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1 mented the antiviral effects of IFN1 against vesicular stomatitis and hepatitis C viruses in human ce
2 ainst Ebola and Lassa fever VLPs, as well as vesicular stomatitis and rabies viruses (VSV and RABV, r
3 including influenza A, Zika, Ebola, Sindbis, vesicular stomatitis, cowpox, and vaccinia, but not muri
4 se surrogate systems such as the rhabdovirus vesicular stomatitis Indiana virus (VSV), lentiviruses o
7 IDLVs pseudotyped with different envelopes (vesicular stomatitis, Rabies, Mokola and Ross River vira
10 Recently, we demonstrated that recombinant vesicular stomatitis virus (rVSV) expressing human NoV c
11 ough not licensed for human use, recombinant vesicular stomatitis virus (rVSV) expressing the filovir
13 development is a system based on recombinant vesicular stomatitis virus (rVSV) that expresses a singl
14 onstrated clinical efficacy of a recombinant vesicular stomatitis virus (rVSV) vaccine vector has sti
15 athology after immunization with recombinant vesicular stomatitis virus (rVSV) vaccine vectors, and i
17 icacy testing of live attenuated recombinant vesicular stomatitis virus (rVSV)-based filovirus vaccin
18 tenuated, replication-competent, recombinant vesicular stomatitis virus (rVSV)-based vaccine candidat
20 approaches is a first-generation recombinant vesicular stomatitis virus (rVSV)-based vaccine expressi
23 In this study, we constructed a recombinant vesicular stomatitis virus (rVSV-VP1) expressing VP1, th
24 EBOV, a replicating, attenuated, recombinant vesicular stomatitis virus (serotype Indiana) whose surf
26 ed vaccine vectors based on live recombinant vesicular stomatitis virus (VSV) and a Semliki Forest vi
27 at intermediate pH for two vesiculoviruses, vesicular stomatitis virus (VSV) and Chandipura virus (C
28 Here we report that two other RNA viruses, vesicular stomatitis virus (VSV) and encephalomyocarditi
29 n of herpes simplex virus type 1 (HSV-1) and vesicular stomatitis virus (VSV) and impaired the replic
30 f green fluorescent protein (GFP)-expressing vesicular stomatitis virus (VSV) and its oncolytically e
31 ve immune functions following infection with vesicular stomatitis virus (VSV) and lymphocytic choriom
32 The active template for RNA synthesis for vesicular stomatitis virus (VSV) and other negative-stra
33 nctional L protein of rhabdoviruses, such as vesicular stomatitis virus (VSV) and rabies virus, catal
35 d infections with enveloped viruses, such as Vesicular Stomatitis Virus (VSV) and Respiratory Syncyti
36 that two RNA viruses with broad host ranges, vesicular stomatitis virus (VSV) and Sindbis virus (SINV
37 h available experimental data on the DMFE of Vesicular stomatitis virus (VSV) and Tobacco etch virus
39 ers, which have been employed here to purify vesicular stomatitis virus (VSV) as a model case, howeve
40 y show the specific detection of pseudotyped vesicular stomatitis virus (VSV) as a model virus on SP-
42 e, we describe such a strategy that utilizes vesicular stomatitis virus (VSV) as a vector for chimeri
43 re we demonstrate that mumps virus (MuV) and vesicular stomatitis virus (VSV) assemble to include CD4
45 g ligands can be displayed on the surface of vesicular stomatitis virus (VSV) by engineering its glyc
48 ion of ACT with systemic administration of a vesicular stomatitis virus (VSV) engineered to express t
50 ralizing antibody titers, measured against a vesicular stomatitis virus (VSV) expressing EBGP or Delt
52 mental vaccine for CHIKV based on a chimeric vesicular stomatitis virus (VSV) expressing the entire C
53 oped a bivalent recombinant vaccine based on vesicular stomatitis virus (VSV) expressing the Zaire eb
55 ecotropic Moloney murine leukemia virus and vesicular stomatitis virus (VSV) G glycoproteins; and (i
56 le retroviral particles pseudotyped with the vesicular stomatitis virus (VSV) G protein with dextran-
61 ecause of its very low human seroprevalence, vesicular stomatitis virus (VSV) has promise as a system
64 ectious autonomously replicating recombinant vesicular stomatitis virus (VSV) in which the glycoprote
65 regions encompassing the appendage region of vesicular stomatitis virus (VSV) Indiana serotype L prot
66 tion of Gp78 results in a robust decrease of vesicular stomatitis virus (VSV) infection and a corresp
82 plication-defective vaccine vectors based on vesicular stomatitis virus (VSV) lacking its envelope gl
