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1 expression, and relies on Set2 and the Set3 histone deacetylase complex.
2 corepressor complex containing Groucho and a histone deacetylase complex.
3 diates the association of MTA2 with the core histone deacetylase complex.
4 activity that is part of an endogenous human histone deacetylase complex.
5 anking regions due to destabilization of the histone deacetylase complex.
6 T3, which encodes a subunit of the Set3/Hos2 histone deacetylase complex.
7 Here, we show that MSI1 is part of a histone deacetylase complex.
8 uitment of nuclear receptor corepressor, and histone deacetylase complex.
9 3 and each of the three subunits of the Hda1 histone deacetylase complex.
10 an integral subunit of a well-characterized histone deacetylase complex.
11 and is formed through the action of the Sir histone deacetylase complex.
12 orthologue of Rb and components of the NuRD histone deacetylase complex.
13 otein, Sap18, which is part of the Sin3/Rpd3 histone deacetylase complex.
14 , a component of the S. cerevisiae Sin3/Rpd3 histone deacetylase complex.
15 cts with SAP18, a component of the mSin3 and histone deacetylase complex.
16 s, possibly by interacting with an MeCPC and histone deacetylase complex.
17 ses in addition to recruiting a co-repressor/histone deacetylase complex.
18 g protein, MBD2, is a component of the MeCP1 histone deacetylase complex.
19 nscription through recruitment of the mSin3A-histone deacetylase complex.
20 shown to directly interact with mSin3 of the histone deacetylase complex.
21 olecular weight Rpd3p.Sin3p containing yeast histone deacetylase complex.
22 ic growth in a parallel pathway to Rpd3-Sin3 histone deacetylase complex.
23 orepressor N-CoR and possibly its associated histone deacetylase complex.
24 and serves as a linker between CBF1 and the histone deacetylase complex.
25 a core complex shared between NuRD and Sin3-histone deacetylase complexes.
26 ne activity, we have characterized two yeast histone deacetylase complexes.
27 tin by bridging interactions between HP1 and histone deacetylase complexes.
28 are important for nucleosome remodelling in histone deacetylase complexes.
29 to the ETO corepressor that associates with histone deacetylase complexes.
30 e expression via the recruitment of multiple histone deacetylase complexes.
31 ein, ZID, which interacts with components of histone deacetylase complexes.
32 ess transcription through the recruitment of histone deacetylase complexes.
33 etylated in response to DNA damage when both histone deacetylase complex 1 (HDAC1)- and Sir2-mediated
35 on and decrease MBD2 association with HDAC1 (histone deacetylase complex 1) and methyl CpG site in th
36 g properties were recently reported for BRAF-histone deacetylase complex 80 and DNA methyltransferase
37 role for Rpd3 and Ume6, two components of a histone deacetylase complex already known to repress ear
38 ted both by potential ERG association with a histone deacetylase complex and by direct EWS/ERG recrui
39 f2/HDAC-containing repressor complex (SHREC) histone deacetylase complex and the anti-silencing prote
40 d that one of these targets is the Sin3-Rpd3 histone deacetylase complex, and that cyclophilin A incr
41 that BRCA1 interacts with components of the histone deacetylase complex, and therefore may explain t
44 ny different components that may control how histone deacetylase complexes are regulated and interact
45 a component of the recently identified NURD histone deacetylase complex, as a protein that binds dir
46 ity to deacetylate histones, termed the BRAF-histone deacetylase complex (BHC), from human cells.
47 native subunit of a repressive mSin3a-HDAC1 histone deacetylase complex, binds with high affinity to
48 translational modification, interacts with a histone deacetylase complex by binding to the corepresso
50 asing evidence indicates that recruitment of histone deacetylase complexes by methyl-CpG-binding prot
51 ese results define SAP30 as a component of a histone deacetylase complex conserved among eukaryotic o
53 mitogenic stimulation, repressive E2F4-p130-histone deacetylase complexes dissociate from, while act
55 bunit of the NuA4 histone acetylase and Rpd3 histone deacetylase complexes, greatly alters the genomi
61 tylation of nucleosomes in coding regions by histone deacetylase complexes (HDACs) Set3C and Rpd3C(S)
63 this repression involves the recruitment of histone deacetylase complexes (HDACs), because R-LANA's
65 highly conserved KRAB domain, which recruits histone deacetylase complexes, histone methylases, and h
66 escribe explains the unanticipated role of a histone deacetylase complex in activating gene expressio
67 involvement of nuclear receptor corepressor/histone deacetylase complex in the molecular pathogenesi
69 transcription was repressed by Max-Mnt-Sin3a-histone deacetylase complexes in proliferating cells.
