ライフサイエンスコーパス: encephalitis virus

1 s to the NS5 protein of the related Japanese encephalitis virus.

2 Louis encephalitis virus.

3 us is related to Powassan virus, a tickborne encephalitis virus.

4 UTR of another alphavirus, Venezuelan equine encephalitis virus.

5 us, dengue virus types 2 and 4, and Japanese encephalitis virus.

6 sely related flaviviruses, such as St. Louis encephalitis virus.

7 rus, Ross River virus, and Venezuelan equine encephalitis virus.

8 om an attenuated strain of Venezuelan equine encephalitis virus.

9 se virus, visna virus, and caprine arthritis encephalitis virus.

10 susceptible virus, the flavivirus tick-borne encephalitis virus.

11 thogens, including dengue virus and Japanese encephalitis virus.

12 WEEV and the unrelated flavivirus St. Louis encephalitis virus.

13 aviruses, such as eastern and western equine encephalitis viruses.

14 of the E proteins from dengue and tick-borne encephalitis viruses.

15 udes West Nile, yellow fever, and tick-borne encephalitis viruses.

16 ic-causing dengue, yellow fever and Japanese encephalitis viruses.

17 and Venezuelan equine encephalitis and other encephalitis viruses.

18 E proteins from dengue type 2 and tick-borne encephalitis viruses.

19 n with neuroinvasive West Nile and La Crosse encephalitis viruses.

20 cluding yellow fever, West Nile and Japanese encephalitis viruses.

21 us 1A4B-6, dengue 2 virus 4G2, and La Crosse encephalitis virus 10G5.4 to capture the specific inacti

22 utilized group-reactive MAbs eastern equine encephalitis virus 1A4B-6, dengue 2 virus 4G2, and La Cr

23 Western equine encephalitis virus, a virus widely distributed throughou

24 fever, tick-borne encephalitis and Japanese encephalitis virus among many others.

25 mary mosquito infection by Venezuelan equine encephalitis virus, an arbovirus causing neurological di

26 c resolution structures of Venezuelan equine encephalitis virus and dengue virus revealed transmembra

27 virus, chikungunya virus, Venezuelan equine encephalitis virus and human immunodeficiency virus type

28 tors of the replication of Venezuelan equine encephalitis virus and other alphaviruses.

29 Previous studies with Venezuelan equine encephalitis virus and Sindbis virus (SINV) indicate tha

30 ephalitic flaviviruses, including tick-borne encephalitis virus and West Nile virus, antagonize IFN-I

31 phalitic arboviruses, such as eastern equine encephalitis virus and West Nile virus, underscore the n

32 ikungunya, and eastern and Venezuelan equine encephalitis viruses and demonstrate that a small ( appr

33 by the E proteins from dengue and tick-borne encephalitis viruses and forms a rod-shaped configuratio

34 avirus 229E), Togaviridae (Venezuelan equine encephalitis virus), and Hepeviridae (HEV), indicating t

35 Except for the vaccine against tick-borne encephalitis virus, and a brief campaign to reduce this

36 ence of a related alphavirus, western equine encephalitis virus, and also by an unrelated sequence fr

37 flavivirus family: West Nile virus, Japanese encephalitis virus, and dengue virus 2.

38 elated helicases from Dengue virus, Japanese encephalitis virus, and humans.

39 s like the hepatitis E virus and the caprine encephalitis virus, and in mRNAs such as those coding fo

40 s of bacteriophage lambda, Venezuelan equine encephalitis virus, and Staphylococcus aureus during sup

41 alphavirus infection with Venezuelan equine encephalitis virus, and this was associated with greater

42 uses include dengue, West Nile, and Japanese encephalitis viruses, and the nonpathogenic flaviviruses

43 Venezuelan, western, and eastern equine encephalitis viruses are New World alphaviruses that are

44 aviruses Sindbis virus and Venezuelan equine encephalitis virus, as well as La Crosse bunyavirus.

