ライフサイエンスコーパス: increased expression of

1 LDH) and was oxidative in nature as shown by increased expression of 8-hydroxydeoxyguanosine (8-OHdg,

2 onsistent with this explanation, we observed increased expression of a GABA transporter, GABA transpo

3 in refractive index in the lens nucleus and increased expression of a particular crystallin protein

4 In addition, increased expression of a serine protease inhibitor, the

5 MLL1) gene rearrangement is characterized by increased expression of a set of homeodomain transcripti

6 risk for schizophrenia and bipolar disorder, increased expression of a ST3GAL3 transcript with risk f

7 VEP is sensitive to changes mediated by the increased expression of alpha-synuclein and especially w

8 compared to naive MDSC control, evMDSC have increased expression of an anti-angiogenic factor thromb

9 pt with risk for schizophrenia and ADHD, and increased expression of an XPNPEP3 transcript with risk

10 iated reduction in drug sensitivity involves increased expression of antiapoptotic proteins and susta

11 ic survivors, nonsurvivors had significantly increased expression of any checkpoint molecule on any c

12 ney HEK293 cells and examined the effects of increased expression of APOL1 (G0, G1, G2, G0G0, G0G1, o

13 arrest, reduced proliferation, migration and increased expression of apoptotic markers.

14 ical analysis of the mouse brain revealed an increased expression of aquaporin4 (AQP4) in the flight

15 Increased expression of Atg5, Atg16, Irgm1, Tlr4, and Ly

16 The increased expression of Atoh1 mRNA after LKB1 loss from

17 anced Zip14-dependent zinc uptake by muscle, increased expression of Atrogin1 and MuRF1 and markedly

18 of Ras, inhibition of Akt/mTOR pathways, and increased expression of autophagy markers, leading to an

19 d cell growth and induced apoptosis and also increased expression of Bax as well as cleaved caspase-3

20 increased brain capillary pericyte density, increased expression of BBB tight junction proteins, red

21 In addition, we find increased expression of beta-site cleaving enzyme (BACE1

22 ersus tumor-infiltrating monocytes and found increased expression of both pro- and anti-inflammatory

23 eads that could not pass the plasma membrane increased expression of both TCSn::GFP and Cytokinin Res

24 We detected increased expression of both tumor-associated truncated

25 SIK1) stabilized the deacetylase, leading to increased expression of c-Myc, which in turn stimulated

26 ediated synaptic engulfment is enhanced with increased expression of C4.

27 RBalpha, and deletion of REV-ERBalpha causes increased expression of C4b transcript in neurons and as

28 These changes are preceded by increased expression of calcium/calmodulin kinase IV (CA

29 d with amplification of Myc target genes and increased expression of canonical Wnt signaling in treat

30 This coincided with increased expression of caspase-8-associated protein 2,

31 Next, we show a significantly increased expression of caspase-mediated apoptosis by si

32 n AAA tissues obtained from surgery revealed increased expression of CCR2 that was co-localized with

33 g repertoires as a result of infection, with increased expression of CD103 in colon NK cells and curt

34 Interestingly, increased expression of CD25 only partially accounted fo

35 cells (Tregs), in contrast, demonstrated an increased expression of CD28 with aging and CTLA4-Ig tre

36 reater competitive advantage as evidenced by increased expression of CD5 and IL-7Ralpha.

37 BCG infection increased expression of CD54, MHC Class I and II molecul

38 , CRP level was 12.5mg/dl and the remarkably increased expression of CD64 on neutrophils was found.

39 Larger and more irregular tumors showed increased expression of cell cycle and DNA damage checkp

40 Diseased endothelium had increased expression of chemokine and alarmin genes incl

41 ylation, aberrant metabolic profiles, and an increased expression of chemokines, indicative of a pers

42 NA-sequencing of DAC-treated tumors revealed increased expression of Chi3l3 (Ym1), reflecting an incr

43 tedly, RNAseq analysis revealed dramatically increased expression of cholecystokinin (CCK) in regener

44 DXR induced increased expression of Cldn2 and Cldn4 in murine small

45 Increased expression of CLIC4 (chloride intracellular ch

46 hosphorylation state, as demonstrated by the increased expression of Collagen-I by HSCs incubated wit

47 d that during desiccation, all three species increased expression of common protective genes.

