ライフサイエンスコーパス: responsive element

1 ferred cis-regulatory element BBRE (BZR1-BAM Responsive Element).

2 lation of this region, which contains a cAMP responsive element.

3 so has characteristics of being an NF-kappaB-responsive element.

4 y Col X promoter activity containing the Bmp-responsive element.

5 on of the nascent viral mRNA transactivation-responsive element.

6 sus binding motifs bearing similarity to Wnt-responsive element.

7 SUPs are frequently associated with ethylene-responsive elements.

8 nd affect hepcidin transcription through BMP-responsive elements.

9 Tcf-4 on hepatocyte nuclear factor 4 (Hnf-4)-responsive elements.

10 ating its transcription through multiple WT1-responsive elements.

11 m [Ca2+]i alongside activation of Ca2+ /cAMP-responsive elements.

12 under the control of well-characterised BMP responsive elements.

13 the ability to induce transcription via BMP-responsive elements.

14 occupancy at the proximal promoter estrogen-responsive elements.

15 nous promoters containing functional ERalpha responsive elements.

16 ctive enzymes through binding to antioxidant responsive elements.

17 2a but reduced the H3K4me3 level at estrogen-responsive elements.

18 es transcription of antioxidant/electrophile responsive elements.

19 pies mammary-specific and universal cytokine-responsive elements.

20 vered pCREs resembling IDE1 (iron deficiency-responsive element 1), a known grass -Fe response CRE.

21 The CRM, termed GRE1 (Gli responsive element 1), can act as both an enhancer and a

22 itro transcription: A-Site (27 nt), the iron responsive elements (29 nt), a fluoride riboswitch from

23 tion of the promoter or mutation of the cAMP responsive element abolished promoter activity and the b

24 sponse pathway, containing the Abscisic Acid Responsive Element (ABRE) element within their promoters

25 a Triticum aestivum promoter containing ABA responsive elements (ABREs) and a Sorghum bicolor NCED t

26 and TLR4-induced IFN-beta and IFN-stimulated responsive element activation.

27 (5) alternative structures for the HIV-1 Rev responsive element also exist in cells, we discover alte

28 alactosidase gene under the control of a BMP-responsive element and BMP4(betagal/+) mice.

29 Here, we identify a polymorphic p53 responsive element and demonstrate its influence on canc

30 tural elements, including the cis-acting Mta responsive element and expression and nuclear retention

31 The data identify a novel redox-responsive element and indicate extensive redox control

32 t that several ERFs also bind to dehydration-responsive elements and act as a key regulatory hub in p

33 rved sequences in the 3'UTR of NSF as miR-33 responsive elements and show that Nsf is specifically re

34 criptional repressor that also binds to cAMP-responsive elements and thereby down-regulates gluconeog

35 d to function as a nontypeable H. influenzae-responsive element, and the proximal AP-1 motif was foun

36 luciferase construct carrying an antioxidant responsive element (ARE) after down-regulation of caveol

37 ed AR binding with PSA promoter and androgen-responsive element (ARE) luciferase activity.

38 and binding, AR is recruited to the androgen responsive element (ARE) sequences on the DNA where AR i

39 ated in oxidative stress via the antioxidant responsive element (ARE), to which nuclear factor-E2-rel

40 64, 605 AA) is essential for the antioxidant responsive element (ARE)-mediated expression of a group

41 expression via binding to specific promoter responsive elements, as assessed by ChIP and luciferase

42 R172C AuxRE::GUS line with two mutated auxin responsive elements (AuxREs), were assayed for nematode-

43 s [cAMP elevation, ERK phosphorylation, cAMP responsive element binding (CREB) phosphorylation, and n

44 causing both beta-catenin (CTNNB1) and cAMP responsive element binding (CREB) protein levels to decr

45 he C-repeat binding factor (CBF)/dehydration-responsive element binding (DREB1) proteins play a promi

46 proteasome-mediated destabilization of cAMP-responsive element binding 2 (CREB2).

47 endoplasmic reticulum Ca2+ -ATPase, and cAMP-responsive element binding activity.

