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1 nd diarrheal diseases, with the exception of viral diarrhea and an increase in diarrheal disease foll
2 a variety of intestinal disorders, including viral diarrhea, antibiotic-associated diarrhea, Clostrid
3 o and persistently infected (PI) with bovine viral diarrhea (BVD) virus (BVDV) constitute the mechani
5 man astrovirus (HAstV) is a leading cause of viral diarrhea in infants and young children worldwide.
7 astroviruses (HAstVs) are a leading cause of viral diarrhea in young children, the immunocompromised,
10 the NS3 proteinase of the pestivirus bovine viral diarrhea virus (BVDV) (NADL strain) is required fo
11 in the helicase/NTPase motifs of the bovine viral diarrhea virus (BVDV) (NADL strain) NS3 protein de
12 olling bovine pestiviruses, including bovine viral diarrhea virus (BVDV) and the emerging HoBi-like v
13 5A and NS5 proteins, respectively, of bovine viral diarrhea virus (BVDV) and yellow fever virus (YF),
15 Nonstructural protein 5B (NS5B) of bovine viral diarrhea virus (BVDV) contains sequence motifs tha
16 s to immunize cattle against selected bovine viral diarrhea virus (BVDV) genes has gained widespread
17 the N-terminal protein encoded by the bovine viral diarrhea virus (BVDV) genome is a cysteine proteas
18 VP32947, inhibits the replication of bovine viral diarrhea virus (BVDV) in cell culture at a 50% inh
19 bi-cistronic subgenomic replicon for bovine viral diarrhea virus (BVDV) in Huh-7 cells, similar to t
20 c screening test for the detection of bovine viral diarrhea virus (BVDV) in pooled bovine serum sampl
23 at the NS5A protein of the pestivirus bovine viral diarrhea virus (BVDV) is a zinc-binding protein.
32 h the N-terminal protease (N(pro)) of bovine viral diarrhea virus (BVDV), a pestiviral interferon ant
33 estigated superinfection exclusion of bovine viral diarrhea virus (BVDV), a positive-sense RNA pestiv
34 e RdRps from hepatitis C virus (HCV), bovine viral diarrhea virus (BVDV), and GB virus-B all can init
35 erases (RdRps) from GB virus-B (GBV), bovine viral diarrhea virus (BVDV), and hepatitis C virus (HCV)
37 g viruses hepatitis C virus (HCV) and bovine viral diarrhea virus (BVDV), lipid droplets, and secrete
44 many origins with the cytopathogenic bovine viral diarrhea virus (cpBVDV) results in the induction o
45 PCR detected parapoxvirus (n = 2) and bovine viral diarrhea virus (n = 2) in clinical samples, demons
46 nfection of calves with noncytopathic bovine viral diarrhea virus (ncpBVDV) was found to induce stron
48 hat RNA-dependent RNA polymerase from bovine viral diarrhea virus and the replicases from three plant
50 ted transmembrane domain derived from bovine viral diarrhea virus could not replace the HCV NS5B tran
53 ty is an inherent function of HCV and bovine viral diarrhea virus RdRps highly purified from both pro
54 7 are highly conserved amino acids in bovine viral diarrhea virus RNA polymerase (BVDV RdRp) and RdRp
55 t RNA-dependent RNA polymerase of the bovine viral diarrhea virus specifically requires a cytidylate
57 yellow fever virus, dengue virus, and bovine viral diarrhea virus) and a human coronavirus (OC43), an
59 TRIMs, TRIM56 inhibits replication of bovine viral diarrhea virus, a ruminant pestivirus of the famil
61 ine herpes virus types 1, 3, 4 and 5, bovine viral diarrhea virus, bovine parainfluenza 3 virus, bovi
62 ulatory beta-hairpin loops, including bovine viral diarrhea virus, dengue virus, and West Nile virus.
63 s, infectious bovine rhinotracheitis, bovine viral diarrhea virus, Mannheimia haemolytica or Mycoplas
65 HCV, classical swine fever virus and bovine viral diarrhea virus; and two unrelated viruses, encepha
66 viruses are recognized as a leading cause of viral diarrhea worldwide in children, immunocompromised
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