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My Father's Shadow: Intergenerational Conflict in African American Men's Autobiography

Dudley, David L

1, 1991

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Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain

The Journal of pharmacology and experimental therapeutics, 2011-07, Vol.338 (1), p.114-124

2011

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The discovery of the benzhydroxamate MEK inhibitors CI-1040 and PD 0325901

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (24), p.6501-6504

2008

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Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition

Nature structural & molecular biology, 2004-12, Vol.11 (12), p.1192-1197

2004

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Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor

ACS medicinal chemistry letters, 2011-02, Vol.2 (2), p.91-96

2011

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Fatty acid amide hydrolase blockade attenuates the development of collagen-induced arthritis and related thermal hyperalgesia in mice

Pharmacology, biochemistry and behavior, 2011-10, Vol.99 (4), p.718-725

2011

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Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo

Nature medicine, 1999-07, Vol.5 (7), p.810-816

1999

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3D matrix platform for the rapid generation of therapeutic anti-human carcinoma monoclonal antibodies

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (41), p.14882-14887

2014

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A Synthetic Inhibitor of the Mitogen-Activated Protein Kinase Cascade

Proceedings of the National Academy of Sciences - PNAS, 1995-08, Vol.92 (17), p.7686-7689

1995

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PD 098059 Is a Specific Inhibitor of the Activation of Mitogen-activated Protein Kinase Kinase in Vitro and in Vivo

The Journal of biological chemistry, 1995-11, Vol.270 (46), p.27489-27494

1995

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Identification of a Novel Mitogen-Activated Protein Kinase Kinase Activation Domain Recognized by the Inhibitor PD 184352

Molecular and Cellular Biology, 2002-11, Vol.22 (21), p.7593-7602

2002

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The development of a Clinician-Administered PTSD Scale

Journal of traumatic stress, 1995-01, Vol.8 (1), p.75-90

1995

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Introduction: The American City in 2017

Forum journal (Washington, D.C.), 2017, Vol.31 (4), p.3-9

Dudley, David

2017

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Design and synthesis of phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3Kinaseγ

Bioorganic & medicinal chemistry letters, 2007-02, Vol.17 (3), p.756-760

2007

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PD98059 Is an Equipotent Antagonist of the Aryl Hydrocarbon Receptor and Inhibitor of Mitogen-Activated Protein Kinase Kinase

Molecular pharmacology, 1998-03, Vol.53 (3), p.438-445

1998

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Suppression of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-mediated CYP1A1 and CYP1B1 induction by 12-O-tetradecanoylphorbol-13-acetate: role of transforming growth factor β and mitogen-activated protein kinases

Biochemical pharmacology, 2001-12, Vol.62 (11), p.1449-1457

2001

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The Development of 800 Days of Solitude: A Conjuring: A Playwriting Thesis

Dudley, David

2018

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Building an enterprise framework for SCADA system for better results

Control Engineering, 2024-07, Vol.71 (4), p.22-24

Dudley, David

2024

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Design of a functional hexapeptide antagonist of endothelin

Journal of medicinal chemistry, 1992-08, Vol.35 (17), p.3301-3303

1992

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Splenic volvulus

Journal of the American College of Surgeons, 2003-12, Vol.197 (6), p.1047-1047

2003

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A Scale for Assessing Sleep Hygiene: Preliminary Data

Psychological reports, 1998-12, Vol.83 (3_suppl), p.1175-1178

1998

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Central role of the MEK/ERK MAP kinase pathway in a mouse model of rheumatoid arthritis: Potential proinflammatory mechanisms

Arthritis and rheumatism, 2007-10, Vol.56 (10), p.3347-3357

2007

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Analysis of the role of N-glycosylation in cell-surface expression and binding properties of angiotensin II type-2 receptor of rat pheochromocytoma cells

Biochemical journal, 1996-01, Vol.313 ( Pt 1) (1), p.297-304

1996

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ROOM TO GROW IN ARIZONA

American Theatre, 2020-05, Vol.37 (4), p.24-28

Dudley, David

2020

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Subclasses of angiotensin II binding sites and their functional significance

Molecular pharmacology, 1990-09, Vol.38 (3), p.370-377

1990

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My Father's Shadow: Intergenerational Conflict in African American Men's Autobiography

Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain

The discovery of the benzhydroxamate MEK inhibitors CI-1040 and PD 0325901

Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition

Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor

Fatty acid amide hydrolase blockade attenuates the development of collagen-induced arthritis and related thermal hyperalgesia in mice

Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo

3D matrix platform for the rapid generation of therapeutic anti-human carcinoma monoclonal antibodies

A Synthetic Inhibitor of the Mitogen-Activated Protein Kinase Cascade

PD 098059 Is a Specific Inhibitor of the Activation of Mitogen-activated Protein Kinase Kinase in Vitro and in Vivo

Identification of a Novel Mitogen-Activated Protein Kinase Kinase Activation Domain Recognized by the Inhibitor PD 184352

The development of a Clinician-Administered PTSD Scale

Introduction: The American City in 2017

Design and synthesis of phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3Kinaseγ

PD98059 Is an Equipotent Antagonist of the Aryl Hydrocarbon Receptor and Inhibitor of Mitogen-Activated Protein Kinase Kinase

Suppression of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-mediated CYP1A1 and CYP1B1 induction by 12-O-tetradecanoylphorbol-13-acetate: role of transforming growth factor β and mitogen-activated protein kinases

The Development of 800 Days of Solitude: A Conjuring: A Playwriting Thesis

Building an enterprise framework for SCADA system for better results

Design of a functional hexapeptide antagonist of endothelin

Splenic volvulus

A Scale for Assessing Sleep Hygiene: Preliminary Data

Central role of the MEK/ERK MAP kinase pathway in a mouse model of rheumatoid arthritis: Potential proinflammatory mechanisms

Analysis of the role of N-glycosylation in cell-surface expression and binding properties of angiotensin II type-2 receptor of rat pheochromocytoma cells

ROOM TO GROW IN ARIZONA

Subclasses of angiotensin II binding sites and their functional significance

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