ライフサイエンスコーパス: be upregulated by

1 In support, the Cdk5 substrate, ATM, is upregulated by 1.5- to 2-fold at P0 and 6 months in p

2 ) and transforming growth factor (TGF)-beta1 was upregulated by 11.7 +/- 1.5% (p < .05) in splenocyte

3 Both RBCK1 and FKBPL are upregulated by 17-beta-estradiol and interact within

4 Moreover, miR-188-3p expression was upregulated by 2-AG or peroxisome proliferator-activ

5 atory shear stress, gp91phox mRNA expression was upregulated by 2.9+/-0.3-fold, and its homologue, No

6 results show that heparan sulfate expression is upregulated by 25% upon HSV-2 infection, which is a s

7 BH3-only members, Bim and Bmf, were upregulated by 2DG, and shRNAs targeting Bim protec

8 Nestin was upregulated by 3 DPI and declined between 7 and 49 D

9 creased by 50%, and cortex VEGF-A expression was upregulated by 30% (P < 0.04).

10 The modulatory subunit of GCL was upregulated by 4-HNE.

11 ITAF and TNF superfamily member 15 (TNFSF15) are upregulated by 5' adenosine monophosphate (AMP)-acti

12 ranscriptional level via ATF-3, which itself was upregulated by 6.9-fold in our cDNA microarray analy

13 sensitive inward rectifier current (IKir,fb) was upregulated by 79%, in HF animals versus controls.

14 tubule (DCT), where Pcbd1 transcript levels are upregulated by a low Mg(2+)-containing diet.

15 We show that MAIT cell cytotoxic responses were upregulated by a combination of both time-dependent

16 the general stress response activator RpoS, were upregulated by a ribosomal error-prone mutation.

17 va) remorin gene, OsREM4.1, whose expression is upregulated by ABA through the transcriptional activa

18 r, our data show that ULBP2/5 expression can be upregulated by accumulation of fumarate, likely by de

19 E. ictaluri type III secretion system (T3SS) is upregulated by acidic pH.

20 ely expressed genes previously identified to be upregulated by activated microglia during aging, neur

21 n molecule high-mobility group box 1 (HMGB1) is upregulated by activated platelets in multiple inflam

22 Furthermore, Siglec-5 levels are upregulated by activation in chimpanzee but not huma

23 activates thyroid hormone in skeletal muscle is upregulated by acute treadmill exercise through a bet

24 A total of 153 genes were upregulated by added trichodiene and were significa

25 nd LS180 colorectal adenocarcinoma cells and is upregulated by agonists of peroxisome proliferator-ac

26 ore, HSF1 target gene hsp70 mRNA and protein are upregulated by alcohol in monocytes.

27 NHE1 was upregulated by alkalinizing SC pH, whereas this anti

28 Several dorsal neural tube genes were upregulated by alleviating Snail2 repression; moreo

29 onociceptin (ppN/OFQ) mRNA has been shown to be upregulated by an increase in cAMP, a treatment that

30 MEF2C was upregulated by and directly interacted with beta-cat

31 Ndrg1 is upregulated by anergic signalling and maintained at h

32 c pyruvate dehydrogenase kinase 4 expression was upregulated by Ang II and PE, resulting in a reducti

33 natriuretic hormones, such as dopamine, and is upregulated by antinatriuretic hormones, such as angi

34 Moreover, TDP-43 mRNA was found to be upregulated by approximately 2.5-fold in the spinal c

35 involved in reducing reactive oxygen species are upregulated by Artemis depletion.

36 we show single-channel activity of TrkH that is upregulated by ATP via TrkA.

37 sangial cell PAI-1 and MCP-1 mRNA expression were upregulated by ATP and UTP but not ADP or adenosine

38 zipper transcription factor-like 1 (LZTFL1) was upregulated by ATRA in a dose- and time-dependent ma

39 RMS1 is known to be upregulated by auxin in the shoot, suggesting a strai

40 sions occurred in nine different tissues and were upregulated by bacterial challenge.

41 dentify a subset of proteins whose synthesis is upregulated by BDNF signaling via MNK1 in neurons.

