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1  with octamer-bound Oct-1 and for subsequent coactivator function.
2 ediated transcriptional activation through a coactivator function.
3 tion, but it is defective in transcriptional coactivator function.
4 insight into the molecular mechanisms of G9a coactivator function.
5 enhances PKM2 binding to HIF-1alpha and PKM2 coactivator function.
6  the importance of APE1's acetylation in its coactivator function.
7 perties of the TAF4 subunit that lead to the coactivator function.
8 nd has been shown to possess transcriptional coactivator function.
9 y, only a selected subset required BAF57 for coactivator function.
10 sed in terms of our present understanding of coactivator function.
11 nfirmed a critical role for them in in vitro coactivator function.
12  (PPAR)-interacting protein) and enhance its coactivator function.
13 e activity of PRMT2 appeared pivotal for its coactivator function.
14 th other proteins that help to mediate CARM1 coactivator function.
15 significant additive inductive effect on PBP coactivator function.
16 MAPK cascade exerts a positive effect on PBP coactivator function.
17 tion of GRIP1 transcriptional activation and coactivator function.
18 tor HNF4) and thus recapitulates partial USA coactivator function.
19 de a more physiologically relevant assay for coactivator function.
20 DR heterodimers bound to DNA and for TRAP220 coactivator function.
21  new tool for investigating the mechanism of coactivator function and demonstrates the importance of
22 However, the mechanism of beta-catenin-GRIP1 coactivator function and synergy is different with AR an
23                       To correlate the E6-AP coactivator function and ubiquitin-protein ligase functi
24 RM1 to AD2 are required for their respective coactivator functions and for their synergy.
25                                          The coactivator functions and physical interactions of Smad4
26  AR that is capable of altering AR activity, coactivator function, and AR-dependent proliferation.
27 eviously been implicated in nuclear receptor coactivator function, and we show that, although BAF57 f
28 th respect to specific polypeptide subunits, coactivator functions, and mechanisms of action (activat
29 2 nuclear protein kinase and transcriptional coactivator functions are abolished.
30       The yeast GCN5 (yGCN5) transcriptional coactivator functions as a histone acetyltransferase (HA
31 c evidence that this generic transcriptional coactivator functions as a positive modifier of prostate
32 sion by NFI-C may occur by interference with coactivator function at the MMTV promoter.
33 er, our findings suggest that the human CRSP coactivator functions, at least in part, by mediating ac
34 sferase inhibitor UNC0646 did not affect G9a coactivator function but selectively decreased G9a corep
35 icate that phosphorylation coordinates SRC-3 coactivator function by linking the probabilistic format
36 ional activation domain which contributes to coactivator function by recruitment of CoCoA.
37 and it has been recently proposed that these coactivators function by modulating chromatin structure
38                                              Coactivator functions can be broadly divide into two cla
39 t competitively inhibit AKR1C3 and block its coactivator function could be developed using reverse-mi
40  Deletion of AD1 only partially reduced p160 coactivator function, due to signaling through AD2, anot
41 tivator binding sites and that dependence on coactivator function for a given activator can vary acco
42                  Our findings reveal a novel coactivator function for Cyc8p/Tup1p at the level of act
43            Our data therefore reveal a novel coactivator function for PIASx(alpha) through reversing
44 ork identified a stimulatory transcriptional coactivator function for the BRCA1 protein, and more rec
45 m changes in TIP60 complex assembly or TIP60 coactivator functions for p53, since a TIP60 complex con
46  acetyl coenzyme A-dependent transcriptional coactivator functions from a chromatin-assembled templat
47 tional activator and suggest that control of coactivator function (i.e. recruitment of CBP and stimul
48 lized TRbeta LBD depleted the extract of the coactivator function in a triiodothyronine-dependent man
49                   To better understand PGC-1 coactivator function in brown fat development, we explor
50 plays a role in breast cancer because of its coactivator function in ER signaling, we determined the
51 steine-rich domain) were unnecessary for G9a coactivator function in ERalpha-mediated transcription.
52  the relevance of its modular nature for its coactivator function in gene regulation.
