ライフサイエンスコーパス: open reading frame

1 cessary to properly enter the capsid protein open reading frame.

2 cessing of a polyprotein encoded in a single open reading frame.

3 s operational when combined with an upstream open reading frame.

4 ate within the coding region of the opposite open reading frame.

5 s via introduction of a TC tag into the muNS open reading frame.

6 is translationally repressed by an upstream open reading frame.

7 ent translation elongation through the viral open reading frame.

8 ond and third in-frame AUG codons in the NS1 open reading frame.

9 mate-induced translation is dependent on Arc open reading frame.

10 e, and in the case of protein coding DNA, an open reading frame.

11 nal AUGs at positions 235 and 241 of the NS1 open reading frame.

12 O) that induces exon skipping to restore the open reading frame.

13 haracteristic gene models yet maintaining an open reading frame.

14 ntranslated regions (NTRs) flanking a single open reading frame.

15 specific activity of target sites within the open reading frame.

16 BpuR-binding site was mapped 5' of the sodA open reading frame.

17 tin is organized into domains in relation to open reading frames.

18 secondary structure motifs but no essential open reading frames.

19 erential translation and the use of multiple open reading frames.

20 gle RNA translation dynamics in frameshifted open reading frames.

21 acetyl-CoA carboxylase subunit D (accD)-like open reading frames.

22 enesis and thereby generate mutations in all open reading frames.

23 such as multi k-mer frequencies and relaxed open reading frames.

24 ange from 22.6-33.0 Kbp, consisting of 27-39 open reading frames.

25 e-encoding RNAs, and dynamic use of upstream open reading frames.

26 oligonucleotides (ASOs) that target upstream open reading frames.

27 sence of gene homologs to all 84 known HHV-7 open reading frames.

28 equences, including 2442 translated upstream open reading frames.

29 encoded by a 3,200-bp genome with only four open reading frames.

30 ribosomal entry sites (IRESs) preceding both open reading frames.

31 aves a clear three nucleotide periodicity in open reading frames.

32 d by GC-rich regions and the absence of long open reading frames.

33 ere confirmed as expressed genes with intact open reading frames.

34 control during the translation of suboptimal open reading frames.

35 particularly those with highly elongated neo open reading frames.

36 54 bp in length, and encodes a predicted 106 open reading frames.

37 ic and have a wide range of genome sizes and open reading frames.

38 uent studies utilized N-terminally truncated open reading frames.

39 infection and the expression of codon-biased open reading frames.

40 on (IGR), and the biosynthetic trpB and trpA open-reading frames.

41 EBV miR-BamHI fragment H rightward open reading frame 1 (BHRF1)-2-5p clustered apart from o

42 P25K to long interspersed element 1 (LINE-1) open reading frame 1 protein (ORF1p), which contains an

43 In this study, we assessed LINE-1 open reading frame 1 protein expression in 12 p53 signat

44 2-hydroxylase, ceruloplasmin, chromosome 19 open reading frame 12 and ATPase type 13A2.

45 2 (Lso2; coiled-coil domain containing short open reading frame 124 [CCDC124] in mammals) was found t

46 detect two separate target sequences in the open reading frame 1ab (ORF1ab) region of the SARS-CoV-2

47 /ml for detecting two regions of the genome (open reading frame 1ab [ORF1ab] and nucleocapsid protein

48 esults on an RNA-dependent RNA polymerase or open reading frame 1b gene assay.

49 ysis showed that amphoterin-induced gene and open reading frame 2 (Amigo2) was overexpressed in LV12

50 mammals), and recently, late-annotated short open reading frame 2 (Lso2; coiled-coil domain containin

51 Open reading frame 2 (ORF2) Ag was detected in both plas

52 Here, an open reading frame 2 deletion mutant of the neuropathoge

53 eactive primer set targeting the overlapping open reading frame 2/3 (ORF2/3) nucleotide sequence of H

54 We identified 220 OR open reading frames, 20 of which are full length, intact

55 ins are essential for viral growth in vitro (open reading frame 32 [ORF32], ORF59, ORF81, ORF83, ORF9

56 at the viral protein kinase (vPK) encoded by open reading frame 36 (ORF36) of Kaposi's sarcoma-associ

57 (KSHV) alkaline exonuclease SOX, encoded by open reading frame 37 (ORF37), is a bifunctional early-l

58 The absence of an equivalent open reading frame 3b (ORF3b) and genetic differences ve

59 f a rodent CoV were also observed at 8.9-kDa open reading frame 4a at the 3' end of the spike gene.