45 Louis encephalitis virus, as well as of nematodes that cause l

46 tron microscopy structure of mature Japanese encephalitis virus at near-atomic resolution, which reve

47 alphaviruses (eastern and Venezuelan equine encephalitis viruses) based upon either fusion of the re

48 uses maedi-visna virus and caprine arthritis-encephalitis virus (CAEV) and human immunodeficiency vir

49 aedi-visna virus (MVV) and caprine arthritis-encephalitis virus (CAEV) cause encephalitis, progressiv

50 The caprine arthritis-encephalitis virus (CAEV) long terminal repeat (LTR) is

51 fected with the lentivirus caprine arthritis-encephalitis virus (CAEV) were evaluated by semiquantita

52 protein and a recombinant Venezuelan equine encephalitis virus capsid protein for HCV IRES-containin

53 mino-terminal subdomain of Venezuelan equine encephalitis virus capsid protein, SD1, plays a critical

54 tent with previous reports on the tick-borne encephalitis virus capsid protein, YFC demonstrates rema

55 h as western, eastern, and Venezuelan equine encephalitis viruses cause serious and potentially fatal

56 ding western, eastern, and Venezuelan equine encephalitis viruses, cause serious and potentially fata

57 rvival of mice given a lethal western equine encephalitis virus challenge.

58 sed plasmid VRC5288 (Zika virus and Japanese encephalitis virus chimera), and the VRC 320, done in on

59 an enzootic member of the Venezuelan Equine Encephalitis Virus complex and belongs to the New World

60 gence from the other members of the Japanese encephalitis virus complex, presumably in Africa, WNV ha

61 n (VEEV), eastern (EEEV), and western equine encephalitis viruses, constitute a continuing public hea

62 small-ruminant lentivirus (caprine arthritis encephalitis virus-Cork strain) and PrP(Sc) demonstrated

63 ally mixed CLPs, but SINV and Western equine encephalitis virus CPs do form mixed cores.

64 f the flavivirus genome (chimeric tick-borne encephalitis virus/dengue virus) abolished virus neurovi

65 Eastern equine encephalitis virus (EEEV) causes human encephalitis in N

66 Eastern equine encephalitis virus (EEEV) causes sporadic but often seve

67 Eastern equine encephalitis virus (EEEV) causes sporadic epidemics of h

68 Eastern equine encephalitis virus (EEEV) is a human and veterinary path

69 Eastern equine encephalitis virus (EEEV) is a representative member of

70 thogenic phenotype.IMPORTANCE Eastern equine encephalitis virus (EEEV) is one of the most pathogenic

71 Eastern equine encephalitis virus (EEEV) produces the most severe human

72 Eastern equine encephalitis virus (EEEV) produces the most severe human

73 encephalitis virus (WEEV), or eastern equine encephalitis virus (EEEV) when given individually or in

74 ne encephalitis virus (VEEV), eastern equine encephalitis virus (EEEV), and western equine encephalit

75 encephalitis virus (VEEV) and eastern equine encephalitis virus (EEEV), evolved separately from those

76 encephalitis virus (WEEV) and eastern equine encephalitis virus (EEEV), two New World alphaviruses, c

77 encephalitis virus (VEEV) and Eastern equine encephalitis virus (EEEV), which have demonstrated poten

78 ncephalitis virus (WEEV), and eastern equine encephalitis virus (EEEV).

79 Eastern and Venezuelan equine encephalitis viruses (EEEV and VEEV, respectively) cause

80 genic mosquito-borne viruses (Eastern equine encephalitis virus [EEEV], Western equine encephalitis v

81 rived from the Sindbis and Venezuelan equine encephalitis viruses encoding either the HCV envelope gl

82 e investigated the ability of western equine encephalitis virus envelope glycoproteins (WEEV GP) to p

83 chikungunya, dengue, yellow fever, Japanese encephalitis virus, GBS, and control datasets.