48 CD11c(+) cells from Sema3E KO mice displayed increased expression of costimulatory molecules and IL-1

49 ation of mouse, human, and porcine APC, with increased expression of costimulatory molecules and secr

50 the brain may increase risk to SCZ only and increased expression of CSE1L is associated with SCZ and

51 criptomic analysis linked elevated injury to increased expression of Cybb, the gene encoding the cata

52 oliferation, rather than cell expansion, and increased expression of CYCLIN D3;1-10.

53 ployed a model of murine BSM tissue in which increased expression of desmin or vimentin was induced b

54 Increased expression of diffuse mHtt sequesters the CREB

55 key second messengers (SMAD-1/5/9) and also increased expression of direct target genes (inhibitors

56 TBI increased expression of DNA sensors cyclic GMP-AMP synth

57 reatment of MDSC-like cells activated STAT3, increased expression of DNMT1 and DNMT3b, and enhanced s

58 migraine trigger, nitroglycerin, we observed increased expression of DOR in cortex, hippocampus, and

59 F-beta3, phospho-AKT and phospho-PRAS40, but increased expression of E-cadherin.

60 a result of tumour cell re-wiring leading to increased expression of EGFR, MAPK, CDK4, CDK2, CDK7, CC

61 in reduced muscle expression of miR-379 and increased expression of EIF4G2 and DAPIT.

62 Ilea of mutant mice displayed increased expression of enterocyte markers, but reduced

63 We identified increased expression of envelope (Env) trimers at the ce

64 Importantly, increased expression of epithelial-derived GSDMD is obse

65 staining of joints from the HFD group showed increased expression of ER stress and apoptotic markers

66 The increased expression of ER stress-associated proteins in

67 Breast cancer progression is accompanied by increased expression of extracellular and cell-surface p

68 esistance but increased cell migration, with increased expression of extracellular matrix-related gen

69 and the transcriptomic level, indicated that increased expression of factors such as interferon-gamma

70 Increased expression of FcgammaRIIB correlated with free

71 from smokers and subjects with COPD display increased expression of ferroportin as well as hepcidin.

72 for acquired resistance to EGFR TKIs through increased expression of FGFR1.

73 ed skeletal muscles, which were confirmed by increased expression of fibroblast growth factor-inducib

74 alpha -> nuclear factor kappaB -> caspase-3, increased expressions of fibrosis-related proteins inclu

75 Increased expression of Filamin-B in podocytes in biopsy

76 Our findings indicate that increased expression of FMR1 mRNA isoforms, including Is

77 ion of primate-conserved LINE-1s, as well as increased expression of full-length hominid-specific LIN

78 nerating crypts from patient biopsies showed increased expression of Gal-9, indicating these processe

79 otrophic factor (GDNF) in injured muscle and increased expression of GDNF family receptor alpha1 (GFR

80 qPCR confirmed increased expression of GDPD1 and increased expression o

81 e WT EBV- versus Delta3A-infected tumors and increased expression of genes associated with T cells, s

82 eq and quantitative RT-PCR analyses revealed increased expression of genes associated with tumor cell

83 Livers of Nod2(-/-) tumorigenic mice had increased expression of genes involved in cell prolifera

84 ssion revealed that downregulation of Rab27a increased expression of genes involved in epithelial-to-

85 ng the pancreas of humans with T1D exhibited increased expression of genes located on misfolded loci

86 ced B cell IgA production in vitro, with the increased expression of genes related with class-switchi

87 r overnight fasting, BAT lacking ALK7 showed increased expression of genes responsive to nutrient str

88 educed EZH2 mRNA and protein levels but also increased expression of genes silenced by EZH2, such as

89 tissues from patients with liver disease had increased expression of genes that define PMC identity c

90 Expansion of tuft cells was associated with increased expression of genes that regulate the tricarbo

91 TDF also increased expression of GFAP and decreased expression of

92 th primary muscle afferent sensitization and increased expression of glial cell line-derived neurotro

93 enitor cells promotes cell proliferation and increased expression of glial markers and glia-enriched

94 ation of mutant TLR4 marrow cells results in increased expression of gluconeogenic genes and impaired

95 (GRM1(+)) melanomas exhibited significantly increased expression of glutaminase (GLS), which catalyz

96 ncreased levels of glycolytic intermediates, increased expression of glycolysis genes, and increased

97 In patients with lung cancer, increased expression of HACE1 correlated with reduced le

98 blood glucose levels that is associated with increased expression of hepatic gluconeogenic enzymes in

