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Chemistry & Biology
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March 26, 2013
Niemann-Pick NPC1: sterols to the rescue and beyond
Tip W Loo, David M Clarke
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 2002
Vanadate trapping of nucleotide at the ATP-binding sites of human multidrug resistance P-glycoprotein exposes different residues to the drug-binding site
Tip W Loo, David M Clarke
Biochemical and Biophysical Research Communications
|
March 6, 2016
P-glycoprotein ATPase activity requires lipids to activate a switch at the first transmission interface
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
August 25, 2017
A short cross-linker activates human P-glycoprotein missing a catalytic carboxylate
Tip W Loo, David M Clarke
The Journal of Biological Chemistry
|
May 20, 2015
The Transmission Interfaces Contribute Asymmetrically to the Assembly and Activity of Human P-glycoprotein
Tip W Loo, David M Clarke
The 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 activity
Tip W Loo, David M Clarke
Biochemistry
|
October 3, 2013
Drug rescue distinguishes between different structural models of human P-glycoprotein
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
April 4, 2017
Corrector VX-809 promotes interactions between cytoplasmic loop one and the first nucleotide-binding domain of CFTR
Tip W Loo, David M Clarke
Biochemistry
|
May 10, 2016
Drugs Modulate Interactions between the First Nucleotide-Binding Domain and the Fourth Cytoplasmic Loop of Human P-Glycoprotein
Tip W Loo, David M Clarke
The Journal of Biological Chemistry
|
September 12, 2002
Location of the rhodamine-binding site in the human multidrug resistance P-glycoprotein
Tip W Loo, David M Clarke
Page
of 7
Search research articles
Search
Showing results (1-10 of 70) with videos related to
Sort By:
Page
of 7
Chemistry & Biology
|
March 26, 2013
Niemann-Pick NPC1: sterols to the rescue and beyond
Tip W Loo, David M Clarke
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 2002
Vanadate trapping of nucleotide at the ATP-binding sites of human multidrug resistance P-glycoprotein exposes different residues to the drug-binding site
Tip W Loo, David M Clarke
Biochemical and Biophysical Research Communications
|
March 6, 2016
P-glycoprotein ATPase activity requires lipids to activate a switch at the first transmission interface
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
August 25, 2017
A short cross-linker activates human P-glycoprotein missing a catalytic carboxylate
Tip W Loo, David M Clarke
The Journal of Biological Chemistry
|
May 20, 2015
The Transmission Interfaces Contribute Asymmetrically to the Assembly and Activity of Human P-glycoprotein
Tip W Loo, David M Clarke
The 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 activity
Tip W Loo, David M Clarke
Biochemistry
|
October 3, 2013
Drug rescue distinguishes between different structural models of human P-glycoprotein
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
April 4, 2017
Corrector VX-809 promotes interactions between cytoplasmic loop one and the first nucleotide-binding domain of CFTR
Tip W Loo, David M Clarke
Biochemistry
|
May 10, 2016
Drugs Modulate Interactions between the First Nucleotide-Binding Domain and the Fourth Cytoplasmic Loop of Human P-Glycoprotein
Tip W Loo, David M Clarke
The Journal of Biological Chemistry
|
September 12, 2002
Location of the rhodamine-binding site in the human multidrug resistance P-glycoprotein
Tip W Loo, David M Clarke
Page
of 7