ライフサイエンスコーパス: virus-encoded

1 bed by a four-subunit RNA polymerase that is virus encoded.

2 f tobacco mosaic virus is facilitated by the virus-encoded 30-kDa movement protein (MP).

3 or structure, they are all recognized by the virus-encoded 3C protein.

4 the ORF1 polyprotein was generated, and the virus-encoded 3C-like (3CL) proteinase (Pro) mediated cl

5 at undergoes autocatalytic processing by the virus-encoded 3C-like proteinase.

6 This virus encoded a single mutation, H316N (numbered relativ

7 Mouse T cells specific to the vaccinia virus-encoded a11r(198-205) could be cross-reactive with

8 ful infection of adult Drosophila requires a virus-encoded activity to suppress RVI.

9 secreting potential unless stimulated with a virus-encoded Ag.

10 As the first example of a virus-encoded alpha chemokine, vCXC-1 may ensure the act

11 The influenza A virus NS1 protein, a virus-encoded alpha/beta interferon (IFN-alpha/beta) ant

12 L4-33K is a virus-encoded alternative RNA splicing factor which acti

13 ion between corresponding family clusters of virus-encoded ANK and Skp1 proteins from three chlorovir

14 e triggered at mitochondria and modulated by virus-encoded anti-apoptotic B cell leukemia (BCL)2-like

15 selection for the evolution of sophisticated virus-encoded anti-CRISPR mechanisms.

16 pase-8, cytokine response modifier A (cowpox virus-encoded antiapoptotic protein), or DN Fas-associat

17 Unexpectedly, virus-encoded antigen was detectable more than 6 weeks a

18 e efficiency difference between cellular and virus-encoded antigens is based on whether the antigen i

19 red thirty-six of the proteins were vaccinia virus-encoded ( approximately 64% of the known vaccinia

20 view the discovery of viral master circuits: virus-encoded autoregulatory gene networks that autonomo

21 by notable sequence homology to the vaccinia virus-encoded B1 kinase (vvB1).

22 wed that CBP interacts with the Epstein-Barr virus-encoded basic region zipper (b-zip) protein, Zta,

23 We previously showed that the vaccinia virus-encoded Bcl-2-like protein, F1L, which suppresses

24 Virulence in animal models depends on the virus-encoded bifunctional Z-DNA/double-stranded RNA (ds

25 (GILGFVFTL) and the dissimilar Epstein-Barr virus-encoded BMLF1(280-288) epitope (GLCTLVAML), that,

26 ression of immune subversion proteins of the virus encoded by genes belonging to the US gene family.

27 RNA transcripts from this cDNA and the viruses encoded by them were infectious for cells of bot

28 Virus-encoded capsid proteins play a major role in the l

29 CMV growth by blocking the expression of the virus-encoded capsid proteins.

30 Given that virus-encoded cation channels play a crucial role in the

31 While these virus-encoded chemokine receptors are necessary for the

32 with diversity-generating retroelements and virus-encoded Clustered Regularly Interspaced Short Pali

33 Recent studies suggest that several virus-encoded components that antagonize RLR signaling i

34 use of the principal, secondary, orphan, and virus-encoded coreceptors for fusion.

35 Here we show that unlike other virus-encoded countermeasures, such as those from primat

36 The virus-encoded cysteine proteinase mediated at least five

37 relevant to understanding the potential of a virus-encoded cytokine-like molecule, HHV8 vIL6, to indu

38 intramolecular disulfide bond formed by the virus-encoded cytoplasmic redox pathway, and is incorpor

39 the formation of which required the vaccinia virus-encoded cytoplasmic redox pathway, and was localiz

40 iated proteins localized to the periphery of virus-encoded cytoplasmic structures, termed virus facto

41 n presented to the immune system as vaccinia virus-encoded cytosolic or endoplasmic reticulum (ER)-ta

42 The vaccinia virus-encoded D5 protein is an essential ATPase involved

43 progress is leading to the identification of virus-encoded determinants responsible for altering fung

44 Finally, identification of virus-encoded dissimilatory sulfite reductase suggests S

45 ori-Lyt in the presence of the Epstein-Barr virus-encoded DNA binding initiator protein, ZTA.

