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T W Loo

Showing results (21-30 of 63) with videos related to

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The Journal of Biological Chemistry|December 10, 1999
Identification of residues in the drug-binding domain of human P-glycoprotein. Analysis of transmembrane segment 11 by cysteine-scanning mutagenesis and inhibition by dibromobimaneT W Loo, D M Clarke
The Journal of Biological Chemistry|March 11, 1994
Functional consequences of glycine mutations in the predicted cytoplasmic loops of P-glycoproteinT W Loo, D M Clarke
The Journal of Biological Chemistry|January 10, 1997
Correction of defective protein kinesis of human P-glycoprotein mutants by substrates and modulatorsT W Loo, D M Clarke
The Journal of Biological Chemistry|August 22, 1997
Drug-stimulated ATPase activity of human P-glycoprotein requires movement between transmembrane segments 6 and 12T W Loo, D M Clarke
Biochemistry|November 29, 1994
Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoproteinT W Loo, D M Clarke
The Journal of Biological Chemistry|January 24, 1998
Identification of residues in the drug-binding site of human P-glycoprotein using a thiol-reactive substrateT W Loo, D M Clarke
The Journal of Biological Chemistry|February 22, 2000
The packing of the transmembrane segments of human multidrug resistance P-glycoprotein is revealed by disulfide cross-linking analysisT W Loo, D M Clarke
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|July 30, 1999
Merck Frosst Award Lecture 1998. Molecular dissection of the human multidrug resistance P-glycoproteinT W Loo, D M Clarke
The Journal of Biological Chemistry|June 29, 2001
Cross-linking of human multidrug resistance P-glycoprotein by the substrate, tris-(2-maleimidoethyl)amine, is altered by ATP hydrolysis. Evidence for rotation of a transmembrane helixT W Loo, D M Clarke
The Journal of Biological Chemistry|May 12, 2000
Drug-stimulated ATPase activity of human P-glycoprotein is blocked by disulfide cross-linking between the nucleotide-binding sitesT W Loo, D M Clarke
Pageof 7

Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
The Journal of Biological Chemistry|December 10, 1999
Identification of residues in the drug-binding domain of human P-glycoprotein. Analysis of transmembrane segment 11 by cysteine-scanning mutagenesis and inhibition by dibromobimaneT W Loo, D M Clarke
The Journal of Biological Chemistry|March 11, 1994
Functional consequences of glycine mutations in the predicted cytoplasmic loops of P-glycoproteinT W Loo, D M Clarke
The Journal of Biological Chemistry|January 10, 1997
Correction of defective protein kinesis of human P-glycoprotein mutants by substrates and modulatorsT W Loo, D M Clarke
The Journal of Biological Chemistry|August 22, 1997
Drug-stimulated ATPase activity of human P-glycoprotein requires movement between transmembrane segments 6 and 12T W Loo, D M Clarke
Biochemistry|November 29, 1994
Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoproteinT W Loo, D M Clarke
The Journal of Biological Chemistry|January 24, 1998
Identification of residues in the drug-binding site of human P-glycoprotein using a thiol-reactive substrateT W Loo, D M Clarke
The Journal of Biological Chemistry|February 22, 2000
The packing of the transmembrane segments of human multidrug resistance P-glycoprotein is revealed by disulfide cross-linking analysisT W Loo, D M Clarke
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|July 30, 1999
Merck Frosst Award Lecture 1998. Molecular dissection of the human multidrug resistance P-glycoproteinT W Loo, D M Clarke
The Journal of Biological Chemistry|June 29, 2001
Cross-linking of human multidrug resistance P-glycoprotein by the substrate, tris-(2-maleimidoethyl)amine, is altered by ATP hydrolysis. Evidence for rotation of a transmembrane helixT W Loo, D M Clarke
The Journal of Biological Chemistry|May 12, 2000
Drug-stimulated ATPase activity of human P-glycoprotein is blocked by disulfide cross-linking between the nucleotide-binding sitesT W Loo, D M Clarke
Pageof 7