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1 is, western equine encephalitis, and eastern equine encephalitis.
2 cephalitic (Venezuelan, Eastern, and Western equine encephalitis) alphaviruses through multiple mecha
3 i) Sindbis, eastern, western, and Venezuelan equine encephalitis and most likely many other alphaviru
6 for Venezuelan equine encephalitis, western equine encephalitis, and eastern equine encephalitis exp
7 ause Venezuelan equine encephalitis, western equine encephalitis, and eastern equine encephalitis.
8 pathological picture in fatal human eastern equine encephalitis, and neuronal cell death is detectab
9 seen with Japanese encephalitis, Venezuelan equine encephalitis, and Rift Valley fever viruses; and
10 lyses placed EILV as a sister to the Western equine encephalitis antigenic complex within the main cl
11 West Nile, tick-borne encephalitis, eastern equine encephalitis, Cache Valley, Jamestown Canyon, and
12 neuroradiographic manifestations of eastern equine encephalitis could hasten the diagnosis of the il
15 he rapid detection of North American eastern equine encephalitis (EEE) and western equine encephaliti
17 osol containing a virulent strain of eastern equine encephalitis (EEE) virus developed neurological s
18 To elucidate the pathogenesis of eastern equine encephalitis (EEE) virus infections, we used hist
20 zuelan equine encephalitis (VEE) and eastern equine encephalitis (EEE) viruses are important, natural
22 is, western equine encephalitis, and eastern equine encephalitis expressing the surface proteins of a
23 e-dependent protection against fatal eastern equine encephalitis, further evidence that IFN is import
24 g evidence of circulating dengue, Venezuelan equine encephalitis, Mayaro, and Oropouche viruses in th
26 ted against Venezuelan, eastern, and western equine encephalitis or Mayaro virus genes were used for
28 Zika virus or Ebola, Chikungunya, or eastern equine encephalitis pseudoviruses was inhibited with gre
29 recently developed and promising Venezuelan equine encephalitis replicon particle (VRP) vector syste
30 oly I:C) and a potential vaccine [Venezuelan equine encephalitis replicon particles expressing MERS-C
31 , or an unrelated, intramuscular, Venezuelan equine encephalitis replicon vaccine expressing EBOV GP.
33 s to infant vaccination, chimeric Venezuelan equine encephalitis/Sindbis virus (VEE/SIN) replicon par
35 co mosaic virus U2, a bacteriophage MS2, and equine encephalitis TRD, is achieved with a combination
40 ressed in mammalian cells using a Venezuelan equine encephalitis (VEE) replicon expression system.
41 the TGEV E gene was cloned into a Venezuelan equine encephalitis (VEE) replicon expression vector and
42 nonstructural proteins (nsPs) of Venezuelan equine encephalitis (VEE) replicon that promoted subgeno
44 nt, epidemic/epizootic strains of Venezuelan equine encephalitis (VEE) virus (VEEV) arise via mutatio
49 mbrane and envelope proteins in a Venezuelan equine encephalitis (VEE) virus replicon particle (VRP)
50 orB (rrPorB), and PorB-expressing Venezuelan equine encephalitis (VEE) virus replicon particles (PorB
51 s necessary for the production of Venezuelan equine encephalitis (VEE) virus replicon particles (VRP)
55 ng human epitopes of HPV16, and a Venezuelan equine encephalitis (VEE) virus-based vector to deliver
57 ern equine encephalitis (EEE) and Venezuelan equine encephalitis (VEE) viruses are pathogens that inf
58 velop a panel useful in subtyping Venezuelan equine encephalitis (VEE) viruses by an indirect fluores
59 ies have indicated that epizootic Venezuelan equine encephalitis (VEE) viruses can evolve from enzoot
60 zed mice with alphavirus vectors (Venezuelan equine encephalitis [VEE] virus replicon particles [VRPs
61 EBOV glycoprotein (GP)-expressing Venezuelan equine encephalitis viral replicon particle vaccine prot
63 ntly related alphaviruses, including Eastern equine encephalitis virus (EEEV) and Semliki Forest viru
64 Naturally circulating strains of eastern equine encephalitis virus (EEEV) bind heparan sulfate (H
75 ghly pathogenic phenotype.IMPORTANCE Eastern equine encephalitis virus (EEEV) is one of the most path
79 y (EM) reconstructions of three anti-Eastern equine encephalitis virus (EEEV) neutralizing human mAbs
