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1 is observed after intranasal challenge with vesicular stomatitis virus.
2 PPRV were able to neutralize RPV-pseudotyped vesicular stomatitis virus.
3 a and IFN-beta, in protection from oncolytic vesicular stomatitis virus.
4 of H1N1, H6N2, and H11N9 IAV strains but not vesicular stomatitis virus.
5 reovirus, HIV-1, human metapneumovirus, and vesicular stomatitis virus.
6 ecting mice from neuropathogenesis caused by vesicular stomatitis virus.
7 ring infection by Listeria monocytogenes and vesicular stomatitis virus.
8 otection from death after CNS infection with vesicular stomatitis virus.
9 vels of RIG-I and resistance to infection by vesicular stomatitis virus.
10 the pseudotypes bearing the glycoprotein of vesicular stomatitis virus.
11 rovide an advantage for host defense against vesicular stomatitis virus.
12 d infectivity assays with BCoV-S-pseudotyped vesicular stomatitis viruses.
13 In this article, we study the polymerase of vesicular stomatitis virus, a member of the rhabdoviruse
15 d vaccinia virus Ankara, complex adenovirus, vesicular stomatitis virus, alphavirus-based chimeras, a
18 n response to infection with the RNA viruses vesicular stomatitis virus and Sendai virus and to trans
19 constructs involving viral vectors (such as vesicular stomatitis virus), and antisense compounds dir
20 ruses, including encephalomyocarditis virus, vesicular stomatitis virus, and influenza virus, in susc
21 rabies virus) and heterologous (inactivated vesicular stomatitis virus) antigens and acceptable accu
24 EBOV is a recombinant, replication competent vesicular stomatitis virus-based candidate vaccine expre
25 laque-forming units (pfu) of the recombinant vesicular stomatitis virus-based candidate vaccine expre
28 observed in phase 1 studies of a recombinant vesicular stomatitis virus-based vaccine expressing a ZE
30 by arboviruses, including Sindbis virus and vesicular stomatitis virus, but this innate restriction
31 d RNA virus, including influenza A virus and vesicular stomatitis virus, by a mechanism independent o
32 ved from viral infections with influenza and vesicular stomatitis virus can persist after resolution
33 al RNA-dependent RNA polymerase L protein of vesicular stomatitis virus catalyzes unconventional pre-
35 source antigens are expressed by vaccinia or vesicular stomatitis virus, either as proteasome-liberat
38 pressing influenza, measles, Ebola, Lassa or vesicular stomatitis virus envelope glycoproteins enable
39 mal human glia, fibroblasts, or melanocytes, vesicular stomatitis virus evoked robust beta interferon
40 tion activity in vitro against a recombinant vesicular stomatitis virus expressing MACV GPC (VSV-MACV
41 in lungs following intranasal infection with vesicular stomatitis virus expressing OVA and influenza
42 ne of those vaccines is based on recombinant vesicular stomatitis virus expressing the EBOV glycoprot
43 ression plasmid followed by infection with a vesicular stomatitis virus expressing the Zaire ebolavir
44 these MAbs to protect from infection with a vesicular stomatitis virus expressing the Zaire ebolavir
45 remaining fully susceptible to X4-tropic and vesicular stomatitis virus G (VSV-G)-pseudotyped viruses
46 transfected secretory membrane glycoprotein, vesicular stomatitis virus G (VSVG) glycoprotein, was re
48 pon infection of the Jurkat T-cell line with vesicular stomatitis virus G glycoprotein (VSV-G)-pseudo
49 F) but, surprisingly, not the trafficking of vesicular stomatitis virus G protein (VSV-G) to the cell
50 "Gectosomes," are designed to co-encapsulate vesicular stomatitis virus G protein (VSV-G) with bioact
52 ination with virus-like particles displaying vesicular stomatitis virus G protein, RNAdjuvant promote
53 gradation of SAMHD1 does not rescue HIV-1 or vesicular stomatitis virus G-pseudotyped lentivectors in
55 hen an alphavirus RNA replicon expresses the vesicular stomatitis virus glycoprotein (VSV G) as the o
56 Forest virus RNA replicons that express the vesicular stomatitis virus glycoprotein (VSV G) has been
58 hy, we found that augmenting fusion with the vesicular stomatitis virus glycoprotein (VSVG) increased
59 g human GBA to an exosome-anchoring protein: vesicular stomatitis virus glycoprotein (VSVG), we demon
60 related class III fusion proteins, including vesicular stomatitis virus glycoprotein G (VSV-G) or bac
62 uction enhancement with LVs pseudotyped with vesicular stomatitis virus glycoproteins and also with m
