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3 in 94% of animals that were seropositive for bovine leukemia virus (BLV) (n = 63) and in 87% of BLV-s
5 ing for the deltaretroviruses, which include bovine leukemia virus (BLV) and human T-cell leukemia vi
6 istent virus infections: sheep infected with Bovine Leukemia Virus (BLV) and humans infected with Hum
7 ly conserved envelope (Env) glycoproteins of bovine leukemia virus (BLV) and its close relative, huma
8 human endogenous retrovirus group K (HERVK), bovine leukemia virus (BLV) and mouse mammary tumor viru
10 To investigate the early establishment of bovine leukemia virus (BLV) infection, we injected BLV-i
11 s) of animals with an early disease stage of bovine leukemia virus (BLV) infection, while IL-10 incre
20 rved charged residues in the deltaretrovirus bovine leukemia virus (BLV) matrix (MA) and NC domains a
21 BMCs) infected with the oncogenic retrovirus bovine leukemia virus (BLV) produce virus when cultured
22 developed genetically simple derivatives of bovine leukemia virus (BLV) that can replicate in tissue
25 ytoplasmic domain of the TM protein (CTM) of bovine leukemia virus (BLV) was regulated by two membran
29 vivo mutation rate is comparable to that of bovine leukemia virus (BLV), another member of the HTLV/
30 herichia coli Shiga toxin (Stx) acts against bovine leukemia virus (BLV)-expressing cells was obtaine
32 Previously, we showed Stx activity against bovine leukemia virus (BLV)-infected cells in vitro and
37 on of B lymphocytes) in cattle infected with bovine leukemia virus (BLV; a retrovirus closely related
40 that peripheral blood mononuclear cells from bovine leukemia virus-infected animals in the alymphocyt
41 with previous findings suggest that IL-12 in bovine leukemia virus-infected animals may regulate prod
42 ipheral blood mononuclear cells (PBMCs) from bovine leukemia virus-infected animals with late-stage d
43 for monocytes/macrophages in progression of bovine leukemia virus infection and, of importance, indi
45 region dispensable for in vivo infectivity, bovine leukemia virus microRNAs represent approximately
46 g of broad windows of small RNA sizes in the bovine leukemia virus ovine model of leukemia/lymphoma,
47 responsive element-independent expression of bovine leukemia virus RNA and supports the hypothesis th
48 scriptase PCR (RT-PCR) consistently detected bovine leukemia virus transcripts in fresh cells, and co