ライフサイエンスコーパス: RNA

1 RNA binding motif protein 25 (RBM25) is a putative splic

2 RNA editing is an essential post-transcriptional process

3 RNA interference (RNAi) is known for its high catalytic

4 RNA interference suppression of NaSIPP in Nicotiana spp.

5 RNA molecules cause the proteins involved in the formati

6 RNA polymerase and ribosomes form a one-to-one complex w

7 RNA quality was also assessed.

8 RNA sequencing analysis was performed and 263 genes were

9 RNA sequencing confirmed that Hh-mediated transcription

10 RNA-binding proteins of the Musashi (Msi) have been impl

11 RNA-mediated interference has been one major approach fo

12 RNA-protein interactions are essential for proper gene e

13 RNA-seq analysis demonstrates differential gene expressi

14 RNA-seq analysis detected aberrant splicing in DONSON du

15 RNA-seq analysis of whole skin identified a larger numbe

16 RNA-seq and RT-qPCR identified potential downstream gene

17 ts maintained virological suppression (HIV-1 RNA <50 copies per mL) at week 24.

18 harbored the highest concentrations of HIV-1 RNA and highest levels of Ki67 expression.

19 h less than 50 copies per mL of plasma HIV-1 RNA at week 48 (by the US Food and Drug Administration s

20 ion was quantified by measuring plasma HIV-1 RNA during MGN1703 administration.

21 Using a single-copy assay, we measured HIV-1 RNA levels in CSF and plasma specimens from 220 HIV-posi

22 virological suppression (<50 copies of HIV-1 RNA per mL) on a stable regimen for at least 6 months, C

23 of known and putative SSP genes based on 144 RNA sequencing data sets covering various stages of macr

24 Using 4sU RNA labelling and RNA-seq, we show this competition resu

25 We employed ChIP-seq and 4sU-RNA-seq to identify aberrant DNA-binding events genome w

26 Escherichia coli (Eco) 6S RNA interacts specifically with the housekeeping sigma(7

27 iologic role of N(6)-methyladenosine (m(6)A) RNA modifications in mRNA requires an understanding of w

28 GreA factors activate RNA cleavage by wild-type RNAPs to similar levels.

29 m6A can also alter RNA structures to affect RNA-protein interactions in cells.

30 uding RNA structure analysis, RNA alignment, RNA annotation, RNA-protein interaction, ribosome profil

31 m6A can also alter RNA structures to affect RNA-protein interactions in cel

32 Decreased DICER1 levels or Alu-RNA accumulation triggers cytosolic escape of mitochondr

33 The Human antigen R protein (HuR) is an RNA-binding protein that recognizes U/AU-rich elements i

34 ific mouse reporter strains, we performed an RNA-seq screen, identifying tip- and stalk-enriched gene

35 dings into preclinical applications using an RNA interference (RNAi)-based approach.

36 NA biology including RNA structure analysis, RNA alignment, RNA annotation, RNA-protein interaction,

37 on, ribosome profiling, RNA-seq analysis and RNA target prediction.

38 Integration of omics data and RNA immunoprecipitation experiments established DGCR8 as

39 Using 4sU RNA labelling and RNA-seq, we show this competition results in reciprocal

40 llected for scanning electron microscopy and RNA sequencing.

41 Here, we used shotgun proteomics, OxICAT and RNA-seq transcriptomics to analyse protein S-mycothiolat

42 gene circuits that combine DNA, protein, and RNA components have demonstrated a range of functions su

43 combined methods of genetics, proteomics and RNA biochemistry, we identified a core set of mRNA m(6)

44 verse transcription (RT) such as RT-qPCR and RNA-Seq.

45 ultiple neurite-targeted non-coding RNAs and RNA-binding proteins with potential regulatory roles.

46 atin immunoprecipitation with sequencing and RNA sequencing, we identify a novel B-lymphoid program f

47 a unique set of non-coding transcripts, and RNAs present at active centromeres are necessary for kin

48 characterization of previously un-annotated RNA transcripts expressed by the spirochete during murin

49 ure analysis, RNA alignment, RNA annotation, RNA-protein interaction, ribosome profiling, RNA-seq ana

50 We developed Yet Another RNA Normalization software pipeline (YARN), that include

51 t study, we test this hypothesis by applying RNA sequencing to CD4(+), CD8(+), and CD19(+) lymphocyte

52 These are then copied as RNA and exported to manufacture new proteins.

53 rlies all secondary genomic analyses such as RNA sequencing (RNA-Seq), chromatin immunoprecipitation,

54 ith other types of experimental data such as RNA-seq or ChIP-seq.

