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نمایش تعداد 1-5 از 5

Synthesis and Modeling of New Benzofuranone Histone Deacetylase Inhibitors that Stimulate Tumor Suppressor Gene Expression

نوع: Journal Paper

نویسنده : Cédric Charrier; Jonathan Clarhaut; Jean-Pierre Gesson; Guillermina Estiu; Olaf Wiest; Joëlle Roche; Philippe Bertrand

سال: 2009

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Residues in the 11 Å Channel of Histone Deacetylase 1 Promote Catalytic Activity: Implications for Designing Isoform-Selective Histone Deacetylase Inhibitorsn †

نوع: Journal Paper

نویسنده : Sujith V. W. Weerasinghe; Guillermina Estiu; Olaf Wiest; Mary Kay H. Pflum

سال: 2008

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Molecular modeling and QSAR analysis of the interaction of flavone derivatives with the benzodiazepine binding site of the GABAA receptor complex

نوع: Journal Paper

نویسنده : Mariel Marder; Guillermina Estiú; Luis Bruno Blanch; Haydee Viola; Cristina Wasowski; Jorge H. Medina; Alejandro C. Paladini

سال: 2001

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Structural Origin of Selectivity in Class II-Selective Histone Deacetylase Inhibitors

نوع: Journal Paper

نویسنده : Guillermina Estiu; Edward Greenberg; Christopher B. Harrison; Nicholas P. Kwiatkowski; Ralph Mazitschek; James E. Bradner; Olaf Wiest

سال: 2008

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A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria

نوع: Journal Paper

نویسنده : Alassane Mbengue; Souvik Bhattacharjee; Trupti Pandharkar; Haining Liu; Guillermina Estiu; Robert V. Stahelin; Shahir S. Rizk; Dieudonne L. Njimoh; Yana Ryan; Kesinee Chotivanich; Chea Nguon; Mehdi Ghorbal; Jose-Juan Lopez-Rubio; Michael Pfrender; Scott Emrich; Narla Mohandas; Arjen M. Dondorp; Olaf Wiest; Kasturi Haldar

سال: 2015

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Synthesis and Modeling of New Benzofuranone Histone Deacetylase Inhibitors that Stimulate Tumor Suppressor Gene Expression

Residues in the 11 Å Channel of Histone Deacetylase 1 Promote Catalytic Activity: Implications for Designing Isoform-Selective Histone Deacetylase Inhibitorsn †

Molecular modeling and QSAR analysis of the interaction of flavone derivatives with the benzodiazepine binding site of the GABAA receptor complex

Structural Origin of Selectivity in Class II-Selective Histone Deacetylase Inhibitors

A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria

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Synthesis and Modeling of New Benzofuranone Histone Deacetylase Inhibitors that Stimulate Tumor Suppressor Gene Expression

Residues in the 11 Å Channel of Histone Deacetylase 1 Promote Catalytic Activity: Implications for Designing Isoform-Selective Histone Deacetylase Inhibitorsn †

Molecular modeling and QSAR analysis of the interaction of flavone derivatives with the benzodiazepine binding site of the GABAA receptor complex

Structural Origin of Selectivity in Class II-Selective Histone Deacetylase Inhibitors

A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria