D M Clarke

The Transmembrane Domains of the Human Multidrug Resistance P-glycoprotein Are Sufficient to Mediate Drug Binding and Trafficking to the Cell Surface*

D. Clarke, T W Loo, D M Clarke, 1999, The Journal of Biological Chemistry.

Correction of Defective Protein Kinesis of Human P-glycoprotein Mutants by Substrates and Modulators*

D. Clarke, T. W. Loo, T W Loo, 1997, The Journal of Biological Chemistry.

Membrane Topology of a Cysteine-less Mutant of Human P-glycoprotein (*)

D. Clarke, T. W. Loo, T W Loo, 1995, The Journal of Biological Chemistry.

Determining the structure and mechanism of the human multidrug resistance P-glycoprotein using cysteine-scanning mutagenesis and thiol-modification techniques.

D. Clarke, T. W. Loo, T W Loo, 1999, Biochimica et biophysica acta.

Superfolding of the Partially Unfolded Core-glycosylated Intermediate of Human P-glycoprotein into the Mature Enzyme Is Promoted by Substrate-induced Transmembrane Domain Interactions*

D. Clarke, T. W. Loo, T W Loo, 1998, The Journal of Biological Chemistry.

Identification of Residues in the Drug-binding Site of Human P-glycoprotein Using a Thiol-reactive Substrate*

D. Clarke, T W Loo, D M Clarke, 1997, The Journal of Biological Chemistry.