ライフサイエンスコーパス: RNA-dependent

1 the binding of NP with RIG-I was found to be RNA dependent.

2 tress granules and interaction with PABP are RNA dependent.

3 on of HDAC1/2 and SRSF1 to the gene body was RNA-dependent.

4 tional activation and assessed their role in RNA-dependent activation.

5 Mtr4 is an essential RNA-dependent adenosine triphosphatase that is required

6 The association between PABPC1 and hEndoV is RNA dependent and furthermore, PABPC1 stimulates hEndoV

7 ranscriptionally active chromatin in both an RNA-dependent and -independent manner and that this asso

8 the complex is composed of subcomplexes with RNA-dependent and independent interactions.

9 FN)-alpha/beta activation pathway using both RNA-dependent and RNA-independent mechanisms.

10 model of multistep FUS aggregation involving RNA-dependent and RNA-independent stages.

11 er, the association of MMTV Gag and YB-1 was RNA dependent, and an MMTV RNA reporter construct coloca

12 rst evidence that astroviruses undergo viral RNA-dependent assembly.

13 DEAD-box proteins are a class of RNA-dependent ATP hydrolysis enzymes that rearrange RNA

14 Rho utilizes its RNA-dependent ATPase activities to translocate along the

15 lex at high pH and increases Delta247-Brr2's RNA-dependent ATPase activity and the extent of RNA unwi

16 l RNA helicase activities, as exemplified by RNA-dependent ATPase activity and unwinding of the DNA-R

17 Prp28 and Prp28-(127-588) have an intrinsic RNA-dependent ATPase activity, albeit with a low turnove

18 An HTS campaign using an RNA-dependent ATPase assay and initial SAR study identif

19 hese Psis interact genetically with Prp5, an RNA-dependent ATPase involved in monitoring the U2 BSRR-

20 Brr2 is an RNA-dependent ATPase required to unwind the U4/U6 snRNA

21 eIF4A is a DEAD-box RNA-dependent ATPase thought to unwind RNA secondary str

22 DEAD-box proteins, a large class of RNA-dependent ATPases, regulate all aspects of gene expr

23 ively charged surfaces on CD1 is involved in RNA-dependent attenuation of A3B catalysis.

24 t recombinant DDX1 binds Rev and RNA and has RNA-dependent catalytic activity.

25 teracts with eRNAs, stimulation manifests in RNA-dependent changes in the histone acetylation mediate

26 ggesting that context is a crucial factor in RNA-dependent chromatin remodeling inhibition.

27 ited to chromatin via RNA and forms a large, RNA-dependent complex with Yra1 and Mex67.

28 se proteins associated with each other in an RNA-dependent complex.

29 Gle1 is a highly conserved regulator of RNA-dependent DEAD-box ATPase proteins, with critical ro

30 Interestingly, RNA-dependent disruption of Gag trafficking required eit

31 RNA dependent DNA-polymerases, reverse transcriptases, a

32 017) describe how the Rad52 protein mediates RNA-dependent DNA double-strand break repair via inverse

33 In Arabidopsis, RNA-dependent DNA methylation and transcriptional silenc

34 n tubes of mutants defective for MET1, DDM1, RNA-dependent DNA methylation, or MSI-dependent histone

35 riEPRV, potentially providing a signature of RNA-dependent DNA methylation.

36 exact mechanism of how Rad52 contributes to RNA-dependent DSB repair remained unknown.

37 Furthermore, we show that KLK3e processes RNA-dependent enhancer activity depending on the integri

38 RNA interference (RNAi) is an RNA-dependent gene silencing approach controlled by an R

39 ment for Aquarius, but not HRDE-1, for small RNA-dependent gene silencing.

40 r protein, VP6, which is known to possess an RNA-dependent helicase activity, may also act as an RNA

41 oswitch action: governing the ability of the RNA-dependent helicase Rho to terminate transcription.

42 n termination events in bacteria rely on the RNA-dependent helicase Rho.

43 ces, called the terminators, or by a nascent RNA-dependent helicase, Rho.

44 he concept that RNA modifications can impair RNA-dependent immune activation.

45 eq, we investigated the functional impact of RNA-dependent interaction between JMJD6 and U2AF65, reve

46 To analyze an RNA-dependent interaction with chromatin, we purified na

47 Moreover, Pum1 and Pum2 display RNA-dependent interaction with fragile X mental retardat

48 We found that Gis2 exhibits RNA-dependent interactions with two proteins involved in

49 mplexes and proteins through RNA-enhanced or RNA-dependent interactions.

