| 1 |
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Correction of defective protein kinesis of human P-glycoprotein mutants by substrates and modulators
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Loo, T. W
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American Society for Biochemistry and Molecular Biology [etc.]
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1980
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| 2 |
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Drug-stimulated ATPase activity of human P-glycoprotein requires movement between transmembrane segments 6 and 12
|
Loo, T. W
|
American Society for Biochemistry and Molecular Biology [etc.]
|
1980
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| 3 |
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Identification of Residues in the Drug-binding Site of Human P-glycoprotein Using a Thiol-reactive Substrate
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Loo, T. W
|
American Society for Biochemistry and Molecular Biology [etc.]
|
1980
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| 4 |
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Inhibition of oxidative cross-linking between engineered cysteine residues at positions 332 in predicted transmembrane segments (TM) 6 and 975 inpredicted TM12 of human P-glycoprotein by drug substrates
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Loo, T. W
|
American Society for Biochemistry and Molecular Biology [etc.]
|
1980
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| 5 |
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Permanent Activation of the Human P-glycoprotein by Covalent Modification of a Residue in the Drug-binding Site/
|
Loo, T. W
|
American Society for Biochemistry and Molecular Biology [etc.]
|
2003
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| 6 |
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Simultaneous Binding of Two Different Drugs in the Binding Pocket of the Human Multidrug Resistance P-glycoprotein/
|
Loo, T. W
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American Society for Biochemistry and Molecular Biology [etc.]
|
2003
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| 7 |
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Substrate-induced Conformational Changes in the Transmembrane Segments of Human P-glycoprotein. DIRECT EVIDENCE FOR THE SUBSTRATE-INDUCED FIT MECHANISM FOR DRUG BINDING/
|
Loo, T. W
|
American Society for Biochemistry and Molecular Biology [etc.]
|
2003
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| 8 |
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The minimum functional unit of human P-glycoprotein appears to be a monomer
|
Loo, T. W
|
American Society for Biochemistry and Molecular Biology [etc.]
|
1980
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