48 utive expression of the C-REPEAT/DEHYDRATION-RESPONSIVE ELEMENT BINDING FACTOR (CBF) transcriptional

49 ract in yeast two-hybrid assays with the ABA responsive element binding factor AREB2/ABF4, which bind

50 ed protein kinase2, and ABA-INSENSITIVE5/ABA-responsive element binding factor family identified spec

51 ed to the nucleus and functioned as ethylene-responsive element binding factor-associated amphiphilic

52 ed HOMEOBOX family members, and the ethylene-responsive element binding factor-associated amphiphilic

53 C2H2 zinc finger encoding gene with ethylene-responsive element binding factor-associated amphiphilic

54 hylene responsive factor), DREB (dehydration responsive element binding gene), RAV (related to ABI3/V

55 APETALA2/ethylene-responsive element binding protein (AP2/EREBP) transcrip

56 h the glucose-responsive factor Carbohydrate-Responsive Element Binding Protein (ChREBP) and GLP-1 se

57 Carbohydrate responsive element binding protein (ChREBP) is central f

58 idence for increased phosphorylation of cAMP-responsive element binding protein (CREB) and activating

59 Here we show that the activity of the cAMP responsive element binding protein (CREB) family of tran

60 en-activated protein kinase (p38 MAPK), cAMP-responsive element binding protein (CREB), and activatin

61 myocyte enhancer factor 2A (MEF2A) and cAMP-responsive element binding protein (CREB), leading to hi

62 ediated by iron-dependent activation of cAMP-responsive element binding protein (CREB), the transcrip

63 er ATM and of the ATM downstream target cAMP-responsive element binding protein (CREB), which was cri

64 cally, APPSw,Ind mice show changes on a cAMP-responsive element binding protein (CREB)-regulated tran

65 eurin activation and phosphorylation of cAMP responsive element binding protein (CREB).

66 and validated the transcription factor cAMP-responsive element binding protein (Creb1) and its trans

67 found reduced levels of phosphorylated cAMP-responsive element binding protein (pCREB) in the CA1s o

68 PAX7 promoter through association with cAMP responsive element binding protein 1 (CREB)/CREB binding

69 LCRL- and RAMP1-dependent activation of cAMP-responsive element binding protein 1 (CREB1) and SP7 (al

70 n-protein interaction between Mesp1 and cAMP-responsive element binding protein 1 (Creb1) in vitro an

71 response: glucocorticoid receptor (GR), cAMP responsive element binding protein 1 (CREB1), peroxisome

72 nd colleagues (Su et al., 2020) identify RAS-responsive element binding protein 1 (RREB1) as a critic

73 We identify RAS-responsive element binding protein 1 (RREB1), a RAS tran

74 C (jumonji domain containing 1C), RREB1 (Ras responsive element binding protein 1), and SEC24C (SEC24

75 RREB1 (RAS-responsive element binding protein 1), identified as a c

76 alpha) levels through interference with cAMP responsive element binding protein 1-mediated transcript

77 vely regulates leptin transcription via cAMP-responsive element binding protein activation (CREB acti

78 a coactivator 1alpha (PGC1alpha), cyclic AMP-responsive element binding protein binding protein (CBP)

79 d kinase 1/2, ribosomal S6 kinase 1, or cAMP responsive element binding protein DNA-binding activity

80 ion pathways and subsequent increase in cAMP responsive element binding protein DNA-binding activity

81 to WRI1 and belong to the APETALA2-ethylene-responsive element binding protein family of transcripti

82 of plasticity-related proteins such as cAMP-responsive element binding protein phosphorylated at Ser

83 l phosphoprotein 32 kDa [DARPP-32], and cAMP responsive element binding protein signaling [CREB]).

84 ENE RESPONSE FACTOR of the APETALA2/ethylene responsive element binding protein superfamily, as a DEL

85 ing into repressor forms, and activates cAMP-responsive element binding protein that in turn represse

86 CBP (CREB (cAMP responsive element binding protein) binding protein (CRE

87 ssion is the transcription factor CREB (cAMP-responsive element binding protein).

