ライフサイエンスコーパス: untranslated region

1 lated miR-194-5p that interacts with AKT2 3' untranslated region.

2 c and direct effect of miR-520g on the TF 3' untranslated region.

3 n of TNF mRNA by GAPDH binding to the TNF 3' untranslated region.

4 24 and miR-503, which directly target its 3' untranslated region.

5 A is differentially regulated through its 3' untranslated region.

6 expression through direct binding to the 3'-untranslated region.

7 d MIE transcript, while others extend the 5' untranslated region.

8 mRNA containing an AU-rich element in its 3'-untranslated region.

9 small upstream open reading frames in its 5' untranslated region.

10 commitment, via binding to the MyoD mRNA 3' untranslated region.

11 sor gene RASSF1A by direct binding to its 3'-untranslated region.

12 aB-rps14 mRNA via specific binding to its 5' untranslated region.

13 vents, consistent with its unusually long 3' untranslated region.

14 interacting with AU-rich sequences in the 3' untranslated region.

15 binding a unique sequence embedded in its 3' untranslated region.

16 open reading frame (uORF) located in its 5' untranslated region.

17 enerally located in close vicinity to the 5' untranslated region.

18 4-truncated transcripts carrying intronic 5' untranslated regions.

19 lecules, with a particular focus on their 3' untranslated regions.

20 d in eukaryotic telomeres, promoters, and 5' untranslated regions.

21 y located in the highly structured 5' and 3' untranslated regions.

22 ticular structural context, especially in 3' untranslated regions.

23 ere attributed to length variations of their untranslated regions.

24 m diversity and changes in the lengths of 3' untranslated regions.

25 oci on several chromosomes, most commonly in untranslated regions.

26 also cryptic peptides encoded in apparently 'untranslated' regions.

27 r cyclin D1 translation by binding to the 3'-untranslated region (3' UTR) of its mRNA.

28 tial of mRNAs via addition or deletion of 3' untranslated region (3' UTR) sequences.

29 and report that they cluster in the HIV-1 3' untranslated region (3' UTR).

30 A-29b (miR-29b) binding sites on the Tet1 3' untranslated region (3' UTR).

31 nhibited the activity of a wild-type CCN2 3' untranslated region (3'-UTR) but not of a mutant CCN2 3'

32 th miR-195 and CUGBP1 interacted with the 3' untranslated region (3'-UTR) of Igf2r mRNA, and the asso

33 g a common GU-rich cis-element within the 3'-untranslated region (3'-UTR) of their mRNA.

34 nd hypertensive nephropathy, and the CHGA 3'-untranslated region (3'-UTR) variant C+87T (rs7610) disp

35 direct interaction with its mRNA three prime untranslated region (3'-UTR).

36 of PpCSP1 is negatively regulated by its 3'-untranslated region (3'-UTR).

37 s suppressor to directly target the SNAI2 3'-untranslated region (3'-UTR).

38 tein (E2 K200R) and a deletion within the 3' untranslated region (3'-UTR).

39 SN5 translation via direct binding to its 3' untranslated region (3'UTR) and 5'UTR, leading to tumor

40 nts of peripheral sensory neurons and the 3' untranslated region (3'UTR) landscapes after unilateral

41 Herein we show the importance of 3 prime untranslated region (3'UTR) non-coding regulatory varian

42 The 3' untranslated region (3'UTR) of mRNA is the binding targe

43 s via binding the AU-rich elements of the 3' untranslated region (3'UTR) of numerous pro-inflammatory

44 s insertion of a retrotransposon into the 3' untranslated region (3'UTR) of the tumor necrosis factor

45 miR-365, a microRNA that targets the PDYN 3'-untranslated region (3'UTR), and is significantly associ

46 ytokine interferon-gamma (IFN-gamma), via 3' untranslated region (3'UTR)-mediated mechanisms.

47 instability through the UG repeats of its 3-untranslated region (3-UTR).

