ライフサイエンスコーパス: AU-rich element

1 tein that destabilizes mRNA by binding to an AU-rich element.

2 smic polyadenylation element and an upstream AU-rich element.

3 and binding was dependent on the 11 residue AU-rich element.

4 tent was present immediately upstream of the AU-rich element.

5 or the rapid degradation of mRNAs containing AU-rich elements.

6 lear localization of mRNA species containing AU-rich elements.

7 RNA is unique in having five IREs, linked by AU-rich elements.

8 1-811 of the 3'UTR, which lack any classical AU-rich elements.

9 ors were required for RNA destabilization by AU-rich elements.

10 nes, many of which are controlled through 3' AU-rich elements.

11 nse mRNAs by recruiting the VHS RNase to the AU-rich elements.

12 three RNP-type concensus motifs and bind to AU-rich elements.

13 r P bodies by host proteins that bind to the AU-rich elements.

14 es and cleaves the mRNAs in proximity to the AU-rich elements.

15 characterized this interaction via conserved AU-rich elements.

16 ding of nucleolin to the instability element AU-rich element 1 of bcl-2 mRNA in a cell-free system an

17 Binding of a bcl-2 mRNA instability element (AU-rich element-1) to nucleolin in S100 extracts from AT

18 cript with a large 3' UTR containing several AU rich elements and poly(U) regions that may regulate m

19 like proteins can bind simultaneously to the AU-rich element and to the poly(A) tail.

20 These results indicate that AU-rich elements and associated proteins can play a role

21 at tristetraprolin recruits VHS RNase to the AU-rich elements and enables the degradation of the stre

22 maintain the expression of genes enriched in AU-rich elements and U-rich elements in the 3'-UTR.

23 in cDNA reporter construct revealed that the AU-rich elements and, in particular the nonameric UUAUUU

24 Of the clones identified, 74% contained AU-rich elements and/or poly-uridine tracts in their 3'

25 The host proteins that bind to the AU-rich elements are either resident in cells (e.g., TIA

26 ver, during stress induced by ATP depletion, AU-rich elements are necessary to maintain stability of

27 An AU rich element (ARE) in the 3' noncoding region promote

28 on at the 5' end of the 136-nucleotide bcl-2 AU-rich element (ARE(bcl-2)).

29 An AU-rich element (ARE) and its cognate RNA-binding protei

30 ied two components of this complex to be the AU-rich element (ARE) binding proteins AUF1 and HuR.

31 matory gene expression can be mediated by an AU-rich element (ARE) cluster present in the 3' untransl

32 An AU-rich element (ARE) consisting of repeated canonical A

33 ein complex, required for the degradation of AU-rich element (ARE) containing messenger RNAs (mRNAs).

34 or previous reports of zinc stabilization of AU-rich element (ARE) containing messenger RNAs.

35 at the level of mRNA decay is mediated by an AU-rich element (ARE) found in the 3'-untranslated regio

36 IEX-1 contains an AU-rich element (ARE) in its 3'-untranslated domains kno

37 egradation of cytokine mRNAs, mediated by an AU-rich element (ARE) in the 3' noncoding region and by

38 ression in monocytes and macrophages, and an AU-rich element (ARE) in the 3' untranslated region (UTR

39 nd TIAR are related proteins that bind to an AU-rich element (ARE) in the 3' untranslated region of t

40 alysis revealed the existence of a conserved AU-rich element (ARE) in the 3'-untranslated region (UTR

41 ciency of TNF transcript are regulated by an AU-rich element (ARE) in the 3'-UTR of messenger RNA.

42 We found a conserved AU-rich element (ARE) in the human LARP4 mRNA 3' untrans

43 alpha mRNA, and TTP can bind directly to the AU-rich element (ARE) in TNF-alpha mRNA.

44 Among previously identified patterns, the AU-Rich Element (ARE) is found here to occur within the

45 ediated through 3' untranslated region (UTR) AU-rich element (ARE) motifs.