70 transcription, Ume6, which acts along with a histone deacetylase complex including Sin3 and Rpd3 to r
72 t functionally associates with the Rpd3-Sin3 histone deacetylase complex involved in transcriptional
73 Our results suggest that the binding to a histone deacetylase complex is an important parameter fo
75 identified, the NuRD (nucleosome remodeling histone deacetylase) complex is unique because it posses
76 a component of the nucleosome-remodeling and histone deacetylase complex, is widely up-regulated in h
77 onent of the NuA4 histone acetylase and Rpd3 histone deacetylase complexes, is important for the glob
79 cription repression domain by recruiting the histone deacetylase complex NuRD and histone H3 lysine 9
80 acterization of a nucleosome remodelling and histone deacetylase complex, NuRD, has suggested that nu
81 Rpd3p, components of one of the predominant histone deacetylase complexes of Saccharomyces cerevisia
83 demethylase 1 (LSD1), a component of several histone deacetylase complexes, plays an important role i
84 l PHD fingers of Rco1, a member of the Rpd3S histone deacetylase complex recruited to transcribing ge
88 e analog technology, we demonstrate that the histone deacetylase complex, Rpd3S, can distinguish the
90 SIN3 and RPD3, which encode components of a histone deacetylase complex, show the same pattern of ge
92 BP, p300, and MOZ) and with component of the histone deacetylase complex (Sin3), and that the interac
93 tive inhibitor of recruitment of N-CoR/mSin3 histone deacetylase complexes, specifically reverse beta
94 tify SAP30 as a novel component of the human histone deacetylase complex that includes Sin3, the hist
95 nt proteomic studies have identified a novel histone deacetylase complex that is upregulated during m
96 interactions of the alpha-HRM with the Sin3-histone deacetylase complex that is utilized by at least
97 ecruiting a complex containing Groucho and a histone deacetylase complex that leads to histone modifi
98 synMuv genes encode components of an Rb and histone deacetylase complex that likely acts to repress
99 o known as BHC80, is a component of the BRAF-histone deacetylase complex that represses target-gene t
100 ined mutations in genes involved in the Rpd3 histone deacetylase complex, the kinetochore, and vesicl
101 is necessary for the activation of the Rpd3S histone deacetylase complex, thereby maintaining the cod
102 se that dCtBP can interfere with corepressor-histone deacetylase complexes, thereby attenuating trans
103 nscription of target genes by recruiting the histone deacetylase complex through a class of silencing
104 d in the functional recruitment of the mSin3-histone deacetylase complex to a specific subset of N-Co
105 Set2 histone methyltransferase and the Set3 histone deacetylase complex to establish repressive chro
106 lex functions in parallel with the Sin3-Rpd3 histone deacetylase complex to repress early meiotic gen
107 riptional elongation by recruiting the Rpd3S histone deacetylase complex to repress intragenic crypti
109 expression by the recruitment of the mSin3A/histone deacetylase complex to the Snail-binding sites i
110 imulates interaction between nucleosomes and histone deacetylase complexes to block cryptic transcrip
111 ors inhibit transcription by recruiting Rpd3 histone deacetylase complexes to promoters and generatin
112 ymphocyte development by recruiting distinct histone deacetylase complexes to specific promoters.
114 d recruitment of repressive, Rpd3-containing histone deacetylase complexes was also seen and at all H
115 reover, cytoplasmic SAP130 (a subunit of the histone deacetylase complex) was expressed in PDA in a R
117 can repress gene expression by recruiting a histone deacetylase complex, whereas liganded TR recruit
118 genetic experiments that the Rpd3/Sin3/Ume6 histone deacetylase complex, which represses meiotic gen
119 nent of the NuRD (nucleosome remodelling and histone deacetylase) complex, which contains additional
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