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| High-affinity binding of chemokine analogs that display ligand bias at the HIV-1 coreceptor CCR5 | Biophysical Journal | | | 2019 | 316 | 216 |
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| Characterisation of preproendothelin-1 derived peptides identifies Endothelin-Like Domain Peptide as a modulator of Endothelin-1 | Scientific Reports | | | 2017 | 452 | 293 |
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| Generating Chemokine Analogs with Enhanced Pharmacological Properties Using Phage Display | Methods in enzymology |  | | 2016 | 576 | 5 |
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| A scalable low-cost cGMP process for clinical grade production of the HIV inhibitor 5P12-RANTES in Pichia pastoris | Protein expression and purification | | | 2016 | 588 | 344 |
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| Enhancing Antitumor Immune Responses by Optimized Combinations of Cell-penetrating Peptide-based Vaccines and Adjuvants | Molecular therapy | | | 2016 | 686 | 406 |
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| The Human Autoantibody Response to Apolipoprotein A-I Is Focused on the C-Terminal Helix: A New Rationale for Diagnosis and Treatment of Cardiovascular Disease? | PloS one | | | 2015 | 565 | 406 |
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| δ-Conotoxins synthesized using an acid-cleavable solubility tag approach reveal key structural determinants for NaV subtype selectivity | The Journal of biological chemistry | | | 2014 | 679 | 1 |
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| Definition of human apolipoprotein A-I epitopes recognized by autoantibodies present in patients with cardiovascular diseases | The Journal of biological chemistry | | | 2014 | 771 | 662 |
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| A novel µ-conopeptide, CnIIIC, exerts potent and preferential inhibition of NaV1.2/1.4 channels and blocks neuronal nicotinic acetylcholine receptors | British journal of pharmacology | | | 2012 | 742 | 0 |
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| Alteration of synaptic network dynamics by the intellectual disability protein PAK3 | The Journal of neuroscience |  | | 2012 | 718 | 0 |
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| Efficient orthogonal bioconjugation of dendrimers for synthesis of bioactive nanoparticles | Bioconjugate chemistry | | | 2011 | 659 | 0 |
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| CC chemokine receptor 5 (CCR5) desensitization: cycling receptors accumulate in the trans-Golgi network | The Journal of biological chemistry | | | 2010 | 665 | 78 |
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| Highly potent HIV inhibition: engineering a key anti-HIV structure from PSC-RANTES into MIP-1 beta/CCL4 | Protein engineering, design & selection | | | 2008 | 680 | 8 |
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| Semisynthetic analogues of PSC-RANTES, a potent anti-HIV protein | Bioconjugate chemistry | | | 2008 | 718 | 5 |
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| Highly potent, fully recombinant anti-HIV chemokines: reengineering a low-cost microbicide | Proceedings of the National Academy of Sciences of the United States of America | | | 2008 | 624 | 2 |
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| Medicinal chemistry applied to a synthetic protein: development of highly potent HIV entry inhibitors | Proceedings of the National Academy of Sciences of the United States of America | | | 2004 | 719 | 1 |
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| Industrial-scale proteomics: from liters of plasma to chemically synthesized proteins | Proteomics | | | 2004 | 637 | 0 |
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| Human immunodeficiency virus type 1 entry inhibitors selected on living cells from a library of phage chemokines | Journal of virology | | | 2003 | 561 | 396 |
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