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In order to demonstrate potential for biological applications, along with compatibility with longer peptides, an i,i + 4 stapled analog of the 11-mer linear peptide ligand that binds the co-activator binding site of estrogen receptor was synthesized

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Since the consumption of NADPH by GSR may compete with NADPH-dependent inflammatory processes, we endeavored to determine NADPH consumption by GSR in macrophages (Ms) stimulated by lipopolysaccharide (LPS), a classical Toll-like receptor 4 ligand

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