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1 a downstream lncRNA, Falcor (Foxa2-adjacent long noncoding RNA).
2 evalent modified base in eukaryotic mRNA and long noncoding RNA.
3 rther expanding the functional repertoire of long noncoding RNA.
4 modifications, and involvement of small and long noncoding RNAs.
5 ul for the study of tertiary interactions in long noncoding RNAs.
6 Most of these loci encoded long noncoding RNAs.
7 ening of genes, gene regulatory regions, and long noncoding RNAs.
8 portant paradigm for chromatin regulation by long noncoding RNAs.
9 ranscripts, ignoring the important impact of long noncoding RNAs.
10 ulature and focus on the developing field of long noncoding RNAs.
11 used in array analyses of messenger RNAs and long noncoding RNAs.
12 ntly we identified a hypermethylation in the long noncoding RNA 299 (LINC00299) gene in blood-derived
14 are aiming at targeting these microRNAs and long noncoding RNAs and exploit their potential as clini
15 ese extended 3' UTRs have characteristics of long noncoding RNAs and likely do not interact with miRN
16 sed genes and their non-coding RNA partners, long noncoding RNAs and microRNAs, provided valuable ins
17 rs, Hedgehog signaling, Hippo-YAP signaling, long noncoding RNAs and somatic drivers, and support a r
18 unctional role of messenger RNAs, microRNAs, long noncoding RNAs, and circular RNAs (ie, regRNAs) in
19 t RNA profiles of mRNAs, primary micro-RNAs, long noncoding RNAs, and enhancer RNAs in a large animal
21 a thousand m(5)C sites in Arabidopsis mRNAs, long noncoding RNAs, and other noncoding RNAs across thr
22 of human cardiomyocytes by a portion of the long noncoding RNA ANRIL, the gene of which is located i
23 coding RNAs such as circular RNAs, YRNAs, or long noncoding RNAs are currently gaining increasing att
26 of miRNAs in AAA is established, studies on long-noncoding RNAs are only beginning to emerge, sugges
28 ng RNAs-short noncoding RNAs (microRNAs) and long-noncoding RNAs-are emerging as new fundamental regu
30 discuss the potential role of microRNAs and long noncoding RNAs as clinical biomarkers and therapeut
32 These results show for the first time that a long noncoding RNA can regulate A-to-I RNA editing, furt
33 We also identified differentially expressed long noncoding RNAs capable of regulating known drug-res
34 scovered that all of its centromeres express long noncoding RNAs (cenRNAs), especially in S phase.
38 Here, we identify an Arabidopsis thaliana long-noncoding RNA, designated ELF18-INDUCED LONG-NONCOD
45 ther regulatory elements, such as miRNAs and long noncoding RNAs, either enhancing or diminishing the
46 altered genome-wide methylation profile: the long noncoding RNA ephemeron, whose rapid upregulation i
48 lated by ischemia, including novel conserved long noncoding RNAs expressed in antisense orientation t
49 lncRNA custom-made array we identified CDF5 LONG NONCODING RNA (FLORE), a circadian-regulated lncRNA
55 odulation of GR ligands and induction of the long noncoding RNA Gas5, leading to c-Myc inhibition.
59 eport the identification of a human-specific long noncoding RNA, Heart Brake LncRNA 1 (HBL1), which r
63 eneity and larger proportion of dysregulated long noncoding RNAs in AD, and illustrated the translati
64 damental resource to deepen our knowledge on long noncoding RNAs in C3 cereals, allowing the Brachypo
65 w discusses the involvement of microRNAs and long noncoding RNAs in cardiac fibrosis and summarizes t
67 or these stress-induced 3' UTR extensions as long noncoding RNAs in the regulation of their neighbori
68 additional layer of complexity, implicating long-noncoding RNAs in the transcriptional regulation of
70 red expression of 284 messenger RNAs and 244 long noncoding RNAs, including those that regulate DNA r
71 t ARIEL (ARID5B-inducing enhancer-associated long noncoding RNA) is a novel enhancer RNA (eRNA) that
73 that tissue-specific expression of the human long noncoding RNA LINK-A in mouse mammary glands initia
74 analyses of RNA sequencing data identify the long noncoding RNA lncNB1 as one of the transcripts most
76 alpha), its translocation and binding to the long noncoding RNA (lncRNA) BACE1-antisense transcript (
79 ncoding genomic elements, including mRNA and long noncoding RNA (lncRNA) core promoters and enhancer
81 X-inactive-specific transcript (Xist) is a long noncoding RNA (lncRNA) essential for inactivating o
83 orming RNA-sequencing to identify changes in long noncoding RNA (lncRNA) expression in human and mous
84 dding an additional layer of complexity, the long noncoding RNA (lncRNA) Flicr (Foxp3 long intergenic
86 is implicated in thyroid development, and a long noncoding RNA (lncRNA) gene, papillary thyroid canc
89 entified H19 as one of the most up-regulated long noncoding RNA (lncRNA) in association with Tgfbr2 i
90 Here we report that the expression of H19 long noncoding RNA (lncRNA) is aberrantly increased in U
91 Emerging evidence highlights the role of the long noncoding RNA (lncRNA) KCNQ1OT1 in fracture healing
92 ymorphism (SNP) located in the intron of the long noncoding RNA (lncRNA) LINC00305 by searching the G
93 Haglr, the Hoxd antisense growth-associated long noncoding RNA (lncRNA) located between Hoxd1 and Ho
94 ed in response to temozolomide and found the long noncoding RNA (lncRNA) MALAT1 as one of the most si
98 entify Pvt1b, a p53-dependent isoform of the long noncoding RNA (lncRNA) Pvt1, expressed 50 kb downst
100 We identified RACER, a novel Tbx5-dependent long noncoding RNA (lncRNA) required for the expression
101 e identify a group of Y chromosome-expressed long noncoding RNA (lncRNA) that are involved in male no
102 00313 as a novel KSHV reactivation-activated long noncoding RNA (lncRNA) that interacts with HIV Tat.
