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Biochemical Pharmacology|May 30, 2006
Biochemical and pharmacological properties of an allosteric modulator site of the human P-glycoprotein (ABCB1)Nazli Maki, Saibal DeyThe Journal of Biological Chemistry|March 19, 2003
Allosteric modulation of human P-glycoprotein. Inhibition of transport by preventing substrate translocation and dissociationNazli Maki, Peter Hafkemeyer, Saibal DeyThe Journal of Biological Chemistry|March 1, 2006
Allosteric modulation bypasses the requirement for ATP hydrolysis in regenerating low affinity transition state conformation of human P-glycoproteinNazli Maki, Karobi Moitra, Pratiti Ghosh, et al.Archives of Biochemistry and Biophysics|April 21, 2006
Allosteric modulation of the human P-glycoprotein involves conformational changes mimicking catalytic transition intermediatesPratiti Ghosh, Karobi Moitra, Nazli Maki, et al.Biochemistry|February 24, 2006
Modulator-induced interference in functional cross talk between the substrate and the ATP sites of human P-glycoproteinNazli Maki, Karobi Moitra, Cara Silver, et al.Pageof 1