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1 farct volume was significantly influenced by 17beta-oestradiol.
2 o that observed for ER's endogenous hormone, 17beta-oestradiol.
4 prague-Dawley rats were ovariectomised and a 17beta-oestradiol (0.25 mg, 21 day release) or placebo p
6 pounds four of them being natural (oestriol, 17beta-oestradiol, 17alpha-oestradiol and oestrone), fou
7 that the biologically active metabolites of 17beta-oestradiol, 2-hydroxyoestradiol (2-OHE2 ) and 4-h
8 europrotective benefits previously seen with 17beta-oestradiol after spinal cord injury may be in par
9 the oxytocin precursor gene as biomarker for 17beta oestradiol and dexamethasone treatment in beef ca
10 by 33.5 and 13.3-fold in cattle treated with 17beta oestradiol and dexamethasone, respectively, in co
11 e is a valid marker for detection of illicit 17beta oestradiol and/or dexamethasone use in beef cattl
12 and 16alpha-hydroxytestosterone to oestrone, 17beta-oestradiol and 17beta,16alpha-oestriol, respectiv
13 ng mechanisms of the catecholoestradiols, to 17beta-oestradiol and catecholamines, we observed that c
14 muscle nNOS correlated directly with plasma 17beta-oestradiol and inversely with the magnitude of sy
15 ER in complex with the endogenous oestrogen, 17beta-oestradiol, and the selective antagonist raloxife
16 ng of MAPKs involved in catecholoestradiol-, 17beta-oestradiol- and catecholamine-induced endothelial
18 sis of this nonapeptide only in cattle after 17beta oestradiol, but not after dexamethasone or placeb
20 vented by chronic treatment of OVX rats with 17beta-oestradiol, but not with chronic progesterone or
22 ptide were measured in beef cattle receiving 17beta oestradiol, dexamethasone or placebo over a perio
27 we report that in human breast cancer cells 17beta-oestradiol (E2)-bound oestrogen receptor alpha (E
29 f the human Msx-2 homologue was regulated by 17beta-oestradiol in the MCF-7 breast cancer cell line.
30 -treatment with a high physiological dose of 17beta-oestradiol increased infarct volume after permane
31 actors which, on binding the steroid hormone 17beta-oestradiol, interacts with co-activator proteins
33 ffects of allopregnanolone, progesterone and 17beta-oestradiol on oxytocin and vasopressin release fr
36 s, rats were either ovariectomized and given 17beta-oestradiol replacement (OVXE2) or sham ovariectom
38 nd they provide increased support that early 17beta-oestradiol replacement is critical in preventing
40 in vitro culture system we demonstrate that 17beta-oestradiol treatment (50 nM) is sufficient to inc
41 CA3 hypersensitivity and amyloidogenesis, if 17beta-oestradiol was initiated at the time of ovariecto
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