84 e was identified in this region of the avian encephalitis virus genome, despite little nucleotide seq

85 The global epidemiology of Japanese encephalitis virus has been further clarified.

86 de viral (for example, HIV, rabies, Japanese encephalitis virus, herpes simplex virus, varicella zost

87 ovirulence and neuroinvasiveness of Japanese encephalitis virus in mice.

88 mosquito-borne North American eastern equine encephalitis virus in myeloid-lineage cells by binding t

89 Louis encephalitis viruses in virus-infected mosquito pools an

90 ifestations characteristic of eastern equine encephalitis virus infection in humans.

91 al for dengue hemorrhagic fever and Japanese encephalitis virus infection, inhibits NLRP3 inflammasom

92 le virus (WNV), Powassan virus, or La Crosse encephalitis virus infections to assess the sensitivity

93 Louis encephalitis virus infections, (ii) differentiates betwe

94 Importance: Tick-borne encephalitis virus is endemic in large parts of Europe a

95 Globally, Japanese encephalitis virus is the most important emerging viral

96 laviviruses may cause encephalitis, Japanese encephalitis virus is the most significant, being respon

97 us (including dengue, West Nile and Japanese encephalitis viruses) is regulated by a wide variety of

98 primer pairs were identified for California encephalitis virus, Jamestown Canyon virus, La Crosse vi

99 Louis encephalitis virus, Japanese encephalitis virus, Kunjin

100 ng genes of an attenuated strain of Japanese encephalitis virus (JE), SA14-14-2.

101 live attenuated vaccines, including Japanese encephalitis virus (JEV) (SA-14-14-2), varicella (Variva

102 BEV), yellow fever virus (YFV), and Japanese encephalitis virus (JEV) and by comparing the resultant

103 presumptive serodiagnosis of acute Japanese encephalitis virus (JEV) and West Nile virus (WNV) infec

104 Four genotypes of Japanese encephalitis virus (JEV) are presently recognized (repre

105 iruses (DENV), West Nile virus, and Japanese encephalitis virus (JEV) are widely used as serodiagnost

106 Using Japanese encephalitis virus (JEV) as a model, we performed a syst

107 A yellow fever virus (YFV)/Japanese encephalitis virus (JEV) chimera in which the structural

108 In recent years, genotype I (GI) of Japanese encephalitis virus (JEV) has displaced genotype III (GII

109 ns against neurotropic flaviviruses.Japanese encephalitis virus (JEV) is a Flavivirus responsible for

110 Japanese encephalitis virus (JEV) is the leading global cause of

111 Plasmid vectors containing Japanese encephalitis virus (JEV) premembrane (prM) and envelope

112 and efficacy of the live-attenuated Japanese encephalitis virus (JEV) SA14-14-2 vaccine are attribute

113 (TBEV), West Nile virus (WNV), and Japanese encephalitis virus (JEV) that could complement each othe

114 Japanese encephalitis virus (JEV), a mosquito-borne flavivirus, r

115 Japanese encephalitis virus (JEV), although confined to Asia, cau

116 g EIIIs from Koutango virus (KOUV), Japanese encephalitis virus (JEV), St. Louis encephalitis virus (

117 three flaviviruses, DENV, WNV, and Japanese encephalitis virus (JEV), using a high-content immunoflu

118 We diagnosed Japanese encephalitis virus (JEV), using antibody detection, cult

119 DENV-4), West Nile virus (WNV), and Japanese encephalitis virus (JEV), were constructed.

120 cation of yellow fever virus (YFV), Japanese encephalitis virus (JEV), West Nile virus (WNV), St.

121 Japanese encephalitis virus (JEV)-specific Fab antibodies were re

122 (WNV), hepatitis C virus (HCV), and Japanese encephalitis virus (JEV).

123 c, mosquito-borne disease caused by Japanese encephalitis virus (JEV).

