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On the Analytical Superiority of 1D NMR for Fingerprinting the Higher Order Structure of Protein Therapeutics Compared to Multidimensional NMR Methods

Analytical chemistry (Washington), 2015-06, Vol.87 (11), p.5539-5545

2015

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Pharmacological characterization of potent and selective NaV1.7 inhibitors engineered from Chilobrachys jingzhao tarantula venom peptide JzTx-V

PloS one, 2018-05, Vol.13 (5), p.e0196791-e0196791

2018

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Hepcidin Revisited, Disulfide Connectivity, Dynamics, and Structure

The Journal of biological chemistry, 2009-09, Vol.284 (36), p.24155-24167

2009

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Broadly Protective Protein-Based Pneumococcal Vaccine Composed of Pneumolysin Toxoid—CbpA Peptide Recombinant Fusion Protein

The Journal of infectious diseases, 2014-04, Vol.209 (7), p.1116-1125

2014

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Ordering of the N‑Terminus of Human MDM2 by Small Molecule Inhibitors

Journal of the American Chemical Society, 2012-10, Vol.134 (41), p.17059-17067

2012

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Current state of biologic pharmacovigilance in the European Union: improvements are needed

Expert opinion on drug safety, 2019-03, Vol.18 (3), p.231-240

2019

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Structural and Biological Identification of Residues on the Surface of NS3 Helicase Required for Optimal Replication of the Hepatitis C Virus

The Journal of biological chemistry, 2006-02, Vol.281 (6), p.3528-3535

2006

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Profiling formulated monoclonal antibodies by (1)H NMR spectroscopy

Analytical chemistry (Washington), 2013-10, Vol.85 (20), p.9623-9629

2013

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Hepatitis C Virus NS3 Helicase Forms Oligomeric Structures That Exhibit Optimal DNA Unwinding Activity in Vitro

The Journal of biological chemistry, 2008-04, Vol.283 (17), p.11516-11525

2008

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Enabling adoption of 2D-NMR for the higher order structure assessment of monoclonal antibody therapeutics

mAbs, 2019-01, Vol.11 (1), p.94-105

2019

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Fragment-Linking Approach Using (19)F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β-Secretase

Journal of medicinal chemistry, 2016-04, Vol.59 (8), p.3732-3749

2016

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Facile Modulation of Antibody Fucosylation with Small Molecule Fucostatin Inhibitors and Cocrystal Structure with GDP-Mannose 4,6-Dehydratase

ACS chemical biology, 2016-10, Vol.11 (10), p.2734-2743

2016

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Correction to On the Analytical Superiority of 1D NMR for Fingerprinting the Higher Order Structure of Protein Therapeutics Compared to Multidimensional NMR Methods

Analytical chemistry (Washington), 2015-07, Vol.87 (14), p.7493-7493

2015

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Correction to Fragment-Linking Approach Using 19 F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β-Secretase

Journal of medicinal chemistry, 2017-04, Vol.60 (7), p.3218-3218

2017

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NSAID-Based γ-Secretase Modulators Do Not Bind to the Amyloid-β Polypeptide

Biochemistry (Easton), 2011-11, Vol.50 (47), p.10328-10342

2011

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Development of a nucleotide sugar purification method using a mixed mode column & mass spectrometry detection

Journal of pharmaceutical and biomedical analysis, 2015-11, Vol.115, p.402-409

2015

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Nonspecificity of Binding of γ-Secretase Modulators to the Amyloid Precursor Protein

Biochemistry (Easton), 2009-12, Vol.48 (50), p.11837-11839

2009

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Profiling Formulated Monoclonal Antibodies by 1H NMR Spectroscopy

Analytical chemistry (Washington), 2013-10, Vol.85 (20), p.9623-9629

2013

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Fragment Based Drug Discovery: Practical Implementation Based on 19F NMR Spectroscopy

Journal of medicinal chemistry, 2012-01, Vol.55 (2), p.678-687

2012

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Three-Dimensional 13C-Detected CH3-TOCSY Using Selectively Protonated Proteins: Facile Methyl Resonance Assignment and Protein Structure Determination

