Skip to search formSkip to main contentSkip to account menu

FANCB gene

Known as: Fanconi Anemia, Complementation Group B Gene, FAAP95, Fanconi anemia complementation group B 
This gene may play a role in DNA repair.
National Institutes of Health

Related topics

Related topics

9 relations
BRCA2 ProteinCell Cycle ControlDNA RepairDNA stability

Narrower (1)

FANCB wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Mutational and Functional Analysis of FANCB as a Candidate Gene for Sporadic Head and Neck Squamous Cell Carcinomas.
BACKGROUND/AIM Head and neck squamous cell carcinomas (HNSCCs) form a heterogeneous tumor entity located throughout the oral… 
Review
2013
Review
2013
VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer.
2013
2013
Multifunctionality of the FA pathway.
In this issue of Blood , Kim and colleagues demonstrate that the Fanconi anemia protein FANCP/SLX4 is multifunctional by… 
2010
2010
Inactivation of the Tumor Suppressor Genes Causing the Hereditary Syndromes Predisposing to Head and Neck Cancer via Promoter Hypermethylation in Sporadic Head and Neck Cancers
Fanconi anemia (FA) and dyskeratosis congenita (DC) are rare inherited syndromes that cause head and neck squamous cell cancer… 
2009
2009
The gene of Bloom's syndrome: an autosomal recessive disorder with male dominance.
2008
2008
Fanconi anemia is a highly penetrant cancer susceptibility syndrome.
2006
2006
The Fanconi anemia gene network is conserved from zebrafish to human.
2006
2006
No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper‐methylation in sporadic childhood leukaemia
Fanconi anaemia (FA) and Nijmegen breakage syndrome (NBS) carry a high risk of haematological cancer. Affected cellular pathways… 
2004
2004
A new gene on the X involved in Fanconi anemia
A new study shows that Fanconi anemia complementation group B is caused by mutations in a previously uncharacterized gene located… 
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… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)