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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 tive RNA transport element CTE of the simian type D retroviruses.
10  the Constitutive Transport Element (CTE) of type D retroviruses.
11            These results demonstrate that in type D retroviruses a PPPY motif plays a key role in a l
12                      In contrast, the simian type D retroviruses act through a cis-acting constitutiv
13   The envelope protein is related to that of type D retroviruses, and SNV appears to use the same rec
14 he constitutive transport elements (CTEs) of type D retroviruses are cis-acting elements that promote
15 fizer monkey virus (M-PMV), the prototypical type D retrovirus, assembles immature capsids within the
16      Jaagsiekte sheep retrovirus (JSRV) is a type D retrovirus associated with a contagious lung tumo
17 n-Pfizer monkey virus (M-PMV), the prototype type D retrovirus, differs from most other retroviruses
18 ve transport element (CTE) encoded by simian type D retroviruses directs unspliced viral RNAs into a
19 ylogenetic analysis distinguished five ovine type D retroviruses: enJSRV groups A and B, ENTV, and tw
20 criptional control element CTE of the simian type D retrovirus has been shown to support replication
21 aEV but only become susceptible to RD114 and type D retroviruses if the cells are pretreated with tun
22  approach for preventing clinically relevant type D retrovirus infection and disease in RMs, with pro
23 endent infection of mouse cells by RD114 and type D retroviruses is caused by deglycosylation of mASC
24           Previous studies have implicated a type D retrovirus (jaagsiekte sheep retrovirus [JSRV]) a
25                                            A type D retrovirus, known as jaagsiekte sheep retrovirus
26            The pp24 and pp16 proteins of the type D retrovirus Mason-Pfizer monkey virus (M-PMV) are
27 whether immature capsids of the prototypical type D retrovirus, Mason-Pfizer monkey virus (M-PMV), ca
28                 We propose that both HIV and type D retroviruses may access the same constitutive RNA
29 - and CTE (constitutive transport element of type-D retrovirus)-mediated transactivation.
30  The constitutive transport element (CTE) of type D retroviruses mediates the nuclear export of unspl
31          The nuclear export of the unspliced type D retrovirus mRNA depends on the cis-acting constit
32                Infection of cells with RD114/type D retroviruses results in impaired amino acid trans
33  The constitutive transport element (CTE) of type D retroviruses serves as a signal of nuclear export
34                                       Simian type D retrovirus (SRV) is enzootic in many populations
35 ian T-cell lymphotropic virus (STLV), simian type D retrovirus (SRV), and simian foamy virus (SFV).
36           Additionally, genetically distinct type D retroviruses such as simian AIDS retrovirus and s
37 unspliced retroviral genomic RNA from simple type-D retroviruses such as SRV-1 that contain a constit
38 t the pulmonary tropic JSRV developed from a type D retrovirus that did not have lung specificity.
39 114, all strains of simian immunosuppressive type D retroviruses, the avian reticuloendotheliosis gro
40                             The RD114/simian type D retroviruses, which include the feline endogenous

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