ライフサイエンスコーパス: replication factor

1 xic stress by inhibition of an essential DNA replication factor.

2 onfunctional and fails to interact with Cut5 replication factor.

3 a regulatory process targeting this key DNA replication factor.

4 y directly targeting expression of the Cdc45 replication factor.

5 k whether it also functions as a specialized replication factor.

6 hat converts the inhibitor into a beneficial replication factor.

7 e in levels and chromatin association of DNA replication factors.

8 bably involved in its interaction with other replication factors.

9 of BPDE on the chromatin association of DNA replication factors.

10 of the cytoskeleton, and, unexpectedly, DNA replication factors.

11 the promoters of other coordinately induced replication factors.

12 alphavirus-like superfamily, encodes two RNA replication factors.

13 poly(A) signal influence expression of viral replication factors.

14 ntrol by regulating the transcription of DNA replication factors.

15 vely repressing mitotic, DNA repair, and DNA replication factors.

16 NUCLEAR ANTIGEN, which encode essential DNA replication factors.

17 r foci that contain HPV genomes and cellular replication factors.

18 c], cyclin D1/3, chromatin licensing and DNA replication factor 1 [Cdt1]), concomitant with increased

19 ases A and B and chromatin licensing and DNA replication factor 1 may explain the reduction in cellul

20 lization of gammaH2AX foci with the telomere replication factor 1 protein in untreated melanoma cells

21 anslation or translation of BMV RNA1-encoded replication factor 1a, and was independent of p20, a cel

22 evels and interactions of brome mosaic virus replication factors 1a and 2a polymerase (2apol) shifted

23 embrane-associated compartments, require BMV replication factors 1a and 2a, and use negative-strand R

24 BMV encodes RNA replication factors 1a, with domains implicated in RNA c

25 Brome mosaic virus (BMV) encodes two RNA replication factors: 1a has a C-terminal NTPase/helicase

26 aromyces cerevisiae) protein subunits of DNA REPLICATION FACTOR A (RFA) were produced.

27 on the heterotrimeric ssDNA-binding molecule replication factor A (RPA).

28 binding protein-Interacting Factor 1 [RIF1], Replication Factor A 3 [RFA3], Cell Division Cycle 13 [C

29 dition of Rta to Z(S186A) and the mixture of replication factors activated viral replication and late

30 serves the activity of several essential DNA replication factors, active processes may contribute to

31 bserved decline in the expression of ten DNA replication factors after the midblastula transition (MB

32 The geminivirus replication factor AL1 interacts with the plant retinobl

33 Earlier studies showed that the viral replication factor, AL1, is sufficient for host inductio

34 n is synthetic lethal with inhibition of DNA replication factors, allowing additional models to be se

35 e findings, we propose that mutations in DNA replication factors alter acetylation of H3 K56.

36 cetylated proteins to include a critical DNA replication factor and provide an additional level of co

37 pathways for induction of this essential DNA replication factor and suggest a mechanism for oncogenic

38 ochondrial DNA (mtDNA) biosynthesis requires replication factors and adequate nucleotide pools from t

39 tool that may facilitate the study of other replication factors and aid in the discovery of novel in

40 We also show that both cellular DNA replication factors and DNA repair DNA polymerases coloc

41 ion by screening an RNAi library against DNA replication factors and identified multiple shRNAs again

42 Notably, key DNA replication factors and major DNA repair DNA polymerases

43 t BIR involves cross-talk between normal DNA replication factors and PRR.

44 heckpoint Rad complexes and the PCNA and RFC replication factors and thus provide further support for

45 ions between the viral genome, virus-encoded replication factors, and host factors.

46 patients with mutations in mitochondrial DNA replication factors, and show that these have distinct d

47 stically to Ty3 cDNA synthesis but that host replication factors antagonize Ty3 replication.