55 luding metabolism and cell cycle, as well as RNA- and protein-modifying enzymes that functionally div

56 43 in the processing of nucleolar-associated RNA.

57 technology is to ligate chromatin-associated RNAs (caRNAs) with their target genomic sequences by pro

58 GreA restarts backtracked RNA polymerase and hence promotes transcription fidelity

59 This direct interaction between RNA polymerase and ribosomes may contribute to the coupl

60 The Ctk1 kinase complex binds RNA in vitro, consistent with direct EF-RNA interaction.

61 r topoisomerase for mRNAs, and requires both RNA binding and catalytic activity to promote neurodevel

62 ic variability is evident between clones, by RNA-sequencing, and at the single-cell level, by RNA-FIS

63 Functional consequences were investigated by RNA studies and on the cellular level using immunofluore

64 sequencing, and at the single-cell level, by RNA-FISH, and is not attributable to differences in repr

65 This removal is controlled in part by RNA-binding proteins that regulate alternative splicing

66 o the expression of all genes transcribed by RNA polymerase II.

67 nscriptomes of individual cells, single-cell RNA sequencing provides unparalleled resolution to study

68 ombine novel mouse reporters and single-cell RNA sequencing to reveal the heterogeneity in IL-4-induc

69 Using single-cell RNA-Seq and multiplexed in situ hybridization, we show h

70 nd their microenvironments using single-cell RNA-seq from 11 primary colorectal tumors and matched no

71 Here, we report that certain RNA template structures and G-rich sequences, ahead of d

72 (2017) demonstrate that endogenous circular RNAs may generate proteins, thereby expanding the eukary

73 gically, the steady-state levels of circular RNAs increased while expression of their associated line

74 as the functions of enhancer RNAs, circular RNAs and chemical modifications to RNA in cellular proce

75 Interest in circulating RNAs for monitoring and diagnosing human health has grow

76 zation of a novel long intergenic non-coding RNA with MyoD-regulated and skeletal muscle-restricted e

77 dentify multiple neurite-targeted non-coding RNAs and RNA-binding proteins with potential regulatory

78 rved regions (T-UCRs) encode long non-coding RNAs implicated in human carcinogenesis.

79 cleotide germ line-specific small non-coding RNAs that have evolutionarily conserved function in mobi

80 MicroRNAs (miRNAs) are small, non-coding RNAs that play critical roles in the post-transcriptiona

81 ly important but not yet standard to combine RNA-centric data and analysis tools with other types of

82 sine (m6A) represents one of the most common RNA modifications in eukaryotes.

83 he unbiased characterization of the complete RNA cargo, including both small- and long-RNAs, in a sin

84 d and accurate structure modeling of complex RNAs.

85 Neuronal protein 3.1 (P311), a conserved RNA-binding protein, represents the first documented pro

86 (cryo-EM) maps of wild type CPMV containing RNA-2, and of naturally-formed empty CPMV capsids.

87 y a set of conserved amino acids that couple RNA and ATP binding to the protein (Motif III).

88 transient cavitation, can be used to deliver RNA to the colonic mucosa of living mice.

89 gests that localization of the APC-dependent RNA subgroup is functionally important for cell migratio

90 ch to specifically mislocalize APC-dependent RNAs suggests that localization of the APC-dependent RNA

91 uencing (RNAseq), we found that host-derived RNAs, most prominently 5S ribosomal RNA pseudogene 141 (

92 cles, about 10 to 15% synthesized detectable RNA.

93 of using a single receptor target to develop RNA aptamers with dual activity for effectively blocking

94 hat recognizes U/AU-rich elements in diverse RNAs through two RNA-recognition motifs, RRM1 and RRM2,

95 s have publicly available, high-quality DNA, RNA, and drug screening data.

96 izes RNA-functionalized AuNPs which form DNA-RNA heteroduplex structures through specific hybridizati

97 mRNA ratios and higher rRNA carryover during RNA-seq analysis.

98 inds RNA in vitro, consistent with direct EF-RNA interaction.

