ライフサイエンスコーパス: internal ribosome entry site

1 d not impair translation directed by the HCV internal ribosome entry site.

2 ation without exhibiting typical features of internal ribosome entry site.

3 downstream expression ratios mediated by an internal ribosome entry site.

4 nes were separated by expressing Tax from an internal ribosome entry site.

5 was driven by an encephalomyocarditis virus internal ribosome entry site.

6 mRNA, indicating that the leader contains an internal ribosome entry site.

7 osis protein expression by translation at an internal ribosome entry site.

8 nucleotides 1 to 43) and a longer element of internal ribosome entry site.

9 s an important role in the hepatitis C virus internal ribosome entry site.

10 regulation is mediated, at least in part, by internal ribosome entry sites.

11 osome entry site was found to bind, with the internal ribosome entry site-40S subunit interaction bei

12 hree of the PPMOs, targeting domain 5 of the internal ribosome entry site (5D PPMO), and the two tran

13 The 5'UTR was tested for internal ribosome entry site activity using a bicistroni

14 prevented the ability of IL-6 to enhance Myc internal ribosome entry site activity, Myc protein expre

15 By homologous recombination of an internal ribosome entry site and Cre recombinase coding

16 Its sequence possesses an internal ribosome entry site and is directly translated

17 show that the JunD mRNA does not possess an internal ribosome entry site and is translated in a cap-

18 ng the PIG-A complementary DNA along with an internal ribosome entry site and the nerve growth factor

19 slation of antiapoptotic protein Bcl-2 at an internal ribosome entry site and this mechanism was iden

20 o human sequences, originally reported to be internal ribosome entry sites and later to instead be pr

21 shown to enhance the translation of several internal ribosome entry sites and upstream ORF-containin

22 rtTA2S-M2-IRES-EGFP vector (where IRES is an internal ribosome entry site) and permits relatively ine

23 on (NCR) of the viral genome functions as an internal ribosome entry site, and its unique 3' NCR is r

24 region showed some attributes of a type IVB internal ribosome entry site, and the polyprotein lacked

25 The regulation of expression from the URE2 internal ribosome entry site appears to be through the l

26 ssays did not validate the possibility of an internal ribosome entry site as a potential mechanism fo

27 etween NS2 and NS3, and second by placing an internal ribosome entry site between the two proteins (a

28 ration and characterization of a novel CXCR3 internal ribosome entry site bicistronic enhanced GFP re

29 ncanonical translation is not mediated by an internal ribosome entry site but requires the interactio

30 A putative internal ribosome entry site can be identified in the co

31 licon but not a Sindbis virus replicon or an internal ribosome entry site containing mRNA.

32 lasmids, and we were able to map a potential internal ribosome entry site-containing region to a 2474

33 The cricket paralysis virus internal ribosome entry site (CrPV-IRES) is a folded str

34 gy, we discovered a specific defect in IRES (internal ribosome entry site)-dependent translation in D

35 By contrast, encephalomyocarditis virus internal ribosome entry site-dependent green fluorescent

36 ltiple proteins required for efficient viral internal ribosome entry site-dependent translation are l

37 ational environment to increase the ratio of internal ribosome entry site-dependent translation to ca

38 their replication was made dependent on the internal ribosome entry sites, derived from other positi

39 treatment, but an encephalomyocarditis virus internal ribosome entry site-driven element exhibited no

40 pendent translation but not bulk cellular or internal ribosome entry site-driven translation.

41 that express the p40 gene linked via a viral internal ribosome entry site element with fluorescent re

42 Using the cricket paralysis virus internal ribosome entry site element, coupled to in vitr

43 Using an internal ribosome entry site element, the green fluoresc

44 nt translation of its own genomic RNA via an internal ribosome entry site element.

