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Cryo-EM structure of human PAPP-A2 and mechanism of substrate recognition

Communications chemistry, 2023-10, Vol.6 (1), p.234-234, Article 234

2023

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IgE epitopes of Ara h 9, Jug r 3, and Pru p 3 in peanut-allergic individuals from Spain and the US

Frontiers in allergy, 2023-01, Vol.3, p.1090114-1090114

2023

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IgE and IgG4 epitopes of the peanut allergens shift following oral immunotherapy

Frontiers in allergy, 2023-11, Vol.4, p.1279290-1279290

2023

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Discovery, Optimization, and Pharmacological Characterization of Novel Heteroaroylphenylureas Antagonists of C−C Chemokine Ligand 2 Function

Journal of medicinal chemistry, 2011-03, Vol.54 (6), p.1667-1681

2011

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A High-Affinity Native Human Antibody Disrupts Biofilm from Staphylococcus aureus Bacteria and Potentiates Antibiotic Efficacy in a Mouse Implant Infection Model

Antimicrobial agents and chemotherapy, 2016-04, Vol.60 (4), p.2292-2301

2016

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IgE and IgG4 Epitope Profiles for the Major Peanut Allergens from Peanut Allergic Patients Undergoing Oral Immunotherapy

Journal of allergy and clinical immunology, 2019-02, Vol.143 (2), p.AB241-AB241

2019

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Epitope Mapping for the Non-Specific Lipid Transfer Proteins (nsLTP) Among Peanut Allergic Patients

Journal of allergy and clinical immunology, 2018-02, Vol.141 (2), p.AB239-AB239

2018

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Chemical Protein Synthesis by Solid Phase Ligation of Unprotected Peptide Segments

Journal of the American Chemical Society, 1999-09, Vol.121 (38), p.8720-8727

1999

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Discovery of Nanomolar Ligands for 7-Transmembrane G-Protein-Coupled Receptors from a Diverse N-(Substituted)glycine Peptoid Library

Journal of medicinal chemistry, 1994-08, Vol.37 (17), p.2678-2685

1994

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Exploratory immunogenicity outcomes of peanut oral immunotherapy: Findings from the PALISADE trial

Clinical and translational allergy, 2024-01, Vol.14 (1), p.e12326-n/a

2024

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Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1

Bioorganic & medicinal chemistry letters, 2002-04, Vol.12 (7), p.1063-1066

2002

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Crystal Structure of Chemically Synthesized [N33A] Stromal Cell-Derived Factor 1α , a Potent Ligand for the HIV-1 ``Fusin" Coreceptor

Proceedings of the National Academy of Sciences - PNAS, 1998-06, Vol.95 (12), p.6941-6946

1998

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Peptoids: A Modular Approach to Drug Discovery

Proceedings of the National Academy of Sciences - PNAS, 1992-10, Vol.89 (20), p.9367-9371

1992

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Peptide Aldehyde Inhibitors of Hepatitis A Virus 3C Proteinase

Biochemistry (Easton), 1995-06, Vol.34 (25), p.8172-8179

1995

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Proteolytic studies of homologous peptide and N-substituted glycine peptoid oligomers

Bioorganic & medicinal chemistry letters, 1994-11, Vol.4 (22), p.2657-2662

1994

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Comparison of the proteolytic susceptibilities of homologous L-amino acid, D-amino acid, and N-substituted glycine peptide and peptoid oligomers

Drug development research, 1995-05, Vol.35 (1), p.20-32

1995

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Novel Cyclooxygenase-1 Inhibitors Discovered Using Affinity Fingerprints

Journal of medicinal chemistry, 2004-09, Vol.47 (20), p.4875-4880

2004

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Engineering and Chemical Synthesis of a Transmembrane Protein: The HCV Protease Cofactor Protein NS4A

Journal of the American Chemical Society, 1999-08, Vol.121 (33), p.7698-7699

1999

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The influence of intramolecular dynamics on branching ratios in thermal rearrangements

