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1 l lineage specification, including FOXA1 and estrogen receptor alpha.
2 ty in E2-exposed HEK293T cells co-expressing estrogen receptor alpha.
3 d the ligand-dependent activation domains of estrogen receptor alpha.
4 receptor coactivator 2, which interacts with estrogen receptor alpha.
5 CD133(hi) CSCs that expressed low levels of estrogen receptor alpha.
6 e genes; vitellogenin, androgen receptor and estrogen receptor alpha.
7 tein-coupled estrogen receptor (GPER/GPR30), estrogen receptor alpha-36 (ERalpha36), epidermal growth
10 egree show a greater effect on the levels of estrogen receptor-alpha activity and nuclear factor eryt
11 confirmed that in hypoxic mice inhibition of estrogen receptor alpha also has a therapeutic effect sp
13 cription activity and directly interact with estrogen receptor alpha, although ACTN4 (Iso) binds ERal
14 ation between maternal LG and mRNA levels of estrogen receptor alpha and beta and the oxytocin recept
15 n regulating the transcriptional activity of estrogen receptor alpha and controlling the expression o
17 ling components and diminished expression of estrogen receptor alpha and progesterone receptor, which
18 iption factor, which interacts directly with estrogen receptor alpha and regulates the expression of
19 stic disease and cancers retained functional estrogen receptor alpha and responded to retreatment wit
20 stone acetylation and recruitment of phospho-estrogen receptor alpha and specificity protein-1 to the
21 rogen binding to nuclear estrogen receptors (estrogen receptor-alpha and estrogen receptor-beta), whi
22 cally, estrogen activity is mediated via the estrogen receptors alpha and beta (ERalpha and ERbeta),
23 ith low micromolar potency, selectivity over estrogen receptors alpha and beta and glucocorticoid rec
25 and glial profiles containing the classical estrogen receptors alpha and beta, and synaptic levels i
27 Furthermore, uterine ILC2s highly expressed estrogen receptor alpha, and in vitro culture of isolate
28 ough repression of E-cadherin, occludin, and estrogen receptor-alpha, and up-regulation of vimentin,
32 r of genome-wide analyses have revealed that estrogen receptor alpha binding to and regulation of its
33 e chromatin architecture and allow FOXA1 and estrogen receptor alpha binding to transcriptional regul
34 entify estrogen receptor 1 (ESR1; previously estrogen receptor alpha) binding sites, and RNA-seq in e
35 ecreases the transcriptional activity of ER (estrogen receptor)-alpha but not ERbeta through the modu
37 tration decreased AIRE thymic expression and estrogen receptor alpha-deficient mice did not show a se
39 isplayed affinity for aromatase (Ki 442 nM), estrogen receptor-alpha (EC50 17 nM), and estrogen recep
40 (E)-norendoxifen were aromatase (Ki 48 nM), estrogen receptor-alpha (EC50 58.7 nM), and estrogen rec
41 we found 3 lncRNA genes are associated with estrogen receptor alpha (ER) positive and ER negative su
44 ox protein A1 (FOXA1) is a pioneer factor of estrogen receptor alpha (ER)-chromatin binding and funct
46 rovides a temporary relief for patients with estrogen receptor alpha (ER)-positive breast cancers.
50 T2 promoter activity when cotransfected with estrogen receptor alpha (ER-alpha) after 17beta-estradio
51 heir abilities to inhibit aromatase, bind to estrogen receptor alpha (ER-alpha) and estrogen receptor
55 ed, dramatic estrogen-induced recruitment to estrogen receptor alpha (ER-alpha)-bound eRNA(+) active
62 e I IGF receptor (IGF1R) in combination with estrogen receptor-alpha (ER) targeting have been complet
63 oligomerization states and mutants of GR and estrogen receptor-alpha (ER), which permitted us to reso
64 hile more than 70% of breast cancers express estrogen receptor-alpha (ER+), endocrine therapies targe
65 ied BRCA1 knockdown resulting in the loss of Estrogen Receptor-alpha (ER-alpha) expression and other
66 cord injury (SCI), or the involvement of the estrogen receptor-alpha (ER-alpha) in locomotor recovery
67 duce tamoxifen resistance through decreasing estrogen receptor-alpha (ER-alpha) level when cultured w
69 s characterized by the lack of expression of estrogen receptor-alpha (ER-alpha), progesterone recepto
70 the expression of luminal markers, including estrogen receptor-alpha (ER-alpha, encoded by ESR1).
74 opment is controlled by the balance of AR to estrogen receptor alpha (ERalpha) activity; either inhib
75 cals and drugs in three independent runs for estrogen receptor alpha (ERalpha) agonist and antagonist
76 demonstrate that Icaritin co-localizes with estrogen receptor alpha (ERalpha) and activates its nucl
77 eural aromatase, androgen receptor (AR), and estrogen receptor alpha (ERalpha) and beta (ERbeta) mRNA
78 Approximately 75% of breast cancers express estrogen receptor alpha (ERalpha) and depend on estrogen
79 plexes involving RNA polymerase II (Pol II), estrogen receptor alpha (ERalpha) and ERalpha-pioneer fa
80 rapidly induced genes are enriched for both estrogen receptor alpha (ERalpha) and FOXA1 binding in t
81 miR-515-5p is transcriptionally repressed by estrogen receptor alpha (ERalpha) and functions as a tum
83 shock protein 27 (Hsp27) binds to a motif in estrogen receptor alpha (ERalpha) and promotes palmitoyl
84 nto account the signaling cross-talk between estrogen receptor alpha (ERalpha) and the human epiderma
85 s between the progesterone receptor (PR) and estrogen receptor alpha (ERalpha) are required for PR ac
90 s direct visualization and quantification of estrogen receptor alpha (ERalpha) DNA binding, co-regula
94 Notably, mice with selective deletion of estrogen receptor alpha (ERalpha) from Kiss1 neurons sho
98 ctions of glucocorticoid receptors (GRs) and estrogen receptor alpha (ERalpha) in breast cancer devel
100 rginine transition at residue 303 (K303R) in estrogen receptor alpha (ERalpha) in invasive breast can
101 that conditional knockout (cKO) mice lacking estrogen receptor alpha (ERalpha) in oviduct and uterine
116 To assess this, we developed a point mutant estrogen receptor alpha (ERalpha) knockin mouse (C451A)
121 imilarly, castration significantly increased estrogen receptor alpha (ERalpha) mRNA expression and de
122 ival rates of breast cancer patients lacking estrogen receptor alpha (ERalpha) negatively correlated
124 capitulated by pharmacological activation of estrogen receptor alpha (ERalpha) or ERbeta in a rat bet
125 thesized that upregulating the expression of estrogen receptor alpha (ERalpha) or estrogen receptor b
128 D538G is common after endocrine therapy for estrogen receptor alpha (ERalpha) positive breast cancer
130 Estrogen triggers transactivation coupled estrogen receptor alpha (ERalpha) proteolysis, but mecha
136 cell line MCF7, which expresses a functional estrogen receptor alpha (ERalpha) signaling pathway.
137 wledge previously unreported, a role whereby estrogen receptor alpha (ERalpha) signaling preferential
139 nd animal model results linking estrogen and estrogen receptor alpha (ERalpha) to CxCa, ERalpha expre
140 lective loss- or gain-of-function mutants of estrogen receptor alpha (ERalpha) to define two distinct
141 P140 in breast cancer and its involvement in estrogen receptor alpha (ERalpha) transcriptional regula
142 ecule antagonist of the transcription factor estrogen receptor alpha (ERalpha) used to treat breast c
143 regulates gene transcription through nuclear estrogen receptor alpha (ERalpha) via 2 activation funct
144 P-Int3/WC/R26 mammary glands contained ample estrogen receptor alpha (ERalpha)+ MECs, but only rare (
146 rogen-based therapies are mainly mediated by estrogen receptor alpha (ERalpha), a nuclear receptor th
147 ivator-6 (NCOA6), a reported coactivator for estrogen receptor alpha (ERalpha), actually attenuates E
148 he genome-wide chromatin-binding profiles of estrogen receptor alpha (ERalpha), along with the epigen
149 strogens drive breast carcinogenesis via the estrogen receptor alpha (ERalpha), androgens play a crit
150 gen-responsive genes, vitellogenin (VTG) and estrogen receptor alpha (ERalpha), as well as the androg
151 Treatment of female rats with antisense to estrogen receptor alpha (ERalpha), but not beta (ERbeta)
152 contribute to the oncogenic potential of the estrogen receptor alpha (ERalpha), but SIRT1 activity ha
153 ons of E2 with one of its cognate receptors, estrogen receptor alpha (ERalpha), estrogen receptor bet
156 campus of female rats through a sex-specific estrogen receptor alpha (ERalpha), mGluR, and endocannab
158 ntermembrane space (IMS) and mediated by the estrogen receptor alpha (ERalpha), was found to upregula
162 ty to antiestrogens and chemotherapeutics in estrogen receptor alpha (ERalpha)-positive and triple-ne
167 s COX-2 activity, is associated with reduced estrogen receptor alpha (ERalpha)-positive breast cancer
168 y used endocrine agents for the treatment of estrogen receptor alpha (ERalpha)-positive breast cancer
170 hway in 20% to 40% of cases, particularly in estrogen receptor alpha (ERalpha)-positive breast cancer
171 ly able to reduce DCIS risk in patients with estrogen receptor alpha (ERalpha)-positive disease.
172 herapy occurs in virtually all patients with estrogen receptor alpha (ERalpha)-positive metastatic br
173 ion and histone modifications, are linked to estrogen receptor alpha (ERalpha)-positive tumors and di
182 ERT) mRNA expression and cell growth through estrogen receptor-alpha (ERalpha) activation in ovarian
184 as a critical role in the regulation of both estrogen receptor-alpha (ERalpha) and c-ErbB2/HER2 (Her2
185 ely 25% of breast cancers do not express the estrogen receptor-alpha (ERalpha) and consequently do no
186 ities of ZYC-26 and ZYC-3 were autonomous of estrogen receptor-alpha (ERalpha) and ERbeta demonstrate
188 ently identified LMTK3 as a regulator of the estrogen receptor-alpha (ERalpha) and wished to understa
189 t regimens for breast cancer that target the estrogen receptor-alpha (ERalpha) are effective, but acq
190 is rescue was accompanied by an induction in estrogen receptor-alpha (ERalpha) expression and that co
191 s to investigate in vivo the role of central estrogen receptor-alpha (ERalpha) expression for bone ma
195 s shown to be a transcriptional activator of estrogen receptor-alpha (ERalpha) in ERalpha-positive br
197 blocked in female mice specifically lacking estrogen receptor-alpha (ERalpha) in serotonin (5-HT) ne
198 as associated with a significant decrease of estrogen receptor-alpha (ERalpha) in the hippocampus but
201 p) on neutralizing epigenetic aberrations in estrogen receptor-alpha (ERalpha) leading to enhanced an
202 that resveratrol acts as a pathway-selective estrogen receptor-alpha (ERalpha) ligand to modulate the
204 1 (GCM1), frizzled 5 (FZD5), WNT2, Sp1, and estrogen receptor-alpha (ERalpha) mRNA, were markedly up
205 models that allow for selective deletion of estrogen receptor-alpha (ERalpha) or selective inhibitio
207 Approximately 75% of breast cancers are estrogen receptor-alpha (ERalpha) positive, underscoring
210 provided a detailed view of the mechanism of estrogen receptor-alpha (ERalpha) regulated gene transcr
212 ly labeled neurons directed to WAT expressed estrogen receptor-alpha (ERalpha), and fewer neurons to
213 males and females is primarily mediated via estrogen receptor-alpha (ERalpha), encoded by the Esr1 g
214 including metalloestrogens that can activate estrogen receptor-alpha (ERalpha), may contribute to bre
215 er subtypes are defined by the expression of estrogen receptor-alpha (ERalpha)-associated genes, many
218 CAF) in both wild-type (WT) and K303R mutant estrogen receptor-alpha (ERalpha)-expressing breast canc
219 ns, and induced proliferation in parallel in estrogen receptor-alpha (ERalpha)-negative mammary cells
220 herapy resistance remains a major problem in estrogen receptor-alpha (ERalpha)-positive breast cancer
221 nefitted tremendously from the generation of estrogen receptor-alpha (ERalpha)-targeted therapies, bu
226 s the estrogen receptor needed for feedback (estrogen receptor alpha [ERalpha]); kisspeptin neurons i
227 e), and mice with knockout of Esr1, encoding estrogen receptor alpha (ERalphaKO mice), to analyze int
229 tion of MCF7 and SK-BR-3 colony formation by estrogen receptor alpha (ESR1) and (ERBB2) siRNA, respec
231 uctal epithelial cells are regulated through estrogen receptor alpha (ESR1) but not estrogen receptor
233 -induced uterine cell growth, we removed the estrogen receptor alpha (Esr1) from mouse uterine stroma
236 ceptor gene, a mutation in the gene encoding estrogen receptor alpha (ESR1) was previously described
237 ear receptors (NRs) [androgen receptor (Ar), estrogen receptor alpha (Esr1), estrogen receptor beta (
238 n receptor (Ahr), interleukin-1 beta (Il1b), estrogen receptor alpha (Esr1), insulin like growth fact
239 ategies enabling neuron-specific deletion of estrogen receptor alpha (Esr1), we examine here whether
242 ntromedial hypothalamus (VMHvl) that express estrogen receptor-alpha (Esr1) and progesterone receptor
244 coid receptor (GR/NR3C1) gene and one in the estrogen receptor-alpha (ESR1) gene were significant (q
246 etic studies highlight the potential role of estrogen receptor-alpha (ESR1) mutations, which show inc
247 5 orders of magnitude more sensitive, by an estrogen receptor alpha (EsRalpha)-dependent mechanism.