48 omic RNA1 (gB1) and RNA2 (gB2), encoding the replication factors, are packaged into two separate viri

49 rotein 7 (MCM7), an E2F-induced cellular DNA replication factor, as a novel biomarker for cervical ca

50 ry subunits, mitochondrial transcription and replication factors, as well as certain heme biosyntheti

51 after pre-RC formation to promote loading of replication factors at origins, a previously unrecognize

52 d origin usage by evaluating the kinetics of replication factor binding in fission yeast and show tha

53 the EBV lytic cycle, is a transcription and replication factor, binding to Zta response elements (ZR

54 nscriptional regulator and mitochondrial DNA replication factor, both in P493-6 lymphocytes with high

55 CDKs are thought to activate one or more replication factors, but the identities of these protein

56 infection induces the accumulation of a host replication factor by activating transcription of its ge

57 The human DNA damage sensors, Rad17-replication factor C (Rad17-RFC) and the Rad9-Rad1-Hus1

58 The five subunit replication factor C (RF-C) complex plays a critical rol

59 Replication factor C (RF-C) complex plays an important r

60 Eukaryotic replication factor C (RF-C) is a heteropentameric comple

61 ating cell nuclear antigen (PCNA) loading by replication factor C (RFC) acts as the initial sensor of

62 oliferating cell nuclear antigen (PCNA), and replication factor C (RFC) and a reconstituted Mlh1-Pms1

63 , proliferating cell nuclear antigen (PCNA), replication factor C (RFC) and DNA polymerase delta.

64 plication clamp PCNA is loaded around DNA by replication factor C (RFC) and functions in DNA replicat

65 Fractions that contained replication factor C (RFC) and proliferating cell nuclea

66 en (PCNA), and show that PCNA, together with replication factor C (RFC) and replication protein A (RP

67 The human clamp loader replication factor C (RFC) and sliding clamp proliferati

68 Replication factor C (RFC) and the proliferating cell nu

69 Replication factor C (RFC) catalyzes assembly of circula

70 The eukaryotic equivalents are the replication factor C (RFC) clamp loader and the prolifer

71 The eukaryotic replication factor C (RFC) clamp loader is an AAA+ spira

72 We find that the replication factor C (RFC) clamp loader specifically inh

73 , and D subunits of Saccharomyces cerevisiae replication factor C (RFC) clamp loader, respectively, a

74 PCNA sliding clamps are loaded onto DNA by a replication factor C (RFC) clamp loader.

75 ell nuclear antigen (PCNA) sliding clamp and replication factor C (RFC) clamp-loading complex, using

76 ELG1 protein, which comprises an alternative replication factor C (RFC) complex and plays an importan

77 The multi-subunit replication factor C (RFC) complex loads circular prolif

78 visiae, this process involves an alternative replication factor C (RFC) complex that contains the fou

79 s, sliding clamps are loaded onto DNA by the replication factor C (RFC) complex, which consists of fi

80 igated the communication between subunits in replication factor C (RFC) from Archaeoglobus fulgidus.

81 e Methanosarcina acetivorans clamp loader or replication factor C (RFC) homolog.

82 s that are loaded onto DNA by clamp loaders [replication factor C (RFC) in eukaryotes].

83 Replication factor C (RFC) is a five-subunit complex tha

84 Replication factor C (RFC) is a heteropentameric AAA+ pr

85 ing cell nuclear antigen loading onto DNA by replication factor C (RFC) is a key step in eukaryotic D

86 Replication factor C (RFC) is an AAA+ heteropentamer tha

87 netic experiments reveal that ATP binding to replication factor C (RFC) is sufficient for loading the

88 Rad17 homologs have extensive homology with replication factor C (RFC) subunits (p36, p37, p38, p40,

89 tin by a complex of Rad17 and the four small replication factor C (RFC) subunits (Rad17-RFC) in respo

90 Pase, is the bacterial homolog of eukaryotic replication factor C (RFC) that loads the sliding clamp

91 24 interacts with the four small subunits of replication factor C (RFC) to form the RFC-Rad24 complex

92 ometry to contain Rfc2 and Rfc3, subunits of replication factor C (RFC), a five subunit protein that

93 Replication factor C (RFC), a heteropentamer of RFC1-5,

94 In addition, DNA replication factor C (RFC), a protein complex that facil

95 and DNA binding by Saccharomyces cerevisiae replication factor C (RFC), and present the first kineti

96 l nuclear antigen (PCNA) and show that PCNA, replication factor C (RFC), and replication protein A (R

97 y the Saccharomyces cerevisiae clamp loader, replication factor C (RFC), and the DNA damage checkpoin

98 When loaded onto primed DNA templates by replication factor C (RFC), PCNA acts to tether the poly

99 tionation of these crude extracts identified replication factor C (RFC), proliferating cell nuclear a

100 several DNA replication proteins, including replication factor C (RFC), proliferating cell nuclear a

101 on, hLigI interacts with and is inhibited by replication factor C (RFC), the clamp loader complex tha

102 is study, we describe an association between replication factor C (RFC), the clamp loader, and DNA li

103 l nuclear antigen, a DNA sliding clamp, and, replication factor C (RFC), the clamp loader.

