The structural requirements of histone deacetylase inhibitors: Suberoylanilide hydroxamic acid analogs modified at the C3 position display isoform selectivity.
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Design and Evaluation of Tumor-Specific Dendrimer Epigenetic Therapeutics.The structural requirements of histone deacetylase inhibitors: suberoylanilide hydroxamic acid analogs modified at the C6 positionMutagenesis studies of the 14 Å internal cavity of histone deacetylase 1: insights toward the acetate-escape hypothesis and selective inhibitor design.Targeted cancer therapy: giving histone deacetylase inhibitors all they need to succeed.The structural requirements of histone deacetylase inhibitors: SAHA analogs modified at the C5 position display dual HDAC6/8 selectivity.The structural requirements of histone deacetylase inhibitors: C4-modified SAHA analogs display dual HDAC6/HDAC8 selectivity.Structural Requirements of Histone Deacetylase Inhibitors: SAHA Analogs Modified on the Hydroxamic Acid.Structural Requirements of HDAC Inhibitors: SAHA Analogues Modified at the C2 Position Display HDAC6/8 Selectivity.
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The structural requirements of histone deacetylase inhibitors: Suberoylanilide hydroxamic acid analogs modified at the C3 position display isoform selectivity.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 12 August 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
The structural requirements of ...... n display isoform selectivity.
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The structural requirements of ...... n display isoform selectivity.
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The structural requirements of ...... n display isoform selectivity.
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The structural requirements of ...... n display isoform selectivity.
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The structural requirements of ...... n display isoform selectivity.
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The structural requirements of ...... n display isoform selectivity.
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The structural requirements of ...... n display isoform selectivity.
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Mary Kay H Pflum
Sujith V W Weerasinghe
Sun Ea Choi
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10.1016/J.BMCL.2011.08.027
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2011-08-12T00:00:00Z