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1 receptor coactivator 2, which interacts with estrogen receptor alpha.
2 e genes; vitellogenin, androgen receptor and estrogen receptor alpha.
3 l lineage specification, including FOXA1 and estrogen receptor alpha.
4 ty in E2-exposed HEK293T cells co-expressing estrogen receptor alpha.
5 d the ligand-dependent activation domains of estrogen receptor alpha.
6 CD133(hi) CSCs that expressed low levels of estrogen receptor alpha.
7 reased autophagy and decreased expression of estrogen receptor-alpha.
8 tein-coupled estrogen receptor (GPER/GPR30), estrogen receptor alpha-36 (ERalpha36), epidermal growth
10 pply our method to dissect the regulation of estrogen receptor-alpha activation in breast cancer to i
12 egree show a greater effect on the levels of estrogen receptor-alpha activity and nuclear factor eryt
13 itro cellular toxicity, devoid of detectable estrogen receptor alpha affinity, displays high aqueous
14 gamma agonist) and 17beta-estradiol (E2; an estrogen receptor alpha agonist) nearly abolished TDCIPP
15 confirmed that in hypoxic mice inhibition of estrogen receptor alpha also has a therapeutic effect sp
16 ation between maternal LG and mRNA levels of estrogen receptor alpha and beta and the oxytocin recept
17 n regulating the transcriptional activity of estrogen receptor alpha and controlling the expression o
19 cellular pathway in both tissues, including estrogen receptor alpha and peroxisome proliferator acti
21 iption factor, which interacts directly with estrogen receptor alpha and regulates the expression of
22 stic disease and cancers retained functional estrogen receptor alpha and responded to retreatment wit
23 and glial profiles containing the classical estrogen receptors alpha and beta, and synaptic levels i
24 hat could be suppressed by inhibitors of the estrogen receptors alpha and beta, fibroblast growth fac
26 Furthermore, uterine ILC2s highly expressed estrogen receptor alpha, and in vitro culture of isolate
27 /progenitor activity, elevated expression of estrogen receptor alpha, and increased DNA damage in cel
29 e expression and proliferation are driven by estrogen receptor alpha, and targeting this transcriptio
30 ough repression of E-cadherin, occludin, and estrogen receptor-alpha, and up-regulation of vimentin,
34 cells within the AVPV/PeN highly co-express estrogen receptor alpha as well as glucocorticoid recept
35 r of genome-wide analyses have revealed that estrogen receptor alpha binding to and regulation of its
36 e chromatin architecture and allow FOXA1 and estrogen receptor alpha binding to transcriptional regul
37 ecreases the transcriptional activity of ER (estrogen receptor)-alpha but not ERbeta through the modu
39 tration decreased AIRE thymic expression and estrogen receptor alpha-deficient mice did not show a se
40 of pharmacology and demonstrated the desired estrogen receptor alpha degrader-antagonist profile and
42 isplayed affinity for aromatase (Ki 442 nM), estrogen receptor-alpha (EC50 17 nM), and estrogen recep
43 (E)-norendoxifen were aromatase (Ki 48 nM), estrogen receptor-alpha (EC50 58.7 nM), and estrogen rec
44 Mutations in ESR1 that confer constitutive estrogen receptor alpha (ER) activity in the absence of
47 ast cancer patients with tumors that express estrogen receptor alpha (ER) generally respond well to h
51 we found 3 lncRNA genes are associated with estrogen receptor alpha (ER) positive and ER negative su
54 ox protein A1 (FOXA1) is a pioneer factor of estrogen receptor alpha (ER)-chromatin binding and funct
55 e success of approved systemic therapies for estrogen receptor alpha (ER)-positive breast cancer, dru
56 rovides a temporary relief for patients with estrogen receptor alpha (ER)-positive breast cancers.
59 T2 promoter activity when cotransfected with estrogen receptor alpha (ER-alpha) after 17beta-estradio
60 heir abilities to inhibit aromatase, bind to estrogen receptor alpha (ER-alpha) and estrogen receptor
64 ed, dramatic estrogen-induced recruitment to estrogen receptor alpha (ER-alpha)-bound eRNA(+) active
69 e I IGF receptor (IGF1R) in combination with estrogen receptor-alpha (ER) targeting have been complet
70 -GAP (GTPase-activating protein), is also an estrogen receptor-alpha (ER) transcriptional co-represso
71 oligomerization states and mutants of GR and estrogen receptor-alpha (ER), which permitted us to reso
72 ied BRCA1 knockdown resulting in the loss of Estrogen Receptor-alpha (ER-alpha) expression and other
73 cord injury (SCI), or the involvement of the estrogen receptor-alpha (ER-alpha) in locomotor recovery
74 duce tamoxifen resistance through decreasing estrogen receptor-alpha (ER-alpha) level when cultured w
76 the expression of luminal markers, including estrogen receptor-alpha (ER-alpha, encoded by ESR1).
