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1 ed and tested in bioassays to evaluate their progestational activities, receptor- and tissue-selectiv
2 marino[3,4-f]quinoline core 1 is the key for progestational activities.
3 eceptor (hPR) in cell-based assays, and anti-progestational activity in a murine model.
4 ects of substitution at C(8) and C(9) on the progestational activity of this pharmacophore.
5              In two in vivo rodent models of progestational activity, a pregnancy maintenance assay a
6  aryl groups resulted in optimization of the progestational activity, affording compounds with in vit
7                         In a third model for progestational activity, the mammary end bud assay, thes
8 rial was developed to compare and contrast a progestational agent, a corticosteroid, and an anabolic
9             Prior trials have confirmed that progestational agents and newer antidepressants effectiv
10 e demonstrated that both corticosteroids and progestational agents do partially alleviate cancer anor
11 in, there is some debate about the safety of progestational agents in patients with a history of brea
12    The decrease in hot flashes achieved with progestational agents is similar to that seen with oestr
13 s been hormone replacement with estradiol or progestational agents, but recent data suggest that anti
14 ppetite stimulation and weight gain, such as progestational agents, cyproheptadines, pentoxifylline,
15  toxic effects associated with androgens and progestational agents.
16 l assess the sequential use of tamoxifen and progestational agents.
17 n combination with each of three regimens of progestational agents: medroxyprogesterone acetate (MPA)
18  patients with congestive heart failure, the progestational and antiandrogenic side effects of the no
19   The aim of this study was to examine how a progestational contraceptive drug (depot medroxyprogeste
20 ging and potentially useful tissue-selective progestational effects.
21 the mouse compared with humans, during which progestational hormones may accentuate the growth of pat
22 R demonstrates full efficacy and an enhanced progestational potency (30-fold) when compared with MPA
23 ted and have long been speculated to provide progestational support in lieu of progesterone itself.

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