ライフサイエンスコーパス: elevated expression of

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

2 uman pathogen Chlamydia trachomatis exhibits elevated expression of a putative iron-transport system

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

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

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

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

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

8 cells exhibit a proapoptotic propensity with elevated expression of activated caspases and are decrea

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

10 Elevated expressions of adipose triglyceride lipase and

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

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

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

14 iated with activation of the Imd pathway and elevated expression of AMP (antimicrobial peptide) genes

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

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

17 Despite the elevated expression of antioxidant transcripts, we obser

18 In mice, this SNP also leads to elevated expression of anxiety-like behaviors that are n

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

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

21 Elevated expression of aromatase (estrogen synthase) in

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

23 otype and transcription factor profile, with elevated expression of B-cell leukemia/lymphoma 6 (Bcl-6

24 Elevated expression of BCL2 is considered a consistent f

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

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

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

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

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

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

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

32 Elevated expression of c-MYC in human colorectal cancer

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

34 Elevated expression of caspases 3 and 7 accounts for the

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

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

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

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

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

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

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

42 exposure, quiescence-defective animals show elevated expression of cellular stress reporter genes an

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

44 c asthma and suggest this may be mediated by elevated expression of CRTh2, leading to higher numbers

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

46 Elevated expression of CXCL2 and MIF and an increased nu

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

48 As in human multiple myelomas, elevated expression of cyclin D genes was common, and p5

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

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

51 itional null (Klf4CN) corneas that displayed elevated expression of cytokines and cytokine receptors,

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

53 Elevated expression of DHHC3 correlated with diminished

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

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

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

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

58 Conversely, elevated expression of DYRK1 phosphorylates Thr27 of ID2

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

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

61 Elevated expression of either Foxp represses the express

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

63 in Drosophila melanogaster demonstrated that elevated expression of either of these genes confers res

64 NSCLC spheroid cultures display elevated expression of EMT master-switch transcription f

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

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

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

68 Elevated expression of EZH2 is common in human cancers a

69 In this study, we found that elevated expression of FASN is associated with advanced

70 sembling squamous cell carcinoma in situ and elevated expression of Fbxw7 target proteins.

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

72 imary adult erythroid progenitors results in elevated expression of fetal gamma-globin.

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

74 Furthermore, elevated expression of FOXM1/SKP2 and c-Myc also contrib

75 Our studies suggest that elevated expression of G1P3 may perturb canonical tumor-

76 More importantly, elevated expression of G1P3 was significantly associated

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

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

79 ibiting an activated phenotype as defined by elevated expression of GARP, CD103, CTLA-4, and IL10, al

80 The DLL1(+) cluster had elevated expression of genes associated with endocytosis

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

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

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

84 Elevated expression of genes encoding putative vacuolar

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

86 Elevated expression of genes involved in synthesis and o

87 domains (NCoRDeltaID) in the liver leads to elevated expression of genes regulated by thyroid hormon

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

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

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

91 raction of CD8 memory phenotype T cells with elevated expression of glucocorticoid-induced TNFR-relat

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

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

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

95 The elevated expression of HbN in Mtb and M. smegmatis facil

96 Elevated expression of Hda impeded growth of the dnaN159

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

98 We found that elevated expression of heparanase by high glucose was as

99 Elevated expression of heparanase is associated with sev

100 Elevated expression of HIF-1alpha was found in peri-impl

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

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

103 HSP90 in muscle cells but as effectively by elevated expression of HSP90 in intestine or neuronal ce

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

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

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

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

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

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

110 Elevated expression of IFNalpha mRNA was limited to lymp

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

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

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

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

115 Loss of Chd4 leads to elevated expression of immature Schwann cell genes (Id2,

116 es (IBDs) and malignancy are associated with elevated expression of indoleamine 2,3 dioxygenase-1 (ID

117 CC development is often associated both with elevated expression of inducible nitric oxide synthase (

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

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

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

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

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

123 , a reduction in mobility and longevity, and elevated expression of innate immune response genes in g

124 MDSCs had elevated expression of iNOS upon exposure to IFN-gamma a

125 oted amyloid clearance mechanisms, including elevated expression of insulin-degrading enzyme.

