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1 or retinoid and thyroid receptor) and N-CoR (nuclear receptor corepressor).
2 cid and thyroid hormone receptor) and N-CoR (nuclear receptor corepressor).
3  mediator for retinoid and thyroid receptors/nuclear receptor corepressor.
4 Atrophin proteins represent a novel class of nuclear receptor corepressors.
5 s to repressed genes by the HDAC activity of nuclear receptor corepressors.
6 acid and thyroid hormone receptor (SMRT) and nuclear receptor corepressor 1 (N-CoR) that accumulated
7        Moreover, targeted inhibition of BCL6/nuclear receptor corepressor 1 (NCoR) complex by peptido
8 ember 1 (Rev-Erbalpha) with its cosuppressor nuclear receptor corepressor 1 (NCOR).
9                                              Nuclear receptor corepressor 1 (NCOR1) and NCOR2 (also k
10                                              Nuclear receptor corepressor 1 (NCoR1) and silencing med
11 hinge region which specifically concentrates nuclear receptor corepressor 1 (NCOR1) at the genome.
12 study, we report that deletion of intestinal nuclear receptor corepressor 1 (NCoR1) completely dimini
13                         Here, we reveal that nuclear receptor corepressor 1 (NCOR1) controls naive an
14                                          The nuclear receptor corepressor 1 (Ncor1) functions as an a
15  which heme binding to Rev-erbalpha recruits nuclear receptor corepressor 1 (NCoR1) into an active re
16                                              Nuclear receptor corepressor 1 (NCoR1) is considered to
17 ction with the histone deacetylase 3 (HDAC3)-nuclear receptor corepressor 1 (NCoR1) repressor complex
18                                          The nuclear receptor corepressor 1 (NCOR1) was reported to m
19     Among the best-known coregulators is the nuclear receptor corepressor 1 (NCoR1).
20 ely ablated in skin keratinocytes for either nuclear receptor corepressor 1 (NCoR1)/silencing mediato
21 ant mice and in mice ablated selectively for nuclear receptor corepressor 1 (NCoR1)/silencing mediato
22 tes the complex mediator of transcription 13/nuclear receptor corepressor 1 axis, which in turn promo
23                                 Knockdown of nuclear receptor corepressor 1 in primary male T cells a
24 e-mediated autophagy - and its co-repressor, nuclear receptor corepressor 1, resulting in changes of
25 nd the nuclear receptor-interacting protein, nuclear receptor corepressor 1, to specific cis-regulato
26 SUMOylation of LXRs, but not the presence of nuclear receptor corepressor 1, was required for repress
27 em, HDAC3 is unique in that interaction with nuclear receptor corepressors 1 and 2 (NCoR1/2) is requi
28 creased the interaction between TR-alpha and nuclear receptor corepressor 2 (NCOR2) and suppressed Pl
29 encing Transcription Factor (CoREST) and the Nuclear Receptor Corepressor 2 (NCOR2).
30 due to loss of glucose homeostasis regulator nuclear receptor corepressor 2 repression, and chromatin
31 due to loss of glucose homeostasis regulator nuclear receptor corepressor 2 repression, and chromatin
32                                       NCOR2 (nuclear receptor corepressor 2) SNP rs150954431 was asso
33 RF7 promoter region through interaction with nuclear receptor corepressor 2/histone deacetylase 3 for
34 l coactivator) and the dissociation of NCoR (nuclear receptor corepressor, a transcriptional corepres
35  expression in vivo and indicates a role for nuclear receptor corepressors and associated histone dea
36 h the deacetylase-activation domain (DAD) of nuclear receptor corepressors and inositol tetraphosphat
37                                       NCoR1 (nuclear receptor corepressor) and SMRT (silencing mediat
38                      The corepressors N-CoR (nuclear receptor corepressor) and SMRT (silencing mediat
39 local chromatin condensation, recruitment of nuclear receptor corepressor, and histone deacetylase co
40 T (switching-defective protein 3, adaptor 2, nuclear receptor corepressor, and transcription factor I
41                             Depletion of the nuclear receptor corepressor by specific short interferi
42  histone deacetylase shown to be part of the nuclear receptor corepressor complex.
43  clock, and regulates its interaction with a nuclear receptor corepressor complex.
