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1 eatures that support its classification as a Nodavirus.
2 ite genomes that are most closely related to nodaviruses.
3 xpected single-domain coat protein of insect nodaviruses.
4 early identical with those observed in T = 3 nodaviruses.
5 usly discovered three RNA viruses related to nodaviruses and here describe a fourth one, called the M
6     The structural similarities between fish nodaviruses and members of the tombusvirus and calicivir
7 ration in the RNA viruses range from subtle (nodaviruses and picornaviruses) to dramatic (tetraviruse
8 is review, we discuss that tombusviruses and nodaviruses are capable of exploiting alternative subcel
9 uence analyses show that Orsay is related to nodaviruses, but molecular characterizations of Orsay re
10 e genomes of a novel parvovirus, astrovirus, nodavirus, circular Rep-encoding single-stranded DNA (CR
11                                    The T = 3 nodaviruses contain prefabricated pentameric helical bun
12 on microscopy (cryo-EM), we show that mature nodavirus crowns comprise two stacked 12-mer rings of mu
13  data for understanding the evolution of the nodavirus family.
14 viously unrecognized features of Flock house nodavirus (FHV) RNA replication compartments.
15    In infected Drosophila cells, Flock House nodavirus (FHV) RNA replication complexes form on outer
16                                          The nodavirus Flock house virus (FHV) has a bipartite, posit
17                                          The nodavirus flock house virus (FHV) has a bipartite, posit
18                          To date, the insect nodavirus flock house virus (FHV) is the only virus of a
19 ansmembrane RNA replication protein A of the nodavirus flock house virus (FHV) recruits FHV genomic R
20                           In the case of the nodavirus Flock House virus (FHV), a bipartite positive-
21                                      For the nodavirus flock house virus (FHV), we recently showed th
22 uring infection of Drosophila cells with the nodavirus Flock House virus (FHV).
23  distinct from that described for the insect nodavirus Flock House virus (FHV).
24            Intact, purified particles of the nodaviruses flock house virus and nodamura virus that we
25                                          The nodavirus genome is composed of two positive-sense RNA s
26 embrane translocation of the ssRNA genome of nodaviruses has been proposed to be mediated by direct l
27 a(1)) of the cleavage peptide in flock house nodavirus increases membrane permeability to hydrophilic
28  assembly, the results have implications for nodavirus interaction with cell RNA silencing pathways a
29 ouper nervous necrosis virus (MGNNV), a fish nodavirus isolated from the grouper Epinephelus malabari
30  possible relevance of these findings to the nodavirus life cycle are presented.
31       Outbreaks of Macrobrachium rosenbergii nodavirus (MrNV), the causative agent of white tail dise
32                      In T=3 particles of the nodavirus Pariacoto virus (PaV), a remarkable 35% of the
33         Here we demonstrate that exposure of nodavirus particles to heat causes the two strands of vi
34    We infer that direct interaction of these nodavirus particles with cytoplasmic components mediated
35      The data support divergent evolution of nodaviruses, picornaviruses, and tetraviruses from a com
36 ruses, the role of heterodimerization in the Nodavirus replication cycle is unclear.
37 ntial, distinct, and selective early step in nodavirus replication.
38  Recent cryoelectron microscopy (cryo-EM) of nodavirus RNA replication complexes revealed that the vi
39         This represents the first endogenous nodavirus sequence, the first nematode endogenous viral
40 acids in a manner reminiscent of other known nodavirus structures.
41                                              Nodavirus studies first revealed viral RNA replication p
42 a region homologous to the capsid protein of nodaviruses, tetraviruses, and birnaviruses.
43 tures can be recapitulated for NoV, the only nodavirus that productively infects mammals.
44                   Pariacoto virus (PaV) is a nodavirus that was recently isolated in Peru from the So
45 a packaging mechanism and is conserved among Nodaviruses, the role of heterodimerization in the Nodav
46 is element derives from a different clade of nodaviruses to the previously reported nematode viruses.
47 e showed that viRNAs derived from a modified nodavirus triggered potent silencing of homologous cellu
48                 Three RNA viruses related to nodaviruses were previously described to naturally infec
49 g differences from insect and fish infecting nodaviruses, which have been shown to assemble trimer-cl