50 ious studies have shown that double-stranded RNA-dependent kinase, PKR, plays an important role in th

51 fic SR-related proteins during splicing in a RNA dependent manner.

52 , a major constituent of paraspeckles, in an RNA-dependent manner and responds in the same way as oth

53 core miRISC silencers Ago2 and Rck/p54 in an RNA-dependent manner and with GW182 in a microtubule-dep

54 roteins interacting with multiple RBPs in an RNA-dependent manner are enriched for RBPs.

55 ion interferes with IFIT1 binding, but in an RNA-dependent manner, whereas translation assays reveal

56 s and to coimmunoprecipitate with NS5A in an RNA-dependent manner.

57 amer that assemble on the DNA template in an RNA-dependent manner.

58 action of RBFox2 with chromatin in a nascent RNA-dependent manner.

59 nRNA loci and interacts with Pol-II in a DNA/RNA-dependent manner.

60 tion to regulate gene expression via a small RNA dependent mechanism.

61 circuits, including multistage cascades and RNA-dependent networks that can be rewired with Csy4 to

62 ells and is retained by interaction with the RNA-dependent nuclear matrix.

63 >950 mRNAs, most of which are distinct from RNAs dependent on TDP-43.

64 These data establish a new RNA-dependent paradigm for myofibroblast formation throu

65 ritical regulator of an unexpected and novel RNA-dependent pathway controlling peripheral B cell surv

66 noprecipitation experiments indicate that an RNA-dependent physical interaction between L1 ORF1p and

67 The EBOV RNA-dependent polymerase complex includes a filovirus-sp

68 t views on evolution and functional roles of RNA-dependent polymerases in living cells.

69 equire the TERT N-terminal (TEN) domain, but RNA-dependent positioning of the TEN domain captures sub

70 RNase L and RNA-dependent protein kinase (PKR) are effectors of the

71 The depletion of double-stranded RNA-dependent protein kinase (PKR) from these MEFs resto

72 situation and show that the double-stranded RNA-dependent protein kinase (PKR) is involved in the lo

73 N-terminal kinase (JNK) and double-stranded RNA-dependent protein kinase (PKR) to induce autophagy w

74 e proteasomal degradation of double-stranded RNA-dependent protein kinase (PKR), little is known abou

75 eIF-2alpha kinases including double-stranded RNA-dependent protein kinase (PKR), which has been recen

76 slational arrest mediated by double-stranded-RNA-dependent protein kinase (PKR).

77 here we identify a role for double-stranded RNA-dependent protein kinase (PKR, also known as EIF2AK2

78 tRNA2-1 and down-regulate the phosphorylated RNA-dependent protein kinase (pPKR), whose activity has

79 rt that in HeLa cells, activation of a PERK (RNA-dependent protein kinase [PKR]-like ER kinase)-eIF2a

80 S, was dependent on CD14 activity but not on RNA-dependent protein kinase and could be inhibited by a

81 d to be effective in blocking binding to the RNA-dependent protein kinase PKR, a cytoplasmic dsRNA-bi

82 uencing reveals that recCas9 catalyzes guide RNA-dependent recombination in human cells with an effic

83 g and simulation to study the dynamics of 6S RNA-dependent regulation, focusing on transitions in gro

84 tral set of peptides active as co-factors in RNA-dependent replication and catalysis.

85 l PPIs including the homodimerization of the RNA dependent RNA polymerase (RdRp), the self-interactio

86 h the only protein present is the poliovirus RNA dependent RNA polymerase (RdRp), which recapitulates

87 nd comprises a methyltransferase (MTase) and RNA dependent RNA polymerase domain.

88 inhibitors of norovirus 3C-like protease and RNA dependent RNA polymerase.

89 , we proposed a model wherein the poliovirus RNA-dependent RNA polymerase (3D(pol)) uses a reiterativ

90 hin P90, focus formation required the entire RNA-dependent RNA polymerase (aa 1700 to 2116).