99 A biology, such as the functions of enhancer RNAs, circular RNAs and chemical modifications to RNA in

100 However, the identity of the ex-RNA responsible for the proinflammatory effect remains u

101 In this study, total extracellular RNA (exRNA) was isolated and sequenced from 183 plasma s

102 Extracted data were as follows: RNA or DNA genome, enveloped or not, primary transmissio

103 q, differential gene expression analysis for RNA-seq, nucleosome positioning for MNase-seq, DNase hyp

104 Despite growing evidence for RNA-based regulation in meningococci, their transcriptom

105 uorescence complementation (AiFC) method for RNA imaging by engineering a green fluorescence protein

106 cleavage is a likely point of regulation for RNA editing, we elucidated endonuclease specificity in v

107 ntified transcriptome-wide binding sites for RNA polymerase II and the exosome cofactors Mtr4 (TRAMP

108 ling the importance of metastable states for RNA-based gene regulation.

109 ossible non-pseudoknotted RNA structures for RNA sequences.

110 mic sequences by proximity ligation, forming RNA-DNA chimeric sequences, which are converted to a seq

111 jects, GXD collects and integrates data from RNA in situ hybridization, immunohistochemistry, RT-PCR,

112 ing differentially expressed (DE) genes from RNA sequencing (RNAseq) studies is among the most common

113 irst time the dynamic connection between FTO RNA binding and demethylation activity that influences s

114 Using next-generation RNA sequencing (RNAseq), we found that host-derived RNAs

115 Injection of Cas9-guide RNA-lipid complexes targeting the Tmc1(Bth) allele into

116 using a tetracycline inducible short hairpin RNA targeting TRAF3IP2.

117 ion consequences of expressing short hairpin RNAs (shRNAs).

118 f NR1D1 were knocked down with small hairpin RNAs in human primary macrophages.

119 nificantly reduced HCV infection but not HCV RNA replication.

120 downstream analysis of large, heterogeneous RNA-Seq data sets and we demonstrate its use with data f

121 By contrast, at a high RNA:protein ratio (>/=1:8), the amorphous aggregation of

122 Active NL genes with higher RNA polymerase II (Pol II) recruitment levels tend to di

123 % of proviruses (range: 2-18%) expressed HIV RNA.

124 Plasma and tissue HIV RNA correlated at baseline and when 9-month declines wer

125 aviremic for 7.4 months, rebounding with HIV RNA of 36 copies/mL that rose to 59,805 copies/mL 6 days

126 ate local human immunodeficiency virus (HIV) RNA levels and the risk of sexual HIV transmission.

127 Here, we report that the sensing of IAV RNA by retinoic acid inducible gene I (RIG-I) initiates

128 We describe opportunities and challenges in RNA structural modeling and design, as recently discusse

129 ruses, and papillomaviruses were detected in RNA-seq data, but proportions were similar (P = .73) acr

130 site dT, predicting frequent A-->G errors in RNA with rates of approximately 10(-4) The A-->C, G-->A,

131 important roles of co-opted host proteins in RNA virus replication have been appreciated for a decade

132 outperform other available transcriptomes in RNA-seq analysis.

133 The assessment metrics used in RNA-Puzzles are briefly described.

134 rent research areas of RNA biology including RNA structure analysis, RNA alignment, RNA annotation, R

135 ector portion of the RdDM pathway, including RNA POLYMERASE V (POL V), DOMAINS REARRANGED METHYLTRANS

136 m(7)G cap that promotes rather than inhibits RNA decay.

137 s accumulation of untrimmed piwi-interacting RNA intermediates with 3' end extension, leading to seve

138 1 mutation in mice inhibits piwi-interacting RNA trimming and causes accumulation of untrimmed piwi-i

139 Piwi-interacting RNAs (piRNAs) are 26-30-nucleotide germ line-specific sm

140 severe reduction of mature piwi-interacting RNAs in the testis.

141 Transfection of Sirtuin-1 small interfering RNA prevented hnRNP F stimulation of Foxo3alpha and down

142 ility complex molecules by small interfering RNA targeting of class II transactivator can reduce the

143 uce trans-acting or phased small-interfering RNA (tasiRNA/phasiRNAs).

144 anti-inflammatory drugs or small interfering RNAs (siRNAs) against COX-1 and COX-2, significantly red

145 ANCI (Nkx2.1-associated noncoding intergenic RNA)-Nkx2.1 gene duplex that is essential for buffering

146 ression of coding, noncoding, and intergenic RNAs in the mature mouse brain with RNA-Seq and validati

147 yladenosine (m(6)A) is an essential internal RNA modification that is critical for gene expression co

148 A receptor target (i.e. GluA1/2R) to isolate RNA aptamers that can potentially inhibit both AMPA and

149 roteins, nearly all essential domains of its RNA, and five stably associated auxiliary proteins.

