ライフサイエンスコーパス: elevated expression of

1 In previous work, we discovered an elevated expression of 14-3-3 proteins in inflammatory a

2 iption factor Ets2 and is accompanied by the elevated expression of a cluster of small nucleolar RNAs

3 tment with three HSP90 inhibitors results in elevated expression of a large number of heat shock prot

4 able to attribute all altered behaviours to elevated expression of a single gene, Cdkn1c.

5 from ERalpha(+) breast cancers demonstrates elevated expression of a UPR gene signature that is a po

6 production and macrophage cell death through elevated expression of A-FABP, thus establishing A-FABP

7 Heat treatment resulted in elevated expression of A3A and A3G in a temperature-depe

8 ricarp appears to be tightly associated with elevated expression of AcMYB123 and AcbHLH42.

9 eurite length and branching, coinciding with elevated expression of actin-cross-linking proteins at t

10 NK cells from HIV-infected individuals have elevated expression of activation markers, spontaneously

11 Elevated expressions of adipose triglyceride lipase and

12 erformance in wild-type mice correlated with elevated expression of aerobic glycolysis enzymes.

13 In vivo data confirmed the elevated expression of AhR by LPS and the LPS-enhanced 2

14 In addition, we observed significantly elevated expression of ALDH1 in lung metastasis and MDR1

15 ion of the CSCs signature, which consists of elevated expression of ALDH1A1 and stem-related genes, h

16 cell extracts from exercised mice, we found elevated expression of Alox15 and Alox5 and higher RvD1

17 We identified a CAF subpopulation with elevated expression of alpha-smooth muscle actin (alphaS

18 K2V617F+ megakaryocytes from patients showed elevated expression of alpha5 subunit, and a neutralizin

19 protected from CVD, there was significantly elevated expression of an esterase, arylacetamide deacet

20 Elevated expression of an ethylene signaling gene, ETHYL

21 The interaction with AR leads to the elevated expression of androgen response genes in androg

22 oliferation, diminished cytokine production, elevated expression of anergy-associated genes, and dimi

23 ce as demonstrated by in vivo imaging and by elevated expression of angiogenesis markers including PE

24 Transcriptomic analyses identified elevated expression of another kinase, protein tyrosine

25 rthermore, this occurred in association with elevated expression of antioxidant enzymes (SOD1, SOD2,

26 Despite the elevated expression of antioxidant transcripts, we obser

27 ession of prostate cancer has been linked to elevated expression of AR in malignant tissue, suggestin

28 Elevated expression of AR-FL alone is sufficient for Abi

29 phages respond to the Th2 cytokine IL-4 with elevated expression of arachidonate 15-lipoxygenase (ALO

30 yB seedlings and mature stem segments showed elevated expression of auxin-responsive genes and expres

31 ributed to a lack of G-protein signaling and elevated expression of betaarr2 and G protein-coupled re

32 Rev-erbalpha ablation led to the robust elevated expression of betaKlotho.

33 horylated Smad 1/5/8 nuclear staining and by elevated expression of Bmp2, Bmpr1b, Bmpr2, and BMP sign

34 In addition, elevated expression of both Axl and 14-3-3zeta showed st

35 low in transformed cells in correlation with elevated expressions of both antioxidant enzymes (catala

36 is very low in AsT cells in correlation with elevated expressions of both antioxidant enzymes and ant

37 forced expression of miR-150 attenuates the elevated expression of brown fat genes caused by KSRP de

38 Knockdown of Anxa4 in zebrafish leads to elevated expression of caspase 8 and Delta113p53, and li

39 d decreased expression of anabolic genes and elevated expression of catabolic and inflammatory genes.

