ライフサイエンスコーパス: single-stranded RNA

1 RNA and how this differs from its action on single-stranded RNA.

2 r by preventing the association of Dbp2 with single-stranded RNA.

3 are monomers that induce tight compaction of single-stranded RNA.

4 uble-stranded DNA, type III complexes target single-stranded RNA.

5 alone (apo) and in complex with a nonameric single-stranded RNA.

6 bits growth by sequence-specific cleavage of single-stranded RNA.

7 ding preferences of NPH-II for duplex versus single-stranded RNA.

8 equential packaging of its three segments of single-stranded RNA.

9 he respective RNA structures, and amounts of single-stranded RNA.

10 age large, defined fragments of its genomic, single-stranded RNA.

11 ith a wide range of sequences and lengths of single-stranded RNA.

12 entially involved TLR7 and TLR8, which sense single-stranded RNA.

13 ng others responsible for the recognition of single-stranded RNA.

14 esis is potently inhibited by the binding of single-stranded RNA.

15 kinase is not activated by and does not bind single-stranded RNA.

16 the Grc3 kinase activity exclusively toward single-stranded RNA.

17 ressed the basic physical properties of long single-stranded RNAs.

18 disposes of or processes viral and cellular single-stranded RNAs.

19 a segmented genome of eight negative-sense, single-stranded RNAs.

20 gher affinity to SL3 RNA than to double- and single-stranded RNAs.

21 ucture remained unaffected by titration with single-stranded RNAs.

22 e RNase L, causing it to dimerize and cleave single-stranded RNAs.

23 the 5'-phosphate and 3'-hydroxyl termini of single-stranded RNAs.

24 Single-stranded RNAs also activate PKR constructs lackin

25 xygen species, NOX2 oxidase, is activated by single stranded RNA and DNA viruses in endocytic compart

26 ows direct visualization of the encapsidated single-stranded RNA and coat protein (CP) N-terminal reg

27 AtRNase J degraded single-stranded RNA and DNA molecules but displays limit

28 he pre-steady-state P(i) release kinetics on single-stranded RNA and DNA substrates of different leng

29 Sen1-HD binds single-stranded RNA and DNA with similar affinity in the

30 rified human PRC2 recognizes G > C,U >> A in single-stranded RNA and has a high affinity for folded g

31 ct sensitivity to pyrimidine-rich regions of single-stranded RNA and is able to process tRNA precurso

32 dered to be linked to the affinity of S1 for single-stranded RNA and its corresponding destabilizatio

33 association was dependent on the presence of single-stranded RNA and mediated by an N-terminal region

34 exit channel, extruding topologically linked single-stranded RNA and preventing the formation of paus

35 ts showed that both SUD-C and SUD-MC bind to single-stranded RNA and recognize purine bases more stro

36 aded from the periphery, TLR7 detected viral single-stranded RNA and triggered immune responses that

37 and mutational analyses show how it threads single-stranded RNA, and structural features suggest how

38 itor the in vitro co-assembly of CCMV CP and single-stranded RNA as a function of the strength of CP-

39 ed and characterized two R-plasmid-dependent single-stranded RNA bacteriophages (RPD ssRNA phages), C

40 In single-stranded RNA bacteriophages (ssRNA phages) a sing

41 Single-stranded RNA bacteriophages (ssRNA phages) infect

42 P L binding were blocked by preannealing the single-stranded RNA bait with miR-122, indicating that t

43 We find single-stranded RNA bases are more chromatin-associated,

44 Here, we demonstrate that single-stranded RNAs bind to PKR with micromolar dissoci

45 tion motif, domains are the largest class of single-stranded RNA binding domains in the human proteom

46 aspects of cellular biology through binding single-stranded RNA binding motifs (RBMs).

47 s a protein conformational change induced by single-stranded RNA binding.

48 In addition to sequence-independent single-stranded RNA-binding and helix-destabilizing acti

49 nd we demonstrate that the complex possesses single-stranded RNA-binding capability.

