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3. Design, synthesis and in vitro evaluation of novel SARS-CoV-2 3CLpro covalent inhibitors

9. Integration of Computational and Experimental Techniques for the Discovery of SARS-CoV-2 PLpro Covalent Inhibitors

14. i-Motif folding intermediates with zero-nucleotide loops are trapped by 2'-fluoroarabinocytidine via F···H and O···H hydrogen bonds

15. A naturally occurring G11S mutation in the 3C‐like protease from the SARS‐CoV‐2 virus dramatically weakens the dimer interface.

35. Design, Synthesis and Biological Evaluation of Novel SARS-CoV-2 3CLpro Covalent Inhibitors

44. COVID-19: Famotidine, Histamine, Mast Cells, and Mechanisms

47. Side-chain interactions in the folding pathway of a Fyn SH3 domain mutant studied by relaxation dispersion NMR spectroscopy

48. NMR dynamics-derived insights into the binding properties of a peptide interacting with an SH2 domain

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