46 ous amounts of methylated nucleotides due to virus-encoded DNA methyltransferases (MTases); about 25%

47 inding protein (OBP), one of seven essential virus-encoded DNA replication proteins, to specific sequ

48 evaded by transcription of highly structured virus-encoded dsRNA inhibitors that bind to and inactiva

49 circumvent PKR function by transcription of virus-encoded dsRNA inhibitors that bind to and inactiva

50 tethering, mediated by Brd4 interaction with virus-encoded E2 protein, facilitates viral genome segre

51 ulated by cellular transcription factors and virus-encoded E2 proteins that act as sequence-specific

52 understanding of the mechanisms by which the virus-encoded E6 oncoproteins contribute to cell transfo

53 hile their direct autoregulatory activity on virus-encoded early gene products is completely preserve

54 The virus-encoded EBNA-1 (EBV nuclear antigen 1) and latent

55 ex mechanism involving interactions with the virus-encoded EBNA1 protein.

56 The identification of virus-encoded effectors of SIE and their transgenic expr

57 The two viruses encoded either wild-type (WT) VP35 protein (recE

58 ircle-like mechanism initiated by a distinct virus-encoded endonuclease.

59 The virus-encoded envelope proteins of human immunodeficienc

60 somal DNA of a host cell and is one of three virus-encoded enzymes that are required for replication.

61 acid motifs as a result of glycosylation by virus-encoded enzymes.

62 adapter-mediated substrate recruitment for a virus-encoded ERAD E3 ligase, mK3.

63 analysis indicated that the mutation in the virus-encoded external scaffolding protein was primarily

64 tein, whereas the fourth mutation alters the virus-encoded external scaffolding protein.

65 We report that vaccinia virus-encoded F1L protein, previously recognized as anti

66 ssociated proteins around the peripheries of virus-encoded factories, interrupting the normal formati

67 The contributions of major Epstein-Barr virus-encoded factors, including proteins, small RNAs, a

68 s previously identified as fcr-1, a putative virus-encoded FcR.

69 both plant and invertebrate hosts requires a virus-encoded function to block the RNA silencing antivi

70 eptibility to cucumber mosaic virus when the virus-encoded function to suppress RNAi was disrupted.

71 ted, by an immediate-early (IE) or early (E) virus-encoded function(s).

72 es is transcribed, including one of the four virus-encoded G protein-coupled receptors (GPCRs), US28.

73 ite of budding by the late (L) domain of the virus-encoded Gag protein.

74 ess ERK activity in the absence of any other virus-encoded gene products.

75 d cells that express a broad spectrum of the virus-encoded genes (type III latency; EBV+/III), EBV-po

76 c analysis reveals that 65% of the predicted virus-encoded genes are expressed during lytic infection

77 ce, host-cell-derived tissue factor (TF) and virus-encoded glycoprotein C (gC) can stimulate protease

78 s initiated by the interaction of the Friend virus-encoded glycoprotein gp55 with the erythropoietin

79 Virus-encoded glycoproteins in the envelope are responsi

80 nd tegument, and a lipid envelope containing virus-encoded glycoproteins.

81 ion of CTL specific for recombinant vaccinia virus-encoded gp160, indicating its ability to bind endo

82 s expressing only US28 but not the remaining virus-encoded GPCRs is phenotypically similar to that of

83 s, in a process that is probably driven by a virus-encoded helicase.

