| 1 |
Attachment of a'molecular spring' restores drug-stimulated ATPase activity to P-glycoprotein lacking both Q loop glutamines
Loo TW, Clarke DM
Biochemical and Biophysical Research Communications, 483(1), 366, 2017 |
| 2 |
Thiol-reactive drug substrates of human P-glycoprotein label the same sites to activate ATPase activity in membranes or dodecyl maltoside detergent micelles
Loo TW, Clarke DM
Biochemical and Biophysical Research Communications, 488(4), 573, 2017 |
| 3 |
P-glycoprotein ATPase activity requires lipids to activate a switch at the first transmission interface
Loo TW, Clarke DM
Biochemical and Biophysical Research Communications, 472(2), 379, 2016 |
| 4 |
Human P-glycoprotein is active when the two halves are clamped together in the closed conformation
Loo TW, Bartlett MC, Clarke DM
Biochemical and Biophysical Research Communications, 395(3), 436, 2010 |
| 5 |
Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"?
Loo TW, Clarke DM
Biochemical and Biophysical Research Communications, 329(2), 419, 2005 |
| 6 |
Thapsigargin or curcumin does not promote maturation of processing mutants of the ABC transporters, CFTR, and P-glycoprotein
Loo TW, Bartlett MC, Clarke DM
Biochemical and Biophysical Research Communications, 325(2), 580, 2004 |