104 MYC stimulates the transcription of DANCR, a long noncoding RNA (lncRNA) that is widely overexpressed
105 pattern was negatively controlled by a novel long noncoding RNA (lncRNA) that we named Stem Cell Inhi
106 telomeric repeat-containing RNA (TERRA), the long noncoding RNA (lncRNA) transcribed from telomeres,
107 IFN-stimulated non-coding RNA 1 (INCR1) as a long noncoding RNA (lncRNA) transcribed from the PD-L1 l
108 and pan-tissue identification of coding and long noncoding RNA (lncRNA) transcripts differentially e
109 ere, we identified and characterized a novel long noncoding RNA (lncRNA), acting as a regulator of th
110 t of these genes, regulated by a p53-induced long noncoding RNA (lncRNA), could control p53's tumor s
112 function involving the regulation of a novel long noncoding RNA (lncRNA), leading to changes in exoso
113 study was designed to determine the role of long noncoding RNA (lncRNA), metastasis-associated lung
114 at Cerox1, an unusually abundant cytoplasmic long noncoding RNA (lncRNA), modulates the levels of mit
117 ified a schizophrenia-associated upregulated long noncoding RNA (lncRNA, AC006129.1) that participate
118 in size from microRNA (20-23 nucleotides) to long noncoding RNA (lncRNA, more than 200 nucleotides).
122 and MYC Accumulating evidence indicates that long noncoding RNAs (lncRNA) contribute to the stem-like
128 oding gene signatures, neither expression of long noncoding RNAs (lncRNA) nor their correlation with
129 sregulation of noncoding RNAs, in particular long noncoding RNAs (lncRNA), appear to play major roles
132 pulmonary disease (COPD) development, while long noncoding RNA (lncRNAs) have been shown to cause CO
133 fied a micropeptide produced from a putative long noncoding RNA (lncRNAs) that is important in contro
136 cRNA classes have been identified, including long noncoding RNAs (lncRNAs) and circular RNAs (circRNA
138 frequently used to functionally interrogate long noncoding RNAs (lncRNAs) and discriminate lncRNA lo
140 lance have been extensively studied; yet how long noncoding RNAs (lncRNAs) and the loci that transcri
142 otic injury, including up- and downregulated long noncoding RNAs (lncRNAs) and transcriptional regula
159 responses to the environment, since several long noncoding RNAs (lncRNAs) are known to quantitativel
162 diabetes mellitus are global emergencies and long noncoding RNAs (lncRNAs) are regulatory transcripts
166 n inhibitor JQ1, or knockdown of overlapping long noncoding RNAs (lncRNAs) blocks AngII-induced genes
173 studies have demonstrated the importance of long noncoding RNAs (lncRNAs) during oncogenic transform
177 ed by numerous mechanisms, but the impact of long noncoding RNAs (lncRNAs) has hardly been studied.
