ライフサイエンスコーパス: regulate the expression of

1 to specify the B-cell lineage, bound to and regulated the expression of 109 lncRNAs in pro-B and mat

2 KstR2, a TetR family repressor (TFR), regulates the expression of 15 genes encoding enzymes th

3 First, SR45 associates with and regulates the expression of 30% of abscisic acid (ABA) s

4 11 expression quantitative trait loci (eQTL) regulating the expression of 4105 genes, including nine

5 osteosarcoma U2OS cells, we found that SRSF3 regulates the expression of 60 genes including ERRFI1, A

6 AdcR regulates the expression of 70 genes involved in zinc ac

7 ERalpha has been shown to regulate the expression of a key mediator of the EnR str

8 that RD26 can act antagonistically to BR to regulate the expression of a subset of BES1-regulated ge

9 tor 1 (IRF-1) is a transcription factor that regulates the expression of a broad range of antiviral h

10 The transcription factor Nrf2 regulates the expression of a large network of cytoprote

11 ucho (Gro) is a Drosophila co-repressor that regulates the expression of a large number of genes, man

12 tein clustered mitochondria homologue (CLUH) regulates the expression of a mitochondrial protein netw

13 For example, Arabidopsis MAP kinase 4 (MPK4) regulates the expression of a subset of defense genes vi

14 Messenger RNA alternative splicing (AS) regulates the expression of a variety of genes involved

15 riaceae, have been implicated in dynamically regulating the expression of a large number of genes upo

16 abditis elegans' life span by differentially regulating the expression of a specific insulin-like pep

17 lling the turnover of basal keratinocytes by regulating the expression of a subset of genes involved

18 cell fate determination and tumorigenesis by regulating the expression of a wide range of target gene

19 vidence that MvfR may also bind and directly regulate the expression of additional 35 loci across the

20 stration of rosiglitazone in T1DM-2W mice up-regulated the expression of AdipoR1 and restored the neu

21 in a non-coding distal enhancer element that regulates the expression of alpha-synuclein (SNCA), a ke

22 bin gene, its enhancers, and POL3RK gene for regulating the expression of alpha-globin in silent cell

23 se lacking STP2, a transcription factor that regulates the expression of amino acid permeases, are im

24 n kinase (AMPK) phosphorylation through down-regulating the expression of AMPK.

25 In neuronal and transformed cells HMGB4 regulated the expression of an oligodendrocyte marker ge

26 rs12459419 C>T in the splice enhancer region regulates the expression of an alternatively spliced CD3

27 not in the dksA mutant, suggesting that DksA regulates the expression of an unknown cofactor(s) requi

28 production in some transgenic lines by down-regulating the expression of an activator of anthocyanin

29 he JAZ2 targets MYC2, MYC3 and MYC4 directly regulate the expression of ANAC19, ANAC55 and ANAC72 to

30 ent miRNAs may independently or coordinately regulate the expression of any given mRNA.

31 er, RANK signaling in tumor cells negatively regulates the expression of Ap2 transcription factors, a

32 SP-PTP also differentially regulates the expression of approximately 50% of the tot

33 Detect was used to identify novel TF modules regulating the expression of Arabidopsis (Arabidopsis th

34 SRSF3 also significantly regulates the expression of at least 20 miRNAs, includin

35 inal NPXY motifs, LRP1 beta-chain positively regulates the expression of ATP binding cassette transpo

36 negative regulator, Keap1 and is able to up-regulate the expression of autophagy-associated proteins

37 Additionally, IL-27 regulated the expression of B7-H4 on HIV MDSC, and contr

38 wth response gene 2 (EGR2) and EGR3 directly regulate the expression of Bcl6 in Tfh cells, which is r

39 Overexpressing NRF-2 up-regulated the expression of Bdnf exon IX, whereas knocki

40 euronal activity and energy metabolism, also regulates the expression of BDNF, which is intimately as

41 ted histone residues, they may independently regulate the expression of BET-sensitive genes.

