Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH
Nature Genetics1998Vol. 20(2), pp. 184–188
Citations Over TimeTop 10% of 1998 papers
Frédéric Coin, Jean‐Christophe Marinoni, Carlo Rodolfo, Sébastien Fribourg, Antonia M. Pedrini, Jean‐Marc Egly
Related Papers
- → Basal Transcription Defect Discriminates between Xeroderma Pigmentosum and Trichothiodystrophy in XPD Patients(2003)196 cited
- → Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene(2001)102 cited
- → How two helicases work together within the TFIIH complex, a perspective from structural studies of XPB and XPD helicases(2013)5 cited
- → The discovery that xeroderma pigmentosum (XP) results from defective nucleotide excision repair(2003)17 cited
- → Gene polymorphisms in the nucleotide excision repair pathway and lung cancer susceptibility(2013)