ライフサイエンスコーパス: negative-strand RNA virus

1 ratory syncytial virus (RSV), a nonsegmented negative-strand RNA virus.

2 feron induction in cells infected with these negative strand RNA viruses.

3 of the RNA polymerase (L) of non-segmented, negative-strand RNA viruses.

4 previously appreciated for the nonsegmented negative-strand RNA viruses.

5 unique GDNQ motif normally characteristic of negative-strand RNA viruses.

6 ts in the design of new therapeutics against negative-strand RNA viruses.

7 ire of targets for antiviral therapy against negative-strand RNA viruses.

8 and possibly other families of nonsegmented negative-strand RNA viruses.

9 which are a characteristic hallmark of many negative-strand RNA viruses.

10 , with implications for many other segmented negative-strand RNA viruses.

11 Arenaviruses are enveloped, negative-strand RNA viruses.

12 let-shaped rhabdovirus and a model system of negative-strand RNA viruses.

13 antiviral therapeutics against nonsegmented negative-strand RNA viruses.

14 virus (VSV), a prototype of the nonsegmented negative-strand RNA viruses.

15 As, which are characteristic of nonsegmented negative-strand RNA viruses.

16 has counterparts in a number of nonsegmented negative-strand RNA viruses.

17 Vesicular stomatitis virus is a negative-stranded RNA virus.

18 hanism of replication of influenza and other negative-stranded RNA viruses.

19 contribute to pathogenicity in a variety of negative-stranded RNA viruses.

20 importance for efficient budding of several negative-stranded RNA viruses.

21 es of a number of L proteins of nonsegmented negative-strand RNA viruses, a cluster of high-homology

22 The large (L) proteins of non-segmented, negative-strand RNA viruses, a group that includes Ebola

23 rate vaccine candidates against nonsegmented negative-strand RNA viruses, a large and expanding group

24 element in control of gene expression of the negative strand RNA viruses and a means by which express

25 e viral genome can form during infections of negative-strand RNA viruses and outgrow full-length vira

26 ation strategy should be applicable to other negative-strand RNA viruses and will promote studies int

27 he largest nucleoprotein of the nonsegmented negative-stranded RNA viruses, and like the NPs of other

28 The phosphoproteins (P) of nonsegmented negative strand RNA viruses are viral RNA polymerase sub

29 The negative-strand RNA viruses are a broad group of animal

30 ratory syncytial virus (RSV), a nonsegmented negative-strand RNA virus, are separated by intergenic r

31 In addition, the use of different negative-strand RNA viruses as vectors to efficiently ex

32 y delineate the evolutionary relationship of negative-strand RNA viruses but also provide insights in

33 Phosphorylation of P proteins in several negative strand RNA viruses by specific cellular kinases

34 tiviral action of IFN against a nonsegmented negative-strand RNA virus by targeting the primary trans

35 that La supports the growth of nonsegmented negative-strand RNA viruses by both IFN suppression and

36 function, against a number of positive- and negative-strand RNA viruses by enhancing type I IFN indu

37 In addition, recombinant negative-strand RNA viruses can now be designed to have

38 dependent RNA polymerase of the nonsegmented negative-strand RNA viruses carries out two distinct RNA

39 Importance: The paramyxovirus family of negative-strand RNA viruses cause significant disease in

40 ses are a large family of membrane-enveloped negative-stranded RNA viruses causing important diseases

41 The nonsegmented negative strand RNA viruses comprise hundreds of human,

42 mal RNA synthesis machinery of non-segmented negative-strand RNA viruses comprises a genomic RNA enca

43 cular stomatitis virus (VSV), a nonsegmented negative-strand RNA virus, directs two discrete RNA synt

44 For some negative-strand RNA viruses (e.g., vesicular stomatitis

45 verse members of the Paramyxovirus family of negative-strand RNA viruses effectively suppress host in

46 Paramyxoviruses and other negative-strand RNA viruses encode matrix proteins that

47 Negative-strand RNA viruses encode their own polymerases

48 irus, which represent viruses from different negative-strand RNA virus families.

49 ttenuate VSV, and perhaps other nonsegmented negative-strand RNA viruses, for potential application a

50 The nucleoprotein of negative-strand RNA viruses forms a major component of t

51 Rescue of negative-stranded RNA viruses from full-length genomic c

52 In contrast to most negative-stranded RNA viruses, hantaviruses and other vi

53 etics techniques to manipulate the genome of negative-strand RNA viruses has contributed enormously t

54 w that the mechanism of RNA encapsidation in negative-strand RNA viruses has many common features.

55 ies to genetically manipulate the genomes of negative-strand RNA viruses has provided us with new too

56 Because monopartite negative strand RNA viruses have not been reported to un

57 Thus, our characterization of this negative-strand RNA virus identified a novel replication

58 The mumps virus is a negative-strand RNA virus in the family Paramyxoviridae.

59 (VSV) is the prototype virus for 75 or more negative-strand RNA viruses in the rhabdovirus family.

