ライフサイエンスコーパス: herpes simplex virus type 1

1 glia) infected with a common viral pathogen (herpes simplex virus type 1).

2 RNA viruses and some DNA viruses, including herpes simplex virus type 1.

3 chnique for mapping O-glycosylation sites on herpes simplex virus type 1.

4 globulin G antibodies to cytomegalovirus and herpes simplex virus type 1.

5 required for the cytoplasmic envelopment of herpes simplex virus type 1.

6 have reduced susceptibility to infection by herpes simplex virus type 1.

7 mmunogenic situations such as infection with herpes simplex virus type 1.

8 Ligands of MARCO dramatically inhibit herpes simplex virus type 1 adsorption and infection of

9 In this work, we modified the herpes simplex virus type 1 amplicon system for efficien

10 sing purified replication factors encoded by herpes simplex virus type 1 and a 70-base minicircle tem

11 Herpes simplex virus type 1 and Alzheimer's disease: pos

12 ling nucleic acid recognition, is usurped by herpes simplex virus type 1 and functions together with

13 ith the corresponding sequences of UL36 from herpes simplex virus type 1 and M48 from murine cytomega

14 o exhibited increased susceptibility to both herpes simplex virus type 1 and murine gammaherpesvirus

15 virus (PRV), an alphaherpesvirus related to herpes simplex virus type 1 and varicella-zoster virus,

16 ediate-early genes of the alphaherpesviruses herpes simplex virus type 1 and varicella-zoster virus.

17 on renders Ksrp(-)(/)(-) cells refractory to herpes simplex virus type 1 and vesicular stomatitis vir

18 vities and underwent serological testing for herpes simplex virus types 1 and 2 (HSV-1 and -2) and co

19 Herpes simplex virus types 1 and 2 (HSV-1 and -2) are si

20 Herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) are

21 Herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) are

22 e = 11.1 weeks) to Epstein Barr virus (EBV), herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), an

23 Trichomonas vaginalis and viral pathogens (herpes simplex virus types 1 and 2 and adenovirus) can c

24 Herpes Simplex Virus types 1 and 2 and Varicella-zoster

25 Plus method for the qualitative detection of herpes simplex virus types 1 and 2 in cerebrospinal flui

26 Seroprevalence of EBV, CMV, herpes simplex virus types 1 and 2, and human herpesviru

27 ein Barr virus (EBV), cytomegalovirus (CMV), herpes simplex virus types 1 and 2, human herpesvirus 8)

28 licate in alpha1,3GT-positive cells, whereas herpes simplex viruses type 1 and type 2 (HSV-1 and HSV-

29 CMV, herpes simplex virus type 1, and human herpesvirus 6 inf

30 on between education and cytomegalovirus and herpes simplex virus type 1 antibody levels remained str

31 Using herpes simplex virus type-1 as a tool to enhance cell-ce

32 These findings demonstrate that herpes simplex virus type 1 binds to MARCO to enhance it

33 otein interactions drive the assembly of the herpes simplex virus type 1 capsid.

34 in UL25 attaches to the external vertices of herpes simplex virus type 1 capsids and is required for

35 o enhance the image contrast of ice-embedded herpes simplex virus type 1 capsids.

36 Talimogene laherparepvec (T-VEC) is a herpes simplex virus type 1-derived oncolytic immunother

37 l structure of a herpesvirus polymerase, the Herpes Simplex Virus type 1 DNA polymerase, at 2.7 A res

38 to activated arrays in cells expressing the herpes simplex virus type 1 E3 ubiquitin ligase, ICP0, w

39 athway are associated with susceptibility to herpes simplex virus type 1 encephalitis (HSE).

40 In contrast to herpes simplex virus type 1-encoded ICP0, bICP0 reduces

41 The Herpes Simplex Virus type-1-encoded E3 ubiquitin ligase,

42 The UL11 gene of herpes simplex virus type 1 encodes a 96-amino-acid tegu

43 Herpes simplex virus type 1 encodes a multifunctional pr

44 gene that has been used previously to study herpes simplex virus type 1 entry.