88 Ethylene-responsive element binding protein, a member of the APET

89 acid biosynthetic genes, APETALA2, ethylene-responsive element binding protein, and no apical merist

90 the selected 10 candidates (AIF, cyclic AMP-responsive element binding protein, ephrin type-A recept

91 Cyclic AMP-responsive element binding protein, hepatocyte specific

92 DK deficiency reduced the activation of cAMP-responsive element binding protein-hepatocyte specific a

93 FACTOR transcription factors, rice ETHYLENE-RESPONSIVE ELEMENT BINDING PROTEIN1 (OsEREBP1) and rice

94 tory networks (i.e. ORYZA SATIVA DEHYDRATION-RESPONSIVE ELEMENT BINDING PROTEIN1 and ORYZA SATIVA No

95 directly transcriptionally regulated by ABA-RESPONSIVE ELEMENT BINDING PROTEIN3 (AREB3), BASIC LEUCI

96 The ABA Binding Factor/ABA-Responsive Element Binding Proteins (ABF/AREB) subfamily

97 The cyclic AMP-responsive element binding- and NMDA-regulated microRNA

98 ance tests and glucagon-stimulated HGP, cAMP-responsive element-binding (CREB) phosphorylation, and e

99 E, FAMA, and inducer of C-repeat/dehydration responsive element-binding factor expression1/scream2 th

100 T, dependent on the presence of the ethylene-responsive element-binding factor-associated amphiphilic

101 irectly reduced expression of the cyclic AMP-responsive element-binding protein (CBP), which as part

102 the fasted state, expression of carbohydrate-responsive element-binding protein (ChREBP) and its glyc

103 Carbohydrate-responsive element-binding protein (ChREBP) is a glucose

104 Carbohydrate-responsive element-binding protein (ChREBP) is a regulat

105 The expression of the carbohydrate-responsive element-binding protein (ChREBP) was decrease

106 Here, we hypothesized that carbohydrate-responsive element-binding protein (ChREBP), a transcrip

107 , termed C24-DS1, binding PTH-sensitive cAMP-responsive element-binding protein (CREB) and a cluster

108 ound to both the BRCA1 promoter and the cAMP-responsive element-binding protein (CREB) complex, a reg

109 known as AKT) depended on activation of cAMP-responsive element-binding protein (CREB) for induction

110 on mediated by the transcription factor cAMP-responsive element-binding protein (CREB) is essential f

111 ative receptors, the phosphorylation of cAMP-responsive element-binding protein (CREB) is strongly de

112 ects were accompanied by maintenance of cAMP responsive element-binding protein (CREB) signaling in n

113 bits E2F transcription factor 3 (E2F3), CAMP-responsive element-binding protein (CREB), and brain-der

114 tion of a downstream substrate of PKAc, cAMP-responsive element-binding protein (CREB), is inhibited

115 ns of glucagon via a cAMP-dependent and cAMP-responsive element-binding protein (CREB)-dependent mech

116 cAMP-responsive element-binding protein (CREB)-regulated tran

117 LKB1 inactivation and subsequent cyclic AMP-responsive element-binding protein (CREB)/CREB-regulated

118 ular signal\x{2013}related kinase (ERK)/cAMP-responsive element-binding protein (CREBP) signaling in

119 lly, KPNA4-mediated nuclear transport of Ras-responsive element-binding protein (RREB1), which sustai

120 asts, one with the transcription factor cAMP-responsive element-binding protein 1 (CREB) and another

121 they activate the transcription factor cAMP-responsive element-binding protein 1 (CREB).

122 ne 36 (H3K36) trimethyltransferase, and cAMP-responsive element-binding protein 1 (CREB1).

123 amb can be replaced by its human homolog Ras-responsive element-binding protein 1 (RREB-1).

124 nscriptional factor CREB1 (cyclic AMP [cAMP]-responsive element-binding protein 1) had the strongest

125 directly binds to the W-boxes of DEHYDRATION-RESPONSIVE ELEMENT-BINDING PROTEIN 2 (GhDREB2), which en

126 We have previously identified iron-responsive element-binding protein 2 (IRP2) as an import

127 ibited iron-dependent protein ALAS2 and iron-responsive element-binding protein 2 expression and redu

128 three protein partners, DREB2A (dehydration-responsive element-binding protein 2A), ANAC013, and ANA

129 specifically induced substance (OASIS)/cAMP responsive element-binding protein 3-like 1 (CREB3l1), a

130 Cyclic AMP-responsive element-binding protein 3-like 3, hepatocyte

131 lipogenesis mediated by hepatic cholesterol responsive element-binding protein and featured portal/l

132 es, including the transcription factors cAMP-responsive element-binding protein and forkhead box O.

