ライフサイエンスコーパス: ribonucleoprotein

1 mbly of a conical capsid enclosing the viral ribonucleoprotein.

2 emblies - a flexuous, helical rod or a loose ribonucleoprotein.

3 (RBPs): lupus La and 70-kDa U1 small nuclear ribonucleoprotein.

4 le by assisting nuclear trafficking of viral ribonucleoproteins.

5 r the assembly of spliceosomal small nuclear ribonucleoproteins.

6 Heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) is a multipurpose RNA-bi

7 We identify heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), a protein with multiple

8 The heterogeneous nuclear ribonucleoprotein A1 (hnRNP-A1) has been implicated in t

9 a cofactor of NOVA2 and heterologous nuclear ribonucleoprotein A1 (HNRNPA1), RNA-binding proteins tha

10 that the UP1 domain of heterogeneous nuclear ribonucleoprotein A1 binds the ISS apical loop site-spec

11 Heterogeneous nuclear ribonucleoprotein A1 stimulates enterovirus 71 (EV71) tr

12 in the UP1 fragment of heterogeneous nuclear ribonucleoprotein A1, and docking analysis suggested a s

13 S trans-acting factor, heterogeneous nuclear ribonucleoprotein A1, with its IRES.

14 Heterogeneous nuclear ribonucleoprotein A2B1 (hnRNPA2B1), hnRNPA0 and ELAV lik

15 inhibits oligomerization and, consequently, ribonucleoprotein activity and viral growth.

16 Stress granules (SGs) are cytoplasmic ribonucleoprotein aggregates that are directly connected

17 Stress granules (SGs) are cytosolic ribonucleoprotein aggregates that are induced during cel

18 holoenzyme proteins that assemble the active ribonucleoprotein and promote its function at telomeres.

19 /Cas9 gene-editing system that combines Cas9 ribonucleoproteins and adeno-associated viral vector del

20 l virus particles, and assembly with genomic ribonucleoproteins and caveolae-associated vesicles prio

21 , such as RNA polymerase II, small nucleolar ribonucleoproteins and mammalian target of rapamycin com

22 s) harbour translationally stalled messenger ribonucleoproteins and play important roles in regulatin

23 roporation of Cas9 nuclease/single-guide RNA ribonucleoproteins and taking advantage of a split-GFP s

24 her by multiple hnRNP (heterogeneous nuclear ribonucleoprotein) and SR (serine-arginine) proteins act

25 characterization of a high molecular weight ribonucleoprotein apparatus participating in psaA mRNA s

26 th repressor function as long as the overall ribonucleoprotein architecture provided by appropriate d

27 sms of HDAg-L-mediated nuclear export of HDV ribonucleoprotein are not clear.

28 les of E2F1, c-Myc and heterogeneous nuclear ribonucleoprotein as intermediary effectors in this feed

29 RNA-dependent RNA polymerization with viral ribonucleoprotein as template, a non-canonical sequence

30 RNP granules are ribonucleoprotein assemblies that regulate the post-tran

31 the mechanism of SMN-assisted small nuclear ribonucleoprotein assembly and the underlying causes of

32 ow that GEMIN2, a spliceosomal small nuclear ribonucleoprotein assembly factor conserved from yeast t

33 Gemin5, which are involved in small nuclear ribonucleoprotein assembly, have an important role in SL

34 SFPS colocalizes with U2 small nuclear ribonucleoprotein-associated factors including U2AF65B,

35 addition of the U4/U6 proteins small nuclear ribonucleoprotein-associated protein 1 (Snu13), pre-mRNA

36 scripts interact with the lupus antigen (La) ribonucleoprotein, avoiding cytoplasmic RNA sensors.

37 liest event, which is followed by Ago2 micro-ribonucleoprotein binding, and translation repression of

38 doplasmic reticulum and impaired dynamics of ribonucleoprotein bodies such as RNA granules that assem

39 binding protein of the heterogeneous nuclear ribonucleoprotein C (hnRNP C) family.

40 facilitate binding of heterogeneous nuclear ribonucleoprotein C (HNRNPC), an abundant nuclear RNA-bi

41 gnition and binding by heterogeneous nuclear ribonucleoprotein C (HNRNPC).

