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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.
11        Here we identify FILNC1 (FoxO-induced long non-coding RNA 1) as an energy stress-induced long
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
15 chanistic link between an activity-dependent long non-coding RNA and epilepsy.
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
27                               Furthermore, a long non-coding RNA antisense to FOXM1 (FOXM1-AS) promot
28 that together with coding genes, (antisense) long non-coding RNAs are deregulated in skin tissue of s
29                                              Long non-coding RNAs are important regulators of biologi
30                       We also find that many long non-coding RNAs are preferentially expressed in ger
31 he secondary structure of the heart-specific long non-coding RNA Braveheart, leading to the discovery
32 on-coding RNA 1) as an energy stress-induced long non-coding RNA by FoxO transcription factors.
33                                            A long non-coding RNA called GRASLND is essential to help
34                                            A long non-coding RNA called lnc-NR2F1 regulates several n
35 herited UBE3A allele is silenced in cis by a long non-coding RNA called UBE3A-ATS.
36                           Modular domains of long non-coding RNAs can serve as scaffolds to bring dis
37                                      Lastly, long non-coding RNAs can serve well as associated genes
38           Many RNAs, including pre-mRNAs and long non-coding RNAs, can be thousands of nucleotides lo
39                 Here, we review the roles of long non-coding RNAs, chromosomal organizational structu
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
42                               Damage-induced long non-coding RNAs (dilncRNA) synthesized at DNA doubl
43 MIR876), and the differential methylation of long non-coding RNA documented for the first time.
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
47                                              Long non-coding RNA expression, but not small non-coding
48 gy stress FoxOs induce the expression of the long non-coding RNA FILNC1, which inhibits survival of R
49 ested binding specificity of PRC2 to certain long non-coding RNAs for recruitment to chromatin.
50 ent findings in human cells where endogenous long non-coding RNAs function to regulate the epigenome.
51                            The X-linked Xist long non-coding RNA functions as an X inactivation maste
52 ain-expressed genes NEXMIF, SLC16A2, and the long non-coding RNA gene FTX.
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
56                           In conclusion, the long non-coding RNA HOTAIR is directly repressed by ER a
57                                              Long non-coding RNAs, however, exhibit more changes in e
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
61         In this study, we identified a novel long non-coding RNA in Lipid Associated Single nucleotid
62                                 The roles of long non-coding RNAs in cancer metabolism remain largely
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
66                      We further identify the long non-coding RNA LeXis as a mediator of this effect.
67 n addition, we identified the human-specific long non-coding RNA, LINKA, as an HNF1A target necessary
68              These include both an antisense long non-coding RNA (lncRNA) and a short PCSK6 isoform p
69                                         As a long non-coding RNA (lncRNA) and a transcriptional regul
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
73                                              Long non-coding RNA (lncRNA) are emerging as contributor
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
77                             Misregulation of long non-coding RNA (lncRNA) genes has been linked to a
78                                        While long non-coding RNA (lncRNA) genes have attracted a lot
79                             The discovery of long non-coding RNA (lncRNA) has dramatically altered ou
80                      Here we report that the long non-coding RNA (lncRNA) HOTAIR (for HOX Transcript
81 r nuclear factor kappa B (NF-kappaB) and the long non-coding RNA (lncRNA) HOTAIR (HOX transcript anti
82                     Here, we show that NEAT1 long non-coding RNA (lncRNA) is a direct transcriptional
83                                              Long non-coding RNA (lncRNA) is a large class of gene tr
84 e other transcript variants, indicating that long non-coding RNA (lncRNA) is processed after transcri
85              We identified a rodent-specific long non-coding RNA (lncRNA) linc1281, hereafter Ephemer
86                                              Long non-coding RNA (lncRNA) loci are known to be import
87                                          The long non-coding RNA (lncRNA) Maternally Expressed Gene 3
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
90                             Herein, based on long non-coding RNA (lncRNA) profiling induced by active
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
93 ized, extracellular messenger RNA (mRNA) and long non-coding RNA (lncRNA) studies are limited.
