Olesya Anatolievna Ulanovskaya
Affiliations: | 2010 | Chemistry | University of Chicago, Chicago, IL |
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"Olesya Ulanovskaya"Mean distance: 8.86 | S | N | B | C | P |
Parents
Sign in to add mentor| Sergey A. Kozmin | grad student | 2010 | Chicago | |
| (Small-molecule modulation of cellular energy metabolism.) | ||||
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Publications
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| Ogasawara D, Ichu TA, Jing H, et al. (2019) Discovery and Optimization of Selective and in Vivo Active Inhibitors of the Lysophosphatidylserine Lipase α/β-Hydrolase Domain-Containing 12 (ABHD12). Journal of Medicinal Chemistry |
| Ogasawara D, Ichu TA, Vartabedian VF, et al. (2018) Selective blockade of the lyso-PS lipase ABHD12 stimulates immune responses in vivo. Nature Chemical Biology |
| Lee HY, Suciu RM, Horning BD, et al. (2018) Covalent inhibitors of nicotinamide N-methyltransferase (NNMT) provide evidence for target engagement challenges in situ. Bioorganic & Medicinal Chemistry Letters |
| Horning BD, Suciu RM, Ghadiri DA, et al. (2016) Chemical Proteomic Profiling of Human Methyltransferases. Journal of the American Chemical Society |
| Efimova EV, Takahashi S, Shamsi NA, et al. (2015) Linking Cancer Metabolism to DNA Repair and Accelerated Senescence. Molecular Cancer Research : McR |
| Deng X, Liang H, Ulanovskaya OA, et al. (2014) Steady-state hydrogen peroxide induces glycolysis in Staphylococcus aureus and Pseudomonas aeruginosa. Journal of Bacteriology. 196: 2499-513 |
| Deng X, Weerapana E, Ulanovskaya O, et al. (2013) Proteome-wide quantification and characterization of oxidation-sensitive cysteines in pathogenic bacteria. Cell Host & Microbe. 13: 358-70 |
| Ulanovskaya OA, Zuhl AM, Cravatt BF. (2013) NNMT promotes epigenetic remodeling in cancer by creating a metabolic methylation sink. Nature Chemical Biology. 9: 300-6 |
| Efimova EV, Labay E, Mauceri HJ, et al. (2012) Abstract LB-162: DNA-damage foci persistence and accelerated senescence as determinants of radiosensitization by glycolysis inhibitors Molecular and Cellular Biology |
| Cui J, Hao J, Ulanovskaya OA, et al. (2011) Creation and manipulation of common functional groups en route to a skeletally diverse chemical library. Proceedings of the National Academy of Sciences of the United States of America. 108: 6763-8 |