ライフサイエンスコーパス: non-coding RNA

1 lity of the RNA product (for both coding and non-coding RNAs).

2 al the formation of an rG4 structure in this non-coding RNA.

3 into mechanisms of chromatin modification by non-coding RNA.

4 in group 1 ILCs that is demarcated by a long non-coding RNA.

5 rted by proteomic analyses, as well as novel non coding RNAs.

6 NAs even in the absence of a training set of non-coding RNAs.

7 and cytoplasmic RBP functions for coding and non-coding RNAs.

8 referentially to mRNAs, rather than unstable non-coding RNAs.

9 hogenesis with a specific focus on antisense non-coding RNAs.

10 ms for the regulation of imprinted genes and non-coding RNAs.

11 n to bias transcription toward coding versus non-coding RNAs.

12 ase modification of unknown function in long non-coding RNAs.

13 slated regions of specific mRNAs and several non-coding RNAs.

14 n shown to be transcriptionally regulated by non-coding RNAs.

15 NA transcripts, likely muscle-expressed long non-coding RNAs.

16 tor for the quality control of mitochondrial non-coding RNAs.

17 mediated by RNA binding proteins (RBPs) and non-coding RNAs.

18 e great promise for functional annotation of non-coding RNAs.

19 , either as protein-encoding molecules or as non-coding RNAs.

20 ot only diverse coding RNA variants but also non-coding RNAs.

21 ast, little is known about the expression of non-coding RNAs.

22 s expression of repeat-associated coding and non-coding RNAs.

23 merase III-associated transcription of small non-coding RNAs.

24 ch as transcription factor-binding sites and non-coding RNAs.

25 concealed using microarrays, including four non-coding RNAs.

26 est genome fraction is encoding thousands of non-coding RNAs.

27 Here we identify FILNC1 (FoxO-induced long non-coding RNA 1) as an energy stress-induced long non-c

28 hereas a subset of gene transcripts and long-non-coding RNAs adjacent to TE insertions are affected b

29 Recently, site-specific small non-coding RNAs, also termed DNA damage response RNAs (D

30 stic link between an activity-dependent long non-coding RNA and epilepsy.

31 ivated as characterized by the appearance of non-coding RNA and histone modifications.

32 adenocarcinoma transcript 1 (MALAT1), a long non-coding RNA and key positive regulator of invasion, e

33 We show that TSS reveals riboswitches, non-coding RNA and novel transcription units.

34 mutations in 20 protein-coding genes, 4 long non-coding RNAs and 10 untranslational regions.

35 ion or mutations in trans factors, including non-coding RNAs and chromatin regulators.

36 are distinct from the previously identified non-coding RNAs and cover 11% of the yeast genome.

37 , we identified a large number of novel long non-coding RNAs and fusion transcripts and found that DN

38 hared liability, we identified multiple long non-coding RNAs and RNA binding protein genes (DA376252,

39 eover, we identify multiple neurite-targeted non-coding RNAs and RNA-binding proteins with potential

40 on nucleic acids, including various kinds of non-coding RNAs and their interactions, molecular dynami

41 ipts, including mRNA, the various classes of non-coding RNA, and small RNA.

42 review, we take a specific look at how TLR7, non-coding RNA, and SSA/Ro60 can contribute to clinical

43 g genes, 508 novel transcribed regions, 5178 non-coding RNAs, and 35 846 small RNA loci that were for

44 about what regulates FKBP5 In recent years, non-coding RNAs, and in particular microRNAs, have been

45 mulating articles are presented: one on long non-coding RNAs, another on the ligand-activated transcr

46 Furthermore, a long non-coding RNA antisense to FOXM1 (FOXM1-AS) promotes th

47 together with coding genes, (antisense) long non-coding RNAs are deregulated in skin tissue of system

48 While a myriad non-coding RNAs are known to be essential in cellular pr

49 We also find that many long non-coding RNAs are preferentially expressed in germ-lin

50 Non-coding RNAs are ubiquitous, but the discovery of new

51 course of this study, we have identified the non-coding RNA BC200 (BCYRN1) as specifically enriched u

52 s in the folding and regulatory functions of non-coding RNAs but their structure proves difficult to

53 es are bound by a large number of coding and non-coding RNAs, but approaches to comprehensively map t

54 ding RNA 1) as an energy stress-induced long non-coding RNA by FoxO transcription factors.

