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1 p of the close turrets observed in mammalian orthoreovirus.
2 mechanism operates during entry of mammalian orthoreoviruses.
3 reoviruses but unlike nonfusogenic mammalian orthoreoviruses.
4 RV) is a member of the fusogenic subgroup of orthoreoviruses.
5 critical step in the life cycle of mammalian orthoreoviruses.
6 al impact of viral pathogens such as Piscine orthoreovirus-1 (PRV-1) on endangered wild salmon popula
7 as Japanese encephalitis virus and mammalian orthoreovirus(4,5), were detected in guinea pigs.
8 es with the p10 FAST protein from Nelson Bay orthoreovirus and found that the N-terminal and transmem
9 has a structure intermediate between that of Orthoreovirus and the CPV virion.
10 cture is equivalent to the core structure of Orthoreovirus and the virion structure of Cytoplasmic po
11  or absence of receptor-binding fibers among orthoreoviruses and aquareoviruses and presence or absen
12 of BRV, which makes BRV like fusogenic avian orthoreoviruses and aquareoviruses but unlike nonfusogen
13 is conserved across muNS homologs from avian orthoreoviruses and aquareoviruses, suggesting this moti
14 olated and characterized bat-borne mammalian orthoreoviruses and paramyxoviruses, demonstrating the u
15  proteins in other dsRNA viruses: lambda1 in orthoreoviruses and VP3 in orbiviruses.
16                                    Mammalian orthoreoviruses are believed to replicate in distinctive
17                                    Mammalian orthoreoviruses are double-stranded RNA viruses that eli
18 rization studies of the newly emerging avian orthoreovirus (ARV) field strains isolated in Pennsylvan
19                Cells infected with mammalian orthoreoviruses contain large cytoplasmic phase-dense in
20 strong structural similarities with those of orthoreoviruses even at the level of secondary-structure
21                                          One orthoreovirus FAST protein, p14, has been shown to hijac
22                                   The use of orthoreoviruses for oncolytic virotherapy was critically
23 single shelled' intermediate for a mammalian orthoreovirus in cryo-preserved infected cells, by cryo-
24 e nonfusogenic mammalian and fusogenic avian orthoreoviruses in having 150 copies of the core clamp p
25                                    Mammalian orthoreoviruses induce apoptosis in vivo and in vitro; h
26 rane (FAST) proteins isolated from fusogenic orthoreoviruses into a well-tolerated lipid formulation,
27                     In contrast, the core of Orthoreovirus is covered by 200 copies of the trimer tha
28                            The turret, as in orthoreoviruses, is likely to play a major role in the c
29 ation of the various stages of the mammalian orthoreovirus life cycle within cytoplasmic inclusion bo
30                                The mammalian Orthoreovirus (mORV) core particle is an icosahedral mul
31        Within infected host cells, mammalian orthoreovirus (MRV) forms viral factories (VFs), which a
32                                    Mammalian orthoreovirus (MRV) infection induces phosphorylation of
33                     In response to mammalian orthoreovirus (MRV) infection, cells initiate a stress r
34                Infection with many mammalian orthoreovirus (MRV) strains results in shutoff of host,
35 we report a complete genome of one mammalian orthoreovirus (MRV) type 3, denoted TO-151/BR, detected
36 we examined the effect of GuHCl on mammalian orthoreovirus (MRV), a double-stranded RNA (dsRNA) virus
37 e cytoplasm of cells infected with mammalian orthoreoviruses (MRV).
38 us (MRV) is the prototypical member of genus Orthoreovirus of family Reoviridae.
39 e identify a new region within the mammalian orthoreovirus outer capsid that regulates particle stabi
40 th a short (<2 nm) ectodomain, the reptilian orthoreovirus p14, accomplishes the same task by hijacki
41 owers the replicative potential of mammalian orthoreovirus populations but increases viral evolutiona
42                                    Mammalian orthoreovirus (reovirus) displays serotype-dependent pat
43                                    Mammalian orthoreovirus (reovirus) encapsidates a segmented, doubl
44 nce to new food antigens.IMPORTANCEMammalian orthoreovirus (reovirus) infects humans throughout their
45                                    Mammalian orthoreovirus (reovirus) infects most mammals and is ass
46                                    Mammalian orthoreovirus (reovirus) is a double-stranded RNA (dsRNA
47                                    Mammalian orthoreovirus (reovirus) is a model system used to study
48                                    Mammalian orthoreovirus (reovirus) is a model to study capsid meta
49                                    Mammalian orthoreovirus (reovirus) is a nonenveloped virus that es
50                                    Mammalian orthoreovirus (reovirus) is a nonenveloped, segmented, d
51                       Nonfusogenic mammalian orthoreovirus (reovirus) is an enteric pathogen of mice
52                                    Mammalian orthoreovirus (reovirus) is commonly used as a model sys
53                                    Mammalian orthoreovirus (reovirus) is composed of two concentric,
54                                    Mammalian orthoreovirus (reovirus) nonstructural protein muNS nucl
55                                The mammalian orthoreovirus (reovirus) outer capsid is composed of 200
56                                    Mammalian orthoreovirus (reovirus) selectively infects and kills t
57                                The mammalian orthoreovirus (reovirus) sigma1 attachment protein forms
58                                The mammalian orthoreovirus (reovirus) sigmaNS protein is required for
59                                    Mammalian orthoreovirus (reovirus) spreads from the site of infect
60                                    Mammalian orthoreovirus (reovirus) strains type 1 Lang (T1L) and t
61 uman NgR1 serves as a receptor for mammalian orthoreovirus (reovirus), but the mechanism of virus-rec
62 lize the dual-layered structure of mammalian orthoreovirus (reovirus).
63 nge, we quantified reassortment in mammalian orthoreovirus (reovirus).
64                                    Mammalian orthoreoviruses (reoviruses) are nonenveloped double-str
65                                    Mammalian orthoreoviruses (reoviruses) are nonenveloped viruses im
66                                    Mammalian orthoreoviruses (reoviruses) are nonenveloped viruses th
67                Early in infection, mammalian orthoreoviruses (reoviruses) build neo-organelles called
68 jor outer capsid protein micro1 of mammalian orthoreoviruses (reoviruses) is also thought to be autoc
69                                    Mammalian orthoreoviruses (reoviruses) serve as potential triggers
70  major outer-capsid protein mu1 of mammalian orthoreoviruses (reoviruses), which are non-enveloped an
71  serotype-independent receptor for mammalian orthoreoviruses (reoviruses).
72                                    Mammalian orthoreoviruses replicate and assemble in the cytosol of
73  to negative impacts on wild salmon: Piscine orthoreovirus, Tenacibaculum spp., and sea lice (Lepeoph
74 we identified a determinant within mammalian orthoreovirus that regulates heat resistance, disassembl
75  and the considerably more complex mammalian orthoreovirus, thus providing an important model for und
76                      Here, we used mammalian orthoreovirus to evaluate the impact of aggregation on t
77                                    Mammalian orthoreoviruses use glycans and junctional adhesion mole
78 Tyr motifs in A36 and the unrelated p14 from Orthoreovirus, we find that only specific spatial arrang