60 riants that contained mutations in the viral open reading frame 5 (ORF5) protein.

61 Despite low-level expression of open reading frame 50 (ORF50), transcripts for the immun

62 ntaneous, tetradecanoyl phorbol acetate-, or open reading frame 50 (ORF50)/replication transactivator

63 We subsequently identified open reading frame 52 (ORF52), a multifunctional and abu

64 In luciferase assays with VZV open reading frame 61 (ORF61) promoter reporter plasmid,

65 The large RNR subunit of KSHV, open reading frame 61 (ORF61), coprecipitated multiple A

66 edicted promoter of the immediate early gene open reading frame 63 (ORF63).

67 elevated expression of CXorf67 (chromosome X open reading frame 67), which frequently occurs in PFA e

68 Open reading frame 7 (ORF7) of VZV has been recognized a

69 ), including but not limited to chromosome 9 open reading frame 72 (C9orf72) repeat expansion carrier

70 85) of a pathogenic mutation in chromosome 9 open reading frame 72 (C9orf72), progranulin (GRN) or mi

71 ncharacterized gene (C17orf99; chromosome 17 open reading frame 99), that is expressed in bone marrow

72 as a 10.3-kb genome that encodes a rare dual open reading frame, a feature uncharacteristic of classi

73 g site of Pfn2 or overexpression of the Pfn2 open reading frame alone in otherwise wild-type cells la

74 ts) translated from nonannotated Alternative Open reading frame (AltORFs) were discovered using custo

75 demonstrated the translation of alternative open-reading frames (altORFs) in addition to annotated p

76 levant to its expression, including a leader open reading frame and an RNA structure overlapping the

77 the Ugandan subtype F, but with different K1 open reading frame and KSHV whole-genome sequences and a

78 hylogenetic clustering within the partial E2 open reading frame and noncoding region 2.

79 quence features: TRmIND by the length of the open reading frame and TRmD both by a approximately 60 n

80 proteins, two ribosomal RNAs, three putative open reading frames and 33 transfer RNAs of 19 amino aci

81 ble-stranded DNA genome coding for up to 250 open reading frames and a fully cytoplasmic replication.

82 ature of indel mutations, which create novel open reading frames and a large quantity of mutagenic pe

83 lly been undertaken through the detection of open reading frames and other genomic motifs, supplement

84 Many maintain intact open reading frames and provirus expression together wit

85 roup of HERV-K elements, still retain intact open reading frames and the capacity to produce certain

86 e amino termini of these proteins to the NP1 open reading frame, and splice site mutations that preve

87 Functional peptides encoded by short open reading frames are emerging as important mediators

88 a phage genome as a network of paths: where open reading frames are favorable, and overlaps and gaps

89 Also, SSP-coding small open reading frames are often expressed at low levels or

90 ing to saturation of inserts adjacent to all open reading frames as well as conventional inactivation

91 may explain why, despite having lost the E6 open reading frame between 20 and 60 million years ago,

92 aled mutations near the N terminus of the G9 open reading frame but none in A16 or other genes.

93 not have evolved by tandem duplication of an open reading frame, but rather originated by fusion betw

94 y inhibit the translation of downstream main open reading frames, but some enhance expression.

95 P24), angiopoietin 4 (ANGPT4), chromosome 11 open reading frame (C11orf30/EMSY), and exocyst complex

96 ubiquitin gene is a unique, highly conserved open reading frame composed solely of tandem repeats, ye

97 species carry a 7.5kb plasmid encoding eight open reading frames conventionally called plasmid glycop

98 ate a sgmRNA encoding a ribosomally occupied open reading frame (dORF) located downstream of the nucl

99 uding an immunogenic peptide derived from an open reading frame downstream of the melanoma stem cell

100 nsmembrane proteins endoregulin (ELN), dwarf open reading frame (DWORF), myoregulin (MLN), and anothe

101 A viruses, and as a likely consequence, most open reading frames encode multifunctional viral protein

102 highlights the functional activity of short open reading frame-encoded peptides and underscores thei

103 is of this envelope transcript revealed long open reading frames encoding putative surface and transm

104 nd DMD mutations that disrupt the dystrophin open reading frame extinguish luciferase expression.

