was correlated with increased expression of soluble Frizzled-related protein

223 We found that Msx gene overexpression increased expression of specific blastemal markers and e

224 ivities results in robust HSR induction with increased expression of specific heat shock proteins tha

225 differentially hydroxymethylated regions and increased expression of specific potassium channels in t

226 d colon tissues from Mefv-/-, which also had increased expression of stem cell markers (OLFM4, BMI1,

227 ytes transiently exposed to the SASP exhibit increased expression of stem cell markers and regenerati

228 ion reduced levels of phosphorylated tau and increased expression of synaptophysin.

229 M. tuberculosis-infected IL-21R KO mice had increased expression of T cell inhibitory receptors, red

230 th the lowest mortality was characterized by increased expression of T-cell immunoglobulin and mucin

231 gn3 stability and DNA binding, promoting the increased expression of target genes that drive differen

232 st, the RIP1-deficient cells were defined by increased expression of tartrate-sensitive prostatic aci

233 ould promote acute skin wound healing though increased expression of TGF beta leading to enhanced for

234 ge >2 and false discovery rate < 0.05), with increased expression of Th2, Th9, Th17/Th22 polar cytoki

235 In MG63 osteoblastic cells, increased expression of the 1,25(OH)2D target gene CYP24

236 associated with disease risk correlate with increased expression of the 7p21 gene TMEM106B and no ot

237 mportant, these changes were associated with increased expression of the antifibrotic protein Smad7 a

238 VIVIT treatment in 5xFAD mice led to increased expression of the astrocytic glutamate transpo

239 aberrant cortical positioning of neurons and increased expression of the astrocytic marker GFAP in th

240 s via divergent regulation of two processes: increased expression of the AtlA murein hydrolase and de

241 strated hypomethylation of MPO and PRTN3 and increased expression of the autoantigens; in remission,

242 -iPSC-CMs under catecholamine-induced stress increased expression of the cardiac stress marker NR4A1;

243 n led to enhanced G2/M cell-cycle arrest and increased expression of the CDK inhibitor 1B (p27Kip1) a

244 increased levels of Il1b, we did measure an increased expression of the chemokine-encoding gene Ccl2

245 in the lung-draining lymph node, as well as increased expression of the costimulatory molecule CD86.

246 Previously we observed increased expression of the critically important beta-ce

247 ed beta-galactosidase (SA-betagal) activity, increased expression of the cyclin-dependent kinase (CDK

248 ptor co-agonist d-serine were accompanied by increased expression of the d-serine degrading enzyme d-

249 ic markers pdx1, glut2, mafA, and nkx6.1 and increased expression of the dedifferentiation markers so

250 methylation, resulting at least in part from increased expression of the DNA methyltransferase DNMT1

251 Increased expression of the EGR1-regulated cardioprotect

252 ot account for all the actions observed with increased expression of the enzyme.

253 F-alpha- and TRAIL-mediated apoptosis due to increased expression of the ER stress mediator tribbles-

254 sitivity to Wnt stimulation, associated with increased expression of the FZD4 receptor.

255 wn-regulation of diabetes-related genes, and increased expression of the genes encoding the myokines

256 Apc-mutant adenomas were characterized by increased expression of the glial nexin Serpine2, the hu

257 ification of the MYC gene is correlated with increased expression of the homologous DNA recombination

258 transcription 1 in the liver and spleen and increased expression of the IFN-gamma-inducible chemokin

259 The Igf1r-deficient mice exhibited an increased expression of the IGF system and surfactant ge

260 ted with brain insulin resistance and showed increased expression of the key downstream messenger ins

261 ced efferocytosis, which was associated with increased expression of the macrophage efferocytosis rec

262 ilial PD patient fibroblasts, accompanied by increased expression of the mitochondrial calcium transp

263 vated mitochondrial-to-nuclear DNA ratio and increased expression of the mitochondrial markers transc

264 Consistently, SCH772984 increased expression of the mitochondrial transcriptiona

265 m airway hyperresponsiveness, due in part to increased expression of the murine ortholog of human chy

266 Increased expression of the mutant GlyR alpha1(Q177K) su

267 sion of angiotensin converting enzyme 2, and increased expression of the Na(+)-K(+)-2Cl(-) cotranspor

268 rimary cortical neurons in culture, ketamine increased expression of the neural plasticity-related pr

269 Additionally, we observed an increased expression of the NLRP3 gene in macrophages an

270 increased expression of CXCL12 downstream of increased expression of the noncanonical NF-kappaB trans

271 calization of the NRF2 transcription factor, increased expression of the NRF2-related antioxidant res

272 post-synaptic SMB motor neuron partners via increased expression of the odr-2 glycosylated phosphati

273 Increased expression of the pluripotency gene Klf4 in th

274 ecause both C57BL/6J and Pde11a KO mice show increased expression of the pro-inflammatory cytokine in

275 n premature depletion of the progenitors and increased expression of the proapoptotic protein Bim (al

276 uent translocations of 9p24.1 and associated increased expression of the programmed cell death protei

277 o kidneys with IRI, which was accompanied by increased expression of the proinflammatory molecules.

278 systems biology approach, is responsible for increased expression of the splicing factor PTBP1 (polyp

279 M-specific TH17 cell differentiation through increased expression of the TH17-instructing cytokines I

280 titis-like phenotype that is triggered by an increased expression of the thymic stromal lymphopoietin

281 otic lesions lacking myeloid CaMKIIgamma had increased expression of the transcription factor ATF6.

282 Analysis of transcriptomes indicated that increased expression of the transcription factor PHYTOCH

283 Moreover, the increased expression of the transcription factors GLI1/G

284 e expression, whereas either no change or an increased expression of these genes was observed in mice

285 nd PDCD1LG2/PD-L2, and copy number-dependent increased expression of these ligands.

286 Increased expression of TLR4 and myeloid differentiation

287 n of oncogenes (PDGFA, PDGFB, and TGFB1) and increased expression of tumor suppressor genes (TNFRSF14

288 We observed increased expression of type 1 IFN-stimulated genes (ISG

289 A recent study from our group showed an increased expression of uncoupling protein-2 (UCP2) in p

290 trols, no change in tumour angiogenesis, but increased expression of vascular cell adhesion molecule-

291 ement and activity, ultimately leading to an increased expression of virulence.

292 n in murine and human macrophages results in increased expression of with-no-lysine kinase 1 (WNK1),

293 Furthermore, the increased expression of Wnt4 elevated the phosphorylatio

294 NFkappaBIZ, in the Treg-DC, together with an increased expression of Wnt5a, a negative regulator of D

295 Here we determined that increased expression of XRN2 induced EMT and promoted me

296 ll adhesion to hCMEC/D3 cells, whereas their increased expression partially prevented THP1, Jurkat an

297 on in the TRAF3 knockout mice was not due to increased expression platelet receptors.

298 at in human tissue data sets, MAE genes show increased expression variability.

299 This increased expression was dependent on glucocorticoid res

300 These 4 gene sets showed increased expression with increasing pathological AMR (p