Journal of the American Chemical Society, 2006-07, Vol.128 (28), p.9119-9128

2006

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Fragment-Linking Approach Using [superscript 19]F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of [beta]-Secretase

Journal of medicinal chemistry, 2016-05, Vol.59 ((8) ; 03, 2016)

2016

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Fragment-Linking Approach Using 19 F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β-Secretase

Journal of medicinal chemistry, 2016-04, Vol.59 (8), p.3732-3749

2016

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Correction to Fragment-Linking Approach Using 19F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β‑Secretase

Journal of medicinal chemistry, 2017-04, Vol.60 (7), p.3218-3218

2017

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Pharmacological characterization of potent and selective Na.sub.V1.7 inhibitors engineered from Chilobrachys jingzhao tarantula venom peptide JzTx-V

PloS one, 2018-05, Vol.13 (5), p.e0196791

2018

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Profiling Formulated Monoclonal Antibodies by ^sup 1^H NMR Spectroscopy

Analytical chemistry (Washington), 2013-10, Vol.85 (20), p.9623

2013

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On the Analytical Superiority of 1D NMR for Fingerprinting the Higher Order Structure of Protein Therapeutics Compared to Multidimensional NMR Methods

Pharmacological characterization of potent and selective NaV1.7 inhibitors engineered from Chilobrachys jingzhao tarantula venom peptide JzTx-V

Hepcidin Revisited, Disulfide Connectivity, Dynamics, and Structure

Broadly Protective Protein-Based Pneumococcal Vaccine Composed of Pneumolysin Toxoid—CbpA Peptide Recombinant Fusion Protein

Ordering of the N‑Terminus of Human MDM2 by Small Molecule Inhibitors

Current state of biologic pharmacovigilance in the European Union: improvements are needed

Structural and Biological Identification of Residues on the Surface of NS3 Helicase Required for Optimal Replication of the Hepatitis C Virus

Profiling formulated monoclonal antibodies by (1)H NMR spectroscopy

Hepatitis C Virus NS3 Helicase Forms Oligomeric Structures That Exhibit Optimal DNA Unwinding Activity in Vitro

Enabling adoption of 2D-NMR for the higher order structure assessment of monoclonal antibody therapeutics

Fragment-Linking Approach Using (19)F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β-Secretase

Facile Modulation of Antibody Fucosylation with Small Molecule Fucostatin Inhibitors and Cocrystal Structure with GDP-Mannose 4,6-Dehydratase

Correction to On the Analytical Superiority of 1D NMR for Fingerprinting the Higher Order Structure of Protein Therapeutics Compared to Multidimensional NMR Methods

Correction to Fragment-Linking Approach Using 19 F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β-Secretase

NSAID-Based γ-Secretase Modulators Do Not Bind to the Amyloid-β Polypeptide

Development of a nucleotide sugar purification method using a mixed mode column & mass spectrometry detection

Nonspecificity of Binding of γ-Secretase Modulators to the Amyloid Precursor Protein

Profiling Formulated Monoclonal Antibodies by 1H NMR Spectroscopy

Fragment Based Drug Discovery: Practical Implementation Based on 19F NMR Spectroscopy

Three-Dimensional 13C-Detected CH3-TOCSY Using Selectively Protonated Proteins: Facile Methyl Resonance Assignment and Protein Structure Determination

Fragment-Linking Approach Using [superscript 19]F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of [beta]-Secretase

Fragment-Linking Approach Using 19 F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β-Secretase

Correction to Fragment-Linking Approach Using 19F NMR Spectroscopy To Obtain Highly Potent and Selective Inhibitors of β‑Secretase

Pharmacological characterization of potent and selective Na.sub.V1.7 inhibitors engineered from Chilobrachys jingzhao tarantula venom peptide JzTx-V

Profiling Formulated Monoclonal Antibodies by ^sup 1^H NMR Spectroscopy

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