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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… 
National Institutes of Health

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5 relations
DNA RepairDNA stabilityFANCG protein, humanFanconi Anemia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
MicroRNA regulation of DNA repair gene expression in 4-aminobiphenyl-treated HepG2 cells.
2006
2006
Continuous in vivo infusion of interferon-gamma (IFN-gamma) enhances engraftment of syngeneic wild-type cells in Fanca-/- and Fancg-/- mice.
Fanconi anemia (FA) is a heterogeneous genetic disorder characterized by bone marrow (BM) failure and cancer susceptibility… 
2006
2006
The Fanconi anemia gene network is conserved from zebrafish to human.
Highly Cited
2004
Highly Cited
2004
The Fanconi Anemia Core Complex Forms Four Complexes of Different Sizes in Different Subcellular Compartments*
Fanconi anemia (FA) is an autosomal recessive disease marked by congenital defects, bone marrow failure, and cancer… 
Highly Cited
2003
Highly Cited
2003
Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems.
Fanconi anemia (FA) is an autosomal recessive syndrome characterized by progressive bone marrow failure and cancer predisposition… 
Highly Cited
2003
Highly Cited
2003
Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport.
2002
2002
Characterization, expression and complex formation of the murine Fanconi anaemia gene product Fancg
Background: Fanconi anaemia (FA) is an autosomal recessive chromosomal instability disorder. Six distinct FA disease genes have… 
Highly Cited
2001
Highly Cited
2001
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway.
Fanconi anaemia (FA) is an autosomal recessive inherited disorder associated with a progressive aplastic anaemia, diverse… 
2000
2000
Carboxy terminal region of the Fanconi anemia protein, FANCG/XRCC9, is required for functional activity.
Fanconi anemia (FA) is an autosomal recessive cancer susceptibility syndrome with eight complementation groups. Four of the FA… 
Highly Cited
1999
Highly Cited
1999
Resistance to Mitomycin C Requires Direct Interaction between the Fanconi Anemia Proteins FANCA and FANCG in the Nucleus through an Arginine-rich Domain*
Fanconi anemia (FA) is a genetically heterogeneous disorder characterized by bone marrow failure, birth defects, and chromosomal… 
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