ライフサイエンスコーパス: single-strand RNA

1 affinity for RNA duplexes compared with the single strand RNA.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 Single-stranded RNAs also activate PKR constructs lackin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

102 nonenveloped icosahedral virions containing single-stranded RNA genomes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 ng a group of more than 1500 short noncoding single-strand RNA molecules of approximately 22 nucleoti

123 Single-stranded RNA molecules fold into extraordinarily

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 8 may be activated by their native ligands, single-stranded RNA, or by small molecules of the imidaz

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

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

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

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

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

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

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

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

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

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

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

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

154 ute a class of non-coding RNAs that catalyze single-strand RNA scission.

155 The first residue of the single strand RNA segment in the backtracked transcripti

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

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

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

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

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

161 serve that ATM silencing results in enhanced single-strand RNA (ssRNA) replication of RSVand Sendai v

162 ic use of chemical modifications to optimize single-strand RNA (ssRNA)-mediated mRNA knockdown.

163 cer for processed products (siRNA) and short single-strand RNAs (ssRNA).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

210 23S rRNA are helices 90-92 and the adjacent single stranded RNA that encompasses A2503.

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

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

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

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

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

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

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

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

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

220 atalyzes intramolecular ligation of 5'-PO(4) single-strand RNA to form a covalently closed circular R

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

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

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

224 Single-stranded RNA transcripts induced interferon-beta

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 stroviruses are nonenveloped, positive-sense single-strand RNA viruses associated with self-limiting

248 f segmented and non-segmented negative-sense single-strand RNA viruses.

249 Single-stranded RNA viruses are recognized by the member

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

251 Single-stranded RNA viruses encompass broad classes of i

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

253 Single-stranded RNA viruses have been thought to encapsi

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

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

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

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

258 Single-stranded RNA viruses package their genomes into c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

300 is triggered by either single strand DNA or single strand RNA, yet the apparent affinity for a DNA a