94                              We identified a long non-coding RNA (lncRNA) that arises from the antise
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
97                                  PCGEM1 is a long non-coding RNA (lncRNA) that is often upregulated i
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
100                                              Long non-coding RNA (lncRNA) transcription into a downst
101 cleotide Metabolism Regulator (lincNMR) is a long non-coding RNA (lncRNA) which is induced in hepatoc
102                          Clustering by mRNA, long non-coding RNA (lncRNA), and miRNA expression conve
103 C, and GC, by targeting and downregulating a long non-coding RNA (lncRNA), LOC553103.
104  Active transcription of the neuron-specific long non-coding RNA (lncRNA), UBE3A-ATS, has been shown
105         The intronless ht-WNT10B resembles a long non-coding RNA (lncRNA), which suggests its involve
106 ect activity of the promoter of LOXL1-AS1, a long non-coding RNA (lncRNA).
107 of uncharacterized non-coding RNAs including long non-coding RNA (lncRNA).
108        A central element of this process are long non-coding RNAs (lncRNA), which in Arabidopsis thal
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.
111                                         Many long non-coding RNAs (lncRNAs) affect gene expression, b
112  RNA exosome and identified a vast number of long non-coding RNAs (lncRNAs) and enhancer RNAs (eRNAs)
113                                              Long non-coding RNAs (lncRNAs) and microRNAs are involve
114  to other non-protein coding RNAs, primarily long non-coding RNAs (lncRNAs) and small nucleolar RNAs
115                                              Long non-coding RNAs (lncRNAs) are a diverse and poorly
116                                              Long non-coding RNAs (lncRNAs) are a diverse class of RN
117                                              Long non-coding RNAs (lncRNAs) are a family of novel gen
118                                              Long non-coding RNAs (lncRNAs) are a fascinating, but st
119                                              Long non-coding RNAs (lncRNAs) are an emerging class of
120                               Alterations in long non-coding RNAs (lncRNAs) are associated with human
121 ies show that the mutation and regulation of long non-coding RNAs (lncRNAs) are associated with vario
122                                              Long non-coding RNAs (lncRNAs) are components of epigene
123  protein-coding genes, the majority of human long non-coding RNAs (lncRNAs) are considered non-conser
124                                              Long non-coding RNAs (lncRNAs) are critical for regulati
125                                              Long non-coding RNAs (lncRNAs) are defined as non-protei
126               In these tumors, expression of long non-coding RNAs (lncRNAs) are deregulated and close
127 these transcriptomic responses and show that long non-coding RNAs (lncRNAs) are dynamically regulated
128                                              Long non-coding RNAs (lncRNAs) are emerging regulators o
129                                              Long non-coding RNAs (lncRNAs) are emerging regulators o
130                                              Long non-coding RNAs (lncRNAs) are expressed in a highly
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
133                                              Long non-coding RNAs (lncRNAs) are important regulators
134                                              Long non-coding RNAs (lncRNAs) are important regulators
135                                              Long non-coding RNAs (lncRNAs) are important regulatory
136                             To identify what long non-coding RNAs (lncRNAs) are involved in non-small
137              RNA-binding proteins (RBPs) and long non-coding RNAs (lncRNAs) are key regulators of gen
138                                              Long non-coding RNAs (lncRNAs) are largely heterogeneous
139                                     Although long non-coding RNAs (lncRNAs) are non-protein-coding tr
140                                              Long non-coding RNAs (lncRNAs) are not translated into p
141                                              Long non-coding RNAs (lncRNAs) are of fundamental biolog
142                                              Long non-coding RNAs (lncRNAs) are often aberrantly expr
143                 To date, Y chromosome-linked long non-coding RNAs (lncRNAs) are poorly characterized
144                                              Long non-coding RNAs (lncRNAs) are post-transcriptional
145                                           As long non-coding RNAs (lncRNAs) are prominent regulators
146                                              Long non-coding RNAs (lncRNAs) are prominently associate
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
149                                              Long non-coding RNAs (lncRNAs) can recruit PRC2 to chrom
150                                              Long non-coding RNAs (lncRNAs) comprise a diverse class
151                                              Long non-coding RNAs (lncRNAs) constitute a large, yet m
152                                              Long non-coding RNAs (lncRNAs) constitute a significant
153                                              Long non-coding RNAs (lncRNAs) contribute to cardiac (pa
154                                              Long non-coding RNAs (lncRNAs) contribute to colorectal
155 ivo, we generated a single-cell landscape of long non-coding RNAs (lncRNAs) during HSC development.
