ライフサイエンスコーパス: feline calicivirus

1 As has been previously demonstrated for feline calicivirus, a member of the Vesivirus genus, PSa

2 Previous studies on feline calicivirus and murine norovirus 1 (MNV1) demonst

3 We have shown for feline calicivirus and rabbit hemorrhagic disease virus

4 NV replication were derived from studies of feline calicivirus and rabbit hemorrhagic disease virus,

5 further divided into the following species: Feline calicivirus and Vesicular exanthema of swine viru

6 tion cryo-electron microscopy structures for feline calicivirus both undecorated and labelled with a

7 of the canonical start/stop site in huNV and feline calicivirus but not in rabbit hemorrhagic disease

8 le-stranded RNA viruses (e.g., Echovirus 12, feline calicivirus) but degraded much faster than MS2 (i

9 el neutralizing B-cell epitope, derived from feline calicivirus capsid protein, and a well characteri

10 irus strains, MD145-12 (genus Norovirus) and feline calicivirus (FCV) (genus Vesivirus), to investiga

11 Feline calicivirus (FCV) and murine norovirus (MNV) are

12 solution structures of the VPg proteins from feline calicivirus (FCV) and murine norovirus (MNV), whi

13 located at the 3' end of the genomic RNA of feline calicivirus (FCV) encodes a small (12.2-kDa) mino

14 s approach is demonstrated by the capture of feline calicivirus (FCV) from cell culture media that is

15 Open reading frame 2 (ORF2) of the feline calicivirus (FCV) genome encodes a capsid precurs

16 Here we show how longitudinal analysis of feline calicivirus (FCV) infection in an animal rescue s

17 Here, we examined the effect of feline calicivirus (FCV) infection on SG accumulation.

18 The genome of feline calicivirus (FCV) is an approximately 7.7-kb sing

19 Feline calicivirus (FCV) nonstructural proteins are tran

20 Expression of the region of the feline calicivirus (FCV) ORF1 encoded by nucleotides 323

21 study was to identify the active form of the feline calicivirus (FCV) RNA-dependent RNA polymerase (R

22 Feline calicivirus (FCV) strains can show significant an

23 mid was engineered in which the LC region of feline calicivirus (FCV) was placed under the control of

24 Feline calicivirus (FCV), a member of the Caliciviridae,

25 Feline calicivirus (FCV), a member of the Vesivirus genu

26 nse was observed in CRFK cells infected with Feline Calicivirus (FCV), a virus released by cell lysis

27 LBC) epitopes in the major capsid protein of feline calicivirus (FCV), an expression library containi

28 structure with that of a related vesivirus, feline calicivirus (FCV), highlighted potentially import

29 qPCR) for feline herpesvirus type 1 (FHV-1), feline calicivirus (FCV), Mycoplasma felis, Chlamydophil

30 ause of infectious acute gastroenteritis and feline calicivirus (FCV), which causes respiratory illne

31 an ATP-regenerating system was isolated from feline calicivirus (FCV)-infected cells.

32 the attachment and infectious viral entry of feline calicivirus (FCV).

33 cule A (fJAM-A) is a functional receptor for feline calicivirus (FCV).

34 We have examined the entry process of feline calicivirus (FCV).

35 lade, which includes the extensively studied feline calicivirus (FCV).

36 in types of feline coronaviruses (FCoVs) and feline caliciviruses (FCVs), respectively, and are impor

37 ed a 99.68% reduction in virus titer against Feline calicivirus in a surface time-kill test using rea

38 Feline calicivirus is a major causative agent of respira

39 gs on the RdRp activity of the norovirus and feline calicivirus Pro(-)Pol enzymes were compared and f

40 Many viruses, including the related feline calicivirus, use terminal sialic acids (SA) as re

41 death in young cats, and virulent, systemic feline calicivirus (vs-FCV) causes a highly fatal diseas

42 we have been exploiting endemic infection of feline calicivirus within five geographically distinct h