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1 substitutions of E3 Y47 and Y48 (Y47/48A) in Semliki Forest virus.
2 licon encoding the nonstructural proteins of Semliki Forest virus.
3 fluenza viruses and nonstructural genes from Semliki Forest virus.
4 E1 ectodomain homotrimer from the alphavirus Semliki Forest virus.
5 alphavirus, Sindbis, and another alphavirus, Semliki Forest virus.
6 subgenomic promoter of the animal-infecting Semliki Forest virus.
7 EEEV, Western equine encephalitis virus, and Semliki Forest virus.
8 as a receptor for the prototypic alphavirus Semliki forest virus.
11 ng rabies virus, vesicular stomatitis virus, Semliki Forest virus, and herpes simplex virus 1, elicit
12 ne vectors derived from Sindbis virus (SIN), Semliki Forest virus, and Venezuelan equine encephalitis
13 us (MAYV) are closely related members of the Semliki Forest virus antigenic complex classified as bel
15 Alphaviruses, particularly Sinbis virus and Semliki Forest virus, are proving to be useful vectors f
17 Furthermore, both Sindbis virus-based and Semliki Forest virus-based vectors could be packaged wit
20 rom a conventional plasmid vector and from a Semliki Forest virus derived, self-replicating vector.
21 ly evident when Gag was expressed by using a Semliki Forest virus-derived vector: under these conditi
22 protein or a ligand-binding antagonist block Semliki forest virus E2-E1-mediated infection of human a
23 that the E2 and E1 glycoproteins (E2-E1) of Semliki forest virus, eastern equine encephalitis virus
27 ver a 25-week span with either a recombinant Semliki Forest virus expressing the SIV-PBj14 Env gp160
32 n RNA replicase polyprotein derived from the Semliki forest virus, in combination with a model antige
34 emonstrate that while transferrin uptake and Semliki Forest virus infection were prevented, influenza
36 thic self-amplifying RNA vector derived from Semliki Forest virus (ncSFV) to generate BHK cell lines
37 at, we demonstrate that a full-length 8.3-kb Semliki Forest virus ribozyme (SFVRz) chimeric RNA maint
38 ated in animal cell lines transfected with a Semliki Forest virus RNA replicon encoding a single vira
39 d, high-titer vaccine platform consisting of Semliki Forest virus RNA replicons that express the vesi
40 in the Togaviridae, including Sindbis virus, Semliki Forest virus, Ross River virus, and Venezuelan e
42 hat fusion and infection by the alphaviruses Semliki Forest virus (SFV) and Sindbis virus were strong
46 ent in the context of avirulent and virulent Semliki Forest virus (SFV) as well as West Nile virus in
47 alphaviruses, except those belonging to the Semliki Forest virus (SFV) clade, have PSs which can be
49 HIKV containing corresponding regions of the Semliki Forest virus (SFV) E2 (domains A, B, and C) subs
54 disease virus (NDV), Sendai virus (SeV), and Semliki Forest virus (SFV) infection and to the TLR3 ago
62 The E1 envelope protein of the alphavirus Semliki Forest virus (SFV) is a class II fusion protein
70 inant vesicular stomatitis virus (VSV) and a Semliki Forest virus (SFV) replicon (SFVG) that propagat
71 ation of additional variants of both SIN and Semliki Forest virus (SFV) replicons encoding the neomyc
73 be infected by vesicular stomatitis (VSV) or Semliki Forest virus (SFV) that require delivery to acid
78 , bovine chromaffin cells were infected with Semliki Forest virus (SFV) vectors containing the rat NC
79 ow that cells expressing genes inserted into Semliki Forest virus (SFV) vectors generate a large frac
80 us we adapted a labelling approach involving Semliki Forest Virus (SFV) vectors to resolve and quanti
81 riggered class II viral fusion protein E1 of Semliki Forest virus (SFV) were fused to target cells.
82 xpressing the E1 and E2 envelope proteins of Semliki Forest virus (SFV) were fused to voltage-clamped
84 biochemical assay to monitor the budding of Semliki Forest virus (SFV), an enveloped alphavirus that
87 on by the alphaviruses Sindbis virus (SINV), Semliki Forest virus (SFV), and chikungunya virus (CHIKV
88 ezuelan equine encephalitis virus (VEEV) and Semliki Forest virus (SFV), can cause encephalitic disea
89 quences from a distantly related alphavirus, Semliki Forest virus (SFV), resulted in nonviable chimer
99 E forms were expressed transiently using the Semliki Forest Virus system, and the culture medium was
100 BPV1) genomes were infected with recombinant Semliki Forest viruses that express the structural prote
101 on of cells expressing recombinant M1 from a Semliki Forest virus vector allowed nuclear export of vR
102 C6 cells and BHK-21 cells transfected with a Semliki Forest virus vector that contains ORF IV demonst
103 -derived vector: under these conditions, the Semliki Forest virus vector-directed mRNA became very ab
106 that combines the nonstructural proteins of Semliki Forest virus with the VSV glycoprotein has been