45 U(L)31 and U(L)34 of herpes simplex virus type 1 form a complex necessary for

46 med at engineering the prefusion form of the herpes simplex virus type 1 gB ectodomain, including mod

47 Herpes simplex virus type 1 glycoprotein C closely co-lo

48 Herpes simplex virus type 1 glycoprotein K (gK) and the

49 We found wide distribution of O-glycans on herpes simplex virus type 1 glycoproteins and demonstrat

50 VZV ORFs transcribed during latency to their herpes simplex virus type 1 homologues reveals that the

51 the critical gamma(1)34.5 virulence genes of herpes simplex virus type 1 (HSV) under translation cont

52 the central 970 residues of this protein for herpes simplex virus type 1 (HSV-1 UL36, 3164 residues).

53 Herpes simplex virus type 1 (HSV-1) acquires its final e

54 The herpes simplex virus type 1 (HSV-1) alkaline nuclease, e

55 transport is essential for the transport of herpes simplex virus type 1 (HSV-1) along axons, yet lit

56 Hybrid replisomes derived from herpes simplex virus type 1 (HSV-1) and equine herpesvir

57 Herpes simplex virus type 1 (HSV-1) and HSV-2 cause very

58 Infection with herpes simplex virus type 1 (HSV-1) and HSV-2 is initiat

59 region of alphaherpesviruses, termed US3 in herpes simplex virus type 1 (HSV-1) and pseudorabies vir

60 n (VP1/2cbd) into assemblons is conserved in herpes simplex virus type 1 (HSV-1) and that this recrui

61 by exploiting the high transgene capacity of herpes simplex virus type 1 (HSV-1) and the episomal ret

62 bution of the neurotropic alphaherpesviruses-herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) a

63 Glycoprotein C (gC) of herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) b

64 the availability of antiviral chemotherapy, herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) i

65 Herpes simplex virus type 1 (HSV-1) and type 2 are commo

66 e-early (IE) genes of the alphaherpesviruses herpes simplex virus type 1 (HSV-1) and varicella-zoster

67 haherpesvirus related to the human pathogens herpes simplex virus type 1 (HSV-1) and varicella-zoster

68 Both cell lines supported the replication of herpes simplex virus type 1 (HSV-1) and vesicular stomat

69 etter define the roles of gE, gI, and Us9 in herpes simplex virus type 1 (HSV-1) anterograde spread u

70 We examine whether APOE determines CMV and herpes simplex virus type 1 (HSV-1) antibody levels and

71 e same subjects, there was no association of herpes simplex virus type 1 (HSV-1) antibody levels with

72 In this report we use lytic infection by herpes simplex virus type 1 (HSV-1) as a model to examin

73 Here we show that herpes simplex virus type 1 (HSV-1) capsids interact wit

74 lectron microscopy (cryo-EM) and compared to herpes simplex virus type 1 (HSV-1) capsids.

75 y in infection of primary human fibroblasts, herpes simplex virus type 1 (HSV-1) disrupts the centros

76 age and packaging of replicated concatemeric herpes simplex virus type 1 (HSV-1) DNA corresponds to a

77 o determine the presence and copy numbers of herpes simplex virus type 1 (HSV-1) DNA in human trigemi

78 though the seven viral proteins required for herpes simplex virus type 1 (HSV-1) DNA replication have

79 Herpes simplex virus type 1 (HSV-1) DNA replication occu

80 estigate possible immune mechanisms in fatal herpes simplex virus type 1 (HSV-1) encephalitis (HSE) a

81 Herpes simplex virus type 1 (HSV-1) encodes a heterotrim

82 Herpes simplex virus type 1 (HSV-1) enters cells by fusi

83 Herpes simplex virus type 1 (HSV-1) envelope proteins ar

84 tations in the thymidine kinase gene (tk) of herpes simplex virus type 1 (HSV-1) explain most cases o

85 at, unlike host FcgammaRs but similar to the herpes simplex virus type 1 (HSV-1) Fc receptor gE-gI, g

86 Reactivation of herpes simplex virus type 1 (HSV-1) from neuronal latenc

87 Egress of herpes simplex virus type 1 (HSV-1) from the nucleus of

88 lutamic acid, or the analogous residues from herpes simplex virus type 1 (HSV-1) gB (HR and RVEA).

