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Rosemary Barrett

Researcher at Harvard University

Publications -  15
Citations -  1505

Rosemary Barrett is an academic researcher from Harvard University. The author has contributed to research in topics: Fms-Like Tyrosine Kinase 3 & Tyrosine kinase. The author has an hindex of 13, co-authored 14 publications receiving 1321 citations. Previous affiliations of Rosemary Barrett include Brigham and Women's Hospital & Novartis.

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Project DRIVE: A Compendium of Cancer Dependencies and Synthetic Lethal Relationships Uncovered by Large-Scale, Deep RNAi Screening

E. Robert McDonald, +99 more
- 27 Jul 2017 - 
TL;DR: A large-scale RNAi screen is conducted in which viability effects of mRNA knockdown were assessed for 7,837 genes using an average of 20 shRNAs per gene in 398 cancer cell lines, outlining the classes of cancer dependency genes and their relationships to genetic, expression, and lineage features.
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The STAT5 inhibitor pimozide decreases survival of chronic myelogenous leukemia cells resistant to kinase inhibitors

TL;DR: Targeting STAT5 with pimozide and the kinase inhibitors imatinib or nilotinib shows enhanced effects in inhibiting STAT5 phosphorylation and in inducing apoptosis, suggesting that targeting STAT5 may be an effective strategy for the treatment of CML and other myeloproliferative diseases.
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FLT3 inhibition and mechanisms of drug resistance in mutant FLT3-positive AML.

TL;DR: Mechanisms whereby AML cells develop resistance to FLT3 inhibitors, and the ways in which combination therapy could potentially be utilized to override drug resistance are discussed.
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Smac mimetics: implications for enhancement of targeted therapies in leukemia.

TL;DR: The results support the idea of using IAP inhibitors in conjunction with targeted tyrosine kinase inhibition to override drug resistance and suppress or eradicate residual disease.
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The STAT5 Inhibitor Pimozide Displays Efficacy in Models of Acute Myelogenous Leukemia Driven by FLT3 Mutations

TL;DR: Pimozide reduces the tumor burden in a mouse model of FLT3-driven AML and may provide a new avenue for the treatment of AML, and these may be effective alone or in combination with tyrosine kinase inhibitors.