Histone deacetylase inhibitors as cancer therapeutics.

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Histone deacetylase inhibitors as cancer therapeutics.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

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2016年學術文章

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Histone deacetylase inhibitors as cancer therapeutics.

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Histone deacetylase inhibitors as cancer therapeutics.

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label

Histone deacetylase inhibitors as cancer therapeutics.

@en

Histone deacetylase inhibitors as cancer therapeutics.

@nl

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Histone deacetylase inhibitors as cancer therapeutics.

@en

Histone deacetylase inhibitors as cancer therapeutics.

@nl

P1476

Histone deacetylase inhibitors as cancer therapeutics.

@en

P2093

Gary A Clawson

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P2860

Histone deacetylases (HDACs): characterization of the classical HDAC family

Histone deacetylases, acetoin utilization proteins and acetylpolyamine amidohydrolases are members of an ancient protein superfamily

Lysine acetylation targets protein complexes and co-regulates major cellular functions

Histone deacetylase inhibitors stimulate dedifferentiation of human breast cancer cells through WNT/β-catenin signaling.

The effect of translocation-induced nuclear reorganization on gene expression.

Genes are often sheltered from the global histone hyperacetylation induced by HDAC inhibitors.

Mutation and genomic deletion status of ataxia telangiectasia mutated (ATM) and p53 confer specific gene expression profiles in mantle cell lymphoma.

Histone deacetylase 3 localizes to the plasma membrane and is a substrate of Src.

HDAC6: a key regulator of cytoskeleton, cell migration and cell-cell interactions.

Augmenting antitumor immune responses with epigenetic modifying agents.

P304

287

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P31

scholarly article

P356

10.21037/ATM.2016.07.22

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P433

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P478

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P577

2016-08-01T00:00:00Z

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P698

27568481

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P932

4980376

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