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1 ructures of the thyroid-hormone receptor and retinoid X receptor alpha.
2 strated that PPARalpha bound FARE-1 with the retinoid X receptor alpha.
3 receptor, retinoic acid receptor alpha, and retinoid X receptor alpha.
4 d miR193 expression via transcription factor retinoid X receptor alpha.
5 eptor, constitutive androstane receptor, and retinoid X receptor alpha.
6 nteract with retinoic acid receptor-gamma or retinoid X receptor-alpha.
7 Although forced expression of PPAR gamma and retinoid X receptor alpha activates the enhancer in HIB-
8 gand-dependent transcriptional activation of retinoid X receptor alpha and to a lesser effect on PPAR
10 homodimerization and heterodimerization with retinoid X receptor alpha, and different dimerization in
11 In gel mobility shift experiments, TRalpha, retinoid X receptor-alpha, and mature SREBP-1 formed a t
12 AAT/enhancer binding protein-alpha, receptor retinoid X receptor-alpha, and peroxisome profilerator-a
13 receptors (RARs) alpha, beta, and gamma; and retinoid X receptors alpha, beta, and gamma but were not
14 y shift assays demonstrate that LXRalpha and retinoid X receptor alpha bind to the two LXREs in intro
16 capable of heterodimerizing with that of the retinoid X receptor alpha but not with that of other rec
17 Ralpha, induced the recruitment of PPARalpha:retinoid x receptor alpha, but not PPARgamma coactivator
21 istent with this suggestion, it appears that retinoid X receptor alpha/farnesoid X receptor alpha and
23 interact with the ligand-binding domains of retinoid X receptor alpha, glucocorticoid receptor, and
24 , such as steroid receptor co-activator 1 or retinoid X receptor alpha, had no effect on S14CAT PUFA
26 ic mobility shift assays showed that the PXR-retinoid X receptor alpha heterodimer binds to the DR3-2
27 specific target genes.The vitamin D receptor/retinoid X receptor-alpha heterodimer (VDRRXRalpha) regu
31 X receptor (FXR) via a direct binding of FXR/retinoid X receptor alpha heterodimers to a highly conse
34 stored the DNA binding activity of PPARalpha/retinoid X receptor alpha, induced mRNA levels of PPARal
35 al cardiac defects such as those seen in the retinoid X receptor alpha knockout (Rxra(-/-)) mouse.
38 d to this site as a monomer, because neither retinoid X receptor alpha nor retinoid X receptor beta a
39 form v-ErbA homodimers and heterodimers with retinoid X receptor alpha on differently oriented core m
41 in D receptor, retinoic acid receptor alpha, retinoid X receptor alpha, peroxisome proliferation-acti
42 e receptors, hepatocyte nuclear factor 4 and retinoid X receptor alpha plus peroxisome proliferator-a
43 itation studies confirmed the recruitment of retinoid X receptor alpha, PPARalpha, and PGC1alpha on t
44 arginal interactions with estrogen receptor, retinoid X receptor alpha, PPARalpha, and PPARgamma.
46 erator-activated receptor gamma (PPARgamma), retinoid X receptor alpha proteins, and all-trans retino
49 to be differentially regulated by the murine retinoid X receptor alpha (RXR alpha) as compared with R
50 ctivated receptor gamma (PPAR gamma) and the retinoid X receptor alpha (RXR alpha) form a heterodimer
53 ne expression, the regulatory effects of the retinoid X receptor alpha (RXR alpha) on atrial naturiet
54 s hepatocyte nuclear factor 4 (HNF4) and the retinoid X receptor alpha (RXR alpha) plus peroxisome pr
55 receptor (VDR) and its heterodimeric partner retinoid X receptor alpha (RXR alpha) specifically bound
56 ide substitutions prevent the binding of the retinoid X receptor alpha (RXR alpha)-peroxisome prolife
57 receptor (VDR) acts as heterodimer with the retinoid X receptor alpha (RXR) to control transcription
59 r expression of vitamin D receptor (VDR) and retinoid X receptor-alpha (RXR) has not been investigate
65 port that Nuclear receptor-related 1 (Nurr1):Retinoid X receptor alpha (RXRalpha) activation has a do
66 three closely related human NRs--HNF4alpha, retinoid X receptor alpha (RXRalpha) and COUPTF2--reveal
67 way that strongly inhibits the expression of retinoid X receptor alpha (RXRalpha) and suppresses the
69 tor activated receptor-gamma (PPARgamma) and retinoid X receptor alpha (RXRalpha) complex was found t
71 , we used the Cre-loxP system to disrupt the retinoid X receptor alpha (RXRalpha) gene specifically i
73 nal activation in the context of a PPARalpha.retinoid X receptor alpha (RXRalpha) heterodimeric compl
75 egulated by activators of both PPARgamma and retinoid X receptor alpha (RXRalpha) in a synergistic ma
76 ns that serve as interacting partners of the retinoid X receptor alpha (RXRalpha) in heart, DNA-prote
77 sactivation of BSEP and SHP promoters by FXR/retinoid X receptor alpha (RXRalpha) in HepG2 cells.