42 SlVRSLip was upregulated by Bemisia tabaci (the TYLCV vector) fee

43 The Hedgehog pathway is upregulated by beta-catenin activation, and inhibitio

44 s4 is expressed within pancreatic islets and is upregulated by beta-cell depolarizing agents.

45 We found the message was upregulated by blood feeding.

46 A BMP antagonist, gremlin, is upregulated by BMP5-8 in dorsolateral, rather than ve

47 oxc2, Connexin37, EphrinB2, and Neuropilin1) was upregulated by BMP9 in LECS.

48 LDH-A gene expression is believed to be upregulated by both HIF and Myc in cancer cells to ac

49 However, CREB transcription is upregulated by both clade B and C gp120, and METH co-

50 HtrA1 expression was upregulated by both cisplatin and paclitaxel treatme

51 ated by hypoxia and that ORF34 transcription was upregulated by both HIFs.

52 imulation, whereas other IFN signature genes were upregulated by both IFN-gamma and IFN-beta.

53 Vitreal IL-1beta, IL-6, and TNF-alpha were upregulated by both the parent and mutant strain 12

54 have shown that the proapoptotic protein BAK is upregulated by butyrate.

55 port a model in which T4P gene transcription is upregulated by c-di-GMP as a result of its binding to

56 sing on the ROS-producing enzyme NOX4, which is upregulated by CAF in many human cancers, and compare

57 ctor of activated T cells (NFAT) control and is upregulated by calcineurin inhibitors.

58 The expression of Samd9L was upregulated by calcitonin, and this was preceded by

59 ion of which is a hallmark of healthy AT and is upregulated by calorie restriction.

60 The feaR gene is upregulated by carbon or nitrogen limitation, which w

61 These results suggest that ICER is upregulated by cardiac hypertrophic stimuli increasin

62 ns in the differentiating TE during cleavage is upregulated by cell contact asymmetry (outside positi

63 (BACE1), the key-enzyme of amyloidogenesis, is upregulated by cerebrovascular insult; moreover, its

64 tabolizing thiolase, the expression of which is upregulated by cholesterol and repressed by KstR, was

65 re- and receptor-operated channels of PASMCs are upregulated by chronic hypoxia and contribute to the

66 t the Na(+)-driven Cl/HCO(3) exchanger NDCBE is upregulated by chronic acid loads in a cell-specific

67 nate transporter NBCn1 (Slc4a7) in rat brain is upregulated by chronic metabolic acidosis.

68 of the Akt substrates whose phosphorylation is upregulated by ClipR-59 is AS160, a negative regulato

69 enriched protein tyrosine phosphatase (STEP) was upregulated by cocaine, prevented by ZM241385, and a

70 STA1 expression is upregulated by cold stress, and the sta1-1 mutant is

71 In mice, VEGF-A165b expression was upregulated by conditions associated with impaired l

72 FKBP5 expression is upregulated by cortisol exposure during stressful epi

73 The ORF35-37 transcript was upregulated by cotransfected hypoxia-inducible facto

74 n by calcineurin, a protein phosphatase that is upregulated by CS.

75 4 1034 References 1034 Copper (Cu) microRNAs are upregulated by Cu deficiency and mediate the post-tr

76 Copper (Cu) microRNAs are upregulated by Cu deficiency and mediate the post-tr

77 tion, likely a cell in which group V sPLA(2) is upregulated by D. farinae, and whose function is also

78 , because inhibiting nuclear-pore genes that are upregulated by DAF-16 blocks p53-dependent cell deat

79 CaTLP1 is upregulated by dehydration and high salinity, and by

80 We show that DTDST is upregulated by dexamethasone stimulation of HT1080 fi

81 In contrast, in other cancers where HIF is upregulated by different mechanisms, including micro-

82 enes, only syt-alpha and syt-beta RNA levels are upregulated by DIMM overexpression.

83 proteins, such as CYCB1;1, whose transcripts are upregulated by DUO POLLEN1 (DUO1).