124 Louis encephalitis virus, Japanese encephalitis virus, Kunjin virus, Murray Valley virus, P

125 sidues in the envelope protein of tick-borne encephalitis virus led Fritz et al. to identify a histid

126 delivered by gene gun and Venezuelan equine encephalitis virus-like replicon particles (VRP), both e

127 iate early promoter or the caprine arthritis-encephalitis virus long terminal repeat (CAEV LTR).

128 ever virus, Sindbis virus, Venezuelan equine encephalitis virus, measles virus, influenza A virus, re

129 River virus (mos-RRV) and Venezuelan equine encephalitis virus (mos-VEE) exhibited enhanced infectio

130 RP) family in clearance of Venezuelan equine encephalitis virus mutants from infected cells.

131 North American eastern equine encephalitis virus (NA-EEEV) is uniquely neurovirulent a

132 ein of natural North American eastern equine encephalitis virus (NA-EEEV) isolates and demonstrated t

133 tial virus, alphavirus and Venezuelan equine encephalitis virus, norovirus, metapneumovirus, yellow f

134 with the corresponding region from Japanese encephalitis virus NS1 to create chimeric DJ NS1 protein

135 presence of dengue virus (DENV) and Japanese encephalitis virus NS1s in the blood of infected interfe

136 e structure determined for Venezuelan equine encephalitis virus nsP2 indicated the presence of a prev

137 llular proteins with which Venezuelan equine encephalitis virus nsP2 interacted.

138 of neurovirulence and stability in Japanese encephalitis virus, opening up new avenues for therapeut

139 Recent work suggests Japanese encephalitis virus originated in the Indonesia-Malaysia

140 etapneumovirus, yellow fever virus, Japanese encephalitis virus, parainfluenza virus and Sendai virus

141 l (influenza virus, Dengue virus, tick-borne encephalitis virus, rabies virus, severe acute respirato

142 gnal from a nonpropagating Venezuelan equine encephalitis virus replicon particle (VRP) delivery syst

143 -vectored vaccine (Kp47/47-Venezuelan equine encephalitis virus replicon particle) for safety, immuno

144 be boosted using HPV16E6E7-Venezuelan equine encephalitis virus replicon particles (HPV16-VRP) and th

145 ng vaccine vector based on Venezuelan equine encephalitis virus replicon particles (VRP) expressing t

146 ne based on nonpropagating Venezuelan equine encephalitis virus replicon particles (VRP) was tested f

147 ystem, footpad delivery of Venezuelan equine encephalitis virus replicon particles (VRP), led to the

148 ter parenteral delivery of Venezuelan equine encephalitis virus replicon particles (VRP).

149 rotein was expressed using Venezuelan equine encephalitis virus replicon particles (VRP-NV1).

150 viously, immunization with Venezuelan equine encephalitis virus replicon particles (VRPs) demonstrate

151 Here, we developed Venezuelan equine encephalitis virus replicon particles (VRPs) encoding hM

152 uated the potential use of Venezuelan equine encephalitis virus replicon particles (VRPs) for in vitr

153 uclear cells in vitro with Venezuelan equine encephalitis virus replicon particles (VRPs) resulted in

154 ped a cell-based assay with a western equine encephalitis virus replicon that expresses a luciferase

155 ing synthetic genomics and Venezuelan equine encephalitis virus replicons (VRPs) expressing spike and

156 ns expressed from packaged Venezuelan equine encephalitis virus replicons elicited protective immunit

157 ered PSCA-cDNA followed by Venezuelan equine encephalitis virus replicons encoding PSCA.

158 7BL/6 mice vaccinated with Venezuelan equine encephalitis virus replicons encoding the Ebola virus nu

159 e inoculated with packaged Venezuelan equine encephalitis virus replicons expressing NV VLPs, blocked

160 00 in cell-based assays using western equine encephalitis virus replicons.