44 ults suggest that atrophin-1 associates with nuclear receptor corepressor complexes and is involved i
45                Cytokine-induced clearance of nuclear receptor corepressor complexes was inhibited by
46 stem, we identified ETO/MTG8, a component of nuclear receptor corepressor complexes, as an atrophin-1
47                  These data suggest that the nuclear receptor corepressors decrease PPARgamma transcr
48     To explore this possibility, we examined nuclear receptor corepressor expression in a panel of no
49 a structurally and functionally more related nuclear receptor corepressor family and suggest an addit
50  HDAC3 complex that contained members of the nuclear receptor corepressor family.
51 ly associated with glutathione S-transferase-nuclear receptor corepressor fragments harboring one of
52 iator retinoid and thyroid hormone receptors/nuclear receptor corepressors), has been reported as the
53 utually exclusive and sequential manner: the nuclear receptor corepressor-HDAC3 complex followed by n
54 ther, our results demonstrate involvement of nuclear receptor corepressor/histone deacetylase complex
55             The Hairless (Hr) gene encodes a nuclear receptor corepressor (HR) that is essential for
56 th coactivators, the GyK gene is targeted by nuclear receptor corepressors in adipocytes.
57 e of another class of nuclear cofactors, the nuclear receptor corepressors, in modulating PPARgamma t
58 in immunoprecipitation assays indicated that nuclear receptor corepressor is present on the endogenou
59                                       N-CoR (nuclear receptor corepressor) is a corepressor for multi
60          Moreover, SMRT, but not the related Nuclear Receptor Corepressor, is required for cellular r
61 -like nuclear export signal that resembles a nuclear receptor corepressor motif (aa 86-95) impaired t
62  oncogenic fusion proteins interact with the nuclear receptor corepressor N-CoR and, in comparison wi
63                                          The nuclear receptor corepressor N-CoR plays a crucial role
64 more, we demonstrate that DAX-1 recruits the nuclear receptor corepressor N-CoR to SF-1, whereas natu
65  the binding of RXR ligands and recruits the nuclear receptor corepressor N-CoR, PPAR permits the bin
66 e we demonstrate that ETO interacts with the nuclear receptor corepressor N-CoR, the mSin3 corepresso
67 ruitment of a corepressor complex, including nuclear receptor corepressor N-CoR, which, unexpectedly,
68 nal sequence that is highly conserved to the nuclear receptor corepressor N-CoR.
69                                              Nuclear receptor corepressors N-CoR and SAFB1 were bound
70 nd cell-based assays to demonstrate that the nuclear receptor corepressors N-CoR and SMRT interact wi
71 ze that corepressor complexes containing the nuclear receptor corepressor (N-CoR) are key factors in
72                                 Detection of nuclear receptor corepressor (N-CoR) association with RA
73  Several lines of evidence indicate that the nuclear receptor corepressor (N-CoR) complex imposes lig
74                                              Nuclear receptor corepressor (N-CoR) depletion increased
75 he tamoxifen-mediated association of ER with nuclear receptor corepressor (N-CoR) in the antiestrogen
76   Reduced H4 acetylation and increased HDAC1/nuclear receptor corepressor (N-CoR) occupancy at some T
77  nuclear receptors correlates with levels of nuclear receptor corepressor (N-CoR) protein.
78 tivated ERalpha, HDAC inhibitor (HDAC1), and nuclear receptor corepressor (N-CoR) that bound the slug
79 knowledge, that the HDAC3 complex, including nuclear receptor corepressor (N-CoR), transducin-beta-li
80 ETO binds to the human homolog of the murine nuclear receptor corepressor (N-CoR).
81 onserved MYND domain that interacts with the nuclear receptor corepressor (N-CoR).
82 TR) actively represses transcription via the nuclear receptor corepressor (N-CoR)/histone deacetylase
83 s similar to the binding motifs proposed for nuclear receptor corepressors (N-CoR and SMRT).