133 itogen-activated protein kinase and the cAMP-responsive element-binding protein consensus binding sit

134 Here we reported that cyclic AMP-responsive element-binding protein H (CREBH) positively

135 gulated by nuclear transcription factor cAMP-responsive element-binding protein H (CREBH) processing.

136 e, liver-enriched transcription factor, cAMP-responsive element-binding protein hepatic-specific (CRE

137 n DC induces protein kinase A-dependent cAMP-responsive element-binding protein phosphorylation, the

138 aled to be critical for ChREBP (carbohydrate-responsive element-binding protein) or SREBP1c (sterol r

139 used by CREB (cyclic adenosine monophosphate-responsive element-binding protein) shut-off and nuclear

140 lasmic reticulum calcium efflux, and of cAMP-responsive element-binding protein, a key transcription

141 ranscription factor 1 (SREBF1), carbohydrate-responsive element-binding protein, and hepatocyte nucle

142 ntly, phosphorylation of the PKA target cAMP-responsive element-binding protein, at serine 133, is ne

143 ed, stress-sensing transcription factor cAMP-responsive element-binding protein, hepatic-specific (CR

144 cAMP responsive element-binding protein, hepatocyte specific

145 hat MondoA, but not its paralog carbohydrate-responsive element-binding protein, is the predominant g

146 Here we show that the mRNA encoding cAMP responsive element-binding protein-3 like-1 (CREB3L1), a

147 accumulation via inhibition of carbohydrate-responsive element-binding protein-beta, pyruvate kinase

148 through the activation of Creb3l3/cyclic AMP-responsive element-binding protein.

149 cks PI3K/Akt signaling, through the ERK/cAMP-responsive element-binding protein/c-Jun pathway.

150 ion of an ABA signaling master effector, ABA-RESPONSIVE ELEMENT-BINDING PROTEIN1, could activate the

151 irectly bound to the promoter of DEHYDRATION-RESPONSIVE ELEMENT-BINDING PROTEIN2A and enhanced its ex

152 EMT, was sufficient to suppress carbohydrate-responsive-element-binding protein (ChREBP, a master lip

153 UT4 regulates the expression of carbohydrate-responsive-element-binding protein (ChREBP; also known a

154 ver-enriched transcription factor cyclic-AMP-responsive-element-binding protein H (CREBH) but not by

155 ion of cyclic adenosine monophosphate (cAMP) responsive-element-binding protein, a crucial mediator i

156 kinase kinase6 (MAP3K6), MAPK5, dehydration-responsive element bindinG2A (DREB2A), and zinc finger p

157 d seeds of two independent maize DEHYDRATION-RESPONSIVE ELEMENT-BINDING2A mutant (zmdreb2a) lines, wi

158 tream sequence (transcription factor B (TFB)-responsive element (BRE)), which are bound by the transc

159 three or more synergistically acting BLIMP1-responsive elements (BRE) within Rp.

160 B15 directly binds to the secondary wall MYB-responsive element consensus sequence, which encompasses

161 KR receptors were characterized using a cAMP-responsive element (CRE)-driven reporter gene assay.

162 c extracellular cues acting via cAMP/calcium-responsive elements (CREs) in Per genes.

163 s led to inhibition of Bmp-2-stimulated, BMP-responsive element-dependent Col X expression and Smad1

164 diminished ATF5-mediated repression of cAMP-responsive element-dependent gene transcription and abro

165 Promoter analysis revealed several responsive elements detected in the promoter region incl

166 erized cold-inducible C-repeat (CRT)/drought-responsive element (DRE) binding factor CBF1/DREB1b is a

167 hat recognize the C-repeat (CRT)/dehydration-responsive element (DRE) DNA regulatory element present

168 53 transcriptional activity, as shown by p53-responsive element-driven luciferase assay and mRNA leve

169 es) to selectively bind to cell membranes or responsive elements (e.g. ultrasound, magnetism, light)

170 dual isoprenoids did not induce electrophile-responsive element (EpRE)-mediated gene expression.

