Id |
Subject |
Object |
Predicate |
Lexical cue |
T1 |
0-95 |
Sentence |
denotes |
Human P-glycoprotein transports cortisol, aldosterone, and dexamethasone, but not progesterone. |
T2 |
96-188 |
Sentence |
denotes |
We expressed human MDR1 cDNA isolated from the human adrenal gland in porcine LLC-PK1 cells. |
T3 |
189-525 |
Sentence |
denotes |
A highly polarized epithelium formed by LLC-GA5-COL300 cells that expressed human P-glycoprotein specifically on the apical surface showed a multidrug-resistant phenotype and had 8.3-, 3.4-, and 6.5-fold higher net basal to apical transport of 3H-labeled cortisol, aldosterone, and dexamethasone, respectively, compared with host cells. |
T4 |
526-717 |
Sentence |
denotes |
But progesterone was not transported, although it inhibited azidopine photoaffinity labeling of human P-glycoprotein and increased the sensitivity of multidrug-resistant cells to vinblastine. |
T5 |
718-814 |
Sentence |
denotes |
An excess of progesterone inhibited the transepithelial transport of cortisol by P-glycoprotein. |
T6 |
815-1053 |
Sentence |
denotes |
These results suggest that cortisol and aldosterone are physiological substrates for P-glycoprotein in the human adrenal cortex and that substances that efficiently bind to P-glycoprotein are not necessarily transported by P-glycoprotein. |
T1 |
0-95 |
Sentence |
denotes |
Human P-glycoprotein transports cortisol, aldosterone, and dexamethasone, but not progesterone. |
T2 |
96-188 |
Sentence |
denotes |
We expressed human MDR1 cDNA isolated from the human adrenal gland in porcine LLC-PK1 cells. |
T3 |
189-525 |
Sentence |
denotes |
A highly polarized epithelium formed by LLC-GA5-COL300 cells that expressed human P-glycoprotein specifically on the apical surface showed a multidrug-resistant phenotype and had 8.3-, 3.4-, and 6.5-fold higher net basal to apical transport of 3H-labeled cortisol, aldosterone, and dexamethasone, respectively, compared with host cells. |
T4 |
526-717 |
Sentence |
denotes |
But progesterone was not transported, although it inhibited azidopine photoaffinity labeling of human P-glycoprotein and increased the sensitivity of multidrug-resistant cells to vinblastine. |
T5 |
718-814 |
Sentence |
denotes |
An excess of progesterone inhibited the transepithelial transport of cortisol by P-glycoprotein. |
T6 |
815-1053 |
Sentence |
denotes |
These results suggest that cortisol and aldosterone are physiological substrates for P-glycoprotein in the human adrenal cortex and that substances that efficiently bind to P-glycoprotein are not necessarily transported by P-glycoprotein. |