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FANCL gene

Known as: Fanconi Anemia, Complementation Group L Gene, Pog, FAAP43 
This gene is involved in the mediation of protein ubiquitination.
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Summary Background The epilepsies are a clinically heterogeneous group of neurological disorders. Despite strong evidence for… Expand
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Highly Cited
2014
Highly Cited
2014
Summary Fanconi anaemia (FA) is a cancer predisposition syndrome characterized by cellular sensitivity to DNA interstrand… Expand
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Highly Cited
2012
Highly Cited
2012
FANCI and FANCD2 form a complex, and play essential roles in the repair of interstrand DNA crosslinks (ICLs) by the Fanconi… Expand
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Highly Cited
2010
Highly Cited
2010
The molecular genetic mechanisms of sex determination are not known for most vertebrates, including zebrafish. We identified a… Expand
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Highly Cited
2008
Highly Cited
2008
A key step in the Fanconi anemia (FA) tumor suppressor pathway is the site-specific monoubiquitination of the FANCD2 protein… Expand
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Highly Cited
2006
Highly Cited
2006
The Fanconi anemia pathway is required for the efficient repair of damaged DNA. A key step in this pathway is the… Expand
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Highly Cited
2005
Highly Cited
2005
Seven Fanconi anemia–associated proteins (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG and FANCL) form a nuclear Fanconi anemia core… Expand
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Highly Cited
2005
Highly Cited
2005
Fanconi anemia (FA) is an autosomal recessive disease marked by bone marrow failure, birth defects, and cancer. The FA proteins… Expand
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Highly Cited
2004
Highly Cited
2004
Monoubiquitination of FANCD2 is a key step in the DNA damage response pathway involving Fanconi anemia proteins and the breast… Expand
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Highly Cited
2003
Highly Cited
2003
Fanconi anemia is a recessively inherited disease characterized by congenital defects, bone marrow failure and cancer… Expand
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