ライフサイエンスコーパス: small nucleolar RNA

1 on of 32 sncRNAs (26 miRNAs, 5 piRNAs, and 1 small nucleolar RNA).

2 ivity of two novel TRF1 targets (7SL RNA and small nucleolar RNAs).

3 e the 5' cap from only one RNA substrate: U8 small nucleolar RNA.

4 NA Pol III genes, and SNR52, which encodes a small nucleolar RNA.

5 the nucleolus caused the redistribution of a small nucleolar RNA.

6 t utilize the biogenesis pathway of an H/ACA small nucleolar RNA.

7 ne is clearly non-coding and appears to be a small nucleolar RNA.

8 tochondrial mt-Nd2, and Snora75, a noncoding small nucleolar RNA.

9 ript 3' end heterogeneity and polyadenylated small nucleolar RNAs.

10 uanosine cap structures of small nuclear and small nucleolar RNAs.

11 stic of certain eukaryotic small nuclear and small nucleolar RNAs.

12 onic sequences as well as generation of some small nucleolar RNAs.

13 268 to 775 nt, including three new H/ACA box small nucleolar RNAs.

14 lethal strain induces the loss of box H/ACA small nucleolar RNAs.

15 es after dimension reduction when applied to small nucleolar RNAs.

16 transcripts including microRNAs, piRNAs and small nucleolar RNAs.

17 microRNAs, piwi-interacting RNA (piRNA), and small nucleolar RNAs.

18 in cells-ribosomal RNAs, transfer RNAs, and small nucleolar RNAs.

19 ocarcinoma transcript 1 (Malat1) and several small nucleolar RNAs.

20 Our recent study demonstrated that small nucleolar RNA 42 (SNORA42) was overexpressed in lu

21 dentified by its high affinity binding to U8 small nucleolar RNA, a small nucleolar RNA required for

22 ne, which contains an orphan box H/ACA class small nucleolar RNA, ACA11, in an intron, is associated

23 t detectably deficient in conventional H/ACA small nucleolar RNA accumulation or function; however, D

24 In addition, nineteen small nucleolar RNAs also revealed differential expressi

25 ssion of a variety of small nuclear RNAs and small nucleolar RNAs, an effect that is also observed in

26 ng strong thermodynamic coupling of Rcl1, U3 small nucleolar RNA and GTP binding to Bms1 that is elim

27 as expression (which is influenced by miRNA, small nucleolar RNA and lncRNA), activation of K-Ras (mu

28 ed introns can be degraded or processed into small nucleolar RNA and microRNA derived from intronic R

29 w that read-through transcription from yeast small nucleolar RNA and small nuclear RNA genes into adj

30 Short duplexes between the U3 small nucleolar RNA and the precursor ribosomal RNA must

31 generated the quantitative Psi map of human small nucleolar RNA and tRNA.

32 itionally, we found a loss of rhythmicity in small nucleolar RNAs and a gain of rhythmicity in glutam

33 -sensitive phenotype with depletion of H/ACA small nucleolar RNAs and defects in rRNA processing.

34 protein that is associated with all Box C/D small nucleolar RNAs and functions in processing and mod

35 As, which are derived by Dicer processing of small nucleolar RNAs and have the potential to function

36 the PWS-related Snord116 repetitive locus of small nucleolar RNAs and host genes, and the antisense t

37 is found associated with the H/ACA class of small nucleolar RNAs and is involved in pseudo-uridylati

38 but not the other regions) are predominantly small nucleolar RNAs and long noncoding RNAs, suggesting

39 ewer than 200 nucleotides, and these include small nucleolar RNAs and microRNAs.

40 ribosomal stress, evidenced by depletion of small nucleolar RNAs and nuclear dispersal of ribosomal

41 Mammalian H/ACA small nucleolar RNAs and telomerase RNA share common seq

42 The DKC1 protein binds to the box H + ACA small nucleolar RNAs and the RNA component of telomerase

43 transcript processed into multiple SNORD116 small nucleolar RNAs and the spliced exons of the host g

44 tructures in the ribosome, box C/D and H/ACA small nucleolar RNAs and U4 small nuclear RNA.

45 all RNAs, including tRNA, small nuclear RNA, small nucleolar RNA, and microRNA.

