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1 observation made for the related pestivirus bovine viral diarrhea virus.
3 known TRIMs, TRIM56 inhibits replication of bovine viral diarrhea virus, a ruminant pestivirus of th
5 trate that RNA-dependent RNA polymerase from bovine viral diarrhea virus and the replicases from thre
6 iridae(yellow fever virus, dengue virus, and bovine viral diarrhea virus) and a human coronavirus (OC
7 ated to HCV, classical swine fever virus and bovine viral diarrhea virus; and two unrelated viruses,
9 are bovine herpes virus types 1, 3, 4 and 5, bovine viral diarrhea virus, bovine parainfluenza 3 viru
11 ow that the NS3 proteinase of the pestivirus bovine viral diarrhea virus (BVDV) (NADL strain) is requ
12 tations in the helicase/NTPase motifs of the bovine viral diarrhea virus (BVDV) (NADL strain) NS3 pro
13 r controlling bovine pestiviruses, including bovine viral diarrhea virus (BVDV) and the emerging HoBi
14 the NS5A and NS5 proteins, respectively, of bovine viral diarrhea virus (BVDV) and yellow fever viru
17 vectors to immunize cattle against selected bovine viral diarrhea virus (BVDV) genes has gained wide
18 ruses, the N-terminal protein encoded by the bovine viral diarrhea virus (BVDV) genome is a cysteine
19 ignated VP32947, inhibits the replication of bovine viral diarrhea virus (BVDV) in cell culture at a
20 ctable, bi-cistronic subgenomic replicon for bovine viral diarrhea virus (BVDV) in Huh-7 cells, simil
21 agnostic screening test for the detection of bovine viral diarrhea virus (BVDV) in pooled bovine seru
24 esis that the NS5A protein of the pestivirus bovine viral diarrhea virus (BVDV) is a zinc-binding pro
33 ted with the N-terminal protease (N(pro)) of bovine viral diarrhea virus (BVDV), a pestiviral interfe
34 we investigated superinfection exclusion of bovine viral diarrhea virus (BVDV), a positive-sense RNA
36 A polymerases (RdRps) from GB virus-B (GBV), bovine viral diarrhea virus (BVDV), and hepatitis C viru
38 -budding viruses hepatitis C virus (HCV) and bovine viral diarrhea virus (BVDV), lipid droplets, and
46 a related transmembrane domain derived from bovine viral diarrhea virus could not replace the HCV NS
47 ells of many origins with the cytopathogenic bovine viral diarrhea virus (cpBVDV) results in the indu
48 lar regulatory beta-hairpin loops, including bovine viral diarrhea virus, dengue virus, and West Nile
51 al virus, infectious bovine rhinotracheitis, bovine viral diarrhea virus, Mannheimia haemolytica or M
52 he mRT-PCR detected parapoxvirus (n = 2) and bovine viral diarrhea virus (n = 2) in clinical samples,
53 ental infection of calves with noncytopathic bovine viral diarrhea virus (ncpBVDV) was found to induc
54 activity is an inherent function of HCV and bovine viral diarrhea virus RdRps highly purified from b
55 d Ile287 are highly conserved amino acids in bovine viral diarrhea virus RNA polymerase (BVDV RdRp) a
56 ombinant RNA-dependent RNA polymerase of the bovine viral diarrhea virus specifically requires a cyti
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