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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
8 ing cholesterol efflux via activation of the liver X receptor-ABCA1 (LXR-ABCA1) pathway.
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
14 s mediated both by TNFalpha signaling and by liver X receptor activation.
15 rophages and lymphocytes but no induction by liver X receptor activation.
16 n CC via suppression of the inflammasome and liver X receptor activation.
17             Treatment of macrophages with an liver X receptor activator results in up-regulation of A
18 e proliferator-activated receptor (PPAR) and liver X receptor activators increase ABCA12 expression i
19 n inflammatory signaling and derepression of liver X receptor activity.
20        Based on this screen, we formulated a liver X receptor agonist (GW3965) and abolished its live
21  biosynthesis pathways by cotreatment with a liver X receptor agonist further augmented forskolin-ind
22                                            A liver X receptor agonist markedly increases macrophage r
23         Stimulation of ABCA1 expression with liver X receptor agonist or overexpression of heterologo
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
26 l subjects was induced by treatment with the liver X receptor agonist TO-901317.
27 This conversion was Abeta-dependent, because liver-X receptor agonist treatment to promote Abeta degr
28                                              Liver X receptor agonists also inhibited the proliferati
29                     Dissociated sterol-based liver X receptor agonists as therapeutics for chronic in
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
32                            Functionally, the liver X receptor agonists TO901317 and GW3965, two known
33                     We found previously that liver X receptor agonists, which regulate intracellular
34 tly with sensitivity to growth inhibition by liver X receptor agonists.
35  cholesterol and by ABC transporter-inducing liver X receptor agonists.
36 s, whereas the HDL pathway is upregulated by liver X receptor agonists.
37                                              Liver X receptor alpha (LXR alpha) agonists and a high c
38 e present study, we investigated the role of liver X receptor alpha (LXR(alpha)) and LXR(beta) in the
39                             Dysregulation of liver X receptor alpha (LXRalpha) activity has been link
40                The nuclear hormone receptors liver X receptor alpha (LXRalpha) and LXRbeta function a
41 s with many NRs, while L2 interacts with the liver X receptor alpha (LXRalpha) and the estrogen recep
42          Here we show the unexpected role of liver X receptor alpha (LXRalpha) as a direct transcript
43                                 Knockdown of liver X receptor alpha (LXRalpha) inhibited ABC transpor
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
46 -sensitive transcription factor SREBP-1c and liver X receptor alpha (LXRalpha).
47 enic transcription factors, most prominently liver x receptor alpha (LXRalpha).
48  level, and its expression is upregulated by liver X receptor alpha (LXRalpha).
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
54                                 The level of liver X receptor alpha expression correlated directly wi
55                     Retroviral expression of liver X receptor alpha in human breast cancer MDA-MB435S
56 ome proliferator-activated receptor alpha or liver X receptor alpha knockout mice were exposed to str
57 PP diet stimulated the hepatic expression of liver X receptor alpha mRNA.
58 ic gluconeogenesis primarily by upregulating liver X receptor alpha through the natriuretic peptide p
59                                     Although liver X receptor alpha was induced, there was no detecta
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
66                                          The liver X receptors alpha and beta (LXRalpha and LXRbeta)
67 2-related factor 2 (NRF2) but not on nuclear liver X receptors alpha and beta (LXRalpha,beta), peroxi
68                    MASs serve as ligands for liver X receptors alpha and beta(LXRalpha and LXRbeta),
69 hese influences of HLP might be mediated via liver-X receptor alpha (LXRalpha)/ATP-binding cassette t
70                         In addition, nuclear liver x receptor-alpha (LXRa), also regulated by TH, ind
71 mRNA and protein expression by up-regulating liver X receptor-alpha (LXRalpha) in macrophages.
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
74              We determined that ATF6 induces liver X receptor-alpha (LXRalpha), an Mertk-inducing tra
75 r-activated receptor-alpha (PPAR-alpha), and liver X receptor-alpha (LXRalpha).
76 l regulatory element-binding protein-1c, and liver X receptor-alpha and the expression of their targe
77 ncoupling protein-1, or transcription factor liver X receptor-alpha.
78                                 CD68, SR-AI, liver-X-receptor-alpha, and PPARgamma were regulated in
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
86 tor-activated receptor, retinoid X receptor, liver X receptor, and activating protein-1.
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-
90                                              Liver X receptors antagonize TLR4-dependent gene activat
91               Estrogen receptors, PPARs, and liver X receptors are members of the nuclear receptor su
92                  Previous studies identified liver X receptor as the transcription factor controlling
93 xisome proliferator-activated receptor-gamma/liver X receptor/ATP-binding cassette transporter A1 pat
94  ATF-1 coinduces heme oxygenase-1 (HO-1) and Liver X receptor beta (LXR-beta).
95 overy of a novel, potent, orally efficacious liver X receptor beta (LXRbeta) agonist (17).
