<p>Drug efflux transporter ATPase activity was examined in P-gp (A and B) and BCRP (D and E) membrane preparations following various concentrations of FLZ exposure and specific drug efflux transport inhibitors. 200 µM Verapamil was used as a positive control in P-gp ATPase assays. Only the P-gp membranes produced a clear concentration dependent response to FLZ. Results are expressed as mean ± SD (n = 3). Inset in panel C shows the P-gp mediated ATPase activity examined in the presence of 10 µM FLZ and 5 µM zosuquidar (P-gp inhibitor) or/and 10 µM FTC (BCRP inhibitor). All data are expressed as the means ± SD (n = 3). *<i>P</i><<i>0.05</i>, **<i>P</i><<i>0.01</i>, significantly different from FLZ alone.</p
P-glycoprotein (ABCB1) prevents absorption (e.g., blood-brain barrier) or enhances excretion (e.g., ...
<p>P-gp ATPase assays were performed according to the instruction of P-gp-Glo™ Assay Systems. Each p...
Adenosine triphosphate (ATP)-binding cassette (ABC) transporters are highly expressed in tumor cells...
<p>Transport was measured in the absence or presence of P-gp inhibitor zosuquidar or BCRP inhibitor ...
The cell membrane P-glycoprotein (P-gp; MDR1, ABCB1) is an energy-dependent efflux pump that belongs...
BCRP / ABCG2 is a key determinant of pharmacokinetics of substrate drugs. Several BCRP substrates an...
ATP-binding cassette sub-family B member 1 (ABCB1) [P-glycoprotein (P-gp), multidrug resistance prot...
Purified Sf9 membrane vesicles containing ABCG2 (Upper panels, A and B) or ABCB1 proteins (lower pan...
The Corning Gentest ATPase assay was used to determine P-gp activity following treatment with R406. ...
International audienceConsiderable interest exists about the localization of P-gp (P-glycoprotein) i...
<p>(A) Stimulation of ATP hydrolysis by verapamil (50 µM), QZ59-<i>SSS</i> (1 µM), valinomycin (10 µ...
AbstractDrug interactions with P-glycoprotein (Pgp) were quantitatively assessed using ATPase assay....
No Heading: Purpose.: P-glycoprotein (P-gp), a membrane ATPase expelling many structurally unrelated...
The effect of (A) verapamil and (B) TMR-Cl was tested on the ATPase activity of TMH1,7 and compared ...
<p>(<i>a</i>) Incubation with EEAC (0.01–200 µg/ml) stimulated the P-gp ATPase activity. Data were a...
P-glycoprotein (ABCB1) prevents absorption (e.g., blood-brain barrier) or enhances excretion (e.g., ...
<p>P-gp ATPase assays were performed according to the instruction of P-gp-Glo™ Assay Systems. Each p...
Adenosine triphosphate (ATP)-binding cassette (ABC) transporters are highly expressed in tumor cells...
<p>Transport was measured in the absence or presence of P-gp inhibitor zosuquidar or BCRP inhibitor ...
The cell membrane P-glycoprotein (P-gp; MDR1, ABCB1) is an energy-dependent efflux pump that belongs...
BCRP / ABCG2 is a key determinant of pharmacokinetics of substrate drugs. Several BCRP substrates an...
ATP-binding cassette sub-family B member 1 (ABCB1) [P-glycoprotein (P-gp), multidrug resistance prot...
Purified Sf9 membrane vesicles containing ABCG2 (Upper panels, A and B) or ABCB1 proteins (lower pan...
The Corning Gentest ATPase assay was used to determine P-gp activity following treatment with R406. ...
International audienceConsiderable interest exists about the localization of P-gp (P-glycoprotein) i...
<p>(A) Stimulation of ATP hydrolysis by verapamil (50 µM), QZ59-<i>SSS</i> (1 µM), valinomycin (10 µ...
AbstractDrug interactions with P-glycoprotein (Pgp) were quantitatively assessed using ATPase assay....
No Heading: Purpose.: P-glycoprotein (P-gp), a membrane ATPase expelling many structurally unrelated...
The effect of (A) verapamil and (B) TMR-Cl was tested on the ATPase activity of TMH1,7 and compared ...
<p>(<i>a</i>) Incubation with EEAC (0.01–200 µg/ml) stimulated the P-gp ATPase activity. Data were a...
P-glycoprotein (ABCB1) prevents absorption (e.g., blood-brain barrier) or enhances excretion (e.g., ...
<p>P-gp ATPase assays were performed according to the instruction of P-gp-Glo™ Assay Systems. Each p...
Adenosine triphosphate (ATP)-binding cassette (ABC) transporters are highly expressed in tumor cells...