ライフサイエンスコーパス: small nuclear

1 e in the levels of regulatory ncRNAs such as small nuclear and nucleolar RNAs (snRNAs and snoRNAs).

2 Small nuclear and nucleolar RNAs that program pre-mRNA s

3 dding far-red light led to the appearance of small nuclear bodies containing phyB.

4 The appearance of small nuclear bodies was rapid, stable, and reversible u

5 of lemurs employed limited mitochondrial or small nuclear data sets, with many relationships poorly

6 viduals, a few of them have been extended to small nuclear families, but none can be applied to large

7 at co-segregates with a disease phenotype in small nuclear families, from genome-wide oligonucleotide

8 ter irradiation, CENP-A is found in multiple small nuclear foci that are mutually exclusive to gammaH

9 In contrast, many unicellular organisms with small nuclear genomes seem to have lost entirely the RNA

10 sformation of European kinship, by promoting small, nuclear households, weak family ties, and residen

11 ys an integral role in catalytic, ribosomal, small nuclear, micro, and transfer RNAs.

12 Hundreds of small nuclear non-coding RNAs, including small nucleolar

13 croRNAs (miRNAs), Piwi-interacting (piRNAs), small nuclear, nucleolar, cytoplasmic (sn-, sno-, scRNAs

14 ed with highly expressed histone genes and U small nuclear or nucleolar RNA (sn/snoRNA) loci that for

15 GRD encodes a small nuclear protein of the RWP-RK family and is broadl

16 We have investigated recruitment of U1 small nuclear ribonuclear protein (snRNP) by G1M2 and IS

17 phase and causes dramatic disorganization of small nuclear ribonuclear protein and serine-arginine ri

18 In yeast, the U2 small nuclear ribonucleic acid (snRNA) component of the

19 ned that RBM20 interacts with both U1 and U2 small nuclear ribonucleic particles (snRNPs) and suggest

20 ibute to a better understanding of Gemin5 in small nuclear ribonucleic protein (snRNP) biogenesis as

21 he present study, we characterized U1-70-kDa small nuclear ribonucleoprotein (70-kDa) autoantigen-spe

22 It exists in inactive small nuclear ribonucleoprotein (7SK snRNP) and active (

23 EFb) via its release from the inhibitory 7SK small nuclear ribonucleoprotein (7SK snRNP).

24 ) kinase, which is suppressed within the 7SK small nuclear ribonucleoprotein (7SK snRNP).

25 scovered an RNA motif that recognizes the U1 small nuclear ribonucleoprotein (snRNP) and is essential

26 issense mutants can rescue iMEF survival and small nuclear ribonucleoprotein (snRNP) assembly, demons

27 compared with SMN likely leading to loss of small nuclear ribonucleoprotein (snRNP) assembly.

28 esting an unknown quality control system for small nuclear ribonucleoprotein (snRNP) assembly.

29 SMN is critical for small nuclear ribonucleoprotein (snRNP) assembly.

30 We previously showed that U1 small nuclear ribonucleoprotein (snRNP) associates with

31 Definition occurs by U1 small nuclear ribonucleoprotein (snRNP) binding the 5' S

32 U6 small nuclear ribonucleoprotein (snRNP) biogenesis is es

33 urney to the spliceosome.The mechanism of U6 small nuclear ribonucleoprotein (snRNP) biogenesis is no

34 Nuclear import is an essential step in small nuclear ribonucleoprotein (snRNP) biogenesis.

35 trates within Cajal bodies (CBs) and impacts small nuclear ribonucleoprotein (snRNP) biogenesis.

36 Interestingly, canonical CB foci and coilin/small nuclear ribonucleoprotein (snRNP) co-localization

37 eoli and bound what we believe to be a novel small nuclear ribonucleoprotein (snRNP) complex composed

38 essential gene encoding a subunit of the U5 small nuclear ribonucleoprotein (snRNP) complex of the s

39 binds 7SK RNA and, as a component of the 7SK small nuclear ribonucleoprotein (snRNP) complex, is recr

40 atalytically inactive state bound to the 7SK small nuclear ribonucleoprotein (snRNP) complex.