82 a chimeric alphavirus expressing the Eastern equine encephalitis virus (EEEV) structural proteins and
83 n microscopy (cryo-EM) structures of eastern equine encephalitis virus (EEEV) under acidic conditions
85 equine encephalitis virus (WEEV), or eastern equine encephalitis virus (EEEV) when given individually
87 an equine encephalitis virus (VEEV), eastern equine encephalitis virus (EEEV), and western equine enc
88 equine encephalitis virus (VEEV) and eastern equine encephalitis virus (EEEV), evolved separately fro
90 equine encephalitis virus (WEEV) and eastern equine encephalitis virus (EEEV), two New World alphavir
91 equine encephalitis virus (VEEV) and Eastern equine encephalitis virus (EEEV), which have demonstrate
93 ed Ross River virus (mos-RRV) and Venezuelan equine encephalitis virus (mos-VEE) exhibited enhanced i
95 ycoprotein of natural North American eastern equine encephalitis virus (NA-EEEV) isolates and demonst
96 usly, we found that chimeric Sindbis-eastern equine encephalitis virus (SINV-EEEV) particles can be r
98 larly cloned attenuated strain of Venezuelan equine encephalitis virus (VEE) has been genetically con
99 (SIN), Semliki Forest virus, and Venezuelan equine encephalitis virus (VEE) have been shown to induc
101 enetic vaccine that is based on a Venezuelan equine encephalitis virus (VEE) replicon launched from p
102 , we hypothesized that attenuated Venezuelan equine encephalitis virus (VEE) replicon particle (VRP)
105 ype 1 (HIV-1) envelope by using a Venezuelan equine encephalitis virus (VEE) replicon system with mic
107 Vaccine vectors derived from Venezuelan equine encephalitis virus (VEE) that expressed simian im
108 date live-virus vaccine strain of Venezuelan equine encephalitis virus (VEE) was configured as a repl
109 The genome from the alphavirus Venezuelan equine encephalitis virus (VEE) was modified to express
110 derived from a vaccine strain of Venezuelan equine encephalitis virus (VEE) were used as a vector fo
111 in mammalian cells infected with Venezuelan equine encephalitis virus (VEE), an important, naturally
112 from Sindbis virus (SIN-Gag) and Venezuelan equine encephalitis virus (VEE-Gag), as well as chimeras
113 the New World viruses, including Venezuelan equine encephalitis virus (VEEV) and eastern equine ence
114 are the encephalitic alphaviruses Venezuelan equine encephalitis virus (VEEV) and Eastern equine ence
115 ns: (1) human cases infected with Venezuelan equine encephalitis virus (VEEV) and Madariaga virus (MA
116 her related alphaviruses, such as Venezuelan equine encephalitis virus (VEEV) and Semliki Forest viru
117 at, the black flying fox, inhibit Venezuelan equine encephalitis virus (VEEV) and strongly bind to Ca
120 ) sequence from capsid protein of Venezuelan equine encephalitis virus (VEEV) binds to importin-alpha
124 usly, a replicon vaccine based on Venezuelan equine encephalitis virus (VEEV) demonstrated protective
125 ginal field isolate of subtype IE Venezuelan equine encephalitis virus (VEEV) demonstrated the presen
127 ons previously vaccinated against Venezuelan equine encephalitis virus (VEEV) exhibited poor neutrali
128 teins of Sindbis virus (SINV) and Venezuelan equine encephalitis virus (VEEV) form cytoplasmic comple
129 encephalitis in humans caused by Venezuelan equine encephalitis virus (VEEV) from natural or aerosol
130 ate that the pathogenic strain of Venezuelan equine encephalitis virus (VEEV) has developed a unique
155 we have developed a noncytopathic Venezuelan equine encephalitis virus (VEEV) mutant that can persist
159 The infectious titer of WNV and Venezuelan equine encephalitis virus (VEEV) TC83 in the brains of A
160 of the attenuated TC-83 strain of Venezuelan equine encephalitis virus (VEEV) to investigate the impa
162 attachment and entry receptor for Venezuelan equine encephalitis virus (VEEV)(1), a New World alphavi
163 Murine infection with wild-type Venezuelan equine encephalitis virus (VEEV), a highly myeloid-cell-
168 d it using an in vivo system with Venezuelan equine encephalitis virus (VEEV), an emerging alphavirus
169 ins drive the assembly of vRCs of Venezuelan equine encephalitis virus (VEEV), and G3BPs were shown t
170 , Rift Valley fever virus (RVFV), Venezuelan equine encephalitis virus (VEEV), and herpes simplex vir
