ライフサイエンスコーパス: type D retrovirus

1 gous RNA export elements, e.g. CTE of simian type D retroviruses.

2 le it to function as a receptor for RD114 or type D retroviruses.

3 he RD114 feline endogenous virus and primate type D retroviruses.

4 ction as an efficient receptor for RD114 and type D retroviruses.

5 EV but are relatively inactive for RD114 and type D retroviruses.

6 the constitutive transport element (CTE) of type D retroviruses.

7 ene therapy using vectors derived from RD114/type D retroviruses.

8 monkey virus (M-PMV) is the prototype of the type D retroviruses.

9 could restrict infection by extant mammalian type D retroviruses.

10 tive RNA transport element CTE of the simian type D retroviruses.

11 the Constitutive Transport Element (CTE) of type D retroviruses.

12 These results demonstrate that in type D retroviruses a PPPY motif plays a key role in a l

13 In contrast, the simian type D retroviruses act through a cis-acting constitutiv

14 The envelope protein is related to that of type D retroviruses, and SNV appears to use the same rec

15 he constitutive transport elements (CTEs) of type D retroviruses are cis-acting elements that promote

16 fizer monkey virus (M-PMV), the prototypical type D retrovirus, assembles immature capsids within the

17 Jaagsiekte sheep retrovirus (JSRV) is a type D retrovirus associated with a contagious lung tumo

18 n-Pfizer monkey virus (M-PMV), the prototype type D retrovirus, differs from most other retroviruses

19 ve transport element (CTE) encoded by simian type D retroviruses directs unspliced viral RNAs into a

20 ylogenetic analysis distinguished five ovine type D retroviruses: enJSRV groups A and B, ENTV, and tw

21 criptional control element CTE of the simian type D retrovirus has been shown to support replication

22 aEV but only become susceptible to RD114 and type D retroviruses if the cells are pretreated with tun

23 approach for preventing clinically relevant type D retrovirus infection and disease in RMs, with pro

24 endent infection of mouse cells by RD114 and type D retroviruses is caused by deglycosylation of mASC

25 Previous studies have implicated a type D retrovirus (jaagsiekte sheep retrovirus [JSRV]) a

26 A type D retrovirus, known as jaagsiekte sheep retrovirus

27 The pp24 and pp16 proteins of the type D retrovirus Mason-Pfizer monkey virus (M-PMV) are

28 whether immature capsids of the prototypical type D retrovirus, Mason-Pfizer monkey virus (M-PMV), ca

29 We propose that both HIV and type D retroviruses may access the same constitutive RNA

30 - and CTE (constitutive transport element of type-D retrovirus)-mediated transactivation.

31 The constitutive transport element (CTE) of type D retroviruses mediates the nuclear export of unspl

32 The nuclear export of the unspliced type D retrovirus mRNA depends on the cis-acting constit

33 Infection of cells with RD114/type D retroviruses results in impaired amino acid trans

34 The constitutive transport element (CTE) of type D retroviruses serves as a signal of nuclear export

35 Simian type D retrovirus (SRV) is enzootic in many populations

36 ian T-cell lymphotropic virus (STLV), simian type D retrovirus (SRV), and simian foamy virus (SFV).

37 Additionally, genetically distinct type D retroviruses such as simian AIDS retrovirus and s

38 unspliced retroviral genomic RNA from simple type-D retroviruses such as SRV-1 that contain a constit

39 t the pulmonary tropic JSRV developed from a type D retrovirus that did not have lung specificity.

40 114, all strains of simian immunosuppressive type D retroviruses, the avian reticuloendotheliosis gro

41 The RD114/simian type D retroviruses, which include the feline endogenous