41 ol II) once released from the inhibitory 7SK small nuclear ribonucleoprotein (snRNP) complex.

42 se mice do not develop autoantibodies to the small nuclear ribonucleoprotein (snRNP) complex.

43 many splicing factors, including the key U2 small nuclear ribonucleoprotein (snRNP) component SF3B1

44 spliceostatin A, sudemycin E binds to the U2 small nuclear ribonucleoprotein (snRNP) component SF3B1.

45 7, 251, 261 and 271 residues of MoSNP1, a U1 small nuclear ribonucleoprotein (snRNP) component, likel

46 The small nuclear ribonucleoprotein (snRNP) core domain, act

47 In eukaryotes, U1 small nuclear ribonucleoprotein (snRNP) forms spliceosom

48 The U2 small nuclear ribonucleoprotein (snRNP) has an essential

49 licing factor Tat-SF1 associates with the U2 small nuclear ribonucleoprotein (snRNP) of the spliceoso

50 ous nuclear ribonucleoproteins (hnRNPs), and small nuclear ribonucleoprotein (snRNP) particles throug

51 The 7SK small nuclear ribonucleoprotein (snRNP) plays a central

52 novo motif analysis shows PAS signals and U1 small nuclear ribonucleoprotein (snRNP) recognition site

53 The 7SK small nuclear ribonucleoprotein (snRNP) sequesters and i

54 olecular recognition of tau pre-mRNA by a U1 small nuclear ribonucleoprotein (snRNP) splicing factor.

55 nisms that regulate P-TEFb involving the 7SK small nuclear ribonucleoprotein (snRNP), factors that co

56 is inhibited by HEXIM1 or HEXIM2 in the 7SK small nuclear ribonucleoprotein (snRNP), which contains,

57 Both the BBR and BPS interact with the U2 small nuclear ribonucleoprotein (snRNP)-associated SF3b

58 eins or release P-TEFb from the inactive 7SK small nuclear ribonucleoprotein (snRNP).

59 ylating the RNA, likely by competing with U1 small nuclear ribonucleoprotein (snRNP).

60 as a base-paired complex within the U4/U6.U5 small nuclear ribonucleoprotein (tri-snRNP).

61 he early spliceosome assembly begins with U1 small nuclear ribonucleoprotein (U1 snRNP) binding to th

62 n the disease, including U1-70K and other U1 small nuclear ribonucleoprotein (U1 snRNP) spliceosome c

63 the U1 small nuclear RNA component of the U1 small nuclear ribonucleoprotein (U1 snRNP) splicing fact

64 components of the spliceosomal subcomplex U1 small nuclear ribonucleoprotein (U1 snRNP).

65 The U1-small nuclear ribonucleoprotein (U1-snRNP) that includes

66 Binding of U1 small nuclear ribonucleoprotein (U1snRNP) to DM20 is gre

67 SF3B1), a key spliceosomal protein of the U2 small nuclear ribonucleoprotein (U2 snRNP).

68 The auxiliary factor of U2 small nuclear ribonucleoprotein (U2AF) facilitates branc

69 t is characterized by high levels of anti-U1 small nuclear ribonucleoprotein 70k autoantibodies and a

70 Basophil activation and IgE anti-U1 small nuclear ribonucleoprotein 70k were also observed i

71 raised against the main MCTD autoantigen U1 small nuclear ribonucleoprotein 70k were found in nearly

72 r messenger RNAs (pre-mRNAs) contains the U7 small nuclear ribonucleoprotein and shares the key cleav

73 to understand the mechanism of SMN-assisted small nuclear ribonucleoprotein assembly and the underly

74 Here we show that GEMIN2, a spliceosomal small nuclear ribonucleoprotein assembly factor conserve

75 pICln, SMN and Gemin5, which are involved in small nuclear ribonucleoprotein assembly, have an import

76 well characterized function in spliceosomal small nuclear ribonucleoprotein assembly.

