ライフサイエンスコーパス: untranslated region

1 ion of specific mRNAs with elongated 3'-UTR (untranslated region).

2 alternative mRNA isoform with a truncated 3' untranslated region.

3 the regulatory sequence in the canonical 3' untranslated region.

4 translation-enhancing element in the manY 5' untranslated region.

5 24 and miR-503, which directly target its 3' untranslated region.

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

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

8 nce to a myeloid-specific microRNA in the 3' untranslated region.

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

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

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

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

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

14 tein expression levels via binding to its 3' untranslated region.

15 otides 2-7, of the miRNA to sites in mRNA 3' untranslated regions.

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

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

18 located AGO2 protein associations within 3'-untranslated regions.

19 d that these sRNAs are processed from the 3' untranslated region (3' UTR) of the oppABCDF and carAB o

20 Sequence-specific features within the 3' untranslated region (3' UTR) often direct mRNAs for deca

21 ore, we identified 16,342 isoforms in the 3' untranslated region (3' UTR), 2640 of which are novel an

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

23 the ribosomal frameshift segment and the 3'-untranslated region (3'-UTR) of the SCoV2 genome, their

24 micro-RNA (miRNA) binding to 3'-untranslated region (3'-UTR) plays an important role in

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

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

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

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

29 e differentiated by mutations in the gene 3'-untranslated region (3'-UTR).

30 radation rates based on the output gene's 3'-untranslated region (3'-UTR): introduction of copies of

31 promotes rapid decay of mRNAs containing 3' untranslated region (3'UTR) AU-rich elements (AREs).

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

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

34 iR-15a/16-1 cluster directly bound to the 3' untranslated region (3'UTR) of Claudin-5, and lentivirus

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

36 to identify microRNAs that would bind the 3' untranslated region (3'UTR) of occludin mRNA; regions th

37 conserved binding site of miR-124 in the 3'-untranslated region (3'UTR) of Parp-1 mRNA.

38 an expansion of a (CTG)n tract within the 3' untranslated region (3'UTR) of the dystrophia myotonica

39 or the fine-tuning of gene expression via 3'-untranslated region (3'UTR) targeting, and we have previ

40 d by miR-21 through distinct sites in its 3' untranslated region (3'UTR), and miR-21 expression in CR

41 led by alternative polyadenylation in the 3' untranslated region (3'UTR), with critical physiological

42 ranslation via reduced miR binding to its 3' untranslated region (3'UTR).

43 r PolH transcripts with various lengths of 3'untranslated region (3'UTR; 427-/2516-/6245-nt).

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

45 Alternative 3' untranslated regions (3' UTRs) are widespread, but their

46 Wu et al characterized small ORFs in the 3' untranslated regions (3' UTRs) of human and zebrafish mR

47 3' Untranslated regions (3' UTRs) of mRNAs emerged as centr

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

49 bility primarily through association with 3' untranslated regions (3' UTRs) of target mRNAs.

50 multiple mRNA transcripts with different 3' untranslated regions (3' UTRs).

51 -310s bind to target binding sites in the 3' untranslated regions (3'-UTR) of both Cyp6g1 and Cyp6g2

52 mouse and human MOR-1Bs that defines the 3'-untranslated regions (3'-UTR) of MOR-1Bs and stabilizes

53 ted the potential binding sites of TTP to 3'-untranslated regions (3'-UTR) of NOX2 mRNA.

54 3'-untranslated regions (3'-UTRs) are the noncoding parts o

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

56 lyadenylation may result in expression of 3'-untranslated regions (3'-UTRs) with varying lengths.

57 le nucleotide polymorphisms (SNPs) in the 3' untranslated regions (3'UTR) of these genes.

58 cells have widespread shortening of mRNA 3'-untranslated regions (3'UTRs) and switches to shorter mR

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

60 The 3' untranslated regions (3'UTRs) of mRNAs include regulator

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

62 polyadenylation (APA) produces transcript 3' untranslated regions (3'UTRs) with distinct sequences, l

63 A genomes share a long, highly structured 5' untranslated region (5' UTR) containing a type I interna

64 e demonstrate that ATXN1's unusually long 5' untranslated region (5' UTR) negatively regulates its ex

65 dies have identified several sites in the 5' untranslated region (5' UTR) of HIV-1 RNA that are bound

66 ured iron-responsive element (IRE) in its 5' untranslated region (5' UTR) that controls its translati

67 out this region of the genome, called the 5' untranslated region (5' UTR), is needed to assist in the

68 XN1 expression and uncover a key role for 5' untranslated region (5' UTR)-miR760 interactions.

69 ely regulates the cobA operon through its 5' untranslated region (5' UTR).