89 The crystal structure of the herpes simplex virus type 1 (HSV-1) gB ectodomain, gB730

90 res of the ectodomains of two FL1 mutants of herpes simplex virus type 1 (HSV-1) gB to clarify whethe

91 entry of the viral genome into the nucleus, herpes simplex virus type 1 (HSV-1) gene expression is r

92 designed to target mRNA of several essential herpes simplex virus type 1 (HSV-1) genes.

93 the chromatin structures associated with the herpes simplex virus type 1 (HSV-1) genome during latenc

94 The herpes simplex virus type 1 (HSV-1) genome is maintained

95 e latency-associated transcript (LAT) of the herpes simplex virus type 1 (HSV-1) genome is transcribe

96 Although the herpes simplex virus type 1 (HSV-1) genome might be expe

97 Herpes simplex virus type 1 (HSV-1) genomes become assoc

98 Herpes simplex virus type 1 (HSV-1) glycoprotein B (gB)

99 PILRalpha is a newly identified herpes simplex virus type 1 (HSV-1) glycoprotein B (gB)

100 Herpes simplex virus type 1 (HSV-1) glycoprotein C (gC)

101 The herpes simplex virus type 1 (HSV-1) glycoprotein gC-1, p

102 have shown previously that immunization with herpes simplex virus type 1 (HSV-1) glycoprotein K (gK)

103 Herpes simplex virus type 1 (HSV-1) glycoprotein K (gK)

104 Studies with herpes simplex virus type 1 (HSV-1) have shown that seco

105 have been shown to complement the growth of herpes simplex virus type 1 (HSV-1) ICP0 mutants.

106 ed to result in partial complementation of a herpes simplex virus type 1 (HSV-1) ICP0 null (ICP0(-))

107 We previously showed that herpes simplex virus type 1 (HSV-1) immediate-early (IE)

108 Early in infection, herpes simplex virus type 1 (HSV-1) immediate-early (IE)

109 Previous studies have shown that the herpes simplex virus type 1 (HSV-1) immediate-early prot

110 Herpes simplex virus type 1 (HSV-1) immediate-early regu

111 Infectious titers of EBOV or herpes simplex virus type 1 (HSV-1) in detergents-treate

112 t this has not been observed previously with herpes simplex virus type 1 (HSV-1) in vitro.

113 igeminal ganglia (TG) latently infected with herpes simplex virus type 1 (HSV-1) indicate the presenc

114 That herpes simplex virus type 1 (HSV-1) induces apoptosis bu

115 Lytic infection with herpes simplex virus type 1 (HSV-1) induces profound mod

116 During productive infection, herpes simplex virus type 1 (HSV-1) induces the formatio

117 innate responses are involved in controlling herpes simplex virus type 1 (HSV-1) infection and that t

118 n important role in the optimal clearance of herpes simplex virus type 1 (HSV-1) infection in mice.

119 sor protein CoREST is involved in repressing herpes simplex virus type 1 (HSV-1) infection in the abs

120 ect of glycoprotein K (gK) overexpression on herpes simplex virus type 1 (HSV-1) infection in two dif

121 Herpes simplex virus type 1 (HSV-1) infection induces an

122 Efficient herpes simplex virus type 1 (HSV-1) infection of human f

123 We show that PRV and herpes simplex virus type 1 (HSV-1) infection of rodent

124 Herpes simplex virus type 1 (HSV-1) infection of the cor

125 We previously showed that herpes simplex virus type 1 (HSV-1) infection rapidly tr

126 During productive herpes simplex virus type 1 (HSV-1) infection, a subset

127 During herpes simplex virus type 1 (HSV-1) infection, the viral

128 mount of virus reactivation following ocular herpes simplex virus type 1 (HSV-1) infection.

129 e clearance), and no evident role for IDO in herpes simplex virus type 1 (HSV-1) infection.