42 NA splicing regulator, heterogeneous nuclear ribonucleoprotein C1/C2 (hnRNPC1/C2) can also bind to do

43 e, we developed a protocol for combined Cas9 ribonucleoprotein (Cas9 RNP)-mediated gene editing and l

44 n CD4(+) T cells using Cas9:single-guide RNA ribonucleoproteins (Cas9 RNPs).

45 res while preserving the co-folded hTERT-hTR ribonucleoprotein catalytic core.

46 oma (FUS) represent one type of membraneless ribonucleoprotein compartment.

47 in (NP) to encapsidate the genome and form a ribonucleoprotein complex (RNP) together with viral poly

48 nd its interaction with the U1 small nuclear ribonucleoprotein complex (snRNP) control male courtship

49 trotransposition and nuclear import of an L1-ribonucleoprotein complex (using L1-encoded ORF1p as a p

50 targeted animals by direct injection of Cas9 ribonucleoprotein complex and short stretches of DNA seq

51 Furthermore, we demonstrated that the FnCas9-ribonucleoprotein complex can be microinjected into mous

52 ing of these proteins was conserved but that ribonucleoprotein complex formation required higher PCBP

53 r the 5'-deleted viral genomes-a less stable ribonucleoprotein complex formed with proteins involved

54 ed by Thoc1, a required component of the THO ribonucleoprotein complex important for RNA processing a

55 y recapitulated the physiologically relevant ribonucleoprotein complex important for selenoprotein fo

56 its viral genome through the formation of a ribonucleoprotein complex in which the nucleoprotein (NP

57 In this study, we show that a ribonucleoprotein complex including the long noncoding R

58 release from the inactive 7SK small nuclear ribonucleoprotein complex is a critical step for P-TEFb

59 (pre-mRNA) splicing is catalyzed by a large ribonucleoprotein complex known as the spliceosome.

60 eated assembly of a large and highly dynamic ribonucleoprotein complex termed the spliceosome, which

61 The human spliceosome is a large ribonucleoprotein complex that catalyzes pre-mRNA splici

62 d is part of the U4/U6.U5 tri-snRNP, a large ribonucleoprotein complex that comprises a major subunit

63 Telomerase is a specialized ribonucleoprotein complex that extends the 3' ends of ch

64 egulatory protein Mena in the formation of a ribonucleoprotein complex that involves the RNA-binding

65 geneous nuclear ribonucleoprotein U (hnRNPU) ribonucleoprotein complex to activate thermogenic gene e

66 oprotein (P), which associate with the viral ribonucleoprotein complex to replicate the genome and, t

67 ion accompanied by the assembly of an exonic ribonucleoprotein complex with a tightly bound U1 but no

68 Since 5' stem-loop I RNA forms a ribonucleoprotein complex with cellular and viral protei

69 l capsid, a conical shell encasing the viral ribonucleoprotein complex, along with its constitutive c

70 tion mobilizes P-TEFb from an inhibitory 7SK ribonucleoprotein complex, but mechanisms targeting phos

71 f nuclear factor of activated T cells (NRON) ribonucleoprotein complex, mediates nuclear translocatio

72 es the concerted action of a large, dynamic, ribonucleoprotein complex, the LSU processome.

73 In the influenza virus ribonucleoprotein complex, the oligomerization of the nu

74 anscriptase is within the RNA subunit of the ribonucleoprotein complex, which in cells contains addit

75 s implicate Rb1 in the regulation of the THO ribonucleoprotein complex.

76 FluPol in the context of a non-transcribing ribonucleoprotein complex.

77 riptase (TERT), the catalytic subunit of the ribonucleoprotein complex.

78 is an essential component of the telomerase ribonucleoprotein complex.

79 e Hsp90 was identified as a component of the ribonucleoprotein complex.

80 cytoplasmic condensates of stalled messenger ribonucleoprotein complexes (mRNPs) that form when eukar

81 ly of the viral replication machinery, large ribonucleoprotein complexes (RNPs) composed of the viral

82 Mouse MX1 interacts with the influenza ribonucleoprotein complexes (vRNPs) and can prevent the

83 yields aberrant particles in which the viral ribonucleoprotein complexes (vRNPs) are eccentrically lo

84 ons yields aberrant particles with the viral ribonucleoprotein complexes (vRNPs) eccentrically locali

85 intracellular trafficking of incoming viral ribonucleoprotein complexes (vRNPs), thereby resulting i

86 nts, including viral glycoproteins and viral ribonucleoprotein complexes (vRNPs), to assemble at thes

87 we demonstrate that LbCpf1, but not AsCpf1, ribonucleoprotein complexes allow efficient mutagenesis

88 using an assay that enables visualization of ribonucleoprotein complexes and faithfully recapitulates

89 ruses could be due to destabilization of the ribonucleoprotein complexes formed.

