ライフサイエンスコーパス: inducible gene

1 enome and successfully identified novel zinc-inducible genes.

2 associated genes and repress differentiation-inducible genes.

3 ), as being encoded by Mlx-dependent glucose-inducible genes.

4 itioned in promoters upstream of most stress-inducible genes.

5 associated macrophage expression of IFNgamma-inducible genes.

6 iating enhancer-promoter looping at ecdysone-inducible genes.

7 and downregulates the expression of hypoxia-inducible genes.

8 ells selectively upregulate a set of hypoxia-inducible genes.

9 s degraded by DCP2 are expressed proximal to inducible genes.

10 xO3a expression and reduced levels of FoxO3a-inducible genes.

11 n transcriptional regulation specifically at inducible genes.

12 cluding CD16A signaling and interferon-gamma-inducible genes.

13 both affect comparable numbers of TNF-alpha-inducible genes.

14 ice showed upregulation of several IFN-gamma-inducible genes.

15 ase activity and increased expression of IFN-inducible genes.

16 al-time polymerase chain reaction of hypoxia-inducible genes.

17 factor is involved in modulating other ATRA-inducible genes.

18 stimulation and is strongly enriched for IFN-inducible genes.

19 other genes that are not recognized as MyoD-inducible genes.

20 loci, which apparently do not accumulate at inducible genes.

21 contributed to basal expression of many LPS-inducible genes.

22 trate that expression of retinoic acid early inducible gene 1 (RAE-1) family NKG2D ligands in cancer

23 Toll-like receptor 3 (TLR-3), retinoic acid-inducible gene 1 (RIG-1), and nucleotide-binding oligome

24 Retinoic acid-inducible gene 1 (RIG-I) and melanoma differentiation-as

25 and Lujo viruses, can inhibit retinoic acid-inducible gene 1 (RIG-i) and Melanoma Differentiation-As

26 The retinoic acid-inducible gene 1 (RIG-I) signaling pathway is essential

27 mRNA fragments produced engage retinoic-acid inducible gene 1 (RIG-I), a cytosolic sensor of RNA viru

28 n-associated protein 5 (MDA5), retinoic acid-inducible gene 1 (RIG-I), and mitochondrial antiviral si

29 al for sustained and amplified retinoic acid-inducible gene 1 (RIG-I)-induced type I interferon expre

30 ted by the cytosolic receptors retinoic acid-inducible gene 1 and melanoma differentiation-associated

31 In particular, the retinoic acid-inducible gene 1 protein (RIG-I) participates in the rec

32 -like receptors (TLRs) and the retinoic acid-inducible gene 1 protein (RIG-I)-like receptors (RLRs) a

33 e we show that MAVS and RIG-I (retinoic acid-inducible gene 1), an RLR family member, also have a rol

34 tors (Toll-like receptor 7 and retinoic acid-inducible gene 1), HCV RNA induced consistent and broad

35 ion of the NKG2D ligand, retinoic acid early inducible gene 1, also increased at the ocular surface a

36 is required for both TRIF- and retinoic acid-inducible gene 1-dependent signaling cascades to induce

37 s that are transmitted via the retinoic acid-inducible gene 1-like receptor (RLR), nucleotide-binding

38 tion induced by TLR2, TLR9, or retinoic acid-inducible gene 1-like receptor agonists.

39 nduced by TLR2, TLR3, TLR9, or retinoic acid-inducible gene 1/melanoma differentiation-associated pro

40 oll-like receptor 7 (TLR7) and retinoic acid inducible gene-1 (RIG-I) for the activation of innate-im

41 bition was dependent on Rig-I (retinoic acid-inducible gene-1), IRF3, and MxA (myxovirus resistance g

42 s and functional analyses identified hypoxia-inducible gene 2 (HIG2), a HIF-1 target, as a new inhibi

43 Here we show that the LD protein hypoxia-inducible gene 2 (Hig2/Hilpda) functions to enhance lipi

44 al cells with KSHV, growth arrest DNA damage-inducible gene 45 beta (GADD45B) is one of the most repr

45 Mitogen-inducible gene 6 (Mig-6) is a critical mediator of proge

46 Mitogen-inducible gene 6 (Mig6) is a tumor suppressor, and the d

47 inib, with a concomitant increase of mitogen-inducible gene 6 (Mig6), a negative regulator of EGFR th

48 lts in upregulated expression of the mitogen-inducible gene 6 (MIG6), a negative regulator of EGFR.

