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Journal of mathematics and the arts, 2023-04, Vol.17 (1-2), p.50-61

Gould, S. L.

2023

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CCR5, CXCR4, and CD4 Are Clustered and Closely Apposed on Microvilli of Human Macrophages and T Cells

Journal of Virology, 2001-04, Vol.75 (8), p.3779-3790

2001

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Binding and Functional Properties of Recombinant and Endogenous CXCR3 Chemokine Receptors

The Journal of biological chemistry, 1998-07, Vol.273 (29), p.18288-18291

1998

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 4: synthesis and structure–Activity relationships for 1-[ N-(Methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-(4-( N-(alkyl)- N-(benzyloxycarbonyl)amino)piperidin-1-yl)butanes

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (18), p.2475-2479

2001

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 1: Discovery and initial structure-activity relationships for 1-amino-2-phenyl-4-(piperidin-1-yl)butanes

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.259-264

2001

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Differences between progeny of beef sires in susceptibility to fescue toxicosis

Journal of animal science, 1993-11, Vol.71 (11), p.3025-3032

1993

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Mycotoxins and Fusarium spp. associated with infected ears of corn in Minnesota

Applied and Environmental Microbiology, 1988-08, Vol.54 (8), p.1930-1933

1988

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Comparison of the functional blockade of rat substance P (NK 1) receptors by GR205171, RP67580, SR140333 and NKP-608

Neuropharmacology, 2003-08, Vol.45 (2), p.231-241

2003

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: Structure-activity relationships for substituted 2-aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.265-270

2001

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1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 1: discovery of the pyrrolidine scaffold and determination of its stereochemical requirements

Bioorganic & medicinal chemistry letters, 2001-06, Vol.11 (11), p.1437-1440

2001

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Discovery of human CCR5 antagonists containing hydantoins for the treatment of HIV-1 infection

Bioorganic & medicinal chemistry letters, 2001-12, Vol.11 (24), p.3099-3102

2001

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1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent Anti-HIV activity

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (20), p.2741-2745

2001

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Design, synthesis, and SAR of heterocycle-containing antagonists of the human CCR5 receptor for the treatment of HIV-1 infection

Bioorganic & medicinal chemistry letters, 2001-12, Vol.11 (24), p.3103-3106

2001

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Combinatorial synthesis of CCR5 antagonists

Bioorganic & medicinal chemistry letters, 2001-12, Vol.11 (24), p.3137-3141

2001

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 3: A proposed pharmacophore model for 1-[ N-(methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-[4-(substituted)piperidin-1-yl]butanes

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (18), p.2469-2473

2001

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Optimization of a Fed-batch Process for Production of a Recombinant Antibody

Annals of the New York Academy of Sciences, 1994-11, Vol.745 (1), p.285-296

1994

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Titration of human-bovine rotavirus reassortants using a tetrazolium-based colorimetric end-point dilution assay

Journal of virological methods, 1995-10, Vol.55 (2), p.199-208

1995

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Use of Lipid Emulsions as Nutritional Supplements in Mammalian Cell Culture

Annals of the New York Academy of Sciences, 1994-11, Vol.745 (1), p.240-243

1994

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First Report of Sudden Death Syndrome (Fusarium solani f. sp. glycines) of Soybean in Minnesota

Plant disease, 2003-04, Vol.87 (4), p.449-449

2003

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Potent 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists: effects of fused heterocycles on antiviral activity and pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 2005-04, Vol.15 (8), p.2129-2134

2005

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Artificial Photosynthetic Reaction Centers: Mimicking Sequential Electron and Triplet-Energy Transfer

Chemphyschem, 2005-11, Vol.6 (11), p.2359-2370

2005

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Time-resolved EPR investigation of charge recombination to a triplet state in a carotene-diporphyrin triad

Molecular physics, 2006-05, Vol.104 (10-11), p.1595-1607

2006

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Watching Television Come of Age: The New York Times Reviews by Jack Gould

Gould, Lewis L

1, 2002

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Artificial photosynthetic reaction centers with carotenoid antennas

Tetrahedron, 2006-02, Vol.62 (9), p.2074-2096

2006

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Antagonists of human CCR5 receptor containing 4-(pyrazolyl)piperidine side chains. Part 1: Discovery and sar study of 4-pyrazolylpiperidine side chains

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (4), p.935-939

2004

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Orbifold jacket

CCR5, CXCR4, and CD4 Are Clustered and Closely Apposed on Microvilli of Human Macrophages and T Cells

Binding and Functional Properties of Recombinant and Endogenous CXCR3 Chemokine Receptors

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 4: synthesis and structure–Activity relationships for 1-[ N-(Methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-(4-( N-(alkyl)- N-(benzyloxycarbonyl)amino)piperidin-1-yl)butanes

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 1: Discovery and initial structure-activity relationships for 1-amino-2-phenyl-4-(piperidin-1-yl)butanes

Differences between progeny of beef sires in susceptibility to fescue toxicosis

Mycotoxins and Fusarium spp. associated with infected ears of corn in Minnesota

Comparison of the functional blockade of rat substance P (NK 1) receptors by GR205171, RP67580, SR140333 and NKP-608

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: Structure-activity relationships for substituted 2-aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 1: discovery of the pyrrolidine scaffold and determination of its stereochemical requirements

Discovery of human CCR5 antagonists containing hydantoins for the treatment of HIV-1 infection

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent Anti-HIV activity

Design, synthesis, and SAR of heterocycle-containing antagonists of the human CCR5 receptor for the treatment of HIV-1 infection

Combinatorial synthesis of CCR5 antagonists

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 3: A proposed pharmacophore model for 1-[ N-(methyl)- N-(phenylsulfonyl)amino]-2-(phenyl)-4-[4-(substituted)piperidin-1-yl]butanes

Optimization of a Fed-batch Process for Production of a Recombinant Antibody

Titration of human-bovine rotavirus reassortants using a tetrazolium-based colorimetric end-point dilution assay

Use of Lipid Emulsions as Nutritional Supplements in Mammalian Cell Culture

First Report of Sudden Death Syndrome (Fusarium solani f. sp. glycines) of Soybean in Minnesota

Potent 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists: effects of fused heterocycles on antiviral activity and pharmacokinetic properties

Artificial Photosynthetic Reaction Centers: Mimicking Sequential Electron and Triplet-Energy Transfer

Time-resolved EPR investigation of charge recombination to a triplet state in a carotene-diporphyrin triad

Watching Television Come of Age: The New York Times Reviews by Jack Gould

Artificial photosynthetic reaction centers with carotenoid antennas

Antagonists of human CCR5 receptor containing 4-(pyrazolyl)piperidine side chains. Part 1: Discovery and sar study of 4-pyrazolylpiperidine side chains

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