ライフサイエンスコーパス: inducible gene

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

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

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

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

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

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

7 enome and successfully identified novel zinc-inducible genes.

8 associated genes and repress differentiation-inducible genes.

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

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

11 and downregulates the expression of hypoxia-inducible genes.

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

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

14 ays a role in stabilizing mRNAs of some heat-inducible genes.

15 anscripts, and enhances activation of stress-inducible genes.

16 , LDGs display the highest expression of IFN-inducible genes.

17 ry elements and maintain low basal levels of inducible genes.

18 ly enriched in ISGs, particularly for highly inducible genes.

19 associated macrophage expression of IFNgamma-inducible genes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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 ion potently increased the levels of mitogen-inducible gene 6 (MIG6), which inhibits EGFR and facilit

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

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

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

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

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

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

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 ion factor to promote the expression of heat-inducible genes and heat tolerance in Arabidopsis.

62 emarkably, a significant proportion of auxin inducible genes and of targets of the AUXIN RESPONSE FAC

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

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

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

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

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

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

69 Type I IFN-inducible genes are abrogated in the absence of IFN-gamm

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

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

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

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

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

75 ase in the expression of a subset of hypoxia-inducible genes at the metastatic site, suggesting the p

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

77 own as a positive elongation factor for many inducible genes by releasing paused RNAPII near the tran

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

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

80 nterface and show its utility using a ligand-inducible gene circuit and toehold switch-based sensors

81 s well as transgenic human cells carrying an inducible gene circuit for the on-demand secretion of er

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

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

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

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

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

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

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

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

90 Highly transcribed and highly inducible genes display strong transcriptional direction

91 Hypoxia-inducible gene domain 1 (HIGD1) proteins are small integ

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

93 xcl10), APC activation (e.g., Cd86), and IFN-inducible genes (e.g., Ifit3, Ifit5, Irf7, Isg15, orMx1)

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

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

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

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

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

99 BdRAM1 showed constitutive expression of AM-inducible genes even in the shoots.

100 To this end, we implemented an inducible-gene excision methodology using a floxed allel

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

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

103 Using inducible gene expression and optogenetics to perturb th

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

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

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

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

108 tively, spatially and temporally controlling inducible gene expression in Arabidopsis that overcomes

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

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

111 Our inducible gene expression PiggyBac transposon system sho

112 o compare expression of 1alpha,25(OH)(2)D(3)-inducible gene expression signatures in clinical samples

113 tergroup differences in 1alpha,25(OH)(2)D(3)-inducible gene expression signatures were modest and var

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

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

116 Inducible gene expression systems are vital tools for th

117 roach to identify transcription factor-based inducible gene expression systems.

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

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

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

121 Further themes include mechanisms of inducible gene expression, the coordination of gene regu

122 To systematically identify regulators of inducible gene expression, we performed high-throughput

123 Using reporter mice with SOX2-driven, inducible gene expression, we show that ONLR-NPCs genera

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

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

126 several transcription factors regulating JA-inducible gene expression.

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

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

129 res the Gadd45 (Growth arrest and DNA-damage-inducible) gene family, very little is known about how t

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

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

132 s LTR12C elements upstream of the interferon-inducible genes GBP2 and GBP5 that encode for broad-spec

133 le-cell RNA sequencing, we found that immune-inducible genes had become constitutively upregulated.

134 ceptor 7 (TLR7) and, possibly, retinoic acid-inducible gene I (RIG-I) after viral sensing.

135 These defective RNAs bind to retinoic acid-inducible gene I (RIG-I) and initiate mitochondrial anti

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

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

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

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

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

141 5 specifically interacted with retinoic acid-inducible gene I (RIG-I) and negatively regulated its ac

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

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

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

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

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

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

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

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

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

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

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

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

154 Using retinoic acid-inducible gene I (RIG-I) signaling as a model, we demons

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

156 al antiviral signaling (MAVS), retinoic acid-inducible gene I (RIG-I), and melanoma differentiation-a

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

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

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

160 tors, such as the RNA helicase retinoic acid-inducible gene I (RIG-I), that sense viral RNA.

