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pubmed-article:17625972pubmed:abstractTextNovel anti-HIV agents that target different stages of the human immunodeficiency virus type 1 (HIV-1) replication cycle are now in clinical trials and have signs of improving our ability to manage HIV-1. This chapter, and the Conference presentation, dealt with the challenges encountered in realizing the optimal benefits of the newer therapeutics to individuals with AIDS and HIV-1 infection receiving highly active antiretroviral therapy (HAART). Emphasis was on the G-protein-coupled seven-transmembrane chemokine receptor, CCR5, as a potentially new therapeutic target and experience with novel CCR5 inhibitors, and the promise from further advancement through structural and molecular analysis of CCR5 inhibitor-CCR5 interactions. The promise in some of the newer protease inhibitors was also discussed.lld:pubmed
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pubmed-article:17625972pubmed:authorpubmed-author:MaedaKenjiKlld:pubmed
pubmed-article:17625972pubmed:authorpubmed-author:MitsuyaHiroak...lld:pubmed
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pubmed-article:17625972pubmed:volume87 Suppl 1lld:pubmed
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pubmed-article:17625972pubmed:dateRevised2009-4-22lld:pubmed
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pubmed-article:17625972pubmed:year2007lld:pubmed
pubmed-article:17625972pubmed:articleTitleDevelopment of therapeutics for AIDS: structure-based molecular targeting.lld:pubmed
pubmed-article:17625972pubmed:affiliationExperimental Retrovirology Section, HIV and AIDS Malignancy Branch, National Cancer Institute, Bethesda, MD 20892, USA. maedak@mail.nih.govlld:pubmed
pubmed-article:17625972pubmed:publicationTypeJournal Articlelld:pubmed
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