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LINGO-1, a Transmembrane Signaling Protein, Inhibits Oligodendrocyte Differentiation and Myelination through Intercellular Self-interactions

The Journal of biological chemistry, 2012-06, Vol.287 (26), p.22184-22195

2012

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Crystal structure of JNK3: a kinase implicated in neuronal apoptosis

Structure (London), 1998-08, Vol.6 (8), p.983-991

1998

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Active-Site Residues of Escherichia coli DNA Gyrase Required in Coupling ATP Hydrolysis to DNA Supercoiling and Amino Acid Substitutions Leading to Novobiocin Resistance

Antimicrobial Agents and Chemotherapy, 2003-03, Vol.47 (3), p.1037-1046

2003

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Targeting the MAPK Signaling Pathway in Cancer: Promising Preclinical Activity with the Novel Selective ERK1/2 Inhibitor BVD-523 (Ulixertinib)

Molecular cancer therapeutics, 2017-11, Vol.16 (11), p.2351-2363

2017

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Iterative Optimization of High-Affinity Protease Inhibitors Using Phage Display. 2. Plasma Kallikrein and Thrombin

Biochemistry (Easton), 1996-06, Vol.35 (24), p.8058-8067

1996

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Iterative Optimization of High-Affinity Protease Inhibitors Using Phage Display. 1. Plasmin

Biochemistry (Easton), 1996-06, Vol.35 (24), p.8045-8057

1996

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Structure-Guided Design of Potent and Selective Pyrimidylpyrrole Inhibitors of Extracellular Signal-Regulated Kinase (ERK) Using Conformational Control

Journal of medicinal chemistry, 2009-10, Vol.52 (20), p.6362-6368

2009

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Abstract 3716: Potent radiation enhancement with VX-984, a selective DNA-PKcs inhibitor for the treatment of NSCLC

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.3716-3716

2016

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Abstract 4693: The selective ERK inhibitor BVD-523 is active in models of MAPK pathway-dependent cancers, including those with intrinsic and acquired drug resistance

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.4693-4693

2015

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Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (23), p.6231-6235

2008

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Directed Evolution of a Protein: Selection of Potent Neutrophil Elastase Inhibitors Displayed on M13 Fusion Phage

Proceedings of the National Academy of Sciences - PNAS, 1992-03, Vol.89 (6), p.2429-2433

1992

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972 VX-950: the discovery of an inhibitor of the hepatitis C NS3·4A protease and a potential hepatitis C virus therapeutic

Hepatology (Baltimore, Md.), 2003, Vol.38, p.624-624

2003

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[2] Selection for protease inhibitors using bacteriophage display

Methods in Enzymology, 1996, Vol.267, p.28-51

1996

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Purification and characterization of the NS3 serine protease domain of hepatitis C virus expressed in Saccharomyces cerevisiae

Journal of general virology, 1997-01, Vol.78 (1), p.39-43

1997

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[4] Affinity maturation of proteins displayed on surface of M13 bacteriophage as major coat protein fusions

Methods in Enzymology, 1996, Vol.267, p.68-82

1996

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Obtaining a family of high-affinity, high-specificity protein inhibitors of plasmin and plasma kallikrein

Molecular diversity, 1996-10, Vol.2 (1-2), p.119-124

1996

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Mutants of polyomavirus middle-T antigen

Biochimica et biophysica acta, 1987-11, Vol.907 (3), p.299-321

1987

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Biochemical Aspects of Xylem Differentiation in Plant Tissue Culture

Markland, William

1983

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Structure–function analysis of tissue-type plasminogen activator by linker-insertion, point and deletion mutagenesis

Protein engineering, 1989-11, Vol.3 (2), p.117-125

1989

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Tissue-type plasminogen activator variants with domain duplications and rearrangements

Protein engineering, 1989-11, Vol.3 (2), p.111-116

1989

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Signal-Dependent Translocation of Simian Virus 40 Large-T Antigen into Rat Liver Nuclei in a Cell-Free System

Molecular and cellular biology, 1987-12, Vol.7 (12), p.4255-4265

1987

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Town planning analysis

Planning outlook, 1952-01, Vol.2 (4), p.43-82

Ogden, William Markland

1952

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Glimpses of Life in Early Oregon

The quarterly of the Oregon Historical Society, 1900-06, Vol.1 (2), p.158-164

Molson, William Markland

1900

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Electrostatic Control of Regioselectivity in Au(I)-Catalyzed Hydroarylation

Journal of the American Chemical Society, 2017-03, Vol.139 (11), p.4035-4041

2017

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Epidemiology, pathophysiology, and classification of fecal incontinence: state of the science summary for the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) workshop

The American journal of gastroenterology, 2015-01, Vol.110 (1), p.127-136

2015

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LINGO-1, a Transmembrane Signaling Protein, Inhibits Oligodendrocyte Differentiation and Myelination through Intercellular Self-interactions

Crystal structure of JNK3: a kinase implicated in neuronal apoptosis

Active-Site Residues of Escherichia coli DNA Gyrase Required in Coupling ATP Hydrolysis to DNA Supercoiling and Amino Acid Substitutions Leading to Novobiocin Resistance

Targeting the MAPK Signaling Pathway in Cancer: Promising Preclinical Activity with the Novel Selective ERK1/2 Inhibitor BVD-523 (Ulixertinib)

Iterative Optimization of High-Affinity Protease Inhibitors Using Phage Display. 2. Plasma Kallikrein and Thrombin

Iterative Optimization of High-Affinity Protease Inhibitors Using Phage Display. 1. Plasmin

Structure-Guided Design of Potent and Selective Pyrimidylpyrrole Inhibitors of Extracellular Signal-Regulated Kinase (ERK) Using Conformational Control

Abstract 3716: Potent radiation enhancement with VX-984, a selective DNA-PKcs inhibitor for the treatment of NSCLC

Abstract 4693: The selective ERK inhibitor BVD-523 is active in models of MAPK pathway-dependent cancers, including those with intrinsic and acquired drug resistance

Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)

Directed Evolution of a Protein: Selection of Potent Neutrophil Elastase Inhibitors Displayed on M13 Fusion Phage

972 VX-950: the discovery of an inhibitor of the hepatitis C NS3·4A protease and a potential hepatitis C virus therapeutic

[2] Selection for protease inhibitors using bacteriophage display

Purification and characterization of the NS3 serine protease domain of hepatitis C virus expressed in Saccharomyces cerevisiae

[4] Affinity maturation of proteins displayed on surface of M13 bacteriophage as major coat protein fusions

Obtaining a family of high-affinity, high-specificity protein inhibitors of plasmin and plasma kallikrein

Mutants of polyomavirus middle-T antigen

Biochemical Aspects of Xylem Differentiation in Plant Tissue Culture

Structure–function analysis of tissue-type plasminogen activator by linker-insertion, point and deletion mutagenesis

Tissue-type plasminogen activator variants with domain duplications and rearrangements

Signal-Dependent Translocation of Simian Virus 40 Large-T Antigen into Rat Liver Nuclei in a Cell-Free System

Town planning analysis

Glimpses of Life in Early Oregon

Electrostatic Control of Regioselectivity in Au(I)-Catalyzed Hydroarylation

Epidemiology, pathophysiology, and classification of fecal incontinence: state of the science summary for the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) workshop

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