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1 is of a precursor of raloxifene, a selective estrogen receptor modulator.
2 ass of drugs recently described as selective estrogen receptor modulators.
3 and retinoid X receptor alpha with selective estrogen receptor modulators.
4 by therapy with any one of several selective estrogen receptor modulators.
5 ther evaluation of carborane-based selective estrogen receptor modulators.
6 ssified as both phytoestrogens and selective estrogen receptor modulators.
7 ) have precipitated a search for alternative estrogen receptor modulators.
8 ogenic actions, characteristics of selective estrogen receptor modulators.
9 nic and antiestrogenic activity of selective estrogen receptor modulators.
10 cer are associated with the use of selective estrogen receptor modulators.
11 Leu-Cys)-Arg-Leu-Leu-Gln-NH2 (peptidomimetic estrogen receptor modulator 1), binds with a Ki of 25 nM
13 ity of ERalpha can be regulated by selective estrogen receptor modulators, a new class of drugs whose
14 nes and patient-derived organoids, selective estrogen receptor modulators, a pure anti-estrogen, and
15 tor degeneration that tamoxifen, a selective estrogen receptor modulator and a drug previously linked
18 s for the differential capacity of selective estrogen receptor modulators and selective estrogen rece
19 the identification of two structurally novel estrogen receptor modulators and the accurate prediction
21 the determination of idoxifene, a selective estrogen receptor modulator, and its pyrrolidinone metab
22 rs, androgen receptor antagonists, selective estrogen receptor modulators, and aromatase inhibitors a
23 d androgen dehydroepiandrosterone, selective estrogen receptor modulators, and the prolactin inhibito
24 tor potentiator (ivacaftor), and a selective estrogen receptor modulator antimicrobial adjuvant (ralo
29 ons among benzothiophene and triarylethylene estrogen receptor modulators can be ascribed to discrete
31 (i.e., agonistic) pharmacology of selective estrogen receptor modulator drugs in this pathway report
38 H) trial showed that raloxifene, a selective estrogen receptor modulator, had no overall effect on th
40 stic differences between different selective estrogen receptor modulators have been translated into i
42 in the brain, including the use of selective estrogen receptor modulators, high soy diets, or isoflav
43 nce: left breast radiation alone), selective estrogen receptor modulators (HR, 2.0 [95% CI, 1.2 to 3.
45 ta and differentially regulated by selective estrogen receptor modulators in a cell line-dependent ma
46 ues can be used for the analysis of selected estrogen receptor modulators in human plasma where more
47 the membrane impermeant E2-BSA and selective estrogen receptor modulators, including a new diphenylac
51 raloxifene (Ral), which is also a selective estrogen receptor modulator, is a complete antiestrogen
55 d to test the ability of the novel selective estrogen receptor modulator lasofoxifene (LAS) to inhibi
58 rapeutic potential of tamoxifen, a selective estrogen receptor modulator, on estrogen-induced lupus.
