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1 ment in group 1 ILCs that is demarcated by a long non-coding RNA.
2 res contains CpG-rich promoters for TERRA, a long non-coding RNA.
3 ble base modification of unknown function in long non-coding RNAs.
4 vel RNA transcripts, likely muscle-expressed long non-coding RNAs.
5 sable element family member, which generates long non-coding RNAs.
6 enes or partially overlapping with annotated long non-coding RNAs.
7 adenosine release and expression of certain long non-coding RNAs.
8 isplaying localization consistent with other long non-coding RNAs.
9 ted upregulation of stress pathway genes and long non-coding RNAs.
10 Oxytricha, producing rearrangement-specific long non-coding RNAs.
12 ve enabled the global mapping of mRNA and of long non-coding RNA 3' ends, quantification of the resul
13 ose antibodies interact with beta-amyloid, a long non-coding RNA AC099552.4 (p = 1.2 x 10(-7)), and a
14 on, whereas a subset of gene transcripts and long-non-coding RNAs adjacent to TE insertions are affec
16 lung adenocarcinoma transcript 1 (MALAT1), a long non-coding RNA and key positive regulator of invasi
17 rray analysis of leukocyte RNA we found that long non-coding RNA and, to a lesser extent, small non-c
18 rent mutations in 20 protein-coding genes, 4 long non-coding RNAs and 10 untranslational regions.
19 ariety of non-coding RNA regions (microRNAs, long non-coding RNAs and antisense transcripts), leading
20 ly 2000s, non-coding RNAs such as microRNAs, long non-coding RNAs and circular RNAs have been assesse
21 works conserved between mouse and human XIST long non-coding RNAs and defined protein communities who
22 ition, we identified a large number of novel long non-coding RNAs and fusion transcripts and found th
23 oding gene transcripts, separating short and long non-coding RNAs and predicting circular RNAs from o
24 his shared liability, we identified multiple long non-coding RNAs and RNA binding protein genes (DA37
25 roRNAs, ribosomal RNA-derived small RNAs and long non-coding RNAs) and associated RNA modifications i
26 e stimulating articles are presented: one on long non-coding RNAs, another on the ligand-activated tr
28 that together with coding genes, (antisense) long non-coding RNAs are deregulated in skin tissue of s
31 he secondary structure of the heart-specific long non-coding RNA Braveheart, leading to the discovery
40 d analysis of changes in genome methylation, long non-coding RNAs, circular RNAs, micro-RNAs and frui
41 cripts, over 90% of which fulfil criteria as long non-coding RNAs correlated with the protein-coding
44 umber of uncharacterized promoter-associated long non-coding RNAs encoded by the mammalian genome, th
45 s with CIZ1, including interaction with XIST long-non-coding RNA, epigenetic maintenance and regulati
46 X-inactive specific transcript), a prototype long non-coding RNA essential for establishing X chromos
48 gy stress FoxOs induce the expression of the long non-coding RNA FILNC1, which inhibits survival of R
50 ent findings in human cells where endogenous long non-coding RNAs function to regulate the epigenome.
53 vation of PPARalpha directly upregulates the long non-coding RNA gene Gm15441 through PPARalpha bindi
54 ciated across all cohorts was located in the long non-coding RNA growth arrest specific five gene (GA
55 iverse classes of RNA, ranging from small to long non-coding RNAs, have emerged as key regulators of
58 tance, and a recent study indicated that the long non-coding RNA HOX transcript antisense RNA (HOTAIR
59 ribed ultraconserved regions (T-UCRs) encode long non-coding RNAs implicated in human carcinogenesis.
