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1 atisfies a number of important criteria as a nuclear receptor coactivator.
2 rginine methyltransferase 1 (PRMT1), another nuclear receptor coactivator.
3 vation surface for binding the p160 class of nuclear receptor coactivators.
4 activation in vivo and suggest redundancy in nuclear receptor coactivators.
5 or 2, thereby establishing a novel family of nuclear receptor coactivators.
6 istence of a new complex of novel functional nuclear receptor coactivators.
7 omoters, which can be further potentiated by nuclear receptor coactivators.
8 NRC and PNRC2 are members of a new family of nuclear receptor coactivators.
9 sitivity, in part, by reducing levels of key nuclear receptor coactivators.
10 ng consistently enables PPARgamma to recruit nuclear receptor coactivators.
11 ceptors is mediated by the 160-kDa family of nuclear receptor coactivators.
12                           ROR-gamma recruits nuclear receptor coactivator 1 and 3 (NCOA1 and NCOA3, a
13 me 8q13 (rs10091374; P=9.06x10(-9)) near the nuclear receptor coactivator 2 (NCOA2) gene.
14                      Here we determined that nuclear receptor coactivator 2 (NCoA2, also known as SRC
15                                      Steroid nuclear receptor coactivator 2 (SRC2) is a member of a f
16                  Increased reactivity toward nuclear receptor coactivator 2 was also observed in pati
17                          PNRC2 (Proline-rich Nuclear Receptor Coactivator 2) was previously identifie
18 ith higher affinity than to the coactivator, nuclear receptor coactivator-2 (Tif2), in coregulator pe
19              Here we show that activation of nuclear receptor coactivator 3 (NCOA3) promotes melanoma
20  regulators, including RNA polymerase II and nuclear receptor coactivator-3.
21                      The interaction between nuclear receptor coactivator 4 (NCOA4) and the iron stor
22 NA-seq in human reticulocytes and identified nuclear receptor coactivator 4 (NCOA4) as a critical reg
23                                              Nuclear receptor coactivator 4 (NCOA4) is a critical car
24 the sole cytosolic iron storage protein, and nuclear receptor coactivator 4 (NCOA4) mediates the auto
25                  Like known cargo receptors, nuclear receptor coactivator 4 (NCOA4) was highly enrich
26  the lysosomes, through its interaction with nuclear receptor coactivator 4 for degradation and relea
27          Finally, we found that silencing of nuclear receptor coactivator 4 prevented accumulation of
28                                       NCOA4 (nuclear receptor coactivator 4) is a widely expressed in
29                      We found overexpressing nuclear receptor coactivator 4, a key adaptor for ferrit
30                    In addition, knockdown of nuclear receptor coactivator 4, the adaptor protein for
31  we report that heterozygous deletion of the nuclear receptor coactivator-5 (Ncoa5) gene resulted in
32                                              Nuclear receptor coactivator 6 (NCOA6) also known as PRI
33                                              Nuclear receptor coactivator 6 (NCOA6) is a multifunctio
34                            Here, we identify Nuclear receptor coactivator 6 (Ncoa6), a subunit of the
35                                          The nuclear receptor coactivator 6 (NCoA6; also AIB3, PRIP,
36                                 We show that nuclear receptor coactivator-6 (NCOA6), a reported coact
37                       We recently found that nuclear receptor coactivator 7 (Ncoa7) and Oxr1 interact
38                                              Nuclear receptor coactivator 7 (NCOA7) deficiency in end
39 ing site of PRMT1 substantially crippled its nuclear receptor coactivator activity.
40                                          The nuclear receptor coactivator AIB1 (amplified in breast c
41 were validated with a probe specific for the nuclear receptor coactivator AIB1 that maps to chromosom
42 y be mediated through MAPK activation of the nuclear receptor coactivator AIB1.