46 example, previous evidence suggests that the AU-rich element (ARE) present in the 3'-UTR of murine tu

47 TTP, and TTP enhances decapping of a target AU-rich element (ARE) RNA in vitro.

48 bcl-2 mRNA contains an AU-rich element (ARE) that functions in regulating bcl-2

49 Reiterations of the AU-rich element (ARE) within the 3'-untranslated region

50 nscriptional regulation mediated through the AU-rich element (ARE) within the COX-2 mRNA 3'-untransla

51 AUF1 is an AU-rich element (ARE)-binding protein that recruits tran

52 proteins such as TIA-1, TIAR and HuR bind to AU-rich element (ARE)-containing mRNAs and control their

53 The destabilization of AU-rich element (ARE)-containing mRNAs mediated by prote

54 We evaluated the expression of over 900 AU-rich element (ARE)-containing transcripts in primary

55 CX(3)H tandem zinc finger protein that binds AU-rich element (ARE)-containing transcripts to enhance

56 We found that this polymorphism influenced AU-rich element (ARE)-mediated decay (AMD) of IFNL3 mRNA

57 ate functions of human mRNA decay enzymes in AU-rich element (ARE)-mediated mRNA decay (AMD) and find

58 and requiring the presence of the TNF-alpha AU-rich element (ARE).

59 tein that destabilizes mRNA by binding to an AU-rich element (ARE).

60 HAMP 3'-UTR harbors a single AU-rich element (ARE).

61 that CSF-1 3' untranslated region containing AU-rich elements (ARE) could regulate CSF-1 posttranscri

62 tion of TNF-alpha mRNA expression identified AU-rich elements (ARE) in the 3' untranslated region as

63 f the mRNAs detected in human saliva contain AU-rich elements (ARE) in their 3' untranslated regions

64 timulating factor mRNAs after binding to the AU-rich elements (ARE) in their 3'-untranslated regions.

65 nger RNA (mRNA) stability and translation by AU-rich elements (ARE) located in its 3' untranslated re

66 We found that the AU-rich elements (ARE) of Xenopus c-myc II and the human

67 Here, we demonstrate that cis-acting AU-rich elements (ARE) present within a 38-base pair reg

68 The 3' UTR region of mda-7 contains AU-rich elements (ARE) that contribute to rapid mda-7 mR

69 eins that can bind to transcripts containing AU-rich elements (ARE), resulting in deadenylation and d

70 Defects in AU-rich elements (ARE)-mediated posttranscriptional cont

71 lity mediated by the 3' untranslated region, AU-rich elements (ARE).

72 AU-rich-element (ARE)-mediated mRNA regulation occurs in

73 uences the stability of key mRNAs containing AU rich elements (AREs) known to be associated with glau

74 variant resembled the mRNA-destabilizing AT(AU)-rich elements (AREs) and resulted in a 10-fold diffe

75 Hsp27 and stabilization of mRNAs containing AU-rich elements (AREs) (ARE-mRNAs).

76 t-transcriptional regulatory motifs, such as AU-rich elements (AREs) and C-rich tracts.

77 is-acting regulatory elements, which include AU-rich elements (AREs) and microRNA (miRNA) targeting s

78 AU-rich elements (AREs) and microRNA target sites are co

79 AU-rich elements (AREs) are cis-acting regulatory region

80 In mammalian cells, mRNAs with AU-rich elements (AREs) are targeted for translational s

81 -untranslated region (UTR) that contains six AU-rich elements (AREs) as well as several uridine-rich

82 trigger the degradation of mRNAs containing AU-rich elements (AREs) at the 3' untranslated regions.

83 8 complex, disassembles mRNPs containing the AU-rich elements (AREs) bound by HuR proteins in a nonde

84 The AU-rich elements (AREs) encoded within many mRNA 3' untr

85 Tristetraprolin (TTP) binds AU-rich elements (AREs) encoded within selected labile m

86 AU-rich elements (AREs) found in the 3' untranslated reg

87 a AU-binding proteins (AUBPs) that recognize AU-rich elements (AREs) found within many transcripts.

