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

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

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

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

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

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

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

9 Double-stranded RNA viruses are ubiquitous in fungi.

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

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

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

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

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

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

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

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

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

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

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

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

22 The double-stranded RNA virus mammalian reovirus displays br

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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