48 ate that, through an interaction with the 3' untranslated regions (3' UTRs) of BCL2 and BIK, LARP1 st

49 The 3' untranslated regions (3' UTRs) of mRNAs play important r

50 cripts that differ in the length of their 3' untranslated regions (3' UTRs) while producing the same

51 3'-untranslated regions (3'-UTRs) are the noncoding parts o

52 ng reporter assays have demonstrated that 3' untranslated regions (3'-UTRs) regulate gene expression

53 transcripts via targeting elements within 3' untranslated regions (3'UTR), and enforced IGF2BP3 expre

54 A) generates mRNA isoforms with different 3' untranslated regions (3'UTRs) and/or coding sequences.

55 Furthermore, NF90 bound to the 3' untranslated regions (3'UTRs) of cyclin E1 mRNA in vitro

56 ate-uridylate-rich elements (AREs) in the 3'-untranslated regions (3'UTRs) of specific mRNAs, such as

57 sRNA) (ADAR), occurs predominantly in the 3' untranslated regions (3'UTRs) of spliced mRNA.

58 t the truncation of segments of the HIV-1 5'-untranslated region (5'-UTR) distinct from the core enca

59 om sequencing analysis of partial VP1 and 5' untranslated region (5'-UTR) sequences of the EV genome.

60 d entirely by alternative splicing in the 5'-untranslated region (5'-UTR).

61 qPCR) targeting a conserved region of the 5' untranslated region (5'-UTR).

62 Here we find that in 5' untranslated region (5'UTR) of human Annexin II receptor

63 dcd4 regulates Sin1 translation, the SIN1 5' untranslated region (5'UTR) was fused with luciferase re

64 upstream open reading frame (uORF) in the 5' untranslated regions (5' UTRs) of both mRNAs.

65 HAdV 5' untranslated regions (5'UTRs) are crucial for cap-indepe

66 Binding of hnRNP C1 to the HPV16 early, untranslated region activated HPV16 late 5'-splice site

67 hrough binding to AU-rich elements in the 3' untranslated region and promoting mRNA decay.

68 ed from a leaderless transcript lacking a 5'-untranslated region and Shine-Dalgarno ribosome binding

69 RNAs containing AU-rich elements in their 3'-untranslated region and target them for degradation.

70 y stabilizing the interaction between the 3'-untranslated region and the RNA-induced silencing comple

71 ntragenic transcripts, leaderless RNAs, long untranslated regions and a unique nucleotide frequency f

72 . vivax genes tend to have unusually long 5' untranslated regions and also present multiple transcrip

73 ding patterns in introns, are enriched in 3' untranslated regions and alter genes distinct from TDP-4

74 t HNRNPR binds MHC class I mRNAs in their 3' untranslated regions and enhances their stability and co

75 insertion sites are within genes (including untranslated regions and introns) and 28% (7217) are wit

76 mRNA-specific activators that bind to the 5' untranslated regions and promote translation on mitochon

77 oplast mRNAs harbor putative SDs in their 5' untranslated regions and the aSD displays strong conserv

78 ASV1 contains a long 5'UTR (untranslated region) and is involved in developmentally

79 of additional genes, predominantly in the 5' untranslated region, and has global effects on the expre

80 HuR bound to the Cdc42 mRNA via its 3' untranslated region, and this association specifically e

81 ence, modified NS5B consensus sequence, pS52 untranslated regions, and coding mutations from a cultur

82 revealed the landscapes of gene structures, untranslated regions, and splicing activities to be more

83 work: both directly through targeting its 3' untranslated region at two distinct seed regions and ind

84 tion initiation when inserted into an mRNA 5 untranslated region, but also generate noise.

85 ational control between cell lines, while 3' untranslated regions can confer cell type-specific expre

86 r pattern (PAMP) motif located within the 3' untranslated region consisting of poly-U/UC.

87 gnition sequence and specific introns and 3' untranslated regions each increased protein expression b

88 tion for genetic parts (promoters, 5' and 3' untranslated regions, etc.) are collected.