60 st represents a paradigm for the function of long non-coding RNA in epigenetic regulation, although h
63 their abundance, the molecular functions of long non-coding RNAs in mammalian nervous systems remain
64 ed for the first time an important role of a long, non-coding RNA in antigenic variation and demonstr
65 on of most eukaryotic pre-messenger RNAs and long non-coding RNAs, introns are removed through the pr
67 n addition, we identified the human-specific long non-coding RNA, LINKA, as an HNF1A target necessary
70 memory T cells, with high expression of this long non-coding RNA (lncRNA) and low expression of the c
71 etic silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vi
72 dence that the mutation and dysregulation of long non-coding RNA (lncRNA) are associated with numerou
74 is regulated by the interaction between the long non-coding RNA (lncRNA) DIGIT and the bromodomain a
75 ak association lies upstream of LOXL1-AS1, a long non-coding RNA (lncRNA) encoded on the opposite str
76 ificant of these are located within BANCR, a long non-coding RNA (lncRNA) exclusively expressed in pr
81 r nuclear factor kappa B (NF-kappaB) and the long non-coding RNA (lncRNA) HOTAIR (HOX transcript anti
84 e other transcript variants, indicating that long non-coding RNA (lncRNA) is processed after transcri
88 MATR3 also binds and regulates the levels of long non-coding RNA (lncRNA) Neat1 and together with PAB
89 yses, including coding-transcript profiling, long non-coding RNA (lncRNA) profiling and coexpression
91 21, P = 5.06 x 10(-8); OR = 1.15) within the long non-coding RNA (lncRNA) RP11-58A18.1 and ~500 kb fr
92 y shown that mice with genetic knockout of a long non-coding RNA (lncRNA) steroid receptor RNA activa
95 ied a cis-regulatory element demarcated by a long non-coding RNA (lncRNA) that controls the function
96 rrelates with the expression of an antisense long non-coding RNA (lncRNA) that has previously been sh
98 sense RNA myeloid-specific 1 (HOTAIRM1) is a long non-coding RNA (lncRNA) that plays a pivotal role i
99 m(6)A alters the local structure in mRNA and long non-coding RNA (lncRNA) to facilitate binding of he
101 cleotide Metabolism Regulator (lincNMR) is a long non-coding RNA (lncRNA) which is induced in hepatoc
104 Active transcription of the neuron-specific long non-coding RNA (lncRNA), UBE3A-ATS, has been shown
109 LLDT-8 on transcriptome including mRNAs and long non-coding RNA (lncRNAs) in rheumatoid arthritis (R
110 g have enabled the discovery of thousands of long non-coding RNAs (lncRNAs) across many species.
112 RNA exosome and identified a vast number of long non-coding RNAs (lncRNAs) and enhancer RNAs (eRNAs)
114 to other non-protein coding RNAs, primarily long non-coding RNAs (lncRNAs) and small nucleolar RNAs
121 ies show that the mutation and regulation of long non-coding RNAs (lncRNAs) are associated with vario
123 protein-coding genes, the majority of human long non-coding RNAs (lncRNAs) are considered non-conser
127 these transcriptomic responses and show that long non-coding RNAs (lncRNAs) are dynamically regulated
131 A transcripts such as microRNAs (miRNAs) and long non-coding RNAs (lncRNAs) are important genetic reg
132 ial, and growing evidence has indicated that long non-coding RNAs (lncRNAs) are important players in
147 We evaluated the potential of circulating long non-coding RNAs (lncRNAs) as biomarkers of subclini
148 ntly known ASD risk genes code for proteins, long non-coding RNAs (lncRNAs) as essential regulators o
155 ivo, we generated a single-cell landscape of long non-coding RNAs (lncRNAs) during HSC development.
174 h a small number of the vast array of animal long non-coding RNAs (lncRNAs) have known effects on cel
178 Further, ethanol-induced upregulation of long non-coding RNAs (lncRNAs) HOTAIR and MALAT1 in endo
180 enocarcinoma (PDAC) progression, the role of long non-coding RNAs (lncRNAs) in PDAC remains largely u
181 Moreover, through screening hypoxia-related long non-coding RNAs (lncRNAs) in PDK1-positive tissue,
186 ealed the transcription of a wide variety of long non-coding RNAs (lncRNAs) in the genomes of several
187 ing to identify binding proteins of specific long non-coding RNAs (lncRNAs) in the native cellular co
188 TA databases indicated similarity with plant long non-coding RNAs (lncRNAs) involved in splicing regu
191 nal to zygotic transition and annotated 1120 long non-coding RNAs (lncRNAs) many of which differentia
194 ding the targeting and spreading patterns of long non-coding RNAs (lncRNAs) on chromatin requires a t
203 roles of multi-protein DNA complexes, so how long non-coding RNAs (lncRNAs) regulate DNA repair is le
208 Despite the overwhelming number of human long non-coding RNAs (lncRNAs) reported so far, little i
211 enome is transcribed and that there are more long non-coding RNAs (lncRNAs) than protein coding genes
212 mammalian genome is transcribed, generating long non-coding RNAs (lncRNAs) that can undergo post-tra
213 c deletion strategy to screen for functional long non-coding RNAs (lncRNAs) that is based on a lentiv
214 ocalization of individual miRNAs, mRNAs, and long non-coding RNAs (lncRNAs) to PBs using intracellula
217 Over 3,000 genes encoding previously unknown long non-coding RNAs (lncRNAs) were revealed through the
219 efforts have vastly expanded the catalog of long non-coding RNAs (lncRNAs) with varying evolutionary
221 ripts, including primary microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and enhancer RNAs (eRNAs
222 nt and gene silencing are thought to involve long non-coding RNAs (lncRNAs), but few specific lncRNAs
223 arcinoma (LUAD) based on multi-omics data of long non-coding RNAs (lncRNAs), microRNAs and mRNAs.