130 Herpes simplex virus type 1 (HSV-1) infects >70% of the

131 Replication of herpes simplex virus type 1 (HSV-1) involves a step in w

132 Herpes simplex virus type 1 (HSV-1) is a leading cause o

133 Virion protein 16 (VP16) of herpes simplex virus type 1 (HSV-1) is a potent transcri

134 Herpes simplex virus type 1 (HSV-1) is a ubiquitous viru

135 Immediate-early protein ICP0 of herpes simplex virus type 1 (HSV-1) is an E3 ubiquitin l

136 toplasmic domain of glycoprotein B (gB) from herpes simplex virus type 1 (HSV-1) is an important regu

137 Herpes simplex virus type 1 (HSV-1) is commonly associat

138 nine (S/T) kinase encoded by the US3 gene of herpes simplex virus type 1 (HSV-1) is conserved in vari

139 Glycoprotein D (gD) of herpes simplex virus type 1 (HSV-1) is one of four glyco

140 The UL28 protein of herpes simplex virus type 1 (HSV-1) is one of seven vira

141 A hallmark of infection with herpes simplex virus type 1 (HSV-1) is the establishment

142 During herpes simplex virus type 1 (HSV-1) latency in mouse dor

143 The mechanism(s) by which herpes simplex virus type 1 (HSV-1) latency is establish

144 riched in acetyl histone H3 (K9, K14) during herpes simplex virus type 1 (HSV-1) latency, whereas all

145 The herpes simplex virus type 1 (HSV-1) latency-associated t

146 The herpes simplex virus type 1 (HSV-1) latency-associated t

147 To study the regulation of herpes simplex virus type 1 (HSV-1) latency-associated t

148 munoglobulin G antibody responses to CMV and herpes simplex virus type 1 (HSV-1) measured in archived

149 Murine herpes simplex virus type 1 (HSV-1) models have shown th

150 Herpes simplex virus type 1 (HSV-1) mutants impaired in

151 Herpes simplex virus type 1 (HSV-1) mutants lacking the

152 Herpes simplex virus type 1 (HSV-1) mutants that fail to

153 The herpes simplex virus type 1 (HSV-1) neurovirulence gene

154 Herpes simplex virus type 1 (HSV-1) not only causes pain

155 rophylaxis, recommended to prevent recurrent herpes simplex virus type 1 (HSV-1) ocular disorders, ma

156 Following herpes simplex virus type 1 (HSV-1) ocular infection of

157 te both adaptive and innate immunity against herpes simplex virus type 1 (HSV-1) ocular infection.

158 interferon signaling gene were infected with herpes simplex virus type 1 (HSV-1) or an attenuated rec

159 Women with primary or secondary syphilis, herpes simplex virus type 1 (HSV-1) or HSV-2 infection,

160 bits latently infected with either wild-type herpes simplex virus type 1 (HSV-1) or the latency-assoc

161 lly occurs during delivery from mothers with herpes simplex virus type 1 (HSV-1) or type 2 (HSV-2) ge

162 Two in-frame, C-terminal isoforms of the herpes simplex virus type 1 (HSV-1) origin binding prote

163 rt the replication of plasmid DNA containing herpes simplex virus type 1 (HSV-1) origin sequences in

164 Herpes simplex virus type 1 (HSV-1) packages its microme

165 The herpes simplex virus type 1 (HSV-1) portal is composed o

166 We previously demonstrated that herpes simplex virus type 1 (HSV-1) preferentially estab

167 Herpes simplex virus type 1 (HSV-1) produces oral lesion

168 The herpes simplex virus type 1 (HSV-1) protein ICP27 has be

169 Viral genes sufficient and required for herpes simplex virus type 1 (HSV-1) reactivation were id

170 Here we show that infection with herpes simplex virus type 1 (HSV-1) reduced CD1d surface

171 Herpes simplex virus type 1 (HSV-1) regulatory protein I

172 n modulating the acquired immune response to herpes simplex virus type 1 (HSV-1) remains ill defined;

173 ological stress.IMPORTANCE Like all viruses, herpes simplex virus type 1 (HSV-1) reproduction relies

174 initial infection and cell-to-cell spread by herpes simplex virus type 1 (HSV-1) require the interact