84 acterization of the aptamers showed that the virus-encoded hemagglutinin, a protein expressed on the

85 The vaccinia virus-encoded heterodimer responsible for poly(A) tail e

86 Moreover, we observed that the virus-encoded HIV transactivator protein Tat cooperated

87 The virus-encoded Holliday junction resolvase is required to

88 s and vaccinia virus specifically, utilize a virus-encoded host range factor(s), such as a member of

89 ropism at the cellular level is regulated by virus-encoded host range proteins acting downstream of v

90 ed of the minor capsid protein (CPm) and the virus-encoded Hsp70 homolog.

91 hermore, the absence of analogous degrons in virus-encoded IAPs explains their relative stability and

92 Over 170 different virus-encoded IFN antagonists from 93 distinct viruses h

93 tiple factors, indicating robustness against virus-encoded immune evasion genes.

94 t has resulted in a delicate balance between virus-encoded immune evasion mechanisms and host antivir

95 PA-X is a fusion protein of influenza A virus encoded in part from a +1 frameshifted X open read

96 sing this assay, we have identified an Ebola virus-encoded inhibitor of the type I IFN response, the

97 Transmitted viruses encoded intact canonical genes (gag-pol-vif-vpr-

98 This enzymatic process is catalyzed by the virus-encoded integrase protein, which is conserved amon

99 nto the host chromosomal DNA directed by the virus-encoded integrase protein.

100 ces correlate with the sequence/structure of virus-encoded integrases, supporting the idea that integ

101 he retroviral life cycle and is catalyzed by virus-encoded integrases.

102 Here we report that the virus-encoded interferon regulatory factor 3 (vIRF3) lat

103 activated KSHV early lytic genes, including virus-encoded interleukin 6 and polyadenylated nuclear R

104 or implicated in transformation and latency, virus-encoded interleukin-8, a CXC chemokine, and pp38 a

105 Viroporins are small virus-encoded ion channel proteins.

106 es suggested that HCV p7 could function as a virus-encoded ion channel.

107 The M1 virus-encoded K1 toxin is primarily but not solely respo

108 ation that bind the origin-binding domain of virus-encoded large T antigen.

109 he latter, (iii) neither viral DNA nor other virus-encoded late proteins are required for the interac

110 In general, virus-encoded late stage structural proteins, such as gB

111 virus (EBV) nuclear antigen 3C (EBNA3C) is a virus-encoded latent antigen essential for primary B-cel

112 The Epstein-Barr virus-encoded latent infection membrane protein 1 (LMP1)

113 al tumor nasopharyngeal carcinoma (NPC), the virus-encoded latent membrane protein LMP2A is consisten

114 nd transmembrane domains of the Epstein-Barr virus-encoded latent membrane protein-1 (LMP1) fused to

115 ng infected cells to differentiate using the virus-encoded LMP1 and LMP2a proteins, which act as func

116 ed that several nonenveloped viruses utilize virus-encoded lytic peptides for host membrane disruptio

117 ty between the HLA-A2-restricted influenza A virus-encoded M1(58-66) epitope (GILGFVFTL) and the diss

118 We propose that the NEC functions as minimal virus-encoded membrane-budding machinery during nuclear

119 e identification and characterization of two virus-encoded methyltransferases (MTases) involved in RN

120 wn-regulated at late times by miR-UL112-1, a virus-encoded microRNA.

121 To date, the vast majority of known virus-encoded microRNAs (miRNAs) are derived from polyme

122 genes in the animal kingdom, although animal virus-encoded microRNAs (miRNAs) are known to guide effi

123 Hundreds of virus-encoded microRNAs (miRNAs) have been uncovered, bu

124 e expression, and there have been reports of virus-encoded microRNAs.

125 n, we report the discovery of three herpes B virus-encoded microRNAs.

126 The Epstein-Barr virus-encoded miR-BART20-5p inhibits T-bet (TBX21), the

127 ese findings imply that some host targets of virus-encoded miRNAs are likely to be of little selectiv

128 Virus-encoded miRNAs have garnered much interest, althou

129 Several virus-encoded miRNAs have unique aspects to their biogen

130 s are continuing but the recent discovery of virus-encoded miRNAs indicates that viruses also use thi

131 Virus-encoded miRNAs seem to evolve rapidly and regulate

132 miRNAs and there is evidence to suggest that virus-encoded miRNAs target specific host genes and path

133 ain LMP1, signal transduction molecules, and virus-encoded miRNAs.

