Evidence of mitochondrial dysfunction and impaired ROS detoxifying machinery in Fanconi Anemia cells
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Molecular Biology
Link
http://www.nature.com/articles/onc2012583.pdf
Reference53 articles.
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2. Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A . Mutations of the SLX4 gene in Fanconi Anemia. Nat Genet 2011; 43: 142–146.
3. Vaz F, Hanenberg H, Schuster B, Barker K, Wiek C, Erven V et al. Mutation of the RAD51C gene in a Fanconi Anemia-like disorder. Nat Genet 2010; 42: 406–409.
4. Vandenberg CJ, Gergely F, Ong CY, Pace P, Mallery DL, Hiom K et al. BRCA1-independent ubiquitination of FANCD2. Mol Cell 2003; 12: 247–254.
5. Meetei AR, de Winter JP, Medhurst AL, Wallisch M, Waisfisz Q, van de Vrugt HJ et al. A novel ubiquitin ligase is deficient in Fanconi anemia. Nat Genet 2003; 35: 165–170.
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