42 on factors including Gli1, Atoh1 and REST to regulate the expression of both oncogenes and tumor supp

43 c-helix-loop-helix transcription factor that regulates the expression of CBF genes, and the phosphory

44 triggered by LPS, as both agents oppositely regulate the expression of CCL19 and TRIB3 Besides, palm

45 In addition, Np63 directly regulates the expression of CD44, the major HA cell memb

46 We found that this is sufficient to regulate the expression of Cdk5 and results in altered b

47 ead ZHOUPI indirectly triggers cell death by regulating the expression of cell wall-modifying enzymes

48 ovis bacillus Calmette-Guerin infection down-regulated the expression of CIITA/MHC-II by inducing hyp

49 et al. (2017) reveal that the gut microbiota regulates the expression of circadian-clock genes to imp

50 hromatin occupancy analyses reveal that Pdx1 regulates the expression of Clec16a, a type 1 diabetes g

51 8 influences flowering time through directly regulating the expression of cmo-MIR156 in the aging pat

52 In correlation, DCs up-regulate the expression of co-stimulatory molecules and

53 Here, we show that Drosophila FOXO (dFOXO) regulates the expression of core small RNA pathway genes

54 stroma plays an important role in negatively regulating the expression of CXLC12 on osteoblasts and t

55 mic and inhibitor significantly down- and up-regulated the expression of CYP3A1, respectively.

56 es the retinoid X receptor, which reportedly regulates the expression of cytochrome P450 aromatase (P

57 ed genes suggested that FoxQ1 may negatively regulate the expression of Dachshund homolog 1 (DACH1),

58 Peg-IFN-alpha up-regulated the expression of DAPK and mTOR, which was ass

59 ruited by specific transcription factors and regulate the expression of developmentally important gen

60 uronal cell types; play an important role in regulating the expression of developmentally important g

61 The H19 long noncoding RNA (lncRNA) regulates the expression of different genes and has been

62 Each isoform regulates the expression of distinct sets of genes and r

63 tiation and the dedifferentiation of INPs by regulating the expression of distinct target genes at di

64 metabolic gene expression, functions to down-regulate the expression of diverse genes encoding secret

65 g chick otocysts, we show that BMP signaling regulates the expression of Dlx5 and Hmx3, both of which

66 that Ilk controls branching morphogenesis by regulating the expression of DUSP8, which inhibits p38MA

67 pression quantitative trait loci (eQTL) that regulate the expression of Egfr between female and male

68 ly in mineralizing dental enamel but also in regulating the expression of EMPs.

69 ng it was demonstrated that Snail positively regulated the expression of EndMT markers (Slug, N-cadhe

70 r stress-sensitive transcription factor that regulates the expression of enzymes which have previousl

71 ng proliferation and cytokine production and regulating the expression of epithelial cytokine recepto

72 intenance of a basal epithelial phenotype by regulating the expression of epithelial-specific genes i

73 Cytosine DNA methylation regulates the expression of eukaryotic genes and transpo

74 is necessary but probably not sufficient to regulate the expression of eve and run-1 Our study there

75 show that inhibition of Notch1 signaling can regulate the expression of fatty acid oxidation genes an

76 w that Transient Receptor Potential (TRP) C3 regulates the expression of fibronectin, a key regulator

77 Together with a second ATPase, FleN, FleQ regulates the expression of flagellar and exopolysacchar

78 Chronic social defeat stress regulates the expression of Fosb in the nucleus accumben

79 la Pathogenicity Island (FPI) and positively regulating the expression of FPI genes, which encode a T

80 alyses have revealed that WNT5a acts to down-regulate the expression of FSH-responsive genesin vitro,

81 ernative splicing functions as a switch that regulates the expression of functionally distinct DmNmna

82 g RNA molecules whose primary function is to regulate the expression of gene products via hybridizati

