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1                                          The equine herpesvirus 1 (EHV-1) alpha-trans-inducing factor
2 -/-) mice infected with the alphaherpesvirus equine herpesvirus 1 (EHV-1) displayed reduced body weig
3 ur findings showed that the alphaherpesvirus equine herpesvirus 1 (EHV-1) efficiently entered and rep
4 the SRT of IE62 was replaced with the SRT of equine herpesvirus 1 (EHV-1) IEP, its trans-activation a
5                                          The equine herpesvirus 1 (EHV-1) immediate-early (IE) and EI
6                                          The equine herpesvirus 1 (EHV-1) immediate-early (IE) phosph
7 (CTL) response to respiratory infection with equine herpesvirus 1 (EHV-1) in CBA (H-2(k)) mice was in
8 accination remains the best option to combat equine herpesvirus 1 (EHV-1) infection, and several diff
9                                              Equine herpesvirus 1 (EHV-1) is a major pathogen affecti
10                                              Equine herpesvirus 1 (EHV-1) is a member of the Alphaher
11              The EICP22 protein (EICP22P) of Equine herpesvirus 1 (EHV-1) is an early protein that fu
12                         The EICP0 protein of equine herpesvirus 1 (EHV-1) is an early, viral regulato
13 rans-activator that activates all classes of equine herpesvirus 1 (EHV-1) promoters but, unexpectedly
14 human cells were efficiently transduced with equine herpesvirus 1 (EHV-1) reconstituted from viral DN
15 hology induced in the lung by the pathogenic equine herpesvirus 1 (EHV-1) strain RacL11 in comparison
16                                    Wild-type equine herpesvirus 1 (EHV-1) strains express a large (25
17                                         Most equine herpesvirus 1 (EHV-1) strains, including the natu
18 ses, herpes simplex virus type 1 (HSV-1) and equine herpesvirus 1 (EHV-1), and of channel catfish vir
19 e genomes of three other alphaherpesviruses: equine herpesvirus 1 (EHV-1), varicella-zoster virus, an
20 ected in the nucleus at 5 h postinfection in equine herpesvirus 1 (EHV-1)-infected HeLa and equine NB
21 s virus to and from T lymphocytes.IMPORTANCE Equine herpesvirus 1 (EHV1) is an ancestral alphaherpesv
22                                              Equine herpesvirus 1 (EHV1) replicates in the respirator
23 bacillus spp., and Mycoplasma equirhinis and equine herpesvirus 1 and 4 infections, after adjustment
24        The sole immediate-early (IE) gene of equine herpesvirus 1 encodes a 1,487-amino-acid (aa) reg
25 e effectively grown on cell lines expressing equine herpesvirus 1 gene 12, a non-HSV homologue of vmw
26      We describe a family of novel vCKBPs in equine herpesvirus 1, bovine herpesvirus 1 and 5, and re
27  herpesviruses: herpes simplex virus type 1, equine herpesvirus 1, guinea pig cytomegalovirus, and mu
28 us type 1 (HSV), varicella-zoster virus, and equine herpesvirus 1.
29 L32 homologs from varicella-zoster virus and equine herpesvirus 1.
30 of turkeys (HVT), and nonavian herpesviruses equine herpesviruses 1 and 4.
31 n linked to the neuropathogenic phenotype of equine herpesvirus-1 (EHV-1).
32 iosum virus proteins MC159 and MC160 and the equine herpesvirus 2 protein E8 share substantial homolo
33 e the cloning of the cellular homolog of the equine herpesvirus-2 protein E10 and show that both prot
34               vCLAP, the E10 gene product of equine herpesvirus-2, is a caspase-recruitment domain (C
35 striking similarity to E10, a product of the equine herpesvirus-2.
36 erpesvirus 1 (BoHV-1), canine herpesvirus 1, equine herpesvirus 4, and pseudorabies virus, establish
37 using a recombinant virus, we found that the equine herpesvirus ICP0 homologue induced the proteasome
38 e most severe disease outcomes, abortion and equine herpesvirus myeloencephalopathy (EHM).
39 HSV-1), as well as two veterinary pathogens, equine herpesvirus type 1 (EHV-1) and bovine herpesvirus
40      Defective interfering (DI) particles of equine herpesvirus type 1 (EHV-1) are capable of mediati
41                                Here, we used equine herpesvirus type 1 (EHV-1) as a model to determin
42                       In this study, we used equine herpesvirus type 1 (EHV-1) as a model to study th
43 from herpes simplex virus type 1 (HSV-1) and equine herpesvirus type 1 (EHV-1) failed to support DNA
44                    To assess the role of the equine herpesvirus type 1 (EHV-1) ICP0 protein (EICP0) i
45                                              Equine herpesvirus type 1 (EHV-1) is a contagious respir
46                                              Equine herpesvirus type 1 (EHV-1) outbreaks continue to
47 ORF2 as a vaccine candidate.IMPORTANCE Nasal equine herpesvirus type 1 (EHV-1) shedding is essential
48                   The cytolytic animal virus equine herpesvirus type 1 (EHV-1) was evaluated for its
49                                              Equine herpesvirus type 1 (EHV-1), a member of the Alpha
50 teins of bovine herpes virus type 1 (BHV-1), equine herpesvirus type 1 (EHV-1), pseudorabies virus (P
51 ular entry receptor for the alphaherpesvirus equine herpesvirus type 1 (EHV-1).
52                 We used the alphaherpesvirus equine herpesvirus type 1 (EHV1) and equine respiratory
53                                              Equine herpesvirus type 1 (EHV1), a well-known member of
54  demonstrate how a central alphaherpesvirus, equine herpesvirus type 1 (EHV1), actually exploits beta
55 host-specific and ancestral alphaherpesvirus equine herpesvirus type 1 (EHV1).
56                          We report here that equine herpesvirus type 2 E8 protein and molluscum conta
57 d 64% similarity) to the CARD of a gene from Equine Herpesvirus type 2.
58 implex virus type 1 (HSV-1) VP22 (HVP22) and equine herpesvirus type 4 (EHV-4) tk (Etk) were construc