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The alpha‐helical rod domain of human lamins A and C contains a chromatin binding site

The EMBO journal, 1993-11, Vol.12 (11), p.4413-4424

1993

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p55CDC25 is a nuclear protein required for the initiation of mitosis in human cells

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (23), p.10500-10504

1991

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Cloning and Pharmacological Characterization of a Fourth Histamine Receptor (H4) Expressed in Bone Marrow

Molecular pharmacology, 2001-03, Vol.59 (3), p.420-426

2001

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Checkpoint Kinase Inhibitors: SAR and Radioprotective Properties of a Series of 2-Arylbenzimidazoles

Journal of medicinal chemistry, 2005-03, Vol.48 (6), p.1873-1885

2005

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Structural analysis of the p62 complex, an assembly of O-linked glycoproteins that localizes near the central gated channel of the nuclear pore complex

Molecular biology of the cell, 1995-11, Vol.6 (11), p.1591-1603

1995

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O-Linked Glycoproteins of the Nuclear Pore Complex Interact with a Cytosolic Factor Required for Nuclear Protein Import

The Journal of cell biology, 1992-01, Vol.116 (2), p.271-280

1992

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Cell Attachment and Motility on Materials Modified by Surface-active RGD-containing Peptides

Annals of the New York Academy of Sciences, 1994-11, Vol.745 (1), p.177-186

1994

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Novel non-benzimidazole chk2 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (7), p.1924-1928

2006

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[26] Therapeutic application of matrix biology

Methods in Enzymology, 1994, Vol.245, p.556-569

1994

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Concept and progress in the development of RGD-containing peptide pharmaceuticals

Biopolymers, 1995, Vol.37 (2), p.157-175

1995

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A Fluorescence-Based High Throughput Screen for the Transporter Associated with Antigen Processing

SLAS discovery, 1999-04, Vol.4 (2), p.87-91

1999

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p55CD25 is a nuclear protein required for the initiation of mitosis in human cells

Proceedings of the National Academy of Sciences - PNAS, 1991, Vol.88 (23), p.10500-10504

1991

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p55 super(CDC25) is a nuclear protein required for the initiation of mitosis in human cells

Proceedings of the National Academy of Sciences - PNAS, 1991-01, Vol.88 (23), p.10500-10504

1991

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Structural Basis of Small-Molecule Aggregate Induced Inhibition of a Protein–Protein Interaction

Journal of medicinal chemistry, 2017-04, Vol.60 (8), p.3511-3517

2017

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Oxysterols are agonist ligands of RORγt and drive Th17 cell differentiation

Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (33), p.12163-12168

2014

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Coupling to Gq Signaling Is Required for Cardioprotection by an Alpha-1A-Adrenergic Receptor Agonist

Circulation research, 2019-09, Vol.125 (7), p.699-706

2019

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Phenotyping drug polypharmacology via eicosanoid profiling of blood[S]

Journal of lipid research, 2015-08, Vol.56 (8), p.1492-1500

2015

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A highly efficient, high-throughput lipidomics platform for the quantitative detection of eicosanoids in human whole blood

Analytical biochemistry, 2013-02, Vol.433 (2), p.181-188

2013

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Polypharmacology of Small-Molecule Modulators of the 5-Lipoxygenase Activating Protein (FLAP) Observed via a High-throughput Lipidomics Platform

Journal of biomolecular screening, 2016-02, Vol.21 (2), p.127-135

2016

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A novel B-RAF inhibitor blocks interleukin-8 (IL-8) synthesis in human melanoma xenografts, revealing IL-8 as a potential pharmacodynamic biomarker

Molecular cancer therapeutics, 2008-03, Vol.7 (3), p.492-499

2008

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Azabenzthiazole inhibitors of leukotriene A4 hydrolase

Bioorganic & medicinal chemistry letters, 2012-12, Vol.22 (24), p.7504-7511

2012

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A highly selective, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor has potent activity in vitro and in vivo

Angiogenesis (London), 2009-09, Vol.12 (3), p.287-296

2009

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2-Aryl benzimidazoles featuring alkyl-linked pendant alcohols and amines as inhibitors of checkpoint kinase Chk2

Bioorganic & medicinal chemistry, 2007-12, Vol.17 (23), p.6467-6471

2007

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Abstract 11086: Isoproterenol Can Act as a Biased Partial Agonist on the Cardiac Myocyte Alpha-1A-Adrenergic Receptors but Does Not Confer Cardioprotection

Circulation (New York, N.Y.), 2018-11, Vol.138 (Suppl_1 Suppl 1), p.A11086-A11086

2018

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Design and operation of a 5000 m3/d reverse osmosis dual product plant

Desalination, 1977-03, Vol.20 (1-3), p.119-141

1977

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The alpha‐helical rod domain of human lamins A and C contains a chromatin binding site

p55CDC25 is a nuclear protein required for the initiation of mitosis in human cells

Cloning and Pharmacological Characterization of a Fourth Histamine Receptor (H4) Expressed in Bone Marrow

Checkpoint Kinase Inhibitors: SAR and Radioprotective Properties of a Series of 2-Arylbenzimidazoles

Structural analysis of the p62 complex, an assembly of O-linked glycoproteins that localizes near the central gated channel of the nuclear pore complex

O-Linked Glycoproteins of the Nuclear Pore Complex Interact with a Cytosolic Factor Required for Nuclear Protein Import

Cell Attachment and Motility on Materials Modified by Surface-active RGD-containing Peptides

Novel non-benzimidazole chk2 kinase inhibitors

[26] Therapeutic application of matrix biology

Concept and progress in the development of RGD-containing peptide pharmaceuticals

A Fluorescence-Based High Throughput Screen for the Transporter Associated with Antigen Processing

p55CD25 is a nuclear protein required for the initiation of mitosis in human cells

p55 super(CDC25) is a nuclear protein required for the initiation of mitosis in human cells

Structural Basis of Small-Molecule Aggregate Induced Inhibition of a Protein–Protein Interaction

Oxysterols are agonist ligands of RORγt and drive Th17 cell differentiation

Coupling to Gq Signaling Is Required for Cardioprotection by an Alpha-1A-Adrenergic Receptor Agonist

Phenotyping drug polypharmacology via eicosanoid profiling of blood[S]

A highly efficient, high-throughput lipidomics platform for the quantitative detection of eicosanoids in human whole blood

Polypharmacology of Small-Molecule Modulators of the 5-Lipoxygenase Activating Protein (FLAP) Observed via a High-throughput Lipidomics Platform

A novel B-RAF inhibitor blocks interleukin-8 (IL-8) synthesis in human melanoma xenografts, revealing IL-8 as a potential pharmacodynamic biomarker

Azabenzthiazole inhibitors of leukotriene A4 hydrolase

A highly selective, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor has potent activity in vitro and in vivo

2-Aryl benzimidazoles featuring alkyl-linked pendant alcohols and amines as inhibitors of checkpoint kinase Chk2

Abstract 11086: Isoproterenol Can Act as a Biased Partial Agonist on the Cardiac Myocyte Alpha-1A-Adrenergic Receptors but Does Not Confer Cardioprotection

Design and operation of a 5000 m3/d reverse osmosis dual product plant

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