171 D3 activated an estrogen responsive element (ERE) luciferase reporter through ERa

172 tivity in endometrial cancer cells, estrogen responsive element (ERE)-luciferase in MCF-7 cells, and

173 group 1) strongly activated ERalpha estrogen responsive element (ERE)-mediated responses.

174 omoter derived with multiple tandem estrogen responsive elements (EREs) and a Gal4ff-UAS system for e

175 Mutation of estrogen responsive elements (EREs) identified in the DEFbeta4 ge

176 terodimers binding DNA at specific oestrogen-responsive elements (EREs) to regulate gene transcriptio

177 owed significant heritability in stimulation-responsive elements from distinct cell types, highlighti

178 transcriptional activity driven by androgen responsive elements from the prostate-specific probasin

179 A glucocorticoid responsive element (GRE) was identified in the Klf13 gen

180 Conserved glycerol-responsive elements (GRE), specific to alba-domain inter

181 the binding of MRs and GRs to glucocorticoid-responsive elements (GREs) within hippocampal glucocorti

182 expression by binding to two glucocorticoid-responsive elements (GREs) within the DPP4 promoter.

183 sible nature and high sensitivity of the B12-responsive element has promising biotechnological applic

184 A novel Hog1 responsive element (HoRE) was identified and shown to be

185 F512 motives responsive to hypoxia (hypoxia-responsive element (HRE)) and inflammation (nuclear fact

186 ng region of miR-98 did not reveal a hypoxia-responsive element (HRE)-containing promoter.

187 start site identified six potential hypoxia-responsive elements (HRE).

188 COPIA78/ONSEN retrotransposons contains heat-responsive elements (HREs), which cause their activation

189 We identify a TGF-beta-responsive element (i.e. SMAD) located on an upstream en

190 Foxc1 interacts directly with a Bmp responsive element in an enhancer upstream of Msx2, and

191 onstrate that a nonconserved functional cAMP-responsive element in BDNF promoter IXa in humans render

192 7 transcription by binding to a negative FXR-responsive element in the 5' MMP7 promoter, an event tha

193 (IRP1), a cytosolic Fe-S protein, to an iron-responsive element in the 5' UTR of ferritin heavy polyp

194 NP F inhibited Bmf transcription via hnRNP F-responsive element in the Bmf promoter.

195 s mediated by the recruitment of CREB to its responsive element in the IL-10 promoter.

196 inding to the GCC box and/or the dehydration-responsive element in the promoter of downstream genes.

197 imulated Sirtuin-1 transcription via hnRNP F-responsive element in the Sirtuin-1 promoter.

198 PR-activation (CRISPRa) identifies a CRISPRa-responsive element in the vicinity of risk variant rs112

199 bution but attenuates its ability to bind AR-responsive elements in promoter region of target genes.

200 In zinc-deficient cells, Zap1 binds to zinc responsive elements in target gene promoters and activat

201 There are 2 androgen-responsive elements in the HBV enhancer I that contribut

202 ntanucleotide 5'-CTAAT-3' sequence, the Pdx1 responsive elements in the human iapp promoter all conta

203 Strikingly, while Pdx1 responsive elements in the human insulin promoter confor

204 her with the identification of the cytokinin-responsive elements in the NIN promoter, strongly sugges

205 h putative upstream activating sequence zinc-responsive elements in the PAH1 promoter.

206 ion of transcription factors bound to the RA-responsive elements in the promoters of RA-targeted gene

207 Finally, we identified two BMP-responsive elements in the proximal region of miR-22 pro

208 The deletion of Nrf2-responsive elements in the rat Agt gene promoter abolish

209 rylated Smad1/5 and Smad3, which bind to BMP-responsive elements in vitro and in vivo and mediate TGF

210 rotein-1 promoter contains three antioxidant responsive elements in which Nrf2 directly binds followi

211 clude that balanced input from many cAMP-CRP-responsive elements, including RpoS, is critical to the

212 eletion analysis and mutation of the hypoxia responsive elements individually or in combination resul

213 R-346 overlaps with active sites for an iron-responsive element (IRE) and an interleukin-1 (IL-1) acu

214 itously, the SNCA mRNA has a structured iron-responsive element (IRE) in its 5' untranslated region (

215 .-160A>G mutation was identified in the iron responsive element (IRE) of FTL, causing ferritin synthe

216 ctively towards the uniquely configured iron-responsive element (IRE) RNA stem loop in the 5' untrans

217 In one mode of operation, IRP1 binds iron-responsive element (IRE) stem-loops in messenger RNAs en

218 The presence of an iron-responsive element (IRE) within the 5' untranslated regi

219 (IRPs) 1 and 2 that bind cis-regulatory iron-responsive elements (IRE) on target messenger RNAs (mRNA

220 ession of iron-related genes by binding iron-responsive elements (IREs) of target mRNAs.

