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1 lies within RP1-13D10.2, an uncharacterized long noncoding RNA.
2 and localizes to the 3' terminus of the 7SK long noncoding RNA.
3 tric carcinoma is in fact a functional viral long noncoding RNA.
4 muscle-specific RNA annotated as a putative long noncoding RNA.
5 s likely to be mediated in part via SSR42, a long-noncoding RNA.
6 ranscripts, ignoring the important impact of long noncoding RNAs.
7 ening of genes, gene regulatory regions, and long noncoding RNAs.
8 ce marked changes in levels of microRNAs and long noncoding RNAs.
9 y infection-specific alterations in multiple long noncoding RNAs.
10 usly uncharacterized, evolutionarily dynamic long noncoding RNAs.
11 amers, pools of random sequences and natural long noncoding RNAs.
12 Most of these loci encoded long noncoding RNAs.
13 portant paradigm for chromatin regulation by long noncoding RNAs.
14 In latently infected ganglia, HSVs express a long noncoding RNA, a latency-associated transcript (LAT
15 ma transcript 1 (MALAT1), a cancer-promoting long noncoding RNA, accumulates in cells by using a 3'-t
16 an left/right pairs identified an intergenic long noncoding RNA adjacent to the PITX2 gene, which we
17 and characterized noncoding species such as long noncoding RNA and circular RNA transcripts whose pr
18 ular Cell challenges the distinction between long noncoding RNAs and enhancer-derived RNAs, and provi
19 ew, we discuss the multifaceted functions of long noncoding RNAs and highlight the current literature
20 ling translated sequences within presumptive long noncoding RNAs and identifying other micropeptides.
21 ese extended 3' UTRs have characteristics of long noncoding RNAs and likely do not interact with miRN
22 , concentrating mainly on recent findings on long noncoding RNAs and microRNAs in cardiac hypertrophy
23 sed genes and their non-coding RNA partners, long noncoding RNAs and microRNAs, provided valuable ins
24 ms of their ability to assemble and quantify long noncoding RNAs and novel coding exons across 20 hum
25 ve and qualitative changes in protein, mRNA, long noncoding RNA, and microRNA composition of extracel
26 and deregulated expression of Tf2 elements, long noncoding RNA, and subtelomeric and stress-related
27 t RNA profiles of mRNAs, primary micro-RNAs, long noncoding RNAs, and enhancer RNAs in a large animal
29 a thousand m(5)C sites in Arabidopsis mRNAs, long noncoding RNAs, and other noncoding RNAs across thr
30 a growing body of evidence demonstrates that long noncoding RNAs are dynamically expressed in differe
32 imately evaluate the futuristic prospects of long noncoding RNAs as biomarkers, and therapeutic targe
33 t suggests studying clinical implications of long noncoding RNAs as possible diagnostic and predictiv
34 ecular Cell, Zhao et al. (2014) identify the long noncoding RNA Blnc1 as a driver of thermogenesis in
38 ented that enhance our view on how small and long noncoding RNAs control developmental timing and onc
40 elucidation of the mechanism of actions for long noncoding RNAs, currently a poorly understood class
41 Here, we identify an Arabidopsis thaliana long-noncoding RNA, designated ELF18-INDUCED LONG-NONCOD
44 ther regulatory elements, such as miRNAs and long noncoding RNAs, either enhancing or diminishing the
45 lated by ischemia, including novel conserved long noncoding RNAs expressed in antisense orientation t
46 lncRNA custom-made array we identified CDF5 LONG NONCODING RNA (FLORE), a circadian-regulated lncRNA
49 odulation of GR ligands and induction of the long noncoding RNA Gas5, leading to c-Myc inhibition.
54 The imprinted, developmentally regulated H19 long noncoding RNA has been implicated in the pathogenes
56 eport the identification of a human-specific long noncoding RNA, Heart Brake LncRNA 1 (HBL1), which r
62 damental resource to deepen our knowledge on long noncoding RNAs in C3 cereals, allowing the Brachypo
63 w discusses the involvement of microRNAs and long noncoding RNAs in cardiac fibrosis and summarizes t
64 this review, we discuss the growing roles of long noncoding RNAs in different aspects of cardiovascul
67 past few years, studies have identified many long noncoding RNAs in the context of cardiovascular bio
69 or these stress-induced 3' UTR extensions as long noncoding RNAs in the regulation of their neighbori
70 inct class of noncoding RNA molecules termed long, noncoding RNAs in the context of the immune system
71 additional layer of complexity, implicating long-noncoding RNAs in the transcriptional regulation of
72 ransposons but also protein-coding genes and long noncoding RNAs, including genes essential for germ
77 s locus encodes two transcript variants of a long noncoding RNA (lncRNA) (rbRosaV1 and rbRosaV2).