88 AU-rich elements (AREs) identified in the 3' untranslate

89 CXCL-8 expression involves AU-rich elements (AREs) in 3' untranslated regions that

90 AU-rich elements (AREs) in 3'-untranslated regions of mR

91 m CCCH zinc finger proteins that can bind to AU-rich elements (AREs) in cellular mRNAs and destabiliz

92 Its mRNA contains three AU-rich elements (AREs) in its 3' untranslated region (3

93 oteins can bind directly to certain types of AU-rich elements (AREs) in mRNA.

94 The widespread occurrence of AU-rich elements (AREs) in mRNAs encoding proteins with

95 dem zinc finger proteins can bind to certain AU-rich elements (AREs) in mRNAs, leading to their deade

96 d that RNPC1 and HuR, both of which can bind AU-rich elements (AREs) in p21 3'-UTR, preferentially bi

97 Stress response RNAs containing AU-rich elements (AREs) in the 3' untranslated region (3

98 AU-rich elements (AREs) in the 3' untranslated region (U

99 Essential signals for this control are AU-rich elements (AREs) in the 3' untranslated region (U

100 ol of cytoplasmic mRNA stability mediated by AU-rich elements (AREs) in the 3' untranslated region of

101 Inherently unstable mRNAs contain AU-rich elements (AREs) in the 3' untranslated regions.

102 AU-rich elements (AREs) in the 3'-untranslated region (U

103 Hu proteins have been shown to bind to AU-rich elements (AREs) in the 3'-untranslated region of

104 rase reporter assay, we demonstrate that the AU-rich elements (AREs) in the 3'-untranslated region of

105 ment RNA-binding protein 1 (AUF1) binding to AU-rich elements (AREs) in the 3'-untranslated regions o

106 AU-rich elements (AREs) in the 3'-UTR of unstable transc

107 s are normally unstable because they contain AU-rich elements (AREs) in their 3' noncoding regions th

108 Inherently unstable mRNAs contain AU-rich elements (AREs) in their 3' untranslated regions

109 of a subset of short-lived mRNAs containing AU-rich elements (AREs) in their 3' untranslated regions

110 level of mRNA turnover contain destabilizing AU-rich elements (AREs) in their 3' untranslated regions

111 destabilize target mRNAs by first binding to AU-rich elements (AREs) in their 3'-untranslated regions

112 Second, Olfr mRNAs have a higher density of AU-rich elements (AREs) in their 3'UTR and upstream open

113 In mammals, rapid mRNA turnover directed by AU-rich elements (AREs) is mediated by selective associa

114 AU-rich elements (AREs) located in the 3' untranslated r

115 en reported to be altered by the presence of AU-rich elements (AREs) located in the 3'-untranslated r

116 s are targeted for rapid degradation through AU-rich elements (AREs) located in their 3' untranslated

117 tem that recapitulates the in vivo effect of AU-rich elements (AREs) on mRNA deadenylation has been d

118 AU-rich elements (AREs) present in the 3' untranslated r

119 slated region of the TNF transcript contains AU-rich elements (AREs) that are targeted by the RNA-bin

120 onferred by 3' untranslated region-localized AU-rich elements (AREs) that associate with RNA-binding

121 The 3'UTR also contains AU-rich elements (AREs) that mediate rapid IL-2 mRNA deg

122 , Hsp70 also binds U-rich RNA including some AU-rich elements (AREs) that regulate the decay kinetics

123 taining the AUUUA pentamer characteristic of AU-rich elements (AREs) that regulate the stability of m

124 selective, and we identified RNAs containing AU-rich elements (AREs) that were upregulated after infe

125 thway in gene regulation subjects mRNAs with AU-rich elements (AREs) to rapid decay by a poorly under

126 n the Spisula 3' UTRs we identified multiple AU-rich elements (AREs) which may control translation ac

127 karyotic mRNA stability can be influenced by AU-rich elements (AREs) within mRNA primary sequences.