40 Hypoxic regions of HCC xenografts displayed elevated expression of Cav1.

41 nd provides an action mechanism that ensures elevated expression of CCA1 at dawn to sustain a robust

42 em and cerebellum, triggering cell death and elevated expression of Ccl2, Il6, and Mmp8 characteristi

43 nes and related molecules revealed 84.6-fold elevated expression of Ccl3 (MIP-1a) 24 h after light ex

44 Taken together, the data demonstrate that elevated expression of CCN1 by dermal fibroblasts functi

45 uding release of pertinent Tc2 cytokines and elevated expression of CD40L.

46 e in peripheral CD8(+) T cells that includes elevated expression of CD44, CD122, and Eomesodermin and

47 +) B cells, and IgM(lo) CD23(-) B cells with elevated expression of CD86.

48 BRAF(V600E) induced elevated expression of CDK2, CDK4, MITF and EST1/2 prote

49 increased inflammatory signature, including elevated expression of chemokines and chemokine receptor

50 n/hypoxia mice and monocrotaline rats showed elevated expression of CLIC4, activation of Arf6 and NF-

51 ctor (MRTF), a fibrogenic RHOA effector, and elevated expression of connective tissue growth factor a

52 We observed elevated expression of crucial injury response factors-i

53 heir citrate accumulation and reversed their elevated expression of CsrB.

54 Elevated expression of CXCL2 and MIF and an increased nu

55 le sclerosis, we find that TH1/17 cells have elevated expression of CXCR3 and reduced expression of I

56 Here, we report that elevated expression of CXorf67 (chromosome X open readin

57 patocellular carcinoma or breast cancer with elevated expression of cyclin D1.

58 ncing reduced LLC-PK1 cell proliferation and elevated expression of cyclin-dependent kinase inhibitor

59 leeding, higher apoptosis of colonic mucosa, elevated expression of cytokines and chemokines, altered

60 We previously reported significantly elevated expression of cytoplasmic Omi/HtrA2, triggers c

61 Elevated expression of DHHC3 correlated with diminished

62 found that neural crest progenitors display elevated expression of DICER, which promotes enhanced ma

63 Surprisingly, elevated expression of different Hox genes and various o

64 degree of hypersensitivity to DNA damage and elevated expression of DNA damage marker genes.

65 Here, we report an elevated expression of DNA polymerase eta (Pol eta) in o

66 We show that elevated expression of DNFA genes is characteristic of m

67 There is elevated expression of DNMT1, Notch1, and the viral gene

68 Conversely, elevated expression of DYRK1 phosphorylates Thr27 of ID2

69 Elevated expression of E2F1 in adipocyte fraction of hum

70 Here we report that elevated expression of each GEF in circulating tumor cel

71 rtalized human breast epithelial cells, that elevated expression of eIF4E translationally activates t

72 trains sensitive to BRD4 inhibition revealed elevated expression of either MYCN or c-MYC, with MYCN e

73 Additionally, we observed elevated expression of endothelial leukocyte adhesion mo

74 nkephalins, which is partly mediated through elevated expression of enkephalinases.

75 Elevated expression of enzymes of the cholesterol pathwa

76 human and mouse atherosclerotic plaques show elevated expression of EphA2, a guidance molecule involv

77 natures, connected loss of CETN3 and SKP1 to elevated expression of epidermal growth factor receptor

78 ry epithelial cell stem/progenitor activity, elevated expression of estrogen receptor alpha, and incr

79 Higher levels of plasma ET-1 and Ang II and elevated expression of ET-1 mRNA in cardiac tissue were

80 Elevated expression of EZH2, the enzymatic subunit of po

81 d toward poorer outcome in CCA patients with elevated expression of ferritin and hepcidin, two major

82 ysis using H&E staining and IF confirmed the elevated expression of fibrosis markers in stenotic comp

83 synthesis, and leads to decreased stress and elevated expression of fimbrial adhesins.

84 a basis to interpret clinical evidence that elevated expression of GADD45B confers poor clinical out

85 as an upstream pathway that accounts for the elevated expression of GALNT14 in lung-metastatic BCCs.

