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Structurally Designedtrans-2-Phenylcyclopropylamine Derivatives Potently Inhibit Histone Demethylase LSD1/KDM1,,§

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Comparative Analysis of Small Molecules and Histone Substrate Analogues as LSD1 Lysine Demethylase Inhibitors

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Phosphorylation of histone H3T6 by PKCβI controls demethylation at histone H3K4

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Dali server: conservation mapping in 3D

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Lysine-specific demethylase 1 (LSD1) is highly expressed in ER-negative breast cancers and a biomarker predicting aggressive biology

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LSD1 Is a Subunit of the NuRD Complex and Targets the Metastasis Programs in Breast Cancer

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Novel Oligoamine Analogues Inhibit Lysine-Specific Demethylase 1 and Induce Reexpression of Epigenetically Silenced Genes

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Crystal structure of histone demethylase LSD1 and tranylcypromine at 2.25Å

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