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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 ModelPharmaceutics
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2024 90 68
Compound K14 inhibits bacterial killing and protease activity in Dictyostelium discoideum phagosomesPloS one
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2024 18 11
Targeted protein degradation reveals BET bromodomains as the cellular target of Hedgehog pathway inhibitor-1Nature communications
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2023 72 68
Targeted Nanofitin-drug Conjugates Achieve Efficient Tumor Delivery and Therapeutic Effect in an EGFRpos Mouse Xenograft ModelMolecular cancer therapeutics
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2023 41 15
Challenges and Opportunities in the Oral Delivery of Recombinant BiologicsPharmaceutics
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2023 23 15
CEMIP ( HYBID , KIAA1199 ): structure, function and expression in health and diseaseThe FEBS journal
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2022 164 164
Discovery of anti-Formin-like 1 protein (FMNL1) antibodies in membranous nephropathy and other glomerular diseasesScientific reports
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2022 258 102
5-ethyl-2’-deoxyuridine fragilizes Klebsiella pneumoniae outer wall and facilitates intracellular killing by phagocytic cellsPloS one
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2022 59 51
Chemoenzymatic synthesis of original stilbene dimers possessing wnt inhibition activity in triple-negative breast cancer cells using the enzymatic secretome of Botrytis cinerea persFrontiers in chemistry
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2022 209 105
Functional and anatomical characterization of atrophic age-related macular degeneration in an aged mouse modelJournal of Ophthalmology and Research
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2021 413 266
Glomerular macrophages in human auto- and allo-immune nephritisCells
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2021 219 135
Heat-stability study of various insulin types in tropical temperature conditions: new insights towards improving diabetes carePLOS ONE
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2021 338 210
Novel Mechanism for an Old Drug: Phenazopyridine is a Kinase Inhibitor Affecting Autophagy and Cellular DifferentiationFrontiers in pharmacology
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2021 118 51
From Conception to Development: Investigating PROTACs Features for Improved Cell Permeability and Successful Protein DegradationFrontiers in Chemistry
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2021 460 580
Platelet Transforming Growth Factor-β1 Induces Liver Sinusoidal Endothelial Cells to Secrete Interleukin-6Cells
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2020 333 147
Identification of anti-mycobacterium and anti-legionella compounds with potential distinctive structural scaffolds from an HD-PBL using phenotypic screens in amoebae host modelsFrontiers in Microbiology
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2020 301 175
Cooperative binding of the tandem WW domains of PLEKHA7 to PDZD11 promotes conformation-dependent interaction with tetraspanin 33Journal of Biological Chemistry
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2020 269 144
Drug repurposing in oncology: Compounds, pathways, phenotypes and computational approaches for colorectal cancerBiochimica et Biophysica Acta. Reviews on Cancer
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2019 469 552
DDR1 role in fibrosis and its pharmacological targetingBiochimica et Biophysica Acta - Molecular Cell Research
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2019 398 3
Identification of novel anti-bacterial compounds from a chemically highly diverse pathways-based library using phenotypic screens in amoebae host models
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2018 604 322
Autoregulation of Class II Alpha PI3K Activity by Its Lipid-Binding PX-C2 Domain ModuleMolecular Cell
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2018 452 0
Antimycobacterial drug discovery using Mycobacteria-infected amoebae identifies anti-infectives and new molecular targetsScientific Reports
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2018 519 195
Tamoxifen prolongs survival and alleviates symptoms in mice with fatal X-linked myotubular myopathyNature Communications
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2018 478 247
Modeling and resistant alleles explain the selectivity of antimalarial compound 49c towards apicomplexan aspartyl proteasesEMBO Journal
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2018 657 15
Inhibitors of Mycobacterium marinum virulence identified in a Dictyostelium discoideum host modelPLOS ONE
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2017 465 215
Mammalian RAD52 Functions in Break-Induced Replication Repair of Collapsed DNA Replication ForksMolecular cell
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2016 51 92
In silico driven design and synthesis of rhodanine derivatives as novel antibacterials targeting the enoyl reductase InhAJournal of medicinal chemistry
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2016 644 6
