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History
- January 31, 2018.
Copyright
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
Author Information
- Emma J. Chory1,2,
- Joseph P. Calarco2,
- Nathaniel A. Hathaway3,
- Oliver Bell4,
- Dana S. Neel2 and
- Gerald R. Crabtree2,5,†
- 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
- 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
- 4Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter (VBC), A-1030 Vienna, Austria
- 5Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
- ↵†Corresponding author. Email: crabtree{at}stanford.edu
Posted January 31, 2018.
Nucleosome turnover is sufficient to establish varied histone methylation states