90 l recognition particles (SRPs) are universal ribonucleoprotein complexes found in all three domains o

91 osslinking and immunoprecipitation (CLIP) of ribonucleoprotein complexes is critical to understanding

92 chanism is to sequester and silence mRNAs in ribonucleoprotein complexes known as stress granules (SG

93 e suitability of MIPs to selectively recover ribonucleoprotein complexes such as ribosomes, founding

94 When RNAi factors bind small RNAs, they form ribonucleoprotein complexes that can be selective for ta

95 estigated the role of stress granules (SGs), ribonucleoprotein complexes that regulate mRNA translati

96 t by a shift of A3G from high-molecular-mass ribonucleoprotein complexes to low-molecular-mass comple

97 They guide ribonucleoprotein complexes to their target nucleic acid

98 sembly of stress granules (SGs), cytoplasmic ribonucleoprotein complexes with cytoprotective and pro-

99 ex (using L1-encoded ORF1p as a proxy for L1-ribonucleoprotein complexes).

100 tially processed, degraded, and regulated by ribonucleoprotein complexes, (ii) how particular miRNA g

101 in gene expression to facilitate changes to ribonucleoprotein complexes, but the cellular mechanisms

102 non-coding RNAs involved in the formation of ribonucleoprotein complexes, including ribosomal RNA, sm

103 virus (IBDV) VP3, a major component of IBDV ribonucleoprotein complexes, on the regulation of VP1, t

104 SMN is critical for the assembly of numerous ribonucleoprotein complexes, yet it is still unclear how

105 ions enriched in microvesicles, exosomes and ribonucleoprotein complexes.

106 pomethylated DRBD18 associate with different ribonucleoprotein complexes.

107 ere detected as part of approximately 45 kDa ribonucleoprotein complexes.

108 ichment of miRNA-targeted messages and micro-ribonucleoprotein components on ER upon reaching a stead

109 ulating the assembly and disassembly of SGs, ribonucleoprotein condensation can influence the surviva

110 ts before nuclear export: rotation of the 5S ribonucleoprotein, construction of the active centre and

111 d indicate that continuous replacement of SL ribonucleoproteins consumed during trans-splicing reacti

112 host cells, it prevented the release of JUNV ribonucleoprotein cores into the cytosol and decreased p

113 d with pre-assembled crRNA + tracrRNA + Cas9 ribonucleoprotein (ctRNP) complexes into mouse zygotes.

114 ith the methylosome components small nuclear ribonucleoprotein D3b (SmD3b) and protein arginine methy

115 La ribonucleoprotein domain family, member 6 (LARP6) is the

116 Binding of La ribonucleoprotein domain family, member 6 (LARP6) to col

117 ces phosphorylation of heterogeneous nuclear ribonucleoprotein E1 (hnRNP E1) at serine-43 (p-hnRNP E1

118 ndependent active sites within the Cas10-Csm ribonucleoprotein effector complex.

119 Telomerase is the ribonucleoprotein enzyme that catalyzes the extension of

120 Telomerase is the ribonucleoprotein enzyme that replenishes telomeric DNA

121 gated the mechanism of heterogeneous nuclear ribonucleoprotein F (hnRNP F) renoprotective action in a

122 plexes are enriched in heterogeneous nuclear ribonucleoprotein F (hnRNPF)-binding sites and near hnRN

123 otein belonging to the heterogeneous nuclear ribonucleoprotein family, which has a known role in proc

124 g RNA sequence to bind heterogeneous nuclear ribonucleoprotein G (HNRNPG).

125 ssion of EA H1 and full complement of pdm/09 ribonucleoprotein genes.

126 P-bodies are cytoplasmic ribonucleoprotein granules involved in posttranscription

127 ctg1 transcript are colocalized in messenger ribonucleoprotein granules responsible for the dendritic

128 ications can become localized to cytoplasmic ribonucleoprotein granules such as stress granules and t

129 Furthermore, heterogeneous nuclear ribonucleoprotein H (hnRNPH) and other RNA-binding prote

130 localization signal of Heterogeneous Nuclear Ribonucleoprotein H2, encoded by HNRNPH2, a gene located

131 on between K17 and the heterogeneous nuclear ribonucleoprotein hnRNP K.

