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1 onic amino acid transporter-1 (mCAT1) in the virus-producing cell.
2 ntity of HIV-1 DNA and replication-competent-virus-producing cells.
3 physically tethers virions to the surface of virus-producing cells.
4 precursor of the Gag (Pr55(Gag)) of HIV-1 in virus-producing cells.
5 essing of Pr55(gag) was largely inhibited in virus-producing cells.
6 ns, confirming the Gag/TSG101 interaction in virus-producing cells.
7 of Vpr also accumulates in the cytoplasm of virus-producing cells.
8 s with rapid turnover of both free virus and virus-producing cells.
9 Vif directly interact with HIV-1 RNA in the virus-producing cells.
12 l and the relationship between the number of virus-producing cells and plasma virus load has not been
13 inhibitory effect of CypA was restricted to virus-producing cells and was TRIM5alpha independent.
14 d with condensed chromatin in the nucleus of virus-producing cells, and cytoplasmic vesicles containi
15 secretion through the exocytic organelles of virus-producing cells, and second after virus binding to
16 cluded from lymphoid B cell follicles, where virus-producing cells are most highly concentrated, sugg
18 pecies-specific interactions between Vif and virus-producing cells, as opposed to between Vif and vir
19 hibit the anti-HIV-1 activity of APOBEC3G in virus-producing cells but not in target cells and APE mo
20 gi or UNG2-specific short-interfering RNA in virus-producing cells but not target cells, the virion-a
21 cent virions, Vif also removes APOBEC3G from virus-producing cells by inducing its ubiquitination and
23 iting virion production; delta, loss rate of virus-producing cells; c, clearance rate of free virions
24 vel of cell-to-cell transmission because the virus-producing cells cannot be easily distinguished fro
25 ermore, we directly demonstrate that >96% of virus producing cells did not express the Ki-67 prolifer
28 ctive APO3G mutants transiently expressed in virus-producing cells exhibited significant antiviral ac
29 acrophages were a significant portion of the virus-producing cells found in LNs, intestinal tissues,
30 riction of Env function may serve to protect virus-producing cells from the membrane-disruptive effec
34 lysis indicated that greater than 95% of the virus-producing cells in these tissues are macrophage an
36 ein are detectable in SIV virions but not in virus-producing cells, indicating that phosphorylation o
38 lthough most HIV originates from short-lived virus-producing cells, it is unlikely that chronic infec
39 t, it was possible to readily isolate stable virus-producing cell lines with titers approaching 10(7)
42 I molecules and costimulators, EC-stimulated virus-producing cells (p24(high) T cells) do not prolife
43 ree distinct times and locations: (i) in the virus-producing cell prior to viral release, yielding a
45 that expression of A3G, A3F, or murine A3 in virus-producing cells resulted in their virion incorpora
46 nt dispersion of genomes was observed around virus-producing cells, suggesting infection of neighbori
47 the Gag, Pol, and Env proteins of virions or virus-producing cells that correlates with virus infecti
48 e therapy to induce a pseudo-latent state in virus-producing cells, thus transforming HIV-1 into a li
51 aMA) HIV-1 precursor Gag (PrGag) proteins in virus-producing cells using a biotin ligase-tagging appr
52 By electron microscopy on thin sections of virus-producing cells, we observed that some NC mutants
53 The majority of mRNA species present in the virus-producing cells were also detected in Psi- particl
55 uman cells, as well as replication-competent-virus-producing cells, were measured to quantified viral
56 rs decreased HIV-1 Gag protein expression in virus-producing cells, while silencing the m(6)A erasers
57 her studies regarding Vif-RNA interaction in virus-producing cells will be important for studying the
59 apture NS2-containing protein complexes from virus-producing cells with streptavidin magnetic beads.
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