Daphne C. Avgousti, Ph.D.
Affiliations: | 2012 | Biochemistry and Molecular Biophysics | Columbia University, New York, NY |
Area:
Biochemistry, General Biophysics, GeneticsGoogle:
"Daphne Avgousti"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Alla Grishok | grad student | 2012 | Columbia | |
| (An analysis of the essential chromatin factor Zinc Finger Protein 1 (ZFP-1), and a study of the involvement of RNAi factors in histone processing in Caenorabditis elegans.) | ||||
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Publications
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| Arnold EA, Kaai RJ, Leung K, et al. (2023) Adenovirus protein VII binds the A-box of HMGB1 to repress interferon responses. Plos Pathogens. 19: e1011633 |
| Lewis HC, Kelnhofer-Millevolte LE, Brinkley MR, et al. (2023) HSV-1 exploits host heterochromatin for nuclear egress. The Journal of Cell Biology. 222 |
| Arnold EA, Kaai RJ, Leung K, et al. (2023) Adenovirus protein VII binds the A-box of HMGB1 to repress interferon responses. Biorxiv : the Preprint Server For Biology |
| Lynch KL, Dillon MR, Bat-Erdene M, et al. (2021) A viral histone-like protein exploits antagonism between linker histones and HMGB proteins to obstruct the cell cycle. Current Biology : Cb |
| Lynch KL, Gooding LR, Garnett-Benson C, et al. (2019) Epigenetics and the dynamics of chromatin during adenovirus infections. Febs Letters |
| Herrmann C, Avgousti DC, Weitzman MD. (2017) Differential Salt Fractionation of Nuclei to Analyze Chromatin-associated Proteins from Cultured Mammalian Cells. Bio-Protocol. 7 |
| Kulej K, Avgousti DC, Sidoli S, et al. (2017) Time-resolved global and chromatin proteomics during herpes simplex virus (HSV-1) infection. Molecular & Cellular Proteomics : McP |
| Avgousti DC, Herrmann C, Kulej K, et al. (2016) A core viral protein binds host nucleosomes to sequester immune danger signals. Nature |
| Avgousti DC, Weitzman MD. (2015) Stress Flips a Chromatin Switch to Wake Up Latent Virus. Cell Host & Microbe. 18: 639-41 |
| Kulej K, Avgousti DC, Weitzman MD, et al. (2015) Characterization of histone post-translational modifications during virus infection using mass spectrometry-based proteomics. Methods (San Diego, Calif.) |