Deficient DNA repair in the human progeroid disorder, Werner syndrome
Open Access
- 4 September 2005
- journal article
- review article
- Published by Elsevier in Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
- Vol. 577 (1-2) , 252-259
- https://doi.org/10.1016/j.mrfmmm.2005.03.021
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Regulation of WRN Helicase Activity in Human Base Excision RepairJournal of Biological Chemistry, 2004
- The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for WRN functionDNA Repair, 2004
- Linkage between Werner Syndrome Protein and the Mre11 Complex via Nbs1Journal of Biological Chemistry, 2004
- Werner Syndrome Protein--Unwinding Function to Explain DiseaseScience of Aging Knowledge Environment, 2004
- Structure and Function of RecQ DNA HelicasesCritical Reviews in Biochemistry and Molecular Biology, 2004
- Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA DamageMolecular and Cellular Biology, 2003
- WRN Interacts Physically and Functionally with the Recombination Mediator Protein RAD52Journal of Biological Chemistry, 2003
- Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.Carcinogenesis: Integrative Cancer Research, 2003
- p53 Modulates the Exonuclease Activity of Werner Syndrome ProteinPublished by Elsevier ,2001
- The Pif1p subfamily of helicases: region-specific DNA helicases?Trends in Cell Biology, 2001