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Biochimica Et Biophysica Acta|December 3, 1999
Determining the structure and mechanism of the human multidrug resistance P-glycoprotein using cysteine-scanning mutagenesis and thiol-modification techniquesT W Loo, D M ClarkeBiochemistry|April 23, 1999
The glycosylation and orientation in the membrane of the third cytoplasmic loop of human P-glycoprotein is affected by mutations and substratesT W Loo, D M ClarkeThe Journal of Biological Chemistry|November 1, 1996
Inhibition of oxidative cross-linking between engineered cysteine residues at positions 332 in predicted transmembrane segments (TM) 6 and 975 in predicted TM12 of human P-glycoprotein by drug substratesT W Loo, D M ClarkeThe Journal of Biological Chemistry|March 30, 2001
Defining the drug-binding site in the human multidrug resistance P-glycoprotein using a methanethiosulfonate analog of verapamil, MTS-verapamilT W Loo, D M ClarkeJournal of the National Cancer Institute|June 8, 2000
Blockage of drug resistance in vitro by disulfiram, a drug used to treat alcoholismT W Loo, D M ClarkeThe Journal of Biological Chemistry|September 15, 1995
P-glycoprotein. Associations between domains and between domains and molecular chaperonesT W Loo, D M ClarkeThe Journal of Biological Chemistry|March 11, 1994
Reconstitution of drug-stimulated ATPase activity following co-expression of each half of human P-glycoprotein as separate polypeptidesT W Loo, D M ClarkeBiochemical and Biophysical Research Communications|June 27, 1998
Nonylphenol ethoxylates, but not nonylphenol, are substrates of the human multidrug resistance P-glycoproteinT W Loo, D M ClarkeThe Journal of Biological Chemistry|August 24, 1999
The transmembrane domains of the human multidrug resistance P-glycoprotein are sufficient to mediate drug binding and trafficking to the cell surfaceT W Loo, D M ClarkeThe Journal of Biological Chemistry|September 15, 1995
Rapid purification of human P-glycoprotein mutants expressed transiently in HEK 293 cells by nickel-chelate chromatography and characterization of their drug-stimulated ATPase activitiesT W Loo, D M ClarkePageof 11