46 g processing of rRNA, small nuclear RNA, and small nucleolar RNA, and mRNA decay.

47 cessing of the U4 small nuclear RNA and some small nucleolar RNAs, and degradation of aberrant mRNAs

48 nate pathogen sensing, response to wounding, small nucleolar RNAs, and the ubiquitin-proteosome and l

49 NA sequences, including long noncoding RNAs, small nucleolar RNAs, and untranslated mRNA regions, acc

50 As such as small-Cajal body associated RNAs, small-nucleolar RNAs, and small-nuclear RNAs traffic to

51 Fragments derived from small RNAs such as small nucleolar RNAs are biologically relevant but remai

52 lized to the yeast nucleolus by using the U3 small nucleolar RNA as a carrier.

53 se loci, we found one encoding a new C/D box small nucleolar RNA, as well as a surprising number that

54 ese mutations also alter the distribution of small nucleolar RNA-associated nucleolar proteins indepe

55 altering the promoter of the Arabidopsis U3 SMALL NUCLEOLAR RNA-ASSOCIATED PROTEIN 18 (UTP18) homolo

56 me, colocalize with 5S ribosomal DNA and U14 small nucleolar RNA at the nucleolus.

57 In eukaryotes, many Box C/D small nucleolar RNAs base pair with ribosomal RNA throug

58 aperoned by a myriad of assembly factors and small nucleolar RNAs, before they reach maturity and ent

59 e and demonstrate that they are deficient in small nucleolar RNA binding.

60 t dyskerin is associated not only with H/ACA small nucleolar RNAs, but also with human telomerase RNA

61 ribonucleoprotein complex guided by C/D box small nucleolar RNAs (C/D box snoRNAs).

62 Here, we identified small nucleolar RNA, C/D box 3 (SNORD3), a specific snoR

63 Several small nucleolar RNAs co-immunoprecipitate with Sen1 but

64 Utp10 is a component of a nucleolar U3 small nucleolar RNA-containing RNP complex that is requi

65 gments and found that small nuclear RNAs and small nucleolar RNAs contributed the most abundant cappe

66 ase in the accumulation of a subset of H/ACA small nucleolar RNAs, correlating with a significant dec

67 A' and A0 sites positionally resemble the U3 small nucleolar RNA-dependent, primary pre-rRNA cleavage

68 Small nucleolar RNAs direct the location of certain meth

69 rRNA through its association with a class of small nucleolar RNAs during ribosomal biogenesis.

70 how that disruption of the box H/ACA SNORA73 small nucleolar RNAs encoded within the small nucleolar

71 NAs are involved in splicing pre-mRNA, while small nucleolar RNAs facilitate ribosome biogenesis.

72 ative endonuclease Rcl1 and the essential U3 small nucleolar RNA form a stable subcomplex thought to

73 RNA candidates, which include four H/ACA box small nucleolar RNAs, four intergenic RNAs and nine RNA

74 we have developed a functional map of the U3 small nucleolar RNA from Saccharomyces cerevisiae.

75 lant snoRNA database provides information on small nucleolar RNAs from Arabidopsis and eighteen other

76 y and of the specific depletion of box H/ACA small nucleolar RNAs from the srp40Delta shm2 ade3 strai

77 ce region contains a cluster of 48 predicted small nucleolar RNA genes, but the comparable region fro

78 of aberrant polyadenylated transcripts from small nucleolar RNA genes.

79 Genes encoding tRNAs, ribosomal RNAs, and small nucleolar RNAs have also been annotated; however,

80 Notably, a specific isoform of small nucleolar RNA host gene 6, enriched in the endopla

81 udy, we uncovered a lipid-associated lncRNA, small nucleolar RNA host gene 9 (SNHG9) as a tumor-promo

82 ession of long noncoding RNA (lncRNA) Snhg9 (small nucleolar RNA host gene 9) in small intestinal epi

83 RA73 small nucleolar RNAs encoded within the small nucleolar RNA hosting gene 3 (Snhg3) causes resist

84 st the 5' external transcribed spacer and U3 small nucleolar RNA in providing an intertwined RNA-prot

85 omosome 15q11-13 that encompasses non-coding small nucleolar RNAs (including HBII-85 snoRNAs) which w

86 Assembly of both proteins with the U3 small nucleolar RNA into a chaperone complex destabilize

87 s such as rRNA, tRNA, small nuclear RNA, and small nucleolar RNA is likely to affect their function.

