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1 gens such as Marburg virus, Nipah virus, and SARS coronavirus.
2 might be unique to the SUD and, thus, to the SARS coronavirus.
3 P-PMO showed low inhibitory activity against SARS coronavirus.
4 ected with H5N1 avian influenza virus or the SARS-coronavirus.
9 og in the severe acute respiratory syndrome (SARS) coronavirus appears to be group 1-like in that it
10 how that the PLpro domains from the MERS and SARS coronaviruses can recognize and process the same su
12 that infection of human airway epithelia by SARS coronavirus correlates with the state of cell diffe
13 zate (PubChem CID 16725315) were tested in a SARS coronavirus (CoV) and Ebola virus-pseudotype infect
16 es of the severe acute respiratory syndrome (SARS) coronavirus (CoV) are sensitive to neutralization
17 lation of severe acute respiratory syndrome (SARS) coronavirus (CoV) from Himalayan palm civets (Pagu
20 oteins of severe acute respiratory syndrome (SARS) coronavirus (CoV) to protective immunity by expres
23 In 2002, severe acute respiratory syndrome (SARS)-coronavirus (CoV) appeared as a novel human virus
24 hat the respiratory tract is a major site of SARS-coronavirus (CoV) infection and disease morbidity.
26 hods by: 1) identifying the sites explaining SARS coronavirus differences between human, bat and palm
31 acting alone, can prevent replication of the SARS coronavirus in the lung, a promising observation fo
32 3 of the severe acute respiratory syndrome (SARS) coronavirus includes a "SARS-unique domain" (SUD)
35 70, was among the best characterized against SARS coronavirus infection, showing weight loss and othe
37 odels for severe acute respiratory syndrome (SARS) coronavirus infection of humans are needed to eluc
39 combinant severe acute respiratory syndrome (SARS) coronavirus lacking the E gene (rSARS-CoV-DeltaE)
41 s) of the severe acute respiratory syndrome (SARS) coronavirus may encode determinants of virus virul
42 me entry site (IRES)-driven mRNAs, including SARS coronavirus mRNAs, hepatitis C virus (HCV), and cri
43 with BHPIV3/SARS-S induced the production of SARS-coronavirus-neutralising serum antibodies, indicati
45 gand that was found to inhibit -1 PRF in the SARS coronavirus on the conformational dynamics of the S
48 rotein of severe acute respiratory syndrome (SARS) coronavirus plays important roles in both viral re
50 tion, the severe acute respiratory syndrome (SARS) coronavirus replicated to high titers in the respi
51 COGs) database, Retroviral Genotyping Tools, SARS Coronavirus Resource, SAGEmap, Gene Expression Omni
52 A vectored mucosal vaccine expressing the SARS-coronavirus S protein alone may be highly effective
54 rotein microarray that harbors proteins from SARS coronavirus (SARS-CoV) and five additional coronavi
55 highly contagious disease that is caused by SARS coronavirus (SARS-CoV) and for which there are curr
56 ar receptor for two divergent coronaviruses, SARS coronavirus (SARS-CoV) and human coronavirus NL63 (
63 , for "middle of the SARS-unique domain") in SARS coronavirus (SARS-CoV) nonstructural protein 3 (nsp
64 pidemiologic studies have suggested that the SARS coronavirus (SARS-CoV) originated from animals.
65 tructures of NL63 coronavirus (NL63-CoV) and SARS coronavirus (SARS-CoV) receptor-binding domains (RB
66 ribe the construction of a panel of isogenic SARS coronavirus (SARS-CoV) strains bearing variant spik
67 evere acute respiratory syndrome (SARS), the SARS coronavirus (SARS-CoV), is a member of this large f
68 in-converting enzyme 2 (ACE2), isolated from SARS coronavirus (SARS-CoV)-permissive Vero E6 cells, th
73 rotein of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) is not only responsible for
74 cation of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) requires proteolytic proces
75 ) against severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) spike (S) glycoprotein conf
76 rotein of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) were mapped by Pepscan anal
77 ks of the severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV), but concerns remain over t
78 TR in the severe acute respiratory syndrome (SARS) coronavirus (SCoV) can each replace the 301-nt 3'
80 he elderly to severe SARS and the ability of SARS coronavirus to replicate in mice led us to examine
81 NL63 and severe acute respiratory syndrome (SARS) coronavirus to determine if DUB activity mediates
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