161 ngat virus (LGTV; a member of the tick-borne encephalitis virus serogroup) and Japanese encephalitis

162 Both viruses belong to the California encephalitis virus serogroup, which causes 70 to 100 cas

163 cell lymphotropic virus type I, and St Louis encephalitis virus), several of which have been suspecte

164 from birds infected with WNV or Saint Louis encephalitis virus (SLEV) and from noninfected control b

165 Differential diagnosis of St. Louis encephalitis virus (SLEV) and West Nile virus (WNV) infe

166 St. Louis encephalitis virus (SLEV) is a mosquito-borne flavivirus

167 Louis encephalitis virus (SLEV) noninfectious recombinant anti

168 Japanese encephalitis virus (JEV), St. Louis encephalitis virus (SLEV), and Bagaza virus (BAGV) were

169 Louis encephalitis virus (SLEV), and dengue virus (DENV) serot

170 Louis encephalitis virus (SLEV), and dengue virus type 2 (DENV

171 Tonate virus and Venezuelan equine encephalitis virus strain 78V3531 also appear to be dist

172 bunyaviruses La Crosse virus and California encephalitis virus, suggesting a conserved role for Wnt

173 (LGTV), one of the members of the tick-borne encephalitis virus (TBEV) complex, was firstly isolated

174 aturally attenuated member of the tick-borne encephalitis virus (TBEV) complex, was tested extensivel

175 Tick-borne encephalitis virus (TBEV) is a flavivirus that is transf

176 Tick-borne encephalitis virus (TBEV) is a vector-transmitted flaviv

177 ly virulent Far Eastern strain of tick-borne encephalitis virus (TBEV) on the backbone of a nonneuroi

178 Tick-borne encephalitis virus (TBEV), a member of the Flaviviridae

179 it less than that associated with tick-borne encephalitis virus (TBEV), the most virulent of the tick

180 mic RNAs (replicons) derived from tick-borne encephalitis virus (TBEV), West Nile virus (WNV), and Ja

181 irus (strain 16681) with those of tick-borne encephalitis virus (TBEV), yellow fever virus (YFV), and

182 nt mice against the most virulent tick-borne encephalitis virus (TBEV).

183 t (REE) within the capsid gene of tick-borne encephalitis virus (TBEV, genus Flavivirus).

184 Seminal studies on tick-borne encephalitis viruses (TBEV), based on partial envelope g

185 g, truncated derivative of Venezuelan equine encephalitis virus that targets dendritic cells (DCs) in

186 pol) inhibited infection of Theiler's murine encephalitis virus (TMEV), a picornavirus from which it

187 ther RNA viruses, including Theiler's murine encephalitis virus (TMEV), vesicular stomatitis virus (V

188 d strain of the alphavirus Venezuelan equine encephalitis virus, to produce virus-like replicon parti

189 e encephalitis virus serogroup) and Japanese encephalitis virus use the nonstructural protein NS5 to

190 Venezuelan equine encephalitis virus (VEE) empty replicon particles (VRPs)

191 loned attenuated strain of Venezuelan equine encephalitis virus (VEE) has been genetically configured

192 Semliki Forest virus, and Venezuelan equine encephalitis virus (VEE) have been shown to induce robus

193 Venezuelan equine encephalitis virus (VEE) is an important equine and huma

194 vaccine that is based on a Venezuelan equine encephalitis virus (VEE) replicon launched from plasmid

195 pothesized that attenuated Venezuelan equine encephalitis virus (VEE) replicon particle (VRP) vaccine

196 Here, utilizing Venezuelan equine encephalitis virus (VEE) replicon particles (VRP) to lim

197 Venezuelan equine encephalitis virus (VEE) replicon particles (VRP) were u

198 HIV-1) envelope by using a Venezuelan equine encephalitis virus (VEE) replicon system with mice and r

199 The initial steps of Venezuelan equine encephalitis virus (VEE) spread from inoculation in the

200 ccine vectors derived from Venezuelan equine encephalitis virus (VEE) that expressed simian immunodef

201 ve-virus vaccine strain of Venezuelan equine encephalitis virus (VEE) was configured as a replication

202 genome from the alphavirus Venezuelan equine encephalitis virus (VEE) was modified to express SHIV89.

