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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… 
National Institutes of Health

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28 relations
Abnormal renal morphologyAnemiaAnemic pallorAutosomal recessive inheritance

Papers overview

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Highly Cited
2011
Highly Cited
2011
Mutations in Fanconi anemia genes and the risk of esophageal cancer
The incidence of esophageal squamous cell carcinoma (ESCC) is very high in northeastern Iran. Previously, we reported a strong… 
Highly Cited
2007
Highly Cited
2007
Downregulation of Fanconi Anemia Genes in Sporadic Head and Neck Squamous Cell Carcinoma
Background/Aims: Much of our understanding of human cancer has come from studies of the hereditary cancer predisposition… 
Highly Cited
2006
Highly Cited
2006
C. elegans FANCD2 responds to replication stress and functions in interstrand cross-link repair.
2006
2006
The Fanconi anemia gene network is conserved from zebrafish to human.
2005
2005
RNAi of FACE1 protease results in growth inhibition of human cells expressing lamin A: implications for Hutchinson-Gilford progeria syndrome
FACE 1 is the endoprotease responsible for cleavage of prelamin A to lamin A. Transfection of HeLa cells with siRNA for human… 
Highly Cited
2003
Highly Cited
2003
Does overweight in infancy persist through the preschool years? An analysis of CDC Pediatric Nutrition Surveillance System data
SummaryObjective:To determine whether overweight in infancy (0-11 months) and young childhood (12-35 months) persists through the… 
Highly Cited
2003
Highly Cited
2003
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition.
Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, progressive bone marrow failure… 
Highly Cited
2002
Highly Cited
2002
Gene therapy of Fanconi anemia: preclinical efficacy using lentiviral vectors.
Fanconi anemia (FA) is an inherited cancer susceptibility syndrome caused by mutations in a DNA repair pathway including at least… 
Highly Cited
2002
Highly Cited
2002
The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC.
Fanconi anemia is an autosomal recessive disorder characterized by aplastic anemia, cancer susceptibility, and cellular… 
Review
2002
Review
2002
Molecular biology of Fanconi anaemia—an old problem, a new insight
Fanconi anaemia (FA) comprises a group of autosomal recessive disorders resulting from mutations in one of eight genes (FANCA… 
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