132 of gene expression via interaction with the ribonucleoprotein hnRNP L-like (hnRNP LL) has prompted a

133 ily in RNA processing, heterogeneous nuclear ribonucleoprotein (hnRNP) A/B proteins.

134 The heterogeneous nuclear ribonucleoprotein (hnRNP) A1 protein is a multifunctiona

135 inc-RoR interacts with heterogeneous nuclear ribonucleoprotein (hnRNP) I and AU-rich element RNA-bind

136 Interestingly, heterogeneous nuclear ribonucleoprotein (hnRNP) L or hnRNP A1 are Akt substrat

137 The heterogeneous nuclear ribonucleoproteins (hnRNP) form a large family of RNA-bi

138 The heterogeneous nuclear ribonucleoprotein, hnRNP A1, is an IRES transacting fact

139 ke domain of the human heterogeneous nuclear ribonucleoprotein hnRNPA2B1 increases the aggregation pr

140 motifs and identified heterogeneous nuclear ribonucleoproteins (hnRNPs) A1 and A2/B1, which are requ

141 MicroRNAs (miRNAs) and heterogeneous nuclear ribonucleoproteins (hnRNPs) are families of sequence-spe

142 of CD1 are involved in heterogeneous nuclear ribonucleoproteins (hnRNPs) binding to A3B.

143 nd some members of the heterogeneous nuclear ribonucleoproteins (hnRNPs) family cause ALS.

144 ations for the role of heterogeneous nuclear ribonucleoproteins (hnRNPs) in the control of alternativ

145 y(ADP-ribosyl)ation of heterogeneous nuclear ribonucleoproteins (hnRNPs) regulates the posttranscript

146 ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs).

147 Ribonucleoprotein immune complexes (RNP ICs), inducers o

148 Here, using ribonucleoprotein immunoprecipitation (RIP) analysis, we

149 Finally, our ribonucleoprotein immunoprecipitation and sequencing (RI

150 HuR ribonucleoprotein immunoprecipitation followed by microa

151 Ribonucleoprotein immunoprecipitation, in vitro associat

152 domain could recover cellular VEGFA mRNA in ribonucleoprotein immunoprecipitations.

153 luding SpoU methylase and U3 small nucleolar ribonucleoprotein IMP3.

154 These transcribed repeats bind to ribonucleoproteins in a conformation-dependent manner.

155 the biogenesis of spliceosomal small nuclear ribonucleoproteins in all tissues.

156 of RNA synthesis, extending our knowledge of ribonucleoprotein interactions that are critical for gen

157 rotein GP2 and required to release the virus ribonucleoprotein into the cell cytoplasm to initiate tr

158 iolistic delivery of pre-assembled Cas9-gRNA ribonucleoproteins into maize embryo cells and regenerat

159 oration-based strategy to deliver Cas9/sgRNA ribonucleoproteins into mouse zygotes with 100% efficien

160 leating proteins promote the condensation of ribonucleoproteins into SGs.

161 TING FACTOR2 (LIF2), a heterogeneous nuclear ribonucleoprotein involved in Arabidopsis thaliana cell

162 s including a group of heterogeneous nuclear ribonucleoproteins involved in WNT5A transcription induc

163 rification analyses further reveal that this ribonucleoprotein is recruited to 5S rRNA genes as a par

164 ntially interacts with heterogeneous nuclear ribonucleoprotein K (hnRNP K) in the nucleus and acts as

165 e transcription factor heterogeneous nuclear ribonucleoprotein K (hnRNP K) was found to bind selectiv

166 ion between TDP-43 and heterogeneous nuclear ribonucleoprotein K (hnRNP K).

167 2 bound specifically to heterogenous nuclear ribonucleoprotein L (hnRNPL) and formed a functional lin

168 ts by interacting with heterogeneous nuclear ribonucleoprotein L via a CANACA motif located in its 3'

169 he RNA-binding protein heterogeneous nuclear ribonucleoprotein M (hnRNPM) promotes breast cancer meta

170 The ribosome is a ribonucleoprotein machine responsible for protein synthe

171 The ribosome is a large two-subunit ribonucleoprotein machine that translates the genetic co

172 In large ribonucleoprotein machines, such as ribosomes and splice

173 nesis as well as new perspectives on dynamic ribonucleoprotein machines.