128 H2 genes, which encode proteins that bind to AU-rich elements (AREs) within the 3' untranslated regio

129 A levels are regulated by proteins that bind AU-rich elements (AREs) within the 3' UTR region of Pth

130 Such regulation depends on AU-rich elements (AREs) within the 3'-untranslated regio

131 ates mRNA turnover after binding to class II AU-rich elements (AREs) within the 3'-untranslated regio

132 Inherently unstable mammalian mRNAs contain AU-rich elements (AREs) within their 3' untranslated reg

133 sized in bacterial systems to many different AU-rich elements (AREs), in vivo studies have pointed to

134 AU-rich elements (AREs), located in the 3'-untranslated

135 P D discriminates among the three classes of AU-rich elements (AREs), most effectively blocking rapid

136 AU-rich elements (AREs), present in mRNA 3'-UTRs, are po

137 tabilization of short-lived mRNAs containing AU-rich elements (AREs), serves as an adapter for c-fos

138 s partner, p54(nrb), binds RNAs that contain AU-rich elements (AREs), such as those for proinflammato

139 Because the GILZ 3'-UTR contains AU-rich elements (AREs), we analyzed the role of the mRN

140 AU-rich elements (AREs), which act as regulators of mRNA

141 on (UTR) of NSPB1 mRNA also contains several AU-rich elements (AREs), which are associated with rapid

142 ed a statistically significant enrichment in AU-rich elements (AREs).

143 y that binds and stabilizes mRNAs containing AU-rich elements (AREs).

144 ing the 3' UTR of COX-2, a region containing AU-rich elements (AREs).

145 urnover of certain mRNAs containing class II AU-rich elements (AREs).

146 AU-rich elements (AREs, usually containing repeated copi

147 Human TZF binds AU-rich elements at the 3' untranslated region and recru

148 Deletion analyses indicated that an AU-rich element (AURE) located between 553 to 625 within

149 d that nucleolin specifically recognized the AU-rich elements (AUUUA) in the 3'-UTR of the Bcl-X(L) m

150 Tristetraprolin (TTP) is an AU-rich element binding protein that regulates the stabi

151 ing protein interacting protein; hnRNP D, an AU-rich element binding protein; and NSAP1, an hnRNP R-l

152 nts, described here, revealed that the known AU-rich element binding proteins, ElrA and ElrB, and TIA

153 to and destabilize certain mRNAs containing AU-rich element binding sites.

154 n PD-L1 mRNA stability via modulation of the AU-rich element-binding protein tristetraprolin (TTP).

155 ically, Pin1 mediated the association of the AU-rich element-binding protein, AUF1, with GM-CSF mRNA,

156 rs could bind to certain isoforms of another AU-rich element-binding protein, HNRNPD/AUF1, as well as

157 AU-rich element-binding proteins (ARE-BP) regulate the s

158 AU-rich element-binding proteins (ARE-BPs) offer post-tr

159 Pin1 regulated the association of the AU-rich element-binding proteins AUF1 and hnRNP C with G

160 TIA-1 and TTP are AU-rich element-binding proteins that prevent the pathol

161 HuR and inactivation of tristetraprolin, two AU-rich element-binding proteins.

162 l line-specific instability does not involve AU-rich elements, but is mediated by several novel eleme

163 quent cleavage near the adenylate-uridylate (AU)-rich elements; (c) it does not effectively degrade v

164 lly disrupt the Nup475-tumor necrosis factor AU-rich element complex.

