ライフサイエンスコーパス: bovine leukemia

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1 in 94% of animals that were seropositive for bovine leukemia virus (BLV) (n = 63) and in 87% of BLV-s

2 The deltaretroviruses, which include bovine leukemia virus (BLV) and human T-cell leukemia vi

3 ing for the deltaretroviruses, which include bovine leukemia virus (BLV) and human T-cell leukemia vi

4 istent virus infections: sheep infected with Bovine Leukemia Virus (BLV) and humans infected with Hum

5 ly conserved envelope (Env) glycoproteins of bovine leukemia virus (BLV) and its close relative, huma

6 In contrast, bovine leukemia virus (BLV) expresses subgenomic RNAP II

7 To investigate the early establishment of bovine leukemia virus (BLV) infection, we injected BLV-i

8 s) of animals with an early disease stage of bovine leukemia virus (BLV) infection, while IL-10 incre

9 MCs from animals with late disease stages of bovine leukemia virus (BLV) infection.

10 The SU and TM proteins of bovine leukemia virus (BLV) initially were reported to b

11 Bovine leukemia virus (BLV) is a complex B-lymphotrophic

12 Bovine leukemia virus (BLV) is a member of the human T-c

13 The bovine leukemia virus (BLV) is an oncogenic retrovirus t

14 The Rex of bovine leukemia virus (BLV) is poorly characterized.

15 rved charged residues in the deltaretrovirus bovine leukemia virus (BLV) matrix (MA) and NC domains a

16 BMCs) infected with the oncogenic retrovirus bovine leukemia virus (BLV) produce virus when cultured

17 developed genetically simple derivatives of bovine leukemia virus (BLV) that can replicate in tissue

18 The correlation between bovine leukemia virus (BLV) unintegrated DNA, viral expr

19 The encapsidation signal of bovine leukemia virus (BLV) was previously shown by dele

20 ytoplasmic domain of the TM protein (CTM) of bovine leukemia virus (BLV) was regulated by two membran

21 Bovine leukemia virus (BLV), a retrovirus related to hum

22 Here we demonstrate that the bovine leukemia virus (BLV), a retrovirus with an RNA ge

23 Bovine leukemia virus (BLV), a transactivating lymphotro

24 vivo mutation rate is comparable to that of bovine leukemia virus (BLV), another member of the HTLV/

25 herichia coli Shiga toxin (Stx) acts against bovine leukemia virus (BLV)-expressing cells was obtaine

26 Bovine leukemia virus (BLV)-induced persistent lymphocyt

27 Previously, we showed Stx activity against bovine leukemia virus (BLV)-infected cells in vitro and

28 iga toxin type 1 (Stx1) has activity against bovine leukemia virus (BLV).

29 ying the virus particle assembly pathway for bovine leukemia virus (BLV).

30 nuclear cells (PBMC) from cows infected with bovine leukemia virus (BLV).

31 on of B lymphocytes) in cattle infected with bovine leukemia virus (BLV; a retrovirus closely related

32 e in application method for the detection of bovine leukemia virus antigen gp51.

33 Bovine leukemia virus contains a pXBL region encoding th

34 e lentivirus and human T-cell leukemia virus/bovine leukemia virus genera.

35 for monocytes/macrophages in progression of bovine leukemia virus infection and, of importance, indi

36 Bovine leukemia virus microRNAs are strongly expressed i

37 region dispensable for in vivo infectivity, bovine leukemia virus microRNAs represent approximately

38 g of broad windows of small RNA sizes in the bovine leukemia virus ovine model of leukemia/lymphoma,

39 responsive element-independent expression of bovine leukemia virus RNA and supports the hypothesis th

40 scriptase PCR (RT-PCR) consistently detected bovine leukemia virus transcripts in fresh cells, and co

41 A recent demonstration that the bovine leukemia virus, a retrovirus, uses RNA polymerase

42 that peripheral blood mononuclear cells from bovine leukemia virus-infected animals in the alymphocyt

43 with previous findings suggest that IL-12 in bovine leukemia virus-infected animals may regulate prod

44 ipheral blood mononuclear cells (PBMCs) from bovine leukemia virus-infected animals with late-stage d

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