86 ogeneous samples in the ASD brain, including elevated expression of gene sets associated with glial a

87 Elevated expression of gene sets such as ECM and cell ad

88 of maturation-related genes and persistent, elevated expression of genes associated with jasmonate a

89 e also observed in the nos mutant, including elevated expression of genes associated with oxidative/n

90 sely, a strain overexpressing ssp1 exhibited elevated expression of genes encoding AAOs and ADD, resu

91 Moreover, CD34(+) SMG cells exhibited elevated expression of genes encoding extracellular matr

92 Elevated expression of genes encoding putative vacuolar

93 Accordingly, elevated expression of genes encoding sets of enzymes in

94 Importantly, the DeltargsD mutant shows elevated expression of genes in the cAMP-dependent prote

95 atocytes, p16-deficiency was associated with elevated expression of genes involved in fatty acid cata

96 formation, we expected to find significantly elevated expression of genes involved in flower and/or f

97 with mutations in C9ORF72 (C9-ALS) suggests elevated expression of genes that pertain to extracellul

98 ) secondary bone marrow plasma cells display elevated expression of genes that promote cell cycle pro

99 hosts, both bacteriocytes and symbionts show elevated expression of genes underlying energy metabolis

100 in HCC-gained active enhancers is linked to elevated expression) of genes regulating HCC proliferati

101 Similarly, elevated expression of GFI1 impedes the in vitro expansi

102 The 1279 T variant has elevated expression of Ghd8, thus conferring increased c

103 revealed that this phenotype is caused by an elevated expression of GL2, thus the mutant was named gl

104 shift with increased lactate production and elevated expression of glycolytic enzymes at the mRNA le

105 These T cells also included an elevated expression of GM-CSF and absence of IL-10 expre

106 In summary, we found elevated expression of GPX4 and higher sensitivity to fe

107 dropout in the small intestine and promoted elevated expression of growth factors with established r

108 Finally, elevated expression of H19 lncRNA due to promoter demeth

109 east cancer patient samples revealed that co-elevated expressions of Hec1 and Nek2 correlated with th

110 Elevated expression of high-mobility group AT hook 2 (HM

111 dipogenic differentiation is associated with elevated expression of histone deacetylase 9 (HDAC9), an

112 We confirmed that a subset of TNBCs have elevated expression of HLA-DR in tumor epithelial cells;

113 In vivo, elevated expression of HTM1 causes glycan trimming on mi

114 Conversely, elevated expression of human ARV1 in HEK293 cells or mou

115 We identified elevated expression of HUWE1 in MM compared with normal

116 Elevated expression of hyaluronan (HA) and HA receptors,

117 esults showed the development of hypoxia, an elevated expression of hypoxia-associated glycolytic gen

118 ype resembling human septic neutrophils with elevated expression of ICAM1, CD11b, PD-L1 as well as en

119 reated with ROCK inhibitor Y-27632 exhibited elevated expression of ICM marker NANOG and reduced expr

120 f IL-6 increased with age and contributed to elevated expression of ICOS on aged Tregs.

121 ulation of infiltrating cells in the dermis, elevated expression of IFN-gamma, CCL5, CCL8, and UBD in

122 ogy in Zc3h12a(+/-) mice was associated with elevated expression of IL-17A- and IL-17C-dependent gene

123 Elevated expression of IL-17RB had a stronger correlatio

124 We found elevated expression of IL-1beta in the lymphoid tissues

125 FURIN-deficient Th cells instead show elevated expression of IL-4R subunit alpha on cell surfa

126 t with BCR-ABL1 kinase inhibitors results in elevated expression of IL7R which enables the survival o

127 Surprisingly, Upf2 fb-KO mice exhibit elevated expression of immune genes and brain inflammati

128 In individuals over 85 years of age, the elevated expression of inflammasome gene modules was ass

129 s that P2X7 receptor activation is linked to elevated expression of inflammation promoting factors, t

