Research Topics
Species | A EmiliSummaryAffiliation: Fred Hutchinson Cancer Research Center Country: USA Publications
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Detail Information
Publications
MEC1-dependent phosphorylation of Rad9p in response to DNA damageA Emili
Division of Molecular Medicine, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA
Mol Cell 2:183-9. 1998..Since the phosphorylated form of Rad9p appears capable of interacting stably with Rad53p in vivo, this phosphorylation response likely controls checkpoint signaling by Rad9p...
Dynamic interaction of DNA damage checkpoint protein Rad53 with chromatin assembly factor Asf1A Emili
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
Mol Cell 7:13-20. 2001..Biochemical and molecular genetic studies suggest that Asf1 is an important target of the Rad53-dependent DNA damage response and that Rad53 may directly regulate chromatin assembly during DNA replication and repair...
A novel yeast protein influencing the response of RNA polymerase II to transcriptional activatorsA Emili
Banting and Best Department of Medical Research and Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada M5G 1L6
Proc Natl Acad Sci U S A 95:11122-7. 1998....
Species-specific interaction of the glutamine-rich activation domains of Sp1 with the TATA box-binding proteinA Emili
Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada
Mol Cell Biol 14:1582-93. 1994..These results support the notion that TBP is a direct and important target of glutamine-rich transcriptional activators...
Characterization of the interaction between the acidic activation domain of VP16 and the RNA polymerase II initiation factor TFIIBR Gupta
Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada
Nucleic Acids Res 24:2324-30. 1996..Taken together our results suggest more evidence is needed to support the notion that TFIIB is a functionally important target for the activator VP16...
