Cerebrospinal fluid HIV-1 RNA, intrathecal immunoactivation, and drug concentrations after treatment with a combination of saquinavir, nelfinavir, and two nucleoside analogues: the... von Yilmaz, Aylin, Fuchs, Dietmar, Hagberg, Lars, Nillroth, Ulrika, Ståhle, Lars, Svensson, Jan-Olof, Gisslén, Magnus

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Cyclic HIV-1 Protease Inhibitors Derived from Mannitol:  Synthesis, Inhibitory Potencies, and Computational Predictions of Binding Affinities von Hultén, Johan, Bonham, Nicholas M, Nillroth, Ulrika, Hansson, Tomas, Zuccarello, Guido, Bouzide, Abderrahim, Åqvist, Johan, Classon, Björn, Danielson, U. Helena, Karlén, Anders, Kvarnström, Ingemar, Samuelsson, Bertil, Hallberg, Anders

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Optimization of P1–P3 groups in symmetric and asymmetric HIV‐1 protease inhibitors von Andersson, Hans O., Fridborg, Kerstin, Löwgren, Seved, Alterman, Mathias, Mühlman, Anna, Björsne, Magnus, Garg, Neeraj, Kvarnström, Ingmar, Schaal, Wesley, Classon, Björn, Karlén, Anders, Danielsson, U. Helena, Ahlsén, Göran, Nillroth, Ullrika, Vrang, Lotta, Öberg, Bo, Samuelsson, Bertil, Hallberg, Anders, Unge, Torsten

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Design and Synthesis of New Potent C 2-Symmetric HIV-1 Protease Inhibitors. Use of l-Mannaric Acid as a Peptidomimetic Scaffold von Alterman, Mathias, Björsne, Magnus, Mühlman, Anna, Classon, Björn, Kvarnström, Ingemar, Danielson, Helena, Markgren, Per-Olof, Nillroth, Ulrika, Unge, Torsten, Hallberg, Anders, Samuelsson, Bertil

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Design and Synthesis of New Potent C2-Symmetric HIV-1 Protease Inhibitors. Use of l-Mannaric Acid as a Peptidomimetic Scaffold von ALTERMAN, Mathias, BJöRSNE, Magnus, MüHLMAN, Anna, CLASSON, Björn, KVARNSTRöM, Ingemar, DANIELSON, Helena, MARKGREN, Per-Olof, NILLROTH, Ulrika, UNGE, Torsten, HALLBERG, Anders, SAMUELSSON, Bertil

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Human immunodeficiency virus type 1 proteinase resistance to symmetric cyclic urea inhibitor analogs von NILLROTH, U, VRANG, L, MARKGREN, P.-O, HULTEN, J, HALLBERG, A, DANIELSON, U. H

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HIV-1 Protease Inhibitors Based on Acyclic Carbohydrates von Zuccarello, Guido, Bouzide, Abderrahim, Kvarnström, Ingemar, Niklasson, Gunilla, Svensson, Stefan C. T, Brisander, Magnus, Danielsson, Helena, Nillroth, Ulrika, Karlén, Anders, Hallberg, Anders, Classon, Björn, Samuelsson, Bertil

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Synthesis of enantiomerically pure cis and trans 2-aminocyclopentanecarboxylic acids. Use of proline replacements in potential HIV-protease inhibitors von Nöteberg, Daniel, Brånalt, Jonas, Kvarnström, Ingemar, Classon, Björn, Samuelsson, Bertil, Nillroth, Ulrika, Danielson, U.Helena, Karlén, Anders, Hallberg, Anders

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A convenient synthesis of 1-(S)-[1′-(S)-( t-butyloxycarbonylamino)-2′-phenylethyl]oxirane. A useful building block in the synthesis of HIV protease inhibitors von Brånalt, Jonas, Kvarnström, Ingemar, Classon, Björn, Samuelsson, Bertil, Nillroth, Ulrika, Danielson, U.Helena, Karlén, Anders, Hallberg, Anders

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Cyclic urea and sulfamide-based inhibitors of HIV-1 protease: Changes in binding mode upon modifications in the P1/P1 side chain von Bäckbro, Kristina, Andersson, Hans, Bonham, Nick M, Classon, Björn, Danielson, U Helena, Hallberg, Anders, Hultén, Johan, Karlén, Anders, Löwgren, Seved, Nillroth, Ulrika, Schaal, Wesley, Unge, Torsten

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The use of 5′-Phosphate Derivatives of Nucleoside Analogues as Inhibitors of HIV-1 Replication von Nillroth, U., Vrang, L., Ahlsen, G., Besidsky, Y., Chattopadhyaya, J., Ugi, I., Danielson, U. H.

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Synthesis of C 2 Symmetric Potential Inhibitors of HIV-1 Protease From D-Mannitol von Niklasson, Gunilla, Kvarnström, Ingemar, Classon, Björn, Samuelsson†, Bertil, Nillroth, Ulrika, Danielson, Helena, Karlén, Anders, Hallberg, Anders

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