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2Multidrug-resistant transporter expression does not always result in drug resistance. 2018;109:3360 doi: 10.1111/cas.13756
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4Intestine-penetrating, pH-sensitive and double-layered nanoparticles for oral delivery of doxorubicin with reduced toxicity. 2019;7:3692 doi: 10.1039/C9TB00212J
5ABCC10 Plays a Significant Role in the Transport of Gefitinib and Contributes to Acquired Resistance to Gefitinib in NSCLC. 2018;9: doi: 10.3389/fphar.2018.01312
6Targeting the Multidrug Transporter Ptch1 Potentiates Chemotherapy Efficiency. 2018;7:107 doi: 10.3390/cells7080107
7Kaempferol-Mediated Sensitization Enhances Chemotherapeutic Efficacy of Sorafenib Against Hepatocellular Carcinoma: An In Silico and In Vitro Approach. 2020;10:472 doi: 10.34172/apb.2020.058
8Optimizing Targeted Inhibitors of P-Glycoprotein Using Computational and Structure-Guided Approaches. 2019;62:10645 doi: 10.1021/acs.jmedchem.9b00966
9Cancer stem cells in hepatocellular carcinoma: an overview and promising therapeutic strategies. 2018;10:175883591881628 doi: 10.1177/1758835918816287
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11Glucose starvation induces resistance to metformin through the elevation of mitochondrial multidrug resistance protein 1. 2019;110:1256 doi: 10.1111/cas.13952
12Active-targeting and acid-sensitive pluronic prodrug micelles for efficiently overcoming MDR in breast cancer. 2020;8:2726 doi: 10.1039/C9TB02328C
13Crystal Structure of the Cyclostreptin-Tubulin Adduct: Implications for Tubulin Activation by Taxane-Site Ligands. 2019;20:1392 doi: 10.3390/ijms20061392
14Pharmacogenetics of treatments for pancreatic cancer. 2019;15:437 doi: 10.1080/17425255.2019.1620731
15Drug metabolizing enzymes-associated chemo resistance and strategies to overcome it. 2019;51:196 doi: 10.1080/03602532.2019.1632886
16The multi-factorial nature of clinical multidrug resistance in cancer. 2019;46:100645 doi: 10.1016/j.drup.2019.100645
17Bimetallic redox nanoprobe enhances the therapeutic efficacy of hyperthermia in drug-resistant cancer cells. 2018;8:1493 doi: 10.1007/s13204-018-0814-9
18Effect of treatment period with LC478, a disubstituted adamantayl derivative, on P-glycoprotein inhibition: its application to increase docetaxel absorption in rats. 2020;50:863 doi: 10.1080/00498254.2019.1700318