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

127 nflammatory cells into the tumors along with elevated expression of interleukin (IL)-6 and IL-11 and

128 ced p38 phosphorylation, CD62L shedding, and elevated expression of interleukin (IL)-6 and IL-1beta m

129 of apoptosis, reduced expression of SOX2 but elevated expression of its antagonist CDX2.

130 Elevated expression of kallikrein was detected in the ki

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

132 By contrast, elevated expression of Lar, a receptor protein tyrosine

133 Western diet-fed L-sIDOL mice had elevated expression of liver X receptor target genes and

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

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

136 ed TAM phenotype, which was characterized by elevated expression of mannose receptor-1, Arginase-1, i

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

138 ic mice at different disease stages revealed elevated expression of markers for endoplasmic reticulum

139 ome-wide microarray analysis revealed highly elevated expression of matrix metalloproteinase 10 and o

140 sed Akt2-deficient mice showed significantly elevated expression of matrix metalloproteinase-9 (MMP-9

141 Elevated expression of matrix metalloproteinase7 (MMP7)

142 c changes in multiple myeloma, which include elevated expression of Mcl-1 and, less frequently, Bcl-2

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

144 Blimp1-deficient DCs exhibited elevated expression of MHC II, and exposure to TLR agoni

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

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

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

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

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

150 As a result of the elevated expression of miR-221, expression of many cell

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

152 ent of mouse intracranial tumors resulted in elevated expression of miR-494.

153 TCN significantly reduced PTH or PGE2 elevated expression of MMP-13 in osteoblastic cells with

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

155 of transcript levels revealed significantly elevated expression of Mn1, and a trend toward increased

156 Together with enhanced NT levels, the elevated expression of modified Trk receptors on skin an

157 white adipose tissue (epididymal WAT) showed elevated expression of mRNA and protein markers of lipol

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

159 o nC60 aggregates with associated Hg(2+) had elevated expression of mt2 when compared to fish exposed

160 ur data indicate that CD34(+) AML cells have elevated expression of multiple glutathione pathway regu

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

162 Elevated expression of MYC is a shared property of many

163 The elevated expression of myelin proteins correlated with a

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

165 In this classifier, elevated expression of NEGR1 was associated with better

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

167 d higher constitutive NF-kappaB activity and elevated expression of NF-kappaB targets of antiapoptoti

168 tive real-time-PCR analysis of gonads showed elevated expression of NF-kappaB-regulated genes.

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

170 hibition of fatty-acid synthesis resulted in elevated expression of numerous markers of ER stress in

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 Deletion of HIF1alpha results in elevated expression of p16(Ink4a) and p19(Arf) in LSCs,

175 rophthalmia-associated transcription factor, elevated expression of p21WAF1 and p27KIP2, hypophosphor

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

177 ion, likely due to the lack of effect on the elevated expression of p53 regulated proapoptotic pathwa

178 widespread apoptosis associated with global elevated expression of p53.

179 nduced senescence, which was associated with elevated expression of p53beta at mRNA and protein level

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

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

182 ia, correlated with cuticle permeability and elevated expression of pathogenesis-related genes PR1a a

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

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

185 Elevated expression of PDGF receptors on stromal CAFs is

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

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 B, a transcription factor for PP2A, leads to elevated expression of PP2A.