99 /-) mutant zebrafish exhibited significantly increased expression of hepatocyte markers with no impac

100 Vs of the HERV-K and -H families, as well as increased expression of HERV-K envelope protein.

101 This loss of activity was associated with increased expression of histamine degrading enzymes and

102 steoarthritic samples, which correlated with increased expression of HS6ST1, a 6-O-sulfotransferase,

103 Stimulation of fibroblasts with TGFbeta1 increased expression of HVEM; subsequent stimulation wit

104 -gamma production in mesenteric lymph nodes, increased expression of Ido1 in the cecum, and a complet

105 nflammatory response that is associated with increased expression of IFN-beta and other IFN-related g

106 NOX2 deficiency results in increased expression of IFN-stimulated genes in response

107 er of bronchoalveolar lavage eosinophils and increased expression of IL-13 mRNA but not expression of

108 ay 6 before RV-A2 infection on day 13 showed increased expression of IL-13, IL-5, Gob5, Muc5b, and Mu

109 We found increased expression of IL15RA and IL21 in duodenal tiss

110 Increased expression of IL17A and associated cytokines w

111 We observed increased expression of IL22 and the IL22 receptor (IL22

112 Increased expression of IL22 by PDACs is associated with

113 g shotgun metagenome sequencing and observed increased expression of immune-modulating microbiota, su

114 -induced mice demonstrated that Hh signaling increased expression of immunoregulatory genes and reduc

115 ponse (UPR) components, which coincides with increased expression of inflammasome components, recruit

116 86 with a serine (VbrK C86S mutant) leads to increased expression of inflammatory cytokines in infect

117 sive tissue infiltration by immune cells and increased expression of inflammatory cytokines.

118 NMT3A mutations demonstrated a significantly increased expression of inflammatory genes compared with

119 st commonly found mutations in CHIP, lead to increased expression of inflammatory genes in innate imm

120 transfected to overexpress LPCAT2 exhibited increased expression of inflammatory genes in response t

121 tory receptor Ly49D on educated NK cells and increased expression of inhibitory receptor NKG2A/CD94 o

122 share a common core phenotype including the increased expression of inhibitory receptors, associated

123 uppressed by the tumor microenvironment, and increased expression of inhibitory receptors, including

124 firmed decreased ERBB3/ERBB4 while revealing increased expression of insulin-like growth factor recep

125 [LLV]) or point mutations in Lpro result in increased expression of interferon (IFN) and IFN-stimula

126 g, we reveal rapid viral replication and the increased expression of interferon-associated genes and

127 patient compared with his normal skin showed increased expression of interferon-gamma and chemokines

128 ion and interleukin-1 signaling pathways and increased expression of interferon-induced protein with

129 Increased expression of interferon-stimulated genes (ISG

130 Removal of SLP increased expression of K1, K10 and K2 in 2D and 3D cult

131 Cox proportional hazard ratio, we found that increased expression of K17 at the IHC level is also ass

132 nontarget microRNA control ZIKV demonstrated increased expression of key cytokines and chemokines cri

133 levated extracellular acidification rate and increased expression of key glycolytic genes (GLUT1, HK2

134 inct in young and older adults; for example, increased expression of killer cell lectin-like receptor

135 bility of release associated with an overall increased expression of L-type voltage-gated Ca(2+) chan

136 human ortholog of MaTAR25, and importantly, increased expression of LINC01271 is associated with poo

137 n revealed that rs2242367 is associated with increased expression of LRRK2 and two long intergenic no

138 Here we demonstrate increased expression of LTbetaR ligands in adaptive and

139 ls results in activation of beta-catenin and increased expression of lymphoid enhancer-binding factor

140 s and Sjogren's syndrome patients identified increased expression of lysosome-associated membrane pro

141 cterized by decreased expression of NRF2 and increased expression of MAFG, which cooperates with MAT2

142 onse to cornea debridement wounding, we find increased expression of MAGP1 throughout the central cor

143 nd that NPCs cultured in BrainPhys displayed increased expression of markers for cortical deep-layer

144 nts during HSC activation and accompanied by increased expression of markers of fibrogenesis; incubat

145 o ductal metaplasia, stem cell features, and increased expression of markers of the epithelial-mesenc

146 llagen due to impaired TGFbeta signaling and increased expression of matrix metalloproteinases drivin

147 quencing of engrafted hESC-CMs confirmed the increased expression of matured ventricular cardiomyocyt

