ライフサイエンスコーパス: antisense RNA

1 is by reducing transcription of an imprinted antisense RNA.

2 ue transcription units and detects prevalent antisense RNA.

3 e first 14 nucleotides at the 5'-pole of the antisense RNA.

4 production was obtained with the RRE-driven antisense RNA.

5 ent by tetracycline-controlled expression of antisense RNA.

6 cillus subtilis in which the antitoxin is an antisense RNA.

7 d by down-regulation of S1P1 expression with antisense RNA.

8 erence, we silenced expression of ap65 using antisense RNA.

9 lar process regulated by naturally occurring antisense RNA.

10 , in most cases, not associated with a known antisense RNA.

11 transcript appears to be an uncharacterized antisense RNA.

12 quences spliced to exons 4 through 7 of this antisense RNA.

13 ative splicing and promoter utilization, and antisense RNA.

14 ce corresponding to the L region of the EMCV antisense RNA.

15 n antitoxin, which, in type I systems, is an antisense RNA.

16 and searched for the presence of RAPs within antisense RNAs.

17 viously described and included noncoding and antisense RNAs.

18 ed sRNAs, two are candidate transposase gene antisense RNAs.

19 s such as microRNA, Piwi-interacting RNA and antisense RNAs.

20 m can be created through engineering minimal antisense RNAs.

21 MHC genes, and both the intergenic sense and antisense RNAs.

22 old to over 900-fold, in response to cognate antisense RNAs.

23 ng or ablating Scl using morpholino-modified antisense RNAs.

24 ny new transcripts, including small RNAs and antisense RNAs.

25 n-coding genes, 21,300 pseudogenes, and 1500 antisense RNAs.

26 in-coding transcripts, including 16 possible antisense RNAs.

27 as been their association with noncoding and antisense RNAs.

28 region of complementarity between sense and antisense RNAs.

29 RNA 2, cyclin-dependent kinase inhibitor 2B antisense RNA 1 (ANRIL), potassium voltage-gated channel

30 e, we demonstrate an essential role of GATA6 antisense RNA 1 (GATA6-AS1) in cardiomyocyte differentia

31 evated levels of hypoxia inducible factor 1A antisense RNA 2 when compared with patients presenting l

32 chain reaction: hypoxia inducible factor 1A antisense RNA 2, cyclin-dependent kinase inhibitor 2B an

33 Levels of hypoxia inducible factor 1A antisense RNA 2, KCNQ1OT1, and metastasis-associated lun

34 To further characterize the antisense RNA, a strand-specific microarray was performe

35 ely, blocking DGD expression in fresh PDH by antisense RNA abolished DHBV infection.

36 conserved; (3) more than 700 distinct small antisense RNAs, about 20 nt long, that are precisely com

37 Small antisense RNAs, about 23 nucleotides in size, were prese

38 tion of CgA expression in vivo by expressing antisense RNA against CgA in transgenic mice led to a si

39 or regulated transgene expression generating antisense RNA also reduced the expression of 22-kD zein

40 icrodissection technique coupled with linear antisense RNA amplification and high density/candidate g

41 ns in the hippocampus and entorhinal cortex, antisense RNA amplification was combined with cDNA array

42 hese data provide an unexpected link between antisense RNA and circadian timing and provide a new exa

43 r region drive the overexpression of a novel antisense RNA and contribute to the development of lymph

44 cellular structure of the tau stem loop with antisense RNA and demonstrate that the stability of the

45 progeny of transduced CD34+ cells expressed antisense RNA and exhibited sustained and significant in

46 In 2004, Flannagan and coworkers used antisense RNA and green fluorescent protein (GFP) expres

47 lease cleavage event that seems to depend on antisense RNA and might implicate endoribonuclease activ

48 s transfected with ALDH1A1- or -3A1-specific antisense RNA and short interfering (Si)RNA.

49 se methods (e.g. antisense oligonucleotides, antisense RNA and small interfering RNA) can be used to

50 d by downregulation of their expression with antisense RNA and small interfering RNA, respectively.

