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4 ctivity, but not pseudorabies virus (PRV) or bovine herpesvirus 1 (BHV-1) entry, did not reduce homot
7 other Alphaherpesvirinae subfamily members, bovine herpesvirus 1 (BHV-1) establishes latency in sens
8 heral nervous system during acute infection, bovine herpesvirus 1 (BHV-1) gene expression is extingui
9 During an infection of nonneuronal cells, bovine herpesvirus 1 (BHV-1) gene expression proceeds in
10 precursors, modified forms, and oligomers of bovine herpesvirus 1 (BHV-1) gI and gE proteins with pol
14 l nervous system during acute infection, the bovine herpesvirus 1 (BHV-1) infection cycle is blocked
22 V) recombinants that efficiently express the bovine herpesvirus 1 (BHV-1) membrane proteins gI and gE
27 study, mammalian expression vectors carrying bovine herpesvirus 1 (BHV-1) VP22 (BVP22) or herpes simp
28 llular attributes of HSV-1 VP22 (HVP22) with bovine herpesvirus 1 (BHV-1) VP22 (BVP22) using green fl
36 2 protein from type 2 (890 strain) BVDV in a bovine herpesvirus 1 (BHV1) vector, we observed that exp
38 orticosteroid dexamethasone (DEX) stimulates bovine herpesvirus 1 (BoHV-1) and herpes simplex virus 1
39 Alphaherpesvirinae subfamily members such as bovine herpesvirus 1 (BoHV-1) and herpes simplex virus 1
40 tion of the ocular, oral, or nasal cavity by bovine herpesvirus 1 (BoHV-1) culminates in lifelong lat
41 e many Alphaherpesvirinae subfamily members, bovine herpesvirus 1 (BoHV-1) expresses an abundant tran
46 ction following stressful stimuli.IMPORTANCE Bovine herpesvirus 1 (BoHV-1) is an important viral path
48 nd acid sphingomyelinase activity.IMPORTANCE Bovine herpesvirus 1 (BoHV-1) is an ubiquitous pathogen
49 incidence of reproductive failure.IMPORTANCE Bovine herpesvirus 1 (BoHV-1) is the most frequently dia
52 uations are predicted to enhance or initiate bovine herpesvirus 1 (BoHV-1) replication and virus spre
53 ion cycle.IMPORTANCE The lifelong latency of bovine herpesvirus 1 (BoHV-1) requires that significant
55 ssion following stressful stimuli.IMPORTANCE Bovine herpesvirus 1 (BoHV-1), an important bovine patho
59 ily of novel vCKBPs in equine herpesvirus 1, bovine herpesvirus 1 and 5, and related alphaherpesvirus
60 the retrograde axonal transport kinetics of bovine herpesvirus 1 and demonstrate that mutation of th
67 f the VZV ORF9a protein, the ortholog of the bovine herpesvirus 1 transporter associated with antigen
68 rus), hUS6 (human cytomegalovirus), bUL49.5 (bovine herpesvirus 1), and CPXV012 (cowpox virus), assem
73 enylated RNA (L1.7 RNA) transcribed from the bovine herpesvirus 4 (BHV-4) HindIII W fragment, in a re
74 virus (HCMV) were inactive, the homolog from bovine herpesvirus 4 (BHV-4), termed HORF1/2, was a very
81 69% with alcelaphine herpesvirus 1, 65% with bovine herpesvirus 4, and 42% with bovine herpesvirus 1.
83 homologues of the "immediate-early" gene of bovine herpesvirus 4, K8 that is a positional homologue
84 one homologue in RRV26-95 except K3 and K5 (bovine herpesvirus-4 immediate-early protein homologues)
86 n that is required for anterograde spread of bovine herpesvirus 5 (BHV-5) infection from the olfactor
89 we present the complete genomic sequence of bovine herpesvirus 5 (BHV-5), an alphaherpesvirus respon
90 vine influenza D virus, bovine parvovirus 2, bovine herpesvirus 6, bovine rhinitis A virus, and multi
92 used to provide sequence evidence for a new bovine herpesvirus in bovine B-lymphoma cells and periph
94 ogens, equine herpesvirus type 1 (EHV-1) and bovine herpesvirus type 1 (BHV-1), and fused them to enh
97 IE1 protein of the gamma-2 class herpesvirus bovine herpesvirus type 4 and a similar motif found in H