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1 er pretreatment with a sequential regimen of cyproterone acetate (50 mg/kg/day for 21 days) and testo
7 tar-Unilever rats by a sequential regimen of cyproterone acetate and testosterone propionate, followe
9 hibited by the addition of the anti-androgen Cyproterone Acetate demonstrating that the effects of FG
10 cells, RU486 revealed a higher potency than cyproterone acetate to prevent responses to dexamethason
11 The agonist activity of the antiandrogen cyproterone acetate was abolished in ebp1 transfectants.
13 ties of weak androgens and an AR antagonist (cyproterone acetate) are still dependent on the AR NH(2)
16 s, hydroxyflutamide, bicalutamide (casodex), cyproterone acetate, and RU58841, and other compounds su
17 ol and medroxyprogesterone) and antagonists (cyproterone acetate, hydroxyflutamide and bicalutamide).
18 ynthetic potent progestigens, norethynodrel, cyproterone acetate, norethindrone, and megestrol acetat
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