Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM052486-01A1
Application #
2191532
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1996-03-01
Project End
2001-02-28
Budget Start
1996-03-01
Budget End
1997-02-28
Support Year
1
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Genetics
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Tan, Wei; Wang, Zheng; Prelich, Gregory (2013) Physical and Genetic Interactions Between Uls1 and the Slx5-Slx8 SUMO-Targeted Ubiquitin Ligase. G3 (Bethesda) 3:771-780
Prelich, Gregory (2012) Gene overexpression: uses, mechanisms, and interpretation. Genetics 190:841-54
Wang, Zheng; Prelich, Gregory (2009) Quality control of a transcriptional regulator by SUMO-targeted degradation. Mol Cell Biol 29:1694-706
Jones, Grace Marie; Stalker, Jim; Humphray, Sean et al. (2008) A systematic library for comprehensive overexpression screens in Saccharomyces cerevisiae. Nat Methods 5:239-41
Chu, Yaya; Simic, Rajna; Warner, Marcie H et al. (2007) Regulation of histone modification and cryptic transcription by the Bur1 and Paf1 complexes. EMBO J 26:4646-56
Wang, Zheng; Jones, Grace Marie; Prelich, Gregory (2006) Genetic analysis connects SLX5 and SLX8 to the SUMO pathway in Saccharomyces cerevisiae. Genetics 172:1499-509
Chu, Yaya; Sutton, Ann; Sternglanz, Rolf et al. (2006) The BUR1 cyclin-dependent protein kinase is required for the normal pattern of histone methylation by SET2. Mol Cell Biol 26:3029-38
Yao, Sheng; Prelich, Gregory (2002) Activation of the Bur1-Bur2 cyclin-dependent kinase complex by Cak1. Mol Cell Biol 22:6750-8
Cang, Yong; Prelich, Gregory (2002) Direct stimulation of transcription by negative cofactor 2 (NC2) through TATA-binding protein (TBP). Proc Natl Acad Sci U S A 99:12727-32
Prelich, Gregory (2002) RNA polymerase II carboxy-terminal domain kinases: emerging clues to their function. Eukaryot Cell 1:153-62

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