45 itiation on picornavirus genomes with type I internal ribosome entry site elements and also for RNA r

46 We identified potential internal ribosome entry site elements located in the 5'

47 Retrovirus transduction of survivin-internal ribosome entry site-enhanced green fluorescent

48 w c-myc was maintained, we studied myc IRES (internal ribosome entry site) function, which does not r

49 PDGF (platelet-derived growth factor)-IRES (internal ribosome entry site)-GFP (green fluorescent pro

50 a dual reporter, pQCXhSSTr2-IRES-GFP (IRES: internal ribosome entry site; GFP: green fluorescent pro

51 lation initiation from the hepatitis C virus internal ribosome entry site (HCV IRES) RNA.

52 presence of upstream open reading frame and internal ribosome entry site in 5' UTR sequences of C. s

53 m the CDK11(p110) mRNA through the use of an internal ribosome entry site in a mitosis-specific manne

54 d due to enhanced translation mediated by an internal ribosome entry site in the 5'-UTR of the c-Myc

55 Here, we provide evidence for an internal ribosome entry site in the DSPP gene that direc

56 An internal ribosome entry site in the HIF-1alpha 5' untran

57 rast to cap-dependent and tobacco etch virus internal ribosome entry site interaction with eIF4F, pol

58 Rz3'X was found to substantially inhibit HCV internal ribosome entry site (IRES) activity and PSMA7 w

59 An internal ribosome entry site (IRES) activity in hTPH2 5'

60 that this leader sequence confers functional internal ribosome entry site (IRES) activity.

61 on codon AUG828, and possesses cross-kingdom internal ribosome entry site (IRES) activity.

62 The dicistrovirus intergenic region internal ribosome entry site (IRES) adopts a triple-pseu

63 tion initiation despite a complex 5' UTR are internal ribosome entry site (IRES) and 5' proximal post

64 onal activity of the hepatitis C virus (HCV) internal ribosome entry site (IRES) and other HCV-like I

65 n D1 mRNA 5' untranslated region contains an internal ribosome entry site (IRES) and that both this I

66 process that requires uncapped RNA, the HCV internal ribosome entry site (IRES) and the 3' region of

67 viral (HCV) genome is translated through an internal ribosome entry site (IRES) as a single polyprot

68 slated region (5'NTR) which folds to form an internal ribosome entry site (IRES) as well as structure

69 We previously discovered an internal ribosome entry site (IRES) at the 5' untranslat

70 taining an encephalomyocarditis virus (EMCV) internal ribosome entry site (IRES) at the same sites as

71 serting an encephalomyocarditis virus (EMCV) internal ribosome entry site (IRES) between these two pr

72 The cricket paralysis virus internal ribosome entry site (IRES) can, in the absence

73 halomyocarditis virus mRNA is mediated by an internal ribosome entry site (IRES) comprising structura

74 dresses the properties of a newly identified internal ribosome entry site (IRES) contained within the

75 athway incorporates 4E-BP resistant cellular internal ribosome entry site (IRES) containing mRNAs, to

76 on on HIV genomic RNA relies on both cap and Internal Ribosome Entry Site (IRES) dependant mechanisms

77 The HCV internal ribosome entry site (IRES) directly regulates t

78 An internal ribosome entry site (IRES) directs internal bin

79 erties of a conserved 75mer RNA motif of the internal ribosome entry site (IRES) element of encephalo

80 bosomal subunit to the mRNA cap structure or internal ribosome entry site (IRES) element, respectivel

81 r proteins identified to interact with viral internal ribosome entry site (IRES) elements and stimula

82 in-based screen to identify small, synthetic internal ribosome entry site (IRES) elements in vivo.

