ライフサイエンスコーパス: corepressor protein

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 ins histone deacetylases 1 and 2, the MIDEAS corepressor protein and a protein called DNTTIP1 whose f

15 through the recruitment of nuclear receptor corepressor protein and silencing mediator of retinoid a

16 the mutant TR constitutively interacts with corepressor proteins and mimics the hypothyroid state, r

17 scriptional regulatory functions, recruiting corepressor proteins and repressing transcription in the

18 egion of Mnt mediates interaction with mSin3 corepressor proteins and that its deletion converts Mnt

19 ormational change that allows the release of corepressor proteins and the binding of coactivator prot

20 yroid hormone, the thyroid receptor releases corepressor proteins and undergoes a conformational chan

21 e of these regulated genes, NR0B1, encodes a corepressor protein, and likely plays a transcriptional

22 In animals and yeast, Groucho/Tup1 corepressor proteins are recruited by diverse transcript

23 the candidates obtained, the transcriptional corepressor protein C-terminal binding protein-1 (CtBP1)

24 sed the possibility that the E1a-interacting corepressor protein C-terminal-binding protein (CtBP) mi

25 tional repression through the recruitment of corepressor proteins containing histone deacetylases in

26 methylase-1 (LSD1/KDM1A) in complex with its corepressor protein CoREST is a promising target for epi

27 specific demethylase-1 (LSD1/KDM1A) with its corepressor protein CoREST is an exceptionally relevant

28 It has been proposed that the cellular corepressor protein CoREST is involved in repressing her

29 H3K4 in peptide substrates, but requires the corepressor protein, CoREST, to demethylate nucleosome s

30 hort-range repressors interact with a common corepressor protein, dCtBP.

31 at the recently identified Groucho and dCtBP corepressor proteins do not function solely through the

32 KAP1/TIF1beta is proposed to be a universal corepressor protein for the KRAB zinc finger protein (KR

33 The binding pattern suggests that the corepressor proteins formed two types of corepressor com

34 factor E4f1 derepresses cdx4 by dissociating corepressor proteins from Tcf3 without inhibiting its bi

35 iation of NF-kappaB with the HDAC1 and HDAC2 corepressor proteins functions to repress expression of

36 ssors, Hairy and Dorsal, recruit a different corepressor protein, Groucho.

37 we show that, in vitro, H directly binds two corepressor proteins, Groucho (Gro) and dCtBP.

38 Mapping the interaction of corepressor proteins (HDAC1, silencing mediator of retin

39 studies with RNA polymerase and the groucho corepressor protein implicate Mam in transcriptional reg

40 essor, BCL-6, can interact with a variety of corepressor proteins in addition to SMRT, including the

41 , HDAC2, and HDAC3) are recruited by cognate corepressor proteins into specific transcriptional repre

42 i, where it mono-ADP ribosylates the nuclear corepressor protein, KAP1, and facilitates KAP1 interact

43 ng a MYC mutant unable to associate with the corepressor protein MIZ1 (ZBTB17).

44 previously shown that p53 interacts with the corepressor protein mSin3a (hereafter designated Sin3) i

45 interaction and in turn for interaction with corepressor proteins N-CoR and SMRT.

46 th increased transcription of genes encoding corepressor proteins NCoR and SMRT.

47 hormone receptor (SMRT) and nuclear receptor corepressor protein (NCoR) are corepressors that interac

48 ue to a family of recently described nuclear corepressor proteins (NCoR and SMRT) which bind to the C

49 t has homology to a repression domain in the corepressor protein NCoR2/SMRTe.

50 bicalutamide) can enhance AR recruitment of corepressor proteins [nuclear receptor corepressor (NCoR

51 Corepressor proteins often have associated histone deace

52 e cancer, with peptides from coactivator and corepressor proteins or random phage display peptides we

53 yeast two-hybrid screen which identified the corepressor protein SAP30 as a LANA binding protein.

54 polymerase II, and an increased presence of corepressor proteins such as histone deacetylases 1 and

55 ssion is mediated through the recruitment of corepressor proteins such as SMRT.

56 OG)-2 is a multi-zinc finger transcriptional corepressor protein that binds specifically to GATA4.

57 NAC1 is a transcriptional corepressor protein that is essential to sustain cancer

58 unction of AF2 is to recruit coactivator and corepressor proteins that allow ERalpha to oscillate bet

59 one deacetylase 3 often forms complexes with corepressor proteins that do not associate with the othe

60 of PTR2 by CUP9 requires TUP1 and SSN6, the corepressor proteins that form a complex with CUP9.

61 ivity is dependent on its ability to recruit corepressor proteins to a unique binding site on its N-t

62 th CSL is thought to both disrupt binding of corepressor proteins to CSL and anchor NICD to CSL, prom

63 2 (MeCP2) binds methylated DNA and recruits corepressor proteins to modify chromatin and alter gene

64 e UNC-4 homeoprotein and its transcriptional corepressor protein UNC-37 regulate SV protein levels in

65 ession in glial cells by stabilizing nuclear corepressor proteins, which reduces binding of p65 to in