51 y, we also observed that the abundance of 52 antisense RNAs and 34 potential noncoding RNAs was affec

52 occurrence and properties of small sense and antisense RNAs and aberrant transcripts in transgenic to

53 on, including inversely regulated modules of antisense RNAs and cognate target messenger RNAs and spe

54 have characterized the association of three antisense RNAs and one intergenically encoded noncoding

55 peutic strategies that target both sense and antisense RNAs and RAN proteins in C9ORF72 ALS/FTD, and

56 e prospects of nanoparticles, immunotherapy, antisense RNA, and drug-resistance-modulation approaches

57 s the interaction between the enzyme and the antisense RNA, and the 5'-phosphate stabilizes the inter

58 e regulation of NOS2 by micromilieu factors, antisense RNAs, and 'unexpected' cytokines.

59 cus aureus, including transcription factors, antisense RNAs, and host elements.

60 ate growth inhibitory proteins, peptides and antisense RNAs, and temperature-sensitive mutant protein

61 ical pathways; up-regulation of pseudogenes, antisense RNAs, and unannotated coding isoforms; and RNA

62 Here we show that many TSGs have nearby antisense RNAs, and we focus on the role of one RNA in s

63 tein, whereas inhibiting miR-503 by using an antisense RNA (antagomir) enhanced CUGBP1 biosynthesis a

64 Three types of primary DCs treated with antisense RNA antagomirs directed against miR-451 secret

65 teraction of nascent prgQ mRNAs with a small antisense RNA (Anti-Q) encoded within prgQ.

66 by using small interfering RNA knockdown or antisense RNA approaches in cells in culture resulted in

67 Transgenic and antisense RNA approaches revealed that RTS gene is requi

68 Using RNA interference and antisense RNA approaches, we show that knock-down of oli

69 wnregulation of this protein using siRNA and antisense RNA approaches.

70 ed with RNA-based agents, such as ribozymes, antisense, RNA aptamers and small interfering RNA, and p

71 ivo, but it is unknown whether the resultant antisense RNAs are a mechanistic by-product of RNA polym

72 RNAseq studies have revealed that bacterial antisense RNAs are abundant, but little is known about t

73 We find that upstream antisense RNAs are cleaved and polyadenylated at poly(A)

74 If all of these reported antisense RNAs are expressed at levels sufficient to reg

75 Natural antisense RNAs are found in a wide range of eukaryotic o

76 We show here that noncoding antisense RNAs are important modulators of proper dosage

77 ogical importance and mode of action of most antisense RNAs are not clear.

78 o increased and the corresponding transposon antisense RNAs are reduced.

79 Various antisense RNAs are reported as non-coding RNAs that regu

80 ng, poorly translated mRNAs, small RNAs, and antisense RNAs are the main substrates, while rRNA, tRNA

81 ify a systematic programme in which elevated antisense RNA arising both from ncRNAs and from 3'-overl

82 d their products, is controlled partly by an antisense RNA arising from a clock component locus.

83 These findings suggest endogenous Kcna2 antisense RNA as a therapeutic target for the treatment

84 ndance, while inhibiting miR-519 by using an antisense RNA [(AS)miR-519] elevated HuR levels.

85 results indicate that the tightly regulated antisense RNA As1_flv4 establishes a transient threshold

86 romoter for the transcription of a noncoding antisense RNA, asDOG1, that is 5' capped, polyadenylated

87 as counteracted by a natural long non-coding antisense RNA, asHSFB2a.