175 Herpes simplex virus type 1 (HSV-1) requires four glycop

176 Herpes simplex virus type 1 (HSV-1) requires four glycop

177 Herpes simplex virus type 1 (HSV-1) shedding from sensor

178 Cells infected with wild-type herpes simplex virus type 1 (HSV-1) show disruption of t

179 lycoprotein E (gE) is required for efficient herpes simplex virus type 1 (HSV-1) spread from the inoc

180 vitro serial passage of a Deltagamma(1)34.5 herpes simplex virus type 1 (HSV-1) strain in SK-N-SH ne

181 Herpes simplex virus type 1 (HSV-1) strain KOS has been

182 ortant phase in the development of an ocular herpes simplex virus type 1 (HSV-1) subunit vaccine is t

183 Evidence for an essential role of the herpes simplex virus type 1 (HSV-1) tegument protein VP1

184 The ability of herpes simplex virus type 1 (HSV-1) to activate NF-kappa

185 The ability of herpes simplex virus type 1 (HSV-1) to suppress silencin

186 A detailed analysis of herpes simplex virus type 1 (HSV-1) transport dynamics i

187 The herpes simplex virus type 1 (HSV-1) U(S)1 gene encodes h

188 The herpes simplex virus type 1 (HSV-1) UL20 gene encodes a

189 The herpes simplex virus type 1 (HSV-1) UL37 gene encodes a

190 The herpes simplex virus type 1 (HSV-1) US3 gene encodes a s

191 Herpes simplex virus type 1 (HSV-1) utilizes a specializ

192 During infection, herpes simplex virus type 1 (HSV-1) utilizes multiple pr

193 we reported a new series of highly defective herpes simplex virus type 1 (HSV-1) vectors that were fu

194 The herpes simplex virus type 1 (HSV-1) virion host shutoff

195 glycoprotein C (gC), a major constituent of herpes simplex virus type 1 (HSV-1) virions, by hijackin

196 Herpes simplex virus type 1 (HSV-1) virions, like those

197 sactivation of VZV genes and has homology to herpes simplex virus type 1 (HSV-1) VP16.

198 erent strains of mice infected ocularly with herpes simplex virus type 1 (HSV-1) was investigated.

199 Cells infected with herpes simplex virus type 1 (HSV-1) were conventionally

200 svirus 8 (HHV-8), cytomegalovirus (CMV), and herpes simplex virus type 1 (HSV-1) were detected in 90%

201 Images of neurons infected with herpes simplex virus type 1 (HSV-1), acquired using elec

202 pathogens, varicella-zoster virus (VZV) and herpes simplex virus type 1 (HSV-1), as well as two vete

203 Here, we use affinity assays to show that herpes simplex virus type 1 (HSV-1), but not HSV-2, bind

204 Other viruses, such as herpes simplex virus type 1 (HSV-1), can additionally re

205 infection of human monocyte-derived DCs with herpes simplex virus type 1 (HSV-1), CYTIP is rapidly de

206 ed States population is infected with either herpes simplex virus type 1 (HSV-1), herpes simplex viru

207 During lytic infection by herpes simplex virus type 1 (HSV-1), histones are presen

208 Viruses, such as herpes simplex virus type 1 (HSV-1), however, go to grea

209 ICP22, an immediate-early protein of herpes simplex virus type 1 (HSV-1), is required for vir

210 In herpes simplex virus type 1 (HSV-1), the immediate-early

211 with viral encephalitic agents: enterovirus, herpes simplex virus type 1 (HSV-1), varicella-zoster vi

212 ormational approach to genome engineering of herpes simplex virus type 1 (HSV-1), which has a large D

213 tion in bacterial lipopolysaccharide (LPS)-, herpes simplex virus type 1 (HSV-1)-, or adenovirus (ser

214 Herpes simplex virus type 1 (HSV-1)-induced cell fusion

215 stress-inducing agents, protein synthesis in herpes simplex virus type 1 (HSV-1)-infected cells is no

216 Analyzing translation factors in herpes simplex virus type 1 (HSV-1)-infected HeLa cells,

217 a protective role in the eyes and brains of herpes simplex virus type 1 (HSV-1)-infected mice.

