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1 (FOG)-2, a cardiac nuclear hormone receptor corepressor protein.
2 VLDLS motif recruits an as yet unidentified corepressor protein.
3 y, which mediate interactions with the dCtBP corepressor protein.
4 motif that mediates interaction with TLE/Gro corepressor proteins.
5 er is acetylated but negatively regulated by corepressor proteins.
6 s distantly related to the Ski/Sno family of corepressor proteins.
7 ASNS transcription, possibly by sequestering corepressor proteins.
8 elA) subunit with histone deacetylase (HDAC) corepressor proteins.
9 g an additional interaction between RPMS and corepressor proteins.
10 ed in part through its association with HDAC corepressor proteins.
11 binding domain, thereby identifying them as corepressor proteins.
12 rs, than to an inherent low affinity for the corepressor proteins.
13 VDR.RXR with transcriptional coactivator or corepressor proteins.
14 get gene expression through association with corepressor proteins.
15 ins histone deacetylases 1 and 2, the MIDEAS corepressor protein and a protein called DNTTIP1 whose f
16 through the recruitment of nuclear receptor corepressor protein and silencing mediator of retinoid a
17 the mutant TR constitutively interacts with corepressor proteins and mimics the hypothyroid state, r
18 scriptional regulatory functions, recruiting corepressor proteins and repressing transcription in the
19 egion of Mnt mediates interaction with mSin3 corepressor proteins and that its deletion converts Mnt
20 ormational change that allows the release of corepressor proteins and the binding of coactivator prot
21 yroid hormone, the thyroid receptor releases corepressor proteins and undergoes a conformational chan
22 e of these regulated genes, NR0B1, encodes a corepressor protein, and likely plays a transcriptional
24 ene transcription through the recruitment of corepressor proteins, B-cell lymphoma 6 (BCL6) protein c
25 emonstrated that engineered BCL6 interacting corepressor protein (Bcor) mutation in hematopoietic ste
26 the candidates obtained, the transcriptional corepressor protein C-terminal binding protein-1 (CtBP1)
27 sed the possibility that the E1a-interacting corepressor protein C-terminal-binding protein (CtBP) mi
28 tional repression through the recruitment of corepressor proteins containing histone deacetylases in
29 methylase-1 (LSD1/KDM1A) in complex with its corepressor protein CoREST is a promising target for epi
30 specific demethylase-1 (LSD1/KDM1A) with its corepressor protein CoREST is an exceptionally relevant
32 H3K4 in peptide substrates, but requires the corepressor protein, CoREST, to demethylate nucleosome s
34 at the recently identified Groucho and dCtBP corepressor proteins do not function solely through the
35 KAP1/TIF1beta is proposed to be a universal corepressor protein for the KRAB zinc finger protein (KR
37 factor E4f1 derepresses cdx4 by dissociating corepressor proteins from Tcf3 without inhibiting its bi
38 iation of NF-kappaB with the HDAC1 and HDAC2 corepressor proteins functions to repress expression of
42 studies with RNA polymerase and the groucho corepressor protein implicate Mam in transcriptional reg
43 essor, BCL-6, can interact with a variety of corepressor proteins in addition to SMRT, including the
45 , HDAC2, and HDAC3) are recruited by cognate corepressor proteins into specific transcriptional repre
46 HP1) isoforms and the generic HP1-associated corepressor protein KAP1 all resulted in growth inhibiti
47 i, where it mono-ADP ribosylates the nuclear corepressor protein, KAP1, and facilitates KAP1 interact
49 previously shown that p53 interacts with the corepressor protein mSin3a (hereafter designated Sin3) i
52 hormone receptor (SMRT) and nuclear receptor corepressor protein (NCoR) are corepressors that interac
53 ue to a family of recently described nuclear corepressor proteins (NCoR and SMRT) which bind to the C
55 bicalutamide) can enhance AR recruitment of corepressor proteins [nuclear receptor corepressor (NCoR
57 e cancer, with peptides from coactivator and corepressor proteins or random phage display peptides we
59 yeast two-hybrid screen which identified the corepressor protein SAP30 as a LANA binding protein.
60 polymerase II, and an increased presence of corepressor proteins such as histone deacetylases 1 and
62 ming complexes with one of several different corepressor proteins, such as FHL1 or SHARP in mammals a
63 OG)-2 is a multi-zinc finger transcriptional corepressor protein that binds specifically to GATA4.
65 unction of AF2 is to recruit coactivator and corepressor proteins that allow ERalpha to oscillate bet
66 one deacetylase 3 often forms complexes with corepressor proteins that do not associate with the othe
68 ivity is dependent on its ability to recruit corepressor proteins to a unique binding site on its N-t
69 th CSL is thought to both disrupt binding of corepressor proteins to CSL and anchor NICD to CSL, prom
70 transcriptional repression by recruiting its corepressor proteins to form a biologically functional t
71 2 (MeCP2) binds methylated DNA and recruits corepressor proteins to modify chromatin and alter gene
72 e UNC-4 homeoprotein and its transcriptional corepressor protein UNC-37 regulate SV protein levels in
73 ession in glial cells by stabilizing nuclear corepressor proteins, which reduces binding of p65 to in