Cell cycle–dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24
Open Access
- 15 May 2008
- journal article
- Published by American Society of Hematology in Blood
- Vol. 111 (10), 5215-5222
- https://doi.org/10.1182/blood-2007-09-113092
Abstract
Fanconi anemia (FA) is a genetic disease characterized by congenital abnormalities, bone marrow failure, and cancer susceptibility. A total of 13 FAKeywords
This publication has 41 references indexed in Scilit:
- Genetic Heterogeneity among Fanconi Anemia Heterozygotes and Risk of CancerCancer Research, 2007
- Identification of the FANCI Protein, a Monoubiquitinated FANCD2 Paralog Required for DNA RepairCell, 2007
- The Fanconi Anemia Signalosome AnchorMolecular Cell, 2007
- PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility geneNature Genetics, 2006
- Evidence for subcomplexes in the Fanconi anemia pathwayBlood, 2006
- Rad54: the Swiss Army knife of homologous recombination?Nucleic Acids Research, 2006
- CSA-dependent degradation of CSB by the ubiquitin–proteasome pathway establishes a link between complementation factors of the Cockayne syndromeGenes & Development, 2006
- A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group MNature Genetics, 2005
- The DNA helicase BRIP1 is defective in Fanconi anemia complementation group JNature Genetics, 2005
- A novel ubiquitin ligase is deficient in Fanconi anemiaNature Genetics, 2003