85 vaccines containing antigens from influenza, vesicular stomatitis virus (VSV) or human immunodeficien
86 n direct cell-to-cell transmission of either vesicular stomatitis virus (VSV) or the retrovirus MoMLV
87 cellular proteins from cells expressing the vesicular stomatitis virus (VSV) P protein identified th
91 entry, 49 constructs were incorporated onto vesicular stomatitis virus (VSV) pseudoparticles and tra
93 adult flies; loss of Toll-7 led to increased vesicular stomatitis virus (VSV) replication and mortali
94 rticle RNA in HEK293 cells stably expressing vesicular stomatitis virus (VSV) replication proteins po
97 stimulated genes within the brain.IMPORTANCE Vesicular stomatitis virus (VSV) shows considerable prom
98 s (MoMLV) spread, and only minimally affects vesicular stomatitis virus (VSV) spread, to adjacent cel
99 In this study, we have engineered a chimeric vesicular stomatitis virus (VSV) that is devoid of its n
100 study, we developed a recombinant strain of vesicular stomatitis virus (VSV) that specifically targe
102 with miRNA inhibitors in cells infected with vesicular stomatitis virus (VSV) to identify miRNAs that
103 zed the ability of a vaccine vector based on vesicular stomatitis virus (VSV) to induce a neutralizin
104 didate that utilizes a replication-defective vesicular stomatitis virus (VSV) vector backbone that la
105 nfluenza vaccine that utilizes an attenuated vesicular stomatitis virus (VSV) vector, to deliver and
107 rements in a simplified system, we generated vesicular stomatitis virus (VSV) virions pseudotyped wit
109 In this work, we developed a pseudotyped vesicular stomatitis virus (VSV) with a glycoprotein of
110 ation method is demonstrated on an RNA-based vesicular stomatitis virus (VSV) with oncolytic properti
113 l proteins potently inhibit the infection of vesicular stomatitis virus (VSV), a prototype member of
121 K-deficient MEFs exhibit impaired control of vesicular stomatitis virus (VSV), a virus sensed by STIN
122 ruses, encephalomyocarditis virus (EMCV) and vesicular stomatitis virus (VSV), activate the NLRP3 inf
123 ly used to pseudotype glycoprotein-deficient vesicular stomatitis virus (VSV), allowing studies of BA
124 this observation, we engineered a strain of vesicular stomatitis virus (VSV), an oncolytic rhabdovir
125 activity of these ISGs against an RNA virus, vesicular stomatitis virus (VSV), and a DNA virus, murin
126 Here, we took a promising oncolytic virus, vesicular stomatitis virus (VSV), and tested the hypothe
127 xpressed using the highly immunogenic vector vesicular stomatitis virus (VSV), cured mice with establ
128 ombinant rabies virus (RABV) and recombinant vesicular stomatitis virus (VSV), expressing either the
129 binant rhabdoviral vectors, rabies virus and vesicular stomatitis virus (VSV), expressing wild-type o
130 ced the replication of a heterologous virus, vesicular stomatitis virus (VSV), in a SOCS1-dependent m
131 RNA of negative-strand RNA viruses, such as vesicular stomatitis virus (VSV), is completely enwrappe
134 ted DNA aptamers against an oncolytic virus, vesicular stomatitis virus (VSV), to protect it from nAb
136 RdRP with those of the related rhabdovirus, vesicular stomatitis virus (VSV), we demonstrate that bo
137 cell lines and primary fibroblasts with the vesicular stomatitis virus (VSV), we detected DNA comple
140 reporter strain of the negative-sense ssRNA vesicular stomatitis virus (VSV), we show that microinje
141 pplication of a novel viral tracer, based on vesicular stomatitis virus (VSV), which directs retrogra
148 antibody repertoire after administration of vesicular stomatitis virus (VSV)-Ebola vaccine at 3 mill
151 a neutralization titer of > or =1:20 against vesicular stomatitis virus (VSV)-HCV pseudotype, 15 of 3
153 -like helicase (RLH) signaling contribute to vesicular stomatitis virus (VSV)-mediated triggering of
154 ue of Blood, Shen et al demonstrate that the vesicular stomatitis virus (VSV)-murine interferon beta
168 results suggested a higher neutralization of vesicular stomatitis virus (VSV)/HCV E1-G pseudotype inf
169 ite-directed mutagenesis of the L protein of vesicular stomatitis virus (VSV, a prototypic NNS RNA vi
170 hanisms by which the transmembrane domain of vesicular stomatitis virus (VSV-TMD) promotes both initi
172 se in early endosomes (SFV, SINV, CHIKV, and vesicular stomatitis virus [VSV]), while viruses that fu
175 n response to infection with the RNA viruses vesicular stomatitis virus and Sendai virus and to trans
