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Biochemistry
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December 25, 2010
The W232R suppressor mutation promotes maturation of a truncation mutant lacking both nucleotide-binding domains and restores interdomain assembly and activity of P-glycoprotein processing mutants
Tip W Loo, M Claire Bartlett, David M Clarke
Biochemical and Biophysical Research Communications
|
April 17, 2010
Human P-glycoprotein is active when the two halves are clamped together in the closed conformation
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
January 30, 2004
Val133 and Cys137 in transmembrane segment 2 are close to Arg935 and Gly939 in transmembrane segment 11 of human P-glycoprotein
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
July 13, 2004
Processing mutations located throughout the human multidrug resistance P-glycoprotein disrupt interactions between the nucleotide binding domains
Tip W Loo, M Claire Bartlett, David M Clarke
Molecular Pharmaceutics
|
October 4, 2005
Rescue of DeltaF508 and other misprocessed CFTR mutants by a novel quinazoline compound
Tip W Loo, M Claire Bartlett, David M Clarke
The Biochemical Journal
|
February 24, 2006
Transmembrane segment 1 of human P-glycoprotein contributes to the drug-binding pocket
Tip W Loo, M Claire Bartlett, David M Clarke
Biochemistry
|
July 27, 2005
ATP hydrolysis promotes interactions between the extracellular ends of transmembrane segments 1 and 11 of human multidrug resistance P-glycoprotein
Tip W Loo, M Claire Bartlett, David M Clarke
Journal of Bioenergetics and Biomembranes
|
May 13, 2006
Rescue of folding defects in ABC transporters using pharmacological chaperones
Tip W Loo, M Claire Bartlett, David M Clarke
Biochemistry
|
July 20, 2013
Bithiazole correctors rescue CFTR mutants by two different mechanisms
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
August 19, 2008
Processing mutations disrupt interactions between the nucleotide binding and transmembrane domains of P-glycoprotein and the cystic fibrosis transmembrane conductance regulator (CFTR)
Tip W Loo, M Claire Bartlett, David M Clarke
Page
of 13
Search research articles
Search
Showing results (41-50 of 123) with videos related to
Sort By:
Page
of 13
Biochemistry
|
December 25, 2010
The W232R suppressor mutation promotes maturation of a truncation mutant lacking both nucleotide-binding domains and restores interdomain assembly and activity of P-glycoprotein processing mutants
Tip W Loo, M Claire Bartlett, David M Clarke
Biochemical and Biophysical Research Communications
|
April 17, 2010
Human P-glycoprotein is active when the two halves are clamped together in the closed conformation
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
January 30, 2004
Val133 and Cys137 in transmembrane segment 2 are close to Arg935 and Gly939 in transmembrane segment 11 of human P-glycoprotein
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
July 13, 2004
Processing mutations located throughout the human multidrug resistance P-glycoprotein disrupt interactions between the nucleotide binding domains
Tip W Loo, M Claire Bartlett, David M Clarke
Molecular Pharmaceutics
|
October 4, 2005
Rescue of DeltaF508 and other misprocessed CFTR mutants by a novel quinazoline compound
Tip W Loo, M Claire Bartlett, David M Clarke
The Biochemical Journal
|
February 24, 2006
Transmembrane segment 1 of human P-glycoprotein contributes to the drug-binding pocket
Tip W Loo, M Claire Bartlett, David M Clarke
Biochemistry
|
July 27, 2005
ATP hydrolysis promotes interactions between the extracellular ends of transmembrane segments 1 and 11 of human multidrug resistance P-glycoprotein
Tip W Loo, M Claire Bartlett, David M Clarke
Journal of Bioenergetics and Biomembranes
|
May 13, 2006
Rescue of folding defects in ABC transporters using pharmacological chaperones
Tip W Loo, M Claire Bartlett, David M Clarke
Biochemistry
|
July 20, 2013
Bithiazole correctors rescue CFTR mutants by two different mechanisms
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
August 19, 2008
Processing mutations disrupt interactions between the nucleotide binding and transmembrane domains of P-glycoprotein and the cystic fibrosis transmembrane conductance regulator (CFTR)
Tip W Loo, M Claire Bartlett, David M Clarke
Page
of 13