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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 nce during persistent infection requires the viral nonstructural protein 1/2 (NS1/2).
9    Herein, we evaluated the effects of three viral nonstructural proteins (2B, 2BC, and 3A) on intrac
10 d by using a monoclonal antibody against the viral nonstructural protein 2C.
11                                          The viral nonstructural protein 3 (NS3) plays a key role in
12 ections also were stained with antibodies to viral nonstructural protein 3 (NS3), separated by LCM, a
13 rovided by the C-terminal helicase domain of viral nonstructural protein 3 (NS3).
14 irus infection, the C-terminal domain of the viral nonstructural protein 3 (nsP3) forms a complex wit
15       Their recruitment is determined by the viral nonstructural protein 3 (nsP3).
16 d genetic adaptation by mutations within the viral nonstructural proteins 3A and 3C.
17  replication via direct interaction with the viral nonstructural protein 4B (NS4B).
18  not understood, but evidence for a role for viral nonstructural protein 5A (NS5A) in IFN resistance
19  viral nonstructural proteins and/or between viral nonstructural proteins and cell proteins are invol
20 ng the possibility that interactions between viral nonstructural proteins and/or between viral nonstr
21                                              Viral nonstructural proteins are often important for vir
22 wn that in both human and animal viruses the viral nonstructural proteins are produced from a polypro
23           Moreover, we demonstrated that the viral nonstructural proteins are responsible for this ef
24 udy provides a unique example of how a small viral nonstructural protein facilitates the multifaceted
25 agosome formation is linked to expression of viral nonstructural proteins, FMDV induced autophagosome
26 e nucleus and is essential for expression of viral nonstructural proteins independent of RNA-activate
27 thermore, simple transient expression of the viral nonstructural proteins is insufficient to induce t
28 associated accessory protein (MAAP), a small viral nonstructural protein, is translated from the same
29 ation of recombinant AAV production, a small viral nonstructural protein, membrane-associated accesso
30                                          The viral nonstructural protein mu NS forms factory-like glo
31                                          The viral nonstructural protein muNS has been implicated in
32                                              Viral nonstructural proteins muNS and sigmaNS and core p
33                                            A viral nonstructural protein, muNS, forms large inclusion
34 tion and revealed a novel mechanism that the viral nonstructural protein NS1 hijacks the host acetylt
35                                          The viral nonstructural protein NS1 interacted with KAT5 and
36                                    The large viral nonstructural protein NS1 is sufficient to induce
37 otein p53 and IAV, in particular through the viral nonstructural protein NS1, has been shown to be su
38  gene promoter, is strictly dependent on the viral nonstructural protein NS1.
39                                NP1 and other viral nonstructural proteins (NS1 to NS4) colocalized wi
40 patocytes induces apoptosis and that the B19 viral nonstructural protein, NS1, may play a critical ro
41 the fluorescent mCherry protein fused to the viral nonstructural protein NS3 (BTV-1/NS3mCherry) was g
42 differ from ncp viruses by the production of viral nonstructural protein NS3.
43  and reproducibly detected low levels of the viral nonstructural protein, NS3.
44 ements for RO formation is the biogenesis of viral nonstructural proteins NS4A and NS4B.
45                                          The viral nonstructural protein NS5 of some flaviviruses fun
46 we identified a novel cellular target of the viral nonstructural protein NS5A and demonstrated its ro
47     We show here that phosphorylation of the viral nonstructural protein NS5A at serine residues is i
48 ng the host response to HCV infection is the viral nonstructural protein NS5A, which, in addition to
49        In this report, we demonstrate that a viral nonstructural protein, nsP2, is a significant regu
50                                   One of the viral nonstructural proteins, nsP2, not only exhibits pr
51 nvaginations (spherules) and accumulation of viral nonstructural proteins (nsPs) at the cytoplasmic n
52 ed between nt 3 and 54; the ORF encoding the viral nonstructural proteins (NSPs) initiates at nt 41 i
53 eplication enzyme complexes (RCs) containing viral nonstructural proteins (nsPs) that mediate the syn
54                                        Three viral nonstructural proteins (nsps), nsp3, nsp4, and nsp
55 xed assay for the detection of antibodies to viral nonstructural proteins (NSPs), raised in cattle in
56 r filaments through interactions between the viral nonstructural protein NSs and the host general tra
57 TSV activated the NLRP3 inflammasome via the viral nonstructural protein NSs through interaction with
58                                              Viral nonstructural protein NSs was inhibitory to the in
59                                              Viral nonstructural protein NSs, a known modulator of im
60 t SFTSV (rHB29NSsKO) that cannot express the viral nonstructural protein (NSs) upon infection of cell
61 e detection of antibodies against either the viral nonstructural proteins or the capsid.
62                                          Two viral nonstructural proteins, sigma NS and micro NS, and
63 remia and did not develop antibodies against viral nonstructural proteins, suggesting that complete p
64  HCV subgenomic RNA replication and suppress viral nonstructural protein synthesis.
65 rus (BSMV) beta(b) gene product is the major viral nonstructural protein synthesized during early sta
66 ated small transmembrane (FAST) proteins are viral nonstructural proteins that mediate cell-cell fusi
67                          In addition to many viral nonstructural proteins, the presence of cell nucle
68 e GPV upstream P9 promoter, which encode the viral nonstructural proteins, were polyadenylated at a h