89 Select 5' untranslated regions exert robust translational control

90 s at the CpG-island overlapping the first 5'-untranslated region exon, paralleling the increased PEAR

91 Study of 5' untranslated region features of these transcripts reveal

92 The study of 5' untranslated region features revealed that GC content an

93 alternative splicing of its terminal exon 3' untranslated region, generating an oncogenic, C-terminal

94 reporter assays demonstrated that FGFRL1 3' untranslated region harboring rs4647940 appears to be hs

95 Additionally, inclusion of the CD40LG 3'-untranslated region in the transgene preserved posttrans

96 Importantly, removal of the Dazl 3'-untranslated region in XY germ cells stabilizes the Dazl

97 ings unveil a role for the translation of 5' untranslated regions in cancer, and expose new targets f

98 ne rich elements (AREs) from various mRNA 3'-untranslated regions in vitro and in vivo despite its la

99 146a/b with mouse and human renalase 3'-UTR (untranslated region) in cultured cells.

100 contained TRs in the promoters, in their 3' untranslated region, in introns, and in exons had higher

101 cis-acting sequence variants in the FAD2 5' untranslated region intron that determine the expression

102 tic production of CaMKII mRNA with a long 3'-untranslated region is necessary for modulating spontane

103 l repression of TNF and that the TNF mRNA 3' untranslated region is sufficient for repression.

104 Here we show that secondary structure in 5' untranslated regions is only a minor determinant for Roc

105 -5p, which directly targeted IkappaBalpha 3' untranslated region, leading to NF-kappaB activation.

106 ifferent sites in last exons and regulate 3' untranslated region length in an opposing manner.

107 microRNA-211 binds to PGC1-alpha 3' untranslated region locus and represses it.

108 The 3' untranslated region luciferase assays performed to deter

109 med by a dose-dependent reduction in HCN4 3'-untranslated region luciferase reporter activity on cotr

110 Subsequent 3' untranslated region luciferase reporter assays confirmed

111 By using an RKIP 3'-untranslated region luciferase reporter construct with a

112 in a 38-base pair region of the PIM1 mRNA 3'-untranslated region mediate a regulatory interaction wit

113 fs, a miRNA collection, defined by shared 3' untranslated region motifs, and a molecular function col

114 uding transcription factor binding sites and untranslated regions mutated in up to approximately 15%

115 located within miRNA-binding sites in the 3'-untranslated region of 155 cardiometabolic genes.

116 ly repressed by p21, directly targets the 3' untranslated region of adenosine monophosphate-activated

117 A target sequence in the 3' untranslated region of an expressed mRNA was detected in

118 The triplex formed within the 5' untranslated region of an mRNA reduces the protein expre

119 Let7 targeted the 3' untranslated region of ARID3B and HMGA2 and suppressed t

120 1b-1, which we show directly binds to the 3' untranslated region of Bcl-2 mRNA leading to its transla

121 We show that miR-30a-5p binds the 3' untranslated region of BDNF, and that overexpression of

122 ture translation events from uORFs in the 5' untranslated region of binding immunoglobulin protein (B

123 The minor allele at rs1883832, in the 5'-untranslated region of CD40, was associated with earlier

124 miR-29 microRNA binding site, within the 3' untranslated region of COL4A1, was identified in the lar

125 Here, we show that the 3' untranslated region of CSR1 contains a target site of mi

126 abrogated the activity of miR-650 on the 3' untranslated region of CSR1.

127 ion by binding the UG-rich element in the 3' untranslated region of Cx43.

128 dentified a G-quadruplex structure in the 5' untranslated region of Gap-43 mRNA that directly interac

129 We used the 3' untranslated region of Gria1, which encodes the AMPA rec

130 endent unwinding of G-quadruplexes in the 5' untranslated region of GW182 mRNA.

131 recognition element of miR-18a-5p in the 3'-untranslated region of hPXR mRNA.

132 iferase reporter assay confirmed that the 3'-untranslated region of IGFBP1 mRNA is targeted by miR-54

133 The 5' untranslated region of irvA mRNA is a trans riboregulato

134 le-nucleotide polymorphisms (SNPs) in the 3' untranslated region of KCNQ1 were recently suggested to

135 oning through direct interaction with the 3' untranslated region of MCL1 mRNA.

136 lements that are generally located in the 5' untranslated region of messenger RNA.

