ライフサイエンスコーパス: canine parvovirus

1 Unexpectedly, a few sequence reads of canine parvovirus 2 and the recently described mouse kid

2 Canine parvovirus and distemper had high annual variatio

3 eceptor TfR as the cell surface receptor for canine parvovirus and feline panleukopenia virus, and al

4 f the H-1PV nucleotides to those observed in canine parvovirus and minute virus of mice, two members

5 Chimeras formed from combinations of canine parvovirus and portions of the parvovirus sequenc

6 , with new host species identified, and that canine parvoviruses are present in the dog population li

7 ng to the canine TfR led to the emergence of canine parvovirus as a new pathogen in dogs.

8 capsid surface loops from R. norvegicus with canine parvovirus assembled, allowing some of that capsi

9 nsferrin receptor, the cellular receptor for canine parvovirus, can bind to only one or a few of the

10 needed to explain the assembly of the T = 1 canine parvovirus capsid, the interactions of the 60-fol

11 Here we examined the protein composition of canine parvovirus capsids and evaluated their structural

12 Canine parvovirus (CPV) and feline panleukopenia virus (

13 cell infection processes and host ranges of canine parvovirus (CPV) and feline panleukopenia virus (

14 Canine parvovirus (CPV) and feline panleukopenia virus (

15 Canine parvovirus (CPV) and feline panleukopenia virus (

16 The structures of canine parvovirus (CPV) and feline parvovirus (FPV) comp

17 Canine parvovirus (CPV) and its relative feline panleuko

18 y and was found to be similar to the related canine parvovirus (CPV) and minute virus of mice (MVM).

19 lthough the emergence and pandemic spread of canine parvovirus (CPV) are well documented, the carnivo

20 ned the role of cytoplasmic transport of the canine parvovirus (CPV) capsid in productive infection b

21 In 1990, the first atomic structure of the canine parvovirus (CPV) capsid revealed a 26-nm-diameter

22 directly visualize the association of single canine parvovirus (CPV) capsids with cellular transferri

23 Canine parvovirus (CPV) emerged in 1978 as a host range

24 Canine parvovirus (CPV) emerged in the late 1970s as a h

25 Canine parvovirus (CPV) enters and infects cells by a dy

26 logous to the four variable surface loops of canine parvovirus (CPV) in individual fragments (pVP2b,

27 examine capsid substitutions that eliminate canine parvovirus (CPV) infectivity and identify how tho

28 Canine parvovirus (CPV) is a highly contagious pathogen

29 Canine parvovirus (CPV) is a highly successful pathogen

30 Canine parvovirus (CPV) is a host range variant of a fel

31 Canine parvovirus (CPV) is a small nonenveloped single-s

32 Canine parvovirus (CPV) is a small, nonenveloped virus t

33 Canine parvovirus (CPV) is an important pathogen causing

34 The DNA-containing capsid of canine parvovirus (CPV) is analyzed following atomic ref

35 es during natural infections of animals with canine parvovirus (CPV) or its ancestor, feline panleuko

36 Canine parvovirus (CPV) outbreaks can have a devastating

37 Serengeti National Park (SNP) and, second, a canine parvovirus (CPV) route of transmission among dome

38 eading to viral attenuation was studied in a canine parvovirus (CPV) strain grown on dog kidney cells

39 We studied the binding kinetics of canine parvovirus (CPV) variants isolated from raccoons-

40 h concentration of anti-VP1-2-13 neutralized canine parvovirus (CPV) when it was incubated with the v

41 We analyzed a region of the capsid of canine parvovirus (CPV) which determines the ability of

42 nized as important hosts in the evolution of canine parvovirus (CPV), a pandemic pathogen of domestic

43 enia virus (FPV) and its host range variant, canine parvovirus (CPV), can bind the feline transferrin

44 ding Aleutian mink disease parvovirus (ADV), canine parvovirus (CPV), minute virus of mice, and bovin

45 MVMi, MVMc, MVM-G17, tumor virus X (TVX), canine parvovirus (CPV), porcine parvovirus (PPV), rat p

46 r feline panleukopenia virus ("FPV-like") or canine parvovirus ("CPV-like").

47 dog contact was associated with exposure to canine parvovirus, Ehrlichia canis, Neospora caninum and

48 sites on the virion, indicating that either canine parvovirus has inherent asymmetry or binding of r

49 three pandemic human influenza A viruses and canine parvovirus in dogs.

50 We recently showed that following canine parvovirus infection of its natural host, the pol

51 Little evidence of transmission of canine parvoviruses into wild carnivore species was foun

52 Canine parvovirus is an important pathogen causing sever

53 The asymmetry of receptor binding to canine parvovirus is reminiscent of the special portal i

54 Substitution of the canine parvovirus NLS rescued the BR3 mutant to wild-typ

55 mplify and sequence the full VP2 gene of 150 canine parvoviruses obtained from a large cross-sectiona

56 ties to nonstructural and capsid proteins of canine parvovirus, respectively.

57 and canine transferrin receptors (TfRs) bind canine parvovirus to host cells and mediate rapid capsid

58 Canine parvovirus type 2 (CPV-2) emerged as a variant of

59 Canine parvovirus type 2 (CPV-2) emerged in 1978 and spr

60 Canine parvovirus type 2 (CPV-2) is a severe enteric pat

61 sis of a partial VP2 sequence of 54 samples, canine parvovirus type 2c (CPV-2c) (n = 26), CPV-2b (n =