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1 olog of the mammalian vitamin D receptor and liver X receptor.
2 upregulation of key lipogenic enzymes by the liver X receptor.
3 eta secretion, suggesting the involvement of liver X receptor.
4 These effects were mediated by liver X receptors.
5 g tissue-specific modulation of estrogen and liver X receptors.
6 rtant model for the vertebrate vitamin D and liver X receptors.
7 genase 1 and reduced foam cell formation via liver X receptor, a potent combination for treating athe
9 erference reduced the expression of ABCG1 in liver X receptor-activated macrophages and caused a para
10 ontrast, lipodystrophy (aP2-SREBP-1c436) and liver X receptor activation (T0901317), which increase d
11 progenitors by reconstituted HDL infusion or liver X receptor activation remain promising approaches
12 lesterol efflux pathways by HDL infusions or liver X receptor activation results in suppression of he
13 , whereas on upregulation of transporters by liver X receptor activation, PM sterol was shifted to th
18 e proliferator-activated receptor (PPAR) and liver X receptor activators increase ABCA12 expression i
21 biosynthesis pathways by cotreatment with a liver X receptor agonist further augmented forskolin-ind
24 ctivity by approximately 5-fold and that the liver X receptor agonist T0901317 (a known activator of
25 e cancer LNCaP cell lines with the synthetic liver X receptor agonist T0901317 decreased the percenta
27 This conversion was Abeta-dependent, because liver-X receptor agonist treatment to promote Abeta degr
30 rolling tumor cell proliferation; therefore, liver X receptor agonists may have utility as antitumori
31 ndent cancers, we investigated the effect of liver X receptor agonists on prostate and breast cancer
38 e present study, we investigated the role of liver X receptor alpha (LXR(alpha)) and LXR(beta) in the
41 s with many NRs, while L2 interacts with the liver X receptor alpha (LXRalpha) and the estrogen recep
44 activation of TLR-mediated innate immune and liver X receptor alpha (LXRalpha) signaling pathways.
45 nuclear hormone receptor for oxysterols, the liver X receptor alpha (LXRalpha), regulates cholesterol
49 ion of the anti-atherogenic nuclear receptor liver X receptor alpha (LXRalpha; Nr1h3) and its downstr
50 Recently, we identified an enrichment of liver X receptor alpha and beta (LXRalpha/beta) in the n
51 o 6-fold increases in foam cells of mRNA for liver X receptor alpha and cholesterol efflux factors AB
52 me proliferator-activated receptor alpha and liver X receptor alpha as well as with the circadian osc
53 e proliferator-activated receptor gamma, and liver X receptor alpha but was unable to reduce accumula
56 ome proliferator-activated receptor alpha or liver X receptor alpha knockout mice were exposed to str
58 ic gluconeogenesis primarily by upregulating liver X receptor alpha through the natriuretic peptide p
60 er for the nuclear hormone receptor known as liver X receptor alpha, (LXRalpha [NR1H3]), which is the
61 ased, as are key lipid metabolism regulators liver X receptor alpha, peroxisome proliferator-activate
62 BP) alpha, C/EBPbeta, C/EBPdelta, PPARgamma, liver X receptor alpha, sterol regulatory element-bindin
63 ompanied by a significant stimulation of the liver X receptor alpha-ATP-binding cassette transporter
64 317 induces dramatic up-regulation of p27 in liver X receptor alpha-overexpressing MDA-MB435S cells.