83 ndicated that compound 1 and DBL exposure up-regulated the expression of gene mcyB and down-regulated

84 highly homologous transcription factors that regulate the expression of genes bearing antioxidant-res

85 ons between these transcription factors also regulate the expression of genes encoding proteins that

86 To regulate the expression of genes encoding these unique p

87 -like family of transcription factors (KLFs) regulate the expression of genes involved in cell prolif

88 Chromatin modifiers regulate the expression of genes involved in metabolism

89 downstream reactive sulfur species (RSS) and regulate the expression of genes mediating sulfide homeo

90 X6 isoforms differentially and cooperatively regulate the expression of genes specific to the structu

91 y of hypoxia-inducible factors (HIFs), which regulate the expression of genes that contribute to angi

92 t, neurons must sense activity over time and regulate the expression of genes that control these para

93 in the nucleus of vitamin D target cells to regulate the expression of genes whose products control

94 c investigations revealed that NURF directly regulated the expression of genes encoding immunoproteas

95 gulated the expression of gene mcyB and down-regulated the expression of genes ftsZ, psbA1, and glmS

96 icated that TDCIPP exposure significantly up-regulated the expression of genes involved in endoplasmi

97 (Glyco(Lo) mice) lowered glycolytic rate and regulated the expression of genes known to promote cardi

98 Notably, apo-pyoverdine positively regulated the expression of genes related to development

99 master xenobiotic receptor that coordinately regulates the expression of genes encoding drug-metaboli

100 ator 1 (Mxr1p) is a zinc finger protein that regulates the expression of genes encoding enzymes of th

101 induced the transcription factor Nrf2, which regulates the expression of genes encoding heme oxygenas

102 neage commitment of T cell precursors, Foxn1 regulates the expression of genes involved in antigen pr

103 scription factor WRINKLED1 (WRI1) positively regulates the expression of genes involved in fatty acid

104 formation of a transcriptional complex that regulates the expression of genes involved in integument

105 WhiB3 regulates the expression of genes involved in lipid anab

106 These data suggested that CLOCK regulates the expression of genes involved in neuronal m

107 (Foxo3a) physically interacts with Tet2 and regulates the expression of genes related to aNSC prolif

108 beta-catenin also regulates the expression of genes that control metabolis

109 ed Tat plays a dual role in HIV infection by regulating the expression of genes belonging to the viru

110 Recently it has emerged that when regulating the expression of genes from mobile genetic e

111 mation of prefrontal cortical minicolumns by regulating the expression of genes involved in early spo

112 e molecular pathways involved and mechanisms regulating the expression of genes involved in inflammat

113 AP2 (ApiAP2) family, that is responsible for regulating the expression of genes involved in RBC invas

114 inhibited gene expression, specifically down-regulating the expression of genes of the late cornified

115 e and regulates adipocyte differentiation by regulating the expression of genes related to insulin se

116 metabolic reprogramming of naive T cells by regulating the expression of glucose transporters, glyco

117 Mechanistically, we showed that BocaSR regulates the expression of HBoV1-encoded nonstructural

118 mmatory stimulants LPS, IL-6 and IL-1beta up-regulated the expression of HCA2 on macrophages.

119 sense iron levels in the blood to positively regulate the expression of hepcidin through activation o

120 jaw (maxilla)-to-mandible transformation by regulating the expression of homeobox transcription fact

121 ctures that interact with the same ligand to regulate the expression of homologous genes in different

122 We found that YAP regulates the expression of Hoxa1 and Hoxc13 in oral and

123 beta-heterodimeric transcription factor that regulates the expression of hundreds of genes in a tissu

124 ntial, pleiotropic transcription factor that regulates the expression of hundreds of genes-is disprop

125 s the human genome at >10,000 sites but only regulates the expression of hundreds of genes.