156                                              Long non-coding RNAs (lncRNAs) exhibit highly cell type-
157                              Discovering new long non-coding RNAs (lncRNAs) has been a fundamental st
158                               More recently, long non-coding RNAs (lncRNAs) have attracted much atten
159                     Non-coding RNAs, such as long non-coding RNAs (lncRNAs) have been found to be dys
160                                  Hundreds of long non-coding RNAs (lncRNAs) have been identified as p
161                                 Thousands of long non-coding RNAs (lncRNAs) have been identified in m
162                                              Long non-coding RNAs (lncRNAs) have been implicated in a
163                                              Long non-coding RNAs (lncRNAs) have been implicated in d
164                                              Long non-coding RNAs (lncRNAs) have been implicated in n
165                                              Long non-coding RNAs (lncRNAs) have been implicated in t
166                   To date, a large number of long non-coding RNAs (lncRNAs) have been recently discov
167                                              Long non-coding RNAs (lncRNAs) have been shown to be cri
168                        For example, although long non-coding RNAs (lncRNAs) have been shown to critic
169                                    Recently, long non-coding RNAs (lncRNAs) have emerged as an import
170                                              Long non-coding RNAs (lncRNAs) have emerged as essential
171                                              Long non-coding RNAs (lncRNAs) have emerged as important
172                                              Long non-coding RNAs (lncRNAs) have emerged as potential
173                                              Long non-coding RNAs (lncRNAs) have emerged as regulator
174 h a small number of the vast array of animal long non-coding RNAs (lncRNAs) have known effects on cel
175       In particular, the biological roles of long non-coding RNAs (lncRNAs) have never been character
176                                              Long non-coding RNAs (lncRNAs) have recently been found
177                     Transcription-regulating long non-coding RNAs (lncRNAs) have the potential to con
178     Further, ethanol-induced upregulation of long non-coding RNAs (lncRNAs) HOTAIR and MALAT1 in endo
179                          The significance of long non-coding RNAs (lncRNAs) in many biological proces
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,
182                 Despite our understanding of long non-coding RNAs (lncRNAs) in primary colon cancer,
183                                 The roles of long non-coding RNAs (lncRNAs) in regulating cancer and
184                                  The role of long non-coding RNAs (lncRNAs) in regulating endothelial
185 m comparable, with a distinct enrichment for long non-coding RNAs (lncRNAs) in snRNA-seq.
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
189                            The expression of long non-coding RNAs (lncRNAs) is dysregulated in hepato
190                                 Thousands of long non-coding RNAs (lncRNAs) lie interspersed with cod
191 nal to zygotic transition and annotated 1120 long non-coding RNAs (lncRNAs) many of which differentia
192             We hypothesized that circulating long non-coding RNAs (lncRNAs) may act as diagnostic mar
193           There is a growing perception that long non-coding RNAs (lncRNAs) modulate cellular functio
194 ding the targeting and spreading patterns of long non-coding RNAs (lncRNAs) on chromatin requires a t
195        As ncRNAs such as microRNAs (miRNAs), long non-coding RNAs (lncRNAs) or circular RNAs (circRNA
196                                              Long non-coding RNAs (lncRNAs) play an important role in
197                                              Long non-coding RNAs (lncRNAs) play an important role in
198                                              Long non-coding RNAs (lncRNAs) play critical roles in di
199                  New evidence indicates that long non-coding RNAs (lncRNAs) play crucial roles in epi
200                                              Long non-coding RNAs (lncRNAs) play crucial roles in reg
201                                              Long non-coding RNAs (lncRNAs) play key roles in human d
202                                              Long non-coding RNAs (lncRNAs) regulate diverse biologic
203 roles of multi-protein DNA complexes, so how long non-coding RNAs (lncRNAs) regulate DNA repair is le
204                                     Although long non-coding RNAs (lncRNAs) regulate various cellular
205                                              Long non-coding RNAs (lncRNAs) regulating gene expressio
206                    Biological roles for most long non-coding RNAs (lncRNAs) remain mysterious.
207 ost response to infection, the roles of many long non-coding RNAs (lncRNAs) remain unknown.
208     Despite the overwhelming number of human long non-coding RNAs (lncRNAs) reported so far, little i
209            Increasing evidence suggests that long non-coding RNAs (LncRNAs) represent a new class of
210                                  Circulating long non-coding RNAs (lncRNAs) serve as valuable biomark
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
215                                 Many nascent long non-coding RNAs (lncRNAs) undergo the same maturati
216 sent here a workflow to identify and analyze long non-coding RNAs (lncRNAs) via RNA-Seq data.