84 hosphoprotein enriched in astrocytes), which is upregulated by E1A in ovarian cancer; PEA15 promotes

85 as an experimental model, we show that Noxa is upregulated by E2 via p53-independent processes that

86 RNPS1, ADD1, rap-2, and SKIIP were upregulated by E2 in HOSE cells but downregulated b

87 at human metallothionein 1G (hMT1G) promoter is upregulated by E2F1 upon VEGF stimulation of human ao

88 Its expression is upregulated by EGF and elevated CTEN mediates EGF-ind

89 n B2 and the canonical UPR promoter elements are upregulated by ELL2 cDNA.

90 ly' expressed in germinal center B cells and was upregulated by engagement of CD40 by CD154, as well

91 nnate and Th2 adaptive immune disorders, and is upregulated by environmental pollutants, including am

92 contrast, cathepsin B3 protein and activity were upregulated by ERFVIIs independent of transcript.

93 xpressed in normal stem cells and tumors and is upregulated by estradiol in MCF7 breast cancer cells.

94 ng sarcoma-associated transcript 1 [EWSAT1]) is upregulated by EWS-FLI1 in pMPCs.

95 of EWS/FLI, the master regulator of ES, and is upregulated by EWS/FLI via a GGAA microsatellite enha

96 echano growth factor (MGF) has been found to be upregulated by exercise or muscle damage.

97 hysiologically, FGF6/9 expression in adipose is upregulated by exercise and cold in mice, and FGF9/FG

98 Both alpha3beta4 and alpha4beta2 nAChRs are upregulated by exposure of cells to AT-1001 for 3 da

99 or its catalytic subunit presenilin 1 (PS1), were upregulated by exposure to either pigment epithelia

100 1 as a direct target of ARID1A and EZH2 that is upregulated by EZH2 inhibition and contributed to the

101 gene expression of innate immunity receptors is upregulated by farming-related exposures.

102 stream terpenoid pathways were also found to be upregulated by FAW feeding.

103 D4(+) T cells, NA-TLRs, TLR3, TLR8, and TLR9 are upregulated by FcgammaRIIIa-pSyk cosignaling and loc

104 drogenase synthesis, was previously shown to be upregulated by FNR (fumarate-nit rate regulator) in t

105 WNT5A and matrix metalloproteinase-7 (MMP7) were upregulated by FOXC1 in TNBC cells.

106 sed gene profiling, we determined that ERBB3 is upregulated by FOXD3, a transcription factor that pro

107 low level in all Arabidopsis tissues but can be upregulated by fumonisin B1 (FB1) treatment and patho

108 in C- and A-fibre nociceptive-type units and is upregulated by G-protein activation.

109 n summary: 1) GPDH, FAS, and ACC mRNA levels are upregulated by glucose; 2) glucose-induced up-regula

110 ncogenic forkhead transcription factor FOXM1 is upregulated by GOF mutant p53s.

111 chemokine specifically expressed in neurons, was upregulated by gp120, and knockout of the FKN recept

112 mediated by the secreted protein Bv8, which is upregulated by granulocyte colony-stimulating factor.

113 NO synthase genes, which characterize MDSCs, were upregulated by GRO-gamma-primed mouse bone marrow c

114 resistant Na+ current, attributed to NaV1.9, is upregulated by GTP and its non-hydrolysable analogue

115 ine-specific transporters (glnH, glnP, glnQ) were upregulated by H(2), and cells grown with H(2) show

116 the mannose uptake system genes (manX, manY) were upregulated by H(2,) and cells grown with H(2) show

117 yzed by targeted proteomics, and 70% of them were upregulated by H2O2.

118 These genes were upregulated by HCV/HIV co-infection but in a greate

119 LCN2 expression is upregulated by HER2/phosphoinositide 3-kinase/AKT/NF-

120 In MCF-7 cells, LMO4 transcripts were upregulated by heregulin, an activator of ErbB rece

121 transcript and protein levels of claudin-14 are upregulated by high Ca(++) diet, while downregulated

122 Importantly, the MzASMT9 gene was found to be upregulated by high light intensity and salt stress.

123 bundance analysis shows that only 5 proteins were upregulated by high iron, 24 proteins had elevated

124 The abundance of cardiac IGF-1 receptor can be upregulated by Hsp60, but how diabetes modulates card

125 n the mammalian heart, including humans, and is upregulated by hypertrophy and cardiac failure.

