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1 ulated genes myxovirus resistance gene 1 and 2',5' oligoadenylate synthetase.
2 to be conserved among all known isozymes of 2'-5'-oligoadenylate synthetase.
3 ear the amino terminus of the 9-2 isozyme of 2'-5'-oligoadenylate synthetase.
4 e genes encoding antiviral proteins, such as 2'-5' oligoadenylate synthetases.
5 an isozyme of the medium size class of human 2'-5' oligoadenylate synthetases.
6 te-binding sites of the P69 isozyme of human 2'-5'-oligoadenylate synthetases.
9 The upregulation of endogenous IFN-beta and 2',5'-oligoadenylate synthetase 1 mRNA expression was al
10 ted increased expression of interferon-beta, 2',5'-oligoadenylate synthetase 1, interferon-alpha, and
12 vidence of concerted evolution of paralogous 2'-5' oligoadenylate synthetase 1 genes was obtained in
14 ne (ISG) expression screening to reveal that 2'-5'-oligoadenylate synthetase 1 (OAS1), through ribonu
16 d IFN-stimulated gene expression (tracked by 2'-5'-oligoadenylate synthetase 1 and myxovirus (influen
17 vels and no significant difference in IFNB1, 2'-5'-oligoadenylate synthetase 1, or myxovirus (influen
18 d in all animals with increased intrahepatic 2'5' oligoadenylate synthetase 1 (2OAS-1) messenger RNA
20 ulation and an IFN-inducible antiviral gene, 2',5'-oligoadenylate synthetase 1a (OAS), were determine
23 Flavivirus is conferred by an allele of the 2'-5' oligoadenylate synthetase 1b gene that encodes the
24 ISG noted on the microarrays, such as STAT1, 2'5'-oligoadenylate synthetase 2, and ISG15, also suppor
25 ins dsRNA-activated protein kinase (PKR) and 2',5'-oligoadenylate synthetase (2',5'-OAS) were down-re
27 The mRNA for IRF-1, p40, and p69 isoforms of 2'-5' oligoadenylate synthetase (2-5 AS) are detectable,
29 Here we report that one of these targets, 2,5 oligoadenylate synthetase (2,5 OAS), is a mediator o
30 , including those coding for MHC I proteins, 2'-5' oligoadenylate synthetase [2'-5'(A)N], and IFN reg
32 o-IFN-beta was supported by induction of the 2'-5' oligoadenylate synthetase, an indicator of IFN act
33 IFN-responsive genes OAS and ISG54 (encoding 2'-5' oligoadenylate synthetase and an IFN-stimulated ge
34 as well as the effector genes, for example, 2'-5'-oligoadenylate synthetase and myxovirus proteins,
35 ted proteins interferon regulatory factor 1, 2',5'-oligoadenylate synthetase, and double-stranded-RNA
36 randed RNA-dependent protein kinase R (PKR), 2',5'-oligoadenylate synthetase, and Mx1 mRNAs in swine
37 s, including myxovirus resistance protein A, 2',5'-oligoadenylate synthetase, and the IFN-stimulated
38 of mRNA for dsRNA-activated protein kinase, 2'5'-oligoadenylate synthetase, and Toll-like receptor 3
42 trong as that of another IFN-inducible gene, 2'-5' oligoadenylate synthetase, but in contrast to 2'-5
43 ed N-terminal domain with the known forms of 2'-5' oligoadenylate synthetases, but differs completely
45 HC class I, IFN regulatory factor-1, MxA and 2',5-oligoadenylate synthetase gene expression, transcri
51 ude the demonstration that the gene encoding 2'-5'oligoadenylate synthetase is responsible for murine
53 ated Gene 15 (ISG15), Interleukin 16 (IL16), 2',5'-Oligoadenylate Synthetase Like (OASL), and Adhesio
54 novel murine cDNA encoding an ovary-specific 2',5'-oligoadenylate synthetase-like protein, OAS1D, whi
57 egulatory role for endothelial expression of 2'-5' oligoadenylate synthetase-like 1 (OASL1) in mainta