78 d unclear whether estrogen signaling through estrogen receptor-alpha (ER-alpha, Esr1) or ER-beta (Esr
79 itutive active/androstane receptor (CAR) KO, estrogen receptor alpha (ERalpha KO, phosphorylation-blo
82 opment is controlled by the balance of AR to estrogen receptor alpha (ERalpha) activity; either inhib
83 cals and drugs in three independent runs for estrogen receptor alpha (ERalpha) agonist and antagonist
84 demonstrate that Icaritin co-localizes with estrogen receptor alpha (ERalpha) and activates its nucl
85 GH-releasing hormone (GHRH) neurons express estrogen receptor alpha (ERalpha) and androgen receptor
86 environmental contaminant that can activate estrogen receptor alpha (ERalpha) and contribute to the
87 Approximately 75% of breast cancers express estrogen receptor alpha (ERalpha) and depend on estrogen
88 Approximately 70% of breast cancers express estrogen receptor alpha (ERalpha) and depend on this key
89 plexes involving RNA polymerase II (Pol II), estrogen receptor alpha (ERalpha) and ERalpha-pioneer fa
90 rficial spinal cord dorsal horn that express estrogen receptor alpha (ERalpha) and explored the behav
91 rapidly induced genes are enriched for both estrogen receptor alpha (ERalpha) and FOXA1 binding in t
92 miR-515-5p is transcriptionally repressed by estrogen receptor alpha (ERalpha) and functions as a tum
94 associates with transcriptional enhancers of estrogen receptor alpha (ERalpha) and that this associat
95 nto account the signaling cross-talk between estrogen receptor alpha (ERalpha) and the human epiderma
96 The development of tamoxifen and subsequent estrogen receptor alpha (ERalpha) antagonists represents
99 s direct visualization and quantification of estrogen receptor alpha (ERalpha) DNA binding, co-regula
102 Notably, mice with selective deletion of estrogen receptor alpha (ERalpha) from Kiss1 neurons sho
105 (CA12) is associated with the expression of estrogen receptor alpha (ERalpha) in breast cancer and i
106 ctions of glucocorticoid receptors (GRs) and estrogen receptor alpha (ERalpha) in breast cancer devel
108 that conditional knockout (cKO) mice lacking estrogen receptor alpha (ERalpha) in oviduct and uterine
124 To assess this, we developed a point mutant estrogen receptor alpha (ERalpha) knockin mouse (C451A)
131 ival rates of breast cancer patients lacking estrogen receptor alpha (ERalpha) negatively correlated
134 thesized that upregulating the expression of estrogen receptor alpha (ERalpha) or estrogen receptor b
137 D538G is common after endocrine therapy for estrogen receptor alpha (ERalpha) positive breast cancer
139 Estrogen triggers transactivation coupled estrogen receptor alpha (ERalpha) proteolysis, but mecha
140 ng nodules are estrogen dependent and retain estrogen receptor alpha (ERalpha) reactivity, but have d
144 cell line MCF7, which expresses a functional estrogen receptor alpha (ERalpha) signaling pathway.