171 ppress replication of SARS-CoV-2, Venezuelan equine encephalitis virus (VEEV), and other emerging vir
173 IMPORTANCE RNA viruses, including Venezuelan equine encephalitis virus (VEEV), have high mutation rat
174 ocess of one of the alphaviruses, Venezuelan equine encephalitis virus (VEEV), to understand its adap
175 se severe encephalitis in humans: Venezuelan equine encephalitis virus (VEEV), western equine encepha
176 potential vaccine candidates for Venezuelan equine encephalitis virus (VEEV), western equine encepha
177 eat infection with the alphavirus Venezuelan equine encephalitis virus (VEEV), which causes flu-like
178 ics are currently unavailable for Venezuelan equine encephalitis virus (VEEV), which elicits flu-like
180 emonstrate that Tc bovine-derived Venezuelan equine encephalitis virus (VEEV)-specific TcPAbs are hig
186 rotropic alphaviruses, which include western equine encephalitis virus (WEEV) and Fort Morgan virus,
187 quine encephalitis virus (EEEV), and western equine encephalitis virus (WEEV) are arthropod-borne pos
188 events that led to the formation of western equine encephalitis virus (WEEV) from SINV- and EEEV-lik
190 nst neurotropic alphaviruses such as western equine encephalitis virus (WEEV) in cultured cells.
195 an equine encephalitis virus (VEEV), western equine encephalitis virus (WEEV), and eastern equine enc
196 an equine encephalitis virus (VEEV), western equine encephalitis virus (WEEV), or eastern equine ence
200 uration utilized group-reactive MAbs eastern equine encephalitis virus 1A4B-6, dengue 2 virus 4G2, an
201 o pathogenic mosquito-borne viruses (Eastern equine encephalitis virus [EEEV], Western equine encepha
202 ition for alphaviruses (ranging from Eastern equine encephalitis virus [EEEV]-specific to alphavirus
203 VEE/SIN alphavirus (derived from Venezuelan equine encephalitis virus [VEE] and the Sindbis virus [S
204 equine encephalitis virus [WEEV], Venezuelan equine encephalitis virus [VEEV], and Chikungunya virus
205 rn equine encephalitis virus [EEEV], Western equine encephalitis virus [WEEV], Venezuelan equine ence
206 E1 fusion loop of Mayaro virus or Venezuelan equine encephalitis virus also resulted in poorly infect
207 r atomic resolution structures of Venezuelan equine encephalitis virus and dengue virus revealed tran
208 st Nile virus, chikungunya virus, Venezuelan equine encephalitis virus and human immunodeficiency vir
212 ins (E2-E1) of Semliki forest virus, eastern equine encephalitis virus and Sindbis virus interact wit
213 er encephalitic arboviruses, such as eastern equine encephalitis virus and West Nile virus, underscor
214 CV core protein and a recombinant Venezuelan equine encephalitis virus capsid protein for HCV IRES-co
215 very amino-terminal subdomain of Venezuelan equine encephalitis virus capsid protein, SD1, plays a c
217 EEV), Madariaga virus (MADV), and Venezuelan equine encephalitis virus complex (VEEV) are New World a
218 IXV) is an enzootic member of the Venezuelan Equine Encephalitis Virus complex and belongs to the New
222 iruses including West Nile virus and Eastern equine encephalitis virus has been detected in wild Atla
223 of the mosquito-borne North American eastern equine encephalitis virus in myeloid-lineage cells by bi
225 ase (PARP) family in clearance of Venezuelan equine encephalitis virus mutants from infected cells.
226 tly, the structure determined for Venezuelan equine encephalitis virus nsP2 indicated the presence of
228 g the EEEV template RNA with EEEV or Western equine encephalitis virus prominently activated expressi
229 tion signal from a nonpropagating Venezuelan equine encephalitis virus replicon particle (VRP) delive
230 a virus-vectored vaccine (Kp47/47-Venezuelan equine encephalitis virus replicon particle) for safety,
231 at can be boosted using HPV16E6E7-Venezuelan equine encephalitis virus replicon particles (HPV16-VRP)
232 opagating vaccine vector based on Venezuelan equine encephalitis virus replicon particles (VRP) expre
233 ) vaccine based on nonpropagating Venezuelan equine encephalitis virus replicon particles (VRP) was t
234 such system, footpad delivery of Venezuelan equine encephalitis virus replicon particles (VRP), led
235 aces after parenteral delivery of Venezuelan equine encephalitis virus replicon particles (VRP).