70 ome binding or subsequent scanning of the 5'-untranslated region (5'-UTR) for the AUG initiation codo

71 5'-flanking region containing the 263 bp 5'-untranslated region (5'-UTR) including the first intron.

72 le-nucleotide polymorphisms (SNPs) in the 5' untranslated region (5'-UTR) of the ferritin light chain

73 eature alternative splicing events in the 5'-untranslated region (5'-UTR) that are favorable for tran

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

75 7me3 and the histone variant H2A.Z at the 5' untranslated region (5'UTR) intron of EIN2.

76 The highly conserved 5' untranslated region (5'UTR) of the HIV-1 RNA genome is c

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

78 promoter, which included a portion of the 5' untranslated region (5'UTR).

79 hesis by engineering sequence elements in 5' untranslated regions (5' UTRs) remains a fundamental cha

80 ) site usage within the coding region and 5' untranslated regions (5'-UTRs), and the lack of FIP1 act

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

82 tiple isoforms characterized by different 5' Untranslated Regions (5'UTRs), whereby translation of a

83 oroplast-specific parts (47 promoters, 38 5' untranslated regions [5'UTRs], nine promoter:5'UTR fusio

84 the gene (enhancer, promoter, and 5' and 3' untranslated regions) account for the majority of activi

85 conserved between virus strains (ie, the 5'-untranslated region and cis-acting replication element)

86 of BCL2 mRNA through AU-rich elements in 3'-untranslated region and consequentially increased BCL2 p

87 ctly interacted with Atg16l1 mRNA via its 3' untranslated region and enhanced ATG16L1 translation, wi

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

89 e novel including a deletion spanning the 5' untranslated region and the first coding part of exon 1.

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

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

92 orly translated, low-stability mRNAs, the 5'-untranslated regions and coding regions of which are enr

93 ourth of these pause sites were localized to untranslated regions and could participate in posttransc

94 s replicate between brain regions, map to 3'-untranslated regions and intronic regions, share common

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

96 resistant allele YrAS2388R has duplicated 3' untranslated regions and is characterized by alternative

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

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

99 were due, in part, to variably annotated 3' untranslated regions and thousands of gene models missin

100 synthesis from non-canonical translation of "untranslated" regions and non-AUG start codons and sensi

101 e expression of CD24 by targeting its 3'UTR (untranslated region) and could be inhibited by SIRT1 via

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

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

104 e Pax3 messenger RNA that differ in their 3' untranslated regions are differentially susceptible to r

105 ts specific to sigma (sigma) factors, and 5'-untranslated region as a determinant for translation eff

106 h have acquired an extra 6 bases in the long untranslated region between the M and F protein coding s

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

108 The cagA 5' untranslated region contains a predicted stem-loop-formi

109 capsid structural proteins as well as the 3' untranslated region, each attenuated virus possessed a d

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

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

112 ering studies of transcriptional regulation, untranslated regions, genome engineering, and expression

113 We identified a 3' untranslated region in the TP53 messenger RNA that bound

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

115 ters, origins of replication, telomeres, and untranslated regions in mRNA, suggesting roles in modula

116 ith m(6) A modification of the FOXO3 mRNA 3'-untranslated region increasing its stability through a Y

117 d a strain-specific +59 motif in the cagA 5' untranslated region influence the levels of cagA express

118 In African Americans, a 5' untranslated region insertion (rs568223361) was associat

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

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

121 Loss of m(6)A from 3' untranslated regions is associated with decreased relati

122 ext suppressed Bdnf transcripts with long 3' untranslated region (L-3'-UTR) using short hairpin RNA a

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

124 The 3' untranslated region luciferase assays performed to deter

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

126 rporating a rbcS gene whose codon use and 5' untranslated-region matched rbcL Additional tobacco geno

127 ssense, nonsense, splice site, and 5' and 3' untranslated region mutations.

128 NA-dependent RNA polymerase to recognize the untranslated region of a genome segment of a related phl

129 with corresponding barcodes placed at the 3' untranslated region of a reporter gene using a lentivira

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

131 gulation of ATM by directly targeting the 3'-untranslated region of ATM mRNA.

132 a direct interaction of miR-181c with the 3' untranslated region of ATM, and the presence of ATM in m

133 1b-1, which we show directly binds to the 3' untranslated region of Bcl-2 mRNA leading to its transla

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

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

136 IP3 interacted with the AU-rich region in 3' untranslated region of Cyclin D1 mRNA and stabilized it.

137 caused by the CTG repeat expansion in the 3'-untranslated region of DMPK gene.

138 satellite repeat expansions (MREs) in the 3' untranslated region of DMPK.

