HDAC3: taking the SMRT-N-CoRrect road to repression
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Molecular Biology
Link
http://www.nature.com/articles/1210612.pdf
Reference125 articles.
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3. Amann JM, Nip J, Strom DK, Lutterbach B, Harada H, Lenny N et al. (2001). ETO, a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain. Mol Cell Biol 21: 6470–6483.
4. Atsumi A, Tomita A, Kiyoi H, Naoe T . (2006). Histone deacetylase 3 (HDAC3) is recruited to target promoters by PML-RAR[alpha] as a component of the N-CoR co-repressor complex to repress transcription in vivo. Biochem Biophys Res Commun 345: 1471–1480.
5. Baek SH, Ohgi KA, Rose DW, Koo EH, Glass CK, Rosenfeld MG . (2002). Exchange of N-CoR corepressor and Tip60 coactivator complexes links gene expression by NF-[kappa]B and [beta]-amyloid precursor protein. Cell 110: 55–67.
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