65 alpha activity (z = 2.0, P = 6.6 x 10(-7)), liver X receptor alpha/beta agonism (z = 2.1, P = 2.8 x
67 2-related factor 2 (NRF2) but not on nuclear liver X receptors alpha and beta (LXRalpha,beta), peroxi
69 hese influences of HLP might be mediated via liver-X receptor alpha (LXRalpha)/ATP-binding cassette t
72 have shown that the nuclear hormone receptor liver X receptor-alpha (LXRalpha) is a major transcripti
73 epatic DNL was due to coactivation by Vpr of liver X receptor-alpha (LXRalpha) with increased express
76 l regulatory element-binding protein-1c, and liver X receptor-alpha and the expression of their targe
79 liferator-activated receptor (PPAR)gamma and liver-X-receptor-alpha, and the cholesterol efflux pump
80 reased activity of RXR heterodimer partners, liver X receptor and peroxisome proliferator-activated r
81 gmented when fed an HFD providing ligands to liver X receptor and peroxisome proliferator-activated r
82 A1 transcription includes the binding of the liver X receptor and retinoid X receptor (LXR/RXR) heter
83 ells, which express low levels of endogenous liver X receptors and are insensitive to T0901317, sensi
84 C on ISR gene expression were independent of liver X receptors and sterol-response element-binding pr
85 ions between TLR-signalling pathways and the liver-X receptor and peroxisome proliferator-activated r
87 erator-activated receptor alpha (PPARalpha), liver X receptor, and their obligate heterodimer partner
88 some proliferator-associated receptor gamma, liver X receptor, and vitamin D receptor in shaping the
89 ocused reviews on estrogen receptors, PPARs, liver X receptors, and the PPARgamma coactivator-1 (PGC-
93 xisome proliferator-activated receptor-gamma/liver X receptor/ATP-binding cassette transporter A1 pat
96 two members of the nuclear receptor family, liver X receptor beta (LXRbeta) and thyroid hormone rece
98 trates a key role for the oxysterol receptor liver X receptor beta (LXRbeta) in the etiology of diabe
100 were associated with increased expression of liver X receptor beta (LXRbeta), a nuclear receptor that
101 However, deletion of the nuclear receptor, liver X receptor beta (LXRbeta), had an adverse effect o
103 The x-ray crystal structures of the human liver X receptor beta ligand binding domain complexed to
105 is via two receptors: retinoic acid receptor/liver X receptor (cholesterol efflux to lumen) and retin
110 hat include a sterol regulatory element, two liver X receptor elements, and a number of conserved GC
112 ts on other related nuclear receptors (i.e., liver X receptor, farnesoid X receptor, estrogen recepto
114 me proliferator-activated receptors, and the liver X receptor have demonstrated significant potential
115 is minimal, regulatory regions responsive to liver X receptor have remained elusive, but no longer; t
117 It is believed that 27HC, acting through the liver X receptor in macrophages and possibly other cells
118 that GX sPLA(2) suppresses activation of the liver X receptor in macrophages, resulting in reduced ex
119 roxisome proliferator-activated receptor and liver X receptor in the control of lipid-dependent gene
120 me proliferator-activated receptor gamma and liver X receptors in coordination with retinoid X recept
121 ated by oxidized low-density lipoprotein and liver X receptors indicates coordinated and reciprocal c
123 hages are stimulated by cholesterol loading, liver X receptor ligands, and cyclic AMP, and N-glycosyl
125 In contrast to FXR, this study showed that liver X receptor (LXR) activation by LXR agonists and ad
126 roliferators-activated receptors (PPARs) and liver X receptor (LXR) activation improved epidermal per
127 ipid-remodeling enzyme LPCAT3 in response to liver X receptor (LXR) activation promoted SREBP-1c proc
129 proliferator-activated receptors (PPARs) and liver X receptor (LXR) activators improve permeability b
132 he increase was mimicked by treatment with a liver X receptor (LXR) agonist and required the transcri
135 an nuclear receptors, the benzenesulfonamide liver X receptor (LXR) agonist N-(2,2,2-trifluoroethyl)-
137 rying amounts of cholesterol, treated with a liver X receptor (LXR) agonist, or injected intravenousl
138 urvival, rendering these tumors sensitive to Liver X receptor (LXR) agonist-dependent cell death.
