HG
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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Prognostic and therapeutic considerations of antibodies against c‐ter apolipoprotein A‐1 in the general population | Clinical & translational immunology | 2020 | 163 | 93 | |||
High-affinity binding of chemokine analogs that display ligand bias at the HIV-1 coreceptor CCR5 | Biophysical Journal | 2019 | 258 | 159 | |||
Characterisation of preproendothelin-1 derived peptides identifies Endothelin-Like Domain Peptide as a modulator of Endothelin-1 | Scientific Reports | 2017 | 410 | 201 | |||
Generating Chemokine Analogs with Enhanced Pharmacological Properties Using Phage Display | Methods in enzymology | 2016 | 541 | 5 | |||
A scalable low-cost cGMP process for clinical grade production of the HIV inhibitor 5P12-RANTES in Pichia pastoris | Protein expression and purification | 2016 | 524 | 237 | |||
Enhancing Antitumor Immune Responses by Optimized Combinations of Cell-penetrating Peptide-based Vaccines and Adjuvants | Molecular therapy | 2016 | 628 | 283 | |||
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 | 521 | 284 | |||
δ-Conotoxins synthesized using an acid-cleavable solubility tag approach reveal key structural determinants for NaV subtype selectivity | The Journal of biological chemistry | 2014 | 636 | 1 | |||
Definition of human apolipoprotein A-I epitopes recognized by autoantibodies present in patients with cardiovascular diseases | The Journal of biological chemistry | 2014 | 728 | 616 | |||
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 | 651 | 0 | |||
Alteration of synaptic network dynamics by the intellectual disability protein PAK3 | The Journal of neuroscience | 2012 | 671 | 0 | |||
Efficient orthogonal bioconjugation of dendrimers for synthesis of bioactive nanoparticles | Bioconjugate chemistry | 2011 | 615 | 0 | |||
CC chemokine receptor 5 (CCR5) desensitization: cycling receptors accumulate in the trans-Golgi network | The Journal of biological chemistry | 2010 | 604 | 8 | |||
Highly potent HIV inhibition: engineering a key anti-HIV structure from PSC-RANTES into MIP-1 beta/CCL4 | Protein engineering, design & selection | 2008 | 625 | 8 | |||
Semisynthetic analogues of PSC-RANTES, a potent anti-HIV protein | Bioconjugate chemistry | 2008 | 662 | 5 | |||
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 | 560 | 2 | |||
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 | 665 | 1 | |||
Industrial-scale proteomics: from liters of plasma to chemically synthesized proteins | Proteomics | 2004 | 586 | 0 | |||
Human immunodeficiency virus type 1 entry inhibitors selected on living cells from a library of phage chemokines | Journal of virology | 2003 | 514 | 346 |