53 d blocks both its enzymatic activity and its coactivator function in regulating basal p21 gene expres
54 re the requirement of ubiquitylation for the coactivator function in regulating HIV-1 transcriptional
55  potent, activator-dependent transcriptional coactivator function in response to VP16, Sp1, and Sp1/S
56           In this study, we investigated PC4 coactivator function in the control of LHR transcription
57 tigate the requirement of lipin-1 PAP versus coactivator function in the establishment of Pparg expre
58 essor binds PPM1G to negatively regulate its coactivator function in the NF-kappaB circuit thereby pr
59   These results strongly suggest that a p160 coactivator functions in CAR-mediated transactivation in
60 insic acetyltransferase activity whose exact coactivator functions in the acetylation of nucleosomal
61                        Here we show that PC4 coactivator function, in contrast to basal (activator-in
62 roles in vivo and suggest a new mechanism of coactivator function, in which a single adaptor protein
63 nts, suggesting that the complex possesses a coactivator function independent from remodeling.
64             Thus, SAF6 is essential for SAGA coactivator function independent of the enzymatic activi
65                          Thus, whereas GRIP1 coactivator function involves direct binding to nuclear
66 eginning E(2) treatment, suggesting that G9a coactivator function is by direct interaction with ERalp
67 scriptional regulation, suggest that SRCAP's coactivator function may depend on its ability to promot
68 the N-terminal domain and that the increased coactivator function of AIB1-Delta4 is due to the loss o
69                                         This coactivator function of atrogin-1 was dependent on its u
70                              The synergistic coactivator function of beta-catenin and CARM1 is not re
71 ption activator target that is essential for coactivator function of both the SAGA and NuA4 histone a
72                                          The coactivator function of cAMP-responsive element-binding
73          We previously demonstrated that the coactivator function of CARM1 depends both on the methyl
74  other domains of CARM1 are required for the coactivator function of CARM1 in addition to the methylt
75  AD, the interaction of CoCoA with p300, the coactivator function of CoCoA for estrogen receptor alph
76 sactivation activity and is required for the coactivator function of CoCoA with nuclear receptors.
77 ding transcriptional activator proteins, the coactivator function of GRIP1 with Lef1 follows a novel
78        Thus, we present evidence for a novel coactivator function of MAML1 for p53, independent of it
79                                          The coactivator function of Mediator-P.5 was not impaired wh
80  only a minor contribution to the long-range coactivator function of Mll3/4.
81 g Ag recognition via direct control over the coactivator function of p300/CBP.
82 n was accompanied by inhibition of the basal coactivator function of PELP1 upon estrogen receptor tra
83 gion of PGC-1alpha abolished the cooperative coactivator function of PGC-1alpha and PRMT1, and compro
84 cted with SRC1 and p300, suggesting that the coactivator function of RIZ1 may be mediated by its inte
85                    These results establish a coactivator function of TAF4 and provide a strategy to d
86  studies have shown that the transcriptional coactivator function of the Mediator involves direct lig
87  that reduced actin binding also reduced the coactivator function of this Fli-I fragment.
88 ely to result in differential effects on the coactivator functions of CBP/p300 for different classes
89 ase 3 and beta-catenin, interfering with Wnt coactivator functions of CCAR2, including in cells harbo
90 ed with the ability of ORF2 to stimulate the coactivator functions of HMGA1.
91                                          The coactivator functions of p300 and CARM1 depended on the
92 on in vivo, we have investigated further the coactivator functions of steroid receptor coactivator-1
93 ce of S675 phosphorylation and transcription coactivator function on BIG2 AKAP-C sequence.
94 TR as well as progesterone receptor-mediated coactivator function on reporter gene expression.
95 e previously shown that yeast TFIID provides coactivator function on the promoters of ribosomal prote
96                         Dual DNA-binding and coactivator functions provide an additional level of com
97                 PHD3 knockdown inhibits PKM2 coactivator function, reduces glucose uptake and lactate
98  mechanisms by which phosphorylation affects coactivator function remains largely undefined.
99                 Finally, we show that mPus1p-coactivator function required SRA, mPus1p-associated mRA
100 mmary tumor virus (MMTV) promoters, and this coactivator function required the methyltransferase acti
101 rmone responses in vivo and that loss of its coactivator function results in partial resistance to ho
102 tivator complex but differentially modulates coactivator function such that inhibition of the CBP/p30
103                                         This coactivator function, surprisingly, is independent of it
104 says identify a domain of TAF3 that mediates coactivator functions targeted by MyoD.
105 owever, the molecular basis underlying MAML1 coactivator function that contributes to Notch signaling
106 role for G9a as a molecular scaffold for its coactivator function, the G9a-specific methyltransferase
107 results are in contrast to the classic ARA55 coactivator function to enhance AR transactivation parti
108  function of E6-AP was defective whereas the coactivator function was intact.
109    GRIP1 mutants deficient in GR binding and coactivator functions were also defective for corepressi
110 ty of CARM1 is important for its synergistic coactivator function with beta-catenin.

 
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