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1 reatment groups received escalating doses of ethinyl estradiol.
2 treated male transgenic rabbits with 17alpha-ethinyl estradiol.
3 and better tolerated than the Yuzpe regimen (ethinyl estradiol, 100 microg, and levonorgestrel, 0.5 m
7 o 1.7 with oral contraceptives that included ethinyl estradiol at a dose of 20 mug and by a factor of
9 ent use of oral contraceptives that included ethinyl estradiol at a dose of 30 to 40 mug was associat
10 actor of 1.3 to 2.3 with those that included ethinyl estradiol at a dose of 30 to 40 mug, with relati
11 eceive either oral contraceptives (triphasic ethinyl estradiol at a dose of 35 microg plus norethindr
12 glucuronidation activity toward lamotrigine, ethinyl estradiol, chenodeoxycholic acid, and lithocholi
13 henol A (BPA) and the pharmaceutical 17alpha-ethinyl estradiol (EE) are synthetic chemicals with estr
14 ted the effectiveness of oral treatment with ethinyl estradiol (EE) on EAE and the mechanisms involve
16 from livers of bile duct ligation (BDL)- or ethinyl estradiol (EE)-injected rats, were viewed and re
18 amine the bioavailability and bioactivity of ethinyl estradiol (EE2) sorbed onto SWCNTs in a fish gas
19 Mice treated with 17beta-estradiol or 17a-ethinyl estradiol had a total uterine tumor incidence of
22 droxyestradiol, 17beta-estradiol, or 17alpha-ethinyl estradiol on days 1-5 of neonatal life (2 microg
24 with maximally efficacious doses of 17-alpha ethinyl estradiol, the benzothiophene SERM, raloxifene,
26 However, the synthetic estrogens, DES and ethinyl estradiol, were detected in various lots of PC-S
27 nicity of bisphenol A, triclosan and 17alpha-ethinyl estradiol without generating obviously toxic byp
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