ライフサイエンスコーパス: leukaemia virus

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

5 uman immunodeficiency virus and human T-cell leukaemia virus are resistant to human complement.

6 The Fv1 gene acts on murine leukaemia virus at a stage after entry into the target c

7 dimensional solution structure of the bovine leukaemia virus (BLV) matrix protein by heteronuclear nu

8 type 1 and 2 (HTLV-1 and HTLV-2) and bovine leukaemia virus (BLV).

9 ific ZFP809 which binds to integrated murine leukaemia virus DNA elements and recruits KAP1 to repres

10 the transmembrane subunit of Moloney murine leukaemia virus (Fig.

11 HIV-1 Nef and the unrelated mouse leukaemia virus glycosylated Gag (glycoGag) strongly enh

12 an endogenous retrovirus unrelated to murine leukaemia virus, implying that the Fv1 protein and its t

13 B-lymphoma Moloney murine leukaemia virus insertion region-1 (BMI1) is a member of

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

17 Moreover, in murine leukaemia virus (MLV), sequence variation in CA confers

18 (n = 100, n = 90 HIV-infected) using murine leukaemia virus (MLV)-based HCV pseudoviruses.

19 shuffling envelope sequences from six murine leukaemia viruses (MLV) followed by selection yielded a

20 mouse strain, which lacks endogenous murine leukaemia viruses (MLVs) able to replicate in murine cel

21 Infection of ESCs by the murine leukaemia viruses (MLVs) results in the normal establish

22 ection of CD2-Runx2 mice with Moloney murine leukaemia virus (Moloney MLV) also led to a dramatic acc

23 e Psi-RNA packaging signal of Moloney murine leukaemia virus (MoMuLV) expose conserved UCUG elements

24 dual hexagonal assembly from N-tropic murine leukaemia virus (N-MLV).

25 ike classical chaperones, the Moloney murine leukaemia virus NC uses a unique mechanism for remodelli

26 es were delivered into ECs by Moloney murine leukaemia virus or human immunodeficiency virus, suggest

27 requirement for Vpu during HIV-1 and murine leukaemia virus particle release.

28 somatic gene therapy by use of a gibbon-ape-leukaemia-virus pseudotyped gammaretroviral vector.

29 e we present the NMR structure of the murine leukaemia virus recoding signal and show that a protonat

30 The xenotropic murine leukaemia virus-related virus (XMRV), a gammaretrovirus,

31 kase (nSpCas9) and engineered Moloney murine leukaemia virus reverse transcriptase (M-MLV RT) collabo

32 against specific RNA viruses such as murine leukaemia virus, Sindbis virus and human immunodeficienc

33 Human feline leukaemia virus subgroup C receptor-related proteins 1 a

34 n of B cells infected with the Friend murine leukaemia virus that form virological synapses with unin

35 Human T cell leukaemia virus type 1 (HTLV-1) and human immunodeficien

36 The human T-cell leukaemia virus type 1 (HTLV-1) subtype c is endemic to

37 wnstream of the splice donor in human T cell leukaemia virus type 1 (HTLV-1) was inserted into a plas