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Molecular Pharmacology|August 23, 2000
Communication between multiple drug binding sites on P-glycoproteinC Martin, G Berridge, C F Higgins, et al.Biochemistry|September 29, 2000
Drug binding sites on P-glycoprotein are altered by ATP binding prior to nucleotide hydrolysisC Martin, G Berridge, P Mistry, et al.British Journal of Pharmacology|October 8, 1999
The molecular interaction of the high affinity reversal agent XR9576 with P-glycoproteinC Martin, G Berridge, P Mistry, et al.British Journal of Pharmacology|January 10, 1998
The multi-drug resistance reversal agent SR33557 and modulation of vinca alkaloid binding to P-glycoprotein by an allosteric interactionC Martin, G Berridge, C F Higgins, et al.Biochimica Et Biophysica Acta|October 7, 1997
The functional purification of P-glycoprotein is dependent on maintenance of a lipid-protein interfaceR Callaghan, G Berridge, D R Ferry, et al.Biochemistry|December 19, 2001
The vinblastine binding site adopts high- and low-affinity conformations during a transport cycle of P-glycoproteinC Martin, C F Higgins, R CallaghanEuropean Biophysics Journal : EBJ|November 23, 2001
The importance of cholesterol in maintenance of P-glycoprotein activity and its membrane perturbing influenceA Rothnie, D Theron, L Soceneantu, et al.British Journal of Cancer|February 1, 1995
Interaction of tamoxifen with the multidrug resistance P-glycoproteinR Callaghan, C F HigginsThe EMBO Journal|October 13, 2001
Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycleM F Rosenberg, G Velarde, R C Ford, et al.British Journal of Cancer|November 11, 1999
The equilibrium and kinetic drug binding properties of the mouse P-gp1a and P-gp1b P-glycoproteins are similarJ C Taylor, D R Ferry, C F Higgins, et al.Pageof 579