ライフサイエンスコーパス: increased expression of

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

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

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

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

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

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

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

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

9 ration of epithelial KIT(+) progenitors, and increased expression of a target gene, Disco-interacting

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

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

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

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

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

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

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

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

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

19 2 suppressed expression of CYP24A1, but also increased expression of an exon 10-skipped CYP24A1 splic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

40 The mpk3 and mpk6 mutants display increased expression of CBF genes and enhanced freezing

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

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

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

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

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

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

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

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

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

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

51 This resulted in sustained, several-fold increased expression of CRRY in the RPE, which significa

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

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

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

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

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

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

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

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

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

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

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

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

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

65 last resulted in decreased proliferation and increased expression of differentiation markers, includi

66 4166 induced phosphorylation of NFkappaB and increased expression of dual specificity phosphatase 6 (

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

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

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

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

71 Increased expression of EGFR in myeloid cells from the c

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

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

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

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

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

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

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

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

80 3H in tumorigenesis have been interested and increased expression of FAM83H and MYC in hepatocellular

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

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

83 DEX-Ac treatment led to increased expression of fibronectin, collagen I, and alp

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

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

86 1 showed increased suppressive function, and increased expression of Foxp3 and TGF-beta.

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

88 ponse, but PD-L1-expressing ILC2s stimulated increased expression of GATA3 and production of IL-13 by

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

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

91 We observed increased expression of genes associated with inflammato

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

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

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

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

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

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

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

99 MCH increased expression of genes regulating hypoxia signall

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 te smoke developed ileitis, characterized by increased expression of interferon gamma, compared to wi

131 ConA-treated HSCs showed increased expression of interferon-beta, tumor necrosis

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

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

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

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

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

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

138 We found increased expression of KIBRA and phosphorylated YAP pro

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

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

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

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

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

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

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

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

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

148 adherence compared to the wild type, due to increased expression of mannose-sensitive type 1 pili.

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

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

151 : enhanced invasion and migration, including increased expression of matrix metalloproteinases and ac

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

153 Increased expression of MCM8 in prostate cancer is assoc

154 Increased expression of mcr-1 results in decreased growt

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

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

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

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

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

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

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

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

163 We validated increased expression of multiple miRNAs, including miR12

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

165 up of double-expressor lymphomas, which have increased expression of MYC and BCL-2 and/or BCL-6 by im

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

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

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

169 ilitated by tumour-associated macrophages or increased expression of negative regulators of cytotoxic

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

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

172 Increased expression of neurotensin receptor 1 (NTR1) ha

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

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

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

176 We observed a significantly increased expression of NKG2D ligands on cells infected

177 These data suggest an increased expression of NLRP12 in association with prost

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

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

180 odocytes in vitro with TGF-beta1 resulted in increased expression of Notch-1, ErbB4, pErbB4, and pEGF

181 We found that LPS increased expression of Nox4, TNF-alpha, and proliferati

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

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

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

185 Interestingly, increased expression of osteogenic differentiation-relat

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

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

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

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

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

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

192 Single ATP injection increased expression of phospho-STAT3 and GAP43, two mar

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

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

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

196 Increased expression of PPP1R11 in p53-deficient CRC cel

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

212 and is also bound by RBM3, which drives the increased expression of RTN3.

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

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

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

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

217 The antennae of R. prolixus showed increased expression of several chemosensory-related gen

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 After radiation, the CD8(+) DCs increased expression of surface molecules required for N

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

252 Increased expression of the EGR1-regulated cardioprotect

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

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

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

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

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

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

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

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

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

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

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

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

265 Consistently, SCH772984 increased expression of the mitochondrial transcriptiona

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

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

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

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

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

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

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

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

274 Increased expression of the pluripotency gene Klf4 in th

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

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

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

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

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

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

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

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

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

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

285 The hearts of FGFR1(DT-cKO) mice showed increased expression of the transient receptor potential

286 re(ERTM);LSL-Kras(G12D);Klf5(fl/fl) mice had increased expression of the tumor suppressor NDRG2 and r

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

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

289 Increased expression of TLR4 and myeloid differentiation

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

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

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

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

294 ion, formation of a continuous EC layer, and increased expression of VE-cadherin.

295 ice, a model of post-traumatic OA in humans, increased expression of VEGF is associated with cataboli

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

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

298 Furthermore, the increased expression of Wnt4 elevated the phosphorylatio

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

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