84                                              Nuclear receptor corepressors (N-CoR) and silencing medi
85 erving to mediate a required exchange of the nuclear receptor corepressors, N-CoR and SMRT, for coact
86 on requires signal-dependent turnover of the nuclear receptor corepressor NCoR from target promoters,
87 alytic activity by missense mutations in the nuclear receptor corepressor (NCOR or SMRT) does not cau
88   Mutations abolishing interactions with the nuclear receptor corepressor (NCOR or SMRT) render HDAC3
89 athway suppressor 2 (GPS2), a subunit of the nuclear receptor corepressor (NCOR) and histone deacetyl
90 irect DNA binding of the receptor along with nuclear receptor corepressor (NCoR) and silencing mediat
91              Here, we report that, while the nuclear receptor corepressor (NCoR) and silencing mediat
92 ance AR recruitment of corepressor proteins [nuclear receptor corepressor (NCoR) and silencing mediat
93 eptor interacting motifs of the corepressors nuclear receptor corepressor (NCoR) and silencing mediat
94                                          The nuclear receptor corepressor (NCoR) and the related fact
95 using a mammalian two-hybrid assay, that the nuclear receptor corepressor (NCoR) and the silencing me
96                Such corepressors include the nuclear receptor corepressor (NCoR) and the silencing me
97  LXRs are dependent on interactions with the nuclear receptor corepressor (NCoR) and the silencing me
98  and thyroid hormone receptor (SMRT) and the nuclear receptor corepressor (NCoR) are negative regulat
99                        HDAC3, HDAC4, and the nuclear receptor corepressor (NCoR) are required for eff
100 ted the binding of the histone deacetylase 3-nuclear receptor corepressor (NCoR) complex to the COX-2
101                          We demonstrate that nuclear receptor corepressor (NCoR) enhances thyroid hor
102 )-dependent derepression of AP-1 by removing nuclear receptor corepressor (NCoR) from the chemokine p
103              We generated adipocyte-specific Nuclear Receptor Corepressor (NCoR) knockout (AKO) mice
104                                          The nuclear receptor corepressor (NCoR) regulates the activi
105                                              Nuclear receptor corepressor (NCoR) was demonstrated to
106 ory proteins in HeLa S3 cells, including the nuclear receptor corepressor (NCoR), TIF1beta/KAP-1, HDA
107 t of two epigenetic modifying complexes, the nuclear receptor corepressor (NCoR)-histone deacetylase
108 -binding domain, which targets PPAR-gamma to nuclear receptor corepressor (NCoR)-histone deacetylase-
109 actions of TH as well as in mice with mutant nuclear receptor corepressor (NCoR).
110 the interaction of the MeCP2 with DNA or the nuclear receptor corepressor (NCoR)/silencing mediator o
111 om repressive to activating functions of the nuclear receptor corepressor (NCoR)/silencing mediator o
112 on of PPRE-bound PV with corepressors [e.g., nuclear receptor corepressor (NCoR)] that led to transcr
113 n in human breast cancer cells by recruiting nuclear receptor corepressors (NCoR and SMRT) and histon
114                             We show that the nuclear receptor corepressor NCoR1 is a key target of pr
115  via downregulation of the tumor-suppressive nuclear receptor corepressor NCOR1.
116  its derived mouse model harboring a mutated nuclear receptor corepressor (NCOR1DeltaID) (Thra1(PV/+)
117                                              Nuclear receptor corepressors (NCORs) are transcription
118       HDAC3 exists in tight association with nuclear receptor corepressors (NCoRs) NCoR1 and NCoR2 (a
119 d the formation of a functional complex with nuclear receptor corepressors (NCORs) were critical in r
120                Transcriptional repression by nuclear receptor corepressors plays a critical role in T
121 noid and thyroid hormone receptor (SMRT) and nuclear receptor corepressor protein (NCoR) are corepres
122 iptional activity through the recruitment of nuclear receptor corepressor protein and silencing media
123 f retinoid and thyroid receptors) and N-CoR (nuclear receptor corepressor) recruit histone deacetylas
124     Results from these studies indicate that nuclear receptor corepressor recruitment is a key featur
125                      MEK1 interacts with the nuclear receptor corepressor silencing mediator of retin
126                                          The nuclear receptor corepressor, silencing mediator of reti
127 using the conserved carboxyl terminus of the nuclear receptor corepressor SMRT as a bait led to the i
128   Histone deacetylase 3 (HDAC3) requires the nuclear receptor corepressor SMRT for HDAC enzyme activi
129                           The recruitment of nuclear receptor corepressor SMRT/N-CoR and subsequent r
130 ne deacetylases (HDAC)5 and 7 along with the nuclear receptor corepressors SMRT (silencing mediator f
131                                              Nuclear receptor corepressors SMRT (silencing mediator o
132 t SMRTER, an insect analog of the vertebrate nuclear receptor corepressors SMRT and N-CoR, interacts
133                           ETO interacts with nuclear receptor corepressors SMRT and N-CoR, which recr
134 on of target genes via interactions with the nuclear receptor corepressors SMRT and NCoR.
135  well as its molecular interactions with the nuclear receptor corepressor, SMRT, and nuclear receptor
136  highlight an unexpected new function of the nuclear receptor corepressor SMRTe for its role in regul
137            We describe here the cloning of a nuclear receptor corepressor that we call SUN-CoR (Small
138 expression, Hr likely defines a new class of nuclear receptor corepressors that serve a more speciali
139 n serve as an adapter molecule that recruits nuclear receptor corepressors to DNA-bound nuclear recep
140 repressor that we call SUN-CoR (Small Unique Nuclear receptor CoRepressor), which shows no homology t

 
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