88 n of the coenzyme A transferase (CoAT) using antisense RNA (asRNA) against ctfB (the second CoAT gene

89 We investigated the effect of antisense RNA (asRNA) structural properties on the downr

90 previously showed that accumulation of PHO84 antisense RNA (asRNA), in cells lacking the nuclear exos

91 h proportion of all eukaryotic genes express antisense RNA (asRNA), which accumulates to varying degr

92 scriptome analyses have revealed hundreds of antisense RNAs (asRNAs) for many bacteria, although few

93 es demonstrated a high number of cis-encoded antisense RNAs (asRNAs) in bacteria, but very little is

94 em from Streptococcus pyogenes and synthetic antisense RNAs (asRNAs) in Escherichia coli strains to r

95 Current approaches to design efficient antisense RNAs (asRNAs) rely primarily on a thermodynami

96 SS) and 5,495 TSS corresponding to potential antisense RNAs (asRNAs).

97 CTCF restricts the extent of the antisense RNA at the wild-type (wt) DM1 locus and constr

98 Clr4 also mediates degradation of antisense RNAs at euchromatic loci, but the underlying m

99 e expression of alternatively polyadenylated antisense RNAs at the locus encoding the floral represso

100 th sense and antisense transcripts, with the antisense RNA being in excess.

101 ch to detect hidden similarities between the antisense RNA-binding protein Rop and other proteins.

102 PrgX is believed to act in concert with an antisense RNA called Qa to inhibit readthrough of transc

103 antisense partners and that perturbation of antisense RNA can alter the expression of the sense gene

104 gulation of yhcSR expression by induced yhcS antisense RNA can inhibit and terminate bacterial growth

105 sgenic plants expressing the three different antisense RNA constructs exhibited abnormal growth and d

106 wo of these vectors were designed to express antisense RNA containing either a Rev response element (

107 tA, reduced rctB translation, most likely by antisense RNA control.

108 Both sense and antisense RNAs corresponding to these miRNA targets accu

109 to regulate the genes encoded opposite them, antisense RNAs could significantly impact gene expressio

110 (DeltaSUB1) mRNA using SUB1 single-stranded antisense RNA coupled with human Argonaute 2.

111 ells, inhibition of Kalirin expression using antisense RNA decreased nerve growth factor (NGF)-induce

112 ction of a much more abundant class of 22 nt antisense RNAs, dependent on a secondary RdRP (RRF-1) an

113 us type 1 (HIV-1)-based vector expressing an antisense RNA directed against HIV-1 is currently in cli

114 We conclude that the processed antisense RNA does not act alone and that Tsix function

115 The antisense RNA does not dimerize, strongly indicating tha

116 siae, results in transcription initiation of antisense RNAs embedded within body of protein-coding ge

117 esults demonstrate that the robust levels of antisense RNAs emerging from shRNA expression systems ca

118 Using antisense RNA encoded by a library of human expressed se

119 Antisense RNAs encoded on the DNA strand opposite anothe

120 Human Ago2 preloaded with the antisense RNA exhibited greater binding affinities for l

121 method to identify a beta-catenin-regulated antisense RNA expressed in HCT116 colorectal carcinoma c

122 Using inducible antisense RNA expression and dominant-negative alleles o

123 We have modelled antisense RNA expression at TFPI-2 in transgenic mouse e

124 Peripheral nerve injury increased Kcna2 antisense RNA expression in injured DRG through activati

125 Reducing mRNA levels of MKK7 by antisense RNA expression not only compromises basal resi

126 In the present study, we utilized an antisense RNA expression strategy to down-modulate const

127 em, modulation of gene function by inducible antisense RNA expression was demonstrated for comC antis

128 methods, namely RNA interference as well as antisense RNA expression, significantly attenuated serum

129 similarly decreased production of sense and antisense RNA foci, as well as DPR proteins, in patient

130 d construct with tetRO driving expression of antisense RNA for the ftsZ gene.

131 The R. palustris asrpaR represents an antisense RNA for which an activity can be measured and

132 we identify a conserved lncRNA, named Kcna2 antisense RNA, for a voltage-dependent potassium channel

133 To obtain additional evidence for antisense RNA function in chloroplasts, we used strain D

134 In leaves, the antisense RNA gene is only expressed after heat stress a

135 transcription factor that binds to the Kcna2 antisense RNA gene promoter.