60 the closest relatives of NYNV and MIDWV are negative-stranded-RNA viruses in the order Mononegaviral

61 Negative-strand RNA viruses include a diverse set of vir

62 is required for the entry of the prototypic negative-strand RNA virus, including influenza A virus a

63 Negative-strand RNA viruses, including paramyxoviruses,

64 rnalized viral ribonucleoproteins (vRNPs) of negative-strand RNA viruses induce an early IFN response

65 Rabies viruses, negative-strand RNA viruses, infect neurons through axon

66 itive-strand RNA virus infections but not in negative-strand RNA virus infections.

67 The nucleocapsid of a negative-strand RNA virus is assembled with a single nuc

68 Gene expression among the nonsegmented negative-strand RNA viruses is controlled by distance fr

69 The genome of nonsegmented negative-strand RNA viruses is tightly embedded within a

70 The viral polymerase of influenza virus, a negative-strand RNA virus, is believed to polyadenylate

71 and reveal the structural organization of a negative-strand RNA virus L protein.

72 The negative-strand RNA virus measles virus (MeV) uses tissu

73 een documented previously for a nonsegmented negative-strand RNA virus (mononegavirus).

74 Vesicular stomatitis virus (VSV) is a negative-stranded RNA virus normally sensitive to the an

75 by modeling crystal structures of homologous negative strand RNA virus Ns in NC.

76 The negative-strand RNA viruses (NSRVs) are unique because t

77 What separates negative-strand RNA viruses (NSVs) from the rest of the

78 nfluenza virus type 3 (PIV3), a nonsegmented negative-strand RNA virus of the Paramyxoviridae family

79 nt to be a previously unrecognized enveloped negative-strand RNA virus of the Paramyxoviridae family,

80 Rhabdoviruses are negative-stranded RNA viruses of the order Mononegaviral

81 r Mononegavirales (comprised of nonsegmented negative-stranded RNA viruses or NNSVs) contains many im

82 eplication and transcription of nonsegmented negative strand RNA viruses (or Mononegavirales) are bel

83 rus (BDV) is a newly classified nonsegmented negative-strand RNA virus (order of Mononegavirales) tha

84 The nonsegmented negative-strand RNA viruses (order Mononegavirales) incl

85 that both the N- and C-terminal regions of a negative-strand RNA virus P are involved in binding the

86 This suggested that negative-strand RNA viruses produce little, if any, dsRN

87 ing those by ssDNA viruses and positive- and negative-strand RNA viruses, produce dsRNAs detectable b

88 of the RNA than the NP protein of some other negative-strand RNA viruses, reflecting the degree of NP

89 However, the impact of TRIM56 on negative-strand RNA viruses remains unclear.

90 h has served in the past as a model to study negative-strand RNA virus replication.

91 Negative-strand RNA viruses represent a significant clas

92 MuV is a negative strand RNA virus, similar to rabies virus or Eb

93 bly diverse family of enveloped nonsegmented negative-strand RNA viruses, some of which are the most

94 The nucleoprotein (NP) of segmented negative-strand RNA viruses such as Orthomyxo-, Arena-,

95 Infection of human dendritic cells (DCs) by negative-strand RNA viruses, such as Newcastle disease v

96 The genomic RNA of negative-strand RNA viruses, such as vesicular stomatiti

97 s instead, suggesting that current segmented negative-strand RNA virus taxonomy may need revision.

98 Borna disease virus (BDV) is a nonsegmented negative-strand RNA virus that replicates and transcribe

99 Paramyxoviruses are enveloped negative-strand RNA viruses that are significant human a

100 Arenaviruses are negative-strand RNA viruses that cause human diseases su

101 Arenaviruses are enveloped negative-strand RNA viruses that cause significant human

102 Influenza virus, a negative-stranded RNA virus that causes severe illness i

103 Arenaviruses are enveloped, negative-stranded RNA viruses that belong to the family

104 Thus, we examined two negative-stranded RNA viruses that have dsRNA intermedia

105 In a negative strand RNA virus, the genomic RNA is sequestere

106 For the nonsegmented negative-strand RNA viruses, the polymerase is comprised

107 virus (VSV), a prototype of the nonsegmented negative-strand RNA viruses, the two methylase activitie

108 In the replication cycle of nonsegmented negative-strand RNA viruses, the viral RNA-dependent RNA

109 A reverse genetics system for negative-strand RNA viruses was first successfully devel

110 Hantaviruses are enveloped, negative-strand RNA viruses which can be lethal to human

111 d vesicular stomatitis virus, a nonsegmented negative-strand RNA virus, which carries out transcripti

112 Vesicular stomatitis virus (VSV) is a negative-strand RNA virus with inherent specificity for

113 se virus (BDV) is a neurotropic nonsegmented negative-strand RNA virus with limited homology to rhabd

114 Newcastle disease virus (NDV) is a negative-strand RNA virus with oncolytic activity agains