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Anti-PEG antibodies compromise the integrity of PEGylated lipid-based nanoparticles via complement

Journal of controlled release, 2022-01, Vol.341, p.475-486

2022

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Editorial: Effector functions of therapeutic antibodies

Frontiers in immunology, 2023-01, Vol.13, p.1126966-1126966

2023

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Dephasing of Majorana qubits due to quasistatic disorder

Physical review. B, 2022-01, Vol.105 (3), Article 035413

2022

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Critical differences in HIV‐1 and HIV‐2 protease specificity for clinical inhibitors

Protein science, 2012-03, Vol.21 (3), p.339-350

2012

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In vivo cytotoxicity of type I CD20 antibodies critically depends on Fc receptor ITAM signaling

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8), p.3209-3217

2010

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Hyperfine-assisted decoherence of a phosphorus nuclear-spin qubit in silicon

Physical review. B, 2019-09, Vol.100 (11), p.1, Article 115435

2019

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High Resolution Crystal Structures of HIV-1 Protease with a Potent Non-peptide Inhibitor (UIC-94017) Active Against Multi-drug-resistant Clinical Strains

Journal of molecular biology, 2004-04, Vol.338 (2), p.341-352

2004

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Novel bis-Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI) UIC-94017 (TMC114) with Potent Activity against Multi-PI-Resistant Human Immunodeficiency Virus In Vitro

Antimicrobial Agents and Chemotherapy, 2003-10, Vol.47 (10), p.3123-3129

2003

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Structural and Kinetic Analysis of Caspase-3 Reveals Role for S5 Binding Site in Substrate Recognition

Journal of molecular biology, 2006-07, Vol.360 (3), p.654-666

2006

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Effectiveness of Nonpeptide Clinical Inhibitor TMC-114 on HIV-1 Protease with Highly Drug Resistant Mutations D30N, I50V, and L90M

Journal of medicinal chemistry, 2006-02, Vol.49 (4), p.1379-1387

2006

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The in vivo mechanism of action of CD20 monoclonal antibodies depends on local tumor burden

Haematologica (Roma), 2011-12, Vol.96 (12), p.1822-1830

2011

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A Novel Bis-Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI), GRL-98065, Is Potent against Multiple-PI-Resistant Human Immunodeficiency Virus In Vitro

Antimicrobial Agents and Chemotherapy, 2007-06, Vol.51 (6), p.2143-2155

2007

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A unified theory of spin-relaxation due to spin-orbit coupling in metals and semiconductors

Scientific reports, 2013-11, Vol.3 (1), p.3233-3233, Article 3233

2013

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Braiding-based quantum control of a Majorana qubit built from quantum dots

Physical review. B, 2024-03, Vol.109 (12), Article 125410

2024

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Valley-enhanced fast relaxation of gate-controlled donor qubits in silicon

Nanotechnology, 2016-08, Vol.27 (31), p.314002-314002

2016

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Both activating and inhibitory Fc gamma receptors mediate rituximab-induced trogocytosis of CD20 in mice

Immunology letters, 2012-03, Vol.143 (1), p.44-52

2012

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Anti-C2 Antibody ARGX-117 Inhibits Complement in a Disease Model for Multifocal Motor Neuropathy

Neurology : neuroimmunology & neuroinflammation, 2022-01, Vol.9 (1)

2022

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Kinetic, Stability, and Structural Changes in High-resolution Crystal Structures of HIV-1 Protease with Drug-resistant Mutations L24I, I50V, and G73S

Journal of molecular biology, 2005-12, Vol.354 (4), p.789-800

2005

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Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 Å resolution crystal structures of HIV‐1 protease mutants with substrate analogs

The FEBS journal, 2005-10, Vol.272 (20), p.5265-5277

2005

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704 Preclinical mechanism of action and pharmacodynamic biomarker studies of DuoBody®-CD3x5T4 in vitro and in vivo in solid cancer models

Journal for immunotherapy of cancer, 2020-11, Vol.8 (Suppl 3), p.A746-A746

2020

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Potent New Antiviral Compound Shows Similar Inhibition and Structural Interactions with Drug Resistant Mutants and Wild Type HIV-1 Protease

Journal of medicinal chemistry, 2007-09, Vol.50 (18), p.4509-4515

2007

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Poor man's topological quantum gate based on the Su-Schrieffer-Heeger model

Physical review. B, 2019-07, Vol.100 (4), p.045414, Article 045414

2019

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Control of valley dynamics in silicon quantum dots in the presence of an interface step

Physical review. B, 2016-07, Vol.94 (3), Article 035438

2016

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Mechanism of Drug Resistance Revealed by the Crystal Structure of the Unliganded HIV-1 Protease with F53L Mutation

Journal of molecular biology, 2006-05, Vol.358 (5), p.1191-1199

2006

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Quantitative analysis of proteins in the tear fluid of patients with diabetic retinopathy

Journal of proteomics, 2012-04, Vol.75 (7), p.2196-2204

2012

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Anti-PEG antibodies compromise the integrity of PEGylated lipid-based nanoparticles via complement

Editorial: Effector functions of therapeutic antibodies

Dephasing of Majorana qubits due to quasistatic disorder

Critical differences in HIV‐1 and HIV‐2 protease specificity for clinical inhibitors

In vivo cytotoxicity of type I CD20 antibodies critically depends on Fc receptor ITAM signaling

Hyperfine-assisted decoherence of a phosphorus nuclear-spin qubit in silicon

High Resolution Crystal Structures of HIV-1 Protease with a Potent Non-peptide Inhibitor (UIC-94017) Active Against Multi-drug-resistant Clinical Strains

Novel bis-Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI) UIC-94017 (TMC114) with Potent Activity against Multi-PI-Resistant Human Immunodeficiency Virus In Vitro

Structural and Kinetic Analysis of Caspase-3 Reveals Role for S5 Binding Site in Substrate Recognition

Effectiveness of Nonpeptide Clinical Inhibitor TMC-114 on HIV-1 Protease with Highly Drug Resistant Mutations D30N, I50V, and L90M

The in vivo mechanism of action of CD20 monoclonal antibodies depends on local tumor burden

A Novel Bis-Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI), GRL-98065, Is Potent against Multiple-PI-Resistant Human Immunodeficiency Virus In Vitro

A unified theory of spin-relaxation due to spin-orbit coupling in metals and semiconductors

Braiding-based quantum control of a Majorana qubit built from quantum dots

Valley-enhanced fast relaxation of gate-controlled donor qubits in silicon

Both activating and inhibitory Fc gamma receptors mediate rituximab-induced trogocytosis of CD20 in mice

Anti-C2 Antibody ARGX-117 Inhibits Complement in a Disease Model for Multifocal Motor Neuropathy

Kinetic, Stability, and Structural Changes in High-resolution Crystal Structures of HIV-1 Protease with Drug-resistant Mutations L24I, I50V, and G73S

Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 Å resolution crystal structures of HIV‐1 protease mutants with substrate analogs

704 Preclinical mechanism of action and pharmacodynamic biomarker studies of DuoBody®-CD3x5T4 in vitro and in vivo in solid cancer models

Potent New Antiviral Compound Shows Similar Inhibition and Structural Interactions with Drug Resistant Mutants and Wild Type HIV-1 Protease

Poor man's topological quantum gate based on the Su-Schrieffer-Heeger model

Control of valley dynamics in silicon quantum dots in the presence of an interface step

Mechanism of Drug Resistance Revealed by the Crystal Structure of the Unliganded HIV-1 Protease with F53L Mutation

Quantitative analysis of proteins in the tear fluid of patients with diabetic retinopathy

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