139 P of highest significance occurred in the 3' untranslated region of gig1, a fish-specific antiviral e

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

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

142 d DNA methylation within the promoter and 5'-untranslated region of Kcna2 gene, rescued Kcna2 express

143 2.5-kb deletion (del2.5) overlapping the 3' untranslated region of LDLR in 7 heterozygous carriers f

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

145 e also identified different motifs in the 3' untranslated region of messenger RNAs that were sex diff

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

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

148 RBP lupus antigen (La) interacts with the 3'-untranslated region of PDCD4 mRNA and prevents miR-21-me

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

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

151 ed N6-methyladenosine modification in the 5'-untranslated region of some highly translated mRNAs.

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

153 open reading frame (uORF) present in the 5' untranslated region of the Arabidopsis (Arabidopsis thal

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

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

156 ding a bright fluorescent marker into the 3'-untranslated region of the endogenous Gata3 locus.

157 The mRNA level depends on the 5'-untranslated region of the first ORF.

158 ns with a reporter plasmid containing the 3' untranslated region of the gene encoding ERalpha (ESR1)

159 an expansion of a GCA-repeat tract in the 5' untranslated region of the gene encoding glutaminase (GL

160 o DNA methylation within the promoter and 5'-untranslated region of the Kcna2 gene, reductions in Kcn

161 coding sequence (CDS) base pairs with the 5' untranslated region of the mRNA to sequester the ribosom

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

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

164 se four known enhancers was active in the 3' untranslated region of the reporter gene.

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

166 We introduced modifications within at the 5' untranslated region of the Sabin2 genome to stabilize at

167 Stem-loop A (SLA), located in the 5' untranslated region of the viral genome, acts as a promo

168 p-independent translation element) in the 3' untranslated region of the viral RNA genome that allows

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

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

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

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

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

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

175 am open reading frames (uORFs) within the 5' untranslated regions of annotated coding genes and 354 s

176 MTHI1 targets the 5' untranslated regions of both the atpH and atpI genes.

177 microRNA recognition elements within the 3' untranslated regions of CAM mRNAs.

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

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

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

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

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

183 mplex assembly and start-site scanning of 5' untranslated regions of mRNAs.

184 utations in the 5' region of TP53, in the 3' untranslated regions of NFKBIZ and TOB1, focal deletions

185 asmic polyadenylation elements within the 3'-untranslated regions of PFKFB3 messenger RNA.

186 nal activators are believed to act on the 5'-untranslated regions of target mRNAs, but the molecular

187 h-affinity binding to AU-rich elements in 3' untranslated regions of target mRNAs, mediated through i

188 Compared to coding sequences, untranslated regions of the transcriptome are not well c

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

190 ing to the complementary sequences within 3'-untranslated regions of those messenger RNAs.

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

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

193 sites within parts of the genome encoding 3'-untranslated regions on the sense strand.

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

195 Mutations located either in the 5' untranslated region or within the open reading frame of

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

197 t binding sites within stem-loop 1 of the 5' untranslated region play important roles in genome packa

198 the RNA-binding protein Raly and the CCR5 3' untranslated region, protecting CCR5 messenger RNA from

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

200 74 strain lacking 30 nucleotides from its 3' untranslated region (rDEN2Delta30) has previously been e

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

202 A transfer DNA insertion in the 3' untranslated region resulted in reduced expression of th

203 n RNase MRP and 2 bacterial messenger RNA 5' untranslated regions reveals functionally important and

204 ta was used to define thousands of 5' and 3' untranslated regions, some of which overlapped with neig

205 are a major class of cis elements within 3' untranslated regions, targeting these mRNAs for rapid de

206 RBPs that we subject to luciferase-based 3'-untranslated-region tethered function assays to pinpoint

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

208 positioning around splicing signals and mRNA untranslated regions that associate with distinct RBP fu

209 y sites (IRES) are segments of mRNA found in untranslated regions that can recruit the ribosome and i

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

211 no loss of attenuation in domain V of the 5'-untranslated region, the primary site of reversion in Sa

212 ) through a targeting sequence at the sty 3' untranslated region, thereby enhancing MAPK signaling an

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

214 3(EGLN3) gene and targeted a site in its 3'-untranslated region to downregulate its transcriptional

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 ences the translation of RhlI through its 5'-untranslated region (UTR) and identified that the sRNA P

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

220 r translational enhancer sequences in the 5' untranslated region (UTR) and rare codons at the beginni

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

222 e that interrogates only the junctions of 3'-untranslated region (UTR) and the poly(A) tails at the t

223 miR-122 binds to two sites in the 5' untranslated region (UTR) and this interaction promotes

