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1 ed through structure-guided modifications of androgen receptor antagonists.
2 ovides strong rationale for developing novel androgen receptor antagonists.
3 ues were prepared and evaluated as potential androgen receptor antagonists against two human prostate
4 NP1 was absent with co-administration of the androgen receptor antagonist bicalutamide and in androge
6 ed males and those receiving the competitive androgen receptor antagonist flutamide had significantly
7 fically, we bilaterally implanted the potent androgen receptor antagonist flutamide in two key brain
9 were reversed by in vivo treatment with the androgen receptor antagonist flutamide, suggesting that
10 Moreover, prenatal administration of the androgen receptor antagonist, flutamide, equalizes devel
11 T4 in vivo and in vitro were reversed by the androgen receptor antagonist, flutamide, indicating that
13 F-0998425, (-)- 6a] is a novel, nonsteroidal androgen receptor antagonist for sebum control and treat
16 ains androgen-receptor dependent, and potent androgen-receptor antagonists induce tumour regression i
18 at mediate a switch in function of selective androgen receptor antagonists/modulators (SARMs) from re
19 osterone was repressed by co-exposure to the androgen receptor antagonist nilutamide supporting a pot
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