ライフサイエンスコーパス: estradiol-17 beta

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1 ansplant recipient rabbits were treated with estradiol 17-beta (100 microg/kg/day) or placebo for 6 w

2 S) on uptake of the model glucuronide 17beta-estradiol 17-(beta-d-glucuronide) (E(2)17betaG) and vice

3 transport amphipathic anions such as 17beta-estradiol 17-(beta-d-glucuronide).

4 ut not glucuronate conjugates such as 17beta-estradiol 17-(beta-D-glucuronide).

5 MgATP-dependent transport of cGMP, cAMP, and estradiol 17-beta-D-glucuronide (E(2)17 beta G).

6 rt into membrane vesicles of the glucuronide estradiol 17-beta-D-glucuronide (E(2)17betaG), the gluta

7 and estrone 3-sulfate, glucuronides such as estradiol 17-beta-D-glucuronide (E(2)17betaG), the monoa

8 d substrates including MK-571, methotrexate, estradiol 17-beta-d-glucuronide, and S(2,4-dinitrophenyl

9 with the MgATP-dependent transport of 17beta-estradiol-(17-beta-D-glucuronide) (E(2)17betaG).

10 shown by vesicular transport of [(3)H]17beta-estradiol-17-beta-(D-glucuronide) and doxorubicin efflux

11 17-beta estradiol (17-beta E(2)) attenuates the expression of va

12 Analogues of estradiol-17 beta (E2) have been evaluated for estrogen

13 kg) or vehicle and twice daily injections of estradiol-17 beta (E2: 1 microgram) for 2 days.

14 r substrates of different molecular weights: estradiol-17-beta-glucuronide (E17betaG), prostaglandin

15 Inhibition by estradiol-17-beta-glucuronide was 35-fold greater than i

16 ed aortic SMCs in the presence or absence of estradiol 17-beta in vitro.

17 t study demonstrates regulation of IGF-IR by estradiol 17-beta in vivo and in vitro in recipient nati

18 Repression of IGF-IR protein and mRNA by estradiol 17-beta in vivo and in vitro suggest that one

19 rhesus monkeys with physiological levels of estradiol-17 beta in combination with medroxyprogesteron

20 In vivo, estradiol-17 beta prevents neointimal thickening after b

21 Earlier, we found estradiol 17-beta treatment of cardiac allograft recipie

22 Estradiol 17-beta treatment of rabbits significantly inh

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