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Solid-phase peptide synthesis in 384-well plates

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Solid-phase peptide synthesis in 384-well plates

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Methods for the generation of large combinatorial macrocycle libraries

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Thiol-to-amine cyclization reaction enables screening of large libraries of macrocyclic compounds and the generation of sub-kilodalton ligands

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Synthesis of asparagusic acid modified lysine and its application in solid-phase synthesis of peptides with enhanced cellular uptake

Development of an albumin-binding ligand for prolonging the plasma half-life of peptide therapeutics

New methods for developing (bi)cyclic peptides by phage display