ライフサイエンスコーパス: ribonucleoprotein

1 averaging to determine the structure of its ribonucleoprotein.

2 y regulated by binding to HNRNPH1, a nuclear ribonucleoprotein.

3 essing of RNA involves heterogeneous nuclear ribonucleoproteins.

4 NBP, DDX21, DDX17) and heterogeneous nuclear ribonucleoproteins.

5 n at the step prior to nuclear import of its ribonucleoproteins.

6 of many tumor-suppressor proteins and viral ribonucleoproteins.

7 ized by high levels of anti-U1 small nuclear ribonucleoprotein 70k autoantibodies and a high incidenc

8 hil activation and IgE anti-U1 small nuclear ribonucleoprotein 70k were also observed in the MCTD-lik

9 t the main MCTD autoantigen U1 small nuclear ribonucleoprotein 70k were found in nearly 80% of the pa

10 elease from the inhibitory 7SK small nuclear ribonucleoprotein (7SK snRNP).

11 We identified heterogenous ribonucleoprotein A1 (hnRNP A1) as a G-quadruplex-unwind

12 binding protein (RBP) heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) as a possible mechanism

13 This work identified heterogenous nuclear ribonucleoprotein A1 (hnRNP-A1) as a pharmacodynamic bio

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

15 ing with nucleolin and heterogeneous-nuclear-ribonucleoprotein-A1.

16 h RNA transport factor heterogeneous nuclear ribonucleoprotein A2 (hnRNP A2) for access to BC RNAs.

17 h RNA transport factor heterogeneous nuclear ribonucleoprotein A2 (hnRNP A2) for DTE access and signi

18 Heterogeneous Nuclear Ribonucleoprotein A2/B1 (HNRNPA2/B1) is a reader of the

19 anscripts depleted DUX4-induced intranuclear ribonucleoprotein aggregates and decreased DUX4-induced

20 Stress granules (SGs) are ribonucleoprotein aggregates that form in response to st

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

22 As (pre-mRNAs) contains the U7 small nuclear ribonucleoprotein and shares the key cleavage module wit

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

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

25 bcellular localization of the incoming viral ribonucleoproteins and measuring the cell's antiviral re

26 add to the toolkit for characterizing native ribonucleoproteins, and open the door to other applicati

27 Our work identifies high-order ribonucleoprotein assemblies with functions outside cell

28 phosphopeptides, proteins, phosphoproteins, ribonucleoprotein assemblies, and large protein complexe

29 al strategy for mechanistic studies of large ribonucleoprotein assemblies.

30 te, and how it relates to co-transcriptional ribonucleoprotein assembly, is abundant with complicated

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

32 d allele of the imprinted gene Small nuclear ribonucleoprotein-associated polypeptide N (Snrpn), cont

33 e we show that light-induced inactivation of ribonucleoprotein attenuates genome editing within cells

34 ulatory proteins, including u2 small nuclear ribonucleoprotein auxiliary factor 65-kDa subunit (U2AF6

35 Here we demonstrate that Cas9-ribonucleoprotein-based genome editors can correct two d

36 in kinase mTOR activates canonical messenger ribonucleoproteins by post-translationally down-regulati

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

38 use this property to develop a new tool for ribonucleoprotein characterization.

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

40 s9 plasmid as well as Cas9 protein/guide RNA ribonucleoprotein complex (RNP), while liposome-coating

41 eudouridylation as part of a small nucleolar ribonucleoprotein complex (snoRNP).

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

43 ein forms a conical lattice around the viral ribonucleoprotein complex (vRNP) consisting of a dimeric

44 to mediate selective packaging of each viral ribonucleoprotein complex (vRNP).

45 g, bioinformatics, 3'-UTR reporter and miRNA ribonucleoprotein complex -immunoprecipitation assays, a

46 components of the U4/U6.U5 tri-small nuclear ribonucleoprotein complex and several splicing factors t

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

48 o study the interaction between a type III-A ribonucleoprotein complex and various RNA substrates.

