John C. Chrivia

Affiliations: 
Pharmacological and Physiological Science Saint Louis University, St. Louis, MO, United States 
Area:
Cell Biology, Molecular Biology
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"John Chrivia"
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Publications

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Bowman TA, Wong MM, Cox LK, et al. (2011) Loss of H2A.Z Is Not Sufficient to Determine Transcriptional Activity of Snf2-Related CBP Activator Protein or p400 Complexes. International Journal of Cell Biology. 2011: 715642
Lunn CL, Chrivia JC, Baldassare JJ. (2010) Activation of Cdk2/Cyclin E complexes is dependent on the origin of replication licensing factor Cdc6 in mammalian cells. Cell Cycle (Georgetown, Tex.). 9: 4533-41
Wong MM, Cox LK, Chrivia JC. (2007) The chromatin remodeling protein, SRCAP, is critical for deposition of the histone variant H2A.Z at promoters Journal of Biological Chemistry. 282: 26132-26139
Ruhl DD, Jin J, Cai Y, et al. (2006) Purification of a human SRCAP complex that remodels chromatin by incorporating the histone variant H2A.Z into nucleosomes. Biochemistry. 45: 5671-7
Eissenberg JC, Wong M, Chrivia JC. (2005) Human SRCAP and Drosophila melanogaster DOM are homologs that function in the notch signaling pathway. Molecular and Cellular Biology. 25: 6559-69
Ruh MF, Chrivia JC, Cox LK, et al. (2004) The interaction of the estrogen receptor with mononucleosomes Molecular and Cellular Endocrinology. 214: 71-79
Monroy MA, Schott NM, Cox L, et al. (2003) SNF2-related CBP activator protein (SRCAP) functions as a coactivator of steroid receptor-mediated transcription through synergistic interactions with CARM-1 and GRIP-1. Molecular Endocrinology (Baltimore, Md.). 17: 2519-28
Xu X, Tarakanova V, Chrivia J, et al. (2003) Adenovirus DNA binding protein inhibits SrCap-activated CBP and CREB-mediated transcription. Virology. 313: 615-21
Sullivan WJ, Monroy MA, Bohne W, et al. (2003) Molecular cloning and characterization of an SRCAP chromatin remodeling homologue in Toxoplasma gondii. Parasitology Research. 90: 1-8
Gusterson R, Brar B, Faulkes D, et al. (2001) The transcriptional co-activators CBP and p300 are activated via phenylephrine through the p42/p44 MAPK cascade. The Journal of Biological Chemistry. 277: 2517-24
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