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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
14 crease in the proportion of cells expressing delta antigen are observed.
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
18                              Since the small delta antigen contains no cysteine residues, treatment o
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).
25                   When the small form of the delta antigen (deltaAg-S) was expressed from a cDNA expr
26  structure that is associated with hepatitis delta antigen (HDAg) in cells replicating HDV.
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
36 nome, and mRNA; the latter encodes hepatitis delta antigen (HDAg), the viral protein.
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
39        However, in the presence of hepatitis delta antigen (HDAg), which is the only protein encoded
40 e that altered the sequence of the hepatitis delta antigen (HDAg).
41 ch encodes the sole viral protein, hepatitis delta antigen (HDAg).
42 NA which encodes a single protein, hepatitis delta antigen (HDAg).
43 l forms of the sole viral protein, hepatitis delta antigen (HDAg).
44 , polyadenylated mRNA encoding the hepatitis delta antigen (HDAg).
45 rms of its principal gene product, hepatitis delta antigen (HDAg).
46                          The large hepatitis delta antigen (HDAg-L) mediates hepatitis delta virus (H
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
49                          The small hepatitis delta antigen (HDAg-S) is expressed throughout replicati
50 ressed in the absence of the small hepatitis delta antigen (HDAg-S).
51  virus (HDV) contains two types of hepatitis delta antigens (HDAg) in the virion.
52  associated with the small (S) and large (L) delta antigens (HDAg).
53                  In contrast to HDV, a large delta antigen is not expressed and the farnesylation mot
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
57                  The large form of hepatitis delta antigen (L-HDAg), which is responsible for virus p
58 ntracellular accumulation of large hepatitis delta antigen (L-HDAg).
59              We observed that HDV genome and delta antigen levels are significantly decreased in the
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
63 are needed for the accumulation of essential delta antigen mRNA species.
64 ned with our previous finding that hepatitis delta antigen mRNA synthesis is likely performed by RNA
65 33-nt downstream of the poly(A) site for the delta antigen mRNA.
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
69 ncode the small and large forms of hepatitis delta antigens (S- and L-HDAg), respectively.
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
73 stranded, circular RNA genome complexed with delta antigen, the viral protein.
74 iting the interaction of the HDV genome with delta antigens through the recruitment of YTHDF1.
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