ライフサイエンスコーパス: untranslated

1 ial lifestyle decisions by binding to the 5' untranslated and/or early coding regions of mRNA targets

2 transcript level through alternate use of 5' untranslated exons (UTRs), promoters, and proinflammator

3 e protein, of which one is located in the 5'-untranslated leader and the other is within the coding s

4 FKFB3 is mediated by binding of CPEB4 to its untranslated messenger RNA.

5 sion of some key genes by targeting their 3'-untranslated mRNA region.

6 ess than 100 codons) have been identified in untranslated mRNA regions (UTRs) across eukaryotes.

7 ng noncoding RNAs, small nucleolar RNAs, and untranslated mRNA regions, accomplish many of their dive

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

42 5'-flanking region containing the 263 bp 5'-untranslated region (5'-UTR) including the first intron.

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

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

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

46 7me3 and the histone variant H2A.Z at the 5' untranslated region (5'UTR) intron of EIN2.

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

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

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

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

51 74 strain lacking 30 nucleotides from its 3' untranslated region (rDEN2Delta30) has previously been e

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 -4.8 kcal/mol) in the middle of the mRNA 5' untranslated region (UTR), our assay robustly detects sm

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

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

97 946a is predicted to bind to the TGFbeta1 3' untranslated region (UTR), thereby inhibiting its transc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

120 The 3' untranslated region luciferase assays performed to deter

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 2.5-kb deletion (del2.5) overlapping the 3' untranslated region of LDLR in 7 heterozygous carriers f

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

170 3(EGLN3) gene and targeted a site in its 3'-untranslated region to downregulate its transcriptional

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

186 24 and miR-503, which directly target its 3' untranslated region.

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

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

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

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

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

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

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

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

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

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

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

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

199 3' Untranslated regions (3' UTRs) of mRNAs emerged as centr

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

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

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

203 -310s bind to target binding sites in the 3' untranslated regions (3'-UTR) of both Cyp6g1 and Cyp6g2

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

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

206 3'-untranslated regions (3'-UTRs) are the noncoding parts o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

291 We show here that a short-complementarity untranslated RNA (scoutRNA), together with crRNA, is req

292 the relative proportions of intronic/exonic/untranslated RNA captured by RNA-seq for most genes.

293 Small, noncoding RNAs are short untranslated RNA molecules, some of which have been asso

294 SPR array transcripts are unusually long for untranslated RNA, suggesting the existence of mechanisms

295 n termination factor that rapidly terminates untranslated RNA.

296 the transcription of tRNAs and other short, untranslated RNAs.

297 used to screen thousands of untranscribed or untranslated sequences and their variants for functional

298 regions including promoters, terminators and untranslated sequences could drive stable luciferase tra

299 tissues, but GLUT8 mRNA exists mostly as an untranslated splice form in tumors.

300 ules, and during stress, when most mRNAs are untranslated, the composition of P-bodies reflects this