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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 of the canonical start/stop site in huNV and feline calicivirus but not in rabbit hemorrhagic disease
7 el neutralizing B-cell epitope, derived from feline calicivirus capsid protein, and a well characteri
8 irus strains, MD145-12 (genus Norovirus) and feline calicivirus (FCV) (genus Vesivirus), to investiga
9                                              Feline calicivirus (FCV) and murine norovirus (MNV) are
10 solution structures of the VPg proteins from feline calicivirus (FCV) and murine norovirus (MNV), whi
11  located at the 3' end of the genomic RNA of feline calicivirus (FCV) encodes a small (12.2-kDa) mino
12 s approach is demonstrated by the capture of feline calicivirus (FCV) from cell culture media that is
13           Open reading frame 2 (ORF2) of the feline calicivirus (FCV) genome encodes a capsid precurs
14    Here we show how longitudinal analysis of feline calicivirus (FCV) infection in an animal rescue s
15              Here, we examined the effect of feline calicivirus (FCV) infection on SG accumulation.
16                                The genome of feline calicivirus (FCV) is an approximately 7.7-kb sing
17                                              Feline calicivirus (FCV) nonstructural proteins are tran
18              Expression of the region of the feline calicivirus (FCV) ORF1 encoded by nucleotides 323
19 study was to identify the active form of the feline calicivirus (FCV) RNA-dependent RNA polymerase (R
20                                              Feline calicivirus (FCV) strains can show significant an
21 mid was engineered in which the LC region of feline calicivirus (FCV) was placed under the control of
22                                              Feline calicivirus (FCV), a member of the Caliciviridae,
23                                              Feline calicivirus (FCV), a member of the Vesivirus genu
24 LBC) epitopes in the major capsid protein of feline calicivirus (FCV), an expression library containi
25 qPCR) for feline herpesvirus type 1 (FHV-1), feline calicivirus (FCV), Mycoplasma felis, Chlamydophil
26 ause of infectious acute gastroenteritis and feline calicivirus (FCV), which causes respiratory illne
27 an ATP-regenerating system was isolated from feline calicivirus (FCV)-infected cells.
28 the attachment and infectious viral entry of feline calicivirus (FCV).
29 cule A (fJAM-A) is a functional receptor for feline calicivirus (FCV).
30        We have examined the entry process of feline calicivirus (FCV).
31 in types of feline coronaviruses (FCoVs) and feline caliciviruses (FCVs), respectively, and are impor
32                                              Feline calicivirus is a major causative agent of respira
33 gs on the RdRp activity of the norovirus and feline calicivirus Pro(-)Pol enzymes were compared and f
34          Many viruses, including the related feline calicivirus, use terminal sialic acids (SA) as re
35  death in young cats, and virulent, systemic feline calicivirus (vs-FCV) causes a highly fatal diseas
36 we have been exploiting endemic infection of feline calicivirus within five geographically distinct h

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