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The Journal of Biological Chemistry|May 20, 2015
The Transmission Interfaces Contribute Asymmetrically to the Assembly and Activity of Human P-glycoproteinTip W Loo, David M ClarkeThe Journal of Biological Chemistry|July 24, 2014
Cysteines introduced into extracellular loops 1 and 4 of human P-glycoprotein that are close only in the open conformation spontaneously form a disulfide bond that inhibits drug efflux and ATPase activityTip W Loo, David M ClarkeBiochemistry|October 3, 2013
Drug rescue distinguishes between different structural models of human P-glycoproteinTip W Loo, David M ClarkeBiochemical Pharmacology|April 4, 2017
Corrector VX-809 promotes interactions between cytoplasmic loop one and the first nucleotide-binding domain of CFTRTip W Loo, David M ClarkePhysical Review. E, Statistical, Nonlinear, and Soft Matter Physics|May 15, 2002
Local optical density of states in finite crystals of plane scatterersMartijn Wubs, A LagendijkPhysical Review Letters|May 21, 2005
Transport of quantum noise through random mediaP Lodahl, A LagendijkBiochemistry|May 10, 2016
Drugs Modulate Interactions between the First Nucleotide-Binding Domain and the Fourth Cytoplasmic Loop of Human P-GlycoproteinTip W Loo, David M ClarkeThe Journal of Biological Chemistry|September 12, 2002
Location of the rhodamine-binding site in the human multidrug resistance P-glycoproteinTip W Loo, David M ClarkeBiochemical and Biophysical Research Communications|March 2, 2005
Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"?Tip W Loo, David M ClarkeBiochemical and Biophysical Research Communications|May 24, 2017
Thiol-reactive drug substrates of human P-glycoprotein label the same sites to activate ATPase activity in membranes or dodecyl maltoside detergent micellesTip W Loo, David M ClarkePageof 70