Miria Stefanini

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

Karla A. Henning, Lei Li, Narayan V. Iyer et al. · Cell · 1995 · 505 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A

Giuseppina Giglia‐Mari, Frédéric Coin, Jeffrey A. Ranish et al. · Nature Genetics · 2004 · 332 citations

Life Sciences, Genetics, Molecular Biology +10

Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

Wim J. Kleijer, Vincent Laugel, Mark Berneburg et al. · DNA repair · 2008 · 271 citations

Life Sciences, Dermatology, Genetics +14

New functions of XPC in the protection of human skin cells from oxidative damage

Mariarosaria D’Errico, Eleonora Parlanti, Massimo Teson et al. · The EMBO Journal · 2006 · 268 citations · Full text

Life Sciences, Cell Biology, Dermatology +14

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the <i>XPD</i> ( <i>ERCC</i> 2) repair/transcription gene

Elaine M. Taylor, Bernard C. Broughton, Elena Botta et al. · Proceedings of the National Academy of Sciences · 1997 · 259 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13