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Fanconi Anemia Complementation Group D2 Protein

Known as: Fanconi Anemia Complementation Group D2 Protein [Chemical/Ingredient], FANCD2, Fanconi Anemia Group D2 Complementing Protein 
A Fanconi anemia complementation group protein that undergoes mono-ubiquitination by FANCL PROTEIN in response to DNA DAMAGE. Also, in response to… 
National Institutes of Health

Related topics

Related topics

15 relations
BARD1 PathwayCell Cycle ControlDNA RepairDNA Repair Gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Hypoxic Stress Facilitates Acute Activation and Chronic Downregulation of Fanconi Anemia Proteins
Hypoxia induces genomic instability through replication stress and dysregulation of vital DNA repair pathways. The Fanconi anemia… 
2014
2014
Fancd2 Is Required for Nuclear Retention of Foxo3a in Hematopoietic Stem Cell Maintenance*
Background: Maintenance of HSCs is challenged by DNA damage and oxidative stress. Results: Fancd2 deficiency promoted cytoplasmic… 
2013
2013
Assessment of FANCD2 nuclear foci formation in paraffin-embedded tumors: a potential patient-enrichment strategy for treatment with DNA interstrand crosslinking agents.
2011
2011
Direct Inhibition of TNF-α Promoter Activity by Fanconi Anemia Protein FANCD2
Fanconi anemia (FA), an inherited disease, is associated with progressive bone marrow failure, predisposition to cancer, and… 
2011
2011
Physical and functional crosstalk between Fanconi anemia core components and the GINS replication complex.
2008
2008
FANCD2 monoubiquitination provides a link between the HHR6 and FA-BRCA pathways
Fanconi Anemia (FA) is a rare genetic disease characterized by chromosome instability mostly resulting from an improper… 
2008
2008
Hepatitis B virus X protein disrupts DNA interstrand crosslinking agent mitomycin C induced ATR dependent intra-S-phase checkpoint.
2007
2007
A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia
Fanconi anemia (FA) is an autosomal recessive disease characterized by pancitopenia, congenital malformations, predisposition to… 
2006
2006
Drosophila homologs of FANCD2 and FANCL function in DNA repair.
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… 
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