65 measles virus, influenza A virus, reovirus, vesicular stomatitis virus, human immunodeficiency virus
66 tent antiviral protection against Sendai and vesicular stomatitis virus in a TLR3 and type I IFN rece
68 In previous work, a prototypic recombinant vesicular stomatitis virus Indiana serotype (rVSIV) vect
69 vity of alpha interferon (IFN-alpha) against vesicular stomatitis virus, Indiana serotype (VSV(IND)),
70 wth inhibition, prolonged protection against vesicular stomatitis virus infection and enhanced transc
71 defect early after Listeria monocytogenes or vesicular stomatitis virus infection but comparable cyto
72 uster activates the IFN pathway and inhibits vesicular stomatitis virus infection by directly targeti
73 e switched Ig in response to immunization or vesicular stomatitis virus infection is strongly impaire
75 with apoptotic triggers such as etoposide or vesicular stomatitis virus infection, but disassemble in
76 osynthetic inhibition during influenza A and vesicular stomatitis virus infection, but not murine hep
81 nfections with encephalomyocarditis virus or vesicular stomatitis virus led to higher levels of autop
82 ction as an entry inhibitor for JUNV and for vesicular stomatitis virus, lymphocytic choriomeningitis
83 inhibition also occurred in the presence of vesicular stomatitis virus M (matrix) protein, another v
84 tu formation of dsRNA in cells infected with vesicular stomatitis virus, measles virus, influenza A v
85 ADAM15 expression enhanced rhinovirus 16 and vesicular stomatitis virus-mediated proinflammatory cyto
86 rms, methyltransferase-defective recombinant vesicular stomatitis virus (mtdVSV) and a DNA vaccine.
88 action results were transiently positive for vesicular stomatitis virus nucleoprotein gene and Ebola
89 s, env-minus viruses pseudotyped with HIV-1, vesicular stomatitis virus, or murine leukemia virus Env
90 dary challenges with Listeria monocytogenes, vesicular stomatitis virus, or Vaccinia virus, but dispe
92 and no impact on antibody neutralization of vesicular stomatitis virus pseudotyped with Ebola virus
93 on virus entry or coreceptor expression, as vesicular stomatitis virus-pseudotyped HIV-1 replication
96 ion conferred by an EBOV vaccine composed of vesicular stomatitis virus pseudovirions that lack nativ
97 sponses than UV-inactivated cytomegalovirus, vesicular stomatitis virus, reovirus, or adenovirus.
98 esis and shows reduced capability to control vesicular stomatitis virus replication and to induce apo
101 ession of HAP2 on the surface of pseudotyped vesicular stomatitis virus results in homotypic virus-ce
102 proteins from La Crosse orthobunyavirus and vesicular stomatitis virus reveal insights into RNA synt
103 lescents and 35% of children had recombinant vesicular stomatitis virus RNA detectable in saliva.
106 Recently, we demonstrated that recombinant vesicular stomatitis virus (rVSV) expressing human NoV c
107 ough not licensed for human use, recombinant vesicular stomatitis virus (rVSV) expressing the filovir
109 onstrated clinical efficacy of a recombinant vesicular stomatitis virus (rVSV) vaccine vector has sti
110 athology after immunization with recombinant vesicular stomatitis virus (rVSV) vaccine vectors, and i
111 ion of VesiculoVax that contains recombinant vesicular stomatitis virus (rVSV) vectors expressing fil
113 icacy testing of live attenuated recombinant vesicular stomatitis virus (rVSV)-based filovirus vaccin
114 tenuated, replication-competent, recombinant vesicular stomatitis virus (rVSV)-based vaccine candidat
116 approaches is a first-generation recombinant vesicular stomatitis virus (rVSV)-based vaccine expressi
118 immunostimulatory properties of recombinant vesicular stomatitis virus (rVSV)-based vaccines make th
120 neurotropic viruses, including rabies virus, vesicular stomatitis virus, Semliki Forest virus, and he
121 EBOV, a replicating, attenuated, recombinant vesicular stomatitis virus (serotype Indiana) whose surf
123 RS-S) but not that of HIV-1 pseudotyped with vesicular stomatitis virus surface glycoprotein G (VSV-G
124 3 vaccine (ChAd3-EBO-Z) and the recombinant vesicular stomatitis virus vaccine (rVSVG-ZEBOV-GP) in L
125 otective efficacy of a bivalent, recombinant vesicular stomatitis virus vaccine expressing both the A
131 een shown to induce G(2)/M arrest.IMPORTANCE Vesicular stomatitis virus (VSV) (a rhabdovirus) and its
133 t on the replication of the (-)ssRNA viruses vesicular stomatitis virus (VSV) (Rhabdoviridae family)
135 at intermediate pH for two vesiculoviruses, vesicular stomatitis virus (VSV) and Chandipura virus (C
