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Fanconi Anemia Group B Protein

Known as: FAAP95, Protein FACB, FANCB 
Fanconi anemia group B protein (859 aa, ~98 kDa) is encoded by the human FANCB gene. This protein may play a role in both ubiquitination and DNA… 
National Institutes of Health

Papers overview

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2020
2020
Fanconi anemia (FA) is the most common genetic cause of bone marrow failure, and is caused by inherited pathogenic variants in… 
2018
2018
BACKGROUND/AIM Head and neck squamous cell carcinomas (HNSCCs) form a heterogeneous tumor entity located throughout the oral… 
2018
2018
VACTERL is a congenital malformation characterized by vertebral defects (V), anal atresia (A), cardiac malformation (C… 
2015
2015
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure, variable congenital malformations and a… 
2010
2010
Fanconi anemia (FA) and dyskeratosis congenita (DC) are rare inherited syndromes that cause head and neck squamous cell cancer… 
Highly Cited
2008
Highly Cited
2008
Recent reports have shown that mutations in the FANCJ/BRIP1 and FANCN/PALB2 Fanconi Anemia (FA) genes confer a moderate breast… 
Review
2005
Review
2005
Fanconi anemia (FA) proteins function in a DNA damage response pathway that appears to be part of the network including breast… 
Highly Cited
2004
Highly Cited
2004
Fanconi anemia is an autosomal recessive syndrome characterized by diverse clinical symptoms, hypersensitivity to DNA…