LS
Scapozza, Leonardo
Affiliation entities
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Enhancing Oral Delivery of Biologics: A Non-Competitive and Cross-Reactive Anti-Leptin Receptor Nanofitin Demonstrates a Gut-Crossing Capacity in an Ex Vivo Porcine Intestinal Model | Pharmaceutics | 2024 | 114 | 98 | |||
| Compound K14 inhibits bacterial killing and protease activity in Dictyostelium discoideum phagosomes | PloS one | 2024 | 41 | 27 | |||
| Targeted protein degradation reveals BET bromodomains as the cellular target of Hedgehog pathway inhibitor-1 | Nature communications | 2023 | 96 | 99 | |||
| Targeted Nanofitin-drug Conjugates Achieve Efficient Tumor Delivery and Therapeutic Effect in an EGFRpos Mouse Xenograft Model | Molecular cancer therapeutics | 2023 | 68 | 26 | |||
| Challenges and Opportunities in the Oral Delivery of Recombinant Biologics | Pharmaceutics | 2023 | 41 | 24 | |||
| CEMIP ( HYBID , KIAA1199 ): structure, function and expression in health and disease | The FEBS journal | 2022 | 182 | 215 | |||
| Discovery of anti-Formin-like 1 protein (FMNL1) antibodies in membranous nephropathy and other glomerular diseases | Scientific reports | 2022 | 280 | 109 | |||
| 5-ethyl-2’-deoxyuridine fragilizes Klebsiella pneumoniae outer wall and facilitates intracellular killing by phagocytic cells | PloS one | 2022 | 78 | 75 | |||
| Chemoenzymatic synthesis of original stilbene dimers possessing wnt inhibition activity in triple-negative breast cancer cells using the enzymatic secretome of Botrytis cinerea pers | Frontiers in chemistry | 2022 | 232 | 127 | |||
| Functional and anatomical characterization of atrophic age-related macular degeneration in an aged mouse model | Journal of Ophthalmology and Research | 2021 | 453 | 297 | |||
| Glomerular macrophages in human auto- and allo-immune nephritis | Cells | 2021 | 241 | 142 | |||
| Heat-stability study of various insulin types in tropical temperature conditions: new insights towards improving diabetes care | PLOS ONE | 2021 | 389 | 307 | |||
| Novel Mechanism for an Old Drug: Phenazopyridine is a Kinase Inhibitor Affecting Autophagy and Cellular Differentiation | Frontiers in pharmacology | 2021 | 146 | 84 | |||
| From Conception to Development: Investigating PROTACs Features for Improved Cell Permeability and Successful Protein Degradation | Frontiers in Chemistry | 2021 | 495 | 665 | |||
| Platelet Transforming Growth Factor-β1 Induces Liver Sinusoidal Endothelial Cells to Secrete Interleukin-6 | Cells | 2020 | 357 | 171 | |||
| Identification of anti-mycobacterium and anti-legionella compounds with potential distinctive structural scaffolds from an HD-PBL using phenotypic screens in amoebae host models | Frontiers in Microbiology | 2020 | 326 | 190 | |||
| Cooperative binding of the tandem WW domains of PLEKHA7 to PDZD11 promotes conformation-dependent interaction with tetraspanin 33 | Journal of Biological Chemistry | 2020 | 294 | 152 | |||
| Drug repurposing in oncology: Compounds, pathways, phenotypes and computational approaches for colorectal cancer | Biochimica et Biophysica Acta. Reviews on Cancer | 2019 | 487 | 637 | |||
| DDR1 role in fibrosis and its pharmacological targeting | Biochimica et Biophysica Acta - Molecular Cell Research | 2019 | 429 | 3 | |||
| Identification of novel anti-bacterial compounds from a chemically highly diverse pathways-based library using phenotypic screens in amoebae host models | 2018 | 643 | 344 | ||||
| Autoregulation of Class II Alpha PI3K Activity by Its Lipid-Binding PX-C2 Domain Module | Molecular Cell | 2018 | 470 | 0 | |||
| Antimycobacterial drug discovery using Mycobacteria-infected amoebae identifies anti-infectives and new molecular targets | Scientific Reports | 2018 | 558 | 205 | |||
| Tamoxifen prolongs survival and alleviates symptoms in mice with fatal X-linked myotubular myopathy | Nature Communications | 2018 | 510 | 273 | |||
| Modeling and resistant alleles explain the selectivity of antimalarial compound 49c towards apicomplexan aspartyl proteases | EMBO Journal | 2018 | 679 | 15 | |||
| Inhibitors of Mycobacterium marinum virulence identified in a Dictyostelium discoideum host model | PLOS ONE | 2017 | 491 | 238 | |||
| Mammalian RAD52 Functions in Break-Induced Replication Repair of Collapsed DNA Replication Forks | Molecular cell | 2016 | 62 | 131 | |||
| In silico driven design and synthesis of rhodanine derivatives as novel antibacterials targeting the enoyl reductase InhA | Journal of medicinal chemistry | 2016 | 670 | 6 | |||
