Histone deacetylases
Zyflamend, a polyherbal mixture, down regulates class I and class II histone deacetylases and increases p21 levels in castrate resistant prostate cancer cells
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Targeting Histone Deacetylases for Cancer Therapy: From Molecular Mechanisms to Clinical Implications
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Class IIa histone deacetylases: conducting development and differentiation
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Histone Deacetylases and the Nuclear Receptor Corepressor Regulate Lytic-Latent Switch Gene 50 in Murine Gammaherpesvirus 68-Infected Macrophages
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Histone Deacetylases with Antagonistic Roles in Saccharomyces cerevisiae Heterochromatin Formation
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Histone deacetylases (HDACs) in XPC gene silencing and bladder cancer
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The yeast Cyc8 Tup1 complex cooperates with Hda1p and Rpd3p histone deacetylases to robustly repress transcription of the subtelomeric FLO1 gene
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Developing selective histone deacetylases (HDACs) inhibitors through ebselen and analogs
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Expression of class I histone deacetylases during chick and mouse development
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Inhibition of Histone Deacetylases Induces Bovine Leukemia Virus Expression In Vitro and In Vivo
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Histone deacetylases 1 and 2 restrain CD4+ cytotoxic T lymphocyte differentiation
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Histone deacetylases 1 and 2 are required for brain development
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Inhibition of histone deacetylases induces formation of multipolar spindles and subsequent p53-dependent apoptosis in nasopharyngeal carcinoma cells
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Histone deacetylases 1 and 2 regulate the transcriptional programs of nephron progenitors and renal vesicles
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Multiple stage dependent roles for histone deacetylases during amphibian embryogenesis: implications for the involvement of extracellular matrix remodeling
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Histone Deacetylases 1 and 2 Are Phosphorylated at Novel Sites during Varicella-Zoster Virus Infection
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A Limited Group of Class I Histone Deacetylases Acts To Repress Human Immunodeficiency Virus Type 1 Expression
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A Conserved Gammaherpesvirus Protein Kinase Targets Histone Deacetylases 1 and 2 To Facilitate Viral Replication in Primary Macrophages
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Original Article Histone deacetylases 3 (HDAC3) is highly expressed in cervical cancer and inhibited by siRNA
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Synthesis and Preclinical Evaluation of a Highly Improved Anticancer Prodrug Activated by Histone Deacetylases and Cathepsin L
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