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Sharyn D. Baker

Researcher at Ohio State University

Publications -  284
Citations -  13815

Sharyn D. Baker is an academic researcher from Ohio State University. The author has contributed to research in topics: Pharmacokinetics & Myeloid leukemia. The author has an hindex of 67, co-authored 260 publications receiving 12638 citations. Previous affiliations of Sharyn D. Baker include University of Texas Health Science Center at San Antonio & University of Texas MD Anderson Cancer Center.

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The genomic landscape of hypodiploid acute lymphoblastic leukemia

TL;DR: Both near-haploid and low-hypodiploid leukemic cells show activation of Ras-signaling and phosphoinositide 3-kinase (PI3K)-signaling pathways and are sensitive to PI3K inhibitors, indicating that these drugs should be explored as a new therapeutic strategy for this aggressive form of leukemia.
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CREBBP mutations in relapsed acute lymphoblastic leukaemia

TL;DR: Analysis of an extended cohort of 71 diagnosis–relapse cases and 270 acute leukaemia cases that did not relapse found that 18.3% of relapse cases had sequence or deletion mutations of CREBBP, which encodes the transcriptional coactivator and histone acetyltransferase CREB-binding protein (CREBBP).
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Differential Metabolism of Gefitinib and Erlotinib by Human Cytochrome P450 Enzymes

TL;DR: The differential metabolizing enzyme profiles suggest that there may be differences in drug-drug interaction potential and that stimulation of CYP3A4 may likely play a role in drug interactions for erlotinib and gefitinib.
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Role of body surface area in dosing of investigational anticancer agents in adults, 1991-2001

TL;DR: It is concluded that body surface area should not be used to determine starting doses of investigational agents in future phase I studies and alternate dosing strategies should be evaluated.
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Irinotecan Pathway Genotype Analysis to Predict Pharmacokinetics

TL;DR: It is concluded that genotyping for ABCB1 1236C>T may be one of the factors assisting with dose optimization of irinotecan chemotherapy in cancer patients and additional investigation is required to confirm these findings in a larger population.