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Computational approaches to therapeutic antibody design: established methods and emerging trends

Briefings in bioinformatics, 2020-09, Vol.21 (5), p.1549-1567

2020

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Structural Insights into FGFR Kinase Isoform Selectivity: Diverse Binding Modes of AZD4547 and Ponatinib in Complex with FGFR1 and FGFR4

Structure (London), 2014-12, Vol.22 (12), p.1764-1774

2014

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N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5- (tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a Novel, Highly Selective, Orally Available, Dual-Specific c-Src/Abl Kinase Inhibitor

Journal of medicinal chemistry, 2006-11, Vol.49 (22), p.6465-6488

2006

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Investigation of (E)‑3-[4-(2-Oxo-3-aryl-chromen-4-yl)oxyphenyl]acrylic Acids as Oral Selective Estrogen Receptor Down-Regulators

Journal of medicinal chemistry, 2015-04, Vol.58 (8), p.3522-3533

2015

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Protein–Ligand Crystal Structures Can Guide the Design of Selective Inhibitors of the FGFR Tyrosine Kinase

Journal of medicinal chemistry, 2012-06, Vol.55 (11), p.5003-5012

2012

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AZD9496: An Oral Estrogen Receptor Inhibitor That Blocks the Growth of ER-Positive and ESR1-Mutant Breast Tumors in Preclinical Models

Cancer research (Chicago, Ill.), 2016-06, Vol.76 (11), p.3307-3318

2016

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Structural approaches to obtain kinase selectivity

Trends in pharmacological sciences (Regular ed.), 2012-05, Vol.33 (5), p.273-278

2012

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Design and Synthesis of Novel Lactate Dehydrogenase A Inhibitors by Fragment-Based Lead Generation

Journal of medicinal chemistry, 2012-04, Vol.55 (7), p.3285-3306

2012

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Characterization of the complex formed between a potent neutralizing ovine-derived polyclonal anti-TNFα Fab fragment and human TNFα

Bioscience reports, 2013-08, Vol.33 (4)

2013

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Landscape of activating cancer mutations in FGFR kinases and their differential responses to inhibitors in clinical use

Oncotarget, 2016-04, Vol.7 (17), p.24252-24268

2016

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Validation of ion mobility spectrometry - mass spectrometry as a screening tool to identify type II kinase inhibitors of FGFR1 kinase

Rapid communications in mass spectrometry, 2021-06, p.e9130-e9130

2021

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Structural and dynamic insights into the energetics of activation loop rearrangement in FGFR1 kinase

Nature communications, 2015-07, Vol.6 (1), p.7877-7877, Article 7877

2015

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The Mycobacterium tuberculosis ino1 gene is essential for growth and virulence

Molecular microbiology, 2004-02, Vol.51 (4), p.1003-1014

2004

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Crystal Structure of Inositol 1-Phosphate Synthase from Mycobacterium tuberculosis, a Key Enzyme in Phosphatidylinositol Synthesis

Structure (London), 2002-03, Vol.10 (3), p.393-402

2002

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Tetrahydroisoquinoline Phenols: Selective Estrogen Receptor Downregulator Antagonists with Oral Bioavailability in Rat

ACS medicinal chemistry letters, 2016-01, Vol.7 (1), p.94-99

2016

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Correction to Investigation of (E)‑3-[4-(2-Oxo-3-aryl-chromen-4-yl)oxyphenyl]acrylic Acids as Oral Selective Estrogen Receptor Down-Regulators

Journal of medicinal chemistry, 2016-04, Vol.59 (7), p.3576-3576

2016

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FGFR1 Kinase Inhibitors: Close Regioisomers Adopt Divergent Binding Modes and Display Distinct Biophysical Signatures

ACS medicinal chemistry letters, 2014-02, Vol.5 (2), p.166-171

2014

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Prevention of MKK6-Dependent Activation by Binding to p38α MAP Kinase

Biochemistry (Easton), 2005-12, Vol.44 (50), p.16475-16490

2005

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Rapid Generation of a High Quality Lead for Transforming Growth Factor-β (TGF-β) Type I Receptor (ALK5)