91 on between arenavirus nucleoprotein (NP) and RNA-dependent RNA polymerase (L protein), the two trans-

92 een the hemagglutinin-neuraminidase (HN) and RNA-dependent RNA polymerase (L) genes of the PIV5 genom

93 ion protein 35 (VP35), glycoprotein (GP) and RNA-dependent RNA polymerase (L) proteins.

94 eries of non-nucleoside boron-containing HCV RNA-dependent RNA polymerase (NS5B) inhibitors are descr

95 the surface of the thumb domain of the viral RNA-dependent RNA polymerase (NS5B).

96 entary sequence of which codes for the viral RNA-dependent RNA polymerase (NS7).

97 nsp14 associates with the CoV RNA-dependent RNA polymerase (nsp12-RdRp), and nsp14-Exo

98 ver the 5-fold vertices, and monomers of the RNA-dependent RNA polymerase (P2) attach to the inner su

99 ithin the N-terminal 270 amino acids and the RNA-dependent RNA polymerase (POL) activity within amino

100 Foot-and-mouth disease virus (FMDV) RNA-dependent RNA polymerase (RdRp) (3D(pol)) catalyzes

101 nce the amplification of the viral siRNAs by RNA-dependent RNA polymerase (RdRP) 1 (RDR1) and RDR6 an

102 s have suggested that multiple copies of the RNA-dependent RNA polymerase (RdRp) 3D are involved in t

103 merase, which has also been reported to have RNA-dependent RNA polymerase (RdRP) activity.

104 of two extensively interacting subunits: an RNA-dependent RNA polymerase (RdRP) and an NTPase VP4.

105 eEF1A) in control of activation of the viral RNA-dependent RNA polymerase (RdRp) and regulation of th

106 wo conserved amino acid substitutions in the RNA-dependent RNA polymerase (RdRp) and six in the capsi

107 n with defined termini, containing the viral RNA-dependent RNA polymerase (RdRp) at one end and a loo

108 The viral RNA-dependent RNA polymerase (RdRp) causes the TSS/surro

109 Recently, we demonstrated that the viral RNA-dependent RNA polymerase (RdRP) complex can be an op

110 pped dsRNAs, the largest of which encodes an RNA-dependent RNA polymerase (RdRP) containing a unique

111 -terminal methyltransferase and a C-terminal RNA-dependent RNA polymerase (RdRp) domain.

112 ich the tandem methyltransferase (MTase) and RNA-dependent RNA polymerase (RdRp) domains stack into o

113 scovered that knockdown of either csr-1, the RNA-dependent RNA polymerase (RdRP) ego-1, or the dicer-

114 These include the sequestration of the RNA-dependent RNA polymerase (RdRp) for functions other

115 fficiently used as primers by the hantaviral RNA-dependent RNA polymerase (RdRp) for transcription in

116 sid (ORF2) genes and occasionally within the RNA-dependent RNA polymerase (RdRP) gene.

117 on sequencing using primers specific for the RNA-dependent RNA polymerase (RDRP) gene.

118 which the respiratory syncytial virus (RSV) RNA-dependent RNA polymerase (RdRp) initiates mRNA trans

119 RNA-dependent RNA polymerase (RdRp) is essential to vira

120 cleotide incorporation fidelity of the viral RNA-dependent RNA polymerase (RdRp) is important for mai

121 The RNA-dependent RNA polymerase (RdRp) of hepatitis C virus

122 The RNA-dependent RNA polymerase (RdRP) of nonsegmented nega

123 a cell-based assay for RNA synthesis by the RNA-dependent RNA polymerase (RdRp) of noroviruses, we p

124 port an in vitro RNA synthesis assay for the RNA-dependent RNA polymerase (RdRP) of rabies virus (RAB

125 The reliance of the viral RNA-dependent RNA polymerase (RdRP) on host factors make

126 ruses (IAV) acquired through the error-prone RNA-dependent RNA polymerase (RdRP) or through genetic r

127 Based on the partial RNA-dependent RNA polymerase (RdRp) region, they cluster

128 a distinct class of siRNAs synthesized by an RNA-dependent RNA polymerase (RdRP) requires the PIR-1 p

129 In this context, the viral RNA-dependent RNA polymerase (RdRP) subunits assembly ha

130 S) in C. elegans also involves RRF-1, a worm RNA-dependent RNA polymerase (RdRP) that is known to pro

131 ny eukaryotic organisms encode more than one RNA-dependent RNA polymerase (RdRP) that probably emerge