50 equence specifically to mRNA targets using a single-stranded RNA-binding domain comprising eight Pumi

51 Phylogenetic analyses revealed that the single-stranded RNA-binding domain is exclusively found

52 his gene modifier screen identified EndoU, a single-stranded RNA-binding protein of ancient origin, a

53 The composite double-stranded/single-stranded RNA-binding region assembles cooperative

54 binding miRNAs function as agonists of these single-stranded RNA-binding TLRs, leading to NF-kappaB s

55 NP both RNA free and a tetrameric form with single-stranded RNA bound.

56 ate that M. tuberculosis RpsA interacts with single stranded RNA, but not with POA.

57 Unlike double-stranded DNA, single-stranded RNA can be spontaneously packaged into s

58 Top3beta is capable of converting two such single-stranded RNA circles into a double-stranded RNA c

59 olism, we designed an assay by annealing two single-stranded RNA circles with complementary sequences

60 The 21-23 nucleotide, single-stranded RNAs classified as microRNAs (miRNA) per

61 structures of apo-D1D2 and post-unwound D1D2:single-stranded RNA complex, and the structure of a D2:d

62 If potent single-stranded RNAs could be identified, they would pro

63 The global epidemic of the single stranded RNA Deformed wing virus (DWV), driven by

64 tion that is distinct from its RNA-activated single-stranded RNA degradation activity.

65 Pase, one of the major enzymes with 3' to 5' single-stranded RNA degradation and processing activitie

66 On the other hand, Cap-0 and 5'ppp single-stranded RNAs did not bind RIG-I and are signalin

67 tably improved module for building models of single-stranded RNA, double-helical DNA, Pauling triplex

68 the HIV-1 genome, which is in the form of a single-stranded RNA enclosed inside a capsid shell, must

69 SIVmac251 single-stranded RNA encoded several uridine-rich sequenc

70 Human astroviruses are single-stranded RNA enteric viruses that cause a spectru

71 pared with plasmacytoid DCs in response to a single-stranded RNA equivalent.

72 sslinks to specific regions characterized by single-stranded RNA flanked by structured elements and t

73 West Nile virus (WNV), a mosquito-borne, single-stranded RNA flavivirus, causes significant human

74 S1 promotes RNA unwinding by binding to the single-stranded RNA formed transiently during the therma

75 l protocols, one involving direct capture of single-stranded RNA fragments and one involving circular

76 eceptor 8 (TLR8) recognizes pathogen-derived single-stranded RNA fragments to trigger innate and adap

77 NA copying to proceed, while also protecting single-stranded RNA from Mg(2+)-catalyzed degradation.

78 ifferential scanning calorimetry showed that single-stranded RNA from satellite tobacco mosaic virus

79 nsation and found that ectopic expression of single-stranded RNAs from 1.688(X) repeats enhanced the

80 The virus possesses a negative-sense single-stranded RNA genome of approximately 13.3 kb enca

81 s C, platelets replicated the positive sense single-stranded RNA genome of DENV by up to approximatel

82 virus particles containing a negative-sense, single-stranded RNA genome packaged within a helical nuc

83 The virus has a negative-sense, single-stranded RNA genome that is encapsidated by the n

84 idae family of nonsegmented, negative-sense, single-stranded RNA genome viruses, is a leading cause o

85 hich the nucleoprotein (NP) encapsidates the single-stranded RNA genome.

86 mall enveloped viruses with a positive-sense single-stranded RNA genome.

87 s (STMV) is a T = 1 icosahedral virus with a single-stranded RNA genome.

88 (HIV-1) is a retrovirus with a ten-kilobase single-stranded RNA genome.

