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N-(2-Amino-phenyl)-4-(heteroarylmethyl)-benzamides as new histone deacetylase inhibitors
Bioorganic & Medicinal Chemistry Letters, 2007A variety of N-(2-amino-phenyl)-4-(heteroarylmethyl)-benzamides were designed and synthesized. These compounds were shown to inhibit recombinant human HDAC1 with IC(50) values in the sub-micromolar range. In human cancer cells growing in culture these compounds induced hyperacetylation of histones, induced the expression of the tumor suppressor protein
Arkadii, Vaisburg +24 more
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Histone Deacetylase 4 is crucial for proper skeletal muscle development and disease
2015Italian Journal of Anatomy and Embryology, Vol. 120, No.
MARRONCELLI, NICOLETTA +7 more
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Histone deacetylase (HDAC) 4 involvement in both Lewy and Marinesco bodies
Neuropathology and Applied Neurobiology, 2006J, Takahashi-Fujigasaki, H, Fujigasaki
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