His primary areas of study are Histone, Chromatin, Genetics, Histone code and Cell biology. His Histone research is multidisciplinary, incorporating elements of Methylation and Epigenetics. The Chromatin study combines topics in areas such as Regulation of gene expression and Transcription.
His studies deal with areas such as SAP30 and Histone methyltransferase as well as Histone code. His Histone methyltransferase research incorporates themes from Epigenomics, Histone H2A, Histone methylation and Histone H1. His Cell biology research is multidisciplinary, incorporating perspectives in Histone H3 and Nucleosome.
Haitao Li mainly focuses on Cell biology, Histone, Chromatin, Epigenetics and Histone code. His work on Plasma protein binding as part of his general Cell biology study is frequently connected to PHD finger, thereby bridging the divide between different branches of science. His Histone study is concerned with Biochemistry in general.
The various areas that Haitao Li examines in his Chromatin study include Carcinogenesis, Regulation of gene expression and Genome instability. In his study, Ternary complex and Stereochemistry is inextricably linked to DNA, which falls within the broad field of Epigenetics. Haitao Li combines subjects such as SAP30 and Histone methyltransferase with his study of Histone code.
Haitao Li spends much of his time researching Cell biology, Histone, Epigenetics, Chromatin and Histone H3. The Cell biology study which covers Regulation of gene expression that intersects with Cell fate determination. His work deals with themes such as H3K4me3, Chondrocyte, Acetylation and Transcription, which intersect with Histone.
The concepts of his Epigenetics study are interwoven with issues in Neuroscience and DNA, SIDD. His Histone H3 research includes themes of Mutation, Gene silencing and Chromatin remodeling. His Epigenomics study integrates concerns from other disciplines, such as Bromodomain and Histone code.
Haitao Li focuses on Cell biology, Histone, Regulation of gene expression, Chromatin and Epigenetics. His studies in Cell biology integrate themes in fields like Histone H3, Transcription, Histone phosphorylation, DNA and HEK 293 cells. His research on Histone H3 frequently links to adjacent areas such as H3K4me3.
His Transcription study combines topics from a wide range of disciplines, such as Epigenomics and Acetylation, Bromodomain. Haitao Li has included themes like Histone methyltransferase, Corepressor and Transcription factor in his Histone phosphorylation study. Many of his studies on Histone apply to Methyltransferase as well.
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How chromatin-binding modules interpret histone modifications: lessons from professional pocket pickers
Sean D Taverna;Haitao Li;Alexander J Ruthenburg;C David Allis.
Nature Structural & Molecular Biology (2007)
Multivalent engagement of chromatin modifications by linked binding modules.
Alexander J. Ruthenburg;Haitao Li;Dinshaw J. Patel;C. David Allis.
Nature Reviews Molecular Cell Biology (2007)
Molecular basis for site-specific read-out of histone H3K4me3 by the BPTF PHD finger of NURF
Haitao Li;Serge Ilin;Wooikoon Wang;Elizabeth M. Duncan.
Nature (2006)
Structure of an argonaute silencing complex with a seed-containing guide DNA and target RNA duplex
Yanli Wang;Stefan Juranek;Haitao Li;Gang Sheng.
Nature (2008)
PRMT5-mediated methylation of histone H4R3 recruits DNMT3A, coupling histone and DNA methylation in gene silencing.
Quan Zhao;Quan Zhao;Gerhard Rank;Yuen T Tan;Haitao Li.
Nature Structural & Molecular Biology (2009)
Nucleation, propagation and cleavage of target RNAs in Ago silencing complexes.
Yanli Wang;Stefan Juranek;Haitao Li;Gang Sheng.
Nature (2009)
WSTF regulates the H2A.X DNA damage response via a novel tyrosine kinase activity
Andrew Xiao;Haitao Li;David Shechter;Sung Hee Ahn.
Nature (2009)
Haematopoietic malignancies caused by dysregulation of a chromatin-binding PHD finger.
Gang G. Wang;Jikui Song;Zhanxin Wang;Holger L. Dormann.
Nature (2009)
Yng1 PHD finger binding to H3 trimethylated at K4 promotes NuA3 HAT activity at K14 of H3 and transcription at a subset of targeted ORFs
Sean D. Taverna;Serge Ilin;Richard S. Rogers;Jason C. Tanny.
Molecular Cell (2006)
Recognition of a Mononucleosomal Histone Modification Pattern by BPTF via Multivalent Interactions
Alexander J. Ruthenburg;Haitao Li;Thomas A. Milne;Scott Dewell.
Cell (2011)
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