150 We find that analysis of large RNA-Seq data sets requires both careful quality control

151 volumes of sRNAs can differ from some larger RNAs.

152 down-regulation of P311 levels by lentiviral RNA interference reproduced the deficits seen in P311(-/

153 gram, and is therefore termed Linc-RAM (Linc-RNA Activator of Myogenesis).

154 te RNA cargo, including both small- and long-RNAs, in a single library preparation step.

155 llectively, these data reveal that mammalian RNAs can harbor a 5' end modification distinct from the

156 in the 5'-untranslated regions of messenger RNA requires the temporal synchronization of RNA synthes

157 posttranscriptional regulation of messenger RNA targets.

158 eric block ASO that binds the SMN2 messenger RNA and promotes exon 7 inclusion and thus increases ful

159 ive expression levels of four host messenger RNAs, was developed to discriminate critically ill adult

160 Safe and efficient delivery of messenger RNAs for protein replacement therapies offers great prom

161 cently been identified in coding (messenger) RNAs as well.

162 dividual role that each has in mitochondrial RNA biology.

163 We monitored the viral load of MJNV RNA in various tissues of shrews, which would reflect th

164 midite for solid-phase synthesis of modified RNA oligonucleotides.

165 Here, we directly monitor RNA proof-reading by RIG-I and we show that it is contro

166 te that L alone initiates synthesis on naked RNA and that P serves to enhance the initiation and proc

167 effector complexes to complementary nascent RNAs to initiate histone H3 lysine 9 di- and trimethylat

168 located in the intron of the long noncoding RNA (lncRNA) LINC00305 by searching the GWAS database.

169 s of modulation by miRNAs and long-noncoding RNA (lncRNA).

170 rs in the interactome of Xist, the noncoding RNA responsible for X inactivation.

171 Noncoding RNAs (ncRNAs) regulate gene expression in all organisms.

172 The question of how noncoding RNAs are involved in Polycomb group (PcG) and Trithorax

173 Many long noncoding RNAs (lncRNAs) are unstable and rapidly degraded in the

174 dences have demonstrated that long noncoding RNAs (lncRNAs) play important roles in many human diseas

175 ally, sRNAs, originating from long noncoding RNAs, guide Argonaute-containing effector complexes to c

176 A bases are not only found in many noncoding RNAs but have also recently been identified in coding (m

177 The discovery of thousands of noncoding RNAs (ncRNAs) has expanded our view on mammalian genomes

178 gnation of more than 87 predicted "noncoding RNAs" to conventional mRNAs coded by protein-coding gene

179 rotein-coding sequences, producing noncoding RNAs, and even supporting evolution of new protein-codin

180 are evolutionarily conserved small noncoding RNAs that display important physiological effects throug

181 anges in the serum levels of these noncoding RNAs are observed in patients with asymptomatic high-gra

182 technology should facilitate revealing novel RNA functions and their genomic target regions.

183 assembly of ribosomal proteins and numerous RNA structural rearrangements.

184 Numerous RNAs are enriched within cellular protrusions, but the u

185 OTEIN6 (ORRM6) result in the near absence of RNA editing of psbF-C77 and the reduction in accD-C794 e

186 are dedicated to different research areas of RNA biology including RNA structure analysis, RNA alignm

187 Characterizing the binding behaviors of RNA-binding proteins (RBPs) is important for understandi

188 The evolution of RNA-protein regulatory networks is far less understood.

189 XR1P) is a member of the fragile X family of RNA-binding proteins, which includes FMRP and FXR2P.

190 rmation to determine the topological fold of RNA.

191 Biological functions of RNA molecules are dependent upon sustained specific thre

192 il 2007, this field remained in the hands of RNA biologists.

193 Cell-specific labeling of RNA can be profiled and imaged using bioorthogonal chemi

194 to investigate the biophysical mechanisms of RNA folding and unfolding, its interactions with ligands

195 n fragmentation and chemical modification of RNA, rendering it less suitable for analysis by techniqu

196 Posttranscriptional modifications of RNA bases are not only found in many noncoding RNAs but

197 The wide range of RNA-seq applications and their high-computational needs

198 h source of information on the regulation of RNA polymerase activity.

199 xtensive study analysing a broad spectrum of RNA-seq workflows.