49 ignaling and decreased expression of mitogen-inducible gene 6 (MIG6), a negative regulator of epiderm

50 on-associated protein, tumor necrosis factor-inducible gene 6 protein, in the extracellular matrix.

51 A deficiency of mitogen-inducible gene-6 (Mig-6) in mice leads to the developmen

52 RNA quantitation, we found that multiple IFN-inducible genes (affecting lymphocyte trafficking, diffe

53 DNA variation in IFN-inducible genes altered T1D risk (P = 0.007), as exempli

54 hat, mechanistically, DDT is a novel hypoxia-inducible gene and direct target of HIF1alpha and HIF2al

55 ng the ribosome binding site strength of the inducible gene and shifts when modifying the plasmid cop

56 transcription elongation of constitutive and inducible genes and associates with coding regions in a

57 n associated with increased expression of GA-inducible genes and decreased ABA accumulation, apparent

58 KAP1 repressed differentiation-inducible genes and derepressed pluripotency-associated

59 reduced responsiveness of jasmonic acid (JA)-inducible genes and enhanced susceptibility to the necro

60 gions of active chromatin in the vicinity of inducible genes and enhancers that regulate immune respo

61 lected per-cell changes in the expression of inducible genes and related more strongly to the subject

62 ratively at the promoters of differentiation-inducible genes and repressed their transcription.

63 Type 1 interferon (IFN)-inducible genes and their inducible products are upregul

64 nduced priming (i.e., high expression of IFN-inducible genes and TLR hyperresponsiveness).

65 d by Suc starvation, downregulation of a Suc-inducible gene, and a reduced Suc content in dormant tin

66 vivo, CHD1 and Mediator are recruited to an inducible gene, and genome-wide binding of the two prote

67 we observed that ATF3 itself is a type I IFN-inducible gene, and that ATF3 further modulates the expr

68 identified two interrelated pathways: 1) IFN-inducible genes, and 2) innate receptors for cellular da

69 manner, indicating that the findings at this inducible gene are likely generalizable to a large set o

70 d serum Type 1 interferons (IFN-1) and IFN-1 inducible genes are gaining traction as disease biomarke

71 interferon gamma (IFN-gamma), many IFN-gamma-inducible genes are induced more rapidly and more strong

72 alysis of active RNAPII reveals that hypoxia-inducible genes are paused and active prior to their ind

73 Altogether these data show that hypoxia-inducible genes are regulated in a multilayered manner t

74 a/ARNT (HIF2) proteins in activating hypoxia-inducible genes are well established, the role of other

75 This gene, termed arsenic inducible gene (arsI), is in an arsenic resistance (ars)

76 we detected up-regulation of a group of IFN-inducible genes as early as 8 h post-T-cell transfer.

77 association to nuclear factor-kappaB and IFN-inducible genes as well as signatures of other transcrip

78 he female birds expressed a set of known IFN-inducible genes at much higher levels than male cells un

79 er gene driven by the promoter from the heat-inducible gene AtHSP18.2.

80 o not affect the expression of retinoic acid-inducible genes but alter the expression levels of sever

81 ovides a new level of regulatory control for inducible genes by lncRNAs.

82 correlate repression of transcription of IFN-inducible genes by the E1B 55-kDa protein with protectio

83 9) impair repression of transcription of IFN-inducible genes, by the E1B, 55-kDa protein, consistent

84 Periostin and TGF-beta inducible gene clone H3 (betaIGH3) mRNA expression from

85 is dominated by overexpression of interferon-inducible genes (consisting of both type I and type II i

86 Ngs1 is targeted to the promoters of GlcNAc-inducible genes constitutively by the transcription fact

87 esults in a rapid down-regulation of hypoxia-inducible genes critical for cancer progression.