132 RNA viruses replicate via a virally encoded RNA-dependent RNA polymerase (RdRP) that uses a unique p

133 However, genes for RNA-dependent RNA polymerase (RdRp), a hallmark of posit

134 Key to the viral life cycle is the RNA-dependent RNA polymerase (RdRp), a heterotrimeric co

135 re dengue genome for interactions with viral RNA-dependent RNA polymerase (RdRp), and we identified t

136 influenza virus genome mainly depend on its RNA-dependent RNA polymerase (RdRP), composed of the PA,

137 SARS-CoV nsp12, the canonical RNA-dependent RNA polymerase (RdRp), exhibits poorly pro

138 ral (HCV) genome is accomplished by the NS5B RNA-dependent RNA polymerase (RdRp), for which mechanist

139 ion of the downstream ORF, which encodes the RNA-dependent RNA polymerase (RdRp), has been proposed t

140 re, we show that transient expression of HCV RNA-dependent RNA polymerase (RdRp), NS5B, in mouse live

141 which encode a putative coat protein and an RNA-dependent RNA polymerase (RdRp), respectively.

142 The VRC consists of the p92 virus-coded RNA-dependent RNA polymerase (RdRp), the viral p33 RNA c

143 etween mitochondrial membranes and the viral RNA-dependent RNA polymerase (RdRp), which is mediated b

144 The virus-coded RNA-dependent RNA polymerase (RdRp), which is responsibl

145 component of the VRC is the virally encoded RNA-dependent RNA polymerase (RdRp), which should be act

146 A expression with a concomitant depletion of RNA-dependent RNA polymerase (RdRP)-derived secondary sm

147 (siRNAs) are amplified from target mRNAs by RNA-dependent RNA polymerase (RdRP).

148 via template switching by the virus-encoded RNA-dependent RNA polymerase (RdRP).

149 and replication of the viral genome by viral RNA-dependent RNA polymerase (RdRp).

150 s is transcribed and replicated by the viral RNA-dependent RNA polymerase (RdRP).

151 tide misincorporation frequency of the viral RNA-dependent RNA polymerase (RdRp).

152 sid protein (N-RNA), and associated with the RNA-dependent RNA polymerase (RdRP).

153 espread conformational shift upon binding to RNA-dependent RNA polymerase (RdRp).

154 l-based assay for the human NoV GII.4 strain RNA-dependent RNA polymerase (RdRp).

155 They all make their own RNA-dependent RNA polymerase (RdRp).

156 hich are known as inhibitors of the HCV NS5B RNA-dependent RNA polymerase (RdRp).

157 on the regulation of VP1, the virus-encoded RNA-dependent RNA polymerase (RdRp).

158 NA) genome, which is replicated by the viral RNA-dependent RNA polymerase (RNAP).

159 re that is recognized and bound by the viral RNA-dependent RNA polymerase (RNAP); however, no 3D stru

160 me and RNA processing enzymes, including the RNA-dependent RNA polymerase (VP1).

161 The viral RNA-dependent RNA polymerase (vRdRp) of paramyxovirus co

162 requires nuclear RNA polymerase IV (Pol IV), RNA-dependent RNA polymerase 2 (RDR2) and DICER-like 3 (

163 -dependent nat-siRNAs were also dependent on RNA-dependent RNA polymerase 2 (RDR2) and plant-specific

164 of a physical association between JMJ24 and RNA-dependent RNA polymerase 2 (RDR2), which represents

165 RNAs are globally reduced by mutation of the RNA-dependent RNA polymerase 2 encoded by modifier of pa

166 analysis of cis and trans activities of the RNA-dependent RNA polymerase 3D.

167 element mRNAs into small RNAs guided by the RNA-dependent RNA polymerase 6 (RDR6) protein and is the

168 However, DCL2 facilitates the recruitment of RNA-DEPENDENT RNA POLYMERASE 6 (RDR6) to ARGONAUTE 1-der

169 econdary short interfering RNAs (siRNAs) via RNA-DEPENDENT RNA POLYMERASE 6 (RDR6), DCL4 and ARGONAUT

170 entified: RNA Polymerase IV (PolIV)-RdDM and RNA-dependent RNA Polymerase 6 (RDR6)-RdDM.

171 ents are converted to double-stranded RNA by RNA-dependent RNA polymerase 6 (RDR6).

