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1 g (approximately 50 differentially expressed circular RNAs).
2 and ligates the processed ends to produce a circular RNA.
3 tracellular SAM dynamics when expressed as a circular RNA.
4 -state output of protein-coding genes toward circular RNAs.
5 drug doxorubicin and their interaction with circular RNAs.
6 ets are a major source of miRNAs, YRNAs, and circular RNAs.
7 ffect of doxorubicin via regulating a set of circular RNAs.
8 native splicing can lead to the formation of circular RNAs.
9 able methods recently used to identify human circular RNAs.
10 uctured 3' UTRs as well as highly structured circular RNAs.
11 genes are noncanonically spliced to produce circular RNAs.
12 uch as long non-coding RNAs, pseudogenes and circular RNAs.
13 g covalently modified RNAs, edited RNAs, and circular RNAs.
14 nerates an RNA pool consisting of lariat and circular RNAs.
15 ously described cases of scrambled exons and circular RNAs.
16 pliced transcripts and the formation of more circular RNAs.
17 via a custom pipeline optimized for handling circular RNAs.
18 encing of small RNAs including microRNAs and circular RNAs.
19 ein-coding genes are able to generate exonic circular RNAs.
20 e alternatively spliced region of linear and circular RNAs.
21 l RNA-seq, our method is also able to detect circular RNAs.
22 anding the function of viral long ncRNAs and circular RNAs.
25 t the first cell type-specific expression of circular RNAs-a neuron-specific and nuclear-enriched RNA
26 le plasma cells have uniquely high levels of circular-RNAs accounted for by and reflecting the combin
27 , including short microRNAs, long ncRNAs and circular RNAs, across various heart diseases indicates t
28 ogy, such as the functions of enhancer RNAs, circular RNAs and chemical modifications to RNA in cellu
30 mFISH), we selectively identified and imaged circular RNAs and their linear counterparts derived from
33 vidence that virus-derived, protein-encoding circular RNAs are biologically functional and linked to
46 eover, discovering biological contexts where circular RNAs are regulated will shed light on potential
51 ments to the current methods used to isolate circular RNAs as well as a way to reveal RNA structures
53 y of minor spliceosome donors to splice into circular RNA at un-annotated, rather than annotated, exo
55 gene encodes an abundant linear and several circular RNAs believed to perform noncoding functions du
57 standing of the mechanisms and regulation of circular RNA biogenesis, the impact that circRNA generat
59 y eukaryotic genes generate linear mRNAs and circular RNAs, but it is largely unknown how the ratio o
64 entification of competing endogenous RNA and circular RNA (circRNA) as important regulators of miRNA
66 in Bank (MSBB)) AD RNA-seq dataset, cortical circular RNA (circRNA) expression was quantified in the
67 expression emerged: ubiquitous expression of circular RNA (circRNA) from genes traditionally thought
78 2, however, a surprising discovery was made: circular RNA (circRNA) was shown to be a transcriptional
83 sed ubiquitination, DNA methylation, and the circular RNA (circRNA)/long noncoding RNA (lncRNA)-miRNA
84 ing endogenous RNAs (ceRNA) including mRNAs, circular RNAs (circRNA) and long noncoding RNAs (lncRNA)
89 the overall profile of miRNA target sites in circular RNAs (circRNA) generated by alternative back sp
109 nal linear RNAs (containing 5' and 3' ends), circular RNAs (circRNAs) are a special type of RNAs that
141 e expression patterns of several circulating circular RNAs (circRNAs) as potential biomarkers in pati
142 (miRNAs), long non-coding RNAs (lncRNAs) or circular RNAs (circRNAs) can be selectively targeted via
149 Blood, Alhasan et al report the existence of circular RNAs (circRNAs) in circulating human platelets,
152 ecent evidence suggests that many endogenous circular RNAs (circRNAs) may play roles in biological pr
161 utational methods estimate the expression of circular RNAs (circRNAs) using the number of sequencing
162 ression profiles; 43 microRNAs (miRNAs), 125 circular RNAs (circRNAs), 366 long noncoding RNAs (lncRN
165 sized an important role for RBM20 in forming circular RNAs (circRNAs), a novel class of noncoding RNA
167 RNAs (ncRNAs), including microRNAs (miRNAs), circular RNAs (circRNAs), and long noncoding RNAs (lncRN
168 ity is elevated further by the production of circular RNAs (circRNAs), another class of mature RNA th
177 agues identify a new class of intron-derived circular RNAs (ciRNAs) and show that they have the poten
179 e experiments demonstrate utilization of the circular RNA class of RNAs across 4 members of the gamma
181 ort that insulin secretion is regulated by a circular RNA containing the lariat sequence of the secon
186 identified regulated expression of specific circular RNAs derived from Ttn (Titin), Fhod3 (Formin ho
187 increases the sensitivity and specificity of circular RNA detection by discovering and quantifying ci
188 expression profiling revealed more than 476 circular RNAs differentially expressed in control brain
189 lic di-guanosine monophosphate (di-GMP) is a circular RNA dinucleotide that functions as a second mes
191 encing and bioinformatics identified several circular RNAs enriched in VSMCs; however, only one, poss
193 ogy to determine confidence in prediction of circular RNA expression, our algorithm uses a statistica
194 sed of multiple genes, termed fusion-derived circular RNAs (fcircRNAs), represent a class of potentia
195 on model trained to predict the formation of circular RNA from a random genomic locus on human genome
196 ntly closed structure to further distinguish circular RNA from linear RNA following in vitro synthesi
198 than 80 percent accurate for distinguishing circular RNAs from other lncRNAs due to difficulty of cl
199 hort and long non-coding RNAs and predicting circular RNAs from other long non-coding RNAs (lncRNAs).