88 ion accumulate point mutations in silent and inducible genes crucial for cell replication and differe

89 Furthermore, the levels of the IFN-inducible genes CXCL10 and TNFSF13B (BAFF) were correlat

90 ce, SP-A inhibited upregulation of IFN-gamma-inducible genes (CXCL10, RARRES3, and ETV7) as well as S

91 ng in transcriptional activation of a highly inducible gene, CYP2C9.

92 To address this, we have implemented an inducible gene deletion system based on a dimerised Cre

93 defects in growth, and in induction of a UV-inducible gene, demonstrating the functional importance

94 Highly transcribed and highly inducible genes display strong transcriptional direction

95 a regulates nearly one-half of all IFN-gamma-inducible genes during infection of macrophages.

96 paradoxical "constitutive plasticity" (fewer inducible genes) during periods of enhanced behavioral r

97 Finally, we show how inducible gene editing can be achieved by combining the

98 We report that Nr4a1, an activity-inducible gene encoding a nuclear receptor, regulates th

99 ISG15 is a type I interferon (IFN)-inducible gene encoding a protein with pleiotropic funct

100 Stronger drought-stimulation of stress-inducible genes encoding late-embryogenesis-abundant pro

101 sulted in increased expression of interferon-inducible genes, especially those involved in type I int

102 In control cells, 3AT-inducible genes exhibit a series of distinct nucleosome

103 nocyte phenotype and function and interferon-inducible gene expression (IFIG).

104 FREEZING6 (SFR6) controls cold- and drought-inducible gene expression and freezing- and osmotic-stre

105 on a combination of stem cell delivery, heat-inducible gene expression and mild heating with high-int

106 ALENs), and has enabled us to insert a 15-kb inducible gene expression cassette at a defined locus in

107 the characterization of an engineered light-inducible gene expression circuit in yeast and compare t

108 of histone acetylation and enhanced ethylene-inducible gene expression in an EIN2-dependent manner.

109 EXPRESSION OF HEAT RESPONSIVE GENE1) in heat-inducible gene expression in Arabidopsis thaliana.

110 S patients induced a significantly lower IFN-inducible gene expression in comparison with healthy con

111 gene expression system to achieve versatile inducible gene expression in hPSC lines.

112 vivo imaging and optogenetic methods and/or inducible gene expression in transgenic mice will facili

113 Our inducible gene expression PiggyBac transposon system sho

114 in NS1 enables the influenza virus to affect inducible gene expression selectively, thus contributing

115 the PiggyBac transposon and a Tet-On 3G drug-inducible gene expression system to achieve versatile in

116 The extension of this chemically inducible gene expression system to sugar cane opens the

117 quantitative cell microscopy tools and drug-inducible gene expression to dissect Msp1 function.

118 st the hypothesis that Smad3 represses Runx2-inducible gene expression to prevent articular cartilage

119 Inducible gene expression underlies the epigenetically i

120 anslation, are commonly used in research for inducible gene expression using Tet-ON/Tet-OFF systems.

121 ate increased IFNAR signaling, increased IFN-inducible gene expression, and enhanced proliferation an

122 several transcription factors regulating JA-inducible gene expression.

123 y and significantly higher levels of ethanol inducible gene expression.

124 VCAM1 These changes are associated with IFN-inducible gene expression.

125 that is required for the regulation JAK-STAT-inducible gene expression.

126 BA responsiveness, thereby activating stress-inducible gene expression.

127 sociated with increased responsiveness of JA-inducible gene expression.

128 repressed sensitivity of jasmonic acid (JA)-inducible gene expression.