176 ved from viral infections with influenza and vesicular stomatitis virus can persist after resolution
177 al RNA-dependent RNA polymerase L protein of vesicular stomatitis virus catalyzes unconventional pre-
180 mal human glia, fibroblasts, or melanocytes, vesicular stomatitis virus evoked robust beta interferon
181 th rVSVDeltaG*/BDVG, a cytolytic recombinant vesicular stomatitis virus expressing BDV G that mimics
182 in lungs following intranasal infection with vesicular stomatitis virus expressing OVA and influenza
183 ne of those vaccines is based on recombinant vesicular stomatitis virus expressing the EBOV glycoprot
184 ression plasmid followed by infection with a vesicular stomatitis virus expressing the Zaire ebolavir
185 these MAbs to protect from infection with a vesicular stomatitis virus expressing the Zaire ebolavir
186 remaining fully susceptible to X4-tropic and vesicular stomatitis virus G (VSV-G)-pseudotyped viruses
187 pon infection of the Jurkat T-cell line with vesicular stomatitis virus G glycoprotein (VSV-G)-pseudo
188 F) but, surprisingly, not the trafficking of vesicular stomatitis virus G protein (VSV-G) to the cell
189 T cells are resistant to both HIV R5 env and vesicular stomatitis virus G protein (VSV-G)-mediated fu
191 ination with virus-like particles displaying vesicular stomatitis virus G protein, RNAdjuvant promote
192 ola virus-like particles (VLPs) that express vesicular stomatitis virus G, wild-type EBOV GP (EBGP),
193 gradation of SAMHD1 does not rescue HIV-1 or vesicular stomatitis virus G-pseudotyped lentivectors in
194 hen an alphavirus RNA replicon expresses the vesicular stomatitis virus glycoprotein (VSV G) as the o
195 Forest virus RNA replicons that express the vesicular stomatitis virus glycoprotein (VSV G) has been
197 hy, we found that augmenting fusion with the vesicular stomatitis virus glycoprotein (VSVG) increased
198 rved with HIV-1 virions pseudotyped with the vesicular stomatitis virus glycoprotein or with the amph
200 uction enhancement with LVs pseudotyped with vesicular stomatitis virus glycoproteins and also with m
203 tent antiviral protection against Sendai and vesicular stomatitis virus in a TLR3 and type I IFN rece
204 In previous work, a prototypic recombinant vesicular stomatitis virus Indiana serotype (rVSIV) vect
205 wth inhibition, prolonged protection against vesicular stomatitis virus infection and enhanced transc
206 defect early after Listeria monocytogenes or vesicular stomatitis virus infection but comparable cyto
208 e switched Ig in response to immunization or vesicular stomatitis virus infection is strongly impaire
210 Furthermore, SLEC differentiation during vesicular stomatitis virus infection was enhanced by adm
211 with apoptotic triggers such as etoposide or vesicular stomatitis virus infection, but disassemble in
212 osynthetic inhibition during influenza A and vesicular stomatitis virus infection, but not murine hep
219 nfections with encephalomyocarditis virus or vesicular stomatitis virus led to higher levels of autop
220 inhibition also occurred in the presence of vesicular stomatitis virus M (matrix) protein, another v
221 mRNA export factors that are targeted by the vesicular stomatitis virus matrix protein to inhibit hos
223 action results were transiently positive for vesicular stomatitis virus nucleoprotein gene and Ebola
224 atic MAVS; challenge of transgenic mice with vesicular stomatitis virus or a synthetic HCV genome ind
225 of TRIM56 did not inhibit the replication of vesicular stomatitis virus or hepatitis C virus, a virus
226 trovirus particles but not HIV-1-pseudotyped vesicular stomatitis virus particles, and E2 Abs immune-
228 and no impact on antibody neutralization of vesicular stomatitis virus pseudotyped with Ebola virus
230 ion conferred by an EBOV vaccine composed of vesicular stomatitis virus pseudovirions that lack nativ
231 esis and shows reduced capability to control vesicular stomatitis virus replication and to induce apo
232 study, we found Newcastle disease virus and vesicular stomatitis virus replication is enhanced in mo
235 ession of HAP2 on the surface of pseudotyped vesicular stomatitis virus results in homotypic virus-ce
236 proteins from La Crosse orthobunyavirus and vesicular stomatitis virus reveal insights into RNA synt
237 lescents and 35% of children had recombinant vesicular stomatitis virus RNA detectable in saliva.