77 hanced complex A formation and binding of U2 small nuclear ribonucleoprotein auxiliary factor 65 kDa

78 d splicing regulatory proteins, including u2 small nuclear ribonucleoprotein auxiliary factor 65-kDa

79 We reveal that the splicing factor U2 small nuclear ribonucleoprotein auxiliary factor 65-kilo

80 PID in the liberation of P-TEFb from the 7SK small nuclear ribonucleoprotein complex (7SK snPNP).

81 ibitor (PSI) and its interaction with the U1 small nuclear ribonucleoprotein complex (snRNP) control

82 luded diverse components of the U4/U6.U5 tri-small nuclear ribonucleoprotein complex and several spli

83 clin T1 and CDK9 are incorporated in the 7SK small nuclear ribonucleoprotein complex containing the i

84 Its release from the inactive 7SK small nuclear ribonucleoprotein complex is a critical st

85 ncode core components of the spliceosomal U6 small nuclear ribonucleoprotein complex, regulate circad

86 plicing complex Bact consisting of the three small nuclear ribonucleoprotein complexes (snRNPs) U2, U

87 ltimeric complex involved in the assembly of small nuclear ribonucleoprotein complexes (snRNPs).

88 ckdown of proteins associated with different small nuclear ribonucleoprotein complexes and by using t

89 tein complex with the methylosome components small nuclear ribonucleoprotein D3b (SmD3b) and protein

90 Brr2 enzyme, which is essential for U4/U6 di-small nuclear ribonucleoprotein disruption during splice

91 of PWS carrying a paternal (p) deletion from small nuclear ribonucleoprotein N (Snrpn (S)) to ubiquit

92 x, SF3B3 and SF3B5, that form part of the U2 small nuclear ribonucleoprotein particle (snRNP) are als

93 The mobile U2 small nuclear ribonucleoprotein particle (snRNP) associa

94 he 5' splice site, and a component of the U2 small nuclear ribonucleoprotein particle (snRNP) complex

95 k9-cyclin T modules from large, inactive 7SK small nuclear ribonucleoprotein particle (snRNP) complex

96 early intron recognition factors U2AF and U1 small nuclear ribonucleoprotein particle (snRNP).

97 ) domain of spliceosomal A protein of the U1 small nuclear ribonucleoprotein particle (U1A) interacti

98 esidues 885-2413) in complex with Aar2, a U5 small nuclear ribonucleoprotein particle assembly factor

99 hat SmD1, a core component of the Drosophila small nuclear ribonucleoprotein particle implicated in s

100 ceosome assembly within the mature U2 snRNP (small nuclear ribonucleoprotein particle), and its displ

101 Prp8, a component of the U5 small nuclear ribonucleoprotein particle, crosslinks ext

102 icing in C. merolae may occur without the U1 small nuclear ribonucleoprotein particle.

103 The U1, U2, U4, U5 and U6 small nuclear ribonucleoprotein particles (snRNPs) are e

104 r messenger RNA substrate bound to U1 and U2 small nuclear ribonucleoprotein particles (snRNPs), and

105 Human spliceosomal U1 small nuclear ribonucleoprotein particles (snRNPs), whic

106 by the spliceosome, a complex of five major small nuclear ribonucleoprotein particles (snRNPs).

