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1 nantiomer has a relatively high affinity for estrogen receptor beta.
2 xes containing retinoic X receptor alpha and estrogen receptor beta.
3 he TSU-PR1 cell line contains high levels of estrogen receptor beta.
4 mice deficient in estrogen receptor alpha or estrogen receptor beta.
14 (betaERKO(-/-)), estrogen receptor-alpha and estrogen receptor-beta (alphabetaERKO(-/-)), and GPER (G
15 e, estrogen receptor alpha (XbaI and PvuII), estrogen receptor beta (AluI), and estrogen receptor bet
17 5 were transcriptionally induced by liganded estrogen receptor beta and inhibited by androgen recepto
20 d fatty acid oxidation, are regulated by the estrogen receptor-beta and consequently contribute to ca
21 common variants in estrogen receptor-alpha, estrogen receptor-beta and the progesterone receptor pro
22 ii) 3beta-Diol is a pro-apoptotic ligand for estrogen receptor beta, and (iii) 3beta-tetrahydrosteroi
23 tifs have diverse affinities for the VDR and estrogen receptor beta, and mutation of specific motifs
24 androgen receptor, estrogen receptor alpha, estrogen receptor beta, and progesterone receptor mRNA a
25 hat are potent and selective agonists of the estrogen receptor beta, and that are selectively cytotox
26 in estrogen receptor-alpha (alphaERKO(-/-)), estrogen receptor-beta (betaERKO(-/-)), estrogen recepto
28 r cells to be transcriptionally regulated by estrogen receptor-beta coupled to Ago2, whereas male Ago
29 d PvuII), estrogen receptor beta (AluI), and estrogen receptor beta(cx) (Tsp509I), endothelial nitric
30 to isoflavones and to placebo was found with estrogen receptor beta(cx) Tsp509I genotype AA, but not
31 ), estrogen receptor-alpha (EC50 17 nM), and estrogen receptor-beta (EC50 27.5 nM), while the corresp
34 n in CNP we used a combination therapy of an estrogen receptor beta (ER beta) inhibitor with a sTNF/T
35 n of the estrogen receptor alpha (ER alpha), estrogen receptor beta (ER beta), progesterone receptor
36 and in vitro models to determine the role of estrogen receptor beta (ER-beta) and its ligands on adip
39 nd to estrogen receptor alpha (ER-alpha) and estrogen receptor beta (ER-beta), and antagonize the act
41 that express the more recently characterized estrogen receptor-beta (ER-beta) has not been examined i
42 It has been shown that the activation of estrogen receptor-beta (ER-beta) plays an important card
43 oughly characterized for its specificity for estrogen receptor-beta (ER-beta), was used to immunoloca
44 DNF, estrogen receptor-alpha (ER-alpha), and estrogen receptor-beta (ER-beta), we found only sparse c
45 e we describe the generation of mice lacking estrogen receptor beta (ERbeta -/-) by insertion of a ne
51 IMP3 expression is repressed specifically by estrogen receptor beta (ERbeta) and its ligand 3betaA-di
54 -length estrogen receptor alpha (ERalpha) or estrogen receptor beta (ERbeta) bound to a fluorescein-l
56 the transcription factors DLX5 and EGR3 and estrogen receptor beta (ERbeta) directly controlling its
60 in vivo from the hearts of wild-type but not estrogen receptor beta (ERbeta) gene-deleted mice admini
65 sion of estrogen receptor alpha (ERalpha) or estrogen receptor beta (ERbeta) in the hippocampus of ag
66 ion of estrogen receptor alpha (ERalpha) and estrogen receptor beta (ERbeta) in the mouse cortex duri
76 rian granulosa cells, we discovered that the estrogen receptor beta (ERbeta) is inducible by activin.