89 ining feature of these viruses is that their single-stranded RNA genomes are of opposite polarity to

90 Leviviruses are bacteriophages with small single-stranded RNA genomes consisting of 3-4 genes, one

91 Bearing the largest single-stranded RNA genomes in nature, coronaviruses are

92 uses replicate by reverse transcribing their single-stranded RNA genomes into double-stranded DNA usi

93 They have positive-sense, single-stranded RNA genomes, and the mechanism(s) by whi

94 HIV and related primate lentiviruses possess single-stranded RNA genomes.

95 ll non-enveloped viruses with positive-sense single-stranded RNA genomes.

96 nonenveloped icosahedral virions containing single-stranded RNA genomes.

97 ase, P4, uses chemical energy to translocate single-stranded RNA genomic precursors into the procapsi

98 Toll-like receptor (TLR), a ligand for single-stranded RNA, has been implicated in the developm

99 Natural single-stranded RNAs have not been reported to activate

100 ch is valid with a culturable positive-sense single-stranded RNA human virus, coxsackievirus B5, by a

101 iviral immune responses by recognizing viral single-stranded RNA in endosomes, but the biosynthetic p

102 ce upon binding with double-stranded DNA and single-stranded RNA in live cells, thereby enabling real

103 hat the NTD possesses the capability to bind single-stranded RNA in solution.

104 rchange in the average probabilities to form single-stranded RNA in the optimal PPT and branch site l

105 al infections and cleaves cellular and viral single-stranded RNAs, including rRNAs in ribosomes.

106 In contrast, HCV single-stranded RNAs, including those derived from the s

107 Moreover, L-RNA complex formation depends on single-stranded RNA, indicating that inter-termini dsRNA

108 the transcription of the relatively flexible single-stranded RNA into a more rigid filamentous struct

109 e reconstruction, suggests that Rsr channels single-stranded RNA into the PNPase cavity.

110 l functional effects from a seemingly simple single-stranded RNA junction and suggest that junction s

111 We have investigated the role of a single-stranded RNA junction, J1/2, that connects the su

112 se testes, most piRNAs are derived from long single-stranded RNAs lacking annotated open reading fram

113 with or without a 5'-triphosphate (ppp), by single-stranded RNA marked by a 5'-ppp and by polyuridin

114 of stroke-inducible tRF-22-WE8SPOX52 using a single-stranded RNA mimic induced down-regulation of imm

115 e KWKK ((+)NH(3)-Lys-Trp-Lys-Lys-NH(2)) to a single-stranded RNA model, polyuridylate (polyU), by cha

116 We show a single-stranded RNA molecule that is antisense to the E-

117 The hepatitis C virus (HCV) genome is a single-stranded RNA molecule.

118 As (miRNAs) are small (20-23 nt), non-coding single stranded RNA molecules that act as post-transcrip

119 s due to RNase T2's preferential cleavage of single-stranded RNA molecules between purine and uridine

120 Single-stranded RNA molecules fold into extraordinarily

121 70) is a demethylase that removes m(6)A from single-stranded RNA molecules in vitro.

122 (CCMV) is capable of packaging both purified single-stranded RNA molecules of normal composition (com

123 inflammatory condition, is a class of short single-stranded RNA molecules termed microRNAs (miRNAs).

124 MicroRNAs (miRNAs) are naturally occurring single-stranded RNA molecules that post-transcriptionall

125 MicroRNAs (miRNAs) are a class of short single-stranded RNA molecules that posttranscriptionally

126 (miRNA) are a novel class of small noncoding single-stranded RNA molecules that regulate gene express

127 microRNAs (miRNAs) are short, single-stranded RNA molecules that silence genes via the

128 amer, whose interaction depended mainly on a single-stranded RNA motif, but not that of the GFP aptam

129 glia of live zebrafish brains, we found that single-stranded RNA of bacterial origin acts as a PAMP a

130 e junction between the stem and the flanking single-stranded RNA of the pri-miRNA hairpin by DGCR8 fo

131 se H activity that act in concert to convert single-stranded RNA of the viral genome to double-strand

132 olutions containing the coat protein and the single-stranded RNA of the virus.