145 wledge previously unreported, a role whereby estrogen receptor alpha (ERalpha) signaling preferential
147 nd animal model results linking estrogen and estrogen receptor alpha (ERalpha) to CxCa, ERalpha expre
148 lective loss- or gain-of-function mutants of estrogen receptor alpha (ERalpha) to define two distinct
149 nding and transcriptional activation through estrogen receptor alpha (ERalpha) to that of 17beta-estr
150 P140 in breast cancer and its involvement in estrogen receptor alpha (ERalpha) transcriptional regula
151 ecule antagonist of the transcription factor estrogen receptor alpha (ERalpha) used to treat breast c
152 regulates gene transcription through nuclear estrogen receptor alpha (ERalpha) via 2 activation funct
153 s missense mutation in the gene encoding the estrogen receptor alpha (ERalpha) was previously identif
154 rogen-based therapies are mainly mediated by estrogen receptor alpha (ERalpha), a nuclear receptor th
155 ivator-6 (NCOA6), a reported coactivator for estrogen receptor alpha (ERalpha), actually attenuates E
156 he genome-wide chromatin-binding profiles of estrogen receptor alpha (ERalpha), along with the epigen
157 otein 14-3-3sigma and a peptide derived from Estrogen Receptor alpha (ERalpha), an important breast c
158 strogens drive breast carcinogenesis via the estrogen receptor alpha (ERalpha), androgens play a crit
159 gen-responsive genes, vitellogenin (VTG) and estrogen receptor alpha (ERalpha), as well as the androg
160 Treatment of female rats with antisense to estrogen receptor alpha (ERalpha), but not beta (ERbeta)
162 ons of E2 with one of its cognate receptors, estrogen receptor alpha (ERalpha), estrogen receptor bet
165 campus of female rats through a sex-specific estrogen receptor alpha (ERalpha), mGluR, and endocannab
166 e-negative breast cancer (TNBC), which lacks estrogen receptor alpha (ERalpha), progesterone receptor
168 ntermembrane space (IMS) and mediated by the estrogen receptor alpha (ERalpha), was found to upregula
173 Obesity is a risk factor for postmenopausal estrogen receptor alpha (ERalpha)-positive (ER(+)) breas
174 ty to antiestrogens and chemotherapeutics in estrogen receptor alpha (ERalpha)-positive and triple-ne
176 hway in 20% to 40% of cases, particularly in estrogen receptor alpha (ERalpha)-positive breast cancer
179 s COX-2 activity, is associated with reduced estrogen receptor alpha (ERalpha)-positive breast cancer
180 y used endocrine agents for the treatment of estrogen receptor alpha (ERalpha)-positive breast cancer
181 ourse of estradiol (E2) stimulation in human estrogen receptor alpha (ERalpha)-positive breast cancer
184 ly able to reduce DCIS risk in patients with estrogen receptor alpha (ERalpha)-positive disease.
185 herapy occurs in virtually all patients with estrogen receptor alpha (ERalpha)-positive metastatic br
186 ion and histone modifications, are linked to estrogen receptor alpha (ERalpha)-positive tumors and di
194 ene has captured ESR1, the gene that encodes estrogen receptor alpha (ERalpha); as a result, this gen
196 ERT) mRNA expression and cell growth through estrogen receptor-alpha (ERalpha) activation in ovarian
198 as a critical role in the regulation of both estrogen receptor-alpha (ERalpha) and c-ErbB2/HER2 (Her2
199 ently identified LMTK3 as a regulator of the estrogen receptor-alpha (ERalpha) and wished to understa
200 t regimens for breast cancer that target the estrogen receptor-alpha (ERalpha) are effective, but acq
201 is rescue was accompanied by an induction in estrogen receptor-alpha (ERalpha) expression and that co
204 s shown to be a transcriptional activator of estrogen receptor-alpha (ERalpha) in ERalpha-positive br
206 blocked in female mice specifically lacking estrogen receptor-alpha (ERalpha) in serotonin (5-HT) ne
209 p) on neutralizing epigenetic aberrations in estrogen receptor-alpha (ERalpha) leading to enhanced an
210 that resveratrol acts as a pathway-selective estrogen receptor-alpha (ERalpha) ligand to modulate the
212 1 (GCM1), frizzled 5 (FZD5), WNT2, Sp1, and estrogen receptor-alpha (ERalpha) mRNA, were markedly up
213 models that allow for selective deletion of estrogen receptor-alpha (ERalpha) or selective inhibitio
215 o differentiates primary tumors to a benign, Estrogen Receptor-alpha (ERalpha) positive, Rictor-negat
216 Approximately 75% of breast cancers are estrogen receptor-alpha (ERalpha) positive, underscoring
217 provided a detailed view of the mechanism of estrogen receptor-alpha (ERalpha) regulated gene transcr
219 or glucose homeostasis primarily through the estrogen receptor-alpha (ERalpha), but the respective im
220 males and females is primarily mediated via estrogen receptor-alpha (ERalpha), encoded by the Esr1 g