107 of Sm core structures of spliceosomal U-rich small nuclear ribonucleoprotein particles (UsnRNPs) requ

108 he U12-type spliceosomes, large complexes of small nuclear ribonucleoprotein particles and associated

109 LIP, which immunoprecipitates SmB along with small nuclear ribonucleoprotein particles and auxiliary

110 autoreactive B cells that recognize self-Ag small nuclear ribonucleoprotein particles with activated

111 important for the biogenesis of spliceosomal small nuclear ribonucleoprotein particles, but downstrea

112 d the spliceosome, which is composed of five small nuclear ribonucleoprotein particles, U1, U2, U4/U6

113 3), insulin-like growth factor 2 (IGF2), and small nuclear ribonucleoprotein polypeptide N, and the l

114 lation site, independent of the U1 snRNP (U1 small nuclear ribonucleoprotein).

115 nts, FLICE-associated huge protein, Mute, U7 small nuclear ribonucleoprotein, and MPM-2 phosphoepitop

116 mic acid, which releases P-TEFb from the 7SK small nuclear ribonucleoprotein, they turned green.

117 the latter, it is incorporated into the 7SK small nuclear ribonucleoprotein, which contains hexameth

118 -COP protein co-immunoprecipitates with SMN, small nuclear ribonucleoprotein-associated assembly fact

119 SFPS colocalizes with U2 small nuclear ribonucleoprotein-associated factors inclu

120 nal transcribed allele of the imprinted gene Small nuclear ribonucleoprotein-associated polypeptide N

121 at sequential addition of the U4/U6 proteins small nuclear ribonucleoprotein-associated protein 1 (Sn

122 ding proteins (RBPs): lupus La and 70-kDa U1 small nuclear ribonucleoprotein.

123 spliceosome is a complex machine composed of small nuclear ribonucleoproteins (snRNPs) and accessory

124 dynamic RNA-protein machinery consisting of small nuclear ribonucleoproteins (snRNPs) and non-snRNP

125 The prespliceosome, comprising U1 and U2 small nuclear ribonucleoproteins (snRNPs) bound to the p

126 5), which are required for the biogenesis of small nuclear ribonucleoproteins (snRNPs) involved in mR

127 The U1 and U2 small nuclear ribonucleoproteins (snRNPs) mark an intron

128 sequential recruitment and rearrangement of small nuclear ribonucleoproteins (snRNPs) on a pre-mRNA

129 rected cross-linking with in vitro assembled small nuclear ribonucleoproteins (snRNPs) or spliceosome

130 lear domains important for the biogenesis of small nuclear ribonucleoproteins (snRNPs) which function

131 onents of the spliceosome, U1, U2, U4 and U5 small nuclear ribonucleoproteins (snRNPs), contain seven

132 on of SMN is as an assembler of spliceosomal small nuclear ribonucleoproteins (snRNPs).

133 splicing, forming the cores of spliceosomal small nuclear ribonucleoproteins (snRNPs).

134 bly of RNA-protein complexes of uridine-rich small nuclear ribonucleoproteins (UsnRNPs).

135 uclear domain important to the biogenesis of small nuclear ribonucleoproteins and telomerase, complex

136 evidence indicates that U1-70K and other U1 small nuclear ribonucleoproteins are Sarkosyl-insoluble

137 ntial role in the biogenesis of spliceosomal small nuclear ribonucleoproteins in all tissues.

138 erlying the conversion of soluble nuclear U1 small nuclear ribonucleoproteins into insoluble cytoplas

139 proteins found in the U1 and U2 spliceosomal small nuclear ribonucleoproteins is highly conserved.

140 ormation of aberrant U11- and U12-containing small nuclear ribonucleoproteins that impair the efficie

141 me proteins associated with the uridine-rich small nuclear ribonucleoproteins U2, U5, and U6 and the

142 The U1A/U2B''/SNF family of small nuclear ribonucleoproteins uses a phylogenetically

143 otein that is found in the U1 and U2 snRNPs (small nuclear ribonucleoproteins) of Drosophila.

144 ex required for the assembly of spliceosomal small nuclear ribonucleoproteins.

145 e complexes with stably bound U2, U5, and U6 small nuclear ribonucleoproteins.

146 that are suppressed, at least in part, by U1 small nuclear ribonucleoproteins.

