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1 he translational potential of XIST, a unique non-coding RNA.
2 into mechanisms of chromatin modification by non-coding RNA.
3 ontains CpG-rich promoters for TERRA, a long non-coding RNA.
4 oteins, post-translational modifications and non-coding RNAs.
5 ying localization consistent with other long non-coding RNAs.
6 also be relevant for the evolution of other non-coding RNAs.
7 into the biology of this important class of non-coding RNAs.
8 n histone modifications, DNA methylation and non-coding RNAs.
9 ry genes and complex circuits also involving non-coding RNAs.
10 NA methylation and the expression of various non-coding RNAs.
11 luding key DDR genes and multiple classes of non-coding RNAs.
12 pregulation of stress pathway genes and long non-coding RNAs.
13 including many protein-coding mRNAs and some non-coding RNAs.
14 essing and/or degradation of both coding and non-coding RNAs.
15 l processes such as alternative splicing and non-coding RNAs.
16 richa, producing rearrangement-specific long non-coding RNAs.
17 ntially targeted by differentially expressed non-coding RNAs.
18 , house-keeping genes, which produce stable, non-coding RNAs.
19 t addition to the ever-expanding pantheon of non-coding RNAs.
20 pharmacologically boosted by acting on such non-coding RNAs.
21 n to bias transcription toward coding versus non-coding RNAs.
22 tor for the quality control of mitochondrial non-coding RNAs.
23 merase III-associated transcription of small non-coding RNAs.
24 tified and characterized on mRNA and various non-coding RNAs.
25 cations, and regulation of transcription via non-coding RNAs.
26 element family member, which generates long non-coding RNAs.
27 osine release and expression of certain long non-coding RNAs.
28 hers function broadly across both coding and non-coding RNAs.
29 nuclear RNA degradation, primarily targeting non-coding RNAs.
31 enes (2.94-fold), GWAS loci (1.52-fold), and non-coding RNAs (1.44-fold), compared with random distri
32 abled the global mapping of mRNA and of long non-coding RNA 3' ends, quantification of the resulting
33 study, we present data that long intergenic non-coding RNA 346 (LINC00346) functions as a promoting
35 ntibodies interact with beta-amyloid, a long non-coding RNA AC099552.4 (p = 1.2 x 10(-7)), and a zinc
40 C across hundreds of residues in rRNA, tRNA, non-coding RNA and mRNA from hyperthermophilic archaea.
41 analysis of leukocyte RNA we found that long non-coding RNA and, to a lesser extent, small non-coding
43 00s, non-coding RNAs such as microRNAs, long non-coding RNAs and circular RNAs have been assessed as
44 conserved between mouse and human XIST long non-coding RNAs and defined protein communities whose bi
45 gene transcripts, separating short and long non-coding RNAs and predicting circular RNAs from other
46 eover, we identify multiple neurite-targeted non-coding RNAs and RNA-binding proteins with potential
47 R, that automates the discovery of expressed non-coding RNAs and UTRs from RNA-seq reads mapped to a
48 s, ribosomal RNA-derived small RNAs and long non-coding RNAs) and associated RNA modifications is exp
49 g genes, 508 novel transcribed regions, 5178 non-coding RNAs, and 35 846 small RNA loci that were for
51 gth, mature tRNAs and other structured small non-coding RNAs, and less abundant tRNA fragments and ma
53 together with coding genes, (antisense) long non-coding RNAs are deregulated in skin tissue of system
58 otential of candidate epigenetic factors and non-coding RNAs as biomarkers and drug targets for DKD.
