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By inhibiting HDAC activity, these drugs aim to reverse the repressive effects of HDACs on gene expression and restore normal cellular function

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Safety, pharmacokinetic, and pharmacodynamic evaluation of a 2-(2-methoxyethyl)-d-ribose antisense oligonucleotide-triantenarry n -acetyl-galactosamine conjugate that targets the human transmembrane protease serine 6

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Analysis of metal coordination behaviors of the Bpy ligands by UVVis absorption spectroscopy indicated the apparent monochelating nature of the dumbbell-shaped Bpy ligands (Kim et al