174 Archaeal RNase P is a ribonucleoprotein made up of one catalytic RNA and five

175 and restricts turnover of cellular microRNA ribonucleoprotein (miRNP) complexes in infected host cel

176 t a specific biological program of messenger ribonucleoprotein (mRNP) assembly, but instead form by c

177 w they determine directionality of messenger ribonucleoprotein (mRNP) complex export from the nucleus

178 egrity and function of cytoplasmic messenger ribonucleoprotein (mRNP) complexes called stress granule

179 rotein targets associated with messenger RNA ribonucleoprotein (mRNP) complexes including stress gran

180 protein, works with other cellular messenger ribonucleoprotein (mRNP) components to ensure the primit

181 l cellular processes by regulating messenger ribonucleoprotein (mRNP) dynamics.

182 NA export factor docking sites and messenger ribonucleoprotein (mRNP) remodeling machinery right over

183 e we showed that REH2C is an mRNA-associated ribonucleoprotein (mRNP) subcomplex with editing substra

184 At the NPC, messenger ribonucleoproteins (mRNPs) first encounter the nuclear b

185 ns and image translation of single messenger ribonucleoproteins (mRNPs) in human cells.

186 ins that assemble into specialized messenger ribonucleoproteins (mRNPs) localized in the germ (pole)

187 RNAs (mRNAs) associate with proteins to form ribonucleoproteins (mRNPs).

188 g a paternal (p) deletion from small nuclear ribonucleoprotein N (Snrpn (S)) to ubiquitin protein lig

189 xample of an enzyme that can occur either as ribonucleoprotein or as protein alone.

190 viral VHHs prevented nuclear import of viral ribonucleoproteins or mRNA transcription, respectively,

191 RF1p, an L1-encoded protein essential for L1 ribonucleoprotein particle (L1RNP) formation and L1 retr

192 F3B5, that form part of the U2 small nuclear ribonucleoprotein particle (snRNP) are also subunits of

193 The mobile U2 small nuclear ribonucleoprotein particle (snRNP) associates with U4/U6

194 ecognition factors U2AF and U1 small nuclear ribonucleoprotein particle (snRNP).

195 criptional regulation and in small nucleolar ribonucleoprotein particle assembly and thus possibly to

196 A high-resolution structure reveals how the ribonucleoprotein particle called U1 snRNP engages with

197 d variably sized RNA fragments obtained from ribonucleoprotein particle footprinting experiments or f

198 l recognition particle (SRP) is an essential ribonucleoprotein particle that mediates the co-translat

199 The small subunit (SSU) processome, a large ribonucleoprotein particle, organizes the assembly of th

200 rolae may occur without the U1 small nuclear ribonucleoprotein particle.

201 onally processed and packaged into messenger ribonucleoprotein particles (mRNPs) in the nucleus.

202 by the ability to form closed-loop messenger ribonucleoprotein particles (mRNPs) via eIF4F-poly(A)-bi

203 anscripts that are physically sequestered in ribonucleoprotein particles (RNPs) and thus subjected to

204 e protein composition and mRNA cargos of the ribonucleoprotein particles (RNPs) that form the substra

205 mRNA that is to be translated is packed into ribonucleoprotein particles (RNPs) where RNA binding pro

206 ly steps of biogenesis and assembly of H/ACA ribonucleoprotein particles (RNPs).

207 In eukaryotic cells, RNAs exist as ribonucleoprotein particles (RNPs).

208 A substrate bound to U1 and U2 small nuclear ribonucleoprotein particles (snRNPs), and transforms int

209 osome, a complex of five major small nuclear ribonucleoprotein particles (snRNPs).

210 also show that, in the cells, IsrA exists as ribonucleoprotein particles (sRNPs), which involve a def

211 uctures of spliceosomal U-rich small nuclear ribonucleoprotein particles (UsnRNPs) requires assembly

212 rgeting the ATP-dependent formation of viral ribonucleoprotein particles (vRNPs).

213 Ro60 and La proteins, which exist in ribonucleoprotein particles and play different roles in

214 Germ granules, specialized ribonucleoprotein particles, are a hallmark of all germ

215 ome, which is composed of five small nuclear ribonucleoprotein particles, U1, U2, U4/U6, and U5.

