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1 of nonadapted wild-type (wt) Ebolavirus and Marburgvirus.
2 appears to be the major virulence factor for marburgviruses.
3 of the secreted ebolavirus glycoproteins on marburgvirus and ebolavirus cell entry, using Fc-tagged
6 m Ebolavirus Zaire and Sudan species and the Marburgvirus Angola strain expressed in a DNA vaccine.
12 n of Reston and Lloviu viruses, filoviruses (marburgviruses, ebolaviruses, and "cuevaviruses") cause
14 1,2), ebolaviruses and cuevaviruses, but not marburgviruses, express two secreted glycoproteins, solu
16 ad-spectrum therapies against members of the Marburgvirus genus, including Marburg virus (MARV) and R
18 151-amino acid fragment of the Lake Victoria marburgvirus GP1 subunit bound filovirus-permissive cell
19 or for the deadly filoviruses Ebolavirus and Marburgvirus has yet to be identified and characterized.
23 s Zaire ebolavirus (ZEBOV) and Lake Victoria marburgvirus (MARV) were not affected by these condition
24 morrhagic fever (MHF), the disease caused by marburgvirus (MARV), and has created a bottleneck in the
25 irus (ZEBOV), Reston Ebolavirus (REBOV), and Marburgvirus (MARV), using transcriptional profiling and
34 f Marburg virus (MARV) species Lake Victoria marburgvirus, strain Musoke, indicate only a few regions
35 potential of all filovirus species: Marburg marburgvirus, Tai Forest ebolavirus, Reston ebolavirus,
36 tely 7%) from the main group of East African marburgviruses than one might expect given the large geo
37 erentiated between the genera Ebolavirus and Marburgvirus The amount of filovirus RNA that could be d
38 species of Ebolavirus and several strains of marburgvirus, the current immunotherapeutics primarily t
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