147 rt that LARP7, BCDIN3, and the noncoding 7SK small nuclear RNA (7SK) are vital for the formation and

148 7), methyl phosphate capping enzyme, and 7SK small nuclear RNA (7SK).

149 The small nuclear RNA (snRNA) activating protein complex (SN

150 Thus, these data suggest that U6 small nuclear RNA (snRNA) and RtcB participate in the fo

151 The human small nuclear RNA (snRNA) and small cytoplasmic RNA (scR

152 with U1 and U2 gene loci, which produce the small nuclear RNA (snRNA) component of the respective sn

153 The small nuclear RNA (snRNA) components of the spliceosome

154 The small nuclear RNA (snRNA) genes have been widely used as

155 re highly enriched at RNA Pol II-transcribed small nuclear RNA (snRNA) genes, and the loss of LEC res

156 ed for the transcription of Pol II-dependent small nuclear RNA (snRNA) genes.

157 tein-coding genes including c-myc and LEC to small nuclear RNA (snRNA) genes.

158 We probe the structure of low-abundance U12 small nuclear RNA (snRNA) in Arabidopsis thaliana and pr

159 Yeast U2 small nuclear RNA (snRNA) nucleotides that form base pai

160 subunit of a protein complex that regulates small nuclear RNA (snRNA) transcription.

161 for the endonucleolytic cleavage of primary small nuclear RNA (snRNA) transcripts within the nucleus

162 se to the catalytic Mg(2+) site in the U2/U6 small nuclear RNA (snRNA) triplex, and the 5'-phosphate

163 vivo association between coilin and rRNA, U small nuclear RNA (snRNA), and human telomerase RNA, whi

164 cleosides from the 3' end of spliceosomal U6 small nuclear RNA (snRNA), directly catalyzing terminal

165 assembled spliceosomal complex comprising U5 small nuclear RNA (snRNA), extensively base-paired U4/U6

166 all nuclear RNP (snRNP), composed of the 7SK small nuclear RNA (snRNA), MePCE, and Larp7, regulates t

167 RNAP II-transcribed cellular RNAs, including small nuclear RNA (snRNA), small nucleolar RNA (snoRNA),

168 , U-rich sequence called the Sm site in each small nuclear RNA (snRNA), to form the core domain of th

169 the survival motor neuron (SMN) protein, U2 small nuclear RNA (snRNA), U5 snRNA, and the small CB-sp

170 The small nuclear RNA (snRNA)-activating protein complex (SN

171 The small nuclear RNA (snRNA)-activating protein complex (SN

172 (RRM1) to bind RNA stemloops in U1 and/or U2 small nuclear RNA (snRNA).

173 y canonical base-pairing to the 5' end of U1 small nuclear RNA (snRNA).

174 wn methyltransferase for the U6 spliceosomal small nuclear RNA (snRNA).

175 lysed at a single catalytic metal site in U6 small nuclear RNA (snRNA).

176 duplex between the authentic pre-mRNA and U7 small nuclear RNA (snRNA).

177 The auxiliary factor of U2 small nuclear RNA (U2AF) is a heterodimer consisting of

178 f noncoding RNAs, including the uridine-rich small nuclear RNA (UsnRNA) and enhancer RNA (eRNA), and

179 iation of the large inactive P-TEFb:7SK RNP (small nuclear RNA 7SK ribonucleoprotein) complex and the

180 pecially dependent on a functional U2 snRNP (small nuclear RNA [snRNA] plus associated proteins), as

181 no oligonucleotide [MO] and an engineered U7 small nuclear RNA [snRNA]) to correct this splicing defe

182 roRNA [miRNA], small nucleolar RNA [snoRNA], small nuclear RNA [snRNA], small Cajal body-specific RNA

183 mal sequence element (PSE) recognized by the small nuclear RNA activating protein complex (SNAPc).

