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1 cture of stem loop IIB is changed within the Rev responsive element.
2 interact with other viral RNAs, such as the Rev-responsive element.
3 ion can be complemented by HIV-1 Rev and the Rev-responsive element.
4 rase fusion protein) and its RNA target, the Rev-responsive element.
5 about 10-fold in the presence of Rev and the Rev-responsive element.
6 ized(5) alternative structures for the HIV-1 Rev responsive element also exist in cells, we discover
7 results indicate that the ESE functions as a Rev-responsive element and demonstrate that EIAV Rev med
8 n the splicing signals or replacement of the Rev-responsive element by the simian retrovirus type 1 c
9 rt of mRNA and that Rev interaction with the Rev-responsive element cannot bypass this requirement.
10 ing and can functionally replace Rev and the Rev-responsive element in the cytoplasmic accumulation o
11 The positive interaction of Rev with the Rev-responsive element in these mRNAs counteracts the ne
12 n-Pfizer monkey virus (MPMV) facilitates Rev/Rev-responsive element-independent expression of HIV-1 g
13 ptional control element that facilitates Rev/Rev-responsive element-independent expression of unsplic
14 ic polyunsaturated diketone to the HIV-1 Rev/Rev-responsive element inhibitor harziphilone under mild
16 structure that is strikingly similar to the Rev responsive element motif when bound to Rev protein.
17 ticle retroelements, that is able to replace Rev-responsive element regulation in human immunodeficie
19 i-HIV-1-genes: the Rev binding domain of the Rev Responsive Element (RRE decoy) (L-RRE-neo), a double
21 de antibiotics in their interaction with the Rev responsive element (RRE) of HIV-1 mRNA has been stud
23 We recently proposed a requirement for HIV-1 Rev responsive element (RRE) RNA binding host nuclear pr
25 tial regulatory HIV-1 protein that binds the Rev responsive element (RRE) within the env gene of the
26 tial HIV-1 regulatory protein that binds the Rev responsive element (RRE) within the env gene of the
30 sduction with a retroviral vector carrying a rev-responsive element (RRE) decoy gene, and reinfused t
32 cts and can functionally replace Rev and the Rev-responsive element (RRE) in the nuclear export of un
33 the activities of these viral elements, the Rev-responsive element (RRE) of the human immunodeficien
35 ognition of the human immunodeficiency virus Rev-responsive element (RRE) RNA by the Rev protein is a
36 t could be targeted to bind and activate the Rev-responsive element (RRE) RNA or heterologous MS2 pha
38 riptional activation directed by Rev and the Rev-responsive element (RRE) when inserted into a Rev- a
39 n requires binding of the Rev protein to the Rev-responsive element (RRE) within the viral transcript
40 Rev binds to a complex RNA structure, the Rev-responsive element (RRE), present in all Rev-respons
41 consisting of Rev and its binding site, the Rev-responsive element (RRE), stands out as particularly
43 spleen necrosis virus (SNV) facilitates Rev/Rev-responsive element (RRE)-independent expression of i
47 has been shown to support replication of Rev-Rev-responsive-element (RRE)-deficient molecular clones
49 234-nucleotide human immunodeficiency virus Rev responsive element (RRE234) was significantly lower.
50 te export through two independent cis-acting Rev-responsive elements (RREs), and differences among Re
51 gh affinity for human immunodeficiency virus Rev responsive element stem loop IIB (RRE-IIB) were prev
52 is dependent on the HIV Rev protein and the Rev-responsive element, the latter located on the env tr
54 f SIVmac239 in which the Rev protein and the Rev-responsive element were replaced by the constitutive