Transcriptional coactivator complexes.
By Anders M. Näär, B. Lemon, R. Tjian. Annual Review of Biochemistry, 2001
605 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/85815d53c20ca57914658651fd15332163da3078
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In Molecular Biology
- Richard A. Young
- Huck-Hui Ng
- Enzo Orlandini
- Davide Marenduzzo
- Kevin Struhl
- D. Michieletto
- D. Reinberg
- Tong Ihn Lee
Citations in the corpus
- Transcriptional regulatory elements in the human genome. (2006, neutral): “, acetyl groups, methyl groups, and phosphates) from histone tails (103, 137).”
- A Polymer Model with Epigenetic Recolouring Reveals a Pathway for the de novo Establishment and 3D organisation of Chromatin Domains (2016, background): “…formation of centromeres in human nuclei occurs through the creation of the centromere-specific nucleosome CENP-A (a modified histone, which can thus be viewed as an “epigenetic mark”) via the concerted action of the chaperone protein HJURP (the “writer”) and the Mis18 complex (the “reader”) [38].”
- Targeted recruitment of Set1 histone methylase by elongating Pol II provides a localized mark and memory of recent transcriptional activity. (2003, background): “…given the distinct genetic requirements for cific and localized chromosomal mark persists for con- transcriptional induction and steady-state maintenance siderable time after transcriptional inactivation and Set1 (Klein and Struhl, 1994; Bhaumik and Green, 2001; dissociation (Figure 7).”