96  two members of the nuclear receptor family, liver X receptor beta (LXRbeta) and thyroid hormone rece
97               Recent studies have implicated liver X receptor beta (LXRbeta) in key neurodevelopmenta
98 trates a key role for the oxysterol receptor liver X receptor beta (LXRbeta) in the etiology of diabe
99                                              Liver X receptor beta (LXRbeta) is a member of the nucle
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
102 tors are estrogen receptor beta (ERbeta) and liver X receptor beta (LXRbeta).
103    The x-ray crystal structures of the human liver X receptor beta ligand binding domain complexed to
104                     Hepatic triglyceride and liver X receptor, carbohydrate response element-binding
105 is via two receptors: retinoic acid receptor/liver X receptor (cholesterol efflux to lumen) and retin
106 n 2 (SREBP2) target genes, and activation of liver X receptor-controlled genes.
107                   A synthetic agonist of the Liver X receptor depleted cholesterol in GBM cells, slow
108                              Upregulation of liver X receptor dramatically reduced foam cell formatio
109 e transcription through the cis-acting GLUT4-liver X receptor element (LXRE) promoter element.
110 hat include a sterol regulatory element, two liver X receptor elements, and a number of conserved GC
111 responsive promoter elements but not through liver X receptor elements.
112 ts on other related nuclear receptors (i.e., liver X receptor, farnesoid X receptor, estrogen recepto
113                                              Liver X receptors function as central transcriptional re
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
116              Stigmasterol also activated the liver X receptor in a cell-based reporter assay.
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
122  vivo in multiple tissues in response to the liver X receptor ligand T0901317.
123 hages are stimulated by cholesterol loading, liver X receptor ligands, and cyclic AMP, and N-glycosyl
124                                              Liver X receptor (LXR) activates fatty acid synthase (FA
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
128                     We reported earlier that liver X receptor (LXR) activation promotes cellular chol
129 proliferator-activated receptors (PPARs) and liver X receptor (LXR) activators improve permeability b
130                                              Liver X receptor (LXR) activators stimulate keratinocyte
131                   We have identified a novel liver X receptor (LXR) agonist (2) that activates the LX
132 he increase was mimicked by treatment with a liver X receptor (LXR) agonist and required the transcri
133       Enhancing cholesterol efflux using the liver X receptor (LXR) agonist GW3965 significantly decr
134                                            A liver X receptor (LXR) agonist induced expression of ABC
135 an nuclear receptors, the benzenesulfonamide liver X receptor (LXR) agonist N-(2,2,2-trifluoroethyl)-
136                                          The liver X receptor (LXR) agonist TO901317 inhibited the sy
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.
139 , including serum, oxysterols, and synthetic liver X receptor (LXR) agonists.
140 r C-23 positions, were designed as potential liver X receptor (LXR) agonists.
141                                              Liver X receptor (LXR) alpha and beta are members of the
142                                              Liver X receptor (LXR) alpha and LXRbeta function as phy
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
149                       Cholesterol sulfate, a liver X receptor (LXR) antagonist, had marked attenuatio
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
153 he GLUT4 promoter was dependent on the GLUT4 liver X receptor (LXR) binding site.
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
160                 The nuclear hormone receptor liver X receptor (LXR) is induced by insulin and is a ke
161                                              Liver X receptor (LXR) is known to promote hepatic lipog
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
166                        The nuclear receptors liver X receptor (LXR) LXRalpha and LXRbeta are differen
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
169               Expression of genes related to liver X receptor (LXR) signaling changed during progress
170 ated pathway functioned independently of the liver X receptor (LXR) sterol-sensing machinery that is
171 ription regulation retinoid X receptor (RXR)-liver X receptor (LXR) system.
172  cholesterol homeostasis, some of them being liver X receptor (LXR) target genes.
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
177                     Ligand activation of the liver X receptor (LXR), a member of the nuclear hormone
178                                              Liver X receptor (LXR), a nuclear hormone receptor, is a
179                            Activation of the liver X receptor (LXR), a nuclear receptor known to up-r
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
187                       Of the two isoforms of Liver X receptor (LXR), LXRbeta has been shown to have m
188                   Synthetic agonists for the Liver X Receptor (LXR), members of the nuclear hormone r
189                Oxysterols, via activation of liver X receptor (LXR), regulate keratinocyte differenti
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
197 crease in expression of the nuclear receptor liver X receptor (LXR).
198 gus-derived compound, as an inhibitor of the liver X receptor (LXR).
199 hinulin B (NeoB) as a novel inhibitor of the liver X receptor (LXR).