136 an adhesin, and in addition, we demonstrate antisense RNA gene silencing in T. vaginalis to study th

137 These results suggest a model where small antisense RNAs generated from the 3' end of the transgen

138 merhead ribozyme flanked by two arms of GPRT antisense RNA (GPRZ) was designed, synthesized and found

139 tide substitutions at the 3' terminus of the antisense RNA had no effect on human Ago2 cleavage activ

140 the fact that therapeutic use of unmodified antisense RNAs has generally been disappointing.

141 ell as the emerging regulatory importance of antisense RNAs, has blurred this distinction.

142 lation of HAS2 mRNA synthesis by the natural antisense RNA HAS2-AS1 has recently been described in os

143 Parallel to Has2 mRNA, Has2 antisense RNA (Has2os2) was up-regulated in co-cultures.

144 ulation, we observe that cis-encoded natural antisense RNAs have a striking preferential complementar

145 n-coding RNA (lncRNA) HOTAIR (HOX transcript antisense RNA) have diverse functional roles in cancer.

146 switch is transcribed as part of a noncoding antisense RNA, herein named AspocR.

147 that the long non-coding RNA HOX transcript antisense RNA (HOTAIR) is overexpressed in pancreatic ca

148 ion of iASPP by RNA-mediated interference or antisense RNA in C. elegans or human cells, respectively

149 Taken together, our results suggest that antisense RNA in chloroplasts can protect otherwise unst

150 The prevalence of antisense RNA in eukaryotes is not known and only a few

151 Its knockdown via antisense RNA in neoplastic epidermoid cells enhanced pr

152 lease, was reduced >90% by the expression of antisense RNA in Nicotiana tabacum.

153 ked out by overexpressing 290-base sense and antisense RNA in NIH 3T3 cells controlled by tetracyclin

154 strand and the relative chance of degrading antisense RNA in the other strand-in the same regions of

155 Moreover, depletion of PN-1 by antisense RNAs in CgA-expressing 6T3 cells resulted in t

156 ding the first evidence of in vivo-expressed antisense RNAs in E. faecalis.

157 The notable lack of antisense RNAs in our non-size selected, directional lib

158 We investigated the effect of several antisense RNAs, including anti-4-1BBL, anti-p100, and an

159 1 for full repression; decreasing Bach1 with antisense RNA increased ferritin expression.

160 IRIP expression by small interfering RNA or antisense RNA increased MPP+ uptake.

161 bryonic stem (ES) cells and demonstrate that antisense RNA induces silencing and deposition of repres

162 ription of the psbN gene, i.e. production of antisense RNA, influences psbT/psbH intergenic processin

163 is-regulatory elements, and we can show that antisense RNAs inhibit PU.1 expression by modulating mRN

164 Our results support the idea that antisense RNAs inhibit retrotransposition by targeting T

165 ncoded negative regulators PrgX and Qa (prgQ antisense) RNA inhibit pCF10 transfer by blocking prgQ t

166 Depletion of TRAF7 by antisense RNA inhibited MEKK3-mediated AP1 and CHOP acti

167 ion by an adenovirus construct encoding p204 antisense RNA inhibited osteoblast-specific gene activat

168 nducing differentiation, whereas ectopic 204 antisense RNA inhibited the differentiation.

169 uction of LDHA expression by interference or antisense RNA inhibits tumorigenesis is not well underst

170 hat seen with mutations that ablate Tsix, an antisense RNA initiated 3' of Xist.

171 ses, including transcriptional interference, antisense RNA interactions between the mRNAs of the two

172 Instead, antisense RNA interactions seem to be the system's drivi

173 Inhibition of p11 expression by inhibitory antisense RNAs (iRNA) treatment resulted in enhanced IFN

174 ranscription of qrf, the long non-coding frq antisense RNA, is induced by light, and its level oscill

175 Similarly, antisense RNA knockdown of Foxg1 expression in the zebra

176 ession of either dominant-negative allele or antisense RNA knockdown of SecA1 or SecA2 dramatically i

177 restingly, the toxic shRNAs generated higher antisense RNA levels, compared with the nontoxic shRNA.