133 We also present modelling of pyrimidine-rich single-stranded RNA onto the highly conserved surface of

134 Aptamers are single-stranded RNA or DNA molecules that have recently

135 e RdRp can initiate de novo from the ends of single-stranded RNA or extend a primed RNA template.

136 st resiquimod (R848; a synthetic analogue of single-stranded RNA) or saline by nasal spray to healthy

137 8 may be activated by their native ligands, single-stranded RNA, or by small molecules of the imidaz

138 viruses distantly related to members of the single-stranded RNA picorna-like virus superfamily were

139 A bacteriophage Phi6, and the positive-sense single-stranded RNA poliovirus (PV) and human rhinovirus

140 roRNAs originate from a stem-loop structured single-stranded RNA precursor.

141 rom the s(2)U-induced preorganization of the single-stranded RNA prior to hybridization.

142 isms that are different from the established single-stranded RNA recognition mode of PPR motifs.

143 ependent RNA endonuclease activity targeting single-stranded RNA regions and demonstrate the function

144 ome, we accurately and simultaneously mapped single-stranded RNA regions in multiple ncRNAs with know

145 ur NMR spectroscopic investigations on short single-stranded RNA revealed a strong preference for C2'

146 ssential host factor for many positive-sense single-stranded RNA (+RNA) viruses including human patho

147 A virus (IAV) genomes are composed of eight single-stranded RNA segments that are coated by viral nu

148 6) and identified two conserved, putatively single-stranded RNA segments, upstream of S1 (nt 2 and 3

149 bp) and small (S) (1608 bp) negative sense, single-stranded RNA segments.

150 ssociated protein that is proposed to confer single-stranded RNA selectivity.

151 ysis of Simple sequences (MIDAS) to identify single-stranded RNA sequences bound by KH domains.

152 KH0, KH1, and KH2 domains bind weakly to the single-stranded RNA sequences suggesting that they may h

153 tures known for their modular recognition of single-stranded RNA sequences with each motif in a tande

154 s of Mss116p in complex with ATP analogs and single-stranded RNA show that the helicase core induces

155 ific and selective recognition of dsRNA over single-stranded RNA (ssRNA) and dsDNA regions at near-ph

156 report the asymmetric reconstruction of the single-stranded RNA (ssRNA) content in one of the three

157 Higher ratios of HCV double-stranded to single-stranded RNA (ssRNA) correlated positively with I

158 show that topological structures containing single-stranded RNA (ssRNA) free of strong base pairing

159 RVFV has a trisegmented single-stranded RNA (ssRNA) genome.

160 Viruses in the Tombusviridae family have single-stranded RNA (ssRNA) genomes with T=3 icosahedral

161 ata from a competition assay between SLA and single-stranded RNA (ssRNA) indicate that SLA competes w

162 ndicates that small phages, particularly the single-stranded RNA (ssRNA) leviviruses, have a previous

163 All RNA interference pathways use small single-stranded RNA (ssRNA) molecules that guide protein

164 A ligase to capture various short 20-24 base single-stranded RNA (ssRNA) oligonucleotides from a targ

165 The recent discovery of the positive-sense single-stranded RNA (ssRNA) Orsay virus (OV) as a natura

166 ose genome is packaged sequentially as three single-stranded RNA (ssRNA) segments into an icosahedral

167 ) binds with 20nM dissociation constant to a single-stranded RNA (ssRNA) sequence adjacent to the bra

168 d protein structures are the active sites of single-stranded RNA (ssRNA) synthesis; (v) at late times

169 e show that Cas9 binds with high affinity to single-stranded RNA (ssRNA) targets matching the Cas9-as

170 ed rotavirus double-layer particles, nascent single-stranded RNA (ssRNA) transcripts (termed in vitro

171 ontal gene transfer may have occurred from a single-stranded RNA (ssRNA) virus (hypovirus) to a dsRNA

172 mes and primarily correspond to unclassified single-stranded RNA (ssRNA) viruses and viruses belongin

173 or Cas13 could be an effective antiviral for single-stranded RNA (ssRNA) viruses because it programma