83 The function of Internal Ribosome Entry Site (IRES) elements is intimate

84 ated GB virus B (GBV-B) genomes is driven by internal ribosome entry site (IRES) elements located wit

85 been demonstrated that selected picornaviral internal ribosome entry site (IRES) elements possess res

86 ranslation of a subgroup of mRNAs containing internal ribosome entry site (IRES) elements such as tho

87 n of translation can be mediated by specific internal ribosome entry site (IRES) elements that are lo

88 For picornavirus RNAs containing type I internal ribosome entry site (IRES) elements, PCBP2 bind

89 In this study, we have identified an internal ribosome entry site (IRES) from the highly infe

90 A replication, and a partial rescue of viral internal ribosome entry site (IRES) function from IFN su

91 vivo, we generated a knockin mouse where an internal ribosome entry site (IRES) green fluorescence p

92 ndent translation mediated by the poliovirus internal ribosome entry site (IRES) in a dose-dependent

93 To determine the role of the HRV2 internal ribosome entry site (IRES) in determining speci

94 C virus (HCV) genomic RNA initiates from an internal ribosome entry site (IRES) in its 5' untranslat

95 RNA genome of hepatitis C virus (HCV) has an internal ribosome entry site (IRES) in its first 370 bas

96 The poliovirus internal ribosome entry site (IRES) in the 5' nontransla

97 The internal ribosome entry site (IRES) in the 5' untranslat

98 ein synthesis, suggesting the presence of an internal ribosome entry site (IRES) in the 5' UTR of VEG

99 g to a region between the cloverleaf and the internal ribosome entry site (IRES) in the 5'-nontransla

100 9 is located within a structurally conserved internal ribosome entry site (IRES) in the 5'-UTR of a n

101 lored cap-independent translation through an internal ribosome entry site (IRES) in the 5'-UTR of the

102 t the CMTX mutation abolished function of an internal ribosome entry site (IRES) in the 5'-UTR of the

103 We report here an internal ribosome entry site (IRES) in the c-Src mRNA th

104 The internal ribosome entry site (IRES) in the hepatitis C v

105 anslation in a cap-independent manner via an internal ribosome entry site (IRES) in their 5' untransl

106 An internal ribosome entry site (IRES) initiates protein sy

107 o alternative translation initiation routes, internal ribosome entry site (IRES) initiation and ribos

108 e under the translational control of the HCV internal ribosome entry site (IRES) into the livers of m

109 These mRNAs contain an internal ribosome entry site (IRES) located in the 5' un

110 In addition, an internal ribosome entry site (IRES) located in the 5'-co

111 NA is translated in neural cell lines via an internal ribosome entry site (IRES) located in the 5'-un

112 to be regulated by an H ferritin-responsive internal ribosome entry site (IRES) located within the c

113 ivity of these two drugs at the level of HCV internal ribosome entry site (IRES) mediated translation

114 An internal ribosome entry site (IRES) mediates translation

115 We tested whether an internal ribosome entry site (IRES) might be located ups

116 t on the foot-and-mouth disease virus (FMDV) internal ribosome entry site (IRES) occurs at two sites

117 of the pGL3-basic vector was replaced by the internal ribosome entry site (IRES) of encephalomyocardi

118 otein (PTB) to stimulate the activity of the internal ribosome entry site (IRES) of foot-and-mouth di

119 A promising target for treatment is the internal ribosome entry site (IRES) of HCV, a highly con

120 The internal ribosome entry site (IRES) of hepatitis C virus

121 type 1 chimera, PV1(RIPO), with the cognate internal ribosome entry site (IRES) of human rhinovirus

122 lating protein translation directed from the internal ribosome entry site (IRES) of the encephalomyoc

123 on factor (eIF) 4F binds tightly to the mRNA internal ribosome entry site (IRES) of tobacco etch viru

124 t RNAs revealed the presence of an efficient internal ribosome entry site (IRES) overlapping ORF 72 c

125 e unknown structure of the hepatitis C virus internal ribosome entry site (IRES) pseudoknot domain.

126 4 nucleotide domain of the Hepatitis C virus internal ribosome entry site (IRES) RNA adopts an indepe

127 itiation, and to the hepatitis C viral (HCV) internal ribosome entry site (IRES) RNA.