216 Piwi-piRNA (Piwi-interacting RNA) ribonucleoproteins (piRNPs) enforce retrotransposon sile

217 nked to germ-cell formation, by forming Piwi ribonucleoproteins (piRNPs) that silence transposable el

218 ing assays show that BEX1 is part of a large ribonucleoprotein processing complex involved in regulat

219 We identified heterogeneous nuclear ribonucleoprotein R (HNRNPR) as an important positive re

220 Naturally occurring mutations in the ribonucleoprotein reverse transcriptase, telomerase, are

221 of their more complex and larger endogenous ribonucleoprotein RNase P.

222 The nucleolus and other ribonucleoprotein (RNP) bodies are membrane-less organel

223 The mobile satBaMV RNA appears to exist as ribonucleoprotein (RNP) complex composed of P20 and fibr

224 mRNA, thereby stabilizing a yet unidentified ribonucleoprotein (RNP) complex that is critical to the

225 CA sheet that associates with the condensed ribonucleoprotein (RNP) complex.

226 diting mammalian genomes when delivered as a ribonucleoprotein (RNP) complex.

227 d the polymerase activity of all possible 16 ribonucleoprotein (RNP) complexes (PB2, PB1, PA, NP) bet

228 eosome assembly through its participation in ribonucleoprotein (RNP) complexes for splice-site recogn

229 dult mouse brain following injection of Cas9 ribonucleoprotein (RNP) complexes in the hippocampus, st

230 ext, we purify and deliver BE3 and HF-BE3 as ribonucleoprotein (RNP) complexes into mammalian cells,

231 y the viral nucleocapsid protein (N) to form ribonucleoprotein (RNP) complexes that are substrates fo

232 or ectopically targeting functional RNAs and ribonucleoprotein (RNP) complexes to genomic loci.

233 , mass spectrometry shows that the Evf2-DLX1 ribonucleoprotein (RNP) contains the SWI/SNF-related chr

234 assembly requires condensation of the viral ribonucleoprotein (RNP) core with the matrix protein (M)

235 Furthermore, affinity-purified MRP ribonucleoprotein (RNP) from HeLa cells cleaves the huma

236 They trap other ribonucleoprotein (RNP) granule components and disrupt R

237 Phase-separated states of proteins underlie ribonucleoprotein (RNP) granules and nuclear RNA-binding

238 Ribonucleoprotein (RNP) granules are enriched in specifi

239 Intracellular ribonucleoprotein (RNP) granules are membrane-less dropl

240 es and the recently identified nonmembranous ribonucleoprotein (RNP) granules.

241 are conserved noncoding RNAs best studied as ribonucleoprotein (RNP) guides in RNA modification.

242 At a pH of ~6, M1 interacts with the viral ribonucleoprotein (RNP) in a putative priming stage; at

243 How and where ribonucleoprotein (RNP) transport granules that support

244 Cas9 mRNA or protein is an efficient RNA- or ribonucleoprotein (RNP)-based delivery method for the CR

245 Such ribonucleoproteins (RNPs) can facilitate the high-fideli

246 tify transcripts associated with cytoplasmic ribonucleoproteins (RNPs) containing the RNA-binding pro

247 Ribonucleoproteins (RNPs) often coassemble into supramol

248 n a stoichiometric manner and stabilized the ribonucleoproteins (RNPs) with a family of polypeptides

249 very and the CRISPR/Cas9 system delivered as ribonucleoproteins (RNPs).

250 les, exosomes (collectively called EVs), and ribonucleoproteins (RNPs).

251 Box C/D small (nucleolar) ribonucleoproteins [s(no)RNPs] catalyze 2'-O-methylation

252 brillarin (FBL, an enzymatic small nucleolar ribonucleoprotein, snoRNP) are frequently overexpressed

253 SMN likely leading to loss of small nuclear ribonucleoprotein (snRNP) assembly.

254 We previously showed that U1 small nuclear ribonucleoprotein (snRNP) associates with RNAP II, and b

255 Definition occurs by U1 small nuclear ribonucleoprotein (snRNP) binding the 5' SS and recognit

256 U6 small nuclear ribonucleoprotein (snRNP) biogenesis is essential for sp

257 pliceosome.The mechanism of U6 small nuclear ribonucleoprotein (snRNP) biogenesis is not well underst

258 , canonical CB foci and coilin/small nuclear ribonucleoprotein (snRNP) co-localization are significan

259 and, as a component of the 7SK small nuclear ribonucleoprotein (snRNP) complex, is recruited to the p

260 nactive state bound to the 7SK small nuclear ribonucleoprotein (snRNP) complex.