104 dogenous and transfected Brd4 interacts with replication factor C (RFC), the conserved five-subunit c

105 utation in RFC4, encoding a small subunit of replication factor C (RFC), was found to display allele-

106 Unlike replication factor C (RFC), which uses the 3' primer/tem

107 proliferating cell nuclear antigen (PCNA) in replication factor C (RFC)-catalyzed loading of the clam

108 e-molecule analysis, we demonstrate that the replication factor C (RFC)-CTF18 clamp loader (RFC(CTF18

109 hat Ctf18, Ctf8, and Dcc1, the subunits of a Replication Factor C (RFC)-like complex, are essential f

110 loaded onto the primer-template junction by replication factor C (RFC).

111 nctions by a clamp loader molecular machine, replication factor C (RFC).

112 tf18, a homologue of the p140 subunit of the replication factor C (RFC).

113 interact with their associated clamp loader, replication factor C (RFC).

114 r antigen (PCNA), and hRad17 has homology to replication factor C (RFC).

115 with proliferating cell nuclear antigen and replication factor C (RFC).

116 DNA requires the activity of a clamp-loader [replication factor C (RFC)] complex and the energy deriv

117 a nucleotide-bound eukaryotic clamp loader [replication factor C (RFC)] revealed a different and mor

118 Replication factor C (RFC, also called activator 1), in

119 ating cell nuclear antigen (PCNA, clamp) and replication factor C (RFC, clamp loader), we have examin

120 The DNA damage clamp loader replication factor C (RFC-Rad24) consists of the Rad24 p

121 ding proteins have been reported previously: replication factor C (the PCNA clamp loader), family B D

122 Our results demonstrate that S. cerevisiae Replication Factor C (yRFC) can load yPCNA onto 5'-ssDNA

123 CTF7/ECO1, POL30 (PCNA), and CHL12/CTF18 (a replication factor C [RFC] homolog) genetically interact

124 pha, proliferating cell nuclear antigen, and replication factor C activate MutLalpha endonuclease to

125 The identification of both replication factor C and DNA helicases as critical for s

126 h three- and four-subunit complexes required replication factor C and proliferating cell nuclear anti

127 rms a replication complex in the presence of replication factor C and proliferating cell nuclear anti

128 PCNA, together with replication factor C and replication protein A, stimulat

129 n A, proliferating cell nuclear antigen, and replication factor C and was active in the SV40 DNA repl

130 Three distinct forms of replication factor C are known to play vital roles in ge

131 repair protein (248kDa) and the five-subunit replication factor C clamp loader (250 kDa).

132 and essential DNA polymerase, and a modified Replication Factor C clamp--loader complex.

133 esis, and the localization and activation of replication factor C complex (RFC) subunits.

134 tion in the large subunit of the replicative replication factor C complex (rfc1-1) increased the expa

135 ase delta/proliferating cell nuclear antigen/replication factor C complex on telomeric templates that

136 pendent phosphorylation; associates with the replication factor C complex, a critical component of th

137 ion: proliferating cell nuclear antigen, the replication factor C complex, DNA polymerase delta, flap

138 rotein family, which include subunits of the Replication factor C complex.

139 rase epsilon, replication protein A, and two replication factor C complexes on chromatin.

140 ng cell nuclear antigen and the clamp loader replication factor C facilitated DNA synthesis with Dpo3

141 ticipation that the discovery of this unique replication factor C homolog will lead to critical insig

142 a its non-conserved C-terminal domain (CTD); replication factor C interaction results in approximatel

143 Replication factor C is required to load proliferating c

144 Eukaryotic replication factor C is the heteropentameric complex tha

145 s two similar small subunits (M. acetivorans replication factor C small subunit (MacRFCS)) and one la

146 lelic intronic AAGGG repeat expansion in the replication factor C subunit 1 (RFC1) gene as the cause

147 mplex, leading to ineffective recruitment of replication factor C to initiate DNA replication.

148 The ATPase activity of replication factor C was characterized and found to be s

149 Complexes of replication factor C with a N-terminal truncation (Delta

150 gammaS), a nonhydrolyzable analog of ATP, to replication factor C with a N-terminal truncation (Delta

151 ohesion establishment factor, the Ctf18-RFC (replication factor C) complex.