126 HIF1-alpha accumulation in nuclear; and down-regulated the expression of hypoxia-associated transcrip

127 maRIIIa-mediated co-signal differentially up-regulated the expression of IFN pathway genes compared w

128 These findings suggest that MTA1 could regulate the expression of IGFBP3 in both DNMT3a-depende

129 In MRSA infection mouse model, MCL down-regulated the expression of IL-6, TNF-alpha, MCP-1/CCL2

130 ucosal immunity and commensal homeostasis by regulating the expression of IL-22 and the antimicrobial

131 Our data show that KRAS regulated the expression of ILK through E2F1-mediated tr

132 matin has emerged as a promising approach to regulate the expression of important disease-relevant ge

133 ysis, we found that in CLL cells, HIF-1alpha regulates the expression of important chemokine receptor

134 model wherein KLK5-mediated PAR-2 activation regulates the expression of inflammation-associated mRNA

135 Activating transcription factor (ATF)3 regulates the expression of inflammation-related genes i

136 Our findings indicate that specific miRNAs regulate the expression of inflammatory cytokines in hum

137 d its phenotype toward pro-atherogenic by up-regulating the expression of inflammatory genes and down

138 , WhiB3 regulates intraphagosomal pH by down-regulating the expression of innate immune genes and blo

139 In addition, antagomir-352 up-regulated the expression of insulin-like growth factor I

140 Furthermore, TR3/Nur77 regulates the expression of integrin beta4 by targeting

141 is at nutritional Se levels not only by down-regulating the expression of integrin beta3 but also by

142 antiviral host factor in hepatocytes, which regulates the expression of interferon (IFN)-stimulated

143 d synaptic input, as evidenced by UNC-3 also regulating the expression of ionotropic neurotransmitter

144 duced by Treg cells at an autoimmune site up-regulates the expression of its own receptor, CCR8, on t

145 sed in microarray analysis, DHI treatment up-regulated the expression of kallikrein and plasma kallik

146 ecules work in part through their ability to regulate the expression of key leukocyte adhesion molecu

147 Rtg3 and Sfp1 regulate the expression of key stress genes such as CTA4

148 the ten-eleven translocation 2 (TET2) enzyme regulates the expression of key cardiac genes, such as M

149 anscriptomic analyses showed that glycolysis regulates the expression of key genes involved in cardia

150 valve is under the control of NOTCH1, which regulates the expression of key pro-osteogenic genes suc

151 p53 controls DNA methylation homeostasis by regulating the expression of key counteracting component

152 gas disease by modulating ROS production and regulating the expression of key physiological regulator

153 ther downstream and control LR production by regulating the expression of LATERAL ORGAN BOUNDARIES-DO

154 Moreover, macroH2A1 isoforms differentially regulate the expression of lipogenic genes by modulating

155 ing controls neuronal network function is by regulating the expression of Lrrtm1 and Lrrtm2.

156 rtant role in endometrial decidualization by regulating the expression of major decidual marker genes

157 PU.1 and SpiB regulate the expression of many components of the B cell

158 -variable regulon) to rapidly and reversibly regulate the expression of many genes, which include kno

159 otspots ': , important genetic variants that regulate the expression of many genes.

160 MicroRNAs regulate the expression of many proteins and require spe

161 cing in macrophages, we discovered that IRE1 regulates the expression of many proatherogenic genes, i

162 F-2 is of special significance because it co-regulates the expressions of mediators of energy metabol

163 odulates activities of H3K27me3 modifiers to regulate the expression of medulloblastoma genes.

164 anscription of PA5471, which subsequently up-regulates the expression of MexXY.

165 Additionally, BDE47 significantly down-regulated the expression of miR-23b in rats and in hepat

166 was to elucidate the mechanism by which VEGF regulates the expression of miR-17-92 cluster in ECs and

167 Heat shock factor (Hsf1) regulates the expression of molecular chaperones to main

168 to traverse through maturation steps and in regulating the expression of most Tcf1 target genes.

