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Tip W Loo

Showing results (51-60 of 70) with videos related to

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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
Biochemistry|July 20, 2007
Nucleotide binding, ATP hydrolysis, and mutation of the catalytic carboxylates of human P-glycoprotein cause distinct conformational changes in the transmembrane segmentsTip W Loo, M Claire Bartlett, David M Clarke
The Biochemical Journal|May 31, 2007
Additive effect of multiple pharmacological chaperones on maturation of CFTR processing mutantsYing Wang, Tip W Loo, M Claire Bartlett, et al.
The Biochemical Journal|January 19, 2006
The chemical chaperone CFcor-325 repairs folding defects in the transmembrane domains of CFTR-processing mutantsTip W Loo, M Claire Bartlett, Ying Wang, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
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
Biochemistry|July 20, 2007
Nucleotide binding, ATP hydrolysis, and mutation of the catalytic carboxylates of human P-glycoprotein cause distinct conformational changes in the transmembrane segmentsTip W Loo, M Claire Bartlett, David M Clarke
The Biochemical Journal|May 31, 2007
Additive effect of multiple pharmacological chaperones on maturation of CFTR processing mutantsYing Wang, Tip W Loo, M Claire Bartlett, et al.
The Biochemical Journal|January 19, 2006
The chemical chaperone CFcor-325 repairs folding defects in the transmembrane domains of CFTR-processing mutantsTip W Loo, M Claire Bartlett, Ying Wang, et al.
Pageof 7