Zinc-dependent histone deacetylases (HDAC) inhibitors represent an important class of biologically active compounds with four of them approved by the FDA. A wide range of molecules has been reported for applications in several human diseases
Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl gro...
Histone deacetylases (HDACs) catalyze the removal of the acetyl group from an e-N-acetyl lysine on ...
Histone deacetylase (HDAC) proteins have become an important target for the treatment of several dis...
There are eleven human isoforms of the zinc-dependent histone deacetylases (HDACs). These proteins a...
In humans, the zinc-dependent histone deacetylases (HDACs) are a family of 11 nonredundant isoforms ...
Histone deacetylases (HDACs) are epigenetic erasers, which are considered as transcriptional repress...
The histone deacetylase (HDAC) enzymes, a class of epigenetic regulators, are historically well esta...
Histone deacetylases (HDACs) are known to deacetylate histones and other proteins, which makes HDAC ...
Histone deacetylases(HDAC)play a critical role in regulating gene expression and thus are considered...
Currently three HDAC inhibitors have been approved by the FDA where the use of vorinostat and romide...
Histone deacetylases (HDACs) are epigenetic drug targets that have gained major scientific attention...
Histone deacetylase (HDAC) inhibitors are a relatively new class of anti-cancer agents that play imp...
Histone deacetylase 6 (HDAC6) is a crucial regulator in various cancer types and several non-oncolog...
Histone deacetylase (HDAC) inhibition has recently emerged as a novel therapy for cancer treatment. ...
Histone deacetylase inhibitors (HDACis) are one of the last frontiers in pharmaceutical research. Se...
Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl gro...
Histone deacetylases (HDACs) catalyze the removal of the acetyl group from an e-N-acetyl lysine on ...
Histone deacetylase (HDAC) proteins have become an important target for the treatment of several dis...
There are eleven human isoforms of the zinc-dependent histone deacetylases (HDACs). These proteins a...
In humans, the zinc-dependent histone deacetylases (HDACs) are a family of 11 nonredundant isoforms ...
Histone deacetylases (HDACs) are epigenetic erasers, which are considered as transcriptional repress...
The histone deacetylase (HDAC) enzymes, a class of epigenetic regulators, are historically well esta...
Histone deacetylases (HDACs) are known to deacetylate histones and other proteins, which makes HDAC ...
Histone deacetylases(HDAC)play a critical role in regulating gene expression and thus are considered...
Currently three HDAC inhibitors have been approved by the FDA where the use of vorinostat and romide...
Histone deacetylases (HDACs) are epigenetic drug targets that have gained major scientific attention...
Histone deacetylase (HDAC) inhibitors are a relatively new class of anti-cancer agents that play imp...
Histone deacetylase 6 (HDAC6) is a crucial regulator in various cancer types and several non-oncolog...
Histone deacetylase (HDAC) inhibition has recently emerged as a novel therapy for cancer treatment. ...
Histone deacetylase inhibitors (HDACis) are one of the last frontiers in pharmaceutical research. Se...
Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl gro...
Histone deacetylases (HDACs) catalyze the removal of the acetyl group from an e-N-acetyl lysine on ...
Histone deacetylase (HDAC) proteins have become an important target for the treatment of several dis...
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