200 y DNA was modeled, the tertiary structure of RNA is constrained using an elastic network.

201 pecific three-dimensional (3D) structures of RNA, with or without the help of proteins.

202 RNA requires the temporal synchronization of RNA synthesis and ligand binding-dependent conformationa

203 However, a general understanding of RNA localization has been hindered by a lack of simple,

204 of these modifications and a dynamic view of RNA structure changes with increased numbers of 2-5-link

205 function to be obtained, the availability of RNAs containing this modification at defined positions t

206 tome analysis, an unbiased approach based on RNA sequencing of resistant subclones, to discover the m

207 sequencing confirmed the effect of hDBR1 on RNA splicing, and metabolite profiling supported the obs

208 fluorescence protein (GFP)-mimicking turn-on RNA aptamer, Broccoli, into two split fragments that cou

209 nfectious virion assembly, ensuring that one RNA dimer is packaged into each nascent virion.

210 -induced nucleosome intermediates using only RNA Polymerase.

211 agnostic (CRISPR-Dx), providing rapid DNA or RNA detection with attomolar sensitivity and single-base

212 Loss-of-function mutations in ORGANELLE RNA RECOGNITION MOTIF PROTEIN6 (ORRM6) result in the nea

213 Overall, RNA sequencing analysis revealed that transcriptomes dur

214 We then performed RNA sequencing to investigate the effect of E2f3a overex

215 We performed RNA-seq on purified peripheral afferent neurons, but fou

216 a plausible structural element in prebiotic RNAs.

217 chromatin in the regulation of premessenger RNA (pre-mRNA) splicing.

218 We extended previous RNA-sequencing and produced a comprehensive annotated tr

219 rate estimated from mistakes in end product RNAs is 10-3-10-5.

220 RNA-protein interaction, ribosome profiling, RNA-seq analysis and RNA target prediction.

221 measurements reveal rapid changes in protein-RNA interactions within 1 min following stress impositio

222 er to compute all possible non-pseudoknotted RNA structures for RNA sequences.

223 onal applications for these small regulatory RNAs in AML.

224 -derived RNAs, most prominently 5S ribosomal RNA pseudogene 141 (RNA5SP141), bound to RIG-I during in

225 its, enable bacterial and archaeal ribosomal RNA gene sequences to be followed across multiple studie

226 or many positive-sense single-stranded RNA (+RNA) viruses including human pathogens hepatitis C virus

227 interaction between positive-strand RNA [(+)RNA] viruses and cellular membranes that contribute to t

228 gh-resolution crystal structures of the same RNA duplex containing four and eight 2-5-linkages at dif

229 Large-scale RNA-binding pockets on protein surfaces are grouped by m

230 The data generated by sci-RNA-seq constitute a powerful resource for nematode biol

231 ions that govern assembly of other segmented RNA viruses.

232 All viruses with positive-sense RNA genomes replicate on membranous structures in the cy

233 e compared using next-generation sequencing (RNA-Seq).

234 ary genomic analyses such as RNA sequencing (RNA-Seq), chromatin immunoprecipitation, and ribosome pr

235 g exome sequencing, whole-genome sequencing, RNA-seq, ChIP-seq, targeted sequencing and single-cell w

236 increased binding of total and phospho-Ser2 RNA polymerase II specifically at the intron retained un

237 t need in rapid, reliable detection of short RNA regions which could open up new opportunities in tra

238 Using chemically synthesized short RNA corresponding to the first 19 nucleotides (nt) of th

239 uses, paving the way for delineating similar RNA-RNA interactions that govern assembly of other segme

240 raining samples, we propose to use simulated RNA-seq datasets to train our model.

241 In this approach, single RNA molecules captured by the nanopore can freely fold f

242 mation was associated with low levels of SIV RNA in the brain as shown by in situ hybridization, and

243 chanism of action and show that mobile small RNAs generate sharply defined domains of target gene exp

244 ome structure and output of regulatory small RNAs (sRNAs) are incompletely understood.

245 Little is known about these small RNAs in litchi (Litchi chinensis), an economically impor

246 They can catalyze site-specific RNA cleavage, and as a result, they have relevance in ge

247 ed protein fold found in several plus-strand RNA viruses that binds to the small molecule ADP-ribose.

