Quantitative characterization of direct P-glycoprotein inhibition by St John's wort constituents hypericin and hyperforin.
- Published in:
- Journal of Pharmacy & Pharmacology, 2004, v. 56, n. 1, p. 123
- By:
- Publication type:
- Article
Works by Er-Jia Wang
Results: 6
1
2
Quantitative evaluation of isothiocyanates as substrates and inhibitors of P-glycoprotein.
- Published in:
- Journal of Pharmacy & Pharmacology, 2003, v. 55, n. 9, p. 1251
- By:
- Publication type:
- Article
3
Many P-glycoprotein substrates do not inhibit the transport process across cell membranes.
- Published in:
- Xenobiotica, 2003, v. 33, n. 2, p. 131, doi. 10.1080/0049825021000035326
- By:
- Publication type:
- Article
4
The Farnesyl Protein Transferase Inhibitor Lonafarnib (SCH66336) Is an Inhibitor of Multidrug Resistance Proteins 1 and 2.
- Published in:
- Chemotherapy (0009-3157), 2003, v. 49, n. 6, p. 303, doi. 10.1159/000074531
- By:
- Publication type:
- Article
5
In Vitro Detection of Drug-Induced Phospholipidosis Using Gene Expression and Fluorescent Phospholipid Based Methodologies.
- Published in:
- Toxicological Sciences, 2007, v. 99, n. 1, p. 162, doi. 10.1093/toxsci/kfm157
- By:
- Publication type:
- Article
6
Temporal Evaluation of CYP mRNA in Mice Administered with Prototypical P450 Inducers: Comparison with Conventional Protein/Enzyme Methods.
- Published in:
- Drug & Chemical Toxicology, 2008, v. 31, n. 4, p. 501, doi. 10.1080/01480540802390825
- By:
- Publication type:
- Article