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A Pathogenic Threshold of Virus Load Defined in Simian Immunodeficiency Virus- or Simian-Human Immunodeficiency Virus-Infected Macaques

Journal of Virology, 1998-12, Vol.72 (12), p.10281-10285

1998

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Highly potent and selective inhibition of human immunodeficiency virus by the bicyclam derivative JM3100

Antimicrobial Agents and Chemotherapy, 1994-04, Vol.38 (4), p.668-674

1994

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The non-immunosuppressive cyclosporin DEBIO-025 is a potent inhibitor of hepatitis C virus replication in vitro

Hepatology (Baltimore, Md.), 2006-04, Vol.43 (4), p.761-770

2006

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Mode of action of SDZ NIM 811, a nonimmunosuppressive cyclosporin A analog with activity against human immunodeficiency virus (HIV) type 1: interference with HIV protein-cyclophilin A interactions

Journal of Virology, 1995-04, Vol.69 (4), p.2451-2461

1995

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Inhibition of human immunodeficiency virus type 1 replication by SDZ NIM 811, a nonimmunosuppressive cyclosporine analog

Antimicrobial Agents and Chemotherapy, 1994-08, Vol.38 (8), p.1763-1772

1994

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Herpesvirus Saimiri vFLIP Provides an Antiapoptotic Function but Is Not Essential for Viral Replication, Transformation, or Pathogenicity

Journal of Virology, 2000-12, Vol.74 (24), p.11919-11927

2000

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Antiviral efficacy in vivo of the anti-human immunodeficiency virus bicyclam SDZ SID 791 (JM 3100), an inhibitor of infectious cell entry

Antimicrobial Agents and Chemotherapy, 1996-03, Vol.40 (3), p.750-754

1996

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Naturally Occurring Capsid Substitutions Render HIV-1 Cyclophilin A Independent in Human Cells and TRIM-cyclophilin-resistant in Owl Monkey Cells

The Journal of biological chemistry, 2005-12, Vol.280 (48), p.40293-40300

2005

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Inhibitors of HIV-1 Proteinase Containing 2-Heterosubstituted 4-Amino-3-hydroxy-5-phenylpentanoic Acid: Synthesis, Enzyme Inhibition, and Antiviral Activity

Journal of medicinal chemistry, 1994-09, Vol.37 (19), p.3079-3089

1994

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Characteristics of a Pathogenic Molecular Clone of an End-Stage Serum-Derived Variant of Simian Immunodeficiency Virus (SIVF359)

Journal of Virology, 2001-10, Vol.75 (19), p.9328-9338

2001

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In vitro activity of inhibitors of late stages of the replication of HIV in chronically infected macrophages

Journal of leukocyte biology, 1994-09, Vol.56 (3), p.381-386

1994

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Purification and partial characterization of poliovirus protease 2A by means of a functional assay

Journal of Virology, 1988-04, Vol.62 (4), p.1243-1250

1988

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Functional association of cyclophilin A with HIV-1 virions

Nature (London), 1994-11, Vol.372 (6504), p.363-365

1994

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SDZ PRI 053, an orally bioavailable human immunodeficiency virus type 1 proteinase inhibitor containing the 2-aminobenzylstatine moiety

Antimicrobial Agents and Chemotherapy, 1995-07, Vol.39 (7), p.1406-1413

1995

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The Use of Cyclosporine, FK506, and SDZ NIM811 to Prevent CD25 Quiescent Peripheral Blood Mononuclear Cells from Producing Human Immunodeficiency Virus

The Journal of infectious diseases, 1996-10, Vol.174 (4), p.850-853

1996

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[Melle4]Cyclosporin, a Novel Natural Cyclosporin with anti-HIV Activity: Structural Elucidation, Biosynthesis and Biological Properties

Antiviral chemistry & chemotherapy, 1994-10, Vol.5 (5), p.331-339

1994

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Measurement of HIV-1 reverse transcriptase by a nonradioactive assay system

Annals of the New York Academy of Sciences, 1992-11, Vol.672 (1 Enzyme Engine), p.252-256

1992

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Measurement of HIV-1 Reverse Transcriptase by a Nonradioactive Assay System

Annals of the New York Academy of Sciences, 1992-11, Vol.672 (1), p.252-256

1992

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Immunostimulatory, but not antiendotoxin, activity of lipid X is due to small amounts of contaminating N,O-acylated disaccharide-1-phosphate: in vitro and in vivo reevaluation of the biological activity of synthetic lipid X

Infection and Immunity, 1991-07, Vol.59 (7), p.2351-2358

1991

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Selective in vitro and in vivo activities of 5-(2-haloalkyl)pyrimidine nucleoside analogs, particularly 5-(2-chloroethyl)-2'-deoxyuridine, against herpes simplex virus