261 leased from the inhibitory 7SK small nuclear ribonucleoprotein (snRNP) complex.

262 The 7SK small nuclear ribonucleoprotein (snRNP) plays a central role in RNA po

263 The 7SK small nuclear ribonucleoprotein (snRNP) sequesters and inactivates the

264 e P-TEFb from the inactive 7SK small nuclear ribonucleoprotein (snRNP).

265 A, likely by competing with U1 small nuclear ribonucleoprotein (snRNP).

266 a complex machine composed of small nuclear ribonucleoproteins (snRNPs) and accessory proteins that

267 rotein machinery consisting of small nuclear ribonucleoproteins (snRNPs) and non-snRNP proteins.

268 required for the biogenesis of small nuclear ribonucleoproteins (snRNPs) involved in mRNA splicing.

269 he DNA interactions of RALY, a heterogeneous ribonucleoprotein that acts as a transcriptional cofacto

270 Telomerase is a ribonucleoprotein that maintains the ends of linear chro

271 Consequently formation of viral ribonucleoproteins that catalyse viral RNA synthesis is

272 f cells is synthesized by ribosomes, complex ribonucleoproteins that in eukaryotes contain 79-80 prot

273 uctures that concentrate proteins, RNAs, and ribonucleoproteins that perform functions essential to g

274 III (Pol III), but the precise role of this ribonucleoprotein therein remains unknown.

275 h releases P-TEFb from the 7SK small nuclear ribonucleoprotein, they turned green.

276 RNAs (snoRNAs) are non-coding RNAs that form ribonucleoproteins to guide covalent modifications of ri

277 ed complex within the U4/U6.U5 small nuclear ribonucleoprotein (tri-snRNP).

278 SIGNIFICANCE STATEMENT Heterogeneous nuclear ribonucleoprotein U (hnRNP U) belongs to a family of RNA

279 that mice lacking the heterogeneous nuclear ribonucleoprotein U (hnRNP U) in the heart develop letha

280 omologous to mammalian heterogeneous nuclear ribonucleoprotein U (hnRNP U), plays an important role i

281 n fat lncRNA 1 (Blnc1)/heterogeneous nuclear ribonucleoprotein U (hnRNPU) ribonucleoprotein complex t

282 estigated roles of the Heterogeneous Nuclear Ribonucleoprotein U (HNRNPU), a nuclear matrix (NM)-asso

283 the spliceosomal subcomplex U1 small nuclear ribonucleoprotein (U1 snRNP).

284 spliceosomal protein of the U2 small nuclear ribonucleoprotein (U2 snRNP).

285 The auxiliary factor of U2 small nuclear ribonucleoprotein (U2AF) facilitates branch point (BP) r

286 tein complexes of uridine-rich small nuclear ribonucleoproteins (UsnRNPs).

287 We show here that the influenza virus ribonucleoprotein (vRNP) complex binds to the CTD of tra

288 Both prevent nuclear import of the viral ribonucleoprotein (vRNP) complex without disrupting nucl

289 les into a conical core containing the viral ribonucleoprotein (vRNP) complex, thought to be composed

290 e further demonstrate that ZBP1 senses viral ribonucleoprotein (vRNP) complexes of IAV to trigger cel

291 Nuclear export of influenza virus ribonucleoprotein (vRNP) from infected cells has been sh

292 Influenza viral ribonucleoprotein (vRNP) is replicated in the nucleus an

293 y, involves core assembly, whereby the viral ribonucleoprotein (vRNP, composed of vRNA and nucleocaps

294 tes the nuclear import of incoming IAV viral ribonucleoproteins (vRNPs) and is important for efficien

295 synthesis results from its binding to viral ribonucleoproteins (vRNPs), the structures containing in

296 cell-penetrating peptide moieties; and Cas9 ribonucleoprotein, whose nucleofection into cells facili

297 ently, all identified RNase P enzymes were a ribonucleoprotein with a conserved catalytic RNA compone

298 rus nucleocapsid (N) protein forms a helical ribonucleoprotein with the viral positive-strand RNA gen

299 tegy, termed S1mplex, to complex CRISPR-Cas9 ribonucleoproteins with a nucleic acid donor template, a

300 t that single-step codelivery of CRISPR/Cpf1 ribonucleoproteins with single-stranded DNA repair templ