130 inflammation and immune suppression through elevated expression of inflammatory adhesion molecules s

131 V-2 immune complexes activate Syk to mediate elevated expression of inflammatory cytokines.

132 d brain are marked by dystrophic morphology, elevated expression of inflammatory markers, and diminis

133 showed increased myocardial infarct size and elevated expression of inflammatory mediators in ischemi

134 ealed that C. perfringens induced (P < 0.05) elevated expression of inflammatory mediators of Infgamm

135 h of the UPR(ER) pathway, in which cells had elevated expression of inositol-requiring enzyme 1 (IRE1

136 ated from the blood of adults with ARDS have elevated expression of interferon (IFN) stimulated genes

137 ammatory phenotypes that are associated with elevated expression of interferon (IFN)-induced genes (I

138 tly lower than in bp, which is likely due to elevated expression of JA inactivating genes.

139 Human Schwann cells showed elevated expression of key proteins such as nerve growth

140 ricular myocytes treated with miR-294 showed elevated expression of Ki67, p-histone H3, and Aurora B

141 f PRSS3/mesotrypsin knockdown, and also that elevated expression of KLK5 is similarly prognostic for

142 TP53 mutations, were associated with highly elevated expression of KRAS mutation-associated genes.

143 ase gene expression, and was associated with elevated expression of late-response cold-related transc

144 ice showed increased phagocytic activity and elevated expression of LDL receptor and pro-inflammatory

145 Elevated expression of LINC00346 was noted in tumor cell

146 y, immunohistochemical analysis revealed the elevated expression of luciferase and Hmox1 in centrilob

147 higher fungal burden within the brain and an elevated expression of M2 macrophage markers than those

148 yeloid-targeted overexpression of MCPIP show elevated expression of M2 markers and reduced response t

149 his chronic inflammation is characterized by elevated expression of many key inflammatory cytokines a

150 sults in immune dysfunction characterized by elevated expression of markers associated with exhaustio

151 Elevated expression of matrix metalloproteinase7 (MMP7)

152 n TAE684-sensitive parental cells led to the elevated expression of mesenchymal markers and invasive

153 iovascular pathologies revealed consistently elevated expression of MICU2, a regulatory subunit of th

154 On the other hand, naturally elevated expression of miR-124 in embryonic carcinoma ce

155 in reaction and in situ hybridization showed elevated expression of miR-143 in calf models of PAH and

156 Moreover, mice with transgenic elevated expression of miR-155 in nestin-positive neural

157 g myeloproliferative neoplasia also revealed elevated expression of miR-155.

158 Elevated expression of miR-223 in these cell lines reduc

159 Elevated expression of miR-31 was observed in Mdr2(-/-)

160 In our experiments, elevated expression of MMP9 in dry eye subjects correlat

161 BP, increased myocardial wall thickness, and elevated expression of mRNAs of several renal ion transp

162 B+CD8+ T cells), a type 1 IFN signature, and elevated expression of multiple immune inhibitory molecu

163 ell repertoire, these data indicate that the elevated expression of multiple TGFbeta-targeting miRNAs

164 neutrophils was specifically associated with elevated expression of myeloid cell leukemia 1 (Mcl1) bu

165 Elevated expression of NAD(P)H:quinone oxidoreductase 1

166 n of regenerated taste buds, as evidenced by elevated expressions of neurofilament and P2X(3) at the

167 pt were detected in the cytoplasm, alongside elevated expression of NF-kappaB pathway genes.

