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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
5       We studied the cytotoxic activity of a vesicular stomatitis/measles hybrid virus (VSV-FH), whic
6 oma cells to infection by Lassa, measles and vesicular stomatitis pseudoviruses.
7  IDLVs pseudotyped with different envelopes (vesicular stomatitis, Rabies, Mokola and Ross River vira
8  with transient detection of the recombinant vesicular stomatitis vaccine virus in blood.
9                    EPNs that incorporate the vesicular stomatitis viral glycoprotein can fuse with ta
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
12                      Previously, recombinant vesicular stomatitis virus (rVSV) pseudotypes expressing
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
16                                  Recombinant vesicular stomatitis virus (rVSV) was shown to be a high
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
19        The replication-competent recombinant vesicular stomatitis virus (rVSV)-based vaccine expressi
20 approaches is a first-generation recombinant vesicular stomatitis virus (rVSV)-based vaccine expressi
21                       Monovalent recombinant vesicular stomatitis virus (rVSV)-based vaccine vectors,
22                  With the use of recombinant vesicular stomatitis virus (rVSV)-based vaccines, guinea
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
25              This study focuses on oncolytic vesicular stomatitis virus (VSV) against pancreatic duct
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
34            The glycoproteins (G proteins) of vesicular stomatitis virus (VSV) and related rhabdovirus
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
38                    Oncolytic viruses such as vesicular stomatitis virus (VSV) are being considered as
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-
41                                        Using vesicular stomatitis virus (VSV) as a model, we coinfect
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
44                                              Vesicular stomatitis virus (VSV) assembly requires conde
45 g ligands can be displayed on the surface of vesicular stomatitis virus (VSV) by engineering its glyc
46                                  Recombinant vesicular stomatitis virus (VSV) encoding the hemaggluti
47                                   VSVFH is a vesicular stomatitis virus (VSV) encoding the MV-Edm F a
48 ion of ACT with systemic administration of a vesicular stomatitis virus (VSV) engineered to express t
49                                              Vesicular stomatitis virus (VSV) exhibits a remarkably r
50 ralizing antibody titers, measured against a vesicular stomatitis virus (VSV) expressing EBGP or Delt
51                 Experiments with recombinant vesicular stomatitis virus (VSV) expressing the EBOV Zai
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
54                  Here we describe the use of vesicular stomatitis virus (VSV) for tracing neuronal co
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-
57 y(C) binding protein 2 (PCBP2) downregulates vesicular stomatitis virus (VSV) gene expression.
58 ll interfering RNA (siRNA) screen to support vesicular stomatitis virus (VSV) growth.
59                                              Vesicular stomatitis virus (VSV) has been extensively st
60                               Replication of vesicular stomatitis virus (VSV) has long served as a mo
61 ecause of its very low human seroprevalence, vesicular stomatitis virus (VSV) has promise as a system
62                                              Vesicular stomatitis virus (VSV) has shown considerable
63                                              Vesicular stomatitis virus (VSV) has shown substantial p
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
67                                       During vesicular stomatitis virus (VSV) infection, pDC depletio
68 vely regulating the host IFN response during vesicular stomatitis virus (VSV) infection.
69 lso known as IFP35) as a factor required for vesicular stomatitis virus (VSV) infection.
70                                              Vesicular stomatitis virus (VSV) is a bullet-shaped rhab
71                                              Vesicular stomatitis virus (VSV) is a highly cytopathic
72                                              Vesicular stomatitis virus (VSV) is a potential oncolyti
73                                              Vesicular stomatitis virus (VSV) is a promising oncolyti
74                                              Vesicular stomatitis virus (VSV) is a promising oncolyti
75                                              Vesicular stomatitis virus (VSV) is a promising oncolyti
76                                  Recombinant vesicular stomatitis virus (VSV) is a promising therapeu
77                                              Vesicular stomatitis virus (VSV) is a prototype nonsegme
78                                              Vesicular stomatitis virus (VSV) is a rhabdovirus that a
79                                              Vesicular stomatitis virus (VSV) is potent and a highly
80                                              Vesicular stomatitis virus (VSV) is the prototype for ne
81 electron cryomicroscopy the structure of the vesicular stomatitis virus (VSV) L protein.
82 plication-defective vaccine vectors based on vesicular stomatitis virus (VSV) lacking its envelope gl
83                          The distribution of vesicular stomatitis virus (VSV) nucleocapsids in the cy
84                                          The vesicular stomatitis virus (VSV) nucleoprotein (N) assoc
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
88                                  Assembly of vesicular stomatitis virus (VSV) particles requires the
89                          Upon treatment with vesicular stomatitis virus (VSV) particles, plasmacytoid
90 diated degree of shielding and the amount of vesicular stomatitis virus (VSV) particles.
