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Spatiotemporal organisation of protein processing in the kidney | Nature Communications
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Discovery of Anilino-1,4-naphthoquinones as Potent EGFR Tyrosine Kinase Inhibitors: Synthesis, Biological Evaluation, and Comprehensive Molecular Modeling | ACS Omega
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Quorum sensing modulates the formation of virulent Legionella persisters within infected cells | Nature Communications
From Angstroms to Nanometers: Measuring Interatomic Distances by Solid-State NMR | Chemical Reviews
Network-based assessment of HDAC6 activity predicts preclinical and clinical responses to the HDAC6 inhibitor ricolinostat in breast cancer | Nature Cancer
Tissue transglutaminase exacerbates renal fibrosis via alternative activation of monocyte-derived macrophages | Cell Death & Disease
Structure Based Drug Design of Crizotinib (PF-02341066), a Potent and Selective Dual Inhibitor of Mesenchymal–Epithelial Transition Factor (c-MET) Kinase and Anaplastic Lymphoma Kinase (ALK) | Journal of Medicinal Chemistry
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Virtual Screening Identifies Irreversible FMS-like Tyrosine Kinase 3 Inhibitors with Activity toward Resistance-Conferring Mutations | Journal of Medicinal Chemistry
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Fluorescence Spectroscopic Profiling of Compound Libraries | Journal of Medicinal Chemistry
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Human Protein-l-isoaspartate O-Methyltransferase Domain-Containing Protein 1 (PCMTD1) Associates with Cullin-RING Ligase Proteins | Biochemistry
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Discovery of 5-Aryl-2,4-diaminopyrimidine Compounds as Potent and Selective IRAK4 Inhibitors | ACS Medicinal Chemistry Letters
A Colorimetric Probe for the Selective Detection of Norepinephrine Based on a Double Molecular Recognition with Functionalized Gold Nanoparticles | ACS Applied Nano Materials
IJMS | Free Full-Text | Bis-Cyclic Guanidine Heterocyclic Peptidomimetics as Opioid Ligands with Mixed μ-, κ- and δ-Opioid Receptor Interactions: A Potential Approach to Novel Analgesics
Molecular architecture of the augmin complex | Nature Communications
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