172 showed that cleavage by nta-miR6019 triggers RNA-dependent RNA polymerase 6- and ribonuclease Dicer-l

173 secondary siRNAs in a manner that depends on RNA-dependent RNA polymerase 6.

174 in, which comprises three enzymatic domains (RNA-dependent RNA polymerase [RdRp], polyribonucleotidyl

175 roles for ncRNAs, as well as a novel Pol II RNA-dependent RNA polymerase activity that regulates an

176 nt RNA polymerase and a DNA ligase to act as RNA-dependent RNA polymerase and RNA ligase, respectivel

177 ce gene was identified, shown to code for an RNA-dependent RNA polymerase and to be allelic with Ty-3

178 hod allows accurate fitting of the monomeric RNA-dependent RNA polymerase bound at the threefold axis

179 on-nucleoside organic inhibitor of the viral RNA-dependent RNA polymerase by means of high-throughput

180 Their viral RNA-dependent RNA polymerase can induce local conformati

181 ily release the RNA genome so that the viral RNA-dependent RNA polymerase can use it as the template

182 pecifically impairs the function of the hRSV RNA-dependent RNA polymerase complex notably by reducing

183 lymerase basic 2 (PB2) proteins comprise the RNA-dependent RNA polymerase complex responsible for vir

184 of polymerase lattices within the multimeric RNA-dependent RNA polymerase complex should facilitate a

185 Influenza virus RNA-dependent RNA polymerase consists of three viral pro

186 The vesicular stomatitis virus (VSV) RNA-dependent RNA polymerase consists of two viral prote

187 ociated N protein in the architecture of the RNA-dependent RNA polymerase domain of L.

188 alternative substrate inhibitor of the NS5B RNA-dependent RNA polymerase during HCV replication.

189 us (HCV) replication as it carries the viral RNA-dependent RNA polymerase enzymatic activity.

190 The RNA-dependent RNA polymerase enzyme NS5B represents one

191 viruses replicate by using a virally encoded RNA-dependent RNA polymerase enzyme that has low fidelit

192 nhibitor of the HCV nonstructural protein 5B RNA-dependent RNA polymerase enzyme, was recently approv

193 protease/helicase and NS5 methyltransferase/RNA-dependent RNA polymerase form part of the viral repl

194 lete match to the nucleotide sequence of the RNA-dependent RNA polymerase from Drosophila X virus (DX

195 The RNA-dependent RNA polymerase from the Hepatitis C Virus

196 ability and poor activity of the avian virus RNA-dependent RNA polymerase in human cells.

197 a A virus mRNAs are transcribed by the viral RNA-dependent RNA polymerase in the cell nucleus before

198 bonucleosides form a novel class of HCV NS5B RNA-dependent RNA polymerase inhibitors, displaying EC50

199 include new NS3/4A protease inhibitors, NS5B RNA-dependent RNA polymerase inhibitors, NS5A inhibitors

200 pecifically, we show that the Nodamura virus RNA-dependent RNA polymerase interacts with the outer mi

201 Influenza virus mRNA synthesis by the RNA-dependent RNA polymerase involves binding and cleava

202 The NS5B RNA-dependent RNA polymerase is an attractive target for

203 his context, heterotrimeric viral PA/PB1/PB2 RNA-dependent RNA polymerase is an attractive target for

204 on of the endonuclease activity of influenza RNA-dependent RNA polymerase is attractive for the devel

205 The RNA-dependent RNA polymerase is responsible for genome r

206 The multifunctional RNA-dependent RNA polymerase L protein of vesicular stom

207 RNA complex constitutes the template for the RNA-dependent RNA polymerase L, which engages the nucleo

208 MuV RNA-dependent RNA polymerase minimally consists of the p

209 ocoris ostravirus 1) with a highly divergent RNA-dependent RNA polymerase missed by conventional BLAS

210 Our data uncover a new role for the viral RNA-dependent RNA polymerase NS5B and p7 proteins in con

211 our results demonstrate a novel role for the RNA-dependent RNA polymerase NS5B in HCV assembly.