91  entry, 49 constructs were incorporated onto vesicular stomatitis virus (VSV) pseudoparticles and tra
92                      A luciferase-expressing vesicular stomatitis virus (VSV) pseudotype that contain
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
95 function by RNAi inhibited an early stage of vesicular stomatitis virus (VSV) replication.
96                                          The vesicular stomatitis virus (VSV) RNA-dependent RNA polym
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
101                           By engineering the vesicular stomatitis virus (VSV) to encode a fluorophore
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
106                                              Vesicular stomatitis virus (VSV) vectors that express he
107 rements in a simplified system, we generated vesicular stomatitis virus (VSV) virions pseudotyped wit
108                           VSV-FH is a hybrid vesicular stomatitis virus (VSV) with a deletion of its
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
111                                              Vesicular stomatitis virus (VSV), a negative-sense RNA v
112                                              Vesicular stomatitis virus (VSV), a negative-strand RNA
113 l proteins potently inhibit the infection of vesicular stomatitis virus (VSV), a prototype member of
114                                 Working with vesicular stomatitis virus (VSV), a prototype of NNS RNA
115                                              Vesicular stomatitis virus (VSV), a prototype of the Rha
116                                    Work with vesicular stomatitis virus (VSV), a prototype, supports
117                                        Using vesicular stomatitis virus (VSV), a prototypic NS RNA vi
118                          Here we show, using vesicular stomatitis virus (VSV), a relative of rabies v
119 aviviridae, but has no appreciable effect on vesicular stomatitis virus (VSV), a rhabdovirus.
120                                  We injected vesicular stomatitis virus (VSV), a transsynaptic tracer
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
132                      The virus studied here, vesicular stomatitis virus (VSV), like its relative, rab
133 al infection with influenza A virus (IAV) or vesicular stomatitis virus (VSV), respectively.
134 ted DNA aptamers against an oncolytic virus, vesicular stomatitis virus (VSV), to protect it from nAb
135                 Here, a prototype RNA virus, vesicular stomatitis virus (VSV), was cultured for three
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
138                                  By studying vesicular stomatitis virus (VSV), we identify the large
139                                 Working with vesicular stomatitis virus (VSV), we previously showed t
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
142       We previously generated an efficacious vesicular stomatitis virus (VSV)-based AIV vaccine expre
143                                  Recombinant vesicular stomatitis virus (VSV)-based chimeric viruses
144                In this study, we developed a vesicular stomatitis virus (VSV)-based human NoV vaccine
145                                      Using a vesicular stomatitis virus (VSV)-based pseudoparticle se
146                                        Here, vesicular stomatitis virus (VSV)-based pseudovirions dis
147                    We produced a recombinant vesicular stomatitis virus (VSV)-based vaccine vector ex
148  antibody repertoire after administration of vesicular stomatitis virus (VSV)-Ebola vaccine at 3 mill
149                     One of these vaccines is vesicular stomatitis virus (VSV)-EBOV, also known as rVS
150  not contain the larger cargoes, collagen or Vesicular stomatitis virus (VSV)-G glycoprotein.
151 a neutralization titer of > or =1:20 against vesicular stomatitis virus (VSV)-HCV pseudotype, 15 of 3
152                                       In the vesicular stomatitis virus (VSV)-induced encephalitis mo
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
155                   We developed a recombinant vesicular stomatitis virus (VSV)-SRV vaccine consisting
156 t cell targets for the matrix (M) protein of vesicular stomatitis virus (VSV).
157 NS RNA viruses comes largely from studies of vesicular stomatitis virus (VSV).
158 r pattern was observed for the IFN-sensitive vesicular stomatitis virus (VSV).
159 al infection by the neurotropic rhabdovirus, vesicular stomatitis virus (VSV).
160 and it inhibits the replication of HSV-1 and vesicular stomatitis virus (VSV).
161  cytopathic viruses, such as the neurotropic vesicular stomatitis virus (VSV).
162  domain of the unrelated glycoprotein (G) of vesicular stomatitis virus (VSV).
163 ensor and effector responses to intratumoral vesicular stomatitis virus (VSV).
164 ve and cells that are resistant to oncolytic vesicular stomatitis virus (VSV).
165 h influenza virus, West Nile virus (WNV), or vesicular stomatitis virus (VSV).
166 ll carcinoma (HNSCC) lines from oncolysis by vesicular stomatitis virus (VSV).
167 mouse model of prostate cancer infected with vesicular stomatitis virus (VSV).
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
171                  Here we show that both RNA (vesicular stomatitis virus [VSV]) and DNA (cytomegalovir
172 se in early endosomes (SFV, SINV, CHIKV, and vesicular stomatitis virus [VSV]), while viruses that fu
173                                              Vesicular stomatitis virus and influenza A virus infecti
174 een after infection of IL-21R(-/-) mice with vesicular stomatitis virus and influenza virus.
