ライフサイエンスコーパス: nodavirus

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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 The structural similarities between fish nodaviruses and members of the tombusvirus and calicivir

6 ration in the RNA viruses range from subtle (nodaviruses and picornaviruses) to dramatic (tetraviruse

7 is review, we discuss that tombusviruses and nodaviruses are capable of exploiting alternative subcel

8 uence analyses show that Orsay is related to nodaviruses, but molecular characterizations of Orsay re

9 The T = 3 nodaviruses contain prefabricated pentameric helical bun

10 data for understanding the evolution of the nodavirus family.

11 viously unrecognized features of Flock house nodavirus (FHV) RNA replication compartments.

12 In infected Drosophila cells, Flock House nodavirus (FHV) RNA replication complexes form on outer

13 The nodavirus Flock house virus (FHV) has a bipartite, posit

14 The nodavirus flock house virus (FHV) has a bipartite, posit

15 To date, the insect nodavirus flock house virus (FHV) is the only virus of a

16 ansmembrane RNA replication protein A of the nodavirus flock house virus (FHV) recruits FHV genomic R

17 In the case of the nodavirus Flock House virus (FHV), a bipartite positive-

18 For the nodavirus flock house virus (FHV), we recently showed th

19 uring infection of Drosophila cells with the nodavirus Flock House virus (FHV).

20 distinct from that described for the insect nodavirus Flock House virus (FHV).

21 Intact, purified particles of the nodaviruses flock house virus and nodamura virus that we

22 The nodavirus genome is composed of two positive-sense RNA s

23 embrane translocation of the ssRNA genome of nodaviruses has been proposed to be mediated by direct l

24 a(1)) of the cleavage peptide in flock house nodavirus increases membrane permeability to hydrophilic

25 assembly, the results have implications for nodavirus interaction with cell RNA silencing pathways a

26 ouper nervous necrosis virus (MGNNV), a fish nodavirus isolated from the grouper Epinephelus malabari

27 possible relevance of these findings to the nodavirus life cycle are presented.

28 Outbreaks of Macrobrachium rosenbergii nodavirus (MrNV), the causative agent of white tail dise

29 In T=3 particles of the nodavirus Pariacoto virus (PaV), a remarkable 35% of the

30 Here we demonstrate that exposure of nodavirus particles to heat causes the two strands of vi

31 We infer that direct interaction of these nodavirus particles with cytoplasmic components mediated

32 The data support divergent evolution of nodaviruses, picornaviruses, and tetraviruses from a com

33 ntial, distinct, and selective early step in nodavirus replication.

34 This represents the first endogenous nodavirus sequence, the first nematode endogenous viral

35 acids in a manner reminiscent of other known nodavirus structures.

36 a region homologous to the capsid protein of nodaviruses, tetraviruses, and birnaviruses.

37 tures can be recapitulated for NoV, the only nodavirus that productively infects mammals.

38 Pariacoto virus (PaV) is a nodavirus that was recently isolated in Peru from the So

39 is element derives from a different clade of nodaviruses to the previously reported nematode viruses.

40 e showed that viRNAs derived from a modified nodavirus triggered potent silencing of homologous cellu

41 g differences from insect and fish infecting nodaviruses, which have been shown to assemble trimer-cl

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