The DNA Repair Helicases XPD and FancJ Have Essential Iron-Sulfur Domains
Open Access
- 1 September 2006
- journal article
- research article
- Published by Elsevier in Molecular Cell
- Vol. 23 (6), 801-808
- https://doi.org/10.1016/j.molcel.2006.07.019
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- DNA-Bound Redox Activity of DNA Repair Glycosylases Containing [4Fe-4S] ClustersBiochemistry, 2005
- Regulation of Murine Telomere Length by RtelCell, 2004
- The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutationsProceedings of the National Academy of Sciences, 2004
- Basal Transcription Defect Discriminates between Xeroderma Pigmentosum and Trichothiodystrophy in XPD PatientsMolecular Cell, 2003
- Structural and Functional Characterization of the Human DNA Repair Helicase XPD by Comparative Molecular Modeling and Site-directed Mutagenesis of the Bacterial Repair Protein UvrBPublished by Elsevier ,2003
- Reduced level of the repair/transcription factor TFIIH in trichothiodystrophyHuman Molecular Genetics, 2002
- BACH1, a Novel Helicase-like Protein, Interacts Directly with BRCA1 and Contributes to Its DNA Repair FunctionCell, 2001
- Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial MembranesHuman Molecular Genetics, 1997
- A regulatedMET3‐GLC7gene fusion provides evidence of a mitotic role forSaccharomyces cerevisiaeprotein phosphatase 1Yeast, 1995
- Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repairCell, 1993