152 ation factors, and the clamp loader complex (replication factor C) remained tethered to chromatin.

153 quirements for DNA polymerase alpha-primase, replication factor C, and PCNA.

154 ntenance (MCM) 3' --> 5' DNA helicase, PolB, replication factor C, and proliferating cell nuclear ant

155 sence of proliferating cell nuclear antigen, replication factor C, and single-stranded binding protei

156 ly loaded around effector DNA by its loader, replication factor C, are ubiquitinated.

157 These functions include loading onto DNA by replication factor C, as well as Okazaki fragment synthe

158 PCNA is loaded onto DNA by replication factor C, but it has been unknown how PCNA i

159 liferating cell nuclear antigen clamp loader replication factor C, DNA polymerase delta, and DNA liga

160 conformations matching the helical pitch of Replication Factor C, it is not biased toward a right-ha

161 ix purified human proteins: AP endonuclease, replication factor C, PCNA, flap endonuclease 1 (FEN1),

162 system comprised of MutS alpha, MutL alpha, replication factor C, proliferating cell nuclear antigen

163 S. pombe Uve1p, Rad2p, DNA polymerase delta, replication factor C, proliferating cell nuclear antigen

164 ating cell nuclear antigen (PCNA) loading by replication factor C, providing a potential mechanism fo

165 loader gamma complex (homolog of eukaryotic Replication Factor C, RFC).

166 loaded onto the template-primer junction by replication factor C, the C-terminal domain of PCNA medi

167 this process through a pathway that includes replication factor C, the chromatin assembly factor Asf1

168 a circular substrate without the addition of replication factor C, which is the protein responsible f

169 nterfaces by the ATP-dependent clamp loader, Replication Factor C, whose clamp-interacting sites form

170 loaded onto DNA by a dedicated complex, the replication factor C, whose mechanism has been studied i

171 d circular DNA do in fact support MutSbeta-, replication factor C-, and PCNA-dependent activation of

172 log 6, Exonuclease 1, replication protein A, replication factor C-Delta1N, proliferating cell nuclear

173 Here we show that the Elg1 replication factor C-like complex (Elg1-RLC) functions i

174 factor is loaded onto DNA by the Rad24-RFC (replication factor C-like complex with Rad24) clamp load

175 es now present data strongly implicating the replication factor C-like complex, Elg1/ATAD5-RLC, in th

176 lity of PCNA to be loaded onto primed DNA by replication factor C.

177 egions of homology with the five subunits of Replication factor C.

178 yeast CHL12 and has similarity to mammalian replication factor C.

179 teracts with multiple subunits of Drosophila replication factor C.

180 provides a binding site for the clamp-loader Replication Factor C.

181 th the 9-1-1 heterotrimer reminiscent of the replication factor C/proliferating cell nuclear antigen

182 ucturally homologous proteins, including the replication factor-C small subunit (RFCS).

183 re of the five-protein clamp loader complex (replication factor-C, RFC) of the yeast Saccharomyces ce

184 Replication-Factor-C (RFC) and RFC-like complexes (RLCs)

185 on factors: replication protein A70 (RPA70), replication factor C1 (RFC1), and DNA polymerase delta.

186 xpansion [(AAGGG)(exp)] in the gene encoding Replication Factor C1 (RFC1).

187 BRCA1/2), Poly-ADP ribose polymerase (PARP), replication factor c2-5 (Rfc2-5), ataxia telangiectasia

188 The top hits based on the combined data-replication factor C3 (RFC3), FAM111A, and interferon re

189 origin firing and concurrent binding of the replication factor Cdc45p to origins.

190 Exogenous expression of replication factors Cdc6 or Cdt1 in RB-proficient cells

191 hat has previously been shown to degrade the replication factor Cdt1 during S phase.

192 Here we show that stabilization of the DNA replication factor Cdt1, a substrate of cullins 1 and 4,

193 -G2-M phases produces high levels of the DNA replication factor Cdt1, and this leads to efficient Mcm

194 DNA replication by inhibiting the essential replication factor Cdt1.

195 The replication factors Cdt1 and Cdc6 are essential for orig

196 of S phase entry in cells overproducing the replication factor, Cdt1.