129 Ad is known to suppress IFN-inducible gene expression; however, we observed that Ad

130 the role of pausing goes well beyond poising-inducible genes for activation and propose that the prim

131 To assess the importance of specific plant-inducible genes for L. lactis growth in ATL, xylose meta

132 We suggest that the GAL lncRNAs poise inducible genes for rapid activation, enabling cells to

133 onjugated beads indicated that retinoic acid-inducible gene I (RIG-I) and interferon gamma-inducible

134 N response by interacting with retinoic acid inducible gene I (RIG-I) and its recruitment to mitochon

135 Retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-as

136 Retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-as

137 interacting with and degrading retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-as

138 5 specifically interacted with retinoic acid-inducible gene I (RIG-I) and negatively regulated its ac

139 f Toll-like receptor 3 (TLR3), retinoic acid-inducible gene I (RIG-I) and several antiviral IFN-stimu

140 e in cancer cells that reduced retinoic acid-inducible gene I (RIG-I) expression and impeded the abil

141 ha and the IFN-stimulated gene retinoic acid-inducible gene I (RIG-I) in response to cyclic GMP-AMP,

142 Retinoic acid-inducible gene I (RIG-I) initiates a rapid innate immune

143 that the sensing of IAV RNA by retinoic acid inducible gene I (RIG-I) initiates ZBP1-mediated cell de

144 Retinoic-acid-inducible gene I (RIG-I) is a cytosolic PRR that senses

145 Retinoic acid-inducible gene I (RIG-I) is a key sensor for viral RNA i

146 Retinoic acid-inducible gene I (RIG-I) is a pattern recognition recept

147 e pattern recognition receptor retinoic acid-inducible gene I (RIG-I) plays a key role in influenza A

148 ucibly binds to the endogenous retinoic acid-inducible gene I (RIG-I) promoter.

149 In infected hepatocytes, the retinoic acid-inducible gene I (RIG-I) protein recognizes 5' triphosph

150 Retinoic acid-inducible gene I (RIG-I) receptor recognizes 5'-triphosp

151 In the cytoplasm, the retinoic acid-inducible gene I (RIG-I) senses the RNA genomes of sever

152 Upon detection of viral RNA, retinoic acid-inducible gene I (RIG-I) undergoes TRIM25-mediated K63-l

153 ion via the cytosolic helicase retinoic acid-inducible gene I (RIG-I), a ubiquitously expressed recep

154 tion of cytosolic RNA sensors, retinoic acid inducible gene I (RIG-I), and melanoma differentiation-a

155 genes following stimulation of retinoic acid-inducible gene I (RIG-I), it could selectively impair th

156 ivation of the RNA sensor, the retinoic acid-inducible gene I (RIG-I), leading to inhibition of IFN p

157 cytoplasmic sensors encoded by retinoic acid-inducible gene I (RIG-I), melanoma differentiation-assoc

158 receptor (TLR) 3, TLR7, TLR8, retinoic acid-inducible gene I (RIG-I), melanoma differentiation-assoc

159 V) persistency are observed in retinoic acid-inducible gene I (RIG-I)-deficient cells and that KSHV O

160 y expressed RdRp can stimulate retinoic acid-inducible gene I (RIG-I)-dependent reporter luciferase p

161 ns homologous to the mammalian retinoic acid inducible gene I (RIG-I)-like helicase (RLH) family of c

162 likely through suppression of retinoic acid-inducible gene I (RIG-I)-like receptor (RLR) activation.

163 tion of viral pathogens by the retinoic acid-inducible gene I (RIG-I)-like receptor (RLR) family resu

164 as viral RNA receptors of the retinoic acid-inducible gene I (RIG-I)-like receptor (RLR) family.

165 Retinoic acid-inducible gene I (RIG-I)-like receptor (RLR) proteins me

166 el, we found that blocking the retinoic acid-inducible gene I (RIG-I)-like receptor pathway or the IF

167 Retinoic acid-inducible gene I (RIG-I)-like receptors (RLRs) are key R

168 on of viral RNA by cytoplasmic retinoic acid inducible gene I (RIG-I)-like receptors initiates signal

169 sensed in the cytoplasm by the retinoic acid-inducible gene I (RIG-I)-like receptors.

170 nfection trigger a coordinated retinoic acid-inducible gene I (RIG-I)-Toll-like receptor (TLR) signal

171 cted with a plasmid expressing retinoic acid-inducible gene I (RIG-I).

