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1 rally unrelated glycosylated Gag from murine leukaemia virus.
2 ot inhibit other retroviruses such as murine leukaemia virus.
3 nic Gag-Abl fusion protein of Abelson Murine Leukaemia Virus and found that in contrast to Gag-Abl, i
4 , human T-cell lymphotropic virus and murine leukaemia virus are believed to spread via sites of cell
7 dimensional solution structure of the bovine leukaemia virus (BLV) matrix protein by heteronuclear nu
9 ific ZFP809 which binds to integrated murine leukaemia virus DNA elements and recruits KAP1 to repres
12 an endogenous retrovirus unrelated to murine leukaemia virus, implying that the Fv1 protein and its t
14 or muscle transduced with the Moloney murine leukaemia virus (M-MLV), a prototypic retroviral based v
15 ins of CA must expand relative to the murine leukaemia virus mature hexamer to accommodate the p10 co
16 s of different genera: HTLV-1, HIV-1, murine leukaemia virus (MLV), avian sarcoma leucosis virus (ASL
18 shuffling envelope sequences from six murine leukaemia viruses (MLV) followed by selection yielded a
19 mouse strain, which lacks endogenous murine leukaemia viruses (MLVs) able to replicate in murine cel
21 ection of CD2-Runx2 mice with Moloney murine leukaemia virus (Moloney MLV) also led to a dramatic acc
22 e Psi-RNA packaging signal of Moloney murine leukaemia virus (MoMuLV) expose conserved UCUG elements
24 ike classical chaperones, the Moloney murine leukaemia virus NC uses a unique mechanism for remodelli
25 es were delivered into ECs by Moloney murine leukaemia virus or human immunodeficiency virus, suggest
28 e we present the NMR structure of the murine leukaemia virus recoding signal and show that a protonat
30 against specific RNA viruses such as murine leukaemia virus, Sindbis virus and human immunodeficienc
31 n of B cells infected with the Friend murine leukaemia virus that form virological synapses with unin
32 wnstream of the splice donor in human T cell leukaemia virus type 1 (HTLV-1) was inserted into a plas
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