79 r partner to class II nuclear receptors, the retinoid X receptor alpha (RXRalpha) plays a vital physi
80 93T, it was possible to demonstrate that the retinoid X receptor alpha (RXRalpha) plus its ligand can
81 epatocyte nuclear factor 4alpha (HNF4alpha), retinoid X receptor alpha (RXRalpha) plus peroxisome pro
82 ediated by hepatocyte nuclear factor 4alpha, retinoid X receptor alpha (RXRalpha) plus peroxisome pro
83 tocyte nuclear factor 4alpha (HNF4alpha) and retinoid X receptor alpha (RXRalpha) plus peroxisome pro
84 ptors hepatocyte nuclear factor 4 (HNF4) and retinoid X receptor alpha (RXRalpha) plus peroxisome pro
86 tor-activated receptor-alpha (PPARalpha) and retinoid X receptor alpha (RXRalpha) stimulate the expre
87 s predicted to interact efficiently with VDR-retinoid X receptor alpha (RXRalpha) was identified in s
88 pharmacologically perturbed the activity of retinoid X receptor alpha (RXRalpha), a key hub within t
91 ctive homodimers to active heterodimers with retinoid X receptor alpha (RXRalpha), and phosphorylatio
92 depends on vitamin A signals mediated by the retinoid X receptor alpha (RXRalpha), as the systemic mu
94 rmone receptor TRalpha1, in combination with retinoid X receptor alpha (RXRalpha), is specifically bo
95 on of RARbeta, but not RARalpha, RARgamma or retinoid X receptor alpha (RXRalpha), on a variety of RA
96 interact in an agonist-dependent manner with retinoid X receptor alpha (RXRalpha), suggesting that th
97 Pbeta), forkhead box protein A2 (FOXA2), and retinoid X receptor alpha (RXRalpha), were markedly decr
98 ln275, Arg316 and Arg371 in nuclear receptor retinoid X receptor alpha (RXRalpha), where berberine co
99 it is very similar in amino acid sequence to retinoid X receptor alpha (RXRalpha), which heterodimeri
100 xisome proliferator-activated receptor alpha-retinoid X receptor alpha (RXRalpha), with which PGC-1be
105 Chinese hamster ovary cells transfected with retinoid X receptor alpha (RXRalpha)/FXR, only chenodeox
106 onstitutive androstane receptor (CAR, NR1I3)/retinoid X receptor alpha (RXRalpha, NR2B1) heterodimer
109 ing protein-alpha (Cebpalpha), Cebpbeta, and retinoid x receptor-alpha (Rxralpha) compared with untre
111 RARalpha formed heterodimers with endogenous retinoid X receptor-alpha (RXRalpha) over RA response el
112 how here that keratinocytic nuclear receptor retinoid X receptor-alpha (RXRalpha) regulates mouse ker
114 brate drugs were abrogated in the absence of retinoid X receptor-alpha (RXRalpha), a molecule known t
115 n availability as hepatic nuclear PPARgamma, retinoid X receptor-alpha (RXRalpha), and PPARgamma/RXRa
120 pha, but were decreased in mice deficient in retinoid X receptor-alpha, the major heterodimerization
121 s, which includes the progesterone receptor, retinoid X receptor alpha, thyroid hormone receptor beta
122 e ability to significantly activate RARs and retinoid X receptor alpha to initiate (TREpal)(2)-tk-CAT
125 mation weight matrix for vitamin D3 receptor/retinoid X receptor alpha (VDR/RXRalpha) binding sites w
126 me proliferator-activated receptor gamma and retinoid-X-receptor alpha, which is further stimulated b
128 e by combining antagonists for PPARgamma and retinoid X receptor alpha with selective estrogen recept
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