105 lgarno (SD) sequences positioned upstream of open reading frames facilitate translation initiation.

106 vectors carrying the full-length dystrophin open-reading frame for transduction of human muscle deri

107 h excludes those lncRNA gene loci with small open reading frames from being regarded as protein-codin

108 sition of the repeat within or outside of an open reading frame has been used to focus research on di

109 citrus-CTV pathosystem, deletion of the p33 open reading frame in a CTV variant resulted in a signif

110 nserted increasing lengths of the dystrophin open reading frame in a foamy virus vector and quantifie

111 omolog repressed the translation of the main open reading frame in cis, independent of the sequence o

112 The nonclassical open reading frame in the FCGR2C gene (FCGR2C.nc-ORF) wa

113 the function of MC021, we replaced the F13L open reading frame in vaccinia virus with an epitope-tag

114 Here, we sequenced the full gyrA and gyrB open reading frames in 240 multidrug-resistant and exten

115 tumors by functional, non-canonical upstream open reading frames in its 5' untranslated region, which

116 g transcript is produced with small upstream open reading frames in its 5' untranslated region.

117 contained as many as around 10% of the total open reading frames in some genomes, substantially incre

118 alignments, we detected at least 175 de novo open reading frames in the focal species O. sativa subsp

119 le we did not find any intact capsid protein open reading frames in the integrated viral sequences, w

120 Finally, we reannotated nine open reading frames in the mitochondrial genome that cod

121 ubjects and sequenced the full gyrA and gyrB open reading frames in their respective sputum TB isolat

122 q allowed for the identification of upstream open reading frames in transcripts, which we predict to

123 genic mutations predicted to restore BRCA1/2 open reading frames, including two patients with multipl

124 ntrol of a strong promoter while leaving its open reading frame intact.

125 e we individually express in human cells 204 open reading frames involved in the DNA damage response

126 th the hypothesis that mutation of the HBeAg open reading frame is an important factor driving CHB pa

127 The virion infectivity factor (Vif) open reading frame is conserved among most lentiviruses.

128 serted downstream from the first ATG and the open reading frame is disrupted by a 1-bp insertion, exp

129 P1, a small NS protein encoded by the middle open reading frame, is required for the expression of th

130 rther analysis demonstrated that KSHV latent open reading frame K12 (ORFK12) gene (kaposin A)-mediate

131 d find that the feature relationship between open reading frame length and guanine-cytosine (GC) cont

132 deletion of uridines to generate functional open reading frames, many of which encode components of

133 he expression of identified and unidentified open reading frames needed to deal with and overcome the

134 Novel open reading frames (nORFs) with coding potential may ar

135 diversification, such as emergence of novel open reading frames (nORFs).

136 An isogenic knockout mutant of the open reading frame NTHI1441 showed a 76.6% +/- 5.5% redu

137 use sgRNA-mediated CRISPR/Cas9 to target the open reading frame of a gene in the genome and analyze t

138 onfirmed by GFP accumulation from the second open reading frame of a polycistronic messenger RNA, whi

139 oxic sequences - most of them located in the open reading frame of CD95L.

140 We discuss that mutations in the open reading frame of CEBPA lead to an altered C/EBPalph

141 ransmembrane protease, serine 2) gene to the open reading frame of ERG, encoding an ETS family transc

142 ating a library of fragments derived from an open reading frame of interest and enriching for the int

143 A mutation at base 1,455 in the open reading frame of Ma1 leads to a premature stop codo

144 in the 5' untranslated region or within the open reading frame of the toxin hamper its translation b

145 The I2L open reading frame of vaccinia virus (VACV) encodes a co

146 otated protein-coding genes, including small open reading frames of less than 100 codons, and the tra

147 l segments combined in which the overlapping open reading frames of matrix 1 (M1)/M2 for the modified

148 splicing impairments that lead to a shift in open reading frames of MLPH and MITF.

149 1 (M1)/M2 for the modified M segment and the open reading frames of nonstructural protein 1 (NS1)/nuc

150 peptides not only from precursors encoded in open-reading frames of mRNA transcripts but also cryptic

151 ent containing transporter genes and several open-reading frames of unknown function.

152 o contain 132,831 bp with 145 putative ORFs (open reading frames) of at least 50 amino acids.