178 siRNAs, there is no change in the transposon antisense RNA levels.

179 apart, in conjunction with a novel cis-bound antisense RNA linked to Polycomb repressor proteins and

180 entified E(2)-induced and RNase H1-sensitive antisense RNAs located at the 5' and 3' ends of the E(2)

181 Thus, natural antisense RNA may be a trigger for heterochromatin forma

182 First, because the antisense RNA mechanism relies on RNA-RNA interactions,

183 Conversely, antisense RNA-mediated attenuation of SIRT2 reversed ROS

184 s this, we demonstrate how naturally derived antisense RNA-mediated transcriptional regulators can be

185 g three unique features of the plasmid pT181 antisense-RNA-mediated transcription attenuation mechani

186 ating embryonic stem cells, transcription of antisense RNA mediates silencing and methylation of the

187 Hence, we targeted ERCC1 by antisense RNA methodologies, and we show that we could s

188 isense transcripts strengthens the view that antisense RNAs might affect a wider variety of processes

189 These antisense RNA molecules originate in the early region of

190 ession is achieved through the production of antisense RNA molecules.

191 HOXA transcript antisense RNA myeloid-specific 1 (HOTAIRM1) is a long no

192 all tissue types tested, we detect a pool of antisense RNA of approximately 35 nt, which derives from

193 Using transgenic plants expressing antisense RNA of CYP79D1 and CYP79D2, Siritunga and Sayr

194 Thus, the L region antisense RNA of EMCV is a key determinant of innate imm

195 Disruption by antisense RNA of endogenous c-Jun expression in LNCaP ce

196 ne endometrial epithelial cells and that the antisense RNA of Scx (Bop1 intronic RNA) accumulates as

197 ge CTG repeat expansions in the untranslated antisense RNA of the Kelch-like 1 gene (KLHL1), but the

198 hat acts on RNA 2 and replacing them with an antisense RNA oligonucleotide, we have engineered a reco

199 tment of NIH3T3 cells with either caspase-12 antisense RNA or dsRNA corresponding to the full-length

200 Targets of antisense RNA or miRNA did not appear to be preferential

201 These data raise the possibility that this antisense RNA or other RpaR-activated noncoding RNAs med

202 tion of ALDH1A1 in HLECs by ALDH1A1-specific antisense RNA or SiRNA was associated with decreased oxi

203 ut functional elements e.g. small RNAs, long antisense RNAs or untranslated regions (UTRs) of mRNA tr

204 y, blocking eIF-4E function by expression of antisense RNA, or overexpression of the inhibitory eIF-4

205 mRNA, the primary transcript (pre-mRNA), the antisense RNA overlapping the MHC genes, and both the in

206 A total of 21 sense/antisense RNA pairs identified in dsRNAs were confirmed

207 Our results provide direct evidence that L1 antisense RNA plays a functional role in chromosome-wide

208 s used as a template for the synthesis of an antisense RNA probe, which is labeled with digoxigenin-l

209 ed by in situ hybridization, by employing an antisense RNA probe; BDNF protein was detected by employ

210 aneous detection of five differently labeled antisense RNA probes and up to seven differ-ent transcri

211 Digoxygenin (dig)-labeled antisense RNA probes are in vitro transcribed from a tem

212 abeled ribonucleotides are incorporated into antisense RNA probes by in vitro transcription.

213 rotocol describes ISH of digoxigenin-labeled antisense RNA probes to whole-mount zebrafish embryos.