134 ies, and a number of previously unidentified virus-encoded miRNAs.

135 similar to those reported for other vaccinia virus-encoded model antigens.

136 These virus-encoded molecules promote cell entry, facilitate d

137 Virus-encoded movement protein (MP) mediates cell-to-cel

138 h plasmodesmata (PD), a process depending on virus-encoded movement protein (MP).

139 itiation factor eIF4E and VP39 (the vaccinia virus-encoded mRNA cap-specific 2'-O-methyltransferase),

140 Virus-encoded mRNA capping enzymes are attractive target

141 e antigen is synthesized from transgene- vs. virus-encoded mRNA.

142 KSHV genomes expressing latent state virus-encoded mRNAs and the LANA1 (latent nuclear antige

143 pect to virus production and accumulation of virus-encoded mRNAs measured by real-time PCR when K-Rta

144 nological, based on T-cell responses against virus-encoded neoantigen(s) expressed in tumor cells.

145 mbinant fusion protein comprised of a cowpox virus encoded NKG2D binding protein (OMCP) and a mutated

146 ied, little is known about the structures of virus-encoded non-structural proteins that are essential

147 involves the contribution of a wide array of virus encoded noncoding RNAs.

148 The virus-encoded nonstructural protein 5B (NS5B) of hepatit

149 A virus-encoded nonstructural protein, termed NSs, is a ma

150 It is thought that virus-encoded nonstructural proteins and RNA genomes int

151 revealed the presence of a substrate for the virus-encoded NS2B-NS3 protease at the carboxy-terminal

152 s observed as discrete foci, associated with virus-encoded NS5A and core proteins and identical in mo

153 The virus-encoded NSs protein acts as a virulence factor by

154 oliferation and the EBV latency Epstein-Barr virus-encoded nuclear antigen (EBNA)2 transcriptional tr

155 -alanine repeat domain (GAr) of Epstein-Barr virus-encoded nuclear antigen 1 (EBNA1) prevents major h

156 a repeat (GAr) within the viral Epstein-Barr virus-encoded nuclear antigen 1 protein.

157 ive sense RNA that are encapsidated with the virus-encoded nucleocapsid (N) protein to form a ribonuc

158 t C6 in the 2'-deoxynucleoside series showed virus-encoded nucleoside kinase-sensitive anti-VZV activ

159 RB) family of tumor suppressor proteins, and virus-encoded oncogenes disrupt the RB-E2F repressor com

160 nd the carcinogenic mechanism of hepatitis B virus-encoded oncoprotein HBx, we explored the function

161 factor receptor family, and the Epstein-Barr virus-encoded oncoprotein latent membrane protein 1 (LMP

162 The human T-cell leukemia virus-encoded oncoprotein Tax is a potent activator of v

163 nducing kinase and the human T-cell leukemia virus-encoded oncoprotein Tax or be constitutively turne

164 rus 40 (SV40) large tumor antigen (Tag) is a virus-encoded oncoprotein which is the target of a stron

165 liomas in vertebrates through the actions of virus-encoded oncoproteins.

166 ombinant PABP in vitro in the absence of any virus-encoded or eukaryotic cellular cofactors.

167 egative costimulatory signal to T cells by a virus-encoded orthologue of CD200.

168 The Tomato bushy stunt virus-encoded P19 forms dimers that bind duplex short in

169 ose induced by p55(gag), which recognize the virus encoded p24(gag) protein.

170 MERS-CoV replication depends in part on a virus-encoded papain-like protease (PL(pro)) that cleave

171 Deletion of 88% [Phe(25) to Pro(243)] of the virus-encoded papain-like protease, p29, in the context

172 to characterize the functional role of this virus-encoded pathway during lytic viral infection.