49 rimidinic endodeoxyribonuclease 1) to form a ribonucleoprotein complex at the MARCKS promoter.

50 ar chromosomes, and they are maintained by a ribonucleoprotein complex called telomerase.

51 DNA for degradation via joint action of the ribonucleoprotein complex Cascade and the helicase-nucle

52 Each ribonucleoprotein complex comprises specific rRNAs and r

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

54 RNase MRP is an essential eukaryotic ribonucleoprotein complex involved in the maturation of

55 hat another component of the JUND-containing ribonucleoprotein complex is NCBP3, a recently identifie

56 study demonstrated that the use of gRNA/Cas9 ribonucleoprotein complex resulted in a high editing eff

57 Telomerase is an enzymatic ribonucleoprotein complex that acts as a reverse transcr

58 ALS) with a mutated version using a DNA-free ribonucleoprotein complex that contains the recombinant

59 Telomerase is a ribonucleoprotein complex that counteracts the shortenin

60 center of this machinery is the ribosome, a ribonucleoprotein complex that depends heavily on Mg(2+)

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

62 ticipates in the regulation of telomerase, a ribonucleoprotein complex that maintains telomere integr

63 The spliceosome is a large ribonucleoprotein complex that removes introns from pre-

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

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

66 when combining microinjection of a gRNA/Cas9 ribonucleoprotein complex with a traditional HR donor te

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

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

69 connecting densities, likely stabilizing the ribonucleoprotein complex, are present between neighbour

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

71 7SK RNA, as part of the 7SK ribonucleoprotein complex, is crucial to the regulation

72 ences which upon incorporation into the RISC ribonucleoprotein complex, play a crucial role in regula

73 Telomerase is a ribonucleoprotein complex, the catalytic core of which i

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

75 cross genomic segments, such as those in the ribonucleoprotein complex.

76 capsid and integrase condensed into a mature ribonucleoprotein complex.

77 mRNA is a component of a previously unknown ribonucleoprotein complex.

78 et mutations using a high-fidelity Cas9 as a ribonucleoprotein complex.

79 the nascent replication product into a viral ribonucleoprotein complex.

80 cross genomic segments, such as those in the ribonucleoprotein complex.

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

82 owerful technology that relies on Cas9/sgRNA ribonucleoprotein complexes (RNPs) to target and edit DN

83 x Bact consisting of the three small nuclear ribonucleoprotein complexes (snRNPs) U2, U5 and U6 and t

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

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

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

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

88 and mammalian cell studies, we describe the ribonucleoprotein complexes and RNA-associated activitie

89 iciencies and low toxicity when delivered as ribonucleoprotein complexes at high concentration.

90 ent role than ZF1 in the accumulation of the ribonucleoprotein complexes at the PM.

91 Diverse ribonucleoprotein complexes control mRNA processing, tra

92 trate that the CA lattice protects the viral ribonucleoprotein complexes from untimely degradation in

93 TRIM5alpha interacts with LINE-1 ribonucleoprotein complexes in the cytoplasm, which is e

94 that microinjection of single-guide RNA/Cas9 ribonucleoprotein complexes into fertilized eggs of the

95 entiating fiber cells, suggesting that TDRD7-ribonucleoprotein complexes may be involved in optimal b

96 n condensates formed from PEG/dextran and in ribonucleoprotein complexes of RNA and the RNA-binding p

97 enzymatic suppressors covalently modify Cas ribonucleoprotein complexes or degrade immune signaling

98 ons resulted in the mislocalization of viral ribonucleoprotein complexes outside the capsid lattice,

99 ing majority of EBP1 interactors are part of ribonucleoprotein complexes regulating many aspects of p

100 ov et al. now uncover two types of premature ribonucleoprotein complexes that are nutrient- and mTOR-

101 The ribosome and RNase P are cellular ribonucleoprotein complexes that perform peptide bond sy

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

103 The HDV genome and antigenome RNAs form ribonucleoprotein complexes with HDAg.

104 polymerase (FluPol) in the context of viral ribonucleoprotein complexes(2,3).