A subset of N-substituted phenothiazines inhibits NADPH oxidasesFree radical biology & medicine
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2015 572 571
A novel biocompatible hyaluronic acid-chitosan hybrid hydrogel for osteoarthrosis therapyInternational journal of pharmaceutics
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2015 828 2
Amoebae-Based Screening Reveals a Novel Family of Compounds Restricting Intracellular Legionella pneumophilaACS infectious diseases
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2015 651 475
Adrenergic antagonists restrict replication of LegionellaMicrobiology
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2015 593 0
Differences in Conformational Dynamics between Plasmodium falciparum and Human Hsp90 Orthologues Enable the Structure-Based Discovery of Pathogen-Selective InhibitorsJournal of medicinal chemistry
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2014 693 626
Establishment and validation of whole-cell based fluorescence assays to identify anti-mycobacterial compounds using the Acanthamoeba castellanii-Mycobacterium marinum host-pathogen systemPloS one
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2014 739 323
Diapocynin, a Dimer of the NADPH Oxidase Inhibitor Apocynin, Reduces ROS Production and Prevents Force Loss in Eccentrically Contracting Dystrophic MusclePloS one
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2014 607 596
Synthesis and in vitro evaluation of a novel radioligand for αvβ3 integrin receptor imaging: [18F]FPPA-c(RGDfK)Bioorganic & medicinal chemistry letters
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2013 665 0
The pharmaceutical biochemistry group: where pharmaceutical chemistry meets biology and drug deliveryChimia
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2012 777 687
NADPH oxidase (NOX) isoforms are inhibited by celastrol with a dual mode of actionBritish journal of pharmacology
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2011 718 0
Noninvasive transdermal iontophoretic delivery of biologically active human basic fibroblast growth factorMolecular pharmaceutics
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2011 597 2
Small-molecule NOX inhibitors: ROS-generating NADPH oxidases as therapeutic targetsAntioxidants & redox signaling
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2009 646 2
Development and validation of a capillary electrophoresis method for the characterization of herpes simplex virus type 1 (HSV-1) thymidine kinase substrates and inhibitorsJournal of chromatography. B
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2007 513 0
Synthesis, in vitro and in silico assessment of organometallic Rhenium(I) and Technetium(I) thymidine complexesJournal of organometallic chemistry
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2007 579 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 familyBiochemical journal
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2006 474 0
Inhibition of RET tyrosine kinase by SU5416Journal of Molecular Endocrinology
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2006 105 0
Calpain-mediated cleavage of Atg5 switches autophagy to apoptosisNature cell biology
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2006 56 0
Structural Insights into the ATP Binding Pocket of the Anaplastic Lymphoma Kinase by Site-Directed Mutagenesis, Inhibitor Binding Analysis, and Homology ModelingJournal of medicinal chemistry
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2006 111 0
Inhibition of Plasmodium falciparum Fatty Acid Biosynthesis: Evaluation of FabG, FabZ, and FabI as Drug Targets for FlavonoidsJournal of medicinal chemistry
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2006 172 1
Tyrosine kinase drug discovery: what can be learned from solved crystal structures?ARKIVOC
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2006 525 396
In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinib-resistant Bcr-Abl+ neoplastic cellsCancer research
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2006 500 1
High-level expression and purification of human thymidine kinase 1: Quaternary structure, stability, and kineticsProtein expression and purification
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2006 53 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 substratesThe Journal of biological chemistry
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2006 144 55
Abl inhibitor BMS354825 binding mode in Abelson kinase revealed by molecular docking studiesLeukemia
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2005 109 0
An enzyme-linked immunosorbent assay to screen for inhibitors of the oncogenic anaplastic lymphoma kinaseHaematologica
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2005 418 145
The crystal structure of PfFabZ, the unique β‐hydroxyacyl‐ACP dehydratase involved in fatty acid biosynthesis of Plasmodium falciparumProtein science
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2005 64 43
Unique substrate specificity of anaplastic lymphoma kinase (ALK): development of phosphoacceptor peptides for the assay of ALK activityBiochemistry
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2005 535 0
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