198 While it is now appreciated that certain long noncoding RNAs (lncRNAs) have important functions i
203 o profile mRNAs and both annotated and novel long noncoding RNAs (lncRNAs) in human naive, central me
205 provide an overview on the emerging role of long noncoding RNAs (lncRNAs) in the regulation of adipo
207 In human cells, little is known about how long noncoding RNAs (lncRNAs) interact with target loci
213 gulatory RNAs such as microRNAs (miRNAs) and long noncoding RNAs (lncRNAs) play crucial roles in the
214 Increasing evidences have demonstrated that long noncoding RNAs (lncRNAs) play important roles in ma
220 that involves many transcription factors and long noncoding RNAs (lncRNAs) that regulate gene express
222 age in chromosomal contacts with a subset of long noncoding RNAs (lncRNAs) we have defined as immune
223 vealed co-activation and accumulation of the long noncoding RNAs (lncRNAs) XACT and XIST on active X
224 (miRNAs), 125 circular RNAs (circRNAs), 366 long noncoding RNAs (lncRNAs), and 3266 messenger RNAs (
225 DNA methylation, transcriptional elongation, long noncoding RNAs (lncRNAs), and CCCTC-binding factor
226 RNAs (miRNAs), circular RNAs (circRNAs), and long noncoding RNAs (lncRNAs), are proposed novel biomar
227 ct the expression and secondary structure of long noncoding RNAs (lncRNAs), but the contribution of t
229 transcriptome profiles, including mRNAs and long noncoding RNAs (lncRNAs), in skeletal muscle of rai
230 ensively understand the interactions between long noncoding RNAs (lncRNAs), mRNAs and micro-RNAs (miR
231 es contain thousands of loci that transcribe long noncoding RNAs (lncRNAs), some of which are known t
232 ied hundreds of regulated protein-coding and long noncoding RNAs (lncRNAs), some of which are regulat
234 for the functional effects of RNA editing in long noncoding RNAs (lncRNAs), we systematically analyze
235 function and a locus regulating hippocampal long noncoding RNAs (lncRNAs), whose expression correlat
249 ersistent accumulation of the oncogenic 7-kb long noncoding RNA MALAT1 is dependent on an unusually l
250 rs for the nuclear speckle localization of a long noncoding RNA, MALAT1, suggesting a dynamic regulat
253 d colleagues revealed that an antisense (AS) long noncoding RNA named GLS-AS, which is negatively reg
256 and transcriptomic data to identify a novel long noncoding RNA Noncoding Intergenic Co-Induced trans
258 functions to the nuclear paraspeckle-forming long noncoding RNA, nuclear enriched assembly transcript
260 ng adenocarcinoma transcript 1 (MALAT1) is a long noncoding RNA overexpressed in various cancers that
261 s upon differentiation, while knockdown of a long noncoding RNA overlapping E1 has no detectable effe
262 x9, and the Bapx2/Nkx3-2 homolog Nkx3-1, the long-noncoding RNA PEAT (Pax1 enhancer antisense transcr
266 ocus that encompasses PTCHD1, DDX53, and the long noncoding RNA PTCHD1-AS is frequently disrupted in
267 eticulum, and further revealed enrichment of long noncoding RNAs, RNAs with retained introns, and a s
269 The expression of TOX2 and a brain-specific long noncoding RNA RP1-269M15.3 in frontal cortex and nu
270 Research, Wang and colleagues show that the long noncoding RNA SATB2-AS1 is dysregulated in colorect
271 tion response (TAR) element, a 59-nucleotide-long, noncoding RNA segment in the 5' long terminal repe
272 cell types of all classes of RNAs, including long noncoding RNAs, several of which were confirmed as
277 0 protein-coding transcripts; and (4) twenty long noncoding RNAs specifically responsive to TRV vecto
279 ct-borne flaviviruses produce a 300-500-base long noncoding RNA, termed subgenomic flavivirus RNA (sf
280 ream of the active VSG is transcribed into a long-noncoding RNA (TERRA), which forms RNA:DNA hybrids
281 amage-induced long noncoding RNA (DINO) is a long noncoding RNA that directly interacts with p53 and
282 ere we demonstrate a novel role of Malat1, a long noncoding RNA that has been originally identified a
284 ll proliferation by identifying an oncogenic long noncoding RNA that is widely overexpressed in human
287 also describe transcription factor-adjacent long noncoding RNAs that define each subclass and valida
289 AR6 and ASAR15 are monoallelically expressed long noncoding RNAs that remain associated with the chro
290 , in turn, reduced the levels of HAS2-AS1, a long-noncoding RNA that epigenetically controls HAS2 mRN
291 chanism, possibly mediated or regulated by a long noncoding RNA, that supports latency III critical f
295 eomic approaches to advance understanding of long noncoding RNAs, we investigate the function of the
297 PK activation, leading to degradation of H19 long noncoding RNA, which normally binds to and inactiva
298 Approximately, 4500 coding genes and 800 long noncoding RNAs, whose levels correlated with the tr
299 nitiate X-Chromosome inactivation (XCI), the long noncoding RNA Xist mediates chromosome-wide gene si