153 results in bicistronic transcripts with two open reading frames, of which only the first, MOCS1A, is

154 luding the repressive effect of the upstream open reading frames on gene expression and the mutationa

155 d a form of B. burgdorferi in which the ospA open reading frame, on lp54, was replaced with the ospC

156 er from SARS-CoV only in containing an extra open reading frame (ORF) (named ORFX), between ORF6 and

157 ue culture, contained a 2,158-bp deletion in open reading frame (ORF) 12.

158 racterized type I IFN antagonism of MERS-CoV open reading frame (ORF) 8b accessory protein.

159 r antibiotic resistance encoded in the first open reading frame (ORF) and accumulation of the reporte

160 reast cancer cells, targeted E-cadherin mRNA open reading frame (ORF) and suppressed E-cadherin prote

161 f the previously annotated Copenhagen strain open reading frame (ORF) as a 17.4-kDa protein.

162 e assessment across pan-cancer fusion genes, open reading frame (ORF) assignment, and retention searc

163 efect in translation of the chloroplast psbJ open reading frame (ORF) but has no effect on psbA expre

164 tic' and harbour an additional uninterrupted open reading frame (ORF) covering almost the entire leng

165 ing genes relied on assumptions, such as one open reading frame (ORF) encodes one protein and minimal

166 e RNA genomes of 2.2 to 4.4 kb with a single open reading frame (ORF) encoding an RNA-dependent RNA p

167 Remarkably, the approximately 1,100 bp open reading frame (ORF) encoding the envelope proteins

168 Turnip crinkle virus (TCV) coat protein (CP) open reading frame (ORF) has been found to promote inter

169 ctions during virus replication, although an open reading frame (ORF) is retained among an unknown pe

170 The integrity of the putative BWRF1 open reading frame (ORF) is retained in over 80% of stra

171 The open reading frame (ORF) lengths of TmELO1 and TmELO2 we

172 While at least one reliable open reading frame (ORF) model has been assigned for eve

173 yvirus, family Potyviridae) contains a large open reading frame (ORF) of 3,494 codons translatable as

174 To address this, we replaced the NSP3 open reading frame (ORF) of the segment 7 (pT7/NSP3) tra

175 is the introduction of a frameshift into the open reading frame (ORF) of the target gene which trunca

176 esponse is quite broad: the median number of open reading frame (ORF) products recognized was nine pe

177 t dsRNA1 dsRNA is 1,683 bp in length with an open reading frame (ORF) that encodes 539 amino acids (m

178 rate that the last 36 nucleotides of the NSs open reading frame (ORF) were needed to ensure the effic

179 Additionally, 594 GENCODE lncRNAs acquire an open reading frame (ORF) when their structure is extende

180 f the frameshift site or by truncating the X open reading frame (ORF), had little effect on the infec

181 functional domains/sites or shifting of the open reading frame (ORF), leading to a variety of human

182 of a conserved 260-triplet-long overlapping open reading frame (ORF), which we call POLGARF (POLG Al

183 these two parts formed a single read-through open reading frame (ORF).

184 the mitochondrial clades based on the mtDNA open reading frame (ORF).

185 ome by assessing the ability of nearly every open reading frame (ORF; approximately 5,300 ORFs) to in

186 enome size of 4248 bp and only four putative open reading frames (ORF), vB_RpoMi-Mini becomes the sma

187 ochorism and to the presence of the atypical open reading frames (ORFans) F-orf and M-orf, respective

188 y quantify the expression of canonical viral open reading frames (ORFs) and to identify 23 unannotate

189 gions downstream of previously annotated EBV open reading frames (ORFs) and viral promoters.

190 nts, the determinants of ribosome flux along open reading frames (ORFs) are not fully understood.

191 Ribo-TISH can also predict novel open reading frames (ORFs) from regular ribosome profili

192 ns conserved (core) and variable (accessory) open reading frames (ORFs) grouped at fixed regions in t

193 me of Bam35, nearly half of the 32 annotated open reading frames (ORFs) have no homologs in databases

194 rganized into operons consisting of discrete open reading frames (ORFs) in a single polycistronic mRN

195 lyses have revealed abundant expressed short open reading frames (ORFs) in bacteria.

196 ave been identified with unusually divergent open reading frames (ORFs) in the conserved region of rp

197 We subjected various open reading frames (ORFs) in the genome of respiratory

198 The open reading frames (ORFs) involved have functions relat

199 ure, 68 substitutions that were localized in open reading frames (ORFs) likely associated with host c

200 The predicted 80 open reading frames (ORFs) of herpes simplex virus 1 (HS

201 ut deletion or interruption of any of the 12 open reading frames (ORFs) of the virus.