217 Over 3,000 genes encoding previously unknown long non-coding RNAs (lncRNAs) were revealed through the
218                                              Long non-coding RNAs (lncRNAs) with a length of > 200 nu
219  efforts have vastly expanded the catalog of long non-coding RNAs (lncRNAs) with varying evolutionary
220                         Here, we report that long non-coding RNAs (lncRNAs), a recently discovered cl
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
226                                              Long non-coding RNAs (lncRNAs), which are non-coding RNA
227                                              Long non-coding RNAs (lncRNAs), which have evolved as im
228 will be translated (mRNAs) from the class of long non-coding RNAs (lncRNAs).
229 oteins, and a significant subset of them are long non-coding RNAs (lncRNAs).
230 anisms that regulate gene expression such as long non-coding RNAs (lncRNAs).
231 mes are transcribed into numerous regulatory long non-coding RNAs (lncRNAs).
232 nal annotation or no protein product such as long non-coding RNAs (lncRNAs).
233 vasively transcribed to produce thousands of long non-coding RNAs (lncRNAs).
234 ammalian genomes encode tens of thousands of long non-coding RNAs (lncRNAs).
235 g both short non-coding RNAs (microRNAs) and long non-coding RNAs (lncRNAs).
236 ing frames (ORFs) and which have been termed long non-coding RNAs (lncRNAs).
237 RNAs and predicting circular RNAs from other long non-coding RNAs (lncRNAs).
238 lements (TEs) comprise a large proportion of long non-coding RNAs (lncRNAs).
239 ts of 799 protein-coding genes (PCGs) and 97 long non-coding RNAs (lncRNAs).
240 nse-associated region contains two genes for long, non-coding RNAs (lncRNAs), AL157359.3 and AL157359
241 nces are disproportionately present in human long, non-coding RNAs (lncRNAs).
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
253                                          The long non-coding RNA NEAT1 serves as a scaffold for the a
254 F4A1, the tumor suppressor gene PTEN and the long non-coding RNA NEAT1.
255 aspeckles are nuclear bodies form around the long non-coding RNA, Neat1, and RNA-binding proteins.
256                        Here we show that the long non-coding RNA, NEAT1, directly modulates neuronal
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
259                                   FHAD1 is a long non-coding RNA overexpressed in heart failure.
260                                          The long non-coding RNA PARTICLE (Gene PARTICL- 'Promoter of
261                                              Long non-coding RNAs play an important role in human com
262          We find that alignments for several long non-coding RNAs previously shown to lack covariatio
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
270                                     Although long non-coding RNAs such as HOTAIR have been implicated
271      Regression analysis identified a single long non-coding RNA that could predict cluster assignmen
272                                  HOTAIR is a long non-coding RNA that is overexpressed, promotes meta
273                  N-BLR is a primate-specific long non-coding RNA that modulates the epithelial-to-mes
274                           Here we identify a long non-coding RNA that we termed Morrbid, which tightl
275                                              Long non-coding RNAs that are expressed from the opposit
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-
279         They describe how a primate-specific long non-coding RNA titrates the levels of a microRNA th
280 , but also reveals a regulatory mechanism by long non-coding RNAs to control energy metabolism and tu
281                      We further identified a long-non coding RNA transcribed at CHPT1 enhancer (also
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
284         Moreover, this study provided global long non-coding RNA transcripts in the blood of patients
285 map to active regulatory regions proximal to long non-coding RNA transcripts.
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
292                                          The long non-coding RNA X-inactive specific transcript (XIST
293 oth X chromosomes are active and express the long non-coding RNAs X active coating transcript (XACT)
294       Notably, expression and coating by the long non-coding RNA XACT are early events in XCI erosion
295                                          The long non-coding RNA Xist establishes an intra-chromosoma
296 genetic silencing in which expression of the long non-coding RNA XIST initiates the heterochromatiniz
297  The master regulator of this process is the long non-coding RNA Xist.
298  is initiated by upregulation of the lncRNA (long non-coding RNA) Xist and recruitment of specific ch
299           Here we discover an Xist antisense long non-coding RNA, XistAR (Xist Activating RNA), which
300                             Interestingly, a long non-coding RNA, ZEB2NAT, was demonstrated to be ess

 
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