60 ining E3 ubiquitin-protein ligase 5 (HERC5); 2'-5'-oligoadenylate synthetase-like (OASL); and helicas
61 ding inflammatory (S100A8/A9/A12, CXCL1, and 2'-5'-oligoadenylate synthetase-like [OASL]) and barrier
63 70-fold and myxovirus resistance gene 1 and 2',5' oligoadenylate synthetase mRNA expression (107- an
64 ed genes for IFN-regulatory factors 1 and 7, 2'5' oligoadenylate synthetase, Mx, and TNF superfamily
65 protein 10, and preferential upregulation of 2',5'-oligoadenylate synthetase, Mx1, and indoleamine 2,
66 nown interferon-stimulated genes such as the 2'5'-oligoadenylate synthetase, MX1, IRF-7, and toll-lik
67 o lack of nitric oxide synthase 2 (NOS2) and 2', 5' oligoadenylate synthetase (OAS) 1 induction in re
68 acokinetics, pharmacodynamic measurements of 2',5'-oligoadenylate synthetase (OAS) activity, and indu
70 h the wild-type (WT) virus uses to block the 2',5'-oligoadenylate synthetase (OAS)-RNase L (RNase L)
72 ivity, which blocks the interferon inducible 2',5'-oligoadenylate synthetase (OAS)-RNase L pathway to
73 response to AZA treatment occurs through the 2',5'-oligoadenylate synthetase (OAS)-RNase L pathway.
74 nterferon response through counteracting the 2',5'-oligoadenylate synthetase (OAS)/RNase L system.
75 luding Myxovirus resistance protein 2 (Mx2), 2',5'-oligoadenylate synthetase (OAS-1), Virus inhibitor
76 2-5A is produced by interferon-inducible 2',5'-oligoadenylate synthetases (OAS) upon activation b
77 RNA-dependent protein kinase (PKR), but not 2',5'-oligoadenylate synthetases (OAS), in vaginal tissu
78 on, the eIF2alpha protein kinase PKR and the 2'-5' oligoadenylate synthetase (OAS) are both activated
81 influenza virus resistance allele Mx(+) and 2'-5' oligoadenylate synthetase (OAS) proteins was not r
82 d cDNAs, including inhibitor of apoptosis-1, 2'-5' oligoadenylate synthetase (OAS), a 2'-5' OAS-like
83 fter CpG and correlated with serum levels of 2'-5' oligoadenylate synthetase (OAS), a validated inter
84 antiviral interferon-stimulated gene product 2'-5' oligoadenylate synthetase (OAS), and the chemokine
85 h includes conventional poly(A) polymerases, 2'-5' oligoadenylate synthetase (OAS), and yeast Trf4p .
86 nes (ISGs) with antiviral properties such as 2'-5' oligoadenylate synthetase (OAS), stimulated trans-
87 NA-responsive defenses controlled by PKR and 2'-5' oligoadenylate synthetase (OAS), which respectivel
95 nce that the host interferon (IFN)-inducible 2'-5'-oligoadenylate synthetase (OAS) and RNase L pathwa
96 ation in the gene encoding the 1b isoform of 2'-5'-oligoadenylate synthetase (OAS), a member of the O
97 p and also functions as an antagonist of the 2'-5'-oligoadenylate synthetase (OAS)/RNase L pathway.
100 ms of IL-29 and IFN-alpha induced equivalent 2'5' oligoadenylate synthetase (OAS) and MX1 gene expres
101 106 (+/-63.3) pg/ml increase (P < 0.01); and 2'5'-oligoadenylate synthetase (OAS) had a 163 (+/-120.6
103 elevation of the IFN-induced antiviral gene 2',5'-oligoadenylate synthetase (OAS1a) but not dsRNA-de
105 kinase (PKR) and the endoribonuclease of the 2',5'-oligoadenylate synthetase-RNase L system (PKR(-/-)
106 clease component of the interferon-regulated 2',5'-oligoadenylate synthetase-RNase L system, demonstr
107 bsence of IFN-stimulated antiviral proteins, 2'-5' oligoadenylate synthetase/RNase L, and dsRNA-depen
108 in the light of both this new member and new 2'-5' oligoadenylate synthetase sequence data from other
109 ligoadenylate synthetase, but in contrast to 2'-5' oligoadenylate synthetase, TP/PD-ECGF mRNA levels