ライフサイエンスコーパス: viral nonstructural protein

1 s dependent on the scaffolding activity of a viral nonstructural protein.

2 ared to be inhibited through interference of viral nonstructural proteins.

3 rmediates in conjunction with many copies of viral nonstructural proteins.

4 esis and strongly depends on the sequence of viral nonstructural proteins.

5 The viral nonstructural protein 1 (NS1) is essential in this

6 In the case of influenza A virus, the viral nonstructural protein 1 (NS1) prevents the inducti

7 resent during different stages of infection (viral nonstructural protein 1 and immunoglobulin M) has

8 Herein, we evaluated the effects of three viral nonstructural proteins (2B, 2BC, and 3A) on intrac

9 d by using a monoclonal antibody against the viral nonstructural protein 2C.

10 The viral nonstructural protein 3 (NS3) plays a key role in

11 ections also were stained with antibodies to viral nonstructural protein 3 (NS3), separated by LCM, a

12 irus infection, the C-terminal domain of the viral nonstructural protein 3 (nsP3) forms a complex wit

13 d genetic adaptation by mutations within the viral nonstructural proteins 3A and 3C.

14 replication via direct interaction with the viral nonstructural protein 4B (NS4B).

15 not understood, but evidence for a role for viral nonstructural protein 5A (NS5A) in IFN resistance

16 viral nonstructural proteins and/or between viral nonstructural proteins and cell proteins are invol

17 ng the possibility that interactions between viral nonstructural proteins and/or between viral nonstr

18 Viral nonstructural proteins are often important for vir

19 wn that in both human and animal viruses the viral nonstructural proteins are produced from a polypro

20 Moreover, we demonstrated that the viral nonstructural proteins are responsible for this ef

21 udy provides a unique example of how a small viral nonstructural protein facilitates the multifaceted

22 agosome formation is linked to expression of viral nonstructural proteins, FMDV induced autophagosome

23 e nucleus and is essential for expression of viral nonstructural proteins independent of RNA-activate

24 thermore, simple transient expression of the viral nonstructural proteins is insufficient to induce t

25 The viral nonstructural protein mu NS forms factory-like glo

26 The viral nonstructural protein muNS has been implicated in

27 Viral nonstructural proteins muNS and sigmaNS and core p

28 A viral nonstructural protein, muNS, forms large inclusion

29 The large viral nonstructural protein NS1 is sufficient to induce

30 gene promoter, is strictly dependent on the viral nonstructural protein NS1.

31 NP1 and other viral nonstructural proteins (NS1 to NS4) colocalized wi

32 patocytes induces apoptosis and that the B19 viral nonstructural protein, NS1, may play a critical ro

33 the fluorescent mCherry protein fused to the viral nonstructural protein NS3 (BTV-1/NS3mCherry) was g

34 differ from ncp viruses by the production of viral nonstructural protein NS3.

35 and reproducibly detected low levels of the viral nonstructural protein, NS3.

36 The viral nonstructural protein NS5 of some flaviviruses fun

37 we identified a novel cellular target of the viral nonstructural protein NS5A and demonstrated its ro

38 We show here that phosphorylation of the viral nonstructural protein NS5A at serine residues is i

39 ng the host response to HCV infection is the viral nonstructural protein NS5A, which, in addition to

40 In this report, we demonstrate that a viral nonstructural protein, nsP2, is a significant regu

41 One of the viral nonstructural proteins, nsP2, not only exhibits pr

42 nvaginations (spherules) and accumulation of viral nonstructural proteins (nsPs) at the cytoplasmic n

43 ed between nt 3 and 54; the ORF encoding the viral nonstructural proteins (NSPs) initiates at nt 41 i

44 Three viral nonstructural proteins (nsps), nsp3, nsp4, and nsp

45 xed assay for the detection of antibodies to viral nonstructural proteins (NSPs), raised in cattle in

46 r filaments through interactions between the viral nonstructural protein NSs and the host general tra

47 Viral nonstructural protein NSs was inhibitory to the in

48 t SFTSV (rHB29NSsKO) that cannot express the viral nonstructural protein (NSs) upon infection of cell

49 Two viral nonstructural proteins, sigma NS and micro NS, and

50 remia and did not develop antibodies against viral nonstructural proteins, suggesting that complete p

51 HCV subgenomic RNA replication and suppress viral nonstructural protein synthesis.

52 rus (BSMV) beta(b) gene product is the major viral nonstructural protein synthesized during early sta

53 In addition to many viral nonstructural proteins, the presence of cell nucle

54 e GPV upstream P9 promoter, which encode the viral nonstructural proteins, were polyadenylated at a h