55 Small non-coding RNAs called piRNAs serve as guides for an ada

56 s, expresses seven small nuclear uracil-rich non-coding RNAs (called HSURs) in latently infected cell

57 d therapeutic targets against gastric cancer.Non-coding RNAs can modify the expression of proteins in

58 Lastly, long non-coding RNAs can serve well as associated genes to in

59 Here, we review the roles of long non-coding RNAs, chromosomal organizational structures a

60 teractions between miRNAs and two classes of non-coding RNAs, circRNAs and lncRNAs.

61 of bacteria and archaea, including abundant non-coding RNAs, cis-antisense transcription and regulat

62 nships among RNAs for mutation detection and non-coding RNA classification.

63 Such bi-functional 'coding and non-coding RNAs' (cncRNAs) have been shown to play impor

64 erase III (Pol III) transcribes medium-sized non-coding RNAs (collectively termed Pol III genes).

65 s encoded by a gene that is transcribed into non-coding RNA containing a 3'-hairpin (HTBS).

66 s, over 90% of which fulfil criteria as long non-coding RNAs correlated with the protein-coding genom

67 Here, we describe an unexpected role in non-coding RNA-directed DNA methylation in Arabidopsis t

68 ions might be attributed to the hypothetical non-coding RNAs embedded within the gene.

69 of uncharacterized promoter-associated long non-coding RNAs encoded by the mammalian genome, the Uph

70 ctive specific transcript), a prototype long non-coding RNA essential for establishing X chromosome i

71 PIWI-interacting RNAs (piRNAs) are small non-coding RNAs essential for animal germ cell developme

72 In addition, 35 maternally expressed non-coding RNAs exhibited the same allele-specific epige

73 em Cell, Qian et al. (2016) demonstrate that non-coding RNAs expressed by the maternal-imprinted locu

74 known structures, we predict contacts in 160 non-coding RNA families.

75 ress FoxOs induce the expression of the long non-coding RNA FILNC1, which inhibits survival of RCC by

76 fining the role of the intronic variants and non-coding RNA for pain in patients with HNSCC.

77 Many non-coding RNAs form structures that interact with cellu

78 indings in human cells where endogenous long non-coding RNAs function to regulate the epigenome.

79 RMRP and NEAT1, two non-coding RNA genes, carry mutations that affect protei

80 he largest family of essential, ever-present non-coding RNA genes.

81 Non-coding RNAs have been drawing increasing attention i

82 Many non-coding RNAs have been identified and may function by

83 Various families of non-coding RNAs have been identified as substrates of th

84 Small non-coding RNAs have emerged as key modulators of viral

85 Recently, non-coding RNAs have emerged as new players in transcrip

86 that satellite DNA, and corresponding small non-coding RNA, helps the dosage compensation machinery

87 In conclusion, the long non-coding RNA HOTAIR is directly repressed by ER and it

88 , and a recent study indicated that the long non-coding RNA HOX transcript antisense RNA (HOTAIR) is

89 s of transcriptional silencing, resulting in non-coding RNA hyperproduction from cryptic RNA polymera

90 ry of: (i) new leads for gene function, (ii) non-coding RNAs; (iii) genes, pathways and ncRNAs that a

91 ultraconserved regions (T-UCRs) encode long non-coding RNAs implicated in human carcinogenesis.

92 the first time an important role of a long, non-coding RNA in antigenic variation and demonstrated a

93 ese findings outline a regulatory role for a non-coding RNA in lipid metabolism and advance our under

94 Here we show that circular antisense non-coding RNA in the INK4 locus (circANRIL), which is t

95 T and suggest a function for major satellite non-coding RNA in the organization of an RNA-nucleosome

96 the functional relevance of the plethora of non-coding RNAs in a given organism is challenging, espe

97 quencing studies have identified hundreds of non-coding RNAs in bacteria, including regulatory small

98 The roles of long non-coding RNAs in cancer metabolism remain largely unex

99 genes and 991 differentially expressed small non-coding RNAs in cortical tubers compared to autopsy c

100 Recent studies posit a role for non-coding RNAs in epithelial ovarian cancer (EOC).

101 ing alternative promoters in gene bodies and non-coding RNAs in intergenic regions.

102 r abundance, the molecular functions of long non-coding RNAs in mammalian nervous systems remain poor

103 gnatures, cell-identity markers, and diverse non-coding RNAs in rodent and human tissue volumes.

104 To address the relevance of small non-coding RNAs in SARS-CoV pathology, we deep sequenced

105 the potential of distal enhancer elements of non-coding RNAs in the prognostication of breast cancer

106 Small non-coding RNAs, in particular microRNAs (miRNAs), regul

107 In addition, we annotated various classes of non-coding RNA including microRNA, long intergenic RNA,

108 samples reveled thousands of uncharacterized non-coding RNAs including long non-coding RNA (lncRNA).

