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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 ClarkeCurrent Protocols in Nucleic Acid Chemistry|June 4, 2011
Resolution of quadruplex polymorphism by size-exclusion chromatographyM Clarke Miller, John O TrentThe Journal of Biological Chemistry|September 29, 1995
Covalent modification of human P-glycoprotein mutants containing a single cysteine in either nucleotide-binding fold abolishes drug-stimulated ATPase activityT W Loo, D M ClarkeNeuropathology and Applied Neurobiology|April 1, 1995
Production and evaluation of syngeneic antibodies showing specificity for the A15 A5 transplantable rat gliomaT M Clarke, G J PilkingtonThe Journal of Biological Chemistry|June 28, 1996
Mutational analysis of the predicted first transmembrane segment of each homologous half of human P-glycoprotein suggests that they are symmetrically arranged in the membraneT W Loo, D M ClarkeThe Journal of the Acoustical Society of America|January 22, 2005
Rapid adaptation to foreign-accented EnglishConstance M Clarke, Merrill F GarrettThe Journal of Biological Chemistry|January 13, 1995
Membrane topology of a cysteine-less mutant of human P-glycoproteinT W Loo, D M ClarkeThe Biochemical Journal|November 1, 1977
Affinity chromatography of aminoacyl-transfer ribonucleic acid synthetases. Small organic ligandsC M Clarke, J R KnowlesThe Journal of Biological Chemistry|November 18, 1994
Prolonged association of temperature-sensitive mutants of human P-glycoprotein with calnexin during biogenesisT W Loo, D M ClarkeThe Journal of Antimicrobial Chemotherapy|February 1, 1984
Clavulanic acid in combination with ticarcillin: an in-vitro comparison with other beta-lactamsA M Clarke, S J ZemcovPageof 190