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FANCI GENE

Known as: Fanconi Anemia, Complementation Group I Gene, FLJ10719, FANCI 
This gene plays a role in the mediation of DNA repair.
National Institutes of Health

Papers overview

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Review
2014
Review
2014
Cyclin-dependent kinases (CDKs) participate in many cellular processes and play a crucial role in the regulation of cell cycle… 
2013
2013
Brachyspina syndrome (BS) is a rare monogenic autosomal recessive hereditary disorder identified in the Holstein breed caused by… 
2013
2013
In this issue of Blood , Kim and colleagues demonstrate that the Fanconi anemia protein FANCP/SLX4 is multifunctional by… 
2013
2013
Fanconi anemia (FA) is a heterogeneous recessive disorder associated with a markedly elevated risk to develop cancer. To date… 
2011
2011
Fanconi anemia (FA) is a rare familial genome instability syndrome caused by mutations in FA genes that results in defective DNA… 
2011
2011
Fanconi anemia (FA) is an inherited chromosomal instability disorder characterized by childhood aplastic anemia, developmental… 
Review
2011
Review
2011
DNA repair defect is one of the hallmarks of tumorigenesis, and is intimately linked to various human cancers, both inherited and… 
1993
1993
3. E. Branum, L. Cummius, M. Bartilson, et aL, Clin. Chem., 34, 110-113 (1988). 4. R. Clark, J. Gallin, and A. Fanci, Blood, 53…