165 EX1 augments the stability and expression of AU-rich element containing mRNAs typically found within

166 ng proteins and miRNAs and how they regulate AU-rich elements containing cytokine mRNA stability/degr

167 mulation, and protein secretion, but not non-AU-rich elements containing cytokine mRNAs, including TG

168 colon cancer, we examined the ability of the AU-rich element-containing (ARE-containing) 3' untransla

169 We propose that HuR first may bind AU-rich element-containing mRNAs in the nucleus and then

170 intermediates generated from the turnover of AU-rich element-containing substrate RNAs.

171 HuA may transiently stabilize a subset of AU-rich element-containing transcripts following T lymph

172 aprolin (TTP), can decrease the stability of AU-rich element-containing transcripts in cell transfect

173 known as KHSRP) interacts with single-strand AU-rich-element-containing mRNAs and is a key mediator o

174 ing factor shown to be capable of regulating AU-rich element-dependent mRNA turnover at the level of

175 ing factor shown to be capable of regulating AU-rich element-dependent mRNA turnover at the level of

176 HuR specifically bound to RNAs containing an AU-rich element derived from the TNF-alpha mRNA in the i

177 AU-rich elements found in the 3'-untranslated regions of

178 containing a strongly destabilizing class II AU-rich element from the GM-CSF mRNA 3'-untranslated reg

179 Interaction of HuR with AU-rich elements, however, was not associated with RNA d

180 In the case of the c-fos AU-rich element, HuD binds to a 27-nucleotide core eleme

181 In the case of the c-fos AU-rich element, HuR binds to a core element of 27 nucle

182 fied recombinant protein binds avidly to the AU-rich element in c-fos and interleukin-3 mRNAs.

183 TTP-directed decay of an mRNA containing an AU-rich element in its 3'-untranslated region.

184 RIG-N stabilized CXCL-8 mRNA via the AU-rich element in the 3' untranslated region of CXCL-8

185 lity shift assays identified a single 125-bp AU-rich element in the 3' untranslated region that forme

186 sults suggest that TTP binds to a functional AU-rich element in the 3'-untranslated region of IFN-gam

187 stimulating factor mRNAs after binding to an AU-rich element in their 3'-untranslated regions.

188 TTP can bind directly to the AU-rich element in TNF-alpha mRNA, increasing its labili

189 The RNA-binding protein AUF1 binds AU-rich elements in 3'-untranslated regions to regulate

190 bility of V-ATPase mRNA is regulated through AU-rich elements in 3'-untranslated regions.

191 of CCCH tandem zinc finger proteins bind to AU-rich elements in certain cellular mRNAs, leading to t

192 Tristetraprolin (TTP) acts by binding to AU-rich elements in certain mRNAs, such as tumor necrosi

193 is an RNA-binding protein that recognizes U/AU-rich elements in diverse RNAs through two RNA-recogni

194 s a mRNA-destabilizing protein that binds to AU-rich elements in labile transcripts, such as the mRNA

195 tandem zinc finger proteins that can bind to AU-rich elements in mRNAs and promote their decay.

196 em zinc finger proteins can bind directly to AU-rich elements in mRNAs and promote transcript deadeny

197 m them showed that TTP could bind to certain AU-rich elements in mRNAs, leading to increases in the r

198 These proteins bind to AU-rich elements in target mRNAs, and promote their dead

199 of mRNA turnover after initially binding to AU-rich elements in target mRNAs.

200 e expression of cytokines through binding to AU-rich elements in the 3' untranslated region and promo

201 tigen R (HuR) and tristetraprolin (TTP) bind AU-rich elements in the 3' untranslated region of many c

202 A-binding proteins (RBPs) that interact with AU-rich elements in the 3' untranslated region of mRNA,

203 conserved in plants and mammals, to specific AU-rich elements in the 3' untranslated region of mRNAs

204 BPs interacted with evolutionarily conserved AU-rich elements in the 3' untranslated region of Notch1

205 er RNAs (mRNAs) are rapidly degraded through AU-rich elements in the 3' untranslated region.