174 ly for adenoviruses, which resembles that of single-stranded RNA (ssRNA) viruses but differs from the

175 Single-stranded RNA (ssRNA) viruses form a major class t

176 While most T=3 single-stranded RNA (ssRNA) viruses package in vivo abou

177 h pump their genome into a preformed capsid, single-stranded RNA (ssRNA) viruses, such as bacteriopha

178 Single-stranded RNA (ssRNA) viruses, which include major

179 en the rates of double-stranded DNA (dsDNA), single-stranded RNA (ssRNA), and ssDNA/reverse-transcrib

180 recognizes guanosine- and uridine-rich viral single-stranded RNA (ssRNA), including influenza virus s

181 zyme Argonaute 2 (hAgo2) and Cryptosporidium single-stranded RNA (ssRNA), we induced specific slicing

182 x measures either ~22 nt from the upper stem-single-stranded RNA (ssRNA, terminal loop) junction or ~

183 ruses, especially those with positive-sense, single-stranded RNA (+ssRNA) genomes, are abundant in tr

184 important roles in inhibiting positive-sense single-stranded RNA (+ssRNA) viral infection, especially

185 les, viruses with a genome of negative-sense single-stranded RNA (-ssRNA).

186 perform similar roles in the positive-sense, single-stranded RNA [ssRNA(+)] arteriviruses.

187 CCHF) virus is a tick-borne, negative-sense, single-stranded RNA [ssRNA(-)] nairovirus that produces

188 sent in all three pathogenic positive-sense, single-stranded RNA [(+)ssRNA] virus families which carr

189 Because replication of positive-sense single-stranded RNA [(+)ssRNA] viruses requires the imme

190 ncoming viral genome, whereas negative-sense single-stranded RNA [(-)ssRNA] viruses carry at infectio

191 cinating features of these highly structured single stranded RNAs (ssRNAs) with emphasis on their pre

192 Single-stranded RNAs (ssRNAs) are ubiquitous RNA element

193 Here we demonstrate that wild-type FUS binds single-stranded RNA stoichiometrically in a length-depen

194 i YbeY exhibits endoribonuclease activity on single-stranded RNA substrate but not on the double-stra

195 w that Rho unidirectionally translocates the single-stranded RNA substrate via a population shift of

196 ystems direct interference complexes against single-stranded RNA substrates.

197 Disordered homopolymeric regions of single-stranded RNA, such as U or A tracts, are found wi

198 minus resemble those seen in the presence of single-stranded RNA suggesting similarities in binding.

199 signaling induced by NOD2 over-expression or single stranded RNA, suggesting specificity for the MDP-

200 strand scission in double-stranded RNA over single-stranded RNA suggests that this chemistry may be

201 lex RNA regardless of the orientation of the single-stranded RNA tail, it preferred a 5' to 3' polari

202 e CRISPR RNA and can be programmed to cleave single-stranded RNA targets carrying complementary proto

203 a unique biochemical activity: the use of a single-stranded RNA template for the synthesis of single

204 es the ability of VP1 to replicate synthetic single-stranded RNA templates containing the 3' untransl

205 red in the presence of substrate analogs and single-stranded RNA templates.

206 the HCV helicase moves with a faster rate on single stranded RNA than on DNA.

207 23S rRNA are helices 90-92 and the adjacent single stranded RNA that encompasses A2503.

208 roRNAs (miRNAs) are small approximately 22nt single stranded RNAs that negatively regulate protein ex

209 MicroRNA are small, non-coding, single-stranded RNAs that are estimated to regulate ~60%

210 Circular RNAs (circRNAs) are single-stranded RNAs that are joined head to tail with l

211 MicroRNAs (miRNAs) are short, single-stranded RNAs that modulate protein expression as

212 NAs (miRNAs) are 19 to 25nt non-coding small single-stranded RNAs that negatively regulate gene expre

213 Microribonucleic acids (RNAs; miRNAs), single-stranded RNAs that typically function as posttran

214 unusually long, high-affinity interface with single-stranded RNA, that this interface provides a func

