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Structural basis of sequence-specific RNA recognition by the antiviral factor APOBEC3G | Nature Communications
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pH-Driven Self-Assembly of Acidic Microbial Glycolipids | Langmuir
Interaction of Zika Virus Envelope Protein with Glycosaminoglycans | Biochemistry
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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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IJMS | Free Full-Text | Factors That Control the Force Needed to Unfold a Membrane Protein in Silico Depend on the Mode of Denaturation
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Fluorescence Spectroscopic Profiling of Compound Libraries | Journal of Medicinal Chemistry
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
A Colorimetric Probe for the Selective Detection of Norepinephrine Based on a Double Molecular Recognition with Functionalized Gold Nanoparticles | ACS Applied Nano Materials
Virtual Screening Identifies Irreversible FMS-like Tyrosine Kinase 3 Inhibitors with Activity toward Resistance-Conferring Mutations | Journal of Medicinal Chemistry
Effect of BHAP on growth of established human breast cancer carcinoma... | Download Scientific Diagram
Design and Synthesis of Dual EZH2/BRD4 Inhibitors to Target Solid Tumors | Journal of Medicinal Chemistry
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Molecular architecture of the augmin complex | Nature Communications
Crystal structure of a bacterial homologue of the bile acid sodium symporter ASBT | Nature
Discovery of Anilino-1,4-naphthoquinones as Potent EGFR Tyrosine Kinase Inhibitors: Synthesis, Biological Evaluation, and Comprehensive Molecular Modeling | ACS Omega
Human Protein-l-isoaspartate O-Methyltransferase Domain-Containing Protein 1 (PCMTD1) Associates with Cullin-RING Ligase Proteins | Biochemistry