81 dding an additional layer of complexity, the long noncoding RNA (lncRNA) Flicr (Foxp3 long intergenic
82 is implicated in thyroid development, and a long noncoding RNA (lncRNA) gene, papillary thyroid canc
85 n somatic copy-number alterations (SCNAs) of long noncoding RNA (lncRNA) in 2,394 tumor specimens fro
89 ymorphism (SNP) located in the intron of the long noncoding RNA (lncRNA) LINC00305 by searching the G
90 Haglr, the Hoxd antisense growth-associated long noncoding RNA (lncRNA) located between Hoxd1 and Ho
93 ) knockout mice, we identify a novel miR-140/long noncoding RNA (lncRNA) NEAT1 signaling network nece
98 We identified RACER, a novel Tbx5-dependent long noncoding RNA (lncRNA) required for the expression
100 ssue of the JCI, Long et al. report that the long noncoding RNA (lncRNA) taurine-upregulated 1 (Tug1)
101 MYC stimulates the transcription of DANCR, a long noncoding RNA (lncRNA) that is widely overexpressed
102 telomeric repeat-containing RNA (TERRA), the long noncoding RNA (lncRNA) transcribed from telomeres,
103 RNA sequencing to study and characterize the long noncoding RNA (lncRNA) transcriptome in lesional sk
105 nal modification of messenger RNA (mRNA) and long noncoding RNA (lncRNA) with roles in RNA processing
106 study was designed to determine the role of long noncoding RNA (lncRNA), metastasis-associated lung
107 activity and binding of a conserved nuclear long noncoding RNA (lncRNA), Rmrp, which is mutated in p
111 in size from microRNA (20-23 nucleotides) to long noncoding RNA (lncRNA, more than 200 nucleotides).
113 and MYC Accumulating evidence indicates that long noncoding RNAs (lncRNA) contribute to the stem-like
115 sregulation of noncoding RNAs, in particular long noncoding RNAs (lncRNA), appear to play major roles
118 pulmonary disease (COPD) development, while long noncoding RNA (lncRNAs) have been shown to cause CO
121 gions corresponding to putative or annotated long noncoding RNAs (lncRNAs) and 154,281 known splicing
123 es from the human neocortex demonstrate that long noncoding RNAs (lncRNAs) are abundantly expressed i
134 s, growing evidence indicates that mRNAs and long noncoding RNAs (lncRNAs) are likewise modified.
135 particularly, the expression profiles of the long noncoding RNAs (lncRNAs) are not fully elucidated.
145 n inhibitor JQ1, or knockdown of overlapping long noncoding RNAs (lncRNAs) blocks AngII-induced genes
150 It has been postulated that a myriad of long noncoding RNAs (lncRNAs) contribute to gene regulat
151 Yet, whether transcription of thousands of long noncoding RNAs (lncRNAs) could play a role in this
152 studies have demonstrated the importance of long noncoding RNAs (lncRNAs) during oncogenic transform
156 ed by numerous mechanisms, but the impact of long noncoding RNAs (lncRNAs) has hardly been studied.
176 stimulate the expression of novel candidate long noncoding RNAs (lncRNAs) in a cell lineage-specific
179 o profile mRNAs and both annotated and novel long noncoding RNAs (lncRNAs) in human naive, central me
180 An emerging theme is the central role of long noncoding RNAs (lncRNAs) in the regulation of this
185 In human cells, little is known about how long noncoding RNAs (lncRNAs) interact with target loci
186 renal cell carcinoma (RCC), yet the role of long noncoding RNAs (LncRNAs) involved in hypoxia-mediat
193 gulatory RNAs such as microRNAs (miRNAs) and long noncoding RNAs (lncRNAs) play crucial roles in the
195 Increasing evidences have demonstrated that long noncoding RNAs (lncRNAs) play important roles in ma
201 e revealed that epigenetic modifications and long noncoding RNAs (lncRNAs) represent an integral part
204 antisense transcripts (NATs) are a class of long noncoding RNAs (lncRNAs) that are complementary to
206 Recent studies have uncovered thousands of long noncoding RNAs (lncRNAs) that populate the cancer g
207 Here we leverage a compendium of 58,648 long noncoding RNAs (lncRNAs) to subtype 947 breast canc
208 es in the experience-dependent expression of long noncoding RNAs (lncRNAs) within the medial prefront
209 vealed co-activation and accumulation of the long noncoding RNAs (lncRNAs) XACT and XIST on active X
210 s, many classes of noncoding RNAs, including long noncoding RNAs (LncRNAs), also undergo changes in t
211 How this regulatory network interfaces with long noncoding RNAs (lncRNAs), an emerging class of deve
212 s), >200-nucleotide long transcripts, namely long noncoding RNAs (lncRNAs), can interfere with gene e
213 associated dysregulation of primate-specific long noncoding RNAs (lncRNAs), downregulation of the alt
215 transcriptome profiles, including mRNAs and long noncoding RNAs (lncRNAs), in skeletal muscle of rai