172 is sensed in the cytoplasm by retinoic acid-inducible gene I (RIG-I, also known as DDX58), which req

173 Retinoic acid (RA)-inducible gene I (RIG-I, encoded by DDX58) forms one cla

174 lus) and 5' poly(U) HCV RNA (a retinoic acid-inducible gene I [RIG-I] stimulus) from two viral genoty

175 ulation with TLR4, TLR7/8, and retinoic acid-inducible gene I agonists.

176 at functions downstream of the retinoic acid-inducible gene I family of pattern recognition receptors

177 ling protein to inactivate the retinoic acid-inducible gene I pathway.

178 tions of each RNP subunit with retinoic acid-inducible gene I protein (RIG-I) from mammalian and avia

179 donors produced IFN-alpha in a retinoic acid-inducible gene I protein (RIG-I)-dependent manner.

180 The cytosolic retinoid-inducible gene I(RIG-I)-like RNA receptor (RLR) RNA sens

181 nd MDA5) or may not be active (retinoic acid-inducible gene I) in mESCs.

182 The cytosolic RIG-I (retinoic acid-inducible gene I) receptor plays a pivotal role in the i

183 ll lines pointed to the RIG-I (retinoic acid inducible gene I)-like receptor Laboratory of Genetics a

184 siology gene 2) but not RIG-I (retinoic acid-inducible gene I).

185 in a significant reduction of retinoic acid-inducible gene I-dependent type I IFN (IFN-I).

186 indicated that TLR as well as retinoic acid-inducible gene I-like helicase (RLH) signaling contribut

187 erferon (IFN) signaling in the retinoic acid-inducible gene I-like receptor (RLR) pathway was blocked

188 ainst RNA viruses that uses an retinoic acid-inducible gene I-like receptor-independent pathway to en

189 r inflammatory cytokines after retinoic acid-inducible gene I-like receptors recognize intracellular

190 t include Toll-like receptors, retinoic acid-inducible gene I-like receptors, and cytosolic DNA senso

191 associated patterns by several retinoic acid-inducible gene I-like receptors, toll-like receptors, an

192 d from Toll-like receptors and retinoic acid-inducible gene I-like receptors.

193 RNA receptors such as TLR3 and retinoid acid-inducible gene I/melanoma differentiation-associated gen

194 of IFN-beta synthesis via the retinoic acid-inducible gene I/melanoma differentiation-associated pro

195 e and independent of the known retinoic acid-inducible gene I/mitochondrial antiviral-signaling prote

196 -like receptors (RLRs), RIG-I (retinoic acid-inducible gene I; encoded by DDX58) and MDA5 (melanoma d

197 Retinoic acid-inducible gene-I (RIG-I) and melanoma differentiation-as

198 y identifying a novel role for retinoic acid-inducible gene-I (RIG-I) as a central regulator of endot

199 allows EBOV VP35 to antagonize retinoic-acid inducible gene-I (RIG-I) like receptors (RLRs) that are

200 by the innate immune receptor Retinoic Acid Inducible Gene-I (RIG-I), whose activation triggers a Ty

201 Retinoic acid inducible gene-I (RIG-I)-like helicases such as melanoma

202 the changes in localization of retinoic-acid-inducible gene-I (RIG-I)-like receptors or the mitochond

203 onse to HBV infection, through retinoic acid-inducible gene-I (RIG-I)-mediated sensing of the 5'-epsi

204 localized with the RNA-binding retinoic acid-inducible gene-I (RIG-I).

205 Retinoic-acid-inducible gene-I (RIG-I; also known as DDX58) is a cytop

206 ntiation-associated gene 5 and retinoic acid-inducible gene-I and their adaptor IFN-beta promoter sti

207 tiation-associated gene 5, and retinoic acid-inducible gene-I provides alternative mechanisms for vir

208 RIG-I (Retinoic Acid Inducible Gene-I) is a cytosolic innate immune receptor

209 ed antiviral immunity, reduced retinoic acid-inducible gene-I, and IFN/cytokine and chemokine respons

210 pendent of the classic TLR and retinoic acid-inducible gene-I-like receptor (RLR) pathways.

211 patterns of TFII-I at active, repressed, or inducible genes, identify novel TFII-I interacting prote

212 We investigated whether interferon-inducible genes (IFIGs) with known anti-human immunodefi

213 ded by a previously uncharacterized arsenite-inducible gene in budding yeast.