203 d from a vaccine strain of Venezuelan equine encephalitis virus (VEE) were used as a vector for expre

204 malian cells infected with Venezuelan equine encephalitis virus (VEE), an important, naturally emergi

205 indbis virus (SIN-Gag) and Venezuelan equine encephalitis virus (VEE-Gag), as well as chimeras betwee

206 N alphavirus (derived from Venezuelan equine encephalitis virus [VEE] and the Sindbis virus [SIN]) en

207 encephalitic alphaviruses Venezuelan equine encephalitis virus (VEEV) and Eastern equine encephaliti

208 w World viruses, including Venezuelan equine encephalitis virus (VEEV) and eastern equine encephaliti

209 ated alphaviruses, such as Venezuelan equine encephalitis virus (VEEV) and Semliki Forest virus (SFV)

210 Neurovirulent Venezuelan equine encephalitis virus (VEEV) causes lethal encephalitis in

211 replicon vaccine based on Venezuelan equine encephalitis virus (VEEV) demonstrated protective effica

212 ield isolate of subtype IE Venezuelan equine encephalitis virus (VEEV) demonstrated the presence of m

213 New attenuated variants of Venezuelan equine encephalitis virus (VEEV) designed in this study combine

214 viously vaccinated against Venezuelan equine encephalitis virus (VEEV) exhibited poor neutralizing an

215 f Sindbis virus (SINV) and Venezuelan equine encephalitis virus (VEEV) form cytoplasmic complexes wit

216 t the pathogenic strain of Venezuelan equine encephalitis virus (VEEV) has developed a unique mechani

217 Venezuelan equine encephalitis virus (VEEV) is a mosquito-borne RNA virus

218 Venezuelan equine encephalitis virus (VEEV) is a mosquito-borne RNA virus

219 Venezuelan equine encephalitis virus (VEEV) is a pathogenic alphavirus, wh

220 Venezuelan equine encephalitis virus (VEEV) is a previously weaponized art

221 Venezuelan equine encephalitis virus (VEEV) is a reemerging pathogen and a

222 Venezuelan equine encephalitis virus (VEEV) is a reemerging virus that cau

223 Venezuelan equine encephalitis virus (VEEV) is a select agent that has bee

224 Venezuelan equine encephalitis virus (VEEV) is a significant human and ani

225 Venezuelan equine encephalitis virus (VEEV) is an alphavirus that is preva

226 Venezuelan equine encephalitis virus (VEEV) is an alphavirus with a wide d

227 Venezuelan equine encephalitis virus (VEEV) is an emerging pathogenic alph

228 Venezuelan equine encephalitis virus (VEEV) is an important human and anim

229 Venezuelan equine encephalitis virus (VEEV) is an important human and anim

230 Venezuelan equine encephalitis virus (VEEV) is an important human and equi

231 Venezuelan equine encephalitis virus (VEEV) is an important human and vete

232 Venezuelan equine encephalitis virus (VEEV) is an important, naturally eme

233 Venezuelan equine encephalitis virus (VEEV) is an important, naturally eme

234 Venezuelan equine encephalitis virus (VEEV) is highly virulent in adult la

235 Venezuelan equine encephalitis virus (VEEV) is one of the most pathogenic

236 Venezuelan equine encephalitis virus (VEEV) is one of the most pathogenic

237 developed a noncytopathic Venezuelan equine encephalitis virus (VEEV) mutant that can persistently r

238 Venezuelan equine encephalitis virus (VEEV) remains a naturally emerging d

239 Venezuelan equine encephalitis virus (VEEV) represents a continuous public

240 nfectious titer of WNV and Venezuelan equine encephalitis virus (VEEV) TC83 in the brains of Asyn-kno

241 Venezuelan equine encephalitis virus (VEEV), a member of the membrane-cont

242 e studied the emergence of Venezuelan equine encephalitis virus (VEEV), an alphavirus pathogen of peo

