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Nucleosome turnover is sufficient to establish varied histone methylation states
View ORCID ProfileEmma J. Chory, Joseph P. Calarco, View ORCID ProfileNathaniel A. Hathaway, View ORCID ProfileOliver Bell, Dana S. Neel, View ORCID ProfileGerald R. Crabtree
doi: https://doi.org/10.1101/256321
Emma J. Chory
1Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
2Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, California 94305, USA
Joseph P. Calarco
2Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, California 94305, USA
Nathaniel A. Hathaway
3Division of Chemical Biology and Medicinal Chemistry, Center for Integrative Chemical Biology and Drug Discovery, UNC Eshelman School of Pharmacy, Chapel Hill, North Carolina 27599, United States
Oliver Bell
4Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter (VBC), A-1030 Vienna, Austria
Dana S. Neel
2Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, California 94305, USA
Gerald R. Crabtree
2Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, California 94305, USA
5Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
Posted January 31, 2018.
Nucleosome turnover is sufficient to establish varied histone methylation states
Emma J. Chory, Joseph P. Calarco, Nathaniel A. Hathaway, Oliver Bell, Dana S. Neel, Gerald R. Crabtree
bioRxiv 256321; doi: https://doi.org/10.1101/256321
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