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Fanconi Anemia Complementation Group A Protein

A Fanconi anemia complementation group protein that is the most commonly mutated protein in FANCONI ANEMIA. It undergoes PHOSPHORYLATION by PROTEIN KINASE B and forms a complex with FANCC PROTEIN in the CELL NUCLEUS.
Also Known As:
FANCA Protein; Fanconi Anemia Group A Complementing Protein; Fanconi Anemia Group A Protein
Networked: 10 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Liu, Johnson M: 2 articles (03/2008 - 03/2002)
2. Chen, Fei: 2 articles (11/2007 - 10/2005)
3. Joenje, H: 2 articles (06/2000 - 04/2000)
4. Lee, Chang-Hun: 1 article (09/2013)
5. Hwang, Soo Kyung: 1 article (09/2013)
6. Son, Kook: 1 article (09/2013)
7. Kim, Sung Hak: 1 article (09/2013)
8. Yang, Jiha: 1 article (09/2013)
9. Lee, Mihee: 1 article (09/2013)
10. Kwak, Heejin: 1 article (09/2013)

Related Diseases

1. Fanconi Anemia (Fanconi's Anemia)
2. Genomic Instability
3. Ataxia Telangiectasia (Louis Bar Syndrome)

Related Drugs and Biologics

1. Mitomycin (Mitomycin-C)
2. Proteins (Proteins, Gene)
3. Nucleic Acids