128 Internal ribosome entry site (IRES) RNAs are elements of

129 Internal ribosome entry site (IRES) RNAs are important r

130 Internal ribosome entry site (IRES) RNAs are necessary f

131 Although structured internal ribosome entry site (IRES) RNAs can manipulate

132 Internal ribosome entry site (IRES) RNAs from the hepati

133 In particular, the tests on the internal ribosome entry site (IRES) segments yield satis

134 was fused in frame with p51, followed by an internal ribosome entry site (IRES) sequence and the p66

135 ation of a bicistronic system, involving the internal ribosome entry site (IRES) sequence from the 5'

136 tes based on the insertion of a picornavirus internal ribosome entry site (IRES) sequence into the ge

137 Enteroviruses use a type I Internal Ribosome Entry Site (IRES) structure to facilit

138 nslation of the HCV RNA is facilitated by an internal ribosome entry site (IRES) that can autonomousl

139 -UTR sequence of mouse PTEN does not have an internal ribosome entry site (IRES) that can mediate cap

140 , RNA upstream of the coding region forms an internal ribosome entry site (IRES) that directly binds

141 hypothesized that this 5'-UTR may contain an internal ribosome entry site (IRES) that facilitates BCL

142 -1 Arg/Lys transporter is translated from an internal ribosome entry site (IRES) that is regulated by

143 Thus, a remarkably short internal ribosome entry site (IRES) that lacks an AUG co

144 ein H2, and CUG-binding protein 1-responsive internal ribosome entry site (IRES) that regulates SHMT1

145 droxymethyltransferase 1 (SHMT1) contains an internal ribosome entry site (IRES) that regulates SHMT1

146 lex secondary structure, and functions as an internal ribosome entry site (IRES) to initiate translat

147 They use a structured RNA element termed an internal ribosome entry site (IRES) to recruit the 40S r

148 SRp20 is an important internal ribosome entry site (IRES) trans-acting factor

149 translation of MPD6 was mediated by a novel internal ribosome entry site (IRES) upstream of the MPD6

150 The dicistrovirus intergenic region internal ribosome entry site (IRES) utilizes a unique me

151 In both lines, an internal ribosome entry site (IRES) was included to faci

152 orescent protein (GFP) transgene fused to an internal ribosome entry site (IRES) was inserted after t

153 This intergenic region contains an internal ribosome entry site (IRES) which directs the sy

154 The BiP mRNA contains an internal ribosome entry site (IRES) which increases the

155 e yeast Saccharomyces cerevisiae contains an internal ribosome entry site (IRES) whose activity is su

156 We define an internal ribosome entry site (IRES) within ELANE and dem

157 e that this isoform results from usage of an internal ribosome entry site (IRES) within exon 5 that i

158 We demonstrate the presence of a functional internal ribosome entry site (IRES) within the 5' leader

159 We previously identified an internal ribosome entry site (IRES) within the 5' leader

160 inine/lysine transporter (cat-1) mRNA via an internal ribosome entry site (IRES) within the mRNA lead

161 gion alone is insufficient to function as an internal ribosome entry site (IRES) without including a

162 ss in detail the recent discovery of the p53 internal ribosome entry site (IRES), its role in p53 tra

163 A recent study indicated that full-length internal ribosome entry site (IRES), present in the 5'-u

164 non-canonical means of initiation, including internal ribosome entry site (IRES), ribosome shunting,

165 and domain II of the hepatitis C virus (HCV) internal ribosome entry site (IRES), we measured the rat

166 planted sequence comprised domain III of the internal ribosome entry site (IRES), which directly bind

167 us 5' nontranslated region (NTR) contains an internal ribosome entry site (IRES), which facilitates t

168 sites as well as the cricket paralysis virus internal ribosome entry site (IRES), which interacts wit

169 5'-untranslated region, is initiated from an internal ribosome entry site (IRES), which is modulated

170 ein through a cap-independent, or rather, an internal ribosome entry site (IRES)-dependent mechanism.