109 re recently, different classes of regulatory non-coding RNAs, including microRNAs.

110 sRNA interactions were also identified with non-coding RNAs, including sRNAs and tRNAs, demonstratin

111 arily conserved enzyme that generates short, non-coding RNAs, including tRNAs and 5S rRNA.

112 se III is essential for the transcription of non-coding RNAs, including tRNAs.

113 RNA processing machinery to cleave its small non-coding RNA into a 22-nt RNA fragment, Sal-1, which

114 machinery to further process bacterial small non-coding RNAs into microRNA-like fragments.

115 furthermore, we identify candidate genes and non-coding RNAs involved in telomere maintenance, immune

116 This small non-coding RNA is also highly expressed within the nucle

117 whether such genomic alterations also affect non-coding RNAs is limited, and their impact on circular

118 We further identify the long non-coding RNA LeXis as a mediator of this effect.

119 LincRNA-p21 is a long intergenic non-coding RNA (lincRNA) involved in the p53-mediated st

120 nct messenger RNA (mRNA) and long intergenic non-coding RNA (lincRNA) profiles compared to hepatocell

121 Long intergenic non-coding RNAs (lincRNAs) are transcribed from non-codi

122 stigation of the capacity of long intergenic non-coding RNAs (lincRNAs) as biomarkers associated with

123 that the mutation and dysregulation of long non-coding RNA (lncRNA) are associated with numerous dis

124 Long non-coding RNA (lncRNA) are emerging as contributors to

125 Here we report that the long non-coding RNA (lncRNA) HOTAIR (for HOX Transcript Antis

126 lear factor kappa B (NF-kappaB) and the long non-coding RNA (lncRNA) HOTAIR (HOX transcript antisense

127 Long non-coding RNA (lncRNA) is a large class of gene transcr

128 We identified a rodent-specific long non-coding RNA (lncRNA) linc1281, hereafter Ephemeron (E

129 also binds and regulates the levels of long non-coding RNA (lncRNA) Neat1 and together with PABPN1 i

130 including coding-transcript profiling, long non-coding RNA (lncRNA) profiling and coexpression netwo

131 wn that mice with genetic knockout of a long non-coding RNA (lncRNA) steroid receptor RNA activator (

132 We identified a long non-coding RNA (lncRNA) that arises from the antisense s

133 cis-regulatory element demarcated by a long non-coding RNA (lncRNA) that controls the function and l

134 tes with the expression of an antisense long non-coding RNA (lncRNA) that has previously been shown t

135 PCGEM1 is a long non-coding RNA (lncRNA) that is often upregulated in pro

136 Long non-coding RNA (lncRNA) transcription into a downstream

137 Clustering by mRNA, long non-coding RNA (lncRNA), and miRNA expression converged

138 The intronless ht-WNT10B resembles a long non-coding RNA (lncRNA), which suggests its involvement

139 characterized non-coding RNAs including long non-coding RNA (lncRNA).

140 A central element of this process are long non-coding RNAs (lncRNA), which in Arabidopsis thaliana

141 e enabled the discovery of thousands of long non-coding RNAs (lncRNAs) across many species.

142 Long non-coding RNAs (lncRNAs) are a diverse and poorly conse

143 Long non-coding RNAs (lncRNAs) are a diverse class of RNAs th

144 Long non-coding RNAs (lncRNAs) are a family of novel genes th

145 Long non-coding RNAs (lncRNAs) are an emerging class of trans

146 Alterations in long non-coding RNAs (lncRNAs) are associated with human carc

147 In these tumors, expression of long non-coding RNAs (lncRNAs) are deregulated and closely as

148 Long non-coding RNAs (lncRNAs) are expressed in a highly tiss

149 nscripts such as microRNAs (miRNAs) and long non-coding RNAs (lncRNAs) are important genetic regulato

150 and growing evidence has indicated that long non-coding RNAs (lncRNAs) are important players in lung

151 Long non-coding RNAs (lncRNAs) are important regulators of di

152 Long non-coding RNAs (lncRNAs) are largely heterogeneous and

153 Although long non-coding RNAs (lncRNAs) are non-protein-coding transcr

154 To date, Y chromosome-linked long non-coding RNAs (lncRNAs) are poorly characterized and t

155 Long non-coding RNAs (lncRNAs) are prominently associated wit

156 evaluated the potential of circulating long non-coding RNAs (lncRNAs) as biomarkers of subclinical c

