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1         Previous studies have shown that the bovine herpesvirus 1 (alphaherpesvirus) UL26.5 homolog w
2           Infected-cell protein 0 encoded by bovine herpesvirus 1 (BHV-1) (bICP0) is necessary for ef
3       Sensory neurons latently infected with bovine herpesvirus 1 (BHV-1) abundantly express latency-
4 ctivity, but not pseudorabies virus (PRV) or bovine herpesvirus 1 (BHV-1) entry, did not reduce homot
5                                              Bovine herpesvirus 1 (BHV-1) establishes a latent infect
6                                              Bovine herpesvirus 1 (BHV-1) establishes a lifelong late
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
11                                              Bovine herpesvirus 1 (BHV-1) induces immune suppression,
12                                              Bovine herpesvirus 1 (BHV-1) induces PCD in peripheral b
13                                              Bovine herpesvirus 1 (BHV-1) infected cell protein 0 (bI
14 l nervous system during acute infection, the bovine herpesvirus 1 (BHV-1) infection cycle is blocked
15                                              Bovine herpesvirus 1 (BHV-1) infection induces clinical
16                                              Bovine herpesvirus 1 (BHV-1) infection induces clinical
17                                              Bovine herpesvirus 1 (BHV-1) is an important pathogen of
18                                              Bovine herpesvirus 1 (BHV-1) is an important pathogen of
19                                              Bovine herpesvirus 1 (BHV-1) is an important pathogen of
20      The latency-related transcript (LRT) of bovine herpesvirus 1 (BHV-1) is the only abundant viral
21 eminal ganglia (TG) are the primary site for bovine herpesvirus 1 (BHV-1) latency.
22 V) recombinants that efficiently express the bovine herpesvirus 1 (BHV-1) membrane proteins gI and gE
23               Acute infection of cattle with bovine herpesvirus 1 (BHV-1) represses cell-mediated imm
24                     Infection of calves with bovine herpesvirus 1 (BHV-1) results in transient immuno
25                                          The bovine herpesvirus 1 (BHV-1) U(L)3.5 gene encodes a 126-
26                                          The bovine herpesvirus 1 (BHV-1) UL49 gene encodes a viral t
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
29                                              Bovine herpesvirus 1 (BHV-1), an alphaherpesvirinae subf
30                                              Bovine herpesvirus 1 (BHV-1), like other Alphaherpesviri
31                                              Bovine herpesvirus 1 (BHV-1), like other members of the
32                                              Bovine herpesvirus 1 (BHV-1), like other members of the
33 viruses porcine pseudorabies virus (PRV) and bovine herpesvirus 1 (BHV-1).
34 and 2, porcine pseudorabies virus (PRV), and bovine herpesvirus 1 (BHV-1).
35  gH, gI, gK, and gL) have been identified in bovine herpesvirus 1 (BHV-1).
36 2 protein from type 2 (890 strain) BVDV in a bovine herpesvirus 1 (BHV1) vector, we observed that exp
37                                    Following bovine herpesvirus 1 (BoHV-1) acute infection of ocular,
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
42      The latency-related (LR) RNA encoded by bovine herpesvirus 1 (BoHV-1) is abundantly expressed in
43                                              Bovine herpesvirus 1 (BoHV-1) is an alphaherpesvirus tha
44                                              Bovine herpesvirus 1 (BoHV-1) is an important pathogen o
45                                              Bovine herpesvirus 1 (BoHV-1) is an important pathogen o
46 ction following stressful stimuli.IMPORTANCE Bovine herpesvirus 1 (BoHV-1) is an important viral path
47                                              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
50                        An important site for bovine herpesvirus 1 (BoHV-1) latency is sensory neurons
51                                 For example, bovine herpesvirus 1 (BoHV-1) reactivation from latency
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
54                                              Bovine herpesvirus 1 (BoHV-1), an important bovine patho
55 ssion following stressful stimuli.IMPORTANCE Bovine herpesvirus 1 (BoHV-1), an important bovine patho
56                                              Bovine herpesvirus 1 (BoHV-1), an important pathogen of
57                                              Bovine herpesvirus 1 (BoHV-1), including modified live v
58                               In the case of bovine herpesvirus 1 (BoHV-1), replication in the epithe
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
61                   Following acute infection, bovine herpesvirus 1 establishes latency in sensory neur
62                                              Bovine herpesvirus 1 impairs TAP-dependent antigenic pep
63          In this report, we demonstrate that bovine herpesvirus 1 infection triggered tyrosine phosph
64      The latency-related (LR) RNA encoded by bovine herpesvirus 1 is abundantly expressed in the trig
65          The ICP0 protein (bICP0) encoded by bovine herpesvirus 1 is the major viral regulatory prote
66                 The bICP0 protein encoded by bovine herpesvirus 1 stimulates productive infection and
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
69                  VP22, a tegument protein of bovine herpesvirus 1, accumulates in the nucleus of infe
70 nd 2 (HSV-1 and -2), pseudorabies virus, and bovine herpesvirus 1.
71  65% with bovine herpesvirus 4, and 42% with bovine herpesvirus 1.
72 irus, encoding gE and gI homologs, is called bovine herpesvirus 1.1 (BHV-1.1).
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
75                     Here, we report that the bovine herpesvirus 4 (BHV4) BORFE2 gene encodes a protei
76 y murine gammaherpesvirus 68 (gammaHV68) and bovine herpesvirus 4 (BHV4), as described here.
77                       Thus, the Bo17 gene of Bovine herpesvirus 4 (BoHV-4) encodes a homologue of the
78                               Interestingly, bovine herpesvirus 4 encodes one such enzyme which is a
79  K5 of KSHV and contains a domain found in a bovine herpesvirus 4 major immediate-early protein.
80                                   Given that bovine herpesvirus 4 protein E1.1 and Kaposi's sarcoma a
81 69% with alcelaphine herpesvirus 1, 65% with bovine herpesvirus 4, and 42% with bovine herpesvirus 1.
82                   This study reports that in bovine herpesvirus 4, glycoprotein B (gB) is a heterodim
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)
85                                          The bovine herpesvirus 5 (BHV-5) gE ectodomain contains a gl
86 n that is required for anterograde spread of bovine herpesvirus 5 (BHV-5) infection from the olfactor
87                                              Bovine herpesvirus 5 (BHV-5) is a neurovirulent alphaher
88         The gE sequence of the neurovirulent bovine herpesvirus 5 (BHV-5) was determined and compared
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
91 vine respiratory syncytial virus (BRSV), and bovine herpesvirus (BHV1).
92  used to provide sequence evidence for a new bovine herpesvirus in bovine B-lymphoma cells and periph
93                                              Bovine herpesvirus type 1 (BHV-1) is an important compon
94 ogens, equine herpesvirus type 1 (EHV-1) and bovine herpesvirus type 1 (BHV-1), and fused them to enh
95                            Unlike equine and bovine herpesvirus type 1 ORF2 homologs that are associa
96 simplex virus (HSV), pseudorabies virus, and bovine herpesvirus type 1.
97 IE1 protein of the gamma-2 class herpesvirus bovine herpesvirus type 4 and a similar motif found in H