171 The activation of this internal ribosome entry site (IRES)-dependent mRNA trans

172 A1 regulates a salvage pathway facilitating internal ribosome entry site (IRES)-dependent mRNA trans

173 chanistically, we demonstrate that decreased internal ribosome entry site (IRES)-dependent Myc mRNA t

174 w that during OIS, a switch between cap- and internal ribosome entry site (IRES)-dependent translatio

175 otein with CCND1 messengerRNA and that CCND1 internal ribosome entry site (IRES)-dependent translatio

176 d that Pdcd4 inhibited cap-dependent but not internal ribosome entry site (IRES)-dependent translatio

177 icistronic cellular reporter system with HCV internal ribosome entry site (IRES)-dependent translatio

178 uced the expression of Runx1 protein from an internal ribosome entry site (IRES)-dependent, cap-indep

179 nhibits the translation of cap-dependent and internal ribosome entry site (IRES)-driven mRNAs, includ

180 e that LSm1 contributes to activation of HCV internal ribosome entry site (IRES)-driven translation b

181 by higher levels of eIF4G1 were found to use internal ribosome entry site (IRES)-mediated alternate t

182 Internal ribosome entry site (IRES)-mediated cap-indepen

183 of the cyclin D1 and c-myc mRNAs occurs via internal ribosome entry site (IRES)-mediated initiation

184 several studies suggest that it may modulate internal ribosome entry site (IRES)-mediated initiation

185 by regulating translation possibly using an internal ribosome entry site (IRES)-mediated mechanism.

186 ic RNA and, at least in part, by stimulating internal ribosome entry site (IRES)-mediated translation

187 All splice variants support internal ribosome entry site (IRES)-mediated translation

188 -cytoplasmic SR protein, SRp20, functions in internal ribosome entry site (IRES)-mediated translation

189 psh-53, psh-274, and psh-375) suppressed HCV internal ribosome entry site (IRES)-mediated translation

190 at the expression of p27kip1 is regulated by internal ribosome entry site (IRES)-mediated translation

191 rine leukemia virus (MLV) vectors containing internal ribosome entry site (IRES)-transgene cassettes

192 tronic expression via translation through an internal ribosome entry site (IRES).

193 criptional level, express mRNA containing an internal ribosome entry site (IRES).

194 s internal recruitment of the ribosome to an internal ribosome entry site (IRES).

195 with the sequence element functioning as an internal ribosome entry site (IRES).

196 he translation of some mRNAs that contain an internal ribosome entry site (IRES).

197 is cotranslated with the OR by virtue of an internal ribosome entry site (IRES).

198 nslation via a stimulatory effect on the myc internal ribosome entry site (IRES).

199 lular mRNAs occurs by ribosome binding to an internal ribosome entry site (IRES).

200 r RNAs (mRNAs) bearing either a 5'-cap or an internal ribosome entry site (IRES).

201 poliovirus (PV) are located within the viral internal ribosome entry site (IRES).

202 in translation initiation by the poliovirus internal ribosome entry site (IRES).

203 , indicating that the TEV leader contains an internal ribosome entry site (IRES).

204 One such element is the internal ribosome entry site (IRES).

205 the CGG repeat element that functions as an internal ribosome entry site (IRES).

206 f the picornavirus genome is regulated by an internal ribosome entry site (IRES).

207 al complex formation with a picornaviral RNA internal ribosome entry site (IRES).

208 eotide substitutions reside within the viral internal ribosome entry site (IRES).

209 We show that each ORF is preceded by one internal ribosome entry site (IRES).

210 , by forming a specific RNA structure called internal ribosome entry site (IRES).