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

106 al that HDACs interact with spliceosomal and ribonucleoprotein complexes, actively control the acetyl

107 ng mRNA, Cas9 mRNA/single guide RNA and Cas9 ribonucleoprotein complexes, and is envisioned to aid th

108 Vault RNAs, found in vault ribonucleoprotein complexes, are known to be one of many

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

110 of any FRET system conjugated to protein or ribonucleoprotein complexes, including those with more c

111 n the selective exclusion of fully assembled ribonucleoprotein complexes, providing a thermodynamic b

112 ization (zipcode) elements to form messenger ribonucleoprotein complexes, which then transport the RN

113 mmune signaling upon interaction with LINE-1 ribonucleoprotein complexes.

114 nt stem (PS) cells mainly employ plasmids or ribonucleoprotein complexes.

115 inly related to translation and formation of ribonucleoprotein complexes.

116 by preserving the ability to form Cas9:gRNA ribonucleoprotein complexes.

117 Stress granules (SGs) are membrane-less ribonucleoprotein condensates that form in response to v

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

119 ive view of NCBP-protein interactions in the ribonucleoprotein context and demonstrates the potential

120 Briefly, CRISPR-Cas9 ribonucleoproteins (crRNPs) are synthesized in vitro and

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

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

123 of influenza A virus is organized into eight ribonucleoproteins, each composed of a distinct RNA segm

124 quires assembly of an enhancer RNA-dependent ribonucleoprotein (eRNP) complex exhibiting properties o

125 ting IAV nucleoproteins and disrupting virus ribonucleoprotein export from the nucleus to the cytosol

126 vesicular and non-vesicular (lipoprotein and ribonucleoprotein) exRNA carriers.

127 fically overexpressing heterogeneous nuclear ribonucleoprotein F (hnRNP F) in their RPTCs and immorta

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

129 that overexpression of heterogeneous nuclear ribonucleoprotein F (Hnrnpf) in renal proximal tubular c

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

131 a splicing regulator, heterogeneous nuclear ribonucleoprotein F1 (PphnRNP-F1), in the nucleus to reg

132 ase family, a group of enzymes that regulate ribonucleoprotein formation and function in every aspect

133 Heterogeneous nuclear ribonucleoprotein G (hnRNPG) is an m(6)A reader protein

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

135 anchors additional components, including the ribonucleoprotein granule components La-related protein

136 through reduced coalescence with cytoplasmic ribonucleoprotein granule components, including FMRP.

137 of DDX3X in cortical neuron development and ribonucleoprotein granule formation.

138 , we report a bottom-up approach to engineer ribonucleoprotein granules composed of a recombinant RNA

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

140 -order assembly of MRJP-3 into extracellular ribonucleoprotein granules that protect RNA from degrada

141 nconventional interface between membraneless ribonucleoprotein granules, such as processing bodies (P

142 nscription factors and cytoplasmic messenger ribonucleoprotein granules.

143 the splicing regulator heterogeneous nuclear ribonucleoprotein H1 (PphnRNP-H1) in the nucleus, a proc

144 ly identified Hnrnph1 (heterogeneous nuclear ribonucleoprotein H1) as a quantitative trait gene under

145 plexes ranging from a 365 kDa CRISPR-Cas Csy ribonucleoprotein hetero-decamer, a 800 kDa GroEL homo-t

146 We identified heterogeneous nuclear ribonucleoproteins hnRNP R and hnRNP U as KPNA7-interact

147 the first report that heterogeneous nuclear ribonucleoprotein (hnRNP) A1 serves as a carrier protein