148 Indeed, SHIP1 activation mediated the increased expression of Mcl-1 and HSP27, two Akt-depende

149 Mutant-clone HSPCs have increased expression of megakaryocyte-associated genes c

150 hagocytic states, such as IL-6 and IL-4, and increased expression of microglial chemokines, such as m

151 on the promoter region of miR-1185-1, which increased expression of miR-1185-1 and further repressed

152 Furthermore, increased expression of miR-9-3p and miR-9-5p in chemore

153 nterocytes isolated from mice given IL1B had increased expression of MIR200C-3p and decreased levels

154 PGE(2) increased expression of miR675-5p by activating expressi

155 nt accumulation of pyruvate, corroborated by increased expression of mitochondrial enzymes and transp

156 tomas with MYCN amplification, 17q gain, and increased expression of mitochondrial ribosome and elect

157 Based on the increased expression of MLO in mycorrhizal roots and its

158 Increased expression of MMPs have been described in trau

159 ssues progressed from BE to HGD to EAC, they increased expression of mRNAs encoding isoform 1 of RNF1

160 ogressive fibrosis and bronchiolization with increased expression of Muc5b in peripheral airways, hon

161 tory response in the lungs, characterized by increased expression of multiple inflammatory markers an

162 igodendrocyte precursor cells (OPCs) rapidly increased expression of myelin genes and myelin proteins

163 maternally separated (MS) pups identified an increased expression of myelin-related genes and a decre

164 rived from JAK2V617F erythrocytes identified increased expression of myeloperoxidase as the likely me

165 reatment increased I(Na) in association with increased expression of Na(V)1.5.

166 heightened transcription factor binding, and increased expression of neighboring genes.

167 This includes increased expression of neuronal-associated transcriptio

168 Here, we observed increased expression of NPY5 receptor (Y5R) in HCC, whic

169 with decreased GULP1 expression, we observed increased expression of NRF2, HMOX1, and other candidate

170 ssion of ER stress and apoptotic markers and increased expression of nuclear protein 1 and tribbles r

171 Muscles of mice with CKD have increased expression of nucleolar protein 66 (NO66), as

172 coincident with improved renal function and increased expression of Ogdhl.

173 rrupt protein-coding genes, resulting in the increased expression of one gene and modest truncation i

174 tance to pathogen infection accompanied with increased expression of one-third of the 207 NLR genes i

175 f cytosolic p16(INK4A) and HMGB1, as well as increased expression of p16Ink4a, p21, and MMP-9.

176 R3(injury) displayed increased expression of parenchymal injury transcripts (

177 The data show increased expression of particular invasion-related gene

178 splayed excess mitochondrial fission and had increased expression of PDK isoforms 1 and 3 that persis

179 Increased expression of perilipin (PLIN) proteins and co

180 utic biomarker for cancer are limited due to increased expression of periostin in non-cancerous infla

181 Increased expression of PFKFB3 is mediated by binding of

182 addition, Hipk2 (-/-) neurons and MEFs show increased expression of PGC-1alpha (peroxisome prolifera

183 ns and mouse embryonic fibroblasts also show increased expression of PGC-1alpha (peroxisome prolifera

184 We detected increased expression of phosphorylated eIF4E, eIF4G, and

185 Our results demonstrated an increased expression of pik3ca, pik3cb, pik3r5 and pik3r

186 /16-1 and MYO1C in TFEB-depleted cells cause increased expression of plasma membrane VEGFR2, but in a

187 motherapy induces BCSC specification through increased expression of pluripotency factors, but how th

188 However, we found that the increased expression of Polkappa was not excessively mut

189 e membrane depolarization and calcium influx increased expression of primiR-199a2 but not of primiR-1

190 violet light exposure and is associated with increased expression of pro-cancer genes and reduced exp

191 There was increased expression of pro-inflammatory markers in cort

192 Chronic tendinopathy was associated with increased expression of pro-inflammatory markers PTX3, C

193 DHA-deficient mice were characterized by an increased expression of pro-inflammatory molecules, name

194 19 and B cell-activating factor receptor and increased expression of proapoptotic BIM.

