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

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

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

5 in a manner that requires a functional STAT3-responsive element.

6 the promoter through this unconventional Tax-responsive element.

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

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

9 nd affect hepcidin transcription through BMP-responsive elements.

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

11 ating its transcription through multiple WT1-responsive elements.

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

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

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

15 occupancy at the proximal promoter estrogen-responsive elements.

16 ctive enzymes through binding to antioxidant responsive elements.

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

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

19 SUPs are frequently associated with ethylene-responsive elements.

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

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

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

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

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

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

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

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

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

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

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

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

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

33 nd mouse Parkin genes contain functional p53 responsive elements, and p53 increases the transcription

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

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

36 throid 2-related factor 2 (Nrf2)-antioxidant responsive element (ARE) pathway by oxidative stress pro

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

38 64, 605 AA) is essential for the antioxidant responsive element (ARE)-mediated expression of a group

39 This repression is mediated by androgen-responsive elements (ARE) and dictated by Polycomb group

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 Ras-responsive element binding protein 1 (Rreb-1) was identi

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

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

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

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

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

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

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

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

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

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

79 ent binding protein-1c, and the carbohydrate responsive element binding protein that govern the expre

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

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

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

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

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

85 Cyclic AMP-responsive element binding protein, hepatocyte specific

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

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

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

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

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

91 behavior are abolished in mice lacking cAMP responsive-element binding (CREB)-1 in the forebrain.

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

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

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

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

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

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

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

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

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

101 red this in mice overexpressing carbohydrate responsive element-binding protein (ChREBP).

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

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

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

105 se, and cyclic adenosine 3',5'-monophosphate-responsive element-binding protein (CREB) phosphorylatio

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

107 depends upon the binding of NF-kappaB, cAMP responsive element-binding protein (CREB), and CBP/p300

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

109 kinase C (PKC)-dependent activation of cAMP-responsive element-binding protein (CREB)-1/ATF-1-like f

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

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

112 he control of the transcription factor, cAMP-responsive element-binding protein (CREB).

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

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

115 Furthermore, despite an intact sterol responsive element-binding protein (SREBP) pathway, Idol

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

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

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

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

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

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

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

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

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

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

126 ort that the transcription factor cyclic AMP-responsive element-binding protein H (CREB-H, encoded by

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

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

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

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

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

132 als in the osteoblasts to inhibit CREB (cAMP-responsive element-binding protein) phosphorylation and

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

134 vated protein kinase phosphorylation of cAMP-responsive element-binding protein, and increased cyclin

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

136 cAMP responsive element-binding protein, hepatocyte specific

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

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

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

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

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

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

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

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

145 PURPOSE OF REVIEW: Cyclic-AMP-responsive-element-binding protein H (CREB-H) is a trans

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

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

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

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

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

151 /AP-1-binding sequences are prototypical RAS-responsive elements, but oncogenic ETS proteins activate

152 on of vIL-6 RNA contains an MRE (MTA [ORF57]-responsive element) composed of two motifs, MRE-A and MR

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

154 genes, expression of which is controlled by responsive elements containing overlapping binding sites

155 We first demonstrated that the cAMP-responsive element (CRE) site in the eotaxin-3 promoter

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

157 ce that CREMalpha physically binds to a cAMP-responsive element, CRE (-111/-104), within the proximal

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

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

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

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

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

163 53 transcriptional activity, as shown by p53-responsive element-driven luciferase assay and mRNA leve

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

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

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

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

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

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

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

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

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

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

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

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

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

177 transactivate IGFBP3 through a novel hypoxia responsive element (HRE) located at 57 kb upstream from

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

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

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

181 Since the ANK promoter contains 2 hypoxia-responsive elements (HREs), we performed site-directed m

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

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

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

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

186 the ATBF1 promoter, and that a half-estrogen-responsive element in the ATBF1 promoter was essential f

187 CD24 expression through a functional hypoxia responsive element in the CD24 promoter.

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

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

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

191 The JMY gene contains HIF-responsive elements in its promoter region and HIF-1alph

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

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

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

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

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

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

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

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

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

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

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

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

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

205 We find LXR-responsive element inside of the promoter region of the

206 .-160A>G mutation was identified in the iron responsive element (IRE) of FTL, causing ferritin synthe

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

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

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

210 synthesis rates of proteins encoded in iron-responsive element (IRE)-mRNAs; metabolic iron ("free,"

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

212 served DNA sequences, 5'-CAAAACA-3' (insulin responsive element, IRE), in rat, mouse and human SCN5a

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

214 -1, decreased ferritin-H, and increased iron-responsive element-iron regulatory protein interaction a

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

216 moter activity via direct binding to the TR4-responsive element located at -243 to -255 on the promot

217 ranscription through homeobox sites in a Wnt-responsive element located between -0.65 to -0.55 Kb of

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

219 -130b expression by binding directly to p63-responsive elements located in close proximity to the ge

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

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

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

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

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

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

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

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

228 Transcription factor cAMP-responsive element modulator (CREM)alpha displays increa

229 of the transcription regulatory factor cAMP-responsive element modulator (CREM)alpha in SLE T lympho

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

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

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

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

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

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

236 effect of the transcriptional repressor cAMP responsive element modulator-alpha on the IL2 promoter.

237 sed assays, we have identified a minimal Mkx-responsive element (MRE) located within the Mkx promoter

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

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

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

241 -1 reactivation to an AP-1 motif in the CD28-responsive element of the HIV-1 long terminal repeat (LT

242 of nuclear proteins that bind to the STAT-3-responsive element of the Hsp70 promoter.

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

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

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

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

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

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

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

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

251 alpha proteins to the two functional hypoxia-responsive elements on the native HSulf-1 promoter.

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

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

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

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

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

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

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

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

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

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

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

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

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

265 By transfecting the cells with a metal-responsive element reporter construct the increase in Cu

266 evident that interaction of HIF with hypoxia-responsive elements resulted in suppression of basal pro

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

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

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

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

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

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

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

274 6a was delineated, and one putative androgen-responsive element site was identified within its promot

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

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

277 of the hrg-1 promoter revealed a 23-bp heme-responsive element that is both necessary and sufficient

278 eat-1 (5'-AGGTCAcAGACCT-3'), as a likely FXR-responsive element that is involved in miR-29a regulatio

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