Edward Seto spends much of his time researching Cell biology, Molecular biology, HDAC11, Transcription factor and Histone deacetylase 2. His study in Cell biology is interdisciplinary in nature, drawing from both Genetics, Acetylation, Histone code, Nuclear receptor co-repressor 2 and Histone. His HDAC11 study deals with the bigger picture of Histone deacetylase.
His Histone deacetylase research incorporates themes from Cancer research, Histone methyltransferase and Immune tolerance. His Histone deacetylase 2 research integrates issues from SAP30 and Histone deacetylase 5. His Histone deacetylase 5 research is multidisciplinary, incorporating perspectives in Histone H2A and HDAC10.
Edward Seto mainly focuses on Cancer research, Molecular biology, Cell biology, HDAC11 and Histone deacetylase. The concepts of his Cancer research study are interwoven with issues in Cancer cell, Chromatin immunoprecipitation, Immune system and HDAC6. Edward Seto focuses mostly in the field of Molecular biology, narrowing it down to matters related to Transcription and, in some cases, YY1.
His Cell biology research incorporates elements of Genetics, Acetylation, Histone code, Nuclear receptor co-repressor 2 and Histone. His HDAC11 study also includes
His primary scientific interests are in Cancer research, Cell biology, HDAC11, Histone and Histone deacetylase. His HDAC11 study incorporates themes from In vitro, Histone deacetylase 5, Knockout mouse, Deacetylase activity and Brown adipose tissue. The Histone deacetylase 5 study combines topics in areas such as SAP30, Histone deacetylase 2, HDAC4 and HDAC10.
The study incorporates disciplines such as Epithelial–mesenchymal transition, Chromatin immunoprecipitation, Epigenetics and Acetylation in addition to Histone. His studies deal with areas such as Molecular biology, Ubiquitin, DNA damage and Phosphorylation as well as Histone deacetylase. As a part of the same scientific study, Edward Seto usually deals with the Molecular biology, concentrating on Histone code and frequently concerns with Histone acetyltransferase and MSH3.
His main research concerns Cancer research, HDAC11, Histone, Histone deacetylase 2 and Histone deacetylase 5. His Cancer research research is multidisciplinary, relying on both Cyclin A2, Signal transduction, HDAC4, HDAC6 and Regulation of gene expression. His research integrates issues of Chromatin, Transcription and Acetylation in his study of Histone.
His studies in Histone deacetylase 2 integrate themes in fields like Histone methylation and HDAC10. He has researched HDAC10 in several fields, including Nuclear receptor co-repressor 2 and Transcriptional regulation. His work focuses on many connections between Histone deacetylase and other disciplines, such as Molecular biology, that overlap with his field of interest in Cell biology, Muscle contraction, Actin and Cortactin.
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Acetylation and deacetylation of non-histone proteins
Michele A. Glozak;Nilanjan Sengupta;Xiaohong Zhang;Edward Seto.
A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression.
Thorsten Heinzel;Robert M. Lavinsky;Tina-Marie Mullen;Mats Söderström.
Erasers of Histone Acetylation: The Histone Deacetylase Enzymes
Edward Seto;Minoru Yoshida.
Cold Spring Harbor Perspectives in Biology (2014)
Lysine acetylation: codified crosstalk with other posttranslational modifications
Xiang Jiao Yang;Xiang Jiao Yang;Edward Seto.
Molecular Cell (2008)
The Rpd3/Hda1 family of lysine deacetylases: from bacteria and yeast to mice and men.
Xiang-Jiao Yang;Edward Seto.
Nature Reviews Molecular Cell Biology (2008)
Transcriptional repression by YY1, a human GLI-Krüppel-related protein, and relief of repression by adenovirus E1A protein.
Yang Shi;Edward Seto;Long Sheng Chang;Thomas Shenk.
Histone Deacetylases Associated with the mSin3 Corepressor Mediate Mad Transcriptional Repression
Carol D Laherty;Wen-Ming Yang;Jian-Min Sun;James R Davie.
HATs and HDACs: from structure, function and regulation to novel strategies for therapy and prevention
Yang Xj;Seto E.
Inhibition of Histone Deacetylase 6 Acetylates and Disrupts the Chaperone Function of Heat Shock Protein 90 A NOVEL BASIS FOR ANTILEUKEMIA ACTIVITY OF HISTONE DEACETYLASE INHIBITORS
Purva Bali;Michael Pranpat;James Bradner;Maria Balasis.
Journal of Biological Chemistry (2005)
Histone deacetylases, transcriptional control, and cancer.
W. Douglas Cress;Edward Seto.
Journal of Cellular Physiology (2000)
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