Sharon Dent

Affiliations: 
The University of Texas Graduate School of Biomedical Sciences at Houston 
Area:
Biochemistry, Molecular Biology, Animal Physiology Biology
Google:
"Sharon Dent"
Mean distance: (not calculated yet)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Koutelou E, Wang L, Schibler A, et al. (2019) Usp22 controls multiple signaling pathways that are essential for vasculature formation in the mouse placenta. Development (Cambridge, England)
Lambies G, Miceli M, Martínez-Guillamon C, et al. (2018) TGFβ-activated USP27X deubiquitinase regulates cell migration and chemoresistance via stabilization of Snail1. Cancer Research
Xi Y, Shi J, Li W, et al. (2018) Histone modification profiling in breast cancer cell lines highlights commonalities and differences among subtypes. Bmc Genomics. 19: 150
Franco HL, Nagari A, Malladi V, et al. (2017) Enhancer transcription reveals subtype-specific gene expression programs controlling breast cancer pathogenesis. Genome Research
Mi W, Guan H, Lyu J, et al. (2017) YEATS2 links histone acetylation to tumorigenesis of non-small cell lung cancer. Nature Communications. 8: 1088
Wang Y, Yun C, Gao B, et al. (2017) The Lysine Acetyltransferase GCN5 Is Required for iNKT Cell Development through EGR2 Acetylation. Cell Reports. 20: 600-612
Gao B, Kong Q, Zhang Y, et al. (2017) The Histone Acetyltransferase Gcn5 Positively Regulates T Cell Activation. Journal of Immunology (Baltimore, Md. : 1950)
Lan X, Atanassov BS, Li W, et al. (2016) USP44 Is an Integral Component of N-CoR that Contributes to Gene Repression by Deubiquitinating Histone H2B. Cell Reports. 17: 2382-2393
Li W, Atanassov BS, Lan X, et al. (2016) Cytoplasmic ATXN7L3B Interferes with Nuclear Functions of the SAGA Deubiquitinase Module. Molecular and Cellular Biology
Schibler A, Koutelou E, Tomida J, et al. (2016) Histone H3K4 methylation regulates deactivation of the spindle assembly checkpoint through direct binding of Mad2. Genes & Development
See more...