148 The heterogeneous nuclear ribonucleoprotein (HNRNP) genes code for a set of RNA-bi

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

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

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

152 s regulated in part by heterogeneous nuclear ribonucleoproteins (hnRNPs) and their viral target seque

153 Heterogeneous nuclear ribonucleoproteins (hnRNPs) are a group of functionally

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

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

156 by electroporation of recombinant Cas9/sgRNA ribonucleoprotein immediately prior to in vivo adoptive

157 Finally, our ribonucleoprotein immunoprecipitation and sequencing (RI

158 mmunofluorescence, immunohistochemistry, and ribonucleoprotein immunoprecipitation assays were perfor

159 HuR ribonucleoprotein immunoprecipitation followed by microa

160 BP1 and RHA both are components of messenger ribonucleoproteins in several cell types.

161 Here, using ribonucleoprotein-inspired polypeptides with low-complex

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

163 unctional protein, and Cas9 single-guide RNA ribonucleoproteins into both adherent and suspension cel

164 for the direct delivery of preassembled Cas9 ribonucleoproteins into protoplasts of F. proliferatum.

165 ure the precise incorporation of these eight ribonucleoproteins into single virus particles, and yet

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

167 ciation with the free form of N and with the ribonucleoprotein is not clear for HMPV or other major h

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

169 Focusing on two RBPs, heterogeneous nuclear ribonucleoprotein K (HNRNPK) and scaffold-attachment fac

170 o, along with its host heterogeneous nuclear ribonucleoprotein K (HNRNPK) gene, encoding an RNA bindi

171 rotein 1) and HNRNP L (heterogeneous nuclear ribonucleoprotein L) protect mRNAs from nonsense-mediate

172 NA processing protein, heterogeneous nuclear ribonucleoprotein-L (hnRNPL).

173 icing is governed by the activity of a large ribonucleoprotein machinery, the spliceosome, whose prot

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

178 esent similarities with eukaryotic messenger ribonucleoprotein (mRNP) granules, membraneless compartm

179 lies is an inherent property of an messenger ribonucleoprotein (mRNP) that is augmented under conditi

180 mbly and activation of a decapping messenger ribonucleoprotein (mRNP) that promotes 5'-3' mRNA degrad

181 We devised ribonucleoprotein networks analyzed by mutational profil

182 d transcripts, the sequestration of mRNAs in ribonucleoprotein partials prior to drying, or the lower

183 R-1 (phosphatase that interacts with RNA and ribonucleoprotein particle 1) family of RNA polyphosphat

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

185 s, with implications for gene regulation and ribonucleoprotein particle assembly throughout the nucle

186 tally important biological role as a site of ribonucleoprotein particle assembly, primarily dedicated

187 factor splicing activator and heterogeneous ribonucleoprotein particle inhibitor genes.

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

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

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

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

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

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

194 NAs that are first transported into axons in ribonucleoprotein particles (RNPs), complexes containing

195 complex facilitates assembly of a number of ribonucleoprotein particles (RNPs).

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

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

198 liceosomes, large complexes of small nuclear ribonucleoprotein particles and associated proteins.

199 unoprecipitates SmB along with small nuclear ribonucleoprotein particles and auxiliary RNA binding pr

200 rmation of mature export-competent messenger ribonucleoprotein particles and to prevent the co-transc

201 by proteins during the evolution of ancient ribonucleoprotein particles.

202 h could regulate the composition and fate of ribonucleoprotein particles.