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

225 t have complex secondary structure in the 5' untranslated region (UTR) are translated more efficientl

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

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

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

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

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

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

232 inds to a U-rich element in the STAT3 mRNA-3'untranslated region (UTR) located within the vicinity of

233 roRNA 33a and 33b (miR-33a/b) bind to the 3' untranslated region (UTR) of ABCA1 and repress its postt

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

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

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

237 validated the miR-744 binding site in the 3' untranslated region (UTR) of PELI3 and demonstrated that

238 ly binds to single-stranded motifs in the 3' untranslated region (UTR) of RNA that contain a UAG trin

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

240 A specific region of the 3'-untranslated region (UTR) of the 14-3-3zeta mRNA is like

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

242 at expansion [r(CUG)(exp)] located in the 3' untranslated region (UTR) of the dystrophia myotonica pr

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

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

245 ss of suppressors was found to map to the 5' untranslated region (UTR) of the rplM-rpsI operon, which

246 (MREs) for both miRNAs are present in the 3'-untranslated region (UTR) of TOP2alpha/170.

247 othesized that unpaired guanosines in the 5' untranslated region (UTR) play an important role in Gag:

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

249 leotide polymorphisms (SNPs) in the HLA-G 3' untranslated region (UTR) regulate HLA-G expression, we

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

251 ISC inhibits mRNA translation through the 3'-untranslated region (UTR) sequence.

252 lternative polyadenylation (APA)-mediated 3'-untranslated region (UTR) shortening is known to increas

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

254 ermed 'regulation elements (RgE)', in the 5'-untranslated region (UTR) to impact translation efficien

255 protein coding regions and one SNV in the 5' untranslated region (UTR) were identified and provided a

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

257 eraction of miR-485-5p within the UGT2B10 3'-untranslated region (UTR), and significant reduction in

258 vy polysomes, probably through the TCF7L2 5'-untranslated region (UTR), as determined by polysome fra

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

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

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

262 -4.8 kcal/mol) in the middle of the mRNA 5' untranslated region (UTR), our assay robustly detects sm

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

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

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

266 946a is predicted to bind to the TGFbeta1 3' untranslated region (UTR), thereby inhibiting its transc

267 Through deletion mutations of the TriMV 5' untranslated region (UTR), we show that the TriMV 5' UTR

268 ver-specific miR-122 binds within the HCV 5' untranslated region (UTR), whereas the broadly expressed

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

270 ript is protected from degradation by its 3' untranslated region (UTR).

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

272 pendent translation element (CITE) in its 3' untranslated region (UTR).

273 rnph1, including four variants within the 5' untranslated region (UTR).

274 e-uridylate-rich elements (ARE) located in 3'untranslated regions (UTR) to mediate mRNA decay.

275 ts with varying lengths, typically of the 3' untranslated regions (UTR).

276 y causative of human diseases, especially in untranslated regions (UTRs) and noncoding RNAs (ncRNAs).

277 This suggests that the M segment untranslated regions (UTRs) are recognized as functional

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

279 lation of E2F1 and E2F3 mRNAs through the 5' untranslated regions (UTRs) of E2F1 and E2F3 (E2F1/3) mR

280 G-quadruplex (G4) sequences are abundant in untranslated regions (UTRs) of human messenger RNAs, but

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

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

283 ents e.g. small RNAs, long antisense RNAs or untranslated regions (UTRs) of mRNA transcripts.

284 In this work, the untranslated regions (UTRs) of mRNAs are systematically

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

286 epression mechanisms targeting the 5' and 3' untranslated regions (UTRs) of utrophin mRNA significant

287 The 5' and 3' untranslated regions (UTRs) regulate crucial aspects of

288 filing of a library of 280,000 randomized 5' untranslated regions (UTRs) with deep learning to build

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

290 lyadenylation site usage, shortening mRNA 3' untranslated regions (UTRs).

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

292 f a positive-sense genome RNA flanked by the untranslated regions (UTRs).

293 els through interactions with both 5' and 3' untranslated regions (UTRs).

294 ng allows the translation of host and viral "untranslated regions" (UTRs) to create N-terminally exte

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

296 nical upstream open reading frames in its 5' untranslated region, which is bypassed in MYC(Tg);KRAS(G

297 s in the miR-33 binding sites of the Abca1 3'untranslated region, which prevents targeting by miR-33.

298 e targeted the PTEN proximal promoter and 5' untranslated region with dCas9 fused to the repressor pr

299 hing genes displayed global shortening of 3' untranslated regions with increased expression in indica

300 We speculated that indels within 5' untranslated regions would be unlikely to have a signifi