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1 eceptor TfR as the cell surface receptor for canine parvovirus and feline panleukopenia virus, and al
2 f the H-1PV nucleotides to those observed in canine parvovirus and minute virus of mice, two members
4 nsferrin receptor, the cellular receptor for canine parvovirus, can bind to only one or a few of the
5 needed to explain the assembly of the T = 1 canine parvovirus capsid, the interactions of the 60-fol
6 Here we examined the protein composition of canine parvovirus capsids and evaluated their structural
8 cell infection processes and host ranges of canine parvovirus (CPV) and feline panleukopenia virus (
13 y and was found to be similar to the related canine parvovirus (CPV) and minute virus of mice (MVM).
14 lthough the emergence and pandemic spread of canine parvovirus (CPV) are well documented, the carnivo
15 ned the role of cytoplasmic transport of the canine parvovirus (CPV) capsid in productive infection b
16 directly visualize the association of single canine parvovirus (CPV) capsids with cellular transferri
20 logous to the four variable surface loops of canine parvovirus (CPV) in individual fragments (pVP2b,
21 examine capsid substitutions that eliminate canine parvovirus (CPV) infectivity and identify how tho
26 es during natural infections of animals with canine parvovirus (CPV) or its ancestor, feline panleuko
28 eading to viral attenuation was studied in a canine parvovirus (CPV) strain grown on dog kidney cells
30 h concentration of anti-VP1-2-13 neutralized canine parvovirus (CPV) when it was incubated with the v
32 nized as important hosts in the evolution of canine parvovirus (CPV), a pandemic pathogen of domestic
33 enia virus (FPV) and its host range variant, canine parvovirus (CPV), can bind the feline transferrin
34 ding Aleutian mink disease parvovirus (ADV), canine parvovirus (CPV), minute virus of mice, and bovin
35 MVMi, MVMc, MVM-G17, tumor virus X (TVX), canine parvovirus (CPV), porcine parvovirus (PPV), rat p
37 dog contact was associated with exposure to canine parvovirus, Ehrlichia canis, Neospora caninum and
38 sites on the virion, indicating that either canine parvovirus has inherent asymmetry or binding of r
42 mplify and sequence the full VP2 gene of 150 canine parvoviruses obtained from a large cross-sectiona
44 and canine transferrin receptors (TfRs) bind canine parvovirus to host cells and mediate rapid capsid
48 sis of a partial VP2 sequence of 54 samples, canine parvovirus type 2c (CPV-2c) (n = 26), CPV-2b (n =
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