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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

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AnemiaBone MarrowFANCG geneFANCG protein, human

Papers overview

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2020
2020
Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation
Fanconi anemia (FA) is phenotypically diverse, hereditary condition associated with bone marrow failure, multiple physical… 
2017
2017
Novel Founder Mutation in FANCA Gene (c.3446_3449dupCCCT) Among Romani Patients from the Balkan Region
Background: Fanconi anemia is a rare autosomal recessive or X-linked disorder characterised by clinical and genetic heterogeneity… 
2017
2017
Loss of heterozygosity in FANCG, FANCF and BRIP1 from head and neck squamous cell carcinoma of the oral cavity.
Recent advances have been made in the understanding of Fanconi anemia (FA), a hereditary disease that increases the risk for head… 
2016
2016
Profiling Fanconi Anemia Gene Mutations among Iranian Patients.
BACKGROUND Fanconi anemia (FA) is a rare genetic syndrome characterized by developmental defects, bone marrow failure, and a high… 
2015
2015
Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.
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… 
Highly Cited
2008
Highly Cited
2008
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3
Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and… 
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… 
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… 
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… 
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