197 nt form of the nuclear matrix-associated DNA replication factor Ciz1 is present in 34/35 lung tumors

198 Further, lethal insertions in replication factor complex 4 (rfc4) and GTPase-activatin

199 biallelic intronic AAGGG repeat expansion in replication factor complex subunit 1 (RFC1) as the cause

200 ors, proliferating cell nuclear antigen, and replication factor complex, was disrupted by DeltaNLA.

201 97-dependent turnover and disassembly of DNA replication factor complexes.

202 We show that four DNA replication factors--Cut5, RecQ4, Treslin, and Drf1--are

203 ver one such metazoa-specific process: a new replication factor, cyclin-dependent kinase 8/19-cyclinC

204 While several transcription/replication factors directly regulate mitochondrial gene

205 of interactions between the Escherichia coli replication factor DnaC protein and the DnaB helicase ha

206 e report that MAT switching requires the DNA replication factor Dpb11, although it does not require t

207 dDP eliminates G(1)-S transcription of known replication factors during embryogenesis and compromises

208 nding model to decipher the roles of various replication factors during metazoan DNA replication.

209 n by interacting with and recruiting the HPV replication factor E1 to the viral origin.

210 The viral replication factors E1 and E2 of papillomaviruses are ne

211 butable to their efficient expression of the replication factors E1 and E2.

212 s bound by a virus-encoded transcription and replication factor E2, which binds to a 12 bp recognitio

213 probably due to a stabilization of the viral replication factor E2.

214 papillomavirus 16 (HPV16) transcription and replication factor E2.

215 Using purified replication factors encoded by herpes simplex virus type

216 ed by competition among origins for limiting replication factors establishes the timing and efficienc

217 These findings make CDC45 the only putative replication factor experimentally proven to be essential

218 been well established, its effects on viral replication factor expression and plasmid replication of

219 re we investigate the role of one of the DNA replication factors, flap endonuclease I (FEN1), in regu

220 DNA replication and to recruit cellular DNA replication factors for viral DNA replication.

221 The E2 proteins are transcription/replication factors from papillomaviruses.

222 Rbf1-dependent repression of E2f1-regulated replication factor genes, which are expressed continuous

223 Saccharomyces cerevisiae, but not other DNA replication factors, greatly reduced PFA at replication

224 RECQ4 is a DNA replication factor important for mtDNA maintenance, and

225 e through S phase and implicated several DNA replication factors in silencing, later works showed tha

226 ion defect is due to dosage insufficiency of replication factors in the nucleus, which stems from two

227 te in vitro plasmid DNA replication, whereas replication factors in the polymerase fractions are stri

228 Vpr indirectly binds MCM10, a eukaryotic DNA replication factor, in a Vpr-binding protein (VprBP) (Vp

229 o a regulator of viral gene expression and a replication factor, in association with the viral E1 pro

230 ve restart was inhibited along with numerous replication factors, including MCM6 and RPA, the latter

231 mutations and the genes encoding several DNA replication factors, including POL1, CTF4, DNA2, and CHL

232 How core replication factors integrate into this phosphorylation

233 The coordinated activity of DNA replication factors is a highly dynamic process that inv

234 identity and order of assembly of eukaryotic replication factors is highly conserved across all speci

235 This motif, named RRF (for repression of replication factors), is conserved in the promoters of o

236 tes polymerase translation relative to other replication factors, just as many single-component RNA v

237 irects cell-specific expression of the viral replication factor large T antigen, and thus transcripti

238 The baculovirus replication factors LEF-1 and LEF-2 of the Autographa ca

239 for optimal replication, encode a conserved replication factor, LEF-7, that manipulates the DDR via

240 on centers where viral proteins and cellular replication factors localize.

241 DNA replication initiation with 16 purified replication factors, made from 42 polypeptides.

242 Another replication factor, Mcm10, mediates the interaction betw

243 that the G1 phase-specific expression of the replication factor Mcm2 is a useful marker for detecting

244 We have applied this method to the DNA replication factor mcm4/cdc21, and find that chromatin a

245 s revealed significantly lower levels of the replication factors Mcm4, Mcm7, and Cdc45 at replication

246 icing factors Rbmx, Sfrs5 and Sfrs7, the DNA replication factors Mcm5 and Brd4, phosphoinositide-3-ki

247 sion, and prevented chromatin recruitment of replication factor Mcm7, demonstrating that JADE1 is req

248 nt cells also retain high levels of tethered replication factors, MCM7 and PCNA, indicating that DNA

249 tions of the DnaB-primase complex with other replication factors might be critical for determining th

250 MDI-Larp's targets include mtDNA replication factors, mitochondrial ribosomal proteins, a

251 proteins, transcription regulation proteins, replication factors, modifying enzymes, and a number of

252 racts with DNA as both a transcription and a replication factor, modulates both intracellular signal

253 lisome) by yet unidentified host factors [Mu replication factors (MRF alpha 2)], which displace the t

254 ation regulates the interaction with another replication factor, MUS-101.

