ライフサイエンスコーパス: cyproterone acetate

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1 th DHT in combination with the anti-androgen cyproterone acetate.

2 orticoid spironolactone and the antiandrogen cyproterone acetate.

3 er pretreatment with a sequential regimen of cyproterone acetate (50 mg/kg/day for 21 days) and testo

4 AR activation by cyproterone acetate, a partial agonist that did not supp

5 This event was blocked by the anti-androgens cyproterone acetate and hydroxyflutamide.

6 Increasing concentrations of cyproterone acetate and mifepristone resulted in more co

7 Molecular docking of cyproterone acetate and RU486 into the homology model fo

8 tar-Unilever rats by a sequential regimen of cyproterone acetate and testosterone propionate, followe

9 s seen only with R1881, dihydrotestosterone, cyproterone acetate, and hydroxyflutamide.

10 s, hydroxyflutamide, bicalutamide (casodex), cyproterone acetate, and RU58841, and other compounds su

11 ties of weak androgens and an AR antagonist (cyproterone acetate) are still dependent on the AR NH(2)

12 The antagonist cyproterone acetate behaved as a full antagonist of D11F

13 Cyproterone acetate (CPA) is a steroidal antiandrogen us

14 tetrachloride (CT), thioacetamide (THA), and cyproterone acetate (CPA).

15 hibited by the addition of the anti-androgen Cyproterone Acetate demonstrating that the effects of FG

16 ol and medroxyprogesterone) and antagonists (cyproterone acetate, hydroxyflutamide and bicalutamide).

17 ta-catenin to the AR DBD in vitro and to the cyproterone acetate-liganded AR in vivo.

18 ynthetic potent progestigens, norethynodrel, cyproterone acetate, norethindrone, and megestrol acetat

19 cells, RU486 revealed a higher potency than cyproterone acetate to prevent responses to dexamethason

20 The agonist activity of the antiandrogen cyproterone acetate was abolished in ebp1 transfectants.

21 The steroid compound cyproterone acetate was identified in a high-throughput

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