The Fanconi Anemia Signalosome Anchor

This publication has 10 references indexed in Scilit:

• First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental Failure
  The American Journal of Human Genetics, 2007
• Identification of FAAP24, a Fanconi Anemia Core Complex Protein that Interacts with FANCM
  Molecular Cell, 2007
• Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
  Nature Genetics, 2006
• A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis
  Nature, 2006
• The Fanconi anemia pathway limits the severity of mutagenesis
  DNA Repair, 2006
• The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway
  Nature Structural & Molecular Biology, 2005
• A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
  Nature Genetics, 2005
• RAD51C Is Required for Holliday Junction Processing in Mammalian Cells
  Science, 2004
• A novel ubiquitin ligase is deficient in Fanconi anemia
  Nature Genetics, 2003
• Interaction of the Fanconi Anemia Proteins and BRCA1 in a Common Pathway
  Molecular Cell, 2001