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FANCG gene

Known as: FANCG, FAG, X-ray repair complementing defective repair in Chinese hamster cells 9 
This gene is involved in the maintenance of genomic integrity and nuclear signal transduction. Allelic variants of the gene are involved in Fanconi… Expand
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
Lung cancer is a leading cause of cancer mortality with an inter-individual difference in susceptibility to the disease. The… Expand
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Highly Cited
2006
Highly Cited
2006
Objectives: We have undertaken a comprehensive study of common polymorphisms in genes of DNA repair, exploring both the risk of… 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 a recessive disorder characterized by congenital abnormalities, progressive bone-marrow failure, and… 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
2001
Highly Cited
2001
Fanconi anemia (FA) is a human autosomal recessive cancer susceptibility disorder characterized by cellular sensitivity to… Expand
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Highly Cited
2000
Highly Cited
2000
To the editor: C-kit mutations in core binding factor leukemias Positivity for CD117(c-kit) expression is present in 80% of… Expand
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Highly Cited
2000
Highly Cited
2000
Fanconi anemia (FA) is a chromosomal instability syndrome associated with a strong predisposition to cancer, particularly acute… Expand
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Highly Cited
1999
Highly Cited
1999
ABSTRACT Fanconi anemia (FA) is an autosomal recessive cancer susceptibility syndrome with at least eight complementation groups… Expand
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Highly Cited
1998
Highly Cited
1998
Fanconi anemia (FA) is an autosomal recessive disease with diverse clinical symptoms including developmental anomalies, bone… Expand
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