200                   We observed enrichment for liver X receptor (LXR)/retinoid X receptor (RXR) and far
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
205                                              Liver X receptors (LXR) alpha and beta are nuclear oxyst
206                                          The liver X receptors (LXR) alpha and beta are regulators of
207                                              Liver X receptors (LXR) are oxysterol-activated nuclear
208                                              Liver X receptors (LXR) are stimulated by cholesterol-de
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
212                         The nuclear receptor liver-X-receptor (LXR) directly regulates expression of
213 liferator activated receptor (PPAR)gamma and liver-X-receptor (LXR)alpha; and the cholesterol efflux
214                                              Liver X receptor (LXRalpha) and RNA polymerase II (RNA P
215 uclear receptor family transcription factors Liver X Receptors (LXRalpha and -beta) are expressed in
216                                              Liver X receptors (LXRalpha and LXRbeta) are important r
217                                          The liver X receptors (LXRalpha and LXRbeta) are members of
218                Here, we show the role of the liver X receptors (LXRalpha and LXRbeta) in preventing a
219                                           As liver X receptors (LXRalpha,beta) regulate genes linked
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
222                                          The liver X receptors, LXRalpha (NR1H3) and LXRbeta (NR1H2),
223                                              Liver X receptors (LXRs) activate triglyceride synthesis
224                                              Liver X receptors (LXRs) alpha and beta are nuclear rece
225                                              Liver X receptors (LXRs) alpha and beta are transcriptio
226                                              Liver X receptors (LXRs) and farnesoid X receptor (FXR)
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
230       The farnesoid X receptor (FXR) and the liver x receptors (LXRs) are bile acid-activated recepto
231                                              Liver X receptors (LXRs) are cholesterol-sensing nuclear
232                                              Liver X receptors (LXRs) are determinants of hepatic ste
233                                              Liver X receptors (LXRs) are involved in maintaining nor
234                                          The liver X receptors (LXRs) are ligand-activated transcript
235                                              Liver X receptors (LXRs) are ligand-activated transcript
236                                          The liver X receptors (LXRs) are ligand-dependent transcript
237                                              Liver X receptors (LXRs) are lipid-activated nuclear rec
238                                              Liver X receptors (LXRs) are members of the nuclear rece
239                                              Liver X receptors (LXRs) are nuclear receptors involved
240                                              Liver X receptors (LXRs) are nuclear receptors that are
241                                          The liver X receptors (LXRs) are nuclear receptors that play
242                                          The liver X receptors (LXRs) are nuclear receptors with esta
243                                              Liver X receptors (LXRs) are one class of nuclear recept
244                                              Liver X receptors (LXRs) are regulators of cholesterol m
245                                              Liver X receptors (LXRs) are transcription factors invol
246                                              Liver X receptors (LXRs) are transcriptional regulators
247                                          The liver X receptors (LXRs) are transcriptional regulators
248                                              Liver X receptors (LXRs) are transcriptional regulators
249                                              Liver X receptors (LXRs) broadly limit cholesterol accum
250                                              Liver X receptors (LXRs) centrally control reverse chole
251                                              Liver X receptors (LXRs) exert key functions in lipid ho
252              Ligand-dependent SUMOylation of liver X receptors (LXRs) has been found to suppress TLR4
253                                              Liver X receptors (LXRs) have been identified as sterol
254                                          The liver X receptors (LXRs) have been known as sterol senso
255                                              Liver X receptors (LXRs) have previously been implicated
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
258                                              Liver X receptors (LXRs) play a critical role in regulat
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
266                                Activation of liver X receptors (LXRs), one cellular mechanism to regu
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
271 ammation, processes that can be modulated by liver x receptors (LXRs).
272 d via SREBPs nor was it sterol-activated via liver X receptors (LXRs).
273 he control of nuclear receptors, such as the liver X receptors (LXRs).
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
277 rotein-dependent gene expression and promote liver X receptor-mediated responses.
278 LA(2) antagonizes StAR promoter activity and liver X receptor-mediated StAR promoter activation.
279 xisome proliferator-activated receptors, and liver X receptors, modulate lipid metabolism.
280                                              Liver X receptors or LXRs are key modulators of macropha
281 1 cholesterol transporter by agonists of the liver X receptor/peroxisome proliferator-activated recep
282 enhanced the ability of GX sPLA2 to suppress liver X receptor reporter activity.
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
287                                         Many liver X receptor/RXR-related genes (e.g., Scd-1 and Sreb
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
290 otide phosphodiesterase activity secreted by liver X receptor-stimulated human macrophages.
291 of lipidated ApoE, through the activation of liver X receptors, stimulates Abeta degradation.
292 -fed L-sIDOL mice had elevated expression of liver X receptor target genes and proinflammatory genes
293 ulatory element 2, and up-regulation of many liver X receptor target 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
297 roxisome proliferator-activated receptor and liver X receptor 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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