Journal of medicinal chemistry, 2009-12, Vol.52 (23), p.7901-7905

2009

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Imidazo[1,2- a]pyridines: A potent and selective class of cyclin-Dependent kinase inhibitors identified through structure-Based hybridisation

Bioorganic & medicinal chemistry letters, 2003-09, Vol.13 (18), p.3021-3026

2003

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Crystal Structure of Human Thymidine Phosphorylase in Complex with a Small Molecule Inhibitor

Structure (London), 2004-01, Vol.12 (1), p.75-84

2004

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The cost-utility of magnetic resonance imaging for breast cancer in BRCA1 mutation carriers aged 30–49

The European journal of health economics, 2007-06, Vol.8 (2), p.137-144

2007

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Imidazo[1,2-b]pyridazines: a potent and selective class of cyclin-dependent kinase inhibitors

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (9), p.2249-2252

2004

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On Humanism

Norman, Richard

2nd Edition, 2012

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Religion and Atheism: Beyond the Divide

1, 2017

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Computational approaches to therapeutic antibody design: established methods and emerging trends

Structural Insights into FGFR Kinase Isoform Selectivity: Diverse Binding Modes of AZD4547 and Ponatinib in Complex with FGFR1 and FGFR4

N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5- (tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a Novel, Highly Selective, Orally Available, Dual-Specific c-Src/Abl Kinase Inhibitor

Investigation of (E)‑3-[4-(2-Oxo-3-aryl-chromen-4-yl)oxyphenyl]acrylic Acids as Oral Selective Estrogen Receptor Down-Regulators

Protein–Ligand Crystal Structures Can Guide the Design of Selective Inhibitors of the FGFR Tyrosine Kinase

AZD9496: An Oral Estrogen Receptor Inhibitor That Blocks the Growth of ER-Positive and ESR1-Mutant Breast Tumors in Preclinical Models

Structural approaches to obtain kinase selectivity

Design and Synthesis of Novel Lactate Dehydrogenase A Inhibitors by Fragment-Based Lead Generation

Characterization of the complex formed between a potent neutralizing ovine-derived polyclonal anti-TNFα Fab fragment and human TNFα

Landscape of activating cancer mutations in FGFR kinases and their differential responses to inhibitors in clinical use

Validation of ion mobility spectrometry - mass spectrometry as a screening tool to identify type II kinase inhibitors of FGFR1 kinase

Structural and dynamic insights into the energetics of activation loop rearrangement in FGFR1 kinase

The Mycobacterium tuberculosis ino1 gene is essential for growth and virulence

Crystal Structure of Inositol 1-Phosphate Synthase from Mycobacterium tuberculosis, a Key Enzyme in Phosphatidylinositol Synthesis

Tetrahydroisoquinoline Phenols: Selective Estrogen Receptor Downregulator Antagonists with Oral Bioavailability in Rat

Correction to Investigation of (E)‑3-[4-(2-Oxo-3-aryl-chromen-4-yl)oxyphenyl]acrylic Acids as Oral Selective Estrogen Receptor Down-Regulators

FGFR1 Kinase Inhibitors: Close Regioisomers Adopt Divergent Binding Modes and Display Distinct Biophysical Signatures

Prevention of MKK6-Dependent Activation by Binding to p38α MAP Kinase

Rapid Generation of a High Quality Lead for Transforming Growth Factor-β (TGF-β) Type I Receptor (ALK5)

Imidazo[1,2- a]pyridines: A potent and selective class of cyclin-Dependent kinase inhibitors identified through structure-Based hybridisation

Crystal Structure of Human Thymidine Phosphorylase in Complex with a Small Molecule Inhibitor

The cost-utility of magnetic resonance imaging for breast cancer in BRCA1 mutation carriers aged 30–49

Imidazo[1,2-b]pyridazines: a potent and selective class of cyclin-dependent kinase inhibitors

On Humanism

Religion and Atheism: Beyond the Divide

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