戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 oxifene, 4-hydroxytamoxifen, nafoxidine, and idoxifene.
2                      A series of homologs of idoxifene [1a, (E)-1-[4-(N-pyrrolidinoethoxy)phenyl]-1-(
3 week, which was maintained for 3 months with idoxifene (3.1 versus 0.48% compared to E2 controls) but
4 ioanalytical method for the determination of idoxifene, a selective estrogen receptor modulator, and
5                                              Idoxifene also inhibits calmodulin, a calcium-binding pr
6            The LOQ obtained was 10 ng/mL for idoxifene and 30 ng/mL for the metabolite.
7 t method was applied to the determination of idoxifene and its metabolite in clinical human plasma sa
8 mn temperatures to perform LC separations of idoxifene and its metabolite within 10 s/sample.
9  internal standard, the results obtained for idoxifene and tamoxifen satisfy current bioanalytical me
10                                         Both idoxifene and tamoxifen significantly inhibited E2-depen
11              In this study, the abilities of idoxifene and tamoxifen to antagonize E2-dependent MCF-7
12  lower relative binding affinity for ER than idoxifene but similar calmodulin-inhibitory activity.
13 ed to a greater extent following 3 months of idoxifene, compared to tamoxifen.
14                                        Using idoxifene-d5 as an internal standard, idoxifene showed a
15                                        Using idoxifene-d5 as an internal standard, the results obtain
16 bited E2-dependent tumor growth, whereas cis-idoxifene had little effect.
17                             In contrast, cis-idoxifene had no effect on either cell proliferation or
18                                              Idoxifene (ID) is a tissue-selective estrogen receptor m
19                           Both tamoxifen and idoxifene initially induced ER expression, whereas prolo
20                                              Idoxifene is a novel selective estrogen (E2) receptor (E
21                       Compared to tamoxifen, idoxifene is metabolically more stable, with a higher re
22 f hormonal therapy with a SERM (tamoxifen or idoxifene) or an aromatase inhibitor (anastrozole or vor
23 cation was 5 and 50 ng/ mL for tamoxifen and idoxifene, respectively.
24                               In conclusion, idoxifene resulted in similar inhibition of E2-dependent
25                                The basis for idoxifene's antitumor activity was examined by comparing
26  Using idoxifene-d5 as an internal standard, idoxifene showed acceptable accuracy and precision value
27                                              Idoxifene showed acceptable results with accuracy rangin
28 ically used transisomer (referred to here as idoxifene) with its cis-isomer, which has a 50-fold lowe

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。