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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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Erapy, and had received methadone or buprenorphine for 3 weeks at the OTP with no plans to discontinue. We also required verbal approval from participants' HIV providers and confirmation of active insurance coverage for ART. Exclusion criteria included ART dosed more frequently than twice daily, use of liquid medication, and use of a regimen that was predicted to have fewer than 1.5 active drugs
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Otein roteininteractions or protein ipid interactions and the other was in the soluble space. The sizes of the pools for such proteins are determined by their rates of membrane-association and membrane-dissociation (Fig. 1A). If membrane-dissociation is faster than membrane-association, then the protein may have a larger soluble pool. Conversely, if membrane-dissociation is slower than membrane-as
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Vioral complications [66-69]. Microglia, as a major target of HIV-1 infection in the CNS, are typically a viral reservoir [70-72] and are also key in HIV-1 neuroinvasiveness-penetration into the CNS by the virus [72,73]. Most importantly, a discrepancy between the localization of HIV-infected cells and the severity of neurocognitive symptoms has been described [74-76]. Thus, other mechanisms secon
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Evaluated. Laboratorial tests included total cholesterol, triglycerides, high density lipoprotein cholesterol, low density lipoprotein cholesterol, hemoglobin A1c, serum creatinine, Creactive protein and microalbuminuria. Body mass index, GFR (MDRD formula) and Framingham risk score [17] were calculated. Hypertension and dyslipidemia were defined by a self-reported history or use of specific thera
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Reclinical opioid-induced central immune signaling literature reviewed here need to be capitalized upon in the short term by conducting quality clinical trials in patient populations. Fortuitously, such trials of opioid-induced central immune signaling and efficacy of central immune signaling-targeted therapies are emerging in the literature. Patient care and quality use of medicine must be at the
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