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Rilpivirine inhibits drug transporters ABCB1, SLC22A1, and SLC22A2 in vitro. , Moss DM., Antimicrob Agents Chemother. November 1, 2013; 57 (11): 5612-8.
Physiological responses of Xenopus laevis tadpoles exposed to cyanobacterial biomass containing microcystin- LR. , Ziková A., Aquat Toxicol. March 15, 2013; 128-129 25-33.
Raltegravir is a substrate for SLC22A6: a putative mechanism for the interaction between raltegravir and tenofovir. , Moss DM., Antimicrob Agents Chemother. February 1, 2011; 55 (2): 879-87.
Involvement of CjMDR1, a plant multidrug-resistance-type ATP-binding cassette protein, in alkaloid transport in Coptis japonica. , Shitan N., Proc Natl Acad Sci U S A. January 21, 2003; 100 (2): 751-6.
Hepatobiliary elimination of certain peptide-mimicking drugs: linear hydrophobic and hydrophilic renin-inhibitors and hydrophobic cyclopeptides. , Ziegler K., J Hepatol. January 1, 1996; 24 Suppl 1 47-52.
A homologue of the mammalian multidrug resistance gene ( mdr) is functionally expressed in the intestine of Xenopus laevis. , Castillo G., Biochim Biophys Acta. June 9, 1995; 1262 (2-3): 113-23.
Functional expression of the renal organic cation transporter and P-glycoprotein in Xenopus laevis oocytes. , Nelson JA., Cancer Chemother Pharmacol. January 1, 1995; 37 (1-2): 187-9.