FANCM and its relatives, Hef, Mph1 and Fml1, are DNA junction-specific helicases/translocases that target and process perturbed replication forks and intermediates of homologous recombination. They have variously been implicated in promoting the activation of the S-phase checkpoint, recruitment of the Fanconi Anemia Core Complex to sites of DNA damage, crossover avoidance during DNA double-strand break repair by homologous recombination, and the replicative bypass of DNA lesions by template switching. This review summarises our current understanding of the biochemical activities and biological functions of the FANCM family
FANCM is a highly conserved DNA remodeling enzyme that promotes the activation of the Fanconi anemia...
FANCD2 is a central player in the DNA damage response, particularly in the repair of spontaneous and...
The DNA damage response in eukaryotes involves multiple, complex, and often redundant pathways that ...
FANCM and its relatives, Hef, Mph1 and Fml1, are DNA junction-specific helicases/translocases that t...
In response to DNA damage, the Fanconi anemia (FA) core complex functions as a signaling machine for...
FANCM is the most highly conserved protein within the Fanconi anaemia (FA) tumour suppressor pathway...
Fanconi anemia (FA) is a genetically heterogeneous cancer-prone disorder associated with chromosomal...
The Fanconi anemia (FA) core complex promotes the tolerance/repair of DNA damage at stalled replicat...
SummaryFanconi anemia (FA) is a disorder associated with a failure in DNA repair. FANCM (defective i...
Fanconi anemia (FA) is a disorder associated with a failure in DNA repair. FANCM (defective in FA co...
Fanconi anemia (FA) is a disorder associated with a failure in DNA repair. FANCM (defective in FA co...
Homologous Recombination (HR) can promote genome stability through its capacity to faithfully repair...
Fanconi anemia (FA) is a genetically heterogeneous chromosome instability syndrome associated with c...
How the Fanconi anaemia (FA) chromosome stability pathway functions to cope with interstrand crossli...
FANCM remodels branched DNA structures and plays essential roles in the cellular response to DNA rep...
FANCM is a highly conserved DNA remodeling enzyme that promotes the activation of the Fanconi anemia...
FANCD2 is a central player in the DNA damage response, particularly in the repair of spontaneous and...
The DNA damage response in eukaryotes involves multiple, complex, and often redundant pathways that ...
FANCM and its relatives, Hef, Mph1 and Fml1, are DNA junction-specific helicases/translocases that t...
In response to DNA damage, the Fanconi anemia (FA) core complex functions as a signaling machine for...
FANCM is the most highly conserved protein within the Fanconi anaemia (FA) tumour suppressor pathway...
Fanconi anemia (FA) is a genetically heterogeneous cancer-prone disorder associated with chromosomal...
The Fanconi anemia (FA) core complex promotes the tolerance/repair of DNA damage at stalled replicat...
SummaryFanconi anemia (FA) is a disorder associated with a failure in DNA repair. FANCM (defective i...
Fanconi anemia (FA) is a disorder associated with a failure in DNA repair. FANCM (defective in FA co...
Fanconi anemia (FA) is a disorder associated with a failure in DNA repair. FANCM (defective in FA co...
Homologous Recombination (HR) can promote genome stability through its capacity to faithfully repair...
Fanconi anemia (FA) is a genetically heterogeneous chromosome instability syndrome associated with c...
How the Fanconi anaemia (FA) chromosome stability pathway functions to cope with interstrand crossli...
FANCM remodels branched DNA structures and plays essential roles in the cellular response to DNA rep...
FANCM is a highly conserved DNA remodeling enzyme that promotes the activation of the Fanconi anemia...
FANCD2 is a central player in the DNA damage response, particularly in the repair of spontaneous and...
The DNA damage response in eukaryotes involves multiple, complex, and often redundant pathways that ...