126 a response regulator that has been shown to be upregulated by hypoxia and other in vitro stress cond

127 Erythropoietin (EPO) is upregulated by hypoxia and causes proliferation and d

128 ntial regulation of microRNA (miR) 21, which is upregulated by hypoxia only in Akt2-expressing cells.

129 show further that beta-catenin transcription is upregulated by hypoxia through hypoxia-inducible fact

130 located in nerve fibers along blood vessels, is upregulated by hypoxia, and induces angiogenesis.

131 in 2), a nucleotide excision repair protein, is upregulated by hypoxia.

132 Here we found OPN expression to be upregulated by hypoxic condition in PC-3 prostate tum

133 in retinal ganglion and photoreceptor cells, was upregulated by IFN-gamma and inhibited proliferation

134 LLT1 expression by chondrocytes could be upregulated by IL-1alpha and TNF.

135 Hence, after being upregulated by IL-1alpha, IL-36alpha acts through

136 13 confirmed that secretion of these enzymes was upregulated by IL-1beta and modulated downward by pr

137 Numerous genes whose expression was upregulated by IL-1beta were modulated downward by I

138 l structures or promote axial elongation and are upregulated by increased RAR-mediated repression.

139 DMSP production and dsyB transcription are upregulated by increased salinity, nitrogen limitati

140 of these supercoiling-dependent early genes is upregulated by increased chlamydial supercoiling leve

141 Bmp6 expression is upregulated by increased iron-levels in the liver.

142 iated with developmental oligodendrogenesis, was upregulated by IndCl and both analogues.

143 es plasma EL concentrations, proving that EL is upregulated by inflammation in humans.

144 Human and mouse RPE cell mCRPs are upregulated by inflammatory cytokines and repetitive

145 Hepcidin transcription is upregulated by inflammatory cytokines, iron, and bone

146 nd, glial-derived neurotrophic factor (GDNF) is upregulated by inflammatory cytokines.

147 CCRL2 is upregulated by inflammatory signals and, unlike other

148 ptidylglycine alpha-amidating monooxygenase, were upregulated by inositol depletion.

149 We now demonstrate that SP100 expression is upregulated by interferons, which have been shown to

150 Neuroendocrine pathway genes are upregulated by intestinal bloating and are required

151 pression of E. coli iron acquisition systems was upregulated by intracellular UPEC.

152 Furthermore, expression of the transgene can be upregulated by intravitreal injection of CNTF.

153 One miR candidate found to be upregulated by ionizing radiation was miR-95, the enf

154 ons, hamartin was unaffected by ischemia but was upregulated by IPC preceding ischemia, which protect

155 -kappaB (NF-kappaBeta) transcription factors are upregulated by IR and have been implicated in radior

156 t decapentaplegic homolog (Bmp-Smad) pathway is upregulated by iron treatment, fail to suppress hepci

157 etal muscle, CHOP-10 mRNA and protein levels were upregulated by ischemia and diabetes mellitus.

158 Interestingly, CXCL10 expression could be upregulated by itself and IL-17 in inflammatory cells

159 These transcripts were upregulated by KCl and downregulated by tetrodotoxi

160 alphavbeta6 expression was upregulated by keratinocytes in vitro and during tum

161 and their corresponding promoter activities were upregulated by Klf4 in transient cotransfection ass

162 ancer factor/T-cell factor promoter activity was upregulated by KM-GSK3beta and diminished by S9A-GSK

163 egulator of LEC differentiation PROX1, which is upregulated by KSHV and directs KSHV-induced lymphati

164 estingly, NKCC1 gene and protein expressions were upregulated by light, which we attribute to the lig

165 class E VPS protein that localizes to ER and is upregulated by lipid imbalance.

166 Interestingly, its expression is upregulated by lipopolysaccharide and poly(I:C), but

167 lity of fatty acids, whereas the HDL pathway is upregulated by liver X receptor agonists.

168 he transcriptional level, and its expression is upregulated by liver X receptor alpha (LXRalpha).

169 The TaHOX1 gene was found to be upregulated by low temperatures, and to have a signif

170 ivation were affected by glucose, with Rankl being upregulated by low glucose.