143 CCAAT/enhancer binding protein (CEBP) alpha, liver X receptor (LXR) and H3K4me3 and microRNA target i
144 osynthesis is transcriptionally regulated by liver X receptor (LXR) and its gene target, sterol regul
145 investigated the regulation of mouse SCD1 by liver X receptor (LXR) and its role in plasma lipoprotei
146 ctivation of C3 expression mainly depends on liver X receptor (LXR) and partly on Toll-like receptor
147 This review summarizes evidence that the liver X receptor (LXR) and peroxisome proliferator-activ
148 hepatocyte nuclear factor (HNF)-4alpha, and liver X receptor (LXR) and the transcription factors ste
150 receptor (PPAR) alpha, beta/delta, gamma and liver X receptor (LXR) are members of the nuclear recept
151 express a specific subset of NRs, including liver X receptor (LXR) beta and peroxisome proliferator-
152 ptional downregulation required the putative liver X receptor (LXR) binding site in the human GLUT4 g
154 element binding protein 2 (SREBP-2) and the liver X receptor (LXR) control antagonistic transcriptio
155 e we show that the sterol-responsive nuclear liver X receptor (LXR) helps maintain cholesterol homeos
156 differentiation due to the formation of RXR/liver X receptor (LXR) heterodimers, which induced expre
157 is report, we reveal a novel function of the liver X receptor (LXR) in preventing APAP-induced hepato
158 ransporter ABCA1, and its upstream regulator Liver X receptor (LXR) in the macrophages exposed to oxL
159 endent) reverse cholesterol transport (RCT), liver X receptor (LXR) is an attractive target for the t
162 mary metabolite of cholesterol and an ER and liver X receptor (LXR) ligand, increases ER-dependent gr
163 d the effect on HIV infection of a synthetic liver X receptor (LXR) ligand, N-(2,2,2-trifluoro-ethyl)
164 overexpressing HSL increased the efficacy of liver X receptor (LXR) ligands on StAR expression and st
165 To examine the therapeutic potential of liver X receptor (LXR) ligands, APP23 mice were fed HF d
167 e show that SIRT1 is a positive regulator of liver X receptor (LXR) proteins, nuclear receptors that
168 we show that activation of nuclear receptor liver X receptor (LXR) sensitized mice to lithogenic die
170 ated pathway functioned independently of the liver X receptor (LXR) sterol-sensing machinery that is
173 ing cassette transporter ABCG1, a macrophage liver X receptor (LXR) target, has been shown to stimula
174 PP)-activated receptor alpha (PPARalpha) and liver X receptor (LXR) through regulation of genes invol
175 s synthetic agonists induce fatty liver, the liver X receptor (LXR) transcription factor remains a ta
176 regulation of IDOL by the sterol-responsive liver X receptor (LXR) transcription factors, induction
180 imulates the transcriptional activity of the liver X receptor (LXR), a nuclear receptor that coordina
181 -hydroxycholesterol, a natural ligand of the liver X receptor (LXR), and the LXR synthetic agonist T0
182 tion of Akr1b7 by PXR was independent of the liver X receptor (LXR), another nuclear receptor known t
183 or-activated receptor gamma (PPARgamma), and liver X receptor (LXR), are potent inhibitors of TLR-ind
184 gulated by thyroid hormone receptor (TR) and liver X receptor (LXR), both of which control hepatic ch
185 SREBP-1c gene expression is induced by the liver X receptor (LXR), but CA-FoxO1 did not block the a
186 ntly the oxysterols, the natural ligands for liver X receptor (LXR), induced these genes via upregula
190 A1), which is regulated by activation of the liver X receptor (LXR), was suppressed in epithelial cel
191 ic cells triggers the lipid-sensing receptor liver X receptor (LXR), which in response upregulates th
192 ol synthesis, and 2) decreased expression of liver X receptor (LXR)-alpha, LXR-beta, and ATP-binding
193 B mediates their beneficial effects, in both liver x receptor (LXR)-dependent and independent manners
194 oxysterols recruit protumor neutrophils in a liver X receptor (LXR)-independent, CXCR2-dependent mann
195 ession of atherosclerotic plaques in part by liver X receptor (LXR)-mediated induction of the chemoki
196 SMILE in the regulation of nuclear receptor liver X receptor (LXR)-mediated sterol regulatory elemen
201 ular cholesterol to apoA-I and is induced by liver X receptor (LXR)/retinoid X receptor (RXR) transcr
202 n of nuclear receptors (NRs), especially the liver X receptor (LXR)/retinoid X receptor heterodimer,
203 deregulation of the miR-155 target gene the liver X receptor (LXR)alpha in lung fibroblasts and macr
