Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng1098_184.pdf
Reference27 articles.
1. Taylor, E. et al. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene. Proc. Natl Acad. Sci. USA 94, 8658– 8663 (1997).
2. Bootsma, D. & Hoeijmakers, J.H.J. DNA repair. Engagement with transcription. Nature 363, 114– 115 (1993).
3. Roy, R. et al. The MO15 cell cycle kinase is ssociated with the TFIIH transcription-DNA repair factor. Cell 79, 1093– 1101 (1994).
4. Serizawa, H. et al. Association of Cdk-activating kinase subunits with transcription factor TFIIH. Nature 374, 280– 282 (1995).
5. Shiekhattar, R. et al. Cdk-activating kinase complex is a component of human transcription factor TFIIH. Nature 374, 283– 287 (1995).
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