157 Long non-coding RNAs (lncRNAs) comprise a diverse class of tr

158 Long non-coding RNAs (lncRNAs) constitute a large, yet mostly

159 Thousands of long non-coding RNAs (lncRNAs) have been identified in mammal

160 Long non-coding RNAs (lncRNAs) have been implicated in numero

161 Long non-coding RNAs (lncRNAs) have been implicated in the re

162 To date, a large number of long non-coding RNAs (lncRNAs) have been recently discovered

163 For example, although long non-coding RNAs (lncRNAs) have been shown to critically

164 Recently, long non-coding RNAs (lncRNAs) have emerged as an important c

165 Long non-coding RNAs (lncRNAs) have emerged as potential key

166 Long non-coding RNAs (lncRNAs) have emerged as regulators of

167 In particular, the biological roles of long non-coding RNAs (lncRNAs) have never been characterized

168 urther, ethanol-induced upregulation of long non-coding RNAs (lncRNAs) HOTAIR and MALAT1 in endotheli

169 over, through screening hypoxia-related long non-coding RNAs (lncRNAs) in PDK1-positive tissue, we fi

170 The roles of long non-coding RNAs (lncRNAs) in regulating cancer and stem

171 parable, with a distinct enrichment for long non-coding RNAs (lncRNAs) in snRNA-seq.

172 the transcription of a wide variety of long non-coding RNAs (lncRNAs) in the genomes of several orga

173 tabases indicated similarity with plant long non-coding RNAs (lncRNAs) involved in splicing regulatio

174 The expression of long non-coding RNAs (lncRNAs) is dysregulated in hepatocellu

175 Thousands of long non-coding RNAs (lncRNAs) lie interspersed with coding g

176 o zygotic transition and annotated 1120 long non-coding RNAs (lncRNAs) many of which differentially e

177 We hypothesized that circulating long non-coding RNAs (lncRNAs) may act as diagnostic markers

178 There is a growing perception that long non-coding RNAs (lncRNAs) modulate cellular function.

179 New evidence indicates that long non-coding RNAs (lncRNAs) play crucial roles in epigenet

180 Long non-coding RNAs (lncRNAs) play key roles in human diseas

181 Although long non-coding RNAs (lncRNAs) regulate various cellular even

182 Long non-coding RNAs (lncRNAs) regulating gene expression at

183 esponse to infection, the roles of many long non-coding RNAs (lncRNAs) remain unknown.

184 espite the overwhelming number of human long non-coding RNAs (lncRNAs) reported so far, little is kno

185 Circulating long non-coding RNAs (lncRNAs) serve as valuable biomarkers i

186 rts have vastly expanded the catalog of long non-coding RNAs (lncRNAs) with varying evolutionary cons

187 sociated region contains two genes for long, non-coding RNAs (lncRNAs), AL157359.3 and AL157359.4.

188 d gene silencing are thought to involve long non-coding RNAs (lncRNAs), but few specific lncRNAs that

189 a cell-type-specific manner, producing long non-coding RNAs (lncRNAs), rather than protein-coding tr

190 h as small nucleolar RNAs (snoRNAs) and long non-coding RNAs (lncRNAs), undergo trans-splicing and po

191 re transcribed into numerous regulatory long non-coding RNAs (lncRNAs).

192 nnotation or no protein product such as long non-coding RNAs (lncRNAs).

193 re disproportionately present in human long, non-coding RNAs (lncRNAs).

194 be translated (mRNAs) from the class of long non-coding RNAs (lncRNAs).

195 s, and a significant subset of them are long non-coding RNAs (lncRNAs).

196 s that regulate gene expression such as long non-coding RNAs (lncRNAs).

197 sts, rs1709393 located in an uncharacterized non-coding RNA locus on chromosomal band 3q12.3 (P=1.65

198 cts generated by ASOs targeting nuclear long non-coding RNA Malat 1 and pre-mRNA were degraded by nuc

199 d ASO potency for reducing expression of the non-coding RNA Malat-1, in Stabilin-expressing cell line

200 s with hypereosinophilic syndrome, this long non-coding RNA may represent a potential therapeutic tar

201 thereby showing that circularization of long non-coding RNAs may alter RNA function and protect from

202 Non-coding RNAs may contribute to this regulatory orches

203 snoRNAs and provided the first evidence that non-coding RNAs may play an important role in regulating

204 ere, recent advances in our understanding of non-coding RNA-mediated regulation of skin development a

