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Predicting the Effect of Amino Acid Single-Point Mutations on Protein Stability—Large-Scale Validation of MD-Based Relative Free Energy Calculations

Journal of molecular biology, 2017-04, Vol.429 (7), p.948-963

2017

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Stapled α−helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy

Proceedings of the National Academy of Sciences - PNAS, 2013-09, Vol.110 (36), p.E3445-E3454

2013

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A general approach to site-specific antibody drug conjugates

Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (5), p.1766-1771

2014

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Functional, Biophysical, and Structural Bases for Antibacterial Activity of Tigecycline

Antimicrobial Agents and Chemotherapy, 2006-06, Vol.50 (6), p.2156-2166

2006

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Discovery of Sulanemadlin (ALRN-6924), the First Cell-Permeating, Stabilized α‑Helical Peptide in Clinical Development

Journal of medicinal chemistry, 2023-07, Vol.66 (14), p.9401-9417

2023

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Identification of a New Member of the Tryptase Family of Mouse and Human Mast Cell Proteases Which Possesses a Novel COOH-terminal Hydrophobic Extension

The Journal of biological chemistry, 1999-10, Vol.274 (43), p.30784-30793

1999

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Modeling mutations in protein structures

Protein science, 2007-09, Vol.16 (9), p.2030-2041

2007

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Peripheral Administration of a Long-Acting Peptide Oxytocin Receptor Agonist Inhibits Fear-Induced Freezing

The Journal of pharmacology and experimental therapeutics, 2016-08, Vol.358 (2), p.164-172

2016

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Mouse Mast Cell Protease 9, a Novel Member of the Chromosome 14 Family of Serine Proteases that is Selectively Expressed in Uterine Mast Cells

The Journal of biological chemistry, 1997-11, Vol.272 (46), p.29158-29166

1997

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Fragment-based drug design

Methods in molecular biology (Clifton, N.J.), 2011, Vol.685, p.241

2011

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CONFIRM: connecting fragments found in receptor molecules

Journal of computer-aided molecular design, 2008-10, Vol.22 (10), p.761-772

2008

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Stapled α-helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy

Proceedings of the National Academy of Sciences - PNAS, 2013-09, Vol.110 (36), p.14519-14519

2013

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Abstract 5691: Novel site-specific antibody drug conjugates based on novel amino acid incorporation technology have improved pharmaceutical properties over conventional antibody drug conjugates

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.5691-5691

2012

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A structural informatics approach to mine kinase knowledge bases

Drug discovery today, 2010-03, Vol.15 (5), p.203-209

2010

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A structural information approach to mine kinase knowledge bases

Drug discovery today, 2010, Vol.15 (5-6), p.203-209

2010

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Synthesis and biological evaluation of ((4-keto)-phenoxy)methyl biphenyl-4-sulfonamides: A class of potent aggrecanase-1 inhibitors

Bioorganic & medicinal chemistry letters, 2009-05, Vol.19 (9), p.2487-2491

2009

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Formation of Enzymatically Active, Homotypic, and Heterotypic Tetramers of Mouse Mast Cell Tryptases

The Journal of biological chemistry, 2000-01, Vol.275 (1), p.351-358

2000

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Protein Relational Database and Protein Family Knowledge Bases to Facilitate Structure-Based Design Analyses

Chemical biology & drug design, 2010-08, Vol.76 (2), p.142-153

2010

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Design and synthesis of 3,3-piperidine hydroxamate analogs as selective TACE inhibitors

Bioorganic & medicinal chemistry letters, 2007-08, Vol.17 (15), p.4333-4337

2007

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Formation of enzymatically active, homotypic, and heterotypic tetramers of mouse mast cell tryptases. Dependence on a conserved Trp-rich domain on the surface

The Journal of biological chemistry, 2000-01, Vol.275 (1), p.351-358

2000

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Influence of a NH2‐terminal extension on the activity of KTX2, a K+ channel blocker purified from Androctonus australis scorpion venom

FEBS letters, 1997-11, Vol.417 (1), p.123-129

1997

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Influence of a NH 2-terminal extension on the activity of KTX2, a K + channel blocker purified from Androctonus australis scorpion venom

FEBS letters, 1997-11, Vol.417 (1), p.123-129

1997

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Lead optimization via high-throughput molecular docking

Current opinion in drug discovery & development, 2007-05, Vol.10 (3), p.264

2007

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L’autonomie de l’établissement, avec ou contre les enseignants ?

2017

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Predicting the Effect of Amino Acid Single-Point Mutations on Protein Stability—Large-Scale Validation of MD-Based Relative Free Energy Calculations

Stapled α−helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy

A general approach to site-specific antibody drug conjugates

Functional, Biophysical, and Structural Bases for Antibacterial Activity of Tigecycline

Discovery of Sulanemadlin (ALRN-6924), the First Cell-Permeating, Stabilized α‑Helical Peptide in Clinical Development

Identification of a New Member of the Tryptase Family of Mouse and Human Mast Cell Proteases Which Possesses a Novel COOH-terminal Hydrophobic Extension

Modeling mutations in protein structures

Peripheral Administration of a Long-Acting Peptide Oxytocin Receptor Agonist Inhibits Fear-Induced Freezing

Mouse Mast Cell Protease 9, a Novel Member of the Chromosome 14 Family of Serine Proteases that is Selectively Expressed in Uterine Mast Cells

Fragment-based drug design

CONFIRM: connecting fragments found in receptor molecules

Stapled α-helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy

Abstract 5691: Novel site-specific antibody drug conjugates based on novel amino acid incorporation technology have improved pharmaceutical properties over conventional antibody drug conjugates

A structural informatics approach to mine kinase knowledge bases

A structural information approach to mine kinase knowledge bases

Synthesis and biological evaluation of ((4-keto)-phenoxy)methyl biphenyl-4-sulfonamides: A class of potent aggrecanase-1 inhibitors

Formation of Enzymatically Active, Homotypic, and Heterotypic Tetramers of Mouse Mast Cell Tryptases

Protein Relational Database and Protein Family Knowledge Bases to Facilitate Structure-Based Design Analyses

Design and synthesis of 3,3-piperidine hydroxamate analogs as selective TACE inhibitors

Formation of enzymatically active, homotypic, and heterotypic tetramers of mouse mast cell tryptases. Dependence on a conserved Trp-rich domain on the surface

Influence of a NH2‐terminal extension on the activity of KTX2, a K+ channel blocker purified from Androctonus australis scorpion venom

Influence of a NH 2-terminal extension on the activity of KTX2, a K + channel blocker purified from Androctonus australis scorpion venom

Lead optimization via high-throughput molecular docking

L’autonomie de l’établissement, avec ou contre les enseignants ?

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