88 The phylogenetically conserved U14 small nucleolar RNA is required for processing of rRNA,

89 ncode the precursors of more than 50 box-C/D small nucleolar RNAs, key regulators of ribosomal biogen

90 letion leads to a specific decrease in H/ACA small nucleolar RNA levels and to defects in ribosomal R

91 Archaeal dual-guide box C/D small nucleolar RNA-like RNAs (sRNAs) bind three core pr

92 nation was associated with the expression of small nucleolar RNAs, long noncoding RNAs, and microRNAs

93 ptome, hallmarked by increased expression of small nucleolar RNAs, long noncoding RNAs, microRNAs (mi

94 RNA including microRNA, long intergenic RNA, small nucleolar RNA, natural antisense transcript, small

95 complex consisting of 40 proteins and the U3 small nucleolar RNA necessary for ribosome biogenesis, i

96 teins, cleavage and polyadenylation factors, small nucleolar RNAs, nucleolar proteins that are probab

97 of four rare variants of SNORA31, encoding a small nucleolar RNA of the H/ACA class that are predicte

98 The U3 small nucleolar RNA participates in early events of euka

99 etylation is dependent on SNORD13, a box C/D small nucleolar RNA predicted to base-pair with 18S rRNA

100 nd RNA-binding affinity and cause defects in small nucleolar RNA processing invivo.

101 ty for coupling of RNAPII transcription with small nucleolar RNA production and rRNA processing.

102 The discovery that disruption of specific small nucleolar RNAs protects against fatty acid-induced

103 y of multiple protein complexes, such as the small nucleolar RNA protein complex.

104 Biogenesis of small nucleolar RNA-protein complexes (snoRNPs) consists

105 3' end pre-rRNA anchoring and folding for U8 small nucleolar RNA recognition and the subsequent remov

106 ffinity binding to U8 small nucleolar RNA, a small nucleolar RNA required for ribosome biogenesis.

107 cerevisiae, including the small nuclear and small nucleolar RNAs, requires distinct RNA elements rec

108 -1 RNA was inserted into the body of the U16 small nucleolar RNA, resulting in accumulation of the ri

109 recent evidence for the roles of microRNAs, small nucleolar RNAs, retrotransposons, the NRSE small m

110 nonribosomal nucleolar proteins, as well as small nucleolar RNA-ribonucleoproteins (sno-RNPs).

111 The hybrid small nucleolar RNA:ribozyme, designated a "snorbozyme,"

112 arious longer structured RNAs such as rRNAs, small nucleolar RNAs, small nuclear RNAs, Y RNAs, and va

113 n polysome profiles and misregulation of the small nucleolar RNA SNORA48.

114 pressants, we found that the expression of a small nucleolar RNA, SNORD90, was elevated following tre

115 C/D box small nucleolar RNAs (SNORDs) are small noncoding RNAs,

116 U3 small nucleolar RNA (snoRNA) and associated proteins are

117 The HMCR sequence has features of a C/D box small nucleolar RNA (snoRNA) and is represented in an ab

118 NA Pol II and share biogenesis pathways with small nucleolar RNA (snoRNA) and small nuclear RNA (snRN

119 , formation of short duplexes between the U3 small nucleolar RNA (snoRNA) and the precursor rRNA (pre

120 ed from the 3' psi pocket of human U65 H/ACA small nucleolar RNA (snoRNA) and the substrate rRNA.

121 In eukaryotes, the highly conserved U3 small nucleolar RNA (snoRNA) base-pairs to multiple site

122 The resulting precipitates contained U3 small nucleolar RNA (snoRNA) but no significant amounts

123 Specifically, the U3 small nucleolar RNA (snoRNA) component of the SSU proces

124 found that ACA11, an orphan box H/ACA class small nucleolar RNA (snoRNA) encoded within an intron of

125 The loss of HBII-52 and related C/D box small nucleolar RNA (snoRNA) expression units have been

126 Finally, we correlate dynamic variations in small nucleolar RNA (snoRNA) gene dosage with changes in

127 nformatic package for computer prediction of small nucleolar RNA (snoRNA) genes in mammalian introns.