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

204 ssembly - the 5' external transcribed spacer ribonucleoprotein - provides a mechanism for how conform

205 e catalytic subunit of the essential RNase P ribonucleoprotein, removes the 5' leader from precursor

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

207 to tRNA recognition by the RNA component of ribonucleoprotein RNase P and other catalytic RNAs, indi

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

209 Stress granules (SGs) are ribonucleoprotein (RNP) assemblies that form in eukaryot

210 ed a nanocapsule (NC), around a preassembled ribonucleoprotein (RNP) complex between a Cas9 nuclease

211 OLE RNAs form a ribonucleoprotein (RNP) complex by partnering with at le

212 e I CRISPR systems rely on the multi-subunit ribonucleoprotein (RNP) complex Cascade to identify DNA

213 (CRISPR)/CRISPR-associated protein 9 (Cas9) ribonucleoprotein (RNP) complex is an RNA-guided DNA-nuc

214 f delivering CRISPR reagents into cells as a ribonucleoprotein (RNP) complex is the ability to edit g

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

216 In the cell, the intron RNA forms a ribonucleoprotein (RNP) complex with the intron-encoded

217 at directly affected the activity of the IDV ribonucleoprotein (RNP) complex, resulting in either att

218 process prior to stable incorporation into a ribonucleoprotein (RNP) complex.

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

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

221 ation of the nuclear lysate resolved several ribonucleoprotein (RNP) complexes containing rRNAs and r

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

223 nd small Cajal body (CB) RNAs (scaRNAs) form ribonucleoprotein (RNP) complexes to mediate 2'-O-methyl

224 ound" molecules, which are active as part of ribonucleoprotein (RNP) complexes, and "unbound," with p

225 and primary human T cells when delivered as ribonucleoprotein (RNP) complexes.

226 The telomerase ribonucleoprotein (RNP) counters the chromosome end repl

227 e, we achieve protein and SpCas9 or AsCas12a ribonucleoprotein (RNP) delivery to cultured human well-

228 , we purified A3A (N57Q)-BE3 base editor for ribonucleoprotein (RNP) electroporation of human-periphe

229 ructure-activity relationships within CRISPR ribonucleoprotein (RNP) enzymes and identify compatible

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

231 The mechanisms underlying ribonucleoprotein (RNP) granule assembly, including the

232 Ribonucleoprotein (RNP) granules are biomolecular conden

233 Ribonucleoprotein (RNP) granules are enriched in specifi

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

235 Ribonucleoprotein (RNP) granules are membrane-less organ

236 Ribonucleoprotein (RNP) granules are membraneless organe

237 Ribonucleoprotein (RNP) granules are non-membrane-bound

238 Ribonucleoprotein (RNP) granules are RNA-protein assembl

239 n colocalize with cytoplasmic, membrane-less ribonucleoprotein (RNP) granules enriched for RNA-proces

240 ransitions in the assembly of large, complex ribonucleoprotein (RNP) granules has become appreciated

241 Partitioning of mRNAs into ribonucleoprotein (RNP) granules supports diverse regula

242 RNA, which is the essential component of all ribonucleoprotein (RNP) granules.

243 hnRNPA2 is a human ribonucleoprotein (RNP) involved in RNA metabolism.

244 In that time, viral ribonucleoprotein (RNP) particles (nucleocapsids) travel

245 CRISPR/Cas9 machinery delivered as ribonucleoprotein (RNP) to the zygote has become a stand

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

247 genome-editing machineries (e.g., Cas9-sgRNA ribonucleoprotein (RNP), and RNP together with donor DNA

248 The vault ribonucleoprotein (RNP), comprising vault RNA (vtRNA) an

249 ochondrial RNA processing (MRP), a catalytic ribonucleoprotein (RNP), recently reported by Lan et al.

250 ry of CRISPR/Cas9, especially in the form of ribonucleoprotein (RNP), remains elusive for clinical tr

251 proportions of extracellular vesicle (EV)-, ribonucleoprotein (RNP)-, and high-density lipoprotein (

252 Here, we demonstrate that Cas9:sgRNA ribonucleoprotein (RNP)-mediated cleavage within a GATA1

253 ich allows efficient packaging of Cas9/sgRNA ribonucleoprotein (RNP).

