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David M Clarke

Showing results (41-50 of 123) with videos related to

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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 mutantsTip 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 conformationTip 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-glycoproteinTip 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 domainsTip 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 compoundTip 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 pocketTip 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-glycoproteinTip 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 chaperonesTip W Loo, M Claire Bartlett, David M Clarke
Biochemistry|July 20, 2013
Bithiazole correctors rescue CFTR mutants by two different mechanismsTip 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
Pageof 13

Showing results (41-50 of 123) with videos related to

Sort By:
Pageof 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 mutantsTip 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 conformationTip 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-glycoproteinTip 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 domainsTip 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 compoundTip 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 pocketTip 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-glycoproteinTip 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 chaperonesTip W Loo, M Claire Bartlett, David M Clarke
Biochemistry|July 20, 2013
Bithiazole correctors rescue CFTR mutants by two different mechanismsTip 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
Pageof 13