137 y the translation of reporters containing 3' untranslated region of Mos or Ccnb1 and the accumulation

138 uR binding to AU-rich elements within the 3' untranslated region of mRNAs encoding oncogenes, growth

139 y, we found that miR-146b-3p binds to the 3'-untranslated region of PAX8 and sodium/iodide symporter

140 n of an atypical and conserved IRE in the 3' untranslated region of Pfn2 mRNA.

141 MAC1 acts through the 5' untranslated region of psaC transcripts and is required

142 miR-26b directly bound the 3'-untranslated region of PTEN, leading to the reduction of

143 iferase reporter assay indicated that the 3' untranslated region of PTPRJ was targeted by this miR.

144 the binding of miR-16 and miR-195 to the 3'-untranslated region of regulatory factor X 5.

145 found that miR-376c-3p encoded within the 3'-untranslated region of RUNX2 played a pivotal role in re

146 at direct interaction of miR-124 with the 3'-untranslated region of SMOX mRNA contributes to this neg

147 Our results show that HuR binds to the 3'-untranslated region of SOX2 mRNA together with the RNA-i

148 n Escherichia coli), or by binding to the 5' untranslated region of target mRNAs (in mammalian cells)

149 es of DIO mice, could directly target the 3'-untranslated region of the APCDD1 gene.

150 Insulin altered DNA methylation in the 3' untranslated region of the calcium pump ATP2A3 gene.

151 Two miR-200b binding sites in the 3'-untranslated region of the CITED2 mRNA were required for

152 The unusually long untranslated region of the cotH in Bacillus subtilis, as

153 G trinucleotide repeats ((CTG)exp) in the 3' untranslated region of the DMPK gene.

154 Expansion of a CGG-repeat tract in the 5'-untranslated region of the FMR1 gene to >200 repeats res

155 The rs6993 located in the 3' untranslated region of the GOT2 locus was significantly

156 capitulate the selective packaging of the 5' untranslated region of the HIV-1 genome in the presence

157 d significantly less 5-hmC binding in the 3' untranslated region of the nestin gene in melanoma compa

158 etically by TET2 via 5-hmC binding at the 3' untranslated region of the nestin gene, providing one po

159 e evasion factors, including CssA, in the 5'-untranslated region of the operon for capsule biosynthes

160 Moreover, the short 5' untranslated region of the oxidative phosphorylation mRN

161 HuR is shown to directly bind the 3' untranslated region of the Rictor transcript and enhance

162 hia coli and many other organisms, in the 5' untranslated region of the target gene.

163 The 3'-untranslated region of the TNF transcript contains AU-ri

164 DENV RT-iiPCR assay targeting a conserved 3' untranslated region of the viral genome was evaluated.

165 ne candidates containing deletions in the 3' untranslated region of the Zika virus genome (ZIKV-3'UTR

166 contains a 10-nucleotide deletion in the 3' untranslated region of the ZIKV genome (10-del ZIKV).

167 egulate gene expression by binding to the 3' untranslated region of their mRNA targets.

168 t by binding to specific sequences in the 3' untranslated region of their target genes and causing th

169 Binding of miR-939 to the 3' untranslated region of these genes was confirmed by repo

170 eracted with a stem-loop structure in the 3' untranslated region of these transcripts through its PIN

171 d to evaluate binding of microRNAs to the 3' untranslated region of TLR7.

172 down-regulated by miR-7 through targeting 3'-untranslated region of VDAC1 mRNA.

173 ion, RIG-I associated specifically to the 3' untranslated region of viral genome.

174 effects, including direct binding to the 3' untranslated region of VWF and targeting FURIN and the h

175 a nuclease-resistant RNA structure in the 3' untranslated region of Zika virus.

176 revealed that PSPC1 binds to intronic and 3'-untranslated regions of a number of adipocyte RNAs, incl

177 Riboswitches, which are embedded in untranslated regions of bacterial messenger RNA (mRNA),

178 iting within long dsRNA stem loops within 3' untranslated regions of endogenous transcripts.

