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FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)

Known as: FANCONI ANEMIA, COMPLEMENTATION GROUP A, FA, FANCA 
Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides… 
National Institutes of Health

Related topics

Related topics

30 relations
Abnormal renal morphologyAnemiaAnemic pallorAutosomal recessive inheritance

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-β1 Production
Transforming growth factor beta (TGF-β) secretion from cells in the bone marrow (BM) niche affects hematopoietic stem cell (HSC… 
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.
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… 
2002
2002
Phosphorylation of Fanconi anemia protein, FANCA, is regulated by Akt kinase.
Phosphorylation of the Fanconi anemia complementation group A (FANCA) protein is thought to be important for the function of the… 
2002
2002
The molecular biology of Fanconi anemia.
Fanconi anemia is a rare autosomal recessive disorder characterized clinically by congenital abnormalities, progressive bone… 
2001
2001
Fanconi anemia protein, FANCG, is a phosphoprotein and is upregulated with FANCA after TNF-alpha treatment.
Fanconi anemia (FA) is a genetic syndrome characterized by bone marrow failure, birth defects, and a predisposition to malignancy… 
2001
2001
Functional analysis of the putative peroxidase domain of FANCA, the Fanconi anemia complementation group A protein.
Fanconi anemia (FA) is an autosomal recessive disorder manifested by chromosomal breakage, birth defects, and susceptibility to… 
2001
2001
A cytoplasmic serine protein kinase binds and may regulate the Fanconi anemia protein FANCA.
Fanconi anemia (FA) is an autosomal recessive disease with congenital anomalies, bone marrow failure, and susceptibility to… 
2000
2000
Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system.
Three of at least 8 Fanconi anemia (FA) genes have been cloned (FANCA, FANCC, FANCG), but their functions remain unknown. Using… 
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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