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ADAM15 Is Functionally Associated with the Metastatic Progression of Human Bladder Cancer

PloS one, 2016-03, Vol.11 (3), p.e0150138-e0150138

2016

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High-Resolution X-Ray Structure and Functional Analysis of the Murine Norovirus 1 Capsid Protein Protruding Domain

Journal of Virology, 2010-06, Vol.84 (11), p.5695-5705

2010

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Bone Marrow Macrophages Induce Inflammation by Efferocytosis of Apoptotic Prostate Cancer Cells via HIF-1α Stabilization

Cells (Basel, Switzerland), 2022-11, Vol.11 (23), p.3712

2022

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High-Resolution Cryo-Electron Microscopy Structures of Murine Norovirus 1 and Rabbit Hemorrhagic Disease Virus Reveal Marked Flexibility in the Receptor Binding Domains

Journal of Virology, 2010-06, Vol.84 (11), p.5836-5841

2010

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Unique Pro-Inflammatory Response of Macrophages during Apoptotic Cancer Cell Clearance

Cells (Basel, Switzerland), 2020-02, Vol.9 (2), p.429

2020

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Design, Synthesis, and Evaluation of Aza-Peptide Epoxides as Selective and Potent Inhibitors of Caspases-1, -3, -6, and -8

Journal of medicinal chemistry, 2004-03, Vol.47 (6), p.1553-1574

2004

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The Tail of KdsC

The Journal of biological chemistry, 2009-10, Vol.284 (44), p.30594-30603

2009

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Molecular Correlates of In Vitro Responses to Dacomitinib and Afatinib in Bladder Cancer

Bladder cancer, 2018-01, Vol.4 (1), p.77-90

2018

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Tail of KdsC: CONFORMATIONAL CHANGES CONTROL THE ACTIVITY OF A HALOACID DEHALOGENASE SUPERFAMILY PHOSPHATASE

The Journal of biological chemistry, 2009-10, Vol.284 (44), p.30594-30603

2009

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An inhibitor of the protein kinases TBK1 and IKK-ɛ improves obesity-related metabolic dysfunctions in mice

Nature medicine, 2013-03, Vol.19 (3), p.313-321

2013

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Isoindolinone enantiomers having affinity for the dopamine D4 receptor

Bioorganic & medicinal chemistry letters, 1998-06, Vol.8 (12), p.1499-1502

1998

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The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (9), p.2337-2340

2006

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Abstract LB-B08: Validation of ADAM15 as a therapeutic target in invasive bladder cancer cells

Molecular cancer therapeutics, 2018-01, Vol.17 (1_Supplement), p.LB-B08-LB-B08

2018

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Structure-based design of caspase-1 inhibitor containing a diphenyl ether sulfonamide

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (20), p.2779-2782

2001

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An inhibitor of the protein kinases TBK1 and IKKζ improves obesity-related metabolic dysfunctions in mice

Nature medicine, 2013-03, Vol.19 (3), p.313

2013

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An inhibitor of the protein kinases TBK1 and IKK-[varepsilon] improves obesity-related metabolic dysfunctions in mice

Nature medicine, 2013-03, Vol.19 (3), p.313

2013

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An inhibitor of the protein kinases TBK1/IKKε improves obesity-related metabolic dysfunctions

Nature medicine, 2013-02, Vol.19 (3), p.313-321

2013

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Isoindolinone enantiomers having affinity for the dopamine D 4 receptor

Bioorganic & medicinal chemistry letters, 1998-06, Vol.8 (12), p.1499-1502

1998

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Progress in the development of inhibitors of SH2 domains

Current pharmaceutical design, 2000-01, Vol.6 (1), p.59-98

2000

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Thiocyanation of alkylanilines. A simple and efficient synthesis of thiosulfonates containing 2-aminobenzothiazole

Tetrahedron letters, 2000-05, Vol.41 (21), p.4065-4068

2000

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A facile synthesis of substituted 3-amino-1H-quinazoline-2,4-diones

Journal of heterocyclic chemistry, 2005-05, Vol.42 (4), p.669-674

2005

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A facile synthesis of substituted 3-amino-1 H -quinazoline-2,4-diones

Journal of heterocyclic chemistry, 2005-05, Vol.42 (4), p.669-674

2005

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Novel cyclohexyl amides as potent and selective D3 dopamine receptor ligands

Bioorganic & medicinal chemistry letters, 1997-09, Vol.7 (18), p.2403-2408

1997

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Novel cyclohexyl amides as potent and selective D 3 dopamine receptor ligands

Bioorganic & medicinal chemistry letters, 1997-09, Vol.7 (18), p.2403-2408

1997

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Structure-based design of novel, dipeptide ligands targeting the pp60Src SH2 domain

Bioorganic & medicinal chemistry letters, 1997-05, Vol.7 (9), p.1107-1112

1997

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ADAM15 Is Functionally Associated with the Metastatic Progression of Human Bladder Cancer

High-Resolution X-Ray Structure and Functional Analysis of the Murine Norovirus 1 Capsid Protein Protruding Domain

Bone Marrow Macrophages Induce Inflammation by Efferocytosis of Apoptotic Prostate Cancer Cells via HIF-1α Stabilization

High-Resolution Cryo-Electron Microscopy Structures of Murine Norovirus 1 and Rabbit Hemorrhagic Disease Virus Reveal Marked Flexibility in the Receptor Binding Domains

Unique Pro-Inflammatory Response of Macrophages during Apoptotic Cancer Cell Clearance

Design, Synthesis, and Evaluation of Aza-Peptide Epoxides as Selective and Potent Inhibitors of Caspases-1, -3, -6, and -8

The Tail of KdsC

Molecular Correlates of In Vitro Responses to Dacomitinib and Afatinib in Bladder Cancer

Tail of KdsC: CONFORMATIONAL CHANGES CONTROL THE ACTIVITY OF A HALOACID DEHALOGENASE SUPERFAMILY PHOSPHATASE

An inhibitor of the protein kinases TBK1 and IKK-ɛ improves obesity-related metabolic dysfunctions in mice

Isoindolinone enantiomers having affinity for the dopamine D4 receptor

The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases

Abstract LB-B08: Validation of ADAM15 as a therapeutic target in invasive bladder cancer cells

Structure-based design of caspase-1 inhibitor containing a diphenyl ether sulfonamide

An inhibitor of the protein kinases TBK1 and IKKζ improves obesity-related metabolic dysfunctions in mice

An inhibitor of the protein kinases TBK1 and IKK-[varepsilon] improves obesity-related metabolic dysfunctions in mice

An inhibitor of the protein kinases TBK1/IKKε improves obesity-related metabolic dysfunctions

Isoindolinone enantiomers having affinity for the dopamine D 4 receptor

Progress in the development of inhibitors of SH2 domains

Thiocyanation of alkylanilines. A simple and efficient synthesis of thiosulfonates containing 2-aminobenzothiazole

A facile synthesis of substituted 3-amino-1H-quinazoline-2,4-diones

A facile synthesis of substituted 3-amino-1 H -quinazoline-2,4-diones

Novel cyclohexyl amides as potent and selective D3 dopamine receptor ligands

Novel cyclohexyl amides as potent and selective D 3 dopamine receptor ligands

Structure-based design of novel, dipeptide ligands targeting the pp60Src SH2 domain

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