202 ding the first detection of products from 27 open reading frames (ORFs) previously designated "predic

203 nting a novel strategy to generate candidate Open Reading Frames (ORFs) resulting from Cytidine to Ur

204 iversity leading to the formation of altered open reading frames (ORFs) that appear to be under relax

205 tic tools, we first identified 315 potential open reading frames (ORFs) within the genome, including

206 forms of HIV-RNA transcripts with competent open reading frames (ORFs), and can be found in the peri

207 GCs usually carry promoter-less open reading frames (ORFs), encoding proteins with vario

208 es for re-evaluating the coding potential of open reading frames (ORFs), including many short ORFs th

209 We identify hundreds of new open reading frames (ORFs), including upstream ORFs (uOR

210 ome sequence containing 128 unique predicted open reading frames (ORFs), many of which were most clos

211 sor encoding distinct repeat epitopes in two open reading frames (ORFs), one translated from the 5' c

212 In addition to canonical open reading frames (ORFs), thousands of translated smal

213 iling, identification of actively translated open reading frames (ORFs), to the quantification of tra

214 quantify translation at the level of single open reading frames (ORFs), using information from Ribo-

215 r double-stranded DNA (dsDNA) genome with 31 open reading frames (ORFs), whose predicted gene product

216 at produce 21 transcripts with nine distinct open reading frames (ORFs).

217 Each genome encodes 21 open reading frames (ORFs).

218 es and analysis of the remaining alleles for open reading frames (ORFs).

219 peptide coding sequence to the Pgd1 and Pgd2 open reading frames (ORFs).

220 gnized that many mRNAs can also encode small open reading frames (ORFs).

221 long single-stranded RNAs lacking annotated open reading frames (ORFs).

222 idae, which bidirectionally encode two major open reading frames (ORFs): Rep and capsid protein (CP)

223 e library (616 overlapping peptides spanning open reading frames [ORFs] 1-3) was used in interferon-g

224 A unique open reading frame (ORFX) was identified in the genomes

225 sm analysis, FX548 contained no mutations in open reading frames other than hgbA We conclude that by

226 Additionally, open reading frame Ov8, unique to OvHV-2, was found to e

227 iptome analysis revealed that an unannotated open reading frame (Percc1) flanks the regulatory sequen

228 Two open reading frames predicted from the genomic islands c

229 The median number of HSV-1 open reading frames recognized per person was 16.

230 ing a premature stop codon in the 33277 fimB open reading frame relative to the 381 fimB allele.

231 nnot express the NSs protein or have the NSs open reading frame replaced with a reporter gene.

232 on enhancing factor (PTEF) relieves upstream open reading frame repression and thereby facilitates VA

233 vel of PTEF, and the alleviation of upstream open reading frame repression requires the proteolytic p

234 xis (PrEP), we performed KSHV typing with K1 open reading frame Sanger and KSHV whole-genome sequenci

235 iginating from DRC (one partial and one full open reading frame sequence).

236 idence has pointed to the existence of small open reading frame (smORF)-encoded microproteins in mamm

237 Small open reading frames (smORFs) and their encoded microprot

238 Small open reading frames (smORFs) encoding 'micropeptides' ex

239 ous lncRNAs have been found to contain short open reading frames (sORFs) which have been overlooked b

240 hese elements include mRNA folding, upstream open reading frames, specific nucleotides flanking the i

241 ed deletions at coding sequence of the ORF8 (open reading frame), spike, and ORF7a proteins, specific

242 One-by-one disruption of each of LINC00261's open reading frames suggests that the RNA, rather than t

243 Both are encoded by a single 870-bp open reading frame that exhibits genetic polymorphisms i

244 oter region was found to contain an upstream open reading frame that is required for Pi-responsive ex

245 that Tug1 contains an evolutionary conserved open reading frame that when overexpressed produces a st

246 transcript variant lacking a small upstream open reading frame that would otherwise inhibit translat

247 The LLT RNA contains multiple upstream open reading frames that can inhibit translation.

248 Short open reading frames that could produces micropeptides we

249 Pseudogenes represent open reading frames that have been damaged by mutations,

250 long RTC4 transcript contains small upstream open reading frames that prevent translation of the down

251 f P3 fused to Pretty Interesting Potyviridae open reading frame), the two PD-localized potyviral prot

252 circular genome of 107,063 bp containing 97 open reading frames, the majority of which share sequenc

253 on our mutant analysis, we revised the rec27 open reading frame: the new start codon is in the previo

254 to dicistronic viruses but contain a single open reading frame, thus likely representing a recent ex

255 CRISPR/Cas9 system despite their lacking an open reading frame to evaluate functional loss.

256 rons, CGG RAN acts as an inhibitory upstream open reading frame to suppress basal FMRP production.