184 C-4, the Myb-like DNA-binding subunit of the small nuclear RNA activating protein complex, binds piRN

185 ~160-nt-long RNAs, including spliceosomal U6 small nuclear RNA and a cyclic-di-AMP binding riboswitch

186 The SL RNA is a small nuclear RNA and a trans splicing substrate for the

187 partmentalization by fluorophore-labeling U1 small nuclear RNA and observing its distribution in the

188 tion of uridine residues to pseudouridine in small nuclear RNA and ribosomal RNA.

189 tein particles (snRNPs), which consist of U1 small nuclear RNA and ten proteins, recognize the 5' spl

190 pression of IRAK4-L is mediated by mutant U2 small nuclear RNA auxiliary factor 1 (U2AF1) and is asso

191 U2 Small Nuclear RNA Auxiliary Factor 1 (U2AF1) forms a het

192 exon and a 'U1 domain' that binds to the U1 small nuclear RNA component of the U1 small nuclear ribo

193 NA for post-transcriptional modification and small nuclear RNA duplexes for splicing.

194 lex SNAP(c) is required for transcription of small nuclear RNA genes and binds to a proximal sequence

195 denylated, RNAPII-dependent, uridylate-rich, small nuclear RNA genes.

196 on factor that is required for expression of small nuclear RNA genes.

197 te snoRNA, small Cajal body RNA (scaRNA) and small nuclear RNA in human and mouse cells by convention

198 ucleotides at the 3' end of the catalytic U6 small nuclear RNA in splicing termination.

199 sequesters the 5'ss residues involved in U1 small nuclear RNA interactions, thereby inhibiting excis

200 abilize U6 ACAGAGA stem-pre-mRNA and Brr2-U4 small nuclear RNA interactions.

201 ibonucleoprotein (U1-snRNP) that includes U1-small nuclear RNA is a highly conserved intranuclear mol

202 The 7SK small nuclear RNA is a highly conserved non-coding RNA t

203 inding protein La recognizes UUU-3'OH on its small nuclear RNA ligands and stabilizes them against 3'

204 ngle-guide RNAs that are expressed from a U6 small nuclear RNA promoter.

205 uired for precursor mRNA splicing through U6 small nuclear RNA stabilization.

206 enzymes and a revised model for CTD-mediated small nuclear RNA termination.

207 th and without the association of 7SK RNA, a small nuclear RNA that is bound to approximately 50% of

208 ffects of the mutants on the synthesis of U5 small nuclear RNA were analyzed.

209 two ncRNAs implicated in RNA processing: U1 small nuclear RNA, a component of the spliceosome, and M

210 damage to noncoding RNAs such as rRNA, tRNA, small nuclear RNA, and small nucleolar RNA is likely to

211 nucleolar RNA, natural antisense transcript, small nuclear RNA, and small RNA using published dataset

212 neuronal identity requires upregulation of a small nuclear RNA, RN7SK, which induces accessibilities

213 tes' most abundant non-coding (spliceosomal) small nuclear RNA, silences proximal PASs and its inhibi

214 irtually any RNA (e.g., mRNA, ribosomal RNA, small nuclear RNA, telomerase RNA and so on).

215 te the suppression of 3' end formation by U1 small nuclear RNA, which is known to bind pre-mRNA at th

216 blating one of its essential components, U11 small nuclear RNA, which resulted in micromelia.

217 We identified a zebrafish snapc4 (small nuclear RNA-activating complex polypeptide 4) muta

218 n a unique transcription factor known as the small nuclear RNA-activating protein complex (SNAPc).

219 The small nuclear RNA-activating protein complex SNAP(c) is

220 A, TFIIB, and TFIIH which, together with the small nuclear RNA-activating protein complex, form a tra

221 The Brr2 RNA helicase disrupts the U4/U6 di-small nuclear RNA-protein complex (di-snRNP) during spli

222 oncanonical mechanisms of base pairing to U1 small nuclear RNA.

223 ox C/D and H/ACA small nucleolar RNAs and U4 small nuclear RNA.

