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1 nd diarrheal diseases, with the exception of viral diarrhea and an increase in diarrheal disease foll
2 glycans and reduce the infectivity of bovine viral diarrhea and dengue viruses in cellular models.
3 a variety of intestinal disorders, including viral diarrhea, antibiotic-associated diarrhea, Clostrid
4 o and persistently infected (PI) with bovine viral diarrhea (BVD) virus (BVDV) constitute the mechani
5 y the virus causes the majority of pediatric viral diarrhea cases.
6 man astrovirus (HAstV) is a leading cause of viral diarrhea in infants and young children worldwide.
7          Astroviruses are a leading cause of viral diarrhea in young children, immunocompromised indi
8 astroviruses (HAstVs) are a leading cause of viral diarrhea in young children, the immunocompromised,
9  astroviruses as the second leading cause of viral diarrhea in young children.
10  circumference) as well as location-specific viral diarrhea seasonality curves.
11                                       Bovine viral diarrhea virus (BVDV) (genus Pestivirus) was repor
12  the NS3 proteinase of the pestivirus bovine viral diarrhea virus (BVDV) (NADL strain) is required fo
13  in the helicase/NTPase motifs of the bovine viral diarrhea virus (BVDV) (NADL strain) NS3 protein de
14 olling bovine pestiviruses, including bovine viral diarrhea virus (BVDV) and the emerging HoBi-like v
15 5A and NS5 proteins, respectively, of bovine viral diarrhea virus (BVDV) and yellow fever virus (YF),
16          The pestivirus noncytopathic bovine viral diarrhea virus (BVDV) can suppress IFN production
17    Nonstructural protein 5B (NS5B) of bovine viral diarrhea virus (BVDV) contains sequence motifs tha
18 s to immunize cattle against selected bovine viral diarrhea virus (BVDV) genes has gained widespread
19 the N-terminal protein encoded by the bovine viral diarrhea virus (BVDV) genome is a cysteine proteas
20 nuated, and killed virus vaccines for bovine viral diarrhea virus (BVDV) have their limitations.
21  VP32947, inhibits the replication of bovine viral diarrhea virus (BVDV) in cell culture at a 50% inh
22  bi-cistronic subgenomic replicon for bovine viral diarrhea virus (BVDV) in Huh-7 cells, similar to t
23 c screening test for the detection of bovine viral diarrhea virus (BVDV) in pooled bovine serum sampl
24                                       Bovine viral diarrhea virus (BVDV) is a positive-strand RNA vir
25                                       Bovine viral diarrhea virus (BVDV) is a positive-stranded RNA v
26 at the NS5A protein of the pestivirus bovine viral diarrhea virus (BVDV) is a zinc-binding protein.
27                                       Bovine viral diarrhea virus (BVDV) is in the Flaviviridae famil
28                                       Bovine viral diarrhea virus (BVDV) is the most insidious and de
29  in epithelial cells by expression of bovine viral diarrhea virus (BVDV) N(PRO) protein targeting IRF
30                           Recombinant bovine viral diarrhea virus (BVDV) nonstructural protein 5B (NS
31                                   The bovine viral diarrhea virus (BVDV) RNA-dependent RNA polymerase
32 S) mediates translation initiation of bovine viral diarrhea virus (BVDV) RNA.
33 K cells infected with a noncytopathic bovine viral diarrhea virus (BVDV) strain, Kyle.
34  Here we investigated the function of bovine viral diarrhea virus (BVDV) uncleaved NS2-3.
35 udies of immune responses elicited by bovine viral diarrhea virus (BVDV) vaccines have primarily focu
36                     A novel mutant of bovine viral diarrhea virus (BVDV) was found with a virion asse
37 h the N-terminal protease (N(pro)) of bovine viral diarrhea virus (BVDV), a pestiviral interferon ant
38 estigated superinfection exclusion of bovine viral diarrhea virus (BVDV), a positive-sense RNA pestiv
39 e RdRps from hepatitis C virus (HCV), bovine viral diarrhea virus (BVDV), and GB virus-B all can init
40 erases (RdRps) from GB virus-B (GBV), bovine viral diarrhea virus (BVDV), and hepatitis C virus (HCV)
41               Pestiviruses, including bovine viral diarrhea virus (BVDV), are important animal pathog
42 g viruses hepatitis C virus (HCV) and bovine viral diarrhea virus (BVDV), lipid droplets, and secrete
43                                       Bovine viral diarrhea virus (BVDV), strain NADL, was originally
44                           Isolates of bovine viral diarrhea virus (BVDV), the prototype pestivirus, a
45 of miRNA dependency of the pestivirus bovine viral diarrhea virus (BVDV).
46 e immunogenicity of the E2 protein of bovine viral diarrhea virus (BVDV).
47 racterized as a specific inhibitor of bovine viral diarrhea virus (BVDV).
48 a broad spectrum of viruses including Bovine viral diarrhea virus (BVDV).
49 aled that the cDNA was amplified from bovine viral diarrhea virus (BVDV).
50  many origins with the cytopathogenic bovine viral diarrhea virus (cpBVDV) results in the induction o
51 PCR detected parapoxvirus (n = 2) and bovine viral diarrhea virus (n = 2) in clinical samples, demons
52 nfection of calves with noncytopathic bovine viral diarrhea virus (ncpBVDV) was found to induce stron
53 fferent viruses associated with BRDC: bovine viral diarrhea virus 1 and 2 (BVDV1 and BVDV2), bovine r
54                 Pestiviruses, such as bovine viral diarrhea virus and classical swine fever virus (CS
55 hat RNA-dependent RNA polymerase from bovine viral diarrhea virus and the replicases from three plant
56                            A chimeric bovine viral diarrhea virus construct containing an HEV RNA ins
57 ted transmembrane domain derived from bovine viral diarrhea virus could not replace the HCV NS5B tran
58              The crystal structure of bovine viral diarrhea virus E2 reveals a unique protein archite
59                         In cytopathic bovine viral diarrhea virus genotype 1 (BVDV1) isolates, insert
60 ty is an inherent function of HCV and bovine viral diarrhea virus RdRps highly purified from both pro
61 7 are highly conserved amino acids in bovine viral diarrhea virus RNA polymerase (BVDV RdRp) and RdRp
62 t RNA-dependent RNA polymerase of the bovine viral diarrhea virus specifically requires a cytidylate
63 ring unrelated viral glycoproteins or bovine viral diarrhea virus were not affected.
64 yellow fever virus, dengue virus, and bovine viral diarrhea virus) and a human coronavirus (OC43), an
65 IM56) as a host restriction factor of bovine viral diarrhea virus, a ruminant pathogen.
66 TRIMs, TRIM56 inhibits replication of bovine viral diarrhea virus, a ruminant pestivirus of the famil
67               Pestiviruses, including bovine viral diarrhea virus, are important animal pathogens and
68 ine herpes virus types 1, 3, 4 and 5, bovine viral diarrhea virus, bovine parainfluenza 3 virus, bovi
69 ulatory beta-hairpin loops, including bovine viral diarrhea virus, dengue virus, and West Nile virus.
70 s, infectious bovine rhinotracheitis, bovine viral diarrhea virus, Mannheimia haemolytica or Mycoplas
71 ation made for the related pestivirus bovine viral diarrhea virus.
72  HCV, classical swine fever virus and bovine viral diarrhea virus; and two unrelated viruses, encepha
73 viruses are recognized as a leading cause of viral diarrhea worldwide in children, immunocompromised
74      Human noroviruses are the main cause of viral diarrhea worldwide in people of all ages.