248 d the distribution of the androgen receptor, estrogen receptor alpha, estrogen receptor beta, and pro
249 i3 channels that selectively mediate SOCE in estrogen receptor alpha-expressing (ERalpha(+)) breast c
252 intra-chromosomal gene fusion involving the estrogen receptor alpha gene ESR1, and another involving
253 leads to demethylation and activation of the estrogen receptor-alpha gene, sensitizing the tumor cell
254 morphisms in the glucocorticoid receptor and estrogen receptor-alpha genes may modify the association
255 hormone receptor family (androgen receptor, estrogen receptor alpha, glucocorticoid receptor, minera
257 e, in the induction of priming, regulated by estrogen receptor alpha in the nociceptor of female rats
259 between STAT3 acetylation and methylation of estrogen receptor-alpha in melanoma, which predicts mela
260 tic variants across the ESR1 locus (encoding estrogen receptor alpha) in 118,816 subjects from three
264 ikewise, renal IRI was exacerbated in female estrogen receptor alpha-KO mice, while female mice recei
266 uR1, depending on its activation by membrane estrogen receptor alpha (mERalpha; during diestrus) vers
267 nvasive cancers from controls were uniformly estrogen receptor alpha negative and undifferentiated, w
268 A7 is associated with the worst prognosis in estrogen receptor alpha-negative (ERalpha(-)) invasive b
269 risk subgroups, and was specific for HER2(+):estrogen receptor alpha-negative (ERalpha(-)) patients (
270 can cause DNA double-strand breaks (DSB) in estrogen receptor-alpha-negative breast cells and that B
273 acts bound to 17beta-estradiol (E2)-liganded estrogen receptor-alpha on estrogen response elements (E
275 .e., liver X receptor, farnesoid X receptor, estrogen receptor alpha, peroxisome proliferator-activat
277 btained from 89 postmenopausal women who had estrogen receptor-alpha positive breast cancer and were
279 o a highly invasive mesenchymal phenotype in estrogen receptor alpha-positive (ERalpha(+)) breast can
280 old subunit in hPAFc, is highly expressed in estrogen receptor alpha-positive (ERalpha(+)) luminal br
281 und develop aggressive, highly aneuploid and estrogen receptor alpha-positive (ERalpha+) mammary aden
282 ndifferentiated, whereas well-differentiated estrogen receptor alpha-positive papillary invasive canc
283 is a well-tolerated, effective treatment for estrogen receptor-alpha-positive (ER+) breast cancer, bu
284 17q23 and 20q13 were frequently amplified in estrogen receptor-alpha-positive luminal breast cancer.
285 variables tested, including staining for the estrogen receptor alpha, progesterone receptor, and c-er
289 however, currently used biomarkers, such as, estrogen receptor-alpha/progesterone receptor (ERalpha/P
290 trate that EMBER confirms a role for the TFs estrogen receptor alpha, retinoic acid receptors alpha a
291 pDC innate functions through cell-intrinsic estrogen receptor alpha signaling, but did not exclude a
293 ymal transition in breast cancer through the estrogen receptor alpha/Slug axis and that it is a poten
294 extracellular signal-related kinase 1/2, and estrogen receptor alpha) that lead to acute cholestasis
295 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 s showed a physical association of Shp2 with estrogen receptor alpha, which is necessary for the syne
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