80 use dihydrotestosterone is the precursor for estrogen receptor beta (ERbeta) ligands, 5AR inhibitors
83 f midbrain DA neurons are immunopositive for estrogen receptor beta (ERbeta) or androgen receptors (A
87 eloped that selectively bind to and activate estrogen receptor beta (ERbeta) rather than estrogen rec
90 of Blood, Yakimchuk and colleagues show that estrogen receptor beta (ERbeta) signaling can act tumor-
91 eviously reported that antiestrogen-liganded estrogen receptor beta (ERbeta) transcriptionally activa
92 for the localization of the newly identified estrogen receptor beta (ERbeta) within the rat paraventr
93 ptors (estrogen receptor alpha (ERalpha) and estrogen receptor beta (ERbeta)) that bind 17beta-estrad
97 eceptors, estrogen receptor alpha (ERalpha), estrogen receptor beta (ERbeta), or the G protein-couple
100 r smooth muscle cells and blood vessels from estrogen receptor beta (ERbeta)-deficient mice exhibit m
115 over, pharmacologic inhibition of microglial estrogen receptor-beta (ERbeta) function corrects the re
120 al of this study was to determine whether an estrogen receptor-beta (ERbeta)-selective agonist (GTx-8
123 ptors [estrogen receptor-alpha (ERalpha) and estrogen receptor-beta (ERbeta)] to promote changes in p
124 s [estrogen receptor alpha (XbaI and PvuII), estrogen receptor beta [ERbeta (AluI) and ERbeta[cx] (Ts
126 ation by steroid receptors, and we show that estrogen receptor beta (ESR2) is the main vector of estr
128 ceptor (Ar), estrogen receptor alpha (Esr1), estrogen receptor beta (Esr2), glucocorticoid receptor (
131 n-related receptor, estrogen receptor-alpha, estrogen receptor-beta, farnesoid X receptor, and mast c
132 the hypothesis that sequence variants of the estrogen receptor beta gene (ESR2) may be associated wit
133 gnition and psychological resources, and the estrogen receptor beta gene (ESR2) polymorphism rs297838
136 ar interactions between these components and Estrogen Receptor Beta, identified as a potential target
138 ch interact with estrogen receptor-alpha and estrogen receptor-beta in multiple tissues, continue to
139 ound that GnRH neurons exclusively expressed estrogen receptor-beta in rats and against the current c
141 found that the vitamin D receptor (VDR) and estrogen receptor beta interact with different alpha-hel
142 sexual motivation through the activation of estrogen receptor beta interacting with the metabotropic
145 ast to ERalphaKO mice, IA performance by OVX estrogen receptor-beta-knockout (ERbetaKO) mice was not
146 nge (HDX) mass spectrometry in analyzing the estrogen receptor beta ligand binding domain (ERbeta LBD
147 taining revealed estrogen receptor-alpha and estrogen receptor-beta localized in the nucleus and cyto
148 overy of a second estrogen receptor subtype, estrogen receptor-beta, may significantly advance our un
149 anslated protein first suggested that murine estrogen receptor beta (mER-beta) is O-GlcNAcylated.
150 Recently, we demonstrated that the murine estrogen receptor-beta (mER-beta) is alternatively O-Glc
151 Expression of estrogen receptor-alpha and estrogen receptor-beta mRNA in lumbar spinal cord was sh
152 ith sulforaphane and diarylpropionitrile, an estrogen receptor beta selective agonist, results in NRF
153 ent with the hypothesis of a joint effect of estrogen receptor beta sequence variants and endogenous
154 and its receptor, oxytocin and its receptor, estrogen receptor beta, serotonin receptors (Htr1a, Htr2
155 BPS on myocyte Ca2+ handling was mediated by estrogen receptor beta signaling and by rapid increases
159 modifications may play a role in regulating estrogen receptor beta transactivation and turnover.
161 suming soy foods, has selective affinity for estrogen receptor-beta, whereas both enantiomers modulat
162 rogen receptors (estrogen receptor-alpha and estrogen receptor-beta), which bind to DNA and function
163 d from women and mice are immunopositive for estrogen receptor beta, with up to 20% being estrogen re