224 ed in a cell-type-specific manner, producing long non-coding RNAs (lncRNAs), rather than protein-codi
225 s such as small nucleolar RNAs (snoRNAs) and long non-coding RNAs (lncRNAs), undergo trans-splicing a
240 nse-associated region contains two genes for long, non-coding RNAs (lncRNAs), AL157359.3 and AL157359
242 products generated by ASOs targeting nuclear long non-coding RNA Malat 1 and pre-mRNA were degraded b
243 somes processed for EXO-NGS, we observed two long non-coding RNAs, malat-1 and CRNDE to be variably e
244 sequences derived from a non-polyadenylated long non-coding RNA (MALAT1), which can form a stabilizi
245 iduals with hypereosinophilic syndrome, this long non-coding RNA may represent a potential therapeuti
246 ion, thereby showing that circularization of long non-coding RNAs may alter RNA function and protect
247 le-based modulation of a triple helix in the long non-coding RNA metastasis-associated lung adenocarc
248 ogical significance of metastasis-associated long non-coding RNA, metastasis-associated lung adenocar
249 transcriptional profiling, we found that the long non-coding RNA MIR100HG and two embedded microRNAs,
250 sine levels, represses the expression of the long non-coding RNA MIR22HG, thus upregulating cMYC prot
251 to this scenario when it was shown that the long non-coding RNA molecule lincRNA-p21, known to be in
252 pression of 110 RNA-binding proteins and 137 long non-coding RNAs, most of them previously not linked
255 aspeckles are nuclear bodies form around the long non-coding RNA, Neat1, and RNA-binding proteins.
257 entified three highly abundant HHV-6 encoded long non-coding RNAs, one of which generates a non-polya
258 actors including regulators of pluripotency, long non-coding RNAs, or the presence of architectural p
263 ependence of high MYC protein levels on PVT1 long non-coding RNA provides a much needed therapeutic t
264 g messenger RNAs and non-coding RNAs such as long non-coding RNAs, pseudogenes and circular RNAs.
265 us, which contains the proto-oncogene c-MYC, long non-coding RNA PVT1, and microRNAs (miRs), is the m
266 (P=1.42 x 10(-12)), 8p12 at lnc-KIF13B-1, a long non-coding RNA (rs643472; P=3.41 x 10(-8)), and 2p2
267 t study, Leucci et al. report a role for the long non-coding RNA SAMMSON in driving mitochondrial fun
268 t advances suggest that chromatin-associated long non-coding RNA scaffolds also recruit chromatin-mod
269 the translation product of the bi-functional long non-coding RNA steroid receptor activator RNA 1 (SR
271 Regression analysis identified a single long non-coding RNA that could predict cluster assignmen
276 over, we predicted several UTRs and lncRNAs (long non-coding RNA) that significantly enriched or depl
277 rial transcription factor binding motifs and long non-coding RNAs, that potentially contribute to org
278 Notably, ZNF750 promoted the expression of a long non-coding RNA (TINCR), which mediated both cancer-
280 , but also reveals a regulatory mechanism by long non-coding RNAs to control energy metabolism and tu
282 luster of nearly 40 microRNAs and their host long non-coding RNA transcript (lnc-MGC) are coordinatel
283 s between the proteins involved in small and long non-coding RNA transcriptional regulatory mechanism
286 s intact but silenced by a nuclear-localized long non-coding RNA, UBE3A antisense transcript (UBE3A-A
287 , the abundance of many miRNA precursors and long non-coding RNAs was dramatically altered in THC-tre
288 y cohort, all protein-coding genes and known long non-coding RNAs were ranked by fold change in expre
289 how that transcription of a Hand2-associated long non-coding RNA, which we named upperhand (Uph), is
290 stantly-acting control elements of antisense long non-coding RNAs, which in turn regulate targeted ge
291 ied 1200 protein coding genes (PCGs) and 100 long non-coding RNAs with domestication-associated haplo
293 oth X chromosomes are active and express the long non-coding RNAs X active coating transcript (XACT)
296 genetic silencing in which expression of the long non-coding RNA XIST initiates the heterochromatiniz
298 is initiated by upregulation of the lncRNA (long non-coding RNA) Xist and recruitment of specific ch