161 se in viral RNA recognition by retinoic acid-inducible gene I (RIG-I), thereby stimulating type I int

162 interferon (IFN) response in a retinoic acid-inducible gene I (RIG-I)-dependent manner and readily ac

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

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

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

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

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

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

169 Retinoic acid-inducible gene I (RIG-I)-like receptors (RLRs) are key s

170 Mammalian retinoic acid-inducible gene I (RIG-I)-like receptors detect viral dou

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

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

173 pathogen recognition receptor, retinoic acid-inducible gene I (RIG-I).

174 outbreak viruses, mediated via retinoic acid-inducible gene I (RIG-I).

175 genome replication can trigger retinoic acid-inducible gene I (RIG-I)/mitochondrial antiviral signali

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

196 l-like receptor 7 and possibly retinoic acid-inducible gene I.

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

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

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

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

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

202 of the TLR4 and the antiviral retinoic acid-inducible gene-I (RIG-I) pathways with clinical outcomes

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

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

205 nsors, Toll-like receptors and retinoic-acid inducible gene-I (RIG-I)-like receptors in particular, w

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

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

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 n sensing cytosolic viral RNA, retinoic acid-inducible gene-I-like receptors (RLRs) interact with the

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

213 IP-Seq analysis identified Klk1b21 as an ICI-inducible gene in AF2ERKI uterus.

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

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

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

217 vate high levels of expression of interferon-inducible genes in glia.

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

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

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

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

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

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

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

225 th increased epithelial expression of IL-6TS-inducible genes in the absence of systemic inflammation.

226 the correct expression of a subset of auxin-inducible genes In this work, we analyzed the response t

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

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

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

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

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

232 tion, which was accompanied by reductions in inducible genes, including Comtd1 in vitro and Fstl1 and

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

234 ession of the recently characterized, immune-inducible gene Induced by Infection (IBIN) was diminishe

235 olism early after activation to regulate TLR-inducible gene induction.

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

237 de that GFAT2 should be considered a new LPS-inducible gene involved in regulation of protein O-GlcNA

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

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

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

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

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

246 r gene OsSULTR1;1 and the sulphur-deficiency-inducible gene OsSDI1.

247 Multiple inducible gene overexpression systems have been develope

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

249 ting protein (TXNIP), an exquisitely glucose-inducible gene previously identified as a critical media

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

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

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

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

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

255 most likely by regulating a subset of auxin inducible genes related to cell expansion.

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

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

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

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

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

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

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

263 ibosomal protein L4 encoded by the cytokinin-inducible genes RPL4A and RPL4D, and that RPL4 loss-of-f

264 rn facilitated the induction of distinct LPS-inducible gene sets.

265 equencing revealed that a number of cytokine-inducible genes shared this heterogeneous response patte

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

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

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

269 In Solomon, the hypersensitive inducible genes such as pathogenesis-related gene PR-1,

270 nds to positively correlate with several IFN-inducible genes, suggesting the potential role of AIM-2

271 Chemically inducible gene switches can provide precise control over

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

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

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

275 es suggest that Mcub is a protective cardiac inducible gene that reduces mitochondrial Ca(2+) influx

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

277 T cells, DNA damage and replication, and IFN-inducible genes that correlated with IL-15 treatment and

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

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

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

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

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

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

284 odifications) that regulate constitutive and inducible gene transcription.

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

286 We find that Vgf nerve growth factor inducible gene up-regulation is a common transcriptional

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

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

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

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

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

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

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

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

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

296 ance of seedlings and the expression of heat-inducible genes whereas knockout of GAPCs has opposite e

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

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

299 , and increased transcript levels of mechano-inducible genes within 60 min.

300 These screens converge upon the p53-inducible gene Zmat3, encoding an RNA-binding protein, a