179 Lower frequency splicing of RE into untranslated regions of gene transcripts was also observ

180 Variants located within untranslated regions of HLA genes are involved in allele

181 find potential G-quadruplexes located in the untranslated regions of human mRNAs (i.e. in the 5' and

182 rden of rare variants in patients within the untranslated regions of known disease-causing genes, dri

183 inds in a sequence-specific manner to the 3' untranslated regions of many proinflammatory mRNAs and r

184 anscriptional riboswitches located in the 5'-untranslated regions of messenger RNA requires the tempo

185 trinucleotide motif predominantly in the 3' untranslated regions of mRNA, and destabilizes target mR

186 RNAs, tRNAs, long noncoding (lnc)RNAs and 3' untranslated regions of mRNAs in human cells.

187 by direct functional interaction with the 3'-untranslated regions of proinvasive alphav- and alpha6-i

188 ers identified so far include elements in 3' untranslated regions of specific mRNAs and several non-c

189 entary sequences and binding affinity for 3' untranslated regions of the Fas ligand (FasL) and Fas, r

190 ent translation enhancers (3'CITE) in the 3' untranslated regions of their genomic (g)RNAs to compete

191 ened for variations in the entire coding and untranslated regions of these 3 genes by resequencing.

192 ase reporter gene activity via binding to 3' untranslated regions of TMEFF2, NTRK2, and SHISA2.

193 binds to AU-rich elements present in the 3' untranslated regions of transcripts that mainly encode p

194 ative nuclear processing within noncoding 3'-untranslated regions of VEGF and CPEB4 messenger RNAs in

195 ificant association between 2 SNPs in the 3' untranslated region or within the adjacent region just 3

196 of the miR-223 binding site in the NLRP3 3' untranslated region, phenocopied the characteristics of

197 iotic transcript isoform with an extended 5'-untranslated region predicted to impair protein translat

198 tly improve the annotations of P. vivax gene untranslated regions, providing an important resource fo

199 74 strain lacking 30 nucleotides from its 3' untranslated region (rDEN2Delta30) has previously been e

200 n an 250 kb haplotype block spanning the 5' untranslated region region of insulin-degrading enzyme i

201 3'-Untranslated region reporter assays, argonaute-2 microri

202 deletion polymorphism (rs3045215) in the 3' untranslated region sequence of human IRF2BP2 mRNA had a

203 3' Untranslated region SNPs are not acting as genetic modif

204 nd CSP41a had been shown to cleave within 3'-untranslated region stem-loop structures, which contain

205 d not bind with high affinity to the ndhA 5' untranslated region, suggesting that PPR53's RNA-stabili

206 e and structural elements in the SMN mRNA 3'-untranslated region that are reminiscent of the snRNP co

207 al design, we engineered a cis-repressing 5' untranslated region that can be activated by this new ri

208 r(CGG) repeat (r(CGG)(exp)) present in a 5' untranslated region that causes fragile X-associated tre

209 ependent translation element (BTE) in the 3'-untranslated region that interacts with host translation

210 anslation of viral or reporter mRNAs with 5' untranslated regions that contain adenosine repeats, so-

211 We extracted a panel of 5' and 3' untranslated regions that control protein production fro

212 is proposed to reflect highly structured 5' untranslated regions that depend strongly on eIF4A-media

213 P2 exons 6 to 11, 1 a PKP2 duplication of 5' untranslated region till exon 1, 1 the desmocollin-2 (DS

214 n the 5b+ annotation build, added additional untranslated regions to 1,393 5b+ gene models, identifie

215 iridae use RNA structures in their 5'- or 3'-untranslated regions to stall and repress XRN1, effectiv

216 among which 23.5% and 5.4% were located in 5 untranslated region (uPSS) and intergenic region (iPSS),

217 identified a novel intron within the LANA 5' untranslated region using a splice acceptor at 127888.