168 The reasons for the elevated expression of NKG2D ligands are unknown.

169 Finally, elevated expression of NMG correlates with mutant p53 st

170 JUNB and FOSB, which is responsible for the elevated expression of oncogenic FAM83A.

171 Oceanospirillaceae ASP10-02a displayed elevated expression of organic matter acquisition and ce

172 RNA in MC3T3-E1 osteoblast precursors we saw elevated expression of osteoblast-related genes such as

173 steocytes, presence of calcified marrow, and elevated expression of osteocalcin in the osteoblasts lo

174 ase in bone regeneration was associated with elevated expression of osteogenic genes, decreased expre

175 cumulation of jasmonic acid (JA) and JA-Ile, elevated expression of over 2,200 different transcripts

176 reported parallel patterns by sex, with male-elevated expression of overlapping sets of glial/immune-

177 with enhanced mRNA stability and subsequent elevated expression of p21.

178 ts into p53-depleted NTera2 cells results in elevated expression of p53 downstream targets and precoc

179 of KLF2, KLF4, VEGF-A, VEGF-C, and FGFR3 and elevated expression of p57.

180 Finally, neuronal nuclear hypertrophy and elevated expression of p75NTR provide evidence of active

181 Mechanistically, an elevated expression of Par-4 induced apoptosis of hypoph

182 We demonstrate that elevated expression of Pav-KLP underlies transport and p

183 s inflammation in autoimmune disease through elevated expression of PD-L1.

184 PDL tissues, which was further confirmed by elevated expression of phosphorylated Smad5 (p-Smad5) by

185 quercetin and myricetin were related to the elevated expression of photoreceptor-specific proteins,

186 e findings, during amino acid starvation the elevated expression of Pim1 overcame the amino acid inhi

187 ownregulation of SUZ12 and ZNF198 along with elevated expression of Plk1, HOTAIR, and EpCAM.

188 n increased ability to form mammospheres and elevated expression of pluripotency-factors (Oct4, Nanog

189 cardial deformation, cardiac hypertrophy via elevated expression of pro-hypertrophic miR-208a, myocar

190 ent in inflammation-related gene signatures, elevated expression of pro-inflammatory tumorigenic cyto

191 of p53 reversed the increased apoptosis and elevated expression of proapoptotic targets Noxa and Pum

192 exhausted HSV-specific CD8(+) T cells, with elevated expression of programmed death ligand-1 (PD-1)

193 and Bregs, respectively) are increased, with elevated expression of programmed death-ligand 1 and IL-

194 Epithelial GR-null mice had elevated expression of proinflammatory chemokines in the

195 esults indicate that NIHL is associated with elevated expression of proinflammatory cytokines and mic

196 ophilus influenza, which was associated with elevated expression of proinflammatory cytokines.

197 palmitate (PA) for 18 h ex vivo also showed elevated expression of proinflammatory genes (Cxcl1, Il6

198 in atopic dermatitis (AD) is associated with elevated expression of proinflammatory genes and activat

199 activation of PI3K/Akt/NF-kappaB pathway and elevated expression of proliferation and anti-apoptosis

200 ealed a unique gene profile characterized by elevated expression of proteins associated with the resp

201 ult neurogenesis, aminergic innervation, and elevated expression of proteins necessary for memory pro

202 Elevated expression of purine synthetic enzymes correlat

203 AC1 and RAC2 and prolonged survival, whereas elevated expression of RAC1 and RAC2 was associated with

204 Their deletion in mice results in elevated expression of Ramp3 in mammary tissue through a

205 Thus, activated effector T cells with elevated expression of rat nonclassic MHC class I C/E16

206 Elevated expression of REGgamma exacerbates local inflam

207 d in tumors from neuroblastoma patients, and elevated expression of Rho-associated kinase (ROCK)2 is

208 The elevated expression of RLN serves as a natural regulator

209 Therefore, the elevated expression of S100A9 and MMPs are observed in C

210 Elevated expression of S100A9, IL1A, MMP3, MMP7, MMP11,

211 Plants with wrky70 mutations have elevated expression of SARD1 in the absence of pathogens

212 This regulation corresponded with elevated expression of serum-response factor (SRF), a ma

213 f macrophages from Tet2 knockout mice showed elevated expression of several chemokine and cytokine ge

214 ling showed that patients with high WBP5 had elevated expression of several HOX cluster genes, such a

215 n associates with high mutational burden and elevated expression of several immune checkpoint genes.

