433 related articles for article (PubMed ID: 11390640)
21. HBP1 and Mad1 repressors bind the Sin3 corepressor PAH2 domain with opposite helical orientations.
Swanson KA; Knoepfler PS; Huang K; Kang RS; Cowley SM; Laherty CD; Eisenman RN; Radhakrishnan I
Nat Struct Mol Biol; 2004 Aug; 11(8):738-46. PubMed ID: 15235594
[TBL] [Abstract][Full Text] [Related]
22. Temporal recruitment of the mSin3A-histone deacetylase corepressor complex to the ETS domain transcription factor Elk-1.
Yang SH; Vickers E; Brehm A; Kouzarides T; Sharrocks AD
Mol Cell Biol; 2001 Apr; 21(8):2802-14. PubMed ID: 11283259
[TBL] [Abstract][Full Text] [Related]
23. Targeting histone deacetylase complexes via KRAB-zinc finger proteins: the PHD and bromodomains of KAP-1 form a cooperative unit that recruits a novel isoform of the Mi-2alpha subunit of NuRD.
Schultz DC; Friedman JR; Rauscher FJ
Genes Dev; 2001 Feb; 15(4):428-43. PubMed ID: 11230151
[TBL] [Abstract][Full Text] [Related]
24. Mad-Max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3.
Ayer DE; Lawrence QA; Eisenman RN
Cell; 1995 Mar; 80(5):767-76. PubMed ID: 7889570
[TBL] [Abstract][Full Text] [Related]
25. ETO, a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain.
Amann JM; Nip J; Strom DK; Lutterbach B; Harada H; Lenny N; Downing JR; Meyers S; Hiebert SW
Mol Cell Biol; 2001 Oct; 21(19):6470-83. PubMed ID: 11533236
[TBL] [Abstract][Full Text] [Related]
26. The homeodomain protein NK-3 recruits Groucho and a histone deacetylase complex to repress transcription.
Choi CY; Kim YH; Kwon HJ; Kim Y
J Biol Chem; 1999 Nov; 274(47):33194-7. PubMed ID: 10559189
[TBL] [Abstract][Full Text] [Related]
27. Histone deacetylases associated with the mSin3 corepressor mediate mad transcriptional repression.
Laherty CD; Yang WM; Sun JM; Davie JR; Seto E; Eisenman RN
Cell; 1997 May; 89(3):349-56. PubMed ID: 9150134
[TBL] [Abstract][Full Text] [Related]
28. Multiple regions of ETO cooperate in transcriptional repression.
Hildebrand D; Tiefenbach J; Heinzel T; Grez M; Maurer AB
J Biol Chem; 2001 Mar; 276(13):9889-95. PubMed ID: 11150306
[TBL] [Abstract][Full Text] [Related]
29. An ERG (ets-related gene)-associated histone methyltransferase interacts with histone deacetylases 1/2 and transcription co-repressors mSin3A/B.
Yang L; Mei Q; Zielinska-Kwiatkowska A; Matsui Y; Blackburn ML; Benedetti D; Krumm AA; Taborsky GJ; Chansky HA
Biochem J; 2003 Feb; 369(Pt 3):651-7. PubMed ID: 12398767
[TBL] [Abstract][Full Text] [Related]
30. Extension of the binding motif of the Sin3 interacting domain of the Mad family proteins.
van Ingen H; Lasonder E; Jansen JF; Kaan AM; Spronk CA; Stunnenberg HG; Vuister GW
Biochemistry; 2004 Jan; 43(1):46-54. PubMed ID: 14705930
[TBL] [Abstract][Full Text] [Related]
31. Recruitment of SMRT/N-CoR-mSin3A-HDAC-repressing complexes is not a general mechanism for BTB/POZ transcriptional repressors: the case of HIC-1 and gammaFBP-B.
Deltour S; Guerardel C; Leprince D
Proc Natl Acad Sci U S A; 1999 Dec; 96(26):14831-6. PubMed ID: 10611298
[TBL] [Abstract][Full Text] [Related]
32. HERP, a novel heterodimer partner of HES/E(spl) in Notch signaling.
Iso T; Sartorelli V; Poizat C; Iezzi S; Wu HY; Chung G; Kedes L; Hamamori Y
Mol Cell Biol; 2001 Sep; 21(17):6080-9. PubMed ID: 11486045
[TBL] [Abstract][Full Text] [Related]
33. The polybasic region that follows the plant homeodomain zinc finger 1 of Pf1 is necessary and sufficient for specific phosphoinositide binding.
Kaadige MR; Ayer DE
J Biol Chem; 2006 Sep; 281(39):28831-6. PubMed ID: 16893883
[TBL] [Abstract][Full Text] [Related]
34. Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis.
Dasen JS; Martinez Barbera JP; Herman TS; Connell SO; Olson L; Ju B; Tollkuhn J; Baek SH; Rose DW; Rosenfeld MG
Genes Dev; 2001 Dec; 15(23):3193-207. PubMed ID: 11731482
[TBL] [Abstract][Full Text] [Related]
35. A feed-forward repression mechanism anchors the Sin3/histone deacetylase and N-CoR/SMRT corepressors on chromatin.
Vermeulen M; Walter W; Le Guezennec X; Kim J; Edayathumangalam RS; Lasonder E; Luger K; Roeder RG; Logie C; Berger SL; Stunnenberg HG
Mol Cell Biol; 2006 Jul; 26(14):5226-36. PubMed ID: 16809761
[TBL] [Abstract][Full Text] [Related]
36. TIS7 interacts with the mammalian SIN3 histone deacetylase complex in epithelial cells.
Vietor I; Vadivelu SK; Wick N; Hoffman R; Cotten M; Seiser C; Fialka I; Wunderlich W; Haase A; Korinkova G; Brosch G; Huber LA
EMBO J; 2002 Sep; 21(17):4621-31. PubMed ID: 12198164
[TBL] [Abstract][Full Text] [Related]
37. Coupled unfolding and dimerization by the PAH2 domain of the mammalian Sin3A corepressor.
Zhang Y; Zhang Z; Demeler B; Radhakrishnan I
J Mol Biol; 2006 Jun; 360(1):7-14. PubMed ID: 16813833
[TBL] [Abstract][Full Text] [Related]
38. The co-repressor mSin3A is a functional component of the REST-CoREST repressor complex.
Grimes JA; Nielsen SJ; Battaglioli E; Miska EA; Speh JC; Berry DL; Atouf F; Holdener BC; Mandel G; Kouzarides T
J Biol Chem; 2000 Mar; 275(13):9461-7. PubMed ID: 10734093
[TBL] [Abstract][Full Text] [Related]
39. A positive regulatory role for the mSin3A-HDAC complex in pluripotency through Nanog and Sox2.
Baltus GA; Kowalski MP; Tutter AV; Kadam S
J Biol Chem; 2009 Mar; 284(11):6998-7006. PubMed ID: 19139101
[TBL] [Abstract][Full Text] [Related]
40. Biological activity of mammalian transcriptional repressors.
Thiel G; Lietz M; Bach K; Guethlein L; Cibelli G
Biol Chem; 2001 Jun; 382(6):891-902. PubMed ID: 11501753
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]