ライフサイエンスコーパス: encephalitis virus

1 ic partners of nsP3 HVD of Venezuelan equine encephalitis virus.

2 ncy virus 1, hepatitis C virus, and Japanese encephalitis virus.

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

4 Louis encephalitis virus.

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

6 UTR of another alphavirus, Venezuelan equine encephalitis virus.

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

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

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

10 om an attenuated strain of Venezuelan equine encephalitis virus.

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

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

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

14 thogens, including dengue virus and Japanese encephalitis virus.

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

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

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

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

19 and Venezuelan equine encephalitis and other encephalitis viruses.

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

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

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

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

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

25 uding Dengue, Zika, West Nile and Tick-borne encephalitis viruses, activate the unfolded protein resp

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

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

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

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

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

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

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

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

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

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

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

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

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

39 lla, Francisella, Powassan virus, tick-borne encephalitis virus, and Colorado tick fever virus.

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

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

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

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

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

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

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

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

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

49 , Jamestown Canyon virus, and eastern equine encephalitis virus, as well as the tick-borne Powassan v

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 Eastern equine encephalitis virus (EEEV) infection was identified durin

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

72 Eastern equine encephalitis virus (EEEV) is a mosquito-transmitted alph

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

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

75 Eastern equine encephalitis virus (EEEV) is one of the most virulent vi

76 Eastern equine encephalitis virus (EEEV) is the most pathogenic member

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

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

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

80 Eastern equine encephalitis virus (EEEV), a mosquito-borne icosahedral

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

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

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

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

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

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

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

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

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

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

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

92 including West Nile virus and Eastern equine encephalitis virus has been detected in wild Atlantic bo

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

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

95 ovirulence and neuroinvasiveness of Japanese encephalitis virus in mice.

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

97 Louis encephalitis viruses in virus-infected mosquito pools an

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

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

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

101 Louis encephalitis virus infections, (ii) differentiates betwe

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

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

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

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

106 Louis encephalitis virus, Japanese encephalitis virus, Kunjin

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

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

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

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

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

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

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

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

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

116 Japanese encephalitis virus (JEV) invades the CNS, resulting in n

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

118 Japanese encephalitis virus (JEV) is a leading cause of viral enc

119 Japanese encephalitis virus (JEV) is a mosquito-borne zoonotic fl

120 Japanese encephalitis virus (JEV) is a zoonotic, mosquito-borne f

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

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

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

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

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

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

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

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

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

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

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

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

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

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

135 rus (DENV; nine isolates analyzed), Japanese encephalitis virus (JEV; one isolate analyzed) and Zika

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

137 Louis encephalitis virus, La Crosse virus, Jamestown Canyon vi

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

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

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

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

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

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

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

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

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

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

148 es with the corresponding region of Japanese encephalitis virus NS1 to generate a chimeric DJ NS1 pro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 7BL/6 mice vaccinated with Venezuelan equine encephalitis virus replicons encoding the Ebola virus nu

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

174 00 in cell-based assays using western equine encephalitis virus replicons.

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

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

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

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

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

180 Louis encephalitis virus (SLEV) noninfectious recombinant anti

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

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

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

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

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

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

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

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

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

190 Tick-borne encephalitis virus (TBEV) is the causative agent of seve

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 Venezuelan equine encephalitis virus (VEEV) is a neurotropic alphavirus tr

230 Venezuelan equine encephalitis virus (VEEV) is a New World Alphavirus that

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 Venezuelan equine encephalitis virus (VEEV) is one of the important human

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

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

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

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

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

253 inally, mice infected with Venezuelan equine encephalitis virus (VEEV) were successfully treated with

254 e infection with wild-type Venezuelan equine encephalitis virus (VEEV), a highly myeloid-cell-tropic

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

256 Venezuelan equine encephalitis virus (VEEV), a New World alphavirus of the

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

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

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

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

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

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

263 NCE RNA viruses, including Venezuelan equine encephalitis virus (VEEV), have high mutation rates that

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

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

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

267 ection with the alphavirus Venezuelan equine encephalitis virus (VEEV), which causes flu-like symptom

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

297 with epidemics, required RelA, and Japanese encephalitis virus, which produced relatively minor cyto

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

299 were seropositive for Zika virus or Japanese encephalitis virus with FRNT.

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