171 iR-155-5p), which increases IL-6 expression, is upregulated by LPS and hyperlipidemia and patients wi

172 and proapoptotic protein and its expression is upregulated by many agents that induce apoptosis.

173 Heat shock protein (Hsp) expression is upregulated by many stimuli and serves to maintain in

174 Because TRAF1 is upregulated by many stimuli, it may modulate the inte

175 In isolated vessels, BPIFB4 is upregulated by mechanical stress, and its knock-down

176 anin content in A. mangostanus seedlings can be upregulated by MeJA and ethylene.

177 assays suggest that the -670/MMP-9 promoter is upregulated by MEK5 and electromobility shift assay f

178 In vitro, the CXCR4 chemokine receptor was upregulated by migratory progenitor cells just as th

179 ere found to be cotranscribed and expression was upregulated by MNNG.

180 vo rat glaucoma model, we show that TNFalpha is upregulated by Muller cells and microglia/macrophages

181 the circumferential marginal zone (CMZ) and is upregulated by Muller glia in acutely damaged retinas

182 Expression of LAMB3 but not FAK was upregulated by mutant KRAS.

183 Conversely, constitutive CXCL12 mRNA levels were upregulated by MyD88 or TRAM knockdown in non-stimu

184 rve that nitrogen catabolite-repressed genes are upregulated by Nab3 depletion.

185 Taken together, KiSS1 expression is upregulated by neuronal activity and activation of GP

186 Genes linked to HMO-utilization were upregulated by neutral HMO and SL, but not by FL in

187 stemic bacterial challenge, TARM1 expression was upregulated by neutrophils and inflammatory monocyte

188 ROS are upregulated by NF-kappaB inhibition and are required

189 pA and ygbA genes, all of which are known to be upregulated by nitrosative stress.

190 Sox17, a transcription factor that is upregulated by Norrin/Fz4/Lrp signaling, plays a cent

191 y regulator in Drosophila melanogaster which is upregulated by Notch in adult muscle progenitors but

192 liest thymic progenitors, and its expression is upregulated by Notch signals.

193 ipts with increased association with HuR and was upregulated by NS3/4A.

194 The LIFR is upregulated by nuclear EGFR, which acts as a transcri

195 We found that these same genes were upregulated by octanoylhomoserine lactone (OHL), wh

196 erived astrocytes showed that LPL expression is upregulated by oleic acid, whereas it is decreased in

197 MTH1 expression is upregulated by oncogenic KRAS and correlates positive

198 e majority of divergent FAD2 genes in tomato are upregulated by one or more stresses.

199 ription of genes encoding ribosomal proteins was upregulated by OPP and at the same time, the genes e

200 ase kinases IkappaB kinase e and TBK1, which are upregulated by overnutrition, and may therefore be s

201 sion oxidize low-density lipoproteins; LOX-1 is upregulated by ox-LDL and ROS, and is involved in cel

202 nally, we show that one of the proteins that is upregulated by OXT is the neuropeptide Y receptor 5.

203 shown by activity and proteomic analyses to be upregulated by oxygen limitation, and aspartate enhan

204 n the synthesis and release of root exudates were upregulated by P-deficient roots, as well as those

205 Transcription of human AMID gene is upregulated by p53 and downregulated in tumors in com

206 In particular, mammalian miR-34 is upregulated by p53 in response to radiation, but litt

207 We show that its receptor, A2B, is upregulated by p53.

208 is a proapoptotic factor and its expression is upregulated by p53.

209 Cell cycle regulators, most notably Cdkn2a, were upregulated by p53 inactivation in gastric premalig

210 -binding activity of NFkappaB, Sp1, and AP-1 was upregulated by PAF with a peak at 1 hour after stimu

211 sion of monocarboxylate transporter 4, which was upregulated by PDT.

212 ded a protein similar to MrgA in B. subtilis was upregulated by peroxide, and a strain containing an

213 Moreover, we found that JNK activity was upregulated by pharmacological inhibition of CFTR in

214 (2+) channel Ca(v)1.2, the activity of which is upregulated by PKA.