128 tein-coding genes, here we analyze noncoding small nucleolar RNA (snoRNA) genes in which introns, rat

129 ink specifically with the chromatin of H/ACA small nucleolar RNA (snoRNA) genes.

130 on of RNAPII-specific spliceosomal snRNA and small nucleolar RNA (snoRNA) genes.

131 r4 in transcription termination at noncoding small nucleolar RNA (snoRNA) genes.

132 zation Elements (NoLEs) of Xenopus laevis U3 small nucleolar RNA (snoRNA) have been defined.

133 anscript 5) as a non-protein-coding multiple small nucleolar RNA (snoRNA) host gene similar to UHG (U

134 ne contained one disrupted allele of the U60 small nucleolar RNA (snoRNA) host gene, resulting in hap

135 U3 small nucleolar RNA (snoRNA) is a member of the Box C/D

136 and structural features of Xenopus laevis U3 small nucleolar RNA (snoRNA) necessary for pre-rRNA clea

137 Correct docking of U3 small nucleolar RNA (snoRNA) on pre-ribosomal RNA (pre-r

138 the exosome-dependent processing of rRNA and small nucleolar RNA (snoRNA) precursors.

139 Mechanistically, DDX41 is essential for small nucleolar RNA (snoRNA) processing, ribosome assemb

140 U14 is a small nucleolar RNA (snoRNA) required for early cleavage

141 Cell, Cheng and Wang et al.(1) show that the small nucleolar RNA (snoRNA) SNORA13 has a non-canonical

142 rain ribosomopathies, caused by mutations in small nucleolar RNA (snoRNA) SNORD118.

143 Vertebrate cells contain a large number of small nucleolar RNA (snoRNA) species, the vast majority

144 cessing (MRP) and mutations in the RNase MRP small nucleolar RNA (snoRNA) subunit of the RNase MRP co

145 age reactions of the pre-rRNA and causes U14 small nucleolar RNA (snoRNA) to remain associated with p

146 rest, DGCR8 controls the stability of mature small nucleolar RNA (snoRNA) transcripts independently o

147 A molecular dissection of U3 small nucleolar RNA (snoRNA) was performed in vivo in Xe

148 In contrast to U3 small nucleolar RNA (snoRNA) which developed strong nucl

149 cribe an expressed pseudogene that encodes a small nucleolar RNA (snoRNA) within an intron and sugges

150 mapping pseudouridinylation sites (Psis) on small nucleolar RNA (snoRNA), 7SL RNA, vault RNA, and tR

151 Although the U3 small nucleolar RNA (snoRNA), a member of the box C/D cl

152 but never directly demonstrated, that the U3 small nucleolar RNA (snoRNA), a nucleolar component requ

153 in the binding of Bms1 to GTP, Rcl1, and U3 small nucleolar RNA (snoRNA), an essential RNA that base

154 r RNAs, including small nuclear RNA (snRNA), small nucleolar RNA (snoRNA), and telomerase RNA, is fur

155 enome-wide screen, we discovered a conserved small nucleolar RNA (snoRNA), SNORA13, that is required

156 cleolar localization elements (NoLEs) of U17 small nucleolar RNA (snoRNA), which is essential for rRN

157 secondary structure like that of a box H/ACA small nucleolar RNA (snoRNA), with a U-rich internal loo

158 ent ADP-ribosylation of histone H2B-Glu35 by small nucleolar RNA (snoRNA)-activated PARP-1 inhibits A

159 ce of an extra domain resembling a box H/ACA small nucleolar RNA (snoRNA).

160 ar precursor containing the RNA chaperone U3 small nucleolar RNA (snoRNA).

161 ntaining RNA in yeast which include mRNA and small nucleolar RNA (snoRNA).

162 tated variants of the 333-nucleotide-long U3 small nucleolar RNA (snoRNA).

163 d 68 Psis on rRNA, which are guided by H/ACA small nucleolar RNAs (snoRNA).

164 Many small nucleolar RNAs (snoRNA)s are processed from intron

165 els of five ncRNA classes (microRNA [miRNA], small nucleolar RNA [snoRNA], small nuclear RNA [snRNA],

166 oprotein complexes, including ribosomal RNA, small nucleolar RNAs (snoRNAs) and 7SK RNA.

