A physiologically-based pharmacokinetic model of methotrexate incorporating hepatic excretion via multidrug-resistance-associated protein 2 (Mrp2) in mice, rats, dogs, and humans-Reference-Cited by-同舟云学术

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A physiologically-based pharmacokinetic model of methotrexate incorporating hepatic excretion via multidrug-resistance-associated protein 2 (Mrp2) in mice, rats, dogs, and humans

Published:2017-07 Issue: Volume: Page:
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Container-title:2017 39th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC)
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Author:

Lohitnavy Manupat,Lu Yasong,Lohitnavy Ornrat,Yang Raymond S.H.

Publisher

IEEE

Link

http://xplorestaging.ieee.org/ielx7/8026122/8036736/08037421.pdf?arnumber=8037421

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Early clinical indicators of acute kidney injury caused by administering high-dose methotrexate therapy to juvenile pigs;Frontiers in Nephrology;2023-09-12

2. Applications of Machine Learning in Rheumatoid Arthritis - An Insight;2022 6th International Conference on Computing Methodologies and Communication (ICCMC);2022-03-29

3. Development of a physiologically based pharmacokinetic (PBPK) model of psilocybin and psilocin from magic mushroom in rats and humans;F1000Research;2021-03-15

4. Comparison of Body Size, Morphomics, and Kidney Function as Covariates of High‐Dose Methotrexate Clearance in Obese Adults with Primary Central Nervous System Lymphoma;Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy;2020-04

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