203 capsid, which consists of a single-stranded, circular RNA genome complexed with delta antigen, the vi
209 of HDV replication: (i) the 1,679-nucleotide circular RNA genome, (ii) its exact complement, the anti
212 igns such as Dicer-substrate RNA, shRNA, and circular RNA have been evaluated in vitro and in preclin
213 such as microRNAs, long non-coding RNAs and circular RNAs have been assessed as potential therapeuti
221 tion of splicing intermediates, we show that circular RNA in Schizosaccharomyces pombe is generated t
223 tions of microRNAs, long non-coding RNAs and circular RNAs in joint tissues and biofluids has increas
224 tudies have revealed thousands of endogenous circular RNAs in mammalian cells, some of which are high
225 le and useful strategy for the generation of circular RNAs in preparative amounts; and (iii) that sel
226 Seq), we compared the expression patterns of circular RNAs in proliferating (early-passage) and senes
227 s the branch sites confirmed lariat RNAs and circular RNAs in the pool generated by constitutive and
229 ing induction of general and tissue-specific circular RNAs, including in the heart and lung, during h
230 regulate the expression of other Drosophila circular RNAs, including Plexin A (PlexA), suggesting a
232 harmacologically, the steady-state levels of circular RNAs increased while expression of their associ
236 H and 2',3'-cyclic phosphate termini to form circular RNA is an essential step in the life cycle of t
240 As, which considers the specific features of circular RNA, is essential to the development of systema
243 n for its biogenesis, we found that Laccase2 circular RNA levels are not controlled by Mbl or the Lac
246 ti et al. (2017) demonstrate that endogenous circular RNAs may generate proteins, thereby expanding t
247 in genome methylation, long non-coding RNAs, circular RNAs, micro-RNAs and fruit metabolites revealed
248 ntial as biomarkers and disease targets, and circular RNA mimics are being explored for use as therap
249 ingle-strand RNA to form a covalently closed circular RNA molecule through ligase-adenylylate and RNA
250 e data also demonstrate the utility of small circular RNA molecules as tools for biochemical studies.
254 epatitis delta virus (HDV), which contains a circular RNA of 1.7 kilobases, is nonetheless able to re
258 containing minimal repeats (<40 nt) generate circular RNAs predominately after 3' end processing.
259 he first examples of developmentally induced circular RNAs processed by the minor spliceosome, and an
260 he past two decades, a circular form of RNA (circular RNA), produced through alternative splicing, ha
263 with previous knowledge that Cdr1as (ciRS-7) circular RNA protects miR-7 from Cyrano-mediated TDMD, w
270 larization of an exon of the PVT1 gene, as a circular RNA showing markedly reduced levels in senescen
271 This was not due to an inability to cut any circular RNA, since Vhs cuts circular mRNAs containing a
272 crease HCC cell invasion via suppressing the circular RNA-SMG1.72 (circRNA-SMG1.72) expression via tr
273 g and long noncoding transcripts, as well as circular RNA species that were also experimentally valid
277 ditionally, GEMORNA's versatility extends to circular RNA, substantially enhancing circular EPO expre
280 ) is a 1,679-nucleotide (nt) single-stranded circular RNA that is predicted to fold into an unbranche
281 tis delta virus (HDV) contains a viroid-like circular RNA that is presumed to replicate via a rolling
282 tis delta virus (HDV) contains a viroid-like circular RNA that replicates via a double rolling circle
283 e utility of orthogonal analytical tests for circular RNA that take advantage of its covalently close
284 of eukaryotic protein-coding genes generate circular RNAs that have covalently linked ends and are r
288 oding species such as long noncoding RNA and circular RNA transcripts whose presence had not been pre
290 tion of single-stranded RNA to form a closed circular RNA via covalent ligase-AMP and RNA-adenylylate
291 ne deaminase acting on RNA (ADAR)-recruiting circular RNAs, we find that guided A>I snRNAs consistent
295 s were molecular precursors in biogenesis of circular RNA which occurred through catalytic role of so
296 e previously characterized Muscleblind (Mbl) circular RNA, which requires the Mbl protein for its bio
297 ne learning method for the identification of circular RNAs, which considers the specific features of
298 g sequences, making linear mRNA as stable as circular RNA while achieving higher translation efficien