218 estigated their suppressive capacities using herpes simplex virus type 1 (HSV-1)-specific effector T

219 Knockout of TRIM14 impairs herpes simplex virus type 1 (HSV-1)-triggered antiviral

220 activation induced by another herpes virus, herpes simplex virus type 1 (HSV-1).

221 protein analysis to examine the tegument of herpes simplex virus type 1 (HSV-1).

222 the nuclei of cells lytically infected with herpes simplex virus type 1 (HSV-1).

223 r in a manner similar to that determined for herpes simplex virus type 1 (HSV-1).

224 responses against many pathogens, including herpes simplex virus type 1 (HSV-1).

225 ression to facilitate reactivation of latent herpes simplex virus type 1 (HSV-1).

226 iates has not been demonstrated in vitro for herpes simplex virus type 1 (HSV-1).

227 We previously demonstrated that a herpes simplex virus type 1 (HSV-1)/adeno-associated vir

228 After replicating in surface epithelia, herpes simplex virus type-1 (HSV-1) enters the axonal te

229 Herpes simplex virus type-1 (HSV-1) induces new lymphati

230 an sulfate (3-OS HS), contribute strongly to herpes simplex virus type-1 (HSV-1) infection in vitro.

231 f herpetic neuralgia using a murine model of Herpes Simplex Virus Type-1 (HSV-1) infection.

232 Herpes simplex virus type-1 (HSV-1) is one of the most w

233 rr virus (EBV), human herpesvirus 6 (HHV-6), herpes simplex virus types 1 (HSV-1) and 2 (HSV-2), and

234 to mimic genital herpes infections caused by herpes simplex virus types 1 (HSV-1) and 2 (HSV-2).

235 ript mapping to open reading frame (ORF) 61 (herpes simplex virus type 1 [HSV-1] ICP0 homolog) was co

236 ts found in the immediate-early promoters of herpes simplex virus type 1(HSV-1).

237 tegument proteins VP13/14, VP22, and VP16 of herpes simplex virus type 1 (HSV1) are components of pri

238 Herein we demonstrate that herpes simplex virus type 1 (HSV1) thymidine kinase (TK)

239 e types of viruses, adenovirus type 5 (AV5), herpes simplex virus type 1 (HSV1), simian virus 40 (SV4

240 Support for the concept that herpes simplex virus type 1 (HSV1), when present in the

241 e association of 4 human herpesviruses (CMV, herpes simplex virus type 1, human herpesvirus type 6, a

242 previously that the plating efficiency of a herpes simplex virus type 1 ICP0-null mutant was enhance

243 ed by subsequent expression of VZV ORF61p or herpes simplex virus type 1 ICP0.

244 Herpes simplex virus type 1 ICP22-/U(S)1.5- mutants init

245 milar activity in the cotransfection assays, herpes simplex virus type 1 ICP27 was inactive.

246 The binding of herpes simplex virus type 1 ICP4, TATA-binding protein (

247 Of the five herpes simplex virus type 1 immediate early (IE) protein

248 Herpes simplex virus type 1 immediate-early protein ICP0

249 therapeutic target to alter pathogenicity of herpes simplex virus type 1 in skin infection.

250 P22 is required for efficient replication of herpes simplex virus type 1 in some cell types (permissi

251 ransneuronal transport of the H129 strain of herpes simplex virus type 1 in the Cebus monkey to label

252 During latency of herpes simplex virus type 1 in the neurons of the periph

253 pathogens were detected by mNGS (4 cases of herpes simplex virus type 1, including 1 case of coinfec

254 e factor 15, Slug, and SPDEF, stimulated the herpes simplex virus type 1-infected cell protein 0 (ICP

255 Increasing MARCO expression enhances herpes simplex virus type 1 infection while MARCO(-/-) m

256 Herpes simplex virus type 1 is a human pathogen responsi

257 The ICP0 protein of herpes simplex virus type 1 is an E3 ubiquitin ligase an

258 Herpes simplex virus type 1 is an important epithelial p

259 UL9, the origin binding protein of herpes simplex virus type 1, is a member of the SF2 fami

260 neration Ad (Ad) vector, which expresses the herpes simplex virus type 1 mutant thymidine kinase (HSV

261 tantially increased replication of oncolytic herpes simplex virus type 1 (oHSV).