167 omes, all mRNAs, and non-coding RNAs such as small nucleolar RNAs (snoRNAs) and long non-coding RNAs

168 otably, a striking finding in humans is that small nucleolar RNAs (snoRNAs) and long non-coding RNAs

169 Box C/D small nucleolar RNAs (snoRNAs) and small Cajal body (CB)

170 Small nucleolar RNAs (snoRNAs) and small Cajal body-spec

171 s are required for processing of a subset of small nucleolar RNAs (snoRNAs) and tRNAs transcribed by

172 We systematically profile small nucleolar RNAs (snoRNAs) and uncover an indispensa

173 Small nucleolar RNAs (snoRNAs) are a class of non-coding

174 Small nucleolar RNAs (snoRNAs) are a diverse group of no

175 Small nucleolar RNAs (snoRNAs) are a large family of euk

176 Small nucleolar RNAs (snoRNAs) are abundant noncoding RN

177 ific tRNAs, small nuclear RNAs (snRNAs), and small nucleolar RNAs (snoRNAs) are all enriched in virio

178 Small nucleolar RNAs (snoRNAs) are also transcribed by R

179 Unexpectedly, we found that a subset of small nucleolar RNAs (snoRNAs) are associated with the m

180 Small nucleolar RNAs (snoRNAs) are conserved noncoding R

181 While small nucleolar RNAs (snoRNAs) are critical for ribosome

182 Small nucleolar RNAs (snoRNAs) are emerging as an import

183 Small nucleolar RNAs (snoRNAs) are emerging as important

184 Box C/D small nucleolar RNAs (snoRNAs) are evolutionarily conser

185 Previously considered "housekeeping" genes, small nucleolar RNAs (snoRNAs) are increasingly understo

186 Small nucleolar RNAs (snoRNAs) are involved in cleavage

187 Small nucleolar RNAs (snoRNAs) are involved in many aspe

188 Small nucleolar RNAs (snoRNAs) are involved in various a

189 Small nucleolar RNAs (snoRNAs) are non-coding RNAs known

190 Small nucleolar RNAs (snoRNAs) are non-coding RNAs that

191 Small nucleolar RNAs (snoRNAs) are non-coding RNAs that

192 Small nucleolar RNAs (snoRNAs) are required for ribose 2

193 Transfer RNAs (tRNAs) and small nucleolar RNAs (snoRNAs) are two of the largest cl

194 ution in human and mouse mRNA and identified small nucleolar RNAs (snoRNAs) as a new class of m6A-con

195 f Molecular Cell, Kim et al. (2019) identify small nucleolar RNAs (snoRNAs) as activators of poly(ADP

196 Alterations in small nucleolar RNAs (snoRNAs) associated with splicing

197 SNORD116 and SNORD115 resemble box C/D small nucleolar RNAs (snoRNAs) but lack known targets.

198 cleolar targeting were identified in Box C/D small nucleolar RNAs (snoRNAs) by fluorescence microscop

199 Small nucleolar RNAs (SnoRNAs) direct chemical modificat

200 For the case of small nucleolar RNAs (snoRNAs) encoded within introns of

201 xpression of one or more of the many C/D box small nucleolar RNAs (snoRNAs) encoded within the comple

202 Most small nucleolar RNAs (snoRNAs) fall into two families, k

203 ication of 17 box C/D fibrillarin-associated small nucleolar RNAs (snoRNAs) from the ancient eukaryot

204 Small nucleolar RNAs (snoRNAs) function in ribosome biog

205 Small nucleolar RNAs (snoRNAs) function mainly as guides

206 Small nucleolar RNAs (snoRNAs) guide chemical modificati

207 Small nucleolar RNAs (snoRNAs) guide nucleotide modifica

208 H/ACA small nucleolar RNAs (snoRNAs) guide pseudouridylation a

209 Most small nucleolar RNAs (snoRNAs) guide rRNA nucleotide mod

210 Emerging evidence suggests that small nucleolar RNAs (snoRNAs) have malfunctioning roles

211 n1-1 exhibit altered accumulation of several small nucleolar RNAs (snoRNAs) immediately upon temperat

212 ve identified homologs of eukaryotic box C/D small nucleolar RNAs (snoRNAs) in Archaea termed sRNAs.

