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Fanconi Anemia Complementation Group D2 Protein

Known as: Fanconi Anemia Complementation Group D2 Protein [Chemical/Ingredient], FANCD2, Fanconi Anemia Group D2 Complementing Protein 
A Fanconi anemia complementation group protein that undergoes mono-ubiquitination by FANCL PROTEIN in response to DNA DAMAGE. Also, in response to… Expand
National Institutes of Health

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Highly Cited
2010
Highly Cited
2010
The Fanconi anemia (FA) pathway is responsible for interstrand crosslink repair. At the heart of this pathway is the FANCI-FAND2… Expand
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Highly Cited
2009
Highly Cited
2009
Fanconi Cross-Links Fanconi anemia is a rare genetic disease characterized by bone marrow failure, developmental abnormalities… Expand
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Highly Cited
2009
Highly Cited
2009
Fanconi anemia (FA) is a human genetic disease characterized by chromosome instability, cancer predisposition, and cellular… Expand
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Highly Cited
2007
Highly Cited
2007
Proteasome inhibitors sensitize tumor cells to DNA-damaging agents, including ionizing radiation (IR), and DNA cross-linking… Expand
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Highly Cited
2005
Highly Cited
2005
Fanconi anemia is a genetic disease characterized by genomic instability and cancer predisposition. Nine genes involved in… Expand
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Review
2003
Review
2003
Fanconi anaemia (FA) is a rare genetic cancer-susceptibility syndrome that is characterized by congenital abnormalities, bone… 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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Highly Cited
2002
Highly Cited
2002
Fanconi anemia (FA) and ataxia telangiectasia (AT) are clinically distinct autosomal recessive disorders characterized by… Expand
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Highly Cited
2002
Highly Cited
2002
Fanconi anemia (FA) is a human autosomal recessive cancer susceptibility disorder characterized by cellular sensitivity to… Expand
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Highly Cited
2001
Highly Cited
2001
Fanconi anemia (FA) is a genetic disease with birth defects, bone marrow failure, and cancer susceptibility. To date, genes for… Expand
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