206 Hu proteins can bind to AU-rich elements in the 3' untranslated regions of unsta

207 egatively regulates PD-L1 expression through AU-rich elements in the 3' UTR of PD-L1 mRNA.

208 y of tandem CCCH finger proteins can bind to AU-rich elements in the 3'-untranslated region of mRNAs,

209 P) plays a central role in PTR by binding to AU-rich elements in the 3'-untranslated region of proinf

210 These proteins bind to AU-rich elements in the 3'-untranslated regions (3'-UTRs

211 first and second RNA binding domains bind to AU-rich elements in the 3'-UTR of mRNA.

212 are unstable (or untranslatable) because of AU-rich elements in the 3'untranslated region.

213 up-regulated by the presence of a variety of AU-rich elements in the body of substrate RNAs.

214 tion mechanism relies on KSRP recognition of AU-rich elements in the mRNA 3'UTR, that is mediated by

215 TTP targets AU-rich elements in the NLRP3 3'-untranslated region (UT

216 ponse mRNAs characterized by the presence of AU-rich elements in their 3' untranslated regions (UTRs)

217 n that can stabilize labile mRNAs containing AU-rich elements in their 3' untranslated regions and ha

218 scripts of mRNA expressed early had abundant AU-rich elements in their 3' untranslated regions, where

219 the stability of target mRNAs by binding to AU-rich elements in their 3' untranslated regions.

220 ponse mRNAs characterized by the presence of AU-rich elements in their 3' UTRs.

221 ger proteins, which bind to mRNAs containing AU-rich elements in their 3'-untranslated region and tar

222 and other mRNAs through the interaction with AU-rich elements in their 3'-untranslated regions.

223 el system for studies of zinc finger protein/AU-rich element interactions that result in mRNA decay.

224 Regulation of messenger RNA stability by AU-rich elements is an important means of regulating gen

225 that the Hro-notch 3' UTR, containing seven AU-rich elements, is key to regulating transcript stabil

226 As are deadenylated and cleaved close to the AU-rich elements, leading to long-term persistence of no

227 invasion, and metastasis by stabilizing the AU-rich element located at the 3'-untranslated region (U

228 e cleavage sites are centered at or near the AU-rich elements located at the 3' untranslated region o

229 stitutions have been introduced into the two AU-rich elements located between 50 and 66 nucleotides u

230 and AUF1 associate with labile mRNAs bearing AU-rich elements located in the 3' untranslated regions

231 acts with high specificity with at least two AU-rich elements located within the 3'-untranslated regi

232 These miRNAs, along with AU-rich-element-mediated decay, suppress IFNL2 and IFNL3

233 cripts that relieves intrinsic microRNA- and AU-rich-element-mediated repression has been observed to

234 A substrate in which the AU-rich element motifs were mutated exhibited minimal de

235 revealed a highly significant enrichment of AU-rich element motifs, with AUUUA pentamers present in

236 AU-rich element mRNA-binding proteins (AUBPs) are key re

237 dependent manner and identify three distinct AU-rich elements necessary to mediate this effect.

238 When this 217-nucleotide nutrient sensor AU-rich element (NS-ARE) is present in a chimeric mRNA i

239 Given that AU-rich elements occur in the 3' UTR of Notch-class gene

240 the 3' stem-loop structure and a downstream AU-rich element of petD pre-mRNA and that its binding af

241 reporter gene activity was dependent on the AU-rich element of the COX-2 3'-untranslated region.

242 red to result from direct TTP binding to the AU-rich element of the TNF-alpha messenger RNA.

243 he stability of target mRNAs via binding the AU-rich elements of the 3' untranslated region (3'UTR) o

244 r 1 (AUF1), a cellular protein that binds to AU-rich elements, or AREs, in the 3' noncoding regions (

245 Nup475 protein bound a tumor necrosis factor AU-rich element over a broad range of pH and salt concen

246 Mutations within one AU-rich element present in the arz1 3'-untranslated regi

247 is exonuclease activity was stimulated by an AU-rich element present in the RNA.

