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Interleukin-11, an inducible cytokine in human articular chondrocytes and synoviocytes, stimulates the production of the tissue inhibitor of metalloproteinases

The Journal of biological chemistry, 1993-10, Vol.268 (29), p.21527-21532

1993

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Characterization of Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2, a fluorogenic substrate with increased specificity constants for collagenases and tumor necrosis factor converting enzyme

Analytical biochemistry, 2004-05, Vol.328 (2), p.166-173

2004

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Discovery of Potent, Selective, and Orally Active Carboxylic Acid Based Inhibitors of Matrix Metalloproteinase-13

Journal of medicinal chemistry, 2009-06, Vol.52 (11), p.3523-3538

2009

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Potent and selective 2-naphthylsulfonamide substituted hydroxamic acid inhibitors of matrix metalloproteinase-13

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6440-6445

2011

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Discovery of CGS 27023A, a Non-Peptidic, Potent, and Orally Active Stromelysin Inhibitor That Blocks Cartilage Degradation in Rabbits

Journal of medicinal chemistry, 1997-08, Vol.40 (16), p.2525-2532

1997

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Characterization of Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH 2, a fluorogenic substrate with increased specificity constants for collagenases and tumor necrosis factor converting enzyme

Analytical biochemistry, 2004, Vol.328 (2), p.166-173

2004

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HIV-1 Transactivator Protein Tat Induces Proliferation and TGFβ Expression in Human Articular Chondrocytes

The Journal of cell biology, 1994-02, Vol.124 (3), p.365-371

1994

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Elevation of plasma hyaluronan and urinary pyridinoline in mouse collagen induced arthritis

Acta orthopaedica, 1995, Vol.66 (S266), p.145-147

1995

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Solution Structure of the Catalytic Domain of Human Stromelysin-1 Complexed to a Potent, Nonpeptidic Inhibitor

Biochemistry (Easton), 1998-10, Vol.37 (40), p.14048-14056

1998

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Reversibility of Tryptic Hydrolysis in a Model Nonapeptide Sequence

Prague, Czechoslovakia, August 29–September 3, 1982, 2019, Vol.17., p.403-406

2019

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Inactivation of trypsin-like proteases by depsipeptides of p-guanidinobenzoic acid

Journal of medicinal chemistry, 1981-06, Vol.24 (6), p.698-700

1981

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Factor C3f is a spasmogenic fragment released from C3b by factors I and H: The heptadeca-peptide C3f was synthesized and characterized

Molecular immunology, 1989-10, Vol.26 (10), p.939-948

1989

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Epoxide hydrase: structure-activity relationships of in vitro stimulators of the microsomal activity

Biochemistry (Easton), 1978-07, Vol.17 (14), p.2876-2881

1978

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Matrix Metalloproteinase Inhibitor CGS 27023A Protects COMP and Proteoglycan in the Bovine Articular Cartilage but not the Release of Their Fragments from Cartilage after Prolonged Stimulation in Vitro with IL-1α

Annals of the New York Academy of Sciences, 1999-06, Vol.878 (1), p.607-611

1999

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Solution structure of the catalytic domain of human collagenase-3 (MMP-13) complexed to a potent non-peptidic sulfonamide inhibitor: binding comparison with stromelysin-1 and collagenase-1 1 1Edited by P. E. Wright

Journal of molecular biology, 2000-08, Vol.301 (2), p.513-524

2000

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HIV-1 transactivator protein Tat induces proliferation and (TGFbeta) expression in human articular chondrocytes

The Journal of cell biology, 1994-02, Vol.124 (3), p.365

1994

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Design and synthesis of thiol containing inhibitors of matrix metalloproteinases

Bioorganic & medicinal chemistry letters, 1999-01, Vol.9 (2), p.195-200

1999

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Bioactive Conformation of Stromelysin Inhibitors Determined by Transferred Nuclear Overhauser Effects

Proceedings of the National Academy of Sciences - PNAS, 1995-01, Vol.92 (2), p.462-466

1995

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Mapping of the C3d Receptor (CR2)-Binding Site and a Neoantigenic Site in the C3d Domain of the Third Component of Complement

Proceedings of the National Academy of Sciences - PNAS, 1985-06, Vol.82 (12), p.4235-4239

1985

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Improved synthetic inactivators of plasmin