43 cer often requires the overexpression of the nuclear receptor coactivator AIB1/SRC-3 acting in conjun
44            The DRIPs are distinct from known nuclear receptor coactivators, although like these coact
45 The amplified-in-breast cancer 3 (AIB3) is a nuclear receptor coactivator amplified and overexpressed
46                                          The nuclear receptor coactivator amplified in breast cancer
47                                          The nuclear receptor coactivator amplified in breast cancer
48                       Here, we show that the nuclear receptor coactivator amplified in breast cancer
49  receptor (GR) is able to interact with both nuclear receptor coactivators and the BRG1 chromatin-rem
50 properties that are consistent with those of nuclear receptor coactivators and with RNA spliceosome c
51 id-, leucine-rich protein 1 (PELP1), a novel nuclear receptor coactivator, and its expression is dere
52 ectly involve, at the transcriptional level, nuclear receptors, coactivators, and proteins of the cel
53 omoted by the estrogen receptor pathway, and nuclear receptor coactivators are thought to participate
54 anism is competition for limiting amounts of nuclear receptor coactivators between the 5' D-I promote
55 omain (TAD) of p53, the TAZ1, TAZ2, KIX, and nuclear receptor coactivator binding domains of CBP, and
56                Our study also reveals that a nuclear receptor coactivator can act in the periphery of
57 naling by the essential C-terminal AD of the nuclear receptor coactivator CoCoA; they indicate that p
58                 Three components of the p160 nuclear receptor coactivator complex, including CARM1, p
59 we report that another component of the p160 nuclear receptor coactivator complex, the coiled-coil co
60 R function by preventing the assembly of CBP-nuclear receptor coactivator complexes, revealing differ
61 (MLL2/ALR), a core component of COMPASS-like nuclear receptor coactivator complexes.
62 ing the probabilistic formation of transient nuclear receptor-coactivator complexes with its molecula
63 e report the cloning and analysis of a novel nuclear receptor coactivator (designated NRIF3) that exh
64                         In common with other nuclear receptor coactivators, DRIP205 interaction occur
65 entification and characterization of a novel nuclear receptor coactivator, ERAP140.
66                       Members of the 160-kDa nuclear receptor coactivator family (p160 coactivators)
67 vator-3 (SRC-3)/AIB1 is a member of the p160 nuclear receptor coactivator family involved in developm
68  in breast cancer 1, is a member of the p160 nuclear receptor coactivator family involved in transcri
69 dies indicate that steroid receptors require nuclear receptor coactivators for efficient transcriptio
70      BAF57 has previously been implicated in nuclear receptor coactivator function, and we show that,
71     AIB1 (amplified in breast cancer 1) is a nuclear receptor coactivator gene amplified and overexpr
72 bind the C-terminal activation domain of the nuclear receptor coactivator GRIP1, we identified a new
73                  In the past few years, many nuclear receptor coactivators have been identified and s
74 d the hSP-B promoter with RARalpha, CBP, and nuclear receptor coactivators in H441 cells.
75                                              Nuclear receptor coactivators include histone acetyltran
76                       TTF-1 is acetylated by nuclear receptor coactivators including the activator of
77                          Members of the p160 nuclear receptor coactivators interact with liganded nuc
78  In this study, we report the isolation of a nuclear receptor coactivator-interacting protein from a
79 new structural parameters for modulating the nuclear receptor-coactivator interaction based on linear
80 -activated receptor binding protein (PBP), a nuclear receptor coactivator, interacts with estrogen re
81      Acetylation of transcription factors by nuclear receptor coactivators is an important mechanism
82 nduced blockade of GR transactivation at the nuclear receptor coactivator level, upstream and indepen
83 rst LXXLL motif is the most potent among all nuclear receptor coactivator motifs tested, and only thi
84 ound receptor, which subsequently recruits a nuclear receptor coactivator (NCoA) complex.