214 hylases, we identified JMJD2B/KDM4B as a p53-inducible gene in response to DNA damage.

215 nges may be due to increased levels of light-inducible genes in cavefish, including clock repressor p

216 n-containing protein recruited to active and inducible genes in Drosophila.

217 IFNAR1 normalized the overexpression of IFN-inducible genes in graft-versus-host disease skin and ma

218 ms of transcriptional elongation in stimulus-inducible genes in humans.

219 quired for activation of many other pathogen-inducible genes in infected plants.

220 er, H3S10ph also marks regulatory regions of inducible genes in interphase mammalian cells, implicati

221 both developmental and inflammatory stimulus-inducible genes in macrophages, but the mechanisms under

222 oietin (Epo), one of the most highly hypoxia-inducible genes in mammals.

223 s correlated with upregulation of type I IFN-inducible genes in monocytes.

224 oinflammatory cytokines and interferon (IFN)-inducible genes in primary human dendritic cells (DCs) t

225 etinoic acid and activation of retinoic acid-inducible genes in RDH10 rafts.

226 revealed that WRKY70 represses many pathogen-inducible genes in the absence of pathogens, yet is requ

227 DNA microarray analysis to identify IFN-beta-inducible genes in vitro and then used this set of genes

228 ctors become sumoylated during activation of inducible genes in yeast, but the identity of these fact

229 ic lung were all dependent on Atf3, a stress-inducible gene, in the noncancer host cells.

230 ngly increased expression of a number of IFN-inducible genes, in addition to enhanced T-bet synthesis

231 The IFN-inducible genes included 3 transcripts involved in trypt

232 primarily increased expression of interferon-inducible genes including ISG15, a marker for increased

233 in stimulating expression of a subset of IFN-inducible genes, including a key regulator of the IFNgam

234 uction of interferon beta (IFN-beta) and IFN-inducible genes, including the melanoma differentiation-

235 In yeast, some inducible genes interact with the nuclear pore complex b

236 ically, STAT3 also suppresses many NF-kappaB-inducible genes involved in innate and adaptive antitumo

237 he B-cell translocation gene-2 (BTG2), a p53-inducible gene, is suppressed in mammary epithelial cell

238 itations by developing single-step optimized inducible gene knockdown or knockout (sOPTiKD or sOPTiKO

239 uman pluripotent stem cell (hPSC) lines with inducible gene knockout (iKO) remains challenging.

240 ockout hPSC lines, as well as stage-specific inducible gene knockout during hPSC differentiation.

241 754 IFN pathway-related genes, including IFN-inducible genes known to be differentially expressed in

242 quences on metal-induced transcription at an inducible gene, metallothionein B.

243 he auxin reporter DR5rev::GFP, and the auxin-inducible genes MONOPTEROS, INDOLE-3-ACETIC ACID INDUCIB

244 that induces myriad target genes, those p53-inducible genes most critical for tumor suppression rema

245 Interestingly, IFNalpha and the IFN inducible gene, MxA were not enhanced, suggesting preven

246 treatment induced the expression of the DEX-inducible gene MYOC only in the perfusion-cultured anter

247 smFISH measurements of the neuronal activity-inducible gene Npas4 in primary neurons.

248 Multiple inducible gene overexpression systems have been develope

249 Another finding was that the list of Spd-inducible genes overlaps almost completely with that of

250 This interlocking analysis of IFN-inducible genes, plasma analytes, and tissue immunohisto

251 Among the IFN-inducible gene products are the protein kinase regulated

252 We propose that altered expression of light-inducible genes provides a selective advantage to cavefi

253 Using cell-specific inducible gene recombination in mice we found that, in t

254 re we show that ablation of Fmrp in aNSCs by inducible gene recombination leads to reduced hippocampa

255 together, these results suggest that hypoxia-inducible genes, regulated by VHL, are essential for nor

256 he same TF can be linked to constitutive and inducible gene regulation via distinct combinations of a

257 has served as a paradigm of tissue-specific, inducible gene regulation.

