Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Neuroscience
Link
http://www.nature.com/articles/nn1990.pdf
Reference50 articles.
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3. Coin, F. et al. Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH. Nat. Genet. 20, 184–188 (1998).
4. Bradsher, J., Coin, F. & Egly, J.M. Distinct roles for the helicases of TFIIH in transcript initiation and promoter escape. J. Biol. Chem. 275, 2532–2538 (2000).
5. Lu, H., Zawel, L., Fisher, L., Egly, J.M. & Reinberg, D. Human general transcription factor IIH phosphorylates the C-terminal domain of RNA polymerase II. Nature 358, 641–645 (1992).
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