169 ence of APEC, and ArcA was shown to directly regulate the expression of motA, motB, and cheA.

170 involved in cancer and immunity and known to regulate the expression of mRNAs differentially expresse

171 Mechanistically, MYC regulates the expression of MTHFD2, and MTHFD2 knockdown

172 duction and biliary cholesterol excretion by regulating the expression of Mtp and Abcg5/Abcg8 via Shp

173 cooperated with DNA methylation to directly regulate the expression of multiple germ cell-specific g

174 nt 32 (RGC32) is a transcription factor that regulates the expression of multiple genes involved in c

175 ted by multiple CNAs and one CNA potentially regulating the expressions of multiple genes.

176 The serine 215 residue, which is known to regulate the expression of Mxr1p-activated genes in a ca

177 Sulfate up-regulated the expression of NCED3, a key step of ABA syn

178 hat many lncRNA loci act locally (in cis) to regulate the expression of nearby genes-for example, thr

179 in the population, and the number of repeats regulates the expression of nearby genes (known as expre

180 JAK1 regulated the expression of nearly 3,000 genes in ABC DL

181 s gene, with or without the loss of elements regulating the expression of neighboring genes, are the

182 umented that transposable elements (TEs) can regulate the expression of neighbouring genes.

183 inly from the salvage pathway, by positively regulating the expression of Neu3, the gene encoding neu

184 the nucleolar remodeling complex (NoRC) that regulates the expression of noncoding RNAs.

185 nt in the second intron of Notch1 locus) and regulates the expression of Notch1 in ventral NSPCs of t

186 tion (PPI) in vitro and in live cells and up-regulate the expression of Nrf2-dependent gene products.

187 We determined that miR-663 regulates the expression of nuclear-encoded respiratory

188 formation of giant multinucleated OCs by up-regulating the expression of nuclear factor of activated

189 ic explanation for the ability of lncRNAs to regulate the expression of numerous genes distributed ac

190 oth endogenous and exogenous PGC-1alpha down-regulate the expression of numerous genes encoding secre

191 L1 TFs work in tandem with KNOTTED1-types to regulate the expression of numerous target genes involve

192 of the disparity in signaling pathways that regulate the expression of Nur77 and CD69.

193 een HMGNs and H1 in chromatin epigenetically regulates the expression of OLIG1&2, thereby affecting o

194 hnRNP and SR proteins also regulate the expression of other Drosophila circular RNA

195 RisA also regulates the expression of other genes, including chemo

196 nscription factor that promotes flowering by regulating the expression of other genes.

197 eQTL analysis suggests that rs1999071 regulates the expression of OXA1L gene.

198 Here we show that p53 regulates the expression of PFKFB4 and that p53-deficien

199 We found that MKL co-regulates the expression of Pfn isoforms indirectly by m

200 MYC post-transcriptionally regulates the expression of PHF8 via the repression of m

201 tion factor Nr2e3, Photoregulin1 (PR1), that regulates the expression of photoreceptor-specific genes

202 ION RESPONSE1, the main transcription factor regulating the expression of Pi starvation-induced genes

203 ations, we find that vegfaa mutant hearts up-regulate the expression of potentially compensating gene

204 zoid and caulonema development by positively regulating the expression of PpLRL1 and PpLRL2, the two

205 es the induction of neural-specific genes by regulating the expression of PRC2 complex components.

206 Interestingly, STAT1 directly regulates the expression of Prdm1 (encodes BLIMP-1) by b

207 1) QSI resistance spreads when QS positively regulates the expression of private or quasi-public good

208 mily proteins are transcription factors that regulate the expression of pro-inflammatory cytokines an

209 PARP1, the most abundant isoform, regulates the expression of proinflammatory mediator cyt

210 y degrading anti-invasive miRNAs so as to up-regulate the expression of proinvasive proteins.