224 ting its association with the inhibitory 7SK small nuclear RNA.

225 l of motor neuron (SMN) complex delivers pre-small nuclear RNAs (pre-snRNAs) to the heptameric Sm rin

226 Expression of modified U1 small nuclear RNAs (snRNA) complementary to the splice d

227 ) hairpins immediately downstream from viral small nuclear RNAs (snRNA).

228 , conditional production of 3'-extensions of small nuclear RNAs (snRNAs) and biogenesis of novel tran

229 It assembles from five U-rich small nuclear RNAs (snRNAs) and over 200 proteins in a h

230 Small nuclear RNAs (snRNAs) are essential factors in mes

231 Uridine-rich small nuclear RNAs (snRNAs) are the basal components of

232 ng genes requiring RNAPII for transcription, small nuclear RNAs (snRNAs) display a further requiremen

233 otspot mutations (r.3A>G) of U1 spliceosomal small nuclear RNAs (snRNAs) in about 50% of Sonic hedgeh

234 risingly, we found that TOE1 associated with small nuclear RNAs (snRNAs) incompletely processed splic

235 Transcription of genes coding for the small nuclear RNAs (snRNAs) is dependent upon a unique t

236 Cross-links identified in the U4 and U6 small nuclear RNAs (snRNAs) suggest U4/U6 stem I as a Br

237 lass of ubiquitously expressed, uridine-rich small nuclear RNAs (snRNAs) transcribed by RNA polymeras

238 ly involves effects of SmD3 on the levels of small nuclear RNAs (snRNAs) U4 and U5.

239 During their biogenesis small nuclear RNAs (snRNAs) undergo multiple covalent mo

240 natching of numerous host RNAs, particularly small nuclear RNAs (snRNAs), and avoidance of host trans

241 bosomal RNAs (rRNAs), transfer RNAs (tRNAs), small nuclear RNAs (snRNAs), and RMRP.

242 the cytoplasm, precursors to specific tRNAs, small nuclear RNAs (snRNAs), and small nucleolar RNAs (s

243 ell-established role in 3' end processing of small nuclear RNAs (snRNAs), attenuates MtnA transcripti

244 mitations, we previously proposed the use of small nuclear RNAs (snRNAs), especially U7snRNA to shutt

245 As (miRNAs), small nucleolar RNAs (snoRNAs), small nuclear RNAs (snRNAs), piwi-associated RNAs (piRNA

246 xes to mediate 2'-O-methylation of rRNAs and small nuclear RNAs (snRNAs), respectively.

247 Although these small nuclear RNAs (snRNAs), termed U1, U2, U4, U5, and

248 e assembly of heptameric Sm protein rings on small nuclear RNAs (snRNAs), which are essential for snR

249 of pseudouridines (Psis) on the spliceosomal small nuclear RNAs (snRNAs), which may enable growth at

250 es (CBs)-subnuclear compartments enriched in small nuclear RNAs (snRNAs)-and promotes efficient splic

251 ynamic machine composed of both proteins and small nuclear RNAs (snRNAs).

252 del comprising 30 proteins plus U4/U6 and U5 small nuclear RNAs (snRNAs).

253 Although uridine-rich small nuclear RNAs (U-snRNAs) are essential for pre-mRNA

254 clease that is crucial for the biogenesis of small nuclear RNAs and enhancer RNAs.

255 equential interactions of pre-mRNA with five small nuclear RNAs and many proteins.

256 ent within snatched fragments and found that small nuclear RNAs and small nucleolar RNAs contributed

257 results in the misexpression of a variety of small nuclear RNAs and small nucleolar RNAs, an effect t

258 the spliceosome, a macromolecule composed of small nuclear RNAs associated with proteins.

259 tural interactions between unspliced RNA and small nuclear RNAs in spliceosomal intermediates.

260 uide covalent modifications of ribosomal and small nuclear RNAs in the nucleus.