| A subset of N-substituted phenothiazines inhibits NADPH oxidases | Free radical biology & medicine | 2015 | 594 | 602 | |||
| A novel biocompatible hyaluronic acid-chitosan hybrid hydrogel for osteoarthrosis therapy | International journal of pharmaceutics | 2015 | 901 | 2 | |||
| Amoebae-Based Screening Reveals a Novel Family of Compounds Restricting Intracellular Legionella pneumophila | ACS infectious diseases | 2015 | 685 | 495 | |||
| Adrenergic antagonists restrict replication of Legionella | Microbiology | 2015 | 616 | 0 | |||
| Differences in Conformational Dynamics between Plasmodium falciparum and Human Hsp90 Orthologues Enable the Structure-Based Discovery of Pathogen-Selective Inhibitors | Journal of medicinal chemistry | 2014 | 711 | 675 | |||
| Establishment and validation of whole-cell based fluorescence assays to identify anti-mycobacterial compounds using the Acanthamoeba castellanii-Mycobacterium marinum host-pathogen system | PloS one | 2014 | 758 | 327 | |||
| Diapocynin, a Dimer of the NADPH Oxidase Inhibitor Apocynin, Reduces ROS Production and Prevents Force Loss in Eccentrically Contracting Dystrophic Muscle | PloS one | 2014 | 626 | 611 | |||
| Synthesis and in vitro evaluation of a novel radioligand for αvβ3 integrin receptor imaging: [18F]FPPA-c(RGDfK) | Bioorganic & medicinal chemistry letters | 2013 | 687 | 0 | |||
| The pharmaceutical biochemistry group: where pharmaceutical chemistry meets biology and drug delivery | Chimia | 2012 | 834 | 732 | |||
| NADPH oxidase (NOX) isoforms are inhibited by celastrol with a dual mode of action | British journal of pharmacology | 2011 | 744 | 0 | |||
| Noninvasive transdermal iontophoretic delivery of biologically active human basic fibroblast growth factor | Molecular pharmaceutics | 2011 | 616 | 2 | |||
| Small-molecule NOX inhibitors: ROS-generating NADPH oxidases as therapeutic targets | Antioxidants & redox signaling | 2009 | 672 | 2 | |||
| Development and validation of a capillary electrophoresis method for the characterization of herpes simplex virus type 1 (HSV-1) thymidine kinase substrates and inhibitors | Journal of chromatography. B | 2007 | 533 | 0 | |||
| Synthesis, in vitro and in silico assessment of organometallic Rhenium(I) and Technetium(I) thymidine complexes | Journal of organometallic chemistry | 2007 | 611 | 0 | |||
| Analysis of the cross-reactivity and of the 1.5 A crystal structure of the Malassezia sympodialis Mala s 6 allergen, a member of the cyclophilin pan-allergen family | Biochemical journal | 2006 | 492 | 0 | |||
| Inhibition of RET tyrosine kinase by SU5416 | Journal of Molecular Endocrinology | 2006 | 121 | 0 | |||
| Calpain-mediated cleavage of Atg5 switches autophagy to apoptosis | Nature cell biology | 2006 | 79 | 0 | |||
| Structural Insights into the ATP Binding Pocket of the Anaplastic Lymphoma Kinase by Site-Directed Mutagenesis, Inhibitor Binding Analysis, and Homology Modeling | Journal of medicinal chemistry | 2006 | 130 | 0 | |||
| Inhibition of Plasmodium falciparum Fatty Acid Biosynthesis: Evaluation of FabG, FabZ, and FabI as Drug Targets for Flavonoids | Journal of medicinal chemistry | 2006 | 189 | 1 | |||
| Tyrosine kinase drug discovery: what can be learned from solved crystal structures? | ARKIVOC | 2006 | 553 | 408 | |||
| In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinib-resistant Bcr-Abl+ neoplastic cells | Cancer research | 2006 | 520 | 1 | |||
| High-level expression and purification of human thymidine kinase 1: Quaternary structure, stability, and kinetics | Protein expression and purification | 2006 | 67 | 0 | |||
| Recombinant expression and biochemical characterization of the unique elongating β-Ketoacyl-acyl carrier protein synthase involved in fatty acid biosynthesis of Plasmodium falciparum using natural and artificial substrates | The Journal of biological chemistry | 2006 | 162 | 82 | |||
| Abl inhibitor BMS354825 binding mode in Abelson kinase revealed by molecular docking studies | Leukemia | 2005 | 118 | 0 | |||
| An enzyme-linked immunosorbent assay to screen for inhibitors of the oncogenic anaplastic lymphoma kinase | Haematologica | 2005 | 431 | 158 | |||
| The crystal structure of PfFabZ, the unique β‐hydroxyacyl‐ACP dehydratase involved in fatty acid biosynthesis of Plasmodium falciparum | Protein science | 2005 | 74 | 82 | |||
| Unique substrate specificity of anaplastic lymphoma kinase (ALK): development of phosphoacceptor peptides for the assay of ALK activity | Biochemistry | 2005 | 557 | 0 |