255 The results showed that the replication factors of PCV1 and PCV2 are fully exchangea

256 in determining the function of the different replication factors once they have been assembled at the

257 ested that the direct interaction of RB with replication factors or sites of DNA synthesis may contri

258 is for negative-strand RNA3 templates, viral replication factors, or common host components.

259 Our data indicate that Cdc2 phosphorylates replication factor Orp2, a subunit of the origin recogni

260 In eukaryotes, the DNA replication factor PCNA is loaded onto primer-template j

261 eckpoint components with limited homology to replication factors PCNA and RF-C, respectively, suggest

262 l, Dzantiev et al. present evidence that the replication factors PCNA and RFC modulate the directiona

263 In human cells, the DNA replication factor proliferating cell nuclear antigen (P

264 Here, we find that the replication factors proliferating cell nuclear antigen (

265 ding potential by supplying the RNA1-encoded replication factor protein A in trans.

266 n S phase and replicates via accumulation of replication factors, rather than recruitment of DNA to p

267 h HPV16 E1, E2, and a number of the cellular replication factors: replication protein A70 (RPA70), re

268 been shown to be structurally similar to the replication factors, RFC clamp loader and proliferating

269 re11/NBS1 complex and Rad51/Rad52 along with replication factors (RPA) and telomere binding proteins

270 NA replication through modulation of crucial replication factor(s) (trans-acting mechanism).

271 xRTS, which bears homology to the yeast replication factors Sld2/DRC1, is essential for DNA repl

272 es a subset of Cdk1 substrates including the replication factors, Sld2 and Dpb2.

273 The loading of essential DNA replication factors such as Cdc45 and proliferating cell

274 ays a direct role in recruiting cellular DNA replication factors, such as replication protein A or po

275 Mcm10 is a DNA replication factor that interacts with multiple subunits

276 Moreover, the viral E2 transcription and replication factor that is expressed at high levels in d

277 the yeast Sld3 protein, is an essential DNA replication factor that is regulated by cyclin-dependent

278 Mcm10 is an essential replication factor that is required for DNA replication

279 Mcm10 is a conserved eukaryotic DNA replication factor that is required for S phase progress

280 drug targets because they are essential DNA replication factors that are highly expressed in cancer

281 some maintenance) proteins are essential DNA replication factors that each contain a putative ATP bin

282 ycle progression, here we identify three DNA replication factors that interact with each other and th

283 herichia coli DnaB helicase complex with the replication factor, the DnaC protein, have been examined

284 RB, we observed the attenuation of multiple replication factors, the complete cessation of DNA synth

285 rongly attenuated the RNA levels of multiple replication factors, their protein expression was not di

286 cation machinery and contribute few, if any, replication factors themselves.

287 cm10) is an essential eukaryotic DNA-binding replication factor thought to serve as a scaffold to coo

288 CDK phosphorylation of the replication factor TICRR (TopBP1-interacting checkpoint

289 d (Dup), the Drosophila homologue of Cdt1, a replication factor to which geminin binds.

290 of dsRNA from host defenses and concentrate replication factors to enhance RNA production.

291 cts in part to facilitate the recruitment of replication factors to oriLyt.

292 wn to recruit many of the necessary cellular replication factors to the viral origin of replication.

293 show that the binding of cellular and viral replication factors to viral RNA is conserved despite ge

294 In particular, expression of the viral DNA replication factor UL84 is affected by the deletion of I

295 alization of the human cytomegalovirus viral replication factor UL84 relative to other proteins invol

296 us DNA polymerase subunit UL44 and the viral replication factor UL84.

297 y, several proteins, including the viral DNA replication factors UL84 and UL57, were identified by ma

298 IE2 40 affect the expression of a viral DNA replication factor, UL84.

299 stein-Barr virus (EBV) encodes a set of core replication factors used during lytic infection in human

300 Mcm10 is a conserved eukaryotic DNA replication factor whose function has remained elusive.