85 d receptor coactivators (SRCs) SRC-1, SRC-2 [nuclear receptor coactivator (NCOA)2], and SRC-3 [amplif
86                                  Steroid and nuclear receptor coactivators (NCoAs) have been implicat
87 , including CREB-binding protein (CBP/p300), nuclear receptor coactivators (NCoAs), and p300/CBP-asso
88                                         p160 nuclear receptor coactivators on the other hand, contrib
89  truncated mutant BRCA2, synergizes with the nuclear receptor coactivator p160 GRIP1 to enhance trans
90 partner of PPAR (retinoid X receptor) or the nuclear receptor coactivators P300 and SRC-1, suggesting
91                                 Furthermore, nuclear receptor coactivators p300/CBP and steroid recep
92                                          The nuclear receptor coactivators participate in the transcr
93                                              Nuclear receptor coactivator PBP (peroxisome proliferato
94                   To investigate the role of nuclear receptor coactivator peroxisome proliferator-act
95 n of the gluconeogenic programme through the nuclear receptor coactivator PGC-1, which is shown here
96 indicates that in addition to functioning as nuclear receptor coactivator, PNRC2 may also play a role
97                          We report that p160 nuclear receptor coactivators potentiate the transactiva
98 iferator-activated receptors (PPARs) and the nuclear receptor coactivator, PPARgamma coactivator-1alp
99                                              Nuclear receptor coactivator PRIP (peroxisome proliferat
100 , has been shown previously to interact with nuclear receptor coactivator PRIP (peroxisome proliferat
101                                              Nuclear receptor coactivator PRIP (peroxisome proliferat
102  (ERalpha) requires the previously described nuclear receptor coactivator protein Flightless-I (Fli-I
103 ) is a putative vitamin D receptor (VDR) and nuclear receptor coactivator protein that is unrelated t
104                                          The nuclear receptor coactivator RAC3 (also known as AIB1/AC
105 activator receptor interacting protein) is a nuclear receptor coactivator required for mammary gland
106 e studies reveal the existence of a distinct nuclear receptor/coactivator signaling pathway that gove
107 determine the functional significance of the nuclear receptor coactivator SRC-1 in developing brain,
108 tor PPARgamma with two peptides derived from nuclear receptor coactivators SRC1 and TRAP220.
109 protein complexes, one of which contains the nuclear receptor coactivator steroid receptor coactivato
110  AIB3 is not redundant with other classes of nuclear receptor coactivators such as PBP and members of
111 gnature motif LXXLL also present in cellular nuclear receptor coactivators, such as steroid receptor
112 to p/CAF or to members of the p160 family of nuclear receptor coactivators, such as steroid receptor
113 hat of the ligand-binding domain-interacting nuclear receptor coactivators, such as TRBP, CBP, and SR
114 hway and specific phosphorylation sites in a nuclear receptor coactivator that can regulate steroid r
115                              NCOA7 encodes a nuclear receptor coactivator that interacts with estroge
116 ar receptor coregulatory protein (PNRC) is a nuclear receptor coactivator that interacts with nuclear
117 GT198 is a tissue-specific, kinase-regulated nuclear receptor coactivator that interacts with the DNA
118 ene amplified in breast cancer 1 (AIB1) is a nuclear receptor coactivator that plays a major role in
119 ceptor coactivator 3 (SRC-3) is an oncogenic nuclear receptor coactivator that plays a significant ro
120  that ERAP140 represents a distinct class of nuclear receptor coactivators that mediates receptor sig
121 tion of ER-alpha activity, whereas two other nuclear receptor coactivators, the p300/CBP-associated f
122  the nuclear receptor corepressor, SMRT, and nuclear receptor coactivator, TRAM-1.
123 high levels of the androgen receptor and two nuclear receptor coactivators, transcriptional intermedi
124 C3/TRAM-1) is a member of the p160 family of nuclear receptor coactivators, which includes SRC-1 (NCo
125 multiple nuclear receptors and with the p160 nuclear receptor coactivators, which upon cloning have p
126        These observations identify AIB1 as a nuclear receptor coactivator whose altered expression ma
127                   PGC-1alpha is an inducible nuclear receptor coactivator with direct functions in bo

 
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