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1 quences are most closely related to those of gibbon ape leukemia virus.
3 sions and was demonstrated with amphotropic, gibbon ape leukemia virus, and vesicular stomatitis viru
5 iruses (MuLVs), feline leukemia viruses, and gibbon-ape leukemia virus, encode an alternate, glycosyl
7 n packaging cell lines containing either the gibbon ape leukemia virus envelope (PG13 cells), the mur
9 y (CHO) cells are resistant to infections by gibbon ape leukemia virus (GALV) and amphotropic murine
12 press distinct but related receptors for the gibbon ape leukemia virus (GALV) and the amphotropic mur
14 kemia virus (MuLV), the related protein from gibbon ape leukemia virus (GaLV) does not form functiona
15 der the direction of MoMSV LTR and using the gibbon ape leukemia virus (GALV) Env for internalization
16 virus (F-MLV) Env, but not with the related gibbon ape leukemia virus (GaLV) Env or with a chimeric
17 ant retroviruses pseudotyped with either the gibbon ape leukemia virus (GaLV) envelope or the vesicul
18 structed functional immunologically reactive gibbon ape leukemia virus (GALV) envelope proteins, tagg
19 g an optimized transduction protocol using a gibbon ape leukemia virus (GaLV) envelope-containing pac
20 e genes from each of the five members of the gibbon ape leukemia virus (GALV) family of type C retrov
22 has remained the only sequence implicated in gibbon ape leukemia virus (GALV) infection, and an acidi
23 ic murine retrovirus-related virus (XMRV) or gibbon ape leukemia virus (GALV) infection, even when th
24 were significantly higher than the level of gibbon ape leukemia virus (GaLV) receptor mRNA in cells
25 s targeting the amphotropic receptor and the gibbon ape leukemia virus (GALV) receptor Pit-1 were use
26 virus preparations of murine leukemia virus, gibbon ape leukemia virus (GALV), and simian sarcoma-ass
27 ity with the exogenous and highly infectious gibbon ape leukemia virus (GALV), the infectivity of KoR
28 y::Fur)] and the fusogenic glycoprotein from gibbon ape leukemia virus (GALV), which it was hoped wou
29 4-enriched marrow cells were cocultivated on gibbon ape leukemia virus (GALV)-based retrovirus vector
30 aging cells FLYRD (LgGLSN and LNX) or by the gibbon ape leukemia virus (GALV)-pseudotype packaging ce
31 nto baboon marrow repopulating cells using a gibbon ape leukemia virus (GALV)-pseudotype retroviral v
39 photropic murine leukemia virus (A-MuLV) and gibbon ape leukemia virus (GALV); E36 cells are highly s
42 ectofusin-1 variants to promote the modified gibbon ape leukemia virus glycoprotein-pseudotyped lenti
45 trast, the slightly different sequences from Gibbon ape leukemia virus, Moloney leukemia virus, PSAPP
46 Here we show that MDEV is also not in the gibbon ape leukemia virus or RD114 virus interference gr
49 generated a human packaging cell line with a gibbon ape leukemia virus pseudotype (Phoenix-GALV), and
52 ll surface phosphate transport proteins, the gibbon ape leukemia virus receptor Glvr-1 (Pit-1) or the
53 B feline leukemia viruses (FeLV-Bs) use the gibbon ape leukemia virus receptor, Pit1, as a receptor
54 For numerous gammaretroviruses, such as the gibbon ape leukemia virus, woolly monkey virus, feline l
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