136 n of herpes simplex virus type 1 (HSV-1) and vesicular stomatitis virus (VSV) and impaired the replic
137 ve immune functions following infection with vesicular stomatitis virus (VSV) and lymphocytic choriom
138 The active template for RNA synthesis for vesicular stomatitis virus (VSV) and other negative-stra
139 The L proteins of rhabdoviruses, such as vesicular stomatitis virus (VSV) and rabies virus (RABV)
140 nctional L protein of rhabdoviruses, such as vesicular stomatitis virus (VSV) and rabies virus, catal
142 d infections with enveloped viruses, such as Vesicular Stomatitis Virus (VSV) and Respiratory Syncyti
143 that two RNA viruses with broad host ranges, vesicular stomatitis virus (VSV) and Sindbis virus (SINV
144 h available experimental data on the DMFE of Vesicular stomatitis virus (VSV) and Tobacco etch virus
146 ers, which have been employed here to purify vesicular stomatitis virus (VSV) as a model case, howeve
147 y show the specific detection of pseudotyped vesicular stomatitis virus (VSV) as a model virus on SP-
149 e, we describe such a strategy that utilizes vesicular stomatitis virus (VSV) as a vector for chimeri
150 re we demonstrate that mumps virus (MuV) and vesicular stomatitis virus (VSV) assemble to include CD4
153 we generate a highly infectious recombinant vesicular stomatitis virus (VSV) bearing the SARS-CoV-2
154 g ligands can be displayed on the surface of vesicular stomatitis virus (VSV) by engineering its glyc
155 on content release and infection by chimeric vesicular stomatitis virus (VSV) containing the envelope
158 ion of ACT with systemic administration of a vesicular stomatitis virus (VSV) engineered to express t
160 iously, we developed a replication-competent vesicular stomatitis virus (VSV) expressing a modified f
162 of neurotropism, we asked whether a chimeric vesicular stomatitis virus (VSV) expressing the EBOV gly
164 mental vaccine for CHIKV based on a chimeric vesicular stomatitis virus (VSV) expressing the entire C
165 usly demonstrated that recombinant wild-type vesicular stomatitis virus (VSV) expressing the HBV midd
166 oV HKU5 expressing the SARS-CoV-1 spike, and vesicular stomatitis virus (VSV) expressing the SARS-CoV
167 ecotropic Moloney murine leukemia virus and vesicular stomatitis virus (VSV) G glycoproteins; and (i
168 le retroviral particles pseudotyped with the vesicular stomatitis virus (VSV) G protein with dextran-
173 ecause of its very low human seroprevalence, vesicular stomatitis virus (VSV) has promise as a system
176 ectious autonomously replicating recombinant vesicular stomatitis virus (VSV) in which the glycoprote
177 itis Indiana virus (VSIV), formerly known as vesicular stomatitis virus (VSV) Indiana (VSV(IND)), is
178 regions encompassing the appendage region of vesicular stomatitis virus (VSV) Indiana serotype L prot
179 tion of Gp78 results in a robust decrease of vesicular stomatitis virus (VSV) infection and a corresp
181 impaired IFN production in macrophages after vesicular stomatitis virus (VSV) infection, and HIPK2-de
194 polymerases since the first structure of the vesicular stomatitis virus (VSV) L protein determined in
199 obial molecule against infection with either vesicular stomatitis virus (VSV) or influenza was demons
200 n direct cell-to-cell transmission of either vesicular stomatitis virus (VSV) or the retrovirus MoMLV
206 entry, 49 constructs were incorporated onto vesicular stomatitis virus (VSV) pseudoparticles and tra
207 ent cell-to-cell fusion assays, and chimeric vesicular stomatitis virus (VSV) recombinants expressing
208 adult flies; loss of Toll-7 led to increased vesicular stomatitis virus (VSV) replication and mortali
211 stimulated genes within the brain.IMPORTANCE Vesicular stomatitis virus (VSV) shows considerable prom
212 s (MoMLV) spread, and only minimally affects vesicular stomatitis virus (VSV) spread, to adjacent cel
213 In this study, we have engineered a chimeric vesicular stomatitis virus (VSV) that is devoid of its n
214 study, we developed a recombinant strain of vesicular stomatitis virus (VSV) that specifically targe
216 with miRNA inhibitors in cells infected with vesicular stomatitis virus (VSV) to identify miRNAs that
217 an immunodeficiency virus type 1 (HIV-1) and vesicular stomatitis virus (VSV) to measure the neutrali
218 resses cytosolic poly(I:C), 5'ppp-dsRNA, and vesicular stomatitis virus (VSV) triggers IFN-I expressi
219 didate that utilizes a replication-defective vesicular stomatitis virus (VSV) vector backbone that la
