Possible involvement of RecQL4 in the repair of double-strand DNA breaks in Xenopus egg extracts
- 30 April 2007
- journal article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Vol. 1773 (4) , 556-564
- https://doi.org/10.1016/j.bbamcr.2007.01.005
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Mochida Memorial Foundation for Medical and Pharmaceutical Research
This publication has 35 references indexed in Scilit:
- The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stabilityJournal of Cell Science, 2005
- Arabidopsis RecQl4A suppresses homologous recombination and modulates DNA damage responsesThe Plant Journal, 2005
- Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 geneJournal of Medical Genetics, 2005
- Initiation of DNA Replication Requires the RECQL4 Protein Mutated in Rothmund-Thomson SyndromeCell, 2005
- Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndromeHuman Molecular Genetics, 2005
- Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseasesHuman Molecular Genetics, 2003
- Rothmund-Thomson syndrome due toRECQ4 helicase mutations: Report and clinical and molecular comparisons with Bloom syndrome and Werner syndromeAmerican Journal of Medical Genetics, 2000
- Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndromeNature Genetics, 1999
- Cloning of Two New Human Helicase Genes of the RecQ Family: Biological Significance of Multiple Species in Higher EukaryotesGenomics, 1998
- Rothmund-Thomson SyndromeDermatologic Clinics, 1995