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On the street, but only in those working in indoor venues, the network developed more quickly among FSW in indoor venues. Considering the transference process of sampling methods in populations to which it is difficult to gain access, conducted by the Global AIDS Program, Centers of Disease Control, a pilot study in Brazil, conducted in the city of Santos, SP, Southeastern Brazil, used the RDS met
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S in the prostasomal lipid raft. Additionally, we found proteins belonging to the ESCRT-III and Vps4 complex, but no proteins from ESCRT-0 and ESCRT-II. Furthermore, we identified ALIX, a protein that interacts with TSG101 (a component of ESCRT-I) and CHMP4 (a component of ESCRT-III) and that is thought to participate in the abscission process (57). ALIX in complex with syntenin (Table I) and synd
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Ns interact with HIV in a manner which could be inhibited by plant lectin interaction, and (iii) that some of these mannosylated proteins could be C-type lectins, considering the blocking effect of man-nan and the relative role of those lectins, syndecans and CD4 in HIV adsorption on MDDC. Interestingly, a recent report has described a selective tissus-specific mannosylation of the mannose recepto
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N, and nebulin molecules). A PDZ domain typically consists of 80 to 100 residues forming six -strands and two -helices. The carboxyl-terminal tail of the 7TMR is believed to interact with an elongated surface groove that is situated between the second -strand and the second -helix in an antiparallel manner. The functional implications of such interactions are as diverse as the PDZ domain-containin
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Istically significant period effect was found (P values i0.52). The primary statistical analysis gave an estimate of the reduction in saquinavir exposure when coadministered with rifabutin, as measured by AUC(0,8 h) and Cmax(0,8 h) of 47 (95 CI 30, 60 ) and 39 (95 CI 11, 59 ), respectively. Figure 1 illustrates the plasma concentrationtime profiles for saquinavir when administered alone (Treat
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Ation MDDC are washed and 2 ?105 cells were adsorbed on a microscopy-adapted slide. Cells were incubated with or without HHA-TRITC or GNA-TRITC (200 /ml; Eylabs) at 4 for 30 min. Cells were washed with PBS 0.01 azide 0.5 BSA and then fixed with 1 paraformaldehyde. The coverslides were mounted in Mowiol (SigmaAldrich). Fluorescence analysis was performed with a Zeiss LSM510 confocal microscope
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