ライフサイエンスコーパス: untranslated

1 n thought to unwind structures formed in the untranslated 5' region via a nonprocessive mechanism.

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

3 d siRNA precursor structures embedded in the untranslated (and translated) regions of the mRNAs.

4 cription of the first translated exon and an untranslated exon in hippocampus (P 1.3 x 10(-8)), front

5 ein-coding sequences are more conserved than untranslated gene regions.

6 cally stimulates pausing at two sites in the untranslated leader of the trpEDCFBA operon.

7 n open reading frames, and fewer occurred in untranslated leader sequences, antisense strands, and in

8 g bipartite element (3'BE) located at the 3' untranslated leader.

9 tion via structural rearrangements in the 5' untranslated (leader) region of the mRNA in response to

10 Untranslated mRNA regions (UTRs) are key mediators of po

11 step process initiated by stable assembly of untranslated mRNPs into core structures, which could pro

12 iculum stress and critically involved in the untranslated protein response, and Sec63, a heat shock p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 74 strain lacking 30 nucleotides from its 3' untranslated region (rDEN2Delta30) has previously been e

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

110 The 3' untranslated region luciferase assays performed to deter

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

112 Subsequent 3' untranslated region luciferase reporter assays confirmed

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

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

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

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

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

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

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

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

121 1b-1, which we show directly binds to the 3' untranslated region of Bcl-2 mRNA leading to its transla

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 3'-Untranslated region reporter assays, argonaute-2 microri

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

178 3' Untranslated region SNPs are not acting as genetic modif

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

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

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

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

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

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

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

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

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

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

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

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

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

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

193 -5p, which directly targeted IkappaBalpha 3' untranslated region, leading to NF-kappaB activation.

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

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

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

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

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

199 24 and miR-503, which directly target its 3' untranslated region.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

214 3'-untranslated regions (3'-UTRs) are the noncoding parts o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

234 3'-untranslated regions (UTRs) specify post-transcriptional

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

254 Select 5' untranslated regions exert robust translational control

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

289 4-truncated transcripts carrying intronic 5' untranslated regions.

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

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

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

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

294 ere attributed to length variations of their untranslated regions.

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

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

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

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

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

300 n many species, CsrA activity is governed by untranslated sRNAs, CsrB and CsrC in Escherichia coli, w