211 Macrophages up-regulated the expression of prolymphangiogenic vascular

212 hat JAK1-mediated signaling cascades in skin regulate the expression of proteases associated with the

213 Nuclear hormone receptors (NHRs) regulate the expression of proteins that control aspects

214 sosomal recruitment and activity by directly regulating the expression of RagD.

215 ntified a new cellular pathway in which ATF4 regulates the expression of RhoGDIalpha that in turn aff

216 uggest that the OT system may play a role in regulating the expression of schizophrenia spectrum diso

217 We show that SMARCE1 drives invasion by regulating the expression of secreted proteases that deg

218 r, EMP2 expression correlates with and helps regulate the expression of several cancer stem cell asso

219 The exposure to TDCIPP significantly up-regulated the expression of several biomarker genes for

220 chanistically, upon CXCL12 exposure, SC down-regulated the expression of several pain-associated targ

221 We found that Nkx6.1 regulates the expression of several beta-cell maturation

222 Mxr1p regulates the expression of several genes involved in th

223 SP signaling regulates the expression of several miRNAs, including mi

224 tein U (hnRNP U), plays an important role in regulating the expression of SLO-2 (a homolog of mammali

225 The EFTF Tbx3 can regulate the expression of some EFTFs; however, its role

226 These results suggest that IL-1 may regulate the expression of specific anti-inflammatory ge

227 poly-U-rich elements within several RNAs and regulates the expression of specific transcripts.

228 or in mediating the hypoxic response by down-regulating the expression of specific genes, including A

229 Further experiments showed that DARPP-32 regulates the expression of SRp20 splicing factor and co

230 DEAF1 and loss of PTA expression in LNSCs by regulating the expression of SRSF10 and PTBP2.

231 ARID5B positively regulates the expression of TAL1 and its regulatory part

232 s activated by the phosphatase Glc7, and can regulate the expression of target genes in concert with

233 in O, and hypoxia inducible factor 1alpha to regulate the expression of target genes.

234 ntrol module that can be used to dynamically regulate the expression of target genes.

235 This complex associates with chromatin and regulates the expression of target genes.

236 four alternatively spliced transcripts that regulate the expression of TH2 cytokines, IL-4, IL-5 and

237 identified gene has been shown to negatively regulate the expression of the caffeine metabolism genes

238 ligand, on the promoters and differentially regulate the expression of the endogenous AR target gene

239 4, Prox1, Sox1, and a few additional factors regulate the expression of the lens structural proteins,

240 g (RS) pathways converge antagonistically to regulate the expression of the nuclear-encoded transcrip

241 uggesting that Znf2 and Pum1 each positively regulate the expression of the other to achieve the fila

242 These miRNAs were found to regulate the expression of the proapoptotic Bcl-2 protei

243 We found that exogenously added HA up-regulated the expression of the BcBOT and all the virule

244 echanistically, we found that PDGF signaling regulated the expression of the E2F transcription factor

245 In zebrafish, dietary Mg(2+) regulated the expression of the highly conserved ARL15 o

246 we observed that c-Met induction markedly up-regulated the expression of the negative co-stimulatory

247 ng through the receptor tyrosine kinase Ret, regulates the expression of the chemosensory fate determ

248 We show Star-PAP-specific PAS usage regulates the expression of the eukaryotic translation i

249 roduction of the anaphylatoxin C3a, and down-regulates the expression of the Foxp3 gene and anergy-re

250 med IB4 cells by RNA interference negatively regulates the expression of the genes downstream of LMP1

251 The protein regulates the expression of the hca catabolic operon in

252 echanistically, we show that AMPK negatively regulates the expression of the integrin-binding protein

253 We also demonstrate that FOXM1 regulates the expression of the microtubulin-associated

254 required for HSPC specification and that it regulates the expression of the Notch ligand Jagged1a in

255 de transcriptional analysis shows that NO up-regulates the expression of the plastid nitrite reductas