173 onformation of gamma, a membrane-disrupting, virus-encoded peptide usually sequestered inside the cap

174 ormation to generate ISVP*s and releases two virus-encoded peptides, mu1N and Phi.

175 This is the first description of a virus-encoded PERK-specific effector and defines a new s

176 In general, the same virus-encoded polymerase is responsible for both genome

177 However, an additional virus-encoded polypeptide referred to as the RPO-associa

178 ermediate transcription factor, comprised of virus-encoded polypeptides A8 and A23, was previously id

179 provide direct evidence that AC4 is a unique virus-encoded posttranscriptional gene-silencing suppres

180 ved after CVB3 infection at G175 and G436 by virus-encoded protease 2A(pro), independent of caspase a

181 ting that 2C is indeed capable of regulating virus-encoded proteases.

182 Cowpox virus encoded protein CPXV203 blocks MHCI surface expres

183 e mechanism of STAT signaling evasion, but a virus-encoded protein called V plays a central role in t

184 mplexes (RNPs) formed by these RNAs with the virus-encoded protein hepatitis delta antigen (HDAg) per

185 The virus-encoded protein pUS9 promotes axonal dissemination

186 assemble in the host cell membrane from the virus-encoded protein PVAP and open at the end of the in

187 nsactivator of transcription (Tat), an early virus-encoded protein required for the efficient transcr

188 to the ability to phosphorylate H5, the only virus-encoded protein shown to be a B1 substrate in vivo

189 The tegument consists of multiple, virus-encoded protein species that together can account

190 We have identified a virus-encoded protein termed gp37/Dip, which directly bi

191 EBV nuclear antigen 1 (EBNA1) is a virus-encoded protein that is critical for the replicati

192 hondria-localized inhibitor of apoptosis), a virus-encoded protein with a unique, albeit poorly under

193 otic function of NSP4 is balanced by another virus-encoded protein, NSP1, which is implicated in PI3K

194 reproduced by ectopic expression of a single virus-encoded protein, Tat.

195 s, and there is increasing evidence that the virus-encoded protein, Tax, plays a primary role in vira

196 icornaviral RNA replication utilizes a small virus-encoded protein, termed 3B or VPg, as a primer to

197 ient cleavage of the capsid precursor by the virus-encoded proteinase is a critical determinant in th

198 ific cleavage of the host factor Gemin3 by a virus-encoded proteinase, 2A(pro).

199 oteins that are proteolytically processed by virus-encoded proteinases to produce mature replicase pr

200 on, several cellular proteins are cleaved by virus-encoded proteinases.

201 Previous studies indicated that two virus-encoded proteins (capping enzyme and VITF-1) and o

202 Several virus-encoded proteins and an activity designated VLTF-X

203 Representative virus-encoded proteins and viral DNA accumulated with no

204 (d) Many chlorella virus-encoded proteins are either the smallest or among

205 At least six virus-encoded proteins are required for synthesis and pr

206 Combined, these analyses revealed 148 unique virus-encoded proteins associated with the virion (about

207 Virus-encoded proteins counteract this innate antiviral

208 The tip contains the virus-encoded proteins genome-linked protein and helper-

209 Despite these findings, no virus-encoded proteins have been identified that directl

210 al response that inhibits the translation of virus-encoded proteins in Nicotiana benthamiana.

211 d heterologous viruses to express individual virus-encoded proteins in wheat.

212 udies have uncovered new mechanisms by which virus-encoded proteins inhibit Ub and Ub-like (Ubl) modi

213 UL25 is one of seven herpes simplex virus-encoded proteins involved specifically in DNA enca

214 duce a restrictive defense response but that virus-encoded proteins may be involved in differential i

215 polyproteins presumed to incorporate all the virus-encoded proteins necessary for viral RNA synthesis

216 that procapsids can be formed in vitro from virus-encoded proteins only without any requirement for

217 e focusing on agents that block Epstein-Barr virus-encoded proteins or induce lytic cycle agents.