213 , our analyses also suggest direct roles for small nucleolar RNAs (snoRNAs) in binding and chaperonin

214 tein-coding potential but expression encodes small nucleolar RNAs (snoRNAs) in its introns.

215 Profiling the expression patterns of small nucleolar RNAs (snoRNAs) in joint ageing and OA ma

216 We examined the expression of miRNAs and small nucleolar RNAs (snoRNAs) in right ventricular myoc

217 t1p functions in the processing of rRNAs and small nucleolar RNAs (snoRNAs) in the nucleus.

218 emonstrated that under lipotoxic conditions, small nucleolar RNAs (snoRNAs) in the rpL13a gene accumu

219 Here, we examined the role of 10 abundant small nucleolar RNAs (snoRNAs) involved in rRNA processi

220 primarily long non-coding RNAs (lncRNAs) and small nucleolar RNAs (snoRNAs) not previously described

221 Small nucleolar RNAs (snoRNAs) orchestrate the modificat

222 ORF57 binds small nucleolar RNAs (snoRNAs) responsible for 18S and 2

223 nalysis of 16 tumors identified a cluster of small nucleolar RNAs (snoRNAs) that are highly up-regula

224 Finally, we discovered a subset of small nucleolar RNAs (snoRNAs) that correlated to indica

225 suggests that they are members of a class of small nucleolar RNAs (snoRNAs) that guide modification a

226 In mammalian cells, all small nucleolar RNAs (snoRNAs) that guide rRNA modificat

227 omal small nuclear RNAs (snRNAs) and certain small nucleolar RNAs (snoRNAs) undergoes hypermethylatio

228 We analyzed the expression of 80 small nucleolar RNAs (snoRNAs) using high-throughput qua

229 Surprisingly, several hundred small nucleolar RNAs (snoRNAs) were identified as coilin

230 Ten ACA yeast small nucleolar RNAs (snoRNAs) were shown to be required

231 The non-coding small nucleolar RNAs (snoRNAs) were subject to the great

232 However, whether small nucleolar RNAs (snoRNAs), a class of non-coding RN

233 locus encodes several imprinted transcripts, small nucleolar RNAs (snoRNAs), and microRNAs.

234 at internal Nm modification can be guided by small nucleolar RNAs (snoRNAs), and that these Nm sites

235 d 15q11, containing all known orphan C/D box small nucleolar RNAs (snoRNAs), are particularly enriche

236 we characterized the box C/D intron-encoded small nucleolar RNAs (snoRNAs), because these both copur

237 The two major families of small nucleolar RNAs (snoRNAs), Box C/D and Box H/ACA, a

238 oncoding RNAs, including small nuclear RNAs, small nucleolar RNAs (snoRNAs), cryptic unstable transcr

239 Three small nucleolar RNAs (snoRNAs), E1, E2 and E3, have been

240 Three human small nucleolar RNAs (snoRNAs), E1, E2 and E3, were repo

241 A is guided by a similar number of box H/ACA small nucleolar RNAs (snoRNAs), each forming a unique sm

242 scovered that all known yeast and vertebrate small nucleolar RNAs (snoRNAs), except for the MRP/7-2 R

243 of small nuclear non-coding RNAs, including small nucleolar RNAs (snoRNAs), have been identified in

244 ies of small RNAs in eukaryotes is the H/ACA small nucleolar RNAs (snoRNAs), most of which guide RNA

245 Noncoding RNAs, including small nucleolar RNAs (snoRNAs), play important roles in

246 producibly found over known binding sites on small nucleolar RNAs (snoRNAs), pre-mRNAs and cryptic, u

247 ncluding tRNAs, small nuclear RNAs (snRNAs), small nucleolar RNAs (snoRNAs), RNase P, RNase MRP, and

248 They contain multiple small nucleolar RNAs (snoRNAs), several of which are ess

249 scape of mRNAs, long noncoding RNAs, snRNAs, small nucleolar RNAs (snoRNAs), small Cajal body-specifi

250 ion of ncRNAs (including microRNAs (miRNAs), small nucleolar RNAs (snoRNAs), small nuclear RNAs (snRN

