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1 st ICI-182780 failed to block the effects of estren.
2  of kinase-mediated actions of the ER with 4-estren-3alpha,17beta-diol (estren) or an estradiol-dendr
3 ver, administration of 17beta-estradiol or 4-estren-3alpha,17beta-diol to ovariectomized mice induces
4                        A synthetic ligand (4-estren-3alpha,17beta-diol) that reproduces the nongenotr
5                     It has been found that 4-estren-3alpha,17beta-diol, a synthetic ligand for the es
6                         We conclude that the estrens act mostly through the AR and, in mice, do not f
7 e effects of a SERM (PSK3471) and 2 estrens (estren-alpha and estren-beta) on bone and reproductive o
8                                              Estren also increased the expression of prostate-specifi
9 stosterone, but differently from raloxifene, estren alters the activity of Elk-1, CCAAT enhancer bind
10                                              Estrens and PSK3471 prevented gonadectomy-induced bone l
11 CI, Windahl et al. provide data showing that estrens are not as suitable a replacement for estrogen a
12 and reproductive organs to determine whether estrens are safe and act via the estrogen receptors and/
13 RM (PSK3471) and 2 estrens (estren-alpha and estren-beta) on bone and reproductive organs to determin
14                                              Estren binds recombinant AR with 10-fold higher affinity
15                                              Estren-bound AR can translocate AR to the nucleus and st
16 munoprecipitation analysis, we show that the estren-bound AR coimmunoprecipitates with a region of th
17       Consistent with the in vitro findings, estren, but not E(2), stimulated Wnt/beta-catenin-mediat
18                        Our results show that estren can bind, translocate, transactivate, and regulat
19                                              Estrens directly activated transcription in several cell
20 mpared the effects of a SERM (PSK3471) and 2 estrens (estren-alpha and estren-beta) on bone and repro
21                                              Estrens have been suggested to not only prevent bone los
22                            Unlike SERMs, the estrens induced reproductive organ hypertrophy in both m
23  an AR antagonist, bicalutamide, blocked the estren-induced increase in PSA expression.
24 e hitherto unidentified genotropic action of estren mediated by AR in androgen-responsive cells and t
25  of the ER with 4-estren-3alpha,17beta-diol (estren) or an estradiol-dendrimer conjugate, each a synt
26                          In vivo analysis of estren's action on male-orchidectomized ICR mice reveale
27 on on male-orchidectomized ICR mice revealed estren's AR agonist actions on the levator ani and semin
28                               Does this mean estrens should not be pursued as a therapy for osteoporo
29                        Though not catabolic, estrens triggered only minor, nonsignificant increases i
30                In 2002, the synthetic ligand estren was described to reproduce the bone anabolic, non
31                     The nongenotropic ligand estren was evaluated for its transcriptional activity me

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