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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
3 ng to the canine TfR led to the emergence of canine parvovirus as a new pathogen in dogs.
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
7                                              Canine parvovirus (CPV) and feline panleukopenia virus (
8  cell infection processes and host ranges of canine parvovirus (CPV) and feline panleukopenia virus (
9                                              Canine parvovirus (CPV) and feline panleukopenia virus (
10                                              Canine parvovirus (CPV) and feline panleukopenia virus (
11                            The structures of canine parvovirus (CPV) and feline parvovirus (FPV) comp
12                                              Canine parvovirus (CPV) and its relative feline panleuko
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
17                                              Canine parvovirus (CPV) emerged in 1978 as a host range
18                                              Canine parvovirus (CPV) emerged in the late 1970s as a h
19                                              Canine parvovirus (CPV) enters and infects cells by a dy
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
22                                              Canine parvovirus (CPV) is a highly contagious pathogen
23                                              Canine parvovirus (CPV) is a host range variant of a fel
24                                              Canine parvovirus (CPV) is a small, nonenveloped virus t
25                 The DNA-containing capsid of canine parvovirus (CPV) is analyzed following atomic ref
26 es during natural infections of animals with canine parvovirus (CPV) or its ancestor, feline panleuko
27                                              Canine parvovirus (CPV) outbreaks can have a devastating
28 eading to viral attenuation was studied in a canine parvovirus (CPV) strain grown on dog kidney cells
29           We studied the binding kinetics of canine parvovirus (CPV) variants isolated from raccoons-
30 h concentration of anti-VP1-2-13 neutralized canine parvovirus (CPV) when it was incubated with the v
31        We analyzed a region of the capsid of canine parvovirus (CPV) which determines the ability of
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
36 r feline panleukopenia virus ("FPV-like") or canine parvovirus ("CPV-like").
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
39 three pandemic human influenza A viruses and canine parvovirus in dogs.
40         The asymmetry of receptor binding to canine parvovirus is reminiscent of the special portal i
41                          Substitution of the canine parvovirus NLS rescued the BR3 mutant to wild-typ
42 mplify and sequence the full VP2 gene of 150 canine parvoviruses obtained from a large cross-sectiona
43 ties to nonstructural and capsid proteins of canine parvovirus, respectively.
44 and canine transferrin receptors (TfRs) bind canine parvovirus to host cells and mediate rapid capsid
45                                              Canine parvovirus type 2 (CPV-2) emerged as a variant of
46                                              Canine parvovirus type 2 (CPV-2) emerged in 1978 and spr
47                                              Canine parvovirus type 2 (CPV-2) is a severe enteric pat
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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