Calla M. Olson
Affiliations: | Harvard Medical School/Dana-Farber Cancer Institute, Boston, MA, United States |
Area:
Cancer Biology, Kinase Inhibition, Cyclin-dependent kinasesGoogle:
"Calla Olson"Mean distance: (not calculated yet)
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Publications
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Meena JK, Wang JH, Neill NJ, et al. (2024) MYC Induces Oncogenic Stress through RNA Decay and Ribonucleotide Catabolism in Breast Cancer. Cancer Discovery. OF1-OF18 |
Richters A, Doyle SK, Freeman DB, et al. (2020) Modulating Androgen Receptor-Driven Transcription in Prostate Cancer with Selective CDK9 Inhibitors. Cell Chemical Biology |
Liu Y, Hao M, Leggett A, et al. (2020) Discovery of MFH290: A Potent and Highly Selective Covalent Inhibitor for Cyclin-Dependent Kinase 12/13. Journal of Medicinal Chemistry |
de Wispelaere M, Carocci M, Burri DJ, et al. (2019) A broad-spectrum antiviral molecule, QL47, selectively inhibits eukaryotic translation. The Journal of Biological Chemistry |
Li Z, Pinch BJ, Olson CM, et al. (2019) Development and Characterization of a Wee1 Kinase Degrader. Cell Chemical Biology |
Olson CM, Liang Y, Leggett A, et al. (2019) Development of a Selective CDK7 Covalent Inhibitor Reveals Predominant Cell-Cycle Phenotype. Cell Chemical Biology |
Olson CM, Jiang B, Erb MA, et al. (2017) Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation. Nature Chemical Biology |
Kalan S, Amat R, Schachter MM, et al. (2017) Activation of the p53 Transcriptional Program Sensitizes Cancer Cells to Cdk7 Inhibitors. Cell Reports. 21: 467-481 |
Winter GE, Mayer A, Buckley DL, et al. (2017) BET Bromodomain Proteins Function as Master Transcription Elongation Factors Independent of CDK9 Recruitment. Molecular Cell |
Zhang T, Kwiatkowski N, Olson CM, et al. (2016) Covalent targeting of remote cysteine residues to develop CDK12 and CDK13 inhibitors. Nature Chemical Biology |