218 man cytomegalovirus (HCMV), contains over 70 virus-encoded proteins that are incorporated during a nu

219 of herpesvirus late genes depends on several virus-encoded proteins whose function is not completely

220 in WDV minichromosomes and/or interaction of virus-encoded proteins with specific host factors are co

221 rus (BMV) RNA replication is directed by two virus-encoded proteins, 1a and 2a.

222 Two other virus-encoded proteins, an HSP70 homolog (HSP70h) and an

223 HCMV gB is also one of the most immunogenic virus-encoded proteins, and a significant fraction of vi

224 Here, we show that two virus-encoded proteins, US2 and US3, coordinate their fu

225 ng live-cell imaging of viral RNA (vRNA) and virus-encoded proteins, we show that the TGB proteins ha

226 xpression, modification, and localization of virus-encoded proteins.

227 pect for therapeutic interventions targeting virus-encoded proteins.

228 localization of active ERK can be altered by virus-encoded proteins.

229 kaging them into an outer shell or capsid of virus-encoded proteins.

230 esumed to be RNA, and is suppressed by plant virus-encoded proteins.

231 kaging them into an outer shell or capsid of virus-encoded proteins.

232 strains the functional analysis of influenza virus-encoded proteins.

233 ific peptides from vaccinia- and influenza A virus-encoded proteins.

234 eparations, >88% of the theoretical vaccinia virus-encoded proteome was detected with high confidence

235 The PBCV-1 proteome reveals that two virus-encoded REases, but not their companion MTases, ar

236 homologous recombination in the absence of a virus-encoded RecA-type protein.

237 During latency, a subset of virus-encoded regulatory proteins is detected; however,

238 V DNA replication, the TRs are nicked by the virus-encoded Rep proteins at the terminal resolution si

239 lving interactions between the viral genome, virus-encoded replication factors, and host factors.

240 luding a requirement of two PCV Oris and the virus-encoded replication initiator Rep protein, suggest

241 auses G(1) cell cycle arrest mediated by the virus-encoded replication-associated protein (RAP) (or K

242 A(1) was found to block the expression of a virus-encoded reporter gene in both infection and transf

243 Holliday junctions, which are cleaved by the virus-encoded resolvase enzyme to form unit-length genom

244 eflects a multistep process catalyzed by the virus-encoded reverse transcriptase (RT).

245 Packaging of virus-encoded RNA is selective, with virions virtually d

246 se is a multiprotein complex, containing the virus-encoded RNA polymerase L and P proteins, and two c

247 belonging to the Picornaviridae, requires a virus-encoded RNA polymerase.

248 provide evidence for a mechanism by which a virus-encoded RNA silencing suppressor represses the tra

249 Neither Bcl-6 protein nor Epstein-Barr virus-encoded RNA was expressed.

250 helioma-like features contained Epstein-Barr virus-encoded RNA-1 by in situ hybridization.

251 trate that deregulated expression of Us11, a virus-encoded RNA-binding, ribosome-associated protein i

252 (HCV) nonstructural protein 5B (NS5B) is the virus-encoded RNA-dependent RNA polymerase (RdRp) essent

253 ation of nearly all RNA viruses depends on a virus-encoded RNA-dependent RNA polymerase (RdRp).

254 ein complexes, on the regulation of VP1, the virus-encoded RNA-dependent RNA polymerase (RdRp).

255 ination occurs via template switching by the virus-encoded RNA-dependent RNA polymerase (RdRP).

