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1 enol red-free media or in the presence of an estrogen receptor antagonist.
2 ot blocked by ICI182780 (50 micro mol/L), an estrogen receptor antagonist.
3 Fulvestrant is a selective estrogen receptor antagonist.
4 This protective effect was abrogated by an estrogen-receptor antagonist.
5 ive effect of E2 was nullified by a specific estrogen-receptor antagonist.
6 mented estrogenic responses not inhibited by estrogen receptor antagonists.
9 he presence of beta-estradiol as well as the estrogen-receptor antagonist 4-Hydroxy-Tamoxifen and the
11 eliminated by ICI 182,780 (10(-7) mol/L), an estrogen receptor antagonist; 5, 6-dichloro-1-beta-D-rib
13 AZD9496 is an oral, nonsteroidal, selective estrogen receptor antagonist and downregulator in ER(+)
14 ential chemopreventive activity of selective estrogen-receptor antagonists as chemopreventives for br
16 Topical treatments with ICI 182,780, a pure estrogen receptor antagonist, caused the hair follicles
17 trogen receptor modulator that is used as an estrogen receptor antagonist for the treatment and preve
20 revent masculine development through various estrogen receptor antagonists have been relatively ineff
25 s of estradiol are completely blocked by the estrogen receptor antagonist ICI 182,780, and the intrac
33 retreatment with indomethacin or the classic estrogen-receptor antagonist ICI 182,780 did not alter t
34 oprotective effects of E2 were blocked by an estrogen receptor antagonist (ICI 182,780) and by a Trx
36 diol-BSA; 1 mg/kg estradiol) with or without estrogen receptor antagonist (ICI 182,780), PI3K inhibit
40 e estrogen receptor, and the addition of the estrogen receptor antagonist, ICI 182,780, to influence
45 port the hypothesis that ICI is an effective estrogen receptor antagonist in the zebra finch brain an
46 ovariectomy or treating female mice with an estrogen receptor antagonist increased mortality, indica
47 ce was eliminated after pretreatment with an estrogen receptor antagonist or ovariectomy but restored
48 single intracerebroventricular injection of estrogen receptor antagonists or aromatase inhibitors, r
49 vessels with 17beta-E2 plus ICI, 182,780, an estrogen receptor antagonist, or wortmannin, an inhibito
50 eptor and mediates the inhibitory effects of estrogen receptor antagonists, such as tamoxifen, suppre
52 at were previously reported as non-steroidal estrogen receptor antagonists with in vitro and in vivo
53 xifen and in designing screens to select for estrogen-receptor antagonists without these side effects
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