211 domain 3 of the foot-and-mouth disease virus internal ribosome entry site (IRES); this junction conta

212 use of molecular tags on viral mRNA such as internal ribosome entry sites (IRES) and genome-linked v

213 imize the coding potential of viral genomes, internal ribosome entry sites (IRES) can be used to bypa

214 ly encode one target protein, but the use of internal ribosome entry sites (IRES) can confer the abil

215 Because internal ribosome entry sites (IRES) have been postulate

216 tion, mitotic raptor promotes translation by internal ribosome entry sites (IRES) on mRNA during mito

217 ciated with protein expression of mRNAs with internal ribosome entry sites (IRES) that are sensitive

218 F mRNA 5'-untranslated region (5'-UTR) bears internal ribosome entry sites (IRES), which confer susta

219 n reading frames that are driven by distinct internal ribosome entry sites (IRES).

220 g regions of six mRNAs were shown to contain internal ribosome entry sites (IRES).

221 Viral internal ribosomes entry site (IRES) elements coordinate

222 equence), or A8-nIRES-A9 (fusion with native internal ribosome entry site [IRES] sequence).

223 ed region of the genome (contiguous with the internal ribosome entry site [IRES]).

224 t (6- to 22-nt) sequences that functioned as internal ribosome entry sites (IRESes) and enhanced tran

225 ndependent translation, which is mediated by internal ribosome entry sites (IRESes) located in the 5'

226 Although the internal ribosome entry sites (IRESes) of viral mRNAs ar

227 urring nucleotide sequences that function as internal ribosome entry sites (IRESes) within the 5' lea

228 eam of ORF1 and ORF2 in mouse L1 function as internal ribosome entry sites (IRESes).

229 oximately 1/400,000) functioned as synthetic internal ribosome entry sites (IRESes).

230 r sequences mediated internal initiation via internal ribosome entry sites (IRESes).

231 The use of bicistronic vectors carrying internal ribosome entry sites (IRESs) allows the coexpre

232 ein syntheses mediated by cellular and viral internal ribosome entry sites (IRESs) are believed to ha

233 Internal ribosome entry sites (IRESs) are powerful model

234 Internal ribosome entry sites (IRESs) are specialized mR

235 Cellular internal ribosome entry sites (IRESs) are untranslated s

236 widespread class of RNA viruses that utilize internal ribosome entry sites (IRESs) for translation in

237 Although the existence of internal ribosome entry sites (IRESs) in viral mRNAs is

238 Internal ribosome entry sites (IRESs) mediate cap-indepe

239 Internal ribosome entry sites (IRESs) promote translatio

240 Internal ribosome entry sites (IRESs) that are required

241 se selective translation of mRNAs containing internal ribosome entry sites (IRESs) that include key p

242 V) messenger RNAs contain related (HCV-like) internal ribosome entry sites (IRESs) that promote 5'-en

243 ve to L13a-mediated silencing when driven by internal ribosome entry sites (IRESs) that require initi

244 Viruses use internal ribosome entry sites (IRESs) to minimize or, li

245 Picornaviruses use internal ribosome entry sites (IRESs) to translate their

246 se structured RNA elements, resembling viral internal ribosome entry sites (IRESs), are found in subs

247 pression were essential for the discovery of internal ribosome entry sites (IRESs), it is becoming in

248 ber of cellular mRNAs are thought to possess internal ribosome entry sites (IRESs), sequences that pe

249 UTR of luciferase reporter mRNAs containing internal ribosome entry sites (IRESs), so that potential

250 ed by recruitment of ribosomes to structured internal ribosome entry sites (IRESs), which are located

251 swine fever virus or cricket paralysis virus internal ribosome entry sites (IRESs), which do not use

252 ncanonical translational mechanisms, such as internal ribosome entry sites (IRESs).

253 al control of HSPG synthetic enzymes through internal ribosome entry sites (IRESs).

254 with cap-independent translation mediated by internal ribosome entry sites (IRESs).

255 nd were not rigorously proven to function as internal ribosome entry sites (IRESs).

256 sis by a cap-independent mechanism involving internal ribosome entry sites (IRESs).

257 that the cricket paralysis virus intergenic internal ribosome entry site is able to support Sec inco

258 n in HCV in detail, mRNAs containing the HCV internal ribosome entry site linked to a luciferase codi

259 Thus, GPR41 expression is mediated via an internal ribosome entry site located in the intergenic r

260 accharomyces cerevisiae, possibly through an internal ribosome entry site-mediated mechanism.