Thrombosis research, 1987-01, Vol.45 (1), p.1-6

1987

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Thick filter neutrophil chemotaxis performed in the absence of albumin

Journal of immunological methods, 1991-03, Vol.137 (1), p.37-46

1991

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HEPATIC EPOXIDE HYDRATASE: STRUCTURE-ACTIVITY RELATIONSHIPS OF IN VITRO ACTIVATORS

GANU, VISHWAS SADASHIV

1977

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Inhibition of interleukin‐1α‐induced cartilage oligomeric matrix protein degradation in bovine articular cartilage by matrix metalloproteinase inhibitors: Potential role for matrix metalloproteinases in the generation of cartilage oligomeric matrix protein fragments in arthritic synovial fluid

Arthritis and rheumatism, 1998-12, Vol.41 (12), p.2143-2151

1998

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Synthesis and properties of cyclic peptides containing the activation site of plasminogen

International Journal of Peptide and Protein Research, 1982-11, Vol.20 (5), p.421-428

1982

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A novel tricyclic pyrazine from lysine hydrochloride pyrolysis

Tetrahedron letters, 1980, Vol.21 (27), p.2679-2680

1980

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Interleukin-11, an inducible cytokine in human articular chondrocytes and synoviocytes, stimulates the production of the tissue inhibitor of metalloproteinases

Characterization of Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2, a fluorogenic substrate with increased specificity constants for collagenases and tumor necrosis factor converting enzyme

Discovery of Potent, Selective, and Orally Active Carboxylic Acid Based Inhibitors of Matrix Metalloproteinase-13

Potent and selective 2-naphthylsulfonamide substituted hydroxamic acid inhibitors of matrix metalloproteinase-13

Discovery of CGS 27023A, a Non-Peptidic, Potent, and Orally Active Stromelysin Inhibitor That Blocks Cartilage Degradation in Rabbits

Characterization of Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH 2, a fluorogenic substrate with increased specificity constants for collagenases and tumor necrosis factor converting enzyme

HIV-1 Transactivator Protein Tat Induces Proliferation and TGFβ Expression in Human Articular Chondrocytes

Elevation of plasma hyaluronan and urinary pyridinoline in mouse collagen induced arthritis

Solution Structure of the Catalytic Domain of Human Stromelysin-1 Complexed to a Potent, Nonpeptidic Inhibitor

Reversibility of Tryptic Hydrolysis in a Model Nonapeptide Sequence

Inactivation of trypsin-like proteases by depsipeptides of p-guanidinobenzoic acid

Factor C3f is a spasmogenic fragment released from C3b by factors I and H: The heptadeca-peptide C3f was synthesized and characterized

Epoxide hydrase: structure-activity relationships of in vitro stimulators of the microsomal activity

Matrix Metalloproteinase Inhibitor CGS 27023A Protects COMP and Proteoglycan in the Bovine Articular Cartilage but not the Release of Their Fragments from Cartilage after Prolonged Stimulation in Vitro with IL-1α

Solution structure of the catalytic domain of human collagenase-3 (MMP-13) complexed to a potent non-peptidic sulfonamide inhibitor: binding comparison with stromelysin-1 and collagenase-1 1 1Edited by P. E. Wright

HIV-1 transactivator protein Tat induces proliferation and (TGFbeta) expression in human articular chondrocytes

Design and synthesis of thiol containing inhibitors of matrix metalloproteinases

Bioactive Conformation of Stromelysin Inhibitors Determined by Transferred Nuclear Overhauser Effects

Mapping of the C3d Receptor (CR2)-Binding Site and a Neoantigenic Site in the C3d Domain of the Third Component of Complement

Improved synthetic inactivators of plasmin

Thick filter neutrophil chemotaxis performed in the absence of albumin

HEPATIC EPOXIDE HYDRATASE: STRUCTURE-ACTIVITY RELATIONSHIPS OF IN VITRO ACTIVATORS

Inhibition of interleukin‐1α‐induced cartilage oligomeric matrix protein degradation in bovine articular cartilage by matrix metalloproteinase inhibitors: Potential role for matrix metalloproteinases in the generation of cartilage oligomeric matrix protein fragments in arthritic synovial fluid

Synthesis and properties of cyclic peptides containing the activation site of plasminogen

A novel tricyclic pyrazine from lysine hydrochloride pyrolysis

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