218 ent, deep-sequencing method targeting the 5' untranslated region (UTR) and P1 genomic region to chara

219 TTP targets AU-rich elements in the NLRP3 3'-untranslated region (UTR) and represses NLRP3 expression

220 ated that MYF5 was capable of binding the 3' untranslated region (UTR) and the coding region (CR) of

221 SLA) and stem-loop B (SLB) located in the 5' untranslated region (UTR) are critical for binding the v

222 Targeting the IL1R1 3' untranslated region (UTR) by EBV miR-BHRF1-2-5p was conf

223 regulated by structural complexity of the 5'untranslated region (UTR) derives from bacterial and oth

224 of CaMKII mRNA, which consists of a short 3'-untranslated region (UTR) form lacking regulatory elemen

225 a common polymorphic variant in the ERCC5 5' untranslated region (UTR) generates an upstream ORF (uOR

226 tion in the asymmetric loop of a critical 3' untranslated region (UTR) hairpin that disrupts local hi

227 Genomic variation in the untranslated region (UTR) has been shown to influence HL

228 KSHV latent infection induces 5' untranslated region (UTR) hypomethylation and 3'UTR hype

229 iscovered four new mutations in the whiB7 5' untranslated region (UTR) in 6/22 samples.

230 We reported that artificially engineered 5' untranslated region (UTR) interspecies rhinovirus/rhinov

231 The eukaryotic 5' untranslated region (UTR) is critical for ribosome recru

232 Given that the CRP 3' untranslated region (UTR) is long and AU rich, we hypoth

233 A nine-nucleotide motif located in the 5' untranslated region (UTR) is required for preferential a

234 in Seb1 resulted in widespread changes in 3' untranslated region (UTR) length as a consequence of inc

235 e subject to tissue-specific APA, such as 3' untranslated region (UTR) lengthening in head and 3' UTR

236 hnRNP E1 promotes its dissociation from a 3' untranslated region (UTR) nucleic acid regulatory motif,

237 her three variants are all located in the 5'-untranslated region (UTR) of an alternative spliced tran

238 Furthermore, the 3' untranslated region (UTR) of bunyaviral mRNA is sufficie

239 inds to and translationally activates the 5' untranslated region (UTR) of G3BP1 mRNAs, thereby contro

240 oRNA 199a2 (miR-199a2), which targets the 3' untranslated region (UTR) of HIF-1alpha mRNA.

241 at predicts the protein expression of the 5' untranslated region (UTR) of mRNAs in the yeast Saccharo

242 The 3' untranslated region (UTR) of mRNAs is the primary regula

243 elicase that unwinds RNA structure in the 5' untranslated region (UTR) of mRNAs.

244 ecular level, CELF1 was found to bind the 3'-untranslated region (UTR) of Myc mRNA and repressed MYC

245 We found that Hrp38 binds to the 3' untranslated region (UTR) of Nanos mRNA, which contains

246 located in a microRNA binding site in the 3'-untranslated region (UTR) of NBS1, was shown to be assoc

247 esence of a G-quadruplex structure in the 5' untranslated region (UTR) of NRF2 mRNA, as measured by c

248 ation of the promotor region, the 5'- and 3'-untranslated region (UTR) of SAMHD1, and the mechanism r

249 terized SLC, a stem-loop structure in the 5' untranslated region (UTR) of the bean pod mottle comovir

250 Although the 5' untranslated region (UTR) of the HIV-1 RNA is known to b

251 erozygosity for a frequent variant in the 3' untranslated region (UTR) of the mutant allele, which di

252 l mRNA stem-loop forming structure in the 5' untranslated region (UTR) of the vacA transcript.

253 Pacman on conserved RNA structures in the 3' untranslated region (UTR) of the viral genomic RNA.

254 The 5' untranslated region (UTR) plays dual roles in CDC20 mRNA

255 criptional regulation of NR4A2, we used a 3' untranslated region (UTR) reporter screen and identified

256 selenoproteins by a mechanism involving a 3 untranslated region (UTR) selenocysteine insertion seque

257 set of messenger RNAs containing distinct 5'-untranslated region (UTR) sequence features.