248 ability of many target mRNAs via binding the AU-rich elements present in the 3' untranslated region o

249 inger protein tristetraprolin (TTP) binds to AU-rich elements present in the 3' untranslated regions

250 destabilization likely occurs via conserved AU-rich elements present in the 3'-untranslated regions

251 these proteins did not appear to bind to the AU-rich elements present in the 3'UTR of CD154.

252 ulated by signaling pathways through an ARE (AU-rich element) present in their 3'-UTRs.

253 ptosis, and inflammation by associating with AU-rich elements residing in their 3'-untranslated regio

254 lu-Ala-His) box RNA helicase associated with AU-rich element (RHAU) (also named DHX36 or G4R1) specif

255 RNA helicase associated with AU-rich element (RHAU) is an ATP-dependent RNA helicase

256 RNA helicase associated with AU-rich element (RHAU), a member of the ATP-dependent DE

257 s including RNA helicase AU (associated with AU rich elements) (RHAU) (G4 resolvase 1), Bloom helicas

258 ammalian cell extracts bound less well to an AU-rich element RNA probe than did the same amount of TT

259 AU-rich element RNA-binding protein 1 (AUF1) binding to

260 AU-rich element RNA-binding protein 1 (AUF1) regulates t

261 eous nuclear ribonucleoprotein (hnRNP) I and AU-rich element RNA-binding protein 1 (AUF1), respective

262 ed proteins including a novel isoform of the AU-rich element RNA-binding protein and KH-type splicing

263 HuR, which in turn is capable of binding an AU-rich element sequence in vitro.

264 itation and site-directed mutagenesis at the AU-rich element sequences of the c-myc mRNA.

265 th longer 3'UTR and with higher density of U/AU-rich elements, suggesting that DHTS inhibits the asso

266 sequence downstream of the single nonameric AU-rich element that is present in its 3'-untranslated r

267 3'-UTR of COX-2 contains a highly conserved AU-rich element that was able to confer lipopolysacchari

268 uR protein has been shown to avidly bind the AU-rich elements that confer instability upon their mRNA

269 kin-2 mRNA is a labile transcript containing AU-rich elements that is transiently stabilized by CD28

270 We previously characterized a 250-nucleotide AU-rich element, the Vg1 translation element (VTE), in t

271 By binding to AU-rich elements via its interaction with tristetraproli

272 hat tristetraprolin directs VHS RNase to the AU-rich elements, we mapped the domains of VHS and trist

273 region of TR3, there are three copies of an AU-rich element which has previously been shown to be in

274 HuD binds to mRNAs that contain an AU-rich element with high affinity.

275 ate that RNPC1 can bind to MIC-1 mRNA via an AU-rich element within MIC-1 3'-UTR and then enhances MI

276 t-1 mRNA stability requires an 11 nucleotide AU-rich element within the distal 217 bases of the 3'-un

277 r, and ZFP36/Tristetraprolin, which binds to AU-rich elements within 3'-untranslated regions to desta

278 P) is a zinc finger protein that can bind to AU-rich elements within certain mRNAs, resulting in dead

279 n translation was shown to involve conserved AU-rich elements within cytokine 3'UTRs.

280 s are selected by their position relative to AU-rich elements within plant introns and by their degre

281 HuR binding to AU-rich elements within the 3' untranslated region of mR

282 he binding of the glycolysis enzyme GAPDH to AU-rich elements within the 3' UTR of IFN-gamma mRNA.

283 TTP can bind to AU-rich elements within the 3'-untranslated regions of t

284 nd recruitment of RNA decay machinery to the AU-rich elements within the 3'-UTR of the target transcr

285 d in a position-dependent manner relative to AU-rich elements within the intron.

286 binds with high specificity to at least two AU-rich elements within the MYCN 3'-untranslated region.

287 proinflammatory cytokine mRNAs by binding to AU-rich elements within their 3' untranslated regions, t