221 er subtypes are defined by the expression of estrogen receptor-alpha (ERalpha)-associated genes, many
224 ns, and induced proliferation in parallel in estrogen receptor-alpha (ERalpha)-negative mammary cells
225 herapy resistance remains a major problem in estrogen receptor-alpha (ERalpha)-positive breast cancer
226 nefitted tremendously from the generation of estrogen receptor-alpha (ERalpha)-targeted therapies, bu
231 s the estrogen receptor needed for feedback (estrogen receptor alpha [ERalpha]); kisspeptin neurons i
232 e), and mice with knockout of Esr1, encoding estrogen receptor alpha (ERalphaKO mice), to analyze int
235 uctal epithelial cells are regulated through estrogen receptor alpha (ESR1) but not estrogen receptor
237 -induced uterine cell growth, we removed the estrogen receptor alpha (Esr1) from mouse uterine stroma
240 ceptor gene, a mutation in the gene encoding estrogen receptor alpha (ESR1) was previously described
241 ear receptors (NRs) [androgen receptor (Ar), estrogen receptor alpha (Esr1), estrogen receptor beta (
242 n receptor (Ahr), interleukin-1 beta (Il1b), estrogen receptor alpha (Esr1), insulin like growth fact
243 ategies enabling neuron-specific deletion of estrogen receptor alpha (Esr1), we examine here whether
248 ntromedial hypothalamus (VMHvl) that express estrogen receptor-alpha (Esr1) and progesterone receptor
251 coid receptor (GR/NR3C1) gene and one in the estrogen receptor-alpha (ESR1) gene were significant (q
253 etic studies highlight the potential role of estrogen receptor-alpha (ESR1) mutations, which show inc
254 5 orders of magnitude more sensitive, by an estrogen receptor alpha (EsRalpha)-dependent mechanism.
255 i3 channels that selectively mediate SOCE in estrogen receptor alpha-expressing (ERalpha(+)) breast c
259 intra-chromosomal gene fusion involving the estrogen receptor alpha gene ESR1, and another involving
260 of this study was to determine the effect of estrogen receptor-alpha gene (ESR1) mutations at the tyr
261 morphisms in the glucocorticoid receptor and estrogen receptor-alpha genes may modify the association
262 hormone receptor family (androgen receptor, estrogen receptor alpha, glucocorticoid receptor, minera
264 e, in the induction of priming, regulated by estrogen receptor alpha in the nociceptor of female rats
266 e used the approach to probe the mobility of estrogen receptor-alpha in the vicinity of an integrated
267 tic variants across the ESR1 locus (encoding estrogen receptor alpha) in 118,816 subjects from three
271 ikewise, renal IRI was exacerbated in female estrogen receptor alpha-KO mice, while female mice recei
273 Dysregulation of hypothalamic-pituitary estrogen receptor alpha-mediated signaling causes episod
274 uR1, depending on its activation by membrane estrogen receptor alpha (mERalpha; during diestrus) vers
275 nvasive cancers from controls were uniformly estrogen receptor alpha negative and undifferentiated, w
276 can cause DNA double-strand breaks (DSB) in estrogen receptor-alpha-negative breast cells and that B
277 acts bound to 17beta-estradiol (E2)-liganded estrogen receptor-alpha on estrogen response elements (E
281 btained from 89 postmenopausal women who had estrogen receptor-alpha positive breast cancer and were
282 o a highly invasive mesenchymal phenotype in estrogen receptor alpha-positive (ERalpha(+)) breast can
283 old subunit in hPAFc, is highly expressed in estrogen receptor alpha-positive (ERalpha(+)) luminal br
284 und develop aggressive, highly aneuploid and estrogen receptor alpha-positive (ERalpha+) mammary aden
285 ndifferentiated, whereas well-differentiated estrogen receptor alpha-positive papillary invasive canc
286 is a well-tolerated, effective treatment for estrogen receptor-alpha-positive (ER+) breast cancer, bu
287 is associated with poor patient outcomes in estrogen receptor-alpha-positive (ERalpha(+)) breast can
288 17q23 and 20q13 were frequently amplified in estrogen receptor-alpha-positive luminal breast cancer.
291 however, currently used biomarkers, such as, estrogen receptor-alpha/progesterone receptor (ERalpha/P
293 pDC innate functions through cell-intrinsic estrogen receptor alpha signaling, but did not exclude a
295 ymal transition in breast cancer through the estrogen receptor alpha/Slug axis and that it is a poten
296 extracellular signal-related kinase 1/2, and estrogen receptor alpha) that lead to acute cholestasis
297 get network, including GPER/GPR30 itself and estrogen receptor alpha, the plasma membrane Ca(2+)-ATPa
299 vity genes primarily sense signaling through estrogen receptor alpha, whereas the resistance genes mo
300 vity of oestrogen signalling is mediated via estrogen receptor alpha within the left gonad epithelium