Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM040118-07S1
Application #
2180185
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1988-04-01
Project End
1997-08-31
Budget Start
1994-09-01
Budget End
1995-08-31
Support Year
7
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Sloan-Kettering Institute for Cancer Research
Department
Type
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10065
Wiest, Nathaniel E; Houghtaling, Scott; Sanchez, Joseph C et al. (2017) The SWI/SNF ATP-dependent nucleosome remodeler promotes resection initiation at a DNA double-strand break in yeast. Nucleic Acids Res 45:5887-5900
Young, Conor P; Hillyer, Cory; Hokamp, Karsten et al. (2017) Distinct histone methylation and transcription profiles are established during the development of cellular quiescence in yeast. BMC Genomics 18:107
Osley, Mary Ann (2014) FACT and the H2B N tail. Mol Cell Biol 34:300-2
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Trujillo, Kelly M; Tyler, Rebecca K; Ye, Chaoyang et al. (2011) A genetic and molecular toolbox for analyzing histone ubiquitylation and sumoylation in yeast. Methods 54:296-303
Nakanishi, Shima; Lee, Jung Shin; Gardner, Kathryn E et al. (2009) Histone H2BK123 monoubiquitination is the critical determinant for H3K4 and H3K79 trimethylation by COMPASS and Dot1. J Cell Biol 186:371-7
Fleming, Alastair B; Kao, Cheng-Fu; Hillyer, Cory et al. (2008) H2B ubiquitylation plays a role in nucleosome dynamics during transcription elongation. Mol Cell 31:57-66
Osley, Mary Ann (2006) Regulation of histone H2A and H2B ubiquitylation. Brief Funct Genomic Proteomic 5:179-89

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