215 Although endosomal TLR7 recognizes single-stranded RNAs, their endogenous RNA ligands have

216 e also show that TRBP can bind 21-nucleotide single-stranded RNAs, though with far lower affinity tha

217 capsidation and reverse transcription from a single-stranded RNA to a double-stranded DNA through the

218 MthRnl) catalyzes intramolecular ligation of single-stranded RNA to form a closed circular RNA via co

219 Single-stranded RNA transcripts induced interferon-beta

220 ed by the complementary association of three single-stranded RNA units, was optimized for improved ge

221 with 10-bp RNA-RNA duplexes and was aided by single-stranded RNA upstream of the duplex but was signi

222 he strength of attraction between CP and the single-stranded RNA viral genome is controlled by ionic

223 Rather, single-stranded RNA viral genomes bearing 5'-triphosphat

224 ributes to the innate immune response during single-stranded RNA viral infection.

225 It is a single stranded (-)RNA virus with a segmented genome.

226 ruses, and Bromo Mosaic Virus (BMV), a T = 3 single stranded RNA virus.

227 Previously, a stochastic model of single-stranded RNA virus assembly was created to model

228 Rift Valley fever virus (RVFV) is a single-stranded RNA virus capable of inducing fatal hemo

229 is E virus (HEV) is a 7.2-kb positive-sense, single-stranded RNA virus containing three partially ove

230 Bacteriophage MS2 is a positive-sense, single-stranded RNA virus encapsulated in an asymmetric

231 Drosophila, encapsidates one of the largest single-stranded RNA virus genomes known.

232 arainfluenza virus (PIV) is a negative-sense single-stranded RNA virus in the Paramyxoviridae family.

233 proach that accurately tracks positive-sense single-stranded RNA virus inactivation without relying o

234 xin (EMR) family have been shown to modulate single-stranded RNA virus infection through regulating s

235 netics and mechanisms of inactivation of the single-stranded RNA virus MS2 under temperature, pH and

236 ect experimental evidence that assembly of a single-stranded RNA virus occurs via a packaging signal-

237 amyxovirus type 1 (APMV-1), a negative-sense single-stranded RNA virus of the genus Avulavirus, famil

238 ry syncytial virus (RSV) is a negative-sense single-stranded RNA virus responsible for lower respirat

239 ry syncytial virus (RSV) is a negative-sense single-stranded RNA virus responsible for lower respirat

240 Ebola virus (EBOV) is an enveloped, single-stranded RNA virus that can cause Ebola virus dis

241 Human respiratory syncytial virus (RSV) is a single-stranded RNA virus that causes acute, and occasio

242 Influenza is a negative-sense single-stranded RNA virus that encodes its own RNA-depen

243 With Coxsackievirus B3 (CVB3) being a single-stranded RNA virus, and the recent evidence that

244 d the RNA content of a purified nonenveloped single-stranded RNA virus, flock house virus (FHV).

245 Vesicular stomatitis virus, a single-stranded RNA virus, triggers activation of the se

246 families, and an unclassified positive-sense single-stranded RNA virus.

247 boo mosaic virus (BaMV) is a positive-sense, single-stranded RNA virus.

248 or the replication of various positive-sense single stranded RNA viruses, which hijack this cellular

249 ) susceptibility compared with other enteric single-stranded RNA viruses (e.g., Echovirus 12, feline

250 In contrast, single-stranded RNA viruses assemble their coat proteins

251 n is a common strategy among positive-sense, single-stranded RNA viruses for bypassing the host cell

252 Single-stranded RNA viruses have been thought to encapsi

253 he members of this family of positive-sense, single-stranded RNA viruses have limited coding capacity

254 The current paradigm for assembly of single-stranded RNA viruses is based on a mechanism invo

255 potentially profound implications for other single-stranded RNA viruses known to have RNA PSs, inclu