261 Interestingly, cap-independent internal ribosome entry site-mediated translation direct

262 hat eIF2A functions as a suppressor of Ure2p internal ribosome entry site-mediated translation in yea

263 c accumulation of hnRNP A1, which attenuates internal ribosome entry site-mediated translation of ant

264 orylation, increased gene transcription, and internal ribosome entry site-mediated translation.

265 rocessing, mRNA localization, stability, and internal ribosome entry site-mediated translation.

266 s yields without substantially affecting HCV internal ribosome entry site-mediated translation.

267 iator ATG and that it can be initiated by an internal ribosome entry site, neither of which has been

268 G, the hepatitis C virus E2 epitope, and the internal ribosome entry site of cricket paralysis virus.

269 inhibited the translation efficiency of the internal ribosome entry site of CSFV.

270 thetic hairpin RNAs (sshRNAs), targeting the internal ribosome entry site of hepatitis C virus (HCV)

271 (sshRNAs) (SG220 and SG273) that target the internal ribosome entry site of the hepatitis C virus (H

272 of translation initiation as directed by the internal ribosome entry sites of certain picornaviruses.

273 whether driven by homologous or heterologous internal ribosome entry sites or from a capped message.

274 and ribosome recruitment found in the viral internal ribosome entry site (PKB223) and the V4 domain

275 enteroviral infection, along with the viral internal ribosome entry site, plays a role in mediating

276 eam of the UTRs demonstrated the presence of internal ribosome entry sites, providing an additional,

277 NA-derived template substrate (complementary internal ribosome entry site), R1479-TP showed similar p

278 ure for the recently discovered human HoxA9D internal ribosome entry site regulon.

279 Dicistroviridae intergenic region (IGR) internal ribosome entry site(s) (IRES) RNAs drive a cap-

280 to the poliovirus type 1 (Mahoney) (PV-1(M)) internal ribosome entry site/segment (IRES)-the question

281 These vectors contain four different internal ribosome entry site-selectable markers, allowin

282 Interestingly, however, the presence of the internal ribosome entry site significantly decreases Sec

283 ue hepatovirus features, including predicted internal ribosome entry site structure, a truncated VP4

284 n for either m(7)G cap or tobacco etch virus internal ribosome entry site, suggesting that the 3' BTE

285 from ORNs expressing P2 receptors in the P2-internal ribosome entry site-tau-lacZ mouse.

286 ways; they are uncapped, and they contain an internal ribosome entry site that allows the ribosome to

287 that the 5'-untranslated region contains an internal ribosome entry site that is constitutively acti

288 Because the VEGF mRNA contains two internal ribosome entry sites, the increased expression

289 egy, we rationally designed two thermosensor internal ribosome entry site (thermo-IRES) elements, who

290 It binds to internal ribosome entry sites to facilitate their use in

291 cIAP1 (cellular inhibitor of apoptosis), an internal ribosome entry site translation-dependent prote

292 rtially overlaps with the site where the HCV internal ribosome entry site was found to bind, with the

293 genomes in which a heterologous picornaviral internal ribosome entry site was inserted at the 2A/2B j

294 which a Cre recombinase gene preceded by an internal ribosome entry site was inserted into the 3' un

295 protein synthesis of LAMB1 by activating its internal ribosome entry site, which in turn led to incre

296 han translation dependent on the HCV or CSFV internal ribosome entry sites, which do not require eIF4

297 mple of a 5-nt bulge, from hepatitis C virus internal ribosome entry site, with a different sequence

298 strated that the differential utilization of internal ribosome entry sites within the mRNAs of these

299 Changes in the internal ribosome entry site, within the 5' noncoding re

300 Mouse embryonic fibroblasts in which an internal ribosome entry site/yellow fluorescent protein