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4. Discovery and characterization of a substrate selective p38alpha inhibitor

6. Binding site elucidation of hydantoin-based antagonists of LFA-1 using multidisciplinary technologies: evidence for the allosteric inhibition of a protein-protein interaction

7. Determination of affinities for lck SH2 binding peptides using a sensitive fluorescence assay: comparison between the pYEEIP and pYQPQP consensus sequences reveals context-dependent binding specificity

11. Design and Synthesis of Dipeptide Nitriles as Reversible and Potent Cathepsin S Inhibitors.

12. Binding Site Elucidation of Hydantoin-Based Antagonists of LFA-1 Using Multidisciplinary Technologies: Evidence for the Allosteric Inhibition of a Protein−Protein Interaction

16. In search of geminites: The synthesis and structural characterization of [Pd{(C 6H 5) 2P(CH 2) nP(C 6H 5) 2}(SeCN) 2] (n= 1,2,3)and [Pd{(C 6H 5) 2PCH 2oC 6H 4CH 2P(C 6H 5) 2}(SeCN) 2]

26. Design and synthesis of dipeptide nitriles as reversible and potent Cathepsin S inhibitors.

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