215 laevis myosin-1c (XlMyo1c) as a myosin that is upregulated by polyadenylation during meiotic maturat

216 such as SM alpha-actin, calponin, and SM-MHC are upregulated by premiR-145 or adenovirus expressing m

217 process, because its expression and activity are upregulated by pressure overload and because myocard

218 CCR2 chemokine receptor, and its expression is upregulated by proinflammatory cytokines.

219 timuli, including tumor necrosis factor, and was upregulated by 'proresolution' lipid mediators, incl

220 f miRs, including miR-30b-5p and miR-30c-5p, are upregulated by proteasome inhibitor PS-341 treatment

221 Although the Mcl-1 protein was upregulated by proteasome inhibition, it was also su

222 ow that cathepsin-B activity in the lysosome is upregulated by RAP and that this allows the expanded

223 econd screen encompassing 946 miRNA, 18 miRs were upregulated by Rapamycin, while eight were downregu

224 hich is well known to encode reward signals, is upregulated by repeated social-defeat stress, a highl

225 chromosomes, a subset of post-meiotic genes was upregulated by resistant Y chromosomes.

226 HOXC9 expression is upregulated by retinoic acid (RA), and knockdown of H

227 Meis1 and Hoxa9 expression is upregulated by retroviral integration in murine myelo

228 Fas expression was upregulated by rituximab as early as 6 h post-treatm

229 eceptors B7-DC and B7-H1, two receptors that are upregulated by ROP16.

230 ntation identified 6 microRNAs, confirmed to be upregulated by RT-qPCR in an expanded cohort (miR-9,

231 rentially expressed genes, pg2131 and pg2167 were upregulated by S. cristatus signaling molecules.

232 r receptor 2 (VEGFR2) was established, which was upregulated by SAHA.

233 he intracellularly transcribed pagC promoter was upregulated by Salmonella in all tissues, defining t

234 DF-1alpha/CXCR4 signaling and let-7a, as YY1 was upregulated by SDF-1alpha and downregulated by treat

235 e II, a protein that phosphorylates cofilin, is upregulated by Sema7A in a Plexin C1-dependent manner

236 s suggest that specific chemokines/receptors are upregulated by sensory neurons following peripheral

237 ts and an inhibitor, we determined that ZEB2 is upregulated by serum and downregulates GAX, while the

238 The oncogenic microRNA miR-155 is upregulated by several oncogenic viruses.

239 SOCS3 is upregulated by several signals in macrophages and has

240 autosomes, and newly acquired X-linked genes are upregulated by similar mechanisms but to a different

241 In this report we showed that p53 level was upregulated by SP600125 in SK-N-SH cell line.

242 In addition, GAS5-AS1 can be upregulated by specific knockdown of HDAC1 or HDAC3.

243 5hmC is upregulated by STAT3 at the promoters of several tumo

244 17 proteins were upregulated by statin therapy, including proteins c

245 analogous mechanisms may apply to genes that are upregulated by statins, but not to downregulated gen

246 reviously showed that p66(Shc) protein level is upregulated by steroid hormones in human carcinoma ce

247 In plants, as in other organisms, sHSPs are upregulated by stress and are proposed to act as mol

248 e ATP-directed mitochondrial protease, LonP1 is upregulated by stress conditions, including hypoxia,

249 n express proenkephalin, but this expression is upregulated by stressful stimuli and can be altered b

250 ied a novel long noncoding RNA (slincR) that is upregulated by strong AHR ligands and is located adja

251 The metabolites are upregulated by subinhibitory levels of the antifolat

252 1A and Sub1C transcript levels were shown to be upregulated by submergence and ethylene, with the Sub

253 -sensitive transcripts, APOC3 and MUC1, that are upregulated by SUMO-less hLRH-1 or by siUBC9 knockdo

254 Further, esgal1 expression was upregulated by symbiosis, a response that was partia

255 (Tconvs) in normal mice, and its expression is upregulated by T cell activation.

