Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH

TFIIH Kinase Places Bivalent Marks on the Carboxy-Terminal Domain of RNA Polymerase II

(2009) Md. Sohail Akhtar et al.   MOLECULAR CELL

DNA repair deficiency and neurological disease

(2009) Peter J. McKinnon   NATURE REVIEWS NEUROSCIENCE

Defective Transcription/Repair Factor IIH Recruitment to Specific UV Lesions in Trichothiodystrophy Syndrome

(2008) V. Chigancas et al.   CANCER RESEARCH

Structure of the DNA Repair Helicase XPD

(2008) Huanting Liu et al.   CELL

XPD Helicase Structures and Activities: Insights into the Cancer and Aging Phenotypes from XPD Mutations

(2008) Li Fan et al.   CELL

Persistence of repair proteins at unrepaired DNA damage distinguishes diseases withERCC2(XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy

(2008) Jennifer Boyle et al.   HUMAN MUTATION

Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in theXPDgene

(2008) Elena Botta et al.   HUMAN MUTATION

Nucleotide Excision Repair Driven by the Dissociation of CAK from TFIIH

(2008) Frédéric Coin et al.   MOLECULAR CELL

Transcription-coupled DNA repair: two decades of progress and surprises

(2008) Philip C. Hanawalt et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Structural basis for group A trichothiodystrophy

(2008) Denis E Kainov et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

(2008) Stefanie C Wolski et al.   PLOS BIOLOGY

p8/TTDA Overexpression Enhances UV-Irradiation Resistance and Suppresses TFIIH Mutations in a Drosophila Trichothiodystrophy Model

(2008) Javier Aguilar-Fuentes et al.   PLoS Genetics