254 The native conformation of the ribonucleoproteins (RNPs) and their higher-order assembl

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

256 ly with extremely high efficiency using Cas9 ribonucleoproteins (RNPs) containing either a sgRNA mole

257 In eukaryotic cells, ribonucleoproteins (RNPs) form mesoscale condensates by

258 s delivery of nucleic acids and gene editing ribonucleoproteins (RNPs) formulated with both commercia

259 rker-free genome editing in hPSCs using Cas9 ribonucleoproteins (RNPs) in combination with AAV6-media

260 nuclear domains involved in the formation of ribonucleoproteins (RNPs) including small nuclear RNPs (

261 we observed an intersection between MIB1 and ribonucleoproteins (RNPs) largely unexplored in mammalia

262 eralizable method of delivering proteins and ribonucleoproteins (RNPs) to cells in vitro and mouse li

263 ted repair (HDR) template interact with Cas9 ribonucleoproteins (RNPs) to shuttle the template to the

264 uence or motif for isolation of cross-linked ribonucleoproteins (RNPs), but rather purifies them base

265 Ro60 ribonucleoproteins (RNPs), composed of the ring-shaped R

266 clusion of larger functional RNA aptamers or ribonucleoproteins (RNPs).

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

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

269 mproved GONAD (i-GONAD) by delivering CRISPR ribonucleoproteins (RNPs; Cas9 protein or Cpf1 protein a

270 NPD interacts with the heterogeneous nuclear ribonucleoprotein SAF-A previously associated with DNA d

271 Here, we used pooled and arrayed Cas9 ribonucleoprotein screens to identify transcription fact

272 odification, is catalyzed by the H/ACA small ribonucleoprotein (snoRNP) complex that shares four core

273 Small nucleolar ribonucleoproteins (snoRNPs) guide the folding, modifica

274 A motif that recognizes the U1 small nuclear ribonucleoprotein (snRNP) and is essential for the local

275 s can rescue iMEF survival and small nuclear ribonucleoprotein (snRNP) assembly, demonstrating intrag

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

277 e encoding a subunit of the U5 small nuclear ribonucleoprotein (snRNP) complex of the spliceosome.

278 d 271 residues of MoSNP1, a U1 small nuclear ribonucleoprotein (snRNP) component, likely in a manner

279 The U2 small nuclear ribonucleoprotein (snRNP) has an essential role in the s

280 Tat-SF1 associates with the U2 small nuclear ribonucleoprotein (snRNP) of the spliceosome.

281 nition of tau pre-mRNA by a U1 small nuclear ribonucleoprotein (snRNP) splicing factor.

282 iceosome, comprising U1 and U2 small nuclear ribonucleoproteins (snRNPs) bound to the precursor messe

283 The U1 and U2 small nuclear ribonucleoproteins (snRNPs) mark an intron and recruit t

284 in P serves as a crucial adaptor between the ribonucleoprotein template and the L protein, which has

285 negative-strand (NNS) RNA viruses possess a ribonucleoprotein template in which the genomic RNA is s

286 are evolutionarily conserved condensates of ribonucleoproteins that assemble in response to metaboli

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

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

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

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

291 1 gene (MARC1) and the heterogeneous nuclear ribonucleoprotein U like 1 gene (HNRNPUL1).

292 ral RNA segments contained in separate viral ribonucleoprotein (vRNP) complexes that are packaged tog

293 nctionally linked to nuclear export of viral ribonucleoprotein (vRNP) complexes, suggesting that vRNP

294 tion in influenza virus morphology and viral ribonucleoprotein (vRNP) localization was observed as an

295 The viral ribonucleoprotein (vRNP) of the influenza A virus (IAV)

296 During entry, the viral ribonucleoproteins (vRNPs) that carry the RNA genome mus

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

298 luenza A virus is organized into eight viral ribonucleoproteins (vRNPs); this provides evolutionary a

299 double-strand DNA break mediated by two Cas9 ribonucleoproteins with microhomology recombination requ

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