212 The Sindbis virus RNA-dependent RNA polymerase nsP4 possesses an amino-ter

213 The RNA-dependent RNA polymerase of influenza virus consists

214 One attractive target is the RNA-dependent RNA polymerase PA subunit.

215 mals may have replaced an ancient eukaryotic RNA-dependent RNA polymerase pathway to control transpos

216 at the local region is completed, the viral RNA-dependent RNA polymerase processes downstream, and t

217 products corresponding to virion-associated RNA-dependent RNA polymerase protein (RdRp), glycoprotei

218 with enzymatic activity, the viral large (L) RNA-dependent RNA polymerase protein.

219 olymerases Pol IV and Pol V and the putative RNA-dependent RNA polymerase RDR2.

220 Hepatitis C virus (HCV) RNA-dependent RNA polymerase replicates the viral genomi

221 NS5B is the RNA-dependent RNA polymerase responsible for replicating

222 The C-terminal domain is an RNA-dependent RNA polymerase responsible for viral RNA s

223 The RDE-10/RDE-11 complex and the RNA-dependent RNA polymerase RRF-1 then engage the targe

224 independent of rde-4 but likely requires the RNA-dependent RNA polymerase RRF-1, suggesting a critica

225 findings further our understanding of viral RNA-dependent RNA polymerase structure-function relation

226 nit, and the RDRC complex, which contains an RNA-dependent RNA polymerase subunit.

227 Non-structural protein 5B (NS5B) is the RNA-dependent RNA polymerase that catalyzes replication

228 (HCV) non-structural protein 5B (NS5B) is an RNA-dependent RNA polymerase that is essentially require

229 Nonstructural protein 9 (Nsp9) is the RNA-dependent RNA polymerase that plays a critical role

230 RSV has an RNA-dependent RNA polymerase that transcribes and replic

231 tered inside the nucleocapsid when the viral RNA-dependent RNA polymerase uses it as the template for

232 agment screen on the dengue virus serotype 3 RNA-dependent RNA polymerase using x-ray crystallography

233 l double-stranded RNA (dsRNA) genome and the RNA-dependent RNA polymerase VP1.

234 P forms the viral RNA-dependent RNA polymerase with the large protein (L).

235 ructures, located in the region encoding the RNA-dependent RNA polymerase, 3D(pol), by site-directed

236 within the Picornaviridae family express an RNA-dependent RNA polymerase, 3D(pol), that is required

237 The poliovirus RNA-dependent RNA polymerase, 3Dpol, replicates the vira

238 ple copies of a major structural protein, an RNA-dependent RNA polymerase, a hexameric NTPase, and an

239 g of heterotypic segments by influenza virus RNA-dependent RNA polymerase, an inhibitory effect of vi

240 iral replicase, on the activity of the viral RNA-dependent RNA polymerase, and an inhibitory effect o

241 ns-acting short interfering RNA3 pathway, an RNA-dependent RNA polymerase, and an XH/XP domain-contai

242 RNA1 encodes the RNA-dependent RNA polymerase, and RNA2 encodes the capsi

243 s is transcribed and replicated by the viral RNA-dependent RNA polymerase, composed of the subunits P

244 f viral RNA synthesis by the recombinant MNV RNA-dependent RNA polymerase, confirming that the stem-l

245 of foot-and-mouth disease virus (FMDV), the RNA-dependent RNA polymerase, forms fibrils in vitro.

246 The RNA-dependent RNA polymerase, glycoprotein precursor, nu

247 logical salt conditions, HCV NS5BDelta21, an RNA-dependent RNA polymerase, has poor affinity for the

248 ular targets for anti-HCV drugs is the viral RNA-dependent RNA polymerase, NS5B.

249 Based on structural data of the RNA-dependent RNA polymerase, rational targeting of key

250 c RNA whose appearance is independent of the RNA-dependent RNA polymerase, suggesting that the telome

251 1 (PA-PB1) subunits of influenza virus (Flu) RNA-dependent RNA polymerase, this paper is devoted to t

252 dies have revealed the position of the viral RNA-dependent RNA polymerase, VP1, within the inner caps

253 s, identified in the p7 polypeptide and NS5B RNA-dependent RNA polymerase, were sufficient to increas

254 lyzed by the NS5B (nonstructural protein 5B) RNA-dependent RNA polymerase, which is a major target of

255 nhibitor of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase, with activity across all H

256 ical, concerted action of RNA POLYMERASE IV, RNA-DEPENDENT RNA POLYMERASE-2, and DICER-LIKE-4.

257 al agent specifically targeting HCV NS5B, an RNA-dependent RNA polymerase.