220 nfluenza vaccine that utilizes an attenuated vesicular stomatitis virus (VSV) vector, to deliver and
222 rements in a simplified system, we generated vesicular stomatitis virus (VSV) virions pseudotyped wit
224 In this work, we developed a pseudotyped vesicular stomatitis virus (VSV) with a glycoprotein of
225 ation method is demonstrated on an RNA-based vesicular stomatitis virus (VSV) with oncolytic properti
226 e, three papers describe the pseudotyping of vesicular stomatitis virus (VSV) with the SARS-CoV-2 spi
227 the antiviral activity of interferon against vesicular stomatitis virus (VSV), a model virus that who
232 K-deficient MEFs exhibit impaired control of vesicular stomatitis virus (VSV), a virus sensed by STIN
233 ks with DNA, modified vaccinia Ankara (MVA), vesicular stomatitis virus (VSV), adenovirus type 5 (Ad5
234 ly used to pseudotype glycoprotein-deficient vesicular stomatitis virus (VSV), allowing studies of BA
235 this observation, we engineered a strain of vesicular stomatitis virus (VSV), an oncolytic rhabdovir
236 activity of these ISGs against an RNA virus, vesicular stomatitis virus (VSV), and a DNA virus, murin
237 ycoproteins of Ebola virus, influenza virus, vesicular stomatitis virus (VSV), and measles virus in G
238 Here, we took a promising oncolytic virus, vesicular stomatitis virus (VSV), and tested the hypothe
239 n immunodeficiency virus type-1 (HIV-1), and vesicular stomatitis virus (VSV), as well as a replicati
240 xpressed using the highly immunogenic vector vesicular stomatitis virus (VSV), cured mice with establ
241 infection limited the cytopathic effect from Vesicular stomatitis virus (VSV), Encephalomyocarditis v
242 ombinant rabies virus (RABV) and recombinant vesicular stomatitis virus (VSV), expressing either the
243 binant rhabdoviral vectors, rabies virus and vesicular stomatitis virus (VSV), expressing wild-type o
247 y, PGAM5 deficient MEFs, upon infection with vesicular stomatitis virus (VSV), revealed diminished IF
248 ted DNA aptamers against an oncolytic virus, vesicular stomatitis virus (VSV), to protect it from nAb
250 RdRP with those of the related rhabdovirus, vesicular stomatitis virus (VSV), we demonstrate that bo
251 cell lines and primary fibroblasts with the vesicular stomatitis virus (VSV), we detected DNA comple
252 prototype of NNS RNA virus gene expression, vesicular stomatitis virus (VSV), we determined the impo
255 reporter strain of the negative-sense ssRNA vesicular stomatitis virus (VSV), we show that microinje
256 pplication of a novel viral tracer, based on vesicular stomatitis virus (VSV), which directs retrogra
258 us (EBOV) crisis of 2013-2016, a recombinant vesicular stomatitis virus (VSV)-based EBOV vaccine was
260 binants carrying large transgenes.IMPORTANCE Vesicular stomatitis virus (VSV)-based oncolytic viruses
261 To address these limitations, we devised a vesicular stomatitis virus (VSV)-based probe to display
264 antibody repertoire after administration of vesicular stomatitis virus (VSV)-Ebola vaccine at 3 mill
268 -like helicase (RLH) signaling contribute to vesicular stomatitis virus (VSV)-mediated triggering of
269 ue of Blood, Shen et al demonstrate that the vesicular stomatitis virus (VSV)-murine interferon beta
282 ite-directed mutagenesis of the L protein of vesicular stomatitis virus (VSV, a prototypic NNS RNA vi
283 hanisms by which the transmembrane domain of vesicular stomatitis virus (VSV-TMD) promotes both initi
287 se in early endosomes (SFV, SINV, CHIKV, and vesicular stomatitis virus [VSV]), while viruses that fu
288 eins via replication incompetent recombinant vesicular stomatitis viruses (VSVs) and human adenovirus
291 sed by two TLR3-dependent viruses (HSV-1 and vesicular stomatitis virus) were high in fibroblasts fro
292 starting with poliovirus and then moving to vesicular stomatitis virus, where he discovered a virion
294 for rapid expanded access to the recombinant vesicular stomatitis virus-Zaire Ebola virus (rVSV-ZEBOV
296 2503202) evaluated the safety of recombinant vesicular stomatitis virus-Zaire Ebola virus envelope gl
297 , lot consistency, and safety of recombinant vesicular stomatitis virus-Zaire Ebola virus envelope gl
298 safety and immunogenicity of the recombinant vesicular stomatitis virus-Zaire Ebola virus envelope gl
299 for rapid expanded access to the recombinant vesicular stomatitis virus-Zaire Ebola virus vaccine (rV
300 uencing backed up the use of the recombinant vesicular stomatitis virus-Zaire Ebola virus vaccine in