261 ntergenic ncRNAs, small cytoplasmic RNAs and small nuclear RNAs show less consistent patterns.

262 for catalysis by unwinding base-paired U4/U6 small nuclear RNAs, a step that must be precisely timed.

263 an intricate network formed by U5, U2 and U6 small nuclear RNAs, and a pre-messenger-RNA substrate.

264 particular spliceosome components, including small nuclear RNAs, cause reproducible uniquely distribu

265 uide chemical modifications of ribosomal and small nuclear RNAs, functions that are carried out in th

266 show that a base-paired complex of U6 and U2 small nuclear RNAs, in the absence of the approximately

267 of nucleotides in ribosomal and spliceosomal small nuclear RNAs, respectively.

268 ed abundant small, noncoding RNAs, including small nuclear RNAs, small nucleolar RNAs (snoRNAs), cryp

269 S and 28S rRNAs and levels of the U-class of small nuclear RNAs.

270 it complex required for 3'-end processing of small nuclear RNAs.

271 rimethylguanosine (TMG) caps on spliceosomal small nuclear RNAs.

272 ng RNAs, which share some of the features of small nuclear RNAs.

273 somes also generates the spliceosomal U-rich small nuclear RNAs.

274 d structural features with cellular Sm-class small nuclear RNAs.

275 increases the levels of spliceosomal and U7 small-nuclear RNAs and corrects RNA processing defects i

276 FLASH (Flice-associated huge protein) and U7 small nuclear RNP (snRNP) are HLB components that partic

277 ufficient for trans-splicing, which binds U1 small nuclear RNP (snRNP) through strong base-pairing wi

278 The 7SK small nuclear RNP (snRNP), composed of the 7SK small nuc

279 ine methyltransferase, methylates Snp1, a U1 small nuclear RNP (snRNP)-specific protein, and that the

280 mice were immunized with 50 mug of U1-70-kd small nuclear RNP fusion protein and 50 mug of U1 RNA ad

281 9-1 associates with the core component of U1 small nuclear RNP in P. patens Genome-wide analyses demo

282 ion, in which the D, E, F, and G proteins of small nuclear RNPs (snRNP) but without other components

283 autoantibody ICs containing apoptotic cells, small nuclear RNPs (snRNPs), or DNA, or directly with TL

284 ation of ribonucleoproteins (RNPs) including small nuclear RNPs (snRNPs).

285 The U1 small nuclear RNPs are common targets of autoantibodies

286 Small nuclear RNPs were fluorescence-labeled, and the ef

287 or the biogenesis of ribosomes, spliceosomal small nuclear RNPs, microRNAs and the telomerase RNP.

288 ore show that mediator is a basal factor for small nuclear SL RNA gene transcription in trypanosomes

289 RNA--protein complexes (RNPs), spliceosomal small nuclear (sn), and small CB-specific (sca)RNPs.

290 The U1 small nuclear (sn)RNA (U1) is a multifunctional ncRNA, k

291 A pseudouridine-modified region of the U2 small nuclear (sn)RNA anneals with the intronic branchpo

292 ereas transcription of small nucleolar (sno)/small nuclear (sn)RNA genes is terminated by the RNA-bin

293 Integrator complex to the Pol II-transcribed small nuclear (sn)RNA genes.

294 The U1 small nuclear (sn)RNA participates in splicing of pre-mR

295 Human U1 small nuclear (sn)RNA, required for splicing of pre-mRNA

296 Spliceosomes comprise small nuclear (sn)RNAs and proteins.

297 denylase TOE1 in distinguishing the fates of small nuclear (sn)RNAs of the spliceosome from unstable

298 ction in posttranscriptional modification of small nuclear (sn)RNAs.

299 embrane proteolysis followed by release of a small nuclear-targeted cytosolic fragment.

300 phomas in non-natural hosts, expresses seven small nuclear uracil-rich non-coding RNAs (called HSURs)