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-
178                          Using a recombinant vesicular stomatitis virus containing LUJV GP as its sol
179                   We generated a recombinant vesicular stomatitis virus encoding Ebola virus Makona v
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
190            By contrast, secretory traffic of vesicular stomatitis virus G protein, recycling of inter
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
196                                              Vesicular stomatitis virus glycoprotein (VSV-G)-pseudoty
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
199 le-cycle RV complemented with a heterologous vesicular stomatitis virus glycoprotein.
200 uction enhancement with LVs pseudotyped with vesicular stomatitis virus glycoproteins and also with m
201 stricted to retroviruses, as it also acts on vesicular stomatitis virus glycoproteins.
202                                              Vesicular stomatitis virus has been shown to bud basolat
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
207         CD8(+) T cell differentiation during vesicular stomatitis virus infection differed significan
208 e switched Ig in response to immunization or vesicular stomatitis virus infection is strongly impaire
209 ce in lymphocytic choriomeningitis virus and vesicular stomatitis virus infection models.
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
213                          Using an intranasal vesicular stomatitis virus infection, we demonstrated th
214 ation and to induce apoptosis in response to vesicular stomatitis virus infection.
215 xpression for EmGFP/IL-15 upregulation after vesicular stomatitis virus infection.
216 efractory to herpes simplex virus type 1 and vesicular stomatitis virus infection.
217 knockdown of tlr13 are highly susceptible to vesicular stomatitis virus infection.
218                         Here, we define that vesicular stomatitis virus L initiates synthesis via a d
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
222 es a rational approach to the attenuation of vesicular stomatitis virus neurovirulence.
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-
227                     Among vaccines, only the vesicular stomatitis virus platform has been successful
228  and no impact on antibody neutralization of vesicular stomatitis virus pseudotyped with Ebola virus
229                                        Using vesicular stomatitis virus pseudovirions bearing EBOV gl
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
233  by IFN in both glioma and melanoma, whereas vesicular stomatitis virus replication was blocked.
234 d-induced interferon production and enhanced vesicular stomatitis virus replication.
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.
238                                 Reovirus and vesicular stomatitis virus single-cycle yields were comp
239                 We have used a collection of vesicular stomatitis virus strains that had been evolvin
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
244 cell lines to infection by the nonretrovirus vesicular stomatitis virus were indistinguishable.
245 whereas other RNA viruses (Sindbis virus and vesicular stomatitis virus) are not.
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
249 ve to the cytoplasmic replicating virus VSV (vesicular stomatitis virus).
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
252                                              Vesicular stomatitis virus, a single-stranded RNA virus,
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
255 enveloped viruses (e.g., HIV, herpesviruses, vesicular stomatitis virus, and influenza virus).
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
258 gion I) of the L protein from a rhabdovirus, vesicular stomatitis virus, at 1.8-A resolution.
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
270                   Remarkably, infection with vesicular stomatitis virus, vaccinia virus, and a variet
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
274         A recombinant, replication-competent vesicular stomatitis virus-based vaccine expressing a su
275 observed in phase 1 studies of a recombinant vesicular stomatitis virus-based vaccine expressing a ZE
276 32gamma protected epithelial WISH cells from vesicular stomatitis virus-induced cell death.
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
279                          The live attenuated vesicular stomatitis virus-vectored Ebola vaccine rVSV-Z
280         The results highlight the ability of vesicular stomatitis virus-vectored vaccines to rapidly
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
283 a and IFN-beta, in protection from oncolytic vesicular stomatitis virus.
284 of H1N1, H6N2, and H11N9 IAV strains but not vesicular stomatitis virus.
285 ecting mice from neuropathogenesis caused by vesicular stomatitis virus.
286 ring infection by Listeria monocytogenes and vesicular stomatitis virus.
287 otection from death after CNS infection with vesicular stomatitis virus.
288 vels of RIG-I and resistance to infection by vesicular stomatitis virus.
289  the pseudotypes bearing the glycoprotein of vesicular stomatitis virus.
290 rovide an advantage for host defense against vesicular stomatitis virus.
291 n with lymphocytic choriomeningitis virus or vesicular stomatitis virus.
292  ligands but instead respond specifically to vesicular stomatitis virus.
293  is observed after intranasal challenge with vesicular stomatitis virus.
294 PPRV were able to neutralize RPV-pseudotyped vesicular stomatitis virus.
295                            These trials used vesicular-stomatitis-virus-G protein (VSV-G)-LVs at high
296                                  Recombinant vesicular stomatitis viruses (VSV) are excellent candida
297           Here we test replication-competent vesicular stomatitis viruses (VSV) on 19 primary human m
298 eins via replication incompetent recombinant vesicular stomatitis viruses (VSVs) and human adenovirus
299                                              Vesicular stomatitis viruses (VSVs) containing wild-type
300                  We are developing oncolytic vesicular stomatitis viruses (VSVs) for systemic treatme

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