60 es are bound by a large number of coding and non-coding RNAs, but approaches to comprehensively map t
65 s, expresses seven small nuclear uracil-rich non-coding RNAs (called HSURs) in latently infected cell
68 ches employed to screen for novel coding and non-coding RNA candidates with diagnostic and therapeuti
69 lysis of changes in genome methylation, long non-coding RNAs, circular RNAs, micro-RNAs and fruit met
73 stem cells revealed changes in a variety of non-coding RNA elements, with significant under expressi
75 ere identified (FDR q < 0.05), including the non-coding RNAs ENTPD3-AS1, LOC102724438, and protein-co
76 h CIZ1, including interaction with XIST long-non-coding RNA, epigenetic maintenance and regulation of
77 PIWI-interacting RNAs (piRNAs) are small non-coding RNAs essential for animal germ cell developme
80 ress FoxOs induce the expression of the long non-coding RNA FILNC1, which inhibits survival of RCC by
81 olymerase II-related enzymes that synthesize non-coding RNAs for RNA-directed DNA methylation (RdDM)
82 n be achieved in three steps: distinguishing non-coding RNAs from protein coding gene transcripts, se
84 n of PPARalpha directly upregulates the long non-coding RNA gene Gm15441 through PPARalpha binding si
87 and global annotation of protein-coding and non-coding RNA genes in a manner orthogonal to gene expr
90 d across all cohorts was located in the long non-coding RNA growth arrest specific five gene (GAS5) (
94 that satellite DNA, and corresponding small non-coding RNA, helps the dosage compensation machinery
95 ry of: (i) new leads for gene function, (ii) non-coding RNAs; (iii) genes, pathways and ncRNAs that a
97 presents a paradigm for the function of long non-coding RNA in epigenetic regulation, although how it
98 In this study, we identified a novel long non-coding RNA in Lipid Associated Single nucleotide pol
99 ently, we discovered a new class of circular non-coding RNAs in metazoans, called tRNA intronic circu
101 e the therapeutic utility of both coding and non-coding RNAs in the context of cardiovascular disease
102 m of m(6)A modifications (in both coding and non-coding RNAs) in cancer pathogenesis and drug respons
105 sRNA interactions were also identified with non-coding RNAs, including sRNAs and tRNAs, demonstratin
106 se H-mediated cleavage, splicing modulation, non-coding RNA inhibition, gene activation and programme
107 most eukaryotic pre-messenger RNAs and long non-coding RNAs, introns are removed through the process
110 ch of these genes, either coding proteins or non-coding RNAs, is or are responsible for DFNA58 HL.
114 ition, we identified the human-specific long non-coding RNA, LINKA, as an HNF1A target necessary for
116 y T cells, with high expression of this long non-coding RNA (lncRNA) and low expression of the cytoki
117 silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vitro a
118 egulated by the interaction between the long non-coding RNA (lncRNA) DIGIT and the bromodomain and ex
119 nt of these are located within BANCR, a long non-coding RNA (lncRNA) exclusively expressed in primate
128 tes with the expression of an antisense long non-coding RNA (lncRNA) that has previously been shown t
129 RNA myeloid-specific 1 (HOTAIRM1) is a long non-coding RNA (lncRNA) that plays a pivotal role in reg
130 ide Metabolism Regulator (lincNMR) is a long non-coding RNA (lncRNA) which is induced in hepatocellul
134 -8 on transcriptome including mRNAs and long non-coding RNA (lncRNAs) in rheumatoid arthritis (RA) fi
135 ancer, the interplay between long intergenic non-coding RNAs (lncRNAs) and chromatin remodeling remai
137 ther non-protein coding RNAs, primarily long non-coding RNAs (lncRNAs) and small nucleolar RNAs (snoR
138 how that the mutation and regulation of long non-coding RNAs (lncRNAs) are associated with various hu
140 ein-coding genes, the majority of human long non-coding RNAs (lncRNAs) are considered non-conserved.
152 known ASD risk genes code for proteins, long non-coding RNAs (lncRNAs) as essential regulators of gen
166 rcinoma (PDAC) progression, the role of long non-coding RNAs (lncRNAs) in PDAC remains largely unknow
169 the transcription of a wide variety of long non-coding RNAs (lncRNAs) in the genomes of several orga
170 o identify binding proteins of specific long non-coding RNAs (lncRNAs) in the native cellular context
171 the targeting and spreading patterns of long non-coding RNAs (lncRNAs) on chromatin requires a techni
172 As ncRNAs such as microRNAs (miRNAs), long non-coding RNAs (lncRNAs) or circular RNAs (circRNAs) ca
177 of multi-protein DNA complexes, so how long non-coding RNAs (lncRNAs) regulate DNA repair is less we
180 espite the overwhelming number of human long non-coding RNAs (lncRNAs) reported so far, little is kno
181 is transcribed and that there are more long non-coding RNAs (lncRNAs) than protein coding genes, sev
182 alian genome is transcribed, generating long non-coding RNAs (lncRNAs) that can undergo post-transcri
183 zation of individual miRNAs, mRNAs, and long non-coding RNAs (lncRNAs) to PBs using intracellular sin
186 rts have vastly expanded the catalog of long non-coding RNAs (lncRNAs) with varying evolutionary cons
188 expression of LRRK2 and two long intergenic non-coding RNAs (lncRNAs), LINC02555 and AC079630.4, in
190 h as small nucleolar RNAs (snoRNAs) and long non-coding RNAs (lncRNAs), undergo trans-splicing and po
196 found not only in messenger RNAs but also in non-coding RNAs, m(6)A affects the fate of the modified
197 processed for EXO-NGS, we observed two long non-coding RNAs, malat-1 and CRNDE to be variably expres
198 ng, we systematically annotated multi-exonic non-coding RNA (mencRNA) genes transcribed from 1.5-Mb i
199 sed modulation of a triple helix in the long non-coding RNA metastasis-associated lung adenocarcinoma
200 criptional profiling, we found that the long non-coding RNA MIR100HG and two embedded microRNAs, miR-
201 levels, represses the expression of the long non-coding RNA MIR22HG, thus upregulating cMYC protein l
202 ional study of EV-mediated transfer of small non-coding RNA molecules at single-cell resolution.
