Fanconi anemia is characterized by hypersensitivity to DNA interstrand crosslinks (ICLs) and susceptibility to tumor formation. Despite the identification of numerous Fanconi anemia (FANC) genes, the mechanism by which proteins encoded by these genes protect a cell from DNA interstrand crosslinks remains unclear. The recent discovery of two DNA helicases that, when defective, cause Fanconi anemia tips the balance in favor of the direct involvement of the FANC proteins in DNA repair and the bypass of DNA lesions
Fanconi anemia is a genetically heterogeneous disorder associated with chromosome instability and a ...
The commonly accepted definition of Fanconi anemia (FA) relying on DNA repair deficiency is submitte...
Interstrand crosslinks (ICLs) are a highly toxic form of DNA damage. ICLs can interfere with vital b...
Fanconi anemia is characterized by hypersensitivity to DNA interstrand crosslinks (ICLs) and suscept...
Mutations in any of at least sixteen FANC genes (FANCA-Q) cause Fanconi anemia, a disorder character...
Mutations in any of at least sixteen FANC genes (FANCA–Q) cause Fanconi anemia, a disorder character...
Fanconi anemia is a human cancer predisposition syndrome caused by mutations in 13 Fanc genes. The d...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital abnormalities, bone marrow...
Interstand crosslinks (ICLs) are DNA lesions where the bases of opposing DNA strands are covalently ...
FANCD2 is a central player in the DNA damage response, particularly in the repair of spontaneous and...
Homologous recombination (also termed homology-directed repair, HDR) is a major pathway for the repa...
Abstract Fanconi Anemia (FA) is a rare, inherited genomic instability disorder, caused by mutations ...
Due to the action of endogenous and exogenous agents, DNA is subject up to 70,000 lesions per day, t...
Fanconi anaemia (FA) is a hereditary, heterogeneous disease that is characterized by chromosomal ins...
Left unrepaired, DNA interstrand crosslinks represent impassable hurdles for DNA replication, and th...
Fanconi anemia is a genetically heterogeneous disorder associated with chromosome instability and a ...
The commonly accepted definition of Fanconi anemia (FA) relying on DNA repair deficiency is submitte...
Interstrand crosslinks (ICLs) are a highly toxic form of DNA damage. ICLs can interfere with vital b...
Fanconi anemia is characterized by hypersensitivity to DNA interstrand crosslinks (ICLs) and suscept...
Mutations in any of at least sixteen FANC genes (FANCA-Q) cause Fanconi anemia, a disorder character...
Mutations in any of at least sixteen FANC genes (FANCA–Q) cause Fanconi anemia, a disorder character...
Fanconi anemia is a human cancer predisposition syndrome caused by mutations in 13 Fanc genes. The d...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital abnormalities, bone marrow...
Interstand crosslinks (ICLs) are DNA lesions where the bases of opposing DNA strands are covalently ...
FANCD2 is a central player in the DNA damage response, particularly in the repair of spontaneous and...
Homologous recombination (also termed homology-directed repair, HDR) is a major pathway for the repa...
Abstract Fanconi Anemia (FA) is a rare, inherited genomic instability disorder, caused by mutations ...
Due to the action of endogenous and exogenous agents, DNA is subject up to 70,000 lesions per day, t...
Fanconi anaemia (FA) is a hereditary, heterogeneous disease that is characterized by chromosomal ins...
Left unrepaired, DNA interstrand crosslinks represent impassable hurdles for DNA replication, and th...
Fanconi anemia is a genetically heterogeneous disorder associated with chromosome instability and a ...
The commonly accepted definition of Fanconi anemia (FA) relying on DNA repair deficiency is submitte...
Interstrand crosslinks (ICLs) are a highly toxic form of DNA damage. ICLs can interfere with vital b...