216 tionally, wood-feeding individuals exhibited elevated expression of several mitochondrial cytochrome

217 R-3189-3p in clinical samples paralleled the elevated expression of SF3B2, which could contribute to

218 Elevated expression of SHMT2 and PSMB4 was found to be a

219 tes exposed to high glucose levels exhibited elevated expression of SHP-1, which was associated with

220 As elevated expression of SNX19 has been associated with SC

221 Elevated expression of SOX2 and its downstream target ge

222 h reporter activity (tagBFP(High)) exhibited elevated expression of stemness and chemoresistance gene

223 growth-inhibiting abiotic stresses and have elevated expression of stress marker genes.

224 onally cold tidal flat might be reflected in elevated expression of stress response and chaperone pro

225 In this study, we show elevated expression of SUB1 in aggressive prostate cance

226 neurons generated on 2D, consistent with the elevated expression of survival markers FOXA2 and EN1 in

227 st, ANA+ healthy African Americans exhibited elevated expression of T-cell activation markers and hig

228 In clinical specimens of TNBC, elevated expression of TDO2 was associated with increase

229 s enhanced neurogenesis correlates well with elevated expression of TGF-beta2 and TGF-beta3, and acti

230 (AD) is a T helper (Th)2-biased disease with elevated expression of Th2 cytokines that responds to Th

231 robust mucoinflammatory features, including elevated expression of Th2-associated markers accompanie

232 Additionally, an elevated expression of the adipogenic marker genes PPARg

233 emorrhage in CCMs is associated with locally elevated expression of the anticoagulant endothelial rec

234 Transcriptome analysis linked Duxbl to elevated expression of the apoptosis-inducing Oas/RNaseL

235 Elevated expression of the ATP7A Cu exporter is known to

236 We show here that elevated expression of the bifunctional DNA glycosylase,

237 eased cell growth arrest was associated with elevated expression of the cell-cycle inhibitor p21.

238 Elevated expression of the chemokine receptor CCR4 in tu

239 protein phosphatase calcineurin (CN) and the elevated expression of the CN-dependent transcription fa

240 T cell stimulation in culture, attributed to elevated expression of the cyclin-dependent kinase inhib

241 Down-regulation of TET1 resulted in elevated expression of the DNA damage marker, suggesting

242 f CD44(+)/CD24(-) cancer stem-like cells and elevated expression of the dual specificity phosphatase

243 d in many soft-tissue sarcomas, resulting in elevated expression of the effector molecule Yes-Associa

244 Elevated expression of the epidermal growth factor recep

245 Microarray analysis identified elevated expression of the ErbB family of receptors and

246 ease in hepatic Fgf21 expression, as well as elevated expression of the FGF21-target gene Igfbp1 Furt

247 wed by long day (LD) photoperiods leading to elevated expression of the floral activator, FT-like gen

248 citatory and inhibitory synapse assembly and elevated expression of the GABAergic synthetic enzyme GA

249 show that in cells overexpressing HRAS(V12), elevated expression of the general transcription factor

250 er Genome Atlas (TCGA) and reveal a markedly elevated expression of the GLUT1 glucose transporter in

251 Chronic stress exposure led to elevated expression of the hypothalamic inhibitory pepti

252 in IFN-gamma responsiveness correlated with elevated expression of the IFN-gamma receptor protein IF

253 While elevated expression of the immunosuppressive cytokine IL

254 sence of tumoral CD8+ T cells was defined by elevated expression of the immunosuppressive marker B7-H

255 nitis and rat pups challenged by LPS/HI have elevated expression of the interleukin-23 (IL-23) recept

256 e to 5-Fluoruracil (5-FU) has been linked to elevated expression of the main target, thymidylate synt

257 Here we report elevated expression of the miR-144-3p/miR-451a cluster i

258 elatively reduced in muscle, where there was elevated expression of the miR486 target genes PTEN and

259 n human airway-infiltrating T cells revealed elevated expression of the miRNA miR-19a in asthma.