216 new class of transcriptional regulators, the long noncoding RNAs (lncRNAs), on MYC ability to influen
217 epigenetic complexes, enhancers, chromatin, long noncoding RNAs (lncRNAs), RNA splicing, nuclear top
218 es contain thousands of loci that transcribe long noncoding RNAs (lncRNAs), some of which are known t
219 for the functional effects of RNA editing in long noncoding RNAs (lncRNAs), we systematically analyze
220 function and a locus regulating hippocampal long noncoding RNAs (lncRNAs), whose expression correlat
221 egrates GRO-seq and RNA-seq data to annotate long noncoding RNAs (lncRNAs), with increased sensitivit
235 at a ribonucleoprotein complex including the long noncoding RNA MALAT1 and the RNA-binding protein Hu
236 tion of PICSAR suppresses tumor growth, this long noncoding RNA may serve as a useful diagnostic mark
239 critical role for transcription kinetics in long noncoding RNA-mediated epigenetic modifications and
240 discoveries, including the identification of long noncoding RNAs, microDNAs, a family of small extrac
241 ncreased expression of small nucleolar RNAs, long noncoding RNAs, microRNAs (miRNAs), and ribosomal g
242 ocused on a lncRNA that we named MYC-induced long noncoding RNA (MINCR), showing a strong correlation
244 thesis of another paraspeckle component, the long noncoding RNA NEAT1, which inhibits paraspeckle for
247 catalog of 1703 predicted microRNAs, 18,882 long noncoding RNAs of which 20% are shown to target col
249 tion, we discuss diverse mechanisms by which long noncoding RNAs orchestrate cardiac transcriptional
251 s upon differentiation, while knockdown of a long noncoding RNA overlapping E1 has no detectable effe
252 x9, and the Bapx2/Nkx3-2 homolog Nkx3-1, the long-noncoding RNA PEAT (Pax1 enhancer antisense transcr
253 om Piipponen et al. provides evidence that a long noncoding RNA, PICSAR, promotes cutaneous squamous
255 Furthermore, as the enormous spectrum of long noncoding RNAs potentially opens up new avenues for
257 We found that depletion of NEAT1 RNA, a long noncoding RNA required for paraspeckle integrity, a
259 The expression of TOX2 and a brain-specific long noncoding RNA RP1-269M15.3 in frontal cortex and nu
260 of all types of RNA, including assemblies of long noncoding RNA, rRNA, mRNA, and mixed RNA samples.
261 nriched migration/differentiation-associated long noncoding RNA (SENCR) were directly associated with
262 icate that a growing number of microRNAs and long noncoding RNAs serve as critical mediators of adapt
263 cell types of all classes of RNAs, including long noncoding RNAs, several of which were confirmed as
266 0 protein-coding transcripts; and (4) twenty long noncoding RNAs specifically responsive to TRV vecto
268 anscriptional enhancers are transcribed into long noncoding RNAs termed "enhancer RNAs" (eRNAs), thei
270 We discovered a putative muscle-specific long noncoding RNA that encodes a peptide of 34 amino ac
271 ere we demonstrate a novel role of Malat1, a long noncoding RNA that has been originally identified a
272 ll proliferation by identifying an oncogenic long noncoding RNA that is widely overexpressed in human
275 m (SNP) associations reside within CASC15, a long noncoding RNA that we define as a tumor suppressor
278 AR6 and ASAR15 are monoallelically expressed long noncoding RNAs that remain associated with the chro
279 ntal cortex, we identified sets of genes and long noncoding RNAs that significantly change during cor
280 g to appreciate the cellular roles played by long noncoding RNAs, the function of transcripts emergin
282 ng significantly with genes regulated by the long noncoding RNA TINCR, its target gene, staufen-1 (ST
288 ion of 145 previously unannotated intergenic long noncoding RNA transcripts (lncRNA) or isoforms that
289 reviously appreciated with hundreds of viral long noncoding RNAs (vlncRNAs) being recently discovered
290 virus (EBV) likely encodes hundreds of viral long noncoding RNAs (vlncRNAs) that are expressed during
291 nriched migration/differentiation-associated long noncoding RNA was recently shown to control the con
292 eomic approaches to advance understanding of long noncoding RNAs, we investigate the function of the
294 PK activation, leading to degradation of H19 long noncoding RNA, which normally binds to and inactiva
295 n (eQTL) and exon use (sQTL), including many long noncoding RNAs, which are enriched in known T2D-ass
296 , loss of SDG7 results in elevated levels of long noncoding RNAs, which are thought to participate in
297 include microRNAs, RNA-binding proteins, and long noncoding RNAs, which dramatically alter the immune
299 osome inactivation (XCI) is initiated by the long noncoding RNA Xist, which coats the inactive X (Xi)
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