221 -1, decreased ferritin-H, and increased iron-responsive element-iron regulatory protein interaction a

222 ression of MTSS1 by binding to a p63-binding responsive element localized in the MTSS1 locus.

223 ly activates the CXCR4 gene via binding to a responsive element located in positions -1376 to -1372 i

224 -130b expression by binding directly to p63-responsive elements located in close proximity to the ge

225 Deletion of three 20E responsive elements located in the let-7-C locus results

226 minal loops of let-7 pre-miRNAs and to Lin28-responsive elements (LREs) in mRNAs are not well defined

227 as a novel Nrf2 activator using antioxidant responsive element luciferase assay in MDA-MB-231 cells.

228 and RNA polymerase II recruitment to the LXR responsive element (LXRE) of SREBP-1c, but not to the LX

229 The YY1 responsive element mapped not to YY1 DNA-binding sites i

230 Compared with the 5 flavone-responsive elements mapped out previously, there are fou

231 rrelation between the ICI-dependent estrogen-responsive element-mediated transcription activity of AF

232 ecently linked the transcription factor cAMP responsive element modulator (CREM) alpha, which is expr

233 of the IFNbeta-induced IL-2 repressor, cAMP-responsive element modulator (CREM) is reduced.

234 ption factor, cyclic adenosine monophosphate-responsive element modulator alpha (CREMalpha) can endor

235 ased expression of transcription factor cAMP-responsive element modulator alpha (CREMalpha), which ha

236 monstrate that the transcription factor cAMP-responsive element modulator alpha (CREMalpha), which is

237 Previous data from our group identified cAMP-responsive element modulator alpha (CREMalpha), which is

238 e atrial remodeling in CREM-IbDeltaC-X (cAMP responsive element modulator isoform IbDeltaC-X) transge

239 explain the sterol profile of testis in cAMP responsive element modulator tau (Crem tau) knockout mic

240 cAMP signaling through CREM (cAMP-responsive element modulator) and its variant ICER (indu

241 cts with PAN RNA via a region termed the Mta responsive element (MRE), stabilizing the transcript and

242 n is its ability to bind to negative calcium responsive elements (nCaRE) of some gene promoters.

243 ch the cyclic binding of Notch1 to the Notch-responsive elements (NREs) on the Rheb promoter is a key

244 In addition, we identify a B12-responsive element of Chlamydomonas reinhardtii METE usi

245 -1 reactivation to an AP-1 motif in the CD28-responsive element of the HIV-1 long terminal repeat (LT

246 The minimal, ERK-responsive element of the SOCS-3 promoter was localized

247 s of CSCs that misappropriate functional and responsive elements of archetypical self-renewal pathway

248 of the luciferase assay identified the core responsive elements of RelA/p65 to be -896/-887 and -424

249 tone H3 lysine 79 (H3K79) methylation at Myc-responsive elements of target gene promoters is a strict

250 experiments identified ICER binding to cAMP-responsive elements of the Per1 promoter.

251 We identified an FXR-responsive element on the Tgr5 gene promoter.

252 uclear translocation and binding to putative responsive elements on IL-10 promoter.

253 cription factors that bind to the cyclic AMP-responsive elements on the Mkp-1 promoter.

254 cRNA-SARCC expression via binding to hypoxia-responsive elements on the promoter of LncRNA-SARCC.

255 riptional regulator of mRNAs containing iron responsive elements, or as a [4Fe-4S] cluster-containing

256 omoter of COX4I2 that functions as an oxygen responsive element (ORE), maximally active at a 4% oxyge

257 Tcf-4/beta-catenin binds Wnt-responsive elements preferentially around beta-catenin-i

258 r augmented by AS by binding to a set of p53 responsive elements (PREs) on the NFATc2 promoter.

