Basal Transcription Defect Discriminates between Xeroderma Pigmentosum and Trichothiodystrophy in XPD Patients

Author:

Dubaele Sandy,De Santis Luca Proietti,Bienstock Rachelle J,Keriel Anne,Stefanini Miria,Van Houten Bennett,Egly Jean-Marc

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference43 articles.

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2. Nucleotide excision repair of DNA with recombinant human proteins;Araujo;Genes Dev.,2000

3. Structural and functional characterization of the human DNA repair helicase XPD by comparative molecular modeling and site-directed mutagenesis of the bacterial repair protein UvrB;Bienstock;J. Biol. Chem.,2002

4. DNA repair. Engagement with transcription;Bootsma;Nature,1993

5. Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy;Botta;Am. J. Hum. Genet.,1998

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