SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
- 16 January 2011
- journal article
- research article
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 43 (2), 138-141
- https://doi.org/10.1038/ng.751
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemiaNature Genetics, 2011
- Mislocalization of XPF-ERCC1 Nuclease Contributes to Reduced DNA Repair in XP-F PatientsPLoS Genetics, 2010
- Selective accumulation of virus-specific CD8+ T cells within the peripheral blood stem cell compartmentBlood, 2009
- The genetic and molecular basis of Fanconi anemiaMutation research. Reviews in mutation research, 2009
- Drosophila MUS312 and the Vertebrate Ortholog BTBD12 Interact with DNA Structure-Specific Endonucleases in DNA Repair and RecombinationMolecular Cell, 2009
- Mammalian BTBD12/SLX4 Assembles A Holliday Junction Resolvase and Is Required for DNA RepairCell, 2009
- Human SLX4 Is a Holliday Junction Resolvase Subunit that Binds Multiple DNA Repair/Recombination EndonucleasesCell, 2009
- Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group MBlood, 2009
- Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humansNature Genetics, 2008
- First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental FailureAmerican Journal of Human Genetics, 2007