257 Sequence analysis of all 41 known ZIKV RNA open reading frames to date indicates that ZIKV has unde

258 nd initiation codon selection by 5' upstream open reading frames, translation initiation factors, and

259 The human cytomegalovirus opening reading frame UL144 is an ortholog of the TNF re

260 Direct sequencing of an HCMV open reading frame UL56 region that included amino acids

261 b plasmid DNA encoding the 3.9 kb human NPC1 open reading frame, under the influence of a 1.5 kb plat

262 10-nucleotide sequence preceding an upstream open reading frame (uORF) and downstream GFP drives a br

263 An upstream open reading frame (uORF) confers the translational cont

264 ntrolled by a single cis-regulatory upstream open reading frame (uORF) in the 5' untranslated regions

265 sttranscriptionally regulated by an upstream open reading frame (uORF) located in its 5' untranslated

266 n this work, we demonstrate that an upstream open reading frame (uORF) present in the 5' untranslated

267 enterovirus genomes also harbour an upstream open reading frame (uORF) that is subject to strong puri

268 ed proteins or translation of upstream small open reading frames (uORF).

269 characterize a complex landscape of upstream open reading frames (uORFs) across 5'-untranslated regio

270 Upstream open reading frames (uORFs) are known to control the tra

271 Upstream open reading frames (uORFs) are potent regulatory elemen

272 Upstream open reading frames (uORFs) are tissue-specific cis-regu

273 Upstream open reading frames (uORFs) are ubiquitous repressive ge

274 observed thousands of AUG-initiated upstream open reading frames (uORFs) that are a major contributor

275 ASOs that bind to mRNA sequences in upstream open reading frames (uORFs) to specifically increase the

276 translation events, including 1,329 upstream open reading frames (uORFs) within the 5' untranslated r

277 sion of Kozak sequence composition, upstream open reading frames (uORFs), and secondary structure.

278 sense-mediated decay (NMD) targets, upstream open reading frames (uORFs), canonical ORFs shorter than

279 Upstream open reading frames (uORFs), located in transcript leade

280 ry 5' leader sequence with multiple upstream Open Reading Frames (uORFs), thereby activating stress-r

281 on reinitiation on mRNAs harbouring upstream open reading frames (uORFs).

282 er but also two pathogen-responsive upstream open reading frames (uORFsTBF1) of the TBF1 gene.

283 slated due to the presence of multiple small open reading frames upstream of the coding region.

284 gions of an antigen or antigens, alternative open reading frame usage, and translation of RNA splicin

285 This RSV F open reading frame was evaluated in rB/HPIV3 in three fo

286 Identical genomic and open reading frame was found to be present in close rela

287 n the CD4+ T-cell response to specific HSV-1 open reading frames was greater between MZ twins than be

288 ere-1), inhibits translation of a downstream open reading frame when bound to amino-tSS.

289 ghly hydrophobic protein from an overlapping open reading frame, which we designate E10.

290 annotation pipelines generally ignore small open reading frames, which are those most likely to enco

291 d multiple microproteins encoded in upstream open reading frames, which form stable complexes with th

292 pathogenic functions of the plasmid-encoded open reading frames, which may motivate further investig

293 As phage Seahorse genome encodes 48 open reading frames with many hypothetical proteins, thi

294 In the former case, these include open reading frames with putative functions in metabolis

295 Here, we describe an alternative open reading frame within human insulin mRNA encoding a

296 nalysis of the i-leader revealed a potential open reading frame within the leader sequence and the te

297 have shown that a fraction of putative small open reading frames within lncRNAs are translated.

298 Among the open reading frames within the viral genome, ORF3, ORF5,

299 protein encoded in part by a +1 frameshifted open reading frame (X-ORF) in segment 3.

300 o far uncharacterized mitochondrial protein (open reading frame YDR381C-A) as an important assembly f