214 tional silencing of FLC and reveal roles for antisense RNA processing and DCL3 function in this regul

215 S gene family: Lym-nNOS1, Lym-nNOS2, and the antisense RNA-producing pseudogene (anti-NOS).

216 unclear whether this repression requires the antisense RNA product or whether the antisense transcrip

217 Inhibition of IFITM3 by antisense RNA promoted OPN protein expression, enhanced

218 studies of the lncRNA HOTAIR (HOX transcript antisense RNA) provide compelling evidence for therapeut

219 e other smaller regulatory RNAs in bacteria, antisense RNAs range in size from tens to thousands of n

220 Non-coding antisense RNAs regulate bacterial genes in response to n

221 erococcus faecalis plasmid pAD1, is the only antisense RNA regulated postsegregational killing system

222 r rapid degradation, as occurs in most other antisense RNA regulated systems, RNA I and RNA II form a

223 terococcus faecalis plasmid pAD1 is the only antisense RNA-regulated addiction module identified to d

224 It is the only antisense RNA-regulated addiction module identified to d

225 E. faecalis plasmid pAD1 encodes an antisense RNA-regulated addiction module that combines f

226 Two antisense RNA-regulated toxin-antitoxin gene families, h

227 de a small hydrophobic protein (ShoB) and an antisense RNA regulator (OhsC).

228 The numbers of antisense RNAs reported for different bacteria vary exte

229 Classic antisense RNA research has focused on detailed examinati

230 nique organization of the par locus, the par antisense RNA, RNA II, binds to its target, RNA I, at re

231 Moreover, induced yhcS antisense RNA selectively increased bacterial susceptibi

232 Conversely, inhibition of miR-34a using antisense RNA sensitized lymphoma cells to therapeutic a

233 RNA interference mediated by RNA such as antisense RNA, short interfering RNA and micro RNA is we

234 Addition of functional uPA protein or LRP antisense RNA significantly increased ERK signaling and

235 kinase, antisense oligodeoxynucleotides and antisense RNA, small inhibitory RNA, triple helix, domin

236 ples are presented in which expression of an antisense RNA specifically reduces its cognate mRNA.

237 rotein Hfq promotes the association of small antisense RNAs (sRNAs) with their mRNA targets, but the

238 was demonstrated that short, single-stranded antisense RNA (ss-siRNA) can also induce RNAi.

239 n PTCs and suggest that transcription of the antisense RNA stabilizes or augments HAS2 mRNA expressio

240 y such host-encoded proteins, we employed an antisense RNA strategy and a lentivirus-based library co

241 These results suggest that the antisense RNA strategy can be useful for identifying nov

242 coccus mutans, we have recently initiated an antisense RNA strategy.

243 egrations driving overexpression of the TERT antisense RNA suggest it may have a role in tumorigenesi

244 ent work on newly identified plasmid-encoded antisense RNAs suggest that there is still much to learn

245 iption site, H3.3 accumulates with sense and antisense RNA, suggesting that it is recruited through a

246 epresented among loci with exosome-sensitive antisense RNAs, suggesting a potential for widespread co

247 Stable transfection of cells with antisense RNA targeted against GRP78 (pkASgrp78 cells) p

248 spoIIE and to decrease spoIIE expression via antisense RNA targeted against spoIIE, respectively.

249 surveillance factor TRAMP, which suppresses antisense RNAs targeted by Clr4 and RNAi.

250 xpressed between the two ecotypes, including antisense RNAs targeting key regulators of root-growth r

251 identification of a cis-encoded 1.2 kb long antisense RNA - termed AmgR - that is complementary to t

252 We propose that the ratA transcript is an antisense RNA that anneals to the 3' end of the txpA mRN

253 pression of a SMN2 trans-splicing RNA and an antisense RNA that blocks a downstream splice site in SM

254 t gene carries within its coding sequence an antisense RNA that drives Xist expression.