203 ircRNAs) are a covalently closed subclass of non-coding RNA molecules formed by back splicing of line
204 ween the primary and secondary structures of non-coding RNA molecules suggests that stem-disrupting k
205 MicroRNAs (miRNAs) are a class of small, non-coding RNA molecules that circulate in blood and are
206 relocalized the Bcl11b enhancer identified a non-coding RNA named ThymoD (thymocyte differentiation f
207 xbp-1 mRNA cleavage is a biologically active non-coding RNA (ncRNA) essential for axon regeneration i
211 CREs could be identified by context-specific non-coding RNA (ncRNA) profiling, based on the observati
213 ed that an entire class of molecules, termed non-coding RNA (ncRNA), plays key regulatory roles in sh
214 r genes, virus-host interactions involved in non-coding RNA (ncRNA), target gene and microRNA express
215 sub-proteomes that interact with coding and non-coding RNAs (ncRNAs) and to identify hundreds of pro
216 rates, while rRNA, tRNA, and other conserved non-coding RNAs (ncRNAs) are excluded from these bodies.
221 e effect of this stress on the expression of non-coding RNAs (ncRNAs) has not been systematically exa
223 (DMD) is a surveillance pathway for certain non-coding RNAs (ncRNAs) including ribosomal RNAs (rRNAs
224 GRID-seq typically finds both coding and non-coding RNAs (ncRNAs) that interact with tissue-speci
231 ied three highly abundant HHV-6 encoded long non-coding RNAs, one of which generates a non-polyadenyl
237 om the screen, progenitor renewal associated non-coding RNA (PRANCR), using RNA interference-mediated
238 We find that alignments for several long non-coding RNAs previously shown to lack covariation sup
241 eate a chromatin environment that influences non-coding RNA production, DNA methylation, and transcri
242 hich contains the proto-oncogene c-MYC, long non-coding RNA PVT1, and microRNAs (miRs), is the most c
244 ing of EVs identifies diverse RBPs and small non-coding RNAs requiring the LC3-conjugation machinery
247 dependent tool evaluates pre-processed small non-coding RNA sequencing (sncRNA-seq) data, i.e. expres
248 sequence-divergent but structurally related non-coding RNAs, share RNP networks and that network hub
249 Recent studies have demonstrated sperm small non-coding RNA (sncRNA) populations vary in response to
254 PARN deficiency affects the stability of non-coding RNAs such as human telomerase RNA (hTR), but
255 quencing technologies since the early 2000s, non-coding RNAs such as microRNAs, long non-coding RNAs
259 Regression analysis identified a single long non-coding RNA that could predict cluster assignment wit
261 ato spindle tuber viroid (PSTVd), a circular non-coding RNA that replicates and spreads systemically
263 ed a large set of tissue-specific coding and non-coding RNAs that are bound to active promoters and e
264 lasma contains > 40,000 different coding and non-coding RNAs that are potential biomarkers for human
268 leolar RNAs (snoRNAs) are a diverse group of non-coding RNAs that direct chemical modifications at sp
271 re 26-30-nucleotide germ line-specific small non-coding RNAs that have evolutionarily conserved funct
278 re focused our attention on microRNAs: small non-coding RNAs that primarily function as post-transcri
279 showed that a subset of introns can work as non-coding RNAs that trap the spliceosome and decrease g
280 we predicted several UTRs and lncRNAs (long non-coding RNA) that significantly enriched or depleted
281 transcription factor binding motifs and long non-coding RNAs, that potentially contribute to organoge
282 modification and chromatin remodelling, and non-coding RNAs, the manipulation of these mechanisms is
283 ly, ZNF750 promoted the expression of a long non-coding RNA (TINCR), which mediated both cancer-inhib
288 Moreover, this study provided global long non-coding RNA transcripts in the blood of patients with
292 ong non-coding RNA expression, but not small non-coding RNA, was largely recapitulated in human endot
293 on-coding RNA and, to a lesser extent, small non-coding RNA were significantly altered in sepsis rela
298 characterization of a novel long intergenic non-coding RNA with MyoD-regulated and skeletal muscle-r
299 chromosomes are active and express the long non-coding RNAs X active coating transcript (XACT) and X