Histone deacetylase inhibitors suppress mutant p53 transcription via histone deacetylase 8

Yan, W, Liu, S, Xu, E, Zhang, J, Zhang, Y, Chen, X, Chen, X·2013·Oncogene

Cited by (156)

Items 101–156 of 156

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  44. Mutational analysis of non-coding genome in prostate cancer using whole genome sequencing
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  45. Characterization and functional analysis of mutant p53 secretome in human cancer
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  46. The effect of matrix stiffness, composition, and three-dimensionality on p53 expression in engineered human bone tumors
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  47. Target Identification of HDAC8 Isoform for the Treatment of Cancer
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  53. BindingDB Entry 50022755: HDAC8 as a target in drug discovery: Function, structure and design.
    BindingDB · 2026 · UC San Diego
  54. BindingDB Entry 50002428: Discovery of meta-sulfamoyl N-hydroxybenzamides as HDAC8 selective inhibitors.
    BindingDB · 2020 · UC San Diego
  55. BindingDB Entry 50010688: Potent non-hydroxamate inhibitors of histone deacetylase-8: Role and scope of an isoindolin-2-yl linker with an α-amino amide as the zinc-binding unit.
    BindingDB · 2021 · UC San Diego
  56. BindingDB Entry 50010426: Histone deacetylase 8 (HDAC8) and its inhibitors with selectivity to other isoforms: An overview.
    BindingDB · 2021 · UC San Diego