258 n plants by a process typically requiring an RNA-dependent RNA polymerase.

259 d but is suggested to target influenza virus RNA-dependent RNA polymerase.

260 ld have arisen as a secondary function of an RNA-dependent RNA polymerase.

261 virus replication, the methyltransferase and RNA-dependent RNA polymerase.

262 targeting an assembly interface of the viral RNA-dependent RNA polymerase.

263 (PIV5) is an essential cofactor of the viral RNA-dependent RNA polymerase.

264 etermine the recognition of viral RNA by the RNA-dependent RNA polymerase.

265 mechanistic understanding of NS5B, the viral RNA-dependent RNA polymerase.

266 f components of the RNA-silencing machinery, RNA-DEPENDENT RNA POLYMERASE1 and SUPPRESSOR OF GENE SIL

267 osttranscriptional gene-silencing components RNA-DEPENDENT RNA POLYMERASE1 and SUPPRESSOR OF GENE SIL

268 riginally targeted region by means of Pol IV/RNA-DEPENDENT RNA POLYMERASE2 (RDR2)-dependent 24-nt sec

269 on P. patens homologs of DICER-LIKE3 (DCL3), RNA-DEPENDENT RNA POLYMERASE2, and the largest subunit o

270 ced by the activity of ARGONAUTE9 (AGO9) and RNA-DEPENDENT RNA POLYMERASE6 (RDR6), two genes involved

271 enance of TE and/or transgene silencing; and RNA-dependent RNA Polymerase6 (RDR6)-RdDM, which was rec

272 RNA viruses encoding high- or low-fidelity RNA-dependent RNA polymerases (RdRp) are attenuated.

273 RNA-dependent RNA polymerases (RdRps) are key to the rep

274 RNA-dependent RNA polymerases (RdRps) are used by RNA vi

275 RNA-dependent RNA polymerases (RdRps) are used by RNA vi

276 Positive-sense RNA viruses encode RNA-dependent RNA polymerases (RdRps) essential for geno

277 Recombinant RNA-dependent RNA polymerases (RdRps) from the human nor

278 All viral RNA-dependent RNA polymerases (RdRps) have a conserved s

279 te for the absence of piRNAs, both involving RNA-dependent RNA polymerases (RdRPs).

280 mplification of initial silencing signals by RNA-dependent RNA polymerases (RdRPs).

281 quires an siRNA amplification step involving RNA-dependent RNA polymerases (RdRPs).

282 oduction of double-stranded RNAs (dsRNAs) by RNA-DEPENDENT RNA POLYMERASEs (RDRs) and proceeds throug

283 Cellular RNA-dependent RNA polymerases (RDRs) catalyze synthesis

284 The viral RNA-dependent RNA polymerases (vRdRps) of nonsegmented,

285 ve identified fidelity determinants in viral RNA-dependent RNA polymerases and have shown that RNA vi

286 Viral RNA-dependent RNA polymerases are considered to be low-f

287 is translocated by the single subunit viral RNA-dependent RNA polymerases is not yet understood.

288 al clamp, conferring steric hindrance on the RNA-dependent RNA polymerases of diverse positive-strand

289 such as influenza, encode large, multidomain RNA-dependent RNA polymerases that can both transcribe a

290 ty in RNA viruses has been attributed to the RNA-dependent RNA polymerases, with mutations in RdRps f

291 ovirus 3D(pol) are a common feature of viral RNA-dependent RNA polymerases.

292 troviral RTs but remarkably similar to viral RNA-dependent RNA polymerases.

293 primers to characterize activities of DNA or RNA-dependent RNA polymerases.

294 ion through initiation to elongation for the RNA-dependent RNA polymerization reaction, explain the r

295 includes Ebola and rabies viruses, catalyze RNA-dependent RNA polymerization with viral ribonucleopr

296 bed and replicated by the heterotrimeric IAV RNA-dependent RNA-polymerase (RdRp).

297 logs were shown to block the activity of the RNA-dependent RNA-polymerase complex of RSV.

298 optimization of non-nucleoside dengue viral RNA-dependent-RNA polymerase (RdRp) inhibitors are descr

299 te in access to the genomic RNA by the viral RNA-dependent-RNA polymerase.

300 we report both genomically local and distal RNA-dependent roles of Dali, a conserved central nervous