59 examine the effects of LY117018, a selective estrogen receptor modulator, on peripheral nerve regener
61 uated the effects of toremifene, a selective estrogen-receptor modulator, on fasting serum lipid leve
62 in combination with more effective selective estrogen receptor modulators or selective receptor downr
64 ratory reported that raloxifene, a selective estrogen receptor modulator, promoted regression of high
66 min after being injected with the selective estrogen receptor modulators, raloxifene, lasofoxifene,
67 Administration of tamoxifen, a selective estrogen-receptor modulator, restored fertility to the D
71 fene, tamoxifen, and nonusers of a selective estrogen receptor modulator (SERM) in the general popula
72 thylene bisphenol analogues of the selective estrogen receptor modulator (SERM) tamoxifen were synthe
73 fficient asymmetric synthesis of a selective estrogen receptor modulator (SERM) that has a dihydroben
74 xifene (BZA) is a third-generation selective estrogen receptor modulator (SERM) that has been approve
75 xyphenyl)]be nzo[b]thiophene) is a selective estrogen receptor modulator (SERM) that is a potent estr
76 eplacement therapy (CRT) (n = 16), selective estrogen receptor modulator (SERM) therapy (n = 8), and
78 benzothiophene raloxifene, 1, is a selective estrogen receptor modulator (SERM) which is currently un
81 SP500263, a novel next-generation selective estrogen receptor modulator (SERM), tamoxifen, and ralox
82 st cancer therapeutic, is a tissue-selective estrogen receptor modulator (SERM), which acts as an ant
83 -a novel, potent, third-generation selective estrogen receptor modulator (SERM)-because this benzothi
86 We tested whether the therapeutic selective estrogen receptor modulators (SERM), raloxifene and tamo
87 , but surprisingly antagonists and selective estrogen receptor modulators (SERMs) activated the AF-2
88 nificant recent findings regarding selective estrogen receptor modulators (SERMs) and selective andro
89 uvant endocrine therapy, including selective estrogen receptor modulators (SERMs) and/or aromatase in
91 the potential of estrogens and 17 Selective Estrogen Receptor Modulators (SERMs) as inhibiting ligan
94 l activity of natural estrogens or selective estrogen receptor modulators (SERMs) has not been determ
96 itional approaches to discovery of selective estrogen receptor modulators (SERMs) have relied on ER b
98 Tamoxifen and its analogues act as selective estrogen receptor modulators (SERMs) in women, with estr
100 enic and antiestrogenic effects of selective estrogen receptor modulators (SERMs) is thought to under
104 of 2,400 compounds, we noted that selective estrogen receptor modulators (SERMs) potently stabilize
107 gen's action and determine whether selective estrogen receptor modulators (SERMs) such as tamoxifen h
108 the mechanism(s) of action of the Selective Estrogen Receptor Modulators (SERMs) tamoxifen and ralox
109 e of a class of compounds known as selective estrogen receptor modulators (SERMs) that possess estrog
113 he ovariectomized rat by estrogen, selective estrogen receptor modulators (SERMs), and bisphosphonate
115 rogram aimed at the development of selective estrogen receptor modulators (SERMs), novel chromene sca
116 eral FDA-approved drugs, including selective estrogen receptor modulators (SERMs), possess selective
117 Current interventions include selective estrogen receptor modulators (SERMs), prophylactic surge
118 en assessed the suitability of the selective estrogen receptor modulators (SERMs), raloxifene and tam
123 n action at the estrogen receptor (selective estrogen receptor modulators (SERMs]); or (2) inhibit es
124 a key determinant of estrogen and selective estrogen receptor modulator signaling in the ERalpha/AP-
126 enyl)-propionitrile (DPN), and the selective estrogen receptor modulator tamoxifen (Tam), inhibit est
127 promoted hormone resistance to the selective estrogen receptor modulator tamoxifen and selective estr
129 east cancer cells were more resistant to the estrogen receptor modulator tamoxifen as a result of inc
134 or breast cancer-specifically, the selective estrogen receptor modulators tamoxifen and raloxifene.
136 ects on uterine development of the selective estrogen receptor modulators, tamoxifen, toremifene, and
137 SCs) into myofibroblasts is inhibited by the estrogen-receptor modulator, tamoxifen, which activates
138 Raloxifene hydrochloride is a selective estrogen receptor modulator that has antiestrogenic effe
141 Phytoestrogens may act as natural selective estrogen receptor modulators that elicit distinct clinic
142 ne and TSE-424 are investigational selective estrogen receptor modulators that have been shown to be
144 ion, tamoxifen and raloxifene, two selective estrogen receptor modulators that have protective effect
146 inhibitors, fenretinide, or other selective estrogen receptor modulators to lower BC risk is not rec
147 tate the design of tissue-specific selective estrogen receptor modulators to treat breast cancers and
149 se 27HC functions as an endogenous selective estrogen receptor modulator, we hypothesize that 27HC bi
150 benzothiophene raloxifene, 1, is a selective estrogen receptor modulator which is currently under cli
152 ell defined forms of estrogens and selective estrogen receptor modulators will continue to provide no
153 s may provide means to develop new selective estrogen receptor modulators with improved profiles.
154 soflavones are naturally occurring selective estrogen receptor modulators, with potential bone protec