260 revealed that Rb/p53-deficient tumors showed elevated expression of the mitochondrial protein transla

261 dent reduction in ER Ca(2+) levels alongside elevated expression of the molecular SOCE components ORA

262 ing area between T-tubules and the SR and an elevated expression of the Na(+)/Ca(2+) exchanger, altho

263 Instrumental training elevated expression of the plasticity marker Zif268 in d

264 Apoptosis-induced tumors displayed elevated expression of the proinflammatory cytokine CXCL

265 BP LARP1 is an mRNA stability regulator, and elevated expression of the protein in hepatocellular and

266 pression was associated with ERK activation, elevated expression of the RAS/RAF downstream co-effecto

267 ciated with mesenchymal-like cell state with elevated expression of the resistant-leading receptor ty

268 High surface thiol density and elevated expression of the ROS scavenger thioredoxin (Tr

269 MYCN, and/or MYCL1 gene expression exhibited elevated expression of the signature genes.

270 ith RA-specific gene expression profiles and elevated expression of the ST6GALNAC1 (p = 0.0023) gene

271 In this regard, elevated expression of the transcription factor X box-bi

272 hat DC-specific Smad7 deficiency resulted in elevated expression of the transcription factors Batf3 a

273 d with increased lipid metabolism, including elevated expression of the transcriptional regulator per

274 actor in the P. aeruginosa arsenal, and also elevated expression of the Type VI (T6) secretion machin

275 ased mammary tumor incidence and burden, and elevated expression of the unfolded protein response and

276 Elevated expression of the Zinc finger E-box binding hom

277 The elevated expression of these cytokines correlated with i

278 Elevated expression of these genes was correlated with h

279 ndicate that there is spatial separation for elevated expression of these important targets in both s

280 Elevated expression of these lncRNAs and c-myc in risk a

281 show that monocyte-derived macrophages have elevated expression of these surface markers, not microg

282 In addition, significantly elevated expression of this enzyme within breast tumors

283 To take advantage of elevated expression of this pathway, we designed drug-lo

284 Our results suggest that an elevated expression of this transcript starting in adole

285 Uniformly elevated expression of TLR-9, occasional MYD88 mutations

286 We report elevated expression of TNFR2 under Th17-polarization con

287 SILAC mass spectrometry indicated that elevated expression of tRNAi(Met) significantly increase

288 They also showed elevated expression of tumor necrosis factor alpha (TNF-

289 of both races displayed T-cell expansion and elevated expression of type I and II interferon pathways

290 n of the integrin alpha4 in mice resulted in elevated expression of UCP1 and beige adipogenesis of su

291 Rbpj in mice results in browning of WAT and elevated expression of uncoupling protein 1 (Ucp1), a ke

292 ed intracellular free fatty acids (FFAs) and elevated expression of uncoupling protein 2 (UCP2) witho

293 systems of acquired resistance to EGFR TKIs, elevated expression of urokinase plasminogen activator (

294 Elevated expression of VEGF and activation of the VEGF r

295 LMSs and 24 leiomyomas showed a significant elevated expression of versican in human LMS versus beni

296 there is competitive selection of cells with elevated expression of virus oncoproteins.

297 in the cerebrovasculature, and substantially elevated expression of WNT inhibitors in the neocortex.

298 Cortical bone of Gnas(+/p-) mice showed elevated expression of Wnt inhibitors sclerostin and Sfr

299 Transcriptional profiling revealed elevated expression of WNT7B occurred in PDAC cell lines

300 Similarly, Elevated expression of ZEB1 and CD117 are found in the p