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  1. Mechanism of Bloom syndrome complex assembly required for double Holliday junction dissolution and genome stability
  2. Preparation and purification of mono-ubiquitinated proteins using Avi-tagged ubiquitin
  3. Monoubiquitination by the Fanconi Anemia core complex locks FANCI:FANCD2 on DNA in filamentous arrays
  4. Author Correction: The FANCM-BLM-TOP3A-RMI complex suppresses alternative lengthening of telomeres (ALT)
  5. ALT control, delete: FANCM as an anti-cancer target in Alternative Lengthening of Telomeres
  6. ATP-dependent helicase activity is dispensable for the physiological functions of Recql4
  7. FANCM limits ALT activity by restricting telomeric replication stress induced by deregulated BLM and R-loops
  8. The FANCM-BLM-TOP3A-RMI complex suppresses alternative lengthening of telomeres (ALT)
  9. Phosphorylation of Drosophila Brahma on CDK-phosphorylation sites is important for cell cycle regulation and differentiation
  10. FANCM-family branchpoint translocases remove co-transcriptional R-loops
  11. ASCIZ/ATMIN is dispensable for ATM signaling in response to replication stress
  12. Granzyme A Deficiency Breaks Immune Tolerance and Promotes Autoimmune Diabetes Through a Type I Interferon–Dependent Pathway
  13. A defined role for multiple Fanconi anemia gene products in DNA-damage-associated ubiquitination
  14. Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway
  15. The FA Core Complex Contains a Homo-dimeric Catalytic Module for the Symmetric Mono-ubiquitination of FANCI-FANCD2
  16. The PTEN phosphatase functions cooperatively with the Fanconi anemia proteins in DNA crosslink repair
  17. The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription
  18. The Architecture and Evolution of Cancer Neochromosomes
  19. The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis
  20. The Fanconi Anemia DNA Repair Pathway: Structural and Functional Insights into a Complex Disorder
  21. Architecture and DNA Recognition Elements of the Fanconi Anemia FANCM-FAAP24 Complex
  22. Cyclin E2 induces genomic instability by mechanisms distinct from cyclin E1
  23. Fanconi proteins get histones moving
  24. The DNA translocase activity of FANCM protects stalled replication forks
  25. DNA interstrand crosslink repair and cancer
  26. Identification of KIAA1018/FAN1, a DNA Repair Nuclease Recruited to DNA Damage by Monoubiquitinated FANCD2
  27. FANCM Connects the Genome Instability Disorders Bloom's Syndrome and Fanconi Anemia
  28. FANCM and FAAP24 Function in ATR-Mediated Checkpoint Signaling Independently of the Fanconi Anemia Core Complex
  29. No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers
  30. Cyclin-Dependent Kinase 2 Functions in Normal DNA Repair and Is a Therapeutic Target in BRCA1-Deficient Cancers
  31. Brca1 inactivation induces p27Kip1-dependent cell cycle arrest and delayed development in the mouse mammary gland
  32. BRCA1-BARD1 Complexes Are Required for p53Ser-15 Phosphorylation and a G1/S Arrest following Ionizing Radiation-induced DNA Damage
  33. MMTV-trBrca1 mice display strain-dependent abnormalities in vaginal development
  34. MAD1 and p27KIP1 Cooperate To Promote Terminal Differentiation of Granulocytes and To Inhibit Myc Expression and Cyclin E-CDK2 Activity