204 ulfonamides were identified in a HTS as dual liver X receptor (LXR, NR1H2, and NR1H3) ligands, and th
209 eptor agonists showed that activation of the liver X receptors (LXR) dramatically promoted lipid accu
210 s, which are ligands for the nuclear hormone liver X receptors (LXR), decrease amyloid beta (Abeta) s
211 The accumulation of desmosterol, a known liver-X receptor (LXR) activator, was associated with in
213 liferator activated receptor (PPAR)gamma and liver-X-receptor (LXR)alpha; and the cholesterol efflux
215 uclear receptor family transcription factors Liver X Receptors (LXRalpha and -beta) are expressed in
220 "cholesterol-sensing" nuclear receptors, the liver X receptors (LXRalpha/LXRbeta), protects against a
221 due to the simultaneous coactivation of the liver X receptor, LXRalpha, a nuclear hormone receptor w
227 egulated by nuclear receptors, including the liver X receptors (LXRs) and peroxisome-proliferator rec
228 Here, we provide evidence that activation of liver X receptors (LXRs) and retinoid X receptors (RXRs)
229 table to accumulation of excess cholesterol, liver X receptors (LXRs) and the farnesoid X receptor (F
256 report studies investigating the role of the liver X receptors (LXRs) LXRalpha and LXRbeta in carbohy
257 Recent studies in rodent models suggest that liver X receptors (LXRs) may play an important role in t
259 that acts in a coupled metabolic cycle with Liver X Receptors (LXRs) to increase brain apolipoprotei
260 retinoid-related orphan receptors (RORs) and liver X receptors (LXRs) were postulated to have distinc
261 oliferator activated receptor (PPAR) family, liver X receptors (LXRs), and farnesoid X receptor (FXR)
262 Idol is a direct target for regulation by liver X receptors (LXRs), and its expression is responsi
263 Proliferator-Activated Receptors (PPARs) and Liver X Receptors (LXRs), are lipid-sensing receptors th
264 hat specific cholestenoic acids activate the liver X receptors (LXRs), enhance islet-1 expression in
265 rally occurring hydroxysterol agonist of the liver X receptors (LXRs), members of the nuclear recepto
267 ptors (PPARs), farnesoid X receptors (FXRs), liver X receptors (LXRs), retinoid-related orphan recept
268 ng through transcription factors such as the liver X receptors (LXRs), sterol regulatory element-bind
269 rly all of the transrepression activities of liver X receptors (LXRs), they can be selectively recrui
270 - to 11-fold) requires two binding sites for liver X receptors (LXRs), which are nuclear receptors th
274 y 1, group H, members 2 and 3 (also known as liver X receptors [LXRs]) regulate genes involved in cho
275 ession and failure to appropriately activate liver X receptor-mediated (LXR-mediated) pathways, ultim
276 ocorticoid production, likely by suppressing liver X receptor-mediated activation of steroidogenic ac
278 LA(2) antagonizes StAR promoter activity and liver X receptor-mediated StAR promoter activation.
281 1 cholesterol transporter by agonists of the liver X receptor/peroxisome proliferator-activated recep
283 Identification and characterization of four liver X receptor response elements in the intron downstr
284 rophages, resulting in reduced expression of liver X receptor-responsive genes including ATP-binding
285 and ATP-binding cassette transporter G1 are liver X receptor-responsive macrophage genes that promot
286 lving inhibition of matrix metalloproteases, liver X receptor/retinoid X receptor, nuclear factor ery
288 Based on these results, modulation of the liver X receptor signaling pathway is a new target for c
289 t occur in response to insulin signaling and liver X receptor signaling would be predicted to increas
292 -fed L-sIDOL mice had elevated expression of liver X receptor target genes and proinflammatory genes
294 expression of transcription factors such as liver X Receptor, the sterol regulatory element binding
295 oxisome proliferator-activated receptors and liver X receptor, these proteins sense the presence of u
296 oxisome proliferator-activated receptors and liver X receptors, this family of transcription factors
298 PPARdelta expression (but not other PPARs or liver X receptors), whereas PPARdelta knockdown by siRNA
299 acons for additional factors, exemplified by liver X receptors, which drive both cell-specific gene e
300 e pathway is sensitive to transrepression by liver X receptors, while the CaMKII-dependent pathway is
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