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1 troviruses such as murine leukemia virus and spleen necrosis virus.
2 ements from Moloney murine sarcoma virus and spleen necrosis virus.
3 inal posttranscriptional control elements in spleen necrosis virus and human foamy virus RNA and supp
4 rated by 1 kb are 4 and 4.7% in one round of spleen necrosis virus and murine leukemia virus replicat
5 avian reticuloendotheliosis group including spleen necrosis virus, and baboon endogenous virus, use
7 he retroviral mutation rates, we developed a spleen necrosis virus-based in vivo system to selectivel
8 ing of RNA and DNA templates, we constructed spleen necrosis virus-based retroviral vectors containin
10 r and intermolecular template switching, two spleen necrosis virus-based vectors were constructed.
11 ructs derived from murine leukemia virus and spleen necrosis virus by replacing an NC flanking region
12 ted into the long terminal repeat (LTR) of a spleen necrosis virus shuttle vector, and proviruses wer
17 The RU5 region at the 5' RNA terminus of spleen necrosis virus (SNV) has been shown to facilitate
20 ucleoside analog 5-azacytidine increased the spleen necrosis virus (SNV) mutation rate 13-fold in one
21 cy direct repeat deletions are not unique to spleen necrosis virus (SNV) or the neomycin drug resista
22 on, we tested whether p12 can be replaced by spleen necrosis virus (SNV) p18, human immunodeficiency
24 ted retroviral vector particles derived from spleen necrosis virus (SNV) that display a single-chain
25 The ability of the nonlentiviral retrovirus spleen necrosis virus (SNV) to cross-package the genomic
26 nd protein analyses determined the 5' UTR of spleen necrosis virus (SNV), reticuloendotheliosis virus
27 ed retroviral vector particles, derived from spleen necrosis virus (SNV), that display the antigen bi
28 eered C-type retroviral vectors derived from spleen necrosis virus (SNV), which are capable of infect
30 otein, an HIV-1-based vector expressing Nef, spleen necrosis virus (SNV)-Nef virus (i.e., SNV vector
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