256 First, c-Myb negatively regulates the expression of the Rag activator Foxo1, an

257 e polycomb repressive complex 1, BMI1, which regulates the expression of the schizophrenia-related ge

258 As showed that Pacman post-transcriptionally regulates the expression of the secreted insulin-like pe

259 l gene which regulates coffee consumption by regulating the expression of the genes linked to caffein

260 of HA levels in cell culture and in vivo by regulating the expression of the HA synthase HAS3 and tw

261 We conclude that miRNAs are involved in regulating the expression of the major T1D autoantigens.

262 tion and survival of the seeded ASCs, and up-regulates the expression of their neurotrophic factors m

263 Since miRNAs exert their functions by regulating the expression of their target mRNAs, several

264 pend on the development of simple methods to regulate the expression of therapeutic genes.

265 CodY regulates the expression of thermonuclease (nuc) via the

266 ontexts, yet the cis and trans elements that regulate the expression of these enzymes remain essentia

267 Egfl7 regulates the expression of these adhesion molecules thr

268 Little is known, however, about what regulates the expression of these autoantigens.

269 suggests that MADS-RIN transcription factor regulates the expression of these genes.

270 However, the mechanisms regulating the expression of these ligands are still not

271 /BZR1 family of transcription factors, which regulate the expression of thousands of downstream genes

272 eracting with co-factors that enable them to regulate the expression of thousands of genes linked to

273 Light regulates the expression of thousands of genes with role

274 NsrR from Streptomyces coelicolor (Sc) regulates the expression of three genes through the prog

275 Down-regulating the expression of three autophagy-related gen

276 Hh signaling through FAP cilia regulated the expression of TIMP3, a secreted metallopro

277 nce that (1) growth arrest-specific 6 (Gas6) regulates the expression of tissue factor during venous

278 Matrine treatment significantly down-regulated the expression of TLR3, TLR4 and TNF-alpha alt

279 We applied our system to regulate the expression of TNFSF10 (TRAIL) in the contex

280 epatocytes that express HCV-NS5A in liver up-regulate the expression of Toll-like receptor 4 (TLR4),

281 this study, we determined whether TGF-beta1 regulated the expression of TREM-1 in a mouse model of p

282 SUMO does not modify Oct-1 directly, but regulates the expression of TRIM21 that enhances Oct-1 u

283 e reporter assay showed that NFATc4 directly regulated the expression of TRPC6 in PASMCs.

284 In addition, we observed that LPS itself up-regulated the expression of TSG6 in TSG6(+/+) mice, sugg

285 Somatically acquired SV may regulate the expression of tumor-related genes and resul

286 onal novel molecular mechanism by which LMP1 regulates the expression of tumor-promoting host genes.

287 Here we show that MYC regulates the expression of two immune checkpoint protei

288 aling keeps Ras targets in check by directly regulating the expression of two key downstream transcri

289 phocyte progenitors and immature lymphocytes regulates the expression of ubiquitous and lymphocyte-sp

290 lpha) controls BAT-mediated thermogenesis by regulating the expression of Ucp1 Inhibitor of different

291 ols macrophage inflammation and ER stress by regulating the expression of UCP2.

292 serve as secondary signaling messengers that regulate the expression of various inflammatory mediator

293 MR-409 also significantly down-regulated the expression of vascular endothelial growth

294 sequently, we found that cyclin F negatively regulates the expression of viral protein Vif (viral inf

295 of AMPK enhances, KSHV lytic replication by regulating the expression of viral genes.

296 NAs) play vital roles in viral infections by regulating the expression of viral or host genes at the

297 hich can interact with the ClpAS-P system to regulate the expression of virulence factors and pathoge

298 The translational GTPase BipA regulates the expression of virulence and pathogenicity

299 human gingival fibroblasts (GFBLs) strongly regulated the expression of wound healing-related genes.

300 ucleotide excision repair through positively regulating the expression of xeroderma pigmentosum compl