Journal of organic chemistry, 1990, Vol.55 (2), p.695-711

1990

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The x-ray structure of flavohemoglobin. A semisynthetic hydroxylase

Journal of the American Chemical Society, 1988-08, Vol.110 (18), p.6261-6263

1988

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Crystal structure of chemically synthesized [N33A] stromal cell-derived factor 1alpha, a potent ligand for the HIV-1 "fusin" coreceptor

Proceedings of the National Academy of Sciences - PNAS, 1998-06, Vol.95 (12), p.6941-6946

1998

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Synthesis, molecular modelling, and NMR structure determination of four cyclic peptide antagonists of endothelin

Bioorganic & medicinal chemistry, 1994-04, Vol.2 (4), p.279-296

1994

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Using Peptoid Libraries [Oligo N-Substituted Glycines] for Drug Discovery

Techniques in Protein Chemistry, 1994, Vol.5, p.533-539

1994

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Efficacy and Safety of Degludec versus Glargine in Type 2 Diabetes

The New England journal of medicine, 2017-08, Vol.377 (8), p.723-732

2017

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Notes from Beethoven’s genome

Current biology, 2024-03, Vol.34 (6), p.R233-R234

2024

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Cryo-EM structure of human PAPP-A2 and mechanism of substrate recognition

IgE epitopes of Ara h 9, Jug r 3, and Pru p 3 in peanut-allergic individuals from Spain and the US

IgE and IgG4 epitopes of the peanut allergens shift following oral immunotherapy

Discovery, Optimization, and Pharmacological Characterization of Novel Heteroaroylphenylureas Antagonists of C−C Chemokine Ligand 2 Function

A High-Affinity Native Human Antibody Disrupts Biofilm from Staphylococcus aureus Bacteria and Potentiates Antibiotic Efficacy in a Mouse Implant Infection Model

IgE and IgG4 Epitope Profiles for the Major Peanut Allergens from Peanut Allergic Patients Undergoing Oral Immunotherapy

Epitope Mapping for the Non-Specific Lipid Transfer Proteins (nsLTP) Among Peanut Allergic Patients

Chemical Protein Synthesis by Solid Phase Ligation of Unprotected Peptide Segments

Discovery of Nanomolar Ligands for 7-Transmembrane G-Protein-Coupled Receptors from a Diverse N-(Substituted)glycine Peptoid Library

Exploratory immunogenicity outcomes of peanut oral immunotherapy: Findings from the PALISADE trial

Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1

Crystal Structure of Chemically Synthesized [N33A] Stromal Cell-Derived Factor 1α , a Potent Ligand for the HIV-1 ``Fusin" Coreceptor

Peptoids: A Modular Approach to Drug Discovery

Peptide Aldehyde Inhibitors of Hepatitis A Virus 3C Proteinase

Proteolytic studies of homologous peptide and N-substituted glycine peptoid oligomers

Comparison of the proteolytic susceptibilities of homologous L-amino acid, D-amino acid, and N-substituted glycine peptide and peptoid oligomers

Novel Cyclooxygenase-1 Inhibitors Discovered Using Affinity Fingerprints

Engineering and Chemical Synthesis of a Transmembrane Protein: The HCV Protease Cofactor Protein NS4A

The influence of intramolecular dynamics on branching ratios in thermal rearrangements

The x-ray structure of flavohemoglobin. A semisynthetic hydroxylase

Crystal structure of chemically synthesized [N33A] stromal cell-derived factor 1alpha, a potent ligand for the HIV-1 "fusin" coreceptor

Synthesis, molecular modelling, and NMR structure determination of four cyclic peptide antagonists of endothelin

Using Peptoid Libraries [Oligo N-Substituted Glycines] for Drug Discovery

Efficacy and Safety of Degludec versus Glargine in Type 2 Diabetes

Notes from Beethoven’s genome

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