256 Genes that were upregulated by TA were associated with increased hi

257 ly member and conserved protein, 14-3-3zeta, is upregulated by tamoxifen and that high expression cor

258 pPD-1 was upregulated by TCR/CD3 + CD28 stimulation and simult

259 eIF2alpha phosphorylation is upregulated by TDP-43 toxicity in flies, and TDP-43 i

260 ed that Hic-5, a focal adhesion protein that is upregulated by TGF-beta1, is expressed persistently i

261 d by the micro (mi)RNA family miR-181, which was upregulated by TGF-beta at the post-transcriptional

262 SPARC was upregulated by TGF-beta2 in the human TM cells (3.8

263 USP27X was upregulated by TGFbeta during EMT and was required f

264 Many TRIM proteins are upregulated by the immunologically important Type I

265 r and Ox40 promoter activities were shown to be upregulated by the NF-kappaB-mediated enhancer activi

266 The enterotoxin B (seb) determinant is upregulated by the Agr system.

267 The enterotoxin D (sed) determinant is upregulated by the Agr system.

268 Rpal_4085 is upregulated by the divalent metals Fe(II), Ni(II), an

269 giotensin receptor gene in the adrenal gland is upregulated by the first week of life resulting in in

270 ABC1 is upregulated by the liver X (LXR) and retinoid X (RXR)

271 Palmitoylation on TMD 2 is upregulated by the palmitoyl acyl transferase GODZ an

272 mma is strongly induced, and Muc1 expression is upregulated by the PPARgamma agonist rosiglitazone.

273 uction of interleukin (IL)-22 by ILC3, which is upregulated by the presence of commensal microorganis

274 SPRR1B is upregulated by the proinflammatory cytokines IL-1beta

275 In the BDE patients, the human lncRNA was upregulated by the disrupted chromosomal association

276 IR2 promoter indicated that the IR2 promoter was upregulated by the EICP0P.

277 0) or mucosal adjuvant properties (IL-1beta) was upregulated by the enterotoxins.

278 EGFR2 expression in vessel endothelial cells was upregulated by the released HMGB1 from PHCCA, result

279 lin isoforms (nrp1a, nrp1b, nrp2a and nrp2b) were upregulated by the activated epicardium and an nrp1

280 ides TRIM21, TRIM22 and TRIM38 were shown to be upregulated by TLR3 and TLR4 ligands as previous repo

281 e CPI-17 promoter and demonstrated that KLF4 was upregulated by TNF, competed with Sp1 for the bindin

282 IL-32 mRNA was upregulated by TNF-alpha and IFN-gamma in primary si

283 Cultured hRPE cell mCRP expression was upregulated by TNF-alpha, IL-1beta, and a repetitive

284 We also identified the gene PA0913, which is upregulated by tobramycin specifically in biofilms gr

285 e expression of antioxidative stress enzymes is upregulated by trans-hydroxytamoxifen (TOT) in breast

286 etion, we establish that retromer expression is upregulated by transcription factor EB (TFEB) and oth

287 pression of TLR2 and TLR4 mRNAs, which could be upregulated by treatment with proinflammatory cytokin

288 Of these, 163 genes (49%) were upregulated by twofold or greater, and 173 genes (5

289 the sufA promoter and levels of SufD protein were upregulated by twofold to threefold in Isc(-) strai

290 Furthermore, SAMHD1 was upregulated by type I and II interferons in hepatic

291 PDRG mRNA was upregulated by ultraviolet radiation (UV) but downre

292 We demonstrate that miRNA396 is upregulated by UV-B radiation in proliferating tissue

293 We show here that expression of the AOX gene is upregulated by various stresses including H(2) O(2) ,

294 Like SOC1, AGL24 mRNA levels are upregulated by vernalization.

295 owever, the final gene in the cluster, MAF5, is upregulated by vernalization.

296 responsive to inflammatory signaling and can be upregulated by viral infections or interferon treatme

297 TSGs (DOC-2/DAB2, CDKN1C and SPARC) and all were upregulated by wild-type pVHL.

298 For example, the oncoprotein c-Myc, which is upregulated by Wnt signaling activity, participates i

299 The expression of HEF1 was upregulated by Wnt-3a, beta-catenin, and Dvl2 in a d

300 gene expression in cultured epithelial cells was upregulated by wounding and neutrophil elastase.