ライフサイエンスコーパス: dsRNA virus

1 the transcription complex in a prototypical dsRNA virus.

2 ruited by the yeast L-A double-stranded RNA (dsRNA) virus.

3 for virion infectivity in many multi-shelled dsRNA viruses.

4 by growth inhibitors, in contrast to fungal dsRNA viruses.

5 and similarities and differences with other dsRNA viruses.

6 ion and diversity of this enormous family of dsRNA viruses.

7 studies and provide much of our knowledge of dsRNA viruses.

8 in the RNA-dependent RNA polymerases of some dsRNA viruses.

9 ly efficient endogenous RNA transcription of dsRNA viruses.

10 negative-strand RNA and double-stranded RNA (dsRNA) viruses.

11 olated, however, in recent structures of two dsRNA viruses, a fungal virus from family Partitiviridae

12 onservation between RdRps of true ssRNA+ and dsRNA viruses and form a minor, deeply separated cluster

13 that is similar in appearance to the RdRP of dsRNA viruses and multiple accessory appendages that may

14 particle-associated transcription cycles of dsRNA viruses and that small molecules are useful tools

15 s a viral nucleic acid sentinel activated by dsRNA viruses and virus replication intermediates within

16 nas vaginalis are persistently infected with dsRNA viruses, and growing evidence indicates that at le

17 Most double-stranded RNA (dsRNA) viruses are transcribed and replicated in a speci

18 machine and a detailed comparison with other dsRNA viruses at the secondary-structure level.

19 Both repress L-A double-stranded RNA (dsRNA) virus copy number, further suggesting that their

20 infection of segmented double-stranded RNA (dsRNA) virus (CPV; Reoviridae) and highlights the import

21 omparison of PcV and other distantly related dsRNA viruses detected preferential insertion sites at w

22 The L-A dsRNA virus expression, replication, and RNA packaging a

23 In double-stranded-RNA (dsRNA) viruses found in animals, bacteria and yeast, the

24 e completion of Koch's postulates for a true dsRNA virus from a filamentous fungus and the descriptio

25 orthoreovirus (MRV), a double-stranded RNA (dsRNA) virus from the family Reoviridae.

26 nfected by nonsegmented double-stranded RNA (dsRNA) viruses from the genus Trichomonasvirus, family T

27 core architecture among a broad spectrum of dsRNA viruses, from the mammalian rotaviruses to the Pse

28 The reovirus polymerase and those of other dsRNA viruses function within the confines of a protein

29 Analysis of bacterial, protozoal, and fungal dsRNA viruses has improved our understanding of their st

30 Most dsRNA viruses have a genome-enclosing capsid that compri

31 NA polymerases from birnaviruses, a group of dsRNA viruses, have their catalytic motifs arranged in a

32 endogenous, persistent double-stranded RNA (dsRNA) virus in each U. maydis subtype.

33 enveloped, nonsegmented double-stranded RNA (dsRNA) virus infecting Giardia lamblia, the most common

34 idae, a large family of double-stranded RNA (dsRNA) viruses infecting plants, insects, fishes and mam

35 rial genome and the presence or absence of a dsRNA virus influence the phenotype of chromosomal varia

36 mRNA transcription in dsRNA viruses is a highly regulated process but the mech

37 ding shells and homologous proteins in other dsRNA viruses: lambda1 in orthoreoviruses and VP3 in orb

38 The endogenous double-stranded RNA (dsRNA) virus Leishmaniavirus (LRV1) has been implicated

39 virus (PcV) shows the progenitor fold of the dsRNA virus lineage and suggests a relationship between

40 ated that the hallmark fold preserved in the dsRNA virus lineage shares a long (spinal) alpha-helix t

41 e many examples of inhibitors acting against dsRNA viruses more generally.

42 Encapsidated dsRNA viruses, most of which are nonenveloped, infect a

43 (LIV), an unclassified, double-stranded RNA (dsRNA) virus of Agaricus bisporus, were associated with

44 c analogs of ssRNA viruses (polyuridine) and dsRNA viruses (polyinosinic-polycytidylic acid) were sig

45 mbles the corresponding enzymatic regions of dsRNA virus polymerases and influenza virus polymerase.

46 antiviral defense modulator are derived from dsRNA viruses (Reoviridae) and dsDNA viruses (Baculoviri

47 olecular mechanism by which infection with a dsRNA virus results in necroptosis.

48 lts were obtained with particles of a second dsRNA virus, rhesus rotavirus, from a divergent taxonomi

49 Here, we have characterized a novel dsRNA virus (Sclerotinia sclerotiorum megabirnavirus 1 [

50 -stranded RNA (ssRNA) virus (hypovirus) to a dsRNA virus, SsMBV1.

51 Moreover, GLV is the only known protozoal dsRNA virus that can transmit efficiently by extracellul

52 Rotavirus is a dsRNA virus that infects epithelial cells that line the

53 Here, we studied a dsRNA virus that infects the fungus Rosellinia necatrix,

54 Here, we investigated the dsRNA virus that infects the widespread enteric parasite

55 and follows the architectural principle for dsRNA viruses that a 120-subunit capsid is a conserved a

56 V) can be infected with double-stranded RNA (dsRNA) viruses that may have important implications for

57 For most dsRNA viruses, the genome-enclosing capsid comprises 120

58 We show that unlike other dsRNA viruses, the VP2 attachment trimer has a triskelio

59 tively induces apoptosis in cells containing dsRNA, virus titers were strongly reduced.

60 ment with its unique capacity as a protozoal dsRNA virus to survive and transmit through extracellula

61 ts the first 9-segment, double-stranded RNA (dsRNA) virus to be isolated in nature.

62 Overall, dsRNA virus was present in 21 (75%) of 28 TV isolates (9

63 might have occurred from an ssRNA virus to a dsRNA virus, which may provide new insights into the evo

64 Bacteriophage 6 is a double-stranded RNA (dsRNA) virus whose genome is packaged sequentially as th

65 read protozoan parasites carry endosymbiotic dsRNA viruses with uncharted implications to the human h

66 BTV is a nonenveloped, double-stranded RNA (dsRNA) virus with two capsids: a well-studied, stable co