256 n the nucleocapsid must be accessible by the virus-encoded RNA-dependent RNA polymerase in order to s

257 equence similarity with RuvC, the absence of virus-encoded RuvA and RuvB to interact with, and the di

258 ted by differential substrate specificity of virus-encoded serine palmitoyltransferase, a key enzyme

259 ted herpesvirus (KSHV) lytic infection, many virus-encoded signaling molecules (e.g., viral G protein

260 Moreover, when the virus encoded SIINFEKL, T cells specific for nonrecombin

261 VX, was not dependent on the presence of the virus-encoded silencing suppressor protein, 25K.

262 ted by rising temperatures but suppressed by virus-encoded silencing suppressors.

263 plication, we recently demonstrated that the virus-encoded single-stranded (ss) DNA-binding protein (

264 d with a multisubunit complex containing the virus-encoded single-stranded DNA-binding protein ICP8.

265 that functioned as binding partners for the virus-encoded Skp1, proteins A682L and A607R.

266 virus (HDV) genome replication requires the virus-encoded small delta protein (deltaAg).

267 ovirus-associated (VA) RNAs and Epstein-Barr virus-encoded small RNAs (EBERs) with respect to RNA seq

268 gest a potential role for either cellular or virus-encoded SSB protein in improving the processivity

269 ing to a better understanding of the role of virus-encoded structural proteins not only in KSHV-relat

270 hat depends upon neither mouse mammary tumor virus-encoded superantigens nor MHC class II expression.

271 en1 mutant plants and in plants expressing a virus-encoded suppressor of RNA silencing (P1/HC-Pro), w

272 clearance in the absence of expression of a virus-encoded suppressor.

273 uses host enzymes, with the exception of the virus-encoded T-antigen (T-ag), to replicate its genome.

274 of how early protein interactions involving virus-encoded tegument proteins are critical for virus a

275 Suppression of viral replication by virus-encoded temperance factors represents a novel mech

276 The genome of this virus encoded the replicative enzymes and the cis-acting

277 acute infection, even after stimulation with virus-encoded TLR7/8 ligand.

278 The virus-encoded transactivating HTLV-I tax gene was demons

279 tes by Epstein-Barr virus (EBV) requires the virus-encoded transactivator EBNA2 and the products of b

280 V gene 62, is the major immediate-early (IE) virus-encoded transactivator of viral gene transcription

281 (HTLV-1) gene expression is mediated by the virus-encoded transactivator protein Tax and three imper

282 responsible for localization of at least one virus-encoded transcript, IRS1 mRNA.

283 coding changes in the core components of the virus-encoded transcription and replication apparatus.

284 This sequence element is bound by a virus-encoded transcription and replication factor E2, w

285 EBNA2 is an Epstein-Barr virus-encoded transcriptional transactivator that mimics

286 irus-transposon vector that stably maintains virus-encoded transgenes in vivo through integration int

287 othelial cell infectivity was dependent on a virus-encoded tropism factor.

288 sform vertebrate cells through the action of virus-encoded tumor antigens that interfere with normal

289 Thus, EBNA3B is a virus-encoded tumor suppressor whose inactivation promot

290 SV40) large tumor antigen (Tag) represents a virus-encoded tumor-specific antigen expressed in many t

291 This is the first structure of a virus-encoded tumour necrosis factor receptor (TNFR).

292 erization of an inhibitor active against the virus-encoded type-1 topoisomerase, an enzyme likely to

293 ntrol of PABP1, Paip2, and EDD1 required the virus-encoded UL38 mTORC1 activator and resulted in augm

294 observations together with the presence of a virus-encoded uracil DNA glycosylase indicates that HSV-

295 -early kinetics, and requires the functional virus-encoded Us3 Ser/Thr protein kinase.

296 annel-forming protein, placing it within the virus-encoded "viroporin" family.

297 ne responses likely drove the evolution of a virus-encoded virulence factor that regulates complement

298 n of translation initiation factors with the virus-encoded VPg protein covalently linked to the 5' en

299 ate transcription factor (VITF)-1 and -3 are virus-encoded, whereas VITF-2 was partially purified fro

300 Hepatitis B virus-encoded X antigen contributes to the development o