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Structural Insights and Biological Effects of Glycogen Synthase Kinase 3-specific Inhibitor AR-A014418

The Journal of biological chemistry, 2003-11, Vol.278 (46), p.45937-45945

2003

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Development of a novel therapeutic vaccine carrier that sustains high antibody titers against several targets simultaneously

The FASEB journal, 2017-03, Vol.31 (3), p.1204-1214

2017

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Relationships between Structure and Interaction Kinetics for HIV-1 Protease Inhibitors

Journal of medicinal chemistry, 2002-12, Vol.45 (25), p.5430-5439

2002

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2-Thioxanthines Are Mechanism-based Inactivators of Myeloperoxidase That Block Oxidative Stress during Inflammation

The Journal of biological chemistry, 2011-10, Vol.286 (43), p.37578-37589

2011

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Kinetic Analysis of the Interaction between HIV-1 Protease and Inhibitors Using Optical Biosensor Technology

Analytical biochemistry, 2000-03, Vol.279 (1), p.71-78

2000

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Determination of Interaction Kinetic Constants for HIV-1 Protease Inhibitors Using Optical Biosensor Technology

Analytical biochemistry, 2001-04, Vol.291 (2), p.207-218

2001

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Screening of Compounds Interacting with HIV-1 Proteinase Using Optical Biosensor Technology

Analytical biochemistry, 1998-12, Vol.265 (2), p.340-350

1998

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Prognostic potential of creatinine and Cystatin C in COVID-19 - a retrospective cohort study from Karolinska University Hospital

Scandinavian journal of clinical and laboratory investigation, 2023-07, Vol.83 (4), p.251-257

2023

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Elucidation of HIV-1 protease resistance by characterization of interaction kinetics between inhibitors and enzyme variants

Antiviral research, 2003-05, Vol.58 (3), p.235-242

2003

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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

Journal of medicinal chemistry, 1998-09, Vol.41 (20), p.3782-3792

1998

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Human immunodeficiency virus type 1 proteinase resistance to symmetric cyclic urea inhibitor analogs

Antimicrobial Agents and Chemotherapy, 1997-11, Vol.41 (11), p.2383-2388

1997

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Characterization of a set of HIV-1 protease inhibitors using binding kinetics data from a biosensor-based screen

Journal of biomolecular screening, 2000-10, Vol.5 (5), p.353-359

2000

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Capture and Analysis of Low Molecular Weight Ligands by Surface Plasmon Resonance Combined with Mass Spectrometry

European journal of mass spectrometry (Chichester, England), 2001-01, Vol.7 (4-5), p.385-391

2001

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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

Journal of medicinal chemistry, 1998-09, Vol.41 (20), p.3782-3792

1998

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P1/P1′ modified HIV protease inhibitors as tools in two new sensitive surface plasmon resonance biosensor screening assays

European journal of pharmaceutical sciences, 2001-05, Vol.13 (2), p.203-212

2001

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Investigation of an allosteric site of HIV-1 proteinase involved in inhibition by Cu2

Advances in experimental medicine and biology, 1998, Vol.436, p.99

1998

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Analysis of the interaction between HIV -1 protease and inhibitors: Applications for drug discovery

Markgren, Per-Olof

2000

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Structural Insights and Biological Effects of Glycogen Synthase Kinase 3-specific Inhibitor AR-A014418

Development of a novel therapeutic vaccine carrier that sustains high antibody titers against several targets simultaneously

Relationships between Structure and Interaction Kinetics for HIV-1 Protease Inhibitors

2-Thioxanthines Are Mechanism-based Inactivators of Myeloperoxidase That Block Oxidative Stress during Inflammation

Kinetic Analysis of the Interaction between HIV-1 Protease and Inhibitors Using Optical Biosensor Technology

Determination of Interaction Kinetic Constants for HIV-1 Protease Inhibitors Using Optical Biosensor Technology

Screening of Compounds Interacting with HIV-1 Proteinase Using Optical Biosensor Technology

Prognostic potential of creatinine and Cystatin C in COVID-19 - a retrospective cohort study from Karolinska University Hospital

Elucidation of HIV-1 protease resistance by characterization of interaction kinetics between inhibitors and enzyme variants

Design and Synthesis of New Potent C2-Symmetric HIV-1 Protease Inhibitors. Use of l-Mannaric Acid as a Peptidomimetic Scaffold

Human immunodeficiency virus type 1 proteinase resistance to symmetric cyclic urea inhibitor analogs

Characterization of a set of HIV-1 protease inhibitors using binding kinetics data from a biosensor-based screen

Capture and Analysis of Low Molecular Weight Ligands by Surface Plasmon Resonance Combined with Mass Spectrometry

Design and Synthesis of New Potent C 2-Symmetric HIV-1 Protease Inhibitors. Use of l-Mannaric Acid as a Peptidomimetic Scaffold

P1/P1′ modified HIV protease inhibitors as tools in two new sensitive surface plasmon resonance biosensor screening assays

Investigation of an allosteric site of HIV-1 proteinase involved in inhibition by Cu2

Analysis of the interaction between HIV -1 protease and inhibitors: Applications for drug discovery

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