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FANCONI ANEMIA, COMPLEMENTATION GROUP E

Known as: FACE, FANCE 
Fanconi anemia caused by mutations of the FANCE gene. This is a protein coding gene. It is required for the nuclear accumulation of FANCC and… Expand
National Institutes of Health

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2014
2014
Background: Monoubiquitination of FANCD2 and FANCI is critical in the FA pathway. Results: Specific mutations in FANCE that… Expand
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Highly Cited
2009
Highly Cited
2009
Fanconi anemia is a cancer-prone inherited bone marrow failure and cancer susceptibility syndrome with at least 13… Expand
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Highly Cited
2007
Highly Cited
2007
ABSTRACT The eleven Fanconi anemia (FA) proteins cooperate in a novel pathway required for the repair of DNA cross-links. Eight… Expand
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2006
2006
Fanconi anemia (FA) is a complex disease involving nine identified and two unidentified loci that define a network essential for… Expand
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Highly Cited
2003
Highly Cited
2003
Ovarian tumor cells are often genomically unstable and hypersensitive to cisplatin. To understand the molecular basis for this… Expand
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Highly Cited
2003
Highly Cited
2003
SummaryObjective:To determine whether overweight in infancy (0-11 months) and young childhood (12-35 months) persists through the… Expand
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Highly Cited
2003
Highly Cited
2003
Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, progressive bone marrow failure… Expand
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Highly Cited
2002
Highly Cited
2002
The Fanconi anaemia (FA) nuclear complex (composed of the FA proteins A, C, G and F) is essential for protection against… Expand
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Highly Cited
2002
Highly Cited
2002
Fanconi anemia (FA) is an inherited cancer susceptibility syndrome caused by mutations in a DNA repair pathway including at least… Expand
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Highly Cited
2002
Highly Cited
2002
Fanconi anemia is an autosomal recessive disorder characterized by aplastic anemia, cancer susceptibility, and cellular… Expand
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