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1 ht correspond to a hypothetical rodent large delta antigen.
2 tion, of its nucleocapsid-like protein large delta antigen.
3 of protein-protein interaction for the large delta antigen.
4 trations and in the context of either intact delta antigen.
5 of the single and essential HDV protein, the delta antigen.
6 lated RNA that could act as the mRNA for the delta antigen.
7 transfected into cells containing the small delta antigen.
8 amate receptor (GluR) subunits and hepatitis delta antigen.
9 el findings were that (i) immunostaining for delta antigen 6 days after infection with 300 genome equ
10 known to express a protein termed the small delta antigen, a structural protein which is also essent
11 en Pol II and HDV RNAs, as well as the small delta antigen, an HDV-encoded protein known to be essent
12 rement for the de novo-synthesized hepatitis delta antigen and temperature dependence, we further sho
13 two essential proteins, the small and large delta antigens, and both are required for viral propagat
15 Two forms of the sole HDV protein, hepatitis delta antigen, are derived from a single open reading fr
16 ave implicated the prenylation site of large delta antigen as a critical determinant of HDV particle
17 ound that, in vivo, both the small and large delta antigens assembled as antiparallel coiled-coil dim
19 es and specific for different regions on the delta antigen (delta Ag), were used to map, via immunopr
20 SC35-like speckle pattern of accumulation of delta antigen deltaAg was maintained for only 6 days, af
21 occurs at a time when the large form of the delta antigen deltaAg-L appears and HDV RNA synthesis be
22 a virus (HDV) encodes one protein, hepatitis delta antigen (deltaAg), a 195-amino-acid RNA binding pr
23 d mRNA that acts as a template for the small delta antigen (deltaAg), the only protein of HDV and ess
24 rylation of the large and small forms of the delta antigen (deltaAg-L and deltaAg-S, respectively).
27 s method to examine the effects of hepatitis delta antigen (HDAg) on the ribozyme activities of HDV R
28 NAs with the virus-encoded protein hepatitis delta antigen (HDAg) perform essential roles in the vira
29 d rodlike structure of HDV RNA and hepatitis delta antigen (HDAg), a basic, disordered, oligomeric pr
30 ngation factor, in the presence of hepatitis delta antigen (HDAg), and in the presence of transcripti
31 t forms of the sole viral protein, hepatitis delta antigen (HDAg), from the same open reading frame.
32 he two forms of the viral protein, hepatitis delta antigen (HDAg), in HDV RNA replication are similar
33 the sole virally encoded protein, hepatitis delta antigen (HDAg), in infected cells; however, the na
34 e coding region whose product, the hepatitis delta antigen (HDAg), is expressed in two isoforms, smal
35 HDV genome encodes two forms of hepatitis delta antigen (HDAg), small HDAg (HDAg-S), which is requ
37 ential forms of the viral protein, hepatitis delta antigen (HDAg), to be synthesized from a single op
38 HDV RNA encodes a single protein, hepatitis delta antigen (HDAg), which is required for viral replic
47 e small delta antigen (HDAg-S) and the large delta antigen (HDAg-L), from a single open reading frame
48 to express two essential proteins, the small delta antigen (HDAg-S) and the large delta antigen (HDAg
54 HDV immunoglobulin G wherein recombinant HDV delta antigen is printed by microarray on slides coated
55 th and incorporation of free large hepatitis delta antigen, it was partially defective in hepatitis d
56 ucture was solved for only a fragment of the delta antigens, it is unknown whether octamers actually
60 her HDV small delta antigen (SHDAg) or large delta antigen (LHDAg), and the self-cleavage of the prim
61 or production of the viral protein hepatitis delta antigen long form (HDAg-L), which is necessary for
62 xperiments, we found that unprenylated large delta antigen molecules could be disulfide cross-linked
64 ned with our previous finding that hepatitis delta antigen mRNA synthesis is likely performed by RNA
66 allel coiled-coils (those from the hepatitis delta antigen (PDB ID code 1A92) and the bovine F(1) ATP
67 roduces HDV-like particles, and we show that delta antigen prenylation can be pharmacologically inhib
68 on has preserved a separate lineage of gamma/delta antigen receptors that share characteristics of bo
70 cted with plasmids encoding either HDV small delta antigen (SHDAg) or large delta antigen (LHDAg), an
71 ould be precipitated together with hepatitis delta antigen, suggesting the association of HDV replica
72 o the production of an elongated form of the delta antigen, the large form, which is essential for vi
75 tion is somehow able to direct the available delta antigen to sites in the nucleoplasm, almost exclus
76 arest to the 5' end of the putative mRNA for delta antigen, was much more sensitive than the other en
77 the HDV genome abrogates the interaction of delta antigens with the HDV genome and inhibits virion a