258 uences located upstream of IFN-I- and IFN-II-inducible genes, respectively, and activate the expressi

259 Sphingosine kinase 1 (SK1) is an FGF-inducible gene responsible for generation of sphingosine

260 of an integrated gene-trap reporter, whereas inducible gene restoration is afforded by Flp-dependent

261 rther, local loss of Yta7 activity at a long inducible gene resulted in accumulation of H3 at the 3'

262 leads to decreased expression of interferon-inducible genes, resulting in significantly compromised

263 tion domain-like receptor, and retinoic acid-inducible gene RIG-like receptor pathways were mapped ba

264 tion domain-like receptor, and retinoic acid-inducible gene RIG-like receptor signaling pathways in r

265 latory factor 3 (IRF3) via the retinoic acid inducible gene (RIG)-I/mitochondrial antiviral signaling

266 regulatory factors (IRFs) and retinoic acid inducible gene (RIG-I).

267 n of dose-dependent induction of Bisphenol A inducible genes showed a weak gene activation peak at a

268 Our work identified a TGF-beta-inducible gene signature specific to CAFs in advanced hi

269 pression of heavy metal-inducible and stress-inducible genes, stress kinase cascades, and apoptosis.

270 The expression of IFN-beta-inducible genes such as CCL5 and CXCL10 was also reduced

271 viability despite reduced levels of hypoxia-inducible genes, such as BNIP3 and BNIP3L.

272 gy allows EcR to be used in chimeric, ligand-inducible gene-switch systems with applications in pest

273 Chemically inducible gene switches can provide precise control over

274 stem is one of the most promising chemically inducible gene switches in plants because of its potenti

275 d Cre protein (CDX2P-CreER(T2)) to allow for inducible gene targeting in intestinal epithelium.

276 ercome these limitations, we designed a new, inducible gene-targeting system by introducing an in-fra

277 e DCs and identify TREM-1 as a novel hypoxia-inducible gene that may amplify inflammatory responses.

278 aled that approximately 85% of the NF-kappaB-inducible genes that are down-regulated by the R30A muta

279 nce the expression of several glucocorticoid-inducible genes that have anti-inflammatory potential.

280 leads to decreased expression of several IFN-inducible genes that mediate important biological functi

281 ed enhancer element present in multiple zinc-inducible genes, the high zinc activation (HZA) element.

282 er study as a more efficient form of hypoxia-inducible gene therapy for the treatment of myocardial i

283 renhancers to preferentially regulate highly inducible genes, thereby providing new insights into the

284 ation significantly inhibits over 60% of TPA-inducible gene transcription and impairs cell proliferat

285 ogen and hypoxia on AR-dependent and hypoxia-inducible gene transcription, protein expression, cell p

286 nflux which modulates mRNA stability of heat-inducible genes under heat stress conditions.

287 Transcription (STAT) 5A/B regulate cytokine-inducible genes upon binding to GAS motifs.

288 ges were seen in the promoter of the hypoxia-inducible gene VEGF.

289 Up-regulation of hypoxia-inducible genes VEGFA, FLT1, VEGFC, HMOX1, and TIE2 was

290 magnifies the specific activation of stress-inducible genes via counteraction of corepressors.

291 ed in cpl1-2, and the expression of some ABA-inducible genes was controlled by Fe availability.

292 As expected, expression of IFN-inducible genes was markedly reduced in the lungs of IFN

293 Upregulation of IFN-inducible genes was transient, temporally associated wit

294 Bbaa1-mediated regulation of IFN-inducible genes was upstream of IFN receptor-dependent a

295 ral SA-dependent and SA-independent pathogen-inducible genes were higher in cbp60a plants than in the

296 The expression levels of salicylic acid (SA)-inducible genes were higher, but those inducible by jasm

297 The discovery that type I interferon (IFN)-inducible genes were strongly upregulated in peripheral

298 , various osmotic stress/abscisic acid (ABA)-inducible genes were up-regulated in cpl1-2, and the exp

299 USP18 is an interferon inducible gene, which is also upregulated by various TLR

300 ays revealed effective inhibition of hypoxia-inducible genes with relatively minimal perturbation of