Skip to search formSkip to main contentSkip to account menu

fanconi anemia complementation group g

Known as: FANCG, FANCONI ANEMIA, COMPLEMENTATION GROUP G 
Fanconi anemia caused by mutations of the FANCG gene.
National Institutes of Health

Related topics

Related topics

5 relations
AnemiaBone MarrowFANCG geneFANCG protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
Current methods for detecting mutations in Fanconi anemia (FA)-suspected patients are inefficient and often miss mutations. We… 
Review
2012
Review
2012
Oxidative stress in Fanconi anaemia: from cells and molecules towards prospects in clinical management
Abstract Fanconi anaemia (FA) is a genetic disease featuring bone marrow failure, proneness to malignancies, and chromosomal… 
2008
2008
Fanconi DNA repair pathway is required for survival and long‐term maintenance of neural progenitors
Although brain development abnormalities and brain cancer predisposition have been reported in some Fanconi patients, the… 
2007
2007
Disruption of the FA/BRCA pathway in bladder cancer
Bladder carcinomas frequently show extensive deletions of chromosomes 9p and/or 9q, potentially including the loci of the Fanconi… 
Highly Cited
2006
Highly Cited
2006
Targeted disruption of FANCC and FANCG in human cancer provides a preclinical model for specific therapeutic options.
BACKGROUND & AIMS How specifically to treat pancreatic and other cancers harboring Fanconi anemia gene mutations has raised great… 
Highly Cited
2004
Highly Cited
2004
The Genetics of FANCC and FANCG in Familial Pancreatic Cancer
Patients with Fanconi anemia (FA) display a wide variety of defects including bone marrow failure and a high risk of developing… 
Highly Cited
2003
Highly Cited
2003
Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
Fanconi anaemia (FA) is an autosomal recessive genetic disorder characterized by progressive bone marrow failure, multiple… 
2003
2003
Spectrum of sequence variation in the FANCG gene: An International Fanconi Anemia Registry (IFAR) study
Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive syndrome associated with chromosomal instability… 
Highly Cited
2002
Highly Cited
2002
The FANCG Fanconi anemia protein interacts with CYP2E1: possible role in protection against oxidative DNA damage.
Fanconi anemia (FA) is a genetic disorder that leads to aplastic anemia and birth defects and predisposes to cancer. FA cells… 
Highly Cited
1999
Highly Cited
1999
A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA.
Fanconi anemia (FA) is a recessively inherited disease characterized at the cellular level by spontaneous chromosomal instability… 
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)