205 criptional profiling, we found that the long non-coding RNA MIR100HG and two embedded microRNAs, miR-

206 hesis, processing and function of coding and non-coding RNA molecules and their interacting proteins

207 The expression of genes and non-coding RNA molecules changed in both fungal resistan

208 lar signaling, and microRNAs which are small non-coding RNA molecules that function in post-transcrip

209 MicroRNA (miRNA) are short non-coding RNA molecules that regulate multiple cellular

210 MicroRNAs (miRNAs) are small non-coding RNA molecules whose primary function is to re

211 MicroRNAs are small and non-coding RNA molecules with the master role in regulat

212 ion of 110 RNA-binding proteins and 137 long non-coding RNAs, most of them previously not linked to s

213 the post-transcriptional processing of other non-coding RNAs (mostly ribosomal RNAs), but have also b

214 Non-coding RNAs must fold into specific structures that

215 relocalized the Bcl11b enhancer identified a non-coding RNA named ThymoD (thymocyte differentiation f

216 idence that promoter demethylation and close non-coding RNAs (namely, CT-ncRNAs) may be two mechanism

217 The brain cytoplasmic (BC1) RNA is a non-coding RNA (ncRNA) involved in neuronal translationa

218 Non-coding RNAs (ncRNAs) are known to regulate gene expr

219 The discovery of structured non-coding RNAs (ncRNAs) in bacteria can reveal new face

220 oRNA highlights the regulatory complexity of non-coding RNAs (ncRNAs), which occupy the bulk of the g

221 nery and further serves as a source of short non-coding RNAs (ncRNAs).

222 e led to the discovery of several classes of non-coding RNAs (ncRNAs).

223 sion levels of both protein coding genes and non-coding RNAs (ncRNAs).

224 the tumor suppressor gene PTEN and the long non-coding RNA NEAT1.

225 kles are nuclear bodies form around the long non-coding RNA, Neat1, and RNA-binding proteins.

226 Here we show that the long non-coding RNA, NEAT1, directly modulates neuronal excit

227 References 1013 MicroRNAs (miRNAs) are small non-coding RNAs, of typically 20-24 nt, that regulate ge

228 The NtcA regulon also included eight non-coding RNAs, of which Ncr1071, Syr6 and NsiR7 were e

229 oli and examined the effect of Hfq-dependent non-coding RNAs on these fusions.

230 hat include fusion proteins, novel exons and non-coding RNAs, one-third of which showed allelically i

231 The long non-coding RNA PARTICLE (Gene PARTICL- 'Promoter of MAT2

232 of differentially expressed genes and their non-coding RNA partners, long noncoding RNAs and microRN

233 Our results suggest that non-coding RNAs play important roles in the regulatory n

234 Non-coding RNAs play indispensable roles in regulating t

235 MiRNAs, a class of small non-coding RNAs, play a pivotal role in regulating gene

236 Here we review how non-coding RNA plays a role in regulation of transcripti

237 tients with type 2 diabetes, long intergenic non-coding RNA predicting cardiac remodeling (LIPCAR) wa

238 s of the complex, underscoring its role as a non-coding RNA processing/degradation unit.

239 kl mutant are correlated with changes in the non-coding RNAs produced by Pol IV and Pol V.

240 Non-coding RNAs produced from active arrays are complexe

241 eate a chromatin environment that influences non-coding RNA production, DNA methylation, and transcri

242 dy, Leucci et al. report a role for the long non-coding RNA SAMMSON in driving mitochondrial function

243 As such, non-coding RNAs should be considered as potential biomar

244 P1 constructs and of assessing the extent of non-coding RNA silencing and histone H4K16 deacetylation

245 is approach, we found that a subset of small non-coding RNAs (sncRNA) is altered in relapse and remis

246 Small non-coding RNAs (sncRNAs) are highly abundant RNAs, typi

247 Small non-coding RNAs (sncRNAs) play critical roles in both va

248 ed the largest class of over-expressed small non-coding RNA species in tubers.

249 MicroRNAs (miRNAs) are small non-coding RNA species that have been shown to have role

250 e recently emerged as a large class of novel non-coding RNA species.

251 n Hfq facilitates interactions between small non-coding RNA (sRNA) and target mRNAs.

