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

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

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

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

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

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

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

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

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

12 268 to 775 nt, including three new H/ACA box small nucleolar RNAs.

13 transcripts including microRNAs, piRNAs and small nucleolar RNAs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 Several small nucleolar RNAs co-immunoprecipitate with Sen1 but

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

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

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

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

56 Small nucleolar RNAs direct the location of certain meth

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

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

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

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

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

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

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

64 of aberrant polyadenylated transcripts from small nucleolar RNA genes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 -1 RNA was inserted into the body of the U16 small nucleolar RNA, resulting in accumulation of the ri

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

135 Small nucleolar RNAs (snoRNAs) are conserved noncoding R

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

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

138 Small nucleolar RNAs (snoRNAs) are involved in cleavage

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

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

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

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

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

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

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

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

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

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

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

150 Small nucleolar RNAs (snoRNAs) function mainly as guides

151 Small nucleolar RNAs (snoRNAs) guide chemical modificati

152 Small nucleolar RNAs (snoRNAs) guide nucleotide modifica

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

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

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

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

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

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

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

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

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

162 Small nucleolar RNAs (snoRNAs) orchestrate the modificat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

199 5q11-q13, including SNURF-SNRPN and multiple small nucleolar RNAs (snoRNAs).

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

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

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

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

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

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

206 3' processing of snoRNAs (small nucleolar RNAs) that are excised from polycistroni

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

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

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

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

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

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

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

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