258 acterial type I toxin mRNAs possess a long 5 untranslated region (UTR) that serves as the target site

259 Luciferase assays wherein the Bcr 3' untranslated region (UTR) was cloned downstream of a luc

260 CCHFV-NP binds to the viral mRNA 5' untranslated region (UTR) with high affinity.

261 ail in mRNAs influences the length of the 3'-untranslated region (UTR), a critical determinant of gen

262 , where auxin reduces PAC distribution in 5'-untranslated region (UTR), but increases in the 3'UTR.

263 (SbCAD2) that has an 8-bp deletion in its 5'-untranslated region (UTR), conferring the spontaneous br

264 Stem-loop A (SLA), a part of the viral 5' untranslated region (UTR), is critical for the initiatio

265 hat DDX3X specifically recognizes the HCV 3' untranslated region (UTR), leading to the activation of

266 rectly to an (AAN)3 motif within the mutS 5' untranslated region (UTR), repressing translation in the

267 hanged when the intron was located in the 5'-untranslated region (UTR), suggesting that the intron af

268 translation via two binding sites in its 3' untranslated region (UTR), thereby ensuring a dual contr

269 and miR-58 family miRNAs within the egl-1 3' untranslated region (UTR), which affect both mRNA copy n

270 responsive elements present in the FOXP1-3' untranslated region (UTR).

271 t of an in vitro-synthesized 365-nt HIV-1 5'-untranslated region (UTR).

272 ich element (ARE) in the human LARP4 mRNA 3' untranslated region (UTR).

273 deleting sequences within both the 3' and 5' untranslated regions (UTR) on each genome segment and sh

274 d repeated Alu elements (IRAlus) in their 3' untranslated regions (UTRs) are inefficiently exported t

275 Each EBOV gene contains exceptionally long untranslated regions (UTRs) flanking the open reading fr

276 ed 3' ends, and genes possessing multiple 3'-untranslated regions (UTRs) generated by alternative cle

277 MBNL1 binds the 3' untranslated regions (UTRs) of DBNL (drebrin-like protei

278 we show that WT1 binds preferentially to 3' untranslated regions (UTRs) of developmental targets.

279 stream open reading frames (uORFs) across 5'-untranslated regions (UTRs) of key signalling components

280 Thus far, only the 3' untranslated regions (UTRs) of MICA, MICB, and UL16-bind

281 to unwind RNA secondary structure in the 5'-untranslated regions (UTRs) of mRNAs to promote their re

282 ed the specific binding of miR-224 to the 3' untranslated regions (UTRs) of SLC4A4 and CFTR mRNAs, th

283 Notably, miR-24-3p targeted the 3' untranslated regions (UTRs) of the major pluripotent fac

284 to all validated human microRNAs and the 3' untranslated regions (UTRs) of ~6000 cancer-associated g

285 3'-untranslated regions (UTRs) specify post-transcriptional

286 e RNA regulons embedded in homeobox (Hox) 5' untranslated regions (UTRs) that confer ribosome-mediate

287 reporters, we show that miR-J8 can target 3' untranslated regions (UTRs) with miR-17-5p or miR-20a co

288 s with polyadenylated 3' ends that map to 5'-untranslated regions (UTRs), introns, and protein-coding

289 ee major domains loosely corresponding to 5' untranslated regions (UTRs), open reading frames, and 3'

290 otide-containing sequences in introns and 3' untranslated regions (UTRs), promotes exon inclusion or

291 mpacts mRNAs with longer, more structured 5' untranslated regions (UTRs).

292 interact with their target genes through 3' untranslated regions (UTRs).

293 , cis-antisense transcription and regulatory untranslated regions (UTRs).

294 and translation through interactions with 3' untranslated regions (UTRs).

295 he presence of transcripts with different 3' untranslated regions (UTRs).

296 ignificant interaction between rs3744165 (5'-untranslated region variant of exon 2 of zinc finger pro

297 etween miR-650 and its target site in the 3' untranslated region was validated through luciferase rep

298 tion initiation sites (uTISs) at the mRNA 5' untranslated regions was strongly associated with improv

299 The large majority of TISs that mapped to 5' untranslated regions were noncanonical and led to N-term

300 roximal APA sites, resulting in shortened 3' untranslated regions, while nonmethylated transcript iso