190 WAT (iWAT) of Ksrp(-/-) mice because of the elevated expression of PR domain containing 16 and perox

191 PKCvarepsilon-depleted NSCLC cells show elevated expression of pro-apoptotic proteins of the Bcl

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

193 at UPR activation in human tumors results in elevated expression of proangiogenic mediators and a con

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

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

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

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

198 Kim1(RECtg) kidneys had elevated expression of proinflammatory monocyte chemotac

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

200 Elevated expression of purine synthetic enzymes correlat

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

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

203 Elevated expression of REGgamma exacerbates local inflam

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

205 s of RpaC function can however be rescued by elevated expression of RpaB, indicative of functional ov

206 persistent activated STAT3 colocalizes with elevated expression of S1PR1, a G-protein-coupled recept

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

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

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

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

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

212 The chd7 morphants show elevated expression of several potent cell-cycle inhibit

213 me profiling of JUB1 overexpressors revealed elevated expression of several reactive oxygen species-r

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

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

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

217 odel was established to mimic the 10-15-fold elevated expression of sIFNAR2a observed in some human d

218 As elevated expression of SNX19 has been associated with SC

219 Elevated expression of ST2, the ligand-binding chain of

220 rticularly at night, and have low sugars and elevated expression of starvation genes at night.

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

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

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

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

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

226 impaired Blimp-1 expression and resulted in elevated expression of Tfh-specific genes.

227 mouse cranial neural crest cells results in elevated expression of TGF-beta2 and TGF-beta receptor t

228 stages of the disease and is associated with elevated expression of the 18 kDa mitochondrial transloc

229 gamma-deficient articular cartilage exhibits elevated expression of the additional catabolic factors

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

231 ceptor (TLR) 9 that similarly localizes with elevated expression of the cathelicidin antimicrobial pe

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

233 Elevated expression of the chemokine receptor CCR4 in tu

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

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

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

237 Elevated expression of the epidermal growth factor recep

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

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

240 ntitative polymerase chain reaction revealed elevated expression of the following molecules in the li

241 titution has wide-ranging effects, including elevated expression of the general stress sigma factor (

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

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

244 Elevated expression of the homeodomain transcription fac

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

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

247 While elevated expression of the immunosuppressive cytokine IL

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

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

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

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

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

253 Elevated expression of the Notch3 receptor has been corr

254 his issue, Chen et al. provide evidence that elevated expression of the nuclear inner membrane protei

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

256 Elevated expression of the proinflammatory cytokine IL-1

257 as the earliest change detected, even before elevated expression of the proinflammatory cytokines, IL

258 Elevated expression of the prostaglandin synthase cycloo

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

260 on between obesity and thrombosis, involving elevated expression of the prothrombotic molecules plasm

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

262 switches to a terminal outcome that features elevated expression of the transcription factor CHOP (GA

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

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

265 blished genome-wide expression data revealed elevated expression of the Wnt receptor FZD2 and the Wnt

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

267 eased rates of O2 consumption, together with elevated expression of thermogenic genes.

268 The elevated expression of these cytokines correlated with i

269 Elevated expression of these genes was correlated with h

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

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

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

273 ic inhibitors targeting cancers that display elevated expression of this kinase.

274 nsistent with a role for RpaC in DNA repair, elevated expression of this protein leads to enhanced re

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

276 d tumor burden and increased survival, while elevated expression of TIGAR in human colon tumors sugge

277 Elevated expression of Tim-3 on virus-specific T cells d

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

279 CHQ elevated expression of TNFR-associated factor 6, a commo

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

281 ultures show CIC characteristics, displaying elevated expression of transcription factors KLF4, SOX2,

282 en-activated protein kinase phosphorylation, elevated expression of transforming growth factor-beta-r

283 Elevated expression of translocator protein (TSPO) has b

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

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

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

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

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

289 r tissue-based antigenic stimulation because elevated expression of UPR components was detected withi

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

291 Elevated expression of VEGF and activation of the VEGF r

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

293 These neurons were characterized by elevated expression of VGCCs and enhanced voltage-gated

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

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

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

297 RP6), phosphorylation of GSK3alpha/beta, and elevated expression of Wnt target genes.

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

299 a growing number of diseases associated with elevated expression of XBP1s.

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