248 e on the interaction between positive-strand RNA [(+)RNA] viruses and cellular membranes that contrib

249 ctor for many positive-sense single-stranded RNA (+RNA) viruses including human pathogens hepatitis C

250 Double-stranded RNAs (dsRNA) produced during human cytomegalovirus (HCMV

251 R-Cas13a as a flexible platform for studying RNA in mammalian cells and therapeutic development.

252 7 achieved SVR and had at least 1 subsequent RNA measurement.

253 anscriptionally regulates the fate of target RNAs.

254 We here show that RNA editing is particularly common in behaviorally sophi

255 The RNA binding protein, LARP1, has been proposed to functio

256 The RNA polymerase II (Pol II) transcription elongation fact

257 ors, the antibody gene deaminase AID and the RNA/DNA editing enzyme APOBEC1 (A1).

258 novel method (RS3D) that can assimilate the RNA secondary structure information, small-angle X-ray s

259 nt idea of pseudoalignment introduced in the RNA-Seq context is highly applicable in the metagenomics

260 f RBPs, including the binding effects of the RNA helicase MOV10 on mRNA degradation, the potentially

261 lustrate that the secondary structure of the RNA molecule-and its absence-plays an essential role in

262 polymerase responsible for synthesis of the RNA primers that are elongated by the replicative DNA po

263 Interestingly, knockdown of the RNA surveillance nuclease, Xrn1, and members of the CCR4

264 eraction between a peripheral element of the RNA that forms a T-loop module and a subset of nucleotid

265 hat the act of transcription rather than the RNA product itself is functionally important in many cas

266 Functional analysis found that the RNA structure in MYB33 correlated with strong silencing

267 raction with a combinatorial approach to the RNA folding problem in order to compute all possible non

268 Whereas the RNA-guided CRISPR interference mechanism varies widely a

269 3 mRNA to a shorter ALE isoform of which the RNA, rather than an encoded protein, is critical for the

270 These RNA-guided nucleases are powerful weapons in the fight a

271 This RNA is found throughout much of the bacterial domain of

272 Through RNA-Seq analyses, we identified 137 genes that are missi

273 on and tissue response were assessed through RNA sequencing.

274 Thus, RNA synthesis by even a single, uncoated particle can in

275 novel, computationally tractable approach to RNA-ligand kinetics, we overcome the two main difficulti

276 applying a gradient-based coarse graining to RNA-ligand systems and solving the process in a pseudo-f

277 circular RNAs and chemical modifications to RNA in cellular processes.

278 g signals from transcriptional regulators to RNA polymerase II in eukaryotes.

279 Total RNA extracted from plasma-derived EXOs of 12 T1DM and 12

280 se embryos and performed whole transcriptome RNA sequencing analyses.

281 d changes in the keratinocyte transcriptome, RNAs isolated from undifferentiated and differentiated c

282 at SIDT1 and SIDT2 not only do not transport RNA, but they are involved in cholesterol transport.

283 dae) are enveloped negative-sense tripartite RNA viruses.

284 ng suggests that the folding path of twister RNA requires proper orientation of the substrate prior t

285 AU-rich elements in diverse RNAs through two RNA-recognition motifs, RRM1 and RRM2, and post-transcri

286 ns illustrates the recognition of unbranched RNA stem loops.

287 each case, we analyzed gene expression using RNA sequencing and assessed differences between conditio

288 d this, we investigated transcriptomes using RNA-seq and amino acid levels with N treatment in tea (C

289 Moreover, no such study has utilized RNA derived from bacterial biofilms, which have potentia

290 The method utilizes RNA-functionalized AuNPs which form DNA-RNA heteroduplex

291 Extensive ex vivo analysis was performed via RNA analysis, Western blot, and histology.

292 specific interactions between Gag and viral RNA are required for the enhancement of particle product

293 vious hypothesis that specific dimeric viral RNA-Gag interactions are the nucleation event of infecti

294 hich included detection of hepatitis D virus RNA among anti-hepatitis D virus seropositive participan

295 ication and transcription of influenza virus RNA.

296 vs. freshwaters), and nucleic acids (DNA vs. RNA), suggesting niche differentiation.

297 ll lines was subjected to transcriptome-wide RNA sequencing analysis.

298 Riboswitches are widespread RNA motifs that regulate gene expression in response to

299 tergenic RNAs in the mature mouse brain with RNA-Seq and validation with independent methods.

300 al proposed that an interaction between Xist RNA and Lamin B receptor (LBR) is necessary and sufficie

301 centiles for the time until the loss of ZIKV RNA detection were 14 days (95% confidence interval [CI]