251 o known mammalian clusters of genes encoding small nucleolar RNAs (snoRNAs), SNRPN through UBE3A(15q1

252 enables detection of NAD(+)-capped intronic small nucleolar RNAs (snoRNAs), suggesting NAD(+) caps c

253 Small nucleolar RNAs (snoRNAs), traditionally implicated

254 rom a variety of genomic loci, which include small nucleolar RNAs (snoRNAs), transfer RNAs (tRNAs) an

255 ncluding tRNAs, small nuclear RNAs (snRNAs), small nucleolar RNAs (snoRNAs), vault RNAs (vtRNAs) and

256 5q11-q13, including SNURF-SNRPN and multiple small nucleolar RNAs (snoRNAs).

257 d transcripts, such as the small nuclear and small nucleolar RNAs (snoRNAs).

258 omal RNAs, is guided by the box C/D class of small nucleolar RNAs (snoRNAs).

259 urally and functionally related to box H/ACA small nucleolar RNAs (snoRNAs).

260 fically associated with the box C+D class of small nucleolar RNAs (snoRNAs).

261 of precursor rRNA is mediated by the box C/D small nucleolar RNAs (snoRNAs).

262 ing with members of the box H + ACA class of small nucleolar RNAs (snoRNAs).

263 d by the elevated expression of a cluster of small nucleolar RNAs (snoRNAs).

264 ins 30 copies of individual SNORD116 C/D box small nucleolar RNAs (snoRNAs).

265 richment for small nuclear RNAs (snRNAs) and small nucleolar RNAs (snoRNAs).

266 /=twofold, false discovery rate </= 5%) were small nucleolar RNAs (snoRNAs).

267 rs to be modulated by a subset of associated small nucleolar RNAs (snoRNAs).

268 to regulate the termination of at least two small nucleolar RNAs (snoRNAs).

269 There are two main classes of small nucleolar RNAs (snoRNAs): the box C/D snoRNAs and

270 U3 and U8 small nucleolar RNAs (snRNAs) participate in pre-rRNA pr

271 precisely map RNase-protected regions within small nucleolar RNAs, spliceosomal RNAs, microRNAs, tRNA

272 xed to the 5' terminal hairpin of one of its small nucleolar RNA substrates, the snR47 precursor.

273 he nucleolar localization element of box C/D small nucleolar RNAs, suggesting that this protein might

274 properties of Tat, we constructed a chimeric small nucleolar RNA-TAR decoy that localizes to the nucl

275 s when targeted to Snord115 genes, which are small nucleolar RNAs that are clustered in the 3' region

276 ases, and most commonly observed on unstable small nucleolar RNAs that are not fully processed at the

277 Here we review processing of small nucleolar RNAs that are transcribed by RNA Polymer

278 3' processing of snoRNAs (small nucleolar RNAs) that are excised from polycistroni

279 a nucleolar localization signal derived from small nucleolar RNAs (the box C/D motif), resulting in r

280 he basis to identify the two main classes of small nucleolar RNAs, the box H/ACA snoRNAs and the box

281 ts several gene classes, including histones, small nucleolar RNAs, the nitrogen discrimination pathwa

282 2'-O-Me on rRNA by directly binding C/D box small nucleolar RNAs, thereby modulating translation.

283 cies with functional significance in cancer: small nucleolar RNAs, transfer RNA, small nuclear RNAs,

284 pes of noncoding small RNAs such as snoRNAs (small nucleolar RNAs), tRNA (transfer RNA) fragments, an

285 of its transcript, which is regulated by the small nucleolar RNA U1.

286 Nop5p is associated with the small nucleolar RNAs U3, snR13, U14, and U18.

287 However, this small nucleolar RNA was not a useful normalizer for canc

288 er long non-coding, micro, small nuclear and small nucleolar RNAs were captured in these libraries.

289 Three microRNAs and three small nucleolar RNAs were differentially methylated; one

290 noncoding RNAs, including multiple tRNAs and small nucleolar RNAs, were revealed.

291 ction of the levels of RNAPII-transcribed U8 small nucleolar RNA, which is essential for 3' rRNA proc

292 ide range of cellular RNAs, including the U3 small nucleolar RNA, which is essential for processing o