252 regulatory function of most bacterial small non-coding RNAs (sRNAs) is base pairing with partially c

253 Although long non-coding RNAs such as HOTAIR have been implicated in b

254 Changes in small non-coding RNAs such as micro RNAs (miRNAs) can serve as

255 In trypanosomes, all mRNAs, and non-coding RNAs such as small nucleolar RNAs (snoRNAs) a

256 Nevertheless, RNA editing in non-coding RNA, such as microRNA (miRNA), have caused gr

257 The technique, referred to as global small non-coding RNA target identification by ligation and seq

258 f different types of RNA (including mRNA and non-coding RNA) targeted by endogenous RNase H1.

259 MicroRNA-7 (miR-7) is a small non-coding RNA that has been found to exhibit a protecti

260 c disorders.Brain cytoplasmic (BC1) RNA is a non-coding RNA that has been implicated in translational

261 HOTAIR is a long non-coding RNA that is overexpressed, promotes metastasi

262 N-BLR is a primate-specific long non-coding RNA that modulates the epithelial-to-mesenchy

263 Here we identify a long non-coding RNA that we termed Morrbid, which tightly con

264 ed a large set of tissue-specific coding and non-coding RNAs that are bound to active promoters and e

265 MicroRNAs (miRNAs) are small non-coding RNAs that are extensively involved in many ph

266 MicroRNAs (miRNAs) are small non-coding RNAs that are involved in post-transcriptiona

267 cting RNAs (piRNAs) are a new class of small non-coding RNAs that are known to be associated with RNA

268 Circular RNAs (circRNAs) are a class of non-coding RNAs that are widely expressed in various cel

269 we describe the presence of rarely studied, non-coding RNAs that exist in high numbers in exosomes.

270 Small nucleolar RNAs (snoRNAs) are non-coding RNAs that form ribonucleoproteins to guide co

271 mall nucleolar RNAs (snoRNAs) are a class of non-coding RNAs that guide the post-transcriptional proc

272 re 26-30-nucleotide germ line-specific small non-coding RNAs that have evolutionarily conserved funct

273 internal RNA modification in both coding and non-coding RNAs that is catalysed by the METTL3-METTL14

274 MicroRNAs (miRNAs) are small, non-coding RNAs that play critical roles in the post-tra

275 MicroRNAs are small non-coding RNAs that regulate gene expression and are ex

276 MicroRNAs (miRNAs) are short non-coding RNAs that regulate gene expression by promoti

277 MicroRNAs (miRNAs) are short single-stranded non-coding RNAs that regulate gene expression, particula

278 MicroRNAs (miRNAs) are short non-coding RNAs that silence mRNAs.

279 s important implications for the function of non-coding RNAs, the translational fidelity of coding RN

280 Viruses express several classes of non-coding RNAs; the functions and mechanisms by which m

281 ly, ZNF750 promoted the expression of a long non-coding RNA (TINCR), which mediated both cancer-inhib

282 also reveals a regulatory mechanism by long non-coding RNAs to control energy metabolism and tumor d

283 uggesting that the early studies using small non-coding RNAs to modulate transcription were making us

284 nd and carry specific subtypes of coding and non-coding RNAs to the exosome.

285 r of nearly 40 microRNAs and their host long non-coding RNA transcript (lnc-MGC) are coordinately inc

286 ween the proteins involved in small and long non-coding RNA transcriptional regulatory mechanisms, su

287 Non-coding RNA transcripts such as microRNAs (miRNAs) an

288 abundance of many miRNA precursors and long non-coding RNAs was dramatically altered in THC-treated

289 hat transcription of a Hand2-associated long non-coding RNA, which we named upperhand (Uph), is requi

290 RNA base modifications in protein-coding and non-coding RNAs, which have energized the emerging field

291 ly-acting control elements of antisense long non-coding RNAs, which in turn regulate targeted gene ex

292 located in the nucleus, is to polyadenylate non-coding RNAs, which undergo trans-splicing and polyad

293 ed fragments) are an abundant class of small non-coding RNAs whose biological roles are not well unde

294 characterization of a novel long intergenic non-coding RNA with MyoD-regulated and skeletal muscle-r

295 MicroRNAs (miRNAs) are small regulatory non-coding RNAs with a diversity of cellular functions,

296 00 protein coding genes (PCGs) and 100 long non-coding RNAs with domestication-associated haplotypes

297 icroRNAs (miRNAs) are a major class of small non-coding RNAs with emerging functions in biotic and ab

298 MicroRNAs (miRNAs) are short non-coding RNAs with key roles in cellular regulation.

299 role in chromosome silencing induced by the non-coding RNA Xist.

300 and-7 modules) with their respective cognate non-coding RNAs (YRNAs and a novel tRNA-like molecule) a