ライフサイエンスコーパス: single-stranded RNA

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

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

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

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

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

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

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

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

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

10 replicative intermediate is represented by a single-stranded RNA.

11 ize the duplex by preferentially binding the single-stranded RNA.

12 ression and/or function of TLR7, a sensor of single-stranded RNA.

13 inding domain confers a general affinity for single-stranded RNA.

14 Argonaute-bound siRNA duplex is converted to single-stranded RNA.

15 dynamic behavior from binding to the random single-stranded RNA.

16 nick and degrade linear as well as circular single-stranded RNA.

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

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

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

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

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

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

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

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

25 tic Hen1 in their ability to methylate small single-stranded RNAs.

26 f these arises by Piwi-catalysed cleavage of single-stranded RNAs.

27 rimer-independent RNA polymerase activity on single-stranded RNAs.

28 generating double-stranded RNA from specific single-stranded RNAs.

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

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

31 the single-stranded DNA Microviridae and the single-stranded RNA Alloleviviridae, accomplish lysis by

32 Single-stranded RNAs also activate PKR constructs lackin

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

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

35 rocessive DExH group often translocate along single-stranded RNA and displace paired strands (or prot

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

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

38 in higher-order structured RNA that contains single-stranded RNA and dsRNA.

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

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

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

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

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

44 Single-stranded RNA and TLR7 generated the most potent e

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

46 x binds nucleic acids, with a preference for single-stranded RNA, and the Tex S1 domain is required f

47 Viral and synthetic single-stranded RNAs are the ligands for Toll-like recep

48 e RISC using pre-miRNAs or long unstructured single stranded RNAs as guides.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 that RNase BN is active on both double- and single-stranded RNA but that duplex RNA is preferred.

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

67 ns and nucleotide-dependent tight binding of single-stranded RNAs by the RNA helicase core.

68 ed molecular patterns, including double- and single-stranded RNA, by pattern recognition receptors in

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

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

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

72 an component has little or no influence over single-stranded RNA cleavage, RI evasion or cytotoxicity

73 response to cytosolic double-stranded RNA or single-stranded RNA containing 5'-triphosphate (5'-ppp).

74 ne motif to mediate high-affinity binding to single-stranded RNAs containing the transcriptional regu

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

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

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

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

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

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

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

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

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

84 m in length and with a width consistent with single-stranded RNA following metal coating.

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

86 he target duplex from truncated duplexes and single-stranded RNA forms.

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

88 Male-specific single-stranded RNA (FRNA) coliphages belong to the fami

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

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

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

92 re critical for reverse transcription of the single-stranded RNA genome into double-stranded DNA.

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

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

95 talyses a series of reactions to convert the single-stranded RNA genome of HIV into double-stranded D

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

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

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

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

100 ensity encompassing approximately 90% of the single-stranded RNA genome.

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

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

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

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

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

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

107 nonenveloped icosahedral virions containing single-stranded RNA genomes.

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

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

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

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

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

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

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

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

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

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

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

119 However, single-stranded RNA is rapidly degraded by ubiquitous RN

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

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

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

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

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

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

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

127 Single-stranded RNA molecules fold into extraordinarily

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

129 ion techniques to isolate small, structured, single-stranded RNA molecules known as aptamers that wer

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

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

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

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

134 miRNAs are a class of 17- to 27-nucleotide single-stranded RNA molecules that regulate gene express

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

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

137 The tripartite genome is packaged as single-stranded RNA molecules via channels on the 5-fold

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

139 propose a mechanism, we demonstrate that the single-stranded RNA of HIV-1 encodes multiple uridine-ri

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

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

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

143 es to study 3C alone and in complex with two single-stranded RNA oligonucleotides derived from the or

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

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

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

147 8 may be activated by their native ligands, single-stranded RNA, or by small molecules of the imidaz

148 ther TLRs (poly(I.C), flagellin, loxoribine, single-stranded RNA, or CpG DNA) in macrophages and HEK-

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

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

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

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

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

154 es limiting the target choice of KSRP within single-stranded RNA regions.

155 Importantly, the single-stranded RNA requirement for association can be u

156 ffinity to tetraloop RNA than to double- and single-stranded RNAs, respectively.

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

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

159 Although RNase II is specific for single-stranded RNA, RNase R readily degrades through st

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

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

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

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

164 The toxin MazF in Escherichia coli cleaves single-stranded RNAs specifically at ACA sequences.

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

166 est Nile virus (WNV), a mosquito-transmitted single-stranded RNA (ssRNA) flavivirus, causes human dis

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

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

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

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

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

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

173 Poly(I:C), but not single-stranded RNA (ssRNA) or a standard DC maturation

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

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

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

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

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

179 ded by either double-stranded RNA (dsRNA) or single-stranded RNA (ssRNA) templates.

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

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

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

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

184 Yet, pDC responses to certain single-stranded RNA (ssRNA) viruses occur only after liv

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

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

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

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

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

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

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

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

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

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

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

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

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

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

199 Chemical shift changes upon the addition of single-stranded RNAs (ssRNAs) identified a group of resi

200 bstantially higher affinity as compared with single-stranded RNA structures unless they contain a 5'-

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

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

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

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

205 Ape1 was found to cleave AP-site-containing single-stranded RNA, suggesting a novel "cleansing" func

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

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

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

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

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

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

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

213 )-fold smaller ribonuclease activity against single-stranded RNA than do the restrictocin homologues,

214 23S rRNA are helices 90-92 and the adjacent single stranded RNA that encompasses A2503.

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

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

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

218 MicroRNAs are short, single-stranded RNAs that arise from a transient precurs

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

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

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

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

223 lex dynamics associated with transition of a single stranded RNA to its secondary and tertiary struct

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

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

226 ay represent a conserved scaffold that binds single-stranded RNA to regulate transcription in both eu

227 Single-stranded RNA transcripts induced interferon-beta

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 nto the genome of the turnip mosaic virus, a single-stranded RNA virus.

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

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

250 Single-stranded RNA viruses are recognized by the member

251 r mechanisms controlling genome packaging by single-stranded RNA viruses are still largely unknown.

252 Single-stranded RNA viruses encompass broad classes of i

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

254 Single-stranded RNA viruses have been thought to encapsi

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

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

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

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

259 Single-stranded RNA viruses package their genomes into c

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

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

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

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

264 ain evolutionary dynamics closer to those of single-stranded RNA viruses than to those of double-stra

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

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

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

268 Noroviruses are positive-sense, single-stranded RNA viruses that cause acute gastroenter

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

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

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

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

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

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

275 double-stranded RNA viruses, positive-sense single-stranded RNA viruses, and the reverse-transcribin

276 hibit the replication of many negative-sense single-stranded RNA viruses, as well as double-stranded

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

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

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

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

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

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

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

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

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

290 efective in signaling with triphosphorylated single-stranded RNAs were perfectly capable of signaling

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

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

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

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

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

296 receptors (RLRs), RIG-I and MDA5, recognize single-stranded RNA with 5' triphosphates and double-str

297 There is a piece of single-stranded RNA with a length of 78 nucleotides in t

298 The influenza virus genome is an 8-segment single-stranded RNA with high potential for in situ reco

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

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