Modulation of Werner Syndrome Protein Function by a Single Mutation in the Conserved RecQ Domain
Open Access
- 1 November 2005
- journal article
- research article
- Published by Elsevier
- Vol. 280 (47) , 39627-39636
- https://doi.org/10.1074/jbc.m506112200
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- Conferring Substrate Specificity to DNA Helicases: Role of the RecQ HRDC DomainStructure, 2005
- Amino Acids of the Sulfolobus solfataricus Mini-chromosome Maintenance-like DNA Helicase Involved in DNA Binding/RemodelingPublished by Elsevier ,2004
- The Werner Syndrome Helicase and Exonuclease Cooperate to Resolve Telomeric D Loops in a Manner Regulated by TRF1 and TRF2Molecular Cell, 2004
- Stimulation of Flap Endonuclease-1 by the Bloom's Syndrome ProteinJournal of Biological Chemistry, 2004
- Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.Carcinogenesis: Integrative Cancer Research, 2003
- Unwinding of a DNA Triple Helix by the Werner and Bloom Syndrome HelicasesJournal of Biological Chemistry, 2001
- Binding and Melting of D-Loops by the Bloom Syndrome HelicaseBiochemistry, 2000
- Oncogenic transformation by the FOX protein Qin requires DNA bindingOncogene, 2000
- Homozygous and compound heterozygous mutations at the Werner syndrome locusHuman Molecular Genetics, 1996
- NMRPipe: A multidimensional spectral processing system based on UNIX pipesJournal of Biomolecular NMR, 1995