262 Herpes simplex virus type 1 packages its DNA genome into

263 we confirm using bacteriophage varphi29 and herpes simplex virus type 1 particles.

264 n is influenced by sequence context and that herpes simplex virus type 1 Pol may dissociate more freq

265 Many viruses (herpes simplex virus type 1, polyomavirus, and human imm

266 Herpes simplex virus type 1 protein ICP0 plays important

267 The human herpes simplex virus type 1 regulatory protein ICP4 bind

268 e, is a multifunctional protein required for herpes simplex virus type 1 replication in vivo.

269 crystal structure of the gB ectodomain from herpes simplex virus type 1 reveals a multidomain trimer

270 meric red fluorescent protein, and truncated herpes simplex virus type 1 sr39 thymidine kinase) by us

271 as used for PET imaging of the reporter gene herpes simplex virus type-1 sr39 thymidine kinase (HSV1-

272 ation of the representative alphaherpesvirus herpes simplex virus type 1, the representative gammaher

273 ed and tested as reporter probes for imaging herpes simplex virus type 1 thymidine kinase (HSV1- tk)

274 nic HC-Ad driving constitutive expression of herpes simplex virus type 1 thymidine kinase (HSV1-TK) a

275 The herpes simplex virus type 1 thymidine kinase (HSV1-tk) g

276 gene encoding the prodrug-converting enzyme herpes simplex virus type 1 thymidine kinase (HSV1-tk) i

277 The herpes simplex virus type 1 thymidine kinase (HSV1-tk) p

278 -MDHT), which can be used for imaging of the herpes simplex virus type 1 thymidine kinase (HSV1-tk) r

279 ydroxymethyl]butyl)guanine ((18)F-FHBG), the herpes simplex virus type 1 thymidine kinase (HSV1-tk) v

280 n (hCEA) and with a fusion reporter gene for herpes simplex virus type 1 thymidine kinase (HSV1tk) an

281 ycytidine kinase double mutant (hdCKDM), and herpes simplex virus type 1 thymidine kinase (hsvTK) rep

282 A hypoxia-inducible dual reporter herpes simplex virus type 1 thymidine kinase and enhance

283 egalovirus (CMV) promoter driving the mutant herpes simplex virus type 1 thymidine kinase reporter ge

284 ssion tomography (PET)-based split reporter (herpes simplex virus type 1 thymidine kinase), cleaved b

285 stably transfected with a mutant version of herpes simplex virus type 1 thymidine kinase, HSV1-sr39t

286 omeric red fluorescent protein, and a mutant herpes simplex virus type 1 thymidine kinase.

287 ceuticals ((18)F-FEAU) comparable to that of herpes simplex virus type-1 thymidine kinase (HSV1-tk)-t

288 gue as a probe for imaging the expression of herpes simplex virus type-1 thymidine kinase (HSV1-TK).

289 mography (PET) is used for the assessment of herpes simplex virus type-1 thymidine kinase gene expres

290 essing a PET reporter gene, the mutant viral herpes simplex virus type 1-thymidine kinase (HSV1-sr39t

291 Ads) carrying the conditional cytotoxic gene herpes simplex virus type 1-thymidine kinase (TK) induce

292 Since herpes simplex virus type 1 transactivator ICP0 and huma

293 Previous studies indicated that the herpes simplex virus type 1 U(L)15 protein (pU(L)15) int

294 The herpes simplex virus type 1 UL25 protein is incorporated

295 The herpes simplex virus type 1 UL25 protein is one of seven

296 Studies on the herpes simplex virus type 1 UL25-null mutant KUL25NS hav

297 identification of charge cluster mutants of herpes simplex virus type 1 UL34 that localize properly

298 The herpes simplex virus type 1 UL6 protein forms a 12-subun

299 tity and similarity with the UL49 prototype, herpes simplex virus type 1 VP22.

300 odds ratio for being in a higher tertile of herpes simplex virus type 1 was 1.63 (95% confidence int