259 ssion by a direct binding to 2 canonical PUM responsive elements present in the FOXP1-3' untranslated

260 binding of iron regulatory proteins to iron-responsive elements present in the UTRs of transferrin r

261 into iron regulatory protein-1 to bind iron-responsive elements present in UTRs of transferrin recep

262 lted in enhanced IFN-beta and IFN-stimulated responsive element promoter activity, whereas silencing

263 a CBFs binding to the C-repeat motif/drought-responsive element promoter motif requires all three Med

264 have remained elusive due to the lack of RA responsive element (RARE) in the 5 half of the HoxB clus

265 eletion analysis characterizes a putative RA-responsive element (RARE) primarily located in the 5'-fl

266 RA and androgen responsive elements (RARE and ARE) were mapped to the hT

267 FBXL5 to physically dislodge IRP2 from iron-responsive element RNA to facilitate its turnover.

268 lpha or RORgamma expression vector and a ROR-responsive element (RORE)-LUC reporter, and a mammalian

269 ancreatic cancer and is dependent on the Ras responsive element (RRE) binding protein (RREB1), which

270 ions of RTA, direct interactions with an RTA-responsive element (RRE) could complement the loss of on

271 goes FRET when binding its corresponding Rev Responsive Element (RRE) RNA aptamer.

272 As opposed to HIV's Rev-responsive element (RRE), the Rex-responsive element (Rx

273 HIV's Rev-responsive element (RRE), the Rex-responsive element (RxRE) is present in all viral mRNAs

274 R mammalian-2-hybrid (M2H) system and in RXR-responsive element (RXRE)-mediated transcriptional exper

275 6a was delineated, and one putative androgen-responsive element site was identified within its promot

276 g transcription factor 2 (ATF-2) to the cAMP-responsive element site was methylation dependent.

277 ed CpG 2), which is juxtaposed to a key cAMP-responsive element site, was significantly demethylated

278 ein (Tat) binds the HIV mRNA transactivation responsive element (TAR), regulating transcription and r

279 ated MICA promoter via its binding to an IE2-responsive element that we identified within the promote

280 13c and Rv1812c may represent general stress-responsive elements that are necessary for aspects of M.

281 t include layer-selective switchable stimuli-responsive elements that control the hydrogel stiffness

282 g assays, we have mapped the functional PPAR-responsive element to a proximal region from -135 to -12

283 sis of the PKCdelta promoter mapped the NaBu-responsive element to an 81-bp minimal promoter region.

284 However, whether the HR provides a responsive element to environmental (i.e., physiologic)

285 f brain-expressed genes, candidate vitamin D responsive elements (VDREs) at -7/-10 kb in human trypto

286 nic cells (C3H10T1/2) transfected with a BMP-responsive element, we sought to determine whether pitui

287 Seven xanthotoxin-responsive elements were localized by analyzing promoter

288 -1 further identified an abscisic acid (ABA)-responsive element, which binds ABA-responsive transcrip

289 IDOL, distinct from that containing the LXR-responsive element, which mediates the response to DUB i

290 nition via specific interactions of the iron-responsive element with a Zn(2+)-containing WRKY-GCM1 do

291 ed of a fusogenic liposome encapsulating ATP-responsive elements with chemotherapeutics and a liposom

292 We identified several CRISPRa-responsive elements with chromatin features of stimulus-

293 ein 1 (LMP1), which is regulated by an EBNA2-responsive element within its ED-L1 promoter.

294 We further report that a functional PPAR-responsive element within the 1.5-kb proximal Gasp-1 pro

295 demonstrate the presence of one p63-specific responsive element within the 15th intronic region of th

296 o a newly identified putative glucocorticoid responsive element within the aromatase promoter II.

297 strated by an evolutionarily conserved Notch-responsive element within the MLCK promoter that binds t

298 We looked for the Hog1-responsive element within the promoter of the most highl

299 ithin rs4972593 and predicted eight estrogen-responsive elements within 5 kb of this locus.

300 on a single cis element in the DNA, the Wnt-responsive element (WRE), at times potentiated by a near