195 This is due to a microbiota-dependent increased expression of proinflammatory factors and decr

196 Increased expression of proinflammatory genes, including

197 TBI increased expression of proinflammatory mediators in the

198 on and proliferation of human aortic SMC and increased expression of proinflammatory molecules and ac

199 Increased expression of protein kinase ULK1 was reported

200 HIF1A-knockout pancreatic cancer cells had increased expression of protein phosphatase 1 regulatory

201 yses revealed that genetic silencing of TBK1 increased expression of proteins and genes essential for

202 Increased expression of proximal AP genes was associated

203 Elevated level of PIP5K1alpha increased expression of pSer-473 AKT (p < 0.001) and inv

204 Increased expression of pulmonary ACE2, the SARS-CoV-2 r

205 These effects were associated with increased expression of purported BMAL1-target genes med

206 s (including those involved with pectin) and increased expression of putative cellulose synthases ind

207 d FGFR siganalling in osteoblasts, including increased expression of RANKL, M-CSF, and osteoprotegeri

208 igh-fat diet-fed ApoE(-/-) mice displayed an increased expression of Rap1 both in aortas and circulat

209 H3K27M mutation led to increased expression of receptor tyrosine kinases (RTK).

210 These findings are further substantiated by increased expression of S100A8 and S100A9 mRNA in whole

211 ical symptoms relative to wild-type mice and increased expression of S100A9 and S100A8 proteins in ke

212 Increased expression of SARS-CoV-2 receptors was blocked

213 Torin1 significantly increased expression of selected sarcomere proteins (inc

214 hese results, transcriptome profiling showed increased expression of several direct p53 targets, redu

215 Here, we report increased expression of several ligands in NF2-null huma

216 her investment into reproduction (including, increased expression of sexually dimorphic traits in mal

217 echanistically, loss of mTORC2 results in an increased expression of signature genes representing imm

218 betaR1, Col1alpha1, and cMyb expression, and increased expression of SMAD7, C/EBPalpha, and C/EBPdelt

219 Increased expression of SPN impeded tumor cell clusterin

220 CO2 activity was significantly elevated, and increased expression of SRC-2 with concomitant reduction

221 cholesterol movement to the ER, evidenced by increased expression of SREBP2-regulated genes.

222 ormation and invasive activity, resulting in increased expression of stem-associated transcription fa

223 We confirmed the increased expression of survivin in CD20(+) lymphocytes

224 te subset of DNMT3A mutation carriers showed increased expression of T-cell stimulating immunoglobuli

225 on 1 upregulation, which subsequently causes increased expression of T-cell-attracting chemokines suc

226 l signature between health and disease, with increased expression of Th17-associated factors in perio

227 Increased expression of the 3.1 isoform of the KCNH2 pot

228 hoice-induced abstinence was associated with increased expression of the activity marker Fos in the O

229 -signaling mode (adipocytes and muscle) with increased expression of the ADAM10/17 metalloprotease th

230 ocrine signaling in adipocytes that promotes increased expression of the adipokine adiponectin and su

231 proliferation, which could be maintained by increased expression of the alternative amino acid trans

232 inflammatory cytokines IL10 and IL12P40, and increased expression of the angiogenic and neurotrophic

233 ion of channel transcripts revealed modestly increased expression of the ATXN1 co-repressor Capicua (

234 ation, was misregulated in male kidneys with increased expression of the canonical Wnt target lymphoi

235 ental infection by P. vranovensis results in increased expression of the cysteine synthases cysl-1 an

236 We found that increased expression of the Drosophila PICALM orthologue

237 ay elevated aminoglycoside resistance due to increased expression of the efflux pump, MexXY.

238 e endothelial activation molecule VCAM-1 but increased expression of the endothelial tight junction p

239 1/Kir5.1 and Nedd4-2 in the kidney exhibited increased expression of the epithelial sodium channel al

240 ecreased expression of the glutamatergic and increased expression of the GABA-ergic synaptic markers,

241 , it declines during ageing concomitant with increased expression of the gap junction protein Gja1.

242 and to localize promoter hypomethylation and increased expression of the growth factor Bmp7 to AgRP n

243 HsmR senses vertebrate heme, leading to increased expression of the hsmRA operon and subsequent

244 rough a positive feed-forward loop involving increased expression of the IL-2 receptor alpha-subunit

245 Increased expression of the immune gene C4 has been link

246 micronuclei formation, reduced Lamin B1, and increased expression of the immune regulators IL6 and IL

247 We also found that Stat3 inactivation led to increased expression of the inflammatory chemokines CCL5

248 tes and developed a thickened epidermis with increased expression of the inflammatory markers Keratin

249 ased growth of xenograft tumors in mice, and increased expression of the integrin subunits ITGA3 and

