ライフサイエンスコーパス: double-stranded RNA virus

1 gastroenteritis, is a prototypical segmented double-stranded RNA virus.

2 virus type 3 Dearing (RT3D) is an oncolytic, double-stranded RNA virus.

3 cytotoxicity caused by reovirus, a prototype double-stranded RNA virus.

4 rticipates in the recognition of single- and double-stranded RNA viruses.

5 l that appears to be common to all groups of double-stranded RNA viruses.

6 Group A rotaviruses (RVs) are 11-segmented, double-stranded RNA viruses and are primary causes of ga

7 Killer strains of S. cerevisiae harbor double-stranded RNA viruses and secrete protein toxins t

8 ne that represses the copy number of the L-A double-stranded RNA virus, and found that it encodes an

9 endothelial cells stimulated by cytokine or double-stranded RNA viruses; and binding of sickle cells

10 Double-stranded RNA viruses are ubiquitous in fungi.

11 were present (positive- and minus-strand and double-stranded RNA viruses), but only one DNA virus was

12 double-stranded RNA, a satellite of the L-A double-stranded RNA virus, encoding a secreted protein t

13 on fibers is one of several common themes in double-stranded RNA virus evolution.

14 Picobirnaviruses (PBVs) are double-stranded RNA viruses frequently detected in human

15 The yeast L-A double-stranded RNA virus furnishes its mRNA with this s

16 Yeast L-A double-stranded RNA virus furnishes its transcript with

17 abases reveals that most positive-strand and double-stranded RNA viruses have ORFs for RNA helicases.

18 s including a newly described non-enveloped, double-stranded RNA virus in the Birnaviridae family we

19 rus (reovirus) is a nonenveloped, segmented, double-stranded RNA virus in the Reoviridae family.

20 tively controls the copy number of L-A and M double-stranded RNA viruses in Saccharomyces cerevisiae.

21 The toxins are encoded by double-stranded RNA viruses in the cell cytoplasm.

22 non-segmented, 4.5-5.5 kilo-base pair (kbp), double-stranded RNA virus infecting T. vaginalis.

23 Bluetongue virus (BTV), a nonenveloped double-stranded RNA virus, is a potent inducer of type I

24 he infectious bursal disease virus (IBDV), a double-stranded RNA virus, is processed at the C-termina

25 in S. cerevisiae causes loss of a beneficial double-stranded RNA virus known as killer virus.

26 ny Leishmania (Viannia) parasites harbor the double-stranded RNA virus Leishmania RNA virus 1 (LRV1),

27 Recently, we reported that a double-stranded RNA virus, Leishmania RNA virus 1 (LRV1)

28 The double-stranded RNA virus mammalian reovirus displays br

29 ription in rotavirus, as with many segmented double-stranded RNA viruses, mRNA is transcribed within

30 isolates of L. braziliensis (>25%) contain a double-stranded RNA virus named Leishmaniavirus 1 (LRV1)

31 Rotavirus, a segmented double-stranded RNA virus of the Reoviridae family, is a

32 Rotavirus, a double-stranded RNA virus of the Reoviridae family, is t

33 The L-A double-stranded RNA virus of yeast encodes its major coa

34 The structure of a double-stranded RNA virus outer shell has revealed unexp

35 ense single-stranded RNA viruses, as well as double-stranded RNA viruses, positive-sense single-stran

36 L-A and L-BC are two double-stranded RNA viruses present in almost all strain

37 In the Saccharomyces cerevisiae double-stranded RNA virus, programmed -1 ribosomal frame

38 vides a powerful system for basic studies of double-stranded RNA virus replication; a nonpathogenic v

39 ach of these in the Saccharomyces cerevisiae double-stranded RNA virus ScVL1 by substituting the cons

40 The Saccharomyces cerevisiae double-stranded RNA virus ScVL1 recognizes a small seque

41 The triennial International Double-Stranded RNA Virus Symposium, this year organized

42 rions derived from the giardiavirus (GLV), a double-stranded RNA virus that infects many Giardia isol

43 eovirus strain type 1 Lang (T1L), which is a double-stranded RNA virus that infects Peyer's patches (

44 Leishmania RNA virus (LRV) is a double-stranded RNA virus that infects some strains of t

45 iruses (RVs) are nonenveloped, 11-segmented, double-stranded RNA viruses that are major pathogens ass

46 Rotaviruses (RVs) are 11-segmented, double-stranded RNA viruses that cause severe gastroente

47 Reoviruses are encapsidated double-stranded RNA viruses that cause systemic disease

48 Mammalian orthoreoviruses are double-stranded RNA viruses that elicit apoptosis in vit

49 Reoviruses are double-stranded RNA viruses that infect hosts via respir

50 rthoreoviruses (reoviruses) are nonenveloped double-stranded RNA viruses that infect most mammalian s

51 Reoviruses are double-stranded RNA viruses that infect the mammalian re

52 Cystoviruses are a class of enveloped double-stranded RNA viruses that use a multiprotein poly

53 The possibility that, similar to some double-stranded RNA viruses, the 1a NTPase/helicase-like

54 d only by strains persistently infected with double-stranded RNA viruses (UmV) in the cell cytoplasm.

55 Trichomonas vaginalis infected with a double-stranded RNA virus undergoes phenotypic variation

56 ers of the Reoviridae family of nonenveloped double-stranded RNA viruses, use at least three proteins

57 s to the replicative cores of retrovirus and double-stranded RNA virus virions.

58 of infectious bursal disease virus (IBDV), a double-stranded RNA virus, we examined the cellular nucl

59 ng efficiencies and the propagation of yeast double-stranded RNA viruses were examined.

60 es suggest that C. parvum harbors a putative double-stranded RNA virus which separately encapsidates

61 hese compounds promote loss of the yeast L-A double-stranded RNA virus, which uses a programmed -1 ri

62 genome is particularly relevant in segmented double-stranded RNA viruses, which exhibit endogenous tr

63 Bluetongue virus is a double-stranded RNA virus with 10 segments of different