240 RS-S) but not that of HIV-1 pseudotyped with vesicular stomatitis virus surface glycoprotein G (VSV-G
241 cipitated HIV-1 gag particles containing the vesicular stomatitis virus type G envelope, HIV-1 envelo
242 3 vaccine (ChAd3-EBO-Z) and the recombinant vesicular stomatitis virus vaccine (rVSVG-ZEBOV-GP) in L
243 otective efficacy of a bivalent, recombinant vesicular stomatitis virus vaccine expressing both the A
246 sed by two TLR3-dependent viruses (HSV-1 and vesicular stomatitis virus) were high in fibroblasts fro
247 constructs involving viral vectors (such as vesicular stomatitis virus), and antisense compounds dir
248 iruses A and B, Newcastle disease virus, and vesicular stomatitis virus), positive-sense RNA viruses
250 In this article, we study the polymerase of vesicular stomatitis virus, a member of the rhabdoviruse
251 he RNA-dependent RNA polymerase L protein of vesicular stomatitis virus, a prototype of nonsegmented
253 nd challenged the animals with a recombinant vesicular stomatitis virus, a synthetic HCV genome, IFN
254 d vaccinia virus Ankara, complex adenovirus, vesicular stomatitis virus, alphavirus-based chimeras, a
256 ruses, including encephalomyocarditis virus, vesicular stomatitis virus, and influenza virus, in susc
257 ent viruses, such as oncolytic adenoviruses, vesicular stomatitis virus, and picornaviruses as well a
259 ot-and-mouth disease virus, two serotypes of vesicular stomatitis virus, bluetongue virus, and bovine
260 by arboviruses, including Sindbis virus and vesicular stomatitis virus, but this innate restriction
261 d RNA virus, including influenza A virus and vesicular stomatitis virus, by a mechanism independent o
262 source antigens are expressed by vaccinia or vesicular stomatitis virus, either as proteasome-liberat
263 measles virus, influenza A virus, reovirus, vesicular stomatitis virus, human immunodeficiency virus
264 ction as an entry inhibitor for JUNV and for vesicular stomatitis virus, lymphocytic choriomeningitis
265 tu formation of dsRNA in cells infected with vesicular stomatitis virus, measles virus, influenza A v
266 s, env-minus viruses pseudotyped with HIV-1, vesicular stomatitis virus, or murine leukemia virus Env
267 dary challenges with Listeria monocytogenes, vesicular stomatitis virus, or Vaccinia virus, but dispe
268 sponses than UV-inactivated cytomegalovirus, vesicular stomatitis virus, reovirus, or adenovirus.
269 otype nonsegmented negative-sense RNA virus, vesicular stomatitis virus, suggest a role for P beyond
271 starting with poliovirus and then moving to vesicular stomatitis virus, where he discovered a virion
272 EBOV is a recombinant, replication competent vesicular stomatitis virus-based candidate vaccine expre
273 laque-forming units (pfu) of the recombinant vesicular stomatitis virus-based candidate vaccine expre
275 observed in phase 1 studies of a recombinant vesicular stomatitis virus-based vaccine expressing a ZE
277 ADAM15 expression enhanced rhinovirus 16 and vesicular stomatitis virus-mediated proinflammatory cyto
278 on virus entry or coreceptor expression, as vesicular stomatitis virus-pseudotyped HIV-1 replication
281 2503202) evaluated the safety of recombinant vesicular stomatitis virus-Zaire Ebola virus envelope gl
282 safety and immunogenicity of the recombinant vesicular stomatitis virus-Zaire Ebola virus envelope gl
298 eins via replication incompetent recombinant vesicular stomatitis viruses (VSVs) and human adenovirus
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