Libin Li, Ph.D.
|2002||Illinois State University, Normal, IL, United States|
Mean distance: 53433
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|Lumen AA, Li L, Li J, et al. (2013) Transport inhibition of digoxin using several common P-gp expressing cell lines is not necessarily reporting only on inhibitor binding to P-gp. Plos One. 8: e69394|
|Ellens H, Deng S, Coleman J, et al. (2013) Application of receiver operating characteristic analysis to refine the prediction of potential digoxin drug interactions. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 41: 1367-74|
|Bentz J, O'Connor MP, Bednarczyk D, et al. (2013) Variability in P-glycoprotein inhibitory potency (IC₅₀) using various in vitro experimental systems: implications for universal digoxin drug-drug interaction risk assessment decision criteria. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 41: 1347-66|
|Holmes EH, Devalapally H, Li L, et al. (2013) Permeability enhancers dramatically increase zanamivir absolute bioavailability in rats: implications for an orally bioavailable influenza treatment. Plos One. 8: e61853|
|Li LB, Chen N, Ramamoorthy S, et al. (2004) The role of N-glycosylation in function and surface trafficking of the human dopamine transporter. The Journal of Biological Chemistry. 279: 21012-20|
|Li LB, Cui XN, Reith MA. (2002) Is Na(+) required for the binding of dopamine, amphetamine, tyramine, and octopamine to the human dopamine transporter? Naunyn-Schmiedeberg's Archives of Pharmacology. 365: 303-11|
|Li LB, Reith ME. (2000) Interaction of Na+, K+, and Cl- with the binding of amphetamine, octopamine, and tyramine to the human dopamine transporter. Journal of Neurochemistry. 74: 1538-52|
|Li LB, Reith ME. (1999) Modeling of the interaction of Na+ and K+ with the binding of dopamine and [3H]WIN 35,428 to the human dopamine transporter. Journal of Neurochemistry. 72: 1095-109|