236 apsid protein was expressed using Venezuelan equine encephalitis virus replicon particles (VRP-NV1).
237 Previously, immunization with Venezuelan equine encephalitis virus replicon particles (VRPs) demo
239 ve evaluated the potential use of Venezuelan equine encephalitis virus replicon particles (VRPs) for
240 f mononuclear cells in vitro with Venezuelan equine encephalitis virus replicon particles (VRPs) resu
241 developed a cell-based assay with a western equine encephalitis virus replicon that expresses a luci
242 Using synthetic genomics and Venezuelan equine encephalitis virus replicons (VRPs) expressing sp
243 proteins expressed from packaged Venezuelan equine encephalitis virus replicons elicited protective
245 that C57BL/6 mice vaccinated with Venezuelan equine encephalitis virus replicons encoding the Ebola v
246 rom mice inoculated with packaged Venezuelan equine encephalitis virus replicons expressing NV VLPs,
249 res, especially against CHIKV and Venezuelan equine encephalitis virus that are major threats, has in
250 pagating, truncated derivative of Venezuelan equine encephalitis virus that targets dendritic cells (
251 ously received an investigational Venezuelan equine encephalitis virus vaccine (previous alphavirus v
253 n coronavirus 229E), Togaviridae (Venezuelan equine encephalitis virus), and Hepeviridae (HEV), indic
254 nly one other NT human arbovirus (Venezuelan equine encephalitis virus), which is also poorly underst
256 ing primary mosquito infection by Venezuelan equine encephalitis virus, an arbovirus causing neurolog
257 ng sequence of a related alphavirus, western equine encephalitis virus, and also by an unrelated sequ
258 tates binding and infection of EEEV, Western equine encephalitis virus, and Semliki Forest virus.
259 arations of bacteriophage lambda, Venezuelan equine encephalitis virus, and Staphylococcus aureus dur
260 lethal alphavirus infection with Venezuelan equine encephalitis virus, and this was associated with
261 he alphaviruses Sindbis virus and Venezuelan equine encephalitis virus, as well as La Crosse bunyavir
262 e virus, Jamestown Canyon virus, and eastern equine encephalitis virus, as well as the tick-borne Pow
263 gly, SKT05 protected mice against Venezuelan equine encephalitis virus, chikungunya virus, and Ross R
264 ellow fever virus, Sindbis virus, Venezuelan equine encephalitis virus, measles virus, influenza A vi
265 y syncytial virus, alphavirus and Venezuelan equine encephalitis virus, norovirus, metapneumovirus, y
266 tenuated strain of the alphavirus Venezuelan equine encephalitis virus, to produce virus-like replico
267 mixture of western, eastern, and Venezuelan equine encephalitis virus-like particles (VLPs), a regim
268 s, cDNA delivered by gene gun and Venezuelan equine encephalitis virus-like replicon particles (VRP),
277 genetic comparison of SA EEEV and Venezuelan equine encephalitis viruses (VEEV) demonstrated similar
278 Epizootic subtype IAB and IC Venezuelan equine encephalitis viruses (VEEV) readily infect the ep
280 bis, Chikungunya, and eastern and Venezuelan equine encephalitis viruses and demonstrate that a small
281 n (VEEV), Eastern (EEEV), and Western (WEEV) equine encephalitis viruses are mosquito-transmitted alp
283 ses such as western, eastern, and Venezuelan equine encephalitis viruses cause serious and potentiall
284 cles derived from the Sindbis and Venezuelan equine encephalitis viruses encoding either the HCV enve
285 halitic alphaviruses (eastern and Venezuelan equine encephalitis viruses) based upon either fusion of
286 , including western, eastern, and Venezuelan equine encephalitis viruses, cause serious and potential
287 nezuelan (VEEV), eastern (EEEV), and western equine encephalitis viruses, constitute a continuing pub
289 astern equine encephalitis (EEE) and western equine encephalitis (WEE) viral RNAs from samples collec
290 8 can act as a receptor for Sindbis, western equine encephalitis (WEEV), and related alphaviruses wit
291 developed a combined vaccine for Venezuelan equine encephalitis, western equine encephalitis, and ea
292 lenge with the viruses that cause Venezuelan equine encephalitis, western equine encephalitis, and ea