256 that the screened ISGs target positive-sense single-stranded RNA viruses more effectively than negati

257 Single-stranded RNA viruses package their genomes into c

258 As part of their life cycle some single-stranded RNA viruses remodel host cytoplasmic mem

259 Flaviviruses are positive-sense, single-stranded RNA viruses responsible for millions of

260 Many single-stranded RNA viruses self-assemble their protein

261 eny, experimental evidence on positive sense single-stranded RNA viruses suggests that the CP also re

262 y of enveloped, negative-sense, nonsegmented single-stranded RNA viruses that account for a significa

263 s (HAstVs) are nonenveloped, positive-sense, single-stranded RNA viruses that are a leading cause of

264 Flaviviruses are single-stranded RNA viruses that cause a wide range of i

265 Astroviruses are small, nonenveloped, single-stranded RNA viruses that cause diarrhea in a wid

266 stroviruses are nonenveloped, positive-sense single-stranded RNA viruses that cause gastrointestinal

267 Noroviruses (NoVs) are single-stranded RNA viruses that infect host organisms v

268 link between platelets and their response to single-stranded RNA viruses that involves activation of

269 s) comprise a large genus of positive-sense, single-stranded RNA viruses whose members cause a number

270 Caliciviruses are single-stranded RNA viruses with 180 copies of capsid pr

271 Alphaviruses are a group of single-stranded RNA viruses with genomes of positive pol

272 a large family of enveloped, negative-sense, single-stranded RNA viruses with significant economic an

273 Like other single-stranded RNA viruses, CMV is known to have a high

274 We found that during sickness behavior, single-stranded RNA viruses, double-stranded RNA ligands

275 During the life cycle of many single-stranded RNA viruses, including many human pathog

276 ite the threat to human health posed by some single-stranded RNA viruses, little is understood about

277 Alphavirus consists of a group of enveloped, single-stranded RNA viruses, many of which are transmitt

278 ation of selected nonenveloped and enveloped single-stranded RNA viruses, retroviruses, bacteriophage

279 ic arthropod-borne viruses (arboviruses) are single-stranded RNA viruses, the most common of which in

280 ve roles of viral genomes in the assembly of single-stranded RNA viruses, we have developed a new ana

281 A large number of single-stranded RNA viruses, which form a major class of

282 ons per site per day, which is comparable to single-stranded RNA viruses.

283 viruses more effectively than negative-sense single-stranded RNA viruses.

284 tudied as a model system for the assembly of single-stranded RNA viruses.

285 organization and apply it to the genomes of single-stranded RNA viruses.

286 which consists of icosahedral, nonenveloped, single-stranded RNA viruses.

287 ovel therapeutic approach against pathogenic single-stranded RNA viruses.

288 ity of identified viruses are positive-sense single-stranded RNA viruses.

289 omically important plant and animal positive single-stranded RNA viruses.IMPORTANCE Uncapped viral RN

290 small, spherical, enveloped, positive-sense, single-stranded, RNA viruses responsible for considerabl

291 Contaminating, single-stranded RNA was precipitated using 4.0 M Lithium

292 structural homology, wild-type MAB21L2 bound single-stranded RNA, whereas this activity was lost in a

293 DNA data is transcribed into single-stranded RNA, which folds into specific molecular

294 roaches for estimating hydrodynamic radii of single-stranded RNAs, which use generic RNA structure pr

295 PCBP2, IGF2BP1, and hnRNP L bound single-stranded RNA, while DHX9, ADAR1, and NF90 bound a

296 c SAMHD1 was found to bind preferentially to single-stranded RNA, while the tetrameric form required

297 These viruses are positive-sense single-stranded RNA with a genome of ~7 to 8 kb, and wer

298 N binds nonspecifically to single-stranded RNA with nanomolar affinity.

299 Circular RNAs (circRNAs) are a class of single-stranded RNAs with a contiguous structure that ha

300 It displays unusual specificity in vitro for single-stranded RNAs with at least one adenosine at the