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Structural Analyses Reveal Phosphatidyl Inositols as Ligands for the NR5 Orphan Receptors SF-1 and LRH- 1

Cell, 2005-02, Vol.120 (3), p.343-355

2005

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Atomic Structure of PDE4: Insights into Phosphodiesterase Mechanism and Specificity

Science (American Association for the Advancement of Science), 2000-06, Vol.288 (5472), p.1822-1825

2000

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Crystal Structures of the Catalytic Domain of Phosphodiesterase 4B Complexed with AMP, 8-Br-AMP, and Rolipram

Journal of molecular biology, 2004-03, Vol.337 (2), p.355-365

2004

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Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: The discovery of GW0385

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (7), p.1788-1794

2006

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Discovery of GSK1997132B a novel centrally penetrant benzimidazole PPARγ partial agonist

Bioorganic & medicinal chemistry letters, 2011-09, Vol.21 (18), p.5568-5572

2011

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Solution Structure of the Amino-Terminal Fragment of Urokinase-Type Plasminogen Activator

Biochemistry (Easton), 1994-04, Vol.33 (16), p.4847-4864

1994

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Discovery of a novel class of PPARδ partial agonists

Bioorganic & medicinal chemistry, 2008-09, Vol.18 (18), p.5018-5022

2008

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NMR Determination of the Structures of Peroxycobalt(III) Bleomycin and Cobalt(III) Bleomycin, Products of the Aerobic Oxidation of Cobalt(II) Bleomycin by Dioxygen

Biochemistry (Easton), 1994-02, Vol.33 (4), p.907-916

1994

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Phenoxyacetic acids as PPARδ partial agonists: Synthesis, optimization, and in vivo efficacy

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (8), p.2345-2350

2011

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Crystallization of cyclic nucleotide phosphodiesterases

Methods in molecular biology (Clifton, N.J.), 2005, Vol.307, p.181

2005

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NMR Structure of a Protein Kinase C-γ Phorbol-Binding Domain and Study of Protein−Lipid Micelle Interactions

Biochemistry (Easton), 1997-09, Vol.36 (35), p.10709-10717

1997

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Heteronuclear 3D NMR studies of water bound to an FK506 binding protein/immunosuppressant complex

Biochemistry (Easton), 1993-03, Vol.32 (10), p.2473-2480

1993

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A Structural Basis for Constitutive Activity in the Human CAR/RXRα Heterodimer

Molecular cell, 2004-12, Vol.16 (6), p.919-928

2004

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Oxidative stress induced by a copper-thiosemicarbazone complex

Biochemistry (Easton), 1990-07, Vol.29 (30), p.7046-7053

1990

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Three-dimensional structure of the FK506 binding protein/ascomycin complex in solution by heteronuclear three- and four-dimensional NMR

Biochemistry (Easton), 1993-01, Vol.32 (3), p.754-765

1993

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Corrigendum to “Discovery of GSK1997132B a novel centrally penetrant benzimidazole PPARγ partial agonist” [Bioorg. Med. Chem. Lett. 21 (2011) 5568–5572]

Bioorganic & medicinal chemistry letters, 2013-02, Vol.23 (4), p.1143-1143

2013

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Genome Duplications and Other Features in 12 Mb of DNA Sequence from Human Chromosome 16p and 16q

Genomics (San Diego, Calif.), 1999-09, Vol.60 (3), p.295-308

1999

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Discovery of GSK1997132B a novel centrally penetrant benzimidazole PPAR[gamma] partial agonist

Bioorganic & medicinal chemistry letters, 2011-09, Vol.21 (18), p.5568-5572

2011

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A general method for assigning NMR spectra of denatured proteins using 3D HC(CO)NH-TOCSY triple resonance experiments

Journal of biomolecular NMR, 1993-03, Vol.3 (2), p.225-231

1993

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Phenoxyacetic acids as PPAR[delta] partial agonists: Synthesis, optimization, and in vivo efficacy

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (8), p.2345-2350

2011

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ADR1a, a zinc finger peptide, exists in two folded conformations

Biochemistry (Easton), 1991-04, Vol.30 (14), p.3365-3371

1991

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NMR studies of an FK-506 analog, [U-carbon-13]ascomycin, bound to FK-506-binding protein

Journal of medicinal chemistry, 1992-06, Vol.35 (13), p.2467-2473

1992

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1H, 13C, and 15N assignments and secondary structure of the FK506 binding protein when bound to ascomycin

Biopolymers, 1993-04, Vol.33 (4), p.535-550

1993

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Side chain and backbone assignments in isotopically labeled proteins from two heteronuclear triple resonance experiments

FEBS letters, 1992-12, Vol.314 (3), p.413-418

1992

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Structural Analyses Reveal Phosphatidyl Inositols as Ligands for the NR5 Orphan Receptors SF-1 and LRH- 1

Atomic Structure of PDE4: Insights into Phosphodiesterase Mechanism and Specificity

Crystal Structures of the Catalytic Domain of Phosphodiesterase 4B Complexed with AMP, 8-Br-AMP, and Rolipram

Substituted 2-[(4-Aminomethyl)phenoxy]-2-methylpropionic Acid PPARα Agonists. 1. Discovery of a Novel Series of Potent HDLc Raising Agents

Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: The discovery of GW0385

Discovery of GSK1997132B a novel centrally penetrant benzimidazole PPARγ partial agonist

Solution Structure of the Amino-Terminal Fragment of Urokinase-Type Plasminogen Activator

Discovery of a novel class of PPARδ partial agonists

NMR Determination of the Structures of Peroxycobalt(III) Bleomycin and Cobalt(III) Bleomycin, Products of the Aerobic Oxidation of Cobalt(II) Bleomycin by Dioxygen

Phenoxyacetic acids as PPARδ partial agonists: Synthesis, optimization, and in vivo efficacy

Crystallization of cyclic nucleotide phosphodiesterases

NMR Structure of a Protein Kinase C-γ Phorbol-Binding Domain and Study of Protein−Lipid Micelle Interactions

Heteronuclear 3D NMR studies of water bound to an FK506 binding protein/immunosuppressant complex

A Structural Basis for Constitutive Activity in the Human CAR/RXRα Heterodimer

Oxidative stress induced by a copper-thiosemicarbazone complex

Three-dimensional structure of the FK506 binding protein/ascomycin complex in solution by heteronuclear three- and four-dimensional NMR

Corrigendum to “Discovery of GSK1997132B a novel centrally penetrant benzimidazole PPARγ partial agonist” [Bioorg. Med. Chem. Lett. 21 (2011) 5568–5572]

Genome Duplications and Other Features in 12 Mb of DNA Sequence from Human Chromosome 16p and 16q

Discovery of GSK1997132B a novel centrally penetrant benzimidazole PPAR[gamma] partial agonist

A general method for assigning NMR spectra of denatured proteins using 3D HC(CO)NH-TOCSY triple resonance experiments

Phenoxyacetic acids as PPAR[delta] partial agonists: Synthesis, optimization, and in vivo efficacy

ADR1a, a zinc finger peptide, exists in two folded conformations

NMR studies of an FK-506 analog, [U-carbon-13]ascomycin, bound to FK-506-binding protein

1H, 13C, and 15N assignments and secondary structure of the FK506 binding protein when bound to ascomycin

Side chain and backbone assignments in isotopically labeled proteins from two heteronuclear triple resonance experiments

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