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The Journal of Biological Chemistry|September 29, 1995
Covalent modification of human P-glycoprotein mutants containing a single cysteine in either nucleotide-binding fold abolishes drug-stimulated ATPase activityT W Loo, D M ClarkeThe Journal of Biological Chemistry|June 28, 1996
Mutational analysis of the predicted first transmembrane segment of each homologous half of human P-glycoprotein suggests that they are symmetrically arranged in the membraneT W Loo, D M ClarkeThe Journal of Biological Chemistry|January 13, 1995
Membrane topology of a cysteine-less mutant of human P-glycoproteinT W Loo, D M ClarkeThe Journal of Biological Chemistry|November 18, 1994
Prolonged association of temperature-sensitive mutants of human P-glycoprotein with calnexin during biogenesisT W Loo, D M ClarkeThe Journal of Biological Chemistry|September 25, 1993
Functional consequences of phenylalanine mutations in the predicted transmembrane domain of P-glycoproteinT W Loo, D M ClarkeThe Journal of Biological Chemistry|June 17, 1998
Superfolding of the partially unfolded core-glycosylated intermediate of human P-glycoprotein into the mature enzyme is promoted by substrate-induced transmembrane domain interactionsT W Loo, D M ClarkeThe Journal of Biological Chemistry|November 26, 1998
Quality control by proteases in the endoplasmic reticulum. Removal of a protease-sensitive site enhances expression of human P-glycoproteinT W Loo, D M ClarkeThe Journal of Biological Chemistry|February 15, 1993
Functional consequences of proline mutations in the predicted transmembrane domain of P-glycoproteinT W Loo, D M ClarkeThe Journal of Biological Chemistry|October 3, 2000
Identification of residues within the drug-binding domain of the human multidrug resistance P-glycoprotein by cysteine-scanning mutagenesis and reaction with dibromobimaneT W Loo, D M ClarkeThe Journal of Biological Chemistry|December 10, 1999
Identification of residues in the drug-binding domain of human P-glycoprotein. Analysis of transmembrane segment 11 by cysteine-scanning mutagenesis and inhibition by dibromobimaneT W Loo, D M ClarkePageof 11