MATE1 regulates cellular uptake and sensitivity to imatinib in CML patients
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Title
MATE1 regulates cellular uptake and sensitivity to imatinib in CML patients
Authors
Keywords
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Journal
Blood Cancer Journal
Volume 6, Issue 9, Pages e470-e470
Publisher
Springer Nature
Online
2016-09-16
DOI
10.1038/bcj.2016.79
References
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Related references
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- (2012) A. Giannoudis et al. BLOOD
- Discovery of Potent, Selective Multidrug and Toxin Extrusion Transporter 1 (MATE1, SLC47A1) Inhibitors Through Prescription Drug Profiling and Computational Modeling
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- Transport Mechanisms and Their Pathology-Induced Regulation Govern Tyrosine Kinase Inhibitor Delivery in Rheumatoid Arthritis
- (2012) Christian Schmidt-Lauber et al. PLoS One
- Interactions of Tyrosine Kinase Inhibitors with Organic Cation Transporters and Multidrug and Toxic Compound Extrusion Proteins
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- Potent and Specific Inhibition of mMate1-Mediated Efflux of Type I Organic Cations in the Liver and Kidney by Pyrimethamine
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- Chronic Myeloid Leukemia CD34+ cells have reduced uptake of imatinib due to low OCT-1 Activity
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