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Structural characterization of nitric oxide synthase isoforms reveals striking active-site conservation

Nature structural biology, 1999-03, Vol.6 (3), p.233-242

1999

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Pharmacological Analysis of Calcium Responses Mediated by the Human A3 Adenosine Receptor in Monocyte-Derived Dendritic Cells and Recombinant Cells

Molecular pharmacology, 2003-02, Vol.63 (2), p.342-350

2003

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Expression of human inducible nitric oxide synthase in Escherichia coli

FEBS letters, 1996-01, Vol.379 (2), p.135-138

1996

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A point mutation of human interferon γ abolishes receptor recognition

Protein engineering, 1992-04, Vol.5 (3), p.253-257

1992

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A point mutation that decreases the thermal stability of human interferon γ

Protein engineering, 1992-04, Vol.5 (3), p.249-252

1992

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Exploiting the cell membrane for the production of heterologous proteins in Escherichia coli

Biotechnology and applied biochemistry, 1990-10, Vol.12 (5), p.567-578

1990

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The carboxyl-terminal region of human interferon γ is important for biological activity: mutagenic and NMR analysis

Protein engineering, 1991-02, Vol.4 (3), p.335-341

1991

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Cytoplasmic and periplasmic expression of a highly basic protein, human interleukin 4, in Escherichia coli

Journal of industrial microbiology, 1990-06, Vol.5 (4), p.215

1990

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Purification and crystallization of a complex between human interferon γ receptor (extracellular domain) and human interferon γ

Proteins, structure, function, and bioinformatics, 1996-09, Vol.26 (1), p.108-114

1996

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Expression of biologically active, mature human granulocyte-macrophage colony stimulating factor with an E. coli secretory expression system

Current microbiology, 1988-11, Vol.17 (6), p.321-332

1988

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The carboxyl-terminal region of human interferon γ is important for biological activity : mutagenic and MNR analysis

Protein engineering, 1991, Vol.4 (3), p.335-341

1991

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A point mutation of human interferon beta abolishes receptor recognition

Protein engineering, 1992-01, Vol.5 (3), p.253-257

1992

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Pharmacological characterization of Sch527123, a potent allosteric CXCR1/CXCR2 antagonist

The Journal of pharmacology and experimental therapeutics, 2007-08, Vol.322 (2), p.477

2007

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Discovery of 2-Hydroxy-N,N-dimethyl-3-{2-[[(R)-1-(5- methylfuran-2-yl)propyl]amino]-3,4-dioxocyclobut-1-enylamino}benzamide (SCH 527123): A Potent, Orally Bioavailable CXCR2/CXCR1 Receptor Antagonist

Journal of medicinal chemistry, 2006-12, Vol.49 (26), p.7603-7606

2006

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Initial optimization and series evolution of diaminopyrimidine inhibitors of interleukin-1 receptor associated kinase 4

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (16), p.3203-3207

2015

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3,4-Diamino-2,5-thiadiazole-1-oxides as potent CXCR2/CXCR1 antagonists

Bioorganic & medicinal chemistry, 2008, Vol.18 (1), p.228-231

2008

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Characterization of Peripheral Human Cannabinoid Receptor (hCB2) Expression and Pharmacology Using a Novel Radioligand, [35S]Sch225336

The Journal of biological chemistry, 2006-09, Vol.281 (38), p.28143-28151

2006

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Pharmacological characterization of human S1P 4 using a novel radioligand, [4,5‐ 3 H]‐dihydrosphingosine‐1‐phosphate

British journal of pharmacology, 2009-01, Vol.142 (5), p.851-860

2009

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Synthesis and structure–activity relationships of heteroaryl substituted-3,4-diamino-3-cyclobut-3-ene-1,2-dione CXCR2/CXCR1 receptor antagonists

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (4), p.1318-1322

2008

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Pharmacological characterization of human S1P4 using a novel radioligand, [4,5‐3H]‐dihydrosphingosine‐1‐phosphate

British journal of pharmacology, 2004-07, Vol.142 (5), p.851-860

2004

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Expression of biologically active, mature human granulocyte-macrophage colony stimulating factor with anE. coli secretory expression system

Current microbiology, 1988-11, Vol.17 (6), p.321-332

1988

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Structural characterization of nitric oxide synthase isoforms reveals striking active-site conservation

Pharmacological Analysis of Calcium Responses Mediated by the Human A3 Adenosine Receptor in Monocyte-Derived Dendritic Cells and Recombinant Cells

Expression of human inducible nitric oxide synthase in Escherichia coli

A point mutation of human interferon γ abolishes receptor recognition

A point mutation that decreases the thermal stability of human interferon γ

Exploiting the cell membrane for the production of heterologous proteins in Escherichia coli

The carboxyl-terminal region of human interferon γ is important for biological activity: mutagenic and NMR analysis

Cytoplasmic and periplasmic expression of a highly basic protein, human interleukin 4, in Escherichia coli

Purification and crystallization of a complex between human interferon γ receptor (extracellular domain) and human interferon γ

Expression of biologically active, mature human granulocyte-macrophage colony stimulating factor with an E. coli secretory expression system

The carboxyl-terminal region of human interferon γ is important for biological activity : mutagenic and MNR analysis

A point mutation of human interferon beta abolishes receptor recognition

Pharmacological characterization of Sch527123, a potent allosteric CXCR1/CXCR2 antagonist

Discovery of 2-Hydroxy-N,N-dimethyl-3-{2-[[(R)-1-(5- methylfuran-2-yl)propyl]amino]-3,4-dioxocyclobut-1-enylamino}benzamide (SCH 527123): A Potent, Orally Bioavailable CXCR2/CXCR1 Receptor Antagonist

Initial optimization and series evolution of diaminopyrimidine inhibitors of interleukin-1 receptor associated kinase 4

3,4-Diamino-2,5-thiadiazole-1-oxides as potent CXCR2/CXCR1 antagonists

Characterization of Peripheral Human Cannabinoid Receptor (hCB2) Expression and Pharmacology Using a Novel Radioligand, [35S]Sch225336

Pharmacological characterization of human S1P 4 using a novel radioligand, [4,5‐ 3 H]‐dihydrosphingosine‐1‐phosphate

Synthesis and structure–activity relationships of heteroaryl substituted-3,4-diamino-3-cyclobut-3-ene-1,2-dione CXCR2/CXCR1 receptor antagonists

Pharmacological characterization of human S1P4 using a novel radioligand, [4,5‐3H]‐dihydrosphingosine‐1‐phosphate

Expression of biologically active, mature human granulocyte-macrophage colony stimulating factor with anE. coli secretory expression system

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