250 TAZ-KO cells exhibited increased expression of the iron exporter ferroportin an

251 as risk variants in STX6 are associated with increased expression of the major transcripts in disease

252 ited the loss of mitochondrial integrity and increased expression of the microtubule-associated prote

253 d fission, decreased membrane potential, and increased expression of the mitochondria-specific protei

254 creases in MDSC accumulation correlated with increased expression of the myeloid cell lineage-specifi

255 hetic neurons: microbiota depletion leads to increased expression of the neuronal transcription facto

256 This however occurs despite increased expression of the nuclear-encoded transcriptio

257 virus infection of the mosquito led to an in increased expression of the odorant binding protein 22 (

258 ibited interleukin 10 (IL-10) expression and increased expression of the p40 subunit shared by IL-12

259 g alveolar bone is resorbed when there is an increased expression of the pro-osteolytic factor termed

260 creased alpha-hemolysin (Hla) production but increased expression of the proteases SspAB and aureolys

261 confirmed increased expression of GDPD1 and increased expression of the retinal enhancer that enters

262 sing age as well as non-cell-autonomously by increased expression of the retinoic acid-degrading enzy

263 These results demonstrate that increased expression of the schizophrenia-associated gen

264 peripheral blood eosinophils accompanied by increased expression of the severe acute respiratory syn

265 Only pgk-Cul3Delta9 mice displayed increased expression of the sodium chloride cotransporte

266 We recently demonstrated that increased expression of the stress response protein regu

267 ation carriers were further characterized by increased expression of the T-cell alpha receptor consta

268 Using an RNA-seq approach, we identified the increased expression of the tetraspanin family member, C

269 re, we show that pre-TCR signalling leads to increased expression of the transcriptional repressor Bc

270 by immunohistochemical validation identified increased expression of the TTSP family member, TMPRSS13

271 However, IEC organoids have increased expression of the type I IFN receptor relative

272 notably, the fusA1 mutant displayed greatly increased expression of the Type III secretion system (T

273 f the i4g1 x i4g2 plant growth phenotype and increased expression of the validated proteins to wild-t

274 otic resistance against tetracycline through increased expression of the xenobiotic transporters mexE

275 While increased expression of these cellular genes defines a p

276 Increased expression of these genes after 3 months' endo

277 at alpha-Syn pathology is reduced due to the increased expression of this protein.

278 tactin, a nonhistone substrate of HDAC8, and increased expression of three fibrotic markers: alpha-sm

279 esult in increased serine degradation and in increased expression of threonine biosynthetic enzymes s

280 On the basis of increased expression of thymidylate synthase (TYMS), thy

281 cell invasion, clinical studies demonstrated increased expression of TIMP-1 and its association with

282 In this study, we confirmed an increased expression of Tlr3, Trif, Tbk1, and Irf7/Irf3

283 NF-kappaB c-Rel and TonEBP essential for the increased expression of TonEBP-dependent osmoprotective

284 e to oxidative stress, which correlated with increased expression of tpx, a gene essential for defens

285 Treatment of hEECs with bovine CAPG increased expression of transcripts previously known to

286 Functional microbiome analysis revealed increased expression of Treg-cell-inducing genes in the

287 AAI is associated with increased expression of TrkA by eosinophils; however, th

288 LPS further increased expression of TSPO and IL-6 in SNCA mice.

289 eptors (PRs) of diseased individuals display increased expression of two key glycolytic genes, sugges

290 Moreover, Th2 cells in presence of IL-3 show increased expression of type 2 effector cytokines, such

291 a transcriptional signature characterized by increased expression of type I and type II IFN-stimulate

292 combinant HMPVs and virion RNAs that induced increased expression of type I interferon, which was dep

293 t dermal endothelial cells in rosacea had an increased expression of VCAM1 and hypothesized that LL-3

294 Increased expression of VEGFB and FLT4 was also associat

295 The increased expression of VIP/VPAC1 in gastric cancer corr

296 fected astrocytes were inducible, leading to increased expression of viral proteins upon reactivation

297 amatergic receptor activity, consistent with increased expression of voltage-gated potassium channel

298 We found that increased expression of WDR-48, but not WDR-20, promotes

299 ly, Tbx3 (+/-) atrioventricular nodes showed increased expression of working myocardial gene programs

300 -mesenchymal transition (EMT) coordinated by increased expression of ZEB-1, an EMT activator.