Antimicrobial Agents and Chemotherapy, 1985-08, Vol.28 (2), p.246-251

1985

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An anti-HIV strategy combining chemotherapy and therapeutic vaccination

Journal of medical primatology, 1999-08, Vol.28 (4-5), p.195-205

1999

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Kinetics and Isotype Profile of Rheumatoid Factor Production During Viral Infection: Organ Distribution of Antibody Secreting Cells

Scandinavian journal of immunology, 1996-09, Vol.44 (3), p.273-284

1996

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HIV-1 Integrase: High-Level Production and Screening Assay for the Endonucleolytic Activity

Antiviral chemistry & chemotherapy, 1992-04, Vol.3 (2), p.113-119

1992

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Mechanism of action of 5-(2-chloroethyl)-2'-deoxyuridine, a selective inhibitor of herpes simplex virus replication

Molecular pharmacology, 1990-05, Vol.37 (5), p.658-664

1990

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Potent and Orally Bioavailable HIV-1 Proteinase Inhibitors Containing the 2-aminobenzylstatine Moiety

Antiviral chemistry & chemotherapy, 1995-10, Vol.6 (5), p.327-336

1995

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A Pathogenic Threshold of Virus Load Defined in Simian Immunodeficiency Virus- or Simian-Human Immunodeficiency Virus-Infected Macaques

Highly potent and selective inhibition of human immunodeficiency virus by the bicyclam derivative JM3100

The non-immunosuppressive cyclosporin DEBIO-025 is a potent inhibitor of hepatitis C virus replication in vitro

Mode of action of SDZ NIM 811, a nonimmunosuppressive cyclosporin A analog with activity against human immunodeficiency virus (HIV) type 1: interference with HIV protein-cyclophilin A interactions

Inhibition of human immunodeficiency virus type 1 replication by SDZ NIM 811, a nonimmunosuppressive cyclosporine analog

Herpesvirus Saimiri vFLIP Provides an Antiapoptotic Function but Is Not Essential for Viral Replication, Transformation, or Pathogenicity

Antiviral efficacy in vivo of the anti-human immunodeficiency virus bicyclam SDZ SID 791 (JM 3100), an inhibitor of infectious cell entry

Naturally Occurring Capsid Substitutions Render HIV-1 Cyclophilin A Independent in Human Cells and TRIM-cyclophilin-resistant in Owl Monkey Cells

Inhibitors of HIV-1 Proteinase Containing 2-Heterosubstituted 4-Amino-3-hydroxy-5-phenylpentanoic Acid: Synthesis, Enzyme Inhibition, and Antiviral Activity

Characteristics of a Pathogenic Molecular Clone of an End-Stage Serum-Derived Variant of Simian Immunodeficiency Virus (SIVF359)

In vitro activity of inhibitors of late stages of the replication of HIV in chronically infected macrophages

Purification and partial characterization of poliovirus protease 2A by means of a functional assay

Functional association of cyclophilin A with HIV-1 virions

SDZ PRI 053, an orally bioavailable human immunodeficiency virus type 1 proteinase inhibitor containing the 2-aminobenzylstatine moiety

The Use of Cyclosporine, FK506, and SDZ NIM811 to Prevent CD25 Quiescent Peripheral Blood Mononuclear Cells from Producing Human Immunodeficiency Virus

[Melle4]Cyclosporin, a Novel Natural Cyclosporin with anti-HIV Activity: Structural Elucidation, Biosynthesis and Biological Properties

Measurement of HIV-1 reverse transcriptase by a nonradioactive assay system

Measurement of HIV-1 Reverse Transcriptase by a Nonradioactive Assay System

Immunostimulatory, but not antiendotoxin, activity of lipid X is due to small amounts of contaminating N,O-acylated disaccharide-1-phosphate: in vitro and in vivo reevaluation of the biological activity of synthetic lipid X

Selective in vitro and in vivo activities of 5-(2-haloalkyl)pyrimidine nucleoside analogs, particularly 5-(2-chloroethyl)-2'-deoxyuridine, against herpes simplex virus

An anti-HIV strategy combining chemotherapy and therapeutic vaccination

Kinetics and Isotype Profile of Rheumatoid Factor Production During Viral Infection: Organ Distribution of Antibody Secreting Cells

HIV-1 Integrase: High-Level Production and Screening Assay for the Endonucleolytic Activity

Mechanism of action of 5-(2-chloroethyl)-2'-deoxyuridine, a selective inhibitor of herpes simplex virus replication

Potent and Orally Bioavailable HIV-1 Proteinase Inhibitors Containing the 2-aminobenzylstatine Moiety

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