243 The structures of human Venezuelan equine encephalitis virus (VEEV), an alphavirus, in complex wit

244 ing an in vivo system with Venezuelan equine encephalitis virus (VEEV), an emerging alphavirus of the

245 ve the assembly of vRCs of Venezuelan equine encephalitis virus (VEEV), and G3BPs were shown to funct

246 Valley fever virus (RVFV), Venezuelan equine encephalitis virus (VEEV), and herpes simplex virus 1 (H

247 The alphaviruses Venezuelan equine encephalitis virus (VEEV), eastern equine encephalitis v

248 f one of the alphaviruses, Venezuelan equine encephalitis virus (VEEV), to understand its adaptation

249 re encephalitis in humans: Venezuelan equine encephalitis virus (VEEV), western equine encephalitis v

250 ial vaccine candidates for Venezuelan equine encephalitis virus (VEEV), western equine encephalitis v

251 currently unavailable for Venezuelan equine encephalitis virus (VEEV), which elicits flu-like sympto

252 heterologous proteins from Venezuelan equine encephalitis virus (VEEV)-based replicons.

253 ate that Tc bovine-derived Venezuelan equine encephalitis virus (VEEV)-specific TcPAbs are highly eff

254 deletion mutant (V3526) of Venezuelan equine encephalitis virus (VEEV).

255 h the envelope proteins of Venezuelan equine encephalitis virus (VEEV).

256 Venezuelan and western equine encephalitis viruses (VEEV and WEEV; Alphavirus; Togavir

257 Venezuelan equine encephalitis viruses (VEEV) belonging to subtype IC have

258 comparison of SA EEEV and Venezuelan equine encephalitis viruses (VEEV) demonstrated similar genetic

259 izootic subtype IAB and IC Venezuelan equine encephalitis viruses (VEEV) readily infect the epizootic

260 encephalitis virus [WEEV], Venezuelan equine encephalitis virus [VEEV], and Chikungunya virus [CHIKV]

261 Because Venezuelan equine encephalitis viruses (VEEVs) are infectious by aerosol,

262 St. Louis encephalitis virus was first identified as the cause of

263 To test this hypothesis, eastern equine encephalitis virus was passaged in BHK or mosquito cells

264 Western equine encephalitis virus (WEEV) and eastern equine encephaliti

265 c alphaviruses, which include western equine encephalitis virus (WEEV) and Fort Morgan virus, are mos

266 ncephalitis virus (EEEV), and western equine encephalitis virus (WEEV) are arthropod-borne positive-s

267 that led to the formation of western equine encephalitis virus (WEEV) from SINV- and EEEV-like ances

268 Western equine encephalitis virus (WEEV) has caused several epidemics t

269 rotropic alphaviruses such as western equine encephalitis virus (WEEV) in cultured cells.

270 Western equine encephalitis virus (WEEV) is an arbovirus from the genus

271 ne encephalitis virus (VEEV), western equine encephalitis virus (WEEV), and eastern equine encephalit

272 ne encephalitis virus (VEEV), western equine encephalitis virus (WEEV), or eastern equine encephaliti

273 ng the neurotropic alphavirus western equine encephalitis virus (WEEV).

274 rosol to a virulent strain of western equine encephalitis virus (WEEV).

275 Western equine encephalitis virus (WEEV; Togaviridae, Alphavirus) is an

276 ne encephalitis virus [EEEV], Western equine encephalitis virus [WEEV], Venezuelan equine encephaliti

277 cted with either Powassan virus or La Crosse encephalitis virus were used to evaluate the cross-react

278 In addition to the plasmids for Japanese encephalitis virus, West Nile virus (WNV), St.

279 other NT human arbovirus (Venezuelan equine encephalitis virus), which is also poorly understood.

280 entiviruses like visna and caprine arthritis-encephalitis viruses, which are mainly macrophage tropic

281 cinated with yellow fever, chimeric Japanese encephalitis virus (YF/JE), or chimeric West Nile virus