255 transcription of a spacer generates a small antisense RNA that is used by RNA-guided Cas nucleases t

256 mids produce plasmid-specific variants of an antisense RNA that regulates conjugation structural gene

257 a-proteobacterial repABC plasmids produce an antisense RNA that regulates the replication initiator i

258 phylococcus aureus plasmid pSK41 produces an antisense RNA that regulates the replication initiator p

259 ermination process requires a 427-nucleotide antisense RNA that spans the intergenic region and acts

260 and H2A.Z show markedly increased levels of antisense RNAs that are normally degraded by the exosome

261 d ~200 long, unspliced and exosome-sensitive antisense RNAs that arise from transcription start sites

262 The antitoxins are proteins or antisense RNAs that counteract the toxins.

263 accumulation of rare 26 nt 5'-phosphorylated antisense RNAs that depend on the RdRP homolog RRF-3, th

264 cient inhibition requires trafficking of the antisense RNA through the Rev/RRE pathway.

265 Its transcription produces antisense RNA to a large part of the psbB pentacistronic

266 t al that proposes regulating Wilm's tumor-1 antisense RNA to control pathological bone resorption.

267 cumulation of the flv4-2 operon mRNA and one antisense RNA to flv4, designated as As1_flv4.

268 ced bidirectionally overexpressing sense and antisense RNA to form dsRNA in vivo.

269 an isogenic RKO cell line expressing stable antisense RNA to GADD45alpha, a significant protection o

270 A recombinant AAV2 (rAAV2) vector encoding antisense RNA to HIV-1 transactivating region (TAR) was

271 hat mir-21 downregulated, whereas a modified antisense RNA to miR-21 upregulated reporter activity.

272 terminal-repeat-driven constructs expressing antisense RNA to the same target region in HIV-1 but con

273 E-1 interacts with trigger-derived sense and antisense RNAs to initiate RNAi, while several other AGO

274 ited by IC2 (potentially through a noncoding antisense RNA) to the paternal chromosome in a region of

275 that relies on the presence of an endogenous antisense RNA, transcribed from the 3'-end of the human

276 normally repressed by a conserved noncoding antisense RNA transcript, BDNF-AS.

277 Antisense RNA transcription attenuators are a key compon

278 in 15 hr after transient induction of a dNR1 antisense RNA transgene.

279 al attenuator from plasmid pT181 and natural antisense RNA translational regulators.

280 e not affected in ALDH3A1-specific SiRNA- or antisense RNA-treated rat lenses, HLECs, or ALDH3A1-null

281 Eliminating cycling of deltaGABA(A)Rs by antisense RNA treatment or gene knockout prevents the lo

282 osome inactivation (XCI) is regulated by the antisense RNA Tsix, which represses Xist on the active X

283 We find that upstream antisense RNAs (uaRNAs) have distinct capped 5' termini

284 turely terminated RNAs (ptRNAs) and upstream antisense RNAs (uaRNAs).

285 CO-2 transfectants expressing keratin 8 (K8) antisense RNA under a tetracycline-responsive element, w

286 Unlike other long ncRNAs, antisense RNAs usually regulate their counterpart sense

287 ntext, when a 121-nucleotide segment of atpB antisense RNA was expressed from an ectopic site, an ele

288 Furthermore, when the RRE-driven antisense RNA was redirected to the Tap/Nxf1 pathway, ut

289 genetic tools, along with optimized RBSs and antisense RNA, we engineered B. marmarensis to produce e

290 ng to protein-coding genes, long ncRNAs, and antisense RNAs were due to DNA contamination on the surf

291 g events and an unexpectedly large number of antisense RNAs were identified, revealing new details of

292 This suggests that the small antisense RNAs were produced from the transgene, which w

293 yabE is negatively regulated by a cis-acting antisense RNA which, in turn, is regulated by two extrac

294 ence of B12, aspocR is transcribed as a long antisense RNA, which inhibits pocR expression.

295 ates in a complex with transcribed sense and antisense RNA, which is distinct from the DNA/chromatin.

296 Ty1 antisense RNAs, which have been reported to inhibit Ty1

297 by widespread transcription of noncoding and antisense RNAs, which is linked to key chromosomal proce

298 We propose that such antisense RNAs will likely be important in the regulatio

299 finities and reduced cleavage activities for antisense RNAs with either a 5'-terminal hydroxyl or aba

300 istronic gene clusters and the generation of antisense RNAs, without cell death.